US3061550A - Textile bleaching composition - Google Patents
Textile bleaching composition Download PDFInfo
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- US3061550A US3061550A US812135A US81213559A US3061550A US 3061550 A US3061550 A US 3061550A US 812135 A US812135 A US 812135A US 81213559 A US81213559 A US 81213559A US 3061550 A US3061550 A US 3061550A
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- bleaching
- weight
- composition
- bleaching composition
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- 238000004061 bleaching Methods 0.000 title claims description 56
- 239000000203 mixture Substances 0.000 title claims description 39
- 239000004753 textile Substances 0.000 title claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 3
- 239000004744 fabric Substances 0.000 description 31
- 239000004677 Nylon Substances 0.000 description 17
- 229920001778 nylon Polymers 0.000 description 17
- 239000007844 bleaching agent Substances 0.000 description 14
- CLFHABXQJQAYEF-UHFFFAOYSA-N 1-benzoylpyrrolidine-2,5-dione Chemical compound C=1C=CC=CC=1C(=O)N1C(=O)CCC1=O CLFHABXQJQAYEF-UHFFFAOYSA-N 0.000 description 13
- 229960001922 sodium perborate Drugs 0.000 description 11
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 11
- 239000000243 solution Substances 0.000 description 7
- 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 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
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 239000003599 detergent Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- -1 alkali metal hypochlorites Chemical class 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 238000002845 discoloration Methods 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 238000004900 laundering Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 239000006172 buffering agent Substances 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000003929 acidic solution Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 229910000397 disodium phosphate Inorganic materials 0.000 description 2
- 235000019800 disodium phosphate Nutrition 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000003949 imides Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
- BUXIEIKHPFAKEW-UHFFFAOYSA-N 1-(3-phenylprop-2-enoyl)pyrrolidine-2,5-dione Chemical compound C(C=CC1=CC=CC=C1)(=O)N1C(CCC1=O)=O BUXIEIKHPFAKEW-UHFFFAOYSA-N 0.000 description 1
- LBBPVMAHZCXFJA-UHFFFAOYSA-N 1-(naphthalene-2-carbonyl)pyrrolidine-2,5-dione Chemical compound C=1C=C2C=CC=CC2=CC=1C(=O)N1C(=O)CCC1=O LBBPVMAHZCXFJA-UHFFFAOYSA-N 0.000 description 1
- AQXYVFBSOOBBQV-UHFFFAOYSA-N 1-amino-4-hydroxyanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2N AQXYVFBSOOBBQV-UHFFFAOYSA-N 0.000 description 1
- HKHHUXCFTMSKOD-UHFFFAOYSA-N 1-benzoyl-5,5-dimethylimidazolidine-2,4-dione Chemical compound O=C1NC(=O)C(C)(C)N1C(=O)C1=CC=CC=C1 HKHHUXCFTMSKOD-UHFFFAOYSA-N 0.000 description 1
- OVXCMDCXMSNGHW-UHFFFAOYSA-N 1-benzoylpiperidine-2,6-dione Chemical compound C=1C=CC=CC=1C(=O)N1C(=O)CCCC1=O OVXCMDCXMSNGHW-UHFFFAOYSA-N 0.000 description 1
- VYXRTZYURDKMLT-UHFFFAOYSA-N 1-benzoylpyrrolidin-2-one Chemical compound C=1C=CC=CC=1C(=O)N1CCCC1=O VYXRTZYURDKMLT-UHFFFAOYSA-N 0.000 description 1
- SDZZWFIVMZCSIB-UHFFFAOYSA-N 2-benzoylisoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1C(=O)C1=CC=CC=C1 SDZZWFIVMZCSIB-UHFFFAOYSA-N 0.000 description 1
- 239000004343 Calcium peroxide Substances 0.000 description 1
