46 results about "Gold(III) chloride" patented technology

The invention discloses citric acid gold potassium used for gold plating and the preparation method thereof. The molecular formular of the citric acid gold potassium is K3Au2C9H5O7N2. The method comprises the steps as follows: gold trichloride is dissolved in water of certain temperature, is concentrated and diluted under the temperature for multiple times, and is reacted with potassium citrate, ethylene diamine tetraacetic acid and malononitrile in a reactor under the certain temperature and the certain time to produce the organic gold salt which has low toxicity and contains no free cyanogen. When the product has the same gold content with the potassium gold cyanide, the total CN- is 5 to 6 percent, being 50 percent lower than that of the CN- in the potassium gold cyanide. The waste liquid after gold plating contains free the CN- in small amount. The invention reduces the cost of waste water treatment for the electroplating plants.

The invention discloses a preparation method of a high-temperature inactivation resistant load type gold catalyst for synthesizing chlorethylene in acetylene hydrochlorination. The catalyst takes active carbon as a carrier, takes aminothiopropionic acid, cystine, methionine and thiocarbamide as active carbon organic surface modifiers and takes auric chloride as an activity center. During the reaction of synthesizing chlorethylene in acetylene hydrochlorination, the active carbon surface modified load type gold catalyst has a high-temperature inactivation resistant performance better than that of an unmodified active carbon load type gold catalyst.

The invention relates to cyanide-free gold electroplating liquid, and belongs to the field of surface modification of metal materials. The cyanide-free gold electroplating liquid has the advantages that: the electroplating liquid is non-toxic, simple in a formula and high in stability, does not have the phenomenon of turbidity and color change after being stood at normal temperature and still can be used. The cyanide-free gold electroplating liquid comprises the following main ingredients: gold trichloride, sodium sulfite or potassium sulfite serving as a main complexing agent, ethylene diamine tetraacetic acid (EDTA) or sodium citrate serving as an auxiliary complexing agent and sodium chloride or potassium chloride serving as inorganic salt. In the cyanide-free gold electroplating liquid, a new formula proportion is adopted, the cost is low, a plating layer is high in bonding force and bright, and the preparation of the functional gold plating layer is realized. The popularization and application of the cyanide-free gold electroplating liquid can create economic and social benefit.

The invention provides a method for enhancing the gold precipitation grade in a gold electrorefining process. According to the method, a coarse gold plate is adopted as an anode, a pure gold plate is adopted as a cathode, and a gold chloride solution is taken as an electrolyte solution to perform electrorefining. Specifically, the outside of the anode is sleeved with a pocket shaped diaphragm made of polypropylene fiber, and the mesh opening of the diaphragm is 800-850 meshes. The cathode is made by the method of: taking the coarse gold plate as the anode, adopting a titanium alloy plate as the cathode, and using a gold chloride solution as an electrolyte solution to conduct electrolysis, precipitating out a pure gold layer on both sides of the titanium alloy plate, and stripping the pure gold layer, thus obtaining a cathode plate used for gold electrorefining. The method provided by the invention effectively avoids adsorption of AgCl and part of insoluble metal impurities on the cathode, thereby enhancing the gold precipitation grade and ensuring the stability of gold electrolysis production. At the same time, by improving the quality of a gold starting sheet, the gold precipitation grade is further improved.

The invention discloses organic gold conductor paste which comprises the following components in percentage by mass: 40%-60% of resin acid gold, 2%-10% of a metal organic matter mixing agent, 30%-60% of an organic carrier and 1%-4% of an oily gold nano solution, wherein the resin acid gold is prepared by reacting sulfurized balsam and gold trichloride; the metal organic matter mixing agent is a mixture of lead caprylate, bismuth 2-hexylhexane, rhodium caprylate, silicon 2-ethylhexanoate, vanadium iso-octoate and trimethyl boron; the concentration of gold in the oily gold nano solution is 40-60 mug/mL, and the diameter is 5-40 nm. By adding the oily gold nano solution, the sheet resistance of the conductor paste is greatly reduced, the adhesive force and the scratch resistance are improved, meanwhile, a sintered film is compact and flat in surface, low in roughness, resistant to acid and alkali, bright yellow and free of light leakage, the roughness Ra is lower than 0.05 mum, the sheet resistance is about 20 momega/square, the adhesive force reaches 64 N/mm<2> or above, and the scratch resistance reaches 3B.

The invention discloses a preparation method of an aromatic halogenated compound. Arene Ar-H and N-halogenated succimide are reacted in an organic solvent under the catalysis of auric chloride to obtain an aromatic halogenated compound Ar-X, wherein Ar represents substituted or unsubstituted non-heterocycle aryl and X represents chlorine, bromine or iodine. The reaction in the method does not need strict water-free and oxygen-free condition and occurs successfully in air. The invention has the advantages of good tolerance and universality to functional groups, little use amount of the catalyst and lower reaction cost, is simple and convenient for operation, and can be widely used for preparing the aromatic halogenated compound.

