WO2011027196A1 - Process for the preparation of expandable vinyl aromatic polymers with a reduced thermal conductivity by polymerization in suspension - Google Patents
Process for the preparation of expandable vinyl aromatic polymers with a reduced thermal conductivity by polymerization in suspension Download PDFInfo
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- WO2011027196A1 WO2011027196A1 PCT/IB2010/001983 IB2010001983W WO2011027196A1 WO 2011027196 A1 WO2011027196 A1 WO 2011027196A1 IB 2010001983 W IB2010001983 W IB 2010001983W WO 2011027196 A1 WO2011027196 A1 WO 2011027196A1
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- vinyl aromatic
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0019—Use of organic additives halogenated
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/08—Styrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0028—Use of organic additives containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/16—Making expandable particles
- C08J9/20—Making expandable particles by suspension polymerisation in the presence of the blowing agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2325/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
- C08J2325/02—Homopolymers or copolymers of hydrocarbons
Definitions
- the present invention relates to a process for the preparation of expandable vinyl aromatic polymers, with a reduced thermal conductivity, by polymerization in suspension .
- the present invention relates to a process for the preparation of expandable vinyl aromatic polymers by polymerization in suspension and the expandable compositions based on vinyl aromatic polymers thus obtained, capable of giving expanded articles with a low density and improved insulating capacity.
- the present invention also relates to expanded articles of vinyl aromatic polymers having a density ranging from 5 to 50 g/1, preferably from 10 to 25 g/1, having excellent thermal insulation properties, expressed by a thermal conductivity ranging from 25 to 50 mW/mK, preferably from 30 to 45 mW/mK, which is generally, on an average, even more 10% lower than that of equivalent expanded articles obtained from conventional materials currently on the market, for example EXTIR A-5000 of Polimeri Europa S.p.A.
- These expanded articles are stable to deformations induced by exposure to solar radiations.
- EPS expandable polystyrene
- These expanded products are obtained by first swelling the polymer beads, in a closed environment, impregnated with an expandable fluid, for example an aliphatic hydrocarbon such as pentane or hexane, and then molding the swollen particles contained inside a mould, by means of the contemporaneous effect of pressure and temperature.
- an expandable fluid for example an aliphatic hydrocarbon such as pentane or hexane
- the swelling of the particles is generally effected with vapour, or another gas, maintained at a temperature slightly higher than the glass transition temperature (Tg) of the polymer.
- expanded polystyrene As already mentioned, a particular applicative field of expanded polystyrene is that of thermal insulation in the building industry where it is generally used in the form of flat sheets.
- the flat expanded polystyrene sheets are normally used with a density of about 25-30 g/1 as the thermal conductivity of the polymer has a minimum at these values. It is not advantageous to fall below this density, even if it is technically possible, as it causes a drastic increase in the thermal conductivity of the sheet which must be compensated by an increase in its thickness.
- thermo-insulating articles with a density even lower than 20 g/1, with a high insulating capacity, without having insulating reductions to be compensated with increases in thickness.
- thermo-insulating articles in expanded polystyrene filled with athermanous materials, in particular graphite and/or carbon black, have the disadvantage of become easily deformed when exposed to solar irradiation, also for short periods of time, as the expanded particles of which they consist tend to collapse .
- the Applicant has now found that it is possible to prepare a flame-retardant expandable polystyrene, without the above drawbacks, i.e. capable of giving articles (e.g. sheets) with a thermal conductivity, for example, of about 34-36 mW/mk at 17 g/1 and with a compression stress, at 10% of deformation, of 75 KPa at 14 g/1, and therefore almost identical to that of a reference EPS, thanks to an optimum cell diameter of about 120-130 microns.
- the thermal conductivity of the sheets is substantially identical to that of EPS modified with athermanous materials. Possible deficits can be compensated by a moderate increase in the thickness .
- An object of the present invention therefore relates to a process for the preparation of beads of flame-retardant expandable vinyl aromatic polymers, capable of producing expanded articles with a reduced thermal conductivity, by means of polymerization in aqueous suspension which comprises polymerizing at least one vinyl aromatic monomer, for example styrene or a mixture of styrene containing up to 25% by weight of -methylstyrene, in aqueous suspension in the presence of a peroxide initiator system, active at a temperature higher than 80°C, an expanding agent, added before, during or after the polymerization, and in the presence of :
- RiCONHCH 2 -CH 2 NHCOR 2 (I) wherein Ri and R 2 , the same or different, represent an (iso)alkyl radical CH 3 (CH 2 ) n with n ranging from 10 to 20, preferably from 16 to 18, a C 6 -C 12 aromatic or C 7 -C 2 5 alkylaromatic radical; and
- a flame-retardant system comprising a brominated additive with a bromine content higher than 30% by weight .
