US3850818A - Antistatic softening composition containing a quaternary ammonium salt and a ethenoxy quaternary ammonium salt - Google Patents
Antistatic softening composition containing a quaternary ammonium salt and a ethenoxy quaternary ammonium salt Download PDFInfo
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- US3850818A US3850818A US00290345A US29034572A US3850818A US 3850818 A US3850818 A US 3850818A US 00290345 A US00290345 A US 00290345A US 29034572 A US29034572 A US 29034572A US 3850818 A US3850818 A US 3850818A
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- quaternary ammonium
- ammonium salt
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- softening composition
- antistatic
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- 239000000203 mixture Substances 0.000 title claims abstract description 40
- -1 ethenoxy quaternary ammonium salt Chemical class 0.000 title claims abstract description 23
- 150000003242 quaternary ammonium salts Chemical class 0.000 title claims abstract description 15
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 24
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 24
- 239000000654 additive Substances 0.000 claims abstract description 15
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 22
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 12
- 230000000996 additive effect Effects 0.000 claims description 8
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 claims description 3
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 claims description 3
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 claims description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract description 8
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract description 5
- 239000004202 carbamide Substances 0.000 abstract description 5
- 239000000600 sorbitol Substances 0.000 abstract description 5
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract description 4
- 150000001298 alcohols Chemical class 0.000 abstract description 4
- 150000002334 glycols Chemical class 0.000 abstract description 4
- 125000000963 oxybis(methylene) group Chemical group [H]C([H])(*)OC([H])([H])* 0.000 abstract 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 14
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 14
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 8
- 239000004753 textile Substances 0.000 description 8
- 239000004902 Softening Agent Substances 0.000 description 7
- 235000019270 ammonium chloride Nutrition 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 150000003839 salts Chemical group 0.000 description 7
- 239000011780 sodium chloride Substances 0.000 description 7
- 230000003068 static effect Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-O Methylammonium ion Chemical compound [NH3+]C BAVYZALUXZFZLV-UHFFFAOYSA-O 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920002972 Acrylic fiber Polymers 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 206010016322 Feeling abnormal Diseases 0.000 description 2
- QGGDXDGBZVPEEG-UHFFFAOYSA-N [NH4+].[Cl-].[Cl-].[NH3+]C Chemical compound [NH4+].[Cl-].[Cl-].[NH3+]C QGGDXDGBZVPEEG-UHFFFAOYSA-N 0.000 description 2
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- FLNKWZNWHZDGRT-UHFFFAOYSA-N azane;dihydrochloride Chemical compound [NH4+].[NH4+].[Cl-].[Cl-] FLNKWZNWHZDGRT-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- GUQGYHBUINQTSV-UHFFFAOYSA-N azane;methanamine Chemical compound N.NC GUQGYHBUINQTSV-UHFFFAOYSA-N 0.000 description 1
- 239000004106 carminic acid Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000003028 elevating effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical compound CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/144—Alcohols; Metal alcoholates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/144—Alcohols; Metal alcoholates
- D06M13/148—Polyalcohols, e.g. glycerol or glucose
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/372—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen containing etherified or esterified hydroxy groups ; Polyethers of low molecular weight
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/432—Urea, thiourea or derivatives thereof, e.g. biurets; Urea-inclusion compounds; Dicyanamides; Carbodiimides; Guanidines, e.g. dicyandiamides
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
Definitions
- R represents an alkyl group of C, ,-C R, represents an alkyl group of C -C or benzyl group
- X represents Cl, Br or C H SO
- m and n each represent an integer of more than 1 inclusive, with the proviso that m n is 20-100, and 05-15 percent by weight of one or more additives selected from the group consisting of alcohols of lower than C inclusive, glycols, glycerol, sorbitol and urea.
- the present invention relates to a softening composition which is stable even at a high concentration and which imparts an excellent antistatic property to the treated textile products.
- Softening agents have been used frequently as finishing agents for textile products. They are used mainly for finishing of washed underwear and diapers to impart a soft feeling to the textile products. Important properties required of softening agents are as follows:
- compositions of softening agents have. been known, but most of them contain quaternary ammonium salts having two long chain alkyl groups as their main ingredients.
- some of the known compositions contain, in addition to said main ingredient, a nonionic surfactant such as an alkylphenol ethylene oxide adduct and a solvent such as an alcohol or glycol to improve the stability of the solution.
- a nonionic surfactant such as an alkylphenol ethylene oxide adduct
- a solvent such as an alcohol or glycol
- the softening agents do not freeze at a low temperature around the freezing point, or even if they are frozen, their viscosities are recovered when the temperature is elevated again to room temperature.
- an antistatic agent for obtaining a composition having an antistatic property.
