US3374177A - Production of a bleaching liquor containing performic acid - Google Patents
Production of a bleaching liquor containing performic acid Download PDFInfo
- Publication number
- US3374177A US3374177A US469897A US46989765A US3374177A US 3374177 A US3374177 A US 3374177A US 469897 A US469897 A US 469897A US 46989765 A US46989765 A US 46989765A US 3374177 A US3374177 A US 3374177A
- Authority
- US
- United States
- Prior art keywords
- bleaching
- acid
- liquor
- hydrogen peroxide
- 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 - Lifetime
Links
- 238000004061 bleaching Methods 0.000 title description 86
- LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical compound NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 title description 18
- 238000004519 manufacturing process Methods 0.000 title description 15
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 102
- 239000002253 acid Substances 0.000 description 50
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 40
- 239000000126 substance Substances 0.000 description 38
- 239000000243 solution Substances 0.000 description 29
- 238000000034 method Methods 0.000 description 25
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 24
- 239000000463 material Substances 0.000 description 24
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 20
- 229910052757 nitrogen Inorganic materials 0.000 description 20
- 239000001301 oxygen Substances 0.000 description 20
- 229910052760 oxygen Inorganic materials 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 18
- 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 14
- 125000004432 carbon atom Chemical group C* 0.000 description 14
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical group C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 14
- 229910052708 sodium Inorganic materials 0.000 description 14
- 239000011734 sodium Substances 0.000 description 13
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 11
- 150000007513 acids Chemical class 0.000 description 11
- 238000004043 dyeing Methods 0.000 description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 210000002268 wool Anatomy 0.000 description 10
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 9
- 230000007935 neutral effect Effects 0.000 description 9
- 125000004430 oxygen atom Chemical group O* 0.000 description 9
- 229910052700 potassium Inorganic materials 0.000 description 9
- 239000011591 potassium Substances 0.000 description 9
- 239000003381 stabilizer Substances 0.000 description 9
- DETXZQGDWUJKMO-UHFFFAOYSA-N 2-hydroxymethanesulfonic acid Chemical compound OCS(O)(=O)=O DETXZQGDWUJKMO-UHFFFAOYSA-N 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
- 229910052783 alkali metal Inorganic materials 0.000 description 7
- -1 alkali metal salts Chemical class 0.000 description 7
- 150000001721 carbon Chemical group 0.000 description 7
- 239000004312 hexamethylene tetramine Substances 0.000 description 7
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 7
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 7
- 229960004011 methenamine Drugs 0.000 description 7
- 229920006395 saturated elastomer Polymers 0.000 description 7
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 7
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 7
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 6
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 6
- 229910001424 calcium ion Inorganic materials 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 229910001414 potassium ion Inorganic materials 0.000 description 6
- 229910001415 sodium ion Inorganic materials 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 5
- 210000003746 feather Anatomy 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 4
- 150000001340 alkali metals Chemical class 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 235000013351 cheese Nutrition 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 4
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 4
- 229940048086 sodium pyrophosphate Drugs 0.000 description 4
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 4
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical group C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 159000000007 calcium salts Chemical class 0.000 description 3
- 238000007865 diluting Methods 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 159000000003 magnesium salts Chemical class 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 229920002239 polyacrylonitrile Polymers 0.000 description 3
- 239000001488 sodium phosphate Substances 0.000 description 3
- 235000011008 sodium phosphates Nutrition 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- DKQAGXDYBRFFLW-UHFFFAOYSA-N (sulfomethylamino)methanesulfonic acid Chemical compound OS(=O)(=O)CNCS(O)(=O)=O DKQAGXDYBRFFLW-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 240000002129 Malva sylvestris Species 0.000 description 2
- 235000006770 Malva sylvestris Nutrition 0.000 description 2
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229920000388 Polyphosphate Polymers 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- MDGWRRISASPFCV-UHFFFAOYSA-N [bis(sulfomethyl)amino]methanesulfonic acid Chemical compound OS(=O)(=O)CN(CS(O)(=O)=O)CS(O)(=O)=O MDGWRRISASPFCV-UHFFFAOYSA-N 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- OBESRABRARNZJB-UHFFFAOYSA-N aminomethanesulfonic acid Chemical compound NCS(O)(=O)=O OBESRABRARNZJB-UHFFFAOYSA-N 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- NMJJFJNHVMGPGM-UHFFFAOYSA-N butyl formate Chemical compound CCCCOC=O NMJJFJNHVMGPGM-UHFFFAOYSA-N 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000001205 polyphosphate Substances 0.000 description 2
- 235000011176 polyphosphates Nutrition 0.000 description 2
- 235000011009 potassium phosphates Nutrition 0.000 description 2
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 2
