子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 一种亚胺连接的发光多孔有机聚合物材料及制备方法 | CN201610207323.7 | 2016-04-05 | CN105754588A | 2016-07-13 | 刘晓明; 李忠平; 夏虹 |
| 本发明的一种亚胺连接的发光多孔有机聚合物骨架材料及制备方法属于多孔材料技术领域，其结构式为：由具有叔丁基取代的芳香多醛化合物与水合肼或对苯二胺通过席夫碱缩合反应得到。本发明利用叔丁基取代的芳香多醛化合物作为反应物，有效防止分子链段间的相互堆积，易于获得高发光的多孔有机聚合物材料，产物具有良好的化学稳定性，可以用于催化剂载体、金属离子识别等领域，具有广泛的应用前景。 | ||||||
| 2 | 制备多亚甲基多苯基多氨基甲酸酯的方法 | CN201180070707.4 | 2011-11-08 | CN103534231B | 2016-04-06 | 李会泉; 柳海涛; 陈家强; 张凯华; 曹妍 |
| 本发明提供一种制备多亚甲基多苯基多氨基甲酸酯的方法，所述方法通过相转移酸性催化剂催化苯氨基甲酸酯与甲基化试剂的缩合而进行，所述方法包括：将苯氨基甲酸酯溶解于与水不互溶的有机溶剂中，以形成溶液A；配制酸催化剂水溶液，以形成溶液B；通过首先将甲基化试剂加入到溶液B中并且随后混合溶液A与溶液B，或者通过在将溶液A与溶液B混合的同时或之后加入甲基化试剂，形成包含有机相和水相的反应体系；在搅拌的同时，将反应体系在30℃-200℃的反应温度和0.05MPa-5MPa的反应压力下进行反应；通过将所述有机相与所述水相静置分层，分离多亚甲基多苯基多氨基甲酸酯混合产物。该方法能够实现产物的高选择性和收率和容易的产物分离。 | ||||||
| 3 | 聚合物，用于制备其的底物、方法和包含其的装置 | CN201480019271.X | 2014-02-06 | CN105339403A | 2016-02-17 | N.B.杜克 |
| 本发明一般涉及用于制备聚合物的底物和用于制备聚合物的方法。本发明一般还涉及聚合物和包含所述聚合物的装置。 | ||||||
| 4 | 聚合物，用于制备其的底物、方法和包含其的装置 | CN201480019443.3 | 2014-02-06 | CN105229054A | 2016-01-06 | N.B.杜克 |
| 本发明一般涉及用于制备聚合物的底物和用于制备聚合物的方法。本发明一般还涉及聚合物和包含所述聚合物的装置。 | ||||||
| 5 | ポリマー、基材、これらを製造する方法およびこれらを備えるデバイス | JP2015557063 | 2014-02-06 | JP2016516098A | 2016-06-02 | ダック，ニコラス・ブレンダン |
| 本発明は、概して、ポリマーを製造するための基材や、ポリマーを製造する方法に関する。また、本発明は、概して、ポリマーおよびこれらを含むデバイスに関する。 | ||||||
| 6 | ポリメチレンポリフェニルポリカーバメートを製造する方法 | JP2014540283 | 2011-11-08 | JP2014532731A | 2014-12-08 | フイクァン リ; ハイタオ リュウ; ジャキン チェン; カイファ チャン; ヤン カオ |
| 本発明は、ポリメチレンポリフェニルポリカーバメートを製造する方法を提供し、前記方法は相転移酸性触媒剤によりフェニルカーバメートとメチル化試薬の縮合を触媒することによって行われ、前記の方法は以下のステップを含む:フェニルカーバメートを水と相互溶解しない有機溶媒に溶解させることにより溶液Aを形成する;酸触媒剤水溶液を調製することにより溶液Bを形成する;まずメチル化試薬を溶液Bに加えた後に溶液AとBを混合することにより、又は溶液Aと溶液Bを混合するとともに又はその後にメチル化試薬を加えることにより、有機相と水相を含む反応システムを形成する;攪拌するとともに、反応システムを30℃〜200℃の反応温度と0.05MPa〜5MPaの反応圧力の条件下で反応を行う;前記の有機相と前記の水相を静置分層することにより、ポリメチレンポリフェニルポリカーバメートの混合生成物を分離する。この方法はにより、生成物の高い選択性と収率及び容易な生成物分離を実現することができる。 | ||||||
| 7 | JPS50104294A - | JP1018075 | 1975-01-25 | JPS50104294A | 1975-08-18 | |
| 8 | Method for preparing homogeneous polymerization catalyst | JP10614495 | 1995-04-28 | JPH08301917A | 1996-11-19 | SHOZAKI HAJIME; TOMOTSU NORIO |
| PURPOSE: To prepare a homogeneous polymerization catalyst having a high catalytic activity by mixing a transition metal compound with a compound which can react with the metal compound to form an ionic complex or a specified oxygenous compound and aging the obtained mixture. CONSTITUTION: A method for preparing a homogeneous polymerization catalyst comprising a transition metal compound (A) and oxygenous compounds (B) represented by formula I (wherein R 1 to R 5 are each 1-8C alkyl; Y 1 to Y 3 are each a group III element; and a and b are each 0-50, provided that a+b≥1) and/or formula II (wherein R 6 and R 7 are each 1-8C alkyl; Y 4 and Y 5 are each a group III element; and c and d are each 0-50, provided that c+d≥1), which comprises mixing catalyst components A and B together and aging the obtained mixture. According to this method, the catalyst can be brought into the state of the highest possible catalytic activity within a short time. The catalyst prepared by this method is used as a polymerization catalyst for, e.g. an aromatic vinyl compound or an α-olefin and, especially when used in the polymerization of an aromatic vinyl compound, it can give a syndiotactic styrene polymer at good efficiency. COPYRIGHT: (C)1996,JPO | ||||||
