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1. 发明授权

US09260575B2 Film and method of preparing the same 有权
标题翻译：电影和制作方法
公开(公告)号：US09260575B2
公开(公告)日：2016-02-16
申请号：US13581719
申请日：2012-08-03
申请人： Jin Ryul Son , Sung Hwan Bang , Jyung Hee Jeon , Sang Youb Lee , Ju Hee Shin
发明人： Jin Ryul Son , Sung Hwan Bang , Jyung Hee Jeon , Sang Youb Lee , Ju Hee Shin
IPC分类号： C09D101/26 , C08J5/18 , B29D7/01 , C08K3/16 , C08L1/28 , B05D1/18 , B05D3/00 , C08J3/28 , B29C41/24 , C08L1/26 , B29K1/00
CPC分类号： C08J5/18 , B05D1/18 , B05D3/007 , B29C41/24 , B29D7/01 , B29K2001/08 , C08J3/28 , C08J2301/28 , C08K3/16 , C08L1/26 , C08L1/284
摘要： A film and a method of preparing the same. The film includes cellulose ether and sodium chloride, wherein an amount of the sodium chloride is from about 0.25 wt % to about 0.6 wt % based on a total weight of the film, and the film has a light-transmission reduction ratio of about 15% or less.
摘要翻译：一种胶片及其制备方法。该膜包括纤维素醚和氯化钠，其中氯化钠的量基于膜的总重量为约0.25重量％至约0.6重量％，并且该膜具有约15重量％的透光率降低率，或更少。

2. 发明授权

US09187595B2 Method for manufacturing biodegradable copolymer by split-injecting aromatic dicarboxylic acid compound 有权
标题翻译：通过分散注入芳族二羧酸化合物制造可生物降解的共聚物的方法
公开(公告)号：US09187595B2
公开(公告)日：2015-11-17
申请号：US14402516
申请日：2013-05-13
申请人： SAMSUNG FINE CHEMICALS CO., LTD
发明人： Jong Pil Chun , Ye Jin Kim , Ki Chull Yun , Min Kyoung Kim
IPC分类号： C08G63/16 , C08G63/183 , C08G63/12 , C08G63/78 , C08G63/52
CPC分类号： C08G63/183 , C08G63/12 , C08G63/181 , C08G63/78
摘要： There is provided a method of preparation for a biodegradable co-polyester, the method including: forming an oligomer through a primary esterification reaction between a hydroxy group of an aliphatic dihydroxy compound and a carboxylic group of an aliphatic dicarboxylic acid compound; performing a secondary esterification reaction between the formed oligomer and an aromatic dicarboxylic acid compound; and performing a polycondensation reaction in a vacuum, in which sequentially divided addition of the aromatic dicarboxylic acid compound is performed and the weight ratio of the aromatic dicarboxylic acid compound with respect to the oligomer for each time of the sequentially divided addition is from 2:8 to 5:5. The method efficiently increases a solubility of aromatic dicarboxylic acid, thereby increasing a reaction rate and reducing a side reaction.
摘要翻译：提供了一种可生物降解的共聚酯的制备方法，其包括：通过脂肪族二羟基化合物的羟基与脂肪族二羧酸化合物的羧基之间的一次酯化反应形成低聚物; 在形成的低聚物和芳族二羧酸化合物之间进行二次酯化反应; 在真空中进行缩聚反应，其中进行依次分配的芳族二羧酸化合物的添加，并且芳香族二羧酸化合物相对于低聚物的重量比分别为2:8 至5：5。该方法有效地提高芳族二羧酸的溶解度，从而提高反应速度并减少副反应。

