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    • 1. 发明授权
    • Controlled polymerization
    • 受控聚合
    • US08178637B2
    • 2012-05-15
    • US12831796
    • 2010-07-07
    • Dane Kenton ParkerFrank James FeherViswanath Mahadevan
    • Dane Kenton ParkerFrank James FeherViswanath Mahadevan
    • C08F36/06C08F36/04C08F36/08
    • C08F297/048C08F2/22C08F2/38C08F12/08C08F293/00C08F293/005C08F2438/00C08F2438/01C08F2438/02C08F2438/03C08G61/08C08G2261/418C08L53/00C08L53/02C08L2666/02
    • The present invention discloses an emulsion polymerization process that comprises: (1) preparing an aqueous polymerization medium which is comprised of (a) at least one monomer, (b) a polymerization control agent, and an emulsifier, wherein the emulsifier is prepared in-situ within the aqueous polymerization medium; and (2) initiating polymerization of said monomer within the aqueous polymerization medium. The subject invention more specifically reveals an emulsion polymerization process that comprises: (1) preparing a monomer solution which is comprised of (a) at least one monomer, (b) a conjugate acid of a surfactant with a pKa of less than 14, and (c) a controlled free radical polymerization agent; (2) preparing an aqueous medium which is comprised of (a) water, and (b) a conjugate base of a weak acid wherein the pKb of the base is less than 14; and (3) mixing the monomer solution with the aqueous medium under conditions that result in the in-situ formation of an emulsifier, and (4) initiating free radical polymerization.
    • 本发明公开了一种乳液聚合方法,其包括:(1)制备由(a)至少一种单体,(b)聚合控制剂和乳化剂组成的水性聚合介质,其中, 位于水性聚合介质中; 和(2)在水性聚合介质中引发所述单体的聚合。 本发明更具体地揭示了乳液聚合方法,其包括:(1)制备单体溶液,其由(a)至少一种单体,(b)pKa小于14的表面活性剂的共轭酸组成,以及 (c)受控自由基聚合剂; (2)制备由(a)水和(b)弱酸的共轭碱组成的水性介质,其中碱的pKb小于14; 和(3)在导致乳化剂原位形成的条件下将单体溶液与水性介质混合,和(4)引发自由基聚合。
    • 2. 发明授权
    • Controlled polymerization
    • 受控聚合
    • US07767775B2
    • 2010-08-03
    • US11454742
    • 2006-06-16
    • Dane Kenton ParkerFrank James FeherViswanath Mahadevan
    • Dane Kenton ParkerFrank James FeherViswanath Mahadevan
    • C08F4/00
    • C08F297/048C08F2/22C08F2/38C08F12/08C08F293/00C08F293/005C08F2438/00C08F2438/01C08F2438/02C08F2438/03C08G61/08C08G2261/418C08L53/00C08L53/02C08L2666/02
    • The present invention discloses an emulsion polymerization process that comprises: (1) preparing an aqueous polymerization medium which is comprised of (a) at least one monomer, (b) a polymerization control agent, and an emulsifier, wherein the emulsifier is prepared in-situ within the aqueous polymerization medium; and (2) initiating polymerization of said monomer within the aqueous polymerization medium. The subject invention more specifically reveals an emulsion polymerization process that comprises: (1) preparing a monomer solution which is comprised of (a) at least one monomer, (b) a conjugate acid of a surfactant with a pKa of less than 14, and (c) a controlled free radical polymerization agent; (2) preparing an aqueous medium which is comprised of (a) water, and (b) a conjugate base of a weak acid wherein the pKb of the base is less than 14; and (3) mixing the monomer solution with the aqueous medium under conditions that result in the in-situ formation of an emulsifier, and (4) initiating free radical polymerization.
    • 本发明公开了一种乳液聚合方法,其包括:(1)制备由(a)至少一种单体,(b)聚合控制剂和乳化剂组成的水性聚合介质,其中, 位于水性聚合介质中; 和(2)在水性聚合介质中引发所述单体的聚合。 本发明更具体地揭示了乳液聚合方法,其包括:(1)制备单体溶液,其由(a)至少一种单体,(b)pKa小于14的表面活性剂的共轭酸组成,以及 (c)受控自由基聚合剂; (2)制备由(a)水和(b)弱酸的共轭碱组成的水性介质,其中碱的pKb小于14; 和(3)在导致乳化剂原位形成的条件下将单体溶液与水性介质混合,和(4)引发自由基聚合。
    • 3. 发明授权
    • Surfactantless synthesis of amphiphilic cationic block copolymers
    • 两亲性阳离子嵌段共聚物的无表面活性合成
    • US07671152B2
    • 2010-03-02
    • US11583424
    • 2006-10-19
    • Dane Kenton ParkerJoseph John Kulig
    • Dane Kenton ParkerJoseph John Kulig
    • C08F2/00C08F236/00
    • C08F293/005C08F293/00C08F2438/03C08L53/00C08L53/02C08L2666/02
    • The present invention is directed to a method of producing an amphiphilic block copolymer, including the steps of: (1) preparing a first aqueous polymerization medium which is comprised of (a) 4-vinylpyridine, (b) a trithiocarbonate RAFT agent, and an emulsifier, wherein the emulsifier is prepared in-situ within the aqueous polymerization medium by the reaction of a latent surfactant with a surfactant activator; (2) polymerizing the 4-vinylpyridine within the first aqueous polymerization medium in the presence of a first free radical initiator to produce a poly(4-vinylpyridine); (3) protonating the poly(4-vinylpyridine) to form a protonated poly(4-vinylpyridine) RAFT macroinitiator; (4) preparing a second aqueous polymerization medium which is comprised of the protonated poly(4-vinylpyridine) RAFT macroinitiator and a monomer containing ethylenic unsaturation but is exclusive of a surfactant; and (5) polymerizing the protonated poly(4-vinylpyridine) RAFT macroinitiator and monomer containing ethylenic unsaturation within the second aqueous medium in the presence of a second free radical initiator and a temperature less than 100° C. to produce an amphiphilic block copolymer of the 4-vinylpyridine and monomer containing ethylenic unsaturation.
