US2947700A - Inhibited chlorite baths and method - Google Patents

Inhibited chlorite baths and method Download PDF

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Publication number
US2947700A
US2947700A US613364A US61336456A US2947700A US 2947700 A US2947700 A US 2947700A US 613364 A US613364 A US 613364A US 61336456 A US61336456 A US 61336456A US 2947700 A US2947700 A US 2947700A
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United States
Prior art keywords
acid
ammonium
baths
chlorite
carboxylic
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Expired - Lifetime
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US613364A
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English (en)
Inventor
Waibel Wilhelm
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Hoechst AG
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Hoechst AG
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Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B11/00Oxides or oxyacids of halogens; Salts thereof
    • C01B11/08Chlorous acid
    • C01B11/10Chlorites
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06LDRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L4/00Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
    • D06L4/20Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen
    • D06L4/22Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen using inorganic agents
    • D06L4/24Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen using inorganic agents using chlorites or chlorine dioxide
    • D06L4/26Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen using inorganic agents using chlorites or chlorine dioxide combined with specific additives

Definitions

  • the proportions in which the above mentioned ammonium salts are to be added per litre of liquor may vary within wide limits. An addition of about 0.5 to about 2 grams per litre of liquor generally suffices. For reasons of economy a proportion within the range of about 0.6 to 1 gram may be used, although proportions smaller'or larger than those mentioned above, for example, 0.3 or 5.0 grams, may be added.
  • the proportions of the sulphonic acid and/or carboxylic acid, or the salts thereof, containing an aliphatic radical of high molecular Weight interrupted by a carboxylic acid amide or carboxylic acid ester group may also vary within wide limits. It is possible to add quantities equal to, inferior to or larger than the quantity of ammonium salt used. In many cases it is sufiicient to use about one fourth of the amount of ammonium salt. Normally, quantities will be used amounting to one fourth up to the equal amount by weightof ammonium salt used. In
  • tities of the surface-active substances claimed Somemethyl-amino acetic acid, hydroxymethaneor hydroxytimes, it is also suflicient to add inferior quantities; in some cases the amount can be reduced to about 3& of the quantity of ammonia salt used.
  • the additions customarily used for adjusting the pH-value for example, hydrochloric acid, formic acid, acetic acid, oxalic acid, phosphoric acid, nitric acid, bisulphates such as sodium bi-' sulfate, acid ortho-phosphates, pyrophosphates, acid polymeric phosphates or mixtures of these acid compounds, and the like.
  • reaction products as are obtained for instance by causing fatty acids ofhigh molecular Weight i.e. such containing more than 8 carbon atoms on amino-sulphonic or aminocarboxylic acids of low molecular weight or on protein decomposition produts.
  • fatty acids ofhigh molecular Weight i.e. such containing more than 8 carbon atoms on amino-sulphonic or aminocarboxylic acids of low molecular weight or on protein decomposition produts.
  • condensation products of the salts from the above-mentionedfatty acids and halogen-sulphonic acids or halogen-carboxylic acids can also be obtained by causing fatty acid derivatives to act upon aliphatic hydroxycarboxylic acids of low molecular weight.
  • Such 'compounds are disclosed, for instance, by Schwartz-Perry Surface Active Agents, 1949, pages 34-39, 94-97 and 102l03.
  • reaction products of fatty acids particularly in the form of their chlorides, containing more than 8 carbon atoms, especial- 1y those containing 12-18 carbon atoms, as, for instance, lauric acid, myristic acid, palmitic acid, stearic acid, or oleic acid with amino acetic acid, taurine, methyltaurine,
  • ethane-sulfonic acid tartaric'acid and the like, for instance lauryl-methyl-tauride, oleyl-methyl-tauride, myristyland palmityl-tauride, stearyl tauride, stearoxy-methane and stearoxy-ethane-sulphonic acid, laurylsarcoside,'
  • stearylsarcoside stearate of tartaric acid obtained by reaction of stearic acid chloride in dry pyridine on tartaric acid, etc.
  • the invention also includes a solid composition suitable for diminishing the formation of chlorine dioxide in' group or a salt of such acid of high molecular weight:
  • composition is stable, and provides a mixture of the ingredients in the appropriate relative proportions
  • a salt of an acidof an oxide of nitrogen advantageously sodium nitrate, may also be incorporated in the above composition.
  • Such compositions are very stable.
  • Example 5 A fabric of staple fibers of viscose was treated for 40 minutes at 75 C. at a goods-to-liquor ratio of 1:20 with a solution containing, per liter, 1 gram of sodium chlorite, 2 grams of ammonium nitrate, 5 grams of ammonium sulphate and 0.2 gram of oleyl-methyl-tauride and having a pH value of 3.5, adjusted by addition of mono-sodium phosphate and then rinsed.
  • the material thus bleached had a whiteness of 79.8 percent.
  • the consumption of sodium chlorite was not more than 0.18 percent. No liberation of chlorine dioxide occurred.
