899 results about "Thio-" patented technology

The invention relates to a hyaluronic acid-polyurethane composite material based on a double dynamic network and a preparation method and application thereof, and the preparation method comprises the following steps: carrying out hydrophobic modification reaction on hyaluronic acid and aminophenylboronic acid to obtain aminophenylboronic acid modified hyaluronic acid; the preparation method comprises the following steps: mixing polytetrahydrofuran ether glycol, polyethylene glycol and isophorone diisocyanate, carrying out a primary reaction, adding trimethylolpropane tri (3-mercaptopropionic acid) ester, carrying out a secondary reaction, adding tannic acid, and carrying out a third reaction to obtain tannic acid-terminated dynamic thionocarbamate polyurethane; and mixing the amino phenylboronic acid modified hyaluronic acid with the tannic acid terminated dynamic thionocarbamate polyurethane for reaction to obtain the hyaluronic acid-polyurethane composite material with the double dynamic networks. Compared with the prior art, by introducing a'thionocarbamate-borate 'double-dynamic network, high toughness, high strength, good self-repairability and repeatable processability in an extreme environment are realized, and the material is particularly suitable for manufacturing and repairing of key components in an LNG ship body and a heat insulation system thereof.

The invention relates to the technical field of polymer photoelectric materials, in particular to a preparation method of a supramolecular gel electrolyte. The method comprises the following steps: esterifying tetraphenylethylene alcohol and methacryloyl chloride to form tetraphenylethylene methacrylate, and performing staged linear heating polymerization on the tetraphenylethylene methacrylate, 3-(methacrylamido) propyl dimethyl 3-thiopropyl ammonium oxide inner salt, acrylic acid, tetraphenylethylene methacrylate and 4-vinylpyridine under the action of ammonium persulfate to obtain a tetraphenylethylene copolymer. And finally, soaking in a lithium chloride aqueous solution to obtain the supramolecular hydrogel electrolyte. The hydrogel obtained by the invention has high mechanical strength and high ionic conductivity, and is suitable for energy storage devices such as flexible supercapacitors and the like.

The invention provides a beta '-sulfo-alpha, beta-unsaturated gamma-lactam derivative as well as a preparation method and application thereof, and belongs to the technical field of organic chemical synthesis. The beta '-thio-alpha, beta-unsaturated gamma-lactam derivative has a structure as shown in a formula I. According to the method disclosed by the invention, cesium carbonate is taken as alkali, and a molecular skeleton of the beta'-thio-alpha, beta-unsaturated gamma-lactam derivative is constructed through free radical coupling and olefin isomerization processes under the condition of blue light irradiation. Bioactivity evaluation shows that the beta '-sulfo-alpha, beta-unsaturated gamma-lactam derivative prepared by the method disclosed by the invention has an inhibition effect on MDA-MB-231 human breast cancer cells.

The invention relates to the technical field of precious metal recovery, in particular to a process for separating precious metal from copper-nickel smelting waste, which comprises the following steps: crushing and grading the waste, adding a sulfuric acid solution containing etidronic acid, leaching, and washing, drying and crushing filter residues to obtain a pretreated material; mixing the pretreated material with a sodium peroxide-sodium carbonate composite flux, roasting, leaching with water, and filtering to obtain a filter residue B; adding a leaching agent containing hydrochloric acid, sodium chlorate and 1, 2-cyclohexanediamine tetraacetic acid into the filter residue B according to the ratio of 1: 3-1: 5, and filtering to obtain filtrate C and filter residue C; adjusting the pH value of the filtrate C to 1.5-2.5, adding an ethanol solution of sodium N, N-diethyldithiocarbamate, precipitating, washing and calcining to obtain sponge palladium; adding ammonium chloride into the filtrate D, precipitating and calcining to obtain sponge platinum; and leaching the filter residue C by using a hydrochloric acid-chloroauric acid mixed solution containing diphenylthiourea, and replacing and calcining zinc powder to obtain crude gold. According to the process, the leaching rates of platinum, palladium and gold and the product purity are greatly improved; flux and reagent systems are optimized, consumption and energy consumption are reduced, waste liquid treatment is matched for up-to-standard discharge, and efficient resource recovery and environment-friendly cooperation are achieved.

