US2860944A - Bleaching fibers of vegetable origin with formamidine sulfinate and alkaline peroxide - Google Patents
Bleaching fibers of vegetable origin with formamidine sulfinate and alkaline peroxide Download PDFInfo
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- US2860944A US2860944A US549537A US54953755A US2860944A US 2860944 A US2860944 A US 2860944A US 549537 A US549537 A US 549537A US 54953755 A US54953755 A US 54953755A US 2860944 A US2860944 A US 2860944A
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- alkaline peroxide
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- 238000004061 bleaching Methods 0.000 title claims description 28
- 239000000835 fiber Substances 0.000 title claims description 22
- 150000002978 peroxides Chemical class 0.000 title claims description 17
- DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 title claims description 16
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical compound NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 title claims description 10
- 235000013311 vegetables Nutrition 0.000 title claims description 10
- 238000000034 method Methods 0.000 claims description 22
- 229920001131 Pulp (paper) Polymers 0.000 claims description 9
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 9
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 4
- 239000002655 kraft paper Substances 0.000 claims description 4
- 239000000243 solution Substances 0.000 description 44
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
- 238000011282 treatment Methods 0.000 description 18
- 229920000742 Cotton Polymers 0.000 description 17
- 239000004744 fabric Substances 0.000 description 17
- 238000000605 extraction Methods 0.000 description 13
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 12
- 235000011121 sodium hydroxide Nutrition 0.000 description 9
- DEDJCHAIBVOQIA-UHFFFAOYSA-N [Na].NC=N Chemical compound [Na].NC=N DEDJCHAIBVOQIA-UHFFFAOYSA-N 0.000 description 6
- 239000000080 wetting agent Substances 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- -1 sodium alkyl sulfate Chemical class 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000012670 alkaline solution Substances 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 238000009991 scouring Methods 0.000 description 3
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 3
- NYYSPVRERVXMLJ-UHFFFAOYSA-N 4,4-difluorocyclohexan-1-one Chemical compound FC1(F)CCC(=O)CC1 NYYSPVRERVXMLJ-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 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 2
- 229940048086 sodium pyrophosphate Drugs 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 230000007928 solubilization Effects 0.000 description 2
- 238000005063 solubilization Methods 0.000 description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 102100027988 GTP-binding protein Rhes Human genes 0.000 description 1
- 101000578396 Homo sapiens GTP-binding protein Rhes Proteins 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 150000002681 magnesium compounds Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 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
- 229920000570 polyether Polymers 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
-
- 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
- D06L4/30—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using reducing agents
-
- 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
- D06L4/70—Multi-step processes
Definitions
- Cotton goods have long been scoured with a solution of a strong alkali and then bleached with an alkaline peroxide solution. Both treatments are usually carried out at an elevated temperature either with the goods immersed in the treating solution or merely saturated or dampened therewith.
- a further object is to provide a method for bleaching cotton goods whereby high brightnesses of improved permanency are readily obtained with excellent absorbencies and mote removal and with relatively little degradation of the cotton.
- Another object is to provide a method whereby the above desirable results can be readily obtained in a shorter time than is possible by methods now used. Still further objects will be apparent from the following description.
- the objects of the invention are accomplished by extracting the vegetable fibers with an aqueous solution of an alkali metal hydroxide containing dissolved therein a iormamidine sulfinate, then bleaching the fibers with an aqueous alkaline peroxide solution.
- Other weaker reducing agents such as the sulfites and sulfides are ineffective for the present purpose.
- the present extraction treatment also appears to swell the cellulose fibers somewhat and softens and opens up the mote structure so that subsequent bleaching with an alkaline peroxide solution is facilitated.
- the alkali component of the extracting solution should be an alkali metal hydroxide.
- Other alkaline materials such as soda ash are too weakly alkaline.
- the concentration of the alkali metal hydroxide, such as potassium or sodium hydroxide, in the solution may be varied considerably, e. g. from about 0.5 to 10%, or even up to 2,860,944 Patented Nov. 18, 1958 20% by weight, but most generally will range from about 2 to 6%.
