CA2547676A1 - Copolymers of vinyl alcohol and itaconic acid for use in paper coatings - Google Patents

Copolymers of vinyl alcohol and itaconic acid for use in paper coatings Download PDF

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CA2547676A1
CA2547676A1 CA002547676A CA2547676A CA2547676A1 CA 2547676 A1 CA2547676 A1 CA 2547676A1 CA 002547676 A CA002547676 A CA 002547676A CA 2547676 A CA2547676 A CA 2547676A CA 2547676 A1 CA2547676 A1 CA 2547676A1
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mol
pva
itaconic acid
composition
copolymer
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CA2547676C (en
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Elliott Echt
Peter A. Morken
G. Michael Collins
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Kuraray Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D129/00Coating compositions based on 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 alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Coating compositions based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Coating compositions based on derivatives of such polymers
    • C09D129/02Homopolymers or copolymers of unsaturated alcohols
    • C09D129/04Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/20Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/36Coatings with pigments
    • D21H19/44Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
    • D21H19/56Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H19/58Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/36Coatings with pigments
    • D21H19/44Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
    • D21H19/56Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H19/60Polyalkenylalcohols; Polyalkenylethers; Polyalkenylesters

Abstract

The present invention is a composition useful for coating the surface of paper wherein the coating composition is an aqueous solution comprising less than 40 wt% water and consisting essentially of a polyvinyl alcohol copolymer that is at least about 95% hydrolyzed, and a process for preparing the same.