- a conventionally known antistatic agent such as stearyl trimethylammonium chloride
- a softening agent composition containing a quaternary ammonium salt having two long chain alkyl SUMMARY OF THE INVENTION The present invention relates to a softening composi tion having an excellent softening effect, particularly a sufficientstability even at a high concentration, and an excellent antistatic effect upon treated textile products.
- the present invention relates to an antistatic softeningcomposition characterized by containing 4-10 percent by weight of a quaternary ammonium salt represented by the following general formula (1):
- R and R each represent an alkyl group of C -C R and R each represent an alkyl group of C -C benzyl group or (C H O),,H (n 1 3) and X represents Cl, Br or C I-I SO. 0.1-5 percent by weight of ethenoxy quaternary ammonium salt represented'by the following general formula (II):
- R represents an alkyl group of C -C
- R represents an alkyl group of C,-C or benzyl group
- X represents Cl, Br or C I-I SO
- m and n each represent an integer of more than 1 inclusive, with the priviso than "1+" is 20-100 and 0.5-15 percent by weight of one or more additives selected from the group consisting of alcohols of lower than C inclusive, glycols, glycerol, sorbitol and urea.
- Preferred R and R are C -C alkyl groups and preferred R and R are C -C alkyl groups and benzyl group.
- Preferred R are those of C -C and the sum of m and n is preferably 30-70.
- the preferred amount of the ethenoxy quaternary ammonium salt of the above general formula (II) is 1.0-5.0 percent by weight and the preferredamount of the additives is 3-8 percent by weight;
- the most preferred quaternary ammonium salts of the above general formula (I) are distearyl dimethylammonium chloride and dihydrogenated tallowalkyl dimethylammonium chloride.
- EXAMPLE 1 (This example is to demonstate the effects based on the constituents of the compositions.)
- compositions A through G are those of the present invention and the compositions H through K are comparative ones. Percentages in the table are shown in weight and the remainder is the amount of water.
- Viscosity, antistatic property and softening property shown in Table l are measured according to the methods which will be described below. The results of the measurements are shown by four grades of G, O, A and X,@ being the most excellent (the lowest in viscosity).
- Quaternary ammonium salts in the table are compounds of the general formula (I) and the ethenoxy quaternary salts are ethenoxy quaternary ammonium salts of the general formula (ll).
- the symbol E indicates ethylene oxide.
- composition directly after blending was allowed to stand at room temperature for 6 months and then at 50 C for 3 months, frozen at 30 C, thawed at room temperature and then frozen again. This procedure was repeated 5 times. Four samples of each composition were measured at 30 C with Brookfield type viscometer. The unit of numerals in the table is centi-poises.
- Pieces of cotton towel, cotton plain fabric for diaper and blanket made from polyacrylonitrile fiber were washed in a usual manner, treated with 0.1 percent and 0.3 percent solutions of each softening composition and finally dried.
- the samples were tested by 5 men and 5 women according to handling (tactile impression) and their feelings were evaluated by the points compared with the standard criteria.
- the numerals in Table 2 are the sums of the points. The larger the nu meral, th softer the textile.
- Viscosity The composition immediately after the blending was allowed to stand at room temperature for one month ter.
- the unit of numerals in the table is centi-poises.
- An antistatic softening composition consisting essentially of 4-10 percent by weight of a quaternary ammonium salt of the formula (1):
- R represents an alkyl group of C -C
- R represents an alkyl group of C -C or benzyl group
- X represents Cl, Br or C H SO
- m and n each represent an integer of more than 1 inclusive, with the privisio that m n is 20-100, 0.5 percent by weight of one or more additives selected from the group consist ing of alcohols of lower than C inclusive, glycols, glycerol, sorbitol and urea, the balance of said composition being water.
- R and R each represents an alkyl group of C -C
- R and R each represents an alkyl group of C -C or benzyl group
- R represents an alkyl group of C -C and the sum of m and n is 30-70.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
An antistatic softening composition, comprising 4-10 percent by weight of a quaternary ammonium salt of general formula (I):
wherein R1 and R2 each represent an alkyl group of C14-C22, R3 and R4 each represent an alkyl group of C1-C3, benzyl group or (C2H4O)nH (n 1 - 3) and X represents Cl, Br or C2H5SO4, 0.1-5 percent by weight of an ethenoxy quaternary ammonium salt of general formula (II):
wherein R5 represents an alkyl group of C10-C22, R6 represents an alkyl group of C1-C3 or benzyl group, X represents Cl, Br or C2H5SO4 and m and n each represent an integer of more than 1 inclusive, with the proviso that m +. n is 20-100, and 0.5-15 percent by weight of one or more additives selected from the group consisting of alcohols of lower than C3 inclusive, glycols, glycerol, sorbitol and urea.
