3832 results about "Hydration reaction" patented technology

The invention discloses a desulfurization waste water zero discharging process. The process comprises a chemical dosing softening process and a microfiltration membrane treatment process; after incoming water is subjected to two-stage softening, nanofiltration and reverse osmosis separation are performed; sodium sulfate decahydrate with the purity of more than 99% is separated out by utilizing freezing crystallization; a reverse osmosis concentrated water regeneration sodium ion exchange device is utilized; sodium chloride with the purity of more than 98% is separated out by utilizing evaporative crystallization; solids are comprehensively utilized, and no liquid is discharged outside. The invention further provides a desulfurization waste water zero discharging system. According to the desulfurization waste water zero discharging process and the system, water in desulfurization waste water can be separated to be reutilized as domestic and industrial usable water, and other impurities in the desulfurization waste water are separated in solid form, so that pollutants harmful to the natural environment do not generate, and the problem that the desulfurization waste water pollutes the environment can be completely solved.

A hydrophobic solid, acid catalyst for the acid catalyzing reaction, such as esterifying reaction, alkylation reaction and hydration reaction, is prepared by attaching the inorganic metal salt to the high-hydrophobicity carrier. Its advantages are high catalyst activity and selectivity, high stability, and high hydrophobicity.

Metal catalysts comprising hollow forms or spheres are made of metal alloy and optionally activated. The metal catalysts can be used for the hydrogenation, dehydrogenation, isomerization reductive alkylation, reductive amination, and/or hydration reaction of organic compounds.

The invention belongs to the material field for removing the arsenic in water by settlement, more particularly relates to polyelement composite metal oxide arsenic removal settlement agent and an application method thereof based on iron oxide, manganese oxide, and aluminum oxide. The invention uses an ectopic preparation method or situ preparation method for preparing and obtaining polyelement composite metal oxide arsenic removal settlement agent which comprises hydrated iron oxide, hydroxyl-hydrated ferric hydroxide, hydrated aluminum oxide, hydroxyl-hydrated alumina, hydrated manganese oxide and the like. The polyelement composite metal oxide arsenic removal settlement agent can be used for removing the arsenic pollutants in water bodies such as lakes, reservoirs, rivers, groundwater, drinking water, industrial waste water, and the like; in addition, the settlement agent can also be used for removing the heavy metals such as copper, chromium, cadmium, lead, and the like, and the pollutants such as iron, manganese, phosphates, and the like in water by settlement.

The invention relates to a clean production process of plateau sulfate type boron-lithium salt lake brine. The process comprises the following steps of: (1) arranging a pre-airing pond, a mirabilite pond, a NaCl pond, a carnallite pond, an epsom salt pond I, a magnesium removing pond, an epsom salt pond II, a boron pond, a lithium pond and an old brine pond; (2) controlling the sodium ion concentration in plateau sulfate type boron-lithium salt lake brine, precipitating mirabilite out in winter to obtain brine A, naturally evaporating the brine A, and salting out to obtain brine B; (3) naturally evaporating the brine B, and precipitating sylvine and carnallite out in sequence to obtain brine C; (4) naturally evaporating the brine C, precipitating an epsom salt out, and performing solid-liquid separation to obtain brine D and a solid A; (5) blending the brine D with mirabilite, removing magnesium to obtain brine E, and naturally evaporating brine E to obtain brine F and a solid B; (6) performing a hydration reaction on brine F, naturally evaporating, and precipitating reservoir water/inderite and brine G out; and (7) evaporating brine G or refrigerating for precipitating lithium sulfate, and processing the lithium sulfate into a corresponding product. The process has the advantages of comprehensive utilization of natural energy, saving in energy and environment friendliness.

In order to reduce incoming atmospheric carbon dioxide levels in compressed air prior to cryogenic distillation, a water spray cooling tower equipped with biocatalytic packing, or fed with absorptive reagents, is used to convert gaseous carbon dioxide into bicarbonate ions which dissolve in the cooling water. The hydration reaction and refrigeration occur synergistically. The bicarbonate ions are subsequently removed from the solution using the heat from the compressed air in a regenerator re-boiler unit, and then fed to a percolation cooling tower for releasing CO₂ and cooling.

