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82 results about "Chloride" patented technology

The chloride ion /ˈklɔːraɪd/ is the anion (negatively charged ion) Cl⁻. It is formed when the element chlorine (a halogen) gains an electron or when a compound such as hydrogen chloride is dissolved in water or other polar solvents. Chloride salts such as sodium chloride are often very soluble in water. It is an essential electrolyte located in all body fluids responsible for maintaining acid/base balance, transmitting nerve impulses and regulating fluid in and out of cells. Less frequently, the word chloride may also form part of the "common" name of chemical compounds in which one or more chlorine atoms are covalently bonded. For example, methyl chloride, with the standard name chloromethane (see IUPAC books) is an organic compound with a covalent C−Cl bond in which the chlorine is not an anion.

Method for preparing ZnWO4 nanorod photocatalysis material

InactiveCN102935360APhotocatalyticWith photocatalytic effectMetal/metal-oxides/metal-hydroxide catalystsTungsten compoundsHeat treatedNanorod
The invention discloses a method for preparing a ZnWO4 nanorod photocatalysis material. The method includes preparing a tungstic acid solution A, a zinc chloride solution B and a sodium citrate solution C; dropwise adding the solution A and the solution C into the solution B to form a solution D; regulating potential of hydrogen (pH) of the solution D to 6-8, and uniformly stirring to obtain a solution E; adding the solution E into a microwave hydrothermal reaction kettle, performing a heating reaction, naturally cooling the solution E to the room temperature after the reaction is finished, and taking out the reaction kettle; and opening the reaction kettle, washing a product for 4-6 times by deionized water and absolute ethyl alcohol, and drying to obtain the ZnWO4 nanorod photocatalysis material. According to the method, the microwave hydrothermal method is utilized to rapidly synthesize the ZnWO4 nanorod with the photocatalysis property, the later crystallization heat treatment is not required, the obtained product is high in purity, and the shape is controllable. The ZnWO4 nanorod with the photocatalysis effect can be synthesized in 10 minutes, and the degradation rate of the prepared ZnWO4 nanorod to rhodamine B in 50-60 minutes can reach to 97%-99%.
Owner:SHAANXI UNIV OF SCI & TECH

Acidic electroplating zinc-nickel alloy electrolyte, preparation method and electroplating method

ActiveCN104694983AReasonable proportionAppropriate ratioJewelleryNickel ionsElectrolyte
The invention discloses an acidic electroplating zinc-nickel alloy electrolyte, a preparation method and an electroplating method thereof; the electrolyte comprises a basic electrolyte and additives; the basic electrolyte is a weakly acidic solution which comprises zinc ions with mass concentration of 27-38g/L, nickel ions with mass centralization of 23-31g/L, chloride ions with mass concentration of 150-220g/L and boric acid with mass concentration of 25-35g/L at Ph value of 4.8-5.4 and at temperature of 28-35 DEG C; and the additives comprise a brightening agent of 1-12 ml/L, a walk agent of 3-30 ml/L and a disodium ethylenediamine tetraacetate complexant of 10-50 ml/L. The acidic electroplating zinc-nickel alloy electrolyte is rational in proportion and proper in matching; the galvanizing efficient is improved by 30-40% compared with the traditional acidic galvanizing; the corrosion resistance of a zinc-nickel coating can be improved remarkably and the service life of the coating is prolonged; the coating is high in hardness, corrosion resistance, abrasive resistance, pyro-oxidation resistance, compactness and comprehensive performance; the electrolyte does not need to the post-treatment technique, so that the adopted electroplating method is saved in cost, efficient and rapid, convenient in operation and far superior to the traditional alkaline zinc-nickel electroplating.
Owner:南通创源电化学科技有限公司

