Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
  • B29D30/00—Producing pneumatic or solid tyres or parts thereof
  • B29D30/06—Pneumatic tyres or parts thereof (e.g. produced by casting, moulding, compression moulding, injection moulding, centrifugal casting)
  • B29D30/52—Unvulcanised treads, e.g. on used tyres; Retreading
  • B29D30/68—Cutting profiles into the treads of tyres
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F2/00—Processes of polymerisation
  • C08F2/46—Polymerisation initiated by wave energy or particle radiation
  • C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
  • C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents

Definitions

• U.S. Patent 4,062,817 discloses polymers of unsaturated copolymerizable carboxylic acids, at least one alkyl acrylate or methacrylate wherein the alkyl group has 10 to 30 carbon atoms and another alkyl acrylate or methacrylate wherein the alkyl group has 1 to 8 carbons. This composition alleviated many of the deficiencies of the earlier compositions. Further improvements in the hydrophilic properties were obtainedby compositions disclosed in U.S. Patent 4,066,583.
• This patent discloses a composition
• a composition comprising (1) a copolymer of the type disclosed in the '817 patent, except that after copolymerization 30 to 90 percent of the carboxylic groups were neutralized with an alkali metal or ammonia and (2) an aliphatic glycol, a plasticizer which is important in facilitating extrusion of the polymer.
• U.S. Patent 4,090,013 discloses a swellable, water absorbent composition which contains a high molecular weight polyelectrolyte which is a synthetic copolymer of an ethylenically unsaturated monomer and a mono-ethylenically unsaturated carboxylic acid such as acrylic acid. Additionally there may be di-functional monomer such as allyl methacrylate used in a very small amount as a chain extender (not a cross-linking agent) and a polyvalent metal cation, preferably aluminum, which complexes the poly-electrolyte. After polymerization the anionic groups of the poly-electrolyte may be neutralized with a base, such as an alkali-metal hydroxide.
• a base such as an alkali-metal hydroxide.
• a cross-linked acrylic acid polymer is prepared by photopolymerizing 20 to 99.9 weight percent of acrylic acid, 50 to 100% of the carboxylic groups of said acid having been neutralized prior to polymerization with an alkaline metal hydroxide, and 0.1 to 80 weight percent of a polyfunctional cross-linking agent. After spreading the monomer mixture to the desired thickness or after spinning it into a fiber it is polymerized upon exposure to a UV light source. The resulting film or fibers have extremely rapid and high degree of absorption of water and body fluids, such as urine or blood.
• DETAILED DISCLOSURE This invention is directed to a photopolymerized interpolymer which has outstanding absorption and retention properties of water and ionic body fluids such as urine or blood.
• the polymer is prepared from a) 20 to 99.9 weight percent of acrylic acid, 50 to 100 percent of the carboxylic groups having been neutralized with an alkali metal hydroxide or ammonia base prior to polymerization, b) 0.1 to 80 weight percent of a polyfunctional cross-linking agent, and c) 0.01 to 5 weight percent of a photoinitiator, said polymer having been polymerized by subjecting the monomer mixture to a UV light source.
• At least 50 weight percent of acrylic acid is employed and more preferably 90 to 99.5 weight percent of acrylic acid and 0.5 to 10 weight percent of a polyfunctional cross-linking agent are employed. Often materials having superior properties are obtained when 0.2 to 5.0 weight percent of a poly-functional cross-linking agent is employed.
• the cross-linking agents that may be employed in this invention are monomeric compounds which contain two or more ethylenically unsaturated groups which can be copolymerized with acrylic acid by UV light.
• the cross-linking agents have two to six ethylenically unsaturated groups such as allyl, acrylate or vinyl groups.
• the nature of that portion of the molecule which does not contain ethylenic unsaturatidn is of no critical consequence as long as it does not possess groups which would interfere with UV polymerization.
• that part of the molecule is made up of a saturated hydrocarbon chain, a glycol or a polyglycol moiety, an aromatic moiety or cyanurate or isocyanurate ring or other non-polymerizable moieties.
• Polyfunctional compounds that may be used as cross-linking agents include, for example, diallyl esters or ethers, allyl or methallyl acrylates and acrylamides, diacrylates and dimethacrylates, divinyl compounds and the like.
