WO2001023460A1 - Film et son procede de fabrication - Google Patents

Film et son procede de fabrication Download PDF

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Publication number
WO2001023460A1
WO2001023460A1 PCT/JP2000/006662 JP0006662W WO0123460A1 WO 2001023460 A1 WO2001023460 A1 WO 2001023460A1 JP 0006662 W JP0006662 W JP 0006662W WO 0123460 A1 WO0123460 A1 WO 0123460A1
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WO
WIPO (PCT)
Prior art keywords
water
film
insoluble material
weight
soluble
Prior art date
Application number
PCT/JP2000/006662
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English (en)
Japanese (ja)
Inventor
Zenpei Meiwa
Hirohiko Hanada
Masafumi Miyamoto
Kenji Ishikawa
Original Assignee
Kao Corporation
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
Priority claimed from JP11278203A external-priority patent/JP3103073B1/ja
Priority claimed from JP2000124521A external-priority patent/JP2001162708A/ja
Application filed by Kao Corporation filed Critical Kao Corporation
Publication of WO2001023460A1 publication Critical patent/WO2001023460A1/fr

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • C11D17/042Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/50Perfumes

Definitions

  • the present invention relates to a film having a function of dissolving or hydrolyzing a film when the film comes into contact with water or the like and releasing contents packaged in the film, and to a method for producing the film.
  • water-soluble films have been functioning in applications such as foods, pharmaceuticals, agricultural chemicals, household goods and the like by dissolving the film when the contents are individually packaged and used, so that the contents can be taken out.
  • Japanese Patent Application Laid-Open No. 61-25771 / 57 describes that by mixing sodium chloride in advance with a water-soluble polymer, sodium chloride can be evenly arranged on the film to make the seasoning uniform.
  • Japanese Patent Application Laid-Open No. HEI 3-1974241 discloses a method in which a water-insoluble polymer is previously blended with a water-soluble polymer to control the release of a drug.
  • there was a sticky feeling when touched by hand was not satisfactory in terms of feel.
  • Japanese Patent Application Laid-open No. Hei 10-725259 Japanese Patent Laid-open No. Hei 9-104 617, Japanese Patent Laid-open No. Hei 5-11998, Japanese Utility Model Laid-open No. Hei 2-444029, Japanese Patent Laid-open Hei 1-2 The same applies to Japanese Patent No. 3713136 and Japanese Patent Application Laid-Open No. 50-73.
  • An object of the present invention is to provide a film having a high storage stability even in a humid environment and a film having a good feeling when touched by hand, and to provide a film manufacturing method.
  • An object of the present invention is to provide a packaging film that can enjoy the smell when Z or is dissolved. Disclosure of the invention The present invention relates to a film comprising a water-insoluble material present on the surface of a water-soluble film, wherein the water-insoluble material is used in an amount of 0.1 to 80 parts by weight based on 10 parts by weight of the water-soluble film.
  • a film in which the water-insoluble material is a powder having an average particle diameter of 500 ⁇ m or less, and a film in which the water-insoluble material is present on the surface of the water-soluble film, and The amount used is 0.1 to 80 parts by weight with respect to 100 parts by weight of the water-soluble film, and the water-insoluble material has a fiber length of 10 ⁇ m to 6 mm in a fibrous form. .
  • a water-soluble film surface a film in which a water-insoluble material is present, wherein the amount of the water-insoluble material used is 0.1 to 80 parts by weight with respect to 100 parts by weight of the water-soluble film,
  • a film in which the water-insoluble material is a powder having an average particle size of 500 ⁇ m or less or a fibrous form having a fiber length of 10 ⁇ m to 6 mm.
  • the present invention is a method for producing a film in which a water-insoluble material is present on the surface of a water-soluble film, and a method for fixing the water-insoluble material on the surface of the water-soluble film by coating or printing.
  • the water-insoluble material may be a powder having an average particle size of 500 ⁇ m or less, or the water-insoluble material may have a fibrous form having a fiber length of 10 ⁇ m to 6 mm.
  • a water-insoluble material is present on the surface of the thin film of the water-soluble polymer having a water content of 50% by weight or more, and then dried.
  • a mixture of the water-insoluble material and the binder solution is applied to the film manufacturing method or the water-soluble film surface. It is a process of making a film that is present and then dried.
  • the production method of the present invention has a water content of 50% by weight. /.
  • a water-insoluble material is present on the surface of the thin film of the water-soluble polymer, and then dried to obtain a film.
  • the amount of the water-insoluble material used is 0.1 to 80 parts by weight based on 100 parts by weight of the thin film of the water-soluble polymer. Parts by weight, and the water-insoluble material is powder or fiber with an average particle size of 5 ⁇ m or less 10 ⁇ !
  • a film production method characterized by having a fibrous morphology of up to 6 mm, A mixture of the soluble material and the binder solution is allowed to exist, and then dried to obtain a film.
  • the amount of the water-insoluble material used is 0.1 to 80 parts by weight with respect to 100 parts by weight of the water-soluble film.
  • the present invention also includes a method for producing a film, wherein the material has a powdery form having an average particle diameter of 500 ⁇ m or less or a fibrous form having a fiber length of 10 m to 6 mm.