The invention relates to a manufacturing method of high-purity gold. The manufacturing method includes the following steps: (1) gold sheets are dissolved, and concentration, purification and extraction are performed to obtain a gold chloride solution; and (2) high-purity gold is obtained through reduction, oxalic acid is added in the solution obtained in the step (1) under the condition of continuous stirring to perform reduction so as to obtain gold sediment, the gold sediment is washed by distilled water for 5-6 times, the distilled water is pumped, the gold sediment is arranged in a drying oven to be dried at the temperature of 80-100 DEG C, and the high-purity gold is obtained. The gold chloride solution is extracted by using high-purity diethyl ether so as to remove impurities to the optimum effect, and the high-purity oxalic acid is used as a reducing agent for restoring the gold chloride to obtain the high-purity gold. Due to the fact that a by-product of the oxalic acid using as the reducing agent is gas CO2, the step of impurity removal is omitted.

The invention discloses a gluconic acid cyanide-free gold-electroplating solution and an electroplating method thereof. The gold-electroplating solution comprises 10-15 g/L by gold of auric chloride, 78-94 g/L by a gluconic acid group of gluconic acid or gluconate, 1-8 g/L of piperidine, and 0.16-0.48 g/L of arsenic trioxide. Gluconic acid or gluconate is taken as a complexant, a complex of piperidine and arsenic trioxide is taken as a brightener, and auric chloride is a main gold salt. The obtained gold-electroplating solution has preferable dispersion and deep electroplating performance; the cathodic current efficiency is high; and performance of the solution is excellent. Through adoption of the gold-electroplating solution in an alkaline condition, an obtained electroplated layer is low in porosity, high in brightness, and excellent in quality.

The invention discloses a supported foamy copper catalyst used for removing acrylonitrile through supercritical water oxidation. A preparation method of the catalyst comprises the following steps: cleaning foamy copper and then modifying foamy copper with AgNO3, thus preparing a substance M; modifying the substance M with mixed liquor prepared from polyvinylpyrrolidone, methanol, palladium dichloride, gold chloride, concentrated hydrochloric acid and sodium borohydride, thus preparing a substance N; modifying the substance N with mixed liquor prepared from PbCl2, SrCl2, concentrated nitric acid, urea and ammonium fluoride, thus preparing a substance O; modifying the substance O with mixed liquor prepared from tetra-n-butyl titanate, tetraethyl orthosilicate and acetylacetone, thus preparing a substance P; modifying the substance P with mixed liquor prepared from ZrCl4, CdCl2 and AlCl3, thus preparing a substance Q; modifying the substance Q with mixed liquor prepared from ZnCl2, BiCl3, NaOH, Na2CO3 and CuCl2, thus obtaining a substance, namely the supported foamy copper catalyst used for removing acrylonitrile through supercritical water oxidation.

The invention discloses electroplate liquid and an electroplate method for cyanide-free gold plating of thallium-contained sulfite. The electroplate liquid is composed of 10-15 g/L of gold chloride in terms of gold, 78-94 g/L of sulfite in terms of sulfite radicals, 1-4 g/L of glycerinum, 0.30-0.65 g/L of organic phosphorus compounds and 0.05-0.14 g/L of thallous salt in terms of thallium. According to the electroplate liquid, the sulfite serves as main coordination agents, the glycerinum serves as stabilizers, the organic phosphorus compounds serve as electron accelerators, the thallous salt serves as brightening agents, and the gold chloride serves as main gold salt, so that the obtained electroplate liquid is good in dispersion capacity and covering capacity, cathode currents are high in efficiency, and the electroplate liquid is excellent in performance. By the adoption of the electroplate liquid, plating obtained through electroplating under the alkaline condition is low in porosity, high in brightness and good in quality.

The invention discloses a plating solution for mercapto sulfonic acid non-cyanogen gold plating and a plating method thereof. The plating solution comprises 10-15g / L of gold trichloride calculated by gold, 35-55g / L mercapto sulfonic acid compound calculated by mercapto group, 11-17g / L citric acid and salts thereof calculated by citrate, and 50-70g / L EDTA. The plating solution uses mercapto sulfonic acid compound as the main complexing agent, uses citric acid and its salts, and EDTA as the auxiliary complexing agent, and uses gold trichloride as the main gold salt, so that the obtained plating solution has good dispersion force, deep plating capability power, high cathodic current efficiency, and excellent performance. The plating layer obtained under basic conditions by using the plating solution has the advantages of low porosity, high brightness and good plating layer quality.