- the use of sodium hydroxide is preferred for cost reasons.
- concentration of the reducing agent can also be varied considerably, but for cost reasons, concentrations greater than about 5% by weight of the solution will not generally be used.
- concentrations range from about 0.1 to 1.0%, although a worthwhile effect can be obtained at a concentration as low as about 0.01%.
- the extraction treatment can be carried out at ordinary temperatures but higher temperatures are preferred since they accelerate the solubilizing action of the alkaline formamidine sulfinate solution on the color bodies.
- an overnight steep of the fibers in the extracting solution at about 25 C. results in eifective solubilization of the color bodies, while treatment times of 1 to 30 minutes at to C. or 20 seconds to 2 minutes at to C. are effective.
- the solution containing the solubilized bodies should be separated from the fibers.
- the fibers are then thoroughly rinsed before being bleached with alkaline peroxide.
- Concentrations of reagents represent percentages by weight, based on the Weight of the treating solution, unless indicated to be otherwise.
- Brightness were determined using a Hunter multipurpose reflectometer.
- the absorbency values reported represent the time in seconds for the absorption on the taut surface of the fabric (held in embroidery hoops) of one drop of water delivered from an eye dropper held 2 inches above the surface.
- Example 1 Strips of unbleached cotton muslin were wet-out for 2 to 3 minutes at 70 to 100 C. with a 0.2% solution of Duponol ME (a sodium alkyl sulfate wetting agent) which also contained 0.3% sodium pyrophosphate. The wet-out strips were rinsed, then extracted by treatment for 1 to 8 minutes at the boiling temperature of the solution with one of the following solutions:
- Example 2 Strips of unbleached cotton muslin were wet-out, rinsed Time for Final, Extraction with Solution (a) or (b) Peroxide Percent Bleach Reflectance (seconds) Mote removal was incomplete in all of the above bleached samples of the (a) series while the corresponding samples of the (b) series were mote-free.
- Example 3 Strips of unbleached cotton muslin were wet-out and rinsed as described in Example 1, extracted 3 to 5 minutes at the boiling temperature with an aqueous solution of 3% sodium hydroxide and sodium formamidine sulfinate equal to 0.2% of the acid, rinsed, then bleached at the boiling temperature for 3 to 30 minutes with a solution containing 1.5% sodium silicate (42 B. solution) and and 0.4% hydrogen peroxide. Results were:
- Cuam fluidity is well recognized as a measure of the degree of cellulose degradation, the higher the Cuam fluidity the greater being the degradation.
- the percent brightness loss in aging represents the loss in brightness (percent reflectance) resulting when a sample in exposed for 1 hour to saturated steam at 15 p. s. i. g.
- the goods can be bleached by any desired method employing an alkaline peroxide bleach solution.
- concentration of hydrogen peroxide H 0 or equivalent peroxygen compound such as sodium peroxide or sodium perborate,
- the solution also will usually contain from about 0.5 to 3% or more of sodium silicate (42 B. solution or equivalent commercial silicate), but other commonly used alkaline agents, such as sodium hydroxide, the alkaline phosphates and borax, or mixtures theerof, can also be used, either alone or in combination with the silicate. Stabilizers such as soluble magnesium compounds and the pyrophosphates can also be added.
- Bleaching can be effected at ordinary temperature but higher temperatures, e. g. to C. (or even up to C. or higher), are preferred. However, because bleaching and mote removal are facilitated by the present extraction treatment, the bleaching time required at any given temperature will generally be substantially shorter than that required when the extraction treatment is omitted or is replaced by the usual caustic scouring treatment. This reduction in bleaching time is important since it frequently will make unnecessary the use of costly storage facilities such as kiers and J-boxes.
- the present method is applicable to wood pulps and other fibers of vegetable origin besides cotton.
- chemical wood pulps such as the kraft and sulfite pulps can be extracted with the present alkali metal hydroxide solution of a formamidine sulfinate, then bleached with alkaline peroxide with resultant advantages similar to those obtained with cotton.
