US3521992A - Method for bleaching with peroxyacids - Google Patents
Method for bleaching with peroxyacids Download PDFInfo
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- US3521992A US3521992A US682557A US3521992DA US3521992A US 3521992 A US3521992 A US 3521992A US 682557 A US682557 A US 682557A US 3521992D A US3521992D A US 3521992DA US 3521992 A US3521992 A US 3521992A
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- fibers
- bleaching
- bleach
- peracetic acid
- goods
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 238000004061 bleaching Methods 0.000 title description 17
- 238000000034 method Methods 0.000 title description 15
- 150000004965 peroxy acids Chemical class 0.000 title description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 44
- 239000000835 fiber Substances 0.000 description 28
- 239000007844 bleaching agent Substances 0.000 description 27
- 239000000243 solution Substances 0.000 description 25
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 24
- 229920000728 polyester Polymers 0.000 description 15
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 12
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 12
- 239000004312 hexamethylene tetramine Substances 0.000 description 12
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- 229920000388 Polyphosphate Polymers 0.000 description 7
- 239000001205 polyphosphate Substances 0.000 description 7
- 235000011176 polyphosphates Nutrition 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- 235000019832 sodium triphosphate Nutrition 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 229920004934 Dacron® Polymers 0.000 description 4
- 238000011065 in-situ storage Methods 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 238000010186 staining Methods 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 101710194948 Protein phosphatase PhpP Proteins 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910001437 manganese ion Inorganic materials 0.000 description 1
- 150000001457 metallic cations Chemical class 0.000 description 1
- 150000001455 metallic ions Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 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 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
- 238000010025 steaming Methods 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000005406 washing Methods 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
- D06L4/15—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen using organic agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- 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
Definitions
- Polyester fibers can be bleached with peracetic acid without developing dark stains by carrying out said bleaching in the presence of at least about 0.025% by weight of either hexamethylenetetramine or trioxane.
- the invention covers bleaching of polyester textile fibers and goods therefrom using a bleach solution containing peracetic acid (also termed peroxyacetic acid).
- peracetic acid also termed peroxyacetic acid
- aqueous solutions of peroxygen compounds are suitable for bleaching textile fibers in the form of loose, fiber material as well as spun, woven or knitted goods consisting of native or artificial fibers of cellulose, or of synthetic fibers.
- peroxy compounds which have been found effective as bleaching agents, monoperacetic acid has been extensively used because it has excellent bleaching activity without damaging the fibers of the bleached goods. This is due, in part, to the fact that monoperacetic acid can bleach goods under acid conditions.
- Other active oxygen bleaches require alkaline solutions which are more prone to attack fibers than are the acidic bleach solutions of peracetic acid.
- polyester fibers and materials containing these fibers can be bleached without developing stains by Wetting the polyester fibers with an aqueous solution containing 0.25 to 1.25% by weight of peracetic acid and atvleast 0.025% (and preferably 0.05 to 0.5%) of hexamethylenetetramine or trioxane, and heating the impregnated fibers or material at temperatures from about 150 to 212 F. for at least one-half hour.
- an aqueous peracetic acid bleach solution is first made up.
- the peracetic acid can be supplied either as preformed peracetic acid or may be made just prior to use by any conventional in-situ method.
- hydrogen peroxide and glacial acetic acid are reacted together in the presence of sulfuric acid, as a catalyst, to form peracetic acid. This is most conveniently sold as 40% peracetic acid and is available to the industry in that concentration.
- peracetic acid is formed by reacting hydrogen peroxide and acetic anhydride to yield a mixture of peracetic acid, residual hydrogen peroxide and acetic acid.
- One in-situ process which is effective is that described in U.S. Pat. 3,227,655, issued to Konrad Prett et al. on Jan. 4, 1966.
- the peracetic acid In the makeup of the bleach solution the peracetic acid, whether in-situ or preformed, is diluted with water so that the solution contains 0.25 to 1.25% of peracetic acid.
- the pH of the bleach solution should be on the order of about 5.5 to about 7.0, and preferably about 5 .5 to about 6.0.
- the pH of the bleach solution is adjusted by adding ammonium hydroxide and acetic acid, as required, to reach the desired pH level.