Provided is a preparation method of a silver-gold alloy nanometer spherical shell based on vapreotide acetate. The preparation method mainly comprises the steps that according to the proportion that 0.91-1.13 mg of vapreotide acetate is added to 1 ml of a hydrochloric acid solution, a vapreotide acetate solution is prepared, and treatment is conducted for 20-24 min at the temperature of 65-67 DEG C; a silver nitrate solution is added according to the ratio of 1 to 3-9, a mixture is put into a water bath constant-temperature oscillator, and incubation is conducted for 24-26 h at the temperature of 24 DEG C; according to the molar ratio of 1 to 1-2 of silver nitrate and sodium borohydride, reducing agent sodium borohydride is added dropwise, and a reaction is conducted for 16-18 min at the temperature of 24 DEG C; the mixture is put into a 100-DEG C boiling water bath, 10 min later, a auric chloride solution is added according to the molar ratio of 1 to 25-45 of auric chloride and the silver nitrate, the mixture is put into the 100-DEG C boiling water bath for 2-4 min, and the silver-gold alloy nanometer spherical shell with the grain size of 90-110 nm is prepared. By the adoption of the preparation method, the morphology is easy to control, the operation is simple, environmental protection is achieved, the reaction condition is gentle, and prepared silver-gold alloys are uniform in grain size and good in dispersity.

The invention discloses a method for preparing gold nano-flowers. The method mainly comprises steps as follows: a vapreotide acetate solution with the concentration being 0.5-0.7 mM is prepared from a hydrochloric acid solution, is placed in a metal bath at 60-64 DEG C for heat treatment for 40-44 min and is subjected to 80-Hz ultrasonic treatment for 30-50 s; then a gold chloride aqueous solution is added with the molar ratio of vapreotide acetate to the gold chloride aqueous solution being 1:(10-13), and the mixture is evenly mixed and is placed into a water-bath thermostatic oscillator for incubation at 110-120 rpm at 23 DEG C for 20-22 h; and sodium borohydride is added to the incubated solution with the molar ratio of sodium borohydride to the gold chloride aqueous solution being 1:(2-5) for a reaction at the reaction temperature of 23 DEG C for 20-24 min until the solution is slowly changed from faint yellow to bluish violet, and the gold nano-flowers with the particle size ranging from 120 nm to 150 nm are prepared. With the method, the preparation technology is simple, reaction conditions are mild, and the prepared gold nano-flowers are uniform in particle size, relatively high in metal loading capacity, regular in shape and good in dispersity.

The invention discloses a loaded type foam aluminum catalyst for removing acrylonitrile through supercritical water oxidation. Foam aluminum is cleaned, is then prepared into a substance M through AgNO3 modification; the substance M is prepared into a substance N through the modification on a mixed solution prepared from polyvinylpyrrolidone, methyl alcohol, gold chloride, concentrated hydrochloric acid and sodium borohydride; the substance N is prepared into a substance O through the modification on a mixed solution prepared from CoCl2, CuCl2, concentrated nitric acid, urea and ammonium fluoride; the substance O is prepared into a substance P through the modification on a mixed solution prepared from tetra-n-butyl titanate, tetraethoxysilane and acetylacetone; the substance P is prepared into a subsequent Q through the modification on a mixed solution prepared from SnCl4, PbCl2 and CeCl3; the subsequent Q is prepared into a substance through the modification on a mixed solution prepared from SrCl2, InCl3, NaOH, Na2CO3 and NiCl2, and the substance is the loaded type foam aluminum catalyst for removing acrylonitrile through supercritical water oxidation.

The invention discloses a load-type foamed aluminum catalyst for removing dimethyl formamide by use of supercritical water oxidization. The load-type foamed aluminum catalyst for removing dimethyl formamide by use of supercritical water oxidization is prepared by virtue of the following steps: washing foamed aluminum, and then modifying the washed foamed aluminum with AgNO3, thereby obtaining a substance M; modifying a mixed solution prepared from polyvinyl pyrrolidone, methanol, gold trichloride, concentrated hydrochloric acid and sodium borohydride by the substance M, thereby obtaining a substance N; modifying a mixed solution prepared from SrCl2, CoCl2, concentrated aqua fortis, urea and ammonium fluoride by the substance N, thereby obtaining a substance O; modifying a mixed solution prepared from tetra-n-butyl titanate, tetraethyl orthosilicate and acetylacetone by the substance O, thereby obtaining a substance P; modifying a mixed solution prepared from ZrCl4, MgCl2 and InCl3 by the substance P, thereby obtaining a substance Q; and modifying a mixed solution prepared from PbCl2, BiCl3, NaOH, Na2CO3 and CdCl2 by the substance Q, thereby obtaining a substance, namely the load-type foamed aluminum catalyst for removing the dimethyl formamide by use of supercritical water oxidization.

The invention discloses an aromatic mercaptan cyanide-free gilding electroplating solution and method. The electroplating solution comprises 10 g/L to 15 g/L of auric chloride by gold, 35 g/L to 55 g/L of aromatic mercaptan by sulfydryl, 0.10 g/L to 0.35 g/L of a dipyridyl compound and 0.30 g/L to 0.60 g/L of selenite by selenious acid radical. The aromatic mercaptan serves as a main coordination agent, the dipyridyl compound serves as an electron acceleration agent, the selenite serves as a brightening agent, and the auric chloride serves as main auric salt, so that the obtained electroplating solution has the good dispersion force and the deep-plating capacity, cathode current efficiency is high, and the performance of the electroplating solution is excellent. The electroplating solution is adopted for electroplating under the alkaline condition, so that an obtained plated layer is low in porosity, high in brightness and good in quality.