3. 发明申请

US20150280223A1 SURFACE-MODIFIED SILICON NANOPARTICLES FOR NEGATIVE ELECTRODE ACTIVE MATERIAL, AND METHOD FOR MANUFACTURING SAME 审中-公开
标题翻译：用于负极电极活性材料的表面改性的硅纳米颗粒及其制造方法
公开(公告)号：US20150280223A1
公开(公告)日：2015-10-01
申请号：US14437387
申请日：2013-08-27
申请人： SAMSUNG FINE CHEMICALS CO., LTD
发明人： Dong Gyu Chang , Ju Myeung Lee , Kyu Eun Shim , Woo Young Yang
IPC分类号： H01M4/36 , H01M10/052
CPC分类号： H01M4/366 , C01B33/02 , C01D15/02 , H01M4/13 , H01M4/386 , H01M4/485 , H01M4/625 , H01M10/052 , H01M2220/20 , H01M2220/30 , Y02T10/7011
摘要： The present invention provides surface-modified silicon nanoparticles comprising a LixSiyOz top film and a carbon (C) coating layer on the surface of the nanoparticles by means of the addition of a lithium source and a carbon source during the manufacture of silicon nanoparticles or a post-treatment thereof. According to the present invention, the surface oxidation of the silicon nanoparticles, which would easily occur during a pulverization process, can be prevented. By using the silicon nanoparticles of which oxidation is prevented as a negative electrode material, problems related to decrease in capacity and electrolyte depletion resulting from an oxidized film can be mitigated. Thus, a deterioration in the properties of a lithium secondary battery can be prevented.
摘要翻译：本发明提供了在制造硅纳米颗粒或柱子期间通过添加锂源和碳源在纳米颗粒的表面上提供包含LixSiyOz顶部膜和碳（C）涂层的表面改性的硅纳米颗粒处理。根据本发明，可以防止在粉碎过程中容易发生的硅纳米颗粒的表面氧化。通过使用防止氧化作为负极材料的硅纳米颗粒，可以减轻由氧化膜引起的容量降低和电解质耗尽的问题。因此，可以防止锂二次电池的性能的劣化。

4. 发明申请

US20150217374A1 METHOD FOR MANUFACTURING METAL NANOPARTICLES BY USING PHASE TRANSITION REDUCTION, AND METAL INK COMPRISING METAL NANOPARTICLES MANUFACTURED THEREBY 审中-公开
标题翻译：通过使用相变过渡制造金属纳米粒子的方法和包含金属纳米粒子的金属油墨制造的
公开(公告)号：US20150217374A1
公开(公告)日：2015-08-06
申请号：US14422425
申请日：2013-05-09
申请人： SAMSUNG FINE CHEMICALS CO., LTD
发明人： Sung Soon Kim , Eui Hyun Ryu , Chan Hyuk Park , Mi Young Kim , Kyung Yol Yon
IPC分类号： B22F9/24 , C22C5/06 , C22B3/00 , H01B1/02
CPC分类号： B22F9/24 , C09C1/62 , C09D11/52 , C22B11/04 , C22C5/06 , H01B1/02
摘要： A method of preparing metal nanoparticles using a phase transfer reduction method in which a reduction reaction is adjusted by distribution equilibrium between an intermediate formed by a coordinate bond between a capping material and various metal precursors in the form of an organic phase and a reducing agent present in an aqueous phase, and a metal ink prepared from the metal nanoparticles. The method of preparing metal nanoparticles includes dissolving a metal precursor and a capping agent in an organic phase, dissolving a reducing agent in an aqueous phase, mixing the organic phase and the aqueous phase to form a precipitate, separating the precipitate, and drying the separated precipitate. The metal nanoparticles prepared using the method can be prepared to have various particle sizes according to the kind of precursors and a length of an alkyl chain of an amine used as the capping agent. As a self-quenching reaction in which growth of the nanoparticles in the aqueous layer is stopped takes place since the nanoparticle precipitate into the aqueous layer from the organic layer due to a difference in density of the metal nanoparticles formed during a reaction, a particle size of the metal nanoparticles can be easily controlled, and excellent processability in which the metal nanoparticles are easily separated/purified from the organic layer in which most reaction by-products are present can be ensured. Also, as the metal nanoparticles having various particle sizes are able to be prepared, a metal ink having various sintering temperatures spanning from a low temperature to a high temperature can be prepared using the metal nanoparticles.
摘要翻译：一种使用相转移还原法制备金属纳米粒子的方法，其中还原反应是通过由封盖材料与各种有机相形式的金属前体之间的配位键形成的中间体与还原剂之间的分布平衡来调节的在水相中，和由金属纳米颗粒制备的金属油墨。制备金属纳米颗粒的方法包括将金属前体和封端剂溶解在有机相中，将还原剂溶解在水相中，混合有机相和水相以形成沉淀物，分离沉淀物，并干燥分离的沉淀。使用该方法制备的金属纳米颗粒可以根据前体的种类和用作封端剂的胺的烷基链的长度制备为具有各种粒径。由于纳米颗粒由于在反应期间形成的金属纳米颗粒的密度差而从有机层沉淀到水层中，所以发生水层中纳米颗粒的生长停止的自熄反应发生，可以容易地控制金属纳米颗粒，并且可以确保金属纳米颗粒容易地从存在大多数反应副产物的有机层中分离/纯化的优异的加工性。另外，由于可以制备具有各种粒径的金属纳米粒子，所以可以使用金属纳米粒子制备具有跨越低温至高温的各种烧结温度的金属油墨。