- SPAGIJMPHSUYSE-UHFFFAOYSA-N Magnesium peroxide Chemical compound [Mg+2].[O-][O-] SPAGIJMPHSUYSE-UHFFFAOYSA-N 0.000 description 1
- 239000012425 OXONE® Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- LHJQIRIGXXHNLA-UHFFFAOYSA-N calcium peroxide Chemical compound [Ca+2].[O-][O-] LHJQIRIGXXHNLA-UHFFFAOYSA-N 0.000 description 1
- 235000019402 calcium peroxide Nutrition 0.000 description 1
- 229910001919 chlorite Inorganic materials 0.000 description 1
- 229910052619 chlorite group Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- BHDAXLOEFWJKTL-UHFFFAOYSA-L dipotassium;carboxylatooxy carbonate Chemical compound [K+].[K+].[O-]C(=O)OOC([O-])=O BHDAXLOEFWJKTL-UHFFFAOYSA-L 0.000 description 1
- CBMPTFJVXNIWHP-UHFFFAOYSA-L disodium;hydrogen phosphate;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound [Na+].[Na+].OP([O-])([O-])=O.OC(=O)CC(O)(C(O)=O)CC(O)=O CBMPTFJVXNIWHP-UHFFFAOYSA-L 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- DLINORNFHVEIFE-UHFFFAOYSA-N hydrogen peroxide;zinc Chemical compound [Zn].OO DLINORNFHVEIFE-UHFFFAOYSA-N 0.000 description 1
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 1
- 229960004995 magnesium peroxide Drugs 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- PNOVPOZTEJDSBU-UHFFFAOYSA-N n-acetyl-n-benzoylbenzamide Chemical compound C=1C=CC=CC=1C(=O)N(C(=O)C)C(=O)C1=CC=CC=C1 PNOVPOZTEJDSBU-UHFFFAOYSA-N 0.000 description 1
- MRIYHLMTPKMDAJ-UHFFFAOYSA-N n-benzoyl-n-formylbenzamide Chemical compound C=1C=CC=CC=1C(=O)N(C=O)C(=O)C1=CC=CC=C1 MRIYHLMTPKMDAJ-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- HJKYXKSLRZKNSI-UHFFFAOYSA-I pentapotassium;hydrogen sulfate;oxido sulfate;sulfuric acid Chemical compound [K+].[K+].[K+].[K+].[K+].OS([O-])(=O)=O.[O-]S([O-])(=O)=O.OS(=O)(=O)O[O-].OS(=O)(=O)O[O-] HJKYXKSLRZKNSI-UHFFFAOYSA-I 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006306 polyurethane fiber Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- PCNRQYHSJVEIGH-ASTDGNLGSA-M sodium;5-benzo[e]benzotriazol-2-yl-2-[(e)-2-phenylethenyl]benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(N2N=C3C4=CC=CC=C4C=CC3=N2)=CC=C1\C=C\C1=CC=CC=C1 PCNRQYHSJVEIGH-ASTDGNLGSA-M 0.000 description 1
- QXADHXQCAQTNGW-UHFFFAOYSA-M sodium;boric acid;hydroxide Chemical compound [OH-].[Na+].OB(O)O QXADHXQCAQTNGW-UHFFFAOYSA-M 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- 229940105296 zinc peroxide Drugs 0.000 description 1
Classifications
-
- 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
-
- 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
- Y10S8/06—Resin bleach
Definitions
- R is aromatic or substituted aromatic and R is an imide radical, preferably derived from a cyclic imide.
- compositions are superior to any presently available home bleach for nylon in that they are highly effective in removing discoloration from nylon fabrics without causing excessive strength losses, and in that they may be conveniently and efiectively used alone or in combination with household soaps or detergents for bleaching purposes. 7
- AE total color difference
- N-benzoyl succinimide and anhydrous sodium perborate' is added to the bath and the fabrics allowed to soak for one hour at a temperature of 45 C.
- the fabric samples are then removed from the bath, rinsed and dried, and the total color (delta E) of the samples before and after bleaching is determined with a differential colorimeter as described above.