wherein R1 and R2 each represent an alkyl group of C14-C22, R3 and R4 each represent an alkyl group of C1-C3, benzyl group or (C2H4O)nH (n 1 - 3) and X represents Cl, Br or C2H5SO4, 0.1-5 percent by weight of an ethenoxy quaternary ammonium salt of general formula (II):
wherein R5 represents an alkyl group of C10-C22, R6 represents an alkyl group of C1-C3 or benzyl group, X represents Cl, Br or C2H5SO4 and m and n each represent an integer of more than 1 inclusive, with the proviso that m +. n is 20-100, and 0.5-15 percent by weight of one or more additives selected from the group consisting of alcohols of lower than C3 inclusive, glycols, glycerol, sorbitol and urea.
Description
United States Patent [191 Katsumi et al.
[ Nov. 26, 1974 1 ANTISTATIC SOFTENING. COMPOSITION CONTAINING A QUATERNARY AMMONIUM SALT AND A ETHENOXY QUATERNARY AMMONIUM SALT [75] Inventors: Mamoru Katsumi; Toshio Sato, both of Wakayama, Japan [73] Assignee: Kao Soap Co. Ltd., Chuo-ku,
Tokyo, Japan [22] Filed: Sept. 19, 1972 [21] Appl. No.: 290,345
[30] Foreign Application Priority Data Primary Examiner-Stephen .1. Lechert, Jr. Attorney, Agent, or Firm-Woodhams, Blanchard and Flynn [57] ABSTRACT An antistatic softening composition, comprising 4-10 percent by weight of a quaternary ammonium salt of general formula (1):
R; R, [y Rt Rt (I) wherein R and R each represent an alkyl group of C,,C R and R each represent an alkyl group of C, -C benzyl group or (C H,O),,H (n 1 3) and X represents Cl, Br or C H SO),, 0.1-5 percent by weight of an ethenoxy quaternary ammonium salt of general formula (11):
(CHzCHzO) H (II) wherein R represents an alkyl group of C, ,-C R, represents an alkyl group of C -C or benzyl group, X represents Cl, Br or C H SO, and m and n each represent an integer of more than 1 inclusive, with the proviso that m n is 20-100, and 05-15 percent by weight of one or more additives selected from the group consisting of alcohols of lower than C inclusive, glycols, glycerol, sorbitol and urea.
7 Claims, No Drawings ANTISTATIC SOFTENING COMPOSITION CONTAINING A QUATERNARY AMMONIUM SALT AND A ETI-IENOXY QUATERNARY AMMONIUM SALT BACKGROUND OF THE INVENTION 1. FIELD OF THE INVENTION The present invention relates to a softening composition which is stable even at a high concentration and which imparts an excellent antistatic property to the treated textile products.
2. DESCRIPTION OF THE PRIOR ART Softening agents have been used frequently as finishing agents for textile products. They are used mainly for finishing of washed underwear and diapers to impart a soft feeling to the textile products. Important properties required of softening agents are as follows:
a. to impart a soft feeling to the treated textile products,
b. to impart antistatic property to the treated textile products,
c. not to reduce hygroscopicity of the treated textile products, and.
d. to maintain stability and low viscosity even at a high concentration of the softening agent solution against possible environmental changes.
Among the above four properties, (a) is indispensable of course and most important, while properties (b) through (d) are also significant in practice.
Various compositions of softening agents have. been known, but most of them contain quaternary ammonium salts having two long chain alkyl groups as their main ingredients.
Further, some of the known compositions contain, in addition to said main ingredient, a nonionic surfactant such as an alkylphenol ethylene oxide adduct and a solvent such as an alcohol or glycol to improve the stability of the solution. Although satisfactory softening effects can be obtained by using such known compositions, the properties and (d), particularly the antistatic property and stability of them are still insufficient.
Recently, the use of fabrics for clothing made of synthetic fibers has been increasing more and more. However, as compared with fabrics of natural fibers, they have serious shortcomings in that they are apt to have a static electric charge, which results in dusty clothing, clinging of the clothing to the body and sparking at the time of putting on or pulling off of the clothing. These serious shortcomings of synthetic fiber clothing fabrics are well known.
Further, during the storage of softening agent solutions under various climate and temperature conditions, an increase in the viscosity of the solution or a,
phase separation is undesirable. In addition, it is desired that the softening agents do not freeze at a low temperature around the freezing point, or even if they are frozen, their viscosities are recovered when the temperature is elevated again to room temperature.
It is expedient to incorporate an antistatic agent for obtaining a composition having an antistatic property. However, if a conventionally known antistatic agent such as stearyl trimethylammonium chloride is incorporated in a softening agent composition containing a quaternary ammonium salt having two long chain alkyl SUMMARY OF THE INVENTION The present invention relates to a softening composi tion having an excellent softening effect, particularly a sufficientstability even at a high concentration, and an excellent antistatic effect upon treated textile products.
