Method of making a polyimide in a low-boiling solvent
    2.
    发明授权
    Method of making a polyimide in a low-boiling solvent 失效
    在低沸点溶剂中制备聚酰亚胺的方法

    公开(公告)号:US06780960B2

    公开(公告)日:2004-08-24

    申请号:US10200825

    申请日:2002-07-22

    CPC classification number: C08G73/106 C08G73/1032

    Abstract: A method of making a solution of a polyimide from a diamine monomer and a dianhydride monomer is disclosed. A solution or slurry of one of the monomers in a solvent that boils at a temperature between about 80° C. and about 160° C. is prepared. The solution or slurry is heated to a temperature between about 80° C. and about 160° C. and the other monomer is slowly added to the solution or slurry. Polyamic acid that is formed quickly imidizes to form the polyimide.

    Abstract translation: 公开了从二胺单体和二酐单体制备聚酰亚胺溶液的方法。 制备在约80℃至约160℃的温度下沸腾的溶剂中的一种单体的溶液或浆液。 将溶液或浆液加热至约80℃至约160℃的温度,并将其它单体缓慢加入到溶液或浆液中。 形成的聚酰胺酸快速酰亚胺化以形成聚酰亚胺。

    Polyimide copolymer
    3.
    发明授权
    Polyimide copolymer 失效
    聚酰亚胺共聚物

    公开(公告)号:US06770733B2

    公开(公告)日:2004-08-03

    申请号:US10336343

    申请日:2003-01-03

    Abstract: A film-formable polyimide copolymer, which comprises two kinds of tetracarboxylic acid dianhydride consisting of (A) pyromellitic acid dianhydride and (B) 3,3′,4,4′-benzophenonetetracarboxylic acid dianhydride, and (C) 6-amino-2-(p-aminophenyl)benzimidazole has a heat-resistant dimensional stability without any deterioration of mechanical properties inherent in the polyimide resin when used as a film.

    Abstract translation: 一种可成膜聚酰亚胺共聚物,其包含由(A)均苯四酸二酐和(B)3,3',4,4'-二苯甲酮四羧酸二酐组成的两种四羧酸二酐和(C)6-氨基-2 - (对 - 氨基苯基)苯并咪唑具有耐热尺寸稳定性,而在用作膜时聚酰亚胺树脂固有的机械性能没有任何劣化。

    Method of synthesizing polyimides
    4.
    发明授权
    Method of synthesizing polyimides 有权
    聚酰亚胺的合成方法

    公开(公告)号:US06737502B2

    公开(公告)日:2004-05-18

    申请号:US10162669

    申请日:2002-06-06

    Inventor: Shean-Jeng Jong

    CPC classification number: C08G73/1039

    Abstract: A solvent-free, catalyst-free and contamination-free method of synthesis of polyimides is disclosed. The method includes polymerizing a diamine with 2,2-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) at a pressure of 0.1-760 mm Hg, preferably a reduced pressure at about 36 mm Hg, and a temperature of 90-400° C., preferably 10-240° C.

    Abstract translation: 公开了无溶剂,无催化剂和无污染的聚酰亚胺的合成方法。 该方法包括在0.1-760mm Hg的压力下,优选在约36mm Hg的减压下,将二胺与2,2-双(3,4-二羧基苯基)六氟丙烷二酐(6FDA) 400℃,优选10-240℃

    Polyimide precursors and polyimides
    8.
    发明授权
    Polyimide precursors and polyimides 有权
    聚酰亚胺前体和聚酰亚胺

    公开(公告)号:US06489431B1

    公开(公告)日:2002-12-03

    申请号:US09806487

    申请日:2001-04-12

    CPC classification number: C08G73/1039 C08G73/10

    Abstract: A polyimide precursor having a repeating unit represented by the following general formula (1), wherein R1 contains a bivalent organic group constituting a diamine having a hexafluoropropylidene group in its molecule represented by the following general formula (2), and the reduced viscosity is from 0.05 to 5.0 dl/g (in N-methylpyrrolidone at a temperature of 30° C., concentration: 0.5 g/dl), and a polyimide obtained by imidizing said precursor: (wherein R1 is a bivalent organic group constituting a diamine, A is a hydrogen atom, a linear alkyl group including a methyl group, or a trifluoromethyl group, and n is the number of a substituent on an aromatic ring and an integer of from 1 to 4).

    Abstract translation: 具有由以下通式(1)表示的重复单元的聚酰亚胺前体,其中R1分子由以下通式(2)表示的分子中包含构成具有六氟亚丙基的二胺的二价有机基团,并且比浓粘度来自 0.05〜5.0dl / g(在N-甲基吡咯烷酮中,温度30℃,浓度:0.5g / dl)和通过酰亚胺化所述前体获得的聚酰亚胺(其中R1是构成二胺的二价有机基团,A 是氢原子,包括甲基或三氟甲基的直链烷基,n是芳环上的取代基数和1至4的整数)。

    Synthetic fiber nonwoven web and method
    10.
    发明授权
    Synthetic fiber nonwoven web and method 失效
    合成纤维非织造纤维网及方法

    公开(公告)号:US06469130B1

    公开(公告)日:2002-10-22

    申请号:US09626014

    申请日:2000-07-26

    Abstract: A nonwoven web and method of preparing a novel nonwoven web of synthetic fiber are disclosed. An aqueous solution amide crosslinked synthetic precursor polymer is extruded under defined conditions through a plurality of die orifices to form a plurality of threadlines. The threadlines are attenuated with a defined primary gaseous source to form fiber under conditions of controlled macro scale turbulence and under conditions sufficient to permit the viscosity of each threadline, as it leaves a die orifice and for a distance of no more than about 8 cm, to increase incrementally with increasing distance from the die, while substantially maintaining uniformity of viscosity in the radial direction, at a rate sufficient to provide fiber having,the desired attenuation and mean fiber diameter without significant fiber breakage. The attenuated threadlines are dried with a defined secondary gaseous source. The resulting fibers are deposited randomly on a moving foraminous surface to form a substantially uniform web. The moving foraminous surface is positioned about 10 to about 100 cm from the last gaseous source to contact the threadlines. The fibers have a mean fiber diameter in the range of about 0.1 to 30 &mgr;m and are substantially free of shot. The attenuating and drying steps are carried out under conditions of controlled macro scale turbulence.

    Abstract translation: 公开了一种制备合成纤维的新的非织造纤维网的非织造纤维网和方法。 将水溶液酰胺交联的合成前体聚合物通过多个模孔在规定的条件下挤出以形成多条丝线。 在受控的大规模湍流的条件下和在足以允许每个丝线的粘度的条件下,当纱线离开模口并且距离不超过约8厘米的条件下,丝线用限定的主要气态源减弱以形成纤维, 随着距离模具的距离的增加而逐渐增加,同时基本上保持径向粘度的均匀性,其速率足以提供具有期望的衰减和平均纤维直径而没有显着纤维断裂的纤维。 衰减的丝线用限定的二次气源干燥。 所得纤维随机地沉积在移动的多孔表面上以形成基本均匀的网。 移动的多孔表面位于离最后气态源约10至约100厘米处以接触线。 纤维的平均纤维直径在约0.1至30μm的范围内,并且基本上没有喷射。 衰减和干燥步骤在受控的大规模湍流条件下进行。

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