• Illustrative examples of polyfunctional cross-linking agents are polyethyleneglycol diacrylate and dimethacrylate, ethylene glycol dimethacrylate, tetraethyleneglycol diacrylate, 1,3-butyleneglycol dimethacrylate, diethyleneglycol divinyl ether, trimethylolpropane diallyl ether, divinyl benzene, trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, triallyl cyanurate, pentaerythritol triacrylate, diallyl itaconate, methylene bis (acrylamide), allyl pentaerithritol, allyl sucrose, 1, 6-hexanediol di
• Acrylic acid must be neutralized prior to polymerization at least 50 percent and preferably 75 percent.
• the most preferred degree of neutralization is 95 to 100 percent because it was noted that with higher degrees of neutralization the resulting polymers exhibit better absorbency properties.
• additional monomers are ⁇ , ⁇ olefinically unsaturated nitriles preferably the monoolefinically unsaturated nitriles having from 3 to 10 carbon atoms such as acrylonitrile, methacrylonitrile, ethacrylonitrile, chloroacrylonitrile, and the like. Most preferred nitriles are acrylonitriles and methacrylonitrile.
• Another useful class of additional monomers which may be incorporated in the interpolymers of this invention is monoethylenically unsaturated amides which have at least one hydrogen on the amide nitrogen and the olefinic unsaturation is alphabeta to the carbonyl group.
• the preferred amides have the structure
• R 3 is a member of the group consisting of hydrogen and an alkyl group having from 1 to 4 carbon atoms and R 4 is a member of the group consisting of hydrogen and an alkyl group having from 1 to 6 carbon atoms.
• amides include acrylamide, methacrylamide, N-methyl acrylamide, N-t-butyl acrylamide, Ncyclohexyl acrylamide, N-ethyl acrylamide and others.
• amides most preferred are acrylamide and methacrylamide.
• acrylic amides include N-alkylol amides of alpha, beta-olefinically unsaturated carboxylic acids including those having from 4 to 10 carbon atoms such as
• N-methylol acrylamide N-ethanol acrylamide, N-propanol acrylamide, and the like.
• the preferred monomers of the N-alkylol amide type are the N-alkylol amides of alpha, beta-monoolefinically unsaturated monocarboxylic acids and the most preferred is N-methylol acrylamide.
• N-alkoxymethyl acrylamides which have the structure
• R 5 is selected from the group consisting of hydrogen and methyl, and R is an alkyl group having from 1 to 8 carbon atoms. It is thus intended that where references are made herein regarding the essential N-substituted alkoxymethyl amides, the term "acrylamide” includes “methacrylamide” within its meaning.
• the preferred alkoxymethyl acrylamides are those wherein R 6 is an alkyl group containing from 2 to 5 carbon atoms, and especially useful is N-butoxymethyl acrylamide.
• the above discussed monomers are copolymerized by subjecting the monomer mixture to UV light. If a film is desired the monomer can be spread on a surface to the desired thickness, e.g. 1 mil to 25 mil, and then subjected to UV light for a short time, e.g. 1 second to several minutes.
• the actual length of ir radiation will depend on a number of factors, such as the thickness of the monomer film, the distance from and the intensity of the source of irradiation, the specific monomers employed and the ratio of such monomers to each other, the presence or absence of additional comonomers and the nature and the amount of the photoinitiator employed.
• the type of photoinitiator employed will depend at least in part on the type of UV irradiation employed (particularly its wave length) since various photoinitiators may be decomposed by UV light of different wavelengths). If it is desired that the material be in the form of fibers, the monomer mixture can be thickened and then spun into fibers which, upon exposure to UV light, are polymerized. In order to effect quick and efficient polymerization under UV light, 0.01 to 5 weight percent of a photoinitiator, preferably 0.1 to 5 percent and more preferably 0.3 to 1.0 weight percent, must be incorporated into the monomer mixture. Any compound which dissociates into free radicals when exposed to UV radiation can be employed.
• photoinitiators or photosensitizers such as acetophenone, propiophenone, benzophenone, xanthone, fluorenone, benzaldehyde, fluorene, a ⁇ thraquinone, triphenylamine, carbozole, 3- or 4-methylacetophenone, 3- or 4-pentylacetophenone, 3-or 4-methoxyacetophenone, 3- or 4- bromoacetophenone, 3- or 4-allylacetophenone, p-di- acetylbenzene, 3- or 4-methoxybenzophenone, 3- or 4- methylbenzophenone, 3- or 4-chlorobenzophenone, 4,4- dimethoxybenzophenone, 4-chloro-4 '-benzylbenzophenone, 3-chloroxanthone, 3, 9-dichloroxanthone, 3-chloro-8- nonyl-xanthone, 3-methoxyxanthone, 3-iodo
• an air cure promoter In addition to the photoinitiator it may be advantageous to employ also from 0.1 to 5.0 percent of an air cure promoter.
