PH27205A - Softening compositions and methods for making and using same - Google Patents
Softening compositions and methods for making and using same Download PDFInfo
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- PH27205A PH27205A PH39082A PH39082A PH27205A PH 27205 A PH27205 A PH 27205A PH 39082 A PH39082 A PH 39082A PH 39082 A PH39082 A PH 39082A PH 27205 A PH27205 A PH 27205A
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- Philippines
- Prior art keywords
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- alkyl
- fabric softening
- fabric
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 24
- 238000000034 method Methods 0.000 title claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- -1 polysiloxane Polymers 0.000 claims description 16
- 229920001296 polysiloxane Polymers 0.000 claims description 15
- 239000004744 fabric Substances 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 238000005406 washing Methods 0.000 claims description 4
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 4
- 239000002253 acid Substances 0.000 claims 3
- 150000001450 anions Chemical class 0.000 claims 2
- 150000002314 glycerols Chemical class 0.000 claims 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 2
- 241000928106 Alain Species 0.000 claims 1
- 101150109517 Camlg gene Proteins 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- UGODCLHJOJPPHP-AZGWGOJFSA-J tetralithium;[(2r,3s,4r,5r)-5-(6-aminopurin-9-yl)-4-hydroxy-2-[[oxido(sulfonatooxy)phosphoryl]oxymethyl]oxolan-3-yl] phosphate;hydrate Chemical compound [Li+].[Li+].[Li+].[Li+].O.C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP([O-])(=O)OS([O-])(=O)=O)[C@@H](OP([O-])([O-])=O)[C@H]1O UGODCLHJOJPPHP-AZGWGOJFSA-J 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 15
- 125000002091 cationic group Chemical group 0.000 description 10
- 239000004753 textile Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000002752 cationic softener Substances 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- IJJWOSAXNHWBPR-HUBLWGQQSA-N 5-[(3as,4s,6ar)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-n-(6-hydrazinyl-6-oxohexyl)pentanamide Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)NCCCCCC(=O)NN)SC[C@@H]21 IJJWOSAXNHWBPR-HUBLWGQQSA-N 0.000 description 1
- 241000219495 Betulaceae Species 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 235000004607 Chlorophora excelsa Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 description 1
- 241000595436 Milicia excelsa Species 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- 101150095197 PALD1 gene Proteins 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920005556 chlorobutyl Polymers 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 235000015250 liver sausages Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005528 methosulfate group Chemical group 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Detergent Compositions (AREA)
Description
I wm ’ Ca ie i. The invention relates to fabric softening
I compositions adapted to be used in the rinse cycle ’ . of an automatic dishwashing machine. More partie Co oularly, this invention is concerned with aqueous . fabric softening compositions which impart improved ‘ softness and other desirable attributes such as bet tar rewettability to the compositions. Speciticale - : 1y, the invention is based on the combination’ of a ’ cationic softener and a unique class of polysiloxanes. - Compositions containing quaternary anmonium - salts having at least one long chain hydrocarboxyl : group such as distearyl dimethyl ammonium chigride or long-chain imidazolinkum salts are commonly used oo to provide fabric softening benefits when employed © 15 | in a laundry rinse operation: for example, see U.S.
Fat. Nos. 3,349,033) 3,644,2031 3,946:1151 3,997,453 4,073,735, and 4,119,545, among many others.
Cr The quaternary ammonium compounds, while . . they are salts, are nevertheless generally charace terized ae water-insoluble since their solubility in water under normal conditions is less than about 5%
Ce "by weight. The usual concentration used by the con- sumer and accepted as the "standard" is 6% by weight. }
“ wap : CE Xe gE % - 0 -
At this and higher concentrations these cationic salte are generally present as ngols" or dispersions, } and stability becomes =a major problem. See for exam- ple U.S. Pat. No. 5,526,299 col. 1, lines 11 to 22.
