Vinyl chloride resin with low viscosity for foaming application and method of preparing the same
    1.
    发明授权
    Vinyl chloride resin with low viscosity for foaming application and method of preparing the same 有权
    用于发泡应用的低粘度氯乙烯树脂及其制备方法

    公开(公告)号:US08691927B2

    公开(公告)日:2014-04-08

    申请号:US13377466

    申请日:2010-06-10

    IPC分类号: C08F114/06 C08F2/24

    摘要: Provided are a vinyl chloride-based resin formed by polymerization of vinyl chloride-based small seed particles having an average particle diameter range of 0.15 μm to 0.5 μm prepared by emulsion polymerization and vinyl chloride-based large seed particles having an average particle diameter range of 0.51 μm to 0.8 μm prepared by micro-suspension polymerization, in which a content ratio (weight ratio) of the large seed particles to the small seed particles is in a range of 1 to 2, and a method of preparing the vinyl chloride-based resin. Excellent low viscosity characteristics of the vinyl chloride resin at high and low shear rates may be obtained by controlling the particle size of the small seed prepared by emulsion polymerization.

    摘要翻译: 本发明提供一种氯乙烯系树脂,其通过聚合具有通过乳液聚合制备的平均粒径范围为0.15μm至0.5μm的氯乙烯基小种子颗粒和平均粒径范围为氯乙烯的大型种子颗粒 通过微悬浮聚合制备的0.51μm〜0.8μm,其中大种子颗粒与小种子颗粒的含量比(重量比)在1至2的范围内,以及制备氯乙烯基 树脂。 通过控制通过乳液聚合制备的小种子的粒度,可以获得高低剪切速率下氯乙烯树脂的优异的低粘度特性。

    METHOD FOR THE MULTI-STEP PREPARATION OF HALOGEN-CONTAINING COMPOSITE LATEX HAVING ASSOCIATIVE GROUPS
    2.
    发明申请
    METHOD FOR THE MULTI-STEP PREPARATION OF HALOGEN-CONTAINING COMPOSITE LATEX HAVING ASSOCIATIVE GROUPS 审中-公开
    具有相关组合的含有氢的复合材料的多步法制备方法

    公开(公告)号:US20110077342A1

    公开(公告)日:2011-03-31

    申请号:US12995768

    申请日:2009-05-11

    摘要: “The invention relates to a method for preparing a composite latex, including(a) a first step of free radical emulsion or microsuspension polymerization or copolymerization, leading to the production of a first polymer latex, and(b) a second step of free radical microsuspension, emulsion, or suspension polymerization or copolymerization in the presence of the first polymer latex obtained in the first step (a), characterized in that the first polymer forming the latex obtained in step (a) is a halogen-containing vinyl polymer and the polymer formed in step (b) is an associative copolymer, preferably compatible with the halogen-containing vinyl polymer, which contains units from a first monomer (A) and units from a second monomer (B) having at least one associative group; however the nature of both polymers are capable of being reversed. The invention also relates to a latex or polymer suspension obtained by said method and to a polymer composition obtained from the latter, as well as to the use of said latex, from said suspension or said polymer composition, for manufacturing rigid or plasticized materials.”

    摘要翻译: “本发明涉及一种制备复合胶乳的方法,包括(a)自由基乳液或微悬浮聚合或共聚的第一步骤,导致制备第一聚合物胶乳,和(b)第二步自由基 在第一步骤(a)中获得的第一聚合物胶乳存在下进行微悬浮,乳液或悬浮聚合或共聚反应,其特征在于,形成步骤(a)中获得的胶乳的第一聚合物是含卤乙烯基聚合物, 在步骤(b)中形成的聚合物是优选与含卤素的乙烯基聚合物相容的缔合共聚物,其含有来自第一单体(A)的单元和具有至少一个缔合基团的第二单体(B)的单元; 然而,两种聚合物的性质都能够被逆转。 本发明还涉及通过所述方法获得的胶乳或聚合物悬浮液和由后者获得的聚合物组合物,以及所述悬浮液或所述聚合物组合物用于制造刚性或增塑材料的所述胶乳的用途。