Method for preparing rod-like magnesium hydroxide from salt lake brine

InactiveCN102674409ALarge particlesImprove filtering effectCalcium/strontium/barium chloridesMagnesium hydroxidePotassiumSodium hydroxide
The invention discloses a method for preparing rod-like magnesium hydroxide from salt lake brine. The method comprises the following steps of: concentrating and crystallizing salt lake brine, from which elements such as potassium and lithium are extracted, serving as a raw material to obtain bischofite; dissolving the bischofite separated by crystallization into water to prepare magnesium chloride solution; introducing ammonia gas to perform magnesium precipitation reaction; when the pH value reaches 7-8, stopping introducing the ammonia gas, reacting at the temperature of 30-50 DEG C for 0.5-2 hours, aging and filtering to obtain alkaline magnesium chloride and magnesium precipitation mother liquor; dispersing the alkaline magnesium chloride in mixed solution of ethanol and water to obtain alkaline magnesium chloride suspension; adding sodium hydroxide to further precipitate to obtain rod-like magnesium hydroxide; filtering and separating to obtain magnesium precipitation mother liquor; replenishing the bischofite and circulating for precipitating the alkaline magnesium chloride; feeding to an ammonia still process along with concentration enrichment of magnesium precipitation mother liquor in ammonia chloride; performing ammonia still with lime; and circulating the produced ammonia gas to precipitate the alkaline magnesium chloride of a next batch and producing byproduct calcium chloride, wherein the magnesium content in the brine is not less than 93.4 g/L. The method has the advantages of high product purity, good economic benefit, no environmental pollution, high operability and easiness for industrial production.
Owner:CENT SOUTH UNIV

Method for preparing high-viscosity chitosan quick hemostatic patch

InactiveCN103386146AIncrease viscosityHigh degree of deacetylationAbsorbent padsBandagesCross-linkFreeze-drying
The invention discloses a method for preparing a high-viscosity chitosan quick hemostatic patch. The method comprises the following steps: preparing chitosan gel from high-viscosity chitosan having a deacetylation degree in the range from 80% to 90%, drying the chitosan gel and then immersing one single side of the chitosan gel into a mixed solution of chloroacetic acid and isopropanol for carboxymethylation, and then soaking the chitosan gel into a 30% glycerol solution for 30 minutes and then draining; and finally, carrying out a cross-linking reaction by using a calcium chloride solution so as to introduce calcium ions and thrombin, and then carrying out vacuum freeze-drying, thereby obtaining the high-viscosity chitosan quick hemostatic patch. Raw materials used for the process of the method are low in cost; the process is simple and convenient, and short in period; the obtained chitosan hemostatic patch is high in adhesiveness, and capable of quickly stopping bleeding of a wound under the promotion effect of the calcium ions and the thrombin.
Owner:黄耀江 +2

Sodium bentonite processing agent for blue-green algae and preparation method thereof

InactiveCN104495960AFast gatheringQuick gather salvageBiocideDisinfectantsSodium BentoniteEutrophication
A sodium bentonite processing agent for blue-green algae is prepared from the following raw materials in parts by weight: 10-20 parts of serpentine, 40-45 parts of sodium-base bentonite, 2-3 parts of magnesium chloride, 8-13 parts of calcium chloride, 15-20 parts of potassium ferrate(VI), 12-16 parts of equisetum hyemale, 13-16 parts of pericarpium granati, 3-5 parts of polymaleic acid, 3-4 parts of sodium pyrophosphate, 2-3 parts of urea, 3-5 parts of anhydrous sodium sulfate, 3-5 parts of boric acid, 4-6 parts of polyvinyl alcohol, proper amount of water, and 3-4 parts of an adsorption auxiliary agent. By adding potassium ferrate(VI), the processing agent for blue-green algae has synergic effects of oxidation, adsorption, flocculating, precipitation, sterilization, disinfection, decoloring and deodoring, also does not generate any toxic and harmful substances, is capable of increasing water dissolved-oxygen content, has good removal effects on ammonia nitrogen, nitrites and algae in water, and is used to remove fulvic acid and suspensions in water and eutrophication phenomenon in fresh water. The processing agent for blue-green algae is good in dispersing suspending property and good in adsorption property, and can help to rapidly aggregate and salvage blue-green algae.
Owner:WUHU XIANGRONG FOOD

Method for enhancing anti-freeze and tensile properties of cellulose ion hydrogel, anti-freeze stretchable cellulose ion hydrogel and application