The present invention-relates to an antistatic softeningcomposition characterized by containing 4-10 percent by weight of a quaternary ammonium salt represented by the following general formula (1):
wherein R and R each represent an alkyl group of C -C R and R each represent an alkyl group of C -C benzyl group or (C H O),,H (n 1 3) and X represents Cl, Br or C I-I SO. 0.1-5 percent by weight of ethenoxy quaternary ammonium salt represented'by the following general formula (II):
wherein R represents an alkyl group of C -C R represents an alkyl group of C,-C or benzyl group, X represents Cl, Br or C I-I SO and m and n each represent an integer of more than 1 inclusive, with the priviso than "1+" is 20-100 and 0.5-15 percent by weight of one or more additives selected from the group consisting of alcohols of lower than C inclusive, glycols, glycerol, sorbitol and urea.
Now a description will be made of particularly preferred compositions. Preferred R and R are C -C alkyl groups and preferred R and R are C -C alkyl groups and benzyl group. Preferred R are those of C -C and the sum of m and n is preferably 30-70. Preferred additives and propylene glycol, ethylene glcol and glycerol. The preferred amount of the ethenoxy quaternary ammonium salt of the above general formula (II) is 1.0-5.0 percent by weight and the preferredamount of the additives is 3-8 percent by weight; vThe most preferred quaternary ammonium salts of the above general formula (I) are distearyl dimethylammonium chloride and dihydrogenated tallowalkyl dimethylammonium chloride. Though the object of the invention can be attained sufficiently with preferably incorporated therein for ensuring the stability of the composition for a long period.
The present invention will be illustrated more concretely by way of examples.
EXAMPLE 1 (This example is to demonstate the effects based on the constituents of the compositions.)
Among the compositions shown in Table 1 given below, the compositions A through G are those of the present invention and the compositions H through K are comparative ones. Percentages in the table are shown in weight and the remainder is the amount of water.
Viscosity, antistatic property and softening property shown in Table l are measured according to the methods which will be described below. The results of the measurements are shown by four grades of G, O, A and X,@ being the most excellent (the lowest in viscosity). Quaternary ammonium salts in the table are compounds of the general formula (I) and the ethenoxy quaternary salts are ethenoxy quaternary ammonium salts of the general formula (ll). The symbol E indicates ethylene oxide.
METHODS OF MEASUREMENT l. Viscosity:
The composition directly after blending was allowed to stand at room temperature for 6 months and then at 50 C for 3 months, frozen at 30 C, thawed at room temperature and then frozen again. This procedure was repeated 5 times. Four samples of each composition were measured at 30 C with Brookfield type viscometer. The unit of numerals in the table is centi-poises.
2. Antistatic property:
Every swatch made from polyester fiber or acrylic fiber was immersed in 0.1 percent or 0.3 percent solution of each softening composition (weight ratio of the composition to the treating solution 1:20) and it was stirred and treated for 5 minutes. The solutions were squeezed out at 100 percent squeeze ratio. The swatches were dried and then allowed to stand at 25 C under percent humidity for 2 days to obtain the samples. The results of frictional static voltage mea sured with a rotatory static tester (the model by the Chemical Laboratory for Kyoto University) are shown in Table 2. Generally, at a frictional static voltage of less than 300 V, a drawback due to the static electricity is negligible. In this connection, frictional static voltages of untreated swatches of polyester and acrylic fibers were 2,200 V and 1,900 V, respectively.
3. Softening property:
Pieces of cotton towel, cotton plain fabric for diaper and blanket made from polyacrylonitrile fiber were washed in a usual manner, treated with 0.1 percent and 0.3 percent solutions of each softening composition and finally dried. The samples were tested by 5 men and 5 women according to handling (tactile impression) and their feelings were evaluated by the points compared with the standard criteria. The numerals in Table 2 are the sums of the points. The larger the nu meral, th softer the textile.
