CA1037658A - Aerosol spray starch formulation - Google Patents
Aerosol spray starch formulationInfo
- Publication number
- CA1037658A CA1037658A CA212,405A CA212405A CA1037658A CA 1037658 A CA1037658 A CA 1037658A CA 212405 A CA212405 A CA 212405A CA 1037658 A CA1037658 A CA 1037658A
- Authority
- CA
- Canada
- Prior art keywords
- weight
- percent
- starch
- formulation
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 56
- 238000009472 formulation Methods 0.000 title claims abstract description 41
- 229920002472 Starch Polymers 0.000 title claims abstract description 40
- 235000019698 starch Nutrition 0.000 title claims abstract description 40
- 239000008107 starch Substances 0.000 title claims abstract description 34
- 239000000443 aerosol Substances 0.000 title claims description 10
- 239000007921 spray Substances 0.000 title description 4
- 229910021538 borax Inorganic materials 0.000 claims abstract description 16
- 239000004328 sodium tetraborate Substances 0.000 claims abstract description 16
- 239000004744 fabric Substances 0.000 claims abstract description 14
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000004327 boric acid Substances 0.000 claims abstract description 12
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 12
- 235000010339 sodium tetraborate Nutrition 0.000 claims abstract description 12
- 239000000463 material Substances 0.000 claims abstract description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 31
- 239000003599 detergent Substances 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- -1 derivatives of aliphatic amines Chemical class 0.000 claims description 19
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 17
- 125000002947 alkylene group Chemical group 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 14
- 239000000839 emulsion Substances 0.000 claims description 14
- 229920001296 polysiloxane Polymers 0.000 claims description 14
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 13
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 13
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 13
- 230000002209 hydrophobic effect Effects 0.000 claims description 11
- 239000003380 propellant Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 239000006185 dispersion Substances 0.000 claims description 10
- 229920001223 polyethylene glycol Polymers 0.000 claims description 10
- 239000002202 Polyethylene glycol Substances 0.000 claims description 9
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 8
- 229920002261 Corn starch Polymers 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000008120 corn starch Substances 0.000 claims description 7
- 125000006353 oxyethylene group Chemical group 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 239000002518 antifoaming agent Substances 0.000 claims description 4
- 238000010409 ironing Methods 0.000 claims description 4
- 239000004753 textile Substances 0.000 claims description 4
- 229920000881 Modified starch Polymers 0.000 claims description 3
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 239000007859 condensation product Substances 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 150000002334 glycols Chemical class 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 239000001282 iso-butane Substances 0.000 claims description 3
- 235000019426 modified starch Nutrition 0.000 claims description 3
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 230000001976 improved effect Effects 0.000 abstract description 5
- 230000000149 penetrating effect Effects 0.000 abstract description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000003139 buffering effect Effects 0.000 description 4
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 235000013847 iso-butane Nutrition 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- PSBDWGZCVUAZQS-UHFFFAOYSA-N (dimethylsulfonio)acetate Chemical compound C[S+](C)CC([O-])=O PSBDWGZCVUAZQS-UHFFFAOYSA-N 0.000 description 2
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000015505 Sorghum bicolor subsp. bicolor Nutrition 0.000 description 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- 125000002015 acyclic group Chemical group 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- 150000003857 carboxamides Chemical class 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 150000005826 halohydrocarbons Chemical class 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
- 239000004299 sodium benzoate Substances 0.000 description 2
- 235000010234 sodium benzoate Nutrition 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229940117986 sulfobetaine Drugs 0.000 description 2
- 150000003456 sulfonamides Chemical class 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- BTANRVKWQNVYAZ-SCSAIBSYSA-N (2R)-butan-2-ol Chemical compound CC[C@@H](C)O BTANRVKWQNVYAZ-SCSAIBSYSA-N 0.000 description 1
- JNYAEWCLZODPBN-KVTDHHQDSA-N (2r,3r,4r)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@@H](O)[C@H]1O JNYAEWCLZODPBN-KVTDHHQDSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical group CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- FRCHKSNAZZFGCA-UHFFFAOYSA-N 1,1-dichloro-1-fluoroethane Chemical compound CC(F)(Cl)Cl FRCHKSNAZZFGCA-UHFFFAOYSA-N 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 1
- JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Chemical compound CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 description 1
- CYXIKYKBLDZZNW-UHFFFAOYSA-N 2-Chloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)CCl CYXIKYKBLDZZNW-UHFFFAOYSA-N 0.000 description 1
- ATEBGNALLCMSGS-UHFFFAOYSA-N 2-chloro-1,1-difluoroethane Chemical compound FC(F)CCl ATEBGNALLCMSGS-UHFFFAOYSA-N 0.000 description 1
- XYYUAOIALFMRGY-UHFFFAOYSA-N 3-[2-carboxyethyl(dodecyl)amino]propanoic acid Chemical compound CCCCCCCCCCCCN(CCC(O)=O)CCC(O)=O XYYUAOIALFMRGY-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 101100184147 Caenorhabditis elegans mix-1 gene Proteins 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
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- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 239000004341 Octafluorocyclobutane Substances 0.000 description 1
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- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- SLDWEJWDVFLQND-UHFFFAOYSA-N acetyloxy-dodecyl-dimethylazanium Chemical compound CCCCCCCCCCCC[N+](C)(C)OC(C)=O SLDWEJWDVFLQND-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
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- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
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- 239000001569 carbon dioxide Substances 0.000 description 1
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- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
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- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- 150000002190 fatty acyls Chemical group 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical class FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
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- 125000001165 hydrophobic group Chemical group 0.000 description 1
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- 150000002500 ions Chemical class 0.000 description 1
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- 125000001421 myristyl 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])[H] 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 1
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000004806 packaging method and process Methods 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
- 239000002245 particle Substances 0.000 description 1
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- 125000005496 phosphonium group Chemical group 0.000 description 1
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- 238000002360 preparation method Methods 0.000 description 1
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- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
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- 238000000926 separation method Methods 0.000 description 1
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- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 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
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000003784 tall oil Chemical class 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
ABSTRACT
An aqueous starch formulation which has improved fabric penetrating power and improved anti-flaking characteristics containing, in addition to the starch component, a polyhydric material, nonionic surfactant, borax and boric acid.
An aqueous starch formulation which has improved fabric penetrating power and improved anti-flaking characteristics containing, in addition to the starch component, a polyhydric material, nonionic surfactant, borax and boric acid.
Description
~3~6S8 The present invention relates to starch formulations of the type typicall~ used by the housewife in finishing home laundered textile garments.
More specifically, the invention provides a starch formulation suitable for spraying from an aerosol container, which formulation has improved fabric penetrating power and improved anti-flaking characteristics.
In the past certain aerosol starch formulations have had a tendency to cause a treated fabric to become unsightly. Apparently, this has been due to the tendency of the formulation to build up deposits on a sole plate of the iron. Upon continued ironing, these deposits would scorch and transfer to the fabric being ironed, leaving portions of the fabric with a blackened appearance.
