WO1998046668A1 - Revetements a degradation regulee et procede de fabrication de ces derniers - Google Patents

Revetements a degradation regulee et procede de fabrication de ces derniers Download PDF

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Publication number
WO1998046668A1
WO1998046668A1 PCT/IE1998/000028 IE9800028W WO9846668A1 WO 1998046668 A1 WO1998046668 A1 WO 1998046668A1 IE 9800028 W IE9800028 W IE 9800028W WO 9846668 A1 WO9846668 A1 WO 9846668A1
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WO
WIPO (PCT)
Prior art keywords
coating
article
water
article according
degradation
Prior art date
Application number
PCT/IE1998/000028
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English (en)
Inventor
Peter John Hurley
Original Assignee
Solplax Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Solplax Limited filed Critical Solplax Limited
Priority to CA002286724A priority Critical patent/CA2286724A1/fr
Priority to EP98917566A priority patent/EP0975692A1/fr
Priority to AU70749/98A priority patent/AU7074998A/en
Publication of WO1998046668A1 publication Critical patent/WO1998046668A1/fr

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Classifications

    • 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
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/0427—Coating with only one layer of a composition containing a polymer binder
    • 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
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
    • 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
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
    • 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
    • C08J2329/00—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 alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Derivatives of such polymer
    • C08J2329/02—Homopolymers or copolymers of unsaturated alcohols
    • C08J2329/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids

Definitions

  • the present invention relates to controlled degradation coatings and in particular to coatings for polyvinylalcohol and poly vinylalcohol/polyvinylacetate copolymers and to a method for their manufacture.
  • Polyvinyl alcohol (PVA) and polyvinylalcohol/polyvinylacetate co-polymers (PVA PVAc) are materials which are subject to aqueous dissolution. Post dissolution, these materials will readily biodegrade on exposure to bacteria present in the environment. These polymers and their part degradation products and degradation products are non-toxic and pose no risk of bio-accumulation or long term hazard to the environment, particularly when the polymers are processed as described in Irish Patent No. S75746.
  • PVA and PVA/PVAc are capable of being processed into a wide variety of useful articles by thermoplastic processes. Once an article has fulfilled its useful life, it is desirable that when it is discarded to waste (landfill or similar), the article will rapidly dissolve and subsequently biodegrade.
  • the application of PVA and PVA PVAc copolymers in the manufacture of many types of articles is limited by the possibility of premature dissolution, which may occur should the article become damp during its working life. Also, the article may absorb atmospheric moisture, rendering it softer and mechanically weaker than designed. There are also problems of handling by humans in that when PVA/PVAc co- polymer materials absorb perspiration, they become sticky to the touch.
  • WO 92/01556 and WO 93/22125 disclose the manufacture of articles of coated PVA/PVAc copolymers by layering or surrounding PVA/PVAc which is water soluble at 20°C with a thin layer of PVA which is insoluble in water at 20°C. Thus an article may be manufactured which would be protected from dissolution until its waterproofing insoluble layer is breached.
  • the copolymer and coating are disclosed as being co-extruded, laminated or moulded, with or without an intervening filler layer.
  • US-A-5.196,247 discloses films of PVA co-extruded or heat laminated with thermoplastic water insoluble polymers and co-polymers, such as polyethylene, polypropylene, ethylvinyl acetate, ethyl methyl acrylate and ethyl acrylic acid.
  • GB 1,271,424 discloses a bed-pan liner consisting of 3 or 4 layers.
  • the layers comprise a water soluble or dispersible base layer, coated by a continuous water repellent layer with a wax based flexible adhesive between.
  • the bed pan liner should fully disintegrate within 5- 10 seconds on immersion in water.
  • EP 0589437A1 discloses a compostable disposable film manufactured by the coating of water soluble polymeric materials with a very thin layer of water insoluble surface coating materials such as polyvinylidene chloride with an intermediate adhesive or primer layer which may consist of polyesters or polyurethanes.
  • US-A-4,939,030 discloses a method for the manufacture of a film to retain the freshness of fruit by coating a PVA film with a thermoplastic film to form a laminate.
  • the outer layer is pierced by pins to create holes of less than 30 microns to form a breathable outer layer over a moisture absorbing inner layer such that the film does not have a moisture permeability lower than 100g/m 2 /24hr.
  • WO 92/15454 discloses a heat bonded laminate of PVA film with a film of polyethylene/ polypropylene non-woven fibre.
  • US-A-5,268,222 discloses a composite fabric of material which is water soluble at room temperature and a second PVA layer which is soluble above 140°F (60°C) and insoluble below 140°F, while US-A-5,500,281 discloses a 2 ply heat bonded laminate of 2-10% water soluble PVA non- woven fibres and an absorbent fibre web.
  • US-A-4,503,098 discloses a disposable film manufactured by the coating of water soluble polymeric materials with a layer of degradable water insoluble surface coating.
  • the insoluble coating consists of 0.5-5 mils (13.2-130 micrometres) thickness of poly(beta- hydroxybutyrate), a dialkanoyl polymer or an ethylene polymer and the coating is susceptible to breakdown by sunlight or bacteria.
  • a PVA/PVAc co-polymeric article may be waterproofed by coating the surface with a phenoxy based surface coating to render it resistant to premature dissolution. A portion of the article may be left uncoated to permit a route by which it may ultimately undergo total dissolution. Alternatively, the entire surface may be coated, in which case the article must be broken prior to disposal to expose the biodegradable co-polymer.
  • WO 93/22125 additionally discloses that a cast/co-extruded article with a cold water soluble inner core and a hot water soluble outer skin may be coated in part with an alcohol based flexographic ink to render the item additionally waterproof.
  • GB 2, 193, 925 A discloses the construction by bonded lamination of a multi-layered polyethylene web/PVA/PVA laminate. The composite sheet is designed for the rapid disintegration of both PVA layers leaving a residue of 19 micron thickness polyethylene web for disposal.
  • US-A-5,283,090 discloses a multi-layer laminated sheet for the construction of disposable sanitary items.
  • the laminate consists of a water impermeable/water insoluble film bonded to one side of an absorbent water swellable layer with a water resistant layer applied to the other surface.
  • the water resistant layer is formed by the application of a fluorine- containing or silicone-type water repellent resin dissolved in an organic solvent.
  • US-A-5, 674,578 discloses a laminate of a water soluble/water dispersible plasticised poly vinyl chloride and polyethylene oxide layer and a layer of a relatively weak water insoluble polymer or copolymer of vinylidene chloride, having a high resistance to liquid and gas.
  • GB 2,195,919A discloses a film for the construction of a disposable ostomy bag which is degradable by immersion in alkali solution (e.g. treatment in a pH 10 solution including triethanolamine and surfactants) then disposed of by flushing down the toilet.
  • the bag is constructed of a three ply sheet of material; the central layer being PVA, the inner layer being a double coating of highly hydrophobic PVC/Acrylonitrile copolymer and the outer layer being carboxylated acrylic acid polymer which is substantively water resistant at neutral pH. On treatment with alkali the carboxylic acid outer coating breaks down and allows dissolution of the central sheet.
