66results about How to "Reduce oxidative degradation" patented technology

The invention relates to the field of calligraphy and painting paper manufacturing, and specifically relates to a water-resisting breaking-resisting oxidation-resisting calligraphy and painting paper. The paper is prepared from raw materials and auxiliary materials through a pulping process and a paper making process. The raw materials comprise components of, by weight: 45-80 parts of bamboo pulp fiber, 10-30 parts of grass pulp fiber, 2-25 parts of wool pulp fiber, and 5-25 parts of viscose fiber. Each ton of the paper comprises auxiliary materials of, by weight: 0.5-2% of an antiseptic, and 3-15% of PVA. The calligraphy and painting paper provided by the invention has excellent water resistance, breaking resistance and oxidation resistance. The water-resisting and breaking-resisting functions are 10 times higher than a wet tensile strength index of a GB / T18739-2008 national standard of rice paper.

A fired product having a luminous function is manufactured by: adhering material-adapting glass frit to a surface of a ceramic material; adhering coating glass frit to the surface of the material-adapting glass frit after drying of the material-adapting glass frit; adhering luminous material particles having a particle size of 50 to 250 μm in one uniform layer to the coating glass frit layer before drying of the coating glass frit so that the upper portions of the luminous material particles are partly exposed from the coating glass frit; alternately stacking coating glass frit and luminous material particles several times; covering the topmost luminous material particles partly exposing from the coating glass frit by adhering coating glass frit; printing an image portion on the surface of the coating glass frit after drying of the coating glass frit; adhering adapting glass frit at a predetermined thickness to the coating glass frit having the printed image portion; uniformly adhering protecting glass frit particles having a large particle size to the surface of the adapting glass frit; and firing the adhered stack at high temperature, wherein the material-adapting glass frit has a coefficient of thermal expansion of an intermediate value between those of the ceramic material and the luminous material particles, the coating glass frit has a coefficient of thermal expansion substantially the same as that of the luminous material particles, and the adapting glass frit has a coefficient of thermal expansion of an intermediate value between those of the luminous material particles and the protecting glass frit particles having a large particle size. This fired product is used in an image forming part of an evacuation route guiding sign device as a fired product layer.

The invention discloses a microencapsulation preparation method of rhodococcus B7740 carotenoids. The method comprises the steps that (1) the rhodococcus carotenoids are extracted through an enzymic method; (2) rhodococcus B7740 carotenoid vegetable oil is prepared; (3) according to the mass ratio of chitosan to Arabic gum, two types of wall material powder are weighed, stirred in hot water to be dissolved and cooled; (4) according to the ratio of the masses of the wall material powder to the volume of the carotenoid vegetable oil, the carotenoid vegetable oil solution is absorbed and homogenized to obtain an o / w type lactescence; (5) a chitosan solution is added and continues to be stirred; (6) the mixture is cooled, curing agent glutaraldehyde is added, the PH is regulated through a NaOH solution, and the mixture continues to be stirred; (7) standing is carried out under the light shading condition, supernate is removed, sediments are washed, and vacuum freezing drying is carried out. The method is easy and convenient to implement, effectively reduces degradation of the carotenoids in the extraction process, reduces carotenoid degradation impurities in core materials and guarantees the physiological activity of carotenoid microcapsules, and the extraction ratio of the carotenoids reaches above 90%.

The invention provides a method for preparing nutritional microspheres. The method comprises the following steps of adsorbing, drying, backfilling, drying, cooling and packaging and the like. A nutrition enhancer is adsorbed by porous starch and covered by starch paste so that the aim that the loss of the nutrition enhancer with the unstable property in processing and storing processes is reduced is realized. The porous starch is in a hollow honeycomb-shaped particle structure so that a semi-closed environment can be provided for nutrients; and a fully-closed environment is provided for the nutrition enhancer by the backfilling of the starch paste. The fully-closed environment can be used for reducing the contact between easily-oxidized nutrients and oxygen, and the loss caused by oxidization is reduced; and the degradation effect on the nutrition enhancer by heat and shearing effects can be hindered. According to the method, the retention rate of the nutrition enhancer in the processing and storing processes can be improved.