Table l Ethenoxy quaternary Com- Quaternary ammonium salt or another Additive Vis- Antistatic Softposition salt quaternary salt cosity property ness A Distearyldimethyl Stearylmethyl Pro- Q Q Q ammonium chloride dipolyoxyethylene pylene ammonium chloride glycol containing 7.0 moles of B0 2.2 6.0 B Distearyldimcthyl Stearylmethyl Pro- Q Q Q ammonium chloride dipoloxyethylene pylene NaCl ammonium chloride containing 50 7.0 moles of EO 2.2 6.0 0.02 c Distearyldimethyl Behenylbenzyldi- O O Q ammonium chloride polyoxyethylene Ethylene ammonium chloride glycol NaBr containing 40 6.0 moles of B0 2.0 7.0 0.03 D Dibchcnyldimcthyl Stearylmethyl Q Q 0 ammonium bromide dipolyoxyethylcne Glycerol NaCl ammonium bromide containing 30 5.0 moles of EO L5 3.0 0.05 E Distearyldihydroxy- Laurylpropyldi- Ethanol NaBr O O 0 ethylammonium polyoxycthylcnc ethosulfatc ammonium chloride containing 7.0 moles of B0 2.5 7.0 0.03 F Dihydrogenated Stearylcthyldi- Sorbitol NaCl Q Q Q tallowalkyl dipolyoxyethylenc methyl ammonium ammonium ethochloride sulfate containing 50 6.0 moles of E0 L0 4.0 0.02 G Dipalmitylbenzyl Stearylmethyldi- Urea Q Q Q methyl ammonium polyoxyethylene 3.0
chloride ammonium chloride Na SO,
containing [00 Pro- 8.0 moles of B0 3.0 pylenc glycol 3.0 0.03 H Dihydrogcnated Stearylmethyldi- Protallowalkyl di polyoxyethylcnc pylcne NaCl methyl ammonium ammonium chloride glycol A Q A chloride containing 8 7.0 moles of E0 [.5 5.0 0.03 l Dihydrogenated Stearyltrimcthyl Protallowalkyl diammonium chloride pylene NaCl methyl ammonium glycol X 0 O chloride Table 1 Continued Ethenoxy quaternary 1 Com- Quaternary ammonium salt or another Additive Vis- Antistatic Softpos1t1on salt quaternary salt cosity property ness .l Dihydrogenated Distearylmethyl Protallowalkyl dipolyoxycthylene pylenc NaCl methyl ammonium ammonium chloride glycol A A O chloride containing 40 7.0 moles of E 2.0 5.0 0.03 K Dihydrogenated Nonylphenolpoly- Protallowalkyl dioxyethylene ether pylcne NaCl methyl ammonium containing 50 glycol O X A chloride 7.0 moles of E0 L0 5.0 0.03
Table 2 Viscosity (centi-poises) Antistatic property Softness (volts) Comimmediately Room temp. 50C 30C Polyester Acrylic position after 6 months 3 months freeze blending 5 times 0.1% 0.3% 0.1% 0.3% 0.l% 0.3%
A 50 170 58 H0 110 75 185 70 100 98 B 50 52 48 40 l 80 I90 66 98 98 C 46 44 46 51 74 62 130 60 97 99 D 64 62 58 58 88 66 100 78 98 97 E 120 145 111 X90 78 66 110 83 l00 97 F 150 145 150 170 85 61 142 70 97 97 G 118 l 145 146 73 S7 96 60 98 98 H 104 270 243 756 130 100 I70 110 90 90 l 350 710 2400 4600 500 370 370 290 79 69 .l 610 590 410 2200 1550 890 900 610 78 81 K H8 135 145 1200 1000 8 I0 830 530 69 72 EXAMPLE 2 and measured at 30 C w1th a Brookfield type v1scome- (This example is to demonstrate the effects based on the proportions of constituents of the compositions.)
Effects of changes in the ethylene oxide units 'of ethenoxy quaternary salts and effects of additives (such as propylene glycol) were examined to obtain the results as shown in Table 3.
METHODS OF MEASUREMENT:
1. Viscosity The composition immediately after the blending was allowed to stand at room temperature for one month ter. The unit of numerals in the table is centi-poises.
2. Recovery after freeze The samples were frozen by allowing them to stand .at C for one day, and thawed by elevating the temperature to a room temperature. This procedure was repeated five times and the state of the samples was examined.
3. Dispersion stability The samples were allowed to stand in a constant temperature bath at 50 C for one month and the phase separation was examined.
The results of evaluation of the above items (2) and (3) were shown by four grades (in the same manner as in Example 1).
The same tendency as in Table 3 was observed also with other ethenoxy quaternary salts, i.e., behenylethyldipolyoxethylene ammonium ethosulfate and laurylbenzyldipolyoxyethylene ammonium chloride. In Table 3, the numerals in the column 1 indicate the numbers of the ethylene oxide unit in 1 mole of the molecule and those in the line 2 indicate wt. percent of PG added.
