WO1997004170A1 - Produits en papier menage a souplesse amelioree - Google Patents
Produits en papier menage a souplesse amelioree Download PDFInfo
- Publication number
- WO1997004170A1 WO1997004170A1 PCT/US1996/011778 US9611778W WO9704170A1 WO 1997004170 A1 WO1997004170 A1 WO 1997004170A1 US 9611778 W US9611778 W US 9611778W WO 9704170 A1 WO9704170 A1 WO 9704170A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- tissue
- following structure
- chloride
- alkyl
- quaternary ammonium
- Prior art date
Links
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/07—Nitrogen-containing compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/22—Agents rendering paper porous, absorbent or bulky
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/10—Phosphorus-containing compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/22—Proteins
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/53—Polyethers; Polyesters
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/59—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon
Definitions
- the invention resides in a tissue which has been topically treated with a hydrophilic softening composition comprising one or more of propylene glycol, polyethylene glycol, polypropylene glycol, and/or other hydrophilic solvents and one or more organic surface modifiers (hereinafter defined).
- the invention resides in a tissue comprising from about 0.5 to about 30 dry weight percent, based on the weight of fiber, of a softening composition comprising one or more hydrophilic solvents selected from the group consisting of water, propylene glycol, polypropylene glycol and polyethylene glycol, and one or more surface modifiers selected from the group consisting of quaternary ammonium compounds, quaternized protein compounds, phospholipids, silicone quaternaries, hydrolyzed wheat protein/polydimethyl siioxane, phosphocopolyol copolymer, quaternized lanolin derivatives, and silicone emulsions.
- Suitabl e quaternary ammonium compounds have the fol l owi ng structures :
- R aliphatic, saturated or unsaturated C 8 - C 22 ;
- X methyl sulfate or other compatible counterion
- R aliphatic, saturated or unsaturated C 8 -C 22 .
- X methyl sulfate, chloride, or other compatible counterion
- R aliphatic, normal, saturated or unsaturated, C 8 - C 22
- R 1 2-hydroxyethyl or 2-hydroxypropyl ;
- R aliphatic, normal or branched, saturated or unsaturated, C 8 - 22'
- X chloride, methyl sulfate, ethyl sulfate, or other compatible counterion;
- R' 2-hydroxyethyl or polyethoxyethanol ; and
- n 1 to 50;
- X methyl sulfate, chloride, or other compatible counterion
- X chloride, sulfate or any other compatible counterion
- R aliphatic alkyl, normal or branched, saturated or unsaturated, C 8 - C 22 ;
- X chloride, methyl sulfate, or other compatible counterion.
- Suitable quaternized protein compounds include the following structures:
- R 1 fatty acid radical, saturated or unsaturated, C 12 - C 22 ;
- R 2 hydrolyzed soy protein, hydrolyzed silk protein, hydrolyzed wheat protein, collagen moiety, or keratin moiety;
- X chloride, lactate, or other compatible counterion
- R fatty acid radical, saturated or unsaturated, C 12 - C 22 ;
- R 2 hydrolyzed collagen or keratin moiety
- X chloride, lactate, or other compatible counterion.
- Suitable phospholipids include, without limitation, those having the following structures:
- A an anion
- n 2 to 6;
- R 3 hydrogen or alkyl , hydroxyalkyl or alkenyl of up to 6 carbons; or cycloalkyl of up to 6 carbon atoms, or polyoxyalkylene of up to 10 carbon atoms; and al kyl , al kenyl , al koxy or hydroxyal kyl , C-
- A an anion
- R 1 is an amidoa ine moiety of the structure:
- n 2 to 6;
- R 3 hydrogen or alkyl , hydroxyalkyl or alkenyl of up to 6 carbons; or cycloalkyl of up to 6 carbon atoms, or polyoxyalkylene of up to 10 carbon atoms; and R 8 has the following structure:
- Suitable silicone quaternaries include those having the following structure:
- R alkyl group, C 12 - C 18 ;
- Suitable organoreactive polysiloxanes include the following structures:
- the add-on amount of the hydrophilic softening composition containing the surface modifier(s) and the hydrophilic solvent(s) can be from about 0.5 to about 30 dry weight percent based on the weight of the tissue, more specifically from about 1 to about 10 dry weight percent. Water can be added to the formulation to reduce the viscosity of the composition and to make the formulation more suitable for application.
- the amount of the surface modifier in the hydrophilic softening composition can be from about 0.2 to about 80 weight percent, more specifically from about 0.5 to about 50 weight percent, and still more specifically from about 1 to about 20 weight percent.
