C01B6/21

METHOD FOR PRODUCING BOROHYDRIDE SALTS

The present invention relates to a method for producing tetrahydridoborate salts with high efficiency at low cost. The method for the production of metal borohydride salts according to the present invention comprises the steps of providing an anhydrous metal borate salt and milling the anhydrous metal borate salt in the presence of a metal material based on magnesium or magnesium alloys in a hydrogen atmosphere at a temperature and for a time sufficient to produce the metal borohydride salt. In another embodiment of the invention, the method for the production of metal borohydride salts according to the present invention comprises the steps of providing an hydrated metal borate salt and milling the hydrated metal borate salt in the presence of a metal material based on magnesium or magnesium alloys in an inert gas atmosphere at a temperature and for a time sufficient to produce the metal borohydride salts. In a still further embodiment of the invention, the metal material based on magnesium or magnesium alloys is a secondary magnesium material, preferably a Class 2, Class 3, or Class 6 secondary magnesium material.

METHOD FOR PRODUCING BOROHYDRIDE SALTS

The present invention relates to a method for producing tetrahydridoborate salts with high efficiency at low cost. The method for the production of metal borohydride salts according to the present invention comprises the steps of providing an anhydrous metal borate salt and milling the anhydrous metal borate salt in the presence of a metal material based on magnesium or magnesium alloys in a hydrogen atmosphere at a temperature and for a time sufficient to produce the metal borohydride salt. In another embodiment of the invention, the method for the production of metal borohydride salts according to the present invention comprises the steps of providing an hydrated metal borate salt and milling the hydrated metal borate salt in the presence of a metal material based on magnesium or magnesium alloys in an inert gas atmosphere at a temperature and for a time sufficient to produce the metal borohydride salts. In a still further embodiment of the invention, the metal material based on magnesium or magnesium alloys is a secondary magnesium material, preferably a Class 2, Class 3, or Class 6 secondary magnesium material.

Method and apparatus for producing sodium borohydride
10472246 · 2019-11-12 · ·

A method and an apparatus for producing sodium borohydride that have excellent energy efficiency and production efficiency are provided. Using a production apparatus 20 comprising: a cylindrical reaction container 21; a cylindrical reaction portion 22 which is rotatably held in this reaction container 21 and in which sodium metaborate that is a raw material 1 and granular aluminum are housed together with a grinding medium 2; and a hydrogen introduction portion 23 for introducing hydrogen gas into the reaction portion 22 directly or via the reaction container 21, the sodium metaborate and the granular aluminum are reacted under a hydrogen atmosphere, while being rolled and ground with the grinding medium, to obtain sodium borohydride.

Method and apparatus for producing sodium borohydride
10472246 · 2019-11-12 · ·

A method and an apparatus for producing sodium borohydride that have excellent energy efficiency and production efficiency are provided. Using a production apparatus 20 comprising: a cylindrical reaction container 21; a cylindrical reaction portion 22 which is rotatably held in this reaction container 21 and in which sodium metaborate that is a raw material 1 and granular aluminum are housed together with a grinding medium 2; and a hydrogen introduction portion 23 for introducing hydrogen gas into the reaction portion 22 directly or via the reaction container 21, the sodium metaborate and the granular aluminum are reacted under a hydrogen atmosphere, while being rolled and ground with the grinding medium, to obtain sodium borohydride.

ELECTROLYTE SEPARATORS INCLUDING LITHIUM BOROHYDRIDE AND COMPOSITE ELECTROLYTE SEPARATORS OF LITHIUM-STUFFED GARNET AND LITHIUM BOROHYDRIDE

Set forth herein are compositions comprising A.(LiBH.sub.4).B.(LiX).C.(LiNH.sub.2), wherein X is fluorine, bromine, chloride, iodine, or a combination thereof, and wherein 0.1A3, 0.1B4, and 0C9 that are suitable for use as solid electrolyte separators in lithium electrochemical devices. Also set forth herein are methods of making A.(LiBH.sub.4).B.(LiX).C.(LiNH.sub.2) compositions. Also disclosed herein are electrochemical devices which incorporate A.(LiBH.sub.4).B.(LiX).C.(LiNH.sub.2) compositions and other materials.

