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1. 发明授权

KR100912495B1 황화아연계 적색형광체 및 이의 제조방법 失效
标题翻译：基于硫化锌的红色磷光体及其制备方法
公开(公告)号：KR100912495B1
公开(公告)日：2009-08-17
申请号：KR1020080125107
申请日：2008-12-10
申请人： 한빔 주식회사 , 서울대학교산학협력단
发明人： 박병우 , 정대룡 , 손동연 , 김종민 , 김천중 , 오병두 , 신현우
IPC分类号： C09K11/57 , C09K11/56 , B82B3/00
摘要： A preparation method of a zinc sulfide-based red phosphor is provided to effectively manufacture a zinc sulfide-based red phosphor with uniform size at a relatively low temperature, and to reduce production costs. A preparation method of a zinc sulfide-based red phosphor comprises the steps of: dissolving zinc acetate, manganese nitrate, and lithium hydroxideÀhydrate in distilled water to prepare a liquid first layer; adding a linoleate-based compound to the liquid first layer mixture to form the liquid first layer and a solid second layer; adding linoleic acid solution dissolved in thioacetamide and ethanol to a mixture formed with the liquid and solid bilayer to form the liquid first layer, the solid second layer, and a liquid third layer; treating a mixture having 3 layers at 85-95 ‹C for 9-12 hours to form Mn-Li-ZnS nano particles; collecting, washing and drying the Mn-Li-ZnS nano particles; heat-treating the dried Mn-Li-ZnS nano particles at 100-600 ‹C to prepare Mn-Li-ZnS fluorescent nano particles represented by chemical formula 1: ZnS : Mn_x, Li_y.
摘要翻译：提供了一种硫化锌系红色荧光体的制备方法，以在相对较低的温度下有效地制造尺寸均匀的硫化锌系红色荧光体，降低生产成本。硫化锌系红磷光体的制备方法包括以下步骤：将乙酸锌，硝酸锰和氢氧化锂 - 水合物溶解于蒸馏水中制备液体第一层; 向所述液体第一层混合物中加入亚油酸酯基化合物以形成液体第一层和固体第二层; 将溶于硫代乙酰胺和乙醇的亚油酸溶液加入到与液体和固体双层形成的混合物中以形成液体第一层，固体第二层和液体第三层; 在85-95℃下处理3层的混合物9-12小时，形成Mn-Li-ZnS纳米颗粒; 收集，洗涤和干燥Mn-Li-ZnS纳米颗粒; 在干燥的Mn-Li-ZnS纳米粒子100-600℃下进行热处理，制备由化学式1表示的Mn-Li-ZnS荧光纳米粒子：ZnS：Mn_x，Li_y。

2. 发明授权

KR100842376B1 망간 도핑된 황화아연 나노입자의 제조방법 失效
标题翻译： ZNS的制备方法：MN纳米颗粒
公开(公告)号：KR100842376B1
公开(公告)日：2008-07-01
申请号：KR1020070022666
申请日：2007-03-07
申请人： 한빔 주식회사 , 재단법인서울대학교산학협력재단
发明人： 박병우 , 손동연 , 정대룡 , 김종민 , 오병두 , 이재승
IPC分类号： B82B3/00 , C01G9/08 , B82Y40/00
CPC分类号： C01G9/08 , B82B3/0038 , B82Y30/00 , B82Y40/00 , C01P2004/64
摘要： A preparation method of even-sized ZnS:Mn nanoparticles is provided to obtain ZnS:Mn nanoparticles having excellent phosphorescence at lower temperature in a simple process economically by employing liquid-solid-solution synthesis method under optimized selections for raw material compounds, Mn concentration and treatment temperature. A preparation method of ZnS:Mn nanoparticles comprises steps of: 1) forming a primary liquid layer by dissolving zinc acetate and manganese nitrate in distilled water; 2) forming a secondary layer by adding linoleate type organic materials to the primary layer; 3) forming a tertiary liquid layer by adding linoleic acid and a solution having thioacetamide in ethanol to the secondary layer; 4) forming ZnS:Mn nanoparticles by treating the prepared primary, secondary and tertiary layers at 85-95deg.C for 9-12 hours; 5) collecting and washing the ZnS:Mn nanoparticles; 6) drying the washed ZnS:Mn nanoparticles; and 7) treating the dried ZnS:Mn nanoparticles at ambient temperature-600deg.C for 9-12 hours. The molar ratio of zinc acetamide in step 1) and thioacetamide in step 3) is 0.9-1.1:0.9-1.1, respectively. The amount of manganese nitrate is 1-10at.% in the solution in step 1). The molar ratio of zinc acetamide and manganese nitrate is 1:0.005-0.02 in step 1).
摘要翻译：提供均匀ZnS：Mn纳米粒子的制备方法，在经过优化选择的原料化合物，Mn浓度和液体固溶体合成方法经济性的基础上，在较低温度下获得了较低的磷光ZnS：Mn纳米粒子，处理温度。 ZnS：Mn纳米颗粒的制备方法包括以下步骤：1）通过将乙酸锌和硝酸锰溶解在蒸馏水中形成主液层; 2）通过将亚油酸盐型有机材料加入到初级层中形成第二层; 3）通过将亚油酸和在乙醇中含有硫代乙酰胺的溶液加入到二级层中形成叔液层; 4）通过在85-95℃下处理制备的初级，二级和三级层9-12小时形成ZnS：Mn纳米颗粒; 5）收集和洗涤ZnS：Mn纳米粒子; 6）干燥洗涤后的ZnS：Mn纳米粒子; 和7）在环境温度为600℃下处理干燥的ZnS：Mn纳米颗粒9-12小时。步骤1）中乙酰胺锌与步骤3）中硫代乙酰胺的摩尔比分别为0.9-1.1：0.9-1.1。在步骤1）的溶液中，硝酸锰的量为1-10at。％。步骤1）中乙酰胺和硝酸锰的摩尔比为1：0.005-0.02。

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