  • the inner coating is considered to be of insufficient strength on its own and liable to tear and break-up on disposal down the toilet without blocking the toilet.
  • the description of the formation of the outer and inner layer indicates that they are a double coatings of 2 x 2.5 micron.
  • US-A-5,277,898 discloses acidic acrylic coatings used in hair perm products, which can be removed under alkaline conditions. Also it discloses an acid soluble coating of alkali-treated shellac.
  • the protective layers described may be applied to PVA.
  • US-A-5,508,101 discloses a multi layered laminate of non- woven webs or films.
  • the inner layer is water soluble and heat bonded on both sides with a web or film of alkali hydrolysable polymers, such that the whole article is dispersable in aqueous alkali.
  • the aforementioned processes seek to protect PVA articles during their working life by fully coating the item with non- degradable or slowly degradable materials and or materials which are non-hydrolysable under normal conditions. It is necessary that the article be physically broken, or that the protective surface be pierced or hydrolysed under caustic or acidic conditions prior to disposal to permit the dissolution of the inner PVA core.
  • the processes seek to leave some area of the PVA item uncoated by the protective layer to permit a route by which dissolution may occur on final disposal. The latter method may not fully protect a PVA or PVA/PVAc article during its working life and may be regarded as complex in application and potentially expensive.
  • the present invention seeks to overcome the disadvantages of known coatings by providing a coating which permits degradation and dissolution of a coated article in a controllable manner.
  • the present invention provides a water soluble article at least partially coated by a water resistant hydratable coating or a chemically and/or physically discontinuous surface coating which is susceptible to breakdown or penetration by water so that the coating resists degradation on contact with or immersion in an aqueous medium under normal conditions which the article is likely to encounter during its useful working life, the coating being susceptible to eventual penetration and degradation by water on prolonged contact with or immersion of the article in an aqueous medium when the article is discarded to waste.
  • the coating becomes hydrated on prolonged exposure to aqueous medium causing it to swell and tear, enabling water to contact the water soluble surface underlying the coating, the degradation of the coating being independent of the prevailing pH.
  • the coating is formed with imperfections comprising microscopic discontinuities or pores which on prolonged exposure enable water to contact the surface underlying the coating.
  • the body of the articles comprises polyvinylalcohol polymer or poly vinyl- alcohol/poly vinylacetate copolymer.
  • the rate of degradation of the coating may be controlled by selection of the thickness and/or physical and/or chemical structure of the coating.
  • the coating includes single or blended surface coating resins having slight hydrophilic character or hydrophobic character. Most preferably, the coating includes material having low or no environmental toxicity.
  • Single or blended acrylic resins may be used in the preparation of the coating, which may further include one or more plasticisers, waxes, surfactants and/or pigments or dyes.
  • the coating includes a non-aqueous solvent selected from esters, ketones, alcohols, white spirit, chlorinated solvents, and aliphatic or aromatic solvent. Decoration of the coating may be achieved by conventional printing methods, including screen, flexographic and gravure printing. Conveniently, the coating is thermoplastic and permits the coated article or material to be welded.
  • the components of the surface coating are selected to permit the article or material to be used in food contact applications.
  • the coating may be coated over by a further aqueous or organic solvent based resin, or by a heat or adhesive bonded layer to provide an additional dissolution resistant, modified surface for purposes of printing, adhesion, smoothness of finish or gloss, or further surface coating.
  • the coating is formed with imperfections comprising microscopic discontinuities or pores which on prolonged exposure enable water to contact the surface underlying the coating.
  • the coating is chemically constituted so that it becomes hydrated on prolonged exposure to aqueous medium causing it to swell and/or tear, enabling water to contact the water soluble surface underlying the coating, irrespective of the prevailing pH.
  • the degradation of the coating and the dissolution of the underlying article is pH independent. Under normal circumstances, the degradation will occur at or near neutral pH.
  • the body of the articles or material may comprise polyvinylalcohol polymer or polyvinylalcohol/ polyvinylacetate copolymer.
  • the rate of degradation of the coating is controlled by selection of the thickness and/or physical and/or chemical structure of the coating.
  • the coating may include single or blended surface coating resins having slight hydrophilic character or hydrophobic character.
  • the material used in manufacturing the coating preferably has low or no environmental toxicity.
  • the coating may include single or blended acrylic resin and one or more plasticisers, waxes and/or surfactants. It may further include a non-aqueous solvent selected from esters, ketones, alcohols, white spirit, chlorinated solvents, aliphatic or aromatic solvents. Also present may be a pigment or dye.
  • a coating according to the invention may be decorated by conventional printing methods, including screen, flexographic and gravure printing.
  • the coating is thermoplastic and permits the coated article or material to be welded to itself or to another article or material.
  • the components of the surface coating are conveniently selected to permit the article or material to be used in food contact applications.