The invention discloses a mixing device for preparing thioacetamide, and relates to the technical field of thioacetamide mixing. Comprising a mixing installation part, an isolation mixing part is installed on the mixing installation part, and the isolation mixing part is used for mixing thioacetamide raw materials; a filler control piece is mounted on the mixed mounting piece; a stored material detection part is mounted on the mixed mounting part; the stored material detection piece is used for detecting melting of solid raw materials; a discharge control part is mounted at the bottom of the mixed mounting part; the discharge control part is used for discharging a thioacetamide raw material mixed solution; by adopting the premixing discharging part, when the discharging electromagnetic valve needs to be opened for discharging work, the mixing motor is kept to be started and is in a driving mixing state; the mixing device is used for solving the problem that the existing mixing device for manufacturing thioacetamide is easy to generate precipitates when discharging thioacetamide raw material mixed liquid intermittently for multiple times.

The invention provides a sulphide ore alkaline desulfurization and cyanidation gold leaching agent system and a method for extracting gold through the sulphide ore alkaline desulfurization and cyanidation gold leaching agent system, and belongs to the technical field of hydrometallurgy. According to the method, a ternary agent system consisting of potassium ferricyanide, low-concentration sodium cyanide and thioguanosine is constructed. An efficient'oxidation-inhibition 'synergistic system is formed between the auxiliary desulfurization agent potassium ferricyanide and the thioguanosine. The rapid and selective oxidation of potassium ferricyanide is smoothly carried out under the synergistic effect of thioguanosine, minerals are thoroughly decomposed, and the surface keeps high activity; meanwhile, due to the existence of the thioguanosine, the local microcell passivation risk and catalytic electron transfer can be eliminated more directionally. The sodium cyanide and the sodium cyanide complement each other, it is jointly guaranteed that the exposed gold can be smoothly and efficiently leached through follow-up low-concentration sodium cyanide, finally, the total consumption of reagents is reduced, environmental pollution is reduced, and meanwhile high-recovery-rate extraction of the gold in the sulfide ore difficult to treat is achieved.

Provided herein is a preparation of a stable drug conjugate containing one or two opened ring structures of thiosuccinimides linked to an antibody or an antibody-like protein for enhancement of targeted treatment of cancers and refractory diseases. In particular, provided herein are preparation of such conjugate homogenously, and its pharmaceutical compositions, as well methods in treatment of refractory diseases.

The invention discloses a tetrathiomolybdate intercalated ternary iron-magnesium-zinc layered double hydroxide catalyst, a preparation method thereof and an application of the tetrathiomolybdate intercalated ternary iron-magnesium-zinc layered double hydroxide catalyst in degrading azo dyes by activating peroxymonosulfate. According to the method, a carbonate intercalated ternary LDH precursor is synthesized through a hydrothermal reaction, interlayer anions are replaced with nitrate and tetrathiomolybdate through ion exchange, and the target catalyst is obtained. In the catalyst, a unique Fe-Mg-Zn ternary metal laminate and a MoS < 2-> intercalation structure cooperatively construct a multi-active center, and MoS < 2-> is used as an electron donor to promote cyclic regeneration of Fe < 3 + > / Fe < 2 + >. The catalyst keeps ultrahigh activity in a wide range of pH (potential of hydrogen) of 3-9, can completely degrade 10 mg / L of acid orange 7 within 5 minutes, and is stable in structure and low in metal dissolution risk. The problems of low activity, slow Fe < 3 + > reduction, metal ion dissolution and the like under neutral and alkaline conditions in an advanced oxidation technology based on peroxymonosulfate are solved, and the method has important application value in the field of printing and dyeing wastewater treatment.