S As a matter of fact stability and viscosity problems become major ones at higher concentrations e.g. above about 7% by weight of the cationic. There have been : oo many proclaimed solutions to providing concentrated (1.0. 5 6-7%) stable cationic formulations within usable and consumer accepteble viscosity ranges e.g. 30 ops to 500 ops. Cee for example U.3. Pate. Nos. bh, 442,013 and 4,661,270. While such concentrated formulations may afford stable and acceptable vis- cosity products their softening characteristics of : 15 gourse at equivalent concentrations, are essentially the same as the 6-7% products. - . It is desirable to provide cationic soften= : | , ing compositions, particularly for use in the rinse ‘cycle of a clothes washing machine, which are of im- proved softening not only at equal concentrations | : with older formulations, but even at lower concen- trations. This concept is not new as evidenced e.g. by U.S. Pat. No, 4,000,077 to Wixon wherein cationic i quaternary softener is combined with alcohol or al- oohol ether sulfate. This patent also demonstrates
/ - that with improved softening, another plus is achieved in terms of enhanced whiteness, the late a “ aw ter often being adversely affected hy cationics. ;
Th Ee It has also been known to employ silicone . - 5 based composition for treating fibers or yarns and - . ‘textiles to soften them. See, in this regard, an / Co article in Colorage-June 29, 1972 entitled "Silicones in the Textile Industry" by H. J. pald p 46 and 53.
Also attention is directed to U.S. Pat. Nos. 3,968,042 and 4,020,212 wherein compositions of or- : oo gano polyxiloxane (and predominantly a poly [dimethyl siloxane/) with a cationic softening surfactant (e.g. distearyl dimethyl ammonium chloride) or conventional imidazolinium softener (Varisoft 475) are described for the treatment of polyolefin fibers. The organo polysiloxanes sre liquid, water-dispersible products with viscosities ranging from "about 100 to about
Co KOO" cps at 77°F. (25°C.). .
Co In British 1,549,180, combinations of cationic and silicone are described, with the silicone proe : | viding in addition to some of the previously known benefits as waterproofing agent and "ironing aids" anti-stat, soil release etc..., softening benefits as well, The silicones are siloxsnes with visco- 2% sities at 25°C. of "at least 100 centistokes and up
Cu vl . to B(XX) centistokes". While this patent appears
Limited to siloxanes with viscosities not abowe 8000 sentistokes disclosures of higher viscosities (e.g. up to 17000 centistokes) are given but data is given allegedly establishing optimum performance in the range of 3000 to 8000 cc. (Ex. 1). In other foreign patents corresponding to British, 1549180, such es French, 2318268, there is generally a similar disclosure but in addition additional examples are given (see also Canadian 1085563, 1102511 and 1118965) : indicating "high viscosity silicones may give supe= rior softeners'. . oo l Further reference is made to U.S. Pat. Nos 3,376,161 which discloses compositions of quaternary ammonium salts and polysiloxanes for impregnating ‘ fibrous material to impart "anti-scruff" charaoteris- : “tios. The only specific viscosity given for ‘a polysilo- ; : 1. Xane is 10,000 cs at 25° C. None of the priof art
Co ispectally in the laundry softener field discldaes a co 20 - copss-linked polysiloxane. J co It has now been discovered that improved softening compositions are provided by a combinae tion of a cationic softener or mixture of cationio . éofteners or mixtures of cationics with anionics (ego alcohol sulfates or alcohol ether sulfates)
- | 937% and/or non-dordos (e.g. fatty alochols, fatty ssid esters), and the like, with a cross-liviced polysiloxens;
The polysilexane may be liquids, semi-woldids or solids’ . The 11quids may have viseosities in the range of less : 8 Ahan about 100 40 several hunired to several thousand to the tens of thousands and up to where it becomes urmeseur- able} the preferred polyeiloxnnes have viscosities about 10,000 cs (25%. ) up to elastomeric types (1.8. no messur- . able viscosity). : The compositions of this invention not only give superior softering, but quite unexpectedly yield treated textiles with improved rewsttebility: : : As 12 well mown, the ontioniec softeners tend to pro- vide Patrios with a degree of wnter-recietmmee or in other 18 words these softensrs tend to render the fabric somewhat hydrophobic, Silicones (or polywiloxanes) also would be - expboted to increase the hydrophobicity of fabrics treated with then as described in British 1,549,180, Notwdihwtend- ne nach tenchings snd expeotations it has now been dis- covered that the compositions of this invention not oly ‘provide improved end outstanding softening of textile es- pecially in the rinse oyole of a washing machine but also do #0 without incrensing the hydrophobicity of the textile.