  • the invention also provides a method of preparing a moisture resistant water soluble article, comprising at least partially coating a water soluble article with a coating material which includes single or blended surface coating resins having slight hydrophilic character or hydrophobic character, the coating being hydratable or being applied in such a way that it has chemical and/or physical discontinuities which render it susceptible to penetration by water so that on exposure to moisture conditions which are not encountered by the article during its normal useful working life but which are encountered when the article is discarded to waste, the coating degrades to permit water to contact and dissolve the article.
  • a coating material which includes single or blended surface coating resins having slight hydrophilic character or hydrophobic character
  • the present invention further provides a coating composition suitable for use as a water resistant hydratable coating or a chemically and/or physically discontinuous surface coating for a water soluble article, the composition comprising single or blended resins having slight hydrophilic character or hydrophobic character, the resultant coating when applied to an article being resistant to degradation by water on contact with or immersion in an aqueous medium under normal conditions which the article is likely to encounter during its useful working life and being susceptible to degradation on prolonged contact with or immersion in the aqueous medium when the article is discarded to waste, enabling water to contact and dissolve the article.
  • the present invention relates to an improved method for the protection of water soluble PVA and PVA/PVAc copolymer articles by surface coating with water resistant surface coatings, which protect the articles from moisture during their working life, yet degrade to expose the article to moisture once the article is discarded.
  • the article may be a formed article or a film or web, or the like. Once the article is exposed to moisture, it dissolves and the solute degrades in the environment.
  • the surface coatings are manufactured from polymeric resin materials (e.g. acrylic resins).
  • the resins can be dissolved in one or more, or blends of non-aqueous solvents, including esters, ketones, alcohols, white spirits, chlorinated solvents or aromatics. Non-toxic or low toxicity solvents are preferred.
  • control of degradation characteristics of these discontinuous surface coatings is achieved by chemical and/or physical weakness being incorporated into the coating by design, i.e. through choice of the type, and quantities of resins and/or solvent components and/or additives used.
  • Resins or blends of resins which are soluble in non-aqueous solvents yet contain polar moieties or moieties which may possess an affinity for water are termed “slightly hydrophilic resins”.
  • Resins which contain no polar moieties are termed "hydrophobic resins”.
  • Surface coatings with designed chemical susceptibility to degradation by moisture may be manufactured from slightly hydrophilic resins, or blends of slightly hydrophilic resins or hydrophobic resins.
  • Surface coatings with designed physical imperfections may be manufactured from slightly hydrophilic resins, or blends of slightly hydrophilic resins and hydrophobic resins, or hydrophobic resins.
  • the occurrence of the size and number of physical imperfections can be regulated by agents which control film formation, e.g. solvents, plasticisers and solvent modifiers.
  • Such coatings can be used fully to coat the PVA/PVAc article and will resist full immersion in water, and in some cases survive total immersion for several hours, thereby rendering PVA/PVAc products practical for many applications.
  • the limited nature of the water resistance permits the plastic articles ultimately to dissolve on disposal and subsequently biodegrade.
  • Any conventional surface coating means including dipping, spraying, smearing, painting, printing, etc, may be used to apply the coating to the article.
  • the present invention also relates to the manufacture of surface coating systems which permit control of the rate of breakdown of the surface coating by the blending of resins with differing degrees of hydrophobic and slight hydrophilic character.
  • the presence of the hydrophilic components in a largely hydrophobic surface coating provides zones of weakness, where moisture can cause breakdown of the coating permitting water to penetrate to the PVA or PVA/PVAc material beneath the coating layer.
  • the present invention also relates to surface coated articles in which the thickness of the applied surface coating is controlled to enable the rate of penetration or breakdown of the surface coating to be controlled. The thinner the coating applied the faster would be the breakdown.
  • the present invention also relates to surface coated articles having discontinuities or imperfections in the surface coating to enable the rate of penetration or breakdown of the surface coating to be controlled. The less perfect is the coating film formation the faster would be the breakdown.
  • Such surface coatings may be made with blends of resins with differing degrees of hydrophobic and slightly hydrophilic character, or be made with single resins with hydrophobic character or made with single resins of slightly hydrophilic character.
  • the depth of surface covering of the PVA/PVAc article is controlled to permit the occurrence of microscopic flaws (or pores). This renders the material highly durable in moisture sensitive applications, yet permits a route for the ultimate breakdown when the article is discarded.
  • the coating may be imparted sufficient flexibility to offer good adhesion to plasticised compounded PVA/PVAc which can be a relatively soft plastic.
  • plasticised compounded PVA/PVAc which can be a relatively soft plastic.
  • the presence of the plasticisers also serves to aid moisture resistance. Also the presence of a plasticiser aids the ultimate breakdown of the surface coating residue.
  • the surface coating plasticiser may be (a) any Cl to CIO mono-, di-or tri- ester of adipic acid, azelaic acid, phthalic acid, trimellitic acid or citric acid or (b) any mono-, di- or tri- Cl to CIO carboxylic acid esters of glycerol, propylene glycol, 1,3-propanediol, ethyl ene glycol, tri-alkyl citrate ester or (c) any blend of (a) and (b). Materials which are non-toxic or of low toxicity, and with low migration properties are preferred.
