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436 results about "Sylvite" patented technology

Sylvite, or sylvine, is potassium chloride (KCl) in natural mineral form. It forms crystals in the isometric system very similar to normal rock salt, halite (NaCl). The two are, in fact, isomorphous. Sylvite is colorless to white with shades of yellow and red due to inclusions. It has a Mohs hardness of 2.5 and a specific gravity of 1.99. It has a refractive index of 1.4903. Sylvite has a salty taste with a distinct bitterness.

Method for tobacco slice cigarette paper coloring by adopting Millard reaction

Disclosed is a method for tobacco slice cigarette paper coloring with Millard reaction. The method comprises the following steps: (1) tobacco patches or stems are put into hot water with temperatures from 40 degrees to 70 degrees and extracted for 20 minutes-40 minutes, and extract liquor is obtained. (2) The extracted tobacco patches or the stems are put into the hot water with 1 to 3 times total weight of the tobacco patches or the stems after being shoved initially by a shoving machine. The temperature of the hot water is controlled at 45 DEG C +/- 5 DEG C. The tobacco patches or the stems are extracted for 20 minutes. The tobacco patches or the stems are pulped from 25 degrees SR to 40 degrees SR by the pulping machine after the tobacco patches or the stems are shoved, thus tobacco syrup is obtained. (3) Additional fibers are pulped by the pulping machine to 40 degrees SR to 75 degrees SR. Cigarette paper is mixtured by mixturing the additional fibers and the tobacco syrup. (4) Extracted liquors are concentrated after the extracted liquors are combined. Sylvite, compound Millard reaction liquid and spices are added to the concentrated extracted liquors and made into coating liquid. The coating liquid is coated on the cigarette paper with the way of coating. (5) The coated cigarette paper is put under temperature condition of from 70 DEG C to 130 DEG C to conduct the Millard reaction.
Owner:HUBEI XINYE TOBACCO SLICE DEV +1

Method for mining sylvite in underground carnallite ore

InactiveCN102434141AAchieving Selective MiningHigh saturationFluid removalPotassiumEngineering
The invention discloses a method for mining sylvite in underground carnallite ore, which comprises the following steps of: (1) building wells, namely, taking three-pipe structures as well bodies, wherein the three pipes include a technical sleeve pipe, a production sleeve pipe and a central pipe; (2) building a groove on a single well, namely, filling normal-temperature water in annular space of the central pipe and the production sleeve pipe, and discharging dissolved brine from the central pipe; (3) mining by non selective dissolution at normal temperature; (4) selectively mining by hot melting at high temperature, namely, communicating two wells or well groups, pulling out the central pipe, filling a sodium chloride and magnesium chloride containing filler of 75 to 90 degrees centigrade into a well, and discharging the brine for processing from the other well in the well group; and (5) refilling a mother solution into the wells. The method for mining the sylvite in the underground carnallite ore provided by the invention realizes selective mining of potassium chloride; and, the method saves energy resources and reduces production cost; moreover, the refilling process of the mother solution realizes zero discharge of the mother solution and facilitates environment protection.
Owner:中水电海外投资有限责任公司 +1

Preparation and application of catalyst for selective hydrodesulfurization of gasoline

The invention relates to preparation and application of a catalyst for selective hydrodesulfurization of gasoline. The catalyst comprises the following components in percentage by weight: 6 to 20 percent of CoO+MoO, 0.1 to 5 percent of K2O, 0.1 to 5 percent of MgO, 0.1 to 5 percent of P2O5, and the balance of ZrO2-Al2O3 composite carrier, wherein the ZrO2 accounts for 0.1 to 20 percent of the weight of the composite carrier. The preparation of the catalyst comprises the following steps of: preparing the composite carrier by adopting a complex precipitation method; adding sylvite, sesbania powder and de-ionized water into the composite carrier, uniformly mixing and kneading, extruding and drying the mixture at the temperature of between 100 and 150 DEG C and roasting the mixture at the temperature of between 450 and 550 DEG C to prepare a catalyst carrier; adding ammonia, EDTA (Ethylene Diamine Tetraacetic Acid) complexing agent to prepare stable Co-Mo co-immersion liquid which contains phosphorus and magnesium; and preparing the catalyst by using an isometric spraying immersion method. The catalyst has high selectivity and stability, and can reduce saturation of olefin to the utmost extent, and has a good desulfurization effect.
Owner:PETROCHINA CO LTD

