US20020159924A1 - Fluorine abatement using steam injection in oxidation treatment of semiconductor manufacturing effluent gases - Google Patents

Fluorine abatement using steam injection in oxidation treatment of semiconductor manufacturing effluent gases Download PDF

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Publication number
US20020159924A1
US20020159924A1 US10/150,468 US15046802A US2002159924A1 US 20020159924 A1 US20020159924 A1 US 20020159924A1 US 15046802 A US15046802 A US 15046802A US 2002159924 A1 US2002159924 A1 US 2002159924A1
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gas
effluent
semiconductor manufacturing
fluid stream
thermal oxidation
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US10/150,468
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Jose Arno
Robert Vermeulen
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Applied Materials Inc
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/68Halogens or halogen compounds
    • B01D53/70Organic halogen compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/68Halogens or halogen compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/20Halogens or halogen compounds
    • B01D2257/204Inorganic halogen compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/20Halogens or halogen compounds
    • B01D2257/206Organic halogen compounds
    • B01D2257/2066Fluorine
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2258/00Sources of waste gases
    • B01D2258/02Other waste gases
    • B01D2258/0216Other waste gases from CVD treatment or semi-conductor manufacturing
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23GCREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
    • F23G2209/00Specific waste
    • F23G2209/14Gaseous waste or fumes
    • F23G2209/142Halogen gases, e.g. silane
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02CCAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
    • Y02C20/00Capture or disposal of greenhouse gases
    • Y02C20/30Capture or disposal of greenhouse gases of perfluorocarbons [PFC], hydrofluorocarbons [HFC] or sulfur hexafluoride [SF6]