- the amount of the silicone emulsion, if included in the hydrophilic softening composition can be from about 1 to about 80 percent, more specifically from about 5 to about 50 percent, and still more specifically from about 5 to about 20 percent.
- humectants include lactic acid and its salts, sugars, glycerin, ethoxylated glycerin, ethoxylated lanolin, corn syrup, hydrolyzed starch hydrolysate, urea, and sorbitol.
- Suitable skin protectants include allentoin, kaolin, aliantoin and zinc oxide.
- Suitable preservatives include Quaternium-15, organic acids, parabens, DMDM hydantoin, diazolidinyl urea, ethylchloroisothiazoline, methyl isothiazolin, sodium hydroxymethyl glycinate, imidazolidinyl urea, and the like.
- Suitable feel modifiers include corn starch, oat flour, talc, boron nitride, and cyclodextrin.
- the hydrophilic softening composition which can be in the form of a solution or suspension, can be applied to the dry tissue surface by any suitable means, such as spraying or printing.
- the tissue to which the hydrophilic formulation is applied can be any tissue useful as facial tissue, bath tissue, or towels. Such can be produced by throughdrying or wet-pressing tissue making processes and can be creped or uncreped, layered or blended (not layered).
- the finished tissue product can be one-ply, two-ply or three or more plies. Either the dryer side or the air side of the tissue can be oriented outwardly in the final tissue product.
- Example 1 A hydrophilic solution consisting of 50 parts by weight propylene glycol, 28.5 parts by weight of a softener/debonder composition (quaternary imidazolinium, fatty acid alkoxylate and polyether with 200- 800 molecular weight, identified as DPSC 5299-8, Witco Corporation) and 21.5 parts by weight water.
- the propylene glycol and DPSC 5299-8 were mixed together until uniform. Then the water was added and the mixture stirred until a homogeneous solution was achieved.
- the resulting hydrophilic solution was applied to the outer surfaces of the two outer plies of a three-ply, blended, wet- pressed creped tissue having a basis weight of 41.6 grams per square meter.
- each ply consisted of a blend of 50 percent eucalyptus hardwood, 14 percent northern hardwood kraft, and 36 percent northern softwood kraft fibers.
- the add-on amount was about 1 dry weight percent based on the total weight of the three-ply tissue.
- the resulting tissue had a fuzzy softness.
- a hydrophilic solution consisting of 90 parts by weight propylene glycol and 10 parts by weight DPSC 5299-8 was prepared.
- the propylene glycol and the DPSC 5299-8 were mixed together until a homogeneous solution was achieved.
- the resulting hydrophilic solution was applied to the outer surfaces of the two outer plies of a three-ply, blended, wet- pressed creped tissue (as described in Example 1) having a basis weight of 41.6 grams per square meter using a gravure printing method.
- the add ⁇ on amounts were about 1, 3, and 10 dry weight percent based on the total weight of the tissue.
- the resulting tissues had a fuzzy softness, with the higher add-on tissues feeling softer.
- a hydrophilic solution was prepared consisting of 80 parts by weight propylene glycol and 20 parts by weight of a quaternary ammonium compound (stearalkonium chloride, 25 percent active, identified as Mackernium SDC- 25, Mclntyre Group, LTD.).
- the propylene glycol and the Mackernium SDC- 25 were mixed together and stirred until homogeneous.
- the resulting Example 3
- a hydrophilic solution was prepared consisting of 80 parts by weight propylene glycol and 20 parts by weight of a quaternary ammonium compound (stearalkonium chloride, 25 percent active, identified as Mackernium SDC- 25, Mclntyre Group, LTD.).
- the propylene glycol and the Mackernium SDC- 25 were mixed together and stirred until homogeneous.
- the resulting hydrophilic solution was applied to the outer surfaces of the two outer plies of a three-ply, wet-pressed creped tissue as described in Example 1 having a basis weight of about 41.6 grams per square meter using a gravure printing method.
- the add-on amounts were about 1, 3, and 10 dry weight percent based on the weight of the tissue.
- the resulting tissue had a fuzzy softness, with the higher add-on tissues being softer.
- Example 4 A hydrophilic solution was prepared consisting of 70 parts by weight propylene glycol, 10 parts by weight DPSC 5299-8 and 20 parts by weight of a second quaternary ammonium compound (olealkonium chloride, 50 percent active, identified as Mackernium KP, Mclntyre Group, LTD.). The propylene glycol and the DPSC 5299-8 were mixed together. The Mackernium KP was added and stirred until homogeneous.
