Magnesium fluoride recovery method
    3.
    发明授权
    Magnesium fluoride recovery method 失效
    氟化镁回收方法

    公开(公告)号:US4874599A

    公开(公告)日:1989-10-17

    申请号:US798080

    申请日:1985-11-14

    IPC分类号: C01F5/28 C22B7/04 C22B60/02

    摘要: A method of obtaining magnesium fluoride substantially free from radioactive uranium from a slag containing the same and having a radioactivity level of at least about 7000 pCi/gm. The slag is ground to a particle size of about 200 microns or less. The ground slag is contacted with an acid under certain prescribed conditions to produce a liquid product and a particulate solid product. The particulate solid product is separated from the liquid and treated at least two more times with acid to produce a solid residue consisting essentially of magnesium fluoride substantially free of uranium and having a residual radioactivity level of less than about 1000 pCi/gm. In accordance with a particularly preferred embodiment of the invention a catalyst and an oxidizing agent are used during the acid treatment and preferably the acid is sulfuric acid having a strength of about 1.0 Normal.

    摘要翻译: 从含有该氟化物的炉渣中获得基本上不含放射性铀的氟化镁的方法,其放射性水平为至少约7000pCi / gm。 将炉渣研磨至约200微米或更小的粒度。 在某些规定的条件下,地渣与酸接触以产生液体产物和颗粒状固体产物。 将颗粒状固体产物与液体分离并用酸处理至少两次以产生基本上由基本上不含铀的氟化镁组成的固体残余物,其残留放射性水平小于约1000pCi / gm。 根据本发明的特别优选的实施方案,在酸处理期间使用催化剂和氧化剂,优选酸是具有约1.0正常强度的硫酸。

    Process for preparing crystalline magnesium fluoride
    4.
    发明授权
    Process for preparing crystalline magnesium fluoride 失效
    制备晶体氟化镁的方法

    公开(公告)号:US3848066A

    公开(公告)日:1974-11-12

    申请号:US41599373

    申请日:1973-11-15

    申请人: GTE SYLVANIA INC

    IPC分类号: C01F5/28

    CPC分类号: C01F5/28

    摘要: 1. A PROCESS SUITABLE FOR PRODUCING CRYSTALLINE MAGNESIUM FLUORIDE COMPRISING: (A) FORMING A REACTION MIXTURE CONSISTING ESSENTIALLY OF AMMONIUM BIFLUORIDE, AN AQUEOUS SOLUTION OF AMMONIUM HYDROXIDE AND MAGNESIUM CARBONATE, SAID AMMONIUM BIFLUORIDE AND AMMONIUM HYDROXIDE BEING IN STOICHIOMETRIC EXCESS OF SAID MAGNESIUM CARBONATE; (B) HEATING THE FOREGOING MIXTURE AT A TEMPERATURE OF AT LEAST ABOUT 60*C. FOR A TIME SUFFICIENT TO FORM AN INTERMEDIATE SOLID COMPLEX; 8C) SEPARATING SAID COMPLEX FROM THE AQUEOUS PHASE; (D) DRYING SAID COMPLEX AT A TEMPERATURE OF AT LEAST ABOUT 100*C. AND (E) HEATING THE DRIED COMPLEX TO AT LEAST ABOUT 350* C. TO FORM MAGNESIUM FLUORIDE.

    Battery-level Ni—Co—Mn mixed solution and preparation method for battery-level Mn solution

    公开(公告)号:US11695170B2

    公开(公告)日:2023-07-04

    申请号:US17789970

    申请日:2019-12-31

    摘要: Provided are a battery-level Ni—Co—Mn mixed solution and a preparation method for a battery-level Mn solution, the steps thereof comprising: acid dissolution (S1), alkalization to remove impurities (S2), synchronous precipitation of calcium, magnesium, and lithium (S3), deep ageing to remove impurities (S4), synergistic extraction (S5), and refining extraction (S6). The steps of deep ageing to remove impurities (S4) and synergistic extraction (S5) comprise: performing deep ageing on a filtrate obtained from the step of synchronous precipitation of calcium, magnesium, and lithium (S3), and after performing filtration to remove impurities, obtaining an aged filtrate; using P204 to extract the aged filtrate and obtain a loaded organic phase, and subjecting the loaded organic phase to staged back-extraction to obtain the battery-level Ni—Co—Mn mixed solution and a Mn-containing solution. By means of the cooperation between the multiple process steps of synchronous precipitation of calcium, magnesium, and lithium (S3), deep ageing to remove impurities (S4), and synergistic extraction (S5), the impurity content of the obtained battery-level Ni—Co—Mn mixed solution is significantly lowered, and the battery-level Ni—Co—Mn mixed solution can be directly used to prepare a lithium battery ternary precursor material. At the same time, the battery-level Mn solution can also be obtained, which is favorable for large-scale applications of the process and increasing economic benefits.

