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US3101323A - Compositions imparting antistatic properties to fibers and method of making same - Google Patents

Compositions imparting antistatic properties to fibers and method of making same Download PDF

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Publication number
US3101323A
US3101323A US55117A US5511760A US3101323A US 3101323 A US3101323 A US 3101323A US 55117 A US55117 A US 55117A US 5511760 A US5511760 A US 5511760A US 3101323 A US3101323 A US 3101323A
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US
United States
Prior art keywords
ethylene oxide
parts
friction
treated
fibers
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
Application number
US55117A
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English (en)
Inventor
Merlo Luigi
Vitelli Giovanni
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Montedison SpA
Original Assignee
Montedison SpA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Montedison SpA filed Critical Montedison SpA
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Publication of US3101323A publication Critical patent/US3101323A/en
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Expired - Lifetime legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53Polyethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/165Ethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40Reduced friction resistance, lubricant properties; Sizing compositions

Definitions

  • these compounds aside from being capable of substantially reducing electrostatic charges, these compounds have the serious disadvantage that they cannot be directly applied to the fibers because of their high viscosity (about 200 centipoises/20 C.) and lack of wetting power and also because they are difficult to remove once they have been applied. Moreover, these compounds have a substantial adverse effect upon the angle of friction of the fibers treated therewith.
  • compositions which have not only antistatic properties that are superior to those of the known condensation products between glycerol or polyglycol and ethylene oxide, but also are characterized by very low viscosity (120 130 centipoises/ 20 C.), emulsifiability with water and very high wetting power.
  • these compositions can be readily removed therefrom. While applied, they do not change the angle of friction or flow of the treated material, as indicated by the electrometer in electrostatic tests.
  • Example 1 -parts of a first condensation product-(obtained according to conventional methods) between ethylene oxide (mol ratio 5.4) and lauryl alcohol (mol ratio 1), and 35 parts polyglycol 200 (ethylene oxide condensate having an average M.W. of 200) are added to 40 parts of a second condensation product (produced according to usual methods) between ethylene oxide (mol ratio 8.36) and glycerol (mol ratio 1). The mixture is stirred until it is homogeneous and, if necessary, is treated with decolorants such as oxidiants or carbon black.
  • decolorants such as oxidiants or carbon black.
  • the preferred range of molar ratios of ethylene oxide to lauryl alcohol is from 5 to 6.
  • the preferred range of molar ratios of ethylene 7 oxide to glycerol in the second is from 8 to 9.
  • Example 2 10 parts of a condensation product between ethylene oxide (mol ratio 5.4) and lauryl alcohol (mol ratio 1) and 30 parts polyglycol 200 are added to 60 parts of a condensation product between ethylene oxide (mol ratio 8.36) and glycerol (mol ratio 1).
  • Example 1 25 g. (Example 1) or 10 g. (Example 2) of the 423.93 g. are used as the first condensation product.
  • glycerol g 92.09 Molecular weight of ethylene oxide g 44 erol and lauryl alcohol and also the molecular weight of the added polyglycol can vary.
  • Example 3 50 parts of a condensation product between ethylene oxide (5.4 mols) and lauryl alcohol (1 mol) are mixed directly in the cold with 35 parts of polyglycol 200 (ethylene oxide condensate having an average M.W. of 200) and 15 parts of a condensation product between ethylene. oxide (8.36 mols) and glycerol (1 mol). Mixing does not require particular expedients, with the exception of good stirring.
  • Example 4 p A polyvinyl chloride yarn is treated with the'cornposition shown in Example 1 or 2, so that a proportion varying from 0.5 to 1% based on the weight of the yarn is absorbed. In electrostatic tests with an electrometer, this yarn shows practically no formation of electric charges, even after passages of 500-1000 meters, while untreated polyvinyl chloride yarn ordinarily produces static charges. Angle of friction of untreated polyvinyl chloride-.. 112 Angle of friction of polyvinyl chloride treated with 0.5% of the composition .Angle of friction of polyvinyl chloride treated with 1% of the composition 110 3
  • Example 5 A viscose rayon yarn is treated with the composition shown in Example 1 or 2, so that a proportion varying from 0.5 to 1% is absorbed.