• air cure promoters are mercaptoacetic acid, mercaptoethanol, Michler's ketone (4, 4'-dimethylaminobenzophenone), diethanolamine, methyl diethanolamine, ethyl p-dimethylaminobenzoate, and the like.
• the monomer mixtures are prepared as aqueous dispersions which eliminates the need for organic solvents . This avoids the pollution problems caused by the removal of organic solvents or the cost associated with the removal of the pollutants.
• the aqueous dispersions contain 0.01 to 5%, and preferably 0.1 to 1%, of a surface active agent such as an anionic, amphoteric, or nonionic dispersing agent or a mixture of dispersants.
• Useful anionic dispersing agents include alkali metal or ammonium salts of the sulfates of alcohols having from 8 to 18 carbon atoms such as sodium lauryl sulfate; ethanolamine lauryl sulfate, ethylamine lauryl sulfate; alkali metal and ammonium salts of sulfonated petroleum and paraffin oils; sodium salts of aromatic sulfonic acids such as dodecane-1-sulfonic acid and octadecane-1-sulfonic acid; aralkyl sulfonates such as sodium isopropyl benzene sulfonate, sodium dodecyl benzene sulfonate and sodium isobutyl naphthalene sulfonate; alkali metal and ammonium salts of sulfonated dicarboxylic acid esters such as sodium dioctyl sulfosuccinate, disodium-
• Nonionic dispersants such as octyl-or nonylphenyl polyethoxyethanol as well as the PLURONIC and the TRITON dispersants may also be used. Also useful are amphoteric dispersants such as dicarboxylic coconut derivatives (MIRANOL). Further examples of useful dispersants are those disclosed beginning on page 102 in J. Van Alphen's "Rubber Chemicals", Elsevier Publishing Co., 1956.
• the copolymers of this invention can be photo polymerized in a film or a fiber form.
• the resulting film or fiber is an elastic, flexible material that has an appreciable degree of strength. If a fine, flaky form is desired, the film can be converted to such a form by drying and then pulverizing or grinding it standard equipment.
• these polymers find many uses in film, fiber, fabric and similar forms. They are of particular utility in the disposable nonwoven industry where there is need for polymers which will absorb and retain water and ionic physiological fluids. An important feature of these polymers is their enhanced thickening property even in the presence of a salt. Specific applications include disposable diapers, medical-surgical supplies and personal care products. Such applications require a polymer which must imbibe the liquid to be absorbed rapidly and be a polymer that will not dissolve. Further, the fluid must be immobilized or congealed in some way to be retained.
• the materials may also be used as suitable additives to greatly increase the absorptive power of conventional absorbents such as cotton, wood pulp and other cellulosic absorbents used in applications such as wiping cloths, surgical sponges, catamenial devices, and the like.
• a disposable diaper there is an inner layer of a soft absorbent nonwoven material that absorbs and passes urine to an inner layer of fluffy fibrous absorbent material, wherein during the construction of this nonwoven fiber agglomerates or fibers of the polymers of this invention may be included and an additional impervious plastic layer, as polyethylene.
• a film of the copolymers of this invention may be used between the outer plastic layer and the inner fluffy absorbent layer.
• the instant copolymers can also be used as flocculants in water treatment, in metallurgical processes, in ore beneficiation and flotation, in agricultural applications such as in soil treatment or seed coating or in any applications where the inherent properties of the polymer are desirable, such as its thickening property in an aqueous medium.
• acrylic acid a cross-linking agent, a dispersant and a photoinitiator are mixed in a vessel. Then either a film or fibers are produced from the monomer mixture which, upon exposure to UV light, are rapidly polymerized.
• a cross-linking agent a cross-linking agent
• a dispersant a photoinitiator
• the monomer mixture can be prepared by following one of two simple procedures.
• One method is to dissolve a previously prepared and dried alkali metal or ammonium acrylate in water to which is then added a dispersant.
• a dispersant To the aqueous solution is then added a cross-linking agent which already contains a photoinitiator.
• Another method is to prepare the acrylate salt in situ by adding acrylic acid to the proper amount of cold aqueous base (e.g. KOH, NaOH or NH 4 OH) with cooling.
• To the aqueous solution is then added a cross-linking agent to which a photoinitiator was previously added; the dispersant is added last.
• aqueous monomer dispersion is spread to a desired thickness (e.g. by the use of Boston-Bradley adjustable blade, by spraying or other known means) on a suitable substrate (e.g. Mylar, polyethylene, paper, etc.).