  • the film of the present invention and the film obtained by the manufacturing method of the present invention are useful for packaging laundry materials in use forms, and the present invention provides laundry articles packaged with these films.
  • the water-soluble film is mainly composed of a water-soluble polymer, but its basis weight is 10 g from the viewpoint of film strength and solubility in water or water-dissolvability (hereinafter referred to as water-disintegrable).
  • Zm 2 or more is preferable, and the range of 15 to 100 g / m 2 is more preferable.
  • the thickness is preferably 9 ⁇ or more, more preferably 13 to 90 zm.
  • the water-soluble polymer has a solubility of 80 parts by weight when one part by weight of a sample is dissolved in 99 parts by weight of water at 25 ° C. /. Refers to the above, with a solubility of 90 weight. /. The above are more preferred.
  • the solubility is calculated by filtering the aqueous solution through filter paper (No. 2) and calculating the solid content in the filter paper.
  • water-soluble polymers examples include polyvinyl alcohol and Z or derivatives thereof (itaconic acid-modified polyvinyl alcohol, sulfonic acid-modified polyvinyl alcohol, maleic acid-modified polyvinyl alcohol, etc.), poly (meth) acrylic acid salts , (Meth) acrylic acid Z Alkali salt of (meth) acrylic acid ester copolymer, (meth) acrylic acid Z Alkaline salt of maleic acid copolymer, synthetic product such as polyvinylpyrrolidone; Semi-synthetic products such as tilcellulose, carboxymethylcellulosic sodium, hydroxyalkylcellulose, and starch derivatives; and natural polymers such as starch, gelatin, agar, seaweed, plant mucilage, and proteins. These may be used alone or in combination of two or more.
  • water-insoluble material a water-insoluble inorganic substance or a water-insoluble organic substance is used.
  • Water-insoluble means that when 1 part by weight of a sample is dissolved in 99 parts by weight of water at 25 ° C, the solubility is 50 parts by weight. /. Refers to the following, 40 weight. /.
  • water-insoluble inorganic substances such as zeolite, bentonite, talc, mai power, force ol, sepiolite, silica, calcium carbonate, titanium oxide, silicic anhydride, hydroxy 'calcium' apatite, phthalocyanine
  • zeolite, bentonite, talc, mica, kaolin, silica, titanium oxide, silicone and the like are preferably used.
  • water-insoluble organic substances include polyethylene, polypropylene, polyamide, polyethylene terephthalate, polystyrene, polyurethane, and Z or a cross-linked product thereof, sodium poly (meth) acrylate or poly (meth) acrylic acid ester, and / or a cross-linked product thereof.
  • Rubbers such as ethylene rubber, propylene rubber, styrene-butadiene rubber, butadiene rubber, silicone rubber, and synthetic polymers such as Z or cross-linked products thereof; cellulose and Z or derivatives thereof, chitosan and Z or derivatives thereof , Starch, natural shells such as fruit shells and Z or its derivatives, such as polyethylene, polyamide, polystyrene, sodium poly (meth) acrylate, poly (meth) acrylate, cellulose and / or cellulose. Derivatives, starch, etc. It used Mashiku. Where "poly (meth) acrylic acid” is replaced with "polyacrylic acid”
  • Polymethacrylic acid means both.
  • the average particle size is 500 ⁇ m or less, preferably 300 m or less, and 0.01 from the viewpoint of the feel of the film and the prevention of powder particles falling off the film. ⁇ 300 ⁇ m is more preferable.
  • the fiber length is 10 ⁇ , due to the feel of the film and the nodling property during film production. ⁇ 6 mm and 20 ⁇ ! ⁇ 5 mm is preferred.
  • the water-insoluble material is paper or non-woven fabric
  • those having a basis weight of 3 to 80 g Zm 2 are preferable, and S SO g / m 2 is more preferable, from the viewpoint of feeling when touching the film by hand and hydrolyzability. .
  • the water-insoluble material may be a true sphere, a substantially sphere, a plate, a bar, a fiber, a paper or a non-woven fabric.
  • a sheet-like material is preferably used, and may also be of an irregular shape by pulverization or the like, and hollow or porous particles may also be used.
  • the water-insoluble material two or more kinds of water-insoluble materials may be used.
  • the water-soluble film retains the water-solubility and water-decomposability, and has no stickiness, has a good feel, and has excellent usability.
  • the water-insoluble material is preferably used in an amount of 0.1 to 80 parts by weight, more preferably 0.3 to 70 parts by weight, based on 100 parts by weight of the water-soluble film.
  • the amount of the water-insoluble material present inside the water-soluble film is preferably 10% by weight or less, more preferably 5% by weight or less, and particularly preferably 0% by weight of the total insoluble material used.
  • the film of the present invention has, for example, a water content of 50% by weight. /.
  • a water-insoluble material is present on the surface of the thin film of the water-soluble polymer described above, and then dried.
  • the water-insoluble material is present when the water content of the water-soluble polymer is less than 50% by weight, the adhesion between the surface of the water-soluble polymer and the water-insoluble material is insufficient, and the water-soluble polymer is easily detached. .
  • water content of the water-soluble polymer is defined by the following equation.
