1610 results about "Thio-" patented technology

The invention provides a salt-responsive temperature-resistant salt-resistant water-based drilling fluid tackifying filtrate reducer as well as a preparation method and application thereof, and belongs to the technical field of drilling. The tackifying filtrate reducer is prepared from the following raw materials in parts by mass: 30 to 50 parts of 1-(2-carboxyethyl)-2-vinylpyridine, 20 to 40 parts of (3-(methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt, 35 to 55 parts of N, N-dimethylacrylamide, 10 to 25 parts of 4-vinylpyridine, 300 to 500 parts of water and 1 to 5 parts of an initiator. According to the filtrate reducer, cations and anions are concentrated on one monomer molecule, so that the synthesized product contains the cations and the anions with the same charge number, has good adsorption capacity and salt response characteristics, is compatible with salt essentially, can effectively resist high temperature and high salt, and can be recycled. And the viscosity-increasing and filtrate-reducing agent has good viscosity-increasing and filtrate-reducing effects on the drilling fluid.

The invention belongs to the field of photocatalytic materials, and particularly relates to a high-entropy sulfide and a preparation method and application thereof. The high-entropy sulfide is granular, the molecular general formula is (MnaFebCocCudZe) xS, x is equal to 1, and the atomic ratio of Mn to Fe to Co to Cu to Zn is a: b: c: d: e of (1-2): (1-2): (1-2): (1-2): (1-2): (1-2): (1-2). The preparation method comprises the following steps: S1, dissolving metal salt in a mixed solvent of isopropanol and glycerol according to the atomic ratio of metal elements, and carrying out solvothermal reaction to obtain a precursor; and S2, dispersing the precursor in ethanol, adding thioacetamide as a sulfur source, and carrying out solvothermal reaction to obtain the high-entropy sulfide. The high-entropy sulfide disclosed by the invention is used as a photocatalytic material and shows excellent photocatalytic performance.

The invention relates to an impact-resistant chlorinated polyvinyl chloride composite material and a preparation method thereof, and belongs to the technical field of polymer composite materials. The composite material comprises the following components: 100 parts of CPVC resin, 6.5 to 9.5 parts of a modified impact modifier, 2.6 to 3.2 parts of a heat stabilizer, 1.5 to 2 parts of a lubricant, 1.2 to 1.6 parts of a processing aid, 0.2 to 0.25 part of a light stabilizer and 8 to 11 parts of a filler, the modified impact modifier takes a POSS cage structure as a core, a branch chain sequentially contains thioamide-secondary amine-tertiary amine structures, a polarity gradient is formed and fully extends into a macromolecular chain of CPVC to transmit and dissipate impact energy, meanwhile, the amine structure interacts with chlorine groups in a molecular chain of CPVC to form molecular anchoring, expansion of crazes is inhibited, and the impact strength of the CPVC is improved. The continuity and the stability of a bonding interface are maintained, so that the composite material keeps relatively high mechanical strength and thermal stability.

The invention relates to an organic molecule, in particular for the application in optoelectronic devices. According to the invention, the organic molecule includes or consists of a structure represented by Formula IwhereinR1 is selected from the group consisting of hydrogen and C6-C12-aryl, which is optionally substituted with one or more C1-C6-alkyl substituents, andRa is at each occurrence independently selected from the group consisting of: hydrogen, deuterium, N(R5)2, OR5, Si(R5)3, B(OR5)2, B(R5)2, OSO2R5, CF3, CN, F, Br, I, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl, and C2-C57-heteroaryl.

Provided are: a crystalline sulfide solid electrolyte, which has an improved ionic conductivity while adopting a liquid phase method, contains predetermined atoms, has a diffraction peak in X-ray diffractometry using a predetermined CuKα ray, and has a thio-LISICON Region II-type crystal structure as a basic structure; and a method for producing a crystalline sulfide solid electrolyte, the method including mixing using predetermined complexing agents and an instant drying step.