Description

TITLE
Copolymers of Vinyl Alcohol and Itaconic Acid for Use in Paper Coatings BACKGROUND OF THE INVENTION
Field of the Invention s This invention relates to polyvinyl alcohol copolymers for use in paper coatings.
Description of the prior art In the process of producing coated paper, paper coatings are applied to the surface of a paper product to obtain the coated paper. The io paper coating can include various components, including polyvinyl alcohol.
Other components may include calcium carbonate, clays such as hydrous aluminum silicates of the kaolin variety or hydrated silica clays, titanium dioxide, blanc fixe, lithopone, and zinc sulfide. Other components of a conventional paper coating composition can include, for example, mineral is pigments, pigment binders, thickeners, humectants, and lubricants - all in various proportions. Paper coatings used to produce coated papers can include high percentages of solids, and such solids levels can approach 70%. Polyvinyl alcohol can be used as a clear coat and also as a co-binder with latex in coated papers. Typically in paper coatings 2o applications polyvinyl alcohol is used and applied as an aqueous composition that typically comprises other components. It can be, and often is, desirable to use high solids paper coatings for more efficient production of coated paper.
However, polyvinyl alcohol (PVA) is difficult to prepare as an 2s aqueous solution of more than 30% solids, and above this level dispersing the polyvinyl alcohol in water becomes very difficult and the resulting solution viscosity very high. To obtain even this degree of solution, an aqueous mixture that includes PVA is typically heated, or "cooked" to achieve complete solution and the resulting PVA solution is then added to 3o a paper coating composition. In paper coatings applications, the amount of water required to deliver an aqueous PVA solution is detrimental, or at least undesirable, in the paper coating composition. It is much preferred for paper coatings applications to use as little water as possible and as a result mixtures having 70% or more of water are not desirable in paper coatings applications. The difficulties in dissolving polyvinyl alcohol in water can cause problems with the process of applying the coating. For example, there can be difficulties getting PVA dispersed into the coating s mixture and evenly distributed on the paper surface with insoluble PVA.
U.S. Pat. No. 5,527,852 describes a particulate PVA slurry as a paper coating agent which can be prepared using PVA having an average particle diameter of from 0.01 to 1 Vim. The PVA slurry described therein is said to be useful when applied to paper as a slurry wherein the PVA is ~o substantially insoluble in cold water, and thereafter dissolves during the drying process to form a film on the surface of the paper.
U.S. Pat. No. 5,057,570 describes a PVA that is partially hydrolyzed, which can be added without additional water to a paper coating composition, and thereby avoids increasing the amount of water in is the paper coating composition. However, it can be desirable to use fully hydrolyzed PVA rather than partially hydrolyzed PVA. Also, it can be desirable to use a higher molecular weight PVA polymer than described in U.S. Pat. No. 5,057,570. Each of these differences can reduce the solubility of the PVA in water, and thus negate the ability to dissolve the 2o dry PVA in a high solids paper coating composition. It is also recognized that if the partially hydrolyzed PVA is not given time to fully dissolve, quality problems with the coating or the coated paper can be encountered.
US 2004/0186034 describes a water-soluble PVA copolymer film composition.
2s It can be desirable to dissolve a fully hydrolyzed PVA having a relatively high degree of polymerization in a high solids paper coating composition.
2 SUMMARY OF THE INVENTION
In one aspect, the present invention is a composition useful for coating the surface of paper wherein the coating composition is an aqueous composition comprising less than 40 wt% water and consisting s essentially of a polyvinyl alcohol copolymer that is at least about 95%
hydrolyzed.
In another aspect, the present invention is a method for preparing a high-solids PVA-containing paper coating composition comprising the step of: adding, as a dry solid component, a PVA copolymer comprising at io least about 1 mol% of itaconic acid as a comonomer and completely dissolving the PVA copolymer.
In another embodiment, the present invention is a method for preparing a high-solids PVA-containing paper coating composition comprising the step of: adding, as a dry solid component, a PVA
is copolymer that is a terpolymer comprising less than about 8 mol% of itaconic acid as a comonomer.
In another aspect the present invention is a terpolymer composition comprising vinyl alcohol, methyl acrylate, and itaconic acid moieties, wherein: (i) the terpolymer comprises less than about 5 mol% of vinyl 2o acetate moieties; (ii) the methyl acrylate fragment is present in an amount of at least about 1 mol% up to about 9 mol%; (iii) the itaconic acid is present in an amount of at least about 1 mol% up to about 9 mol%, and, (iv) the methyl acrylate is in the form of a lactone.
DETAILED DESCRIPTION
2s In one embodiment, the present invention is a high solids paper coating composition comprising fully hydrolyzed PVA. For the purposes of the present invention, "high solids" as the term is used herein shall denote aqueous compositions which are prepared by dissolving or dispersing solid materials in water, and where water is the only component that is a 30 liquid at 25 °C and 1 atmosphere pressure. A high solids coating composition of the present invention is one that comprises less than about 40 wt% water. It can be desirable in the practice of the present invention to use as little water as possible, and so any amount of water which is less
3 than about 40 wt% of the total coating composition is desirable, with the proviso that the composition comprises fully hydrolyzed PVA copolymer that is completely dissolved in the aqueous phase of the coating composition.
s A coating composition of the present invention can comprise or consist essentially of other materials such as minerals and pigments, for example, that are not completely dissolved and thus provide a coating suspension, slurry, or dispersion. For the purposes of the present invention no distinction will be made between a suspension, slurry, or io dispersion and each will be considered as included in the term "coating composition".
A coating composition of the present invention can additionally comprise other components that are known and conventional for use in paper coating applications. For example pigments, minerals, fillers, pH
is control agents, surfactants, latexes, or dyes -- any of which can be considered conventional to paper coatings applications -- are contemplated as useful in the practice of the present invention.
A coating composition of the present invention can comprise PVA
