EP0701640B1 - Wasserfrei selbstemulgierbare chemische weichmachende zusammensetzung anwendbar in faserigen materialien aus zellulose - Google Patents

Wasserfrei selbstemulgierbare chemische weichmachende zusammensetzung anwendbar in faserigen materialien aus zellulose Download PDF

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Publication number
EP0701640B1
EP0701640B1 EP94918091A EP94918091A EP0701640B1 EP 0701640 B1 EP0701640 B1 EP 0701640B1 EP 94918091 A EP94918091 A EP 94918091A EP 94918091 A EP94918091 A EP 94918091A EP 0701640 B1 EP0701640 B1 EP 0701640B1
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EP
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Prior art keywords
quaternary ammonium
weight
web
compound
mixture
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Expired - Lifetime
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EP94918091A
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English (en)
French (fr)
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EP0701640A1 (de
Inventor
Robert Gene Laughlin
Dean Van Phan
Paul Dennis Trokhan
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Procter and Gamble Co
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Procter and Gamble Co
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/07Nitrogen-containing compounds
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/06Alcohols; Phenols; Ethers; Aldehydes; Ketones; Acetals; Ketals
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-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
    • D21H21/14Non-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
    • D21H21/22Agents rendering paper porous, absorbent or bulky
    • D21H21/24Surfactants

Definitions

  • This invention relates to a method of producing a substantially waterless self-emulsifiable chemical softener composition. More particularly, it relates to a method of producing a substantially waterless self-emulsifiable chemical softener compositions useful for treating fibrous cellulose materials, such as tissue paper webs.
  • the treated tissue webs can be used to make soft, absorbent paper products such as toweling, napkin, facial tissue, and toilet tissue products.
  • Armak Company of Chicago, Illinois, in their bulletin 76-17 (1977) disclose the use of dimethyl di(hydrogenated)tallow ammonium chloride in combination with fatty acid esters of polyoxyethylene glycols to impart both softness and absorbency to tissue paper webs.
  • quaternary ammonium compounds such as the well known dialkyl dimethyl ammonium salts (e.g. ditallow dimethyl ammonium chloride, ditallow dimethyl ammonium methyl sulfate, di(hydrogenated)tallow dimethyl ammonium chloride etc ). are effective chemical debonding agents. Unfortunately, these quaternary ammonium compounds are not hydrophilic. Applicants have discovered that the chemical softening compositions of the present invention enhance both softness and absorbency rate of fibrous cellulose materials.
  • dialkyl dimethyl ammonium salts e.g. ditallow dimethyl ammonium chloride, ditallow dimethyl ammonium methyl sulfate, di(hydrogenated)tallow dimethyl ammonium chloride etc .
  • the ultimate users of the chemical softening composition simply dilute the mixture with a liquid carrier (i.e., water) to form an aqueous dispersion of the quaternary ammonium compound / polyhydroxy compound mixture, which is then added to the papermaking furnish.
  • a liquid carrier i.e., water
  • the homogenous mixture of the quaternary ammonium compound and the polyhydroxy compound can exist either in a solid state or in a fluid state before being dispersed in the aqueous media.
  • the mixture of the quaternary ammonium compound and polyhydroxy compound is diluted with a liquid carrier such as water to a concentration of from about 0.01% to about 25% by weight of the softening composition before being added to the papermaking furnish.
  • the transition from the X ⁇ to the X ⁇ crystal occurs at 27°C in DHTDMAMS instead of 47°C as in DODMAMS.
  • calorimetric data indicate that several crystal ⁇ Lam phase transitions occur in DHTDMAMS rather than one as in DODMAMS. The onset temperature of the highest of these transitions is 56°C, in good agreement with the X-ray data.
  • Analysis of the amount of treatment chemicals used herein or retained on tissue paper webs can be performed by any method accepted in the applicable art.
  • wet strength additives typically result in paper products with permanent wet strength, i.e., paper which when placed in an aqueous medium retains a substantial portion of its initial wet strength over time.
  • permanent wet strength in some types of paper products can be an unnecessary and undesirable property.
  • Paper products such as toilet tissues, etc., are generally disposed of after brief periods of use into septic systems and the like. Clogging of these systems can result if the paper product permanently retains its hydrolysis-resistant strength properties.
  • manufacturers have added temporary wet strength additives to paper products for which wet strength is sufficient for the intended use, but which then decays upon soaking in water. Decay of the wet strength facilitates flow of the paper product through septic systems.
  • the substantially waterless self-emulsifiable chemical softener composition of (5) can be pre-mixed (steps 1-5 above) at the chemical supplier (e.g. Sherex company of Dublin, Ohio) and then economically shipped to the ultimate users of the chemical softening composition where it can then be diluted to the desired concentration.
  • the chemical supplier e.g. Sherex company of Dublin, Ohio
  • the embryonic wet web is transferred from the photo-polymer wire, at a fiber consistency of about 15% at the point of transfer, to a photo-polymer fabric having 0.87 cells per mm 2 (562 Linear Idaho cells per square inch), 40 percent knuckle area and 0.23 mm (9 mils) of photo-polymer depth. Further dewatering is accomplished by vacuum assisted drainage until the web has a fiber consistency of about 28%.
  • the patterned web is pre-dried by air blow-through to a fiber consistency of about 65% by weight.
  • the web is then adhered to the surface of a Yankee dryer with a sprayed creping adhesive comprising 0.25% aqueous solution of Polyvinyl Alcohol (PVA).
  • PVA Polyvinyl Alcohol
  • the fiber consistency is increased to an estimated 96% before the dry creping the web with a doctor blade.
  • the doctor blade has a bevel angle of about 25 degrees and is positioned with respect to the Yankee dryer to provide an impact angle of about 81 degrees; the Yankee dryer is operated at about (800 fpm, feet per minute) 244 meters per minute.
  • the dry web is formed into roll at a speed of (700 fpm) 214 meters per minutes.
  • the fiber consistency is increased to an estimated 96% before the dry creping the web with a doctor blade.
  • the doctor blade has a bevel angle of about 25 degrees and is positioned with respect to the Yankee dryer to provide an impact angle of about 81 degrees; the Yankee dryer is operated at about (800 fpm, feet per minute) 244 meters per minute.
  • the dry web is formed into roll at a speed of (700 fpm) 214 meters per minute