Table 3 G Viscosity at room temperature Recovery after freeze Dispersion stability P E0 0 3 5 10 15 20 0 5 10 15 20 0 3 5 10 15 20 2 3600 1120 750 460 860 980 A A A A A A A A A A A A 8 125 90 104 180 420 1390 A 6 O 6 A A 6 A A A A 20 114 72 80 75 240 1350 A 8 A A O A 84 102 80 80 140 1440 A O O A A O A 70 110 105 1750 A O 0 1 8 A O I O A 50 H8 52 48 98 2250 A O O y A O 1 o 8 A 60 240 190 51 53 110 2500 A O 0 O A o 0' A 976 540 5:18 230 240 2410 A A O O A A O O O A 780 558 414 390 410 2400 A A O O A A A O O O O A 710 690 390 440 610 2250 A A O O A A A O O O A A 1200 1100 980 780 830 2150 A A A A A A A A A A A A none 12000 9800 3700 1200 1100 980 x x x A A A x A O Q A A The embodiments of the invention in which the exclusive property or privelege is claimed are defined as follows:
1. An antistatic softening composition, consisting essentially of 4-10 percent by weight of a quaternary ammonium salt of the formula (1):
weight of an ethenoxy quaternary ammonium salt of the formula (II):
wherein R represents an alkyl group of C -C R represents an alkyl group of C -C or benzyl group, X represents Cl, Br or C H SO and m and n each represent an integer of more than 1 inclusive, with the privisio that m n is 20-100, 0.5 percent by weight of one or more additives selected from the group consist ing of alcohols of lower than C inclusive, glycols, glycerol, sorbitol and urea, the balance of said composition being water.
2. An antistatic softening composition according to claim 1, in which R and R each represents an alkyl group of C -C R and R each represents an alkyl group of C -C or benzyl group, R represents an alkyl group of C -C and the sum of m and n is 30-70.
3. An antistatic softening composition according to claim 1, in which the additive is selected from propylene glycol, ethylene glycol and glycerol.
4. An antistatic softening composition according to claim 1, in which the amount of said ethenoxy quaternary ammonium salt of the formula (II) is 1.0 to 5.0 percent by weight.
5. An antistatic softening composition according to claim 1, in which the amount of the additive is 3 to 8 percent by weight.
6. An antistatic softening composition according to claim 3, in which the amount of the additive is 3 to 8 percent by weight.
7. An antistatic softening composition according to claim 1, in which said quaternary ammonium salt of the formula (I) is selected from distearyldimethylammonium chloride and dihydrogenated tallowalkyl dimethylammonium chloride.
Claims (7)
1. AN ANTISTATIC SOFTENING COMPOSITION, CONSISTING ESSENTIALLY OF 4-10 PERCENT BY WEIGHT OF A QUATERNARY AMMONIUM SALT OF THE FORMULA (I):
2. An antistatic softening composition according to claim 1, in which R1 and R2 each represents an alkyl group of C16-C18, R3 and R4 each represents an alkyl group of C1-C3 or benzyl group, R5 represents an alkyl group of C12-C18 and the sum of m and n is 30-70.
3. An antistatic softening composition according to claiM 1, in which the additive is selected from propylene glycol, ethylene glycol and glycerol.
4. An antistatic softening composition according to claim 1, in which the amount of said ethenoxy quaternary ammonium salt of the formula (II) is 1.0 to 5.0 percent by weight.
5. An antistatic softening composition according to claim 1, in which the amount of the additive is 3 to 8 percent by weight.
6. An antistatic softening composition according to claim 3, in which the amount of the additive is 3 to 8 percent by weight.
7. An antistatic softening composition according to claim 1, in which said quaternary ammonium salt of the formula (I) is selected from distearyldimethylammonium chloride and dihydrogenated tallowalkyl dimethylammonium chloride.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP46074276A JPS5124638B2 (en) | 1971-09-23 | 1971-09-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3850818A true US3850818A (en) | 1974-11-26 |
Family
ID=13542413
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00290345A Expired - Lifetime US3850818A (en) | 1971-09-23 | 1972-09-19 | Antistatic softening composition containing a quaternary ammonium salt and a ethenoxy quaternary ammonium salt |