solids up to about 20 wt% of the mineral portion of the coating. In one 2o embodiment, the PVA solids of the present invention is a PVA/acid copolymer consisting essentially of the copolymer obtained by copolymerization of vinyl acetate with itaconic acid, followed by complete hydrolysis of the acetate moieties to yield the PVA/acid copolymer. For the purposes of the present invention, complete hydrolysis shall mean 2s hydrolysis of at least about 95% of the acetate moieties. Preferably, the coating composition comprises from about 0.5% to about 20 wt% PVA
solids relative to the weight of the pigment. More preferably, the coating composition comprises from about 1 % to about 2 wt% PVA solids.
PVA copolymers of the present invention can be obtained by known 3o and conventional methods. PVA is typically obtained by polymerization of vinyl acetate monomer, followed by conversion of the vinyl acetate polymer to the vinyl alcohol polymer. PVA copolymers are obtained by introducing one or more additional monomers into the polymerization vessel with vinyl acetate, and hence the term is inclusive of dipolymers,
4 terpolymers, and/or higher degrees of copolymers. Terpolymers are obtained by copolymerization of three monomers.
As used herein, the term complete hydrolysis shall mean that a sufficient amount of reagent has been added to convert at least about s 95%, preferably at least about 97%, and most preferably at least about 99% of the acetate groups of a polyvinyl acetate copolymer. PVA
copolymers of the present invention may include other carboxylic acid or carboxylic ester functional groups. In such copolymers, vinyl alcohol moieties can react with acid or ester groups to form lactone functional io groups. Therefore, in the practice of the present invention the extent of PVA hydrolysis is indicated by the presence of either or both vinyl alcohol and/or lactone structures. A PVA copolymer of the present invention can comprise some residual un-hydrolyzed acetate moieties. Preferably a PVA copolymer of the present invention comprises less than about 5 is mol% residual acetate moieties, more preferably less than about 3 mol%, and most preferably less than about 1 mol%.
The PVA/acid copolymer of the present invention comprises from about 1 mol% to about 10 mol% itaconic acid. Preferably the PVA acid copolymer comprises from about 2 to about 8 mol% itaconic acid, and 2o most preferably from about 3 to about 6 mol% itaconic acid.
The degree of polymerization of the PVA acid copolymer is from about 400 to about 4000. Preferably the degree of polymerization of the PVA copolymer is from about 500 to about 2000.
In another embodiment, the PVA acid copolymer of the present 2s invention is a terpolymer comprising vinyl alcohol and itaconic acid components, and additionally comprising a second acid polymer component that is either an acrylic or methyl acrylate unit. A PVA mixed acid terpolymer of the present invention can be preferred in some cases.
For the purposes of the present invention, functional equivalents of 3o itaconic acid can include mono- and/or diesters of itaconic acid.
In another embodiment, the present invention is a method for preparing high solids aqueous paper coating compositions from a completely hydrolyzed PVA acid copolymer. In the practice of the present invention, the completely hydrolyzed PVA acid copolymer can be added as a dry solid to water, or alternatively added in any manner that will provide an aqueous PVA paper coating solution comprising less than 40 wt% water. In the practice of the present invention, a heating step is not required for effective dissolution of the PVA acid copolymer described s herein.
The PVA paper coating solution composition can be prepared at a temperature of less than about 30°C. Particularly, the paper coating composition can be prepared at a temperature above about 15 °C up to and including a temperature of about 30°C. Preferably, paper coating io composition can be prepared at a temperature of from about 18 °C to about 30°C.
The method of the present invention can comprise various other steps or procedures that are known and/or conventional in processes for preparing high solids paper coatings. Such steps as mixing or dispersing is the components are considered conventional.
In still another embodiment, the present invention is an article comprising a coated paper, wherein the paper comprises a coating of a PVA acid copolymer, wherein the copolymer comprises itaconic acid.
In still another embodiment, the present invention is a polyvinyl 2o alcohol terpolymer composition wherein the terpolymer comprises vinyl alcohol, an alkyl acrylate, and itaconic acid moieties. The terpolymer comprises at least about 90 mol% vinyl alcohol. Preferably the vinyl alcohol is present in an amount of at least about 91 mol%, more preferably the vinyl alcohol is present in an amount of at least about 92 2s mol%, and most preferably at least about 94 mol%. The terpolymer further comprises itaconic acid in an amount of from at least about 1.0 mol% up to about 9 mol%, and an alkyl acrylate is present in an amount of from at least about 1 mol% up to about 9 mol%.
Equivalents of itaconic acid can be useful in the practice of the 3o present invention. For example, 2-acrylamido 2-methylpropane sulfonic acid (AMPS) is a commercially available monomer that can be used in the same manner as itaconic acid in the practice of the present invention.
The preparation of PVA/AMPS copolymers is described in T. Moritani and J.Yamauchi, Polymer, v39, p553-557 (1998). Terpolymers of the present invention can be obtained by including alkyl acrylates in the copolymerization reaction. The salt form of AMPS is preferably used in the practice of the present invention, and preferred for use is the sodium salt (SAMPS), although any organic salt form would suffice for use herein.
s AMPS salts such as SAMPS can be included in an amount of from 1 to 7 mol%, preferably from 2 mol% to 6 mol%, most preferably from 3 mol% to mol%.
Alkyl acrylates suitable for use in the practice of the present invention include alkyl groups having from 1 to 10 carbon atoms. Such io alkyl groups can be selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl isomers including iso-butyl, n-butyl, and t-butyl, and isomers of pentyl, hexyl, heptyl octyl, nonyl and decyl alkyl groups.
Preferably the alkyl group has from 1 to 4 carbon atoms, more preferably from 1 to 3 carbon atoms, and most preferably the alkyl group is methyl.
is A terpolymer composition as described herein is soluble in a cold aqueous solution at a temperature of less than or equal to about 25°C.
Without being held to theory, the terpolymer comprises an alkyl acrylate that essentially exists in the lactone form rather than in the acid or carboxylate form. In a composition of the present invention, itaconic acid Zo can exist in various forms, such as an acid, salt, lactone, or any combination of these forms, depending on the chemical environment of the terpolymer. The capacity of the terpolymer to change form under various chemical conditions is contemplated herein, and does not negate the function of the presently claimed invention as described and practiced 2s herein.
EXAMPLES
The Examples are for illustrative purposes only, and are not intended to limit the scope of the invention.