- phosphates particularly the water-soluble polyphosphates, such as sodium tripolyphosphate, tetrasodium pyrophosphate, sodium hexametaphosphate and long-chained polyphosphates normally termed, polyphosphate glasses.
- water-soluble polyphosphates such as sodium tripolyphosphate, tetrasodium pyrophosphate, sodium hexametaphosphate and long-chained polyphosphates normally termed, polyphosphate glasses.
- These glasses are produced by condensing molecules of sodium orthophosphate to form long chains of molecules having POP bonds, and should have a chain length sufficiently small to allow sufficient solubility in the solution.
- Typical polyphosphates include Sodaphos, having a chain length of about 6 and a P 0 content of 63.8% by Weight, Hexaphos, having a chain length of about 13 and a P 0 content of 67.5% by Weight and other such glasses having chain lengths up to about 20.
- the phosphates are added in amounts sufficient to supply about 0.1 to 0.5% of the bleach solution.
- To the above solution is then added at least 0.025% (and preferably 0.05 to 0.5%) of hexamethylenetetramine or trioxane. Larger amounts of either hexamethylenetetramine or trioxane can be employed but do not improve the stain-inhibiting eifect.
- the polyester-containing fibers or goods which are to be bleached are placed in a saturator containing the above solution and removed with a 50 to 150% by weight pickup of the bleach solution.
- the exact bleach solution pickup is not critical, but about has been found eifective in obtaining the desired bleach without removing excessive bleach solution from the saturation.
- the temperature of bleach solution being applied is not critical, so long as it is below that at which peracetic acid becomes unstable, and ambient temperatures are most conveniently used.
- the polyester fibers or goods After saturating the polyester fibers or goods, they are heated by contact with steam or steam-air mixtures at temperatures of from to 212 F.
- the time of treatment will vary depending upon the degree of bleach desired and the original condition of the fibers and/or cloth.
- the time of bleaching may vary from thirty minutes up to four hours; however, most bleaching is conducted within a period of about forty minutes to about two hours.
- the goods After steaming of the bleach-impregnated goods, the goods may be washed, dried and packaged. In some cases, washing of the cloth is not necessary, and it is directly fed to subsequent stages, e.g., dyeing, etc. for further processing.
- polyester fibers which are most responsive to bleaching by the above bleach solution without staining are the polyester fibers, particularly those such as Dacron and Avlin. These polyesters are of the terephthalic acid type.
- metal catalysts which are used in the production of the polyester fiber remain in the fiber after manufacture.
- These metal catalysts are believed to discolor the cloth during the bleaching process.
- the degree of discoloration apparently depends in part on the intensity of the bleaching process. That is, when bleaching takes place at higher temperatures, i.e., 190 to 212 F. for extended periods up to three hours, there appears to be a greater tendency for these metallic cations to stain the cloth during the bleaching process. It is believed that in some way the hexamethylenetetramine, or trioxane additive, prevents these metallic ions from reacting with the bleach solution and being converted into forms which stain the polyester fiber or goods formed from the fibers.
- this additive in the case of hexamethyllenetetramine, this additive must be introduced into the bleach solution in a preformed state in order to be operative. That is, the addition of ammonia and formaldehyde (which are the precursors of hexamethylenetetramine) to the bleach solution does not have this etfect of preventing staining as does hexamethylenetetramine. This is somewhat surprising, since ammonia and formaldehyde will react under normal, ambient conditions to form hexamethylenetetramine.
- EXAMPLE 1 A number of bleaching runs were carried out as follows. Bleach solutions were made up by mixing peracetic acid and water to give the concentrations set forth in Table 1. The bleach solutions also had varying amounts of sodium tripolyphosphate, hexamethylenetetramine and/ or trioxane as set forth in Table 1. The residual hydrogen peroxide content of these bleach solutions is set forth in Table 1. Woven fabrics constructed of blended yarns containing 65% Dacron and cotton were saturated in the various bleach solutions until they picked up 100% of their weight of the bleach solution.