AS a matter of foot the goods exiibit improved wettability, 2 An mowt are aswere, oe 0f the ubiquitous complaints of / oo Ce. . BAD OF:IGINAL J oo ap cationic softeners is that, in particular, towels wofbemed vith such softeners do not sbscrb wader ss well es virgin of untreated towels, Mis is also a compledrrt with syn~
Ahetion vhers the comfort factor is often directly Fo- lubed to the ability 10 sbeord moleture; Tus as sa exes ple, nylon goods tend to be unaomforteble in wars elimates dud 40 their lower ability %o absorb perapiration han aot tous Boftening theme synthetics with scetiondes exsserbates this problem, ) The oationics which are useful herein incinde dhe entire class of quaternary montium odmpounds viieh nay, : | only in part, be represmted by the following gental fore rl ~ | x(a i — . vs - ~a wherein at least one of the R groups ond preferably two oo (vege R amd R,) represents an aliphatic from 12 to 30 ver- bon atoms and the other R groups (eig: R, md Ry) nay be ower aliphatic e.g. from 0, to Oy preferably C, 40 9% end preferably, alkyl or eralkyl as methyl, ethyl ed pro- 0 prior bel, The "other" R groups (1.0, By md By) may - ‘BAD ORIGINAL 9
“ Co apes . © algo together with the nitrogen and/or one ox more than neterostcns and (preferably nitrogen) fom a §= or b= nesbered heterocyclic ring snd X= 48 ay sion oie hale, : eulato, methyl sulfate, nd trate, sosbatey phosphate; ben : 8 abate, oleate, etc, The symbol "g' represents the derde « valence of the enon snd alNo, therefore, the mmber of quaternary catiordo moieties in association therewith!
Ptusly with a sulfate anion we would have : nt | 80,~2 © 10 fypiosl ccapounis of the foregoing formula I inahide ethyl- dimethyl-stearyl smonium chloride, cetyl-d4 netifyl~bensyl wont chloride, dimethyl distemryl smnonium chleride, benzyl-dinsthyl-stearyl gamordun chloride, bensyl-dimethyl » ~ stearyl amordum bromide, trimethyl-stesryl senor chlo 13 ride, trimethyl-cetyl emmonium bromide, diethyldistearyl ' gmmomdum chloride, a1 ethyl-ootyl-stearyl smonium chloride, d4mothyl-ethyl-leuryl emordium chloride, a4methyl-methyl~ othyl-leuryl-cetyl smoniun chloride, propyl myristyl m= © mordum chloride, ditallow-dimethyl emonium chloride, md the corresponding methosulfates, acetates, ete, Imideso- 4ntum oanpounds of the Pormilas -fB =
BAD ORIGINAL 9 oo amor oo I oo o Ra rb bor, § nT x . xa” oo (rg)a” (Rg Jb
Ry wherein the R, groups represent independermtly hydrogen or €, to C, alkyl with hydrogen being preferred: Ry re presents aliphatic, prefersbly alkyl or acyloxyelkyl of 's Og to Cy and more preferably allyl of Oj to Gyo By : represents aliphatic, preferably Cy to 04 alkyl sod move preferably methyl or sthyl; a ad bd represent sero oF / ong end n 4 b 21 Ry mney be selected 8 Rgy the suse oo different, or mey be lower alkyl or substitubed alkyl of 0 0 Yo 04 such as haloalkyl, hydroxyalkyl, eminoellkyl; ale : kylmminoalkyl, scyleminoalkyl and the lilef end X= ix ~~ any sion similar to the formula I quaternsry enionw ~ . iy , the more preferred cumpounds of formula IY are the asyl- ’ LA eminoethyl oompounds of the formila ~ a ny 0 11(a) ~. 1s RB ~ ® ; (Rg)a 7 Nes (Rg)b