| 9 | Method of storing homogeneous polymerization catalyst | JP10614295 | 1995-04-28 | JPH08301915A | 1996-11-19 | SHOZAKI HAJIME; TOMOTSU NORIO |
| PURPOSE: To provide a method of storing a homogeneous polymerization catalyst, whereby the catalyst is supressed in the decrease in its activity during the period from the time when the respective catalyst components are mixed together to the time when the mixture is fed to the polymerization step. CONSTITUTION: A method of storing a homogeneous polymerization catalyst comprising a transition metal compound (A) and a compound (B) which reacts with component A to form an ionic complex, and further optionally an alkylated metal compound, wherein the respective catalyst components are mixed together and the obtained mixture is stored below 35°C. COPYRIGHT: (C)1996,JPO | ||||||
| 10 | New acrylic derivative of urea | JP11187389 | 1989-04-28 | JPH0249760A | 1990-02-20 | ROJIE GARIIGU; JIYATSUKU RARO |
| NEW MATERIAL: Monomethylolacrylamidemethyleneurea of the formula. USE: Useful as an additive to aminoplastic resins and phenol resins, especially resins used as adhesives for wood. PREPARATION: Equimolar amounts of acrylamidomethyleneurea, and water and aqueous solution of formaldehyde are reacted together to give a compound of the formula. The reaction is carried out by heating at 60°C for about one hour in the presence of a polymerization inhibitor such as hydroquinone methyl ether or triethylamine. The compound of the formula is a white solid, whose physical state changes at 190-200°C. COPYRIGHT: (C)1990,JPO | ||||||
| 11 | Modified aminoplast and method of making wood chip board or laminated sheet by using it | JP15354176 | 1976-12-22 | JPS5280396A | 1977-07-06 | KARURU SHIYUNEE; SHIYUTETSUFUEN PIISHIYU; DEIITERU TEIHIII |
| 12 | POLYMERS, SUBSTRATES, METHODS FOR MAKING SUCH, AND DEVICES COMPRISING THE SAME | EP14748738 | 2014-02-06 | EP2953993A4 | 2016-12-28 | DUCK NICHOLAS BRENDAN |
| The present invention relates generally to substrates for making polymers and methods for making polymers. The present invention also relates generally to polymers and devices comprising the same. | ||||||
| 13 | POLYMERS, SUBSTRATES, METHODS FOR MAKING SUCH, AND DEVICES COMPRISING THE SAME | EP14749541 | 2014-02-06 | EP2953987A4 | 2016-09-28 | DUCK NICHOLAS BRENDAN |
| The present invention relates generally to substrates for making polymers and methods for making polymers. The present invention also relates generally to polymers and devices comprising the same. | ||||||