- Process for bleaching terephthalate polyester fibers and goods containing these fibers comprising wetting said fibers with an aqueous solution consisting essentially of 0.25 to 1.25% of peracetic acid and at least 0.025% of a member selected from the group consisting of trioxane and hexamethylenetetramine, heating the impregnated fibers at a temperature of from about to 212 F., and recovering bleached fibers which are free of stains.
- aqueous solution containing peracetic acid also contains from 0.1 to 0.5% of a water-soluble alkali metal polyphosphate.
- alkali metal polyphosphate is sodium tripolyphosphate
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
Description
United States Patent 3,521,992 METHOD FOR BLEACHING WITH PEROXYACIDS Bernard K. Easton, Pennington, N.J., assignor to FMC Corporation, New York, N.Y., a corporation of Delaware No Drawing. Filed Nov. 13, 1967, Ser. No. 682,557 Int. Cl. D061 3/02 U.S. Cl. 8-111 Claims ABSTRACT OF THE DISCLOSURE Polyester fibers can be bleached with peracetic acid without developing dark stains by carrying out said bleaching in the presence of at least about 0.025% by weight of either hexamethylenetetramine or trioxane.
BACKGROUND OF THE INVENTION Field of the invention The invention covers bleaching of polyester textile fibers and goods therefrom using a bleach solution containing peracetic acid (also termed peroxyacetic acid).
Description of the prior art It is known that aqueous solutions of peroxygen compounds are suitable for bleaching textile fibers in the form of loose, fiber material as well as spun, woven or knitted goods consisting of native or artificial fibers of cellulose, or of synthetic fibers. Among the peroxy compounds which have been found effective as bleaching agents, monoperacetic acid has been extensively used because it has excellent bleaching activity without damaging the fibers of the bleached goods. This is due, in part, to the fact that monoperacetic acid can bleach goods under acid conditions. Other active oxygen bleaches require alkaline solutions which are more prone to attack fibers than are the acidic bleach solutions of peracetic acid.
One problem that has arisen in using peracetic acid to bleach polyester fibers, or spun, woven or knitted goods containing polyester fibers, is that dark brown stains often develop on the bleached goods. These stains are of varying diameters and are sporadically located over the surface of the goods without any apparent pattern. Moreover, it has been noticed that these stains do not occur in cloths produced from natural cellulosic fibers, e.g., cotton, but instead appear in one type of synthetic fiber, namely the polyester fiber-containing goods, e.g., Dacron or Dacron and cotton blends.
OBJECTS OF THE INVENTION It is an object of the present invention to bleach polyester fiber-containing goods with aqueous, peracetic acidcontaining bleach solutions without the formation of dark stains on the bleached goods.
This and other objects will be apparent from the fol lowing description of the invention.
SUMMARY OF THE INVENTION It has now been found that polyester fibers and materials containing these fibers can be bleached without developing stains by Wetting the polyester fibers with an aqueous solution containing 0.25 to 1.25% by weight of peracetic acid and atvleast 0.025% (and preferably 0.05 to 0.5%) of hexamethylenetetramine or trioxane, and heating the impregnated fibers or material at temperatures from about 150 to 212 F. for at least one-half hour.
It has been found further that best bleaching is obtained when the above bleaching process is carried out in the presence of from 0.1 to 0.5% of a water-soluble, alkali metal polyphosphate, preferably, sodium tripolyphosphate.
3,521,992 Patented July 28, 1970 In carrying out the present invention, an aqueous peracetic acid bleach solution is first made up. The peracetic acid can be supplied either as preformed peracetic acid or may be made just prior to use by any conventional in-situ method. In producing preformed peracetic acid, hydrogen peroxide and glacial acetic acid are reacted together in the presence of sulfuric acid, as a catalyst, to form peracetic acid. This is most conveniently sold as 40% peracetic acid and is available to the industry in that concentration. In the in-situ process, peracetic acid is formed by reacting hydrogen peroxide and acetic anhydride to yield a mixture of peracetic acid, residual hydrogen peroxide and acetic acid. One in-situ process which is effective is that described in U.S. Pat. 3,227,655, issued to Konrad Prett et al. on Jan. 4, 1966.
