WO1997039097A1 - Amido- and imido- peroxycarboxylic acid bleach granules - Google Patents
Amido- and imido- peroxycarboxylic acid bleach granules Download PDFInfo
- Publication number
- WO1997039097A1 WO1997039097A1 PCT/EP1997/001459 EP9701459W WO9739097A1 WO 1997039097 A1 WO1997039097 A1 WO 1997039097A1 EP 9701459 W EP9701459 W EP 9701459W WO 9739097 A1 WO9739097 A1 WO 9739097A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- acid
- surfactant
- group
- bleach
- peroxycarboxylic acid
- Prior art date
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- 239000008187 granular material Substances 0.000 title claims abstract description 47
- 239000007844 bleaching agent Substances 0.000 title claims abstract description 42
- 239000004094 surface-active agent Substances 0.000 claims abstract description 34
- 239000000203 mixture Substances 0.000 claims abstract description 20
- 239000002253 acid Substances 0.000 claims abstract description 16
- 238000000034 method Methods 0.000 claims abstract description 12
- 125000003368 amide group Chemical group 0.000 claims abstract description 11
- 239000011872 intimate mixture Substances 0.000 claims abstract description 7
- 239000000758 substrate Substances 0.000 claims abstract description 6
- FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical compound CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 claims abstract description 5
- KCAZSAYYICOMMG-UHFFFAOYSA-N 6-hydroperoxy-6-oxohexanoic acid Chemical compound OOC(=O)CCCCC(O)=O KCAZSAYYICOMMG-UHFFFAOYSA-N 0.000 claims abstract description 4
- ADKBGLXGTKOWIU-UHFFFAOYSA-N butanediperoxoic acid Chemical compound OOC(=O)CCC(=O)OO ADKBGLXGTKOWIU-UHFFFAOYSA-N 0.000 claims abstract description 4
- LDCLYCYEPBDTIV-UHFFFAOYSA-N 6-[[4-[(6-hydroperoxy-6-oxohexyl)carbamoyl]benzoyl]amino]hexaneperoxoic acid Chemical compound OOC(=O)CCCCCNC(=O)C1=CC=C(C(=O)NCCCCCC(=O)OO)C=C1 LDCLYCYEPBDTIV-UHFFFAOYSA-N 0.000 claims abstract description 3
- SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- -1 carbonyl radical Chemical class 0.000 claims description 11
- 150000003254 radicals Chemical class 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 6
- 239000012736 aqueous medium Substances 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 238000004061 bleaching Methods 0.000 claims description 3
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 claims 2
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 claims 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 claims 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 claims 1
- 150000004965 peroxy acids Chemical class 0.000 abstract description 14
- 238000004140 cleaning Methods 0.000 abstract description 3
- 239000004744 fabric Substances 0.000 description 16
- 239000000975 dye Substances 0.000 description 13
- 239000011230 binding agent Substances 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 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
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 238000005469 granulation Methods 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- LMYSNFBROWBKMB-UHFFFAOYSA-N 4-[2-(dipropylamino)ethyl]benzene-1,2-diol Chemical compound CCCN(CCC)CCC1=CC=C(O)C(O)=C1 LMYSNFBROWBKMB-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 101000581940 Homo sapiens Napsin-A Proteins 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 102100027343 Napsin-A Human genes 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000000988 sulfur dye Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- CFPOJWPDQWJEMO-UHFFFAOYSA-N 2-(1,2-dicarboxyethoxy)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)OC(C(O)=O)CC(O)=O CFPOJWPDQWJEMO-UHFFFAOYSA-N 0.000 description 1
- 241000219307 Atriplex rosea Species 0.000 description 1
- 241001677188 Coccus viridis Species 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-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
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 150000001335 aliphatic alkanes Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- JHUXOSATQXGREM-UHFFFAOYSA-N dodecanediperoxoic acid Chemical compound OOC(=O)CCCCCCCCCCC(=O)OO JHUXOSATQXGREM-UHFFFAOYSA-N 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000004028 organic sulfates Chemical class 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
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 159000000000 sodium salts Chemical group 0.000 description 1
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3945—Organic per-compounds
Definitions
- the invention concerns bleach granules, compositions and a method for cleaning colored fabrics without causing localized dye damage.
- Peroxyacid granulation has been the subject of much research.
- the literature has described a variety of ways to improve chemical stability, prolong storage life and enhance releasability.
- US Patent 5,049,298 inhibits peroxyacid decomposition through co-granulation with a hydratable inorganic material.
- Diperoxydodecanedioic acid (“DPDA”) and N,N- phthaloylaminoperoxycaproic acid (“PAP”) are typical of the peroxyacids.