Ty . vhare Ry) Rey (a) and (b) sre en defined for Formulae II oo -9 = . ; | BAD ORIGINAL I ind By in hydrogen or selected from the nae group es
Ry ad Ry, is hydrexyl (whence the free a0id) or alkyl of q to Oye
Nlustrative compounds of Formulas IT ad IIa ine $ oludes oo 2<heptedeqyl-1-methyl-1-oleylandoethyl imddnzolindum othosultate : 2-hiaptadecy 1-1-mathyl-1-(2-stenraylarids Yethylimidano- drdin sulfate, 3 10 2«heptadecyl-1-mathyl-l~(2-stenroylumido ethylind dexolim shloride, oo 940000-1-(2-hydroxysthyl )~1~bensyl imidasolinim @ilérite, oo 2edoao=1~ (hydroxyethyl )-1-(4-chlorobutyl Mai dasclintum . shioride, ia 1 8ec000-1=(2-hydronyetil }-1-ostadeceryl Amd dwrolintim chloride, ; 24al1 oil fatty-l1-(2-hydroxyethyl )-1-bensyl fd d mio) dnive ) | . ¢hioride, eT 2-kall oil fabty=1-(2-hydraryethyl )-1~(4-chlorobutyl )= dmidarodirdum chloride, " 2-hisptrdeceny1-1-(2-hydroxyetiyl)-1-(4=chlorobutyl wilde . Holinium chloride, g-heptadecenyl-1-(2«hydroxysthyl )=1-bensyl imidazolium oo ; ohloride, Lo "” Bebaptadecyl-1- (hydroxyethyl -1-octedeayl imi danokdin ethyl ) EE = :
BAD ORIGINAL i
CooL .
4 pegs on { wd fate. ; rolyoationtcs of the following formula IIX sre aldo useful: — -, 111 nolo rt yr a fo 1m 3 wherein the R group is selected from %9 to %0 aliphatic, prefernbly alkyl or alkenyls or RO (01, ) - where R hes seis menning ns above, 1.0, Cj to Oy, aliphatic wd pre~ furably alkyl or alkenyly the R's may be hydrogen) 0 0 0, alkyl or hydroxynlkyl group; n 48 m integer of 2 to 6 od n is m integer from 1 to B53 md X 18 an defined in
Pormla (A). The preferred compounds sre thome where R 49
Og 10 0g and By is lower alkyl, especinlly methyll
Of the compounds within formila IIT mention may be mnde of the following i 1 Hoffa lowy1-¥, ¥, FL, Nlotetrometiy1-1, S~propanedi ankonitm : dinethom1 fate
Al Lomy 1-H, Kb, Fl-trinethyl-1, S-propenedd amondius dimethos i ‘sulfate
NeOley1-N, 8, N%, NL, ro pentrmethy1-1, S-propanadi somonium 81+ - méthosulfate : N-Re1lowy1-H, BURY, 1, Nl. pent cmethy1-1, S~propenedl amond wom cu
BAD ORIGINAL 9 a a, 29905” | . } dinethomlfate :
Newtoaryl-N, N,N,N}, pont emethy1-1; S~propmeds emmordum dimethomul fate 3 N-stearyloxypropyl-¥, Nt, tran (3-hydroxypropyl )-1, 3« : . or $ propansdi emondwm dimethopulfate ’ lh . / BER
RE The cross-linked polysilaxanes which may be used i are generally represented by a reticulated structure com prising the following unites nm | | R Cn | O~Bi~0 | md ohio 0 | I co _ F a _ F ~ 3 5 _P "W' und 4 "D" und ¢ "Mum wherein R represents alkyl, partioulsrly lower (oy $0 0, alkyl), substituted alkyl (e.g. with alkoxy, sno, halogen ebCeas )y aralkyl (e.gs benzyl) and the 11)ey the preferred R group is methyl, the "M" unit comprises from 0 #6 about 10% (e.g. OF, 2%, %) of the mmber of units.