In the makeup of the bleach solution the peracetic acid, whether in-situ or preformed, is diluted with water so that the solution contains 0.25 to 1.25% of peracetic acid. The pH of the bleach solution should be on the order of about 5.5 to about 7.0, and preferably about 5 .5 to about 6.0. The pH of the bleach solution is adjusted by adding ammonium hydroxide and acetic acid, as required, to reach the desired pH level.
It is also desirable to add phosphates, particularly the water-soluble polyphosphates, such as sodium tripolyphosphate, tetrasodium pyrophosphate, sodium hexametaphosphate and long-chained polyphosphates normally termed, polyphosphate glasses. These glasses are produced by condensing molecules of sodium orthophosphate to form long chains of molecules having POP bonds, and should have a chain length sufficiently small to allow sufficient solubility in the solution, Typical polyphosphates include Sodaphos, having a chain length of about 6 and a P 0 content of 63.8% by Weight, Hexaphos, having a chain length of about 13 and a P 0 content of 67.5% by Weight and other such glasses having chain lengths up to about 20. The phosphates are added in amounts sufficient to supply about 0.1 to 0.5% of the bleach solution. To the above solution is then added at least 0.025% (and preferably 0.05 to 0.5%) of hexamethylenetetramine or trioxane. Larger amounts of either hexamethylenetetramine or trioxane can be employed but do not improve the stain-inhibiting eifect.
The polyester-containing fibers or goods which are to be bleached are placed in a saturator containing the above solution and removed with a 50 to 150% by weight pickup of the bleach solution. The exact bleach solution pickup is not critical, but about has been found eifective in obtaining the desired bleach without removing excessive bleach solution from the saturation. The temperature of bleach solution being applied is not critical, so long as it is below that at which peracetic acid becomes unstable, and ambient temperatures are most conveniently used.
After saturating the polyester fibers or goods, they are heated by contact with steam or steam-air mixtures at temperatures of from to 212 F. The time of treatment will vary depending upon the degree of bleach desired and the original condition of the fibers and/or cloth. The time of bleaching may vary from thirty minutes up to four hours; however, most bleaching is conducted within a period of about forty minutes to about two hours. After steaming of the bleach-impregnated goods, the goods may be washed, dried and packaged. In some cases, washing of the cloth is not necessary, and it is directly fed to subsequent stages, e.g., dyeing, etc. for further processing.
The fibers which are most responsive to bleaching by the above bleach solution without staining are the polyester fibers, particularly those such as Dacron and Avlin. These polyesters are of the terephthalic acid type.
The operation of the present process to yield a bleached cloth which is free of dark stains is not completely understood. Without in any way intending to limit or restrict the scope of the invention, the following theory is offered by way of explanation.
with steam at the temperatures and for the period of time set forth in Table 1. In order to reduce the temperature in the steam tube below 212 F., air was mixed with steam before it was passed into the steam tube in contact with the saturated woven fabrics. The bleached samples were then removed and observed for stains prior to being rinsed and dried.
TABLE 1 Run 1 Run 2 Run 3 Run 4 Run 5 Run 6 Control Control Control Control Control Control Hydrogen Peroxide (100% basis) 0. 040 0. 040 0.051 0.051 0. 051 0.051 0. 019 0. 010 0.051 0.051 0.051 0.051 Pei-acetic Acid (100% basis) 0. 52 0. 52 0. 53 0. 52 0. 52 0. 52 0. 52
IIMT 1 Hydrogen Peroxide (100% basis) Peracetic Acid (100% basis) lIMT l STPP Temperature F.) Time thrs.) Staining Run 13 Run 14 Run 15 Run 16 Run 17 Control Control Control Control C ontrol Hydrogen Peroxide (100% basis). 0.10 0. 10 0. 10 0. 10 0. 049 0. 049 0. 040 0. 049 0. 049 0. 040 gqrlaiz etic Acid (100% basis) 0. 53 0. 53 0. 53 0. 5 0. 52 0. 52 O. 52 0. 52 0. 52 0. 52
Trioxane Temperature C F.) Time (hrs.) Staining 1 Hexamethylenetetramino. 2 Sodium tripolyphosphate. No'rE.St=Strains; No St=N0 Stains.
