会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明申请
    • PROCESS FOR PREPARING A POLYESTER RESIN
    • 制备聚酯树脂的方法
    • WO2006063908A1
    • 2006-06-22
    • PCT/EP2005/055955
    • 2005-11-14
    • AKZO NOBEL N.V.WINTERS, RobinDE VOS, Siebe, CornelisVENDERBOSCH, Rudolf, Anthonius, MariaPARDOEN, Johannes, Adrianus
    • WINTERS, RobinDE VOS, Siebe, CornelisVENDERBOSCH, Rudolf, Anthonius, MariaPARDOEN, Johannes, Adrianus
    • C08G63/91C08G63/16C08G81/00G03G9/087
    • C08G63/914C08G63/78
    • The present invention relates to a process for preparing a polyester resin having a gel content of less than 0.45 wt%, based on the total weight of the polyester resin, and a glass transition temperature of between 40 and 70°C, comprising the step of reacting a polyester resin precursor with a chain extender which is different from the building blocks of the polyester precursor resin, optionally in the presence of a catalyst, at a temperature between 170 and 300 °C in a continuous reactor, wherein the polyester resin precursor comprises a functional group present as end group selected from hydroxyl or carboxyl, and optionally a functional group in the polyester resin precursor backbone selected from hydroxyl, carboxyl, amine, and carbonate, and the molar ratio of the functional group in the polyester resin precursor backbone to the functional group present as end group is at most 10:1. The invention further pertains to a polyester resin having a gel content of less than 0.45 wt%, based on the total weight of the polyester resin, and a glass transition temperature of between 40 and 70°C, which is prepared from a polyester resin precursor and a chain extender which is different from the building blocks of the polyester precursor resin.
    • 本发明涉及一种制备聚酯树脂的方法,该聚酯树脂的凝胶含量基于聚酯树脂的总重量小于0.45重量%,玻璃化转变温度在40-70℃之间,包括以下步骤: 任选地在催化剂存在下,在连续反应器中使聚酯树脂前体与不同于聚酯前体树脂的结构单元的增链剂反应,其中聚酯树脂前体包括 存在于作为选自羟基或羧基的端基的官能团,以及选自羟基,羧基,胺和碳酸酯的聚酯树脂前体骨架中的官能团,以及聚酯树脂前体骨架官能团与 作为末端基团的官能团最多为10:1。 本发明还涉及一种聚酯树脂,该聚酯树脂的凝胶含量基于聚酯树脂的总重量小于0.45重量%,玻璃化转变温度为40-70℃,其由聚酯树脂前体 和与聚酯前体树脂的结构单元不同的扩链剂。
    • 9. 发明申请
    • PROCESS FOR PREPARING ORGANICALLY MODIFIED LAYERED DOUBLE HYDROXIDE
    • 制备有机改性层状双氢氧化物的方法
    • WO2007065859A1
    • 2007-06-14
    • PCT/EP2006/069204
    • 2006-12-01
    • Akzo Nobel N.V.WINTERS, RobinSCHOMAKER, ElwinDE VOS, Siebe CornelisREEDIJK, Marianne FrederikaZIJTVELD-VAN DER WIEL, Johanna Henriëtte
    • WINTERS, RobinSCHOMAKER, ElwinDE VOS, Siebe CornelisREEDIJK, Marianne FrederikaZIJTVELD-VAN DER WIEL, Johanna Henriëtte
    • C01B13/36C01F7/00
    • C01F7/005C01B13/363C01F7/002C01P2002/22C01P2002/78
    • The invention relates to a process for preparing an organically modified layered double hydroxide having a distance between the individual layers of the layered double hydroxide of above 1.5 nm and comprising an organic anion as charge-balancing anion, the process comprising the steps of: (a) preparing a precursor suspension comprising a divalent metal ion source and a trivalent metal ion source; (b) solvothermally treating the precursor suspension to obtain the layered double hydroxide, wherein an organic anion is added before or during the formation of the layered double hydroxide of step (b), or following the formation of the layered double hydroxide, so as to obtain the organically modified layered double hydroxide, with the proviso that deoxycholic acid is not the sole organic anion. The invention further pertains to a process for preparing an organically modified layered double hydroxide having a distance between the individual layers of the layered double hydroxide of above 1.5 nm and comprising an organic anion as charge-balancing anion, the process comprising the steps of: (a) preparing a precursor suspension comprising a divalent metal ion source and a trivalent metal ion source; (b) thermally treating the precursor suspension to obtain the layered double hydroxide, wherein an organic anion is added before or during the formation of the layered double hydroxide of step (b), or following the formation of the layered double hydroxide, so as to obtain the organically modified layered double hydroxide, with the proviso that in step a) the trivalent metal ion source is not reacted with the organic anion at a temperature of between 60 and 85°C for 4 to 8 hours prior to the addition of the divalent metal ion source and step b) is subsequently carried out at a temperature of 90 to 95°C for 4 to 8 hours.
    • 本发明涉及一种制备有机改性层状双氢氧化物的方法,其具有1.5nm以上层状双氢氧化物的各层之间的距离,并且包含作为电荷平衡阴离子的有机阴离子,该方法包括以下步骤:(a )制备包含二价金属离子源和三价金属离子源的前体悬浮液; (b)溶剂化处理前体悬浮液以获得层状双氢氧化物,其中在步骤(b)的层状双氢氧化物的形成之前或期间,或在形成层状双氢氧化物之后加入有机阴离子,以便 获得有机改性的层状双氢氧化物,条件是脱氧胆酸不是唯一的有机阴离子。 本发明还涉及一种制备有机改性的层状双氢氧化物的方法,其具有1.5nm以上层状双氢氧化物的各层之间的距离,并且包含有机阴离子作为电荷平衡阴离子,该方法包括以下步骤:( a)制备包含二价金属离子源和三价金属离子源的前体悬浮液; (b)热处理前体悬浮液以获得层状双氢氧化物,其中在步骤(b)的层状双氢氧化物形成之前或期间,或在形成层状双氢氧化物之后加入有机阴离子,以便 获得有机改性的层状双氢氧化物,条件是在步骤a)中,三价金属离子源在60至85℃的温度下不与有机阴离子反应4至8小时,然后加入二价 金属离子源和步骤b)随后在90至95℃的温度下进行4至8小时。