The present invention is directed to a new spray starch formulation with a substantially reduced tendency to build up deposits on the sole plate of an iron. In this way the fabric discoloration problem of the prior art is practically eliminated. The improvement is accomplished by using an aqueous, starch containing solution or dispersion which includes, in addition to the starch component, a boric acid-borax buffering system, a nonionic-surfactant and a polyhydric compound as set forth hereinbelow.
According to the present invention, there is provided an aerosol starch formulation for use in finishing laundered textile garments comprising from about 2 to about 10 parts by weight of a liquefied normally gaseous pro-pellent and from about 98 to about 90 parts by weight of an aqueous starch composition comprising at least about 85 percent by weight of water, from about 2 to about 6 percent by weight of starchJ said starch being present as a solution or dispersion, from about 0.05 to about 1.0 percent by weight of a polyhydric material selected from the group of polymeric glycols of alkanes and olefins having from 2 to about 6 carbon atoms, from about 0.01 to about 0.5 percent by weight of a nonionic surfactant selected from the group consist-ing of condensation products of an organic aliphatic or alkyl aromatic hydro-phobic compound and a hydrophilic group comprising ethylene oxide, water-soluble salts of derivatives of aliphatic amines which contain at least one cationic group, one alkyl group of 8 to 18 carbon atoms and an anionlc water-~LQ371~
solublizing carboxyl, sulfo, sulfato, phosphato, or phosphono group in their molecular structure, zwitterionic detergents having the structural formula
More specifically, the invention provides a starch formulation suitable for spraying from an aerosol container, which formulation has improved fabric penetrating power and improved anti-flaking characteristics.
In the past certain aerosol starch formulations have had a tendency to cause a treated fabric to become unsightly. Apparently, this has been due to the tendency of the formulation to build up deposits on a sole plate of the iron. Upon continued ironing, these deposits would scorch and transfer to the fabric being ironed, leaving portions of the fabric with a blackened appearance.
The present invention is directed to a new spray starch formulation with a substantially reduced tendency to build up deposits on the sole plate of an iron. In this way the fabric discoloration problem of the prior art is practically eliminated. The improvement is accomplished by using an aqueous, starch containing solution or dispersion which includes, in addition to the starch component, a boric acid-borax buffering system, a nonionic-surfactant and a polyhydric compound as set forth hereinbelow.
According to the present invention, there is provided an aerosol starch formulation for use in finishing laundered textile garments comprising from about 2 to about 10 parts by weight of a liquefied normally gaseous pro-pellent and from about 98 to about 90 parts by weight of an aqueous starch composition comprising at least about 85 percent by weight of water, from about 2 to about 6 percent by weight of starchJ said starch being present as a solution or dispersion, from about 0.05 to about 1.0 percent by weight of a polyhydric material selected from the group of polymeric glycols of alkanes and olefins having from 2 to about 6 carbon atoms, from about 0.01 to about 0.5 percent by weight of a nonionic surfactant selected from the group consist-ing of condensation products of an organic aliphatic or alkyl aromatic hydro-phobic compound and a hydrophilic group comprising ethylene oxide, water-soluble salts of derivatives of aliphatic amines which contain at least one cationic group, one alkyl group of 8 to 18 carbon atoms and an anionlc water-~LQ371~
solublizing carboxyl, sulfo, sulfato, phosphato, or phosphono group in their molecular structure, zwitterionic detergents having the structural formula
2 \ ~
R _ N R4 X - 0
R _ N R4 X - 0
3 0 wherein R is an alkyl group containing about 10 to L8 carbon atoms, R2 and R3 are each Cl to C3 alkyl, R4 is an alkylene or hydroxy alkylene group contain-ing 1 to 4 carbon atoms and X is C or S:0 and polar nonionic detergents of the formula Rl R2 R Y~ 0 wherein Rl is an alkyl, alkenyl or monohydroxyalkyl radical having about 10 to 20 carbon atoms, R2 and R3 are each selected rom the group consisting oE
methyl, ethyl, propyl, ethanol and propanol radicals and Y is N or P, from about 0.05 to about 0.15 percent by weight of boric acid and from about 0.2 to about 0.6 percent by weight of borax, the weight ratio of borax to boric acid being from about 5:1 to about 3:1, said formulation having a substantially reduced tendency of flake when applied onto fabric which is then ironed.
An aqueous solution or dispersion of any type of starch, e.g. those derived from corn, wheat, rice, grain sorghum, waxy grain sorghum, waxy maize or tapioca, or mixtures thereof and water soluble or dispersible modifications or derivatives thereof, containing more than about 85 percent by weight of water and from about 2 percent to about 6 percent by weight of starch may be employed in the new formulations of the invention. Modified starches that may be used in the new formulations include natural starches that have been de-graded to obtain a lower viscosity by acidic, oxidative or enzymic depolymeri-zation. Additionally, low viscosity commercially available propoxylated and ethoxylated starches are useable in the new formulations and are presently pre-ferred since their low viscosity at relatively high solids concentrations make them very adaptable to spraying processes. Suitable alkoxylated, low viscosity starches are submicron sized particles of hydrophobic starch that are readily dispersed in water and are prepared by alkoxylation of granular starch with a monofunctional alkoxylating agent which provides the starch with ether linked 1~76~g3 hydrophobic groups. A suitable method for their preparation is taught in United States Patent 3,462,283. In accordance with the invention, the pro-poxylated or ethoxylated starch derivatives are dispersed in the aqueous medium in an amount of from about 2 percent to about 6 percent by weight of the spray formulation.
The polyhydric component of the new formulation, which enhances the wetting and anti-clogging properties of the composition, is typically present in quantities of from about 0.05% to about 1% by weight of the mixture, pre-ferably about 0.1 to 0.5% by weight. The polyhydric compound is chosen from the group of polymeric glycols of alkanes and olefins having from 2 to about 6, preferably 2 carbon atoms. Representative and preferred members of this group of compounds are polyethylene glycols having molecular weights from about 1000 to about 12,000. ~ost preferable among this group of polyhydric components is a polyethylene glycol having a molecular weight of 6,000 present in the composition.
Another component of the new formulation is a nonionic surfactant which enhances the penetration of the composition into the fabric. This diminishes the sole plate build up and helps reduce the amount of flaking which may occur. The nonionic surfactants of the present formulation are generally present in quantities of from about 0.01% to about 0.5% by weight of the mix-ture.
As used herein the term "nonionic surfactant" refers to a compound used in the formulation which compound is other than the polymeric polyhydric material which is also required. Amphoteric, zwitterionic and polar nonionic surfactants are useful surfactants which may be substituted for the nonionic surfactant in the practice of this invention.
