WO1992007722A1

WO1992007722A1 - Coating of hydrophilic interpenetrating networks

Info

Publication number: WO1992007722A1
Application number: PCT/US1991/006686
Authority: WO
Inventors: Mohammad Iqbal; Alan G. Miller; Terrance P. Smith; John J. Stofko, Jr.
Original assignee: Minnesota Mining And Manufacturing Company
Priority date: 1990-10-24
Filing date: 1991-09-13
Publication date: 1992-05-14
Also published as: AU8905191A; EP0554370A1; BR9107009A; ES2060416T5; AU653757B2; ES2060416T3; KR930702162A; DE69103534T3; JPH06502358A; CA2093514A1; DE69103534D1; EP0554370B2; EP0554370B1; DE69103534T2

Abstract

This invention relates to transparent materials that are capable of absorbing liquids, and, more particularly, to materials that can be used as ink-receptive layers for transparent imageable materials. Compositions useful as transparent liquid absorbent materials have been formed by blending a liquid-insoluble polymeric material with a liquid-soluble polymeric material. The liquid-insoluble material is presumed to form a matrix, within which the liquid soluble material resides. A problem that frequently arises in the formulation of polymer blends is the incompatibility of the polymers being blended. When attempts are made to blend polymers that are incompatible, phase separation occurs, resulting in haze, lack of transparency, and other forms of nonhomogeneity. This invention provides polymeric networks comprising blends of polymers wherein at least one of the polymers of the blend is crosslinked, after blending, to form a continuous network throughout the bulk of the blend, the uncrosslinked components of the blend being intertwined in such a way as to form a macroscopically homogeneous composition. Substantially all of the crosslinking occurs after the polymeric blend is coated and dried to a continuous film in contrast to crosslinking in solution, thereby providing an easily coatable solution without gelation. The integrity of such networks persist even after absorption of solvent. These materials can be used to form durable, non-tacky, ink-absorbent, transparent coatings for graphical materials.

Description

COATING OF HYDROPHILIC INTERPENETRATING NETWORKS

Background of the Invention

1. Field of the Invention

This invention relates to transparent materials that are capable of absorbing liquids, and, more particularly, to materials that can be used as ink-receptive layers for transparent imageable materials.

2. Discussion of the Art

Transparent materials that are capable of absorbing significant quantities of liquid, while maintaining some degree of durability and transparency, are useful in contact lenses, priming layers for coatings coated out of aqueous solutions, fog-resistant coatings, and transparent imageable materials for use with mechanized ink depositing devices, such as pen plotters and ink-jet printers. Transparent imageable materials are used as overlays in technical drawings and as transparencies for overhead projection. It is desirable that the surface of liquid absorbent materials for use in transparent graphical applications be tack free to the touch even after absorption of significant quantities of ink.

During normal use of pen plotters and ink-jet printers, the inks used in such machines are exposed to open air for long periods of time prior to imaging. After such exposure to ai_:r, the ink must still function in an acceptable manner, without loss of solvent. To meet this requirement, ink formulations typically utilize solvents of very low volatility, such as water, ethylene glycol , propylene glycol, and so on. Inks that contain water or water-miscible solvents are commonly referred to as aqueous inks, and the solvents for these inks are commonly referred to as aqueous liquids.

Because of the low volatility of aqueous liquids, drying of an image by means of evaporation is very limited. In the case of imaging onto a paper sheet, which has a fibrous nature, a significant amount of the liquid diffuses into the sheet, and the surface appears dry to the touch within a very short time. In the case of imaging onto polymeric film, some means of absorbing aqueous liquids is needed if satisfactory drying of the image is to occur.

Compositions useful as transparent liquid absorbent materials have been formed by blending a liquid-insoluble polymeric material with a liquid-soluble polymeric material. The liquid-insoluble material is presumed to form a matrix, within which the liquid soluble material resides. Examples of such blends are the transparent water-absorbent polymeric materials disclosed in U.S. Patent Nos. 4,300,820 and 4,369,229, and in European Patent Application No. 0 233 703.

Because of the low volatility of aqueous liquids, drying of an image by means of evaporation is very limited. In the case of imaging onto a paper sheet which has a fibrous nature, a significant amount of the liquid diffuses into the sheet, and the surface appears dry to the touch within a very short time. In the case of imaging onto polymeric film, some means of absorbing aqueous liquids is needed if satisfactory drying of the image is to occur. A problem that frequently arises in the formulation of polymer blends is the incompatibility of the polymers being blended. When attempts are made to blend polymers that are incompatible, phase separation occurs, resulting in haze, lack of transparency, and other forms of inho ogeneity. Compatibility between two or more polymers in a blend can often be improved by incorporating into the liquid-insoluble matrix-forming polymer chains monomeric units that exhibit some affinity for the liquid-soluble polymer. Polymeric materials having even a small amount of acid functionality are more likely to exhibit compatibility with polyvinyl lactams. Generally, the compatibility of polymers being blended is improved if the polymers are capable of hydrogen bonding to one another. A second form of incompatibility noted in using blends of liquid-absorbent polymers is the incompatibility of the matrix forming insoluble polymer with the liquid being absorbed. For example, if the liquid being absorbed is water, and if the water-insoluble polymers are hydrophobic, some inhibition of water absorption ability can be expected. One method of overcoming this difficulty is to utilize hydrophilic matrix polymers that are water-insoluble at the temperatures at which they are to be used, though they may be water-soluble at a different temperature. In U.S. Patent No. 4,503,111, ink-receptive coatings comprising either polyvinyl alcohol or gelatin blended with polyvinyl pyrrolidone are disclosed. Both polyvinyl alcohol and gelatin, being water-insoluble at room temperature, are able to act as matrix-forming polymers for these coatings, and the coatings are quite receptive to aqueous inks. However, the coatings do exhibit a tendency to become tacky, either because of imaging, or because of high humidity.