The invention discloses an oligonucleotide synthesis process of a sulfo-PMO structure. In the oligonucleotide synthesis process of the sulfo-PMO structure, the molecular structural formula of sulfo-PMO is shown in the specification. According to the invention, the molecular structure of thio-PMO is specifically limited, and the synthesis of nucleotide phosphate amide and (thio) phosphoric acid amide in the solid-phase synthesis oligonucleotide is carried out along the direction from 5'to 3 ', that is, in each cycle period, the O5'or O6' position of the nucleotide phosphate amide and (thio) phosphoric acid amide monomer is firstly subjected to coupling reaction, and then the protecting group is removed at the O3 'or N3' position, so that the oligonucleotide phosphate amide and (thio) phosphoric acid amide are obtained. And releasing active hydroxyl or amino / amido to enter the next cycle. The protecting group adopted by the sulfo-PMO molecule is consistent with the protecting groups of other nucleotides, so that the conversion rate of each step of coupling reaction can be conveniently detected on line.

The invention discloses a preparation method of olmacycline tosylate for injection, belongs to the technical field of pharmaceutical preparations, and provides a special preparation and a preparation method of the olmacycline tosylate for injection in order to solve the problems that the olmacycline tosylate for injection is prone to epimerization and oxidative degradation and the room temperature stabilization time is short after redissolution. According to the preparation, omagazines tosylate is used as a main component and matched with glycerol, vitamin C, thioglycerol, sodium acetate and water for injection, and the pH is adjusted to a proper range through hydrochloric acid or sodium hydroxide. According to the method, by means of the synergistic effect of glycerin and vitamin C, glycerin fixes medicine molecules and protects vitamin C, vitamin C removes oxidation inducements, and thioglycerin is matched to assist in inhibiting degradation, so that the medicine stability is greatly improved, the redissolved liquid medicine can be stabilized at 25 DEG C for 72 hours, the total impurities are controlled at a low level, and the clinical actual requirements are met.

The invention relates to an optical monomer and a preparation method and application thereof, the structural general formula of the optical monomer is shown as G1, G2, G3, G4, G5, G6, G7 and G8, R1 is selected from one of the formulas, and R2 is hydrogen or methyl; n is a positive integer selected from 1-10. The optical monomer provided by the invention contains a plurality of aromatic rings with high molar refractive index and low molar volume, and also contains sulfur atoms with relatively high molar refractive index, so that the whole molecule of the whole monomer is extremely high in refractive index; the polymer also has a phenyl dithiocarbamate structure, and has good compatibility with film-forming resin with carbamate when being used for a photopolymer holographic recording medium. The monomer structure provided by the invention has a plurality of branched chains, the overall molecular weight is small, and the molecules are not easy to agglomerate.

An oil-in-water cosmetic composition comprising: compound of thipyridinone type; one or more Polyglyceryl Fatty Acid Ester; an oil phase; and wherein the oil-in-water cosmetic composition is a macroemulsion and wherein the compound of thipyridinone type penetrates rapidly and in a high amount.

This invention relates to a method for the recovery of metal from a material comprising: contacting a material with a first reagent comprising a thiocarbonyl group and a second reagent under various conditions. The metal may be a base metal, a precious metal, or a combination thereof. The conditions include, but are not limited to, recovery in the presence of a microbe; optimal material size and / or shape; geolocation parameters; elemental sulfur; added pyrite; or a combination thereof.

The invention relates to a nano bismuth agent for preventing and / or treating gastritis infection as well as a preparation method and application thereof, the preparation method comprises the following steps: respectively dissolving soluble bismuth salt and a sulfur-containing compound, mixing, and reacting to obtain the nano bismuth agent after the reaction is finished, the sulfur-containing compound is any one or a combination of at least two of thioamino acid, vitamin B1, thioacetamide, sodium sulfide, sodium thiosulfate, bovine serum albumin, whey protein, ovalbumin or metallothionein. The prepared nano bismuth agent has efficient antibacterial performance, shows an excellent curative effect which is two orders of magnitude higher than that of an existing bismuth complex on clinically separated drug-resistant helicobacter pylori, and does not further induce increase of drug resistance of the helicobacter pylori.