  • this yarn shows no formation of electric charges, even after pas sages of 500-1000 m., while untreated viscose rayon yarn ordinarily produces static charges.
  • this yarn shows no formation of electric charges, even after pa..- sages of 500-1000 111., while untreated acetate rayon yarn ordinarily produces high static charges.
  • Angle of friction of untreated acetate rayon 107-110 Angle of friction of acetate rayon treated with 0.5% of the composition 107-105
  • Angle of friction of acetate rayon treated with 1% of the composition 105 Static electric charge values expressed in coulombs/meter:
  • Untreated nylon yarn 4.8 10-- Nylon yarn treated with this composition 3X10- Example 8 A linen or silk yarn is treated with the composition shown in Example 1 or 2, so that a proportion varying from 0.5 to 1% is absorbed. In electrostatic tests with an electrometer, this yarn shows no formation of electric charges, even after passages of 500-1000 m., while untreated linen or silk yarn produces ordinarily static charges.
  • Angle of friction of untreated linen 100 Angle of friction of linen treated with 0.5% of the composition 98 Angle of friction of linen treated with 1% of the composition 98 Angle of friction of untreated silk 110 (A Angle of friction of silk treated with 0.5% of the composition 108 Angle of friction of silk treated with 1% of the composition 108 Static electric charge values expressed in coulombs/meter:
  • the ethylene oxide-glycerol condensation product imparts the antistatic property. This is improved by the ethylene oxide-lauryl alcohol condensation product, which has wetting properties and facilitates adhesion of the mixture to the fiber.
  • the polyglycol improves lubrication and fluidity, which reduces the coefiicient of friction.
  • a polyvinyl chloride yarn was treated with 0.5% (by weight) of a condensation product between ethylene oxide and glycerol.
  • a polyvinyl chloride yarn was treated with a condensation product between ethylene oxide and lauryl alcohol with 0.5% based on the weight of the yarn.
  • the same yarn was treated with an equal amount by weight of the composition of this invention under the same conditions.
  • compositions of this application not only have antistatic properties that are superior to those of the known condensation products, but are also characterized by very low viscosity, emulsitiability with water and very high wetting power. After having been applied to fibers, yarns or fabrics, these compositions can be readily removed therefrom. While applied they do not change the angle of friction or flow.
  • polyglycol-s made by condensation of polyhydric alcohols or ethylene oxide can be substituted for polyglycol 200, and the molecular weight may be in a wide range, viz. 100 to 10,000. Polyglycols liquid at ordinary temperature are preferred.
  • a composition capable of preventing the development of static electric charges in yarns made from natural and synthetic textile fibers when applied to said fibers at a ratio of about 0.5 to 1.0 percent by weight said composition consisting of a homogeneous mixture of to 25 parts of a liquid condensation product of ethylene oxide and lauryl alcohol, and 60 to 40 parts of a liquid condensation product of ethylene oxide and of glycerol, homogeneously mixed with a polyglycol, said polyglycol being polymerized ethylene oxide having an average molecular weight of about 200, said condensation products each being formed With a molar predominance of ethylene oxide, the molar ratio in said condensation products being not greater than about 8.36 mols of ethylene oxide to one mol of the other ingredient, the said polyglycol comprising to parts of the mixture.
  • a composition capable of preventing the development of static electric charges in yarns made fromnatural and synthetic textile fibers when applied to said fibers at a ratio of about 0.5 to 1.0 percent by weight said composition consisting of a homogeneous mixture of 10 to 25 parts of a condensation product of 5.4 mols of ethylene oxide and 1 mol of lauryl alcohol, and 6'0 to 40 parts of a condensation product of 8.36 mols of ethylene oxide and 1 mol of glycerol, homogeneously mixed with 30 to 35 parts of a polyglycol, said polyglycol being polymerized ethylene oxide having an average molecular weight of about 200.
  • a composition capable of preventing the development of static electric changes in yarns made from natural and synthetic textile fibers when applied to said fibers at a ratio of about 0.5 to 1.0 percent by weight said composition consisting of parts of a condensation product between 5.4 mols of ethylene oxide and 1 mol of lauryl alcohol and of a condensation product between 8.36 mols ethylene oxide and 1 mol of glycerol, homogeneously mixed with 35 parts of a polyglycol having an average molecular weight of 200.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
US55117A 1956-03-29 1960-09-12 Compositions imparting antistatic properties to fibers and method of making same Expired - Lifetime US3101323A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT353123X 1956-03-29