- Table I shows the results obtained with various molar ratios of sodium perborate to N-benzoyl succinimide and with various concentrations of the bleaching composition. The concentration of bleaching composition is expressed as percent based on the weight of the fabric sample.
- bleach composition is added to give a concentration in th fabrc gzlcnliflgase of 0 34%, based on the weight of e 1 Table V Table 11 M 1 AE B to e Aft G 1 er na tiii B A More er Fresh bleaching composition 13.
- the pH of the bleach bath is varied by changing the relative concentration of the buffers.
- a citric acid-disodium phosphate buffer is Concentmhon Percent used, while for pH 8 and 9, a boric acid-sodium hydroxide Bef After buffer is employed to give the values shown below.
- the reduction in total color and yellowness (-l-b) at various m g5 L7 pH levels and various molar ratios is shown in Table 3:2 3:? ⁇ g VI-A below.
- a bleaching composition is prepared by mixing 42% by weight of N-benzoyl succinimide, 12.5% by weight of sodium perborate, 42.5% by weight of sodium carbonate, 2.6% by weight of a detergent (sodium l auryl' sulfate) and 0.4% of a fluorescent whitener (Tinopal RBS). Swatches (6 x 6 inches) cut from a heat-yellowed commercial cotton percale sheet are bleached in a solution to which has been added 1% (based on fabric weight) of the above bleach composition for one hour at 45 C.
- Example VII is repeated using the bleaching composition of Example V with substantially the same results.
- a Wide range of pH values can be used in bleaching fabrics with the compositions of this invention without appreciable damage to the fabrics.
- the desired pH may be achieved by adding suitable well-known buffering agents to the bleaching solution or by mixing the buffering agents with the bleaching composition in the dry state, if desired.
- the bleaching efiectiveness of these compositions at high'pH values permits their use in combination With common household laundry soaps and detergents for preventive bleaching of nylon and other fibers.
- almost any of the commercially available optical whiteners may be used in combination with these compositions.
- the bleach is most efiective and fiber degradation is minimized considerably.
- Suitable N-acylimides include: N,N-dibenzoylformamide, N,N-dibenzoyl acetamide, 1,3-dibenzoyl dimethylhydantoin, N-benzoylphthalimide, N-benzoylpyrrolidone, N-cinnamoylsuccinimide, and N m nitrobenzoylsuccinimide.
- cyclic N-substituted irnides are employed.
- R in the formula ll R-C-Ri I is preferably an aromatic or substituted aromatic radical
- a textile bleaching composition consisting essentially of a solid, stable pcroxygen compound and a water soluble N-acylimide having the general formula:
- a textile bleaching composition consisting essentially of sodium perborate and N-benzoyl succinimide in a molar ratio of from about 0.1 to about 12.4.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
Description
United States Patent Office 3,%l,550 Patented Oct. 30, 1962 3,061,550 TEXTILE BLEACHING CGMPOSITION Melvin Myron Baevsky, Wilmington, Del., assignor to E. I. du Pont de Nernours and Company, Wilmington, DeL, a corporation of Delaware No Drawing. Filed May 11, 1959, Ser. No. 812,135. 6 Claims. (Cl. 252-99) This invention relates to compositions of matter which are useful for the bleaching of textiles and other materials, particularly those made of the synthetic linear polyamides known as nylon.
The bleaching of nylon materials, especially textile materials which are to be used in the white or undyed state, has presented a problem which has not been heretofore satisfactorily solved. U-ndyed nylon fabrics which have been used for some time may become slightly yellow or otherwise discolored. The use of alkaline peroxide bleach solutions results in excessive damage to nylon fabrics, while other bleaching compositions which have been proposed are either not sufficiently effective or are very inconvenient to use. The use of hydrogen peroxide in mildly acidic solutions, as described in US. 2,720,441, requires an excessive length of time for bleaching, while its use in strongly acidic solutions leads to excessive strength losses. The most effective bleach available heretofore has included alkali metal hypochlorites and acetic acid. This method of bleaching, however, is inconvenient and the results are dependent on accurate measurement of the ingredients in home laundering. Thus, the lack of a convenient and eflective home bleach for nylon reduces the potential of nylon in several of the larger markets for white goods and also in the full utilization of nylon in many of its present end uses, such as end blends with cotton.