The invention belongs to the technical field of a biologically medical material, and concretely relates to a medical absorbable oxycellulose material and a preparation method thereof. The material has dual functions of stopping bleeding and restoring wound. The material takes natural cellulose as a raw material, and is oxidized by an oxidation system under certain technology condition, the obtained product is subjected to acid treatment, washing by water and drying to prepare the medical absorbable oxycellulose material. The oxidation system has the advantages of strong selectivity, mild and controllable condition, and environmental protection of preparation technology. The prepared material has the advantages of rapidly stopping bleeding and rapidly being absorbed, has wound restoration function, can promote the healing of wound, and has wide application value on medical science.

The invention discloses a high pressure hydrogenation naphthenic lubricating oil light stabilizer composition. The composition comprises, by mass, 80-90% of an ultraviolet light absorbent and a hindered amine light stabilizer 3,5-bis(1,1-dimethylethyl)-4-octadecyl hydroxybenzene phenylpropionate, and 10-20% of a tri[2,4-di-t-butylphenyl]phenyl phosphite chelating agent. The light stability of high pressure hydrogenation naphthenic lubricating oil can be obviously improved by adding 0.5-1% of the high pressure hydrogenation naphthenic lubricating oil light stabilizer composition to base oil ofa high pressure hydrogenation naphthenic lubricating oil composition.

A glycine metal chelate complex belongs to the technical field of amino acid and trace element complexing and comprises an auxiliary material and two or more glycine metal chelates, the metal chelates include calcium glycinate, magnesium glycinate, zinc glycinate, ferrous glycinate, iron glycinate, copper glycinate and manganese glycinate. Also disclosed is a preparation method of the glycine metal chelate complex, the prepared metal chelate complex can supplement trace elements in a balanced manner for the purpose of meeting the needs of a human body for elements such as calcium, magnesium, zinc, iron, copper and manganese, and the preparation method is simple and easy to perform.

The invention belongs to the technical field of analysis chemistry, specifically to a method for extracting ascorbic acid from vegetables and fruits by using a nitrogen protection micro wave-assisted extracting technology. The method comprises the following steps of: taking fresh vegetables and fruits, adding a weak acid solution with certain concentration in 1:6-1:12 g / ml times of volume as an extracting solvent, discharging the oxygen in the system via a nitrogen protecting device, extracting at a micro wave condition with certain power for a certain time, cooling, compensating weight, uniformly mixing, centrifuging, taking out supernatant fluid, diluting, analyzing and detecting the content of the ascorbic acid in the vegetables and fruits via high performance liquid chromatography. According to the method, nitrogen protection is combined with micro wave-assisted extraction to discharge the oxygen in the system, thus the oxidization of the ascorbic acid is reduced and the extracting rate is greatly improved. The method is combined with the high performance liquid chromatography for exactly detecting the content of the ascorbic acid in the vegetables and fruits, and is applicable to extracting and separating other components which are easy to oxidize by heating.

The invention provides a tobramycin solution for inhalation. The tobramycin solution is prepared from tobramycin and a pH regulator, wherein the tobramycin is dissolved in a sodium chloride aqueous solution with concentration of 2.25-4.5mg / ml, the concentration of the tobramycin is 60-75 mg / ml, the pH regulator is sulfuric acid, and pH of the tobramycin solution for inhalation is 5.8-6.2. The tobramycin solution for inhalation is simple in composition, pH of the solution is controlled to be near-neutral and osmotic pressure is near-isotonic by controlling dosage of sulfuric acid, and bronchospasm and cough caused by irritation of the tobramycin solution for inhalation are reduced; after the tobramycin solution for inhalation is stored at room temperature for 1 year, the content of tobramycin is reduced slightly, the content of related substances is lower than 1.0%, requirements of the USP (United States Pharmacopeia) for the tobramycin solution for inhalation are met, the problem thatthe conventional tobramycin solution for inhalation is required to be stored at 2-8 DEG C is solved, drug use for a patient is facilitated, and storage cost and transport cost are reduced.