  • a method of causing the water-insoluble material to be present on the surface of the water-soluble polymer thin film a method of spraying or spraying the water-insoluble material on the surface of the water-soluble polymer thin film is preferably used.
  • the water-soluble polymer when a water-insoluble material is present on the surface of a thin film of a water-soluble polymer, the water-soluble polymer contains a plasticizer, particularly in order to more reliably fix the water-insoluble material to the water-soluble film. It may be.
  • the plasticizer is water; phenolic compounds such as methanolic, ethanolic, isopropynoleanolic, etc .; glycols such as ethyleneglycol, diethyleneglycolone, triethyleneglycolone, polyethyleneglycol; glycerin, polyglycerin, G
  • glycols such as polyethylene glycol; at least one selected from polyhydric alcohols such as glycerin, polyglycerin, trimethylolpropane, and pentaerythritol is preferably used for improving the plasticizing effect, drying speed, and production speed. obtain.
  • the amount of the plasticizer is 1 part by weight or more based on 100 parts by weight of the water-soluble polymer from the viewpoint of the plasticizing effect, and 100 parts by weight from the viewpoint of the film forming property of the polymer sheet ⁇ ⁇ ⁇ the strength of the polymer sheet. Parts by weight or less, more preferably 3 to 60 parts by weight.
  • the plasticizer is removed by a method such as drying if necessary.
  • the water-insoluble plastic material may be fixed on the film surface by a binder.
  • a binder Such films are obtained by making a film from a water-soluble polymer, then presenting a mixture of a water-insoluble material and a binder solution on the surface of the film, and then drying. At this time, it is preferable to plasticize only the surface of the film or to mix a water-soluble water-soluble polymer and a plasticizer before the water-insoluble material is present on the film surface together with the binder.
  • the binder is previously dissolved or dispersed in water and / or an alcohol such as methanol, ethanol, propanol or butanol; or a petroleum such as hexane, heptane, tonolen, xylene or thinner, and then the water-insoluble material is dissolved or dispersed. Then, paint or ink (print) on a water-soluble film prepared in advance. That is, the water-insoluble material is fixed on the surface of the water-soluble film by coating or printing. For example, a water-insoluble material dispersed or dissolved in an organic solvent or the like is applied or printed on the surface of a previously prepared water-soluble film.
  • an alcohol such as methanol, ethanol, propanol or butanol
  • a petroleum such as hexane, heptane, tonolen, xylene or thinner
  • a general mixer or disperser is used to mix the water-insoluble material into the binder solution.
  • a general mixer or disperser is used as a method of causing the water-insoluble material to be present on the surface of the water-soluble film together with a binder.
  • a coating or printing method for example, spray coating, comma coater, lip coater, gravure coater 1.
  • Coating methods such as mouth-coating, flow-coating, and kiss coating; printing methods such as gravure printing and flexographic printing are preferably used.
  • the binder for fixing the water-insoluble material to the surface of the water-soluble film examples include a water-soluble polymer, an alcohol-soluble polymer, and a petroleum-soluble polymer.
  • the organic solvent is preferably one that does not dissolve the water-soluble film, and alcohols such as methanol, ethanol, and propanol, depending on the type of water-soluble polymer constituting the water-soluble film; Petroleum solvents such as hexane, heptane, octane, toluene and xylene are used.
  • the amount of the organic solvent is 0.5 to 20 times the weight of the water-insoluble material.
  • organic solvents are removed by a method such as drying after fixing the water-insoluble material on the surface of the water-soluble film.
  • additives such as a thickener can be used to improve the dispersibility of the water-insoluble material in an organic solvent.
  • Ethyl cellulose, hydroxypropyl cellulose or an oil-soluble polymer is preferably used as a thickener.
  • the addition amount of such a thickener is preferably 0.1 to 10% by weight based on the water-insoluble tenacious material.
  • binders examples include polyvinyl alcohol and / or its derivatives (itaconic acid-modified polyvinyl alcohol, sulfonic acid-modified polyvinyl alcohol, maleic acid-modified polyvinyl alcohol, etc.), poly (meth) acrylate alkali salt, ) Alkaline salt of acrylic acid / (meth) acrylic acid ester copolymer, alkali salt of (meth) acrylic acid Z maleic acid copolymer, polyvinylpyrrolidone, polyethylene oxide, polyamide, polyethylene terephthalate, polystyrene , Polyurethane, ethylene rubber, propylene rubber, styrene-butadiene rubber, butadiene rubber, silicone-based polymers, etc .; methylcenorellose, ethylethylenolose, sodium carboxymethylcellulose, hydroxya Semi-synthetic products such as ruquilcellulose and starch derivatives; natural polymers such as chi
  • the amount of the binder is preferably 1 to 50 parts by weight, more preferably 3 to 40 parts by weight, based on 100 parts by weight of the water-insoluble material.
  • the film thus obtained contains water or a solvent, it is dried by a method such as a drum drying method, a belt drying method, or a hot air drying method.
  • the film of the present invention can be provided with an embossed pattern on its surface by embossing.
  • the feel when touching the hand can be further improved.
  • the surface area of the concave portion on the film surface is preferably 40% or less.
  • the thickness of the film after embossing is preferably at least 1.3 times the thickness of the film before embossing.