It therefore becomes clear that while blends of soluble and insoluble polymers may be useful as liquid absorbent compositions, they suffer major limitations in liquid absorption ability and in durability.

Summary of the Invention This invention provides a coatable composition capable of forming hydrophilic liquid-absorbent, semi-interpenetrating networks, hereinafter referred to as SIPNs. The SIPNs of this invention are formed from polymer blends comprising (a) at least one crosslinkable polymer, (b) at least one liquid-absorbent polymer comprising a water-absorbent polymer, and (c) optionally, a crosslinking agent. Substantially all crosslinking of the crosslinkable polymer takes place after the composition is coated onto a substrate and allowed to dry. These SIPNs are continuous networks wherein the crosslinked polymer forms a continuous matrix throughout the bulk of the material and through which the liquid-absorbent polymer is intertwined in such a way as to form a macroscopically homogeneous composition. The SIPNS of this invention are capable of absorbing significant quantities of those liquids that are solvents or swelling agents of the uncrosslinked portion of the SIPN without loss of physical integrity and without leaching or other forms of phase separation. In cases where the SIPNS are initially transparent, they also remain transparent after absorption of significant quantities of liquids. The nature of the crosslinking used in the formation of the matrix component SIPN is such that it provides durability in the presence of the liquids encountered during use with compatibility toward the liquid-absorbent component. The crosslinked matrix component and the liquid-absorbent component are miscible, exhibit little or no phase separation, and generate little or no haze upon coating. The nature of the crosslinking should not cause phase separation or other inhomogeneity in the SIPN, or gelation of coating solutions before use or coating.

The present invention further provides transparent compositions capable of providing improved ink absorption and durability, while at the. same time retaining transparency and being amenable to the types of processing commonly used in producing transparent graphical materials.

SUB ^• Detailed Description The crosslinked portion of the SIPN will hereinafter be called the matrix component, and the liquid-absorbent portion will hereinafter be called the absorbent component.

The term "hydrophilic", as used herein, is used to describe a material that is generally receptive to water, either in the sense that its surface is wettable by water or in the sense that the bulk of the material is able to absorb significant quantities of water. More specifically, materials that exhibit surface wettability by water are said to have hydrophilic surfaces, while materials that have surfaces not wettable by water will be said to have hydrophobic surfaces. The term "hydrophilic liquid-absorbing materials" as used herein, describes materials that are capable of absorbing significant^* quantities of water, blends of water and other liquids, including those materials that are water-soluble. When molecular structures are being discussed, monomeric units will be referred to as hydrophilic units if they have a water-sorption capacity of at least one mole of water per mole of monomeric unit. Sorption capacities of various monomeric units are given, for example, in D. w. Van Krevelin, with the collaboration of P. J. Hoftyzer, Properties of Polymers: Correlations With Chemical Structure Elsevier Publishing Company (Amsterdam, London, New York: 1972) pages 294-296. Monomeric units will be referred to as hydrophobic if they form water-insoluble polymers capable of absorbing only small amounts of water when polymerized by themselves.

The matrix component of the SIPN of the present invention comprises crosslinkable polymers that are either hydrophobic or hydrophilic in nature, and can be derived- from the copolymerization of acrylic or other hydrophobic or hydrophilic ethylenically unεaturated monomeric units with monomers having acidic groups, or if pendant ester groups are already present in these acrylic or ethylenically unsaturated monomeric units, by hydrolysis.

Hydrophobic monomeric units suitable for preparing crosslinkable matrix components are preferably selected from:

(1) acrylates and methacrylates having the structure :

wherein R¹ represents H or -CH, and R² represents an alkyl group having up to ten carbon atoms, preferably up to four carbon atoms, and more preferably one to two carbon atoms, a cycloaliphatic group having up to nine carbon atoms, a substituted or unεubεtituted aryl group having up to 14 carbon atoms, and an oxygen containing heterocyclic group having up to ten carbon atoms;

(2) acrylonitrile or methacrylonitile; (3) styrene or α-methylstyrene having the structure:

where X and Y independently represent hydrogen or alkyl groups having up to 4 carbon atoms, preferably 1 or 2 carbon atoms, a halogen atom, alkyl halide group, or OR™ where R^m represent hydrogen or an alkyl group having up to 4 carbon atoms, preferably 1 or 2 carbon atoms, and Z represents hydrogen or methyl; and (4) vinyl acetate.