5. 发明申请

US20150210546A1 METHOD FOR PREPARING LITHIUM METAL PHOSPHOR OXIDE 审中-公开
标题翻译：制备锂金属磷酸氧化物的方法
公开(公告)号：US20150210546A1
公开(公告)日：2015-07-30
申请号：US14419289
申请日：2013-05-10
申请人： SAMSUNG FINE CHEMICALS CO., LTD
发明人： Hyun A Song , Dong Gyu Chang , Woo Young Yang
IPC分类号： C01B25/45
摘要： The present invention relates to a method for preparing a lithium metal phosphor oxide, the method including: mixing an iron salt solution and a phosphate solution in a reactor; applying a shearing force to the mixed solution in the reactor during the mixing to form a suspension containing nano-sized iron phosphate precipitate particles; obtaining the nano-sized iron phosphate particles from the suspension; and mixing the iron phosphate with a lithium raw material and performing firing, and the lithium metal phosphor oxide according to the present invention has an Equation of LiMnFePO4. Herein, M is selected from the group consisting of Ni, Co, Mn, Cr, Zr, Nb, Cu, V, Ti, Zn, Al, Ga, and Mg, and n is in a range of 0 to 1. According to the present invention, since calcination is performed at a temperature that is lower than that of another existing method, there is an effect of reducing a process cost, and the obtained lithium metal phosphor oxide prepared according to the method of the present invention has an olivine structure type.
摘要翻译：本发明涉及一种制备锂金属磷光体的方法，该方法包括：在反应器中混合铁盐溶液和磷酸盐溶液; 在混合期间对反应器中的混合溶液施加剪切力以形成含有纳米尺寸磷酸铁沉淀颗粒的悬浮液; 从悬浮液中获得纳米尺寸的磷酸铁颗粒; 并将磷酸铁与锂原料混合并进行焙烧，根据本发明的锂金属荧光体具有LiMnFePO4的方程式。这里，M选自Ni，Co，Mn，Cr，Zr，Nb，Cu，V，Ti，Zn，Al，Ga和Mg，n在0〜1的范围内。在本发明中，由于在低于另一现有方法的温度下进行煅烧，所以具有降低加工成本的效果，所得到的根据本发明方法制备的锂金属荧光体具有橄榄石结构类型。

6. 发明申请

US20150203354A1 METHOD FOR PREPARING NANO-SIZED IRON PHOSPHATE PARTICLES 审中-公开
标题翻译：制备纳米尺寸磷酸铁锂颗粒的方法
公开(公告)号：US20150203354A1
公开(公告)日：2015-07-23
申请号：US14419607
申请日：2013-05-13
申请人： SAMSUNG FINE CHEMICALS CO., LTD , NANOMATERIALS TECHNOLOGY PTE LTD
发明人： Hyun A Song , Dong Gyu Chang , Woo Young Yang , Wei Kian Soh , Zhigang Shen , Jiyao Zhang , Lingyan Gao
IPC分类号： C01B25/37
CPC分类号： C01B25/375 , B82Y30/00 , B82Y40/00 , C01P2002/72 , C01P2004/03 , C01P2004/64
摘要： The present invention relates to a method for preparing nano-sized iron phosphate particles, the method including the steps of: mixing an iron salt solution and a phosphate solution in a reactor in order to prepare a suspension containing amorphous or crystalline iron phosphate precipitate; and applying a shearing force to the mixed solution inside the reactor during the step of mixing, wherein the suspension containing nano-sized iron phosphate precipitate particles is formed by means of the shearing force and the conditions inside the reactor. According to the present invention, micro-mixing takes place faster than nucleation, which provides an advantage for preparing nanoparticles and for preparing particles having a uniform particle size distribution.
摘要翻译：本发明涉及一种制备纳米尺寸磷酸铁颗粒的方法，所述方法包括以下步骤：在反应器中混合铁盐溶液和磷酸盐溶液，以制备含有无定形或结晶磷酸铁沉淀物的悬浮液; 以及在混合步骤期间对反应器内的混合溶液施加剪切力，其中通过剪切力和反应器内部的条件形成含有纳米尺寸的磷酸铁沉淀颗粒的悬浮液。根据本发明，微混合比成核更快，这为制备纳米颗粒和制备具有均匀粒度分布的颗粒提供了一个优点。

