摘要:
A process for preparing a mesoporous material, e.g., transition metal oxide, sulfide, selenide or telluride, Lanthanide metal oxide, sulfide, selenide or telluride, a post-transition metal oxide, sulfide, selenide or telluride and metalloid oxide, sulfide, selenide or telluride. The process comprises providing an acidic mixture comprising a metal precursor, an interface modifier, a hydrotropic or lyotropic ion precursor, and a surfactant; and heating the acidic mixture at a temperature and for a period of time sufficient to form the mesoporous material. A mesoporous material prepared by the above process. A method of controlling nano-sized wall crystallinity and mesoporosity in mesoporous materials. The method comprises providing an acidic mixture comprising a metal precursor, an interface modifier, a hydrotropic or lyotropic ion precursor, and a surfactant; and heating the acidic mixture at a temperature and for a period of time sufficient to control nano-sized wall crystallinity and mesoporosity in the mesoporous material. Mesoporous materials and a method of tuning structural properties of mesoporous materials.
摘要:
An electrically conductive member of the present disclosure includes a base member containing chromium (Cr), and a first layer provided on a surface of the base member and containing chromium(III) oxide (Cr2O3). The first layer also contains titanium (Ti).
摘要:
The present invention concerns specific new compounds of formula Li(2−x)Na(x)MO(2−y/2)F(1+y) (where 0≤x≤0.2 and −0.6≤y≤0,8 and M is a transition metal), cathode material comprising the new compounds, batteries and lithium-cells comprising said new compound or cathode material, a process for the production of the new compound and their use.
摘要:
A article made by vacuum deposition, includes a substrate; and a color layer deposited on the substrate, wherein the color layer has an L* value between about 75 to about 80, a a* value between about −5 to about −10, and a b* value between about 15 to about 20 in the CIE LAB color space.
摘要:
Methods and systems for processing metal oxides from metal containing solutions. Metal containing solutions are mixed with heated aqueous oxidizing solutions and processed in a continuous process reactor or batch processing system. Combinations of temperature, pressure, molarity, Eh value, and pH value of the mixed solution are monitored and adjusted so as to maintain solution conditions within a desired stability area during processing. This results in metal oxides having high or increased pollutant loading capacities and/or oxidation states. These metal oxides may be processed according to the invention to produce co-precipitated oxides of two or more metals, metal oxides incorporating foreign cations, metal oxides precipitated on active and inactive substrates, or combinations of any or all of these forms. Metal oxides thus produced are, amongst other uses; suitable for use as a sorbent for capturing or removing target pollutants from industrial gas streams or drinking water or aqueous streams or for personal protective respirators.
摘要:
The invention relates to a method for producing lithium-transition metal mixtures of general formula Lix(M1yM21-y)nOnz, wherein M1 represents nickel, cobalt or manganese, M2 represents chromium, cobalt, iron, manganese, molybdenum or aluminium, and is different from M1, n is 2 if M1 represents manganese and is 1 otherwise, x is comprised between 0.9 and 1.2, y is comprised between 0.5 and 1.0 and z is comprised between 1.9 and 2.1. According to the inventive method, an intimate mixture composed of transition metal compounds containing oxygen and of a lithium compound containing oxygen is calcinated, said mixture being obtained by processing a solid powder transition metal compound with a solution of said lithium compound, and then drying. At least the M1 compound is used in powder form having a specific surface of at least 20 m2/g (BET) and calcination is carried out in a fluidised bed.
摘要翻译:本发明涉及一种制备通式为Lix(M 1 yM 2-y)n O n z的锂 - 过渡金属混合物的方法,其中M 1表示镍,钴或锰,M 2表示铬 ,钴,铁,锰,钼或铝,并且不同于M 1,如果M 1表示锰,则n为2,否则为1,x为0.9至1.2,y为0.5至1.0 z在1.9和2.1之间。 根据本发明的方法,煅烧由含有氧的过渡金属化合物和含氧化合物的锂化合物组成的紧密混合物,所述混合物通过用所述锂化合物的溶液处理固体粉末过渡金属化合物,然后干燥而获得。 至少M 1化合物以比表面积至少为20m 2 / g(BET)的粉末形式使用,并且在流化床中进行煅烧。
摘要:
Advantageous processes are disclosed for the production of vinyl fluoride. Also disclosed are advantageous methods which may be employed for the preparation of catalysts useful in such processes. Included are methods which involve (i) reducing surface B.sub.2 O.sub.3 present in a bulk chromium oxide composition containing surface B.sub.2 O.sub.3 by treating said composition with HF at an elevated temperature and/or (ii) treating a bulk chromium oxide composition containing B.sub.2 O.sub.3 to enrich the B.sub.2 O.sub.3 present on its surface by heating said composition in oxygen or an oxygen-containing environment (e.g., air) at an elevated temperature for a time sufficient to enrich the B.sub.2 O.sub.3 on the surface of the composition by at least a factor of two compared to the surface analysis of the untreated bulk composition. Processes are provided herein which involve contacting 1,1-difluoroethane in the vapor phase with a trivalent chromium catalyst (preferably a trivalent chromium catalyst having primarily the morphology of alpha-chromium oxide and/or containing less than 1000 ppm alkali metal as the alkali metal oxide) wherein chromium is at least 95 atom percent of the metallic cations of said catalyst, at a temperature between about 225.degree. C. and 375.degree. C. Advantageous embodiments of these processes are disclosed wherein (i) the catalyst is prepared by reducing B.sub.2 0.sub.3 present in a bulk chromium oxide composition as indicated above, (ii) chromium is at least 99 atom percent of the metallic cations of the catalyst and/or (iii) the space velocity is from about 200 volumes to 2000 volumes of 1,1-difluoroethane per volume of catalyst per hour.