Composite fine particles of forward osmosis driving solution system and application thereof

The invention relates to composite fine particles of a forward osmosis driving solution system. Fine particle cores are fully or partially coated by a separable outer layer; an outer layer shell provides an osmotic pressure; and the cores provide a separable characteristic. The solution system has the characteristics that: (1) the system has the composite fine particles having core-shell structures; (2) the diameters of the composite fine particles are less than 500 microns; and (3) the cores of the fine particles comprise particle cores of polymer particles, chitosan, nonmetal particles, metal or alloy; the shells of the fine particles comprise sodium polystyrene sulfonate, polyvinylamine hydrochloride, polyacrylic acid sodium salt, sylvite, calcium salt, polymethylacrylic acid sodium salt or sylvite, polyvinyl alcohol or polyaniline hydrochloride; the surfaces of the fine particle shells are provided with grafted groups, namely, chemical substances having ionization performance are grated on the surfaces of the particle shells by a chemical method; chemical structures having ionization performance are selected from the following chemical substances: Cl<->, COO<-> or SO<3->; and corresponding counter ions are H<+>, Na<+>, K<+>, Ca<2+> or quaternary ammonium salt according to the properties of the groups.
Owner:NANJING UNIV OF TECH +1

New method for producing propiconazole

ActiveCN101781290ASolve the problems of long reaction time, high water content and sticky materialsSimple processOrganic chemistryPropiconazoleBromine
The invention discloses a new method for producing propiconazole, comprising the following steps of: cyclizing 2,4-dichloroacetophenone and 1,2-pentanediol, brominating with bromine to generate 2-brooethyl-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolane, then condensing with 1,2,4-tolyltriazole sylvite to prepare a crude product, and desolventizing, washing and distilling the crude product in vacuum to obtain the propiconazole. When the brominating reaction is carried out after the cyclizing reaction is finished, the bromine is added for twice, firstly the bromine accounting for 1%-10% of the total weight of the bromine is added in a reaction system for brominating induction reaction, and then the residual bromine is added. The bromine is added for twice during brominating reaction, firstly the bromine accounting for 1%-10% of the total weight of the bromine is added for initiating the whole system, the brominating induction reaction guides the direction of the brominating reaction so that monobromides and dibromides generating ketone due to the repeated resolution of cyclized matter are reduced, and finally the method achieves the purpose of improving the yield of the brominating reaction; and the conversion rate of the bromides is high and can be greater than 97%.
Owner:利民化学有限责任公司

Multi-ion health-preserving solution and preparation method and application thereof

The invention discloses a multi-ion health-preserving solution, which contains alkaline concentrated solution and acidic concentrated solution; and the multi-ion health-preserving solution is characterized in that: the alkaline concentrated solution contains the following components in part by weight: 800 to 1200 parts of concentrated seawater mother liquor; 280 to 420 parts of sylvite; 18 to 33 parts of wollastonite; and 0.15 to 0.45 parts of germanium oxide; and the acidic concentrated solution contains the following components in part by weight: 400 to 600 parts of calcium ion water; 145 to 225 parts of citric acid solution; 0.4 to 0.6 parts of germanium oxide; 14 to 26 parts of tourmaline; 24 to 36 parts of sugar; and 280 to 420 parts of white vinegar. The invention also discloses a preparation method and application of the multi-ion health-preserving solution. The multi-ion health-preserving solution has the effects of radical conversion, toxin expulsion and balance-circulation synergism, and products made from the multi-ion health-preserving solution as additive, such as drinking water, cosmetic solution, washing water, food and antialcoholic products, have disease-preventing-and-treating, senility-deferring, cosmetic and body-building effects.
Owner:上海心动能科技有限公司