    • 本发明涉及一种制备两亲性嵌段共聚物的方法,包括以下步骤:(1)制备第一种水性聚合介质,其包含(a)4-乙烯基吡啶,(b)三硫代碳酸酯RAFT试剂和 乳化剂,其中乳化剂通过潜在表面活性剂与表面活性剂活化剂的反应在水性聚合介质中原位制备; (2)在第一含水聚合介质中在第一自由基引发剂存在下聚合4-乙烯基吡啶以产生聚(4-乙烯基吡啶); (3)使聚(4-乙烯基吡啶)质子化以形成质子化的聚(4-乙烯基吡啶)RAFT大分子引发剂; (4)制备由质子化的聚(4-乙烯基吡啶)RAFT大分子引发剂和含有烯属不饱和单体但不包括表面活性剂的单体组成的第二水性聚合介质; 和(5)在第二自由基引发剂和低于100℃的温度存在下,在第二水性介质中聚合质子化聚(4-乙烯基吡啶)RAFT大分子引发剂和含有烯属不饱和单体的单体,以产生两亲性嵌段共聚物 4-乙烯基吡啶和含有烯属不饱和单体的单体。
    • 4. 发明授权
    • Oxathiazaphospholidine free radical control agent
    • Oxathiazaphospholidine自由基控制剂
    • US07462674B2
    • 2008-12-09
    • US11975313
    • 2007-10-18
    • Dane Kenton Parker
    • Dane Kenton Parker
    • C08F2/00
    • C08F2/38C07F9/6584
    • This invention discloses a process for producing a polymer by controlled polymerization which comprises polymerizing at least one monomer in the presence of a free radical control agent of the structural formula: (Z)-(R1)n, wherein n represents an integer from 1 to about 6; wherein Z represents an aromatic or aliphatic moiety containing from 1 to about 20 carbon atoms; wherein R1 represents a moiety of the structural formula: wherein R2 represents a moiety selected from the group consisting of alkyl groups, alkenyl groups, alkynyl groups, aryl groups, heteroaryl groups, and alkaryl groups; wherein the alky groups, alkenyl groups, alkynyl groups, aryl groups, heteroaryl groups, and alkaryl groups can be substituted, unsubstituted, linear, branched or cyclic; and wherein Ar represents a p-alkoxyphenyl group having an alkoxy moiety that contains from 1 to 8 carbon atoms.
    • 本发明公开了一种通过控制聚合制备聚合物的方法,该方法包括在结构式为(Z) - (R1)n的自由基控制剂存在下使至少一种单体聚合,其中n表示1至 约6; 其中Z表示含有1至约20个碳原子的芳族或脂族部分; 其中R1表示结构式的部分:其中R2表示选自烷基,烯基,炔基,芳基,杂芳基和烷芳基的部分; 其中烷基,烯基,炔基,芳基,杂芳基和烷芳基可以是取代的,未取代的,直链的,支链的或环状的; 并且其中Ar表示具有含有1至8个碳原子的烷氧基部分的对 - 烷氧基苯基。
    • 10. 发明授权
    • Synthesis of stable nitrile oxide compounds
    • 稳定的氧化腈化合物的合成
    • US06355826B1
    • 2002-03-12
    • US09603590
    • 2000-06-26
    • Dane Kenton Parker
    • Dane Kenton Parker
    • C07C29106
    • C08K5/32C07C291/06C08L21/00
    • This invention discloses a process for the synthesis of stable aryl nitrile oxides which comprises the sequential steps of (1) halomethylating a halomethyl group onto a substituted aromatic compounds wherein said halomethyl group is halomethylated onto a position that is ortho to at least one of the substituent groups on the substituted aromatic compound; (2) converting the ortho halomethylated-substituted aromatic compound into an ortho-substituted aromatic aldehyde by reacting the ortho halomethylated-substituted aromatic compound with a salt selected from the group consisting of sodium 2-nitropropane and potassium 2-nitropropane in a lower alcohol solvent; (3) converting the ortho-substituted aromatic aldehyde into an ortho-substituted aromatic; and (4) converting the ortho-substituted aromatic oxime into the ortho-substituted aryl nitrile oxide by reacting the ortho-substituted aromatic oxime with an aqueous sodium hypochlorite solution.
    • 本发明公开了一种用于合成稳定的芳基氧化腈的方法,其包括以下顺序步骤:(1)将卤代甲基卤化成取代的芳族化合物,其中所述卤代甲基被卤甲基化至至少一个取代基的位置 取代芳族化合物上的基团; (2)通过邻位卤代甲基取代的芳族化合物与选自2-羟基丙烷钠和2-硝基丙烷钾的盐在低级醇溶剂中反应,将邻甲基取代的芳族化合物转化为邻位取代的芳族醛 ; (3)将邻位取代的芳族醛转化为邻位取代的芳香族; 和(4)通过使邻位取代的芳族肟与次氯酸钠水溶液反应,将邻位取代的芳族肟转化成邻位取代的芳基氧化腈。