181 |
Preparation of condensation products and addition products of water-soluble having an amino group and use thereof |
JP52483597 |
1997-01-03 |
JP2000505124A |
2000-04-25 |
ヘトヒェ アルベルト; ロイター ヴォルフガング; シュトイエルレ ウルリヒ; シェア ギュンター; カンター ハルトムート; マイクスナー フーベルト; ヴァイザー ユルゲン; ディリク―ブレンツィンガー ライナー |
(57)【要約】 アミノ基を有する水溶性の縮合物又は付加生成物の溶液から、膜による限外濾過によって、縮合物又は付加生成物の5〜95重量%を透過液として分離し、改善された作用を有する、アミノ基を有する縮合物又は付加生成物を、場合により透過液から単離する、製紙の際の、高められた脱水促進作用及び歩留まり向上作用を有する、アミノ基を有する水溶性の縮合物及び付加生成物の製造法及び製紙の際の歩留まり向上剤、脱水促進剤及び定着剤、アルキルジケテンを用いる紙料のサイジングの際のプロモータ、下水スラッジ用の凝集剤、複合フィルムの製造の際の付着剤、ヘアケア剤及びスキンケア剤中の添加剤及び陰イオン性有効成分の不動化用の薬剤としての、透過液中に含有されている高分子量ポリマー成分の使用。 |
182 |
Charge transfer polymer and its electroluminescence device |
JP31593898 |
1998-11-06 |
JPH11246660A |
1999-09-14 |
HSIEH BING R |
PROBLEM TO BE SOLVED: To obtain a charge transfer polymer capable of forming an electroluminescence device emitting an orangey red light with high brightness and stable mechanically and electrically by introducing a group connected to an aromatic group into a repeating unit through a nitrogen atom.
SOLUTION: This polymer comprises a repeating unit selected from the group consisting of formula I [G is nothing, O, S, a group of the formula N-Ph (Ph is a phenyl), vinylene, ethynylene, o-, m- or p-phenylene, a group of the formula -CH=CH-Ph-CH=CH (Ph is a phenylene); R is H, a methyl, methoxy; p-Ar is a para-substituted aromatic group; and G' is an unsaturated double bonding group], formula II (R' is an aryl, alkyl, alkoxy; R" is H, a halogen, aryl, alkyl; and X is nothing, CH
2, O or S) and formula III. The polymer has pref. a weight average molecular weight of 3,000 to 100,000 and number average molecular weight of 300 to 10,000, and an organic solvent solubility.
COPYRIGHT: (C)1999,JPO |
183 |
Electrode for lithium secondary battery and lithium secondary battery |
JP27707297 |
1997-10-09 |
JPH11121011A |
1999-04-30 |
MOTOMURA HIKARI; HASEZAKI KAZUHIRO |
PROBLEM TO BE SOLVED: To enhance adhesion between active materials and between an active material and a metal collecting body by binding the electrode active material by a binding agent composed of bisallylnadiimide compound or allylnadiimide compound, which are addition polymerization type imide monomer of water dispersive low molecular weight.
SOLUTION: In manufacturing a positive electrode, bis-allylnadiimide compound or allylnadiimide compound is mixed to a mixture with electric conductor powder of carbon, etc., as necessary to positive electrode active material powder of LiMn
2O
4, etc., as a binding agent and water is added thereto prepare a uniform water slurry. This water slurry is applied to the surface of a collecting body composed of a conductive metal foil using such a method as coating by a doctor blade and dried. It is pressed as necessary and heat treated by heating to 100-500°C. One hour or more heating treating is usually sufficient. An Al or Ni foil, or a mesh material is especially suited to the collecting body.
