Patents
Literature
Patsnap Copilot is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Patsnap Copilot

1763 results about "Carbonation" patented technology

Carbonation is the chemical reaction of carbon dioxide to give carbonates, bicarbonates, and carbonic acid. In chemistry, the term is sometimes used in place of carboxylation, which refers to the formation of carboxylic acids.

Hydrogen production from carbonaceous material

Hydrogen is produced from solid or liquid carbon-containing fuels in a two-step process. The fuel is gasified with hydrogen in a hydrogenation reaction to produce a methane-rich gaseous reaction product, which is then reacted with water and calcium oxide in a hydrogen production and carbonation reaction to produce hydrogen and calcium carbonate. The calcium carbonate may be continuously removed from the hydrogen production and carbonation reaction zone and calcined to regenerate calcium oxide, which may be reintroduced into the hydrogen production and carbonation reaction zone. Hydrogen produced in the hydrogen production and carbonation reaction is more than sufficient both to provide the energy necessary for the calcination reaction and also to sustain the hydrogenation of the coal in the gasification reaction. The excess hydrogen is available for energy production or other purposes. Substantially all of the carbon introduced as fuel ultimately emerges from the invention process in a stream of substantially pure carbon dioxide. The water necessary for the hydrogen production and carbonation reaction may be introduced into both the gasification and hydrogen production and carbonation reactions, and allocated so as transfer the exothermic heat of reaction of the gasification reaction to the endothermic hydrogen production and carbonation reaction.
Owner:BOARD OF SUPERVISORS OF LOUISIANA STATE UNIV & AGRI & MECHANICAL COLLEGE +1

Separation of Carbon Dioxide (Co2) From Gas Mixtures By Calcium Based Reaction Separation (Cars-Co2) Process

A reaction-based process has been developed for the selective removal of carbon dioxide (CO2) from a multicomponent gas mixture to provide a gaseous stream depleted in CO2 compared to the inlet CO2 concentration in the stream. The proposed process effects the separation of CO2 from a mixture of gases (such as flue gas / fuel gas) by its reaction with metal oxides (such as calcium oxide). The Calcium based Reaction Separation for CO2 (CaRS—CO2) process consists of contacting a CO2 laden gas with calcium oxide (CaO) in a reactor such that CaO captures the CO2 by the formation of calcium carbonate (CaCOa). Once “spent”, CaCO3 is regenerated by its calcination leading to the formation of fresh CaO sorbent and the evolution of a concentrated stream of CO2. The “regenerated” CaO is then recycled for the further capture of more CO2. This carbonation-calcination cycle forms the basis of the CaRS—CO2 process. This process also identifies the application of a mesoporous CaCO3 structure, developed by a process detailed elsewhere, that attains >90% conversion over multiple carbonation and calcination cycles. Lastly, thermal regeneration (calcination) under vacuum provided a better sorbent structure that maintained reproducible reactivity levels over multiple cycles.
Owner:THE OHIO STATES UNIV

Method for producing aluminum oxide and co-producing active calcium silicate through high-alumina fly ash

The invention provides a method for producing aluminum oxide and co-producing active calcium silicate through high-alumina fly ash. The method comprises the following steps that: the high-alumina fly ash firstly reacts with a sodium hydroxide solution to carry out pre-desilication to obtain a liquid-phase desiliconized solution and a solid-phase desiliconized fly ash; lime cream is added to the liquid-phase desiliconized solution to carry out a causticization reaction, the resulting solid phase is active calcium silicate which is prepared through carrying out filter pressing, flash evaporation and drying to obtain the finished product; limestone and a sodium carbonate solution are added to the desiliconized fly ash to blend qualified raw slurry, then the blend qualified raw slurry is subjected to baking into the clinker, the liquid phase generated from dissolution of the clinker is a crude solution of sodium aluminate; the crude solution of the sodium aluminate is subjected to processes of first-stage deep desilication, second-stage deep desilication, carbonation, seed precipitation, baking and the like to obtain the metallurgical grade aluminum oxide meeting requirements. According to the present invention, the defects in the prior art are overcome; purposes of less material flow and small amount of slaggling are achieved; energy consumption, material consumption and production cost are relative low; extraction rate of the aluminum oxide is high; the calcium silicate with high added value is co-produced; the method provided by the present invention can be widely applicable for the field of chemical engineering.
Owner:INNER MONGOLIA DATANG INT RENEWABLE RESOURCES DEV

Separation of carbon dioxide (CO2) from gas mixtures by calcium based reaction separation (CaRS-CO2) process

A reaction-based process has been developed for the selective removal of carbon dioxide (CO2) from a multicomponent gas mixture to provide a gaseous stream depleted in CO2 compared to the inlet CO2 concentration in the stream. The proposed process effects the separation of CO2 from a mixture of gases (such as flue gas/fuel gas) by its reaction with metal oxides (such as calcium oxide). The Calcium based Reaction Separation for CO2 (CaRS—CO2) process consists of contacting a CO2 laden gas with calcium oxide (CaO) in a reactor such that CaO captures the CO2 by the formation of calcium carbonate (CaCO3). Once “spent”, CaCO3 is regenerated by its calcination leading to the formation of fresh CaO sorbent and the evolution of a concentrated stream of CO2. The “regenerated” CaO is then recycled for the further capture of more CO2. This carbonation-calcination cycle forms the basis of the CaRS—CO2 process. This process also identifies the application of a mesoporous CaCO3 structure, developed by a process detailed elsewhere, that attains >90% conversion over multiple carbonation and calcination cycles. Lastly, thermal regeneration (calcination) under vacuum provided a better sorbent structure that maintained reproducible reactivity levels over multiple cycles.
Owner:THE OHIO STATES UNIV