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229910052572 stoneware Inorganic materials 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- NQPJDJVGBDHCAD-UHFFFAOYSA-N 1,3-diazinan-2-one Chemical class OC1=NCCCN1 NQPJDJVGBDHCAD-UHFFFAOYSA-N 0.000 description 1
- MGGVALXERJRIRO-UHFFFAOYSA-N 4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-2-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-1H-pyrazol-5-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2)O MGGVALXERJRIRO-UHFFFAOYSA-N 0.000 description 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Natural products CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- GHOBJYIMFCJMPZ-UHFFFAOYSA-M N=CS(=O)(=O)[O-].[Na+] Chemical compound N=CS(=O)(=O)[O-].[Na+] GHOBJYIMFCJMPZ-UHFFFAOYSA-M 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001669 calcium Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 1
- GFVMLYBCWPLMTF-UHFFFAOYSA-N disodiomagnesium Chemical compound [Na][Mg][Na] GFVMLYBCWPLMTF-UHFFFAOYSA-N 0.000 description 1
- XPHAQQHTRIJDJJ-UHFFFAOYSA-L disodium;(sulfonatomethylamino)methanesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)CNCS([O-])(=O)=O XPHAQQHTRIJDJJ-UHFFFAOYSA-L 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229960001484 edetic acid Drugs 0.000 description 1
- BEGBSFPALGFMJI-UHFFFAOYSA-N ethene;sodium Chemical group [Na].C=C BEGBSFPALGFMJI-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- KLKFAASOGCDTDT-UHFFFAOYSA-N ethoxymethoxyethane Chemical compound CCOCOCC KLKFAASOGCDTDT-UHFFFAOYSA-N 0.000 description 1
- 150000003948 formamides Chemical class 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- TVHALOSDPLTTSR-UHFFFAOYSA-H hexasodium;[oxido-[oxido(phosphonatooxy)phosphoryl]oxyphosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O TVHALOSDPLTTSR-UHFFFAOYSA-H 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical class O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 150000002680 magnesium Chemical class 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 1
- 239000004137 magnesium phosphate Substances 0.000 description 1
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 1
- 229960002261 magnesium phosphate Drugs 0.000 description 1
- 235000010994 magnesium phosphates Nutrition 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000009896 oxidative bleaching Methods 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
- 229950005308 oxymethurea Drugs 0.000 description 1
- 229920002866 paraformaldehyde Polymers 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
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- OQZCJRJRGMMSGK-UHFFFAOYSA-M potassium metaphosphate Chemical compound [K+].[O-]P(=O)=O OQZCJRJRGMMSGK-UHFFFAOYSA-M 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000019828 potassium polyphosphate Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- OEOJZPJDGUSIBL-UHFFFAOYSA-M sodium;azanylidynemethanesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C#N OEOJZPJDGUSIBL-UHFFFAOYSA-M 0.000 description 1
- UOULCEYHQNCFFH-UHFFFAOYSA-M sodium;hydroxymethanesulfonate Chemical compound [Na+].OCS([O-])(=O)=O UOULCEYHQNCFFH-UHFFFAOYSA-M 0.000 description 1
- 239000008234 soft water Substances 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- UHLICHJXSLXXRV-UHFFFAOYSA-N triazinan-4-one Chemical class O=C1CCNNN1 UHLICHJXSLXXRV-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/0024—Dyeing and bleaching in one process
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
- D06L4/12—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen combined with specific additives
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
- D06L4/15—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen using organic agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/06—Material containing basic nitrogen containing amide groups using acid dyes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/916—Natural fiber dyeing
- Y10S8/917—Wool or silk
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/93—Pretreatment before dyeing
- Y10S8/931—Washing or bleaching
Definitions
- the present invention relates to a process for the production from hydrogen peroxide of a bleaching liquor containing performic acid for the treatment of textile fibrous material.
- keratinous fibrous material may be bleached with aqueous liquors containing performic acid as the oxidizing bleaching agent.
- aqueous liquors containing performic acid as the oxidizing bleaching agent.
- the bleaching action and stability of such liquors is dependent on the method by which the performic acid has been prepared.
- more stable performic acid bleaching liquors can be prepared from formaldehyde and hydrogen peroxide in the presence of acids than from formic acid and hydrogen peroxide.
- liquors having a particularly strongbleaching action are moreover obtained when a concentrated stock bleaching solution is first prepared and then diluted for use.
- an active and surprisingly stable bleaching liquor containingperformic acid can be pre- Patented Mar. 19, 1968 ice pared without using free formaldehyde by reacting (a) hydrogen peroxide and (b) at least one substance yielding formaldehyde or a low molecular weight formic ester or a low molecular weight formamide in an acid to neutral aqueous solution at a temperature of up to 60 C. the resultant solution may then be diluted if desired and adjusted to a pH value of 1 to 8.5, preferably 2 to 8.5.
- Substances yielding formaldehyde are defined as substances which contain at least once a group having the general formula:
- Y denotes a nitrogen or oxygen atom
- X denotes a nitrogen or oxygen atom or the group SO M
- M being a proton, an ammonium ion, an alkali metal ion or half an alkaline earth metal ion, andthe valencies of the said nitrogen and/or oxygen atoms which are not attached to the central carbon atom being, in the absence of a $0 M group, at the most partly saturated by hydrogen.