Hydrophilic monomeric units suitable for preparing crosslinkable polymers are preferably selected from:

(1) vinyl lactamε having the repeating structure:

where n represents the integer 2 or 3; (2) acrylamide or methacrylamide having the structure:

CH =C

C=0

I

N

R³

where R¹ is as defined previously, R³ represents H or an alkyl group having up to ten carbon atoms, preferably from one to four carbon atoms, and R^" represents H or an alkyl group, having up to ten carbon atoms, preferably from one to four carbon atomε, or an hydroxyalkyl group, or an alkoxy alkyl group having the structure of -(CH₂ ) -OR³ , where p represents an integer from 1 to 3, inclusive; (3) tertiary amino alkylacrylates or tertiary 5 amino alkylmethacrylateε having the structure:

R¹

I

CH. •c

10 ' -

I

0

(CH, ),

.N

15 where represents the integer 1 or 2 and

R¹ and R³ are as defined previously, and R⁵ represents H or an alkyl group having up to ten carbon atoms, preferably from one to

20 four carbon atoms;

(4) hydroxy alkylacrylates, alkoxy alkylacrylates, hydroxy alkyl methacrylates, or alkoxy alkyl methacrylateε having the structure:

where R and R⁴ are as defined previouεly, q represents an integer from 1 to 4 , inclusive, preferably 2 to 3; and (5) alkoxy acrylates or alkoxy methacrylateε having the εtructure: R^J I CH =C

C=0

I

0

(CH₂CH-0)_rH

where r represents an integer from 5 to 25, inclusive, and R¹ is defined previously.

Some of the previously mentioned structures of both the hydrophobic and hydrophilic monomeric units contain pendant ester groups that can readily be rendered crosslinkable by hydrolysis. For the others, monomeric units containing acidic groups must be incorporated into the polymeric structure to render them crosslinkable. Polymerization of these monomers can be carried out by typical free radical solution, emulsion, or suspension polymerization techniques. Suitable monomeric units containing acidic groups include acrylic acid or methacrylic acid, other copolymerizable carboxyclic acids, and ammonium salts.

The crosslinking agent is preferably selected from the group of polyfunctional aziridines possessing at least two crosslinking sites per molecule, such as trimethylol propane-tris-( β-(N-aziridinyl )propionate )

CH -CH -C- ( CH -O-

CH.

pent a e rythri tol-tri ε- ( β- ( N-az i ridinyl ) propionate ) HO-CH- -C ( CH. , --0O--

CH.

trimethylolpropane-tris-( β-(N-methylaziridinyl propionate)

CH,

CH

CH. -CH₂-C(CH₂-0-C-CH₂-CH₂-N

CH.

and so on. Crosεlinking can alεo be brought about by meanε of metal ions, such as provided by multivalent metal ion salts, provided the composition containing the crosslinkable polymer is made from 80 to 99 parts by weight of- monomer and from 1 to 20 parts by weight of a chelating compound.

The metal ions can be selected from ions of the following metals: cobalt, calcium, magnesium, chromium, aluminum, tin, zirconium, zinc, nickel, and so on, with the preferred compounds being selected from aluminum acetate, aluminum ammonium εulfate dodecahydrate, alum, aluminum chloride, chromium (III) acetate, chromium till) chloride hexahydrate, cobalt acetate, cobalt (II) chloride hexahydrate, cobalt (II) acetate tetrahydrate, cobalt sulfate hydrate, copper εulfate pentahydrate, copper acetate hydrate, copper chloride dihydrate, ferric chloride hexahydrate, ferric ammonium εulfate dodecahydrate, ferrous chloride, tetrahydrate, magnesium acetate tetrahydrate, magnesium chloride hexahydrate, magnesium nitrate hexahydrate, manganese acetate tetrahydrate, manganeεe chloride tetrahydrate, nickel chloride hexahydrate, nickel nitrate hexahydrate, stannous chloride dihydrate', stannic chloride, tin (II) acetate, tin (IV) acetate, strontium chloride hexahydrate, strontium nitrate, zinc acetate dihydrate, zinc chloride, zinc nitrate, zirconium (IV) chloride, zirconium acetate, zirconium oxychloride, zirconium hydroxychloride, ammonium zirconium carbonate, and so on.

The preferred chelating compounds can be selected from:

(1) alkaline metal salts of acrylic or methacrylic acid having the structure:

R¹

CH,-C

² I

C=0

I

OM where R¹ is described previously and M represents Li^*, Na,

K, Rb, Cε, or NH₄ , preferably NH₄ , Na, or K;

(2) N-substituted acrylamido or methacrylamido monomers containing ionic groups having the structure:

where R¹ is described previously, R⁶ represents H or an alkyl group having up to four carbon atoms, preferably H, R represents COOM or -SO. M where M is described previously;

(3) alkali metal salt of p-styrene sulfonic acid; (4) sodium salt of 2-sulfo ethyl acrylate and sodium salt of 2-sulfo ethyl methacrylate;

(5) 2-vinyl pyridine and 4-vinyl pyridine;

(6) vinyl imidazole;

(7) N-(3-aminopropyl ) methacrylamide hydrochloride; and

(8) 2-acetoacetoxy ethyl acrylate and 2-acetoacetoxy ethyl methacrylate.