| 14 | Harnstoff-Formaldehydharz, seine Herstellung und seine Verwendung | EP82104543.2 | 1982-05-25 | EP0066233A1 | 1982-12-08 | Schöllhorn, Wolf-Dietrich |
Harnstoff-Formaldehydharz, welches durch Zugabe eines Härtungskatalysators unter stark exothermer Bildungsreaktion zu einem Aminoplasten polykondensiert, dessen Herstellung und Verfahren zur Weiterverarbeitung, sowie daraus gewonnenen Schaumprodukten. |
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| 15 | P-NITROPHENOLE-FORMALDEHYDE POLYCONDENSATE FOR MEASUREMENT, METHOD OF PRODUCTION AND USE | US15515697 | 2015-09-29 | US20170307572A1 | 2017-10-26 | Barna KOVÁCS; Katalin BALOGH; Aleksandar SECENJI |
| The invention relates to a wide range optical sensor for measuring pH, wherein said optical sensor contains a carrier and one or more p-nitro-phenyl/formaldehyde condensed polymer of formula (I) bounded to said carrier wherein n is 1-20, and Z is H or binding group. | ||||||
| 16 | Polymers, substrates, methods for making such, and devices comprising the same | US14173269 | 2014-02-05 | US09193819B2 | 2015-11-24 | Nicholas Brendan Duck |
| The present invention relates generally to substrates for making polymers and methods for making polymers. The present invention also relates generally to polymers and devices comprising the same. | ||||||
| 17 | Polymers, substrates, methods for making such, and devices comprising the same | US14173452 | 2014-02-05 | US20140220477A1 | 2014-08-07 | Nicholas Brendan Duck |
| The present invention relates generally to substrates for making polymers and methods for making polymers. The present invention also relates generally to polymers and devices comprising the same. | ||||||
| 18 | Novel amino resins useful in sizing paper and their use | US56920 | 1987-06-03 | US4847315A | 1989-07-11 | Thord G. G. Hassler |
| A water-soluble, thermosetting resin comprising units derived from tris(2-aminoethyl)amine, and preferably units derived from dicyandiamide and/or epichlorohydrin, is useful as an accelerator in paper sizing, e.g. using an alkyl ketene dimer. | ||||||
| 19 | Process for the production of amino silicate compounds and their condensation products | US786617 | 1977-04-08 | US4169930A | 1979-10-02 | David H. Blount |
| Silicic-amino compounds are formed by the chemical reaction of silicic acid with amino compounds in the presence of a suitable alkali at a suitably elevated temperature, and then by reacting the resultant compounds with an aldehyde, a condensation product is formed. | ||||||
| 20 | Process for the production of amino silicate compounds and their condensation products | US652338 | 1976-01-26 | US4033935A | 1977-07-05 | David H. Blount |
| Silicic-amino compounds are formed by the chemical reaction of silicic acid with amino compounds in the presence of a suitable alkali at a suitably elevated temperature, and then by reacting the resultant compounds with an aldehyde, a condensation product is formed. | ||||||
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