  • the film of the present invention may be scented, and may be scented on the surface and / or inside of the film. By perfuming the film surface and / or inside, the fragrance duration after opening the package can be freely controlled.
  • Examples of the method of perfumery include a method of dispersing or mixing a fragrance component and a fragrance-containing material into a water-soluble film, and a method of dispersing a fragrance component and a fragrance-containing material when a water-insoluble material is present on the surface of the water-soluble film. There is a method of mixing and making it exist on the surface of the water-soluble film.
  • fragrances and fragrances terpene-based hydrocarbons such as ⁇ -binene,] 3-binene, myrcene, limonene, 1,8-cineole, and hydrophobic fragrances such as amyl acetate and amyl probionet (for example, — No. 3,266,734, page 3, upper left column, line 19 to the same page lower left column, line 13).
  • ⁇ -binene 3-binene
  • myrcene myrcene
  • limonene 1,8-cineole
  • hydrophobic fragrances such as amyl acetate and amyl probionet (for example, — No. 3,266,734, page 3, upper left column, line 19 to the same page lower left column, line 13).
  • amyl acetate and amyl probionet for example, — No. 3,266,734, page 3, upper left column, line 19 to the same page lower left column, line 13).
  • a releasing agent besides the plasticizer, a releasing agent, an anti-blocking agent, a solubility improving agent, a coloring component and the like may be used as additives.
  • Nonionic surfactants such as polyoxyethylene alkyl ethers, polyoxyethylene phenols, polyoxypropylene propylene glycols, polyoxyethylene polyoxypropylene alkyl ethers, etc. , Alkyl trimethylammonium chloride, salt Cationic surfactants such as nickel are preferably used.
  • the amount of these release agents is 0.1 parts by weight or more based on 100 parts by weight of the water-soluble polymer from the viewpoint of release properties, and 5 parts by weight or less from the viewpoint of film-forming properties and strength of the water-soluble film. Is preferred.
  • the antiblocking agent inorganic substances such as bentonite, talc, kaolin, zeolite and the like, and organic substances such as starch and cellulose powder are preferably used.
  • the amount of the anti-booking agent added is preferably 1 part by weight or less, particularly 0.1 part by weight, based on 100 parts by weight of the water-soluble polymer from the viewpoint of handling properties such as winding property and productivity. The following is preferred. '
  • a water-soluble inorganic salt As the solubility improver, a water-soluble inorganic salt, a water-soluble organic salt, a water-insoluble inorganic substance, and a water-insoluble organic substance are used.
  • water-soluble inorganic salts include chlorides such as sodium chloride, potassium chloride, and magnesium chloride; sulfates such as sodium sulfate, potassium sulfate, magnesium sulfate, and aluminum sulfate; carbonates such as sodium carbonate and sodium hydrogen carbonate.
  • water-soluble organic salts such as citrate, conodate, maleate, fumarate, and malate, fatty acid salts, ester phosphates, acylated amino acid salts, and the like. Examples include sulfosuccinates.
  • the water-insoluble inorganic substance include inorganic substances such as bentonite, talc, kaolin, and zeolite.
  • water-insoluble organic substance include cellulose powder and starch.
  • the addition amount of these solubility improvers is preferably 1 to 30 parts by weight with respect to 100 parts by weight of the water-soluble polymer in order to improve the solubility and obtain a uniform film.
  • J, a non-liquid finishing agent, a washing composition such as a sizing agent is divided into this film and used as a laundry article.
  • the laundry composition to be packaged can be in the form of tablets, powders, powders, and pastes. Pastes and doughs are more preferred in terms of feel. In the case of pastes and doughs, the contact area between the gas (especially oxygen) and the laundry composition can be reduced, which is also preferable from the viewpoint of improving the stability (deterioration such as discoloration and generation of an odor).
  • the dough-like material it enters the hardness 0 0 5 to 2 0 kg / cm 2 is preferably at 2 5 ° C, 0 1 ⁇ 1 5 kg / cm:.. , More preferably, 0 5-10 kg / cm 2 is more preferable.
  • the adapter can be determined by measuring the stress when penetrating 2 cm into the laundry composition at a penetration speed of 30 cm / min.
  • “dough” means a kneaded product of a powdery composition and a fluid substance such as a liquid, paste, or gel composition. And those having fluidity due to stress.
  • the dough can be produced using a universal stirrer, such as a universal stirrer suitable for high-viscosity stirring.
  • a universal stirrer such as a universal stirrer suitable for high-viscosity stirring.
  • the viscosity of the laundry composition used in the present invention is preferably 100,000 mPa's or more, and 200,000 mPas or more. mPas or more is more preferable.
  • the thickness of the packaged laundry composition is preferably 15 mm or less, more preferably 10 mm or less, and even more preferably 5 mm or less from the viewpoint of solubility.
  • the thickness is preferably 1 mm or more, more preferably 2 mm or more, from the viewpoint of strength and ease of handling. From the viewpoint of the convenience of use, it is preferable to use one packaged for each use.
  • the laundry composition to be packaged is preferably from 10 to 100 g, more preferably from 15 to 50 g.
