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65results about "Varying alkali metal carbonate water content" patented technology

Carbonate recycling in a hydrogen producing reaction

A process for producing hydrogen gas from a reaction of an organic substance and a base with a recycling of a carbonate or bicarbonate by-product and a regeneration of the base. In one embodiment, reaction of an organic substance and a base produces hydrogen gas and a metal carbonate. The instant invention provides recycling of the metal carbonate by-product. In a preferred embodiment, the metal carbonate by-product is soluble and recycling includes a three step process. In a first step, the soluble metal carbonate is reacted with a metal hydroxide to form a weakly soluble or insoluble metal carbonate that precipitates in a metathesis reaction. The metal hydroxide reactant of the hydrogen producing reaction is also formed in the metathesis reaction and remains in solution. Precipitation of the carbonate thus permits ready isolation of the carbonate by-product, while leaving behind an aqueous metal hydroxide phase that can be returned to and further utilized in the hydrogen producing reaction. The metal carbonate precipitate of the metathesis reaction is thermally decomposed to form a metal oxide solid in a second step. In a third step, the metal oxide is reacted with water to reform the metal hydroxide reactant of the metathesis reaction. The hydrogen producing reaction and recycling process are sustainable in that the metal hydroxide reactant of each reactant is regenerated in the recycling process. In an alternative embodiment, the hydrogen producing reaction produces a metal carbonate precipitate directly and recycling occurs through thermal decomposition of the metal carbonate to form a metal oxide followed by reaction of the metal oxide with water to reform the metal hydroxide employed in the hydrogen producing reaction. In yet another embodiment, a bicarbonate by-product is formed by a hydrogen producing reaction of an organic substance and a base and bicarbonate recovery occurs by heating the bicarbonate to form a carbonate and recycling according to the instant carbonate recycling process.
Owner:TACTICAL FUEL CELLS

System and process for preparing low-salt dense soda ash by liquid-phase hydration

The invention discloses a system and a process for preparing low-salt dense soda ash by liquid-phase hydration. The method comprises the following steps of: adding light soda ash with the temperature of more than 93 DEG C, condensate water and saturated solution of sodium carbonate according to a mass ratio of 1:0.22:1.4-1:0.22:2.0 into a hydration tank for hydration, wherein the reaction temperature is controlled to be between 100 and 104 DEG C and the reaction time is 20 to 25 minutes, and crystallizing the soda ash in a form of a monohydrate soda, namely Na2CO3.H2O after the reaction; after separating the monohydrate soda crystal slurry with a hydrocyclone separator, feeding the top liquid into a mother liquor storing barrel and feeding the bottom liquid into a centrifuge; after dehydrating the bottom liquid with the centrifuge to obtain a monohydrate soda filter cake; and drying, cooling and screening the monohydrate soda filter cake to obtain the finished product, namely the low-salt dense soda ash, wherein when the centrifuge is used for dehydrating, water is added to wash off a part of salts. The system can guarantee the constant material level of a material bin so that the feeding of the soda ash is stable. The obtained soda ash product has the advantages of large crystallization granule size, high first-rate product rate and high added value, wherein the product with crystallization granule size of more than 180 mu m is up to over 75 percent; the qualification rate is up to 100 percent; and the first-rate product rate is up to 95 percent.
Owner:内蒙古博源工程有限责任公司

Sodium carbonate recovery from waste streams and impounded sodium carbonate decahydrate deposits

A process is described for recovering sodium carbonate or other sodium-based chemicals from sodium-bearing streams, including in particular mine water, evaporative pond water and sodium carbonate decahydrate deposits, recycle and purge streams, and other waste streams. In the process sodium bicarbonate-bearing streams are decarbonized to reduce the sodium bicarbonate concentration in a combination with other sodium-bearing streams, resulting in a liquor suitable as feed to a sodium carbonate decahydrate or sodium carbonate monohydrate process. The sodium bicarbonate stream is combined in a mix tank with other sodium carbonate bearing streams where the concentration is adjusted to form a liquor suitable to feed a sodium decahydrate or sodium carbonate monohydrate evaporation / crystallization step. In the process the combination of the various sodium-bearing streams is decarbonized to below 3.5% sodium bicarbonate when fed to a sodium decahydrate process and to below 1% sodium bicarbonate when fed to a sodium carbonate monohydrate process. The feed streams are adjusted in sodium carbonate concentration by higher concentrated sodium carbonate-bearing streams or by addition of sodium carbonate decahydrate produced from said streams or recovered form evaporation pond deposits, are then processed to produce sodium carbonate decahydrate or sodium carbonate monohydrate or further processed to form other sodium carbonate salts.
Owner:TATA CHEM NORTH AMERICA INC