COPYRIGHT: (C)1999,JPO |
184 |
Gas separation membrane with polycarbodiimide resin layer |
JP26519297 |
1997-08-19 |
JPH1157381A |
1999-03-02 |
MAEDA MASATOSHI; YOSHIOKA MASAHIRO; FUKUOKA TAKAHIRO; SAKAMOTO YUKIE; MOCHIZUKI SHU |
PROBLEM TO BE SOLVED: To obtain a gas separation membrane having high permeability and selectivity of separation and also having superior heat and chemical resistances and durability by disposing a polycarbodiimide resin layer having a specified repeating structural unit. SOLUTION: The gas separation membrane used for separating and recovering hydrogen in ammonia synthesis is formed by disposing a polycarbodiimide resin layer having a repeating structural unit represented by the formula (where R is a divalent org. group) i.e., consists of a laminated film having an active separation layer of polycarbodiimide resin and a porous support layer. An org. diamine forming the divalent org. group in the structure of the polycarbodiimide resin is, e.g. m- and -p-xylene-7,8-diamine, 1,4-bis(2- ethylamine)benzene or the like. The porous support layer is made of polyamide resin, polyimide resin, polysulfone resin, etc. |
185 |
New polyalkylene guanidine salt or biguanidine salt with branched silane, its production and use thereof as antimicrobial agnet |
JP19638997 |
1997-07-08 |
JPH111556A |
1999-01-06 |
LEE BYUNG-HYUNG; KIM WOO-SUN; KIM YOUNG-JUN; BANG SANG-GU; LIM KWANG-MIN; CHOI SANG-RAK; JOO KEUM-CHAN |
PROBLEM TO BE SOLVED: To obtain the subject compound adhesive to various materials, and useful for antimicrobial treatment of synthetic/natural fibers, woods, paper, glass, metals, etc., by reacting a specific compound with a specific silane compound under agitation. SOLUTION: This compound of formula III is obtained by reaction of a compound of formula I [A is oxyethylene with a repeating number of 1-100,000, a 1-20C alkyl, etc.; Y is HCl, etc.; B is a 0-20C alkyl; Z is OR (R is methyl, etc.); X is I, etc.; (x) is guanidine, etc.; (m) is an integer of >=0; (n) is an integer of >=1] with a silane compound of formula II at an equivalent ratio to the guanidine group, etc., of 0.01-1.0 pref. at 0-200 deg.C in the presence of a catalyst (e.g. alkali metal alkoxide) and a solvent (e.g. organic acid) under agitation. The other objective antimicrobial composition is obtained by including 0.1-80 wt.% of this compound and 20-99.9 wt.% of water or an organic solvent with a boiling point of 25-30 deg.C. |
186 |
Aromatic polycarbodimide and sheet made therefrom |
JP15576297 |
1997-05-28 |
JPH1067840A |
1998-03-10 |
SAKAMOTO YUKIE; MOCHIZUKI SHU; YOSHIOKA MASAHIRO |
PROBLEM TO BE SOLVED: To obtain an aromatic polycarbodiimide which can be bonded in a short time even at low temperatures and shows excellent moisture resistance and heat resistance even under humid, high temperatures and high pressure conditions by introducing siloxane bonds into the main chain. SOLUTION: This resin is a polycarbodiimide containing siloxane bonds in the main chain and comprising structural units each represented by formula I (wherein R is a single bond or a 1-4C alkylene; x is an integer of 1-20; and n is an integer of 2-200). A polycarbodiimide comprising structural units each represented by formula II (wherein R and n are as defined above) corresponding to formula I (wherein x is 1) has a high content of carbodiimide units and shows excellent thermosetting properties. A varnish of this polycarbodiimide is molded by a usual method into a film which can be used as an adhesive sheet. This film may be formed on a support. |
187 |
Photolabile polymer with triazene and/or pentazadiene structural units |
JP6738794 |
1994-04-05 |
JPH06322117A |
1994-11-22 |
STEBANI JUERGEN; NUYKEN OSKAR; SLUKA PETER; FINCKH PETER |
PURPOSE: To provide a polymer comprising triazene and/or pentazadiene structural units and being the most suitable as a biochemical reagent used as a photoresist, especially a positive photoresist.
CONSTITUTION: A triazene and/or pentazadiene polymer is used as a photoresist, especially a positive photoresist. This is a polymer obtained by diazotizing a difunctional aromatic amino compound to convert it into the corresponding bisdiazonium salt and polycondensing this with an amino-containing compound. The amino-containing compound used is a difunctional primary or secondary amine of the formula: R
1-NH-Z-NH-R
2 (wherein Z is a non-aromatic hydrocarbon group; and R
1 and R
2 are each H or the like).
COPYRIGHT: (C)1994,JPO |
188 |
JPH04502369A - |
JP51050090 |
1990-08-01 |
JPH04502369A |
1992-04-23 |
|
|
189 |
Electric conductor and its manufacture |
JP22986089 |
1989-09-05 |
JPH0393106A |
1991-04-18 |
SAITO KAZUO |
PURPOSE: To improve the oxidation resistance, mechanical strength and flexibility of an electric conductor by doping an insoluble and infusible basic body, obtained through the process of heat-treating a polycarbodiimide resin, with an electron-donative doping agent or an electron-acceptable doping agent.