- the amide having general formula (I) is added in a quantity ranging from 5 to 5,000 ppm, with respect to the weight of the monomeric base, preferably 10 to 500 ppm.
- the preferred product is N, ' ethylene-bis-stearamide .
- vinyl aromatic monomer as used in the present description and claims, essentially means a product corresponding to the following general formula (ID :
- R is a hydrogen or a methyl group
- n is zero or an integer ranging from 1 to 5
- Y is a halogen, such as chlorine or bromine, or an alkyl or alkoxyl radical having 1 to 4 carbon atoms .
- vinyl aromatic monomers having the general formula identified above are: styrene, a- methylstyrene, para-methylstyrene, ethylstyrene , butylstyrene , dimethylstyrene , mono-, di-, tri-, tetra- and penta-chlorostyrene, bromo- styrene , methoxystyrene , acetoxystyrene, etc.
- Preferred vinyl aromatic monomers are styrene, a-methylstyrene and para-methylstyrene.
- the vinyl aromatic monomers having general formula (II) can be used alone or in a mixture of up to 50% by weight with other co-polymerizable monomers.
- said monomers are (meth) acrylic acid, Ci - C 4 alkyl esters of (meth) acrylic acid such as methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, isopropyl acrylate, butyl acrylate, amides and nitriles of (meth) acrylic acid such as acrylamide, methacrylamide , acrylonitrile , methacrylonitrile, butadiene, ethylene, divinyl benzene, maleic anhydride, etc.
- Preferred co- polymerizable monomers are acrylonitrile and methyl methacrylate .
- expanding agent capable of being englobed in the polymeric vinyl aromatic matrix can be used in the process, object of the present invention.
- Typical examples of expanding agents are aliphatic hydrocarbons, Freon, carbon dioxide, alcohols such as ethyl alcohol, etc..
- the expanding agents can be selected from aliphatic or cyclo-aliphatic hydrocarbons containing 3 to 6 carbon atoms such as n-pentane, iso-pentane, cyclopentane or mixtures thereof; halogenated derivatives of aliphatic hydrocarbons containing 1 to 3 carbon atoms, such as, for example, dichlorodifluoromethane, 1, 2 , 2-trifluoro-ethane , 1,1,2- trifluoroethane ; carbon dioxide; and ethyl alcohol.
- the expanding agents are added in a quantity ranging from 1 to 10% by weight, with respect to the monomeric base, preferably during the polymerization phase, or subsequently by means of the re-suspension technology.
- the latter comprises the phases of :
- additives for example a flame- retardant system
- a flame-retardant system can be added, containing from 0.1 to 3% by weight, with respect to the monomeric base, preferably from 0.4 to 2.2%, of a self- extinguishing brominated additive containing at least 30% by weight of bromine, preferably from 50 to 90% by weight, and 0 to 1% by weight, with respect to the monomeric base, preferably 0.01 to 0.4%, of a synergic product containing at least one C-C or C-O-O-C thermolabile bond, as described hereunder.
- Flame- retardant agents particularly suitable for the present invention are brominated aliphatic, cycloaliphatic , aromatic compounds, for example C 6 - Ci 8 , such as hexabromocyclododecane (EBCD) , pentabromomonochlorocyclohexane and pentabromophenyl allyl ether, bis -tetrabromobisphenol-A allyl ether, the latter known on the market as "Chemtura BE51" , of the company Chemtura, etc.
- EBCD hexabromocyclododecane
- pentabromomonochlorocyclohexane and pentabromophenyl allyl ether
- bis -tetrabromobisphenol-A allyl ether the latter known on the market as "Chemtura BE51" , of the company Chemtura, etc.
- Synergic products which can be used are dicumyl peroxide (DCP) , cumene hydroperoxide, 3 , 4 -dimethyl-3 , 4 -diphenyl-hexane , 2 , 3 -dimethyl- 2 , 3- diphenyl butane, 3 , 6 , 9- triethyl-3 , 6 , 9 - trimethyl-1 , 4 , 7 - triperoxynonane , etc.