Process for producing sodium hydrogencarbonate crystal particles having low caking property

InactiveUS20070178037A1Longer treatment timeReduce cakingVarying alkali metal carbonate water contentAlkali metal carbonates moisture absorption preventionSodium bicarbonateGas concentration
A process for producing sodium hydrogencarbonate crystals, which comprise subjecting sodium hydrogencarbonate crystal powder having an average particle size of from 50 to 500 μm based on the mass to heat treatment at a temperature of from 70 to 95° C. by a heating gas having a carbon dioxide gas concentration of at most the concentration calculated by the following formula (1):
Carbon dioxide gas concentration=0.07l×e(0.1×T)×R(−0.0005×T−0.9574)  (1)
(wherein T is the temperature (%) of sodium hydrogencarbonate crystals, and R is the relative humidity (%), provided that the upper limit of the carbon dioxide gas concentration is 100 vol %) with reference to the graph of FIG. 1 wherein the horizontal axis (X-axis) represents the relative humidity and the vertical axis (Y-axis) represents the carbon dioxide gas concentration, to form anhydrous sodium carbonate on the surface of the sodium hydrogencarbonate crystal particles with a content of anhydrous sodium carbonate of from 0.03 to 0.40 mass % in the sodium hydrogencarbonate crystals.
A process for producing sodium hydrogencarbonate crystal particles having a low caking property, which are useful in the field of food products, pharmaceuticals, bath additives, etc., which require no necessity to contain an anticaking agent, can be provided.
Owner:ASAHI GLASS CO LTD

Method for preparing high-purity anhydrous sodium carbonate by using membrane method

The invention discloses a method for preparing high-purity anhydrous sodium carbonate by using a membrane method. The method comprises the following steps: (1) dissolving industrial sodium carbonate with distilled water of 55-65 DEG C, and stirring to ensure that calcium impurities in the industrial sodium carbonate are fully deposited; (2) adding a sodium hydroxide solution into the solution, and stirring at 55-65 DEG C to ensure that magnesium ions in the solution are fully deposited until the magnesium ion content of the solution is lower than 5ppm; (3) filtering the solution by using a ceramic membrane; (4) evaporating a filtrate after filtration, putting an obtained magma solution into a centrifuge for separation, and adding deionized water into the centrifuge to wash filter cakes until no chloride ion is generated in the filter cakes; and (5) drying the product obtained by centrifuging to obtain high-purity anhydrous sodium carbonate, wherein in the high-purity anhydrous sodium carbonate, Ca<2+> is less than or equal to 1ppm, Mg<2+> is less than or equal to 1ppm, SS is less than or equal to 1ppm, and Cl<-> is less than or equal to 2ppm. In the high-purity anhydrous sodium carbonate prepared by the method disclosed by the invention, Ca<2+> is less than or equal to 1ppm, Mg<2+> is less than or equal to 1ppm, SS is less than or equal to 1ppm, and Cl<-> is less than or equal to 2ppm.
Owner:TIANJIN BOHUA YONGLI CHEM IND

Method for comprehensively utilizing solid waste in methyl carbonate production

The invention discloses a method for comprehensively utilizing solid waste in the methyl carbonate production, comprising the following steps: adding solvent in the solid waste, stirring and evenly mixing the mixture according to the volume ratio of 1:1.5; carrying out filter pressing separation to obtain organic phase solution and sodium carbonate solidoid substance containing crystallization water; distillating the organic phase solution at normal pressure under the condition that the temperature is lower than 70 DEG C to reclaim the solvent and simultaneously obtain about 40 percent of organic phase solution relative to the weight of waste residue; carrying out vacuum distillation on organic matters to obtain 5 percent of methyl carbonate relative to the organic phase, which is more than 85 percent of 1,2-propanediol and 1 percent of ice carbon; and baking the solidoid substance to volatilize to obtain 50 percent of industrial sodium carbonate relative to the weight of solid waste residue. The method overcomes the defects that the prior method causes the environment pollution and influences the safe running of a boiler, sodium carbonate, propanediol and methyl carbonate in the waste are burnt out and cannot be recovered so as to cause waste. The method can energy sources and change wastes into valuables.
Owner:张青
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