摘要翻译:PCT No.PCT / US96 / 09752 Sec。 371日期1997年12月3日第 102(e)日期1997年12月3日PCT提交1996年6月7日PCT公布。 公开号WO96 / 41679 日期1996年12月27日公开了用于生产氟乙烯的有利的方法。 还公开了可用于制备可用于这些方法的催化剂的有利方法。 包括以下方法:(i)通过在高温下用HF处理所述组合物和/或(ii)处理含有B 2 O 3的本体氧化铬组合物以富集B 2 O 3,从而减少存在于含有表面B 2 O 3的本体氧化铬组合物中的表面B 2 O 3 在表面上通过在氧气或含氧环境(例如空气)中在升高的温度下加热所述组合物足以使组合物表面上的B 2 O 3与表面分析相比至少增加2倍的时间 的未处理的散装组合物。 本文提供了将气相中的1,1-二氟乙烷与三价铬催化剂(优选主要具有α-氧化铬形态的三价铬催化剂和/或含有少于1000ppm碱金属作为碱金属的三价铬催化剂) 氧化物),其中铬为所述催化剂的金属阳离子的至少95原子%,温度为约225℃至375℃。公开了这些方法的有利实施方案,其中(i)催化剂通过还原B 2 O 3 存在于如上所述的本体氧化铬组合物中,(ii)铬是催化剂的金属阳离子的至少99原子%,和/或(iii)空间速度为约200体积至2000体积的1,1- 每单位体积催化剂每小时二氟乙烷。
摘要:
A process is disclosed for producing chromium oxide powders, which comprises forming an aqueous slurry wherein the solids content is a mixture which consists essentially of in percent by weight about 5 to 15 chromium acetate and the balance chromium oxide, agglomerating the mixture, sintering the resulting agglomerated mixture in a hydrogen atmosphere at a temperature at about 1400.degree. C. to about 1550.degree. C. in metallic vessels, entraining the sintered chromium oxide powder in a carrier gas, passing the sintered chromium oxide powder and the carrier gas through a plasma flame at a power of about 10 to about 80 KW using an inert gas as the plasma gas, and cooling the resulting plasma heated chromium oxide powder to produce free flowing chromium oxide powder having a free chromium content of less than about 1% by weight.
摘要:
Chromium(III) oxide and hydroxide aerogels are produced by the reaction of chromium(VI) oxide with a solvent which is reducing to chromium(VI), such as methanol, heating the solution to hypercritical conditions, and venting the solvent hypercritically. The product aerogels exhibit surface areas above 400 m.sup.2 /g, pore volumes of at least 2 cm.sup.3 /g and a substantially uniform pore size distribution. Also disclosed is a unique process which employs high pore volume, high surface area chromium(III) oxide or hydroxide as a fluorination catalyst. More particularly, reaction of C.sub.2 Cl.sub.3 F.sub.3 with HF over these catalysts produced high yields of C.sub.2 Cl.sub.2 F.sub.4 and C.sub.2 ClF.sub.5.
摘要:
A process for producing ultrafine particles of a ceramic, which comprises heating a ceramic having substantially the same components as the final ultrafine ceramic particles, a metal constituting the metal component of the final ultrafine ceramic particles, a mixture of said ceramic with said metal or carbon, or a mixture of said metal with carbon by an arc plasma or a high frequency induction plasma generated in hydrogen, nitrogen, oxygen, a gaseous mixture of hydrogen and nitrogen, or a gaseous mixture of nitrogen and oxygen.