EP0116512A1 - Fiber debonder formulation comprising diamido quaternary ammonium compound and alkoxylated fatty acid - Google Patents

Fiber debonder formulation comprising diamido quaternary ammonium compound and alkoxylated fatty acid Download PDF

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Publication number
EP0116512A1
EP0116512A1 EP84630017A EP84630017A EP0116512A1 EP 0116512 A1 EP0116512 A1 EP 0116512A1 EP 84630017 A EP84630017 A EP 84630017A EP 84630017 A EP84630017 A EP 84630017A EP 0116512 A1 EP0116512 A1 EP 0116512A1
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Prior art keywords
fatty acid
formulation
fatty alcohol
debonding
cellulose fiber
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EP84630017A
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German (de)
French (fr)
Inventor
William John Zeman
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Witco Corp
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Sherex Chemical Co Inc
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/001Modification of pulp properties
    • D21C9/002Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives
    • D21C9/005Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives organic compounds

Definitions

  • the present invention relates to paper debonders and more particularly to a novel paper or fiber debonding formulation.
  • tissue debonder reduces the tensile strength of the tissue by weakening the cellulosic fiber-to-fiber bond. Desirably, the ability of the tissue to absorb moisture is not adversely effected by the paper debonder.
  • paper debonders are being employed in two consumer product lines.
  • One line is the disposable tissue (facial and bathroom) product line where debonders are added to the pulp slurry in the wet end of the tissue manufacturing operation.
  • the debonders are expected to provide a finished tissue of improved softness.
  • Disposable diapers are the second consumer product line employing debonders and their use is somewhat different than the use of debonders in disposable tissue production.
  • the paper debonder is added to the pulp slurry at the wet end of the disposable diaper manufacturing operation (ie. at the same manufacturing juncture as in the disposable tissue manufacturing operation), but the debonder functions as a processing aid to assist in the fluffing of the finished paper sheet into the bulky diaper sheeting.
  • the reduced tensile strength of the pulp fibers thus, aids mechanical pickers in fluffing the dried pulp into a bulky sheeting which is soft yet retains excellent water absorbency.
  • the present invention is directed to a novel fiber debonding formulation which is not only effective in reducing the cellulosic fiber-to-fiber bond, but also is non-toxic and safe (very low eye and skin irritation).
  • the present invention is a method for treating cellulosic pulp fibers to reduce interfiber bonding and to reduce the mechanical strength of webs formed therefrom.
  • the method is characterized by blending with an aqueous cellulosic pulp slurry a debonding formulation comprising:
  • the resulting debonded cellulosic fiber pulp web possessing reduced interfiber bonding and reduced mechanical strength results from the foregoing method and additionally comprises an aspect of the present invention.
  • Advantages of the present invention include the excellent performance imparted by the paper debonders of the present invention in reducing interfiber bonding and reducing mechanical strength for providing fluffy webs of treated pulp which webs or sheets additionally possess excellent moisture absorbency characteristics. Another advantage is that the ingredients of the debonder formulation are non-toxic and are non-irritants. A further advantage is the debonding formulation is fluid at room temperature and is easily handleable by the fluffed pulp or tissue manufacturer.
  • alkoxylated fatty acids or fatty alcohols employed in the debonding formulation of the present invention traditionally have not been recognized as effective paper debonders themselves.
  • the disclosed quaternary ammonium compounds and alkoxylated fatty acids or fatty alcohols provide a unique (synergistic) fiber debonding formulation which is extremely effective and its effectiveness is quite unexpected based upon the prior art.
  • such quaternary amido ammonium compounds can be represented by the general formula :
  • R will comprise a CS-C 30 aliphatic group and preferably such groups are hydrocarbyl (fatty) groups. It must be recognized, however, that the occasional presence of oxygen or nitrogen in such substituents may be encountered and their presence is permissible provided that the resulting quaternary ammonium compound in combination with the alkoxylated fatty acid will provide a debonding formulation which possesses the requisite fluidity for use as a paper debonder at commercial scale operations.
  • R1 is a C 12 -C 18 aliphatic group typically being a fatty group derived from natural and synthetic fatty acids.
  • R 2 comprises a (polyoxy alkylene) hydroxy alkyl group which results from the alkoxylation of the amine nitrogen to which it is attached. Desirably, R 2 will result from the ethoxylation or propoxylation of the amine nitrogen to which it is attached.