REDUCTION KIT, REDUCING COMPOSITION AND USE OF SAID KIT AND COMPOSITION

Disclosed is a reduction kit including a reducing compound and an open-cell polymer foam, the surface of which includes a polymer having a catechol unit. Also disclosed is a reducing composition including an open-cell foam, the surface of which includes a polymer having a catechol unit, the foam being functionalized by a reducing compound. The use of the kit or composition as a reagent in reduction reactions is also disclosed.

Method for catalytically induced hydrolysis and recycling of metal borohydride solutions

The process for obtaining M.sup.1BH.sub.4, the process comprising contacting M.sup.1-B0.sub.2 with a metal M.sup.2 in the presence of molecular hydrogen (H.sub.2) under conditions permitting the formation of M.sup.1-BH.sub.4 and M.sup.2-oxide, wherein the M.sup.1 is a metal selected from column I of the periodic table of elements or alloys of metals selected from column I of the periodic table of elements and M.sup.2 is a metal or an alloy of metals selected from column II of the periodic table of elements, provided that M.sup.2 is not Mg and M.sup.1 is different from M.sup.2.

Method for catalytically induced hydrolysis and recycling of metal borohydride solutions

The process for obtaining M.sup.1BH.sub.4, the process comprising contacting M.sup.1-B0.sub.2 with a metal M.sup.2 in the presence of molecular hydrogen (H.sub.2) under conditions permitting the formation of M.sup.1-BH.sub.4 and M.sup.2-oxide, wherein the M.sup.1 is a metal selected from column I of the periodic table of elements or alloys of metals selected from column I of the periodic table of elements and M.sup.2 is a metal or an alloy of metals selected from column II of the periodic table of elements, provided that M.sup.2 is not Mg and M.sup.1 is different from M.sup.2.

Graphene/Metal or Metalloid Core-Shell Composite and Manufacturing Method Thereof
20190185391 · 2019-06-20 ·

The present invention relates to a manufactured graphene/metal or metalloid core-shell composite and manufacturing method thereof. The method comprising: using a modified graphene oxide as a base, then performing concentration and steam drying followed by organic solvent replacement to obtain a modified graphene oxide organic solvent; using a liquid-phase self-assembly method to coat the modified graphene oxide onto a surface of the metal or metalloid to form a graphene/metal or metalloid coated particle solution, then filtering and drying to obtain the graphene metal/metalloid core-shell composite. The method improves upon a conventional organic and inorganic material coating technique, and reduces an impact of a water-based solvent and high temperature on a highly reactive metal and metalloid, thereby expanding the feasibility of the coating technique and addressing a barrier of applicability of graphene and reactive metal or metalloid in the field of energetic materials.

Ionic conductor containing high-temperature phase of LiCB.SUB.9.H.SUB.10., method for manufacturing same, and solid electrolyte for all-solid-state battery containing said ion conductor

A method for manufacturing an ion conductor including LiCB.sub.9H.sub.10 and LiCB.sub.11H.sub.12 is provided. The method includes mixing LiCB.sub.9H.sub.10 and LiCB.sub.11H.sub.12 in a molar ratio of LiCB.sub.9H.sub.10/LiCB.sub.11H.sub.12=1.1 to 20. An ion conductor including lithium (Li), carbon (C), boron (B) and hydrogen (H) is also provided. The ion conductor has X-ray diffraction peaks at at least 2?=14.9?0.3 deg, 16.4?0.3 deg and 17.1?0.5 deg in X ray diffraction measurement at 25? C., and has an intensity ratio (B/A) of 1.0 to 20 as calculated from A=(X-ray diffraction intensity at 16.4?0.3 deg)?(X-ray diffraction intensity at 20 deg) and B=(X-ray diffraction intensity at 17.1?0.5 deg)?(X-ray diffraction intensity at 20 deg).