- a second quaternary ammonium compound olealkonium chloride, 50 percent active, identified as Mackernium KP, Mclntyre Group, LTD.
- the resulting hydrophilic solution was applied to the outer surfaces of the two outer plies of a three-ply blended, wet-pressed creped tissue as described in Example 1 and a three-ply layered, wet- pressed creped tissue having a basis weight of about 41.6 grams per square meter.
- Each of the plies of the layered tissue contained three layers.
- the dryer side outer layer consisted of eucalyptus fibers.
- the inner layer contained 28 percent northern hardwood kraft and 72 percent northern softwood kraft fibers.
- the air side outer layer contained northern hardwood kraft and northern softwood kraft fibers.
- Kymene 557H (Hercules, Inc.) was added at 0.16 - 0.34 weight percent based on dry fiber in all layers.
- a wet strength agent (Parez 631NC from Cytec Industries, Inc.) was added at 0.45 - 0.55 weight percent based on dry fiber in the inner layer and the airside layer.
- the three-ply tissue was plied together such that the two outer surfaces were dryer side layers.
- the add-on amounts of the hydrophilic solution were about 1 and 2 dry weight percent based on the total weight of the tissue.
- the resulting tissue products were very soft, with the higher add-on tissues being softer.
- a hydrophilic solution was prepared consisting of 50 parts by weight propylene glycol, 20 parts by weight DPSC 5299-8 and 30 parts by weight Mackernium KP.
- the propylene glycol and the DPSC 5299-8 were mixed together.
- the Mackernium KP was added and stirred until homogeneous.
- the resulting hydrophilic solution was applied to the outer surfaces of the two outer plies of a three-ply, blended, wet-pressed creped tissue as described in Example 1 and a three- ply layered, wet-pressed creped tissue as described in Example 4.
- the add-on amounts were about 1 and 2 dry weight percent based on the weight of the tissue.
- the resulting tissue products were very soft, with the higher add-on tissues being softer.
- a hydrophilic solution consisting of 80 parts by weight propylene glycol, 10 parts by weight of DPSC 5299-8 and 10 parts by weight of an organoreactive polysiloxane (identified as FTS-226, 40 percent active, OSi Specialties, Inc.).
- the propylene glycol and DPSC 5299-8 were mixed together until uniform.
- the FTS-226 was added and the mixture stirred until a homogeneous solution was achieved.
- the resulting hydrophilic solution was applied to the outer surfaces of the two outer plies of a three-ply, blended, wet- pressed creped tissue as described in Example 1.
- the add-on amount was about 1 and 5 dry weight percent based on the weight of the tissue.
- the resulting tissue had a flannelly softness.
- a hydrophilic solution consisting of 40 parts by weight propylene glycol, 10 parts by weight DPSC 5299-8 and 50 parts by weight FTS-226.
- the propylene glycol and the DPSC 5299-8 were mixed together until uniform.
- the FTS-226 was added and the mixture stirred until a homogeneous solution achieved.
- the resulting hydrophilic solution was applied to a blended three-ply, wet- pressed creped tissue as described in Example 1 and a layered, three- ply, wet-pressed creped tissue as described in Example 4.
- the add-on amount was about 1 and 2 dry weight percent based on the weight of the tissue.
- the resulting tissues had a flannelly softness.
- a hydrophilic solution consisting of 55 parts by weight propylene glycol, 20 parts by weight DPSC 5299-8 and 25 parts by weight FTS-226.
- the propylene glycol and the DPSC 5299-8 were mixed together until uniform.
- the FTS-226 was added and the mixture stirred until a homogeneous solution achieved.
- the resulting hydrophilic solution was applied to both a blended, three-ply, wet-pressed creped tissue as described in Example 1 and a layered, three- ply, wet-pressed creped tissue as described in Example 4.
- the add-on amount was about 1 and 2 dry weight percent based on the weight of the tissues.
- the resulting tissues had a flannelly softness with the higher add-on tissue being softer.
- a one-ply, uncreped, through-air-dried tissue was made using a layered headbox.
- the two outer layers contained bleached eucalyptus hardwood kraft pulp processed through a Maule shaft disperser with a power input of 80 kilowatts at a consistency of about 34 percent and at a temperature of 184 * F.
- the two outer layers made up 70 percent of the tissue sheet by weight of fiber.
- the remaining 30 percent of the tissue web constituted the middle layer and consisted of bleached northern softwood kraft pulp.
- the total basis weight of the sheet was 33.9 grams per square meter of air-dried tissue.