The embodiment of the specification provides a modification identification method of a thio-phosphorylated nucleic acid sequence, which comprises: performing enzymolysis on a to-be-identified nucleic acid sequence by using a nucleic acid mixed enzyme to obtain an enzymolysis product; performing secondary mass spectrum analysis on the enzymolysis product based on first mass spectrum information; and determining whether a target sequence fragment exists in the to-be-identified nucleic acid sequence based on the first mass spectrum information and the second mass spectrum information. At least the to-be-identified nucleic acid sequence modified by thio-phosphorylation is actually obtained based on a preset modification rule. The first mass spectrum information comprises a theoretical analysis result generated by analyzing a theoretical sequence fragment, and the theoretical sequence fragment is determined based on the preset modification rule, the to-be-identified nucleic acid sequence and the nucleic acid mixed enzyme. The modification identification method can accurately and efficiently identify the chemical modification of the thio-phosphorylated nucleic acid sequence.

The application provides a synthesis process of metrafenone, in which inorganic alkali KOH is used as a catalyst, a key intermediate 4-(((5,5-dimethyl-dihydroisoxazole-4-yl)thio)methyl)-1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-ol can be obtained at low production cost and high yield, metrafenone is prepared through substitution reaction and oxidation reaction, the reaction yield is high, raw materials are simple and easy to obtain, three-waste emissions are small, and the process is beneficial to industrial mass production.

The present invention relates to a novel polymorph of (1R,2R,3aS,3bR,10aS,10bR,11S,12aS)-5,10b-difluoro-1-(((fluoromethyl)thio)carbonyl)-11-hydroxyl-2,10a,12a-trimethyl-7-phenyl-1,2,3,3a,3b,7,10,10a,10b,11,12,12a-dodecylhydrocyclapenta[5,6]napththo[1,2-F]indazole-1-furan-2-carboxylate ester as shown in formula (I), a preparation method therefor, and a use thereof. The crystal form of the present invention has characteristics such as a significant pharmaceutical effect, good stability, high yield, and high purity, and is beneficial for the selection and design of a drug administration route and the determination of a drug preparation process parameter, thereby improving drug production quality.

The invention belongs to the technical field of electromagnetic wave absorbing materials, and discloses a composite coating with electromagnetic protection and explosion-proof functions as well as a preparation method and application of the composite coating. The coating comprises 40 to 60 parts of polycarbodiimide modified diphenylmethane diisocyanate, 40 to 60 parts of a semi-prepolymer which is synthesized from polycarbonate diol with the equivalent weight of 1000 and has the NCO content of 10 to 20 percent, 73 to 100 parts of a polyether amine curing agent, 15 to 20 parts of diethyl toluenediamine or dimethyl thio toluenediamine, 0.5 to 2 parts of calcium carbonate and 3 to 6 parts of magnetic powder. And the two components are quickly reacted and molded through a spraying process. According to the invention, the polyurea elastomer is used as a matrix, so that the coating is endowed with excellent impact resistance, explosion-proof characteristics, water impermeability, oil resistance, low temperature resistance and other environmental tolerance; meanwhile, an adjustable electromagnetic wave absorption function is realized by doping specific magnetic powder. The coating is simple in preparation process and excellent in comprehensive performance, and is particularly suitable for equipment surfaces with high requirements on stealth and survival protection, such as oil storage equipment.

The present invention relates generally to improved formulations of 6- thioguanine (6-TG), their methods of preparation, and their use in treatment methods. The invention provides a pharmaceutical composition comprising 6-TG, and a polyethylene oxide polymer having a molecular weight of between about 900,000 g / mol and about 9,000,000 g / mol, their methods of preparation, and their use in methods for treating a disease or condition of the distal intestine that responds to 6-TG, wherein the 6-TG is released in the distal intestine.

