1923 results about "Copper chloride" patented technology

The invention relates to a method for producing copper chloride hydroxide and blue vitriod by using cupriferous etching wastewater; the method comprises the following steps: acidic copper chloride etching wastewater and alkaline copper chloride etching wastewater are neutralized and crystallized to get acidic copper chloride crystal under the condition of strictly controlling filling liquid and the Ph range of a reaction kettle, and then pumped and filtrated, and centrifugated; part of the obtained alkaline copper chloride crystal is dried to obtain finished products while the other is added with NaOH solution for alkali conversion to obtain copper oxide, and then is acidulated by sulphuric acid, crystallized, washed, centrifugated, and dried to obtain blue vitriod products. The method for producing blue vitriod by directly using sulphuric acid-oxyful etching wastewater includes the following steps: sulphuric acid-oxyful etching wastewater and composition brass wasterwater in a PCB manufacture are blended together and added with NaOH to form cupric hydroxide precipitation which filtrated, washed, and then acidulated by sulphuric acid to obtain copper sulphate solution; after the copper sulphate solution is cooled, crystallized, centrifugated and dried, and the blue vitriod is obtained.

Compositions having antimicrobial activity contain particles comprising at least one inorganic copper salt; and at least one functionalizing agent in contact with the particles, the functionalizing agent stabilizing the particle in a carrier such that an antimicrobially effective amount of ions are released into the environment of a microbe. The average size of the particles ranges from about 1000 nm to about 3 nm. Preferred copper salts include copper iodide, copper bromide and copper chloride, most preferred being copper iodide. Preferred functionalizing agents comprise materials with a molecular weight of 60 or above, which include amino acids, other acidic materials, thiols, hydrophilic polymers, emulsions of hydrophobic polymers and surfactants. The functionalized particles are preferably made by a grinding process.

Embodiments of the invention are directed to a composition having antimicrobial activity comprising particles comprising at least one inorganic copper salt; and at least one functionalizing agent in contact with the particles, the functionalizing agent stabilizing the particle in a carrier such that an antimicrobially effective amount of ions are released into the environment of a microbe. The average size of the particles ranges from about 1000 nm to about 4 nm. Preferred copper salts include copper iodide, copper bromide and copper chloride. Preferred functionalizing agents include amino acids, thiols, hydrophilic polymers, emulsions of hydrophobic polymers and surfactants.

The invention discloses a preparation method of nano cuprous oxide. In the method, copper chloride and copper nitrate are taken as copper sources, hydrazine hydrate, glucose and an ascorbic acid and the like are taken as reducing agents, and cuprous oxide materials in the shape of an octahedron, a hollow sphere, a cube and a hollow cube and the like are successfully obtained by using a liquid-phase reduction method and a hydrothermal method. Required raw materials for preparation are rich, the cost is low, and no waste is produced. The preparation process is simple, and the repeatability is good. Cuprous oxide nano-materials have wide applications in the aspects of photocatalysis, gas-sensing materials, antibacterial materials, and the like.

An improved process calcining a gypsum/cellulosic fiber slurry to produce a composite gypsum/cellulosic fiber product resides in adding a selected crystal modifier to the gypsum/cellulosic fiber slurry prior to the heating step to reduce the time necessary to carry out the calcination process, to reduce the temperature at which the calcination process is run or to increase the aspect ratio of the acicular calcium sulfate alpha hemihydrate crystals formed during the calcination process. Useful crystal modifiers include aluminum sulfate, aluminum chloride, chlorine, zinc sulfate, iron (III) sulfate, aluminum sulfate hexadecahydrate, iron (II) sulfate heptahydrate, iron (III) sulfate pentahydrate, zinc sulfate heptahydrate, copper sulfate pentahydrate, copper chloride dehydrate, manganese sulfate monohydrate and trisodium phosphate.

The invention relates to a pig feed, in particular to a nursery pig concentrated feed, comprising the following raw materials by weight proportion: 30-50 of sucking pig composite vitamin, 30-50 of low copper mineral element, 60-100 of peeled soybean meal, 100-180 of fermented soybean meal, 100-150 of extruded soybean, 110-180 of steam fish meal, 50-100 of dried porcine soluble, 60-120 of acid whey powder, 80-90 of glucose powder, 5-10 of glutamine, 80-100 of chyle fat powder, 40-49 of calcium carbonate, 12-14 of basic zinc chloride, 4-6 of salt, 55-60 of calcium biphosphate, 6-10 of sodium butyrate, 12-15 of lysine, 6-8 of threonine, 4-6 of TP-100 enzyme, 4-5 of cysteine, 5-7 of se-enriched yeast and 6-10 of copper chloride hydroxide. The nursery pig concentrated feed has the advantages of milk nutrition composition simulation, good palatability, high digestibility, large feed intake because the baby pigs like to eat and improvement of survival rate as well as immunity of the nursery pigs.