The nonionic synthetic organic detergents are generally the condensa-tion product of an organic aliphatic or alkyl aromatic hydrophobic compound and hydrophilic alkylene oxide groups. Practically any hydrophobic compound having a carboxy, hydroxy, amido, or amino group with a free hydrogen attached to the nitrogen can be condensed with an alkylene oxide such as ethylene oxide or with the polyhydration products thereof, e.g., polyethylene glycoL, to form 37~S~
a nonionic detergent. Further, the length of the polyalkyleneoxy chain can be adjusted to achieve the desired balance between the hydrophobic and hydrophilic elements.
Useful for the nonionic compound types of hydrophobes are higher aliphatic alcohols and alkyl phenols, although others may be used such as carboxylic acids, carboxamides, mercaptans~ sulphonamides, etc. The ethylene oxide condensates with higher alkyl phenols represent a preferred class of nonionic compounds. Usually the hydrophobic moiety should contain at least about 6 carbon atoms, and preferably at least about 8 carbon atoms, and may contain as many as about 50 carbon atoms or more. The amount of alkylene oxide will vary considerably depending upon the hydrophobe, but as a general guide a rule, at least about 5 moles of alkylene oxide per mole of hydrophobe should be used. The upper limit of alkylene oxide will vary, also, but no particular criticality can be ascribed thereto. As much as 200 or more moles of alkylene oxide per mole of hydrophobe may be employed. While ethylene oxide is the preferred and prodominating oxyalkylating reagent, other lower alkylene oxides such as propylene oxide, butylene oxide, and the like may also be used or substituted in part for the ethylene oxide.
Other nonionic compounds which are suitable are the polyoxyalkylene esters of the organic acids such as the higher fatty acids, the rosin acids, tall oil acids, acids from petroleum oxidation products, etc. These esters will u~ually contain from about 10 to about 22 carbon atoms in the acid moiety and from about 12 to about 30 moles of ethylene oxide or its equivalent.
Still other nonionic surfactants are the alkylene oxide condensates with the higher fatty acid amides. The fatty acid group will generally con-tain from about 8 to about 22 carbon atoms and this will be condensed with about 10 to about 50 moles of ethylene oxide. The corresponding carboxamides and sulphonamides may also be used as substantial equivalents.
Still another class of nonionic products are the oxyalkylated higher aliphatic alcohols. The fatty alcohols should contain at least 6 carbon atoms, and preferably at least about 8 carbon atoms. The most preferred alcohols are lauryl, myristyl, cetyl, stearyl and oleyl alcohols and should be condensed _ ~ _ 1~)37~S~
with at least about 6 moles of ethylene oxide and, preferably, about 10 to 30 moles of ethylene oxide. A typical nonionic procluct is oleyl alcohol con-densed with 15 moles of ethylene oxide. The corresponding alkyl mercaptans when condensed with ethylene oxide are also admirably suitable in the composi-tions of the present invention.
Still other suitable nonionics are the polyoxyethylene polyoxypropy-lene adducts of l-butanol. The hydrophobe of these nonionics has a minimum molecular weight of 1,000 and consists of an aliphatic monohydric alcohol containing from 1 to 8 carbon atoms to which is attached a heteric chain of oxyethylene and oxypropylene. The weight ratio of oxypropylene to oxyethylene covers the range o~ 95:5 to 85:15. Attached to this is the hydrophilic poly-oxyethylene chain which is from 44.4 to 54.6 percent of the total molecular weigh~ of 1,~00 to 4,000.
A particularly useful group of nonionics is marketed under the trade mark "Pluronics." The compounds are formed by condensing ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol. The molecular weight of the hydrophobic portion of the molecule is of the order of 950 to 4,000 preferably 1,200 to 2,500. The addition of poly-oxyethylene radicals to the hydrophobic portion tends to increase the solubili-ty of the molecule as a whole. The molecular weight of the block copolymers varies from 1,100 to 15,000 and the polyethylene oxide content may comprise 20 to 80 percent by weight.
Suitable nonionics may be derived by the condensation of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine. The molecular weight varies from 500 to 4,500.
Other nonionic detergents include the ethylene oxide addends of mono-esters of hexahydric alcohols and inner ethers thereof with higher fatty acids containing about 10 to 20 carbon atoms, e.g., sorbitan monolaurate,sorbitan mono-oleate, and mannitan monoalmitate.
The amphoteric detergent which can be used in the compositions of this invention are generally water-soluble salts of derivatives of aliphatic amines which contain at least one cationic group, e.g., non-quaternary nitrogen, ~Q376~
quaternary ammonium, or quaternary phosphonium group, at least one alkyl group of about 8 to 18 carbon atoms and an anionic ~ater-solubili~ing carboxyl, sulfo, sulfato, phosphato or phosphone group in their molecular structure.
The alkyl group may be straight chain or branched and the specific cationic atom may be part of a heterocyclic ring.
Examples of suitable ampholytic detergents include the alkyl beta-aminopropionates, RN~H)C2H4COOM; the alkyl beta-aminodipropionates, RN(C2H4COOM)2; the alkyl and hydroxy alkyl taurinates, RN~CH3)C2H4503M; and the long-chain imidazole derivatives having the following formula:
INl \ CIH2 ~I) R - C ~ N _ W
N 2\
R _ C _ N ~II) wherein R is an acyclic group of about 7 to 17 carbon atoms, W is selected from the group of R20H, R2COOM, and R20R2COOM, Y is selected from the group consisting of OH, R30S03, R2 is an alkylene or hydroxyalkylene group contain-ing 1 to 4 carbon atoms, R is selected from the group consisting of alkyl, alkyl aryl and fatty acyl glyceride groups having 6 to 18 carbon atoms in the alkyl or an acyl group; and M is a water-soluble cation, e.g., sodium potassi-um, ammonium or alkylolammonium.
Formula I detergents are disclosed in Volume II of "Surface Active Agents and Detergents" and in French Patent 1,412,921 and Formula II deter-gents are described in United States 2,773,068; United States 2,781,354; and United States 2,781,357. The acyclic groups may be derived from coconut oil fatty acids ~a mixture of fatty acids containing 8 to 18 carbon atoms), lauric fatty acid, and oleic fatty acid and the preferred groups are C7-C17 alkyl groups. Preferred detergents of this type are sodium N-lauryl beta-amino-propionate, disodium N-lauryl iminodipropionate, and the disodium salt o 2-lauryl-cycloimidium-l-hydroxyl, l-ethoxy-ethanoic acid, l-ethanoic acid.
~376~B
Zwitterionic detergents such as the betaines and sulfo-betaines having the follo~ing formula are also useful:
R / N~) R4 - -X = O
R3 ~ ) wherein R is an alkyl group containing about 10 to L8 carbon atoms, R2 and R3 are each Cl-~3 alkyl, R4 is an alkylene or hydroxyaLkylene group containing about 1 to 4 carbon atoms, and X is C or S:O. The alkyl group can contain one or more intermediate linkages such as amido, ether or polyether linkages or nonfunctional substituents such as hydroxyl or halogen which do not substan-tially affect the hydrophobic character of the group. When X is c, the deter-gent is called a betaine; and when X is S:O, the detergent is called a sulfo-betaine or sultaine. Preferred betaine and sulfobetaine detergents are 1-(lauryl dimethylammonio) acetate, l-myristyl dimethylammonio) propane-3-sul-fonate, and l-~myristyl dimethylammonio)-2-hydroxypropane-3-sulEonate.