Definitions

  • the present invention generally relates to an effluent abatement system for the treatment of gas streams from processes such as manufacturing of semiconductor materials, devices and products.
  • the invention relates more specifically to abatement of halogens such as fluorine and fluorinated chemical species, by reaction thereof with water vapor during thermal oxidation treatment of a halogen-containing effluent gas.
  • Gaseous effluents from the manufacture of semiconductor materials, devices, products and memory articles may contain a wide variety of chemical species from the process facility. These chemical species include inorganic and organic compounds, breakdown products of photo-resist and other reagents, and a wide variety of other gases that must be removed from the waste gas streams before being vented from the process facility into the atmosphere.
  • the effluent gas in such instances may be subjected to any of a wide variety of treatments to abate the various undesirable components of the gas.
  • Such effluent gas treatment may for example include scrubbing of the effluent gas to remove acid gas components and/or particulates from the gas stream.
  • the gas may also be thermally oxidized to remove organic components and other oxidizable components, by mixing the effluent with an oxidant, such as high purity oxygen, air or nitrous oxide, and flowing the resulting gas mixture through a thermal oxidation reaction chamber.
  • an oxidant such as high purity oxygen, air or nitrous oxide
  • halogens e.g., fluorine (F 2 ) and fluorinated compounds are particularly problematic among the various components requiring abatement.
  • fluorine (F 2 ) and fluorinated compounds are particularly problematic among the various components requiring abatement.
  • the electronics industry uses perfluorinated compounds (PFCs) in wafer processing tools to remove residue from deposition steps and to etch thin films. PFCs are recognized to be strong contributors to global warming and the electronics industry is working to reduce the emissions of these gases.
  • the most commonly used PFCs include CF 4 , C 2 F 6 , SF 6 , C 3 F 8 , and NF 3 . These PFCs are dissociated in a plasma to generate highly reactive F 2 and fluorine radicals, which do the actual cleaning, and etching.
  • the products from these processing operations include mostly fluorine, silicon tetrafluoride (SiF 4 ), and to a lesser extent hydrogen fluoride (HF) and carbonyl fluoride (COF 2 ).
  • HF hydrogen fluoride
  • COF 2 carbonyl fluoride
  • a number of reagents have been used for reaction with PFCs to convert them to compounds that are less corrosive, can easily be scrubbed from the exhaust stream, or pose less of a danger to health and the environment.
  • hydrogen H 2
  • Hydrogen can be introduced as a reagent to convert the fluorine to HF, which can then be removed using a wet scrubber.
  • Hydrogen poses a potential problem due to its explosive nature, and hydrogen has been banned from some semiconductor processing operations because of this danger.
  • Methane is not as explosive as H 2 , but suffers from other problems.
  • the combustion of CH 4 at high temperatures in the presence of oxygen produces oxides of nitrogen (NO x ).
  • NO x oxides of nitrogen
  • the CH 4 can be converted to fluorine substituted methanes (of the formula CH x F y , wherein x and y may range from 0 to 4).
  • fluorine substituted methanes of the formula CH x F y , wherein x and y may range from 0 to 4).
  • Both anhydrous ammonia (NH 3 ) and aqueous ammonia (NH 4 OH) can also be used as reagents for F 2 abatement.
  • Ammonia increases the cost of ownership for the effluent treatment system in which it is used, and thus has a corresponding economic disadvantage. Further, the presence of ammonia can be a factor in the generation of oxygen difluoride if pH is not rigorously controlled in the effluent treatment system.
  • the present invention relates to the abatement of halogen in a halogen-containing effluent gas stream.
  • the invention relates to an apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools, comprising: an oxidizing unit having one or more inlet units at one end, downstream from at least one semiconductor manufacturing process tool, arranged to elevate the temperature of the effluent fluid stream, effect oxidation of at least a portion of the oxidizable components of the effluent fluid stream, and utilize water vapor to effect conversion of at least a portion of the halogen-containing components of the effluent fluid stream at the inlet end.
  • Such apparatus may in one embodiment further include a post-treatment unit, downstream from the oxidizing unit, arranged to remove acidic components from the effluent fluid stream.
  • thermal oxidation reactor for abatement of oxidizable halogen components in an effluent gas
  • thermal oxidation reactor comprising: a housing defining a flow passage therein for flow of effluent gas therethrough; an inlet coupled to the housing for introduction of effluent gas to the central flow passage, such inlet comprising (1) a shrouding gas flow passage arranged to flow shrouding gas into the central flow passage cocurrently with the effluent gas and surrounding the effluent gas, and (2) a reagent gas flow passage arranged to flow a reagent gas into the central flow passage cocurrently with the shrouding gas and surrounding the shrouding gas, wherein the reagent gas is reactive with halogen species in the effluent gas, with the central flow passage being of sufficient length downstream of the inlet to permit the reagent gas to mix and react with the halogen species of the effluent gas.
  • the invention relates to a method for treating the effluent fluid stream from one or more semiconductor manufacturing process tools using a system that includes an oxidizing unit having one or more inlet units at one end, comprising the steps of:
  • the above-described method may further comprise in a particular embodiment the additional step of removing acidic components from the effluent fluid stream.
  • Another aspect of the invention relates to a method of thermally oxidizing a halogen-containing effluent gas in a thermal oxidation reactor including a gas flow path bounded by a liner susceptible to corrosion in exposure to halogen species in the halogen-containing effluent gas, such method comprising introducing the halogen-containing effluent gas into the thermal oxidation reactor and flowing water vapor between the introduced halogen-containing effluent gas and the liner to thereby protect the liner by reaction of the water vapor with the halogen species in the halogen-containing effluent gas.
  • FIG. 1 is a schematic representation, in partial section, of an effluent abatement system receiving a halogen-containing effluent gas from a semiconductor manufacturing plant, according to one embodiment of the invention.
  • FIG. 2 is a schematic representation of gas flows in the inlet portion of a thermal oxidizer apparatus, according to one aspect of the invention.
  • FIG. 3 is a cross-sectional elevation view of an inlet of a thermal oxidizer unit, according to one embodiment of the invention.
  • FIG. 4 is a cross-sectional elevation view of an inlet of a thermal oxidizer unit, according to another embodiment of the invention.
  • the present invention utilizes the introduction of water vapor as a reagent in the thermal oxidation abatement treatment of halogen-containing gases, e.g., fluorine-containing gases.
  • halogen-containing gases e.g., fluorine-containing gases.
  • the use of water vapor for such oxidation treatment of the halogen-containing gas offers the advantage of providing a source of hydrogen to react with the halogen, in addition to having a lower impact on cost of ownership than other reagents that might be used.
  • Introduction of the water vapor at the beginning of the thermal section of the effluent abatement system allows a maximum reaction time (relative to any downstream addition of water vapor) and by early reaction with the halogen components of the effluent gas serves to protect the sections of the abatement system that are most vulnerable to corrosion.
  • the thermal oxidation unit employed in the practice of the invention may be utilized in conjunction with an upstream pretreatment unit (with the pre-treatment unit being downstream from one or more semiconductor process tools).
  • the pre-treatment unit may be arranged to remove water-soluble components and particulates from the effluent gas, prior to treatment of the effluent gas in the thermal oxidation unit, wherein the halogen-containing components of the effluent stream are converted to a form that is more treatment, e.g., by post-oxidation treatment scrubbing, optionally with quenching of the effluent gas discharged from the thermal oxidation unit.
  • the introduced water vapor effects the conversion of diatomic halogens (e.g., F 2 , I 2, Cl 2 , Br 2 ) to their more readily treatable mineral acid form.
  • the water vapor may be utilized to provide a hydrogen source to effect such conversion, heat to keep the surfaces in the oxidation unit above dewpoint and overcome the latent heat of vaporization of the water.
  • Oxidation may be added to the effluent in or upstream of the oxidation unit, or the effluent may already contain an oxidizer medium deriving from its upstream source (semiconductor tool(s)).
  • FIG. 1 is a schematic representation, in partial section, of an effluent abatement system 10 receiving a halogen-containing effluent gas from a semiconductor manufacturing plant 74 , according to one embodiment of the invention.
  • the semiconductor manufacturing plant 74 may comprise semiconductor manufacturing process tools of any suitable type.
  • the semiconductor manufacturing process tools may comprise high density plasma chemical vapor deposition tools that use a remote plasma source to effect disassociation of fluorine from fluorine containing gases used during the cleaning process.
  • the effluent abatement system 10 includes main process section A-D, comprising thermal reaction section A, primary cooling/scrubbing section B, lower secondary cooling/scrubbing section C and upper secondary cooling/demister section D.
  • the effluent abatement system 10 includes a thermal oxidation reactor 12 , to which is joined an inlet assembly 14 for delivery of process gases and ancillary fluids to the reactor.
  • the thermal oxidation reactor 12 includes an exterior wall 16 and an interior wall 20 enclosing an annular heating element 18 .
  • the interior wall 20 encloses a central flow passage 22 of the reactor.
  • the annular heating element may for example be electrically heated to provide a hot surface at the interior wall 20 , for elevated temperature treatment of the effluent being treated.
  • the inner wall 20 or “liner,” may be formed of any suitable material, such as Inconel® metal alloy.
  • the thermal oxidation reactor 12 may alternatively be of any suitable type.
  • Examples of alternative types include flame-based thermal oxidizers (e.g., using oxygen as an oxidizer and hydrogen or methane as the fuel), catalytic oxidizers, transpirative oxidizers, etc.
  • the thermal oxidizer may be heated in any suitable manner, such as by electrical resistance heating, infrared radiation, microwave radiation, convective heat transfer or solid conduction.
  • the thermal oxidization reactor 12 may as shown be equipped with a control thermocouple 24 .
  • the thermocouple is used to monitor the temperature of the heating element 18 .
  • the thermocouple may be arranged in suitable signal transmission relationship to a thermal energy controller (not shown).
  • Such thermal energy controller may in turn be arranged to responsively modulate the electrical heating energy to the annular heating element 18 , and thereby achieve a desired temperature of the hot wall surface of interior wall 20 . In such manner, the wall surface can be maintained at a desired temperature level appropriate for the thermal oxidation treatment of the effluent flowed through the thermal oxidizer unit (in the direction indicated by arrow F in FIG 1 .)
  • the thermal oxidation reactor 12 in the embodiment shown is adapted to receive clean dry air (CDA) from CDA supply line 26 .
  • the CDA supply line 26 may be joined in supply relationship to a suitable source of clean dry air (e.g., CDA source 72 ).
  • CDA source 72 e.g., CDA source 72 .
  • the thus-introduced air flows into the annular space between outer wall 16 and inner wall 20 of the thermal oxidizer unit, and is heated to suitable temperature in contact with the annular heating element 18 .
  • Resultant heated air then may flow through orifices or pores in the inner wall 20 into the central flow passage 22 of the reactor.
  • the oxidant may be added to mix with the effluent gas an form an oxidizable effluent gas mixture for thermal oxidation in the reactor.
  • the oxidant may be added at the inlet, as another introduced fluid stream, to support the oxidation reactions in the thermal oxidation reactor.
  • the thermal oxidizer unit 12 is joined to a quench inlet section 28 of quench unit 32 .
  • an array of water spray nozzles 30 is provided, supplied with water by an associated water feed conduit, as shown.
  • the water spray nozzles serve to provide initial quench cooling to the hot effluent gas stream as the stream is discharged from the thermal oxidizer unit into the quench unit.
  • the quench unit is arranged with the quench inlet section 28 joined to a transverse section 34 of the quench unit.
  • the transverse section 34 in turn is joined to the sump section 36 of the quench unit.
  • the sump section 36 at its lower end is coupled to a slope drain/vapor barrier 38 .
  • a conductivity liquid level sensor/chamber purge assembly is joined to the sump section 36 , and is coupled to CDA branch line 42 which provides clean dry air to the assembly.
  • the sump section 36 of the quench unit 32 is joined to the lower end of the scrubber demister column 44 .
  • the scrubber demister column is filled, in the lower secondary cooling/scrubbing section thereof, with a secondary scrubbing packing 46 , and the upper portion of such section of the column is equipped with a water spray nozzle 48 for effecting scrubbing of the upflowing effluent gas therein, by countercurrently flowing water downwardly over the packing 46 .
  • the water spray nozzle 48 is supplied with water by water feed line 50 .
  • the upper portion of the lower section of the scrubber demister column is equipped with a vapor relief port 52 to which is coupled a vapor relief line 54 , for venting overpressure in the column.
  • An exhaust temperature sensor 56 is mounted on the upper portion of the lower section of the scrubber demister column, to provide temperature monitoring capability for the column.
