Patent classifications
C01C1/164
LIGNOCELLULOSIC CONVERSION PROCESS COMPRISING SULFUR DIOXIDE AND/OR SULFUROUS ACID PRETREATMENT
Provided herein is a process for producing one or more products from a lignocellulosic feedstock. The process comprises treating the lignocellulosic feedstock by contacting the feedstock at least sulfur dioxide, sulfurous acid, or a combination thereof to produce a pretreated feedstock comprising one or more sulfonic acids. A process stream comprising one or more sulfonic acids is subsequently treated in a wet oxidation step to produce a stream comprising at least soluble oxidized phenolic compounds. The soluble oxidized phenolic compounds are then fed to an anaerobic digestion to produce methane. Optionally, hydrogen sulfide is produced during the anaerobic digestion. The hydrogen sulfide may then be converted to an acid selected from sulfur dioxide, sulfurous acid or a combination thereof in one or more steps. The acid may then be re-used in treatment as desired.
PROCESS FOR REDUCING THE CORROSIVENESS OF A BIOCIDAL COMPOSITION CONTAINING IN SITU GENERATED SODIUM HYPOCHLORITE
A process for substantially reducing the corrosiveness of a composition containing in situ generated sodium hypochlorite in which the sodium hypochlorite is substantially converted to a haloamine.
DEVICE AND METHOD FOR HARMLESS TREATMENT AND REGENERATION OF WASTE LIQUID DISCHARGE DURING WATER GLASS MOLD SHELL HARDENED WITH AMMONIUM CHLORIDE SOLUTION
A harmless treatment and regeneration device and method thereof of waste liquid discharge from failed hardener solution during hardening of water glass mold shell via ammonium chloride solution are provided. The device includes a waste liquid storage tank, a filtering mechanism, a regeneration mechanism, and a regeneration liquid storage tank. A fluid outlet end of the waste liquid storage tank is in fluid communication with a fluid inlet end of the filtering mechanism, a fluid outlet end of the filtering mechanism is in fluid communication with a fluid inlet end of the regeneration mechanism, and a fluid outlet end of the regeneration mechanism is in fluid communication with a fluid inlet end of the regeneration liquid storage tank.
A PROCESS FOR PRODUCING ALUMINA
A process for extracting values from a leach residue from lithium extraction comprising:
(a) mixing the leach residue with a chloride containing compound to form a first mixture;
(b) calcining the first mixture to form a calcined mixture rich in calcium aluminosilicate and a hydrochloric acid containing off gas;
(c) acid leaching the calcined mixture to form an aluminium bearing liquor and a silicon rich solid residue;
(d) recovering values selected from the group consisting of aluminium compounds, silicon compounds and compounds containing silicon and aluminium.
Methods and systems for utilizing carbide lime or slag
Provided herein are methods comprising a) treating a slag solid or carbide lime suspension with an ammonium salt in water to produce an aqueous solution comprising calcium salt, ammonium salt, and solids; b) contacting the aqueous solution with carbon dioxide from an industrial process under one or more precipitation conditions to produce a precipitation material comprising calcium carbonate and a supernatant aqueous solution wherein the precipitation material and the supernatant aqueous solution comprise residual ammonium salt; and c) removing and optionally recovering ammonia and/or ammonium salt using one or more steps of (i) recovering a gas exhaust stream comprising ammonia during the treating and/or the contacting step; (ii) recovering the residual ammonium salt from the supernatant aqueous solution; and (iii) removing and optionally recovering the residual ammonium salt from the precipitation material.
PROCESS FOR TREATING LIGNOCELLULOSIC FEEDSTOCK COMPRISING WET OXIDATION
A process for producing one or more products from a lignocellulosic feedstock comprising treating the lignocellulosic feedstock to produce sugar in one or more stages comprising addition of acid, base or a combination thereof and introduction of heat. The addition of the acid, base, or a combination thereof produces a salt. The sugar is fermented to produce a fermentation product and the fermentation product is recovered. A stream comprising the salt is treated by wet oxidation with the introduction of heat. A stream comprising salt resulting from the wet oxidation is provided for use as a salt product or a process chemical for introduction within the process. Heat from the wet oxidation may be supplied to any stage of the process in which heat is introduced.
Recovery of Valuable Resources from Produced Water and Coal Combustion Products
The present invention relates to processes employing water produced from wells that, after suitable purification steps, is processed to recover resources that can be used to treat other waste streams, such as flue gases and ashes from combustion of fossil fuels.
Process for the preparation of trisilylamine from monochlorosilane and ammonia
The present invention relates to a specific process for producing trisilylamine from monochlorosilane and ammonia in the liquid phase. The invention further relates to a plant in which such a process can be carried out with advantage.
Production of trisilylamine from monochlorosilane and ammonia by use of inert solvent
The present invention relates to a specific process for producing trisilylamine from monochlorosilane and ammonia in the liquid phase. The invention further relates to a plant wherein such a process can be carried out with advantage.
RARE EARTH AND GROUP 4 CATALYSTS FOR AMBIENT CONVERSION OF DINITROGEN TO SECONDARY SILYLAMINES
Catalysts and methods for dinitrogen conversion to secondary silyamines or ammonia (N.sub.2RR) are provided. The catalysts are a metalacyclic platform characterized by a pocket with tunable dimensions and conditions. The catalysts show dramatically improved N.sub.2RR activity compared to previously reported early d-block catalysts. The tetraphenolate-supported bimetallic lanthanide or group IV metal complex undergoes multiple two-electron reductions, the last of which leads to the reductive activation of dinitrogen. The inclusion of a weak acid and silyl electrophiles during the reduction enables the catalytic conversion of N.sub.2 to purely secondary amines.