The polar nonionic detergents are those in which the hydrophilic group contains a semi-polar bond directly between two atoms, for example, N--~O; P-~O; As-~ 0; and S~~ O. There is charge separation between the two directly bonded atoms, but the detergent molecule bears no net charge and does not dissociate into ions.
The polar nonionic detergents of this invention include open-chain aliphatic amine oxides of the general formula RlR3R3N -~O. For the purpose of this invention Rl is an alkyl, alkenyl, or monohydroxyalkyl radical having about 10 to 20 carbon atoms. R2 and R3 are each selected from the group con-sisting of methyl, ethyl, propyl, ethanol, and propanol radicals.
Other operable polar nonionic detergents are the open-chain aliphatic phosphine oxides having the general formula RlR2R3P-~O wherein Rl is an alkyl, alkenyl~ or monohydroxyalkyl radical ranging in chain length from 10 to 18 carbon atoms, and R2 and R3 are each alXyl and mono-hydroxyalkyl radicals con-taining from 1 to 3 carbon atoms.
The boric acid-borax buffering system is present in the formulation 3Q of the present invention at about 0.25% to about 0.75% by weight of the mix-1~376~
ture, more preferably from about 0.4 to about 0.5% of the mixture. It has been found that by keeping the ratio of borax to boric acid within specific limits significant improvement in the flaking properties of the spray starch can be obtained. More specifically, it has been found that when the ratio of borax to boric acid is between the range of about 5:]L to about 3:1, more pre-ferably about 4:1, an unexpected improvement is achieved in that a reduced tendency to scorch and flake is obtained when the formulation is applied to fabrics and ironed.
~ther materials, having specific functional characteristics may also be present in the new formulations in addition to the aqueous solution or dis-persion of starch, boric-acid-borax buffering system, nonionic surfactant, and polyhydric component. These additional materials may include starch preserva-tives such as sodium benzoate; perfumes; anti-foaming agents such as silicone emulsions, e.g., dimethyl polysiloxane emulsion ~10% silicone); colloidal dis-persants; bactericides, such as formalin; ironing aids such as silicone and fluorocarbon compounds; anti-corrosion agents such as sodium nitrite; sizing agents, such as alkali metal, e.g. sodium, carboxymethyl cellulose; and a host of other functional materials known in the art.
The following examples include preferred and typical sprayable starch formulations that may be prepared in accordance with the invention.
1~376~i~
EXAMPLE 1 and COMPARATIVE EXAMPLE A
The following sprayable starch formulations are prepared.
Ingredients Percent by Weight Comparative Example 1 _Example A
Ethoxylated corn starch 4.00 4.00 Sodium carboxymethylcellulose 0.2 0.2 Boric acid 0.1 Borax 0-4 Formalin (27%) 0.042 0.042 Silicone anti-foam /dimethyl poly-siloxane emulsion ~10% silocone7** 0.5 Polyethylene glycol (m.w. 6000) 0.2 Octyl phenoxy polyethoxy ethanol (9-10 oxyethylene groups per molecule) 0.05 NaN02 0.1 0.1 Dimethyl polysiloxane emulsion ~37% silicone)*** 0.5 0.5 Perfume 0.015 0.015 Propylene glycol - 1.0 Sodium benzoate - 0.10 Deionized water Bal. Bal.
* The ethoxylated corn starch of Example 1 and Comparative Example A is a Corn Products Low Viscosity Starch which can be characteri2ed as follows:
** Union Carbide SAG-470 General Electric SM-2061 Degree of Ethoxylation A mixture of compounds having 0.05 to 0.07 oxyethylene units per 100 glucose units Color White Texture Free flowing powder pH ~lO percent dispersion) 5.5-6.0 Viscosityl 17.5+5.0 cps.
Moisture 12.5 percent max.
Ash 0. 5 percent max.
Viscosity of 10 percent dispersion cooled for 30 minutes at 200F using Brooksfield R.V.F., Spindle No. 1 @20 RPM @ 80F.
_ g _ ~V3~
In preparing the foregoing formulations the starch ingredient is first either dispersed ~propoxylated and ethoxylated starches) or dissolved ~soluble starches) in hot water. The remaining ingredients are then added to the starch solution and the mixture i5 thoroughly blended in a suitable appara-tus.
From about 98 parts to about 90 parts of the ultimate formulation and about 2 parts to about l0 parts of a suitable propellant can then be packaged in a suitable aerosol container. In these examples, 94 parts of the formulation and 6 parts of isobutane were combined to produce the aerosol formulations. Among the propellant fluids that are preferably used are the liquefied gases, materials which at atmospheric temperature and pressure will usually be in the gaseous state. Preferred useful propellants are liquefied gases or mixtures thereof of the hydrocarbon and/or halohydrocarbon types, preferably of 1 to 4 carbon atoms, with the halohydrocarbons having chlorine and/or fluorine as the halogen~s) thereof. Other liquefied gas propellants of the hydrocarbon and halogenated hydrocarbon types may also be employed in desired ratios to yield the dispensing pressure, which is normally from 10 to 100 lbs./sq. in., more preferably 30 to 60 lbs./sq. in. and often ideally about 50 lbs./sq. in. Such pressures are given at 25C. (room temperature).
Among the propellants which may be employed are chlorodifluoro~ethane; di-chlorodifluoromethane; difluoroethane; vinyl chloride; chlorodifluoroethane;
dichlorotetrafluoroethane; ~asymmetrical); dichlorotetrafluoroethane ~symmetri-cal); chlorotrifluoroethane; dichlorofluoroethane; "Chlorothene" ~CC13.CH3);
and octafluorocyclobutane; all of which are examples of halogenated hydrocarbon propellants. Among the hydrocarbon propellants may be mentioned propane; 2-methyl propane ~isobutane); n-butane and cyclobutane. Other such propellants are discussed in the text Pressurized Packaging ~Aerosols) by Herzka and Pickthall ~1958, Academic Press Inc., New York) at pages 19-77. Other useful propellants include inorganic gaseous propellants such as nitrogen, nitrous oxide and carbon dioxide.
The starch formulations of Example 1 and Comparative Example A are tested and compared as follows:
~1137~5~3 Ten pre-washed cotton swatches were ironed consecutively at the ~otton setting using various conventional irons as indicated below, at 50%
wet pickup level (on fabric). Visual observations are made and rà tings are assigned on a scale.