  • the upper section of the scrubber demister column is likewise filled with a secondary scrubbing packing 58 and is equipped with a water spray nozzle 60 coupled to water feed line 50 .
  • the water feed line 50 has an air operated valve 101 therein. The valve is normally in a closed condition, and may be actuated as necessary to provide additional scrubbing capability for treatment of a specific effluent gas stream.
  • the upper section of the scrubber demister column is coupled to an exhaust temperature sensor 62 , for monitoring the temperature of the effluent gas stream.
  • a magnehelic pressure display 64 is also joined to the upper section of the scrubber demister column.
  • a clean dry air line 70 is joined to clean dry air source 72 .
  • the CDA line 70 supplies CDA to the column, e.g., for dilution of the effluent stream being discharged from the upper end of the column in the direction indicated by the arrow R.
  • the CDA line 70 has a restricted flow orifice 68 therein and a flow control valve upstream of the orifice, for selectively restricting flow of CDA to the upper end of the column.
  • the inlet assembly 14 for delivery of process gases and ancillary fluids to the thermal oxidation reactor 12 is arranged as shown, with process gas inlet conduits 88 and 90 receiving process exhaust gas in lines 84 and 86 from the gas flow router/manifold 82 , which in turn receives gas streams 76 , 78 and 80 from the semiconductor manufacturing plant 74 .
  • the semiconductor manufacturing plant 74 may be arranged to carry out any suitable operations for the production of semiconductor materials, devices and products.
  • Examples of specific operations of such semiconductor manufacturing plant 74 may include one or more process steps, such as for example:
  • Specific manufacturing operations may for example comprise photolithography steps in the manufacture of VLSI and ULSI circuits, epitaxial deposition of film materials such as silicon from dispensed Si source gases, ion implantation and doping in the fabrication of CMOS, NMOS, BiCMOS and other structures, and manufacture of devices such as DRAMs, SRAMs, FeRAMs, etc.
  • the semiconductor manufacturing plant 74 may be employed to fabricate electronic device structures such as for example:
  • the semiconductor manufacturing plant 74 may be constructed and arranged to produce electronic device structures.
  • the products may for example comprise memory chip devices, such as:
  • the process gas inlet conduits 88 and 90 flow the influent process exhaust gas into the thermal oxidation reactor 12 .
  • These process gas inlet conduits are constructed with ancillary fluid addition lines 92 and 94 , for addition of ancillary process fluids to the main effluent stream being flowed through the process gas inlet conduits 88 and 90 .
  • the inlet assembly 14 also includes a shroud gas feed line 96 and a hydrogen source feed line 98 .
  • the hydrogen source feed line 98 is joined to a hydrogen source gas supply 100 .
  • the shroud gas may be a purge gas for the thermal oxidation reactor, or the inlet or associated piping and channels of the effluent abatement system.
  • Illustrative shroud or purge gas species include nitrogen, helium, argon, etc.
  • water vapor (steam) is introduced as a hydrogen source gas to the thermal oxidation reactor 12 .
  • the water vapor is utilized at elevated temperature appropriate to the thermal oxidation process being carried out in the thermal oxidation reactor and the halogen components being abated in the effluent gas.
  • the hydrogen source gas supply 100 therefore may comprise a vaporization unit that is supplied with water from a suitable feed source, such as a water line in the semiconductor manufacturing facility, a municipal or industrial water supply, or the like.
  • the hydrogen source gas supply 100 may alternatively comprise a steam line in the semiconductor manufacturing facility or other source of water vapor.
  • the hydrogen source gas supply 100 may comprise a chemical reaction vessel for reacting reagent materials to form water vapor.
  • a hydrocarbon reagent such as methane, propane, natural gas, etc.
  • an oxygen-containing gas such as air, oxygen, oxygen-enriched air, ozone, or the like
  • Water vapor is employed in accordance with the present invention to provide a source of hydrogen in the thermal oxidation reactor, for reaction with the halogen constituents of the effluent gas.
  • halogen e.g., bromine, iodine and chlorine
  • the invention is not thus limited, and extends in utility to the abatement of other halogens, e.g., bromine, iodine and chlorine, and to corresponding other halogen-containing compounds, complexes and radicals.
  • the invention therefore provides water vapor as a source of hydrogen gas for reaction with the halogen species, e.g., converting fluorine species to forms that are amenable to removal by wet scrubbing.
  • fluorine gas is readily converted by reaction with steam, to yield hydrogen fluoride, which is easily removed from the effluent gas in the scrubbing step.
  • the scrubbing step also removes various other acid gas components of the effluent, to produce a halogen-reduced/acid gas-reduced effluent.
  • the present invention overcomes these deficiencies.
  • water vapor is injected between the stream of process gas and the liner of the thermal oxidation reactor, thereby protecting the liner from attack.
  • FIG. 2 there is shown a schematic representation of gas flows in the inlet portion of a thermal oxidizer apparatus (such as that shown in FIG. 1), according to one aspect of the invention.
  • FIG. 2 shows the liner 20 of the thermal oxidation reactor as bounding the central flow passage of the thermal oxidation reactor.
  • a fluorine-containing effluent gas stream, indicated by the arrow G, is flowed from the inlet into and through the central flow passage of the thermal oxidation reactor.
  • a shrouding gas Concurrent with the flow of the effluent gas stream through the inlet into the central passage of the thermal oxidation reactor, a shrouding gas, indicated by arrows H, is introduced, to surround the effluent gas stream in downflow through the central flow passage of the thermal oxidation reactor.
  • the shrouding gas may for example be nitrogen, or other inert gas.
  • the inlet introduces water vapor, indicated by arrows I, for flow downwardly in the thermal oxidation reactor.
  • the shrouding gas separates the effluent gas stream from the water vapor and prevents premature reactions that could otherwise generate solids and clog the gas feed tubes of the inlet.
  • the water vapor may optionally be introduced with air or nitrogen mixture.
  • the hydrogen deriving from the steam will react with the fluorine or other halogen components of the effluent gas.
  • the hot reaction products will be quenched in the primary section B (see FIG. 1) and will travel to the secondary sections C and D (see also FIG. 1) where they will be scrubbed.
  • the arrows I instead of representing water vapor, may represent an alternative hydrogen source material, such as methane.
  • oxygen, air or other oxygen-containing gas indicated by arrow J, may be introduced to the thermal oxidation reactor for reaction with the methane or other hydrogen source material, to produce water vapor as a reaction product, for reaction with fluorine and fluorinated species.
  • the nitrogen or other inert gas indicated by arrow H will serve the same function in this variant arrangement, of separating the effluent from the water vapor (and methane combustion products).
  • FIG. 3 is a cross-sectional elevation view of an inlet of a thermal oxidizer unit of the type shown in FIG. 1, according to one embodiment of the invention.
  • the same reference numerals are used in FIG. 3 as employed for the corresponding elements in FIG. 1.
  • the inlet structure 14 includes a process gas inlet conduit 90 for introducing effluent gas from a process facility, such as a semiconductor manufacturing tool, to a thermal oxidation reactor 12 .
  • the process gas inlet conduit 90 features an inlet pressure monitoring port 112 for coupling with a suitable pressure monitoring device to sense the pressure of the process gas.
  • the process gas inlet conduit 90 is provided with fluid addition lines 92 and 94 , for addition of oxygen, air, nitrogen, and/or any other gas species, to assist the thermal oxidation reaction in the reactor 12 .
  • the fluid addition lines may be employed to add a co-reactant species for specific components of the effluent gas being treated.
  • the process gas inlet conduit 90 terminates in a lower tubular wall 122 enclosing a cylindrical flow passage 120 , within an outer tubular wall 124 .
  • the outer tubular wall 124 is in spaced relationship to tubular wall 122 , defining an annular space 126 therebetween.
  • a shroud gas feed line 96 Communicating with annular space 126 is a shroud gas feed line 96 , to which shroud gas such as nitrogen is introduced, for downward flow around the discharged effluent gas in the central flow passage defined by outer tubular wall 124 .
  • the outer tubular wall 124 thus defines an effluent flow passage and is open-ended at its lower end.
  • Water vapor is introduced in hydrogen source gas feed line 98 and flows downwardly, exiting the inlet structure at its lower end as indicated by arrows K. Subsequently, in flow below the inlet 12 , in the thermal oxidation reactor, the water vapor mixes with the effluent gas and fluorine and fluorinated species in the effluent gas are reacted with hydrogen deriving from the injected water vapor. Hydrogen fluoride and other reaction products thereby are formed, which are readily removable in the subsequent scrubbing operation of the effluent treatment system.
  • methane or other hydrogen source gas may be introduced in line 98 to the inlet.
  • methane is introduced in line 98
  • oxygen, air, or other oxygen-containing gas may be concurrently introduced in the same line, or in a different line of the inlet, e.g., in line 92 or line 94 .
  • a steam generator may additionally be coupled with hydrogen source gas feed line 98 , to provide hydrogen for reaction with the halogen in the effluent gas.
  • FIG. 4 is a cross-sectional elevation view of an inlet 140 of a thermal oxidizer unit, according to another embodiment of the invention.
  • the inlet comprises an inlet body 141 constructed with a first tubular feed conduit 142 and a second tubular feed conduit 144 , defining enclosed interior passages 146 and 148 , respectively.
  • Effluent gas indicated by arrows L, is introduced to the first tubular feed conduit 142 and second tubular feed conduit 144 , for flow through the inlet into the thermal oxidation reactor.
  • the inlet body 141 also comprises nitrogen feed passages 150 and 152 , through which nitrogen gas, indicated by arrows M, is flowed. These nitrogen feed passages communicate with central nitrogen feed passage 154 . As shown, at the bottom of the inlet body, the nitrogen gas (arrows M) flows downwardly as a shrouding gas for the effluent gas stream (arrows L).
  • a hydrogen source gas is introduced to the inlet body by hydrogen source gas passages 156 and 158 , for entry into the annular hydrogen source gas reservoir 160 .
  • the hydrogen source gas is flowed from the reservoir through the hydrogen source gas outlet slots 162 and 164 , and flows downwardly (arrows N) around the effluent gas stream (arrows L), so that the effluent gas stream is shrouded by the shrouding gas stream (arrows M), to thereby prevent premature reaction between the effluent gas and the hydrogen source gas.
  • the relative flow rates of the hydrogen source gas and the effluent gas stream may be suitably selected so as to minimize the incidence of corrosion of the liner in the thermal oxidation reactor and to effect the desired reaction and removal of the halogen content of the effluent gas stream being treated.
  • the relative rates of flow of all gas streams in a given treatment application may be readily determined without undue experimentation, by the simple expedient of independently varying the flow rate of each stream in sequence and determining the corresponding destruction removal efficiency (DRE) of the halogen component(s) of interest in the treated effluent gas.
  • DRE destruction removal efficiency
  • Suitable temperature and pressure levels for the effluent abatement process of the invention can be similarly determined, to achieve a desired level of abatement of the halogen component in the effluent gas.
  • Preferred temperatures for the use of water vapor or CH 4 as a hydrogen source reagent are between 650° C. and 950° C., with the lower temperatures decreasing the corrosion rate and F 2 attack on the liner.
  • the invention will therefore be appreciated as providing a simple and effective technique for the abatement of fluorine and fluorinated species, as well as of other halogen species, from effluent gases generated in industrial processes, such as manufacturing of semiconductor materials, devices and products.
  • F 2 abatement from an effluent derived from a semiconductor manufacturing plant was evaluated in a Delatech CDOTM thermal oxidation unit (Ecosys Corporation, San Jose, Calif.), using NH 4 OH as the abatement reagent.
  • F 2 abatement from a corresponding effluent was evaluated using water flushed through the NH 4 OH injection lines of the thermal oxidation reactor.
  • the Destruction Removal Efficiency (DRE) for F 2 when water was flushed through the NH 4 OH injection lines was between DRE value for NH 4 OH reagent and the DRE value when no reagent was used.
  • a fluorine abatement effluent treatment system of the type shown in FIG. 1 and equipped with an inlet of the type shown in FIG. 3 is operated, to effect treatment of an effluent gas stream from a semiconductor manufacturing facility.
  • Water vapor is used as the fluorine abatement agent.
  • the process gas flows down the center tube, with N 2 flowing into the surrounding tube and out the annulus formed by the two concentric tubes. This N 2 flowing out the annulus separates the process gases from the water vapor and prevents premature reactions that could generate solids and clog the inlet tubes.
  • the water is vaporized into steam using the same heater used for the NH 4 OH testing in Example 2.
  • the steam and air or N 2 mixture is introduced into the hydrogen source gas feed tube to flow around the tube carrying the effluent gas and mix with the process gases in the thermal section of the CDOTM thermal oxidation reactor.
  • the hot reaction products are quenched in the primary section and travel through the secondary section where they are scrubbed.