Other crosslinkable polymers suitable for the matrix component of the hydrophilic SIPNs of the present invention are polymers having crosslinkable tertiary amino groups, wherein said groups can be provided either as part of the monomeric units used in the formation of the polymer, or grafted onto the polymer after the formation of the polymeric backbone. These have the general structure of:

-[/VVVCH\/\/\/\]-

R⁸ N

R⁹^ R¹⁰

wherein R⁸ represents a member selected from the group consisting of substituted and unsubstituted alkyl groups, substituted and unsubstituted amide groups, and substituted and unsubstituted ester groups, the foregoing groups preferably having no more than ten carbon atoms, more preferably having no more than five carbon atoms, substituted and unsubstituted aryl groups, preferably having no more than 14 carbon atoms, R⁹ and R¹⁰ independently represent a member. selected from the group consisting of substituted and unsubεtituted alkyl groups, preferably having no more than ten carbon atoms, more preferably having no more than five carbon atoms, and substituted and unsubstituted aryl groups, preferably havi-ng no more than 14 carbon atoms. Additionally, R⁹ and R¹ ° can be connected to form the εubstituted or unsubεtituted cyclic structure -R⁹ -R¹ ° -. The symbol /\/\/\ represents a plurality of unsubstituted or substituted -CH. - groups linked together to form the backbone of the chain. Where water or other aqueous liquids are to be

^• absorbed, it is preferred that R⁸ be selected to be -(C=0)NH(R¹¹ )-, wherein R¹¹ represents a εubstituted or unsubstituted divalent alkyl group, preferably having no more than ten carbon atoms, and more preferably having no more than five carbon atoms. Preferred substituents for R¹¹ are those capable of hydrogen bonding, including -COOH, -CN, and -N0₂. Additionally, R¹¹ can include in its structure hydrogen bonding groupε, εuch as -CO-, -S=0, -0-, )N-, -S-, and )P-. Crosslinkable polymers suitable for the matrix component wherein R⁸ is -(C=0)NH(R^{1 x} )- can be prepared by treating polymerε or copolymerε containing maleic anhydride, with an amine having the εtructure:

wherein, R⁹ , R¹° , and R¹¹ are as described previously.

A particularly useful example of a crosslinkable matrix component is a copolymer of polymethyl vinyl ether and maleic anhydride, wherein these two monomeric units are present in approximately equimolar amounts. This copolymer can be formed in the following manner:

(a) (b; OCH, I ³ — > [ ( CH, _; -CH-) f C i H C , H ) ] s

0=C c=o

OH . N

H .1 1

N

/ \ R⁹ R^{1 0}

( C )

wherein R⁹ , R¹ ° , and R¹ are aε deεcribed previouεly, and ε preferably represents a number from about 100 to about 600. This reaction can be conveniently performed by disεolving the polymethyl vinyl ether/maleic anhydride copolymer, i.e., reactant (a), in methyl ethyl ketone, dissolving the amine, i.e., reactant (b), in an alcohol, such aε methanol or ethanol, and mixing the two solutions. This reaction proceedε rapidly at room temperature, with agitation. The product of thiε reaction may begin to form a cloudy εuspension, which can be cleared by the addition of water to the solution. Crosslinking agents suitable for this type of polymer are multi-functional alkylating agents, each functional group of which forms a bond with a polymer chain through a tertiary amino group by quaternization of the trivalent nitrogen of the tertiary amino group. Difunctional alkylating agents are εuitable for thiε purpose. In the case where the tertiary amino group iε pendant to the backbone of the polymer, thiε crosslinking reaction can be depicted aε follows:

R^{1 2}

2[/\/\/\/CH\/\/\/\], l o

Q-R^{1 2} -Q R -N _^■+ -R 9

R I N N /WWCHW N

\ i

( d ) ( e ) ( f )

where R⁸ , R , R¹ ° , and ε are aε deεcribed previouεly, R can be the εame as R⁸ , R⁹ , or R¹° , and Q^~ can be a halide, an alkyl εulfonate, preferably having no more than 5 carbon atoms, or any aryl sulfonate, preferably having no more than 14 carbon atoms.

Other crosslinkable polymers suitable for forming the matrix component of the SIPNs of the present invention include polymerε having εilanol groups, wherein the silanol groups can either be part of the monomeric units used in the formation of the polymer or be grafted onto the polymer after the formation of the polymeric backbone. If grafting is preferred, the polymeric backbones generally contain monomeric units of maleic anhydride, which can be converted into graftable sites by reaction with compounds having primary amino groups. Silanol side groups can be grafted onto these sites by heating a solution containing the backbone polymer with an aminoalkoxysilane.. The alkoxysilane can εubεequently be hydrolyzed by the addition of water. The reaction scheme can be depicted aε follows: 4

- A- 17

(CH- -CH)-}- + (R¹⁵-Si-R¹³-NH, ) (R -NH. )^■

'16

0=C C=0

\ /

(a) (b) (c)