- Examples of substances which contain at least once a group having the Formula I are: formaldehyde polymers, such as trioxymethylene, tetraoxymethylene and paraformaldehyde; formals, such as dimethylformal and diethylformal; hydroxymethanesulfonic acid; aminomethanesulfonic acid; imino-bis-methanesulfonic acid and N-alkyl and N-hydroxyalkyl derivatives of these two acids; nitrilotrismethanesulfonic acid, ammonium salts, alkali metal salts and alkaline earth metal salts of these acids, such as preferably the sodium, potassium and calcium salts; N-methylol compounds of carbamides, such as particularly urea, imidazolidones, tetrahydrotriazinones, hexahydropyrimidones and urones; of melamines, of dicyanodiamide; and also ethers of such N-methylol compounds with alcohol
- Examples of low molecular weight formic esters and formamides are substances having the general formula:
- Q denotes a radical OR or R being an alkyl radical having one to five carbon atoms, R being a hydrogen atom or an alkyl radical having one to five carbon atoms and R being a hydrogen atom or an alkyl radical having one to five carbon atoms.
- substances having the Formula II are: methyl formate, ethyl formate, propyl formate, butyl formate and diethylformamide.
- the drop in the pH value during bleaching may be prevented or minimized by employing or additionally employing substances containing at least one group having the Formula I or substances having the Formula II which form amines or preferably ammonia by reaction With hydrogen peroxide.
- a particularly suitable and therefore preferred substance of this type is hexamethylene tetramine.
- Formamide, dimethylformamide, aminomethanesulfonic acid, iminobismethanesulfonic acid, their alkyl derivatives, particularly their methyl derivatives, and their salts however act in this way.
- formaldehyde polymers such as trioxymethylene, tetraoxymethylene and paraformalclehyde; hydroxymethanesulfonic acid and its sodium, potassium and calcium salts; the reaction products of this acid with ammonia, i.e., aminomethanesultonic acid, aminobismethanesul-fonic acid and nitrilotrismethanesulfonic acid and the sodium, potassium and calcium salts of these acids and hexamethylene tctramine.
- Substances of the abovementioned type are reacted with hydrogen peroxide in aqueous medium.
- the speed of this reaction is dependent on the hydrogen ion concentration of the medium.
- An acid or neutral range is used to achieve rapidly a bleaching solution which is ready for use.
- the acid reaction may be produced by adding inorganic or organic acids or acid salts.
- the acids may be chosen at will. Strong acids are very suitable, such as sulfuric acid and sulfonic acids, and acid salts such as sodium bisulfite and sodium bisulfate.
- the amount of acid substance required depends on its acidity. Amounts of 0.5 to of strong acids, with reference to the weight of hydrogen peroxide to be reacted, are adequate, whereas 10 to 50% of weaker acids or acid salts may be necessary.
- stabilizers for active oxygen have proved to be very suitable to coemploy stabilizers for active oxygen in the present process. These stabilizers are particularly advantageous when it is intended to carry out bleaching at elevated temperature, particularly above 50 C. because under these conditions they prevent too rapid delivery of the active oxygen with consequent yellowing and even damage to the material being bleached.
- Stabilizers for active oxygen are known per se; examples are alkali metal polyphosphates, such as tetrasodium pyrophosphate, and more highly condensed phosphates such as sodium tripolyphosphate, sodium tetraphosphate and sodium hexapolyphosphate; magnesium silicate; magnesium phosphate; and complex-forming aminopolycarboxylic acids, such as particularly nitrilotriacetic acid and ethylene dia'minotetracetic acid and their ammonium salts, magnesium-alkali metal salts and alkali metal salts.
- Alkali metal polyphosphates particulary those of sodium and potassium, nit-rilotriacetic acid, ethylene diaminotetracetic acid and the sodium, potassium and magnesium salts of these acids are preferred.
- the stabilizers for active oxygen may be used singly or more than one of them may be additionally used. Generally it is not necessary to use them in amounts of more than with reference to the weight of anhydrous hydrogen peroxide.
- wetting agents, detergents and/ or softening agents and also optical brighteners which are stable to peroxides may be added to the liquor at any stage during its production.
- Hydrogen peroxide is advantageously used in the process according to this invention in amounts which are one to twelve times, preferably three to ten times the amount which is equivalent to the substance (b).
- Hydrogen peroxide is advantageously used in the process according to this invention in amounts which are one to twelve times, preferably three to ten times the amount which is equivalent to the substance (b).
- the ratio betwen substances which contain at least one group having the Formula I or substances having the Formula II and hydrogen peroxide is preferably chosen so that for each mole of groups having the Formula I or of substance having the Formula II, one to twelve moles of hydrogen peroxide are available; particularly successful results are achieved with a molar ratio of 1:3 to 1:10.
- the amount of hydrogen peroxide depends on whether it is desired to bleach in a long liquor or with a padding liquor. Amounts of hydrogen peroxide of from 10 i to 30 cc./l. have proved to be particularly useful for long liquors and from 40 to 130 cc./l. for padding liquors.