  • the surface coating may include a wax material (eg Ceraflour waxes of BYK Cera) for added water resistance and improved anti-scratch properties. Also, if desired, surface active agents may be employed to assist wetting on application.
  • a wax material eg Ceraflour waxes of BYK Cera
  • surface active agents may be employed to assist wetting on application.
  • Solvent modifiers may be included in the coating to control the rate of solvent evaporation, thereby yielding improved coating film formation and by implication effecting the occurrence of flaws (or pores) in the surface coating.
  • Such modifiers include propylene glycol, 1,3-propanediol, ethylene glycol or any Cl to C4 mono- or di- ethers, or mono- or di- esters of the aforementioned.
  • a coated surface may be decorated by conventional means, e.g. Flexographic and Gravure printing inks. Also it may be coloured by pigments or dyes. The components of the surface coating may be chosen to permit varying degrees of gloss or matt finish.
  • the surface coating may be thermoplastic in nature to permit heat sealing systems to be applied, such that coated articles or materials may be welded, e.g. to form bags from coated film materials.
  • the components of the surface coating may be chosen to permit a coated article to be used for food contact applications.
  • the size and distribution of the physical discontinuities can be controlled by the appropriate selection of resins or resin blends and in this way, the dissolution characteristics of the coated article may be controlled.
  • Hydrophobic resins suitable for use in the invention include
  • NeoCryl B-842 of Zeneca Resins eg. NeoCryl B-842 of Zeneca Resins
  • Slightly Hydrophilic Resins useful in the invention include:
  • the present invention also relates to the preparation of PVA and PVA/PVAc surface coatings from acrylic based polymers.
  • Acrylic based polymeric materials are preferred as they are potentially biodegradable and present a low risk to the environment.
  • the present invention also relates to the subsequent over-coating of the physically discontinuous coating.
  • the over-coating may comprise one or more layers of aqueous and/or organic solvent based surface coatings, and/or covering the same by a heat bonded or adhesive bonded layer which may provide additional dissolution resistance or may modify the surface printing properties, adhesion properties, anti-blocking properties, smoothness of finish or gloss characteristics, or permit further surface coating.
  • the subsequent coatings will have a faster rate of breakdown than the discontinuous layer.
  • Such a composite film as described above would appear as a physically continuous film but contain zones of greater and lesser resistance to hydration and hence the article would be protected by a combined chemically and physically discontinuous coating.
  • the invention will now be described more particularly with reference to the following non- limiting examples.
  • 'NeoCryl' is a Trademark of Zeneca Resins
  • 'Surcol' is a Trademark of Allied Colloids
  • 'Bisoflex' is a Trademark of British Petroleum Co. and used under license by International Speciality Chemicals
  • 'Dowinol' is a Trademark of Dow Chemicals
  • NeoCryl B-842 Surcol 836
  • Coated Film Results - Films coated with formulations A-D had good retention of strength on light exposure to moisture, whereas uncoated film control rapidly absorbed moisture and reverted to a semi-liquid paste.
  • Formulations A-C had good adhesion to PVA/PVAc film on stretching and creasing with A and B having the best performance.
  • Formulations D and E tended to have less flexibility and form microscopic cracks on creasing and stretching, which lead to mechanical weakness on immersion in water. Coatings A to E above were diluted 1 :1 with ethyl acetate and a test PVA/PVAc injection moulding was fully immersed into the resin and allowed to dry.
  • the test moulding was a thimble shaped injection moulding of approximate dimensions; 43mm high, 16mm dia, wall thickness 1mm, base thickness 5mm and weighing approximately 3 gram.
  • the thickness of the dry surface coatings was typically 3 to 5 microns.
  • the dried coated mouldings were immersed in 500 ml of pure water and the dissolution observed against an uncoated test moulding as control.
  • TM dissolves as control leaving a thin, friable residue of flexible clear film.
  • TM dissolves as control leaving a thin, friable residue of flexible clear film.
  • TM dissolves as control leaving a thin, very friable residue of opaque film.
  • TM dissolves as control leaving dispersed particles of a thin friable residue of opaque film.
  • Figures 1 to 6 represent a region 575 x 435 micron (10 m).
  • the surface of the control ( Figure 1) indicates a flat surface scored by fine straight lines. These details are attributed to fine linear abrasions on the mould of the test plaque.
  • Example A illustrates a smoother surface than the control, where the test plaque abrasions have been covered. There are numerous fine pores or depressions (1-7 micron in diameter) randomly distributed over the surface coating at an approximate number of 2-300 per mm 2 .
  • Example B ( Figure 3) illustrates a gently undulating surface, where the test plaque abrasions have been covered. There are numerous fine pores or depressions (1-15 micron in diameter) distributed in clusters over the surface, being typically situated in depressions in the undulating surface coating. The approximate number of pores is 3-400 per mm 2 .
  • Example C illustrates a gently undulating surface, where the test plaque abrasions have been covered. There are numerous round or ovate pores or depressions (30- 100 micron in diameter) distributed evenly over the surface. The approximate number of pores being 34-45 per mm 2 .
  • Example D illustrates an undulating surface where numerous ridges have formed, roughly running parallel and 2-300 micron apart. The test plaque abrasions have been covered. Though distributed evenly over the surface, the pores or depressions have increased in size (typically 100-150 micron in diameter) and are more irregular in shape, with some forming channels of up to 500 micron length. The approximate number of pores being 5-10 per mm 2 . In these larger pores, there are numerous smaller pores or depressions (1-20 micron in diameter).