Metal Metal Teflon Teflon Steam Steam Iron Iron Iron Iron w/o Steam w/Steam ~Dry) (Steam) Flat Iron Example 1 0 O
Comparative 3 2 l 2 2 Example A
Scale: 0 - hardly noticeable 1 - slight 2 - moderate 3 - bad A comparison of the formulations of Example 1 and Example A clearly indicate the improved effects that are obtained by use of the boric acid-borax buffer-ing system, nonionic surfactant, and polyhydric component.
Other sprayable formulations in accordance with the invention are prepared in Examples 2 to 4.
Example 2 Ingredients Percent by Weight Propoxylated Corn Starch* 6.0 Sodium carboxymethylcellulose 0,05 Boric acid 0.05 Borax 0.25 - 20 Formalin (27%) 0.042 Polyethylene glycol (M.w. 2000) 1.0 Octylphenoxy polyethoxy ethanol o.s (as in Example 1) NaNo2 0.3 Dimethyl polysiloxane emulsion 1.0 (37% siliccne)***
Dimethyl polysiloxane emulsion 0.75 (10% silicone)***
Perfume 0.015 Deionized water Balance ~37~i5~
*-The propoxylated corn starch of Example 2 is sold as a Corn Products low Viscosity Starch and can be characterized as follows:
Degree of Propoxylation 0.05 to 0.07 oxypropylene units per 100 glucose units Color White Texture Free flowing powder pH ~10% dispersion) 5.5-7.0 Viscosityl 17.5-~5.0 cps.
Moisture 12.5 percent max.
Ash 0.5 percent max.
lViscosity of lO percent dispersion cooled for 30 minutes at 200F using~
Brookfeld R,S.F. Spindle No. 1 ~ 20 RPM ~ 80F.
** and *** - As in Example 1 Example 3 Ingredients Percent by Weight Hypochlorite Oxidized Corn Starch* 2.0 Boric acid 0.15 Borax 0-5 Polyethylene glycol ~m.w. 4000) 0.05 Nonyl phenol ~condensed with 9 moles of 0.01 ethylene oxide) 2a NaN2 0.05 Dimethyl polysiloxane emulsion (37% silicone)*** - 0.1 Dimethyl polysiloxane emulsion ~10% silicone)** 0.25 Deioni~ed water Balance The degree of hypochlorite oxidation is in the range of about 10 to about 20 scott. The scott viscosity test is run at a solids content of a~out 4%.
** and - As in Example 1.
~lQ3~7~5B
ExampIe 4 Ingredients Percent by Weight ~thoxylated corn starch 4.0 Boric acid 0.1 Borax 0 4 Polyethylene glycol ~m.w. 6000) 0.2 Dinonyl phenol (condensed with 15 moles of ethylene oxide) 0.05 Dimethyl polysiloxane emulsion ~37% silicone)*** 0-5 Dimethyl polysiloxane emulsion ~10~ silicone)** 0.5 Deionized water Balance , ** and * - As in ~xampie 1 When sprayed onto cotton fabrics, the above formulations are virtually free of any flaking problem. Further no significant problem of aerosol valve clogging is experienced. The above formulations provide fabrics with a smooth "hand" as opposed to the somewhat harsh feel usually associated with starched garments.
Although the invention has been described and illustrated with re~erence to certain specific embodiments, modifications can be made without departing from the spirit and scope of the invention as defined by the follow-ing claims.
methyl, ethyl, propyl, ethanol and propanol radicals and Y is N or P, from about 0.05 to about 0.15 percent by weight of boric acid and from about 0.2 to about 0.6 percent by weight of borax, the weight ratio of borax to boric acid being from about 5:1 to about 3:1, said formulation having a substantially reduced tendency of flake when applied onto fabric which is then ironed.
An aqueous solution or dispersion of any type of starch, e.g. those derived from corn, wheat, rice, grain sorghum, waxy grain sorghum, waxy maize or tapioca, or mixtures thereof and water soluble or dispersible modifications or derivatives thereof, containing more than about 85 percent by weight of water and from about 2 percent to about 6 percent by weight of starch may be employed in the new formulations of the invention. Modified starches that may be used in the new formulations include natural starches that have been de-graded to obtain a lower viscosity by acidic, oxidative or enzymic depolymeri-zation. Additionally, low viscosity commercially available propoxylated and ethoxylated starches are useable in the new formulations and are presently pre-ferred since their low viscosity at relatively high solids concentrations make them very adaptable to spraying processes. Suitable alkoxylated, low viscosity starches are submicron sized particles of hydrophobic starch that are readily dispersed in water and are prepared by alkoxylation of granular starch with a monofunctional alkoxylating agent which provides the starch with ether linked 1~76~g3 hydrophobic groups. A suitable method for their preparation is taught in United States Patent 3,462,283. In accordance with the invention, the pro-poxylated or ethoxylated starch derivatives are dispersed in the aqueous medium in an amount of from about 2 percent to about 6 percent by weight of the spray formulation.
The polyhydric component of the new formulation, which enhances the wetting and anti-clogging properties of the composition, is typically present in quantities of from about 0.05% to about 1% by weight of the mixture, pre-ferably about 0.1 to 0.5% by weight. The polyhydric compound is chosen from the group of polymeric glycols of alkanes and olefins having from 2 to about 6, preferably 2 carbon atoms. Representative and preferred members of this group of compounds are polyethylene glycols having molecular weights from about 1000 to about 12,000. ~ost preferable among this group of polyhydric components is a polyethylene glycol having a molecular weight of 6,000 present in the composition.
Another component of the new formulation is a nonionic surfactant which enhances the penetration of the composition into the fabric. This diminishes the sole plate build up and helps reduce the amount of flaking which may occur. The nonionic surfactants of the present formulation are generally present in quantities of from about 0.01% to about 0.5% by weight of the mix-ture.
As used herein the term "nonionic surfactant" refers to a compound used in the formulation which compound is other than the polymeric polyhydric material which is also required. Amphoteric, zwitterionic and polar nonionic surfactants are useful surfactants which may be substituted for the nonionic surfactant in the practice of this invention.
The nonionic synthetic organic detergents are generally the condensa-tion product of an organic aliphatic or alkyl aromatic hydrophobic compound and hydrophilic alkylene oxide groups. Practically any hydrophobic compound having a carboxy, hydroxy, amido, or amino group with a free hydrogen attached to the nitrogen can be condensed with an alkylene oxide such as ethylene oxide or with the polyhydration products thereof, e.g., polyethylene glycoL, to form 37~S~
a nonionic detergent. Further, the length of the polyalkyleneoxy chain can be adjusted to achieve the desired balance between the hydrophobic and hydrophilic elements.