- the perforrnic acid bleaching liquor may be prepared by adding the ingredients direct to the liquor in the amounts desired for bleaching.
- a concentrated stock bleaching solution may first be prepared which is diluted to the concentration for use immediately prior to use.
- Stock bleaching solutions may be prepared in concentrations which are equivalent to 100 to 500 cc./l. of 35% hydrogen peroxide.
- the temperature should not exceed 40 C.; bleaching liquors to which the ingredients are added direct may however be prepared at higher temperatures up to about 60 C.
- the bleaching liquor which if necessary has been cliluted to the concentration required for use, may be adjusted to a pH value of from 1 to 8.5, preferably from 4 to 6, if it does not have such a pH value by virtue of its method of production.
- the usual alkaline or acid reacting reagents particularly weak or medium strength bases or acids, may be used for the purpose. It is preferable to adjust the pH value in the presence of the material to be bleached because the latter sometimes contains acid or alkaline substances which may change the pH value of the bleaching liquor.
- a particularly advantageous agent of this type contains 50 to 20% by weight of condensed alkali metal phosphate, by weight of hydroxymethanesulfonic acid or its ammonium, alkali metal (particularly sodium or potassium), or alkaline earth metal (particularly calcium) salts, 10 to 20% by weight of condensed alkali metal phosphate, particularly sodium or potassium phosphates, and 10 to 0% by weight of ethylene diaminotetracetic acid or its ammonium, alkali metal (particularly sodium or potassium), or alkaline earth metal (particularly magnesium) salts.
- the agent may also contain solid acids or acid salts.
- Such an agent may be used for example as follows: for each liter of bleaching liquor, 20 cc. of 35% hydrogen peroxide is mixed with 20 cc. of water, 3 to 7 g. of the agent is dissolved therein and the solution is made up to 1 liter with water. The bleaching liquor thus prepared is ready for immediate use without further measures.
- the process according to this invention yields performic acid bleaching liquors which are distinguished by remar"- able stability and bleaching power in a particularly simple and convenient way.
- the liquors may be used for example for bleaching textile materials of polyamide, polyester, polyacrylonitrile, cellulose, cellulose ester and regenerated cellulose fibers. They are particularly suitable for bleaching textile material which contains or consists of protein fibers, for example, wool, silk and animal hairs, and also feathers, bristles and the like.
- the liquors may be used for the said purpose in conventional ways.
- bleaching conditions have proved to be suitable for bleaching wool: A high degree of whiteness is obtained in a long liquor at 50 C. in two to six hours. Equally good results are achieved at C. in about thirty minutes and in the neighborhood of the boiling point in ten to twenty minutes.
- the batchwise and continuous padding method is particularly suitable for piece goods and tops.
- the material is padded with the bleaching solution on a padding machine.
- the padded material can then be rolled up, Wrapped round with a waterproof sheet and kept in slow rotary movement at room temperature for five to fifteen, preferably five to ten, hours.
- the padded material may be heated in a tunnel (to 40 C. or more) and then kept in movement in a reaction chamber at elevated temperature. A considerable shortening of the bleaching period is thus achieved.
- This bleaching method may also be carried out continuously by passing the padded material in open width at temperatures of 80 to 105 C. through a steamer at such a rate that the optimum bleaching period corresponding to the temperature is achieved.
- EXAMPLE 1 An agent for the production of a bleaching liquor containing performic acid has the following composition:
- the winch dyeing machine is charged with 50 kg. of unbleached piece goods of wool and polyacrylonitrile (70:30) for bleaching. The whole is left for five minutes at room temperature, the pH value of the liquor is controlled and if necessary adjusted to 5.5 with ammonia or formic acid. The temperature is then raised in about fifteen minutes to 80 C. and kept steady for thirty minutes. The pH value remains practically constant during this bleaching. The material is then thoroughly rinsed hot and cold and further treated in any desired way. The material has a high degree of whiteness after this bleach.
- EXAMPLE 2 A cheese dyeing machine of alloyed steel (liquor capacity 750 liters) is filled with 50 kg. of dry blended yarn (wool and rayon staple 70:30) in the form of cheeses on the material carrier. 15 liters of 35% hydrogen peroxide is added to 735 liters of water in an attached container and there is dissolved therein 3.5 kg. of a mixture having the following composition:
- r onr CH CzH O which is stable to peroxides and goes on to both fibers from a weak acid medium is dissolved in water and added to the bleaching solution made as described above.
- the liquor thus prepared is pumped into the machine. To expel enclosed air, the liquor is allowed to circulate for about ten minutes. Then 0.15 kg. of nonylphenol monoglycol ether, dissolved in a little water, is added and dispersed as a wetting agent. While the liquor is circulated it is heated in fifteen minutes to 70 C. and the material is treated for forty-five minutes at this temperature.
- the pH value of the bleaching liquor is 5.3 at the beginning and 5.6 at the end of the bleaching period.
- the material is rinsed hot and cold.