Abstract

An apparatus and process for abatement of halogen in a halogen-containing effluent gas, such as is produced by a semiconductor manufacturing plant utilizing perfluorocompounds in the operation of the plant. Halogen-containing effluent gas is contacted with water vapor in a thermal oxidation reactor to convert halogen species to reaction products that are readily removed from the effluent gas by subsequent scrubbing. A shrouding gas may be employed to separate the halogen-containing effluent gas from the water vapor at the inlet of the thermal oxidation reactor, to thereby prevent premature reaction that would otherwise produce particulates and reaction products that could clog the inlet of the reactor.

Description

  • This is a divisional of U.S. application Ser. No. 09/420,080, filed on Oct. 18, 1999.[0001]
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention [0002]
  • The present invention generally relates to an effluent abatement system for the treatment of gas streams from processes such as manufacturing of semiconductor materials, devices and products. The invention relates more specifically to abatement of halogens such as fluorine and fluorinated chemical species, by reaction thereof with water vapor during thermal oxidation treatment of a halogen-containing effluent gas. [0003]
  • 2. Description of the Related Art [0004]
  • Gaseous effluents from the manufacture of semiconductor materials, devices, products and memory articles may contain a wide variety of chemical species from the process facility. These chemical species include inorganic and organic compounds, breakdown products of photo-resist and other reagents, and a wide variety of other gases that must be removed from the waste gas streams before being vented from the process facility into the atmosphere. [0005]
  • The effluent gas in such instances may be subjected to any of a wide variety of treatments to abate the various undesirable components of the gas. Such effluent gas treatment may for example include scrubbing of the effluent gas to remove acid gas components and/or particulates from the gas stream. The gas may also be thermally oxidized to remove organic components and other oxidizable components, by mixing the effluent with an oxidant, such as high purity oxygen, air or nitrous oxide, and flowing the resulting gas mixture through a thermal oxidation reaction chamber. [0006]
  • In such effluent treatment systems, halogens, e.g., fluorine (F[0007] 2) and fluorinated compounds are particularly problematic among the various components requiring abatement. The electronics industry uses perfluorinated compounds (PFCs) in wafer processing tools to remove residue from deposition steps and to etch thin films. PFCs are recognized to be strong contributors to global warming and the electronics industry is working to reduce the emissions of these gases.
  • The most commonly used PFCs include CF[0008] 4, C2F6, SF6, C3F8, and NF3. These PFCs are dissociated in a plasma to generate highly reactive F2 and fluorine radicals, which do the actual cleaning, and etching. The products from these processing operations include mostly fluorine, silicon tetrafluoride (SiF4), and to a lesser extent hydrogen fluoride (HF) and carbonyl fluoride (COF2). The toxic nature of these gases poses considerable health and environmental hazards, in addition to being highly corrosive to exhaust systems.
  • Optimization of the operating conditions in the semiconductor manufacturing process tool to increase the conversion efficiencies (of PFCs to end products) has been the primary focus in reducing PFC emissions. An example of this approach is the Applied Materials HDP-CVD process. The improvements that have been made in PFC conversions by process optimization has enabled the use of shorter clean cycles to be achieved, and consequently higher wafer throughputs to be obtained. [0009]
  • The current trend in the semiconductor manufacturing industry to 300 mm wafer manufacturing will increase the amounts of PFCs used in semiconductor manufacturing facilities. The increase in usage of PFCs and their conversion to highly reactive products have led to an increase in the corrosion rate of the abatement equipment and associated exhaust ductwork. In particular the corrosion attributable to fluorine has necessitated more frequent replacement of equipment components upstream of the typically employed wet scrubber unit in the effluent treatment system. [0010]
  • A number of reagents have been used for reaction with PFCs to convert them to compounds that are less corrosive, can easily be scrubbed from the exhaust stream, or pose less of a danger to health and the environment. For example, hydrogen (H[0011] 2) can be introduced as a reagent to convert the fluorine to HF, which can then be removed using a wet scrubber. Hydrogen, however, poses a potential problem due to its explosive nature, and hydrogen has been banned from some semiconductor processing operations because of this danger.
  • As a result of the explosive hazard associated with H[0012] 2, other reagents can be dissociated to provide hydrogen to abate the F2. Methane (CH4) can be employed to abate fluorine and fluorinated species by combustion thereof using added air or oxygen (O2). The water vapor and reactive hydrogen produced from this combustion react with the F2 and fluorinated species to convert them to HF and SiO2, which can then be readily removed from the exhaust stream.
  • Methane is not as explosive as H[0013] 2, but suffers from other problems. The combustion of CH4 at high temperatures in the presence of oxygen produces oxides of nitrogen (NOx). Under combustion conditions where insufficient oxygen is present, the CH4 can be converted to fluorine substituted methanes (of the formula CHxFy, wherein x and y may range from 0 to 4). These fluoromethanes are of concern because of their strong global warming potential.
  • Both anhydrous ammonia (NH[0014] 3) and aqueous ammonia (NH4OH) can also be used as reagents for F2 abatement. Ammonia increases the cost of ownership for the effluent treatment system in which it is used, and thus has a corresponding economic disadvantage. Further, the presence of ammonia can be a factor in the generation of oxygen difluoride if pH is not rigorously controlled in the effluent treatment system.
  • It would therefore be an advance in the art to provide a method of abatement of fluorine and other halogen species, which overcomes the various above-described deficiencies of the prior art. [0015]
  • SUMMARY OF THE INVENTION
  • The present invention relates to the abatement of halogen in a halogen-containing effluent gas stream. [0016]
  • In one aspect, the invention relates to an apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools, comprising: an oxidizing unit having one or more inlet units at one end, downstream from at least one semiconductor manufacturing process tool, arranged to elevate the temperature of the effluent fluid stream, effect oxidation of at least a portion of the oxidizable components of the effluent fluid stream, and utilize water vapor to effect conversion of at least a portion of the halogen-containing components of the effluent fluid stream at the inlet end. [0017]
  • Such apparatus may in one embodiment further include a post-treatment unit, downstream from the oxidizing unit, arranged to remove acidic components from the effluent fluid stream. [0018]
  • Another aspect of the invention relates to a thermal oxidation reactor for abatement of oxidizable halogen components in an effluent gas, such thermal oxidation reactor comprising: a housing defining a flow passage therein for flow of effluent gas therethrough; an inlet coupled to the housing for introduction of effluent gas to the central flow passage, such inlet comprising (1) a shrouding gas flow passage arranged to flow shrouding gas into the central flow passage cocurrently with the effluent gas and surrounding the effluent gas, and (2) a reagent gas flow passage arranged to flow a reagent gas into the central flow passage cocurrently with the shrouding gas and surrounding the shrouding gas, wherein the reagent gas is reactive with halogen species in the effluent gas, with the central flow passage being of sufficient length downstream of the inlet to permit the reagent gas to mix and react with the halogen species of the effluent gas. [0019]
  • In one method aspect, the invention relates to a method for treating the effluent fluid stream from one or more semiconductor manufacturing process tools using a system that includes an oxidizing unit having one or more inlet units at one end, comprising the steps of: [0020]
  • providing water vapor to the inlet end of the oxidizing unit; [0021]
  • effecting, at the inlet end of the oxidizing unit, the conversion of at least a portion of the halogen-containing components of the effluent fluid stream to a form that is more treatable using such water vapor; and [0022]
  • effecting, in the oxidizing unit, the oxidation of at least a portion of the oxidizable components of the effluent fluid stream. [0023]
  • The above-described method may further comprise in a particular embodiment the additional step of removing acidic components from the effluent fluid stream. [0024]
  • Another aspect of the invention relates to a method of thermally oxidizing a halogen-containing effluent gas in a thermal oxidation reactor including a gas flow path bounded by a liner susceptible to corrosion in exposure to halogen species in the halogen-containing effluent gas, such method comprising introducing the halogen-containing effluent gas into the thermal oxidation reactor and flowing water vapor between the introduced halogen-containing effluent gas and the liner to thereby protect the liner by reaction of the water vapor with the halogen species in the halogen-containing effluent gas. [0025]
  • Other aspects, features and embodiments will be fully apparent from the ensuing disclosure.[0026]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a schematic representation, in partial section, of an effluent abatement system receiving a halogen-containing effluent gas from a semiconductor manufacturing plant, according to one embodiment of the invention. [0027]
  • FIG. 2 is a schematic representation of gas flows in the inlet portion of a thermal oxidizer apparatus, according to one aspect of the invention. [0028]
  • FIG. 3 is a cross-sectional elevation view of an inlet of a thermal oxidizer unit, according to one embodiment of the invention. [0029]
  • FIG. 4 is a cross-sectional elevation view of an inlet of a thermal oxidizer unit, according to another embodiment of the invention. [0030]
  • DETAILED DESCRIPTION OF THE INVENTION, AND PREFERRED EMBODIMENTS THEREOF
  • The disclosures of U.S. patent application Ser. No. 08775,838 filed Dec. 31, 1996 in the names of Mark Holst, et al. for “Effluent Gas Stream Treatment System Having Utility for Oxidation Treatment of Semiconductor Manufacturing Effluent Gases,” issued Sep. 21, 1999 as U.S. Pat. No. 5,955,037 and the disclosure of U.S. patent application Ser No. 09/228,706 filed Jan. 12, 1999 in the names of Robert R. Moore, et al. for “Apparatus and Method for Controlled Decomposition of Gaseous Pollutants” are hereby incorporated herein by reference in their respective entireties. [0031]
  • The present invention utilizes the introduction of water vapor as a reagent in the thermal oxidation abatement treatment of halogen-containing gases, e.g., fluorine-containing gases. The use of water vapor for such oxidation treatment of the halogen-containing gas offers the advantage of providing a source of hydrogen to react with the halogen, in addition to having a lower impact on cost of ownership than other reagents that might be used. Introduction of the water vapor at the beginning of the thermal section of the effluent abatement system allows a maximum reaction time (relative to any downstream addition of water vapor) and by early reaction with the halogen components of the effluent gas serves to protect the sections of the abatement system that are most vulnerable to corrosion. [0032]
  • The thermal oxidation unit employed in the practice of the invention may be utilized in conjunction with an upstream pretreatment unit (with the pre-treatment unit being downstream from one or more semiconductor process tools). The pre-treatment unit may be arranged to remove water-soluble components and particulates from the effluent gas, prior to treatment of the effluent gas in the thermal oxidation unit, wherein the halogen-containing components of the effluent stream are converted to a form that is more treatment, e.g., by post-oxidation treatment scrubbing, optionally with quenching of the effluent gas discharged from the thermal oxidation unit. [0033]
  • In the thermal oxidation unit, the introduced water vapor effects the conversion of diatomic halogens (e.g., F[0034] 2, I2, Cl2, Br2) to their more readily treatable mineral acid form. The water vapor may be utilized to provide a hydrogen source to effect such conversion, heat to keep the surfaces in the oxidation unit above dewpoint and overcome the latent heat of vaporization of the water. Oxidation may be added to the effluent in or upstream of the oxidation unit, or the effluent may already contain an oxidizer medium deriving from its upstream source (semiconductor tool(s)).
  • Referring now to the drawings, FIG. 1 is a schematic representation, in partial section, of an [0035] effluent abatement system 10 receiving a halogen-containing effluent gas from a semiconductor manufacturing plant 74, according to one embodiment of the invention.
  • The [0036] semiconductor manufacturing plant 74 may comprise semiconductor manufacturing process tools of any suitable type. For example, the semiconductor manufacturing process tools may comprise high density plasma chemical vapor deposition tools that use a remote plasma source to effect disassociation of fluorine from fluorine containing gases used during the cleaning process.
  • The [0037] effluent abatement system 10 includes main process section A-D, comprising thermal reaction section A, primary cooling/scrubbing section B, lower secondary cooling/scrubbing section C and upper secondary cooling/demister section D.
  • In the thermal reaction section A, the [0038] effluent abatement system 10 includes a thermal oxidation reactor 12, to which is joined an inlet assembly 14 for delivery of process gases and ancillary fluids to the reactor.
  • The [0039] thermal oxidation reactor 12 includes an exterior wall 16 and an interior wall 20 enclosing an annular heating element 18. The interior wall 20 encloses a central flow passage 22 of the reactor. The annular heating element may for example be electrically heated to provide a hot surface at the interior wall 20, for elevated temperature treatment of the effluent being treated. The inner wall 20, or “liner,” may be formed of any suitable material, such as Inconel® metal alloy.
  • The [0040] thermal oxidation reactor 12, although illustratively shown as an electrically heated unit, may alternatively be of any suitable type. Examples of alternative types include flame-based thermal oxidizers (e.g., using oxygen as an oxidizer and hydrogen or methane as the fuel), catalytic oxidizers, transpirative oxidizers, etc. The thermal oxidizer may be heated in any suitable manner, such as by electrical resistance heating, infrared radiation, microwave radiation, convective heat transfer or solid conduction.
  • The [0041] thermal oxidization reactor 12 may as shown be equipped with a control thermocouple 24. The thermocouple is used to monitor the temperature of the heating element 18. The thermocouple may be arranged in suitable signal transmission relationship to a thermal energy controller (not shown). Such thermal energy controller may in turn be arranged to responsively modulate the electrical heating energy to the annular heating element 18, and thereby achieve a desired temperature of the hot wall surface of interior wall 20. In such manner, the wall surface can be maintained at a desired temperature level appropriate for the thermal oxidation treatment of the effluent flowed through the thermal oxidizer unit (in the direction indicated by arrow F in FIG 1.)
  • The [0042] thermal oxidation reactor 12 in the embodiment shown is adapted to receive clean dry air (CDA) from CDA supply line 26. The CDA supply line 26 may be joined in supply relationship to a suitable source of clean dry air (e.g., CDA source 72). The thus-introduced air flows into the annular space between outer wall 16 and inner wall 20 of the thermal oxidizer unit, and is heated to suitable temperature in contact with the annular heating element 18. Resultant heated air then may flow through orifices or pores in the inner wall 20 into the central flow passage 22 of the reactor. In such manner, the oxidant may be added to mix with the effluent gas an form an oxidizable effluent gas mixture for thermal oxidation in the reactor. Alternatively, the oxidant may be added at the inlet, as another introduced fluid stream, to support the oxidation reactions in the thermal oxidation reactor.
  • At its lower end, the [0043] thermal oxidizer unit 12 is joined to a quench inlet section 28 of quench unit 32. In the quench inlet section, an array of water spray nozzles 30 is provided, supplied with water by an associated water feed conduit, as shown. The water spray nozzles serve to provide initial quench cooling to the hot effluent gas stream as the stream is discharged from the thermal oxidizer unit into the quench unit.
  • The quench unit is arranged with the quench [0044] inlet section 28 joined to a transverse section 34 of the quench unit.
  • The [0045] transverse section 34 in turn is joined to the sump section 36 of the quench unit. The sump section 36 at its lower end is coupled to a slope drain/vapor barrier 38. A conductivity liquid level sensor/chamber purge assembly is joined to the sump section 36, and is coupled to CDA branch line 42 which provides clean dry air to the assembly.
  • At its upper end, the [0046] sump section 36 of the quench unit 32 is joined to the lower end of the scrubber demister column 44. The scrubber demister column is filled, in the lower secondary cooling/scrubbing section thereof, with a secondary scrubbing packing 46, and the upper portion of such section of the column is equipped with a water spray nozzle 48 for effecting scrubbing of the upflowing effluent gas therein, by countercurrently flowing water downwardly over the packing 46. The water spray nozzle 48 is supplied with water by water feed line 50.
  • The upper portion of the lower section of the scrubber demister column is equipped with a [0047] vapor relief port 52 to which is coupled a vapor relief line 54, for venting overpressure in the column. An exhaust temperature sensor 56 is mounted on the upper portion of the lower section of the scrubber demister column, to provide temperature monitoring capability for the column.
  • The upper section of the scrubber demister column is likewise filled with a secondary scrubbing packing [0048] 58 and is equipped with a water spray nozzle 60 coupled to water feed line 50. The water feed line 50 has an air operated valve 101 therein. The valve is normally in a closed condition, and may be actuated as necessary to provide additional scrubbing capability for treatment of a specific effluent gas stream.
  • The upper section of the scrubber demister column is coupled to an [0049] exhaust temperature sensor 62, for monitoring the temperature of the effluent gas stream. A magnehelic pressure display 64 is also joined to the upper section of the scrubber demister column. A clean dry air line 70 is joined to clean dry air source 72. The CDA line 70 supplies CDA to the column, e.g., for dilution of the effluent stream being discharged from the upper end of the column in the direction indicated by the arrow R. The CDA line 70 has a restricted flow orifice 68 therein and a flow control valve upstream of the orifice, for selectively restricting flow of CDA to the upper end of the column.