The invention relates to the technical field of non-ferrous metal beneficiation, in particular to a flotation reagent composition for recycling micro-fine particle copper sulfide from copper oxide acid leaching residues and a beneficiation method of the flotation reagent composition. The flotation reagent composition for recovering copper sulfide from copper oxide acid leaching residues is characterized by comprising a collecting agent, a hydrophobic agglomeration agent and a foaming agent, and the collecting agent is ethyl thioacetate; the hydrophobic agglomeration agent is prepared from octadecyl triethoxy silane and kerosene; and the foaming agent is selected from terpilenol, methyl isobutyl carbinol or sec-octanol. The ethyl thioacetate serving as a collecting agent is stable in chemical property in an acid environment, weak in gangue mineral collecting capacity and good in selectivity in the copper sulfide mineral flotation process, and therefore the grade and the recovery rate of obtained copper sulfide concentrate are higher.

This invention discloses a method for preparing a cyclic peptide compound containing a cisamide bioelectron isosteric cyclic peptide. The method involves introducing a thioamide unit at a specific position on the peptide backbone, making it a potential activatable reaction site. This site is selectively activated by a metal salt and undergoes an intramolecular condensation reaction with an acylhydrazine group located in the same peptide chain, generating a 1,2,4-triazole heterocyclic structure in situ. In a single reaction process, the cyclization of the peptide and the precise construction of the cisamide bioelectron isosteric group in the peptide backbone are achieved simultaneously.

This invention belongs to the field of environmental chemistry and relates to a method for quantitatively analyzing the concentrations of cystine and cysteine ​​in a mixed solution. Based on the theoretical characteristics of the reaction between the disulfide bond in cystine, a representative amino acid, and the thiol group in cysteine, and persulfate, this invention expands the detection capability of the traditional 5,5-dithio-bis-(2-nitrobenzoic acid) (DTNB), providing support for the quantitative analysis of cystine and cysteine ​​concentrations and the study of their transformation processes.

The invention discloses a method for green and efficient recovery of gold from refractory gold ore. The green and efficient gold recovery method for the refractory gold ore comprises the following steps that biological oxidation pretreatment is conducted on the refractory gold ore, and biological oxidation ore pulp is obtained; adjusting the pH value of the biological oxidation ore pulp, standing for 1-3 days to carry out bacterial inactivation on the biological oxidation ore pulp, then adding a proper amount of iron-based ligand to adjust the potential of the biological oxidation ore pulp to a proper range, and then adding a proper amount of thiosulfate to carry out in-situ leaching to obtain leached ore pulp; and the leaching ore pulp is filtered and separated, and gold leaching liquid and leaching residues are obtained. According to the method for green and efficient gold recovery from the refractory gold ore, a biological oxidation pretreatment method and a weakly acidic iron-based thiosulfate in-situ leaching process are combined, acid-base conversion of ore pulp is not needed, and green and efficient leaching of gold in the refractory gold ore can be achieved with the low production cost and the short process.

The present invention relates to novel compounds of formula (I), optionally conjugated to peptide or protein molecules, and the synthesis thereof. The invention also relates to the use of the novel compounds for coupling reactions with linkers and other molecules. The invention also relates to the use of the novel compounds in bio-orthogonal strain promoted cycloaddition (copper-free), i.e. Click reaction. (I).

The invention is directed to a crosslinkable polyethylene composition comprising an additive composition consisting of polyethylene glycol and a mixture of 4,4′-thiobis (2-tertbutyl-5-methylphenol) plus thiodiethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate].

COSMETIC COMPOSITION COMPRISING THIOPYRIDINONE COMPOUNDS, A REDUCING AGENT, AND ARGININE. The present invention relates to a composition, preferably a cosmetic composition, comprising at least one thiopyridinone compound of formula (I) or formula (I'), with at least one reducing agent of formula (II) and arginine. The composition of the present invention lightens or depigments keratinous material, preferably skin. The present invention provides a composition including a thiopyridinone compound of formula (I) or formula (I') with increased stability of the thiopyridinone compound of formula (I) or formula (I') against exposure to light. Figure for the abstract: none