  • the water content in the laundry composition of the present invention is preferably 0.1 to 15% by weight, more preferably 0.5 to 10% by weight, particularly preferably 0.5 to 10% by weight, from the viewpoint of preventing blocking and drying. Preferably, it is 2.3 to 7% by weight.
  • the water content excludes water of crystallization such as zeolite, carbonate and citrate.
  • the non-liquid detergent among the laundry compositions used in the present invention mainly contains a surfactant and a builder.
  • the surfactant include a higher alcohol or an ethylene oxide thereof (hereinafter referred to as “EO”), a sulfate salt of an adduct, an alkyl benzene sulfone salt, and a no.
  • Anionic surfactants such as rough-insolephonic rooster salt, ⁇ -olefinsorephonic salt, ⁇ -sulfofatty acid salt, ⁇ -sulfofatty acid alkyl ester salt or fatty acid salt; ⁇ / propylene Oxide (hereinafter referred to as "PII") adducts, nonionic surfactants such as fatty acid alcohol amides and alkylpolyglycosides; amphoteric surfactants; cation surfactants and the like.
  • PII propylene Oxide
  • amine salts of straight-chain alkyl benzene sulfonic acids having an alkyl chain of 10 to 14 carbon atoms, and amine salts of ester sulfates of higher alcohols having 12 to 18 carbon atoms are preferred in terms of detergency and foam properties.
  • POO. 1-4 mol adducts ( However, EO and P ⁇ may be either random polymerization or block polymerization) from the viewpoints of removing sebum stains, hard water resistance, and biodegradability.
  • the content of the surfactant is preferably 5 to 80% by weight, more preferably 20 to 60% by weight in the non-liquid detergent in terms of detergency. /. Particularly preferred is 30-50 weight. /. It is. It is also preferable to use a combination of a nonionic surfactant and an anionic surfactant. In this case, the total of both is 50 to 100% by weight, particularly 70 to 100% by weight in the surfactant, and the detergency is good. It is preferred in that respect.
  • builders include inorganic builders such as carbonates, crystalline or amorphous aluminosilicates, crystalline or amorphous silicates, phosphates, and phosphates, and tri-triacetates, and ethylenediaminetetraacetic acid.
  • examples thereof include sodium such as organic builder such as salt, tartrate, citrate, acrylic acid polymer and copolymer, and alkali metal salt such as potassium.
  • a crystalline aluminosilicate is preferred in terms of the ability to capture polyvalent metal ions such as calcium ions and the ability to absorb oil to nonionic surfactants.
  • the content of the builder is preferably 5 to 70% by weight, more preferably 10 to 60% by weight, and particularly preferably 15 to 55% by weight in the non-liquid detergent from the viewpoint of improving the detergency. /. It is.
  • the content ratio of the surfactant and the builder is preferably from 1 ⁇ 5 to 10 ⁇ 1 (weight ratio), more preferably from the viewpoint of producing a dough having detergency and flexibility. 1/3 to 3/1, particularly preferably lZ2 to 3/2.
  • the non-liquid detergent in the present invention includes a bleaching agent (percarbonate, perborate, bleach activator, etc.), a re-staining inhibitor (carboxymethyl cellulose, etc.), which are known in the field of clothing detergents.
  • a bleaching agent percarbonate, perborate, bleach activator, etc.
  • a re-staining inhibitor carboxymethyl cellulose, etc.
  • Softener softener, reducing agent (sulfite, etc.), fluorescent whitening agent, foam inhibitor (silicone Etc.) and fragrances and the like.
  • the bleaching agent and the softening agent are respectively less than 20% by weight, preferably less than 2% and less than 4% by weight in the non-liquid detergent.
  • a softening agent such as an amine salt or a quaternary ammonium salt can be used.
  • a quaternary ammonium salt of a di-long-chain alkyl type is preferable, and the alkyl group contains a linking group such as one CO—, —C—, —NHC—, or one CONH— in the alkyl group.
  • the softener content is 4 to 70% by weight in the non-liquid finish. /. It is.
  • a fragrance, a pigment, a silicone compound, an antibacterial agent, a solvent, a water-soluble salt, and the like may be contained.
  • an oxygen-based bleaching agent is suitable.
  • the oxygen-based bleach contains a compound containing a peroxide that generates hydrogen peroxide in water.
  • peroxide sodium peroxide, Tripoli-phosphate sodium peroxide adduct, sodium pyrophosphate-hydrogen peroxide adduct, urea-hydrogen peroxide adduct, 4 N a S 0 4 ⁇ 2 H 2 N ⁇ NaC1, sodium perborate ⁇ monohydrate, sodium perborate, tetrahydrate, sodium peroxide, sodium peroxide, calcium peroxide, etc.
  • Sodium sodium borate monohydrate and sodium perborate tetrahydrate are preferred.
  • the bleach content is 2 to 90% by weight, preferably 20 to 90% by weight, in the non-liquid bleach.
  • a compound having an appropriate leaving group tetraacetylethylenediamine, acetooxybenzenesulfonate, JP-A-59-22999, JP-A- Bleaching of a metal catalyst or the like in which an organic peracid precursor or a transition metal is stabilized with a sequestering agent described in JP-A-6-316840, JP-A-6-316700 It may be contained as an activator.
