Patent classifications
C01B9/02
Method and apparatus for extracting high-purity gold from ore
A method and plant for gold recovery from any gold-bearing ore by low-temperature chlorination, wherein the finely-divided gold-bearing feedstock is chlorinated gaseous chlorine at a temperature of about 245 C. to form a highly volatile chloride compound, which after leaving a reactor is directed to a low-temperature nitrogen plasma unit having a temperature of 900-1100 C., wherein the said compound decomposes and turns into high-purity gold powder, which is cooled with gaseous nitrogen at a cooling reactor's inlet, which is equipped with a water chamber, and collected in a dumping hopper. Some embodiments allow recovery of high-purity 999.9 fine gold using an environmentally friendly, cost effective and inexpensive method implemented on an industrial scale.
Method and Apparatus for Extracting High-Purity Gold from Ore
A method and plant for gold recovery from any gold-bearing ore by low-temperature chlorination, wherein the finely-divided gold-bearing feedstock is chlorinated gaseous chlorine at a temperature of about 245 C. to form a highly volatile chloride compound, which after leaving a reactor is directed to a low-temperature nitrogen plasma unit having a temperature of 900-1100 C., wherein the said compound decomposes and turns into high-purity gold powder, which is cooled with gaseous nitrogen at a cooling reactor's inlet, which is equipped with a water chamber, and collected in a dumping hopper. Some embodiments allow recovery of high-purity 999.9 fine gold using an environmentally friendly, cost effective and inexpensive method implemented on an industrial scale.
Systems and methods for removal and sequestration of acidity from surface seawater
A method by which an environmental energy (e.g., wave energy) is harvested, converted into electrical power, and thereafter used to electrolyze seawater into hydrogen and chlorine gases. Those gases are recombined into hydrogen chloride from which is formed hydrochloric acid solution which is diluted and deposited at a depth sufficient to ensure its neutralization and sequestration for a significant period of time (e.g., for over a millennium). By removing chloride ions from a portion of the sea adjacent to its upper surface and depositing them into a portion of the sea more adjacent to its bottom, acidity is shifted from the surface to base of the sea, and the surface ocean is given a greater ability to absorb and buffer atmospheric carbon dioxide without a corresponding increase in acidity.
Systems and methods for removal and sequestration of acidity from surface seawater
A method by which an environmental energy (e.g., wave energy) is harvested, converted into electrical power, and thereafter used to electrolyze seawater into hydrogen and chlorine gases. Those gases are recombined into hydrogen chloride from which is formed hydrochloric acid solution which is diluted and deposited at a depth sufficient to ensure its neutralization and sequestration for a significant period of time (e.g., for over a millennium). By removing chloride ions from a portion of the sea adjacent to its upper surface and depositing them into a portion of the sea more adjacent to its bottom, acidity is shifted from the surface to base of the sea, and the surface ocean is given a greater ability to absorb and buffer atmospheric carbon dioxide without a corresponding increase in acidity.
Salt production via hydrohalite decomposition
Salt production can include preparing hydrohalite particles by crystallization from saturated brine, adding the hydrohalite particles to a salt brine, thereby forming a hydrohalite-salt brine mixture, agitating the hydrohalite-salt brine mixture until the hydrohalite particles have decomposed into NaCl crystals, and filtering out the NaCl crystals from the salt brine. In some instances, an initial temperature of the salt brine prior to adding the hydrohalite particles is at least 0? C. In some instances, a ratio of salt brine to hydrohalite particles, by weight, is from 0.4 to 29.
Salt production via hydrohalite decomposition
Salt production can include preparing hydrohalite particles by crystallization from saturated brine, adding the hydrohalite particles to a salt brine, thereby forming a hydrohalite-salt brine mixture, agitating the hydrohalite-salt brine mixture until the hydrohalite particles have decomposed into NaCl crystals, and filtering out the NaCl crystals from the salt brine. In some instances, an initial temperature of the salt brine prior to adding the hydrohalite particles is at least 0? C. In some instances, a ratio of salt brine to hydrohalite particles, by weight, is from 0.4 to 29.
Production of heavy brines by calcination of carbonates using plasma arc reactor
Embodiments relate to systems and methods directed towards arrangements of a preheater, a heat exchanger, a plasma recovery system, and at least one processing stage configured to use steam output of a calciner for heating incoming wastewater that is being processed.
Production of heavy brines by calcination of carbonates using plasma arc reactor
Embodiments relate to systems and methods directed towards arrangements of a preheater, a heat exchanger, a plasma recovery system, and at least one processing stage configured to use steam output of a calciner for heating incoming wastewater that is being processed.
METAL CHLORIDES AND METALS OBTAINED FROM METAL OXIDE CONTAINING MATERIALS
Method and apparatus for preparing at least one metal chloride from metal oxide containing material comprising calcining the metal oxide containing material under temperature conditions sufficient to obtain a calcined product comprising at least one metal oxide; and selectively chlorinating the calcined product to form at least one metal chloride.
METAL CHLORIDES AND METALS OBTAINED FROM METAL OXIDE CONTAINING MATERIALS
Method and apparatus for preparing at least one metal chloride from metal oxide containing material comprising calcining the metal oxide containing material under temperature conditions sufficient to obtain a calcined product comprising at least one metal oxide; and selectively chlorinating the calcined product to form at least one metal chloride.