  • R3 preferably is a C l -C 4 alkyl group and results from the conventional alkylation of a tertiary amine for forming a quaternary ammonium compound.
  • X is a monovalent anion typically encountered in the formation of quaternary ammonium compounds and most often will be halogen, nitrate, acetate, hydroxide, sulfate, or the like though chlorine and sulfate are the most prevelant.
  • Synthesis of the quaternary ammonium compounds is based upon diethylene triamine (2,2'-diaminodiethylamine).
  • the diethylene triamine molecule is reacted with a C 8 -C 30 carboxylic acid for forming amide groups.
  • carboxylic or fatty acids gives rise to the R l substituent.
  • the resulting diamidoamine then is alkoxylated in conventional fashion and to such an extent that essentially a 100 percent tertiary amine contentresults in the reaction mixture. While theoretically only about one mole of alkylene oxide is required for this reaction, generally an excess, eg. up to 50 percent, will be used to ensure the tertiary amine content requirement.
  • ethylene oxide and propylene oxide are the reactants of choice and will result in formation of the R 2 substituent.
  • the diamido tertiary amine molecule is alkylated in conventional fashion to form the resulting quaternary ammonium structure.
  • Alkyl halogens, alkyl nitrates, alkyl sulfates, etc. will be used for this reaction in conventional fashion and will result in the R 3 substituent and the X monovalent anion.
  • the resulting quaternary ammonium compound can be cut in an alcohol, glycol, or similar solvent for increasing its handling characteristics and/or to supply a desired actives concentration of the quaternary ammonium compound for formulating the debonder formulation of the present invention.
  • the proportion of quaternary ammonium compound in the ultimate debonding formulation generally will be from between about 10% or 50% by weight of the debonding formulation.
  • the fatty acids or alcohols are conventional in nature broadly ranging from C S -C 30 fatty acids or alcohols, advantageously C 12 -C 22 and preferably C 18 fatty acids or alcohols.
  • the fatty acids or alcohols are alkoxylated in conventional fashion, advantageously with ethylene oxide, though propylene oxide, butylene oxide, and other conventional alkylene oxides may be used in this reaction scheme.
  • the proportion of alkoxy groups generally should be from between about 2 and 12 moles of alkoxy group per mole of fatty acid or alcohol and advantageously from between about 4 and 7 moles per mole of fatty acid or alcohol.
  • the proportion of alkoxylated fatty acid or alcohol in the debonding formulation will range from between about 90% to 50% by weight of the debonding formulation.
  • the debonding formulation optionally may contain minor proportions of solvents for improving the fluidity and handling characteristics of the debonding formulation.
  • solvents for improving the fluidity and handling characteristics of the debonding formulation.
  • propylene glycol orthe like may be used in the debonding formulation for improving handling characteristics of the debonding formulation without imparting any adverse effects to the debonded pulp.
  • Additional such fluidity-improving solvents include, for example, alkanols, other alkyleneglycols, ethers and the like.
  • the proportion of alkoxylated fatty acid or alcohol is rediced to accommodate such solvents for providing between about 40 and 60weight percent alkoxylated fatty acid or alcohol and between about 5 and 20 percent fluidity-enhancing solvent.
  • the debonding formulation is manufactured readily by mechanical blending of the quaternary ammonium compound and alkoxylated fatty acid or fatty alcohol in conventional fashion, optionally also containing a fluidity-enhancing solvent.
  • the debonding formulation is applied to an aqueous pulp slurry in conventional fashion.
  • the type of pulp employed is not a limitation on use of the debonding formulations and can be conventional Kraft pulp or sulfitepulp.
  • the debonding formulation is added to the aqueous slurry in a proportion of between about 0.1 and 2% (by weight of the dry pulp solids),advantageously from between about 0.2 and 1%, and preferably between about 0.2 and 0.4 weight percent.
  • the pulp slurry can be intended for tissue production, disposable diaper production, or any other cellulosic fiber product wherein reduced tensile strength is desired.
  • the pulp slurry will be fluffed for production of disposable diapers, sanitary absorbents, and the like.
  • the sheets were removed from the mold and pressed between dry blotters at a pressure of 3.5 kg/cm 2 (50 psi) for a period of 5 minutes on a first press followed by 2 minutes on a second press.
  • the pressed sheets then were placed in TAPPI drying ring which were housed under standardized conditions of a constant temperature of 21.1 0 C (70°F) and 50% relative humidity for drying overnight.
  • the conditioned hand sheets were tested in accordance with standard test methods set forth below :
  • the debonders were added to the pulp at the rate of 1.5 g per kilogram of pulp.
  • the pulp was softwood Kraft pulp (Albacel) for the first text series and softwood sulfite pulp (Puget S) for the second test series. The following test results were recorded.