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 provides a method for promoting acquisition of clean fuel by light / sound concerted catalytic degradation of waste plastics and upgrading and conversion thereof, which comprises the following steps: uniformly mixing g-C3N4, cadmium acetate and thioacetamide according to a predetermined proportion, pouring into a reaction kettle, placing in a high-temperature oven for a predetermined time, centrifuging, cleaning and drying to obtain a catalyst, the method comprises the following steps: loading a catalyst on the surface of aerogel, hydrogel or non-woven fabric to obtain an MTSJA-loaded catalyst, treating waste plastic with NaOH, adding the MTSJA-loaded catalyst, stirring under irradiation of a xenon lamp, starting ultrasound for reaction, and carrying out light / sound synergistic catalytic degradation on the waste plastic. According to the method, energy consumption is not needed, toxic and harmful gas is not generated, the purposes of energy conservation and environmental protection can be achieved, meanwhile, carbon dioxide in water can be catalytically reduced to generate clean energy such as methane in the process of degrading the waste plastic, and further obtaining of the energy is promoted.

The invention belongs to the technical field of anticorrosive coatings, and particularly relates to a high-temperature-resistant hydrophobic anticorrosive coating as well as a preparation method and application thereof. The invention provides a high-temperature-resistant hydrophobic anticorrosive coating, which is prepared from the following raw material components in parts by weight: 100 to 140 parts of epoxy resin; 3 to 7 parts of 2-benzothiazole thiosuccinic acid; 2 to 6 parts of hydrophobically modified ZIF-67 (at) MgAlCeFe-LDH (layered double hydroxide); 4-8 parts of a filler; 2-6 parts of a dispersant; 1-3 parts of a defoaming agent; 2-4 parts of a coalescing agent; 15-35 parts of a curing agent; 20 to 30 parts of water; and 10 to 20 parts of ethanol. The hydrophobic property of the coating can be improved by adding hydrophobic modified ZIF-67 (at) MgAlCeFe-LDH, and the corrosion resistance of the anticorrosive coating is remarkably improved by matching with 2-benzothiazole thiosuccinic acid and utilizing the interaction between the ZIF-67 (at) MgAlCeFe-LDH and the 2-benzothiazole thiosuccinic acid. The anti-corrosion coating prepared by the method has excellent corrosion resistance, hydrophobic performance and high temperature resistance.

The invention belongs to the field of food processing, and particularly relates to an ostrich meat preservative and a preservation method. The ostrich meat preservative provided by the invention is prepared by matching and mixing the chitosan, the nisin and the tea polyphenol according to a specific proportion, so that the refrigeration refreshing time of the ostrich meat treated by the preservative can be effectively prolonged, the ostrich meat can maintain a relatively high L * value and a * value within 16 days of storage, the deterioration of meat color is delayed, the water-retaining property is remarkably improved, and the quality of the ostrich meat is improved. The content of thiobarbituric acid reactants and volatile basic nitrogen is obviously reduced, and fat oxidation and protein degradation are inhibited; the total number of bacterial colonies and the number of microorganisms such as coliform bacteria, pseudomonas, mould and saccharomycetes are obviously reduced. The growth and reproduction of putrefying bacteria can be effectively inhibited, and the cold fresh shelf life is prolonged.

The invention discloses a composite collecting agent and a preparation method and application thereof, and relates to the technical field of solid waste recycling. The composite collecting agent comprises a main agent, an auxiliary agent and a synergist, and the mass ratio of the main agent to the auxiliary agent is (3-1): (1-2). The mass of the synergist is 0.1%-2.5% of the total mass of the composite collecting agent; the structural formula of the main agent is as shown in formula (I): R-O-C (= S)-NH-R '(I); in the formula (I), R is alkyl, and R'is 3-chloro-1, 2-epoxypropane; the auxiliary agent is a mercaptobenzothiazole derivative. The thiocarbamate and the mercaptobenzothiazole derivative are compounded according to a specific proportion for the first time, a Zn-S shielding layer is destroyed through an intermolecular synergistic effect, and the silver recovery rate is increased; the preparation method is simple and easy to operate, facilitates reduction of the dosage of a single agent and reduces environmental pollution. The foam stability is improved, the flotation efficiency is improved, the selective collection efficiency of the silver-zinc ore is remarkably improved, and the flotation index is improved.