- a surface active wetting agent When bleaching cotton fabrics, it is generally preferred to wet-out the fabric with a solution of a surface active wetting agent prior to the extraction treatment, since such a wet-out treatment improves the absorbency of the bleached fabric.
- Anionic, cationic and nonionic wetting agents can be used for this purpose. Examples are the usual soaps and the synthetic surface active wetting agents such as the alkyl aryl sulfonates, the fatty alcohol sulfates, quaternary ammonium salts such as cetyl pyridinium chloride, fatty alcohol amine condensates, alkoxylated aryl polyether alcohols and polyethylene oxide condensates.
- the wet-out solution most preferably will also contain a water-soluble phosphate, e. g. a molecularly dehydrated phosphate such as sodium pyrophosphate, sodium tripolyphosphate or sodium hexametaphosphate.
- a water-soluble phosphate e. g. a molecularly dehydrated phosphate such as sodium pyrophosphate, sodium tripolyphosphate or sodium hexametaphosphate.
- the wet-out treatment is preferably carried out at an elevated temperature, e. g. 50 to 100 C., with immersion times ranging from 1 to 30 minutes.
- a method of bleaching vegetable fibers of the group consisting of cotton, kraft wood pulp and sulfite Wood pulp comprising extracting naturally occurring color bodies from said fibers with an aqueous alkali metal hydroxide solution of a formamidine sulfinate and then bleaching said fibers with an alkaline solution of hydrogen peroxide.
- a method of bleaching cotton fabric comprising extracting naturally occurring color bodies from said fabric with an aqueous alkali metal hydroxide solution of a formamidine sulfinate and then bleaching the fabric with an aqueous alkaline solution of hydrogen peroxide.
- the method of bleaching cotton fabric comprising (a) wetting-out said fabric with a solution of a surface active wetting agent, (b) rinsing the fabric, (c) extracting naturally occurring color bodies from the fabric with an aqueous sodium hydroxide solution of sodium formamidine sulfinate, (d) rinsing the fabric, then (e) bleaching the fabric with an aqueous alkaline solution of hydrogen peroxide.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Paper (AREA)
- Detergent Compositions (AREA)
Description
United States Patent 1 2,860,944 BLEACHING FIBERS 0F VEGETABLE ORIGIN WITH FORMAMIDINE SULFINATE AND AL- KALINE PEROXIDE James H. Young, Niagara Falls, N. Y., assignor to E. L du Pont de Nemours and Company, Wilmington, Del., a corporation of Delaware N0 Drawing. Application November 28, 1955 Serial N 0. 549,537 9 Claims. (Cl. 8-104) This invention relates to a method of bleaching fibers of vegetable origin, particularly cotton goods.
Cotton goods have long been scoured with a solution of a strong alkali and then bleached with an alkaline peroxide solution. Both treatments are usually carried out at an elevated temperature either with the goods immersed in the treating solution or merely saturated or dampened therewith.
Methods have been devised for carrying out such scouring and bleaching treatments continuously, but whether practiced batchwise or continuously each treatment has usually required a treating time of the order of 1 hour or longer, necessitating the use of costly kiers or J-boxes for storing the goods the required time in contact with the hot treating solution. The prior methods degrade the cotton significantly, and such degradation, and a somewhat impermanent final brightness, are normally expected of such methods. Bleaching to a high permanent brightness without degradation of the goods but with good absorbency and complete mote removal would be highly desirable. The present invention relates to a practical method whereby these objectives may be largely achieved.
It is an object of the invention to provide an improved method for bleaching fibers of vegetable origin. A further object is to provide a method for bleaching cotton goods whereby high brightnesses of improved permanency are readily obtained with excellent absorbencies and mote removal and with relatively little degradation of the cotton. Another object is to provide a method whereby the above desirable results can be readily obtained in a shorter time than is possible by methods now used. Still further objects will be apparent from the following description.