The invention discloses a lithium-based concrete sealing solidifying agent. The lithium-based concrete sealing solidifying agent comprises the following components in percentage by weight: 50.0-90.0 percent of lithium silicate sol, 0.01-1.0 percent of wetting and dispersing agent, 0.01-1.0 percent of defoaming agent, 0.01-1.0 percent of permeability-resistant agent, 0.0-10.0 percent of stabilizing agent, 0.0-1.0 percent of accelerating agent and the balance of water. The lithium-based concrete sealing solidifying agent can produce C-S-H gel through the effective permeability and the hydration reaction with dissociative calcium ions in concrete to seal capillary pores in the concrete, so that the permeability resistance, the wear resistance, the hardness and other performance of the concrete can be improved.

The invention provides a curing agent and a curing method for heavy metals in fly ash from mswi (municipal solid waste incineration). The curing agent comprises an aluminum-rich high-silicon material and an alkaline exciting agent, wherein the mass of the aluminum-rich high-silicon material is 15% to 25% of the mass of the fly ash from mswi; the mass of the alkaline exciting agent is 3% to 5% of the mass of the fly ash from mswi. The curing agent adopts industrial waste residues, and raw materials are cheap and easy to obtain; according to the curing method, lots of calcium oxide, chloride and sulfide existing in the fly ash from mswi have a hydration reaction with the aluminum-rich high-silicon material to generate a C-S-H (calcium silicate hydrate), Friedel (calcium chloroaluminate) phase and Aft (ettringite) phase system; during the formation process of the mineral system, a solid solution is formed through ion exchange, a new phase is formed through coprecipitation, and a relatively strong stable constraint effect can be played on heavy metals through physical adsorption and coating, so that wastes can be treated by using wastes, and harmless treatment of the fly ash from mswi and resource utilization of the industrial waste residues are realized.

The present invention is a formable dental treatment tray utilizing poly(2-ethyl-2-oxazoline) and a gelatinous active. Blending of the active is accomplished by mixing the Poly(2-ethyl-2-oxazoline) with an active ingredient, such as a peroxide like hydrogen peroxide, carbamide peroxide, sodium perborate, or sodium percarbonate, usually also with water or an appropriate organic solvent. Peroxide concentrations in these new gels can reach a 30% concentration of hydrogen peroxide while maintaining a shelf life of six months at room temperature without developing peroxide decomposition. The gels are applied to an appropriate backing and dried to a gelatinous state. In use, the active is hydrated and regains adhesiveness. Then the tray is pressed and formed around a user's dental arch to form the customizable tray. Multiple active ingredients may be used, with or without peroxide, for accomplishing desired treatment regimens.

A macroreticular alumina carrier contains alumina and halogen and is prepared through mixing hydrated aluminium oxide with pore enlarging agent, shaping and calcining at 600-850 deg.C

A fiber cement composite material providing improved rot resistance and durability, the composite material incorporating biocide treated fibrous pulps to resist microorganism attacks. The biocide treated fibers have biocides attached to inner and outer surfaces of individualized fibers to protect the fibers from fungi, bacteria, mold and algae attacks. The biocides selected have strong affinity to cellulose and do not interfere with cement hydration reactions. This invention also discloses the formulation, the method of manufacturing and the final fiber cement products using the biocide treated fibers.

Flowable concrete mixtures have an aqueous foam admixture mixed therein to give the concrete mixture desired strength, flowability, and density. The concrete mixtures include a hydration stabilizer to stabilize the aqueous foam. The hydration stabilizer inhibits the reaction between the hydraulic cement and the water in the aqueous foam. The aqueous foam can be further stabilized using a fluorochemical surfactant. Preferred fluorochemical surfactants comprise an oligomer having at least one hydrophilic nonionic monomer and at least one hydrophilic anionic monomer.

The invention relates to a carbon loaded noble metal catalyst, which is characterized in that the catalyst consists of a carrier and palladium and ruthenium which are loaded on the carrier, wherein the carrier is powdery fruit shell active carbon and is between 85 and 99.7 percent by weight; the palladium is between 0.2 and 10 percent by weight; and the ruthenium is between 0.1 and 10 percent by weight. The catalyst is obtained by performing acid treatment, ash removal and oxidation treatment on the carrier, namely the active carbon for removing surface reduction functional groups first, using a solution of the palladium and the ruthenium to perform soakage treatment, and using one or more among hydrogen, potassium borohydride or hydrazine hydrate to perform reduction treatment. The catalyst has high activity and selectivity and good stability in hydrogenation reaction of organic compounds containing carbonyl.