Table 1 Properties of Coated Paper Ex Est. BrightnessWhiteness)FluorescenceFluorescence Coat TAPPI CIE TAPPI vs. Base Weight'(points) (points) Paper (g/mz) C1 none 86.9 82.9 2.0 0.0 C2 12 87.9 82.3 1.0 -1.0 C3 12 89.8 89.1 3.0 1.0 C4 12 90.4 92.2 4.0 2.0 C5 12 90.5 92.6 4.1 2.1 C6 12 90.5 93.1 4.4 2.4 1 12 90.3 92.1 4.1 2.1 2 12 90.2 92.0 4.1 2.1 3 12 90.3 92.4 4.2 2.2 4 12 90.5 92.3 4.0 2.0 'Laboratory hand draw-downs done on pre-coated wood-free paper base stock 2807-20.
zTesting done using Technidyne Brightimeter Micro S-5.
'Fluorescence was measured according to TAPPI standard test method T-452.

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a ~n 'These ~Xarnple namb~ers correspond to Table I
Comparative Example 1 (C1) An uncoated base paper was tested for Brightness, Whiteness, Hunter s Color, and TAPPI Fluorescence, giving the results shown in Table 1.
Comparative Example 2 (C2) A coating was made without any polyvinyl alcohol or fluorescent dye applied to the base sheet and tested.
Comparative Example 3 (C3) to The surface of an uncoated basepaper substrate was coated with 12 g/m2 with the coating described in Table 2 with fluorescent dye and CMC but no polyvinyl alcohol promoter. The coated paper was tested for Brightness, Whiteness, Color, and Fluorescence, giving the results shown in Table 1.
Comparative Example 4 (C4) is The process of Example C3 was repeated except that in addition 1.0 parts per hundred of Celvol 203S solution was included in the mixture.
Comparative Example 5 (C5) The process of Example C3 was repeated except that in addition 1.5 parts per hundred of Celvol 203S solution was included in the mixture.
2o Comparative Example 6 (C6) The process of Example C3 was repeated except that in addition 2.0 parts per hundred of Celvol 103 solution was included in the mixture.
Example 1 The process of Example C3 was repeated except that in addition 1.0 parts 2s per hundred of 6.4 mole% Itaconic acid copolymer, 60% neutralization was added dry to the mixture.
Examale 2 The process of Example C3 was repeated except that in addition 1.0 parts per hundred of 4.2 mole% itaconic acid copolymer, 60% neutralization so was included in the mixture as a dry component.