Abstract

A debonded cellulose fibre pulp web possessing reduced interfibre bonding and reduced mechanical strength is made by blending with an aqueous cellulose pulp slurry, a debonding formulation comprising:
  • (a) a quaternary ammonium compound having the general formula :
    Figure imga0001
    where
    • R1 = C8-C30 aliphatic group,
    • R2 = (polyoxy alkylene) hydroxyl alkyl group
    • R3 = C1-C4 alkyl group
    • X- = monovalent anion; and
  • (b) an alkoxylated C8-C30 fatty acid or fatty alcohol.

Description

    Background of the Invention
  • The present invention relates to paper debonders and more particularly to a novel paper or fiber debonding formulation.
  • Due in part to effective advertising, consumers expect soft, fluffy facial tissue and toilet tissue which possesses excellent water absorbency. Additionally, an objective of some major tissue producers is to offer a single-ply bathroom tissue which has the appearance of a standard two-ply tissue in fluffiness, softness, and overall appearance. One method for treating wood pulp to achieve the softness and fluffiness expected by the consumer without losing the ability of the tissue to absorb moisture is to employ a paper debonder during the tissue manufacturing operation. Paper debonders reduce the tensile strength of the tissue by weakening the cellulosic fiber-to-fiber bond. Desirably, the ability of the tissue to absorb moisture is not adversely effected by the paper debonder.
  • Presently, paper debonders are being employed in two consumer product lines. One line is the disposable tissue (facial and bathroom) product line where debonders are added to the pulp slurry in the wet end of the tissue manufacturing operation. The debonders are expected to provide a finished tissue of improved softness. Disposable diapers are the second consumer product line employing debonders and their use is somewhat different than the use of debonders in disposable tissue production. The paper debonder is added to the pulp slurry at the wet end of the disposable diaper manufacturing operation (ie. at the same manufacturing juncture as in the disposable tissue manufacturing operation), but the debonder functions as a processing aid to assist in the fluffing of the finished paper sheet into the bulky diaper sheeting. The reduced tensile strength of the pulp fibers, thus, aids mechanical pickers in fluffing the dried pulp into a bulky sheeting which is soft yet retains excellent water absorbency.
  • A variety of paper debonders have been employed commercially and proposed in the literature. For example, U.S. Pat. No. 3,554,862 proposes a debonder which is a cationic long-chain fatty alkyl compound having at least 12 carbon atoms in at least one of the alkyl chains while U.S. Pat. No. 3,930,933 employs the same cationic compound in combination with a natural non-drying oil. British Pat. 1,407,134 describes the use of imidazolines as paper debonders. U.S. Pat. No. 4,144,122 proposes the use of bis(alkoxy)-(2-hydroxy propylene) quaternary ammonium compounds which contain both cationic and non-ionic hydrophilic groups as paper debonders. Even though prior paper debonders function effectively in reducing the cellulosic fiber-to-fiber bond, toxicity suspicions concerning them are prevelant.
  • The present invention is directed to a novel fiber debonding formulation which is not only effective in reducing the cellulosic fiber-to-fiber bond, but also is non-toxic and safe (very low eye and skin irritation).
  • Broad Statement of the Invention
  • The present invention is a method for treating cellulosic pulp fibers to reduce interfiber bonding and to reduce the mechanical strength of webs formed therefrom. The method is characterized by blending with an aqueous cellulosic pulp slurry a debonding formulation comprising:
    Figure imgb0001
    • where Rl =C8-C30 aliphatic group,
    • R2 = (polyoxy alkylene) hydroxyl alkyl group
    • R 3 = C1-C4 alkyl group
    • X = monovalent anion; and