7. 发明申请

US20150197655A1 AQUEOUS COMPOSITION FOR PREPARING HARD CAPSULE, PREPARATION METHOD THEREFOR, HARD CAPSULE, AND METHOD FOR RECYCLING HARD CAPSULE SCRAPS 审中-公开
标题翻译：用于制备硬质胶囊的水性组合物，其制备方法，硬化胶囊和用于回收硬质胶囊的方法
公开(公告)号：US20150197655A1
公开(公告)日：2015-07-16
申请号：US14415006
申请日：2013-07-04
申请人： SAMSUNG FINE CHEMICALS CO., LTD.
发明人： Jin Ryul Son , Sang Youb Lee , Jyung Hee Jeon , Sung Hwan Bang , Ju Hee Shin
IPC分类号： C09D101/28 , C09D105/06 , C09D105/00
摘要： Disclosed are an aqueous composition for preparing a hard capsule, a preparation method therefor, a hard capsule, and a method for recycling hard capsule scraps. The disclosed aqueous composition for preparing a hard capsule comprises a water-soluble cellulose ether, an alcohol, and water. In addition, the method for recycling hard capsule scraps comprises the step of dissolving hard capsule scraps comprising a water-soluble cellulose ether into a mixture solution comprising water and an alcohol so as to prepare an aqueous composition for preparing a recycled hard capsule.
摘要翻译：公开了一种制备硬胶囊的水性组合物，其制备方法，硬胶囊和回收硬胶囊废料的方法。所公开的用于制备硬胶囊的水性组合物包含水溶性纤维素醚，醇和水。此外，回收硬胶囊废料的方法包括将包含水溶性纤维素醚的硬胶囊废料溶解在包含水和醇的混合溶液中以制备用于制备再循环硬胶囊的水性组合物的步骤。

8. 发明申请

US20150194701A1 SOLID ELECTROLYTE CONTAINING IONIC LIQUID 有权
标题翻译：固体电解液含有离子液体
公开(公告)号：US20150194701A1
公开(公告)日：2015-07-09
申请号：US14421055
申请日：2013-09-30
申请人： SAMSUNG FINE CHEMICALS CO., LTD
发明人： Sang Mi Kim , Hyun Cheol Lee , Jin Hee Lee
IPC分类号： H01M10/0564 , H01M10/0566 , H01G11/56 , H01M10/052
CPC分类号： H01M10/0564 , H01B1/06 , H01G11/56 , H01M10/052 , H01M10/0565 , H01M10/0566 , H01M2300/0045 , H01M2300/0065 , H01M2300/0085 , H01M2300/0091 , Y02E60/13
摘要： The present invention is intended to provide a gel-type solid electrolyte having flexibility while maintaining the advantages of an ionic liquid by effectively internalizing the ionic liquid into a porous metal oxide. To this end, the present invention provides the gel-type solid electrolyte which includes an ionic liquid in a porous metal oxide prepared from a silane compound represented by the following Chemical Formula 1: Si(R1)x(OR2)y(CR3═CR4R5)(4-x-y) [Chemical Formula 1] in the Formula, R1 and R2 are alkyl groups with carbon numbers in the range of 1 to 3, which are independent from each other; R3, R4 and R5 are each independently hydrogen, a halogen element or an alkyl group having 1 to 5 carbon atoms; and x is an integer in the range of 0≦x≦3, y is an integer in the range of 1≦y≦4 and x+y is an integer in the range of 2≦x+y≦4.
摘要翻译：本发明旨在提供具有柔性的凝胶型固体电解质，同时通过有效地使离子液体内化为多孔金属氧化物，同时保持离子液体的优点。为此，本发明提供了一种凝胶型固体电解质，其包括由以下化学式1表示的硅烷化合物制备的多孔金属氧化物中的离子液体：Si（R1）x（OR2）y（CR3 = CR4R5 ）（4-xy）式中的[化学式1] R 1和R 2为碳数为1〜3的烷基，它们彼此独立; R 3，R 4和R 5各自独立地为氢，卤素元素或具有1至5个碳原子的烷基; 并且x是0≤n1E的整数; x和nlE; 3，y是1≤n1E的整数; y和nlE; 4和x + y是2≤n1E的范围内的整数; x + y和nlE; 4。