Embodiments of the invention are directed to a composition having antimicrobial activity comprising particles comprising at least one inorganic copper salt; and at least one functionalizing agent in contact with the particles, the functionalizing agent stabilizing the particle in a carrier such that an antimicrobially effective amount of ions are released into the environment of a microbe. The average size of the particles ranges from about 1000 nm to about 4 nm. Preferred copper salts include copper iodide, copper bromide and copper chloride. Preferred functionalizing agents include amino acids, thiols, hydrophilic polymers emulsions of hydrophobic polymers and surfactants.

The invention provides a boiler coal combustion-improving desulfurizing and denitrifying agent composition. The composition comprises the following raw materials in parts by weight: 2-7 parts of sodium carbonate, 1-3 parts of alumina, 2-8 parts of aluminium hydroxide, 2-5 parts of ferric trichloride, 2-6 parts of ferric oxide, 3-10 parts of potassium permanganate, 3-10 parts of potassium chlorate, 10-35 parts of activated attapulgite clay, 15-30 parts of urea, 2-4 parts of ammonium formate, 2-4 parts of ammonium chloride, 6-23 parts of ammonium acetate, 3-9 parts of manganese oxide, 9-12 parts of copper chloride, 1-3 parts of copper oxide, 2-4 parts of zinc sulfate, 1-3 parts of zinc nitrate, 7-18 parts of potassium dichromate, 1.0-1.5 parts of titanium dioxide, 0.5-1.0 part of barium molybdate, 0.5-1.5 parts of cobalt sulfate, 0.5-1.5 parts of vanadium pentoxide, 0.3-0.7 part of cerium oxide, 0.1-0.2 part of sodium dodecyl benzene sulfonate and 0.1-0.2 part of alkyl glyceryl ether. The composition is convenient to use, has stable properties, plays roles of combustion improving, desulfurization and denitrification, has coal saving rate of 8-25% and can remove fixed sulfur by 50-70%.

The invention relates to a method for preparing a core-shell structure metal/polymer nanofiber membrane. The prepared fiber membrane uses a polymer as a nuclear layer and uses a nano-metal as a shell layer; the polymer can be polyvinyl pyrrolidone, polyvinyl alcohol, polyoxyethylene, polylactic acid, polyacrylonitrile, hyaluronic acid, chitosan and the like; the nano-metal shell layer comes from metal salt silver nitrate or copper chloride. The core-shell structure metal/polymer nanofiber is prepared by utilizing the electrospinning technique; by controlling the process parameters, the concentration of polymer, the content of metal salt and the proportioning of solvents, the metal/polymer nanofiber membrane is prepared; the fiber membrane has high application value on tissue engineering, recovery of wound, drug transportation, photoelectricity and the like.

The invention discloses a process for manufacturing a 12OZ thick copper multilayer circuit board. In an inner layer etching process, the concentration of CU2+ in an acid copper chloride etching solution is controlled to be 150+/-20g/l, the temperature is 50+/-3 DEG C, total acidity is 2.8+/-0.6N, specific gravity is 1.30+/-0.10, etching speed is 1.2+/-m/min, and the number of etching times is 4 times; a plate pressing process comprises a hot pressing step and a cold pressing step, wherein the hot pressing time is 200 minutes, a system is vaccumized at absolute pressure of 10mbar between the fifth minute and the ninety-fifth minutes, the maximum press plate pressure is controlled to be 21.42Kgf/cm2, and the temperature is 190 DEG C; the time for cold pressing is 110 minutes, and the maximum press plate pressure is controlled to be 18.36Kgf/cm2; when the diameter D of a prebored hole is more than or equal to 2.0mm and is less than 4.8mm, a drill bit with diameter d of less than or equal to 1.7mm is used to prebore 4 holes, and the holes are redrilled by using a drill bit with the diameter D. The process has the advantages of improving the etching factors of the plate material of the inner layer, reducing the side etching effect with good plate pressing effect and protecting the bored holes from the phenomenon that the holes are blocked by copper scarp.

The invention relates to a method for recycling ammonian in ammonian waste water with high concentration, in particular to a method for recycling ammonian in printed wiring board waste water; crystallization mother liquid containing ammonium chloride with high concentration which is generated from processes such as producing alkaline copper chloride, Alpha crystallization type alkaline copper, blue vitriod and the like by using wiring board etching waster water, firstly is evaporated, concentrated and crystallized by one or two combination in multiple effect evaporation technique of mechanical compression, evaporating and compression with heat so as to recycle most ammonium chloride; secondly, Ph is adjusted and ammonian is evaporated so as to recycle ammonia or ammonium sulphate; ammonian waste water generated from removing tin water from ammonia and recycling tin mud are treated by evaporating ammoniac after directly adjusting Ph; and the residual sewage is further treated in the sewage treatment system. By using the method, both of the removal rates of ammonian waste water for wiring board and the recovery rate of ammonia are more than 99.8 percent; the method has good treatment effect, high efficiency, little amount of steam usage, low running cost, and good popularization and application prospect.