Claims (6)

  1. Verfahren zum Herstellen einer im wesentlichen wasserfreien, selbstemulgierfähigen, chemischen Weichmacherverbindung mit einem Gemisch aus:
    (a) einer quartären Ammoniumverbindung mit der Formel
    Figure 00380001
    in welcher jeder R2 Substituent eine C1 - C6 Alkyl- oder Hydroxidalkyl-Gruppe oder ein Gemisch daraus, insbesondere ein C1 - C3 Alkyl, vorzugsweise Methyl, ist; wobei jeder R1 Substituent eine C14 - C22 Hydrocarbyl-Gruppe oder ein Gemisch daraus, vorzugsweise ein C16 - C18 Alkyl ist, und X- ein geeignetes Anion, vorzugsweise Chlorid oder Methylsulfat ist; und
    (b) einer Polyhydroxiverbindung ausgewählt aus Glycerol, Polyglycerolen mit einem mittleren Molekulargewicht von 150 bis 800 g/mol und Polyoxiethylenglykolen und Polyoxipropylenglylolen mit einem mittleren Molekulargewicht von 200 bis 4000 g/mol, insbesondere von 200 bis 1000 g/mol, vorzugsweise von 200 bis 600 g/mol;
    in welchem das Gewichtsverhältnis der quartären Ammoniumverbindung zu der Polyhydroxiverbindung von 1 : 0,1 bis 0,1 : 1, insbesondere von 1 : 0,3 bis 0,3 : 1, vorzugsweise von 1 : 0,7 bis 0,7 : 1 reicht,
    wobei dieses Verfahrens die folgenden Verfahrensschritte umfaßt:
    a) die Polyhydroxiverbindung wird mit der quartären Ammoniumverbindung bei einer Temperatur gemischt, bei welcher die quartäre Ammoniumverbindung und die Polyhydroxiverbindung mischbar sind, wobei der Feuchtigkeitsgehalt der chemischen Weichmacherverbindung weniger als 20 Gew.% beträgt,
    b) bilden eines homogenen Gemisches aus der quartären Ammoniumverbindung und der Polyhydroxiverbindung, und
    c) abkühlen des homogenen Gemisches auf eine feste Form bei Raumtemperatur.
  2. Verfahren nach Anspruch 1, in welchem die quartäre Ammoniumverbindung Di(hydriertes)talgdimenthylammoniumchlorid oder Di(hydriertes)talgdimethylammoniummethylsulfat ist.
  3. Verfahren nach Anspruch 1 oder 2, in welchem die quartäre Ammoniumverbindung mit der Polyhydroxiverbindung bei einer Temperatur von wenigstens 40°C, vorzugsweise von 56°C bis 68°C gemischt wird.
  4. Verfahren nach einem der Ansprüche 1 -3, in welchem die quartäre Ammoniumverbindung in einem flüssigkristallinen Zustand oder in einem flüssigen Zustand vorliegt, wenn sie mit der Polyhydroxiverbindung gemischt wird.
  5. Im wesentlichen wasserfreie, selbst-emulgierfähige, chemische Weichmacherverbindung, die durch ein Verfahren gemäß einem der Ansprüche 1 - 4 erhältlich ist, in welcher die chemische Weichmacherverbindung bei Raumtemperatur ein stabiler, homogener Festkörper ist.
  6. Im wesentlichen wasserfreie, selbst-emulgierfähige, chemische Weichmacherverbindung nach Anspruch 5, in welcher der Feuchtigkeitsgehalt der chemischen Weichermacherverbindung weniger als 10 Gew.% beträgt.
EP94918091A 1993-06-03 1994-05-23 Wasserfrei selbstemulgierbare chemische weichmachende zusammensetzung anwendbar in faserigen materialien aus zellulose Expired - Lifetime EP0701640B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US7229993A 1993-06-03 1993-06-03
US72299 1993-06-03
PCT/US1994/005777 WO1994029520A1 (en) 1993-06-03 1994-05-23 Waterless self-emulsifiable chemical softening composition useful in fibrous cellulosic materials