It is accordingly an object of this invention to provide an improved bleaching composition. Another object is to provide a composition of matter which may be conveniently and effectively used for home bleaching of nylon textile materials. A further object is to provide a bleach ing composition which may be used in conjunction with soaps and detergents which are commonly used in home laundering of nylon and other textiles.
The above objects are accomplished according to this invention by a bleaching composition comprising a solid, stable peroxygen compound and an N-acylimide having the general formula:
wherein R is aromatic or substituted aromatic and R is an imide radical, preferably derived from a cyclic imide.
The above compositions are superior to any presently available home bleach for nylon in that they are highly effective in removing discoloration from nylon fabrics without causing excessive strength losses, and in that they may be conveniently and efiectively used alone or in combination with household soaps or detergents for bleaching purposes. 7
Although it has been customary to judge fabric color by eye, it is much more satisfactory to use precise instrumental methods whereby a numerical value can be obtained. In the following examples, color measurements are made using a differential colorimeter as described by L. B. Glasser and D. I. Troy in the Journal of the Optical Society 42, 652660 (1952). These authors describe a method whereby reflectance measurements can be converted into the color coordinates, L for lightness, a for greenesS-redness, and b for yellowness-blueness.
Using this system, negative values of b representv blue shades, while positive values represent yellow shades. The depth or intensity of color will be proporfabrics before discoloration.
tional to the numerical magnitude of the b value. Also described is a method for determining the total color difference (AE) between a sample and a white standard when the sample contains an admixture of colors which cannot be described in terms of any single color coordinate.
In the following examples, bleaching tests are carried out on fabrics which have been discolored by either dye transfer or heat yellowing, since these are the most common sources of garment discoloration encountered in actual use. The dye transferred fabrics are discolored by laundering white fabrics in the presence of blue, red, and yellow fabrics which had been dyed to saturation with certain dyes of poor washfastness. The fabrics used for this purpose in the following examples are dyed with a'blue dye, Anthraquinone Blue SWF (Prototype No. 12, Technical Manual and Yearbook, A.A.T.C.C., 1955), a red dye, Celanthrene Red 3BN (Prototype No. 234), and a yellow dye, Celanthrene Fast Yellow GL (Prototype No. 534). The color of the dye transferred fabrics is numerically described in the examples in terms of the total color difference (AB) when compared to the same Thus, the lower the total color difference (AE), after treatment with an oxidizing agent, the greater the color removal and the more effective the bleach. The heat-yellowed fabrics described in the following examples are discolored by exposure to excessive heat. The color of these fabrics is described in terms of the +b value (yellowness). The effectiveness of the bleaching action of the various compounds given in the examples can be clearly determined by comparison of the magnitude of the +b values of a fabric, before and after bleaching.