Phe "D" unit from about 20 to about 9% of the mmbeyr of = units end the "1 unit from about 2 to about BOF, Fre tarred ranges are 0 to % for "™ unites about 40% 4s about B07 "D" unites end about 107 to about 607 "I unite:
Most preferred are ranges of OF to less them 9% (ele? 3%, - 1? = oo vay ol : : BAD ORIGINAL £1
Coe i oo of or 1) oz "™" unite; 60 to 80% "I" units} end about 20% to about 407 "™ units, m,n, and p represent integers ex . pressing the relative content of the "ut, fp and no oo unite respectively. Fxpressed as a ratio where "unite s are present, we have nip nay range from gbout 100.1 $0 10.1 end prefer- = ” ably about 100.1 to 20.1, with no "M' wn ta the ratio is oo : ~ _n. may range from about 49.1 to 1.4 md prafer- vo 7 ably about 4.1 to 1.3
The compositions of this invention sre resiily pre o paced in the ususl 6-87 active ingredient level hid oh is
Co tb oustomery ons for the reasons sivanced shove, . I% is Lo . | quite apparent that higher levels may be used resdrting : 13 $0 the techniques of the prior srt and, as ‘demonstrated : oo alder, levels up to 60% hy weight of motive ingredients wre rendily obteined, Regardless, however, of the Level of active ingredients, of more sigmificemce in mobi ving : thy maximm benefits of this invention is the ratdo of -- | 20 aston o softener $0 polysilaxeme, Ratios of cations to polysiloxane may range from bout 10011 to about 1110 | oo with ratio fram about 1511 to 1110 being preferredy Tid + 117 more preferred, 511 to 1:5 more highly preferred
Co with outstanding results gohievable at ratios of $13; 211,
F Cn. | T - | ponies oo ges 111, 112 and 49.
As for viscosity preferences the range of frem abouk 10,000 up $0 about 100,000 (e.g. 60,000 ops) 48 out- . sanding for softening, but also, up to and above 1,000,000 ’ opé 18 equally useful, Of unique significance are the elavbomerie products which have, one might say, infinite viscosity: They are not only eulstanding softeners but aise impart rewettability sheracteristios woh are even bother then those given ty the lower viscosity msberisls: | In addition $0 the eationle softensr and polysile~- : xan, one muy add, as well, ss aloohol sulfate (esgs softener sdfitvents or otherwise for exmmple, O)q V0 On slochol sul- fade), an alochol ether sulfate (e.g) Oy to Cy alechel and 2 or 3 or 4 moles of ethylene oxide snd then sulfated), 13 sodium paraffin (e.g. Oyg $0 Oy) sulfonate; nomienie mate- rial such es peraffine, fuatly acid ester glycol md gliy- : ceryl esters, a fatty aloohol ¢.g. Og ¥0 Oy slechel; mm : ethoxylated fatty, wxine salt of a higher (0yq Vo Qyo-eis! shouric) fatty solid and wo forth! These miliary mate- rials may be present in a ostionic to mxiliary ratio of abot 2051 0 115 preferably from about 1511 4 111 snd oo more prefursbly 10:1 40 311 The eomposition may eembein the usual mjuvarts of perfume, eolor opasifiers (ep resin emulsions), sequestremt;, viscosity oomirel sgenty muh a 2s inirganio salts 1.0, sodium nitrate, sodim chloride; 6al- , BAD ORIGINAL 9 odum chloride end the like, wolubiliwers e.g. hydre-
Axopen, elo. ” A partieularly preferred miditionsl component of popresented by the genersl elass of high molecular weight s alothols and especially the fatty alachols of Oy 40 Cyn typically Oy, $0 GO, Wuch es n-dodesyl aleohel, n-deire~ desylalechol, oxo-trideaylalochol; nehexsiécylaloshol, n~ oetedecyl alochol, elcomyl alechol; and mived fubly l= echals of synthetic or natursl derivation ¢.g. stemyl = 10 alechol: /n especially preferred ratio of cationic 40 fatty aloohol ranges from 611 $0 211 end more prefered $11 40 311 and most preferred 47511 Yo 3.351 (e.gl 401)
The following exmaple will serve to flluwirabe ¥he jesent drverkion without being deemdd lindtative thereot, . 13 Paris sre by weight unless otherwise indowteds so | ..* A ‘moftering ecmposition of the following demponentis
A8 provides oo
Ditallow dimethyl smoniua chloride We 0,¢-Cyg Tatty alochol oy
Silaxene (orows-lirked X2-7589 oy
A rt Br rr lr A, Atm tn et Stee tb ie on = . | BAD ORjGinAL 9
- Win product when compared $0 a 180 eps subirfun-
ALally Liner poly silaxsne yields drastically sofver
Surry oloth towels and improved rewsttedility in the bo= ) walks The softening gvalustion ests may be rn spooning $ $6 a conventional laboratory procedure uring six tines hardened cotton $exry cloth towels at a doseage of 10 n1/wath with 8 repliostes or in a stendmd washing machine with ferry oloth towels, The remetiability is sebernined by partially immersing thin, treated sirips of cloth iwto - 10 a Solum of water and measuring the wicking height of ihe quia : : ; BN © Beasple Tin Tepested using the following axtdontes ond amounts thereof in place of he DIDM AC (3:00). v
Co © (a) DENIC ict) 7 (p)pmmne (5:26) © (eo) Dimethyl dimtesryl samoniue metho- sulfate (3i01) (4) 2-heptodecyl-1-methyl=l-olyl~ - smidoethyl inidasolirdum ethomifate (3.6%) ee -16- : | Cd ae ORIGINAL ar
Bach of Exemples I end II{a) to 1X(e) is repested - feplacing the mixed Oy ~Oy, fatty alochol with the follow- ing non-donios in the indionted amounts | # ch ——fir etre ede ee r SS (a) hexadecyl sleehol) (0dvF) . (b) oatadeayl aloohol (009k) * (e) glyceryl monostearate (039%) oo (4) 0,405 Patty slochol (Lia) .