The invention discloses an oxidation-resistant cable and a production method thereof, the cable including a conductor, a shield, an insulation layer and an outer sheath, the shield is arranged on theouter surface of the conductor, the insulation layer is located outside the shield, and a fill layer is arranged between the insulation layer and the outer sheath. a water blocking tape is arranged between the fill layer and the outer sheath; the insulation layer takes polypropylene as a base material, supplemental polyolefin elastomer POE, antioxidant 1010, 168 and magnesium oxide crosslink polyethylene nanocomposites are also used, polypropylene has high impact resistance and mechanical toughness and is resistant to various organic solvents and acid-base corrosion and is strongly heat-resistance, flame-resistant and acid and alkli-resistant, and the polyolefin elastomer POE enhances the strength and toughness of polypropylene. The addition of magnesium oxide crosslinked polyethylene nanocomposites improves the thermal properties of polypropylene, and good heat resistance and oxidation resistance are guaranteed. The antioxidant can delay the oxidation degradation of tree materials.

The invention discloses water-soluble oxidized chitosan and a finishing method of the water-soluble oxidized chitosan on a fabric. The water-soluble oxidized chitosan is prepared by the following steps: dissolving chitosan in a 1-carboxymethyl-3-methylimidazolium hydrogen sulfate aqueous solution, oxidizing C2 and C3 sites of the chitosan by sodium periodate under microwave radiation to generate aldehyde groups, and then oxidizing primary hydroxyl at C6 site of the dialdehyde chitosan in an ionic liquid by concentrated nitric acid-concentrated phosphoric acid to generate carboxyl. The water-soluble oxidized chitosan can be used for modifying fabrics. Compared with a traditional chemical cross-linking agent modified fabric, the method has the advantages that the grafting efficiency of the oxidized chitosan is high, the enzyme treatment condition is mild, the reaction process is simple, the fabric is crease-resistant, antibacterial, efficient and lasting, the fabric is comfortable to wear, and the requirements of people on lasting functional ecological textiles are met.

The invention relates to a method for preparing a high-performance irradiation cross-linking ultrahigh polyethylene extrusion plate. The method specifically comprises the following steps that: in the presence of a flow modifier, a sensitizer, a nucleating agent and antioxidant auxiliaries, an ultrahigh polyethylene plate is formed through melt extrusion, subjected to cross-linking reaction under high-performance X-ray irradiation and annealed in a vacuum drying oven so as to obtain the ultrahigh molecular weight polyethylene (UHMWPE) plate. The inherent performance stability of the polyethylene plate is ensured, and furthermore, the temperature resistance and mechanical properly of the polyethylene plate are improved.

The invention discloses a processing method of euphausia superba powder with enriched lipid. The processing method comprises the following steps that 1, euphausiacea raw materials are pretreated to obtain an euphausiacea pretreatment material; 2, the euphausiacea pretreatment material is heated to obtain an euphausiacea boiling material A and boiling liquid A; 3, the euphausiacea boiling material A and the boiling liquid A are mixed with the euphausiacea pretreatment material in a stirred mode according to the proportion to obtain a mixed euphausiacea material; 4, the mixed euphausiacea material continues to be heated to obtain an euphausiacea boiling material B and boiling liquid B; 5, the euphausiacea boiling material B and the boiling liquid B are separated; 6, the euphausiacea boiling material B is preliminarily dehydrated to obtain predried euphausiacea powder; 7, the boiling liquid B is concentrated, and concentrated liquor is sprayed back to the predried euphausiacea powder; 8, the predried euphausiacea powder is dried fast to obtain the euphausia superba powder with the enriched lipid. The processing method has the advantages that the output rate of the euphausia superba powder is increased; oxidative degradation of astaxanthin and lipid in the euphausia superba powder is reduced; the content of the lipid in the euphausia superba powder is increased, and quality is improved.