The objects of the invention are accomplished by extracting the vegetable fibers with an aqueous solution of an alkali metal hydroxide containing dissolved therein a iormamidine sulfinate, then bleaching the fibers with an aqueous alkaline peroxide solution.
Any water-soluble formamidine sulfinatecan be used for the present purpose but sodium formamidine sulfinate is preferred. Other weaker reducing agents such as the sulfites and sulfides are ineffective for the present purpose.
In experimenting with formamidine sulfinic acid, it was discovered that aqueous sodium hydroxide solutions thereof, in which the acid is of course present as sodium formamidine sulfinate, reduce and solubilize dyes which are similar to the color bodies naturally occurring in vegetable fibers such as cotton and wood pulp. It was further found that a substantial part of such color bodies can be solubilized and extracted from such fibers by means of the above solutions with the result that the extracted fibers are more readily bleached with an alkaline peroxide solution.
The present extraction treatment also appears to swell the cellulose fibers somewhat and softens and opens up the mote structure so that subsequent bleaching with an alkaline peroxide solution is facilitated.
The alkali component of the extracting solution should be an alkali metal hydroxide. Other alkaline materials such as soda ash are too weakly alkaline. The concentration of the alkali metal hydroxide, such as potassium or sodium hydroxide, in the solution may be varied considerably, e. g. from about 0.5 to 10%, or even up to 2,860,944 Patented Nov. 18, 1958 20% by weight, but most generally will range from about 2 to 6%. The use of sodium hydroxide is preferred for cost reasons.
The concentration of the reducing agent can also be varied considerably, but for cost reasons, concentrations greater than about 5% by weight of the solution will not generally be used. The preferred concentrations range from about 0.1 to 1.0%, although a worthwhile effect can be obtained at a concentration as low as about 0.01%.
The extraction treatment can be carried out at ordinary temperatures but higher temperatures are preferred since they accelerate the solubilizing action of the alkaline formamidine sulfinate solution on the color bodies. As a general guide, an overnight steep of the fibers in the extracting solution at about 25 C. results in eifective solubilization of the color bodies, while treatment times of 1 to 30 minutes at to C. or 20 seconds to 2 minutes at to C. are effective. After suitable solubilization of the color bodies has resulted, the solution containing the solubilized bodies should be separated from the fibers. Preferably, the fibers are then thoroughly rinsed before being bleached with alkaline peroxide.
The invention is illustrated by the following examples. Concentrations of reagents represent percentages by weight, based on the Weight of the treating solution, unless indicated to be otherwise. Brightness (percent reflectances) were determined using a Hunter multipurpose reflectometer. The absorbency values reported represent the time in seconds for the absorption on the taut surface of the fabric (held in embroidery hoops) of one drop of water delivered from an eye dropper held 2 inches above the surface.
Example 1 Strips of unbleached cotton muslin were wet-out for 2 to 3 minutes at 70 to 100 C. with a 0.2% solution of Duponol ME (a sodium alkyl sulfate wetting agent) which also contained 0.3% sodium pyrophosphate. The wet-out strips were rinsed, then extracted by treatment for 1 to 8 minutes at the boiling temperature of the solution with one of the following solutions:
(a) A 3% aqueous solution of sodium hydroxide.
(b) A 3% aqueous solution of sodium hydroxide containing the sodium salt of formamidine sulfinic acid, HN=C(NH )SO H, in an amount equivalent to 0.2% of the acid.
BLEAGHED WITH 0.2% H202 SOLUTION Extraction Treatment Percent Reflectance Extraction After Bleach SOLUTION In those samples bleached with the 0.2% peroxide solution, the samples of the (a) series were distinctly poorer than the corresponding samples of the (b) series both with respect to final brightness and the completeness of mote removal. Mote removal was substantially complete in all samples of the (b) series which were bleached at the higher peroxide concentrations.
Example 2 Strips of unbleached cotton muslin were wet-out, rinsed Time for Final, Extraction with Solution (a) or (b) Peroxide Percent Bleach Reflectance (seconds) Mote removal was incomplete in all of the above bleached samples of the (a) series while the corresponding samples of the (b) series were mote-free.