  • the content of bleach activator is 0 to 30% by weight, preferably 1 to 20% by weight in the non-liquid bleach.
  • p-toluenesulfonate in addition to surfactants, builders, and softeners used in non-liquid detergents or non-liquid finishes, p-toluenesulfonate, xylenesulfonate, alkenylsuccinate, urea, etc. It may contain a solubilizer, a penetrant, a suspending agent such as clay, an abrasive, a chelate, a pigment, a dye, a fragrance, and the like.
  • the sizing agent is described in JP-B-48-239. No.
  • T-330 maleic acid-modified polyvinyl alcohol, Nippon Synthetic Chemical Industry Co., Ltd. 150 g, water 850 g, and glycerin 15 g as a plasticizer are dissolved, defoamed, and put on a polyethylene terephthalate film. It was applied to a thickness of 200 ⁇ m using an applicator. Next, after spraying zeolite powder (average particle size: 7.6 m, manufactured by Kao Corporation), drying it with hot air at 110 ° C for 10 minutes, the release film was removed, and the film (F — 1) was obtained. The thickness of the film 3 0 / m, Zeorai preparative composite weight: 1. One is 4 g / m 2 7 this.
  • K-60 polyvinylpyrrolidone, manufactured by Wako Pure Chemical Industries, Ltd.
  • A-55 Solfalex A-55, hydroxyalkyl starch, manufactured by Matsutani Chemical Co., Ltd.
  • W—100 G Cellulose powder, average fiber length 150 m, manufactured by Nippon Paper Industries Co., Ltd.
  • Kaolin average particle size 4.2 m, manufactured by Wako Pure Chemical Industries, Ltd.
  • KM-118 carboxylic acid-modified polybutyl alcohol, manufactured by Kuraray Co., Ltd.
  • 150 g water at 800 g
  • polyethylene glycol as plasticizer PEG # 400, Wako Pure Chemical Industries, Ltd.
  • Emulgen 135 nonionic surfactant, manufactured by Kao Corporation
  • TSA732 silicone-based defoamer as a defoamer 0.75 g was dissolved and defoamed.
  • the film was dried with hot air at 140 ° C (drying residence time: 2 minutes) to obtain a long water-soluble film having a film thickness of 40.
  • the surface of the water-soluble film (A) is coated with a coating (a) using a comma coater (manufactured by Hirano Tecseed Co., Ltd.), dried for 10 seconds in a hot air dryer at 60 ° C, and wound up. Obtained.
  • the composite amount of calcium carbonate, binder and fragrance in this film is 7.1 g / m "C S.
  • the paint (b) was applied to the surface of the water-soluble film (A) prepared in the same manner as in Example 5 using a Daravia printing machine (manufactured by Hirano Teksid Co., Ltd.), and dried at 60 ° C with hot air. The film was dried for 1 second for 2 seconds to obtain a wound film. The composite amount of calcium carbonate and titanium oxide in this film was 4.2 g / m 2 .
  • a gravure printing machine (a picture printed on a Mary's backsheet, Kao Corporation) was used as a gravure printing machine on the surface of the film obtained by compounding the carbonated titanium oxide and titanium oxide obtained in Example 6 with a binder.
  • the film was obtained by overprinting with ink (c) using The composite amount of titanium oxide and lid mouth cyanine blue in this film was 0.3 g / m 2 .
  • a film was prepared in the same manner as in Example 1 except that the film was prepared without spraying the zeolite powder.
  • a film was prepared in the same manner as in Example 1, except that a water-soluble salt (manufactured by Naikai Salt Industry Co., Ltd.) was used instead of the water-insoluble zeolite powder.
  • the amount of complexed salt was 1.4 g Zn.
  • Table 1 shows the compositions of the films obtained in Examples 1 to 7 and Comparative Examples 1 and 2, and Table 2 shows the results of evaluation by the following methods.
  • the amount of compounding of the water-insoluble materials in Examples 5 to 7 includes the weight of the fragrance and the fragrance.
  • Example 8 Production of a packaged detergent
  • Nonidet R-7 polyoxyethylene (7) alkyl (C 12 to C 15 ) ether] manufactured by Mitsubishi Chemical Corporation Sulfuric oxide (Na salt) 10 g, “Sophthanol EP 7045” manufactured by Nippon Shokubai Chemical Industry Co., Ltd.
  • the obtained dough is stretched to a thickness of 2 mm, cut into 7 cm ⁇ 13 cm, and placed between two sheets of the film (F-1) obtained in Example 1 (with the zeolite composite surface facing outside). It was sandwiched and heat-sealed to obtain a packaging detergent for clothing.
  • the obtained dough is stretched to a thickness of 2 mm, cut into 7 cm ⁇ 13 cm, and between the two films (F-1) obtained in Example 1. (The zeolite composite surface is the outer surface) And heat-sealed to obtain a packaging detergent for clothing.
  • Japanese Patent Application Laid-Open No. 06-306769 discloses 15% of the softener composition of Example 1, 46% of Emargen 120 (manufactured by Kao Corporation), 33% of polyethylene glycol (molecular weight: 6000), 33%, and 20% of carbon atoms.