- 5 kg. of previously dissolved condensation product of 2 moles of stearic acid and 1 mole of diethylene triamine, which has been partly acetylated with 1 mole of acetic anhydride, is added to the final rinsing liquor as a softener, the liquor is made slightly acid with acetic acid (pH 5 .5 to 6.5) and allowed to circulate for ten minutes at room temperature.
- a yarn is thus obtained which has a high degree of whiteness and a soft, pleasant handle.
- EXAMPLE 3 Precleaned dry woollen piece goods are padded at room temperature on a padding machine with a liquor (liquor retention which contains 80 cc./l. of 35% hydrogen peroxide, 20 g./l. of the mixture described in paragraph 1 of Example 1 and 1.5 g./l. of octylphenol heptaglycol ether and has a pH value of 5.5.
- the hydrogen peroxide is first mixed with an equal amount of water and then the solids are dissolved in this solution by stirring at room tempera! ture.
- the goods After the goods have been padded, they are heated to 60 C. in a shaft, then rolled up, wrapped round with a moisture-proof plastics sheet and left rotating in a reaction chamber for two hours at 60 C.
- the bleached material is then rinsed on an open width Washing machine. The material exhibits a good bleaching effect.
- EXAMPLE 4 Precleaned piece goods of wool and polyester (60:40) having a moisture content of 60% are padded with the same solution as described in Example 3 at room temperature (squeezed out to 100%) and heated in a shaft to C. After the goods have been padded they are not rolled up but proceed continuously into a steamer in which they remain for a total of fifteen to twenty minutes at C. or for ten minutes at C. They are then rinsed. The goods thus acquire a beautiful white color.
- EXAMPLE 5 A pack dyeing machine (600 liters capacity), which contains washed, moist pig bristles having a dry Weight of 35 kg, is charged with 500 liters of a bleaching solution which has been prepared from 7.5 liters of 35% hydrogen peroxide and 1.5 kg. of a mixture which has been prepared from 50 parts of sodium nitrilomethanesulfonate, 20 parts of hexamethylene tetramine, 20 parts of sodium phosphate, 5 parts of sodium ethylene diaminotetracetate and 5 parts of ethylene diamine tetracetic acid.
- the pH value of the bleaching liquor adjusts itself to 7.3.
- the circulating liquor is brought to a temperature of 85 C. in fifteen minutes and kept at this temperature for twenty-five minutes.
- the pH value of the liquor falls during bleaching into the acid region and remains at 6.1.
- the material is then rinsed thoroughly both hot and cold. Very beautifully bleached bristles are obtained.
- EXAMPLE 6 25 liters of 35 hydrogen peroxide is added in an alloyed steel winch dyeing machine (capacity 2,500 liters) to 2,000 liters of water at 35 C., well dispersed and 6 kg. of the mixture described in Example 5 is dissolved therein. Then 0.4 kg. of octylphenyl heptaglycol ether is added. The winch dyeing machine is then charged with 75 kg. of nylon-6 piece goods, the pH value of the bleaching liquor is tested and, if necessary, adjusted to 7.0 with ammonia or formic acid. The temperature of the bleaching liquor is then raised to 80 C. in fifteeen minutes and kept at this temperature for thirty minutes. The pH value of the liquor changes during this period to 6.3.
- EXAMPLE 7 Precleaned dry woollen piece goods are padded as described in Example 3. After having been padded, the material is rolled up, wrapped in a moistureproof sheet of plastic and left to rotate for eight hours at room temperature (22 C.). The bleached material is then rinsed on an open Width washing machine, squeezed out and dried. The Woollen piece goods thus bleached exhibit a very high degree of whiteness.
- EXAMPLE 9 100 kg. of blended yarn of wool and polyacrylonitrile (90: in the form of cheeses is introduced on a material carrier into a cheese dyeing machine of alloyed steel (liquor capacity 1,500 liters). In an attached container, 30 liters of 35% hydrogen peroxide is added to 1,455 liters of water. 6 kg. of a mixture of 50 parts of dimethylolurea, 8 parts of sodium bisulfite, 18 parts of sodium bisulfate, 5 parts of hexamethylene tetramine, 10 parts of sodium pyrophosphate and 9 parts of ethylenediaminotetra-cetic acid is dissolved in this liquor. The liquor is allowed to circulate for five minutes to expel the enclosed air. Then 0.2 kg.
- nonylphenol monoglycol ether is dissolved in a little water and added and dispersed in the liquor. While the liquor is circulating, the temperature is raised to 90 C. in fifteen minutes and maintained for twenty minutes. The pH value of the bleaching liquor is 5.3 at the commencement and rises to 5.7 at the end of the bleaching. The goods thus bleached exhibit a high degree of whiteness.
- EXAMPLE 10 5 liters of 35% hydrogen peroxide, 0.75 liter of 10% sulphuric acid, 0.5 liter of formamide and 1.35 liters of water are mixed at C. A stock bleaching solution is thus formed.