The invention provides a packaging shape-stabilizing method of an inorganic hydrated salt phase-change heat storage material, which comprises the following steps: (1) adding a nucleator and deionized water into the inorganic hydrated salt phase-change material, and heating until the inorganic hydrated salt phase-change material achieves the molten state; (2) adding a porous propping material into the molten-state inorganic hydrated salt phase-change material, and stirring sufficiently and uniformly; (3) putting the molten-state mixture obtained in the step (2) in a vacuum environment to enhance the adsorptivity of the porous propping material for the inorganic hydrated salt phase-change material; and (4) moving the molten-state mixture out of the vacuum environment, and immediately putting the molten-state mixture into a low-temperature environment suitable for crystallization to perform recrystallization. The composite shape-stabilized phase-change material obtained by the method has the advantages of stable structure, high latent heat, no toxicity, simple preparation process, short time consumption and low cost.

The invention relates to a method for low-pressure processing of coal bed gas, comprising the steps of: introducing the coal bed gas into a hydration reactor from the bottom part of a hydration reactor so as to be contacted with hydrate working liquid in the hydration reactor, leading methane contained in the coal bed gas and water in the hydrate working liquid to generate hydration reaction to form a hydrate which is removed from the coal bed gas; meanwhile, the purified gas is obtained after the methane in the coal bed gas is removed; wherein the operation pressure of the hydration reactor is 0.11-0.85MPa, and the temperature is 3-18 DEG C. The formed hydrate can be further introduced into a hydrate decomposition device for decomposition, thereby obtaining the methane with high concentration. The invention simultaneously relates to a device for realizing the method for low-pressure processing of the coal bed gas. The invention can safely purify the oxygen-containing coal bed gas under lower pressure and remove the contained methane to be lower than 0.05 molar fraction, thereby reducing the emission of the methane, reducing the greenhouse effect and simultaneously avoiding the risk of explosion.

The invention relates to a magnetic cation exchange resin catalyzer and a preparation method and application thereof. In the method, nanometer magnetic metal oxide and long-chain fatty acid are mixed in the water the pH of which is 9-12, the pH is regulated to 4-5, and modified nanometer magnetic particulate is obtained after the nanometer magnetic metal oxide and the long-chain fatty acid react; monomer, evocating agents, crosslinking agents and pore-foaming agents are mixed with the modified nanometer magnetic particulate which accounts for 5-65% of the total weight of the monomer and the crosslinking agents, magnetic resin is obtained after polymerization, and the catalyzer is obtained through sulphur reaction of the magnetic resin. The catalyzer can be used for catalyzing olefin hydration reaction, ether hydrolysis reaction, esterification reaction, etherealization reaction, condensation reaction or aromatic hydrocarbon alkylation reaction in a magnetic reactor.

Neutral electrolytes, relatively neutral electrolytes, metal oxides, metal hydroxides and/or organic exothermic hydration chemicals may be hydrated with water at a controlled location in a subterranean formation to generate sufficient exothermic heat to at least soften and possibly melt and flow bitumen at or near the location. This controlled and localized heating would be useful in drilling through relatively thick bitumen or “tar” beds. In one non-limiting embodiment the exothermic hydration reaction does not generate appreciable amounts of gas. Alternatively, the exothermic reaction may be used to liberate hydrocarbons from gas hydrates in an embodiment where the evolution of gas is acceptable.

The invention provides a method for producing caprolactam by taking high-purity benzene as a raw material, and the method comprises the following steps of: A. preparing cyclohexene from the raw material benzene through hydrogenation; B. separating and purifying cyclohexene; C. carrying out hydration on the cyclohexene for preparing cyclohexanol; D. separating and purifying cyclohexanol; E. carrying out dehydrogenation on cyclohexanol for preparaing cyclohexanone; F. refining cyclohexanone; G. carrying out oximation on cyclohexanone so as to prepare cyclohexanone-oxime; H. refining cyclohexanone-oxime; I. carrying out rearrangement on refined cyclohexanone-oxime so as to prepare caprolactam; and J. refining caprolactam, wherein the high-purity benzene is adopted as a raw material, so that the purity of benzene is more than 99.95%, the sulphur content is less than 5ppm, and the methylbenzene is not more than 100ppm. The method has the beneficial effects that the high-purity benzene is adopted as a raw material, so that the impurity is less, and the product quality is high; the raw material is high in comprehensive utilization rate and low in hydrogen consumption; and the mass of the raw material and intermediate products generated in all the steps of reaction can be strictly controlled, so that the direct commercial value of the intermediate products is fully exerted, and the optimal quality of the product caprolactam can be reached.