BX (PIA IV
A ommposition similar to Hxmple I is prepared excepd a. shat in place of ¥2-T809 cross-liried polysiloxane st equal ’ moms of a linear (VFL44SE-Welker Chemical Co) pelydi- / néthyl-siloxeane 18 used, While this partiouler éompositien 38 softens well, its rewstisMlity is significantly pover than oo 0 "that of Exemple I. In the wicking tess, Example I test wem- ple gives » wicking height of 44.0 ma whereas in his exon : ~ ple the test smple goes only 35.4 ma, A differsnes of 3.3 1 .
A. a mm in test yesults is considered signi ficemt. :
Pw ELNPLA ¥
Rrsaple I sd II are repeated except that he fatly ~/ © dlodhol 18 eliminated and in the case of Example TI(n) sd
Cf X¥(b) the level of cations is raved 30F. Ersellent re- suits are sbkained’ r a. BAD CRIGINAL 9
Claims (1)
- - EY RN ny bo Ce : AOC on : Yo : | ES APPS : Caml aD ren . : oo Lan aT nn . » CEL at | 2 0 5 Too RE EL es "7 HAT WE CLAIM 18: : CT 1, A fabric softening composition comprising Cot (A) a quaternary armonius salt fabric soften~ , ing compound, and5. (B) a cross-linked polysiloxane ropresented by i | | a structure containing the following die "i . ’ . , . ! Lo functional units D and tri-functional units an . ; Tj and, optionally, monofunctional units, oo - / OR > (M unit) h © 10 Re 81 «=0 : ; ’ ! | ' - ’ | Aamo de : Co fun . R n Me - . 7 ' " Sl R i (D unit) oo / EE Omer 1 we0 : R f , | (T unit) . R odio oo oo b P vhere ‘ R represents alkyl of from 1 to 4 carbon atoms, : “18 « : he ter cae ety ! oe Ce eee ‘ Ta | p= REYr . et i : a PAE A i rai ———y 5 iC2 ws : ’ { © which may be substituted, or benyl, : ¥, n and p sre mmbers expressing the relative . i content of the "M', "D" smd "#' units, respivtive- ly, ed (n 4 p)/n ranges from 10011 to 1011 enCs . options] units "0" are present md n/p ranges from 4911 t0 114 when optional urdts "™ mre not pre- pent, the mount of the tri-functional crowi-iinke ing units "I" ranges fram shout 2 40 80% of the bo- tal units] the emourt of di-fimotionsl wdds "I" 18 from sbout 20 to sbout 99 of the totel units, ad the amount of units "N" rengss from 0 40 about 5% of the total units, md the weight ratio of (4) to (B) ranges from abork 20051 $0 11107 2, 1 fabric eoftering composition as defined in 13 Olaim 1 further comprising a nordorde softener adhivent melegted from the group consisting of peraffins, fatty BE acid ester glycol, glycerol esters, fatty (ag to tp) al~ cohol, ond ethoxylated mmine sels of a higher (0,,+0,,) Latty solid.3. A fabric softening composition as defined in Cledm 1 wherein the ratio of (A) to (B) ranges from about sri to 111,4. A fabric softening ocmpomition es defined in Olaim © wherein the ratio of (A) $0 (B) renges fram edout -19 - oo oo BAD ORIGINAL 9 : hee511 to 111, ‘8, A fabrie softening composition as defined in ; Olaim 4 wherein the quaternary ammonium salt is represented by the formla ~~ ) (a) : R R bo v7 2 x{=)n ~~ J ~N i 5 Ry R,* . i 3 Tr J “5 AY L. : SO wherein R, represents a O10 to Oso alkyl moiety, BP repre~ . | | sents a Gy to Oy, alkyl molety, lower alkyl of 