- DCP dicumyl peroxide
- cumene hydroperoxide 3 , 4 -dimethyl-3 , 4 -diphenyl-hexane
- 2 , 3 -dimethyl- 2 3- diphenyl butane
- bearings as used in the present description and claims, essentially refers to the form of
- This process can alternatively also comprise the dissolution/dispersion of the flame-retardant system, and/or other additive, in the vinyl aromatic monomer, as previously defined, and the suspension in water of the monomeric mixture, followed by polymerization in the presence of possible polymerization additives, known to experts in the field, among which stabilizing agents of the suspension, chain transfer agents, expansion coadjuvants, nucleating agents, plasticizers , etc.
- the "beads" thus obtained have a substantially spherical form, both before and after expansion.
- the beads are prepared by polymerization in aqueous suspension using inorganic salts of phosphoric acid, for example tri-calcium phosphate or magnesium pyrophosphate, as suspending agents. These salts can be added to the polymerization mixture either already finely subdivided or synthesized in situ by reaction, for example, between sodium pyrophosphate and magnesium sulfate .
- inorganic salts of phosphoric acid for example tri-calcium phosphate or magnesium pyrophosphate
- Said inorganic salts can be assisted in their suspending action by anionic surface-active agents, for example sodium dodecylbenzene sulfonate or their precursors such as sodium metabisulfite , as described in US patent 3,631,014.
- anionic surface-active agents for example sodium dodecylbenzene sulfonate or their precursors such as sodium metabisulfite , as described in US patent 3,631,014.
- the polymerization can also be carried out in the presence of organic suspending agents such as polyvinylpyrrolidone, polyvinyl alcohol, etc..
- the polymerization reaction is generally triggered by an initiating system.
- the initiating system normally comprises two peroxides, the first with a halving time of an hour at 85-95°C (for example dibenzoyl peroxide) and the other with a halving time of an hour at 110-120°C (examples are tert-butylperoxy-2-ethylhexanoate and tert- butylperbenzoate) .
- the vinyl aromatic polymer which is obtained at the end of the polymerization has an average molecular weight Mw ranging from 50,000 to 300,000, preferably from 70,000 to 250,000.
- Mw average molecular weight
- the viscosity of the reagent mixture (vinyl aromatic monomeric base plus possible additives) , to be suspended in water, by dissolving vinyl aromatic polymer therein, up to a concentration of 1 to 30% by weight, preferably 5 to 20%, calculated with respect to the monomeric base.
- the solution can be obtained by dissolving a preformed polymer in the reagent mixture (for example fresh polymer or waste- products from previous polymerizations and/or expansions) or by a mass pre-polymerization of the monomer, or mixture of monomers, until the previously mentioned concentrations are obtained, and subsequently continuing the polymerization in aqueous suspension, possibly in the presence of the remaining additives .
- substantially spherical beads of expandable polymer are obtained, with an average diameter ranging from 0.2 to 2 mm, preferably from 1 to 1.5 mm.
- the beads are then discharged from the polymerization reactor and washed, in continuous or batchwise, with non-ionic surface-active agents or, alternatively, with acids, as described in US patent 5,041,465.
- the polymer beads can then be treated thermally with hot air ranging from 30 to 60°C.
- the expandable beads obtained are subjected to pre-treatment which is generally applied to conventional expandable compositions and which essentially consists in:
- a liquid antistatic agent selected from amines, ethoxylated tertiary alkylamines, ethylene oxide/propylene oxide copolymers, etc.. Said agent is used to adhere the coating and to facilitate the screening of the beads prepared in suspension;
- said coating essentially consisting of a mixture of mono-, di- and tri-esters of glycerine (or other alcohols) with fatty acids, and metal stearates such as zinc and/or magnesium stearate .
- a further object of the present invention relates to expandable compositions in vinyl aromatic-based beads capable of providing low-density expanded products and with an improved insulating capacity which comprise :
- a a matrix obtained by polymerizing 50-100% by weight of one or more vinyl aromatic monomers, for example styrene or a mixture of styrene containing up to 25% by weight of a- methylstyrene, and 0-50% by weight of at least one copolymerizable monomer; b. 1-10% by weight, calculated with respect to the polymeric matrix (a), of an expanding agent;
- thermolabile C-O-O-C or C-C bond d. 0-1% by weight, preferably 0.01-0.4%, calculated with respect to the polymeric matrix (a) , of a synergic agent (c) containing at least one thermolabile C-O-O-C or C-C bond;
- a mixture is charged into a closed and stirred container, consisting of 150 parts by weight of water, 0.2 parts of sodium pyrophosphate, 97 parts of styrene, 3 parts of alpha-methylstyrene , 0.30 parts of dibenzoyl peroxide, 0.25 parts of tert-butylperbenzoate, 0.70 parts of hexabromocyclododecane Saytex HP 900 sold by Albemarle, 0.2 parts of dicumyl peroxide and 0.002 parts of N, N' ethylene-bis-stearamide wax sold by Sogis with the trade-name of Waxo . The mixture is heated under stirring to 90°C.