    (b) an alkoxylated C8-C30 fatty acid or fatty alcohol
  • The resulting debonded cellulosic fiber pulp web possessing reduced interfiber bonding and reduced mechanical strength results from the foregoing method and additionally comprises an aspect of the present invention.
  • Advantages of the present invention include the excellent performance imparted by the paper debonders of the present invention in reducing interfiber bonding and reducing mechanical strength for providing fluffy webs of treated pulp which webs or sheets additionally possess excellent moisture absorbency characteristics. Another advantage is that the ingredients of the debonder formulation are non-toxic and are non-irritants. A further advantage is the debonding formulation is fluid at room temperature and is easily handleable by the fluffed pulp or tissue manufacturer. These and other advantages readily will become apparent to those skilled in the art based upon the disclosure contained herein.
  • Detailed Description of the Invention
  • The alkoxylated fatty acids or fatty alcohols employed in the debonding formulation of the present invention traditionally have not been recognized as effective paper debonders themselves. However, in combination,the disclosed quaternary ammonium compounds and alkoxylated fatty acids or fatty alcohols provide a unique (synergistic) fiber debonding formulation which is extremely effective and its effectiveness is quite unexpected based upon the prior art. Thus, it is the unique combination of ingredients comprising the debonding formulation which must be viewed in assessing the present invention rather than the individual ingredients themselves.
  • Initially, referring to the quaternary ammonium compounds, such quaternary amido ammonium compounds can be represented by the general formula :
    Figure imgb0002
  • In the foregoing general formula, R, will comprise a CS-C30 aliphatic group and preferably such groups are hydrocarbyl (fatty) groups. It must be recognized, however, that the occasional presence of oxygen or nitrogen in such substituents may be encountered and their presence is permissible provided that the resulting quaternary ammonium compound in combination with the alkoxylated fatty acid will provide a debonding formulation which possesses the requisite fluidity for use as a paper debonder at commercial scale operations. Thus, preferably R1 is a C12-C18 aliphatic group typically being a fatty group derived from natural and synthetic fatty acids. R2 comprises a (polyoxy alkylene) hydroxy alkyl group which results from the alkoxylation of the amine nitrogen to which it is attached. Desirably, R2 will result from the ethoxylation or propoxylation of the amine nitrogen to which it is attached. R3 preferably is a Cl-C4 alkyl group and results from the conventional alkylation of a tertiary amine for forming a quaternary ammonium compound. X is a monovalent anion typically encountered in the formation of quaternary ammonium compounds and most often will be halogen, nitrate, acetate, hydroxide, sulfate, or the like though chlorine and sulfate are the most prevelant.
  • Synthesis of the quaternary ammonium compounds is based upon diethylene triamine (2,2'-diaminodiethylamine). The diethylene triamine molecule is reacted with a C8-C30 carboxylic acid for forming amide groups. Such carboxylic or fatty acids gives rise to the Rl substituent. The resulting diamidoamine then is alkoxylated in conventional fashion and to such an extent that essentially a 100 percent tertiary amine contentresults in the reaction mixture. While theoretically only about one mole of alkylene oxide is required for this reaction, generally an excess, eg. up to 50 percent, will be used to ensure the tertiary amine content requirement. As noted above, ethylene oxide and propylene oxide are the reactants of choice and will result in formation of the R2 substituent. Finally, the diamido tertiary amine molecule is alkylated in conventional fashion to form the resulting quaternary ammonium structure. Alkyl halogens, alkyl nitrates, alkyl sulfates, etc. will be used for this reaction in conventional fashion and will result in the R3 substituent and the X monovalent anion.The resulting quaternary ammonium compound can be cut in an alcohol, glycol, or similar solvent for increasing its handling characteristics and/or to supply a desired actives concentration of the quaternary ammonium compound for formulating the debonder formulation of the present invention. The proportion of quaternary ammonium compound in the ultimate debonding formulation generally will be from between about 10% or 50% by weight of the debonding formulation.
  • Referring to the alkoxylated C8-C30 fatty acid or fatty alcohol,the fatty acids or alcohols are conventional in nature broadly ranging from CS-C30 fatty acids or alcohols, advantageously C12-C22 and preferably C18 fatty acids or alcohols. The fatty acids or alcohols are alkoxylated in conventional fashion, advantageously with ethylene oxide, though propylene oxide, butylene oxide, and other conventional alkylene oxides may be used in this reaction scheme. The proportion of alkoxy groups generally should be from between about 2 and 12 moles of alkoxy group per mole of fatty acid or alcohol and advantageously from between about 4 and 7 moles per mole of fatty acid or alcohol. The proportion of alkoxylated fatty acid or alcohol in the debonding formulation will range from between about 90% to 50% by weight of the debonding formulation.