Example 3 Strips of unbleached cotton muslin were wet-out and rinsed as described in Example 1, extracted 3 to 5 minutes at the boiling temperature with an aqueous solution of 3% sodium hydroxide and sodium formamidine sulfinate equal to 0.2% of the acid, rinsed, then bleached at the boiling temperature for 3 to 30 minutes with a solution containing 1.5% sodium silicate (42 B. solution) and and 0.4% hydrogen peroxide. Results were:
Extraction Bleaching Ahsorh- Cuam Percent Tirne Time Percent Reency Fluidity Brightness (mm.) (min) fleetance (seconds) (Rhos) Loss in Aging 1 These are average values for 23 cotton fabrics bleached in a continuous commercial system in which fabric was secured with a caustic soda solution, washed, then bleached with alkaline peroxide solution. Both the scouring and the bleaching treatments involved saturating the goods with the treating solution, heatingthe staurated goods with live steam to about the boiling point, then storing the heated goods in an insulated J-box [or 1 hour.
It is seen from the above data that the samples treated by the present method were distinctly superior to the commercially bleached goods in every respect, and that these superior results were obtained in much shorter times.
Cuam fluidity (rhes) is well recognized as a measure of the degree of cellulose degradation, the higher the Cuam fluidity the greater being the degradation. The percent brightness loss in aging represents the loss in brightness (percent reflectance) resulting when a sample in exposed for 1 hour to saturated steam at 15 p. s. i. g.
Following the present extraction treatment the goods can be bleached by any desired method employing an alkaline peroxide bleach solution. The concentration of hydrogen peroxide (H 0 or equivalent peroxygen compound such as sodium peroxide or sodium perborate,
in such solutions can be varied considerably depending upon the results desired but generally will range from about 0.05 to 1.5% or somewhat higher. Hydrogen peroxide concentrations of at least about 0.3% are preferred when complete removal of motes is desired. The solution also will usually contain from about 0.5 to 3% or more of sodium silicate (42 B. solution or equivalent commercial silicate), but other commonly used alkaline agents, such as sodium hydroxide, the alkaline phosphates and borax, or mixtures theerof, can also be used, either alone or in combination with the silicate. Stabilizers such as soluble magnesium compounds and the pyrophosphates can also be added.
Bleaching can be effected at ordinary temperature but higher temperatures, e. g. to C. (or even up to C. or higher), are preferred. However, because bleaching and mote removal are facilitated by the present extraction treatment, the bleaching time required at any given temperature will generally be substantially shorter than that required when the extraction treatment is omitted or is replaced by the usual caustic scouring treatment. This reduction in bleaching time is important since it frequently will make unnecessary the use of costly storage facilities such as kiers and J-boxes.
The present method is applicable to wood pulps and other fibers of vegetable origin besides cotton. Thus, chemical wood pulps such as the kraft and sulfite pulps can be extracted with the present alkali metal hydroxide solution of a formamidine sulfinate, then bleached with alkaline peroxide with resultant advantages similar to those obtained with cotton.
When bleaching cotton fabrics, it is generally preferred to wet-out the fabric with a solution of a surface active wetting agent prior to the extraction treatment, since such a wet-out treatment improves the absorbency of the bleached fabric. Anionic, cationic and nonionic wetting agents can be used for this purpose. Examples are the usual soaps and the synthetic surface active wetting agents such as the alkyl aryl sulfonates, the fatty alcohol sulfates, quaternary ammonium salts such as cetyl pyridinium chloride, fatty alcohol amine condensates, alkoxylated aryl polyether alcohols and polyethylene oxide condensates. The wet-out solution most preferably will also contain a water-soluble phosphate, e. g. a molecularly dehydrated phosphate such as sodium pyrophosphate, sodium tripolyphosphate or sodium hexametaphosphate. The wet-out treatment is preferably carried out at an elevated temperature, e. g. 50 to 100 C., with immersion times ranging from 1 to 30 minutes.