•> -[A- — (CH — CH) ]-, [A- — (CH- -CH) ]- i I 0=C C«0 O-C C=0 i

OH NH OH NH

I 13

R in

,14 -έi-i 16

1 ,15

(pendant group 1) (pendant group 2)

(d)

wherein A represents a monomeric unit preferably selected from the group consisting of acrylonitrile, allyl acetate, ethylene, methyl acrylate, methyl methacrylate, methyl vinyl ether, stilbene, isostilbene, styrene, vinyl acetate, vinyl chloride, vinylidene chloride, vinylpyrrolidone, divinylether, norbornene, and chloroethyl vinyl ether;

R¹³ represents a divalent alkyl group, preferably having up to ten carbon atoms, more preferably having not more than five carbon atomε; R¹⁴ , R¹⁵, and R¹⁶ independently represent alkoxy groupε having up to about five carbon atomε, more preferably having not more than about three carbon atoms; and R¹⁷ represents a member selected from the group consisting of substituted or unsubstituted alkyl groups, preferably having up to ten carbon atoms, more preferably having not more than five carbon atoms, and subεtituted or unsubstituted aryl groups, preferably having up to 14 carbon atoms.

Suitable substituents for R¹ include alkoxy, -OH, -COOH, -COOR, halide, and -NR₂ , wherein R represents an alkyl group, preferably having up to five carbon atoms, more preferably having not more than three carbon atoms. The relative amounts of the two types of side groups in polymer (d) are determined by the relative amounts of compounds (b) and (c) used in the grafting εolutionε. The molar ratio of compound (c) to compound (b) in the reaction rangeε from about 3 to about 6, preferably from about 4 to about 5.

A diεcuεεion of the copolymerization of these monomeric units with maleic anhydride and the properties of the resulting copolymerε can be found in Brownell, G. L., "Acids, Maleic and Fumaric," in Encyclopedia of Polymer Science and Technology, Vol. 1, John Wiley & Sons, Inc., (New York:1964), pp. 67-95.

Once the silanol groups are formed by hydrolysiε, the reεulting polymer can be crosslinked by the removal of water and other solvents from the system without addition of further crosslinking agent, according to the reaction:

ΛΛΛΛΛCBΛΛΛΛΛ l VWCHWW\ OH-S i-OH

OH-Si-OH 0 OH > HO-Si-OH

ΛΛΛΛΛ iCHΛΛΛΛΛ

Additionally, crosslinking can occur at more than one of the -OH groups attached to the silicon atom.

While it is the primary function of the matrix component of the SIPN to impart physical integrity and durability to the SIPN without adversely affecting the overall liquid absorbency of the SIPN, it is the primary function of the liquid-absorbent component to promote absorption of liquids. When aqueous liquids are to be absorbed, as is in the case of most inks, the liquid-absorbent component must be capable of absorbing water, and preferably be water-soluble. The liquid-absorbent component can be selected from polymers formed from the following monomers:

(1) vinyl lactams having the repeating structure:

where n is as described previously; (2) alkyl tertiary amino alkylacrylates and alkyl tertiary amino alkylmethacrylates having the structure:

where m, R¹ and R³ are aε deεcribed previously;

(3) alkyl quaternary amino alkylacrylates or alkyl quaternary amino alkyl methacylates having the structure:

R¹

1 CH,-C

² I

C-0

where p represents the integer 1 or 2; and R¹ is as described previously, R¹ , R , R²° independently represent hydrogen or an alkyl group having up to 10 carbon atoms, preferably having from 1 to 6 carbon atomε, and Q represents a halide, R SO.,

R¹⁹SO. or R²⁰SO,

Polymerization of these monomers can be carried out by conventional typical free radical polymerization techniques as mentioned previously.

Alternately, the liquid-absorbent component can be selected from commercially available water-soluble or water-εwellable polymers such as polyvinyl alcohol, polyvinyl alcohol/poly(vinyl acetate) copolymer, poly(vinyl formal) or poly(vinyl butyral) , gelatin, carboxy methylcellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxyethyl starch, polyethyl oxazoline, polyethylene oxide, polyethylene glycol, polypropylene oxide, and so on. The preferred polymers are polyvinyl lactams, eεpecially polyvinyl pyrrolidone, and polyvinyl alcohol.

SIPNs of the present invention to be used for forming ink-receptive layerε typically comprise from about 0.5 to 6.0% by weight of crosslinking agent, preferably from about 1.0 to 4.5% by weight, when crosslinking agents are needed. The crosslinkable polymer can comprise from about 25 to about 99% by weight, preferably from about 30 to about 60% by weight, of the total SIPNs. The liquid-absorbent component can comprise from about 1 to about 75% by weight, preferably from about 40 to about 70% by weight, of the total SIPNs. Such ink-receptive layers are generally borne by a substrate, such as transparent polymeric sheet. To form an ink-receptive layer, it is convenient to apply a composition for preparing such a layer to the substrate by means of a coating solution, which is subsequently dried to form a solid layer. A coatable liquid composition can be prepared by dissolving polymers of the matrix component and the liquid-absorbent component in a common solvent, which can be water, or water- iscible solvents, in appropriate proportions depending on the solubility of the components. The appropriate crosslinking agent, if used, is then added, and mixed until a uniform solution is obtained.