CONSTITUTION: A polycarbodiimide resin can be manufactured through a process of condensation reaction involving decarbonation of an organic diisocyanate. An electron-donative doping agent is selected from the First Group A metal including lithium, sodium, potassium, rubidium and cesium, and an electron- acceptive doping agent on the other hand is selected from anions selected from such materials as fluorine, chlorine, bromine, a halogen of iodine, halides of As, F
5, PF
5, BF
5, BC1
3, BBr
2 and the like, the oxides of such uon-metallic elements as SO
3, N
2O
3 and the like or the inorganic acids of H
2SO
4, HNO
3, HC1O
4 and the like. Thus, an electric conductor can be obtained with excellence in oxidation resistance, mechanical strength and flexibility.
COPYRIGHT: (C)1991,JPO&Japio |
190 |
JPS6151941B2 - |
JP5139276 |
1976-05-07 |
JPS6151941B2 |
1986-11-11 |
GYUNTAA BAATSU; MANFURETSUTO DAAMU; BARUTAA SHEEFUAA |
|
191 |
Azomethine (co)polymer and manufacture |
JP21966483 |
1983-11-24 |
JPS59113033A |
1984-06-29 |
POORU UINSUROTSUPU MOOGAN |
|
192 |
Polyphosphazene polymer containing substituted alkyl or cycloalkyl substituent |
JP9087383 |
1983-05-25 |
JPS5930824A |
1984-02-18 |
UIRIAMU RII HAAGENROOZAA; AADERU FUAAHAN HARASA |
|
193 |
JPS5856566B2 - |
JP12071580 |
1980-09-02 |
JPS5856566B2 |
1983-12-15 |
UIRIAMU RII HAAGENROOZAA; AADERU FUAAHAN HARASA |
|
194 |
Novel water-soluble polymer and manufacture |
JP6044982 |
1982-04-13 |
JPS57180632A |
1982-11-06 |
BORUFUUDEIITAA SHIYUREEAA; YANOSU MUSUTSUIIKU; GIYUNTAA KORUPU; KURUTO TORIIBENETSUKU; KARURU RAIRITSUTSU |
|
195 |
JPS549521B1 - |
JP6353971 |
1971-08-20 |
JPS549521B1 |
1979-04-25 |
|
|
196 |
Hardenable mixture |
JP7340177 |
1977-06-22 |
JPS53300A |
1978-01-05 |
HANSUUDEIITAA YAKOBU; RORUFU KUBENSU; HAINRITSUHI HAINE |
|
197 |
JPS5097700A - |
JP195575 |
1974-12-26 |
JPS5097700A |
1975-08-02 |
|
|
198 |
JPS49105000A - |
JP565774 |
1974-01-10 |
JPS49105000A |
1974-10-04 |
|
|
199 |
水性銅めっき浴および基板上での銅または銅合金の析出方法 |
JP2018510935 |
2016-08-30 |
JP2018529841A |
2018-10-11 |
ハイコ ブルナー; ラース コールマン; アグニエシュカ ヴィチャク; オリヴィエ マン |
本発明は、ビスウレア誘導体、ならびに電子用途のためのプリント回路板、IC基板、半導体およびガラスデバイスの製造において、銅および銅合金を析出させるための水性めっき浴における前記誘導体の使用に関する。本発明によるめっき浴は少なくとも1つの銅イオン源およびビスウレア誘導体を含む。このめっき浴はリセス構造を銅で充填することおよびピラーバンプ構造のビルドアップに特に有用である。 |
200 |
フタロニトリル化合物 |
JP2018513250 |
2016-05-20 |
JP2018515625A |
2018-06-14 |
スン・ヒ・イ; サン・ウ・キム; キ・ホ・アン |
本出願は、新規なフタロニトリル化合物及びその用途に関する。前記フタロニトリル化合物は、新規な構造を有し、フタロニトリル化合物が適用され得るものと公知された用途で優れた効果を示すことができる。このようなフタロニトリル化合物の用途には、いわゆるフタロニトリル樹脂、フタロシアニン染料、蛍光増白剤、写真増感剤又は酸無水物等の原料或いは前駆体が例示され得る。 |