Publications (1)

Publication Number Publication Date
US3101323A true US3101323A (en) 1963-08-20

Family

ID=11241205

Family Applications (1)

Application Number Title Priority Date Filing Date
US55117A Expired - Lifetime US3101323A (en) 1956-03-29 1960-09-12 Compositions imparting antistatic properties to fibers and method of making same

Country Status (7)

Country Link
US (1) US3101323A (hu)
BE (1) BE556197A (hu)
CH (1) CH353123A (hu)
DE (1) DE1067403B (hu)
FR (1) FR1173346A (hu)
GB (1) GB804964A (hu)
NL (2) NL215802A (hu)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4066558A (en) * 1974-02-11 1978-01-03 Ici Americas Inc. Low viscosity spin finish systems for neat finish application
US4153561A (en) * 1976-12-31 1979-05-08 Hoechst Aktiengesellschaft Conditioning agent
US4297407A (en) * 1978-06-05 1981-10-27 Snia Viscosa Societa Nazionale Industria Applicazioni Viscosa S.P.A. Finish composition for the spinning of highly crimped cellulose fibers using a composition cont. fatty acid ester, organic phosphoric acid ester, fatty acid ethylene oxide cond. prod. and fatty acid salt

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL97682C (hu) * 1956-03-29
NL262325A (hu) * 1960-03-15
US4624793A (en) * 1984-06-20 1986-11-25 National Distillers And Chemical Corporation Fiber finishes

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1970578A (en) * 1930-11-29 1934-08-21 Ig Farbenindustrie Ag Assistants for the textile and related industries
US2316258A (en) * 1939-02-23 1943-04-13 Kummel Paul Production of softening agents
GB665914A (en) * 1948-09-01 1952-02-06 Wakefield & Co Ltd C C Improvements in or relating to the anti-static treatment of textile fibres, filaments and yarns
US2690426A (en) * 1950-03-07 1954-09-28 Atlas Powder Co Lubricating compositions
GB804964A (en) * 1956-03-29 1958-11-26 Montedison Spa Antistatic compositions and their preparation and use

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1970578A (en) * 1930-11-29 1934-08-21 Ig Farbenindustrie Ag Assistants for the textile and related industries
US2316258A (en) * 1939-02-23 1943-04-13 Kummel Paul Production of softening agents
GB665914A (en) * 1948-09-01 1952-02-06 Wakefield & Co Ltd C C Improvements in or relating to the anti-static treatment of textile fibres, filaments and yarns
US2690426A (en) * 1950-03-07 1954-09-28 Atlas Powder Co Lubricating compositions
GB804964A (en) * 1956-03-29 1958-11-26 Montedison Spa Antistatic compositions and their preparation and use

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4066558A (en) * 1974-02-11 1978-01-03 Ici Americas Inc. Low viscosity spin finish systems for neat finish application
US4153561A (en) * 1976-12-31 1979-05-08 Hoechst Aktiengesellschaft Conditioning agent
US4297407A (en) * 1978-06-05 1981-10-27 Snia Viscosa Societa Nazionale Industria Applicazioni Viscosa S.P.A. Finish composition for the spinning of highly crimped cellulose fibers using a composition cont. fatty acid ester, organic phosphoric acid ester, fatty acid ethylene oxide cond. prod. and fatty acid salt

Also Published As

Publication number Publication date
BE556197A (hu)
NL215802A (hu)
FR1173346A (fr) 1959-02-24
CH353123A (de) 1961-03-31
NL97682C (hu)
GB804964A (en) 1958-11-26
DE1067403B (de) 1959-10-22

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