  • The [0050] inlet assembly 14 for delivery of process gases and ancillary fluids to the thermal oxidation reactor 12 is arranged as shown, with process gas inlet conduits 88 and 90 receiving process exhaust gas in lines 84 and 86 from the gas flow router/manifold 82, which in turn receives gas streams 76,78 and 80 from the semiconductor manufacturing plant 74.
  • The [0051] semiconductor manufacturing plant 74 may be arranged to carry out any suitable operations for the production of semiconductor materials, devices and products.
  • Examples of specific operations of such [0052] semiconductor manufacturing plant 74 may include one or more process steps, such as for example:
  • (a) ion implantation; [0053]
  • (b) epitaxial growth; [0054]
  • (c) plasma etching; [0055]
  • (d) reactive ion etching; [0056]
  • (e) metallization; [0057]
  • (f) physical vapor deposition; [0058]
  • (g) chemical vapor deposition; [0059]
  • (h) photolithography; [0060]
  • (i) cleaning; and [0061]
  • (j) doping. [0062]
  • Specific manufacturing operations may for example comprise photolithography steps in the manufacture of VLSI and ULSI circuits, epitaxial deposition of film materials such as silicon from dispensed Si source gases, ion implantation and doping in the fabrication of CMOS, NMOS, BiCMOS and other structures, and manufacture of devices such as DRAMs, SRAMs, FeRAMs, etc. [0063]
  • The [0064] semiconductor manufacturing plant 74 may be employed to fabricate electronic device structures such as for example:
  • (a) transistors; [0065]
  • (b) capacitors; [0066]
  • (c) resistors; [0067]
  • (d) memory cells; [0068]
  • (e) dielectric material; [0069]
  • (f) buried doped substrate regions; [0070]
  • (g) metallization layers; [0071]
  • (h) channel stop layers; [0072]
  • (i) source layers; [0073]
  • (j) gate layers; [0074]
  • (k) drain layers; [0075]
  • (l) oxide layers; [0076]
  • (m) field emitter elements; [0077]
  • (n) passivation layers; [0078]
  • (o) interconnects; [0079]
  • (p) polycides; [0080]
  • (q) electrodes; [0081]
  • (r) trench structures; [0082]
  • (s) ion implanted material layers; [0083]
  • (t) via plugs; [0084]
  • (u) precursor structures for the foregoing (a)-(t) electronic device structures; and [0085]
  • (v) device assemblies comprising more than one of the foregoing (a)-(t) electronic device structures. [0086]
  • With regard to products, the [0087] semiconductor manufacturing plant 74 may be constructed and arranged to produce electronic device structures. The products may for example comprise memory chip devices, such as:
  • (i) ROM chips; [0088]
  • (ii) RAM chips; [0089]
  • (iii) SRAM chips; [0090]
  • (iv) DRAM chips; [0091]
  • (v) PROM chips; [0092]
  • (vi) EPROM chips; [0093]
  • (vii) EEPROM chips; and [0094]
  • (viii) flash memory chips. [0095]
  • In the FIG. 1 effluent abatement system, the process [0096] gas inlet conduits 88 and 90 flow the influent process exhaust gas into the thermal oxidation reactor 12. These process gas inlet conduits are constructed with ancillary fluid addition lines 92 and 94, for addition of ancillary process fluids to the main effluent stream being flowed through the process gas inlet conduits 88 and 90.
  • The [0097] inlet assembly 14 also includes a shroud gas feed line 96 and a hydrogen source feed line 98. The hydrogen source feed line 98 is joined to a hydrogen source gas supply 100. The shroud gas may be a purge gas for the thermal oxidation reactor, or the inlet or associated piping and channels of the effluent abatement system. Illustrative shroud or purge gas species include nitrogen, helium, argon, etc.
  • In accordance with a preferred aspect of the present invention, water vapor (steam) is introduced as a hydrogen source gas to the [0098] thermal oxidation reactor 12. The water vapor is utilized at elevated temperature appropriate to the thermal oxidation process being carried out in the thermal oxidation reactor and the halogen components being abated in the effluent gas. The hydrogen source gas supply 100 therefore may comprise a vaporization unit that is supplied with water from a suitable feed source, such as a water line in the semiconductor manufacturing facility, a municipal or industrial water supply, or the like. The hydrogen source gas supply 100 may alternatively comprise a steam line in the semiconductor manufacturing facility or other source of water vapor. As a still further alternative, the hydrogen source gas supply 100 may comprise a chemical reaction vessel for reacting reagent materials to form water vapor. For example, a hydrocarbon reagent, such as methane, propane, natural gas, etc., may be introduced to the chemical reaction vessel for mixing and reaction with an independently introduced oxidant, e.g., an oxygen-containing gas such as air, oxygen, oxygen-enriched air, ozone, or the like, to produce water vapor as a reaction product.
  • Water vapor is employed in accordance with the present invention to provide a source of hydrogen in the thermal oxidation reactor, for reaction with the halogen constituents of the effluent gas. Although the invention is described hereinafter primarily in reference to fluorine and fluorinated species being the halogen components of interest, it will be appreciated that the invention is not thus limited, and extends in utility to the abatement of other halogens, e.g., bromine, iodine and chlorine, and to corresponding other halogen-containing compounds, complexes and radicals. [0099]
  • The invention therefore provides water vapor as a source of hydrogen gas for reaction with the halogen species, e.g., converting fluorine species to forms that are amenable to removal by wet scrubbing. For example, fluorine gas is readily converted by reaction with steam, to yield hydrogen fluoride, which is easily removed from the effluent gas in the scrubbing step. The scrubbing step also removes various other acid gas components of the effluent, to produce a halogen-reduced/acid gas-reduced effluent. [0100]
  • Fluorine in the effluent gas flowed into an effluent abatement system of the type shown in FIG. 1, with steam injection at the inlet of the reactor, will be abated in the upper section of the reactor. [0101]
  • In conventional systems comprising thermal oxidation treatment of the effluent followed by water scrubbing, but lacking the steam addition (or other hydrogen source injection/addition) capability of the system of the present invention, fluorine will be abated in the primary and secondary stages of the cooling and scrubbing sections, however, prior to being converted to HF, the reactive fluorine can corrode components in the thermal section of the thermal oxidation reactor. In some cases this has led to failure of the thermal section liners and primary cooling sections in less than two months. The most common failure mode in the liners is erosion of the center of the liner. For the primary cooling sections the failures are typically due to attack on the hot areas not contacted by the water quench. [0102]
  • The present invention overcomes these deficiencies. Introduction of steam as a hydrogen source at the inlet, as for example in [0103] line 98 in the system of FIG. 1, allows the reactive F2 and fluorinated species to be reacted before they have a chance to attack the thermal section.
  • In preferred practice of the present invention, water vapor is injected between the stream of process gas and the liner of the thermal oxidation reactor, thereby protecting the liner from attack. [0104]
  • Referring now to FIG. 2, there is shown a schematic representation of gas flows in the inlet portion of a thermal oxidizer apparatus (such as that shown in FIG. 1), according to one aspect of the invention. [0105]
  • FIG. 2 shows the [0106] liner 20 of the thermal oxidation reactor as bounding the central flow passage of the thermal oxidation reactor. A fluorine-containing effluent gas stream, indicated by the arrow G, is flowed from the inlet into and through the central flow passage of the thermal oxidation reactor.
  • Concurrent with the flow of the effluent gas stream through the inlet into the central passage of the thermal oxidation reactor, a shrouding gas, indicated by arrows H, is introduced, to surround the effluent gas stream in downflow through the central flow passage of the thermal oxidation reactor. The shrouding gas may for example be nitrogen, or other inert gas. [0107]
  • Concurrently, the inlet introduces water vapor, indicated by arrows I, for flow downwardly in the thermal oxidation reactor. [0108]
  • By such arrangement, the shrouding gas separates the effluent gas stream from the water vapor and prevents premature reactions that could otherwise generate solids and clog the gas feed tubes of the inlet. The water vapor may optionally be introduced with air or nitrogen mixture. [0109]
  • In the thermal section of the reactor, the hydrogen deriving from the steam will react with the fluorine or other halogen components of the effluent gas. The hot reaction products will be quenched in the primary section B (see FIG. 1) and will travel to the secondary sections C and D (see also FIG. 1) where they will be scrubbed. [0110]
  • In a variant of the foregoing water vapor introduction arrangement described above in connection with FIG. 2, the arrows I, instead of representing water vapor, may represent an alternative hydrogen source material, such as methane. Concurrently, oxygen, air or other oxygen-containing gas, indicated by arrow J, may be introduced to the thermal oxidation reactor for reaction with the methane or other hydrogen source material, to produce water vapor as a reaction product, for reaction with fluorine and fluorinated species. The nitrogen or other inert gas indicated by arrow H will serve the same function in this variant arrangement, of separating the effluent from the water vapor (and methane combustion products). [0111]
  • FIG. 3 is a cross-sectional elevation view of an inlet of a thermal oxidizer unit of the type shown in FIG. 1, according to one embodiment of the invention. For ease of description, the same reference numerals are used in FIG. 3 as employed for the corresponding elements in FIG. 1. [0112]
  • As shown in FIG. 3, the [0113] inlet structure 14 includes a process gas inlet conduit 90 for introducing effluent gas from a process facility, such as a semiconductor manufacturing tool, to a thermal oxidation reactor 12.
  • The process [0114] gas inlet conduit 90 features an inlet pressure monitoring port 112 for coupling with a suitable pressure monitoring device to sense the pressure of the process gas. The process gas inlet conduit 90 is provided with fluid addition lines 92 and 94, for addition of oxygen, air, nitrogen, and/or any other gas species, to assist the thermal oxidation reaction in the reactor 12. For example, the fluid addition lines may be employed to add a co-reactant species for specific components of the effluent gas being treated.
  • The process [0115] gas inlet conduit 90 terminates in a lower tubular wall 122 enclosing a cylindrical flow passage 120, within an outer tubular wall 124. The outer tubular wall 124 is in spaced relationship to tubular wall 122, defining an annular space 126 therebetween.
  • Communicating with [0116] annular space 126 is a shroud gas feed line 96, to which shroud gas such as nitrogen is introduced, for downward flow around the discharged effluent gas in the central flow passage defined by outer tubular wall 124. The outer tubular wall 124 thus defines an effluent flow passage and is open-ended at its lower end.
  • Water vapor is introduced in hydrogen source [0117] gas feed line 98 and flows downwardly, exiting the inlet structure at its lower end as indicated by arrows K. Subsequently, in flow below the inlet 12, in the thermal oxidation reactor, the water vapor mixes with the effluent gas and fluorine and fluorinated species in the effluent gas are reacted with hydrogen deriving from the injected water vapor. Hydrogen fluoride and other reaction products thereby are formed, which are readily removable in the subsequent scrubbing operation of the effluent treatment system.
  • Instead of water vapor, methane or other hydrogen source gas may be introduced in [0118] line 98 to the inlet. For example, if methane is introduced in line 98, then oxygen, air, or other oxygen-containing gas may be concurrently introduced in the same line, or in a different line of the inlet, e.g., in line 92 or line 94. A steam generator may additionally be coupled with hydrogen source gas feed line 98, to provide hydrogen for reaction with the halogen in the effluent gas.
  • FIG. 4 is a cross-sectional elevation view of an [0119] inlet 140 of a thermal oxidizer unit, according to another embodiment of the invention. The inlet comprises an inlet body 141 constructed with a first tubular feed conduit 142 and a second tubular feed conduit 144, defining enclosed interior passages 146 and 148, respectively. Effluent gas, indicated by arrows L, is introduced to the first tubular feed conduit 142 and second tubular feed conduit 144, for flow through the inlet into the thermal oxidation reactor.
  • The [0120] inlet body 141 also comprises nitrogen feed passages 150 and 152, through which nitrogen gas, indicated by arrows M, is flowed. These nitrogen feed passages communicate with central nitrogen feed passage 154. As shown, at the bottom of the inlet body, the nitrogen gas (arrows M) flows downwardly as a shrouding gas for the effluent gas stream (arrows L).
  • Concurrently, a hydrogen source gas is introduced to the inlet body by hydrogen [0121] source gas passages 156 and 158, for entry into the annular hydrogen source gas reservoir 160. The hydrogen source gas is flowed from the reservoir through the hydrogen source gas outlet slots 162 and 164, and flows downwardly (arrows N) around the effluent gas stream (arrows L), so that the effluent gas stream is shrouded by the shrouding gas stream (arrows M), to thereby prevent premature reaction between the effluent gas and the hydrogen source gas.
  • Subsequently, as the gas streams (arrows L, M and N) pass downwardly, the respective streams mix and the hydrogen source gas reacts with the fluorine and fluorinated species in the effluent gas stream, to abate the fluorine content thereof. [0122]
  • In the broad practice of the invention, the relative flow rates of the hydrogen source gas and the effluent gas stream may be suitably selected so as to minimize the incidence of corrosion of the liner in the thermal oxidation reactor and to effect the desired reaction and removal of the halogen content of the effluent gas stream being treated. [0123]
  • The same is true of the shrouding gas used to protect the effluent gas from premature reaction with the hydrogen source gas. [0124]
  • The relative rates of flow of all gas streams in a given treatment application may be readily determined without undue experimentation, by the simple expedient of independently varying the flow rate of each stream in sequence and determining the corresponding destruction removal efficiency (DRE) of the halogen component(s) of interest in the treated effluent gas. [0125]
  • Suitable temperature and pressure levels for the effluent abatement process of the invention can be similarly determined, to achieve a desired level of abatement of the halogen component in the effluent gas. [0126]
  • Preferred temperatures for the use of water vapor or CH[0127] 4 as a hydrogen source reagent are between 650° C. and 950° C., with the lower temperatures decreasing the corrosion rate and F2 attack on the liner.
  • The invention will therefore be appreciated as providing a simple and effective technique for the abatement of fluorine and fluorinated species, as well as of other halogen species, from effluent gases generated in industrial processes, such as manufacturing of semiconductor materials, devices and products. [0128]
  • The features and advantages of the invention will be more fully apparent from the following non-limiting examples. [0129]
  • EXAMPLE 1
  • F[0130] 2 abatement from an effluent derived from a semiconductor manufacturing plant was evaluated in a Delatech CDO™ thermal oxidation unit (Ecosys Corporation, San Jose, Calif.), using NH4OH as the abatement reagent.
  • F[0131] 2 abatement from a corresponding effluent was evaluated using water flushed through the NH4OH injection lines of the thermal oxidation reactor.
  • The Destruction Removal Efficiency (DRE) for F[0132] 2 when water was flushed through the NH4OH injection lines was between DRE value for NH4OH reagent and the DRE value when no reagent was used.
  • The improved DRE for water flushing relative to performance with no F[0133] 2 abatement reagent indicated that some of the F2 was being abated by the water in the heated section of the CDO™ thermal oxidation reactor. Table 1 below shows the fluorine abatement with injection of water into the inlet section of the thermal oxidation reactor.
    TABLE 1
    Fluorine abatement with injection of water into thermal
    oxidation reactor inlet section.
    NH3 aq. H2O NH3 in F2 in Total Flow Water F2 in F2 out F2 DRE
    g/min g/min slpm slpm slpm pH (ppm) (ppm) %
    4.0 2.9 1.6 2.0 182 3.4 11,013 1 99.99
    0.0 4.0 0.0 2.0 180 3.3 11,111 3 99.97
    0.0 4.0 0.0 2.0 172 3.2 11,628 10 99.91
    0.0 0.0 0.0 2.0 172 3.2 11,628 40 99.66
  • EXAMPLE 2
  • Long term testing with NH[0134] 4OH as a F2 abatement reagent revealed a problem with corrosion on the bottom of the inlet section of the thermal oxidation reactor. This corrosion was traced to cooling by the NH4OH being vaporized in the inlet section. To prevent this cooling due to the change of state from liquid to vapor, a heater was installed before the inlet section to vaporize the incoming NH4OH prior to injection. This heater consisted of a tubular housing with a heating element inside the housing. The NH4OH was metered, mixed with air and entered the side of the housing where it was vaporized by the heater element. The NH4OH vapor mixed with air exited the housing and flowed to the inlet assembly. This modification resolved the corrosion problem. NH4OH may be employed as an adjunctive fluorine abatement agent in the broad practice of the present invention.
  • EXAMPLE 3
  • A fluorine abatement effluent treatment system of the type shown in FIG. 1 and equipped with an inlet of the type shown in FIG. 3 is operated, to effect treatment of an effluent gas stream from a semiconductor manufacturing facility. Water vapor is used as the fluorine abatement agent. The process gas flows down the center tube, with N[0135] 2 flowing into the surrounding tube and out the annulus formed by the two concentric tubes. This N2 flowing out the annulus separates the process gases from the water vapor and prevents premature reactions that could generate solids and clog the inlet tubes. The water is vaporized into steam using the same heater used for the NH4OH testing in Example 2. The steam and air or N2 mixture is introduced into the hydrogen source gas feed tube to flow around the tube carrying the effluent gas and mix with the process gases in the thermal section of the CDO™ thermal oxidation reactor. The hot reaction products are quenched in the primary section and travel through the secondary section where they are scrubbed.
  • EXAMPLE 4
  • Another test is conducted using the combustion of CH[0136] 4 in air or O2 to generate water vapor to react with the F2 and fluorinated species. In this case the same inlet configuration as shown in FIG. 3 is used. The process gases flow through the same center tube as in the water vapor injection in Example 3. CH4 is injected. The flow of N2 separates the process gases from the water vapor and CH4 combustion products. O2 or clean dry air (CDA) is added to support the combustion of the CH4.
  • While the invention has been described with reference to illustrative embodiments, it will be recognized that other variations, modification and other embodiments are contemplated, as being within the spirit and scope of the invention, and therefore the invention is to be correspondingly broadly construed with respect to such variations, modifications and other embodiments, as being within the spirit and scope of the invention as claimed. [0137]