I claim:
1. In a method of bleaching vegetable fibers of the group consisting of cotton, kraft wood pulp and sulfite wood pulp with an alkaline peroxide solution, the improvement comprising extracting naturally occurring color bodies from said fibers with an aqueous alkali metal hydroxide solution of a formamidine sulfinate prior to bleaching said fibers with the alkaline peroxide solution.
2. A method of bleaching vegetable fibers of the group consisting of cotton, kraft wood pulp and sulfite Wood pulp comprising extracting naturally occurring color bodies from said fibers with an aqueous alkali metal hydroxide solution of a formamidine sulfinate and then bleaching said fibers with an alkaline solution of hydrogen peroxide.
3. The method of claim 2 wherein both the extraction and the bleaching treatments are carried out at a temperature in the range 80 to 130 C.
4. The method of claim 2 employing sodium formamidine sulfinate.
5. A method of bleaching cotton fabric comprising extracting naturally occurring color bodies from said fabric with an aqueous alkali metal hydroxide solution of a formamidine sulfinate and then bleaching the fabric with an aqueous alkaline solution of hydrogen peroxide.
6 111? method of claim 5 wherein both the extraction and the bleaching treatments are carried out at a temperature in the range of 80 to 130 C.
7. The method of claim 5 employing sodium formamidine sulfinate.
8. The method of claim 5 wherein the fabric is wetout with a solution of a surface active wetting agent prior to extraction of color bodies from said fabric with the alkali metal hydroxide solution of a formamidine sulfinate.
9. The method of bleaching cotton fabric comprising (a) wetting-out said fabric with a solution of a surface active wetting agent, (b) rinsing the fabric, (c) extracting naturally occurring color bodies from the fabric with an aqueous sodium hydroxide solution of sodium formamidine sulfinate, (d) rinsing the fabric, then (e) bleaching the fabric with an aqueous alkaline solution of hydrogen peroxide.
References Cited in the file of this patent UNITED STATES PATENTS 1,501,553 Bochter July 15, 1924 2,072,665 Campbell Mar. 2, 1937 2,134,679 Allen Nov. 1, 1938 2,206,535 Lubs July 2, 1940 2,508,714 Harris May 23, 1950 2,685,496 Harris Aug. 3, 1954
Claims (1)
1. IN A METHOD OF BLEACHING VEGETABLE FIBERS OF THE GROUP CONSISTING OF COTTON, KRAFT WOOD PULP AND SULFITE WOOD PULP WITH AN ALKALINE PEROXIDE SOLUTION, THE IMPROVEMENT COMPRISING EXTRACTING NATURALLY OCCURING COLOR BODIES FROM SAID FIBERS WITH AN AQUEOUS ALKALI METAL HYDROXIDE SOLUTION OF A FORMAMIDINE SULFINATE PRIOR TO BLEACHING SAID FIBERS WITH THE ALKALINE PEROXIDE SOLUTION.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US549537A US2860944A (en) | 1955-11-28 | 1955-11-28 | Bleaching fibers of vegetable origin with formamidine sulfinate and alkaline peroxide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US549537A US2860944A (en) | 1955-11-28 | 1955-11-28 | Bleaching fibers of vegetable origin with formamidine sulfinate and alkaline peroxide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2860944A true US2860944A (en) | 1958-11-18 |
Family
ID=24193405
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US549537A Expired - Lifetime US2860944A (en) | 1955-11-28 | 1955-11-28 | Bleaching fibers of vegetable origin with formamidine sulfinate and alkaline peroxide |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2860944A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3382149A (en) * | 1964-10-29 | 1968-05-07 | Du Pont | Bleaching of hardwood sulfite pulp with hydrogen peroxide, including pretreatment with alkali |