Common solvents can be selected by making use of Hansen parameters, which are numerical values that characterize the individual contributions to cohesive energy density made by the inter olecular dispersion forces, dipole forces, and hydrogen bonding forces of a particular compound. Soluble solid materials tend to be more readily dissolved by liquids having Hansen parameters within a specified range, this range being called the solubility envelope, and less readily dissolved by liquids having Hansen parameters outside of the solubility envelope. Because of this tendency, Hansen parameters can be used as a basis for selecting single solvents or for formulating solvent blends capable of disεolving a particular solid material or combination of solid materials.

Experimentally determined Hansen parameters and solubility envelopes for a variety of solid materials, along with Hansen parameters for many commonly used

SUBSTITUTESHEET solvents, aε well aε formulae for mathematically estimating Hansen parameters of materials not listed, can be found in Barton, A.F.M. CRC Handbook of Solubility Parameters and Other Cohesion Parameters CRC Press, Inc., (Boca Raton: 1983), incorporated herein by reference. Systematic methods for utilizing Hansen parameters to compute formulations for solvent blends capable of dissolving particular combinations of solid materials in more complicated systems can be found in Teas, J.P., "Solubility Parameters", Treatis.e on Coatinqs, R.R. Myers and J.S. Long, ed.. Vol. 2, Part II, Marcel

Dekker (New York: 1976), p. 413-448, incorporated herein by reference. Because such computational methods often result in more than one possible solvent formulation, additional experimental evaluation may be needed to arrive at an optimal formulation.

Additional constraints upon the choice of solvents may arise from practical requirements involving coating, drying, toxicity, or other considerations.

While in solution prior to coating, little or no crosslinking of the matrix polymer takes place. The components remain uniformly dissolved in solution, retaining good coating characteristics without gelation and having adequate pot life to allow coating onto a transparent substrate-, such as a polymeric film, and subsequent drying to form a continuous layer. The amount of heat required to accomplish the drying in a reasonable time is usually sufficient for causing crosslinking of the matrix component to occur. In this way, the problems of dealing with volatile monomers, some of which can be toxic, and unreacted monomers resulting from incomplete conversion are eliminated.

SIPN solutions of the present invention may contain additional modifying ingredients such as adhesion promoters, particles, surfactantε, viεcosity modifiers, and like materials, provided that such additives do not adversely affect the liquid-absorbing capability of the invention.

TESHEET Coating can be conducted by any suitable means, such as knife coating, rotogravure coating, reverse roll coating, or other conventional means. Drying can be accomplished by means of heated air. If preferred, an adhesion promoting priming layer can be applied to the subεtrate prior to coating. Such priming layers can include primer coatings, surface treatments such as corona treatment, or other appropriate treatment. Adhesion of the SIPN layer can alεo be promoted by providing a gelatin sublayer of the type used in photographic film backingε between the priming layer and the SIPN layer. Film backings having both a priming layer and a gelatin sublayer are commercially available, and are frequently designated aε primed and subbed film backingε.

When the SIPNs of the present invention are to be used to form the ink absorbing layer of a film for use with an ink-jet printer, it is preferred that the backing of the film have a caliper in the range of about 50 to about 125 micrometers. Films having calipers below about 50 micrometers tend to be too fragile for graphic arts films, while films having calipers over about 125 micrometers tend to be too stiff for easy feeding through many of the imaging machines currently in uεe. Materials suitable for backingε for graphic arts films include polyesters, e.g., polyethylene tetrephthalate, cellulose acetates, polycarbonates, poly(vinyl chlorides), polystyreneε, and polysulfones.

When the SIPNs of the present invention are to be used to form the ink absorbing layer of a film for uεe with- an ink-jet printer, the SIPN layer may further be overcoated with an ink-permeable, anti-tack protective layer, εuch aε, for example, a layer compriεing polyvinyl alcohol in which starch particles have been dispersed, or a semi-interpenetrating polymeric network in which polyvinyl alcohol is the absorbent component. Such overcoat layerε can provide surface properties that help to properly control the spread of ink droplets so as to optimize image quality.

SUBSTITUTE SHEET In addition to ^"the polymeric materials comprising the SIPN, other modifying ingredients, such as εurfactantε, particles, or the like, can be added to the formulation for the overcoat layer to improve ink flow, dot spread, or other aspects of ink receptivity to improve image appearance.

In order to more fully illustrate the various embodiments of the preεent invention, the following non-limiting, examples are provided.

Example 1

A polymeric material εuitable for the matrix of an SIPN was prepared by combining N-vinyl-2-pyrrolidone (75 parts by weight), N,N-dimethyl acrylamide (2 parts by weight), the ammonium salt of acrylic acid (5 parts by weight), azo-biε-isobutyronitrile (0.14 part by weight, "Vazo", available from E. I. DuPont de Nemours and Company), and deionized water (566 parts by weight) in a one-liter brown bottle. The mixture was purged with dry nitrogen gas for five minutes; polymerization was then effected by immersing the bottle for between 18 to 24 hours in a constant temperature bath maintained at a temperature of 60°C. The resulting polymerized mixture was then diluted with deionized water to give a 10% aqueous solution. The resulting solution will hereinafter be called Solution A.