Claims (23)

We claim:
1. An apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools, comprising:
an oxidizing unit having one or more inlet units at one end, downstream from at least one semiconductor manufacturing process tool, arranged to elevate the temperature of the effluent fluid stream, effect oxidation of at least a portion of the oxidizable components of the effluent fluid stream, and utilize water vapor to effect conversion of at least a portion of the halogen-containing components of the effluent fluid stream to a form that is more treatable at the inlet end.
2. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 1, further comprising a post-treatment unit downstream from the oxidizing unit, arranged to remove acidic components from the effluent fluid stream.
3. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 1, further comprising a pre-treatment unit upstream from the oxidizing unit and downstream from said one or more semiconductor manufacturing process tools.
4. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 3, wherein the pre-treatment unit is arranged to remove water-soluble components and particulates.
5. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 1, wherein the water vapor is used to effect the conversion of diatomic halogens to their more readily treatable mineral acid form.
6. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 1 further comprising a vaporizing unit arranged to provide water vapor to the inlet end of the oxidizing unit.
7. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 1 wherein the oxidizing unit is further arranged to utilize a purge gas to preclude the conversion of at least a portion of the halogen-containing components of the effluent fluid stream from being effected at the one or more inlet units.
8. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 1 wherein the one or more inlet units are arranged to introduce the effluent fluid stream into the oxidizing unit, introduce the purge gas into the oxidizing unit close to the one or more inlet units, and introduce a reagent into the oxidizing unit at the inlet end of the oxidizing unit.
9. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 8, wherein the reagent is water vapor.
10. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 8 wherein the reagent is a hydrocarbon gas and the oxidizing unit is further arranged to mix an oxygen containing gas with the hydrocarbon gas at the inlet end of the oxidizing unit.
11. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 1 wherein the effluent fluid stream is heated to within the temperature range of about 650° C. to about 950° C.
12. The apparatus for treating the effluent fluid stream from one or more semiconductor manufacturing process tools of claim 1 wherein the semiconductor manufacturing process tools comprise high density plasma chemical vapor deposition tools which use a remote plasma source to effect disassociation of diatonic halogen gas from halogen containing gases used during the cleaning process.
13. A thermal oxidation reactor for abatement of oxidizable halogen components in an effluent gas, said thermal oxidation reactor comprising: a housing defining a flow passage therein for flow of effluent gas therethrough; an inlet coupled to the housing for introduction of effluent gas to the central flow passage, said inlet comprising (1) a shrouding gas flow passage arranged to flow shrouding gas into the central flow passage cocurrently with the effluent gas and surrounding the effluent gas, and (2) a reagent gas flow passage arranged to flow a reagent gas into the central flow passage cocurrently with the shrouding gas and surrounding the shrouding gas, wherein the reagent gas is reactive with halogen species in the effluent gas, with said central flow passage being of sufficient length downstream of the inlet to permit the reagent gas to mix and react with the halogen species of the effluent gas.
14. The thermal oxidation reactor of claim 13, wherein the housing comprises a liner susceptible to corrosion in contact with said halogen species in the absence of said reagent gas to react with said halogen species.
15. The thermal oxidation reactor of claim 13, wherein the inlet is arranged to receive effluent gas from a semiconductor manufacturing plant.
16. The thermal oxidation reactor of claim 13, wherein the semiconductor manufacturing plant utilizes at least one perfluorocompound as a reagent therein, and produces effluent gas containing fluorine and/or fluorinated species.
17. The thermal oxidation reactor of claim 13, wherein the housing includes a heating element arranged to maintain a temperature of effluent gas flowed through the central flow passage in the range of from about 650° C. to about 950° C.
18. The thermal oxidation reactor of claim 13, coupled in effluent gas flow supply relationship to a scrubbing unit.
19. The thermal oxidation reactor of claim 18, wherein the scrubbing unit comprises a water scrubbing unit.
20. The thermal oxidation reactor of claim 19, wherein the water scrubbing unit comprises a packed bed column equipped with at least one water spray nozzle.
21. The thermal oxidation reactor of claim 13, wherein the central flow passage comprises an elongate cylindrical passage.
22. The thermal oxidation reactor of claim 13, coupled in effluent gas supply relationship to a quench unit, with the quench unit coupled in effluent gas supply relationship to a scrubbing unit.
23. The thermal oxidation reactor of claim 22, wherein the scrubbing unit comprises a water scrubbing unit.
US10/150,468 1999-10-18 2002-05-17 Fluorine abatement using steam injection in oxidation treatment of semiconductor manufacturing effluent gases Abandoned US20020159924A1 (en)

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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050135984A1 (en) * 2003-12-19 2005-06-23 Shawn Ferron Apparatus and method for controlled combustion of gaseous pollutants
US20070166205A1 (en) * 1996-12-31 2007-07-19 Mark Holst Effluent gas stream treatment system having utility for oxidation treatment of semiconductor manufacturing effluent gases
US20090149996A1 (en) * 2007-12-05 2009-06-11 Applied Materials, Inc. Multiple inlet abatement system
US20090314626A1 (en) * 2006-03-03 2009-12-24 Pascal Moine Method for treating effluents containing fluorocompounds like pfc and hfc
WO2010006181A2 (en) * 2008-07-11 2010-01-14 Applied Materials, Inc. Methods and apparatus for abating electronic device manufacturing process effluent
US7700049B2 (en) 2005-10-31 2010-04-20 Applied Materials, Inc. Methods and apparatus for sensing characteristics of the contents of a process abatement reactor
US7736599B2 (en) 2004-11-12 2010-06-15 Applied Materials, Inc. Reactor design to reduce particle deposition during process abatement
US20120100491A1 (en) * 2009-01-30 2012-04-26 Central Glass Company, Limited Semiconductor Production Equipment Including Fluorine Gas Generator
GB2515017A (en) * 2013-06-10 2014-12-17 Edwards Ltd Process gas abatement
JP2015525332A (en) * 2012-04-30 2015-09-03 ハイバック コーポレイション Double coaxial processing module
WO2016048526A1 (en) * 2014-09-25 2016-03-31 Applied Materials, Inc. Vacuum foreline reagent addition for fluorine abatement
WO2018185469A1 (en) * 2017-04-04 2018-10-11 Edwards Limited Purge gas feeding means, abatement systems and methods of modifying abatement systems
WO2018212940A1 (en) * 2017-05-19 2018-11-22 Applied Materials, Inc. Apparatus for collection and subsequent reaction of liquid and solid effluent into gaseous effluent
US11114285B2 (en) 2016-04-13 2021-09-07 Applied Materials, Inc. Apparatus for exhaust cooling
WO2023097105A1 (en) * 2021-11-29 2023-06-01 Evoqua Water Technologies Llc Pfas treatment using gac, reactivation and thermal destruction