    Rigid, closed-cell, graft-polymer foam; rigid flexible cellular foam; rigid flexible cellular foam mixtures; and method for manufacturing a rigid, closed-cell, graft-polymer foam
    3.
    发明授权
    Rigid, closed-cell, graft-polymer foam; rigid flexible cellular foam; rigid flexible cellular foam mixtures; and method for manufacturing a rigid, closed-cell, graft-polymer foam 有权
    刚性,闭孔,接枝聚合物泡沫; 刚性柔性细胞泡沫; 刚性柔性细胞泡沫混合物; 以及用于制造刚性,闭孔,接枝聚合物泡沫的方法

    公开(公告)号:US07879922B2

    公开(公告)日:2011-02-01

    申请号:US11942979

    申请日:2007-11-20

    IPC分类号: C08F2/48 C08F259/04 C08J9/04

    摘要: Expanded products, more specifically, rigid or semi-flexible foams of low density from 1.5 to 12 lbs/ft3 or more, with closed cells can be manufactured. The products have a PVC backbone with branches with methacrylate crosslinked with isocyanate through a reaction activated by ultraviolet or microwave radiation. The use of polyfunctional monomers that are sensitive to irradiation yields a higher cross-link density, which improves the physical and mechanical properties such as hardness, resistance to abrasion, ductility, and resistance to friction. The selection of monomers and oligomers allows the manufacturer to determine of the final properties of the foam. The process yields foams with extreme hardness and better shear factors making the foam an ideal product for aerospace and windmill use. These physical properties emerge during the post-curing process, preferably by use of compounds based on methacrylates in dispersion with PVC and isocyanates.

    摘要翻译: 可以制造具有闭孔的膨胀产品,更具体地,具有1.5至12磅/平方英尺或更小的低密度的刚性或半柔性泡沫。 该产品具有通过紫外线或微波辐射激活的反应通过异氰酸酯与甲基丙烯酸酯交联的具有支链的PVC骨架。 使用对辐射敏感的多官能单体产生更高的交联密度,这提高了物理和机械性能,例如硬度,耐磨性,延展性和耐摩擦性。 单体和低聚物的选择允许制造商确定泡沫的最终性能。 该方法产生具有极高硬度和更好的剪切因子的泡沫,使泡沫成为航空航天和风车使用的理想产品。 这些物理性质在后固化过程中出现,优选通过使用与PVC和异氰酸酯分散的基于甲基丙烯酸酯的化合物。

    Living radical graft copolymerization of vinyl monomers initiated from the structural defects of polyvinylchloride
    6.
    发明授权
    Living radical graft copolymerization of vinyl monomers initiated from the structural defects of polyvinylchloride 失效
    从聚氯乙烯的结构缺陷引发乙烯基单体的活性自由基接枝共聚

    公开(公告)号:US06437044B1

    公开(公告)日:2002-08-20

    申请号:US09770141

    申请日:2001-01-26

    IPC分类号: C08F400

    摘要: A graft copolymer composition and the preparation of the composition by living radical polymerization is disclosed. The polymerization reaction can be initiated at active chlorine sites on the poly(vinyl chloride) backbone in conjunction with a transition metal catalyst and an optional ligand. The graft copolymers are useful as, among others, compatibilizers for blends and alloys, as high heat distortion temperature poly(vinyl chloride) materials, as impact modifiers, and permanently plasticized materials.

    摘要翻译: 公开了接枝共聚物组合物和通过活性自由基聚合制备组合物。 聚合反应可以在聚(氯乙烯)主链的活性氯位上与过渡金属催化剂和任选的配体一起引发。 接枝共聚物尤其可用作混合物和合金的增容剂,作为高热变形温度聚(氯乙烯)材料,作为抗冲改性剂和永久增塑的材料。

    Multiple phase polymeric vinyl chloride systems and related core-shell particles
    7.
    发明申请
    Multiple phase polymeric vinyl chloride systems and related core-shell particles 失效
    多相聚合氯乙烯体系和相关的核 - 壳颗粒