Useful for the nonionic compound types of hydrophobes are higher aliphatic alcohols and alkyl phenols, although others may be used such as carboxylic acids, carboxamides, mercaptans~ sulphonamides, etc. The ethylene oxide condensates with higher alkyl phenols represent a preferred class of nonionic compounds. Usually the hydrophobic moiety should contain at least about 6 carbon atoms, and preferably at least about 8 carbon atoms, and may contain as many as about 50 carbon atoms or more. The amount of alkylene oxide will vary considerably depending upon the hydrophobe, but as a general guide a rule, at least about 5 moles of alkylene oxide per mole of hydrophobe should be used. The upper limit of alkylene oxide will vary, also, but no particular criticality can be ascribed thereto. As much as 200 or more moles of alkylene oxide per mole of hydrophobe may be employed. While ethylene oxide is the preferred and prodominating oxyalkylating reagent, other lower alkylene oxides such as propylene oxide, butylene oxide, and the like may also be used or substituted in part for the ethylene oxide.
Other nonionic compounds which are suitable are the polyoxyalkylene esters of the organic acids such as the higher fatty acids, the rosin acids, tall oil acids, acids from petroleum oxidation products, etc. These esters will u~ually contain from about 10 to about 22 carbon atoms in the acid moiety and from about 12 to about 30 moles of ethylene oxide or its equivalent.
Still other nonionic surfactants are the alkylene oxide condensates with the higher fatty acid amides. The fatty acid group will generally con-tain from about 8 to about 22 carbon atoms and this will be condensed with about 10 to about 50 moles of ethylene oxide. The corresponding carboxamides and sulphonamides may also be used as substantial equivalents.
Still another class of nonionic products are the oxyalkylated higher aliphatic alcohols. The fatty alcohols should contain at least 6 carbon atoms, and preferably at least about 8 carbon atoms. The most preferred alcohols are lauryl, myristyl, cetyl, stearyl and oleyl alcohols and should be condensed _ ~ _ 1~)37~S~
with at least about 6 moles of ethylene oxide and, preferably, about 10 to 30 moles of ethylene oxide. A typical nonionic procluct is oleyl alcohol con-densed with 15 moles of ethylene oxide. The corresponding alkyl mercaptans when condensed with ethylene oxide are also admirably suitable in the composi-tions of the present invention.
Still other suitable nonionics are the polyoxyethylene polyoxypropy-lene adducts of l-butanol. The hydrophobe of these nonionics has a minimum molecular weight of 1,000 and consists of an aliphatic monohydric alcohol containing from 1 to 8 carbon atoms to which is attached a heteric chain of oxyethylene and oxypropylene. The weight ratio of oxypropylene to oxyethylene covers the range o~ 95:5 to 85:15. Attached to this is the hydrophilic poly-oxyethylene chain which is from 44.4 to 54.6 percent of the total molecular weigh~ of 1,~00 to 4,000.
A particularly useful group of nonionics is marketed under the trade mark "Pluronics." The compounds are formed by condensing ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol. The molecular weight of the hydrophobic portion of the molecule is of the order of 950 to 4,000 preferably 1,200 to 2,500. The addition of poly-oxyethylene radicals to the hydrophobic portion tends to increase the solubili-ty of the molecule as a whole. The molecular weight of the block copolymers varies from 1,100 to 15,000 and the polyethylene oxide content may comprise 20 to 80 percent by weight.
Suitable nonionics may be derived by the condensation of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine. The molecular weight varies from 500 to 4,500.
Other nonionic detergents include the ethylene oxide addends of mono-esters of hexahydric alcohols and inner ethers thereof with higher fatty acids containing about 10 to 20 carbon atoms, e.g., sorbitan monolaurate,sorbitan mono-oleate, and mannitan monoalmitate.
The amphoteric detergent which can be used in the compositions of this invention are generally water-soluble salts of derivatives of aliphatic amines which contain at least one cationic group, e.g., non-quaternary nitrogen, ~Q376~
quaternary ammonium, or quaternary phosphonium group, at least one alkyl group of about 8 to 18 carbon atoms and an anionic ~ater-solubili~ing carboxyl, sulfo, sulfato, phosphato or phosphone group in their molecular structure.
The alkyl group may be straight chain or branched and the specific cationic atom may be part of a heterocyclic ring.
Examples of suitable ampholytic detergents include the alkyl beta-aminopropionates, RN~H)C2H4COOM; the alkyl beta-aminodipropionates, RN(C2H4COOM)2; the alkyl and hydroxy alkyl taurinates, RN~CH3)C2H4503M; and the long-chain imidazole derivatives having the following formula:
INl \ CIH2 ~I) R - C ~ N _ W
N 2\
R _ C _ N ~II) wherein R is an acyclic group of about 7 to 17 carbon atoms, W is selected from the group of R20H, R2COOM, and R20R2COOM, Y is selected from the group consisting of OH, R30S03, R2 is an alkylene or hydroxyalkylene group contain-ing 1 to 4 carbon atoms, R is selected from the group consisting of alkyl, alkyl aryl and fatty acyl glyceride groups having 6 to 18 carbon atoms in the alkyl or an acyl group; and M is a water-soluble cation, e.g., sodium potassi-um, ammonium or alkylolammonium.
Formula I detergents are disclosed in Volume II of "Surface Active Agents and Detergents" and in French Patent 1,412,921 and Formula II deter-gents are described in United States 2,773,068; United States 2,781,354; and United States 2,781,357. The acyclic groups may be derived from coconut oil fatty acids ~a mixture of fatty acids containing 8 to 18 carbon atoms), lauric fatty acid, and oleic fatty acid and the preferred groups are C7-C17 alkyl groups. Preferred detergents of this type are sodium N-lauryl beta-amino-propionate, disodium N-lauryl iminodipropionate, and the disodium salt o 2-lauryl-cycloimidium-l-hydroxyl, l-ethoxy-ethanoic acid, l-ethanoic acid.
~376~B
Zwitterionic detergents such as the betaines and sulfo-betaines having the follo~ing formula are also useful:
R / N~) R4 - -X = O
R3 ~ ) wherein R is an alkyl group containing about 10 to L8 carbon atoms, R2 and R3 are each Cl-~3 alkyl, R4 is an alkylene or hydroxyaLkylene group containing about 1 to 4 carbon atoms, and X is C or S:O. The alkyl group can contain one or more intermediate linkages such as amido, ether or polyether linkages or nonfunctional substituents such as hydroxyl or halogen which do not substan-tially affect the hydrophobic character of the group. When X is c, the deter-gent is called a betaine; and when X is S:O, the detergent is called a sulfo-betaine or sultaine. Preferred betaine and sulfobetaine detergents are 1-(lauryl dimethylammonio) acetate, l-myristyl dimethylammonio) propane-3-sul-fonate, and l-~myristyl dimethylammonio)-2-hydroxypropane-3-sulEonate.
The polar nonionic detergents are those in which the hydrophilic group contains a semi-polar bond directly between two atoms, for example, N--~O; P-~O; As-~ 0; and S~~ O. There is charge separation between the two directly bonded atoms, but the detergent molecule bears no net charge and does not dissociate into ions.
The polar nonionic detergents of this invention include open-chain aliphatic amine oxides of the general formula RlR3R3N -~O. For the purpose of this invention Rl is an alkyl, alkenyl, or monohydroxyalkyl radical having about 10 to 20 carbon atoms. R2 and R3 are each selected from the group con-sisting of methyl, ethyl, propyl, ethanol, and propanol radicals.