  • The debonding formulation optionally may contain minor proportions of solvents for improving the fluidity and handling characteristics of the debonding formulation. For example, propylene glycol orthe like may be used in the debonding formulation for improving handling characteristics of the debonding formulation without imparting any adverse effects to the debonded pulp. Additional such fluidity-improving solvents include, for example, alkanols, other alkyleneglycols, ethers and the like. When the fluidity-enhancing solvents are used in the formulation, the proportion of alkoxylated fatty acid or alcohol is rediced to accommodate such solvents for providing between about 40 and 60weight percent alkoxylated fatty acid or alcohol and between about 5 and 20 percent fluidity-enhancing solvent.
  • In practicing the present invention, the debonding formulation is manufactured readily by mechanical blending of the quaternary ammonium compound and alkoxylated fatty acid or fatty alcohol in conventional fashion, optionally also containing a fluidity-enhancing solvent. The debonding formulation is applied to an aqueous pulp slurry in conventional fashion. The type of pulp employed is not a limitation on use of the debonding formulations and can be conventional Kraft pulp or sulfitepulp.The debonding formulation is added to the aqueous slurry in a proportion of between about 0.1 and 2% (by weight of the dry pulp solids),advantageously from between about 0.2 and 1%, and preferably between about 0.2 and 0.4 weight percent. As noted above, the pulp slurry can be intended for tissue production, disposable diaper production, or any other cellulosic fiber product wherein reduced tensile strength is desired. Preferably, the pulp slurry will be fluffed for production of disposable diapers, sanitary absorbents, and the like.
  • The following examples show how the present invention can be practiced but should not be construed as limiting. In this application, all percentages and proportions are by weight and all units are in the metric system, unless otherwise expressly indicated. Also, all citations are expressly incorporated herein by reference.
  • IN THE EXAMPLES
  • 50g of wood pulp (Albacel Bleached Kraft or Puget S Bleached Sulfite) for each debonder evaluated was placed in a TAPPI Standard 300 rpm disintegrator having a 4 L capacity. Approximately 3L of tap water was added and allowed to disperse in the wood pulp for about 5 minutes. The debonder sample then was added at a rate of either 1.5 or 4.0 g/kg of pulp and agitation continued for an additional 2 minutes. The slurry from the disintegrator was diluted with tap water for use in hand sheet production. The hand sheets (nominally at 60 g/m2) were produced in a TAPPI sheet mold. The sheets were removed from the mold and pressed between dry blotters at a pressure of 3.5 kg/cm2 (50 psi) for a period of 5 minutes on a first press followed by 2 minutes on a second press. The pressed sheets then were placed in TAPPI drying ring which were housed under standardized conditions of a constant temperature of 21.10 C (70°F) and 50% relative humidity for drying overnight.
  • The conditioned hand sheets were tested in accordance with standard test methods set forth below :
    • (a) Hand sheet formation, TAPPI test method T 205 om-81;
    • (b) Physical testing of hand sheets, TAPPI test method T 220 os-71;
    • (c) Z-directional tensile test, TAPPI test method T 506 su-68; and
    • (d) Absorption of water by lightweight creped paper, Canadian test method CPPA F.7P(PM-74).
    EXAMPLE 1
  • Debonder candidates were formulated as follows:
  • DEBONDER
  • Figure imgb0003
  • The debonders were added to the pulp at the rate of 1.5 g per kilogram of pulp. The pulp was softwood Kraft pulp (Albacel) for the first text series and softwood sulfite pulp (Puget S) for the second test series. The following test results were recorded.
    Figure imgb0004
    Figure imgb0005
  • The above-tabulated results show the debonding effect achieved by the debonder formulation of the present invention. In order to place this data in an easier to understand form, the percentage loss in strength of the handsheets is given below:
    Figure imgb0006
  • The above-tabulated results demonstrate the strength decrease imparted by the novel debonder formulation. Even though the overall strength decreased significantly, the water absorbency rate remained substantially constant.
  • EXAMPLE 2
  • Next, in order to demonstrate the synergistic effect achieved by combining the diamido-ammonium quaternary debonder with the alkoxylated fatty acid, debonder formulations with and without the alkoxylated fatty acid were evaluated at a dosage of 4g/kg of pulp.
  • The debonder formulations appear below:
    Figure imgb0007
    Figure imgb0008
  • The percentage loss in strength based upon the above-tabulated results appear below:
    Figure imgb0009
  • The above-tabulated results show that the addition of the alkoxylated fatty acid to the quaternary debonder resulted in a 40% loss in Mullen Burst strength and a 67% loss in Tensile Strength. The dramatic effect of the debonder formulation is demonstrated.