Solution A (8 g of a 10% aqueous solution) was mixed with surfactant (0.2 g of a 2% aqueous εolution, "Triton X100", Rohm and Haas Co.), polyvinyl alcohol(8 g of a 5"% aqueous εolution, "Vinol 540", Air Products and Chemicals, Inc.), and polyfunctional aziridine crosslinking agent (0.5 g of a 10% aqueous solution, XAMA-7, Sanncor Ind. Inc. ) in a separate vessel.

The resultant solution was coated onto a backing of polyethylene terephthalate film having a caliper of 100 micrometers, which had been primed with polyvinylidene chloride, over which had been coated a gelatin sublayer of the type used in photographic films for improving gelatin adhesion ("Scotchpar" Type PH primed and subbed film, available from Minnesota Mining and Manufacturing Company) . Coating was carried out by means of a knife coater at a wet thickness of 200 micrometers. The coating was then dried by exposure to circulating heated air at a temperature of 90°C for five minutes to form a clear SIPN layer.

Printing was performed with an ink-jet printer and pen using ink containing Direct Blue 99 dye (3% solution in water). After six minutes, the imaged film was immersed in water and no dye was removed from image. The SIPN layer remained intact.

Example 2 A solution of matrix component of the present invention was prepared by firεt dissolving 1.3 g of a copolymer of methyl vinyl ether and maleic anhydride ("Gantrez" AN-169, available from GAF Chemicals Corporation) in 24.6 g of methyl ethyl ketone. In a separate vessel, 1.3 g of aminopropyl morpholine

(available from Aldrich Chemical Company, Inc.) were dissolved in 11.6 g of methanol. The previously prepared εolution of copolymer waε then added, dropwise, to the aminopropyl morpholine/methanol solution, after which 36.6 of distilled water were added to the resulting combined solutions. The resulting εolution will hereinafter be called matrix component Solution B.

In yet another vessel, 2.5 g of polyvinyl pyrrolidone (K90, available from GAF Chemicals Corporation) were dissolved in 22.1 g of distilled water. This solution was then added to matrix component Solution B and agitated until a uniform εolution was obtained. The resulting solution, hereinafter called blend Solution B, was then divided into 5 samples of 20.0 g each. The dihalo compound 3,3-bis-(iodomethyl )-oxetane was prepared according to the ^'procedure described in

SUBSTITUTESHEET Sorenεon, W.R., and Campbell, T.W., Preparative Methods of Polymer Chemiεtry, 2nd Edition, New York, Interscience Publishers, Inc., 1968, p. 376, incorporated herein by reference. A εolution of 10 parts by weight of this compound and 90 parts by weight of dimethyl formamide (DMF) was prepared for use aε an alkylating agent for crosslinking the matrix component.

Crosslinkable solutionε according to the present invention were prepared by adding 0.35 g of the 3, 3-bis-( iodomethyl )-oxetane/DMF solution to one of the 20.0 g samples of blend Solution B, 0.70 g of■ the

3,3-bis-( iodomethyl )-oxetane/DMF εolution to a second 20.0 g sample of blend Solution B, and 1.4 g of the 3 , 3-bis-( iodomethyl )-oxetane/DMF εolution to a third 20.0 g εample of blend Solution B. These solutions were each coated onto a backing of polyethylene terephthalate film having a caliper of 100 micrometers which had been primed with polyvinylidene chloride, over which had been coated a gelatin sublayer of the type uεed in photographic films for improving gelatin adhesion ("Scotchpar" Type PH primed and εubbed film, available from Minneεota Mining and Manufacturing Company). Coating was carried out by means of a knife coater, with the wet thickness of the solution coated onto the film being 75 micrometers. Drying was carried out by exposure to circulating heated air at a temperature of 90°C for five minutes.

After drying, all three of the solutionε reεulted in clear SIPN layerε that retained their physical integrity when washed with a moving stream of water at room temperature. Exposure to water in selected areas resulted in detectable water absorption, as indicated by swelling of the SIPN layer. Swelling of the SIPN layer was detected by the bump that could be felt by running a finger over the surface of the coated film in such a way aε to paεε from the portion of the layer not exposed to water to the portion that was exposed to water. Because the amount of crosεlinking agent used could be varied over a wide range without failure of crosεlinking and without losε of hydrophilicity, it was concluded that thiε type of crosslinking is sufficiently tolerant of variability to be uεeful in a manufacturing proceεε.

Example 3 The polymeric material for the matrix of the SIPN was prepared by combining N-vinyl-2-pyrrolidone (28 parts by weight), N,N-dimethyl acrylamide (20 parts by weight), 2-acrylamido-2-methyl propanesulfonic acid (2 parts by weight of the ammonium salt), azo-bis-isobutyronitrile (0.07 part by weight, "Vazo", available from E. I. du Pont de Nemours and Company), and deionized water (280 parts by weight) in a one-liter brown bottle.- After the mixture was purged with dry nitrogen gaε for five minuteε, polymerization was effected by immersing the bottle in a constant temperature bath maintained at 60°C for eight hours to give a very viscous clear εolution (97.8% converεion). The resulting polymerized mixture waε then diluted with deionized water to give a 10% εolution in water, hereinafter called Solution C.