EXAMPLE I N-benzoyl succinimide and anhydrous sodium perborate' is added to the bath and the fabrics allowed to soak for one hour at a temperature of 45 C. The fabric samples are then removed from the bath, rinsed and dried, and the total color (delta E) of the samples before and after bleaching is determined with a differential colorimeter as described above. Table I below shows the results obtained with various molar ratios of sodium perborate to N-benzoyl succinimide and with various concentrations of the bleaching composition. The concentration of bleaching composition is expressed as percent based on the weight of the fabric sample. Total color measurements before and after bleaching are shown for Table I Concentra- AE tion, Per- 7 cent Molar Ratio I Before After When the buffering agents, citric acid and disodium phosphate, are mixed with the dry bleaching composition and the weight of bleaching composition increased sufficiently to provide the same concentration of N-benzoyl succinimide and sodium perborate in the bleaching lauryl sulfate) and 0.26% by weight of a commercial fluorescent whitening agent. Nylon taffeta fabric samples are bleached with this composition, using the conditions given in Example Iexcept that sufficient bleach bath, similar results are obtained. 5 is added to the bath to give a concentration of 1.0%, based on the weight of the fabric sample. The total EXAMPLE H color of the samples is determined before and after Samples of nylon taffeta fabric are treated as described bl hi as d ib d i Example I, T bl V b l in Example I except that Various Nfiuhstitllted lfIlldeS shows results obtained with the freshly prepared bleachwere substituted for N-benzoyl succinimide. Table II ing composition and after storage for six and ten Weeks below Shows the compounds used, the molar ratio of in both glass containers and cardboard cartons. As hydrous Sodium pefhofate t0 imide and the total 60101 shown in the table, no substantial loss in bleaching power before and after bleaching. A sufficient amount of the is observed. bleach composition is added to give a concentration in th fabrc gzlcnliflgase of 0 34%, based on the weight of e 1 Table V Table 11 M 1 AE B to e Aft G 1 er na tiii B A More er Fresh bleaching composition 13. 8 1. 8 iger goweekli stigragg in glass... g g e 4. er wee ssora ein ass 13-21fiii zgh h g l li inimide 9.2 After 6 weeks storage in c rdboardfl 13. 8 3. 3 N -beta-naphthoylsuccinimide 7. 5 9,4 27 4 Af er 10 Weeks storage in cardboard 13. 8 3. 3 N-benzoylglutarimide. 6.4 8.5 4.1 N-p-ch]orobenzoylsuocinimide 7. 0 14. 5 7. 2
T l E Z F bl h d f EXAMPLE v1 1 a on i i g 2 o fig i ggi gg i i iii; g fi 30 This example illustrates the efiectiveness of the bleachadded a mixuire of Ndbenzoyl 5 dimgthylhy dant01-n ing compositions of this invention at various concentraand sodium perborate, the total weight of the bleaching Hons and Y molar ratlos of peroxygen compomld bath being 100 times the Weight of the sample The to N-substituted 1rn1de. Samples of nylon taffeta fabric bleach bath is maintained at a pH of 6.7 by the addition f bleached hour at 45 infaqueous i of citric acid and disodiumphosphate. Table III shows mg bath contamlilg N'benzoyl p i and sodium the reduction in color obtained with various concentraz g the welght of bath belpg 50 the Welght tions of N-benzoyl 5,5-dimethylhydantoin based on the f 3 The concentration of N'benzoyl i weight of the fabric and various molor ratios of sodium cmlml e 15 .kept Constant based Weight Perborate to N benzoyl dimethylhydantom 40 of the fabric sample, while the molar ratio of SOdIUlTl perborate to N-benzoyl succinimide is varied as shown Table III in Table VI below. The pH of the bleach bath is varied by changing the relative concentration of the buffers. I For pH 6 and 7, a citric acid-disodium phosphate buffer is Concentmhon Percent used, while for pH 8 and 9, a boric acid-sodium hydroxide Bef After buffer is employed to give the values shown below. The reduction in total color and yellowness (-l-b) at various m g5 L7 pH levels and various molar ratios is shown in Table 3:2 3:? {g VI-A below. Table VI-B shows the reduction in total 1.4 8.5 1.0 color and yellowness obtained with various concentrations of N-benzoyl succinimide and various molar ratios of EXAMPLE IV sodium perborate to N-benzoyl succinimide when the Example I is repeated except that potassium mono aqueous bleaching bath is maintained at a pH of 10. persulfate, KHSO is substituted for sodium perborate. Table IV below shows the molar ratio of potassium monopersulfate to N-benzoyl succinimide in the bleach- Table ing composition, the concentration of the bleaching composltlon based on the weight of the fabric and the total DH Molar AE yellowness color before and after bleaching. Ratio Table IV 18. 4 7. 2 1.0 6.5 4.6
Molar Ratio tiiiii f e r AE 0 4 3 cent l8 2'2 it Before After 0 3 6 EXAMPLE V V 610 1014 31s A bleaching composition is prepared by mixing 24.9% iii 2:; by weight of N-benzoyl succinimide, 39.0% by weight of 2-2 2' anhydrous sodium perborate, 33.3% by weight of citric 6:0 16:8 5:?