Other operable polar nonionic detergents are the open-chain aliphatic phosphine oxides having the general formula RlR2R3P-~O wherein Rl is an alkyl, alkenyl~ or monohydroxyalkyl radical ranging in chain length from 10 to 18 carbon atoms, and R2 and R3 are each alXyl and mono-hydroxyalkyl radicals con-taining from 1 to 3 carbon atoms.
The boric acid-borax buffering system is present in the formulation 3Q of the present invention at about 0.25% to about 0.75% by weight of the mix-1~376~
ture, more preferably from about 0.4 to about 0.5% of the mixture. It has been found that by keeping the ratio of borax to boric acid within specific limits significant improvement in the flaking properties of the spray starch can be obtained. More specifically, it has been found that when the ratio of borax to boric acid is between the range of about 5:]L to about 3:1, more pre-ferably about 4:1, an unexpected improvement is achieved in that a reduced tendency to scorch and flake is obtained when the formulation is applied to fabrics and ironed.
~ther materials, having specific functional characteristics may also be present in the new formulations in addition to the aqueous solution or dis-persion of starch, boric-acid-borax buffering system, nonionic surfactant, and polyhydric component. These additional materials may include starch preserva-tives such as sodium benzoate; perfumes; anti-foaming agents such as silicone emulsions, e.g., dimethyl polysiloxane emulsion ~10% silicone); colloidal dis-persants; bactericides, such as formalin; ironing aids such as silicone and fluorocarbon compounds; anti-corrosion agents such as sodium nitrite; sizing agents, such as alkali metal, e.g. sodium, carboxymethyl cellulose; and a host of other functional materials known in the art.
The following examples include preferred and typical sprayable starch formulations that may be prepared in accordance with the invention.
1~376~i~
EXAMPLE 1 and COMPARATIVE EXAMPLE A
The following sprayable starch formulations are prepared.
Ingredients Percent by Weight Comparative Example 1 _Example A
Ethoxylated corn starch 4.00 4.00 Sodium carboxymethylcellulose 0.2 0.2 Boric acid 0.1 Borax 0-4 Formalin (27%) 0.042 0.042 Silicone anti-foam /dimethyl poly-siloxane emulsion ~10% silocone7** 0.5 Polyethylene glycol (m.w. 6000) 0.2 Octyl phenoxy polyethoxy ethanol (9-10 oxyethylene groups per molecule) 0.05 NaN02 0.1 0.1 Dimethyl polysiloxane emulsion ~37% silicone)*** 0.5 0.5 Perfume 0.015 0.015 Propylene glycol - 1.0 Sodium benzoate - 0.10 Deionized water Bal. Bal.
* The ethoxylated corn starch of Example 1 and Comparative Example A is a Corn Products Low Viscosity Starch which can be characteri2ed as follows:
** Union Carbide SAG-470 General Electric SM-2061 Degree of Ethoxylation A mixture of compounds having 0.05 to 0.07 oxyethylene units per 100 glucose units Color White Texture Free flowing powder pH ~lO percent dispersion) 5.5-6.0 Viscosityl 17.5+5.0 cps.
Moisture 12.5 percent max.
Ash 0. 5 percent max.
Viscosity of 10 percent dispersion cooled for 30 minutes at 200F using Brooksfield R.V.F., Spindle No. 1 @20 RPM @ 80F.
_ g _ ~V3~
In preparing the foregoing formulations the starch ingredient is first either dispersed ~propoxylated and ethoxylated starches) or dissolved ~soluble starches) in hot water. The remaining ingredients are then added to the starch solution and the mixture i5 thoroughly blended in a suitable appara-tus.
From about 98 parts to about 90 parts of the ultimate formulation and about 2 parts to about l0 parts of a suitable propellant can then be packaged in a suitable aerosol container. In these examples, 94 parts of the formulation and 6 parts of isobutane were combined to produce the aerosol formulations. Among the propellant fluids that are preferably used are the liquefied gases, materials which at atmospheric temperature and pressure will usually be in the gaseous state. Preferred useful propellants are liquefied gases or mixtures thereof of the hydrocarbon and/or halohydrocarbon types, preferably of 1 to 4 carbon atoms, with the halohydrocarbons having chlorine and/or fluorine as the halogen~s) thereof. Other liquefied gas propellants of the hydrocarbon and halogenated hydrocarbon types may also be employed in desired ratios to yield the dispensing pressure, which is normally from 10 to 100 lbs./sq. in., more preferably 30 to 60 lbs./sq. in. and often ideally about 50 lbs./sq. in. Such pressures are given at 25C. (room temperature).
Among the propellants which may be employed are chlorodifluoro~ethane; di-chlorodifluoromethane; difluoroethane; vinyl chloride; chlorodifluoroethane;
dichlorotetrafluoroethane; ~asymmetrical); dichlorotetrafluoroethane ~symmetri-cal); chlorotrifluoroethane; dichlorofluoroethane; "Chlorothene" ~CC13.CH3);
and octafluorocyclobutane; all of which are examples of halogenated hydrocarbon propellants. Among the hydrocarbon propellants may be mentioned propane; 2-methyl propane ~isobutane); n-butane and cyclobutane. Other such propellants are discussed in the text Pressurized Packaging ~Aerosols) by Herzka and Pickthall ~1958, Academic Press Inc., New York) at pages 19-77. Other useful propellants include inorganic gaseous propellants such as nitrogen, nitrous oxide and carbon dioxide.
The starch formulations of Example 1 and Comparative Example A are tested and compared as follows:
~1137~5~3 Ten pre-washed cotton swatches were ironed consecutively at the ~otton setting using various conventional irons as indicated below, at 50%
wet pickup level (on fabric). Visual observations are made and rà tings are assigned on a scale.
Metal Metal Teflon Teflon Steam Steam Iron Iron Iron Iron w/o Steam w/Steam ~Dry) (Steam) Flat Iron Example 1 0 O
Comparative 3 2 l 2 2 Example A
Scale: 0 - hardly noticeable 1 - slight 2 - moderate 3 - bad A comparison of the formulations of Example 1 and Example A clearly indicate the improved effects that are obtained by use of the boric acid-borax buffer-ing system, nonionic surfactant, and polyhydric component.
Other sprayable formulations in accordance with the invention are prepared in Examples 2 to 4.
Example 2 Ingredients Percent by Weight Propoxylated Corn Starch* 6.0 Sodium carboxymethylcellulose 0,05 Boric acid 0.05 Borax 0.25 - 20 Formalin (27%) 0.042 Polyethylene glycol (M.w. 2000) 1.0 Octylphenoxy polyethoxy ethanol o.s (as in Example 1) NaNo2 0.3 Dimethyl polysiloxane emulsion 1.0 (37% siliccne)***
Dimethyl polysiloxane emulsion 0.75 (10% silicone)***
Perfume 0.015 Deionized water Balance ~37~i5~
*-The propoxylated corn starch of Example 2 is sold as a Corn Products low Viscosity Starch and can be characterized as follows:
Degree of Propoxylation 0.05 to 0.07 oxypropylene units per 100 glucose units Color White Texture Free flowing powder pH ~10% dispersion) 5.5-7.0 Viscosityl 17.5-~5.0 cps.