The invention discloses a preparation method of FePS3, which comprises the following steps: mechanically mixing pyrite powder, sulfur-containing small molecules and elemental phosphorus, calcining the fully mixed powder in two temperature stages under a protective atmosphere, and cooling to obtain FePS3 nano-powder; wherein in the first temperature stage, the temperature is 200-300 DEG C, and the heat preservation time is 120-240 minutes, and in the second temperature stage, the temperature is 400-600 DEG C, and the heat preservation time is 120-180 minutes; the sulfur-containing small molecules are thiourea, thioacetamide or a mixture of the thiourea and the thioacetamide; the molar ratio of sulfur atoms to phosphorus atoms in FeS2 molecules and sulfur-containing small molecules in the pyrite powder is (1: 3: 5)-(1: 1: 5). According to the method, pyrite is used as an iron source and a sulfur source, sulfur-containing small molecules are used as a second sulfur source, and the FePS3 nano-powder is directly obtained through solid-phase reaction with the simple substance phosphorus without additional purification treatment. The method is low in solid-phase reaction temperature and simple in process, does not need harsh reaction conditions, and is easy for large-scale production.

The invention relates to a sulfur-containing tryptophan cyclic peptide compound as well as a synthesis method and application thereof. The synthesis method comprises the following steps: carrying out electrolytic reaction on a tryptophan peptide compound with a structure as shown in a formula I or a stereoisomer thereof and a thiosulfonate compound with a structure as shown in a formula II to obtain the sulfur-containing tryptophan cyclic peptide compound with a structure as shown in a formula III or a stereoisomer thereof. The sulfur-containing tryptophan cyclic peptide compound can be obtained by directly electrolyzing the tryptophan peptide compound by adopting an electrochemical method, so that the use of a transition metal catalyst and stoichiometric alkali is avoided, the generation of chemical wastes is avoided, and the realization of atom economy is facilitated. The method has the advantages of simple operation, high product purity, easy purification, high efficiency and yield, low production cost, mild reaction conditions, no need of inert gas protection, greener reaction system, environmental protection, safety, economy, energy saving and environmental protection, and is more conducive to realization of industrial production.

The application discloses a gold leaching method for pyrite-containing gold ore, and comprises the following steps: after the pyrite-containing gold ore is finely ground, water is added to obtain a slurry; a gold leaching reagent solution is added into the slurry to obtain a mixed leaching solution; the pH value of the mixed leaching solution is adjusted to alkaline, and leaching treatment is performed; and after filtration, a gold-containing leaching solution is obtained; the gold leaching reagent solution comprises polyphosphate, copper salt and thiosulfate; in the gold leaching reagent, polyphosphate is added; under alkaline conditions, polyphosphate ions can be selectively adsorbed or complexed on the surface active sites of pyrite to form a physical or chemical masking layer, thereby effectively blocking the direct contact of pyrite with dissolved oxygen and thiosulfate in the solution, inhibiting the catalytic decomposition of pyrite, significantly reducing the invalid consumption of thiosulfate, stabilizing the pH value and potential of the leaching system, and guaranteeing the efficient leaching of gold.

This invention belongs to the field of mineral flotation technology, and discloses a flotation collector for non-ferrous metal sulfide ores, its preparation method, and its application. The collector uses O,O-dialkyldithiophosphate as a starting material, and reacts sequentially with a halocarboxylic acid ester, hydrazine hydrate, potassium hydroxide, and carbon disulfide in anhydrous ethanol in a three-step reaction to obtain the target product, O,O-dialkyldithiophosphate hydrazide-N′-dithiocarbamate potassium. Its molecular structure simultaneously contains three active groups: a dithiophosphate group, an hydrazide group, and a dithiocarbamate group. This invention achieves efficient process connection and smooth transition by optimizing the material ratio, temperature, and time of each reaction step, and has advantages such as mild reaction conditions, simple operation, few side reactions, high yield, and stable product. The prepared collector exhibits excellent collecting performance and good selectivity for non-ferrous metal sulfide ores such as chalcopyrite, and is suitable for widespread application in sulfide ore flotation processes.