41 results about "Thiodiethylene Glycol" patented technology

The invention discloses zinc-aluminum coating anti-corrosion paint. The paint is composed of two-components of A and B in a mass ratio of 3:1, wherein a component A comprises the following raw materials: zinc aluminum alloy powder, nano-silica, sodium lignosulphonate, benzotriazole, thiodiethylene glycol, amino trimethylene phosphonic acid, sodium carboxymethylcellulose and deionized water; a component B comprises the following raw materials: zircinium fluoride, gamma-aptes, inositol hexaphosphate, cellaburate, ethanol and the deionized water, wherein the zinc aluminum alloy powder is composedof Zn, Al, Ti, Ni, Mg and Mn. According to the zinc-aluminum coating anti-corrosion paint and the preparation method thereof, excellent corrosion resistance and impact resistance are acquired and a deficiency that the production process of triphenylphosphine in the prior art has potential dangers on environmental safety and operators is compensated by means of adjusting mass ratio of each component of the zinc aluminum alloy powder on the basis of replacing the triphenylphosphine with the amino trimethylene phosphonic acid and the sodium carboxymethylcellulose.

The invention relates to the food and medical industries, medical cosmetics, dermatology, agriculture and the mixed feed industry. According to the invention vicinal dithioglycole (common formula RCH(SH)CH(SH)R−1 (I)) is used as a food additive, a food product, physiologically-active substances and active ingredients of forage additives and of forage, in cosmetic and / or dermatological and skin-therapeutic remedies. The invention comprises methods for producing such additives, products and remedies. The substance of formula (I) stimulates physiological processes, increases human and animal immunity, inhibits undesirable process in organisms and food products, produces curative and preventive action of skin, hair and nails and after vicinal dithioglycole is administered the intoxication effect of alcohol consumption known as hang-over is completely remored.

The invention discloses a synthetic method for epoxy end group polythioether liquid rubber. The method comprises the following steps: synthesizing sulphydryl end group polythioether liquid rubber by using thiodiglycol, hydroxyethyl-2-hydroxypropyl thioether and the like as main monomers; then using polyethylene glycol diglycidyl ether resin as a transforming agent so as to transform a sulphydryl end group into an epoxy end group so as to finally generate the end group polythioether liquid rubber. The technology has the advantages that the polyethylene glycol diglycidyl ether resin is adopted as the transforming agent of the end group, the defects that the viscosity of a sulphydryl in traditional epoxy modification technology is high, solvents of toluene, butanone and the like are needed to perform dilution, the reaction exotherm is violent, and a side effect is easy to generate are overcome; reactions are smooth, the product quality is easy to control, the viscosity of the generated epoxy end group polythioether liquid rubber is moderate, and the stability is good; the strength of epoxy resin and the toughness and the heat resistance of polythioether rubber are reserved after the end group is transformed, so that the brittleness of the epoxy resin is improved, and the adhesive property of materials is improved.

The invention relates to a method for synthesizing 9-hydroxy-4-oxa-7-thianonene. The method is characterized by comprising the following steps: A, adding solid caustic soda and thiodiglyco into a reaction kettle, slowly raising the temperature to 30 to 50DEG C, and reacting for 1 to 3 hours to generate thiodiglycolic sodium; B, adding chloropropene into a metering tank, then charging materials into the reaction kettle, and dropwise adding the chloropropene at the temperature of 30 to 50DEG C for 1 to 4 hours; after adding, raising the temperature to 80 to 130DEG C, reacting for 1 to 3 hours, and cooling a reaction solution; C, carrying out acidizing, filtering and desalting treatment on the cooled reaction solution to obtain a crude product of 9-hydroxy-4-oxa-7-thianonene; then rectifying, and collecting fractions to obtain colorless or pale yellow transparent 9-hydroxy-4-oxa-7-thianonene. The method disclosed by the invention has the advantages that the raw materials are low in price and easily obtained, and the yield of a product is high; the method is suitable for industrially producing the 9-hydroxy-4-oxa-7-thianonene.

The invention relates to a preparation method of a thiophenol compound antioxidant product, relating to the technical field of preparation of antioxidant products. A process technical method of the thiophenol compound antioxidant product comprises the following steps of: taking 3, 5-methyl ester and thiodiglycol as raw materials, performing ester exchange reaction under the actions of a catalyst and a color blocking agent, and generating a reaction product mixed solution containing 2, 2'-thiodiethyl bis(3-(3, 5-di-tert-butyl-4-hydroxyphenyl) propionate by continuously removing a byproduct, namely methanol during the reaction process; adding an appropriate amount of phosphite ester-like compound into the reaction product mixed solution, and generating a new phosphite ester-like compound by secondary ester exchange reaction; and selecting a recrystallization solvent, performing recrystallization and refining on the reaction product mixed solution, and performing solid-liquid separation to obtain a while granular crystal product.