Classifications

• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
  • C08K5/0058—Biocides
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/13—Phenols; Phenolates
  • C08K5/132—Phenols containing keto groups, e.g. benzophenones
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/13—Phenols; Phenolates
  • C08K5/136—Phenols containing halogens
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
  • C08K5/37—Thiols
  • C08K5/375—Thiols containing six-membered aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
  • C08L33/18—Homopolymers or copolymers of nitriles
  • C08L33/20—Homopolymers or copolymers of acrylonitrile
• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F1/00—General methods for the manufacture of artificial filaments or the like
  • D01F1/02—Addition of substances to the spinning solution or to the melt
  • D01F1/10—Other agents for modifying properties
  • D01F1/103—Agents inhibiting growth of microorganisms
• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
  • D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D01F6/18—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide
• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
  • D01F6/28—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D01F6/38—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising unsaturated nitriles as the major constituent
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
  • Y10S8/929—Carpet dyeing
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
  • Y10T428/2913—Rod, strand, filament or fiber
  • Y10T428/298—Physical dimension

Definitions

• This invention relates to bacteriostatic compositions of polyacrylonitrile or of copolymers containing at least 85 weight percent of acrylonitrile in the polymer molecule and minor but effective amounts of 2-chloro-4-phenylphenol, and to articles made from such compositions.
• Polyacrylonitrile and many of the fiber and film-forming copolymers of acrylonitrile may advantageously be fabricated by a wet spinning process wherein the polymer composition is extruded from compositions of the polymer in polyacrylonitrile-dissolving aqueous saline solvents, particularly aqueous solutions of zinc chloride and its saline equivalents.
• aqueous saline solvents particularly aqueous solutions of zinc chloride and its saline equivalents.
• the fiber-forming, aqueous saline spinning solution or other composition of the polymer is extruded during the spinning operation into a non-polymer dissolving coagulation liquid or spin bath, which frequently is a solution of the same salt or salts as are in the spinning solution.
• Acrylonitrile polymers including fiber-forming copolymers, particularly polyacrylonitrile, that are saltspun in the referred-to manner are generally formed initially as aquagel intermediates. Such intermediates have a water-swollen or hydrated structure prior to their being finally irreversibly dried to the desired, characteristi cally hydrophobic, product.
• the aquagel structure of polyacrylonitrile and other fiber and film-forming acrylonitrile polymers may be derived by the extrusion of a solution of the acrylonitrile polymer that is dissolved in an aqueous zinc chloride saline solvent therefor into and coagulation in an aqueous coagulating spin bath. It is usually desirable for zinc chloride to be at least the principal (it not the entire) saline solute in the aqueous saline solvent solution.
• various of the saline equivalents for zinc chloride may also be employed in the aqueous saline solvent medium for the spinning solution and the coagulating bath utilized.
• These zinc chloride equivalents include various of the thiocyanates (such as calcium thiocyanate), lithium bromide and the salts and salt mixtures that are solvent members of the so-called lyotropic series as are disclosed, among other places, in US. 2,140,921; 2,425,192; 2,648,592; 2,648,593; 2,548,646; 2,648,648; and 2,648,649.
• Fibers produced from acrylonitrile polymers have excellent physical properties but do not have the inherent ability to inhibit the growth of bacteria.
• the textile industry is particularly interested in a fibrous material useful for the production of blankets, carpeting and the like, which has the desirable properties of polyacrylonitrile or fiber-forming copolymers containing at least 85 weight percent of acrylonitrile in the polymer molecule and in addition has the ability to inhibit the growth of bacteria and to destroy existing bacteria. It is also highly desirable to prepare heat-shrinkable, flexible films useful for bottle closures and the like applications which have long-losting bacteriostatic properties.
• Fabricated acrylonitrile polymer films, textile fibers and like filamentous articles derived from salt-spinning processes are generically described as being capable of lying substantially in a single plane, having at least one major dimension, and at least one minor dimension less than about 0.1 inch, said articles being characterized by having orientation of the molecules parallel to one another and to a major axis of the article.
• compositions of matter containing at least weight percent of acrylonitrile in the polymer molecule which have longlasting bacteriostatic properties.
• a further object is to provide shaped articles from the compositions of the invention which have long-lasting bacteriostatic properties.
• Articles made from the resulting compositions show pronounced bacteriostatic properties even after prolonged treatment with a heated aqueous detergent system.
• a polymer containing at least 85 percent acrylonitrile in the polymer molecule, as described herein, is spun from an aqueous saline solution thereof into an aqueous coagulant.
• the coagulated product is stretched to ellect orientation and is washed in any conventional manner to extract saline constituents and is finally irreversibly dried.
• the compound 2-chloro-4-phenylphenol can be incorporated in the spun article during the course of its manufacture or after it is reduced to its final dimensions and irreversibly dried.
• the invention is applicable to products made by dry spinning or wet-spinning from organic solutions of the polymer, as well as wet-spinning of aqueous saline solutions of the polymer.
• the acrylonitrile polymer employed in practice of the present invention is advantageously, polyacrylonitrile, although, as is readily apparent, any of the Well known fiber and film-forming copolymers thereof that contain, polymerized in the polymer molecule, at least 85 weight percent of .acrylonitrile with at least one other ethylenically unsaturated monomer that is copolymerizable with acrylonitrile may, beneficially, be utilized.
• the aciylonitrile polymer employed is soluble in an aqueous saline solvent which, usually, has therein at least about 5060 weight percent of zincchloride or its saline equivalents. US.