| US3384534A (en) * | 1964-12-16 | 1968-05-21 | Fmc Corp | Bleaching of wood pulps with thiourea dioxide |
| US3709778A (en) * | 1971-01-12 | 1973-01-09 | Atlantic Richfield Co | Method for bleaching groundwood pulp with tertiary butyl hydroperoxide |
| US4610802A (en) * | 1983-12-29 | 1986-09-09 | Tokai Denka Kogyo Kabushiki Kaisha | Method of activating thiourea dioxide |
| US5458737A (en) * | 1993-07-27 | 1995-10-17 | Hoechst Celanese Corporation | Quaternary compounds as brightness enhancers |
| US5560805A (en) * | 1993-07-27 | 1996-10-01 | Hoechst Celanese Corporation | Enhanced decolorization of waste paper with selected amines |
| US5580422A (en) * | 1993-07-27 | 1996-12-03 | Hoechst Celanese Corporation | Brightening color dyed wastepaper with a bleaching agent and a quaternary compound |
| US20060270581A1 (en) * | 2003-04-25 | 2006-11-30 | David Toms | Fabric whitener |
| US20120031575A1 (en) * | 2010-04-28 | 2012-02-09 | Savage Services Corporation | Pulp Bleaching and Alkaline Extraction Method |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1501553A (en) * | 1921-05-23 | 1924-07-15 | Bochter Carl | Process of preparing raw linen for bleaching operations |
| US2072665A (en) * | 1934-09-25 | 1937-03-02 | Du Pont | Bleaching process |
| US2134679A (en) * | 1935-10-17 | 1938-11-01 | Health Res Foundation Inc | Process for treating biologic material |
| US2206535A (en) * | 1939-05-19 | 1940-07-02 | Du Pont | Stripping dyed textile |
| US2508714A (en) * | 1946-10-07 | 1950-05-23 | Harris Res Lab | Process of treating keratinous materials |
| US2685496A (en) * | 1951-05-22 | 1954-08-03 | Harris Res Lab Inc | Method for stripping color from keratinous material |
-
1955
- 1955-11-28 US US549537A patent/US2860944A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1501553A (en) * | 1921-05-23 | 1924-07-15 | Bochter Carl | Process of preparing raw linen for bleaching operations |
| US2072665A (en) * | 1934-09-25 | 1937-03-02 | Du Pont | Bleaching process |
| US2134679A (en) * | 1935-10-17 | 1938-11-01 | Health Res Foundation Inc | Process for treating biologic material |
| US2206535A (en) * | 1939-05-19 | 1940-07-02 | Du Pont | Stripping dyed textile |
| US2508714A (en) * | 1946-10-07 | 1950-05-23 | Harris Res Lab | Process of treating keratinous materials |
| US2685496A (en) * | 1951-05-22 | 1954-08-03 | Harris Res Lab Inc | Method for stripping color from keratinous material |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3382149A (en) * | 1964-10-29 | 1968-05-07 | Du Pont | Bleaching of hardwood sulfite pulp with hydrogen peroxide, including pretreatment with alkali |
| US3384534A (en) * | 1964-12-16 | 1968-05-21 | Fmc Corp | Bleaching of wood pulps with thiourea dioxide |
| US3709778A (en) * | 1971-01-12 | 1973-01-09 | Atlantic Richfield Co | Method for bleaching groundwood pulp with tertiary butyl hydroperoxide |
| US4610802A (en) * | 1983-12-29 | 1986-09-09 | Tokai Denka Kogyo Kabushiki Kaisha | Method of activating thiourea dioxide |
| US5458737A (en) * | 1993-07-27 | 1995-10-17 | Hoechst Celanese Corporation | Quaternary compounds as brightness enhancers |
| US5560805A (en) * | 1993-07-27 | 1996-10-01 | Hoechst Celanese Corporation | Enhanced decolorization of waste paper with selected amines |
| US5580422A (en) * | 1993-07-27 | 1996-12-03 | Hoechst Celanese Corporation | Brightening color dyed wastepaper with a bleaching agent and a quaternary compound |
| US20060270581A1 (en) * | 2003-04-25 | 2006-11-30 | David Toms | Fabric whitener |
| US20120031575A1 (en) * | 2010-04-28 | 2012-02-09 | Savage Services Corporation | Pulp Bleaching and Alkaline Extraction Method |
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