Publications (2)

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EP0701640A1 EP0701640A1 (de) 1996-03-20
EP0701640B1 true EP0701640B1 (de) 2000-03-08

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EP94918091A Expired - Lifetime EP0701640B1 (de) 1993-06-03 1994-05-23 Wasserfrei selbstemulgierbare chemische weichmachende zusammensetzung anwendbar in faserigen materialien aus zellulose

Country Status (19)

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EP (1) EP0701640B1 (de)
JP (1) JP3194958B2 (de)
KR (1) KR100336444B1 (de)
CN (1) CN1052050C (de)
AU (1) AU694433B2 (de)
BR (1) BR9406738A (de)
CA (1) CA2162848A1 (de)
CZ (1) CZ321395A3 (de)
DE (1) DE69423352T2 (de)
FI (1) FI955789A (de)
HK (1) HK1013134A1 (de)
HU (1) HUT74116A (de)
MY (1) MY111219A (de)
NO (1) NO954868L (de)
NZ (1) NZ267305A (de)
PE (1) PE53894A1 (de)
PH (1) PH31624A (de)
SG (1) SG66237A1 (de)
WO (1) WO1994029520A1 (de)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19711452A1 (de) 1997-03-19 1998-09-24 Sca Hygiene Paper Gmbh Feuchtigkeitsregulatoren enthaltende Zusammensetzung für Tissueprodukte, Verfahren zur Herstellung dieser Produkte, Verwendung der Zusammensetzung für die Behandlung von Tissueprodukten sowie Tissueprodukte in Form von wetlaid einschließlich TAD oder Airlaid (non-woven) auf Basis überwiegend Cellulosefasern enthaltender flächiger Trägermaterialien
CN103233380B (zh) * 2013-05-07 2016-08-03 金红叶纸业集团有限公司 纸张的制备工艺
KR101800510B1 (ko) * 2015-10-28 2017-11-22 김철성 수납장
US11286620B2 (en) 2019-01-11 2022-03-29 The Procter & Gamble Company Quaternary ammonium compound compositions and methods for making and using same
JP7359365B2 (ja) 2019-03-29 2023-10-11 学校法人神奈川大学 柔軟剤及び繊維の洗浄方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5223096A (en) * 1991-11-01 1993-06-29 Procter & Gamble Company Soft absorbent tissue paper with high permanent wet strength
US5217576A (en) * 1991-11-01 1993-06-08 Dean Van Phan Soft absorbent tissue paper with high temporary wet strength
US5240562A (en) * 1992-10-27 1993-08-31 Procter & Gamble Company Paper products containing a chemical softening composition
US5279767A (en) * 1992-10-27 1994-01-18 The Procter & Gamble Company Chemical softening composition useful in fibrous cellulosic materials

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WO1994029520A1 (en) 1994-12-22
AU6955994A (en) 1995-01-03
JP3194958B2 (ja) 2001-08-06
PH31624A (en) 1999-01-12
DE69423352D1 (de) 2000-04-13
BR9406738A (pt) 1996-03-12
FI955789A0 (fi) 1995-12-01
CN1052050C (zh) 2000-05-03
HU9503464D0 (en) 1996-01-29
FI955789A (fi) 1996-01-18
CN1128550A (zh) 1996-08-07
KR100336444B1 (ko) 2002-11-20
NZ267305A (en) 1997-11-24
SG66237A1 (en) 1999-07-20
CA2162848A1 (en) 1994-12-22
DE69423352T2 (de) 2000-10-19
HK1013134A1 (en) 1999-08-13
MY111219A (en) 1999-09-30
KR960702877A (ko) 1996-05-23
PE53894A1 (es) 1995-01-02
NO954868D0 (no) 1995-11-30
AU694433B2 (en) 1998-07-23
HUT74116A (en) 1996-11-28
EP0701640A1 (de) 1996-03-20
NO954868L (no) 1996-02-02
JPH08511068A (ja) 1996-11-19
CZ321395A3 (en) 1996-07-17

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