Country Status (8)
Country | Link |
---|---|
US (1) | US3850818A (en) |
JP (1) | JPS5124638B2 (en) |
AU (1) | AU468515B2 (en) |
CH (1) | CH544181A (en) |
DE (1) | DE2246866C3 (en) |
ES (1) | ES406891A1 (en) |
FR (1) | FR2153434B1 (en) |
GB (1) | GB1404494A (en) |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3958059A (en) * | 1973-10-01 | 1976-05-18 | The Procter & Gamble Company | Fabric treatment composition |
US3959155A (en) * | 1973-10-01 | 1976-05-25 | The Procter & Gamble Company | Detergent composition |
US3974076A (en) * | 1974-01-11 | 1976-08-10 | The Procter & Gamble Company | Fabric softener |
US4038196A (en) * | 1975-03-12 | 1977-07-26 | Kao Soap Co., Ltd. | Softening agent for woven fabrics |
US4076632A (en) * | 1977-02-22 | 1978-02-28 | The Procter & Gamble Company | Fabric softener |
US4084034A (en) * | 1976-08-23 | 1978-04-11 | Nalco Chemical Company | Sodium chloride and polydiallyl dimethyl ammonium chloride as an electroconductive additive |
US4102825A (en) * | 1976-10-01 | 1978-07-25 | Kao Soap Co., Ltd. | Liquid light-duty detergent composition |
US4157307A (en) * | 1978-08-07 | 1979-06-05 | The Procter & Gamble Company | Liquid fabric softener |
US4174304A (en) * | 1975-08-01 | 1979-11-13 | Bullen Chemical Company Midwest, Inc. | Surfactant system |
US4330526A (en) * | 1976-03-22 | 1982-05-18 | Kao Soap Co., Ltd. | Shampoo composition |
US4399045A (en) * | 1980-11-18 | 1983-08-16 | The Procter & Gamble Company | Concentrated fabric softening compositions |
DE3324056A1 (en) * | 1982-07-05 | 1984-01-19 | Lion Corp., Tokyo | ADDITIONAL FOR GRAINY DETERGENTS AND CLEANERS |
US4439335A (en) * | 1981-11-17 | 1984-03-27 | The Procter & Gamble Company | Concentrated fabric softening compositions |
US4485048A (en) * | 1982-08-09 | 1984-11-27 | Akzona Incorporated | Ethoxylated quaternary benzyl compounds |
US4844822A (en) * | 1987-07-06 | 1989-07-04 | The Dial Corporation | Softener/antistat compositions |
US6369159B1 (en) | 1987-05-13 | 2002-04-09 | Pdm Holdings Corp. | Antistatic plastic materials containing epihalohydrin polymers |
WO2023239891A1 (en) | 2022-06-10 | 2023-12-14 | Lubrizol Advanced Materials, Inc. | Thermoplastic polyurethanes with high temperature stability and uses thereof |
WO2024102687A1 (en) | 2022-11-08 | 2024-05-16 | Lubrizol Advanced Materials, Inc. | High resilient thermoplastic polyurethanes and uses thereof |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5126372A (en) * | 1974-08-26 | 1976-03-04 | Kasuga Electric Co | Chojakusokotaino soko hisokokenchisochi |
JPS5126373A (en) * | 1974-08-26 | 1976-03-04 | Kasuga Electric Co | Chojakusokotaino soko hisokokenchisochi |
DE2459354C2 (en) * | 1974-12-16 | 1986-03-27 | Hoechst Ag, 6230 Frankfurt | SOFT SOFT CONDENSER CONCENTRATE WITH DISINFECTING PROPERTIES |
DE2525610C2 (en) * | 1975-06-09 | 1985-04-11 | Henkel KGaA, 4000 Düsseldorf | Cationic softeners with improved cold water solubility |
GR67665B (en) | 1979-05-21 | 1981-09-02 | Unilever Nv | |
JPS5713958U (en) * | 1980-06-24 | 1982-01-25 | ||
US4401577A (en) * | 1980-09-25 | 1983-08-30 | Akzona Incorporated | Quaternary ammonium dihydroborates in fabric softener formulations |
DE3263800D1 (en) * | 1981-01-16 | 1985-07-04 | Procter & Gamble | Textile treatment compositions |
GB2115847B (en) * | 1982-03-02 | 1984-04-04 | Derek James Frost | Antistatic composition for synthetic textile materials |
NZ207932A (en) * | 1983-05-11 | 1986-03-14 | Colgate Palmolive Co | Fabric softener compositions containing quaternary ammonium compounds |
JPS60263384A (en) * | 1984-06-11 | 1985-12-26 | Mitsubishi Plastics Ind Ltd | Cover for housing magnetic disk |
GB8500959D0 (en) * | 1985-01-15 | 1985-02-20 | Unilever Plc | Fabric conditioning method |
GB8500958D0 (en) * | 1985-01-15 | 1985-02-20 | Unilever Plc | Fabric conditioning composition |
JPH0533493Y2 (en) * | 1988-08-24 | 1993-08-25 | ||
EP0890671A3 (en) * | 1997-07-10 | 2000-02-23 | Ciba SC Holding AG | Use of modified fatty amines for preventing deposition of low molecular weight by-products on textile materials |
Citations (4)