Families Citing this family (158)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4102547B2 (en) * 1998-12-01 2008-06-18 株式会社荏原製作所 Exhaust gas treatment equipment
TW506852B (en) * 2000-08-28 2002-10-21 Promos Technologies Inc Device and method for processing exhaust from process chamber
US7220396B2 (en) * 2001-07-11 2007-05-22 Battelle Memorial Institute Processes for treating halogen-containing gases
US6962679B2 (en) * 2001-07-11 2005-11-08 Battelle Memorial Institute Processes and apparatuses for treating halogen-containing gases
US7578883B1 (en) * 2001-08-29 2009-08-25 Lsi Corporation Arrangement and method for abating effluent from a process
JP4374814B2 (en) * 2001-09-20 2009-12-02 株式会社日立製作所 Treatment method for perfluoride treatment
TW497986B (en) * 2001-12-20 2002-08-11 Ind Tech Res Inst Dielectric barrier discharge apparatus and module for perfluorocompounds abatement
US7488460B2 (en) * 2004-01-05 2009-02-10 Innovative Engineering Solutions, Inc. Combined chemical agent and dynamic oxidation treatment of hazardous gas
US7534399B2 (en) * 2004-03-10 2009-05-19 Innovative Engineering Solutions, Inc. Hazardous gas abatement system using electrical heater and water scrubber
US7074034B2 (en) * 2004-06-07 2006-07-11 Air Products And Chemicals, Inc. Burner and process for combustion of a gas capable of reacting to form solid products
JP2008546525A (en) * 2005-06-13 2008-12-25 アプライド マテリアルズ インコーポレイテッド Method and apparatus for detoxifying treatment
DE102006027882B4 (en) * 2005-09-02 2009-04-30 Clean Systems Korea Inc., Seongnam Scrubber for treating semiconductor waste gas
KR100623368B1 (en) 2005-09-02 2006-09-12 크린시스템스코리아(주) Direct burn-wet scrubber for semiconductor manufacture equipment
GB0521944D0 (en) * 2005-10-27 2005-12-07 Boc Group Plc Method of treating gas
JP4937998B2 (en) * 2006-03-07 2012-05-23 カンケンテクノ株式会社 HCD gas removal method and apparatus
EP1930034B1 (en) 2006-12-07 2012-11-14 Thoratec LLC An integrated centrifugal blood pump-oxygenator, an extracorporeal life support system and a method of de-bubbling and priming an extracorporeal life support system
KR100888044B1 (en) * 2007-07-04 2009-03-10 스템코 주식회사 Apparatus for manufacturing semiconductor unit
TWI355964B (en) * 2007-12-05 2012-01-11 Ind Tech Res Inst Method for catalytic treating perfluorocompound ga
US8192693B2 (en) * 2008-02-12 2012-06-05 Innovative Engineering Solutions, Inc. Apparatus for dynamic oxidation of process gas
KR101682583B1 (en) 2008-03-25 2016-12-05 어플라이드 머티어리얼스, 인코포레이티드 Methods and apparatus for conserving electronic device manufacturing resources
GB0806730D0 (en) * 2008-04-14 2008-05-14 Edwards Ltd Detection of halogens
KR100992752B1 (en) 2008-11-14 2010-11-05 주식회사 동부하이텍 Scrubber of semiconductor manufacturing apparatus
US9324576B2 (en) 2010-05-27 2016-04-26 Applied Materials, Inc. Selective etch for silicon films
US10283321B2 (en) 2011-01-18 2019-05-07 Applied Materials, Inc. Semiconductor processing system and methods using capacitively coupled plasma
US8999856B2 (en) 2011-03-14 2015-04-07 Applied Materials, Inc. Methods for etch of sin films
US9064815B2 (en) 2011-03-14 2015-06-23 Applied Materials, Inc. Methods for etch of metal and metal-oxide films
US8808563B2 (en) 2011-10-07 2014-08-19 Applied Materials, Inc. Selective etch of silicon by way of metastable hydrogen termination
US9267739B2 (en) 2012-07-18 2016-02-23 Applied Materials, Inc. Pedestal with multi-zone temperature control and multiple purge capabilities
US9373517B2 (en) 2012-08-02 2016-06-21 Applied Materials, Inc. Semiconductor processing with DC assisted RF power for improved control
US9034770B2 (en) 2012-09-17 2015-05-19 Applied Materials, Inc. Differential silicon oxide etch
US9023734B2 (en) 2012-09-18 2015-05-05 Applied Materials, Inc. Radical-component oxide etch
US9390937B2 (en) 2012-09-20 2016-07-12 Applied Materials, Inc. Silicon-carbon-nitride selective etch
US9132436B2 (en) 2012-09-21 2015-09-15 Applied Materials, Inc. Chemical control features in wafer process equipment
US8969212B2 (en) 2012-11-20 2015-03-03 Applied Materials, Inc. Dry-etch selectivity
US8980763B2 (en) 2012-11-30 2015-03-17 Applied Materials, Inc. Dry-etch for selective tungsten removal
US9111877B2 (en) 2012-12-18 2015-08-18 Applied Materials, Inc. Non-local plasma oxide etch
US8921234B2 (en) 2012-12-21 2014-12-30 Applied Materials, Inc. Selective titanium nitride etching
US10256079B2 (en) 2013-02-08 2019-04-09 Applied Materials, Inc. Semiconductor processing systems having multiple plasma configurations
US9362130B2 (en) 2013-03-01 2016-06-07 Applied Materials, Inc. Enhanced etching processes using remote plasma sources
US9040422B2 (en) 2013-03-05 2015-05-26 Applied Materials, Inc. Selective titanium nitride removal
US20140271097A1 (en) 2013-03-15 2014-09-18 Applied Materials, Inc. Processing systems and methods for halide scavenging
US9493879B2 (en) 2013-07-12 2016-11-15 Applied Materials, Inc. Selective sputtering for pattern transfer
GB2516267B (en) * 2013-07-17 2016-08-17 Edwards Ltd Head assembly
US9773648B2 (en) 2013-08-30 2017-09-26 Applied Materials, Inc. Dual discharge modes operation for remote plasma
US9576809B2 (en) 2013-11-04 2017-02-21 Applied Materials, Inc. Etch suppression with germanium
US9520303B2 (en) 2013-11-12 2016-12-13 Applied Materials, Inc. Aluminum selective etch
US9245762B2 (en) 2013-12-02 2016-01-26 Applied Materials, Inc. Procedure for etch rate consistency
US9287095B2 (en) 2013-12-17 2016-03-15 Applied Materials, Inc. Semiconductor system assemblies and methods of operation
US9287134B2 (en) 2014-01-17 2016-03-15 Applied Materials, Inc. Titanium oxide etch
US9259683B2 (en) 2014-01-22 2016-02-16 Micron Technology, Inc. Methods and apparatus for treating fluorinated greenhouse gases in gas streams
US9396989B2 (en) 2014-01-27 2016-07-19 Applied Materials, Inc. Air gaps between copper lines
US9293568B2 (en) 2014-01-27 2016-03-22 Applied Materials, Inc. Method of fin patterning
US9385028B2 (en) 2014-02-03 2016-07-05 Applied Materials, Inc. Air gap process
US9499898B2 (en) 2014-03-03 2016-11-22 Applied Materials, Inc. Layered thin film heater and method of fabrication
US9299575B2 (en) 2014-03-17 2016-03-29 Applied Materials, Inc. Gas-phase tungsten etch
US9299538B2 (en) 2014-03-20 2016-03-29 Applied Materials, Inc. Radial waveguide systems and methods for post-match control of microwaves
US9299537B2 (en) 2014-03-20 2016-03-29 Applied Materials, Inc. Radial waveguide systems and methods for post-match control of microwaves
US9903020B2 (en) 2014-03-31 2018-02-27 Applied Materials, Inc. Generation of compact alumina passivation layers on aluminum plasma equipment components
US9309598B2 (en) 2014-05-28 2016-04-12 Applied Materials, Inc. Oxide and metal removal
US9406523B2 (en) 2014-06-19 2016-08-02 Applied Materials, Inc. Highly selective doped oxide removal method
US9378969B2 (en) 2014-06-19 2016-06-28 Applied Materials, Inc. Low temperature gas-phase carbon removal
US9425058B2 (en) 2014-07-24 2016-08-23 Applied Materials, Inc. Simplified litho-etch-litho-etch process
US9496167B2 (en) 2014-07-31 2016-11-15 Applied Materials, Inc. Integrated bit-line airgap formation and gate stack post clean
US9378978B2 (en) 2014-07-31 2016-06-28 Applied Materials, Inc. Integrated oxide recess and floating gate fin trimming
US9659753B2 (en) 2014-08-07 2017-05-23 Applied Materials, Inc. Grooved insulator to reduce leakage current
US9553102B2 (en) 2014-08-19 2017-01-24 Applied Materials, Inc. Tungsten separation
US9355856B2 (en) 2014-09-12 2016-05-31 Applied Materials, Inc. V trench dry etch
US9368364B2 (en) 2014-09-24 2016-06-14 Applied Materials, Inc. Silicon etch process with tunable selectivity to SiO2 and other materials
US9478434B2 (en) 2014-09-24 2016-10-25 Applied Materials, Inc. Chlorine-based hardmask removal
US9613822B2 (en) 2014-09-25 2017-04-04 Applied Materials, Inc. Oxide etch selectivity enhancement
US9966240B2 (en) 2014-10-14 2018-05-08 Applied Materials, Inc. Systems and methods for internal surface conditioning assessment in plasma processing equipment
US9355922B2 (en) 2014-10-14 2016-05-31 Applied Materials, Inc. Systems and methods for internal surface conditioning in plasma processing equipment
US11637002B2 (en) 2014-11-26 2023-04-25 Applied Materials, Inc. Methods and systems to enhance process uniformity
US10224210B2 (en) 2014-12-09 2019-03-05 Applied Materials, Inc. Plasma processing system with direct outlet toroidal plasma source
US10573496B2 (en) 2014-12-09 2020-02-25 Applied Materials, Inc. Direct outlet toroidal plasma source
US9502258B2 (en) 2014-12-23 2016-11-22 Applied Materials, Inc. Anisotropic gap etch
US9343272B1 (en) 2015-01-08 2016-05-17 Applied Materials, Inc. Self-aligned process
US11257693B2 (en) 2015-01-09 2022-02-22 Applied Materials, Inc. Methods and systems to improve pedestal temperature control
US9373522B1 (en) 2015-01-22 2016-06-21 Applied Mateials, Inc. Titanium nitride removal
US9449846B2 (en) 2015-01-28 2016-09-20 Applied Materials, Inc. Vertical gate separation
US9728437B2 (en) 2015-02-03 2017-08-08 Applied Materials, Inc. High temperature chuck for plasma processing systems
US20160225652A1 (en) 2015-02-03 2016-08-04 Applied Materials, Inc. Low temperature chuck for plasma processing systems
KR20160105653A (en) 2015-02-27 2016-09-07 (주)써스텍 Color change agent and method of manufacturing thereof
US9881805B2 (en) 2015-03-02 2018-01-30 Applied Materials, Inc. Silicon selective removal
US9691645B2 (en) 2015-08-06 2017-06-27 Applied Materials, Inc. Bolted wafer chuck thermal management systems and methods for wafer processing systems
US9741593B2 (en) 2015-08-06 2017-08-22 Applied Materials, Inc. Thermal management systems and methods for wafer processing systems
US9349605B1 (en) 2015-08-07 2016-05-24 Applied Materials, Inc. Oxide etch selectivity systems and methods
US10504700B2 (en) 2015-08-27 2019-12-10 Applied Materials, Inc. Plasma etching systems and methods with secondary plasma injection
TWI599395B (en) * 2015-11-26 2017-09-21 Orient Service Co Ltd Method and device for purifying fluoride in semiconductor process exhaust gas
US10504754B2 (en) 2016-05-19 2019-12-10 Applied Materials, Inc. Systems and methods for improved semiconductor etching and component protection
US10522371B2 (en) 2016-05-19 2019-12-31 Applied Materials, Inc. Systems and methods for improved semiconductor etching and component protection
US9865484B1 (en) 2016-06-29 2018-01-09 Applied Materials, Inc. Selective etch using material modification and RF pulsing
TWI637780B (en) * 2016-07-18 2018-10-11 東服企業股份有限公司 Method and device for capturing products after sintering reaction of semiconductor process exhaust gas
US10062575B2 (en) 2016-09-09 2018-08-28 Applied Materials, Inc. Poly directional etch by oxidation
US10629473B2 (en) 2016-09-09 2020-04-21 Applied Materials, Inc. Footing removal for nitride spacer
US10062585B2 (en) 2016-10-04 2018-08-28 Applied Materials, Inc. Oxygen compatible plasma source
US9721789B1 (en) 2016-10-04 2017-08-01 Applied Materials, Inc. Saving ion-damaged spacers
US9934942B1 (en) 2016-10-04 2018-04-03 Applied Materials, Inc. Chamber with flow-through source
US10546729B2 (en) 2016-10-04 2020-01-28 Applied Materials, Inc. Dual-channel showerhead with improved profile
US10062579B2 (en) 2016-10-07 2018-08-28 Applied Materials, Inc. Selective SiN lateral recess
US9947549B1 (en) 2016-10-10 2018-04-17 Applied Materials, Inc. Cobalt-containing material removal
US9768034B1 (en) 2016-11-11 2017-09-19 Applied Materials, Inc. Removal methods for high aspect ratio structures
US10163696B2 (en) 2016-11-11 2018-12-25 Applied Materials, Inc. Selective cobalt removal for bottom up gapfill
US10242908B2 (en) 2016-11-14 2019-03-26 Applied Materials, Inc. Airgap formation with damage-free copper
US10026621B2 (en) 2016-11-14 2018-07-17 Applied Materials, Inc. SiN spacer profile patterning
US10566206B2 (en) 2016-12-27 2020-02-18 Applied Materials, Inc. Systems and methods for anisotropic material breakthrough
US10403507B2 (en) 2017-02-03 2019-09-03 Applied Materials, Inc. Shaped etch profile with oxidation
US10431429B2 (en) 2017-02-03 2019-10-01 Applied Materials, Inc. Systems and methods for radial and azimuthal control of plasma uniformity
US10043684B1 (en) 2017-02-06 2018-08-07 Applied Materials, Inc. Self-limiting atomic thermal etching systems and methods
US10319739B2 (en) 2017-02-08 2019-06-11 Applied Materials, Inc. Accommodating imperfectly aligned memory holes
CN114797403A (en) * 2017-02-09 2022-07-29 应用材料公司 Plasma abatement technique using water vapor and oxygen reagents
US10943834B2 (en) 2017-03-13 2021-03-09 Applied Materials, Inc. Replacement contact process
GB2561191B (en) * 2017-04-04 2020-08-26 Edwards Ltd Apparatus for treating gases and a method of reducing deposition on a surface in such apparatus
US10319649B2 (en) 2017-04-11 2019-06-11 Applied Materials, Inc. Optical emission spectroscopy (OES) for remote plasma monitoring
US11276559B2 (en) 2017-05-17 2022-03-15 Applied Materials, Inc. Semiconductor processing chamber for multiple precursor flow
US11276590B2 (en) 2017-05-17 2022-03-15 Applied Materials, Inc. Multi-zone semiconductor substrate supports
US10497579B2 (en) 2017-05-31 2019-12-03 Applied Materials, Inc. Water-free etching methods
US10049891B1 (en) 2017-05-31 2018-08-14 Applied Materials, Inc. Selective in situ cobalt residue removal
TWI646279B (en) * 2017-06-01 2019-01-01 華邦電子股份有限公司 Piping system
US10920320B2 (en) 2017-06-16 2021-02-16 Applied Materials, Inc. Plasma health determination in semiconductor substrate processing reactors
US10541246B2 (en) 2017-06-26 2020-01-21 Applied Materials, Inc. 3D flash memory cells which discourage cross-cell electrical tunneling
US10727080B2 (en) 2017-07-07 2020-07-28 Applied Materials, Inc. Tantalum-containing material removal
US10541184B2 (en) 2017-07-11 2020-01-21 Applied Materials, Inc. Optical emission spectroscopic techniques for monitoring etching
US10354889B2 (en) 2017-07-17 2019-07-16 Applied Materials, Inc. Non-halogen etching of silicon-containing materials
US10043674B1 (en) 2017-08-04 2018-08-07 Applied Materials, Inc. Germanium etching systems and methods
US10170336B1 (en) 2017-08-04 2019-01-01 Applied Materials, Inc. Methods for anisotropic control of selective silicon removal
US10297458B2 (en) 2017-08-07 2019-05-21 Applied Materials, Inc. Process window widening using coated parts in plasma etch processes
US10283324B1 (en) 2017-10-24 2019-05-07 Applied Materials, Inc. Oxygen treatment for nitride etching
US10128086B1 (en) 2017-10-24 2018-11-13 Applied Materials, Inc. Silicon pretreatment for nitride removal
KR102362761B1 (en) * 2017-11-22 2022-02-15 씨에스케이(주) Gas treating apparatus
US10256112B1 (en) 2017-12-08 2019-04-09 Applied Materials, Inc. Selective tungsten removal
US10903054B2 (en) 2017-12-19 2021-01-26 Applied Materials, Inc. Multi-zone gas distribution systems and methods
US11328909B2 (en) 2017-12-22 2022-05-10 Applied Materials, Inc. Chamber conditioning and removal processes
US10854426B2 (en) 2018-01-08 2020-12-01 Applied Materials, Inc. Metal recess for semiconductor structures
US10964512B2 (en) 2018-02-15 2021-03-30 Applied Materials, Inc. Semiconductor processing chamber multistage mixing apparatus and methods
US10679870B2 (en) 2018-02-15 2020-06-09 Applied Materials, Inc. Semiconductor processing chamber multistage mixing apparatus
TWI766433B (en) 2018-02-28 2022-06-01 美商應用材料股份有限公司 Systems and methods to form airgaps
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GB2579197B (en) * 2018-11-22 2021-06-09 Edwards Ltd Abatement method
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US10920319B2 (en) 2019-01-11 2021-02-16 Applied Materials, Inc. Ceramic showerheads with conductive electrodes
GB2593722A (en) * 2020-03-31 2021-10-06 Edwards Ltd Apparatus