    METHOD FOR PRODUCING HOLLOW PARTICLES, HOLLOW PARTICLES, ANTIREFLECTION COATING, AND OPTICAL ELEMENT
    8.
    发明申请
    METHOD FOR PRODUCING HOLLOW PARTICLES, HOLLOW PARTICLES, ANTIREFLECTION COATING, AND OPTICAL ELEMENT 审中-公开
    生产中空颗粒的方法,中空颗粒,抗反射涂层和光学元件

    公开(公告)号:US20150225569A1

    公开(公告)日:2015-08-13

    申请号:US14415576

    申请日:2013-07-12

    IPC分类号: C09D5/00

    摘要: A hollow particle and a method for producing hollow particles are provided. The shell of the particle(s) is a continuous layer containing magnesium fluoride and thus is strong.A hollow particle has a continuous shell containing magnesium fluoride and an at least partially removed hollow core. A method for producing hollow particles includes forming core-shell particles having a core particle and a continuous shell containing magnesium fluoride and removing at least a portion of the core particle from the core-shell particles to produce a hollow core. The core-shell particles can be formed by adding an aqueous solution of a magnesium salt and an aqueous solution containing fluoride ions to an aqueous dispersion containing the core particles at a temperature of 10 degrees Celsius to 30 degrees Celsius, both inclusive, and then heating the combined liquid at a temperature of 50 degrees Celsius to 80 degrees Celsius, both inclusive.

    摘要翻译: 提供中空粒子和中空粒子的制造方法。 颗粒的壳是含有氟化镁的连续层,因此是强的。 中空颗粒具有包含氟化镁和至少部分去除的中空芯的连续壳。 制造中空粒子的方法包括形成具有核心粒子的核 - 壳粒子和含有氟化镁的连续壳体,并从核 - 壳粒子中除去至少一部分核心粒子,得到中空核。 核 - 壳颗粒可以通过将镁盐水溶液和含有氟离子的水溶液加入到含有核颗粒的水分散体中,在10℃至30℃的温度下加热,然后加热 在50摄氏度至80摄氏度的温度下的组合液体。

    Method of synthesizing a fluoride growth material for improved outgassing
    9.
    发明申请
    Method of synthesizing a fluoride growth material for improved outgassing 审中-公开
    合成氟化物生长材料以改进除气的方法

    公开(公告)号:US20060249072A1

    公开(公告)日:2006-11-09

    申请号:US11122703

    申请日:2005-05-05

    摘要: Improved contaminant removal from alkaline- or alkali-earth metal fluoride crystal growth material can be obtained by coprecipitating an alkaline- or alkali-earth metal fluoride with a scavenging agent during synthesis of the fluoride growth material. The coprecipitation of the alkaline- or alkali-earth metal fluoride and scavenging agent can be performed using at least one of chloride, nitrate, hydroxide and carbonate salts of the alkaline- or alkali-earth metal fluoride and scavenging agent. This provides a more intimate mixture or dispersion of the scavenging agent in solid solution or as a mechanical mixture with the alkaline- or alkali-earth metal fluoride for improved outgassing and fewer trapped impurities, leading to improved radiation hardness and bulk absorption.

    摘要翻译: 通过在合成氟化物生长材料期间用清除剂共沉淀碱金属或碱土金属氟化物,可以获得从碱金属或碱土金属氟化物晶体生长材料中去除改进的污染物。 碱金属或碱土金属氟化物和清除剂的共沉淀可以使用碱金属或碱土金属氟化物和清除剂中的至少一种氯化物,硝酸盐,氢氧化物和碳酸盐来进行。 这提供了清除剂在固溶体中或作为与碱土金属或碱土金属氟化物的机械混合物的更加密切的混合物或分散体,用于改善除气和较少的捕获的杂质,导致改进的辐射硬度和体积吸收。

    Method of making high purity optical fluoride crystals
    10.
    发明授权
    Method of making high purity optical fluoride crystals 失效
    制备高纯度氟化物晶体的方法

    公开(公告)号:US06802901B2

    公开(公告)日:2004-10-12

    申请号:US10198526

    申请日:2002-07-18

    IPC分类号: C30B1114

    摘要: The present invention relates to the manufacturing of high purity optical flouride crystals, the making of purified optical flouride crystal feedstocks and to the anionic purification of optical fluoride crystalline materials. The invention relates generally to methods for removing oxide impurities from optical fluoride crystal feedstocks. More specifically, the invention relates to a method for preparing purified optical fluoride crystal feedstocks and the use of the feedstock in manufacturing VUV

    摘要翻译: 本发明涉及高纯度光学荧光晶体的制造,纯化的光学氟化物晶体原料的制备以及氟化物结晶材料的阴离子净化。 本发明一般涉及从光氟化物晶体原料中除去氧化物杂质的方法。 更具体地说,本发明涉及一种制备纯化的氟化物氟化物晶体原料的方法,以及在制备用于VUV光刻/激光系统的VUV <200nm透射光氟化物晶体中的原料的使用。