The invention discloses an energy-saving cooling toughening filling master batch and a preparation method thereof. The master batch comprises, by weight, 60 to 80% of heavy calcium carbonate, 6 to 10% of a dispersant, 10 to 20% of a carrier resin, 1 to 5% of a cooling agent, 0.3 to 1% of an anti-oxidant, 1 to 5% of a flexibilizer and 1 to 2% of a coupling agent. The preparation method comprises the following steps: placing the weighed components except the cooling agent into a high-speed mixer for high-speed mixing and discharging an obtained mixture until the components are completely coated; after the mixture is completely cooled, putting the mixture into the high-speed mixer for low-speed mixing, adding the weighed cooling agent and discharging an obtained mixture for subsequent usage after uniform mixing; and putting the mixture into a double screw extruder for extrusion and carrying out granulation and packaging so as to obtain the finished product--the master batch. According to the invention, consumption and cost are reduced, tensile strength of a plastic woven bag is substantially improved, and quality is enhanced.

The invention discloses a waterproof corrosion-resistant antiaging high-flexibility rich mineral paper and a preparation method thereof. The rich mineral paper is composed of the following raw materials in parts by weight: 15-20 parts of synthetic resin, 1-5 parts of EVA / EAA (ethylene-vinyl acetate / ethylene-acrylic acid) copolymer, 55-60 parts of inorganic powder, 5-10 parts of shielding agent, 1-4 parts of preservative, 0.1-1 part of antiaging agent and 1-10 parts of assistant. The preparation method comprises the following steps: weighing raw materials according to the formula proportion, uniformly mixing, sending into an 80-120-DEG C mixer, mixing for 5-15 minutes to activate the materials, mixing by a 100-240-DEG C Banbury mixer for 5-10 minutes, pressing the obtained material into a single screw / double screw extruder through a bi-wrist / bipyramid feeder, carrying out extrusion forming at 130-190 DEG C, cooling, granulating, introducing the master batch into a drying machine, drying until the water content is less than 0.3%, extruding by a 190-230-DEG C DEG C, calendering by a 40-70-DEG C calender, carrying out cooling to form, and trimming to obtain the rich mineral paper finished product. The rich mineral paper has the advantages of water resistance, corrosion resistance, aging resistance, long use period, high / low temperature resistance, simple production technique and very high popularization value.

The invention relates to an edaravone sodium chloride injection liquid and a preparation method thereof. 100 ml of the injection liquid comprises 20-40 mg of edaravone, 0.6-1.0 g of sodium chloride, 100-150 mg of propylene glycol, 2.5-3.5 g of vitamin C, and 0.3-1.0 g of sodium hydrogen carbonate, wherein the pH is adjusted to 3.5-5.0. The preparation process of the injection liquid comprises thesteps: liquid preparation, filtration, filling, capping, sterilization and lamp inspection; liquid preparation adopts a two-step preparation method, and the preparation process adopts low temperaturepreparation. The adopted method is simple to operate and low in cost, and the prepared edaravone sodium chloride injection liquid has good drug stability and fewer side effects, can effectively reducethe generation of impurities, has high patient compliance with medication and safety, can be used for improving neurological symptoms, daily living activities and function disorder caused by acute cerebral infarction, and can effectively prevent and treat brain injury.

The invention discloses a titanium sol modified geogrid, which is composed of the following raw materials in parts by weight: aluminum nitride powder 2-3, polypropylene imine 10-17, tert-butyl acrylate 6-8, Lithium aluminum hydride 0.1‑0.3, 4‑dimethylaminopyridine 0.3‑1, antioxidant 10100.4‑1, multi-walled carbon nanotubes 10‑15, antioxidant 1680.6‑1, high density polyethylene 140‑160, lignin Sodium sulfonate 1‑2, butyl benzyl phthalate 4‑7, dibasic lead phosphite 0.04‑0.1, triethanolamine 1‑2, microcrystalline paraffin 3‑4, silane coupling agent kh5600.6‑1 , Tetrabutyl titanate 3‑4. The combination of antioxidant 1010 and antioxidant 168 added in the present invention can eliminate alkyl free radicals, peroxyl free radicals, alkoxyl free radicals and hydroperoxides, and greatly reduce the freedom to participate in polymer autooxidation chain reactions. The base content can delay the oxidative degradation process of the polymer and improve the oxidation resistance of the finished material.