9. 发明授权

US09035108B2 Method for preparing chlorohydrins composition and method for preparing epichlorohydrin using chlorohydrins composition prepared thereby 有权
标题翻译：制备氯代醇组合物的方法和由其制备的氯代醇组合物制备表氯醇的方法
公开(公告)号：US09035108B2
公开(公告)日：2015-05-19
申请号：US13806969
申请日：2011-06-08
申请人： Won Seob Song , Sung Yul Woo , Boo Weon Song , Seong Han Park , Myoung Suk Kwon
发明人： Won Seob Song , Sung Yul Woo , Boo Weon Song , Seong Han Park , Myoung Suk Kwon
IPC分类号： C07C31/34 , C07D301/02 , C07C29/62 , C07C29/80 , C07D303/08
CPC分类号： C07D301/02 , C07C29/62 , C07C29/80 , C07D303/08 , C07C31/36
摘要： Provided are a method of preparing a chlorohydrin composition and a method of preparing epichlorohydrin by using a chlorohydrin composition prepared by using the method. The method of preparing chlorohydrins in which polyhydroxy aliphatic hydrocarbon is reacted with a chlorination agent in the presence of a catalyst includes performing at least one combination of a series of unit operations comprising a first reaction step, a water removal step, and a second reaction step in this stated order, wherein the method further includes mixing a chlorohydrin concentrate obtained by purifying the reaction mixture discharged from the final reaction step from among the reaction steps and a water-rich layer discharged from the water-removal step and diluting the mixture with water. The method of preparing epichlorohydrin includes contacting the chlorohydrin composition prepared by using the method of preparing a chlorohydrin composition with an alkaline agent.
摘要翻译：提供了通过使用通过使用该方法制备的氯代醇组合物制备氯代醇组合物的方法和制备表氯醇的方法。制备其中多羟基脂族烃与氯化剂在催化剂存在下反应的氯氢化物的方法包括进行一系列单元操作的至少一种组合，其中包括第一反应步骤，脱水步骤和第二反应步骤按照所述顺序，其中所述方法还包括将通过纯化从反应步骤中排出的最终反应步骤的反应混合物和从除水步骤排出的富水层中获得的氯代醇浓缩物混合并用水稀释混合物。制备表氯醇的方法包括使通过使用氯醇组合物与碱性试剂的制备方法制备的氯代醇组合物接触。

10. 发明授权

US08969631B2 Method for preparing chlorohydrins composition and method for preparing epichlorohydrin using chlorohydrins composition prepared thereby 有权
标题翻译：制备氯代醇组合物的方法和由其制备的氯代醇组合物制备表氯醇的方法
公开(公告)号：US08969631B2
公开(公告)日：2015-03-03
申请号：US13806911
申请日：2011-06-08
申请人： Won Seob Song , Sung Yul Woo , Boo Weon Song , Seong Han Park , Myoung Suk Kwon
发明人： Won Seob Song , Sung Yul Woo , Boo Weon Song , Seong Han Park , Myoung Suk Kwon
IPC分类号： C07C31/34 , C07D301/28 , C07C29/62 , C07C29/80 , C07D303/08 , C07D301/24
CPC分类号： C07D301/28 , C07C29/62 , C07C29/80 , C07D303/08 , C07C31/36
摘要： A method of preparing a chlorohydrin composition and a method of preparing epichlorohydrin by using a chlorohydrin composition prepared by using the method are provided. The method of preparing a chlorohydrin composition in which a polyhydroxy aliphatic hydrocarbon is reacted with a chlorination agent in the presence of a catalyst includes performing at least one combination of a series of unit operations comprising a first reaction step, a water removal step, and a second reaction step in this stated order, wherein the method further includes mixing a chlorohydrin concentrate obtained by purifying the reaction mixture discharged from the final reaction step from among the plurality of reaction steps and a water-rich layer discharged from the water-removal step. The method of preparing epichlorohydrin includes contacting the chlorohydrin composition prepared by using the method of preparing a chlorohydrin composition with an alkaline agent.
摘要翻译：提供了一种制备氯代醇组合物的方法和通过使用通过使用该方法制备的氯代醇组合物制备表氯醇的方法。制备其中多羟基脂族烃与氯化剂在催化剂存在下反应的氯代醇组合物的方法包括进行一系列单元操作的至少一种组合，该组合操作包括第一反应步骤，脱水步骤和第二反应步骤，其中所述方法还包括混合通过纯化从多个反应步骤中排出的最终反应步骤的反应混合物获得的氯代醇浓缩物和从除水步骤排出的富含水层。制备表氯醇的方法包括使通过使用氯醇组合物与碱性试剂的制备方法制备的氯代醇组合物接触。

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