Claims (20)

1. A debonded cellulose fiber pulp web possessing reduced interfiber bonding and reduced mechanical strength characterized by said web being impregnated with a debonding formulation comprising:
(a) a quaternary ammonium compound having the general formula:
Figure imgb0010
where Rl = C8-C30 aliphatic group,
R2 =(polyoxy alkylene)hydroxyl alkyl group
R3= C1-C4 alkyl group
X = monovalent anion; and
(b) an akoxylated C8-C30 fatty acid or fatty alcohol .
2. The debonded cellulose fiber pulp web of claim 1 which is impregnated with between about 0.1% and 2% of said debonding formulation by weight of said dry pulp solids.
3. The debonded cellulose fiber pulp web of claim 2 which is impregnated with between about 0.2% and 1% of said debonding formulation.
4. The debonded cellulose fiber pulp web of claim 1 wherein for said quaternary ammonium compound (a), RI is a C12-C18 aliphatic group and R2 is an ethoxylate, polyethoxylate, propoxylate, or polypropoxylate residue.
5. The debonded cellulose fiber pulp web of claim 1 wherein said alkoxylated fatty acid or fatty alcohol (b) is an ethoxylated C12-C22 fatty acid or fatty alcohol.
6. The debonded cellulose fiber pulp web of claim 5 wherein said fatty acid or fatty alcohol is ethoxylated with between about 2 and 12 moles of ethylene oxide per mole of said fatty acid.
7. The debonded cellulose fiber pulp web of claim 4 wherein said alkoxylated fatty acid or fatty alcohol (b) is an ethoxylated C12-C22 fatty acid or fatty alcohol which is ethoxylated with between about 4 and 7 moles of ethylene oxide per mole of said fatty acid or fatty alcohol.
8. The debonded cellulose fiber pulp web of claim 1 wherein said debonding formulation comprises from between about 10% and 50% by weight of said quaternary ammonium compound (a) and between about 90% and 50% by weight of said alkoxylated fatty acid or fatty alcohol(b).
9. The debonded cellulose fiber pulp web of claim 1 which additionally contains a fluidity-enhancing solvent.
10. The debonded cellulose fiber pulp web of claim 9 wherein said fluidity-enhancing solvent comprises an alkylene glycol.
11. A method for treating cellulose pulp fibers to reduce interfiber bonding and to reduce the mechanical strength of webs formed therefrom, characterized by blending with an aqueous cellulose pulp slurry and debonding formulation comprising:
Figure imgb0011
where R1 = C8-C30 aliphatic group,
R2 = (polyoxy alkylene)hydroxyl alkyl group
R 3 = C1-C4 alkyl group
X = monovalent anion; and