Citations (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US566317A (en) * 1896-08-25 Wheat-steamer
US3898040A (en) * 1972-06-29 1975-08-05 Universal Oil Prod Co Recuperative form of thermal-catalytic incinerator
US4083607A (en) * 1976-05-05 1978-04-11 Mott Lambert H Gas transport system for powders
US4519999A (en) * 1980-03-31 1985-05-28 Union Carbide Corporation Waste treatment in silicon production operations
US4661056A (en) * 1986-03-14 1987-04-28 American Hoechst Corporation Turbulent incineration of combustible materials supplied in low pressure laminar flow
US4719088A (en) * 1985-02-12 1988-01-12 Mitsubish Denki Kabushiki Kaisha Apparatus for removing at least one acidic component from a gas
US4886444A (en) * 1987-06-19 1989-12-12 L'air Liquide Process for treating gaseous effluents coming from the manufacture of electronic components and incineration apparatus for carrying out said process
US4908191A (en) * 1987-07-21 1990-03-13 Ethyl Corporation Removing arsine from gaseous streams
US4986838A (en) * 1989-06-14 1991-01-22 Airgard, Inc. Inlet system for gas scrubber
US5009869A (en) * 1987-12-28 1991-04-23 Electrocinerator Technologies, Inc. Methods for purification of air
US5045288A (en) * 1989-09-15 1991-09-03 Arizona Board Of Regents, A Body Corporate Acting On Behalf Of Arizona State University Gas-solid photocatalytic oxidation of environmental pollutants
US5123836A (en) * 1988-07-29 1992-06-23 Chiyoda Corporation Method for the combustion treatment of toxic gas-containing waste gas
US5160707A (en) * 1989-08-25 1992-11-03 Washington Suburban Sanitary Commission Methods of and apparatus for removing odors from process airstreams
US5183646A (en) * 1989-04-12 1993-02-02 Custom Engineered Materials, Inc. Incinerator for complete oxidation of impurities in a gas stream
US5238656A (en) * 1990-10-26 1993-08-24 Tosoh Corporation Treatment equipment of exhaust gas containing organic halogen compounds
US5252007A (en) * 1992-05-04 1993-10-12 University Of Pittsburgh Of The Commonwealth System Of Higher Education Apparatus for facilitating solids transport in a pneumatic conveying line and associated method
US5271908A (en) * 1992-04-07 1993-12-21 Intel Corporation Pyrophoric gas neutralization chamber
US5407647A (en) * 1994-05-27 1995-04-18 Florida Scientific Laboratories Inc. Gas-scrubber apparatus for the chemical conversion of toxic gaseous compounds into non-hazardous inert solids
US5510093A (en) * 1994-07-25 1996-04-23 Alzeta Corporation Combustive destruction of halogenated compounds
US5533890A (en) * 1992-12-17 1996-07-09 Thermatrix, Inc. Method and apparatus for control of fugitive VOC emissions
US5599508A (en) * 1993-06-01 1997-02-04 The Babcock & Wilcox Company Flue gas conditioning for the removal of acid gases, air toxics and trace metals
US5650128A (en) * 1994-12-01 1997-07-22 Thermatrix, Inc. Method for destruction of volatile organic compound flows of varying concentration
US5649985A (en) * 1995-11-29 1997-07-22 Kanken Techno Co., Ltd. Apparatus for removing harmful substances of exhaust gas discharged from semiconductor manufacturing process
US5693293A (en) * 1993-06-17 1997-12-02 Das-Dunnschicht Anlagen Systeme Gmbh Dresden Apparatus for the purification of waste gas
US5756052A (en) * 1995-12-26 1998-05-26 Mitsubishi Jukogyo Kabushiki Kaisha Flue gas treatment system
US5779998A (en) * 1994-04-06 1998-07-14 Atmi Ecosys Corporation Method and apparatus for concentration and recovery of halocarbons from effluent gas streams
US5800792A (en) * 1994-11-29 1998-09-01 Teisan Kabushiki Kaisha Exhaust gas treatment unit and method
US5891404A (en) * 1995-10-16 1999-04-06 Teisan Kabushiki Kaisha Exhaust gas treatment unit
US5900217A (en) * 1995-01-23 1999-05-04 Centrotherm Elektrische Anlagen Gmbh & Co. Apparatus for purifying waste gases
US5914091A (en) * 1996-02-15 1999-06-22 Atmi Ecosys Corp. Point-of-use catalytic oxidation apparatus and method for treatment of voc-containing gas streams
US5955037A (en) * 1996-12-31 1999-09-21 Atmi Ecosys Corporation Effluent gas stream treatment system having utility for oxidation treatment of semiconductor manufacturing effluent gases
US6072227A (en) * 1998-02-11 2000-06-06 Applied Materials, Inc. Low power method of depositing a low k dielectric with organo silane

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5982927A (en) 1982-11-04 1984-05-14 Toyo Sanso Kk Treatment of waste gas
JPH0365218A (en) 1989-08-04 1991-03-20 Asahi Glass Co Ltd Removal of harmful effect from nitrogen trifluoride
JPH04209524A (en) 1990-12-04 1992-07-30 Fujitsu Ltd Manufacture of semiconductor device
JP2915754B2 (en) 1993-06-25 1999-07-05 三菱重工業株式会社 Control method of strip storage device
US5665317A (en) 1995-12-29 1997-09-09 General Electric Company Flue gas scrubbing apparatus
JP3648539B2 (en) * 1996-12-31 2005-05-18 アドバンスド.テクノロジー.マテリアルス.インコーポレイテッド Exhaust flow treatment system for oxidation treatment of semiconductor manufacturing exhaust
DE29712026U1 (en) 1997-07-09 1998-11-12 Ebara Germany Gmbh Burner for the combustion of exhaust gases with at least one condensable component
JPH11276860A (en) 1998-03-27 1999-10-12 Japan Pionics Co Ltd Treatment of fluorocarbon by decomposition and decomposition treatment device

Patent Citations (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US566317A (en) * 1896-08-25 Wheat-steamer
US3898040A (en) * 1972-06-29 1975-08-05 Universal Oil Prod Co Recuperative form of thermal-catalytic incinerator
US4083607A (en) * 1976-05-05 1978-04-11 Mott Lambert H Gas transport system for powders
US4519999A (en) * 1980-03-31 1985-05-28 Union Carbide Corporation Waste treatment in silicon production operations
US4719088A (en) * 1985-02-12 1988-01-12 Mitsubish Denki Kabushiki Kaisha Apparatus for removing at least one acidic component from a gas
US4661056A (en) * 1986-03-14 1987-04-28 American Hoechst Corporation Turbulent incineration of combustible materials supplied in low pressure laminar flow
US4886444A (en) * 1987-06-19 1989-12-12 L'air Liquide Process for treating gaseous effluents coming from the manufacture of electronic components and incineration apparatus for carrying out said process
US4908191A (en) * 1987-07-21 1990-03-13 Ethyl Corporation Removing arsine from gaseous streams
US5009869A (en) * 1987-12-28 1991-04-23 Electrocinerator Technologies, Inc. Methods for purification of air
US5123836A (en) * 1988-07-29 1992-06-23 Chiyoda Corporation Method for the combustion treatment of toxic gas-containing waste gas
US5183646A (en) * 1989-04-12 1993-02-02 Custom Engineered Materials, Inc. Incinerator for complete oxidation of impurities in a gas stream
US4986838A (en) * 1989-06-14 1991-01-22 Airgard, Inc. Inlet system for gas scrubber
US5160707A (en) * 1989-08-25 1992-11-03 Washington Suburban Sanitary Commission Methods of and apparatus for removing odors from process airstreams
US5045288A (en) * 1989-09-15 1991-09-03 Arizona Board Of Regents, A Body Corporate Acting On Behalf Of Arizona State University Gas-solid photocatalytic oxidation of environmental pollutants
US5238656A (en) * 1990-10-26 1993-08-24 Tosoh Corporation Treatment equipment of exhaust gas containing organic halogen compounds
US5271908A (en) * 1992-04-07 1993-12-21 Intel Corporation Pyrophoric gas neutralization chamber
US5252007A (en) * 1992-05-04 1993-10-12 University Of Pittsburgh Of The Commonwealth System Of Higher Education Apparatus for facilitating solids transport in a pneumatic conveying line and associated method
US5533890A (en) * 1992-12-17 1996-07-09 Thermatrix, Inc. Method and apparatus for control of fugitive VOC emissions
US5599508A (en) * 1993-06-01 1997-02-04 The Babcock & Wilcox Company Flue gas conditioning for the removal of acid gases, air toxics and trace metals
US5693293A (en) * 1993-06-17 1997-12-02 Das-Dunnschicht Anlagen Systeme Gmbh Dresden Apparatus for the purification of waste gas
US5779998A (en) * 1994-04-06 1998-07-14 Atmi Ecosys Corporation Method and apparatus for concentration and recovery of halocarbons from effluent gas streams
US5407647A (en) * 1994-05-27 1995-04-18 Florida Scientific Laboratories Inc. Gas-scrubber apparatus for the chemical conversion of toxic gaseous compounds into non-hazardous inert solids
US5603905A (en) * 1994-07-25 1997-02-18 Alzeta Corporation Apparatus for combustive destruction of troublesome substances
US5510093A (en) * 1994-07-25 1996-04-23 Alzeta Corporation Combustive destruction of halogenated compounds
US5800792A (en) * 1994-11-29 1998-09-01 Teisan Kabushiki Kaisha Exhaust gas treatment unit and method
US5650128A (en) * 1994-12-01 1997-07-22 Thermatrix, Inc. Method for destruction of volatile organic compound flows of varying concentration
US5900217A (en) * 1995-01-23 1999-05-04 Centrotherm Elektrische Anlagen Gmbh & Co. Apparatus for purifying waste gases
US5891404A (en) * 1995-10-16 1999-04-06 Teisan Kabushiki Kaisha Exhaust gas treatment unit
US5649985A (en) * 1995-11-29 1997-07-22 Kanken Techno Co., Ltd. Apparatus for removing harmful substances of exhaust gas discharged from semiconductor manufacturing process
US5716428A (en) * 1995-11-29 1998-02-10 Kanken Techno Co., Ltd. Method for removing harmful substances of exhaust gas discharged from semiconductor manufacturing process
US5756052A (en) * 1995-12-26 1998-05-26 Mitsubishi Jukogyo Kabushiki Kaisha Flue gas treatment system
US5914091A (en) * 1996-02-15 1999-06-22 Atmi Ecosys Corp. Point-of-use catalytic oxidation apparatus and method for treatment of voc-containing gas streams
US5955037A (en) * 1996-12-31 1999-09-21 Atmi Ecosys Corporation Effluent gas stream treatment system having utility for oxidation treatment of semiconductor manufacturing effluent gases
US6072227A (en) * 1998-02-11 2000-06-06 Applied Materials, Inc. Low power method of depositing a low k dielectric with organo silane

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070166205A1 (en) * 1996-12-31 2007-07-19 Mark Holst Effluent gas stream treatment system having utility for oxidation treatment of semiconductor manufacturing effluent gases
US20070212288A1 (en) * 1996-12-31 2007-09-13 Mark Holst Effluent gas stream treatment system having utility for oxidation treatment of semiconductor manufacturing effluent gases
US20090010814A1 (en) * 1996-12-31 2009-01-08 Mark Holst Effluent gas stream treatment system having utility for oxidation treatment of semiconductor manufacturing effluent gases
US7695700B2 (en) 1996-12-31 2010-04-13 Applied Materials, Inc. Effluent gas stream treatment system having utility for oxidation treatment of semiconductor manufacturing effluent gases
US20050135984A1 (en) * 2003-12-19 2005-06-23 Shawn Ferron Apparatus and method for controlled combustion of gaseous pollutants
US7736599B2 (en) 2004-11-12 2010-06-15 Applied Materials, Inc. Reactor design to reduce particle deposition during process abatement
US7985379B2 (en) 2004-11-12 2011-07-26 Applied Materials, Inc. Reactor design to reduce particle deposition during process abatement
US7700049B2 (en) 2005-10-31 2010-04-20 Applied Materials, Inc. Methods and apparatus for sensing characteristics of the contents of a process abatement reactor
US7736600B2 (en) 2005-10-31 2010-06-15 Applied Materials, Inc. Apparatus for manufacturing a process abatement reactor
US20090314626A1 (en) * 2006-03-03 2009-12-24 Pascal Moine Method for treating effluents containing fluorocompounds like pfc and hfc
US20090149996A1 (en) * 2007-12-05 2009-06-11 Applied Materials, Inc. Multiple inlet abatement system
WO2010006181A2 (en) * 2008-07-11 2010-01-14 Applied Materials, Inc. Methods and apparatus for abating electronic device manufacturing process effluent
WO2010006181A3 (en) * 2008-07-11 2010-04-08 Applied Materials, Inc. Methods and apparatus for abating electronic device manufacturing process effluent
US20120100491A1 (en) * 2009-01-30 2012-04-26 Central Glass Company, Limited Semiconductor Production Equipment Including Fluorine Gas Generator
JP2015525332A (en) * 2012-04-30 2015-09-03 ハイバック コーポレイション Double coaxial processing module
GB2515017A (en) * 2013-06-10 2014-12-17 Edwards Ltd Process gas abatement
GB2515017B (en) * 2013-06-10 2017-09-20 Edwards Ltd Process gas abatement
TWI675699B (en) * 2014-09-25 2019-11-01 美商應用材料股份有限公司 Vacuum foreline reagent addition for fluorine abatement
WO2016048526A1 (en) * 2014-09-25 2016-03-31 Applied Materials, Inc. Vacuum foreline reagent addition for fluorine abatement
US11114285B2 (en) 2016-04-13 2021-09-07 Applied Materials, Inc. Apparatus for exhaust cooling
WO2018185469A1 (en) * 2017-04-04 2018-10-11 Edwards Limited Purge gas feeding means, abatement systems and methods of modifying abatement systems
US10888817B2 (en) 2017-04-04 2021-01-12 Edwards Limited Purge gas feeding means, abatement systems and methods of modifying abatement systems
US10861681B2 (en) 2017-05-19 2020-12-08 Applied Materials, Inc. Apparatus for collection and subsequent reaction of liquid and solid effluent into gaseous effluent
WO2018212940A1 (en) * 2017-05-19 2018-11-22 Applied Materials, Inc. Apparatus for collection and subsequent reaction of liquid and solid effluent into gaseous effluent
WO2023097105A1 (en) * 2021-11-29 2023-06-01 Evoqua Water Technologies Llc Pfas treatment using gac, reactivation and thermal destruction

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