- DPDA diperoxydodecanedioic acid
- PAP N,N- phthaloylaminoperoxycaproic acid
- Binders such as lauric acid or sodium dodecylbenzene sulphonate (“LAS”) are added to enhance cohesiveness.
- US Patent 4,909,953 stabilizes amidoperoxyacids, especially the monononylamide of peroxysuccinic acid (“NAPSA”) and the monononylamide of peroxyadipic acid (“NAPAA”) by contact with a phosphate buffer solution.
- a related disclosure is US Patent 5,055,218 which describes bleach granules of NAPAA and linear alkyl benzene sulfonate paste.
- US Patent 4,126,573 reports avoidance of fabric dye damage by forming granules having a peroxyacid particle as an inner core surrounded by an outer coating of a surfactant compound.
- the process involves dissolving a surfactant such as LAS in water followed by dispersing finely divided DPDA and subsequent drying of the mixture.
- a surfactant such as LAS
- DPDA finely divided DPDA
- This technology area is crowded for reasons that small process or formulation changes can have significant impact upon the resultant bleach particles.
- Most of the related art has focused upon stabilizing peroxy acid against decomposition. Relatively little attention has been given to the equally serious problem of localized dye damage.
- Amido- and imidoperoxy acids are generally more storage stable than their equivalent non-nitrogen containing analogues. However they do suffer from the localized dye damage problem. The problem occurs during hand or machine washing when high concentrations of dissolved peracid come into contact with fabric surfaces prior to agitation. Previous attempts to control the problem through particle size and co-granulated/binder systems have generally been unsuccess ul .
- a bleach granule including from 20 to 100% by weight of an intimate mixture of :
- a surfactant (ii) a surfactant, the peroxycarboxylic acid and surfactant being present in a weight ratio from 20:0 to 1:20.
- a bleach composition including:
- a bleach granule including from 20 to 100% by weight of an intimate mixture of : (i) an amido or imido C 4 -C 30 peroxycarboxylic acid and (ii) a surfactant, the peroxycarboxylic acid an surfactant being present in a weight ratio from 20:1 to 1:20; and
- a method for bleaching a stained substrate including contacting the stained substrate in an aqueous medium with a bleach granule formed from 60 to 100% by weight of an intimate mixture of an amido or imido C 4 -C 30 peroxycarboxylic acid and a surfactant, the peroxycarboxylic acid and surfactant being dosed into a weight ratio from 20:1 to 1:20, the bleach granule being dosed into the aqueous medium to provide peroxycarboxylic acid at a level from 0.05 to 100 ppm active oxygen.
- a method for preparing a bleach granule is also provided involving the steps of :
- the process is best performed either in the absence or with relatively small amounts of water. These amounts will usually be less than the combined amounts of peroxycarboxylic acid and surfactant, most especially amounts less than 15% by weight .
- Peroxyacids of the present invention may be selected from mono- or di- percarboxylic amido or imido acids.
- the mono- percarboxylic acids are of the general formula:
- R is selected from the group consisting of C ⁇ -C ⁇ alkyl, C ⁇ -C ⁇ cycloalkyl and C 6 -C 12 aryl radicals;
- R 1 is selected from the group consisting of hydrogen, C ⁇ -C 16 alkyl, C ⁇ C ⁇ cycloalkyl and C 6 -C 12 aryl radicals
- R 2 is selected from the group consisting of hydrogen, C 1 -C 16 alkyl, C x -C 16 cycloalkyl and C 6 -C 12 aryl radicals and a carbonyl radical that can form a ring together with R;
- R 3 is selected from the group consisting of C x -C 16 alkylene
- M is selected from the group consisting of hydrogen, alkali metal, alkaline earth metal, ammonium and alkanolammonium cations and radicals.
- the di-percarboxylic acids of the present invention may be of the general formula:
- R 4 is selected from the group consisting of C 1 -C 12 alkylene ,
- R 5 is selected from the group consisting of hydrogen, C ⁇ C ⁇ alkyl and C 6 -C 12 aryl radicals and a carbonyl radical that can form a ring together with R 3 ;
- R 6 is selected from the group consisting of hydrogen, C x -C 16 alkyl and C 6 -C 12 aryl radicals and a radical that can form a
- R 3 is selected from the group consisting of C ⁇ -C ⁇ alkylene ,
- n 1 and n" each are an integer chosen such that the sum thereof is 1
- m and m' each are an integer chosen such that the sum thereof is 1;
- M is selected from the group consisting of hydrogen, alkali metal, alkaline earth metal, ammonium and alkanolammonium cations and radicals.
- the most preferred peroxyacids are N,N- phthaloylaminoperoxycaproic acid (PAP) ; monononylamide of either peroxysuccinic acid (NAPSA) or peroxyadipic acid (NAPAA) ; and N,N' -terephthaloyl-di (6-aminoperoxycaproic acid) (TPCAP) .