Method for preparing lithium salt ore from plateau sulfate type salt lake brine

The invention discloses a method for preparing lithium salt ore from plateau sulfate type salt lake brine. The method comprises the following steps of: evaporating sulfate type salt lake brine to be in the sodium chloride saturated state, freezing in winter to separate out mirabilite, and carrying out solid-liquid separation when the content of the sulfate ion in the brine is controlled to be 1g / L to 7g / L; evaporating the brine from which the mirabilite is separated out, so as to separate sodium chloride; evaporating the brine from which the sodium chloride is separated out, so as to separate out sylvine, carnallite and epsomite, carrying out solid-liquid separation when the lithium ion concentration in the brine is controlled to be greater than or equal to 6g / L, wherein the brine subjected to solid-liquid separation is the brine with high magnesium chloride content; mixing the brine with high magnesium chloride content with the mirabilite to react so as to separate out sodium salt and magnesium salt, and carrying out solid-liquid separation when the magnesium-lithium ratio in the solution is controlled to be less than or equal to 8:1, so as to obtain boron-lithium-rich brine; and reacting the boron-lithium-rich brine with water to separate out boron rock, carrying out solid-liquid separation so as to obtain lithium-rich brine; and introducing the lithium-rich brine into a lithium salt pool, and evaporating so as to separate out the lithium salt ore.
Owner:QINGHAI INST OF SALT LAKES OF CHINESE ACAD OF SCI +1

Mechanical crystallizer for sylvite industry

The invention relates to a mechanical crystallizer for sylvite industry. The mechanical crystallizer for sylvite industry comprises a crystallizer body, an outer barrel, a guide cylinder, a feeding baffle plate, a main stirring apparatus, a bowl-shaped baffle plate and a discharged material stirring device, wherein the outer barrel, the guide cylinder, the feeding baffle plate and the bowl-shaped baffle plate are fixedly connected with the crystallizer body, the main stirring apparatus and the discharged material stirring device are connected with the crystallizer body by a support and a bearing, a mother solution overflow opening is formed at the upper end of the crystallizer body, a discharge hole is formed at the bottom of the crystallizer body, the bowl-shaped baffle plate is arranged just under the guide cylinder, and the bottom of the bowl-shaped baffle plate is of an arched-shaped structure which is high in the middle and low at the periphery and is provided with material communication holes at the periphery. The mechanical crystallizer is used for crystallization production of potassium chloride and potassium sulfate and makes the feeding size of raw materials be increased to 8mm, circulating paste for crystallization is relatively separated from crystallized products, the mass concentration of the circulating paste and the handling capacity of the crystallizer can be effectively increased, the particle size of the crystallized products is increased, the entrainment rate of the raw material in the crystallized products is reduced and good crystallization effect is achieved.
Owner:CHANGSHA DESIGN & RES INST OF CHEM IND MIN

Automobile exhaust soot particle trapping burner

The invention discloses an automobile exhaust soot particle trapping burner. The automobile exhaust soot particle trapping burner comprises a shell, a cellular carrier and a three-way catalyst. The shell is filled with the cellular carrier. The three-way catalyst is attached to the carrier and prepared through a method which includes the steps that water-soluble copper salt, water-soluble manganese salt, water-soluble sylvite, water-soluble cerium salt and water-soluble zircon salt are taken and are then dissolved in water, citric acid and polyethylene glycol are added, the water is removed through evaporation after the water-soluble copper salt, the water-soluble manganese salt, the water-soluble sylvite, the water-soluble cerium salt and the water-soluble zircon salt are completely dissolved to obtain gel, and the gel is dried and roasted to obtain the three-way catalyst. The automobile exhaust soot particle trapping burner has a low activation temperature, can be externally connected to the tail end of an automobile exhaust pipeline to trap and burn soot, can remove 80%-95% of soot, 70%-90% of CO, 80%-90% of HC and 50%-70% of NOx at the early use stage, and is easy and convenient to install; the automobile exhaust soot particle trapping burner can still work after an automobile runs for twenty thousand to thirty thousand kilometers, and the cost of the automobile exhaust soot particle trapping burner is far lower than that of an existing three-way catalytic converter.
Owner:广东联南环保科技有限公司