• the compound 2 chloro 4 phenylphen-ol hereafter called bacteriostatic agent, is a readily available material which is well known to those skilled in the art.
• the bacteriostatic agent must be present in the shaped article in amounts of at least about 0.5 percent by weight, preferably 0.5 to 20 percent by weight based on the Weight of the polymer.
• the permissible maximum proportion depends on the limit of its compatibility with the organic spinning solution or aqueous saline solution, as well as the polymeric material contained therein. The maximum limit is generally about 20 weight percent, based on the weight of the acrylonitrile polymer.
• the bacteriostatic agent can be added to the acrylonitrile polymer spinning solution in a mutual solvent therefore, or by milling said bacteriostatic agent to finely divided particles which are suspended in a small amount of the spinning solution media to form a concentrate thereof, followed by addition of said concentrate to the spinning solution with stirring. 7
• the basteriostatic agent can be incorporated into the water-swollen aquagel or finally oriented, irreversibly dried article by soaking the article in an aqueous solution of the bacteriostatic agent.
• the time required for the aquagel or irreversibly dried article to absorb the bacteriostatic agent is very brief, and varies with the concentration of the liquid from which the bacteriostatic agentisapplied, and the temperature of the application. Generally, enough of the bacteriostatic agent defined herein, is absorbed by the aquagel or irreversibly dried article in about minutes or less. No adverse efiect is found when the polymeric article is soaked in the aqueous bacteriostatic solution for periods of several days.
• bacteriostatic agent useful for the purposes of the present invention may be used in aqueous solutions which may be of any desired or convenient concentration. Thus, solutions containing 'as little as 0.1 percent by weight or less of the bacteriostatic agent defined herein have been used successfully.
• the time and temperature of treatment for incorporating the bacteriostatic agent of the present invention into the polymeric article either in its water-swollen aquagel form or completely oriented finally dried form should bercorrelated as to cause the article to absorb at least about 0.5 weight percent of the bacteriostatic agent, based on the weight of the fiber-forming polymer. Amounts as high as 20 percent are unobjectionable.
• the temperature of treatment may be any temperature at which the aqueous bacteriostatic solution is a liquid, however, it is convenient to efiiect the treatment at temperatures of about 95 C.
• compositions of the present invention include typically, for example, plasticizers, lubricants, dye assistants, dyes and pigments.
• Example 1 A length (4inches) of water-swollen, unstretchedtow, formed by extrusion of an aqueous saline solution of polyacrylonitrile through a mil, 300 hole metal spinneret into, an aqueous coagulating bath, .was washed thoroughly to remove salt. It was then allowed to stand in 10 milliliters of a 0.05 percent aqueous solution of 2- chloro-4-phenylphenol at 95 C. for a period of about 10 minutes, until the fibers had absorbed at least about 0.5 weight percent of the 2-chloro-4-phenylphenol based on the weight of the fiber-forming polymer. The tow was removed from thejimpregnating solution, rinsed briefly in tap water and dried over night under normal room temperatures.
• the dried, impregnated tow was immersed in an aqueous bath containing 0.1 weight percent of Igepon T (sodium N-methyl-N-oleyl taurate), and heated with stirring at 95 C. for a period of about 0.5 hour. The tow was then rinsed with tap water and dried overnight at normal room temperatures.
• Igepon T sodium N-methyl-N-oleyl taurate
• the dried filament tow was placed on the surface of a nutrient agar seeded with Staphylococcus aureus con- I tained on the surface of a hardened agar media plate, and subsequently incubated for a period of about 48 hours at a temperature between about 30 C. and 37 C. A zone of inhibition was observed around the test specimen following the incubation period.
• composition of matter the essential constituents of which are (1) a fiber-forming acrylonitrile polymer which polymer contains in the polymer molecule at least about 85 weight percent of acrylonitrile, the balance being another monoethylenically unsaturated monomer that is compatible with acrylonitrile and (2) at least about 0.5 weight percent based on the weight of said fiber-forming polymer of 2-chloro-4-phenylphenol.
• composition of claim 1 wherein the 2-chlorot-phenylphenol is present in amounts between about 0.5
• composition of claim 1, wherein said fiber forming polymer is polyacrylonitrile.
• a polymeric article of manufacture having bacteriostatic properties said article capable of lying substantially in a single plane, having at least one major dimension, and at least one minor dimension less than about 0.1 inch, comprised of (l) a fiber-forming acrylonitrile polymer which contains in the polymer molecule at least about 85 weight percent of acrylonitrile, the balance being another monoethylenically unsaturated monomeric material that is copolymerizable with acrylonitrile and (2) dispersed therein at least about 0.5 Weight percent, based on the weight of the fiber-forming polymer of 2-chloro-4-phenylphenol.
• V a fiber-forming acrylonitrile polymer which contains in the polymer molecule at least about 85 weight percent of acrylonitrile, the balance being another monoethylenically unsaturated monomeric material that is copolymerizable with acrylonitrile and (2) dispersed therein at least about 0.5 Weight percent, based on the weight of the fiber-forming polymer of 2-chloro-4-

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• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Polymers & Plastics (AREA)
• General Chemical & Material Sciences (AREA)
• Textile Engineering (AREA)
• Life Sciences & Earth Sciences (AREA)
• Biochemistry (AREA)
• Microbiology (AREA)
• Biodiversity & Conservation Biology (AREA)
• Toxicology (AREA)
• Manufacturing & Machinery (AREA)
• Artificial Filaments (AREA)

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• 1962
  • 1962-03-16 US US180341A patent/US3197430A/en not_active Expired - Lifetime
  • 1962-03-16 US US180305A patent/US3192180A/en not_active Expired - Lifetime
  • 1962-03-16 US US180308A patent/US3198764A/en not_active Expired - Lifetime
• 1965
  • 1965-06-21 NL NL6507931A patent/NL6507931A/xx unknown
  • 1965-06-21 DE DE1544788A patent/DE1544788C3/de not_active Expired
  • 1965-06-21 BE BE665711A patent/BE665711A/xx unknown

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