ActiveCN110041538AImprove frost resistanceImprove tensile propertiesCellulosePhysical chemistry
The invention provides a method for enhancing the anti-freeze and tensile properties of cellulose ion hydrogel, anti-freeze stretchable cellulose ion hydrogel and application, relating to the technical field of ion hydrogel. The method for enhancing the anti-freeze and tensile properties of the cellulose ion hydrogel comprises steps as follows: enabling the cellulose ion hydrogel to be immersed into a chlorinated metal salt solution, and dipping for 10-40min to obtain the anti-freeze stretchable cellulose ion hydrogel. Current cellulose ion hydrogel has the technical problems that the tensileproperty is poor and tensile and wire properties can lose at low temperature as well. According to the method, by enabling the cellulose ion hydrogel to be immersed in the chlorinated metal salt solution, metal ions and chloride ions in chlorinated metal salt enter the cellulose ion hydrogel, so that the anti-freeze property of the cellulose ion hydrogel is effectively improved, and the prepared anti-freeze stretchable cellulose ion hydrogel still has good mechanical property and chemical property at the low temperature.
Owner:SOUTH CHINA UNIV OF TECH

Fiber radical sewage decoloration and purification material and preparing method thereof

InactiveCN103466731AWide variety of sourcesEasy to manufactureOther chemical processesWaste water treatment from textile industryFlocculationReclaimed water
The invention discloses a fiber radical sewage decoloration and purification material which is characterized by comprising a component (I) and a component (II). The component (II) occupies 5%-10% of the total mass. The component (1) is a product obtained by reaction of 36% formaldehyde solutions, dicyandiamide, ammonium chloride and property-modifying additives A, wherein the mass ratios of the 36% formaldehyde solutions, the dicyandiamide, the ammonium chloride and the property-modifying additives A are sequentially 1.0-1.3:0.50-0.65:0.60-0.70:0.06-0.09. The property-modifying additives A are a mixture obtained by mixing magnesium sulfate and magnesium chloride according to a proportion, wherein the mass ratio of the magnesium sulfate and the magnesium chloride is 2.0-3.5:8.0-6.5. The component (II) is a natural fiber (plant and / or animal) which is modified by cation modifiers. The fiber radical sewage decoloration and purification material integrates multiple functions such as decoloration, flocculation, entanglement and COD removing. The decoloration ratio of sewage can reach more than 93%, the COD value removing rate is higher than that of the prior art by more than 10%, reclaimed water reusing can be achieved, and sewage discharging is reduced.
Owner:HEFEI DONGFANG MEIJIE MOLECULAR MATERIAL TECH CO LTD

Phosphorus-free corrosion and scale inhibitor applicable to high-chlorine high-concentration-multiple circulating cooling water and preparation method of phosphorus-free corrosion and scale inhibitor

InactiveCN110655206AStrong targetingLow toxicitySpecific water treatment objectivesScale removal and water softeningMeth-Biology
The invention relates to a phosphorus-free corrosion and scale inhibitor applicable to high-chlorine high-concentration-multiple circulating cooling water and a preparation method of the phosphorus-free corrosion and scale inhibitor, belonging to the technical field of water treatment. The technical problem to be solved by the invention is to provide the phosphorus-free corrosion and scale inhibitor with low toxicity, chloride resistance and low cost for high-concentration-multiple circulating cooling water containing high-concentration chloride ions. The phosphorus-free corrosion and scale inhibitor is prepared from the following raw materials in parts by weight: 3 to 5 parts of zinc sulfate, 4 to 7 parts of sodium gluconate, 2 to 4 parts of sodium molybdate, 0.5 to 2 parts of benzotriazole, 5 to 9 parts of and acrylic acid-2-acrylamide-2-methylpropanesulfonic acid copolymer, 7 to 12 parts of polyepoxysuccinic acid and 3 to 5 parts of hydrolyzed polymaleic anhydride. Compared with similar corrosion and scale inhibitors, the phosphorus-free corrosion and scale inhibitor for high-concentration-multiple circulating cooling water provided by the invention has the advantages of strongtargeting performance, low toxicity, chloride resistance, low cost, simple operation, convenience, rapidness, environmental friendliness, safety, high efficiency and the like.
Owner:RUITIAN SECURITY & ENVIRONMENTAL PROTECTION CO LTD PANZHIHUA GANGCHENG GRP