  • a paste was obtained by mixing 2% of fatty acid, 2% of Gerbe AS having 16 carbon atoms, 0.5% of fragrance, and 1.5% of water. 2 m of paste obtained Stretched to a thickness of 7 m, cut to 7 cm x 13 cm, sandwiched between two sheets of the film (F-1) obtained in Example 1 (with the zeolite composite surface as the outer surface), and heat-sealed.
  • a packaging finish for clothing was obtained.
  • a suspension consisting of 100 parts of starch, 2 parts of mono-tallow alkyltrimethylammonium chloride, and 10 parts of water was alpha-solidified with a 150 ° C heating roller, dried, crushed, and sieved. 25%, Emalgen 120 (manufactured by Kao Corp.) 40%, polyethylene glycol (molecular weight 6000) 30%, carbon number 20
  • a paste was obtained by mixing 1.5% of fatty acid, 1.5% of Gerbe AS having 16 carbon atoms, 0.5% of flavor and 1.5% of water. The obtained paste is stretched to a thickness of 2 mm, cut into 7 cm ⁇ 13 cm, and the film (F-1) obtained in Example 1 is placed between two sheets (the zeolite composite surface is removed). On the outer surface) and heat sealed to obtain a packaging paste for clothing.
  • T-330 maleic acid-modified polyvinyl alcohol, manufactured by Nippon Synthetic Chemical Industry Co., Ltd.
  • 8500 g of water 200 g of glycerin as plasticizer (manufactured by Wako Pure Chemical Industries, Ltd.), and emulgen 135 as a release agent
  • glycerin as plasticizer
  • emulgen 135 as a release agent
  • Example 13 While unwinding the water-soluble film (F-2), cellulose powder (W-400G, average fiber length 27 ⁇ , Japan, using a Daravia coating machine (Hirano Rexid Co., Ltd., gravure roll 200 mesh) was used. While stirring a dispersed solution of 50 g of papermaking (manufactured by K-200 Cures), 10 g of ethylcellulose (manufactured by K-200 Cures), 890 g of isopropyl alcohol (manufactured by Wako Pure Chemical Industries, Ltd.), and 50 g of water Worked. Subsequently, hot air drying was performed at 110 ° C for 20 seconds. As a result, a film in which cellulose powder (W-400G) was composited with the water-soluble film was obtained. The compounded amount of W-400G was 2.5 g Zm 2 .
  • a gravure printing machine Hirano Lecce Co., Ltd., gravure roll 100 mesh
  • a cellulose fiber yarn PLUS W-50G, average fiber length 300 111, Nippon Paper Industries
  • MFG hydroxypropyl cellulose
  • ethyl alcohol manufactured by Wako Pure Chemical Industries, Ltd.
  • hot air drying was performed at 110 ° C for 20 seconds.
  • the amount of W-50G complexed in this product was 8.5 g Zm 2 .
  • Example 14 100 g of cellulose fiber (W-50G) was changed to 100 g of Zeolite (manufactured by Kao Corporation), and the same operation as in Example 14 was performed to combine zeolite with a water-soluble film. The obtained film was obtained. The zeolite composite amount of this product was 4.5 g Zm 2 .
  • the water-soluble film (F-2) was used as a comparative sample as it was.
  • Example 13 and Comparative Example 3 were compared with those of Example 17 and Comparative Example 3. Evaluation was performed in the same manner as in Comparative Examples 1-2. Table 3 shows the results.
  • the film of the present invention is one in which the film is dissolved or hydrolyzed by contact of the film with water or the like, and the contents packaged in the film function. When used, the contents of foods, agricultural chemicals, household goods, etc. can be easily and conveniently taken out.
  • This film is excellent in water solubility and water dissolvability, not only enables long-term storage and storage in high humidity environments, but also has no stickiness when touched by hand and is excellent in the touch surface.

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  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
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Abstract

Cette invention concerne un film qui est doté d'une grande stabilité au stockage, même en atmosphère très humide, et qui est agréable au toucher; un procédé de fabrication pour ce film; et un film de conditionnement qui renferme un parfum et qui dégage donc une odeur agréable lorsqu'on l'ouvre ou qu'on le dissout. Ce film comprend une pellicule hydrosoluble et un matériau insoluble dans l'eau sur une de ses faces. Le matériau insoluble dans l'eau représente de 0, 1 à 80 parties en poids pour 100 parties en poids du film hydrosoluble et se présente sous la forme de paricules dont le diamètre moyen est de 500 νm ou moins, ou sous la forme de fibres d'une longueur comprise entre 10 νm et 6 mm. L'invention concerne également un produit de lavage dont les emballages individuels sont constitués par ledit film. Le procédé de fabrication de ce film consiste plus précisément à fixer le matériau insoluble dans l'eau sur une face de la pellicule hydrosoluble par application en couche ou par impression.