acid, 2.54% by weight of an anionic detergent (sodium Table VI-B Concentration of N-benzoyl Molar Total Yellowness succinimide, percent Ratio Color EXAMPLE Vll A bleaching composition is prepared by mixing 42% by weight of N-benzoyl succinimide, 12.5% by weight of sodium perborate, 42.5% by weight of sodium carbonate, 2.6% by weight of a detergent (sodium l auryl' sulfate) and 0.4% of a fluorescent whitener (Tinopal RBS). Swatches (6 x 6 inches) cut from a heat-yellowed commercial cotton percale sheet are bleached in a solution to which has been added 1% (based on fabric weight) of the above bleach composition for one hour at 45 C. Colorimeter analysis showed the original fabric to have a yellowness value of 0.3 unit, which is increased to 3.5 units after exposure to heat. After bleaching, the fabrics have a yellowness value of 0.4 unit. Measurement of the fluidity of the sample, which is a measure of the extent of degradation due to bleaching, using test method 82-54 of the Technical Manual and Year Book of the American Association of Textile Chemists and Colorists, showed no appreciable change after three bleaching cycles. When the same fabric was bleached with alkali-chlorite'and vinegar, the fluidity after one bleaching increased markedly and after three bleachings was up to a value of 20.2,
as compared to 3.7 for the bleaching composition of this invention.
EXAMPLE VIII Example VII is repeated using the bleaching composition of Example V with substantially the same results. A Wide range of pH values can be used in bleaching fabrics with the compositions of this invention without appreciable damage to the fabrics. The desired pH may be achieved by adding suitable well-known buffering agents to the bleaching solution or by mixing the buffering agents with the bleaching composition in the dry state, if desired. The bleaching efiectiveness of these compositions at high'pH values permits their use in combination With common household laundry soaps and detergents for preventive bleaching of nylon and other fibers. Likewise, almost any of the commercially available optical whiteners may be used in combination with these compositions. At a pH in the range of about 6 to about 10, the bleach is most efiective and fiber degradation is minimized considerably.
Preferably, the bleaching composition comprises N- benzoyl succinimide and sodium perborate, either anhydrous or hydrated, since this composition is highly effective and the ingredients are readily available and relatively inexpensive.
Suitable N-acylimides, in addition to those givenin the examples, include: N,N-dibenzoylformamide, N,N-dibenzoyl acetamide, 1,3-dibenzoyl dimethylhydantoin, N-benzoylphthalimide, N-benzoylpyrrolidone, N-cinnamoylsuccinimide, and N m nitrobenzoylsuccinimide. Preferably, cyclic N-substituted irnides are employed. R in the formula ll R-C-Ri I is preferably an aromatic or substituted aromatic radical,
aliphatic radicals being much less eiiective.
Any pcroxygen compound which is stable in the dry state and which liberates active oxygen readily when dissolved in aqueous media may be employed. Suitable pcroxygen compounds, in addition to those given in the examples, include alkali percarbonates such as sodium and potassium percarbonate, urea peroxide, Zinc peroxide, calcium peroxide, magnesium peroxide, tetrasodium pyroperphosphate, and disodium perphosphate and others.
The molar ratio of pcroxygen compound to N-acylimide may vary widely depending on the conditions employed. As little as 0.1 mol of peroxygen compound per mol of N-acylimide is efiective, while as much as '12 mols of pcroxygen compound per mol of 'N-acylimide is not harmful at the lower pH levels. However, when the bleach composition is used at high pH values, e.g., pH 10, the molar ratio is preferably no higher than about 2 for optimum bleaching.
The bleaching compositions of this invention are particularly suitable for bleaching nylon textiles but may also be used for bleaching cotton, regenerated cellulose, and textile materials made from various synthetic fibers such as polyesters, polyacrylonitrile and polyurethane fibers.