The invention discloses a preparation method of a high-purity ultra-clean hydroxylamine aqueous solution. A four-stage purification process comprises the following steps: 1) low-temperature chelation-ceramic membrane metal removal; 2) molecular sieve membrane rectification decomposition prevention; 3) pulse electrodialysis reversal deep desalination; and 4) gradient filtration terminal refining. According to the preparation method of the high-purity ultra-clean hydroxylamine aqueous solution, a low-temperature molecular sieve membrane rectification technology is adopted, hydroxylamine liquid-phase thermal decomposition is avoided through a vapor phase separation mechanism, and the decomposition rate is reduced to 1t from 15% of a traditional process; the method comprises the following steps of: removing metal through chelation-electrodialysis synergistically, ensuring that Fe and Cu ion residues are less than or equal to 0.05 ppb through a thiosemicarbazide-bipolar membrane system, ensuring the nitrogen environment in the whole process, ensuring that the dissolved oxygen is less than or equal to 5ppb, replacing liquid phase distillation with molecular sieve membrane vapor phase separation, solving hydroxylamine liquid phase thermal decomposition, and breaking through the trace metal removal limit by combining thiosemicarbazide-bipolar membrane synergistically removing impurities. And then through nanoscale terminal filtration, the metal / particle control reaches ppb-level limit which is superior to the SEMI standard, and double spanning of quality and cost is realized.

The invention provides a modified sulfide solid electrolyte and a preparation method and application thereof.The modified sulfide solid electrolyte comprises lithium thioborate crystals, composite grain boundaries are contained between the lithium thioborate crystals, and lithium iodide is contained in the composite grain boundaries. The structures of crystal lattices and composite crystal boundaries in the modified sulfide solid electrolyte are stable, so that the lithium ion migration capability of the modified sulfide solid electrolyte can be improved, and the ionic conductivity of the modified sulfide solid electrolyte is obviously improved.

The invention discloses a foamed nickel loaded cobalt sulfide / nickel sulfide NF-CoS / NiS. The foamed nickel loaded cobalt sulfide / nickel sulfide NF-CoS / NiS is prepared by the following steps: firstly, taking foamed nickel NF as a substrate, loading cobalt hydroxide on the surface of the NF through first electrodeposition, then converting the NF into ZIF-67 through an impregnation method, then vulcanizing through thioacetamide and hydrothermal reaction, and finally loading Ni3S2 nanoparticles through second electrodeposition. The nickel foam loaded cobalt sulfide / nickel sulfide NF-CoS / NiS can be obtained. The preparation method comprises the following steps: 1, preparing foamed nickel electro-deposition cobalt hydroxide; 2, preparation of the foamed nickel loaded cobalt hydroxide / ZIF-67; 3, cobalt hydroxide / cobalt sulfide NF-Co / CoS is loaded on the foamed nickel; and 4, preparation of the foamed nickel loaded cobalt sulfide / nickel sulfide NF-CoSX / Ni3S2. When the material is used as a supercapacitor material, charging and discharging are carried out in a voltage window range of 0-0.5 V, and when the current density is 1mA cm <-2 >, the area specific capacitance is 8-9F cm <-2 >; and when the current density is 10mA cm <-2 >, 70-80% of the initial capacity is still kept after 5000 charge-discharge cycles are carried out.

The invention discloses a chilled beef freshness rapid detection model training method and a freshness detection method.The chilled beef freshness rapid detection model training method comprises the steps that a chilled beef sample is obtained, and the freshness index of the chilled beef sample is measured, the freshness indexes comprise the sensory score, the color a *, the pH value, the volatile basic nitrogen TVB-N, the thiobarbituric acid reactant TBARS, the total bacterial count TVC, the carbonyl content, the total sulfydryl content and the solubility of the chilled beef sample; establishing a chilled beef freshness grade evaluation standard according to the freshness index; collecting multi-modal data of the chilled beef sample, wherein the multi-modal data comprises near infrared spectrum data NIR, hyperspectral data HSI and low-field nuclear magnetic resonance LF-NMR relaxation time data; performing feature extraction on the multi-modal data through a feature extraction method to obtain multi-modal feature data; and carrying out preprocessing on the multi-modal characteristic data through a standardization SS and a Savitzky-Golay smooth filtering SG preprocessing method so as to obtain preprocessed data.

The invention relates to a coumarin-based fluorescent probe as well as a preparation method and application thereof in the aspect of HClO detection, and belongs to the technical field of HClO detection. The invention discloses a coumarin-based fluorescent probe W (O-(3-((2-morpholinyl ethyl) carbamoyl)-2-oxo-2hydrogen-benzopyran-7-yl) dimethyl thiocarbamate) prepared on the basis of an intramolecular charge transfer (ICT) mechanism, and a preparation method of the coumarin-based fluorescent probe W. The novel lysosome targeting fluorescent probe contains coumarin as a fluorophore, a morpholine group as a targeting group and a dimethyl thiocarbamate group as a recognition group, is a novel lysosome targeting fluorescent probe, and has excellent performances of high selectivity, low detection limit, low cytotoxicity, high resolution and the like in the aspect of HClO detection; the method can be used for detecting the content of endogenous and exogenous hypochlorous acid in living cells.