Example 3 The process of Example C3 was repeated except that in addition 1.0 parts per hundred of 1.8 mole % itaconic acid copolymer, 40% neutralization was added dry to the mixture.
s Example 4 The process of Example C3 was repeated except that in addition 1.0 parts per hundred of 2.7 mole% itaconic acid, 2.9 mole% methyl acrylate copolymer, 30% neutralization was added dry to the mixture.
Example 5 to A 2 L polymer kettle was assembled with an overhead stirrer, a Claisen head with a multi-inlet port fitting connected to 2 syringe pumps and a tap-H20 condenser further attached to a N2 bubbler, an overhead thermowell with a thermocouple device, and a septum. The agitator was a single PTFE paddle and the stir rate was set to 80 rpm. The kettle was charged is with 1000 g vinyl acetate (Aldrich Chemical co., Milwaukee, WI, USA) 401 g MeOH (EM Science), 1.5 g itaconic acid (Aldrich), and 0.6 g methyl acrylate (Aldrich) then degassed at rt for 20 minutes with a sparging tube.
The kettle was then heated to reflux (ca. 65 °C) with an oil bath.
Syringe pump #1 was charged with neat methyl acrylate. Syringe pump #2 was zo charged with a 24.7 wt% solution of itaconic acid in MeOH. 2 g of VAZO-64 (DuPont, Wilmington, DE, USA) dissolved in 100 g of MeOH was added to the reactor. Syringe pump #1 was then activated~to feed at 0.0262 cc/min and syringe pump #2 was activated to feed at 0.46 cc/min.
The polymerization was refluxed for 159 minutes, then a solution of 2s sodium nitrite (Aldrich) in 80 g of MeOH was added all at once to halt the polymerization. The solids were determined to be 17.8% at this time. The polymer is thus 4.1 mol% itaconic acid and 1.6 mol% methyl acrylate. The polyvinyl acetate terpolymer was transferred to a 3 L round bottom flask.
The flask was attached to a rotary evaporator and MeOH/vinyl acetate 3o azeotrope was removed at reduced pressure. Addition of 500 g of MeOH
followed by azeotropic distillation was repeated 3 times, at which time removal of vinyl acetate was judged substantially complete. The polyvinyl acetate was dissolved in 700 g of MeOH and charged to a 1 gallon explosion-proof stainless steel blender (Eberbach Corp., Ann Arbor, MI).
The blender was set to stir at 10,000 rpm then 430 g of 25 wt% sodium methoxide in methanol (Aldrich) was added through a small hole in the blender's cover. The ensuing heterogeneous mixture was stirred for 10 s minutes, then 143 g of glacial acetic acid (EM Science) was slowly added.
The mixture was stirred 2 minutes, then filtered. The polymer product was rinsed 3 times with MeOH and once with acetone, then dried in a vacuum oven at 80 °C overnight. 151 g of white terpolymer powder were isolated.
The viscosity was determined to be 21.8 mPa-s (cP) (4% solids aqueous ~o solution at 20 °C (68 °F), determined by Hoeppler falling ball method).
Infrared analysis in ATR mode of the polymer showed the presence of a lactone carbonyl peak at 1745 cm-~, an acid carboxyl at 1705 cm-', and a sodium carboxylate at 1572 cm-'.
Is Examples 6-10 were prepared in the same manner as described for Example 5, except that the polymerization time was 175 minutes and the precharge and feed rates of itaconic acid (IA) and methyl acrylate (MA) were modified as shown in Table 3.
2o The itaconic acid copolymer of Example 11 was prepared by precharging the vessel with 1.41 g IA and 1.46 g MA then feeding a mixture of 21.3:14.4:64.3 solution of IA: MA:MeOH at 0.393 cc/min for 163 minutes.
Itaconic acid copolymers of Examples 12-14 were prepared as described 2s in Example 5 except that polymerizations were halted after 175, 134, and 159 minutes, respectively. The copolymers of Examples 1 and 2 were prepared on a 20 liter scale, feeding IA comonomer at a rate to afford 6.4 and 4.2 mol% comonomer, respectively.

Table 3 Example IA Pre-MA MeOH Pump 1 Pump 2 IA MA
charge Pre- Pre- (cc/min.)(cc/min.)mol mol (g) charge charge (g) (g) 6 1.24 0.72 400 0.0314 0.368 2.3 1.4 7 1.51 0.83 400 0.0380 0.442 2.9 1.7 8 1.49 1.47 400 0.064 0.442 3.0 3.0 9 1.00 2.50 400 0.11 0.300 2.1 5.4 1.40 1.48 420 0.066 0.425 2.7 2.9 11 1.41 1.46 420 see text see text 2.0 2.1 12 1.41 0 400 0 0.41 2.4 0 13 2.43 0 400 0 0.26 1.8 0 14 2.41 0 400 0 0.46 3.1 0 Example 15 s Test of solubility of polymers. The cold water solubility of the resins was measured by charging a 20 mL vial with 50 mg of polymer, a magnetic stir-bar, and 3.0 mL of deionized water. The mixture was stirred at 22-25 °C and the time to dissolve >95% of the polymer was measured. The results are tabulated in Table 4.
to C7 is a 5-6 mol% methyl acrylate polyvinyl alcohol copolymer, >99%
hydrolyzed, 17-23 cP viscosity.
C8 is a commercially available polyvinyl alcohol homopolymer, ca. 88%
is hydrolyzed, which is cold water soluble and is equivalent to Celvol 203S.
C9 is a polyvinyl alcohol homopolymer >99% hydrolyzed with 27-33 cP
viscosity.
Methyl acrylate copolymer or homopolymer are not cold water soluble.

Table 4 Polymer of IA MA Dissolution Example mol% mol% time 6 2.3 1.4 30 min.

7 2.9 1.7 30 min.