Preparation method of graphite sheet surface chemical plating iron-nickel alloy layer

InactiveCN104195532AImprove bindingHigh hardnessLiquid/solution decomposition chemical coatingChemical platingGraphite
The invention relates to a preparation method of a graphite sheet surface chemical plating iron-nickel alloy layer. The preparation method comprises the following steps of 1, carrying out degreasing treatment on a graphite sheet; 2, carrying out oxidation treatment on the graphite sheet subjected to degreasing treatment; 3, carrying out the following sensitized treatment on the graphite sheet by utilizing a stannous chloride solution; 4, carrying out activating treatment on the graphite sheet by utilizing a palladium chloride solution; 5, sequentially adding 8-10 parts of C6H5Na3O7.2H2O powder, 4-5 parts of NH4Cl2 powder, 3-6 parts of FeSO4.7H2O powder, 2-3 parts of NiSO4.6H2O powder and 2-4 parts of NaH2PO2.H2O powder into ultra-pure water according to the mass ratio so as to fully dissolve the powder, adopting a NaOH aqueous solution as a pH adjustment solution, and dropwise adding the pH adjustment solution with the pH being controlled in a range of 9-9.5 to prepare a plating solution for surface chemical plating of the graphite sheet; 6, carrying out chemical plating treatment on the graphite sheet subjected to preliminary treatment. The preparation method is convenient in manufacturing and simple in process, and a compact and uniform plating layer with controllable thickness can be obtained on the surface of the graphite sheet.
Owner:TIANJIN UNIV

Preparation method of sodium ibandronate

InactiveCN102898466AEasy to operateMeet the quality requirements of raw materialsGroup 5/15 element organic compoundsSkeletal disorderPhosphorous acidChlorobenzene
The invention relates to the technical field of pharmaceutical chemistry, particularly relates to a method of pharmaceutical synthesis, and specifically relates to a preparation method of sodium ibandronate. To overcome the disadvantages of high content of chlorides and phosphites in sodium ibandronate prepared by a conventional preparation method of sodium ibandronate, the preparation method of sodium ibandronate with extremely low content of chlorides and phosphites is provided. In the preparation method, 3-(N-methylpentylamino) propionic acid hydrochloride, phosphorus trichloride and phosphorous acid are employed as raw materials and reacted in a chlorobenzene solvent, so as to obtain sodium ibandronate with extremely low content of the chlorides and the phosphites. The obtained sodium ibandronate can not only meet impurity control standards of the chlorides and the phosphites in a sodium ibandronate crude drug, but also prevent low yield, long period and huge harm to human body and environment which are brought by a lot of refining steps.
Owner:JIANGSU AOSAIKANG PHARMA CO LTD

Method for preparing lithium manganate by wet-doping method

InactiveCN103337619AIncrease the average oxidation stateSuppress purityCell electrodesManganates/permanganatesOxidation stateManganate
The invention discloses a method for preparing lithium manganate by a wet-doping method. By the wet-doping method, manganese chloride solution, ammonium bicarbonate solution and lanthanum nitrate solution are reacted in aqueous solution. Lanthanum hydroxide and manganese carbonate are generated in a coprecipitation way. Manganic manganous oxide-doped crystals are obtained after high-temperature calcination, crushing and grading. Lithium carbonate and the manganic manganous oxide-doped crystals are mixed according to the molar ratio of lithium to manganese, and the molar ratio is 1.15:2. After being mixed effectively and uniformly, the above mixture is put into a kiln to be sintered at a high temperature. After cooling, crushing, grading, sieving and deironing of the sintered materials, spinel-shaped and lanthanum-doped lithium manganate is obtained. The method can combine materials and doping elements tightly. During the high-temperature calcination reaction, the doping elements can be inserted into crystal structures to be doped completely and fused with the doped crystals together. The doping of lanthanum element can raise the average oxidation state of manganese ions, inhibit Jahn-Teller effect effectively, reduce the capacity fading and raise the cycle performance.
Owner:HUNAN DAHUA NEW ENERGY