Provided herein are compositions and methods for removing / recovering heavy metal ions in a phosphoric acid-containing stream by mixing a dialkyldithiophosphate compound having at least one alkyl chain length of C8 to C18, a dialkyldithiophosphate compound having at least one alkyl chain length of C8 to C18, and a dialkyldithiophosphate compound having at least one alkyl chain length of C18 to C18, reagents of at least one dialkyldithiophosphinate compound and at least one surfactant are added to a phosphoric acid solution or slurry to form heavy metal ion complexes, and the heavy metal ion complexes are separated from the solution or slurry.

The invention provides a method for preparing high-purity hafnium tetrachloride by wet extraction and separation, which comprises the following steps: stirring and leaching hafnium alloy waste serving as a raw material by using HNO3 and HF mixed acid, then adding thioacetamide, adjusting the pH value to 4-5, stirring and filtering; compounding tributyl phosphate, trioctylphosphine oxide and sulfonated kerosene to obtain a composite extracting agent, and stirring and mixing to form a homogeneous organic phase; in a hydrochloric acid medium, controlling the volume ratio of an organic phase to a water phase to be (2.5-3.5): 1, carrying out three-stage counter-current extraction, and standing for phase splitting; the extracted organic phase passes through an adsorption column filled with iminodiacetic acid modified silica gel; and carrying out reverse extraction by using a hydrochloric acid solution, and then carrying out reduced pressure evaporation concentration, cooling crystallization and dehydration to obtain hafnium tetrachloride. According to the method, the zirconium and hafnium separation efficiency in the hafnium tetrachloride preparation process is improved, and the problem that the content of zirconium and hafnium impurities in the product is too high is solved.

The invention provides a pharmaceutical wastewater treatment process. The pharmaceutical wastewater treatment process comprises the following steps: A1, pretreatment, A2, adsorption treatment, A3, oxidation treatment and A4, filtration treatment. In the step A2, a composite adsorbent comprising the following raw materials: attapulgite, activated carbon, carbon nanotubes, 4-carboxyphenylboronic acid, polyethyleneimine, sodium dithiocarbamate, epoxy resin E-44, deionized water and modified nano zero-valent iron is used, and self-repairing is realized through dynamic chemical bonds such as boric acid ester bonds, imine bonds and thiol-disulfide bonds; the adsorbent can be self-repaired during microscopic damage, so that the service life is prolonged, and relatively high adsorption capacity is kept. In the step A3, a gel microsphere oxidant comprising the following raw materials: hydrogen peroxide, potassium persulfate, copper-iron sulfide, nitrogen-doped carbon quantum dots, sodium alginate powder, sodium polyacrylate and a phosphate buffer solution is used, and efficient degradation is realized through a synergistic mechanism of free radical oxidation, non-free radical oxidation and photocatalysis.

The invention belongs to the technical field of mineral flotation, and particularly discloses a method for recovering whole-fraction iron lepidolite through combination of multi-stage magnetic separation and synergistic flotation. Comprising a matched compound collecting agent which is composed of sodium dodecenesulfonate, amino acid methyl thiohydracrylate, an amphoteric polyacrylamide polymer, carboxyethylidene diphosphonic acid and polyethylene glycol, and efficient recovery of whole-size-fraction iron lepidolite is achieved by matching with a corresponding magnetic separation-flotation combined process. The compound collecting agent generates static electricity and physical and chemical adsorption on the iron lepidolite through specific groups such as sulfonic acid groups, carboxyl groups, amino groups, acylamino groups and phosphate groups, exerts excellent selectivity and collecting functions, generates a dispersion effect and a chelating flocculation effect on micro-fine-particle iron lepidolite, and well cooperates with multi-stage magnetic separation to recover whole-particle-size iron lepidolite, so that the recovery rate of the whole-particle-size iron lepidolite is increased, and the recovery rate of the whole-particle-size iron lepidolite is increased. And the existing combined beneficiation process of the iron lepidolite is optimized, the cost and the environmental influence are reduced, and technical support is provided for sustainable development of lithium resources.

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.

A pyrazine thio-biphenyl compound and its application, specifically discloses the compound of formula (II) or a pharmaceutically acceptable salt thereof.