- the beads of expandable polymer thus produced are subsequently recovered and washed with demineralized water containing 0.05% of a non-ionic surface-active agent consisting of a fatty alcohol condensed with ethylene oxide and propylene oxide, sold by Huntsman under the trade-name of Empilan 2638.
- the granules are then dried in a stream of warm air, with the addition of 0.02% of a non- ionic surface-active agent, consisting of a condensate of ethylene oxide and propylene oxide on a glycerine base, sold by Dow (Voranol CP4755) and are screened separating the fraction with a diameter ranging from 1 to 1.5 mm. This fraction proved to represent 40%, 30% being the fraction between 0.5 and 1 mm, 15% the fraction between 0.2 and 0.5 mm, and 15% the gross fraction, between 1.5 and 3 mm.
- the product is pre-expanded with vapour at a temperature of 100°C, at two densities, i.e. 14 and 17 g/1, left to age for 1 day and used for the moulding of blocks (having dimensions of 1040 x 1030 x 550 mm)
- the diameter of the cells of beads expanded at 17 g/1 was 120-130 microns.
- the blocks were then cut to prepare flat sheets on which the thermal conductivity and compression stress at 10% of deformation are measured.
- the thermal conductivity measured after 5 days of residence in an oven at 70°C, was 36.5 mW/mK at 14 g/1 and 34 mW/mK at 17 g/1.
- the compression stress at 10% of deformation, measured at 14 g/1 was 75 KPa.
- Test-samples were taken from a sheet for the fire behaviour test according to the regulation DIN 4102. The test-samples passed the test .
- Example 1 is repeated but increasing the axo wax to 0.01 parts. The thermal conductivity and all the other characteristics, including the fire behaviour test, remained unvaried.
- Example 1 was repeated, but substituting the axo wax with 0.002 parts of polyethylene wax having a low molecular weight ( ⁇ 5,000 g/mol) and a melting point of 113 °C.
- the thermal conductivity proved to be comparable to that of Example 1 (37 mW/mk at 14 g/1) as also the fire behaviour test (passed) .
- the compression stress at 10% of deformation, measured at 14 g/1 proved to be lower (60 KPa) , the cell diameter of the expanded beads was in fact 220-230 microns.
- Example 1 was repeated, but without the addition of hexabromocyclododecane .
- the expandable polymer beads thus produced were then recovered and subjected to the same processing as Example 1.
- the thermal conductivity proved to be 41 mW/mk at 14 g/1.
- the compression stress at 10% of deformation, measured at 14 g/1 proved to be 80 KPa - the cell diameter of the expanded beads was 90-100 microns.
- Test samples were taken from a sheet for the fire behaviour test according to the regulation DIN 4102: the test samples did not pass the test.
Abstract
Description
Claims
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES10754550.1T ES2526997T3 (en) | 2009-09-07 | 2010-08-06 | Process for the preparation of expandable aromatic vinyl polymers with reduced thermal conductivity by suspension polymerization |
RU2012110977/04A RU2526045C2 (en) | 2009-09-07 | 2010-08-06 | Method of producing foamed vinyl aromatic polymers with low thermal conductivity by suspension polymerisation |
PL10754550T PL2475709T3 (en) | 2009-09-07 | 2010-08-06 | Process for the preparation of expandable vinyl aromatic polymers with a reduced thermal conductivity by polymerization in suspension |
JP2012528461A JP2013503959A (en) | 2009-09-07 | 2010-08-06 | Process for producing foamable vinyl aromatic polymers with low thermal conductivity by polymerization in suspension |
EP20100754550 EP2475709B1 (en) | 2009-09-07 | 2010-08-06 | Process for the preparation of expandable vinyl aromatic polymers with a reduced thermal conductivity by polymerization in suspension |