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Laminated Bodies (AREA)

Abstract

La présente invention concerne un revêtement pour articles biodégradables comprenant un revêtement pouvant être hydraté ou un revêtement présentant une discontinuité chimique ou physique. Les imperfections du revêtement, qui peuvent comprendre des pores dans le revêtement, permettent à l'eau de pénétrer jusqu'à la surface sous-jacente de l'article hydrosoluble. La nature et l'étendue des imperfections permettent de réguler la vitesse de pénétration de l'eau dans le revêtement. Dans un autre mode de réalisation, le revêtement est un revêtement pouvant être hydraté qui gonfle et se déchire lorsqu'il est hydraté afin d'exposer l'article sous-jacent à l'humidité. La présente invention permet de protéger l'article d'une dissolution prématurée au cours de sa durée de vie normale, article qui se dégradera cependant lorsqu'il sera éliminé avec les déchets et que le revêtement de surface, en se dégradant, permettra à l'eau d'atteindre et de dissoudre l'article sous-jacent. En général, le corps de l'article comprend un poly(alcool de vinyle) ou un copolymère poly(alcool de vinyle)/poly(acétate de vinyle) hydrosoluble biodégradable. On peut former la discontinuité chimique/physique en recouvrant d'un revêtement pouvant être hydraté une surface déjà couverte d'un revêtement comportant des défectuosités physiques.
PCT/IE1998/000028 1997-04-15 1998-04-15 Revetements a degradation regulee et procede de fabrication de ces derniers WO1998046668A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
CA002286724A CA2286724A1 (fr) 1997-04-15 1998-04-15 Revetements a degradation regulee et procede de fabrication de ces derniers
EP98917566A EP0975692A1 (fr) 1997-04-15 1998-04-15 Revetements a degradation regulee et procede de fabrication de ces derniers
AU70749/98A AU7074998A (en) 1997-04-15 1998-04-15 Controlled degradation coatings and a method for their manufacture