(b) alkoxylated C8-C30 fatty acid or fatty alcohol .
12. The method of claim 11 wherein said cellulose pulp fibers are blended with between about O.1% and 2% of said debonding formulation by weight of the dry pulp fibers.
13. The method of claim 12 wherein said cellulose pulp fibers are blended with between about 0.2% and 1% of said debonding formulation.
14. The debonded cellulose fiber pulp web of claim 1 wherein for said quaternary ammonium compound (a), R1 is a C12-C18 aliphatic group and R2 is an ethoxylate, polyethoxylate, propoxylate, or polypropoxylate residue.
15. The method of claim 11 wherein said blended alkoxylated fatty acid or fatty alcohol is an ethoxylated C12-C22 fatty acid or fatty alcohol.
16. The method of claim 15 wherein said fatty acid or fatty alcohol is ethoxylated with between about 2 and 12 moles of ethylene oxide per mole of said fatty acid or fatty alcohol.
17. The method of claim 14 wherein said alkoxylated fatty acid or fatty alcohol is an ethoxylated C12-C22 fatty acid or fatty alcohol which is ethoxylated with between about 4 and 7 moles of ethylene oxide per mole of said fatty acid.
18. The method of claim 11 wherein said debonding formulation which is blended with said aqueous cellulose pulp slurry comprises between about 10% and 50% by weight of said quaternary ammonium compound (a) and between about 90ù and 50% by weight of said alkoxylated fatty acid or fatty alcohol (b).
19. The method of claim 18 wherein said debonding formulation additionally contains a fluidity-enhancing solvent.
20. The method of claim 19 wherein said fluidity-enhancing solvent is an alkylene glycol.
EP84630017A 1983-02-10 1984-02-08 Fiber debonder formulation comprising diamido quaternary ammonium compound and alkoxylated fatty acid Withdrawn EP0116512A1 (en)

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WO1997049858A1 (en) * 1996-06-25 1997-12-31 Ildiko Tanczos Method of manufacturing paper pulp/cellulose
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US6156157A (en) * 1995-07-21 2000-12-05 Kimberly-Clark Worldwide, Inc. Method for making soft tissue with improved bulk softness and surface softness
US6379498B1 (en) 2000-02-28 2002-04-30 Kimberly-Clark Worldwide, Inc. Method for adding an adsorbable chemical additive to pulp during the pulp processing and products made by said method
US6582560B2 (en) 2001-03-07 2003-06-24 Kimberly-Clark Worldwide, Inc. Method for using water insoluble chemical additives with pulp and products made by said method
US7749356B2 (en) 2001-03-07 2010-07-06 Kimberly-Clark Worldwide, Inc. Method for using water insoluble chemical additives with pulp and products made by said method
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DE2254120A1 (en) * 1972-11-04 1974-05-16 Pelz & Co Kg W Absorbent fibrous wadding for medical purposes - contains cation-active and ionogenic emulsifiers with good wetting capacity
US4144122A (en) * 1976-10-22 1979-03-13 Berol Kemi Ab Quaternary ammonium compounds and treatment of cellulose pulp and paper therewith
FR2431569A1 (en) * 1978-07-21 1980-02-15 Kenogard Ab PROCESS FOR THE MANUFACTURE OF DOWN PULP
US4233164A (en) * 1979-06-05 1980-11-11 The Proctor & Gamble Company Liquid fabric softener
EP0049924A1 (en) * 1980-10-15 1982-04-21 THE PROCTER & GAMBLE COMPANY Process for manufacture of soft absorbent tissue paper and paper made thereby

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US5552020A (en) * 1995-07-21 1996-09-03 Kimberly-Clark Corporation Tissue products containing softeners and silicone glycol
US5730839A (en) * 1995-07-21 1998-03-24 Kimberly-Clark Worldwide, Inc. Method of creping tissue webs containing a softener using a closed creping pocket
US6156157A (en) * 1995-07-21 2000-12-05 Kimberly-Clark Worldwide, Inc. Method for making soft tissue with improved bulk softness and surface softness
WO1997049858A1 (en) * 1996-06-25 1997-12-31 Ildiko Tanczos Method of manufacturing paper pulp/cellulose
US6379498B1 (en) 2000-02-28 2002-04-30 Kimberly-Clark Worldwide, Inc. Method for adding an adsorbable chemical additive to pulp during the pulp processing and products made by said method
US6582560B2 (en) 2001-03-07 2003-06-24 Kimberly-Clark Worldwide, Inc. Method for using water insoluble chemical additives with pulp and products made by said method
US7749356B2 (en) 2001-03-07 2010-07-06 Kimberly-Clark Worldwide, Inc. Method for using water insoluble chemical additives with pulp and products made by said method
US7993490B2 (en) 2001-03-07 2011-08-09 Kimberly-Clark Worldwide, Inc. Method for applying chemical additives to pulp during the pulp processing and products made by said method
WO2015165783A1 (en) * 2014-04-28 2015-11-05 Mondi Ag Modified pulp

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PT78086B (en) 1986-04-17
PT78086A (en) 1984-03-01

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