8 3.0 3.0 30 min.

9 2.1 5.4 17 min.

2.7 2.9 10 min.

11 2.0 2.1 24 min.

12 2.4 0 20 min.

13 1.8 0 5 days 14 3.1 0 20 min.

C7 0 5-6 insoluble C8 0 0 4 min.

C9 0 0 insoluble

Claims (14)

1. A composition useful for coating the surface of paper wherein the coating composition is an aqueous coating composition comprising less than 40 wt% water and comprising polyvinyl alcohol (PVA) acid copolymer that includes at least about 90 mol% vinyl alcohol and from about 1 to about 10 mol% itaconic acid, wherein the copolymer comprises less than about 5 mol% residual vinyl acetate moieties, and the PVA copolymer is completely dissolved in the aqueous phase of the coating composition.
2. The composition of Claim 1 wherein the PVA acid copolymer comprises from about 1 mol% to about 9 mol% of itaconic acid.
3. The composition of Claim 2 wherein the PVA comprises less than about 3 mol% residual vinyl acetate moieties and from about 2 mol% to about 8 mol% itaconic acid.
4. The composition of Claim 3 wherein the PVA comprises less than about 1 mol% residual vinyl acetate moieties and from about 3 mol% to about 6 mol% Itaconic acid.
5. The composition of Claim 1 wherein the PVA copolymer comprises from about 1 mol% to about 9 mol% itaconic acid and from about 1 mol%
to about 9 mol% of an alkyl acrylate.
6. The composition of Claim 5 wherein the PVA copolymer comprises from about 2 mol% to about 8 mol% itaconic acid and from about 1 mol%
to about 9 mol% of an alkyl acrylate.
7. The composition of Claim 6 wherein the PVA copolymer comprises from about 3 mol% to about 6 mol% itaconic acid and from about 1 mol%
to about 9 mol% of an alkyl acrylate.
8. A method for preparing a paper coating composition wherein the coating composition is an aqueous coating composition comprising less than 40 wt% water and comprising polyvinyl alcohol (PVA) acid copolymer that includes at least about 90 mol% vinyl alcohol and from about 1 to about 10 mol% itaconic acid, wherein the copolymer comprises less than about 5 mol% residual vinyl acetate moieties, and the PVA copolymer is completely dissolved in the aqueous phase of the coating composition, the method comprising the step of: adding as a dry solid component the PVA

copolymer wherein the PVA copolymer further comprises at least about 1 mol% of itaconic acid.
9. A method of coating a paper article comprising the steps of: (1)~
preparing a high-solids PVA-containing paper coating composition by adding, as a dry solid component, a PVA/itaconic acid copolymer comprising at least about 1 mol% of itaconic acid to an aqueous coating composition; and (2) applying the aqueous PVA-containing paper coating to the surface of a paper article.
10. A terpolymer composition comprising vinyl alcohol, methyl acrylate, and itaconic acid moieties, wherein: (i) the terpolymer comprises less than about 5 mol% of vinyl acetate moieties; (ii) the methyl acrylate comonomer is present in an amount of at least about 1 mol% up to about 9 mol%; (iii) the itaconic acid comonomer is present in an amount of at least about 1 mol% up to about 9 mol%, and, (iv) the methyl acrylate of the terpolymer exists in the form of a lactone.
11. A water-soluble film comprising the copolymer composition of Claim 1.
12. An article comprising the water-soluble film of Claim 11.
13. A water-soluble film comprising the composition of Claim 10.
14. An article comprising the water-soluble film of Claim 13.
CA2547676A 2003-12-15 2004-12-15 Copolymers of vinyl alcohol and itaconic acid for use in paper coatings Expired - Fee Related CA2547676C (en)

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US20050154120A1 (en) 2005-07-14
US7608660B2 (en) 2009-10-27
EP2273010B1 (en) 2018-07-04
US20080171825A1 (en) 2008-07-17
EP1694918A1 (en) 2006-08-30
JP2007514075A (en) 2007-05-31
US7608661B2 (en) 2009-10-27
CA2547676C (en) 2016-09-13
US7371796B2 (en) 2008-05-13
US7608662B2 (en) 2009-10-27
EP2273010A1 (en) 2011-01-12
DE602004031257D1 (en) 2011-03-10
US20080176993A1 (en) 2008-07-24
WO2005059248A1 (en) 2005-06-30
US20080176998A1 (en) 2008-07-24

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