Abstract: An adsorbent comprising a porous copolymer produced by copolymerizing a cross-linkable monomer and a mono-ethylenically unsaturated monomer, said copolymer having pores of an average pore diameter (d) of 500 A to 6,000 A and having such a broad pore diameter distribution that the pore volume having a pore diameter in the range of from 0.5 d to 2 d is not more than 60% of the total pore volume in the copolymer. By the use of such a porous copolymer having a specific composition and pore characteristics, organic compounds (e.g. toxic compounds) adsorbed on the proteins (e.g. plasma proteins) present in intercellular and/or extracellular liquids (e.g. blood) can be effectively adsorption-removed. Especially when the present adsorbent is used for purification of blood, it is advantageously subjected to such a pretreatment that plasma proteins are adsorbed on the adsorbent and then crosslinked with a crosslinking agent.
Type:
Grant
Filed:
June 22, 1978
Date of Patent:
May 13, 1980
Assignee:
Asahi Kasei Kogyo Kabushiki Kaisha
Inventors:
Tsutomu Abe, Akihiko Ikeda, Tokio Sakurai
Abstract: Hard, infusible, discrete beads of crosslinked copolymer are prepared by free-radical catalyzed polymerization of a monomer mixture in aqueous dispersion wherein oxygen is incorporated in the monomer mixture. Ion exchange resins having improved mechanical strength are obtained by attaching functional groups to the copolymer.
Abstract: What is disclosed is a pearl polymer product, a method of making the same, and the use thereof as a carrier for biologically active materials, said product being composed of hollow pearl particles having a diameter from 5 to 1000 microns and consisting of a cross-linked polymer which is a cross-linked homopolymer or copolymer comprising at least one member selected from the group consisting of acrylamide, methacrylamide, methylene-bis-acrylamide and methylene-bis-methacrylamide, said polymer containing at least 5 percent by weight of a monomer having at least two carbon-carbon double bonds which are activated by a neighboring phenyl group or carbonyl group, said polymer further being of a composition such that x+3y.gtoreq.40, where x is the percent by weight in the polymer of acrylamide and methacrylamide and y is the percent by weight in the polymer of methylene-bis-acrylamide and methylene-bis-methacrylamide.
Type:
Grant
Filed:
May 15, 1978
Date of Patent:
February 26, 1980
Assignee:
Rohm GmbH
Inventors:
Dieter Kraemer, Hermann Plainer, Waldemar Schleier
Abstract: An ion-exchange hollow fiber is prepared by introducing into the wall of the fiber polymerizable liquid monomers, and polymerizing the monomers therein to form solid, insoluble, cross-linked, ion-exchange resin particles which embed in the wall of the fiber. Excess particles blocking the central passage or bore of the fiber are removed by forcing liquid through the fiber. The fibers have high ion-exchange capacity, a practical wall permeability and good mechanical strength even with very thin wall dimensions. Experimental investigation of bundles of ion-exchange hollow fibers attached to a header assembly have shown the fiber to be very efficient in removing counterions from solution.
Type:
Grant
Filed:
March 5, 1975
Date of Patent:
February 5, 1980
Assignee:
California Institute of Technology
Inventors:
Alan Rembaum, Shiao-Ping S. Yen, Elias Klein
Abstract: Hybrid copolymers are prepared by at least partially filling the macropores of a macroreticular copolymer with a guest crosslinked copolymer of either the same monomers or a copolymer of different type monomers. The hybrid copolymers can be readily converted into ion exchange resins. Such resins have markedly improved physical and chemical properties, including improved ion exchange properties.
Abstract: This invention relates to nitrogenous vinylbenzyl and bis-(vinylbenzyl) compounds for use in the preparation of polymers, especially ion exchange resins, and to processes for the preparation of the monomers and polymers. More particularly, it relates to the preparation, polymerization, and use of the new nitrogenous compounds as crosslinking agents and/or function-introducing agents.
Type:
Grant
Filed:
October 13, 1977
Date of Patent:
February 20, 1979
Assignee:
Rohm and Haas Company
Inventors:
David H. Clemens, Frank J. Glavis, deceased
Abstract: The invention relates to preparation of synthetic macroporous ion-exchanaging materials by a ternary copolymerization of hydrophilic monomers containing non-ionogenous groups with monomers containing ionogenous groups and cross-linking monomers in an aqueous dispersion in the presence of inert components and suspension stabilizers. Hydroxyalkyl, oligoglycol and polyglycol esters and N-substituted or unsubstituted amides of acrylic and methacrylic acid are used as the hydrophilic monomers; compounds CH.sub.2 .dbd.C(R)COX, where R = H or CH.sub.3, X = --OR.sub.1 N(R.sub.2)R.sub.3, --OR.sub.1 SO.sub.3 H, --NHR.sub.1 N(R.sub.2)R.sub.3 or --HNR.sub.1 SO.sub.3 H, R.sub.1 = alkylene and R.sub.2 and R.sub.