  • the same quantity of ammonium chloride or ammonium acetate may be used.
  • Example 6 A fabric of staple fibers of viscose was treated for 40 minutes at 75 C, at a goods-to-liquor ratio of 1:20 with a solution containing, per liter, 1 gram of sodium chlorite, 0.3 gram of ammonium chloride and 3 grams of lauryl-methyltauride and having a pH value of 3.5 adjusted by addition of formic acid, and then rinsed.
  • the material thus bleached had a whiteness of 80.2 percent.
  • the consumption of sodium chloride did not exceed 0.21 percent. No chlorine dioxide escaped during the bleaching process.
  • the same quantity of ammonium sulphate, ammonium chlorate or ammonium acetate may be used.
  • Example 7 Knit goods of staple fibers of cellulose acetate were treated for 20 minutes at 70 C., at a goods-to-liquor ratio of 1:25, with a solution containing per liter 1.5 grams of calcium chlorite, 0.4 gram of ammonium chloride and 2 grams of lauric acid methyl tauride, as well as 1 gram of stearic acid sarcoside.
  • the pH value of ,the bleaching bath was adjusted to 3.0 by means of a (mixture consisting of sodium acetate and hydrochloric acid in a proportion of 1:1.
  • Example 8 Yellowed yarn of polyamide fibers consisting of hexamethylene diarnine and adipic acid were treated for 1 7
  • Example 9 A fabricof polyester fibers from polyethylene glycol terephthalate was treated in a goods-to liquor ratio of 1:30 with a solution containing per liter 2 grams of sodium chlorite, 3 grams of ammonium phosphate, 2 grams of a condensation product of fatty acids of tallow and hydrolized protein and 1 gram of acid sodium hexa- -methaphosphate and adjusted to a pH value of 2 .5 by
  • a method of diminishing the formation of chlorine dioxide in acid sodium chlorite baths used for bleaching textile materials and having a pH of about 2.5 to 4.5 comprising adding to said baths an ammonium salt selected from the group consisting of ammonium chloride, ammonium sulphate, ammonium chlorate and ammonium acetate in a concentration of about 0.3 to 5 grams per liter and fiurther adding a compound selected from the group consisting of sulfonic acids and carboxylic acids containing an aliphatic radical having eight to eighteen carbon atoms which is interrupted by 'a carboxylic amide group and of sulphonic acids and carboxylic acids containing an aliphatic radical having eight to eighteen carbon atoms which is interrupted by a carboxylic ester group and the salts thereof.
  • an ammonium salt selected from the group consisting of ammonium chloride, ammonium sulphate, ammonium chlorate and ammonium acetate in a concentration of about 0.3 to 5 grams per liter
  • a method of diminishing the formation of chlorine dioxide in acid sodium chlorite baths used for bleaching textile materials and having a pH of about 2.5'to 4.5 comprising adding to said baths ammonium chloride in a concentration of about 0.3 to 5 grams per liter and further adding the sodium salt of a sulfonic acid containing an aliphatic radical having eight to eighteen carbon atoms which is interrupted by a carboxylic amide group.
  • ammonium sulphate in g a concentration of about 0.3 to 5 grams per liter and further adding the sodium salt of a sulfonic acid containing an aliphatic radical having eight to eighteen carbon atoms which is interrupted by a carboxylic amide group.
  • a method of diminishing the formation of chlorine dioxide in acid sodium chlorite baths used for bleaching textile materials and having a pH of about 2.5 to 4.5 comprising adding to said baths ammonium chlorate in a concentration of about 0.3 to 5 grams per liter and further adding the sodium salt of a sulfonic acid containing an aliphatic radical having eight to eighteen carbon atoms which is interrupted by a carboxylic amide group.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Detergent Compositions (AREA)
US613364A 1953-12-15 1956-10-02 Inhibited chlorite baths and method Expired - Lifetime US2947700A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF13471A DE1086665B (de) 1953-12-15 1953-12-15 Verfahren zur Verminderung des Entweichens von Chlordioxyd aus sauren Chloritbaedern oder Chlordioxydloesungen

Publications (1)

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US2947700A true US2947700A (en) 1960-08-02

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US613364A Expired - Lifetime US2947700A (en) 1953-12-15 1956-10-02 Inhibited chlorite baths and method

Country Status (6)

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US (1) US2947700A (sr)
BE (1) BE534142A (sr)
DE (1) DE1086665B (sr)
FR (1) FR1117236A (sr)
GB (1) GB760206A (sr)
NL (1) NL95065C (sr)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3063782A (en) * 1960-02-29 1962-11-13 Olin Mathieson Bleaching cellulosic materials
US3065040A (en) * 1957-09-24 1962-11-20 Hoechst Ag Textile bleaching process using chlorite bleaching baths
US3111358A (en) * 1961-04-14 1963-11-19 Olin Mathieson Hydrazine salt for activation and stabilization of chlorite bleach for cellulosic textiles
US3967039A (en) * 1972-05-04 1976-06-29 Solvay & Cie Coated alkali metal chlorite particles
US4236891A (en) * 1979-02-05 1980-12-02 Olin Corporation Process for textile bleaching with dibasic magnesium hypochlorite
US4790950A (en) * 1988-03-07 1988-12-13 The Drackett Company Aqueous alkali metal halogenite compositions containing a colorant stabilized by NH4 OH
US4873013A (en) * 1988-03-07 1989-10-10 The Dracket Company Aqueous alkali metal halogenite compositions containing a colorant stabilized by ammonium hydroxide
EP0482811A1 (en) * 1990-10-26 1992-04-29 Diversey Limited Chlorous acid solutions