- the stock solution obtained according to paragraph 1 is added to 500 liters of water in the attached container of an alloyed steel or stoneware pack dyeing machine which is charged with 50 kg. of precleaned loose wool.
- the diluted liquor is pumped onto the material to be bleached, adjusted with sulphuric acid to a pH value of 5 and, while the liquor is circulating, heated to 50 C. and kept at this temperature for 2 /2 hours; the pH value changes only slightly to 5.3.
- the goods are rinsed hot and cold.
- bleaching may also be carried out in thirty minutes at 80 C.
- 0.5 liter of a solution of the magnesium disodium salt of ethylene diaminotetracetic acid is added to the bleaching liquor as an oxygen stabilizer.
- the goods are bleached excellently after this treatment.
- EXAMPLE 11 25 liters of a stock bleaching solution (previously prepared from 2.5 liters of 10% sulfuric acid, 16.75 liters of hydrogen peroxide and 5.75 liters of dimethylformamide) is aded to 1,000 liters of water in a tops dyeing machine. Then 2 kg. of tetrasodium pyrophosphate is added as an oxygen stabilizer and 0.2 kg. of nonylphenol heptaglycol ether as a wetting agent. The material carrier, with 75 kg. of wool tops on bobbins, is then introduced. The pH value of the bleaching liquor adjusts itself to 4.8. The liquor is allowed to circulate for ten minutes to expel the air and is then heated to 90 C. and left for twenty minutes at this temperature. The pH value of the liquor rises during this period to 5.7. The material is slowly cooled and thoroughly rinsed by adding water. The goods thus treated are bleached excellently.
- EXAMPLE 12 A wooden feather washer provided with a stirring means and having a liquor capacity of 1,200 liters is charged with 25 kg. of washed unbleached bed feathers which are still moist and then charged with 1,000 liters of a bleaching solution which contains 25 liters of stock bleaching solution prepared as described in Example 11. The pH value of the bleaching solution is 4.7. The bleaching liquor is heated to 50 C. and left at this temperature for 2 /2 hours, the pH value thus rising to 5.3. The feathers are then rinsed hot and cold, hydroextracted and dried in a steamer. Excellently bleached feathers are obtained.
- EXAMPLE 13 30 liters of a stock bleaching solution composed as follows: 3 parts of methyl formate, 60 parts of 35 hydrogen peroxide, 2 parts of 10% sulfuric acid and 35 parts or" water, is added to 2,000 liters of water (12 hardness, German scale) at 20 C. in a wooden winch dyeing machine having a capacity of 2,500 liters.
- this bleaching liquor there are dissolved 1.5 kg. of tetrasodium pyrophosphate and 1.5 kg. of a 35% solution of sodium ethylenediaminotetracetate as stabilizer for the active oxygen and 0.3 kg. of octylphenol heptaglycol ether.
- 60 kg. of woollen piece goods is introduced.
- the pH value of the bleaching liquor is 7.0.
- the temperature is raised in fifteen minutes from 20 to C. and maintained for thirty-five minutes.
- the pH value of the liquor undergoes only slight change (to 6.7) during bleaching.
- the goods bleached in this way exhibit an excellent degree
- EXAMPLE l4 Precleaned dry piece goods of wool and polyester (55:45) are padded in a padding machine with cc./l. of a bleaching solution (liquor retention 80%) having the following composition: 10 parts of diethylformamide, 65 parts of 35% hydrogen peroxide, 15 parts of 10% sulfuric acid and 10 parts of water.
- the padding liquor also contains 1.2 g./l. of octylphenol heptaglycol ether and 5 g./l. of sodium pyrophosphate.
- the goods after they have been padded, are heated to 80 C. in a shaft, then rolled up, wrapped in a moistureproof plastics film and allowed to rotate for thirty minutes at 80 C. in a thermo-dwell chamber. The goods are then rinsed. The goods exhibit an excellent bleaching effect.
- EXAMPLE 15 Precleaned dry woolen piece goods are padded as described in Example 14 with the same bleaching solution. The liquor retention is The padded goods are rolled up, wrapped in a moistureproof sheet and allowed to rotate for seven hours at 22 C. Excellently bleached goods are thus obtained.