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IE970278 IES80667B2 (en) 1997-04-15 1997-04-15 Controlled degradation coatings and a method for their manufacture
IES970278 1997-04-15

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WO1998046668A1 true WO1998046668A1 (fr) 1998-10-22

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AU (1) AU7074998A (fr)
CA (1) CA2286724A1 (fr)
IE (1) IES80667B2 (fr)
WO (1) WO1998046668A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6713140B2 (en) 2001-12-21 2004-03-30 Kimberly-Clark Worldwide, Inc. Latently dispersible barrier composite material
US6783826B2 (en) 2001-12-21 2004-08-31 Kimberly-Clark Worldwide, Inc. Flushable commode liner
WO2020161254A1 (fr) 2019-02-06 2020-08-13 Fostag Formenbau Ag Article en matière plastique soluble dans l'eau

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Publication number Priority date Publication date Assignee Title
US4372311A (en) * 1980-09-12 1983-02-08 Union Carbide Corporation Disposable articles coated with degradable water insoluble polymers
US4503098A (en) * 1980-09-12 1985-03-05 Union Carbide Corporation Disposable articles coated with degradable water insoluble polymers
WO1991017202A1 (fr) * 1990-05-01 1991-11-14 Courtaulds Packaging Limited Materiaux d'emballage
WO1993022125A1 (fr) * 1992-04-23 1993-11-11 British Technology Group Inter-Corporate Licensing Limited Materiaux et articles polymeres
EP0703265A1 (fr) * 1994-07-22 1996-03-27 Hoechst Aktiengesellschaft Hydrogels hydrophiles à capacité de gonflement élevée

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4372311A (en) * 1980-09-12 1983-02-08 Union Carbide Corporation Disposable articles coated with degradable water insoluble polymers
US4503098A (en) * 1980-09-12 1985-03-05 Union Carbide Corporation Disposable articles coated with degradable water insoluble polymers
WO1991017202A1 (fr) * 1990-05-01 1991-11-14 Courtaulds Packaging Limited Materiaux d'emballage
WO1993022125A1 (fr) * 1992-04-23 1993-11-11 British Technology Group Inter-Corporate Licensing Limited Materiaux et articles polymeres
EP0703265A1 (fr) * 1994-07-22 1996-03-27 Hoechst Aktiengesellschaft Hydrogels hydrophiles à capacité de gonflement élevée

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6713140B2 (en) 2001-12-21 2004-03-30 Kimberly-Clark Worldwide, Inc. Latently dispersible barrier composite material
US6783826B2 (en) 2001-12-21 2004-08-31 Kimberly-Clark Worldwide, Inc. Flushable commode liner
WO2020161254A1 (fr) 2019-02-06 2020-08-13 Fostag Formenbau Ag Article en matière plastique soluble dans l'eau

Also Published As

Publication number Publication date
IES80667B2 (en) 1998-11-18
AU7074998A (en) 1998-11-11
CA2286724A1 (fr) 1998-10-22
EP0975692A1 (fr) 2000-02-02
IES970278A2 (en) 1998-10-21

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