• a suitable substrate e.g. Mylar, polyethylene, paper, etc.
• UV irradiation which polymerizes the monomer mixture into a soft, pliable form.
• this film can be dried in an oven at about 50°C for 1 to 15 min. After drying the film may still retain some flexibility or become brittle and flaky, depending on the length of drying.
• the aqueous monomer dispersion is thickened to the desired degree with a nonreactive thickening agent such as a cellulose derivative as for example hydroxypropyl cellulose, high molecular weight polyvinyl pyrrolidone. and the like; natural gums such as guar gum, locust bean gum, gum tragacanth; agar, naturally occuring hydrocolloids such as alginates and the like. Fibers are then spun from a spinneret in a regular manner and immediately exposed to UV irradiation.
• a nonreactive thickening agent such as a cellulose derivative as for example hydroxypropyl cellulose, high molecular weight polyvinyl pyrrolidone. and the like
• natural gums such as guar gum, locust bean gum, gum tragacanth
• agar naturally occuring hydrocolloids such as alginates and the like. Fibers are then spun from a spinneret in a regular manner and immediately exposed to UV ir
• DVT Demand Wettability Test
• a test diaper is constructed frcm a 4 inch diameter pad (10.16. cm.) using materials from a commercial diaper.
• a film prepared from a polymer to be tested for absorbency is placed in the center of the test diaper between two layers of fluff (wood pulp).
• a diaper without the polymer film is used as a blank.
• the demand-wettabiiity apparatus is a burette filled with the test fluid and firmly stoppered at the top, with an air bleed on the side, and a delivery orifice on the bottom connected by a flexible tube to the sample holder.
• the sample holder has an opening in the center which is connected to the flexible tube that leads to the delivery orifice of the burette.
• the sample holder is level with the air bleed opening in the burette.
• CT Compression Test
• Said pressure corresponds to the maximum pressure that is exerted on portions of a diaper when a toddler is picked up or held. This is 10 to 15 times the pressure that the diaper normally would experience.
• the sample is then weighed to determine the amount of fluid in grams retained per one gram of polymer.
• Static Test (ST) A weighed film sample is iinmersed in a test liquid for 10 minutes. It is then removed from the liquid, the excess liquid drained for a few seconds and then shaken lightly several times. The swelled sample is weighed again to determine the weight of liquid absorbed by the polymer.
• Table II below is presented data showing the absorbency properties of the various polymers of this invention. Each polymer in Table II is identified by the Example No. in which it was prepared. The absorbency tests in the Table below were carried out with simulated urine which had the following compositions: 97.09% distilled water, 1.94% urea, 0.80% sodium chloride, 0.11% magnesium sulfate heptahydrate and 0.06% calcium chloride. The values expressed in the Table are grams or milliliters of liquid (as indicated) absorbed per one gram of the copolymer.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Mechanical Engineering (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Absorbent Articles And Supports Therefor (AREA)
• Tyre Moulding (AREA)
• Materials For Medical Uses (AREA)
• Manufacture Of Macromolecular Shaped Articles (AREA)
• Polymerisation Methods In General (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

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• 1980
  • 1980-11-20 JP JP81500443A patent/JPS56501807A/ja active Pending
  • 1980-11-20 BR BR8009002A patent/BR8009002A/pt not_active IP Right Cessation
  • 1980-11-20 WO PCT/US1980/001567 patent/WO1981001850A1/en not_active Ceased
  • 1980-11-20 JP JP81500443A patent/JPS6221365B2/ja not_active Expired
  • 1980-11-20 DE DE8181900236T patent/DE3070797D1/de not_active Expired
  • 1980-11-20 EP EP81900236A patent/EP0042406B1/en not_active Expired
  • 1980-12-10 CA CA000366477A patent/CA1160984A/en not_active Expired
  • 1980-12-15 IE IE2625/80A patent/IE51167B1/en not_active IP Right Cessation
  • 1980-12-17 GR GR63674A patent/GR72805B/el unknown
  • 1980-12-18 BE BE0/203224A patent/BE886737A/fr not_active IP Right Cessation
  • 1980-12-19 IT IT8026838A patent/IT1209292B/it active
  • 1980-12-23 ES ES498118A patent/ES8205821A1/es not_active Expired
• 1981
  • 1981-01-05 MX MX185376A patent/MX156880A/es unknown
  • 1981-08-14 DK DK362981A patent/DK160254C/da not_active IP Right Cessation
• 1988
  • 1988-07-26 JP JP63186688A patent/JPS6465108A/ja active Pending

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