0; 40 0, or bensyl, R, end Ry independently represent lower alkyl of dy to 0, or benzyl, or R, md Ry together with the ritro- gen atom to which they ere bonded form a %=- or G-membersd : heterocyclic ring, X~ 1s am anion, and n represents the - valence of the anion X-, : “7 8, A fabric softening composition comprising a quaternary ammonium salt fabric softening compound (a ) a 1s cross-linked polysiloxane (8) represented by a stribture gowbedning the following di~functional units D snd ¥ri- Sanctions) urdts Ty ed, optionally; moncfimotional units CW Co . : BAD ORIGINAL 9 : hn iii — 4 i - $0 = L )EEL ee ree ee oo | CEE ef ny CA Cs bE ! < i i z 2 (x ds) : \ | CD . s p-8” 0 Lo ; R (v urd ®) : o— 83 © ERE : os oo g R In x : NL n \ AT unit) - | | o—81—0 ny vo \ 0 P . - . CF ere i - - $ Rr yopronent® elxyl of from 140 4 saxon sony IE He wich may be pabetitutieds or vensy 4 no " g, n od P yimbers ccpronsiag 460 TLE oo a. : SA 3 } — wT gon of tbe mt, "O" sod ne dil ropes? o ad (0 ¥ p)/a reves from yoord 46,3012 yh 69 " gional ude met gre present ad 8/ p TeniEe® trod } abe \ 4911 © 114 when optional ond tit we not Wt ; ody . 3 penty the ount of 0 rs -Amotdonsd orost™ ; A 14 pking und ts ne penge® gron. $H0U 2 %o oof of oo : tne botel ard bey the amount of apumostonss unis . ; 13 ‘ wph 4s from about 20 ¥0° abound Gul of Me vol } CS qa . . & Ct . Co | mer - ; EEE H : Wt : CL RIG ig : Ce BAD OF 7 vo oo 27205 To | ~ Ce . . Ty a units, snd the smount of wits" ranges from 0 ~~ © 40 shout UL of the total nmits, esd a non-domio softener evhmiser (E) melected frem the : group consisting of peraffine, fatly acid ssher : $ glycol, glycerol esters, tatiy (0, to Oy) alechel, © and ethoxylated mine salt of ‘a higher (0,4=0,,) © fatky acid in a weight ratio of Q151E ranging frem © 200613840 111051,~ 7. A method for treating lamdry to softer the - SE Laouiry in the rinse cycle of a clothes washing racing ) which camprines adding to the rinse cycle weter a Tadic he softening composition es defined in Oledm 1, . uM Bo ye 1 ; uo Co CL i NORMAN BIDMSIKORY - “ JRAR.PAUL GRANDMAYRR - ge ALAIN JAOUES:" lo VIVIANR 2408 = i i a ar .J . po .. i ~ a ' . <0). _ : Co . : Co . “ ow
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US23234688A | 1988-08-12 | 1988-08-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
PH27205A true PH27205A (en) | 1993-05-04 |
Family
ID=22872742
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PH39082A PH27205A (en) | 1988-08-12 | 1989-08-10 | Softening compositions and methods for making and using same |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP0354856A3 (en) |
JP (1) | JPH02154069A (en) |
AU (1) | AU616990B2 (en) |
BR (1) | BR8904038A (en) |
DK (1) | DK395589A (en) |
GR (1) | GR1000488B (en) |
MX (1) | MX170216B (en) |
MY (1) | MY105007A (en) |
NZ (1) | NZ230238A (en) |
PH (1) | PH27205A (en) |
PT (1) | PT91429A (en) |
TR (1) | TR24991A (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5336419A (en) * | 1990-06-06 | 1994-08-09 | The Procter & Gamble Company | Silicone gel for ease of ironing and better looking garments after ironing |