The invention relates to the technical field of mercury removal, in particular to a compound heavy metal chelating agent and a preparation method and application thereof. The preparation method of the compound heavy metal chelating agent comprises the following steps: mixing N-dithio carboxyl-amino phenyl formic acid, a cyclohexyl-3, 5-diene-1, 2-dicarboxylic acid solution, a propionic acid solution and a sodium hydroxide solution, stirring until complete dissolution and standing, then completing evaporative crystallization, and separating and purifying the separated chelating agent. The N-dithio carboxyl-amino phenyl formic acid, the cyclohexyl-3, 5-diene-1, 2-dicarboxylic acid, the propionic acid and a proper amount of sodium hydroxide are mixed to form a compound reagent, the chelating absorption effect on the heavy metal Hg in the natural gas wastewater is better, and the formed chelate is very stable and not easy to decompose.

The invention relates to the technical field of bird repelling agents, in particular to a bird repelling agent based on thiocyanuric acid and a preparation method thereof, and the bird repelling agent is prepared from the following raw materials: thiocyanuric acid, modified beta-cyclodextrin, a magnetic powder synergist, a gel matrix, a synergistic aid, a solvent and a surfactant. The invention discloses a bird repellent based on thiocyanuric acid and a preparation method thereof, thiocyanuric acid is included through monoisocyanate modified beta-cyclodextrin, a magnetic powder synergist and a gel matrix are combined to form a'molecular inclusion-magnetic response-gel fixation 'triple-action system, and the problems that an existing bird repellent is short in time efficiency and poor in weather resistance are solved. The release time of the bird repellent is prolonged, the high bird repelling rate is still kept under the conditions of high temperature and rainwater, and the bird repellent is suitable for scenes such as farmlands and electric power facilities and has remarkable technical progress and practical value.

The invention discloses a precious metal leaching agent based on thiosulfate and a precious metal leaching process. The leaching agent contains thiosulfate, a thiourea-based catalyst and an iron-based oxidizing agent, and the molar ratio of the thiosulfate to the thiourea-based catalyst to the iron-based oxidizing agent is (0.05-5): (0.005-1): (0.005-1). According to the leaching agent, on the basis of the synergistic effect of all the components, the dissolution efficiency of precious metal is improved, generation of polysulfate in side reaction is greatly reduced, and follow-up precious metal recovery is facilitated. A leaching process adopting the leaching agent comprises the following steps: exposing precious metal sites of a precious metal-containing material, adding the leaching agent, adjusting the pH value of a leaching system, carrying out a leaching reaction, and carrying out solid-liquid separation after the reaction is finished, so as to obtain a precious metal leachate. According to the technology, by controlling the pH value of the system and the adding amount of the leaching agent, leaching of different grades and types of precious metal-containing materials can be achieved under the normal temperature condition, and tests show that by taking gold ore as an example, the gold recovery rate of the technology can reach 100% at most.

The invention discloses a preparation method and application of chalcogenide doped graphdiyne, chalcogenide is implanted into a chalcogenide cavity in a simple thermal driving mode by using a chalcogenide cavity formed in para-nitrogen substituted graphdiyne as an anchoring site, so that the chalcogenide is distributed in a lattice shape, and a high-load monatomic graphdiyne material is obtained. The nano-enzyme sensor is constructed by utilizing the activity of peroxidase-like enhanced by the chalcogenide doped graphdiyne to detect bisphenol and thiosulfate ions, and powerful support is provided for monitoring of food safety and environmental safety.

The invention relates to the technical field of conditioning meat products, and provides a method for controlling and researching frozen storage quality deterioration of conditioned chicken wings by steady-state EGCG (epigallocatechin gallate), which comprises the following steps: step 1, sample treatment: conditioning unfrozen chicken wings; step 2, measuring the color, the unfreezing loss, the ferrimyoglobin, the sulfydryl, the Shore band, the thiobarbituric acid value TBARS and the volatile basic nitrogen TVB-N of the conditioned chicken wings; 3, analyzing a result; changes of color, unfreezing loss, ferrimyoglobin content, sulfydryl, Shore band, thiobarbituric acid value TBARS and volatile basic nitrogen TVB-N in the chicken wing freezing and thawing process are analyzed and conditioned; and 4, performing sensory evaluation according to the sensory evaluation table. According to the method, the control of the steady-state EGCG on the frozen storage quality deterioration of the conditioned chicken wings can be better studied.

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.