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE569085A (sr) * 1957-07-05

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB461328A (en) * 1934-08-14 1937-02-15 Ig Farbenindustrie Ag Improvements in washing and cleansing
US2353823A (en) * 1941-09-26 1944-07-18 Mathieson Alkali Works Inc Bleaching cellulosic materials
US2415657A (en) * 1942-11-04 1947-02-11 Pennsylvania Salt Mfg Co Stable hypochlorite composition
US2526839A (en) * 1947-02-01 1950-10-24 Olin Mathieson Method of repressing the generation of chlorine dioxide
US2607738A (en) * 1948-06-25 1952-08-19 Monsanto Chemicals Bleaching, sterilizing, disinfecting, and deterging compositions
US2691637A (en) * 1949-12-27 1954-10-12 Hoechst Ag Bleaching and disinfecting agents
US2694059A (en) * 1951-05-17 1954-11-09 Hercules Powder Co Ltd Corrosion inhibition in chlorite bleaching of cellulose derivatives
US2739032A (en) * 1953-03-30 1956-03-20 William K Wilson Iron-catalyzed decomposition of sodium chlorite
US2747734A (en) * 1953-06-12 1956-05-29 Milton F Rose Composition of matter for removing abradant substances from exfoliated vermiculite and process of using same

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT173427B (de) * 1949-12-27 1952-12-27 Hoechst Ag Verfahren zur Verhütung von Korrosionen beim Arbeiten mit wäßrigen Lösungen von Chloriten oder Chlordioxyd sowie haltbares Bleichmittel

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB461328A (en) * 1934-08-14 1937-02-15 Ig Farbenindustrie Ag Improvements in washing and cleansing
US2353823A (en) * 1941-09-26 1944-07-18 Mathieson Alkali Works Inc Bleaching cellulosic materials
US2415657A (en) * 1942-11-04 1947-02-11 Pennsylvania Salt Mfg Co Stable hypochlorite composition
US2526839A (en) * 1947-02-01 1950-10-24 Olin Mathieson Method of repressing the generation of chlorine dioxide
US2607738A (en) * 1948-06-25 1952-08-19 Monsanto Chemicals Bleaching, sterilizing, disinfecting, and deterging compositions
US2691637A (en) * 1949-12-27 1954-10-12 Hoechst Ag Bleaching and disinfecting agents
US2711363A (en) * 1949-12-27 1955-06-21 Hoechst Ag Bleaching and disinfecting agents
US2694059A (en) * 1951-05-17 1954-11-09 Hercules Powder Co Ltd Corrosion inhibition in chlorite bleaching of cellulose derivatives
US2739032A (en) * 1953-03-30 1956-03-20 William K Wilson Iron-catalyzed decomposition of sodium chlorite
US2747734A (en) * 1953-06-12 1956-05-29 Milton F Rose Composition of matter for removing abradant substances from exfoliated vermiculite and process of using same

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3065040A (en) * 1957-09-24 1962-11-20 Hoechst Ag Textile bleaching process using chlorite bleaching baths
US3063782A (en) * 1960-02-29 1962-11-13 Olin Mathieson Bleaching cellulosic materials
US3063783A (en) * 1960-02-29 1962-11-13 Olin Mathieson Bleaching cellulosic materials
US3111358A (en) * 1961-04-14 1963-11-19 Olin Mathieson Hydrazine salt for activation and stabilization of chlorite bleach for cellulosic textiles
US3967039A (en) * 1972-05-04 1976-06-29 Solvay & Cie Coated alkali metal chlorite particles
US4236891A (en) * 1979-02-05 1980-12-02 Olin Corporation Process for textile bleaching with dibasic magnesium hypochlorite
US4790950A (en) * 1988-03-07 1988-12-13 The Drackett Company Aqueous alkali metal halogenite compositions containing a colorant stabilized by NH4 OH
US4873013A (en) * 1988-03-07 1989-10-10 The Dracket Company Aqueous alkali metal halogenite compositions containing a colorant stabilized by ammonium hydroxide
EP0482811A1 (en) * 1990-10-26 1992-04-29 Diversey Limited Chlorous acid solutions

Also Published As

Publication number Publication date
DE1086665B (de) 1960-08-11
NL95065C (sr)
BE534142A (sr)
GB760206A (en) 1956-10-31
FR1117236A (fr) 1956-05-18

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