Type:
Grant
Filed:
January 29, 1975
Date of Patent:
February 13, 1979
Assignee:
Ceskoslovenska akademie ved
Inventors:
Jiri Coupek, Otakar Mikes, Petr Strop, Miroslava Krivakova
Abstract: A fluorinated copolymer having 1 to 50 mole % of a component having functional group of carboxylic acid group or a group which can be converted to carboxylic acid group, is produced by copolymerizing a fluorinated ethylenic unsaturated monomer and a functional monomer having the functional group in the presence of a polymerization initiator source in an aqueous medium under the pressure of higher than 7 kg/cm.sup.2 whereby the copolymer having high molecular weight (T.sub.Q of higher than 150.degree. C.) and an ion exchange capacity of 0.5 to 4 meq/g dry polymer is produced.
Abstract: This invention relates to vinylbenzyl and crosslinking bis-(vinylbenzyl) monomers for use in the preparation of polymers, especially ion exchange resins, and to methods for the preparation of the monomers and polymers. It is particularly concerned with the preparation, polymerization, and use of new nitrogenous monomers as crosslinking agents and/or function-introducing agents.
Abstract: A process for the production of a particulate ion exchange material which comprises heating an inorganic material to produce a porous inert inorganic substrate, adsorbing an organic monomer into the substrate and polymerizing the adsorbed monomer so that the resultant polymer is retained within the pores of the substrate, and, if necessary, introducing ion exchange functional groups into the polymer.
Type:
Grant
Filed:
February 19, 1976
Date of Patent:
December 19, 1978
Assignee:
National Research Development Corporation
Abstract: Novel crosslinked ion exchange resins derived from dimethylaminoethyl methacrylate are disclosed together with their process of manufacture by suspension polymerization preferably utilizing a trialkylamine phase extender. Trialkylamines are found to be useful generally as phase extenders for the preparation of other polymeric materials by the known methods of suspension polymerization.
Abstract: A process of polymerizing a monomer mixture containing from 3 to 100% of amines containing two or more allyl groups which method comprises reacting a solution of the monomer mixture in a concentrated mineral acid in the presence of a polymerization initiator and isolating the polymer salt so formed.
Type:
Grant
Filed:
April 21, 1976
Date of Patent:
October 24, 1978
Assignees:
ICI Australia Limited, Commonwealth Scientific and Industrial Research Organization
Abstract: A process for producing carboxyl cationites which comprises dissolution of comonomers such as methacrylic or acrylic acid and a vinyl-containing amide such as hexahydro-1,3,5-triacryloyltriazine, N, N'-methylenediacrylamide, N, N'-ethylenedimethacrylamide or N, N'-hexamethylenedimethacrylamide as well as an initiator of radical polymerization in a 5-50% acetic acid. Weight ratio between the unsaturated carboxylic acid and vinyl-containing amide is varied from 3:1 to 12:1; concentration of said comonomers in a 5-50% acetic acid is varied within the range of from 10 to 30%. The resulting reaction mixture is dispersed in polyethylsiloxane or polymethylphenylsiloxane liquid at a weight ratio between the reaction mixture and said silicone liquid ranging from 1:3 to 1:5 respectively. Thereafter, copolymerization is effected in a suspension at a temperature ranging from 20.degree. to 100.degree. C.
Abstract: The phosphonated fluorotelomers of this invention are, or can easily be made to be, hydrophilic. When blended with inert fibrous materials they can be used to make diaphragms for electrolytic cells, particularly for chlor-alkali cells used in the production of chlorine, hydrogen and sodium hydroxide from brine. Ion-exchange membranes can also be made from these fluorotelomers. The fluorotelomers can be made by using free radical phosphonyl esters to terminate the polymerization of the selected fluorocarbons.
Abstract: Anion exchange resins containing borohydride counter ions display essentially the same chemical activity as solutions of sodium borohydride but have the added advantage that products treated therewith are not contaminated with sodium ions or borate ions. Thus, alcohols can now be freed of carbonyl components without thereby being contaminated with borate; metal ions, such as silver, can be reduced to the free element; metal ions of groups IV-A to VI-A can be converted to volatile metal hydrides; and transition metal ions can be converted to the boride. The anion exchange resin is prepared by treating a strong base anion exchanger with aqueous sodium borohydride or sodium cyanoborohydride. Regeneration of the borohydride form from the borate proceeds directly with aqueous sodium borohydride.
Abstract: Disclosed is an improved hydraulically impermeable cation exchange membrane for an electrolytic cell and a method for the preparation of such a membrane using a copolymeric substrate and applying to the surface thereof by means of plasma polymerization, a very thin top coating of a second polymeric material to drastically reduce the permeability of the substrate material with a minimal effect upon the bulk properties of the resultant membrane. Such top coatings may be applied over the basic substrate or over surface treated substrates to enhance the chemical resistivity of the membrane to chemical breakdown occasioned by the electrolyte within the electrolytic cell.