The concentration of the bleaching composition in an aqueous solution, as well as the time and temperature involved, may be adjusted according to the particular use anticipated. For example, as a preventive bleach to be used during laundering of nylon fabrics to prevent the build-up of discoloration, a concentration between about 0.02 and about 0.2%, based on the Weight of solution, is satisfactory. For the latter use, an average Washing cycle (10 -20 minutes) of a home automatic washing machine using water at a temperature of about 30 to about 60 C.,' is satisfactory. As a corrective bleach to whiten badly discolored fabrics, a concentration of about 0.1 to about 2.0%, based on the weight of solution, with a washing cycle of about 20 to about 60 minutes with water at about 30 to about C., is satisfactory.
I claim:
1. A textile bleaching composition consisting essentially of a solid, stable pcroxygen compound and a water soluble N-acylimide having the general formula:
n R-O-Ih wherein R comprises an aromatic group and R comprises an imide radical, the molar ratio of the pcroxygen compound to imide being in the range of from about 0.1 to about 12.4.
2. The bleaching composition of claim 1 wherein the pcroxygen compound is sodium perborate.
3. The bleaching composition of claim 1 wherein the N-acylirnide is N-benzoyl succinimide.
4. A textile bleaching composition consisting essentially of sodium perborate and N-benzoyl succinimide in a molar ratio of from about 0.1 to about 12.4.
5. The bleaching composition of claim 4 in aqueous solution, said solution containing at least about 0.1% by weight thereof.
6. The bleaching solution of claim 5 buffered to a pH of 6-10.
References Cited in the file of this patent UNITED STATES PATENTS 825,883 Heinrici July 10, 1906 2,717,878 Malkemus Sept. 13, 1955 2,898,181 Dithmar et al Aug. 4, 1959 FOREIGN PATENTS 16,151 Great Britain Jan. 4, 1906 782,898 Great Britain Sept. 18, 1957
Claims (1)
1. A TEXTILE BLEACHING COMPOSITION CONSISTING ESSENTIALLY OF A SOLID, STABLE PEROXYGEN COMPOUND AND A WATER SOLUBLE N- ACYLIMIDE HAVING THE GENERAL FORMULA:
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US812135A US3061550A (en) | 1959-05-11 | 1959-05-11 | Textile bleaching composition |
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Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3163606A (en) * | 1959-06-19 | 1964-12-29 | Konink Ind Mij Vorheen Noury & | Textile bleaching composition |
US3177148A (en) * | 1958-05-09 | 1965-04-06 | Lever Brothers Ltd | Bleaching processes and compositions |
US3349035A (en) * | 1964-05-12 | 1967-10-24 | Degussa | Activated bleaching composition |
DE1294919B (en) * | 1964-12-18 | 1969-05-14 | Fmc Corp | Process for the activation of peroxygen compounds in aqueous bleach solutions |
US3462344A (en) * | 1966-05-31 | 1969-08-19 | Fmc Corp | Superbleaching of wood pulps |
US3637339A (en) * | 1968-03-07 | 1972-01-25 | Frederick William Gray | Stain removal |
US3655567A (en) * | 1967-11-01 | 1972-04-11 | Colgate Palmolive Co | Bleaching and detergent compositions |
US3969257A (en) * | 1971-07-23 | 1976-07-13 | Colgate-Palmolive Company | Washing and bleaching composition containing bleach, activator and a nitrilotricarboxylic acid compound |
US4859800A (en) * | 1986-11-06 | 1989-08-22 | The Clorox Company | Phenoxyacetate peracid precursors |
US4956117A (en) * | 1986-11-06 | 1990-09-11 | The Clorox Company | Phenoxyacetate peracid precursors and perhydrolysis systems therewith |