    公开(公告)号:US20020051884A1

    公开(公告)日:2002-05-02

    申请号:US09954371

    申请日:2001-09-17

    IPC分类号: B32B005/16

    CPC分类号: C08F259/04 Y10T428/2998

    摘要: An emulsion or suspension polymer comprising a vinyl chloride polymeric core and an acrylic ester-acrylonitrile polymeric shell is disclosed. The emulsion polymer is preferably prepared using a two-stage process. In the first stage, a vinyl chloride monomer is polymerized or copolymerized to form a first phase of a polymeric hard core having a relatively high chlorine content. In a second stage, the soft acrylic ester-acrylonitrile copolymer is made in situ in a reaction mixture comprising the first phase. The product provides both flame retardancy and low MFFT, and is useful in a variety of coating and binding applications.

    摘要翻译: 公开了一种包含氯乙烯聚合物芯和丙烯酸酯 - 丙烯腈聚合物壳的乳液或悬浮聚合物。 乳液聚合物优选使用两阶段方法制备。 在第一阶段中,将氯乙烯单体聚合或共聚以形成具有较高氯含量的聚合物硬核的第一相。 在第二阶段中,软质丙烯酸酯 - 丙烯腈共聚物在包含第一相的反应混合物中原位制备。 该产品提供阻燃性和低MFFT,并且可用于各种涂层和结合应用。

    Graft copolymerization in supercritical media

    公开(公告)号:US5663237A

    公开(公告)日:1997-09-02

    申请号:US490954

    申请日:1995-06-15

    摘要: A supercritical graft copolymerization process is described which includes the steps of: adding a polymer into a high pressure reactor; adding a free radically polymerizable monomer into the reactor; adding a free radical polymerization initiator; adding a sufficient amount of a supercritical solvent to dissolve at least a portion of the polymer and the monomer when supercritical conditions are achieved inside the reactor; and heating and pressurizing the reactor to achieve supercritical conditions therein for a time sufficient to effect a graft copolymerization on the polymer by the polymerizing monomer which forms at least one side chain on the polymer. In general, the reaction pressure will range from 70 atm. to 200 atm. and the reaction temperature will range from 50.degree. C. to 90.degree. C. In the examples provided above, the supercritical solvent was carbon dioxide. However, there is no need to limit the application to such in that the process steps will be equally applicable to other supercritical solvents which have the ability to dissolve at least a portion of the polymer and grafting monomer when at supercritical conditions in the reactor. In general, the reaction time will range from one to six hours, although shorter and longer reaction times are contemplated within the scope of this invention, the range merely being listed as the best mode known to the inventors at the time of the filing of this application. Specifically, the graft copolymerization process has been demonstrated when the polymer is a polyolefin, particularly polypropylene and poly(vinyl chloride), although other backbone polymers are certainly contemplated as within the scope of this invention. Specific examples are discussed wherein the monomer used to effect the graft copolymerization are selected from the group consisting of styrene and acrylic acid when the polyolefin polymer is polypropylene and also specifically discussed is a poly(vinyl chloride) polymer wherein the grafted polymer is based on a monomer of vinyl acetate.

    Heat resistant polyvinyl chloride copolymer and preparation process of
the copolymer
    10.
    发明授权
    Heat resistant polyvinyl chloride copolymer and preparation process of the copolymer 失效
    共聚物耐热聚氯乙烯共聚物及其制备方法

    公开(公告)号:US5166271A

    公开(公告)日:1992-11-24

    申请号:US401833

    申请日:1989-09-01

    IPC分类号: C08F259/04

    CPC分类号: C08F259/04

    摘要: A heat resistant polyvinyl chloride copolymer or a heat and impact resistant polyvinyl chloride copolymer is prepared by conducting graft copolymerization of N-substituted maleimide on a vinyl chloride resin or a rubber containing vinyl chloride resin.The graft copolymerization reaction is carried out in the presence of a radical polymerizable monomer which is (1) liquid at the polymerization temperature, (2) capable of dissolving the N-substituted maleimide at the temperature, (3) 70.degree. C. or more in glass transition temperature of the polymer thereof, and (4) used in an amount sufficient to dissolve the N-substituted maleimide.