PCT/JP2000/006662 1999-09-30 2000-09-27 Film et son procede de fabrication WO2001023460A1 (fr)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP27820299 1999-09-30
JP11278203A JP3103073B1 (ja) 1999-09-30 1999-09-30 フィルムの製法
JP11/278202 1999-09-30
JP11/278203 1999-09-30
JP2000124521A JP2001162708A (ja) 1999-09-30 2000-04-25 フィルム
JP2000/124521 2000-04-25

Publications (1)

Publication Number Publication Date
WO2001023460A1 true WO2001023460A1 (fr) 2001-04-05

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008004200A1 (fr) * 2006-07-05 2008-01-10 The Procter & Gamble Company Substrat hydrosoluble possédant une résistance à la dissolution avant son immersion dans l'eau
WO2008004198A2 (fr) * 2006-07-05 2008-01-10 The Procter & Gamble Company Substrat soluble dans l'eau résistant à la dissolution avant d'être immergé dans l'eau
WO2008004201A2 (fr) * 2006-07-05 2008-01-10 The Procter & Gamble Company Substrat hydrosoluble disposant d'une résistance à la dissolution avant son immersion dans l'eau
WO2008053379A2 (fr) * 2006-11-03 2008-05-08 The Procter & Gamble Company Substrat hydrosoluble présentant une résistance à la dissolution avant son immersion dans l'eau.
JP2010507714A (ja) * 2006-11-03 2010-03-11 ザ プロクター アンド ギャンブル カンパニー 水に浸漬されるより前に溶解耐性を有する水溶性基材
US7727946B2 (en) 2005-05-13 2010-06-01 The Procter & Gamble Company Process for making functionalized films for cleaning products
US7972589B2 (en) 2004-05-17 2011-07-05 Akzo Nobel N.V. Hair fixative film
WO2016043009A1 (fr) * 2014-09-17 2016-03-24 積水化学工業株式会社 Film d'emballage soluble dans l'eau

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51138772A (en) * 1975-05-28 1976-11-30 Kuraray Co Method of modification of surface property of polyvinyl alcohol film
JPH01237136A (ja) * 1988-03-17 1989-09-21 Lion Corp 水分散性防水フィルム及び吸収性物品
JPH01249343A (ja) * 1988-03-30 1989-10-04 Kuraray Co Ltd 表面被覆されたポリビニルアルコール系フイルム及びその製造方法
JPH0244029U (fr) * 1988-09-22 1990-03-27
JPH11179279A (ja) * 1997-12-18 1999-07-06 Kansai Paint Co Ltd 樹脂成型品の塗装方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51138772A (en) * 1975-05-28 1976-11-30 Kuraray Co Method of modification of surface property of polyvinyl alcohol film
JPH01237136A (ja) * 1988-03-17 1989-09-21 Lion Corp 水分散性防水フィルム及び吸収性物品
JPH01249343A (ja) * 1988-03-30 1989-10-04 Kuraray Co Ltd 表面被覆されたポリビニルアルコール系フイルム及びその製造方法
JPH0244029U (fr) * 1988-09-22 1990-03-27
JPH11179279A (ja) * 1997-12-18 1999-07-06 Kansai Paint Co Ltd 樹脂成型品の塗装方法

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7972589B2 (en) 2004-05-17 2011-07-05 Akzo Nobel N.V. Hair fixative film
JP2012162081A (ja) * 2005-05-13 2012-08-30 Procter & Gamble Co 機能化フィルム
JP2016135478A (ja) * 2005-05-13 2016-07-28 ザ プロクター アンド ギャンブル カンパニー 機能化フィルム
US7727946B2 (en) 2005-05-13 2010-06-01 The Procter & Gamble Company Process for making functionalized films for cleaning products
WO2008004198A2 (fr) * 2006-07-05 2008-01-10 The Procter & Gamble Company Substrat soluble dans l'eau résistant à la dissolution avant d'être immergé dans l'eau
WO2008004201A2 (fr) * 2006-07-05 2008-01-10 The Procter & Gamble Company Substrat hydrosoluble disposant d'une résistance à la dissolution avant son immersion dans l'eau
WO2008004200A1 (fr) * 2006-07-05 2008-01-10 The Procter & Gamble Company Substrat hydrosoluble possédant une résistance à la dissolution avant son immersion dans l'eau
WO2008004198A3 (fr) * 2006-07-05 2008-05-15 Procter & Gamble Substrat soluble dans l'eau résistant à la dissolution avant d'être immergé dans l'eau
WO2008004201A3 (fr) * 2006-07-05 2008-07-10 Procter & Gamble Substrat hydrosoluble disposant d'une résistance à la dissolution avant son immersion dans l'eau
US8440318B2 (en) 2006-07-05 2013-05-14 The Procter & Gamble Company Water-soluble substrate with resistance to dissolution prior to being immersed in water
WO2008053379A2 (fr) * 2006-11-03 2008-05-08 The Procter & Gamble Company Substrat hydrosoluble présentant une résistance à la dissolution avant son immersion dans l'eau.
JP2010507714A (ja) * 2006-11-03 2010-03-11 ザ プロクター アンド ギャンブル カンパニー 水に浸漬されるより前に溶解耐性を有する水溶性基材
WO2008053379A3 (fr) * 2006-11-03 2009-03-26 Procter & Gamble Substrat hydrosoluble présentant une résistance à la dissolution avant son immersion dans l'eau.
WO2016043009A1 (fr) * 2014-09-17 2016-03-24 積水化学工業株式会社 Film d'emballage soluble dans l'eau
US10351685B2 (en) 2014-09-17 2019-07-16 Sekisui Chemical Co., Ltd. Water-soluble packaging film

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