- the inner layer was refined to obtain sufficient dry strength in the final product.
- the one-ply tissue was printed with a formulation consisting of about 12 percent Mackernium SDC, about 30 percent glycerin, about 50 percent polypropylene glycol and about 8 percent water.
- the resulting tissue contained about 0.5 weight percent DPSC-5299-8 and approximately 4 weight percent of the printed formulation based on fiber.
- the resulting tissue had a smooth, silky, surface feel.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Paper (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
- Materials For Medical Uses (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sanitary Thin Papers (AREA)
Abstract
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP09506800A JP2001502760A (ja) | 1995-07-21 | 1996-07-16 | 柔軟性を改良したティシュー製品 |
HU9901712A HUP9901712A2 (hu) | 1996-07-16 | 1996-07-16 | Megnövelt lágyságú törlőkendő-termék |
BR9611422A BR9611422A (pt) | 1995-07-21 | 1996-07-16 | Produtos de papel fino com maciez aperfeiçoada |
EP96925328A EP0840823B1 (fr) | 1995-07-21 | 1996-07-16 | Produits en papier menage a souplesse amelioree |
PL96326892A PL326892A1 (en) | 1995-07-21 | 1996-07-16 | Paper tissues of improved softness |
AU65465/96A AU710263B2 (en) | 1995-07-21 | 1996-07-16 | Tissue products with improved softness |
DE69629031T DE69629031T8 (de) | 1995-07-21 | 1996-07-16 | Tissueprodukte mit verbesserter weichheit |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US50584095A | 1995-07-21 | 1995-07-21 | |
US08/505,840 | 1995-07-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997004170A1 true WO1997004170A1 (fr) | 1997-02-06 |
Family
ID=24012090
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1996/011778 WO1997004170A1 (fr) | 1995-07-21 | 1996-07-16 | Produits en papier menage a souplesse amelioree |
Country Status (14)
Country | Link |
---|---|
EP (1) | EP0840823B1 (fr) |
JP (1) | JP2001502760A (fr) |
KR (1) | KR19990035770A (fr) |
CN (1) | CN1207785A (fr) |
AR (1) | AR002886A1 (fr) |
AU (1) | AU710263B2 (fr) |
BR (1) | BR9611422A (fr) |
CA (1) | CA2223807A1 (fr) |
CO (1) | CO4560507A1 (fr) |
DE (1) | DE69629031T8 (fr) |
PL (1) | PL326892A1 (fr) |
TR (1) | TR199800096T2 (fr) |
WO (1) | WO1997004170A1 (fr) |
ZA (1) | ZA965677B (fr) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998019010A1 (fr) * | 1996-10-25 | 1998-05-07 | Kimberly-Clark Worldwide, Inc. | Tissu-papier a base de composes contenant une amidoamine cationique |
WO1998019013A1 (fr) * | 1996-10-25 | 1998-05-07 | Kimberly-Clark Worldwide, Inc. | Tissu-papier contenant des composes quaternaires silicones |
US6146494A (en) * | 1997-06-12 | 2000-11-14 | The Procter & Gamble Company | Modified cellulosic fibers and fibrous webs containing these fibers |
US6228223B1 (en) | 1997-08-06 | 2001-05-08 | Akzo Nobel Nv | Composition for treatment of cellulosic material |
US6416624B1 (en) | 1997-10-10 | 2002-07-09 | Union Carbide Chemicals & Plastics Technology Corporation | Spray application of an additive composition to sheet materials |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4200476B2 (ja) * | 2002-05-22 | 2008-12-24 | 星光Pmc株式会社 | 家庭用薄葉紙用柔軟剤、それを使用した製紙方法、及び家庭用薄葉紙 |
TW201734278A (zh) * | 2016-03-24 | 2017-10-01 | 金百利克拉克國際公司 | 包含軟化組成物之紙巾 |
CN107286302A (zh) * | 2017-06-28 | 2017-10-24 | 常州市瑞泰物资有限公司 | 一种纸用柔软剂及其制备方法 |
CN109183504B (zh) * | 2018-09-30 | 2021-01-29 | 广州旭太材料科技有限公司 | 一种造纸柔软剂及其制备方法 |
CN110699995A (zh) * | 2019-10-16 | 2020-01-17 | 东莞市凯柔纸业有限公司 | 一种柔纸巾的制作方法 |