BR112012004860A BR112012004860A2 (en) | 2009-09-07 | 2010-08-06 | process for the preparation of flame retardant expandable aromatic vinyl polymer beads, expandable bead compositions, and expanded articles |
CN2010800390093A CN102575037A (en) | 2009-09-07 | 2010-08-06 | Process for the preparation of expandable vinyl aromatic polymers with a reduced thermal conductivity by polymerization in suspension |
US13/393,843 US9115253B2 (en) | 2009-09-07 | 2010-08-06 | Process for the preparation of expandable vinyl aromatic polymers with a reduced thermal conductivity by polymerization in suspension |
MX2012002778A MX342325B (en) | 2009-09-07 | 2010-08-06 | Process for the preparation of expandable vinyl aromatic polymers with a reduced thermal conductivity by polymerization in suspension. |
HK12109382.3A HK1168615A1 (en) | 2009-09-07 | 2012-09-24 | Process for the preparation of expandable vinyl aromatic polymers with a reduced thermal conductivity by polymerization in suspension |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITMI2009A001543 | 2009-09-07 | ||
ITMI2009A001543A IT1395379B1 (en) | 2009-09-07 | 2009-09-07 | PROCEDURE FOR THE PREPARATION OF EXPANDABLE VINYLAROMATIC POLYMERS WITH REDUCED THERMAL CONDUCTIVITY BY MEANS OF SUSPENSION POLYMERIZATION |
Publications (1)
Publication Number | Publication Date |
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WO2011027196A1 true WO2011027196A1 (en) | 2011-03-10 |
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ID=42061118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/IB2010/001983 WO2011027196A1 (en) | 2009-09-07 | 2010-08-06 | Process for the preparation of expandable vinyl aromatic polymers with a reduced thermal conductivity by polymerization in suspension |
Country Status (13)
Country | Link |
---|---|
US (1) | US9115253B2 (en) |
EP (1) | EP2475709B1 (en) |
JP (1) | JP2013503959A (en) |
CN (1) | CN102575037A (en) |
BR (1) | BR112012004860A2 (en) |
ES (1) | ES2526997T3 (en) |
HK (1) | HK1168615A1 (en) |
IT (1) | IT1395379B1 (en) |
MX (1) | MX342325B (en) |
PL (1) | PL2475709T3 (en) |
PT (1) | PT2475709E (en) |
RU (1) | RU2526045C2 (en) |
WO (1) | WO2011027196A1 (en) |
Families Citing this family (1)
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CN108137845B (en) * | 2015-10-20 | 2021-08-17 | 巴斯夫欧洲公司 | System and method for producing cast-in-place foam |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4393147A (en) * | 1982-11-22 | 1983-07-12 | Cosden Technology, Inc. | Expandable polymeric styrene particles |
WO2002012377A2 (en) * | 2000-08-08 | 2002-02-14 | The Dow Chemical Company | Flame retardant foam from blends of vinyl aromatic and olefinic polymers |
WO2008141767A2 (en) * | 2007-05-18 | 2008-11-27 | Polimeri Europa S.P.A. | Composite material based on vinyl aromatic polymers having enhanced thermal insulation properties and process for the preparation thereof |
EP2025691A2 (en) * | 2007-07-26 | 2009-02-18 | Korea Kumho Petrochemical Co., Ltd. | Method for producing expandable polystrene beads which have excellent heat insulation properties |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
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GB2048276B (en) * | 1979-03-20 | 1983-03-30 | Labofina Sa | Fireretardant polystyrenic compositions |
US4692471A (en) * | 1986-08-11 | 1987-09-08 | Atlantic Richfield Company | Expandable polypropylene interpolymer particles |
IT1289606B1 (en) | 1997-01-30 | 1998-10-15 | Enichem Spa | PROCEDURE FOR THE PRODUCTION OF EXPANDABLE PARTICLES OF STYRENE POLYMERS |
JP4035979B2 (en) | 2000-10-20 | 2008-01-23 | 株式会社カネカ | Expandable polystyrene resin particles and method for producing the same |
ITMI20012168A1 (en) | 2001-10-18 | 2003-04-18 | Enichem Spa | EXPANDABLE VINYLAROMATIC POLYMERS AND PROCEDURE FOR THEIR PREPARATION |