Solution C (21.94 g of a 10% aqueous εolution) waε thoroughly mixed with polyvinyl alcohol( "Vinol 540", available from Air Productε and Chemical, Inc., 28.6 g of a 5% aqueous solution), and chromium chloride crosεlinking agent (0.29 g of a 10% aqueouε εolution) in a εeparate veεsel. The reεultant solution was coated onto a backing of polyethylene terephthalate film having a caliper of 100 micrometers, which had been primed with polyvinylidene chloride, over which had been coated a gelatin sublayer of the type used in photographic films for improving gelatin adheεion ("Scotchpar" Type PH primed and subbed film, available from Minnesota Mining and Manufacturing Company) . Coating was carried out by means of a knife coater at a wet thickness of 200 micrometers. The coating

SUBSTITUTE SHEET waε then dried by exposure to circulating heated air at a temperature of 90°C for five minutes. After drying, a clear SIPN layer formed.

Printing was performed with an ink-jet printer and a pen plotter using ink containing dye (3 to 5% εolution in water). After one minute, the imaged film waε dry to the touch. The SIPN layer remained intact.

Example 4 The purpose of this example is to illuεtrate the uεe of an SIPN of the preεent invention aε a single layer hydrophilic coating that is capable of absorbing aqueous ink.

A solution of the grafting material was prepared by first dissolving 0.07 g of 3-aminopropyltriethoxyεilane (Aidrich Chemical Co., Inc.) and 0.22 g of

2-methoxyethylamine (Aldrich Chemical Co., Inc.) in 7.9 g of methanol. In a εeparate vessel, a solution of the backbone polymer waε prepared by diεsolving 0.5 g of a copolymer of methyl vinyl ether and maleic anhydride ("Gantrez AN-169", GAF Chemicalε Corporation) in 9.5 g of methyl ethyl ketone. The solutions of the grafting material and the backbone polymer were then combined and stirred to provide a clear, viscous liquid. A solution of absorbent component was prepared in a separate vessel by adding 1.5 g of polyvinyl pyrrolidone, (K-90, GAF Chemicalε Corporation) to 13.5 g of deionized water and stirring the resulting mixture until a clear solution waε formed. The solution of absorbent component, along with 15.0 g of water, waε added to the previouεly prepared combined εolutions of grafting material and backbone polymer, and the resulting mixture stirred at room temperature until a clear εolution waε obtained.

An ink-receptive layer was formed by coating the εolution εo prepared onto a sheet of polyvinylidene chloride-primed and gelatin-subbed polyethylene terephthalate film having a caliper of 100 micrometers ("Scotchpar" Type PH primed and subbed film, available from Minnesota Mining and Manufacturing Company) by means of a knife coater adjusted so as to apply a liquid layer having a wet thicknesε of 125 micrometerε. The liquid layer waε dried in a forced air oven at a temperature of 90°C for a period of five minutes.

The ink receptivity of the dried coating waε tested by writing on it with a pen which uεed an aqueouε ink ("Expresεo" brand pen, Sanford Corp. Bellwood, IL). The ink image dried εufficiently in 10 εeconds to be non-smearable when gently rubbed with the finger. The

SIPN layer tended to become tacky at relative humidities of about 90% or greater.

Various modifications and alterations of this invention will become apparent to those skilled in the art without departing from the scope and spirit of this invention, and it εhould be underεtood that thiε invention iε not to be unduly limited to the illuεtrative embodimentε set forth herein.

SUBSTITUTESHEET

Claims

WHAT IS CLAIMED IS:

1. An article comprising a εubεtrate bearing on at least one major surface thereof a hydrophilic liquid-absorbent, semi-interpenetrating network formed from a polymer blend comprising:

(a) at least one crosslinkable polymer; and

(b) at least one liquid-absorbent polymer comprising a water-absorbent polymer.

2. The article of Claim 1, wherein said croεεlinkable polymer is crosslinked after it has been applied to said εubεtrate.

3. Method of preparing the article of Claim 1, compriεing the steps of:

(1) blending said at least one croεεlinkable polymer with said at leaεt one liquid-abεorbent polymer in a liquid medium to form a solution;

(2) applying εaid εolution to εaid substrate; and

(3) drying εaid εolution, whereby εaid croεslinkable polymer becomes crosslinked.

4. The article of Claim 1, further including a crosslinking agent.

5. The article of Claim 4, wherein said croεεlinkable polymer iε croεslinked after it has been applied to εaid εubεtrate.

SUBSTITUTE SHEET

6. Method of preparing the article of Claim 4, comprising the stepε of:

(1) blending εaid at leaεt one croεεlinkable polymer with εaid at least one liquid-abεorbent polymer and a croεεlinking agent in a liquid medium to form a εolution;

(2) applying εaid εolution to said εubεtrate; and

(3) drying εaid εolution, whereby εaid crosslinkable polymer becomes crosεlinked.

SUBSTITUTESHEET