The invention discloses a corrosive capable of displaying an ultra low carbon solidification arborescent structure and a preparation method thereof. The corrosive is prepared from the following components: picric acid, stannous chloride, copper chloride, hydrochloric acid, surfactant, absolute ethyl alcohol and distilled water. The preparation method is as follows: taking a specified amount of the distilled water, and equally dividing the distilled water into two parts; mixing and putting solid medicament into a glass container according to fixed quantity, and adding one part of the distilledwater into the solid mixed medicament to dissolve the medicament; adding a specified amount of the absolute ethyl alcohol into another part of spare distilled water; adding a hydrochloric acid solution into the absolute ethyl alcohol solution; mixing the ethyl alcohol and the hydrochloric acid solution which are poured into an aqueous solution containing the solid medicament; fully stirring; and finally adding the surfactant to finish preparing. By utilizing the reagent provided by the invention, the solidified arborescent structure forms of ultra low C, S, P continuous casting steel billets can be displayed clearly, a finish requirement on sample surface is lowered, the sample preparation working procedure is simplified and the larbour intensity of operators is lowered.

The invention discloses a method for producing tribasic copper chloride. The method for producing the tribasic copper chloride includes the following steps of: (1) removing impurities from an acidic etching waste solution; (2) adding clean water or a tirbasic copper chloride production mother solution to a synthesis reactor, performing preheating, and then, preheating the acidic etching waste solution whose impurities have been removed and an alkaline solution of sodium hydroxide and mixing the two solutions for a reaction with the pH value and temperature of the reaction being controlled so as to gradually form the tribasic copper chloride, and discharging partial materials after a certain amount of reaction time; (3) filtering the materials discharged from the reaction system, and performing washing, suction filtration, centrifugation and drying on the filtrated residues to obtain the tribasic copper chloride; and (4) performing ammonia nitrogen removal treatment on filtrated liquid. By adopting the method for producing the tribasic copper chloride in the invention, continuous production can be achieved and the tribasic copper chloride with large particle size and high purity can be produced; further, production cost can be reduced and overall process can be integrated; and the method for producing the tribasic copper chloride is advantaged in simple ultimate steps of ammonia nitrogen removal, easiness in operation as well as reduced difficulty and cost of ammonia nitrogen treatment.

The invention discloses a non-noble metal mercury-free catalyst for hydrochlorination of acetylene and a preparation method thereof. The catalyst mainly contains copper, chlorine, a carrier and the balance of catalysis-promoting metallic elements, wherein the copper exists in the form of copper chloride, the chlorine exists in the form of an inorganic salt of chlorine, the carrier is activated carbon or nitrided activated carbon which is subjected to acid cleaning, and the catalysis-promoting metallic elements are one of or a mixture of any of alkali metals, alkaline-earth metals and non-noble metals of which the chloride is non-volatile in transition metallic elements. The preparation method comprises the process steps of preparing impregnation motor liquor, adding a catalyst carrier to perform equivalent-volume impregnation, drying the mixture and the like. The non-noble metal mercury-free catalyst prepared by adopting the method is better in activity, high in selectivity, long in service life, low in cost and environment-friendly, and can be used for hydrochlorination of acetylene during the production of vinyl chloride by using a calcium carbide method.

The invention discloses a three-dimensional nitrogen-doped graphene platinoid-loaded composite electro-catalyst. A preparation method comprises the following steps of ultrasonically dispersing graphene oxide sheet in an aqueous solution, adding urea and soluble nickel salt for full and uniform mixing, transferring the mixture into a hydrothermal reaction kettle for reaction, performing freeze-drying to obtain three-dimensional nitrogen-doped graphene, dissolving the three-dimensional nitrogen-doped graphene in ethylene glycol, sequentially adding chloroplatinic acid, copper chloride dehydrate and glutamic acid, and performing microwave reaction to obtain the catalyst. The method has the characteristics of that energy is saved, the speed is high, and the operation is simple; the raw materials are easy to obtain, the yield is high, the capability of platinum in the direct electro-catalytic oxidation of methanol under an acidic condition can be remarkably improved, peak current is 3 to 4 times than that of a commercial carbon black platinum-loaded electro-catalyst and a commercial carbon black platinum-ruthenium-loaded electro-catalyst, and the prepared catalyst is widely applied to a methanol fuel cell.