ITMI20020584A1 (en) | 2002-03-20 | 2003-09-22 | Polimeri Europa Spa | COMPOSITIONS BASED ON VINYLAROMATIC POLYMERS EXPANDABLE WITH IMPROVED EXPANDABILITY |
JP2003335891A (en) * | 2002-05-21 | 2003-11-28 | Kanegafuchi Chem Ind Co Ltd | Expandable polystyrene resin particle, polystyrene expansion molded product and its preparation process |
ITMI20021711A1 (en) * | 2002-07-31 | 2004-02-01 | Polimeri Europa Spa | VINYLAROMATIC POLYMERS EXPANDABLE IN PEARLS AND PROCEDURE FOR THEIR PREPARATION. |
ITMI20030627A1 (en) * | 2003-03-31 | 2004-10-01 | Polimeri Europa Spa | EXPANDABLE VINYLAROMATIC POLYMERS AND PROCEDURE FOR THEIR PREPARATION. |
JP4990814B2 (en) * | 2008-02-18 | 2012-08-01 | 積水化成品工業株式会社 | Process for producing modified polystyrene resin particles, pre-expanded particles, and expanded molded article. |
ITMI20080823A1 (en) | 2008-05-07 | 2009-11-08 | Polimeri Europa Spa | COMPOSITIONS OF VINYLAROMATIC POLYMERS EXPANDABLE TO IMPROVED THERMAL INSULATION CAPACITY, PROCEDURE FOR THEIR PREPARATION AND ITEMS EXPANDED BY THEM |
IT1392391B1 (en) | 2008-12-19 | 2012-03-02 | Polimeri Europa Spa | COMPOSITIONS OF VINYLAROMATIC POLYMERS EXPANDABLE TO IMPROVED THERMAL INSULATION CAPACITY, PROCEDURE FOR THEIR PREPARATION AND ITEMS EXPANDED BY THEM OBTAINED |
IT1393962B1 (en) | 2009-05-05 | 2012-05-17 | Polimeri Europa Spa | EXPANDED ITEMS WITH EXCELLENT SOLAR IRRADIATION RESISTANCE AND EXCELLENT THERMO-INSULATING AND MECHANICAL PROPERTIES |
-
2009
- 2009-09-07 IT ITMI2009A001543A patent/IT1395379B1/en active
-
2010
- 2010-08-06 MX MX2012002778A patent/MX342325B/en active IP Right Grant
- 2010-08-06 CN CN2010800390093A patent/CN102575037A/en active Pending
- 2010-08-06 RU RU2012110977/04A patent/RU2526045C2/en active
- 2010-08-06 BR BR112012004860A patent/BR112012004860A2/en active IP Right Grant
- 2010-08-06 US US13/393,843 patent/US9115253B2/en not_active Expired - Fee Related
- 2010-08-06 JP JP2012528461A patent/JP2013503959A/en active Pending
- 2010-08-06 PL PL10754550T patent/PL2475709T3/en unknown
- 2010-08-06 PT PT107545501T patent/PT2475709E/en unknown
- 2010-08-06 EP EP20100754550 patent/EP2475709B1/en active Active
- 2010-08-06 ES ES10754550.1T patent/ES2526997T3/en active Active
- 2010-08-06 WO PCT/IB2010/001983 patent/WO2011027196A1/en active Application Filing
-
2012
- 2012-09-24 HK HK12109382.3A patent/HK1168615A1/en not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4393147A (en) * | 1982-11-22 | 1983-07-12 | Cosden Technology, Inc. | Expandable polymeric styrene particles |
WO2002012377A2 (en) * | 2000-08-08 | 2002-02-14 | The Dow Chemical Company | Flame retardant foam from blends of vinyl aromatic and olefinic polymers |
WO2008141767A2 (en) * | 2007-05-18 | 2008-11-27 | Polimeri Europa S.P.A. | Composite material based on vinyl aromatic polymers having enhanced thermal insulation properties and process for the preparation thereof |
EP2025691A2 (en) * | 2007-07-26 | 2009-02-18 | Korea Kumho Petrochemical Co., Ltd. | Method for producing expandable polystrene beads which have excellent heat insulation properties |
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RU2526045C2 (en) | 2014-08-20 |
US20120184636A1 (en) | 2012-07-19 |
ITMI20091543A1 (en) | 2011-03-08 |
RU2012110977A (en) | 2013-10-20 |
BR112012004860A2 (en) | 2016-04-05 |
MX2012002778A (en) | 2012-06-25 |
US9115253B2 (en) | 2015-08-25 |
HK1168615A1 (en) | 2013-01-04 |
JP2013503959A (en) | 2013-02-04 |
MX342325B (en) | 2016-09-26 |
CN102575037A (en) | 2012-07-11 |
EP2475709B1 (en) | 2014-10-01 |
PL2475709T3 (en) | 2015-04-30 |
EP2475709A1 (en) | 2012-07-18 |
IT1395379B1 (en) | 2012-09-14 |
ES2526997T3 (en) | 2015-01-19 |
PT2475709E (en) | 2015-01-14 |
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