- a bleaching liquor containing performic acid from hydrogen peroxide comprising bringing together at a temperature of up to 60 C. in an acid to neutral aqueous solution (a) hydrogen peroxide and (b) a compound selected from the group consisting of at least one substance yielding formaldehyde, said substance containing at least one group having the general formula in which Y is a member selected from the group consisting of nitrogen and oxygen, X is a member selected from the group consisting of nitrogen, oxygen, and SO M, M being a member selected from the group consisting of a proton, an ammonium ion, a sodium ion, a potassium ion, and half a calcium ion, and the valencies of the said nitrogen and/ or oxygen atoms which are not attached to the central carbon atom being, in the absence of an 80 M group, at the most partly saturated by hydrogen, a formic ester having up to six carbon atoms in the molecule, and a formamide having up
- a bleaching liquor containing performic acid from hydrogen peroxide
- the improvement which comprises bringing together at a temperature of up to 60 C. in an acid to neutral aqueous solution (a) hydrogen peroxide and (b) a compound selected from the group consisting of at least one substance yielding formaldehyde, said substance containing at least one group having the general formula in which Y is a member selected from the group consisting of nitrogen and oxygen, X is a member selected from the group consisting of nitrogen, oxygen, and SO M, M being a member selected from the group consisting of a proton, an ammonium ion, a sodium ion, a potassium ion, and half a calcium ion, and the valencies of the said nitrogen and/or oxygen atoms which are not attached to the central carbon atom being, in the absence of an SO M group, at the most partly saturated by hydrogen, a formic ester having up to six carbon atoms in the molecule, and a formamide
- a bleaching liquor from hydrogen peroxide comprising bringing together at a temperature of up to 60 C. in acid to neutral aqueous solution (a) hydrogen peroxide and (h) a compound selected from the group consisting of at least one substance yielding formaldehyde, said substance containing at least one group having the general formula Y-CH X, in which Y is a member selected from the group consisting of nitrogen and oxygen, X is a member selected from the group consisting of nitrogen, oxygen, and SO M, M being a member selected from the group consisting of a proton, an ammonium ion, a sodium ion, a potassium ion, and half a calcium ion, and the valencies of the said nitrogen and/or oxygen atoms which are not attached to the central carbon atom being, in the absence of an $0 M group, at the most partly saturated by hydrogen, a formic ester having up to six carbon atoms in the molecule and 21 formamide having up
- a bleaching liquor contairing performic acid from hydrogen peroxide
- the improvement which comprises bringing together at a temperature of up to 60 C. in an acid to neutral aqueous solution (a) hydrogen peroxide and (b) a compound selected from the group consisting of at least one substance yielding formaldehyde, said substance containing at least one group having the general formula in which Y is a member selected from the group consistiig of nitrogen and oxygen, X is a member selected from the group consisting of nitrogen, oxygen, and SO M, M being a member selected from the group consisting of a proton, an ammonium ion, a sodium ion, a potassium ion, and half a calcium ion, and the valencies of the said nitrogen and/ or oxygen atoms which are not attached to the central carbon atom being, in the absence of an $0 M group, at the most partly saturated by hydrogen, a formic ester having up to 6 carbon atoms in the molecule and a
- An agent for the production of a bleaching liquor containing performic acid comprising 50 to 20% by weight of hexamethylene tetramine, 30 to 60% by weight of a member selected from the group consisting of hydroxymethanesulfonic acid and an ammonium, alkali 1116131 and alkaline earth metal salt thereof, 10 to 20% by Weight of a phosphate selected from the group consisting of condensed sodium phosphate, condensed potassium phosphate and 10 to 0% by weight of a member selected from the group consisting of ethylenediaminotetracetic acid and an ammonium, sodium, potassium or magnesium salt thereof.
- a bleaching liquor containing perforrnic acid from hydrogen peroxide comprising bringing together at a temperature of up to 60 C. in an acid to neutral aqueous solution (a) hydrogen peroxide and (b) a compound selected from the group consisting of at least one substance yielding formaldehyde, said substance containing at least one group having the general formula in which Y is a member selected from the group consisting of nitrogen and oxygen, X is a member selected from the group consisting of nitrogen, oxygen, and SO M, M being a member selected from the group consisting of a proton, an ammonium ion, a sodium ion, a potassium ion, and half a calcium ion, and the valencies of the said nitrogen and/or oxygen atoms which are not attached to the central carbon atom being, in the absence of an 50 M group, at the most partly saturated by 11 12 hydrogen, a formic ester having up to six carbon atoms 2,860,945 11/19
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Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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DEB0077610 | 1964-07-10 | ||