Antistatic agent for polyester elasticizing oiling agent and manufacturing method thereof

The invention discloses an antistatic agent for a polyester elasticizing oiling agent. The antistatic agent comprises the following components in part by weight: 30 to 40 parts of fatty alcohol, 10 to 12 parts of ethylene oxide, 40 to 50 parts of phosphorus pentoxide, 1 to 3 parts of potassium hydroxide and 2 to 5 parts of deionized water. The manufacturing method comprises the follow steps of: firstly, synthesizing the fatty alcohol and the ethylene oxide to obtain fatty alcohol-polyoxyethylene ether; secondly, synthesizing the fatty alcohol-polyoxyethylene ether and the phosphorus pentoxide to obtain fatty alcohol-polyoxyethylene ether organic phosphate; thirdly, synthesizing the fatty alcohol-polyoxyethylene ether organic phosphate and the ethylene oxide to obtain fatty alcohol-polyoxyethylene ether organic phosphate alcohol-polyoxyethylene ester; and fourthly; and fourthly, synthesizing the fatty alcohol-polyoxyethylene ether organic phosphate alcohol-polyoxyethylene ester and the potassium hydroxide to obtain fatty alcohol-polyoxyethylene ether organic phosphate alcohol-polyoxyethylene ester sylvite. The antistatic agent produced by the method has the advantages of high efficiency, low cost, strong frost resistance, easiness in emulsification and capability of meeting series of requirements of post-processing such as elasticizing.
Owner:TONGXIANG HENGLONG CHEM CO LTD

Garbage leachate reverse-osmosis concentrate treatment method

The invention relates to a garbage leachate reverse-osmosis concentrate treatment method, which comprises the following steps: pouring acid into a reverse-osmosis concentrate to reduce alkalinity of the concentrate, introducing the feed liquid into a degassing membrane tube, removing carbon dioxide gas and discharging the degassed concentrate into a sealed neutralization tank, pouring alkali into the neutralization tank, adjusting pH of the feed liquid to 6.5-7.5, preheating and letting the feed liquid enter a first-stage mechanical compression evaporator to carry out forced-circulation heat-exchange evaporation, carrying out forced-circulation heat-exchange evaporation by a second-stage mechanical compression evaporator, controlling liquid-solid rate to 28-35%, carrying out quality-based crystallization to obtain sodium salt and sylvite, processing high-concentration mother liquor and recovering humus, and pumping a separating medium or a supernatant inside a coagulative precipitation tank back into the second-stage mechanical compression evaporator and continuously evaporating. Operation load of each stage can be effectively reduced, the influence of humus accumulation in the concentrate and other unfavorable factors is reduced, continuous and stable operation of the evaporation system can be guaranteed, and zero emission of the reverse-osmosis concentrate can be realized.
Owner:WELLE ENVIRONMENTAL GRP CO LTD

Method for raising hydrogen production efficiency of microalgae

The invention discloses a method for raising hydrogen production efficiency of microalgae and belongs to the field of a biological energy source. The method comprises the following steps: hydrogen-production microalgae cells are cultured in a medium until the exponential growth phase; the microalgae cells are collected, and the microalgae cells are transferred to a microalgae hydrogen-production medium containing organic matters, deoxygenization and sealing are carried out, and the microalgae cells are continuously cultured in a dark environment for a certain time, wherein the organic matters contain at least one of glucose, fructose, acetate, pyruvic acid, 3-phosphoglycerate, malic acid and amino acid and at least one of sodium salts and sylvite of the above organic matters; and finally, the microalgae cells are again placed in a light environment to induce water decomposition to produce hydrogen. It is verified through experiments that hydrogen production efficiency of microalgae can be remarkably raised by adding the organic matters to the microalgae hydrogen-production medium. The method has characteristics of novel technology and remarkable effect and the like, is simple and reliable, and has important practical application value in the field of new energy.
Owner:NINGBO INST OF MATERIALS TECH & ENG CHINESE ACADEMY OF SCI
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