US4957647A (en) * | 1986-11-06 | 1990-09-18 | The Clorox Company | Acyloxynitrogen peracid precursors |
US5049305A (en) * | 1986-11-06 | 1991-09-17 | Zielske Alfred G | Phenoxyacetate peracid precursors and perhydrolysis systems therewith |
US5328634A (en) * | 1986-11-06 | 1994-07-12 | The Clorox Company | Acyloxynitrogen peracid precursors |
US20080034511A1 (en) * | 2004-09-23 | 2008-02-14 | Batchelor Stephen N | Laundry Treatment Compositions |
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US825883A (en) * | 1905-07-10 | 1906-07-10 | Walter Heinrici | Stable solution of peroxid of hydrogen. |
GB190616151A (en) * | 1906-07-17 | 1907-02-21 | Francis Alfred Manly | An Improved Continuing or Loud Pedal for Pianofortes. |
US2717878A (en) * | 1949-05-26 | 1955-09-13 | Colgate Palmolive Co | Surface active compositions containing imides |
GB782898A (en) * | 1954-05-19 | 1957-09-18 | Unilever Ltd | Improvements in detergent compositions |
US2898181A (en) * | 1953-05-20 | 1959-08-04 | Degussa | Process for washing and bleaching compositions therefor |
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US825883A (en) * | 1905-07-10 | 1906-07-10 | Walter Heinrici | Stable solution of peroxid of hydrogen. |
GB190616151A (en) * | 1906-07-17 | 1907-02-21 | Francis Alfred Manly | An Improved Continuing or Loud Pedal for Pianofortes. |
US2717878A (en) * | 1949-05-26 | 1955-09-13 | Colgate Palmolive Co | Surface active compositions containing imides |
US2898181A (en) * | 1953-05-20 | 1959-08-04 | Degussa | Process for washing and bleaching compositions therefor |
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Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3177148A (en) * | 1958-05-09 | 1965-04-06 | Lever Brothers Ltd | Bleaching processes and compositions |
US3163606A (en) * | 1959-06-19 | 1964-12-29 | Konink Ind Mij Vorheen Noury & | Textile bleaching composition |
US3349035A (en) * | 1964-05-12 | 1967-10-24 | Degussa | Activated bleaching composition |
DE1294919B (en) * | 1964-12-18 | 1969-05-14 | Fmc Corp | Process for the activation of peroxygen compounds in aqueous bleach solutions |
US3462344A (en) * | 1966-05-31 | 1969-08-19 | Fmc Corp | Superbleaching of wood pulps |
US3655567A (en) * | 1967-11-01 | 1972-04-11 | Colgate Palmolive Co | Bleaching and detergent compositions |
US3637339A (en) * | 1968-03-07 | 1972-01-25 | Frederick William Gray | Stain removal |
US3714050A (en) * | 1968-03-07 | 1973-01-30 | Colgate Palmolive Co | Stain removal |
US3969257A (en) * | 1971-07-23 | 1976-07-13 | Colgate-Palmolive Company | Washing and bleaching composition containing bleach, activator and a nitrilotricarboxylic acid compound |
US4859800A (en) * | 1986-11-06 | 1989-08-22 | The Clorox Company | Phenoxyacetate peracid precursors |
US4956117A (en) * | 1986-11-06 | 1990-09-11 | The Clorox Company | Phenoxyacetate peracid precursors and perhydrolysis systems therewith |
US4957647A (en) * | 1986-11-06 | 1990-09-18 | The Clorox Company | Acyloxynitrogen peracid precursors |
US5049305A (en) * | 1986-11-06 | 1991-09-17 | Zielske Alfred G | Phenoxyacetate peracid precursors and perhydrolysis systems therewith |
US5328634A (en) * | 1986-11-06 | 1994-07-12 | The Clorox Company | Acyloxynitrogen peracid precursors |
US5380457A (en) * | 1986-11-06 | 1995-01-10 | The Clorox Company | Acyloxynitrogen peracid precursors |
US20080034511A1 (en) * | 2004-09-23 | 2008-02-14 | Batchelor Stephen N | Laundry Treatment Compositions |
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