Moisture 12.5 percent max.
Ash 0.5 percent max.
lViscosity of lO percent dispersion cooled for 30 minutes at 200F using~
Brookfeld R,S.F. Spindle No. 1 ~ 20 RPM ~ 80F.
** and *** - As in Example 1 Example 3 Ingredients Percent by Weight Hypochlorite Oxidized Corn Starch* 2.0 Boric acid 0.15 Borax 0-5 Polyethylene glycol ~m.w. 4000) 0.05 Nonyl phenol ~condensed with 9 moles of 0.01 ethylene oxide) 2a NaN2 0.05 Dimethyl polysiloxane emulsion (37% silicone)*** - 0.1 Dimethyl polysiloxane emulsion ~10% silicone)** 0.25 Deioni~ed water Balance The degree of hypochlorite oxidation is in the range of about 10 to about 20 scott. The scott viscosity test is run at a solids content of a~out 4%.
** and - As in Example 1.
~lQ3~7~5B
ExampIe 4 Ingredients Percent by Weight ~thoxylated corn starch 4.0 Boric acid 0.1 Borax 0 4 Polyethylene glycol ~m.w. 6000) 0.2 Dinonyl phenol (condensed with 15 moles of ethylene oxide) 0.05 Dimethyl polysiloxane emulsion ~37% silicone)*** 0-5 Dimethyl polysiloxane emulsion ~10~ silicone)** 0.5 Deionized water Balance , ** and * - As in ~xampie 1 When sprayed onto cotton fabrics, the above formulations are virtually free of any flaking problem. Further no significant problem of aerosol valve clogging is experienced. The above formulations provide fabrics with a smooth "hand" as opposed to the somewhat harsh feel usually associated with starched garments.
Although the invention has been described and illustrated with re~erence to certain specific embodiments, modifications can be made without departing from the spirit and scope of the invention as defined by the follow-ing claims.
Claims (7)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. An aerosol starch formulation for use in finishing laundered textile garments comprising from about 2 to about 10 parts by weight of a liquefied normally gaseous propellent and from about 98 to about 90 parts by weight of an aqueous starch composition comprising at least about 85 percent by weight of water, from about 2 to about 6 percent by weight of starch, said starch being present as a solution or dispersion, from about 0.05 to about 1.0 percent by weight of a polyhydric material selected from the group of polymeric glycols of alkanes and oelfins having from 2 to about 6 carbon atoms, from about 0.01 to about 0.5 percent by weight of a nonionic surfactant selected from the group consisting of condensation products of an organic aliphatic or alkyl aromatic hydrophobic compound and a hydrophilic group comprising ethylene oxide, water-soluble salts of derivatives of aliphatic amines which contain at least one cationic group, one alkyl group of 8 to 18 carbon atoms and an anionic water-solublizing carboxyl, sulfo, sulfato, phos-phato, or phosphono group in their molecular structure, zwitterionic detergents having the structural formula wherein R is an alkyl group containing about 10 to 18 carbon atoms, R2 and R3 are each C1 to C3 alkyl, R4 is an alkylene or hydroxy alkylene group containing 1 to 4 carbon atoms and X is C or S:O and polar nonionic detergents of the formula R1 R2 R3 Y ?O
wherein R1 is an alkyl, alkenyl or monohydroxyalkyl radical having about 10 to 20 carbon atoms, R2 and R3 are each selected from the group consisting of methyl, ethyl, propyl, ethanol and propanol radicals and Y is N or P, from about 0.05 to about 0.15 percent by weight of boric acid and from about 0.2 to about 0.6 percent by weight of borax, the weight ratio of borax to boric acid being from about 5:1 to about 3:1, said formulation having s substantially reduced tendency of flake when applied onto fabric which is then ironed.
wherein R1 is an alkyl, alkenyl or monohydroxyalkyl radical having about 10 to 20 carbon atoms, R2 and R3 are each selected from the group consisting of methyl, ethyl, propyl, ethanol and propanol radicals and Y is N or P, from about 0.05 to about 0.15 percent by weight of boric acid and from about 0.2 to about 0.6 percent by weight of borax, the weight ratio of borax to boric acid being from about 5:1 to about 3:1, said formulation having s substantially reduced tendency of flake when applied onto fabric which is then ironed.
2. The formulation of claim 1 which further contains, as an anti-foaming agent, from about 0.25 to about 0.75 percent by weight of a dimethyl polysiloxane emulsion containing about 10% by weight of silicone.
3. The formulation of claim 1 which further contains, as an ironing aid, from about 0.1 to about 1.0% by weight of a dimethyl polysiloxane emulsion containing about 37% by weight of silicone.
4. The formulation of claim 1 wherein said starch is a low viscosity starch derivative chosen from the group consisting of propoxylated and ethoxylated starches.
5. The formulation of claim 1 wherein said polyhydric material is a polyethylene glycol.
6. The formulation of claim 5 wherein the polyethylene glycol has a molecular weight from about 1,000 to about 12,000.
7. An aerosol starch formulation for use in finishing laundered textile garments comprising about 6 parts by weight of a liquefied isobutane propellant and about 94 parts by weight of an aqueous starch solution or dispersion comprising at least about 85 percent by weight of water, about 4 percent by weight of an ethoxylated corn starch, about 0.2 percent by weight of polyethylene glycol having a molecular weight of about 6,000, about 0.05 percent of octylphenoxy polyethoxy ethanol having about 9 to 10 oxyethy-lene groups per molecule, about 0.4 percent by weight of borax, about 0.1 percent by weight of boric acid, as an anti foaming agent and an ironing aid about 0.5 percent of a dimethyl polysiloxane emulsion containing about 10%
silicone andaabout 0.5 percent of a dimethyl polysiloxane emulsion containing about 37% silicone respectively, said formulation having a substantially reduced tendency to flake when applied to a fabric which is then ironed.
silicone andaabout 0.5 percent of a dimethyl polysiloxane emulsion containing about 37% silicone respectively, said formulation having a substantially reduced tendency to flake when applied to a fabric which is then ironed.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US41059773A | 1973-10-29 | 1973-10-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1037658A true CA1037658A (en) | 1978-09-05 |
Family
ID=23625419
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA212,405A Expired CA1037658A (en) | 1973-10-29 | 1974-10-28 | Aerosol spray starch formulation |
Country Status (1)
Country | Link |
---|---|
CA (1) | CA1037658A (en) |
-
1974
- 1974-10-28 CA CA212,405A patent/CA1037658A/en not_active Expired
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