DEB0077609 | 1964-07-10 | ||
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US491441A Expired - Lifetime US3551087A (en) | 1964-07-10 | 1965-09-29 | Simultaneous dyeing and bleaching of proteinaceous fibrous material |
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US491441A Expired - Lifetime US3551087A (en) | 1964-07-10 | 1965-09-29 | Simultaneous dyeing and bleaching of proteinaceous fibrous material |
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DE (2) | DE1469608A1 (enrdf_load_stackoverflow) |
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NO (1) | NO121715B (enrdf_load_stackoverflow) |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3912447A (en) * | 1973-03-07 | 1975-10-14 | Basf Ag | Dyeing natural polyamide fibers |
US4964870A (en) * | 1984-12-14 | 1990-10-23 | The Clorox Company | Bleaching with phenylene diester peracid precursors |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9302441D0 (en) * | 1993-02-08 | 1993-03-24 | Warwick Int Group | Oxidising agents |
GB9302442D0 (en) * | 1993-02-08 | 1993-03-24 | Warwick Int Group | Oxidising agents |
GB9302443D0 (en) * | 1993-02-08 | 1993-03-24 | Warwick Int Group | Oxidising agents |
WO1995021283A1 (en) * | 1994-02-07 | 1995-08-10 | Warwick International Group Limited | Process for bleaching textiles |
US5616616A (en) * | 1994-06-01 | 1997-04-01 | Minntech Corporation | Room Temperature sterilant |
US5589507A (en) * | 1995-11-17 | 1996-12-31 | Minntech Corporation | Method for sterilizing medical devices utilizing a room temperature sterilant |
US6200355B1 (en) | 1999-12-21 | 2001-03-13 | Basf Corporation | Methods for deep shade dyeing of textile articles containing melamine fibers |
US7008177B2 (en) * | 2002-11-14 | 2006-03-07 | Cummins Inc. | Centrifugal pump with self cooling and flushing features |
EP1607430A1 (en) * | 2004-06-09 | 2005-12-21 | Nederlandse Organisatie voor toegepast-natuurwetenschappelijk Onderzoek TNO | Fibre-reinforced polymer composites and processes for preparing the same |
US20080087390A1 (en) * | 2006-10-11 | 2008-04-17 | Fort James Corporation | Multi-step pulp bleaching |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1063679A (en) * | 1913-01-27 | 1913-06-03 | Max Hartmann | Process of producing stable hydrogen-peroxid compounds. |
US2720440A (en) * | 1952-12-26 | 1955-10-11 | Du Pont | Bleaching polyacrylonitrile fibers |
US2860945A (en) * | 1955-07-28 | 1958-11-18 | Du Pont | Bleaching cyanoethylated cotton fibers with hydrogen peroxidephosphate solution and optionally with water-soluble sulfoxylate solution |
GB923845A (en) * | 1960-03-30 | 1963-04-18 | Shell Int Research | A stock solution for the stabilization of hydrogen peroxide |
US3193445A (en) * | 1962-07-16 | 1965-07-06 | Pittsburgh Plate Glass Co | Method of bleaching cellulosic materials with hydrogen peroxide |
-
1964
- 1964-10-02 DE DE19641469608 patent/DE1469608A1/de active Pending
- 1964-10-02 DE DE19641469609 patent/DE1469609A1/de active Pending
-
1965
- 1965-06-17 NO NO65158556A patent/NO121715B/no unknown
- 1965-06-23 CH CH241266A patent/CH479750A/de not_active IP Right Cessation
- 1965-06-23 CH CH880165A patent/CH450343A/de unknown
- 1965-07-06 US US469897A patent/US3374177A/en not_active Expired - Lifetime
- 1965-07-07 BE BE666517D patent/BE666517A/xx unknown
- 1965-07-09 GB GB29131/65A patent/GB1064534A/en not_active Expired
- 1965-07-09 SE SE9139/65A patent/SE310872B/xx unknown
- 1965-07-09 NL NL6508903A patent/NL6508903A/xx unknown
- 1965-09-29 US US491441A patent/US3551087A/en not_active Expired - Lifetime
-
1968
- 1968-12-11 SE SE1694968A patent/SE318251B/xx unknown
-
1969
- 1969-10-23 NL NL6916024A patent/NL6916024A/xx unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1063679A (en) * | 1913-01-27 | 1913-06-03 | Max Hartmann | Process of producing stable hydrogen-peroxid compounds. |
US2720440A (en) * | 1952-12-26 | 1955-10-11 | Du Pont | Bleaching polyacrylonitrile fibers |
US2860945A (en) * | 1955-07-28 | 1958-11-18 | Du Pont | Bleaching cyanoethylated cotton fibers with hydrogen peroxidephosphate solution and optionally with water-soluble sulfoxylate solution |
GB923845A (en) * | 1960-03-30 | 1963-04-18 | Shell Int Research | A stock solution for the stabilization of hydrogen peroxide |
US3193445A (en) * | 1962-07-16 | 1965-07-06 | Pittsburgh Plate Glass Co | Method of bleaching cellulosic materials with hydrogen peroxide |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3912447A (en) * | 1973-03-07 | 1975-10-14 | Basf Ag | Dyeing natural polyamide fibers |
US4964870A (en) * | 1984-12-14 | 1990-10-23 | The Clorox Company | Bleaching with phenylene diester peracid precursors |
Also Published As
Publication number | Publication date |
---|---|
DE1469608A1 (de) | 1968-12-19 |
DE1469609A1 (de) | 1969-03-27 |
CH450343A (de) | 1968-04-30 |
NL6916024A (enrdf_load_stackoverflow) | 1970-01-26 |
BE666517A (enrdf_load_stackoverflow) | 1966-01-07 |
CH880165A4 (enrdf_load_stackoverflow) | 1967-10-14 |
US3551087A (en) | 1970-12-29 |
SE310872B (enrdf_load_stackoverflow) | 1969-05-19 |
NO121715B (enrdf_load_stackoverflow) | 1971-04-05 |
CH479750A (de) | 1969-10-15 |
GB1064534A (en) | 1967-04-05 |
SE318251B (enrdf_load_stackoverflow) | 1969-12-08 |
NL6508903A (enrdf_load_stackoverflow) | 1966-01-11 |
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