CN114263068B (zh) * | 2021-12-30 | 2022-10-04 | 福建恒安集团有限公司 | 一种柔软抗菌整理剂、制备方法及其应用工艺 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4943350A (en) * | 1987-08-06 | 1990-07-24 | Scott Paper Company | Chemically treated paper products - towel and tissue |
US5217576A (en) * | 1991-11-01 | 1993-06-08 | Dean Van Phan | Soft absorbent tissue paper with high temporary wet strength |
EP0688901A2 (fr) * | 1994-06-21 | 1995-12-27 | Kimberly-Clark Corporation | Papier de soie contenant de la glycérine et des composés d'ammonium quaternaire |
-
1996
- 1996-07-04 ZA ZA965677A patent/ZA965677B/xx unknown
- 1996-07-15 CO CO96037086A patent/CO4560507A1/es unknown
- 1996-07-16 EP EP96925328A patent/EP0840823B1/fr not_active Expired - Lifetime
- 1996-07-16 BR BR9611422A patent/BR9611422A/pt not_active Application Discontinuation
- 1996-07-16 AU AU65465/96A patent/AU710263B2/en not_active Ceased
- 1996-07-16 KR KR1019980700426A patent/KR19990035770A/ko not_active Ceased
- 1996-07-16 CA CA002223807A patent/CA2223807A1/fr not_active Abandoned
- 1996-07-16 JP JP09506800A patent/JP2001502760A/ja active Pending
- 1996-07-16 DE DE69629031T patent/DE69629031T8/de not_active Expired - Fee Related
- 1996-07-16 WO PCT/US1996/011778 patent/WO1997004170A1/fr not_active Application Discontinuation
- 1996-07-16 CN CN96198797A patent/CN1207785A/zh active Pending
- 1996-07-16 PL PL96326892A patent/PL326892A1/xx unknown
- 1996-07-16 TR TR1998/00096T patent/TR199800096T2/xx unknown
- 1996-07-19 AR ARP960103653A patent/AR002886A1/es unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4943350A (en) * | 1987-08-06 | 1990-07-24 | Scott Paper Company | Chemically treated paper products - towel and tissue |
US5217576A (en) * | 1991-11-01 | 1993-06-08 | Dean Van Phan | Soft absorbent tissue paper with high temporary wet strength |
EP0688901A2 (fr) * | 1994-06-21 | 1995-12-27 | Kimberly-Clark Corporation | Papier de soie contenant de la glycérine et des composés d'ammonium quaternaire |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998019010A1 (fr) * | 1996-10-25 | 1998-05-07 | Kimberly-Clark Worldwide, Inc. | Tissu-papier a base de composes contenant une amidoamine cationique |
WO1998019013A1 (fr) * | 1996-10-25 | 1998-05-07 | Kimberly-Clark Worldwide, Inc. | Tissu-papier contenant des composes quaternaires silicones |
US5904810A (en) * | 1996-10-25 | 1999-05-18 | Kimberly-Clark Worldwide, Inc. | Tissue containing cationic amidoamine compounds |
US6030675A (en) * | 1996-10-25 | 2000-02-29 | Kimberly-Clark Worldwide, Inc. | Tissue containing silicone amidoamine esters and phosphates |
US6146494A (en) * | 1997-06-12 | 2000-11-14 | The Procter & Gamble Company | Modified cellulosic fibers and fibrous webs containing these fibers |
US6228223B1 (en) | 1997-08-06 | 2001-05-08 | Akzo Nobel Nv | Composition for treatment of cellulosic material |
US6416624B1 (en) | 1997-10-10 | 2002-07-09 | Union Carbide Chemicals & Plastics Technology Corporation | Spray application of an additive composition to sheet materials |
Also Published As
Publication number | Publication date |
---|---|
CN1207785A (zh) | 1999-02-10 |
AR002886A1 (es) | 1998-04-29 |
EP0840823B1 (fr) | 2003-07-09 |
AU6546596A (en) | 1997-02-18 |
JP2001502760A (ja) | 2001-02-27 |
TR199800096T2 (xx) | 1998-07-21 |
EP0840823A1 (fr) | 1998-05-13 |
DE69629031D1 (de) | 2003-08-14 |
PL326892A1 (en) | 1998-10-26 |
CA2223807A1 (fr) | 1997-02-06 |
AU710263B2 (en) | 1999-09-16 |
KR19990035770A (ko) | 1999-05-25 |
CO4560507A1 (es) | 1998-02-10 |
ZA965677B (en) | 1997-01-24 |
BR9611422A (pt) | 1999-02-23 |
MX9800373A (es) | 1998-07-31 |
DE69629031T8 (de) | 2004-07-29 |
DE69629031T2 (de) | 2004-04-22 |
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