It is known that some of the metal catalysts which are used in the production of the polyester fiber remain in the fiber after manufacture. These metal catalysts, particularly manganese ions, are believed to discolor the cloth during the bleaching process. Further, the degree of discoloration apparently depends in part on the intensity of the bleaching process. That is, when bleaching takes place at higher temperatures, i.e., 190 to 212 F. for extended periods up to three hours, there appears to be a greater tendency for these metallic cations to stain the cloth during the bleaching process. It is believed that in some way the hexamethylenetetramine, or trioxane additive, prevents these metallic ions from reacting with the bleach solution and being converted into forms which stain the polyester fiber or goods formed from the fibers. It is further noted that in the case of hexamethyllenetetramine, this additive must be introduced into the bleach solution in a preformed state in order to be operative. That is, the addition of ammonia and formaldehyde (which are the precursors of hexamethylenetetramine) to the bleach solution does not have this etfect of preventing staining as does hexamethylenetetramine. This is somewhat surprising, since ammonia and formaldehyde will react under normal, ambient conditions to form hexamethylenetetramine.
The following examples are given to illustrate the invention but are not deemed to be limiting thereof.
EXAMPLE 1 A number of bleaching runs were carried out as follows. Bleach solutions were made up by mixing peracetic acid and water to give the concentrations set forth in Table 1. The bleach solutions also had varying amounts of sodium tripolyphosphate, hexamethylenetetramine and/ or trioxane as set forth in Table 1. The residual hydrogen peroxide content of these bleach solutions is set forth in Table 1. Woven fabrics constructed of blended yarns containing 65% Dacron and cotton were saturated in the various bleach solutions until they picked up 100% of their weight of the bleach solution. The saturated fabrics then were placed in a steam tube and contacted Pursuant to the requirements of the patent statutes, the principle of this invention has been explained and exemplified in a manner so that it can be readily practiced by those skilled in the art, such exemplification including what is considered to represent the best embodiment of the invention. However, it should be clearly understood that, within the scope of the appended claims, the invention may be practiced by those skilled in the art, and having the benefit of this disclosure otherwise than as specifically described and exemplified herein.
What is claimed is:
1. Process for bleaching terephthalate polyester fibers and goods containing these fibers comprising wetting said fibers with an aqueous solution consisting essentially of 0.25 to 1.25% of peracetic acid and at least 0.025% of a member selected from the group consisting of trioxane and hexamethylenetetramine, heating the impregnated fibers at a temperature of from about to 212 F., and recovering bleached fibers which are free of stains.
2. Process of claim 1 wherein said member selected from the group consisting of hexamethylenetetramine and trioxane is present in amounts of about 0.05 to 0.5%.
3. Process of claim 1 wherein said aqueous solution containing peracetic acid also contains from 0.1 to 0.5% of a water-soluble alkali metal polyphosphate.
4. Process of claim 3 wherein said alkali metal polyphosphate is sodium tripolyphosphate.
5. Process of claim 1 wherein said aqueous solution contains at least 0.025% of hexamethylenetetramine.
References Cited UNITED STATES PATENTS MAYER WEINBLATT, Primary Examiner US. Cl. X.R. 8-101
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US68255767A | 1967-11-13 | 1967-11-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3521992A true US3521992A (en) | 1970-07-28 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US682557A Expired - Lifetime US3521992A (en) | 1967-11-13 | 1967-11-13 | Method for bleaching with peroxyacids |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1655409A1 (en) * | 2004-11-04 | 2006-05-10 | Zimmer Aktiengesellschaft | Method for the treatment of silver-containing textile substrates |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2833814A (en) * | 1952-12-18 | 1958-05-06 | Du Pont | Preparation of peracetic acid |
US3049394A (en) * | 1959-01-05 | 1962-08-14 | Du Pont | Process of dyeing a linear polyester |
-
1967
- 1967-11-13 US US682557A patent/US3521992A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2833814A (en) * | 1952-12-18 | 1958-05-06 | Du Pont | Preparation of peracetic acid |
US3049394A (en) * | 1959-01-05 | 1962-08-14 | Du Pont | Process of dyeing a linear polyester |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1655409A1 (en) * | 2004-11-04 | 2006-05-10 | Zimmer Aktiengesellschaft | Method for the treatment of silver-containing textile substrates |
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