- Amounts of the amido or imido peroxycarboxylic acid in the granule may range from 25 to 95%, preferably from 40 to 80% by weight .
- Intimately mixed with the amido or imido peroxyacids will be a surfactant to ensure against dye damage to colors on the cloth subjected to bleaching.
- the surfactant may be naturally derived, such as soap or certain synthetic material selected from anionic, nonionic, amphoteric, zwitterionic, cationic actives and mixtures thereof.
- the total level of the surfactant in the granule may range up to 90% by weight, preferably being from 1% to 50%, most preferably from 8 to 20%.
- the synthetic anionic surfactants will be water- soluble alkali metal salts of organic sulfates and sulfonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher aryl radicals.
- the preferred anionic surfactants are sodium (C 1:l -C 15 ) alkylbenzene sulphonates and sodium (C 16 -C 18 ) alkyl sulfates.
- the acid form of sulfuric and sulfonic surfactants have proved effective.
- Illustrative is the linear secondary alkyl C 10 -C 15 benzene sulfonic acid, found more effective than its sodium salt form.
- nonionic surfactants are the alkyl polyglucosides, fatty acid sugar amides (e.g. methyl glucamides) and C 18 -C 8 alkyl di-C ⁇ C-, alkyl tertiary amine oxides or C 18 -C 12 fatty amidopropyl di-C ⁇ C ? alkyl tertiary amine oxides, the amine oxides being preferred.
- the ratio of peroxycarboxylic acid to surfactant will usually range from 20:1 to 1:20, preferably from 10:1 to 1:1, optimally from 2:1 to 7:1 by weight.
- Bleach granulations of this invention may optionally contain at least one granulate adjunct such as a stabilizer, exotherm control agent or binder.
- the stabilizers may be phosphate or phosphonate chelants (e.g. Dequest ® ) and ethylenediaminetetraacetic acid. Amounts of these materials may range from 0.1 to 20% by weight of the granule. Exotherm control agents may be included to prevent autodecomposition of the peroxyacid. Amounts of the exotherm control agent may range from 1 to 80% by weight. Suitable examples of such agents are boric acid, citric acid and hydrated inorganic salts (e.g. magnesium sulfate) . In certain instances it is advantageous not to include hydrated inorganic salts such as sodium sulfate, at least in amounts limited to below 10% by weight.
- hydrated inorganic salts such as sodium sulfate
- Binders for the granule may be fatty acids (e.g. lauric acid) , polyacrylates and mixtures of these. Amounts of binder may range from 0.1 to 10% by weight.
- Bleach compositions of the present invention which incorporate the bleach granules will also include a builder.
- Builders may be selected from calcium sequestrant materials, precipitating materials, calcium ion-exchange materials and mixtures thereof. Illustrative are sodium or potassium tripolyphophosphate, sodium carbonate, sodium citrate, tartrate mono- and di- succinates, oxydisuccinate, crystalline or amorphous alumino silicates (i.e. zeolites) and mixtures thereof.
- Amounts of the builder may range from 1 to 80% by weight, preferably from 10 to 60%. Fabrics and other stained substrates may be cleaned by dispersal of the bleach granule in an aqueous medium.
- the bleach granule should be dosed at levels to achieve peroxycarboxylic acid concentrations that range from 0.05 to 100 ppm, preferably from 2 to 50 ppm in the medium.
- the amount of builder may range from about 0.1 to 3.0 grams per liter of aqueous medium.
- a series of granules according to the present invention were prepared by mixing the peroxycarboxylic acid bleach known as PAP with dimethyl C 16 alkyl amine oxide.
- PAP peroxycarboxylic acid bleach
- dimethyl C 16 alkyl amine oxide was formulated at 50% while the level of amine oxide to PAP was varied in weight ratio.
- the granules further included approximately 1% binder (secondary alkane sulfonate and polyacrylic acid) with the remainder of the composition being citric acid.
- a mixture of the bleach granule and a commercial detergent powder were placed at the center of a sulfur dye test cloth of either black or prune color.
- a piece of cotton ballast was rolled into a tube and placed on top of the bleach granules. The sides of the test cloth were then raised so that the granules sat within a valley of the test cloth, with the ballast cloth tube entrapping the granules.
- This bundle was then placed in the bottom of a terg-o-tometer pot, with the remaining pieces of ballast cloths placed on top. Water was slowly added to the pot. A soak period of 30 minutes at 25°C was followed by 2 minutes of agitation (100 rpm) . The target active oxygen level was 5 ppm.
- the test cloths were then rinsed and air dried. This test was meant to simulate entrapment of the bleach granule/detergent at the bottom of a hand wash bowl or in a washing machine. Wash conditions and materials are as outlined below.