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US3154489A (en) * | 1960-07-18 | 1964-10-27 | Armour & Co | Surface active compositions |
US3178366A (en) * | 1962-05-28 | 1965-04-13 | Armour & Co | Treating compositions for softening fibers |
US3546115A (en) * | 1967-02-28 | 1970-12-08 | Cargill Inc | Fabric softener |
US3573091A (en) * | 1967-11-13 | 1971-03-30 | Armour & Co | Method of preparing water-dispersible softener compositions and products thereby |
-
1971
- 1971-09-23 JP JP46074276A patent/JPS5124638B2/ja not_active Expired
-
1972
- 1972-09-19 US US00290345A patent/US3850818A/en not_active Expired - Lifetime
- 1972-09-20 GB GB4354972A patent/GB1404494A/en not_active Expired
- 1972-09-21 CH CH1377972A patent/CH544181A/en not_active IP Right Cessation
- 1972-09-21 ES ES406891A patent/ES406891A1/en not_active Expired
- 1972-09-21 AU AU46960/72A patent/AU468515B2/en not_active Expired
- 1972-09-22 FR FR7233715A patent/FR2153434B1/fr not_active Expired
- 1972-09-23 DE DE2246866A patent/DE2246866C3/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3154489A (en) * | 1960-07-18 | 1964-10-27 | Armour & Co | Surface active compositions |
US3178366A (en) * | 1962-05-28 | 1965-04-13 | Armour & Co | Treating compositions for softening fibers |
US3546115A (en) * | 1967-02-28 | 1970-12-08 | Cargill Inc | Fabric softener |
US3573091A (en) * | 1967-11-13 | 1971-03-30 | Armour & Co | Method of preparing water-dispersible softener compositions and products thereby |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3959155A (en) * | 1973-10-01 | 1976-05-25 | The Procter & Gamble Company | Detergent composition |
US3958059A (en) * | 1973-10-01 | 1976-05-18 | The Procter & Gamble Company | Fabric treatment composition |
US3974076A (en) * | 1974-01-11 | 1976-08-10 | The Procter & Gamble Company | Fabric softener |
US4038196A (en) * | 1975-03-12 | 1977-07-26 | Kao Soap Co., Ltd. | Softening agent for woven fabrics |
US4174304A (en) * | 1975-08-01 | 1979-11-13 | Bullen Chemical Company Midwest, Inc. | Surfactant system |
US4330526A (en) * | 1976-03-22 | 1982-05-18 | Kao Soap Co., Ltd. | Shampoo composition |
US4084034A (en) * | 1976-08-23 | 1978-04-11 | Nalco Chemical Company | Sodium chloride and polydiallyl dimethyl ammonium chloride as an electroconductive additive |
US4102825A (en) * | 1976-10-01 | 1978-07-25 | Kao Soap Co., Ltd. | Liquid light-duty detergent composition |
US4076632A (en) * | 1977-02-22 | 1978-02-28 | The Procter & Gamble Company | Fabric softener |
US4157307A (en) * | 1978-08-07 | 1979-06-05 | The Procter & Gamble Company | Liquid fabric softener |
US4399045A (en) * | 1980-11-18 | 1983-08-16 | The Procter & Gamble Company | Concentrated fabric softening compositions |
US4439335A (en) * | 1981-11-17 | 1984-03-27 | The Procter & Gamble Company | Concentrated fabric softening compositions |
DE3324056A1 (en) * | 1982-07-05 | 1984-01-19 | Lion Corp., Tokyo | ADDITIONAL FOR GRAINY DETERGENTS AND CLEANERS |
US4485048A (en) * | 1982-08-09 | 1984-11-27 | Akzona Incorporated | Ethoxylated quaternary benzyl compounds |
US6369159B1 (en) | 1987-05-13 | 2002-04-09 | Pdm Holdings Corp. | Antistatic plastic materials containing epihalohydrin polymers |
US4844822A (en) * | 1987-07-06 | 1989-07-04 | The Dial Corporation | Softener/antistat compositions |
WO2023239891A1 (en) | 2022-06-10 | 2023-12-14 | Lubrizol Advanced Materials, Inc. | Thermoplastic polyurethanes with high temperature stability and uses thereof |
WO2024102687A1 (en) | 2022-11-08 | 2024-05-16 | Lubrizol Advanced Materials, Inc. | High resilient thermoplastic polyurethanes and uses thereof |
Also Published As
Publication number | Publication date |
---|---|
DE2246866A1 (en) | 1973-03-29 |
FR2153434B1 (en) | 1976-05-21 |
ES406891A1 (en) | 1975-10-01 |
JPS4841095A (en) | 1973-06-16 |
AU468515B2 (en) | 1976-01-15 |
AU4696072A (en) | 1974-03-28 |
GB1404494A (en) | 1975-08-28 |
FR2153434A1 (en) | 1973-05-04 |
DE2246866B2 (en) | 1978-08-17 |
CH544181A (en) | 1973-11-15 |
DE2246866C3 (en) | 1979-04-12 |
JPS5124638B2 (en) | 1976-07-26 |
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