The invention discloses a low-mercury catalyst used for synthesizing vinyl chloride. The low-mercury catalyst takes mercuric chloride as a main active component, one or more of precious metals such as Au, Pd, Pt, Ru, Rh, Os and Ir salts or complexes thereof as active regulators, and one or more of potassium chloride, ferric chloride, zinc chloride and copper chloride as cocatalysts. By adding trace amount of precious metal salt into the mercuric chloride, the low-mercury catalyst forms a stable composite metal compound, plays a role in fixing and activating mercuric chloride, and still maintains very high catalytic activity and stability when the load capacity of the mercuric chloride is reduced to 0.1-2%.

The invention discloses an acidic copper chloride etching liquid electrolytic regeneration recycling and copper plate recovery device and method. The device comprises an electrolytic bath which is divided into a cathode region and an anode region by virtue of a composite conductive macromolecular membrane, an etching auxiliary cylinder, an etching liquid waste liquid collecting cylinder, a regenerated liquid collecting cylinder and an exhaust treatment device, wherein the cathode region is internally provided with a cathode electrolytic sheet, the anode region is internally provided with an anode electrolytic sheet, and the etching auxiliary cylinder is internally provided with a gas dissolving device; a waste liquid generated by the etching cylinder is fed to the cathode region of the electrolytic bath by virtue of the etching liquid waste liquid collecting cylinder, a water inlet and a gas outlet are formed in the anode region of the electrolytic bath, the water outlet is communicated with the etching auxiliary cylinder by virtue of the regenerated liquid collecting cylinder, gases generated by the anode region are introduced to the etching auxiliary cylinder by virtue of the gas dissolving device at the gas outlet, the etching auxiliary cylinder is communicated with the etching cylinder, and exhaust gases generated by the etching auxiliary cylinder are fed to the exhaust gas treatment device. The device and method disclosed by the invention solve the problem that an existing acidic copper chloride etching liquid is high in energy consumption of regeneration recycling, low in reuse rate, more in copper impurities of the cathode and the like.

The invention discloses a dendritic crystal corrosion macroscopic examination reagent for solidification structures and defects of a continuous cast blank and a preparation method thereof. The reagent comprises the following components by mass percent: 0.28-1.09% of copper chloride, 0.17-0.27% of magnesium chloride, 0.56-1.60% of ferric chloride, 1.28-1.30% of hydrochloric acid with the mass concentration of 36-38%, 54.70-55.80% of absolute ethyl alcohol and the balance of water. The preparation method comprises the following steps: adding the water into a container, and then adding the copper chloride, magnesium chloride, ferric chloride and hydrochloric acid; and adding the absolute ethyl alcohol after all the added raw materials are fully dissolved, and evenly stirring. Compared with the prior art, the invention solves the problem that other corrosive reagents can not clearly display the dendritic crystal solidification structures of a continuous cast blank; and the reagent has the characteristic of original-size display without expansion or reduction for interior defects of a continuous cast blank when used for dendritic crystal corrosion macroscopic examination on the solidification structures and defects of the continuous cast blank.

The invention relates to a method for preparing monoclinic crystal system crystalline copper oxide and an application of the monoclinic crystal system crystalline copper oxide. The method comprises the following steps: a. a sodium hydroxide or potassium hydroxide water solution with a concentration of between 5 and 50 percent and a volume of between 30 and 80 percent of the volume of a reaction vessel is added into the reaction vessel, preheated to between 30 and 100 DEG C, added with crystalline copper chloride hydroxide with the addition between 1/6 and 1/3 of the mol number of sodium hydroxide, and reacted for 10 to 60 minutes at a reaction temperature of between 30 and 100 DEG C and under the condition of stirring; b. crystalline copper oxide is prepared after washing, pumping filtration, centrifugation and drying of reacted materials; and c. the crystalline copper oxide is crushed by the physical method, and the activated copper oxide with fine granularity are prepared. The method is easy to realize separation of the copper chloride hydroxide and the copper oxide with other water-soluble background salts, and has a simple technique and low production cost; and the crystalline copper oxide prepared has high yield, high purity, high activity, good quality and is suitable for mass production.

Embodiments of the invention are directed to a composition having antimicrobial activity comprising particles comprising at least one inorganic copper salt; and at least one functionalizing agent in contact with the particles, the functionalizing agent stabilizing the particle in a carrier such that an antimicrobially effective amount of ions are released into the environment of a microbe. The average size of the particles ranges from about 1000 nm to about 4 nm. Preferred copper salts include copper iodide, copper bromide and copper chloride. Preferred functionalizing agents include amino acids, thiols, hydrophilic polymers emulsions of hydrophobic polymers and surfactants.