Separation of carbon dioxide (CO2) from gas mixtures by calcium based reaction separation (CaRS-CO2) process

A reaction-based process has been developed for the selective removal of carbon dioxide (CO2) from a multicomponent gas mixture to provide a gaseous stream depleted in CO2 compared to the inlet CO2 concentration in the stream. The proposed process effects the separation of CO2 from a mixture of gases (such as flue gas/fuel gas) by its reaction with metal oxides (such as calcium oxide). The Calcium based Reaction Separation for CO2 (CaRS-CO2) process consists of contacting a CO2 laden gas with calcium oxide (CaO) in a reactor such that CaO captures the CO2 by the formation of calcium carbonate (CaCO3). Once “spent”, CaCO3 is regenerated by its calcination leading to the formation of fresh CaO sorbent and the evolution of a concentrated stream of CO2. The “regenerated” CaO is then recycled for the further capture of more CO2. This carbonation-calcination cycle forms the basis of the CaRS-CO2 process. This process also identifies the application of a mesoporous CaCO3 structure, developed by a process detailed elsewhere, that attains >90% conversion over multiple carbonation and calcination cycles. Lastly, thermal regeneration (calcination) under vacuum provided a better sorbent structure that maintained reproducible reactivity levels over multiple cycles.
Owner:THE OHIO STATES UNIV

Method of treating cement kiln dust for recovery and recycle

InactiveUS6331207B1SolubilityAmmonium compounds
Fresh or stockpiled cement kiln dust is moistened with sufficient water so that the amount of total free and combined water relative to dust is about 3 parts water to 1 part dust by mass, or less. The wet solids are treated with carbon dioxide to convert compounds, such as calcium hydroxide, to carbonates, such as calcium carbonate. The degree of carbonation is controlled so that the solubility of calcium becomes minimum for the dust being treated; this is also when hydroxyl and bicarbonate ions in solution are about at their minima. As the carbonation reactions occur, the water combined in hydroxides is released as free water so that the mixture becomes a slurry and the potentially soluble alkalies and sulfate (and any chlorides present) are released to the liquid phase. The solids are separated from the liquid, and the solids, which may be washed, provide a material suitable for return as feed to the kiln. The liquid, which contains the dissolved alkali compounds, is recycled to reclaim additional dust or treated to recover alkali salts when the alkali salts are sufficiently concentrated.While any source of carbon dioxide may be used, the preferred source is exit gases from the kiln. The gases are conditioned by condensation of water and removal of ammonium compounds, such as sulfate and chloride. The conditioning condensate may be treated to recover useful byproduct salts.
Owner:GEBHARDT RONALD FR

Method for preparing high-alkali value (TBN400) synthesized calcium alkyl benzene sulfonate

The invention provides a method for preparing high base number (TBN400) synthetic calcium alkyl-benzene sulfonate. The method comprises the following steps of: adopting a mixed acid of long-chain linear alkyl-benzene sulfonic acid and high-boiling heavy alkyl-benzene sulfonic acid, calcium oxide and/or calcium hydroxide, low-carbon alcohol, alkaline-earth metal halide or nitrate, and a mixture of alkaline-earth metal alkylphenol or alkaline-earth metal alkylphenate and polyisobutylene succinic anhydride for a neutralization reaction in the presence of a solvent and cutback oil at a temperature of between 40 and 80 DEG C; then, passing through carbon dioxide to a product of the neutralization reaction at a temperature of between 40 and 60 DEG C for a carbonation reaction; and producing high base synthetic alkyl-benzene sulfonate with a total base number (TBN) of 400mgKOH/g by adopting a process of a one-step method. The product is divided into high-base number (TBN400) synthetic alkyl-benzene sulfonate containing chlorine and high-base number (TBN400) synthetic alkyl-benzene sulfonate without the chlorine. The product produced by adopting the method with low viscosity, small turbidity, easy filtration, light color and no skin formation has the advantages of excellent high-temperature detergency, excellent anti-foaming property and excellent heat storage stability.
Owner:JINZHOU DPF TH CHEM CO LTD

Spherical calcium carbonate and method for producing thereof

InactiveUS20060165583A1Inferior physical propertyLow blowing rateCalcium/strontium/barium carbonatesCosmetic preparationsCalcium hydroxideO-Phosphoric Acid
When spherical calcium carbonate is produced by blowing a carbon dioxide gas or a carbon dioxide-containing gas into an aqueous suspension containing calcium hydroxide to react them, after start of the reaction, an aqueous solution or suspension of a water-soluble phosphoric acid compound or a water-soluble salt thereof is added to the reaction mixture when carbonation ratio reaches 2 to 10%, and the reaction is further allowed to continue at a low gas blowing rate of 1.0 NL/minute or lower (step (a)). Subsequently, an aqueous suspension containing calcium hydroxide and an aqueous solution or suspension of a water-soluble phosphoric acid compound or a water-soluble salt thereof are added to the reaction mixture, and a carbon dioxide gas or a carbon dioxide-containing gas is introduced to allow to react and thereby produce spherical calcium carbonate having a mean particle diameter of 10 μm or larger. This production method is performed under high velocity revolution from the start of the reaction to the end of the step (a) This method provides calcite type spherical calcium carbonate showing high brightness and small friction coefficient, and having a shape comparatively close to a true sphere and a mean particle diameter of 10 μm or larger.
Owner:OKUTAMA IND
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products