Method for electroplating goldfinger with thick gold layer

ActiveCN103233250AAvoid Bubble ProblemsInhibit sheddingJewellerySolder maskGold layer
The invention discloses a method for electroplating a goldfinger with a thick gold layer. The method comprises the following processes: a, using copper-clad plate to etch an outer circuit, and forming a goldfinger leading wire; b, coating a coating material so as to form a gold-plating finger area; c, carrying out electronickelling on the gold-plating finger; d, electrogilding on the nickel layer of the gold-plating finger area; and e, removing the goldfinger leading wire and forming a solder mask, wherein a nickel aminosulfonate electroplating liquid is used in the process c for the electronickelling of the gold-plating finger area; and a nickel sulfonic acid electroplating liquid is a mixed solution of 300-600g/L nickel aminosulfonate, 20-50g/L boric acid and 30-70g/L nickel chloride. According to the method, the nickel aminosulfonate electroplating liquid is selected for the electronickelling of the gold-plating finger area, so that the electronickelling efficiency is high, the surface of the electronickelling layer is smooth and does not have residual stress, and the subsequent gold layer can be stably plated without gold throwing; and the goldfinger plated by the method is particularly suitable for electroplating gold layers with the thickness above 30 microinches, the nickel layer can be effectively prevented from being exposed, and the quality of the produced goldfinger can be greatly improved.
Owner:VICTORY GIANT TECH HUIZHOU CO LTD

Sodium alginate adsorption support and preparation method and application thereof

PendingCN112191234AOvercoming pollutionOvercoming productivityOther chemical processesWater contaminantsFreeze-dryingChloride
The invention provides a sodium alginate adsorption support as well as a preparation method and application thereof, and relates to the field of adsorption materials. The preparation method comprisesthe following steps: preparing a sodium alginate solution with a mass fraction of 2-13% by using sodium alginate as a solute and water as a solvent; then, pouring the sodium alginate solution into a culture plate, standing to remove bubbles, freezing at -35--25 DEG C for 8-12 hours first, and then, carrying out secondary freezing at a60--50 DEG C for 3-5 hours, and carrying out freeze drying in avacuum freeze dryer for 36-60 hours to obtainsodium alginate freeze-dried blocks; soaking the obtained sodium alginate freeze-dried blocks into an ethanol solution, then taking out sodium alginate, removing ethanol attached to the surface, then putting sodium alginate into a calcium chloride solution for a cross-linking reaction, taking out a sodium alginate product after the reaction, and removing calcium chloride on the surface so as to obtain the sodium alginate adsorption support. The sodium alginate adsorption support is low in preparation cost and high in heavy metal adsorption efficiency, and various problems of environmental pollution and production and operation cost are effectively solved.
Owner:XIAMEN UNIV OF TECH +1

Black rice-white peach flavor yoghourt and preparation method thereof

InactiveCN106578054AReduce brittlenessAvoid breakingMilk preparationFood flavorFermentation
The invention relates to a flavor yoghourt with black rice and a white peach and a preparation method thereof, belonging to the technical field of processing of dairy products and beverages. The preparation method mainly comprises the following steps: cooking the black rice, then soaking the black rice in a sodium alginate solution with a concentration of 1%, then adding the black rice into a calcium chloride solution with a concentration of 1%, carrying out curing so as to obtain QQ black rice, then mixing the QQ black rice with a sugar solution according to a ratio of 1: 1 and carrying out filling and sterilization so as to obtain QQ black rice jam; cleaning and peeling the white peach, cutting the white peach into peach blocks with sizes of 5*5*5, preparing white peach jam, and then uniformly mixing the QQ black rice jam with the white peach jam according to a ratio of 1: 1 so as to prepare black rice-white peach jam; adjusting the content of protein in raw milk to no less than 3.6%, carrying out fermentation to prepare a yoghourt base-material, mixing the yoghourt base-material with the black rice-white peach jam and carrying out filling so as to obtain the black rice-white peach flavor yoghourt. The black rice-white peach flavor yoghourt is chewy, allows people to feel burst in their mouth and endows people with totally different mouthfeel experience.
Owner:河北新希望天香乳业有限公司
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