- the reflectance of the dye damage monitor cloths was measured using the Colorgard System /05 (manufacturer: BYK Gardner), set to the CIE Lab scale; where is a measure of the
- subscript f represents the fabric after application of the PAP containing detergent
- subscript i represents the untreated fabric
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
Description
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU22903/97A AU2290397A (en) | 1996-04-12 | 1997-03-20 | Amido- and imido- peroxycarboxylic acid bleach granules |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1532396P | 1996-04-12 | 1996-04-12 | |
| US60/015,323 | 1996-04-12 | ||
| US08/699,314 | 1996-08-19 | ||
| US08/699,314 US5770551A (en) | 1996-08-19 | 1996-08-19 | Amido- and imido- peroxycarboxylic acid bleach granules |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1997039097A1 true WO1997039097A1 (en) | 1997-10-23 |
Family
ID=26687237
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1997/001459 WO1997039097A1 (en) | 1996-04-12 | 1997-03-20 | Amido- and imido- peroxycarboxylic acid bleach granules |
Country Status (2)
| Country | Link |
|---|---|
| AU (1) | AU2290397A (en) |
| WO (1) | WO1997039097A1 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999061572A1 (en) * | 1998-05-29 | 1999-12-02 | Unilever Plc | Process and product for the treatment of textile fabrics |
| EP1760141A1 (en) * | 2005-09-06 | 2007-03-07 | SOLVAY (Société Anonyme) | Coated peroxycarboxylic acid granules, process for their preparation and their use in detergent, bleach or disinfection applications |
| US7531498B2 (en) | 2003-06-13 | 2009-05-12 | Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) | Peroxycarboxylic acid-based bleach compositions having a long shelf life |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5049298A (en) * | 1988-11-25 | 1991-09-17 | Akzo Nv | Process for the preparation of bleaching granules |
| US5055218A (en) * | 1990-04-13 | 1991-10-08 | The Procter & Gamble Company | Bleach granules containing an amidoperoxyacid |
| EP0450587A2 (en) * | 1990-04-06 | 1991-10-09 | Hoechst Aktiengesellschaft | Stable granules of peroxycarboxylic acid |
| US5098598A (en) * | 1988-12-24 | 1992-03-24 | Interox Chemicals Limited | Percarboxylic acids |
| WO1992011238A2 (en) * | 1990-12-22 | 1992-07-09 | Solvay Interox Limited | Peroxycarboxylic acids |
| WO1995003276A1 (en) * | 1993-07-26 | 1995-02-02 | Unilever N.V. | Amido peroxycarboxylic acids for bleaching |
-
1997
- 1997-03-20 WO PCT/EP1997/001459 patent/WO1997039097A1/en active Application Filing
- 1997-03-20 AU AU22903/97A patent/AU2290397A/en not_active Abandoned
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5049298A (en) * | 1988-11-25 | 1991-09-17 | Akzo Nv | Process for the preparation of bleaching granules |
| US5098598A (en) * | 1988-12-24 | 1992-03-24 | Interox Chemicals Limited | Percarboxylic acids |
| EP0450587A2 (en) * | 1990-04-06 | 1991-10-09 | Hoechst Aktiengesellschaft | Stable granules of peroxycarboxylic acid |
| US5055218A (en) * | 1990-04-13 | 1991-10-08 | The Procter & Gamble Company | Bleach granules containing an amidoperoxyacid |
| WO1991016411A1 (en) * | 1990-04-13 | 1991-10-31 | The Procter & Gamble Company | Bleach granules containing an amidoperoxyacid |
| WO1992011238A2 (en) * | 1990-12-22 | 1992-07-09 | Solvay Interox Limited | Peroxycarboxylic acids |
| WO1995003276A1 (en) * | 1993-07-26 | 1995-02-02 | Unilever N.V. | Amido peroxycarboxylic acids for bleaching |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999061572A1 (en) * | 1998-05-29 | 1999-12-02 | Unilever Plc | Process and product for the treatment of textile fabrics |
| US7531498B2 (en) | 2003-06-13 | 2009-05-12 | Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) | Peroxycarboxylic acid-based bleach compositions having a long shelf life |
| EP1760141A1 (en) * | 2005-09-06 | 2007-03-07 | SOLVAY (Société Anonyme) | Coated peroxycarboxylic acid granules, process for their preparation and their use in detergent, bleach or disinfection applications |
| WO2007028806A1 (en) * | 2005-09-06 | 2007-03-15 | Solvay (Societe Anonyme) | Coated peroxycarboxylic acid granules, process for their preparation and their use in detergent, bleach or disinfection applications |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2290397A (en) | 1997-11-07 |
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