US5064543A (en) * | 1990-06-06 | 1991-11-12 | The Procter & Gamble Company | Silicone gel for ease of ironing and better looking garments after ironing |
EP0749469A1 (en) * | 1994-03-11 | 1996-12-27 | The Procter & Gamble Company | Fabric softener compositions |
CA2204887C (en) * | 1994-11-10 | 2001-08-07 | Alice Marie Vogel | Wrinkle reducing composition |
US5532023A (en) * | 1994-11-10 | 1996-07-02 | The Procter & Gamble Company | Wrinkle reducing composition |
GB9503596D0 (en) * | 1995-02-23 | 1995-04-12 | Unilever Plc | Cleaning composition comprising quaternised poly-dimethylsiloxane and nonionic surfactant |
TW313595B (en) * | 1995-04-21 | 1997-08-21 | Danaklon As | |
GB2318364B (en) * | 1996-10-21 | 2000-09-13 | Kao Corp | Detergent composition |
GB0212157D0 (en) | 2002-05-27 | 2002-07-03 | Unilever Plc | Fabric conditioning composition |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB991597A (en) * | 1960-05-25 | 1965-05-12 | Wallace Cameron & Co Ltd | Improvements in or relating to detergent solutions |
DE2631114C3 (en) * | 1975-07-14 | 1981-11-26 | The Procter & Gamble Co., 45202 Cincinnati, Ohio | Fabric softeners |
US4128484A (en) * | 1975-07-14 | 1978-12-05 | The Procter & Gamble Company | Fabric softening compositions |
DE2631419A1 (en) * | 1975-07-16 | 1977-02-03 | Procter & Gamble Europ | COMPOSITIONS FOR TEXTILE TREATMENT |
GB1549180A (en) * | 1975-07-16 | 1979-08-01 | Procter & Gamble | Textile treating compositions |
DE3427496A1 (en) * | 1984-07-26 | 1986-01-30 | Henkel KGaA, 4000 Düsseldorf | METHOD FOR PRODUCING A POLYSILOXANE BLOCK POLYMERISATE |
-
1989
- 1989-08-07 NZ NZ230238A patent/NZ230238A/en unknown
- 1989-08-08 AU AU39411/89A patent/AU616990B2/en not_active Ceased
- 1989-08-10 PT PT91429A patent/PT91429A/en unknown
- 1989-08-10 PH PH39082A patent/PH27205A/en unknown
- 1989-08-10 BR BR898904038A patent/BR8904038A/en not_active Application Discontinuation
- 1989-08-10 MX MX017161A patent/MX170216B/en unknown
- 1989-08-11 MY MYPI89001099A patent/MY105007A/en unknown
- 1989-08-11 GR GR890100506A patent/GR1000488B/en unknown
- 1989-08-11 DK DK395589A patent/DK395589A/en not_active Application Discontinuation
- 1989-08-11 TR TR89/0920A patent/TR24991A/en unknown
- 1989-08-11 EP EP89402291A patent/EP0354856A3/en not_active Withdrawn
- 1989-08-14 JP JP1210000A patent/JPH02154069A/en active Pending
Also Published As
Publication number | Publication date |
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JPH02154069A (en) | 1990-06-13 |
DK395589A (en) | 1990-02-13 |
AU616990B2 (en) | 1991-11-14 |
BR8904038A (en) | 1990-03-20 |
MX170216B (en) | 1993-08-11 |
GR1000488B (en) | 1992-07-30 |
DK395589D0 (en) | 1989-08-11 |
MY105007A (en) | 1994-07-30 |
TR24991A (en) | 1992-08-21 |
EP0354856A3 (en) | 1990-05-02 |
AU3941189A (en) | 1990-02-15 |
PT91429A (en) | 1990-03-08 |
GR890100506A (en) | 1990-08-22 |
EP0354856A2 (en) | 1990-02-14 |
NZ230238A (en) | 1991-10-25 |
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