The invention relates to a production technology of cellulose carbamate fiber filaments, and belongs to the technical field of production of cellulose carbamate fibers. A complete cellulose carbamate fiber filament production process with high completeness is formed through specific cellulose activation, cellulose carbamate preparation, cellulose carbamate solution preparation and spinning steps, a prepared spinning stock solution has good spinnability, and the final product has good performances, so the technology is very suitable for industrial large-scale production, and considers the production cost, the production efficiency and the product quality.

The invention belongs to the technical field of treatment of carbon dioxide in flue gas through an absorption solvent, and discloses a method for capturing carbon dioxide in flue gas of a power plant, which comprises the following steps: firstly, removing mechanical impurities in the flue gas of the power plant in a gravity settling manner, and then enabling the flue gas of the power plant to pass through activated carbon to obtain filtered flue gas; introducing the filtered flue gas into a decarburization absorption tower to be in contact with a semi-lean amine solution to complete removal of carbon dioxide to obtain wet purified gas; and finally, carrying out gas-liquid separation on the wet purified gas, and discharging the gas. The semi-lean amine solution is prepared from deionized water, N-methyldiethanolamine, monoethanolamine, 1-hydroxyethylidene-1,1-diphosphonic acid, etidronate disodium, polyacrylic acid, hydroxyl silicone oil, tetradecyldimethylbenzylammonium chloride and sodium sulfite. The method solves the problems that MEA is used as a trapping solvent in the prior art, the trapping efficiency is about 90%, and the trapping efficiency is low.

The invention provides a making method of smoked flavored fish. The making method comprises the following steps of taking fishes as a raw material, taking the flesh of the fishes and cutting the fleshof the fishes into slices, performing pickling with a smoking solution, performing low-temperature smoking, performing vacuum packaging, and performing curing and sterilization to obtain smoked flavored Spanish mackerel products. The national standard GB1886.127-2016 is used as a reference to screen the high-quality smoking solution, the natural smoking solution is adopted for liquid smoking, antioxidants such as bamboo leaf extract, curcumin, tea polyphenol and rosemary are added into the liquid smoking process, and the functions of removing fishy smell and keeping freshness are achieved. The liquid smoking process adopted by the invention can effectively avoid the generation of carcinogenic substances such as polycyclic aromatic hydrocarbon and heterocyclic amine in traditional smoked aquatic products. The smoked Spanish mackerel product obtained by the method effectively retains the flavor and taste of the traditional smoked Spanish mackerel, and the similarity is up to 90% or above. Besides, the method disclosed by the invention is simple in process and convenient to prepare, the damage to nutritional ingredients of the Spanish mackerel is small, the nutritional value of the Spanish mackerel is effectively reserved, the taste is delicious, the meat quality is fine and smooth and extremely traditional characteristics and high nutrition are achieved.

The invention discloses a geogrid resistant to heat and humidity, which is composed of the following raw materials in parts by weight: zinc dihydrogen phosphate 4-5, phosphite 2-3, dimethyl diallyl chloride Ammonium 0.6‑1, polypropylene imine 10‑17, tert-butyl acrylate 6‑8, lithium aluminum hydride 0.1‑0.3, 4‑dimethylaminopyridine 0.3‑1, antioxidant 10100.4‑1, multi-walled carbon nanotubes 10-15, antioxidant 1680.6-1, high-density polyethylene 140-160, chlorinated paraffin 4-6, titanium dioxide 10-12, butyltin trioctoate 0.4-1, amino trimethylene phosphonic acid 0.1-0.2, di Phenylsilanediol 2‑3, calcium hexafluoroacetylacetonate 0.4‑1. The geogrid of the invention has good resistance to heat and humidity, good impermeability, and is not easy to corrode.

The invention provides a method of separating vanadium and chromium quickly by means of centrifugal extraction and preparing ammonium metavanadate. The method comprises the following steps: (1) mixinga vanadium and chromium-containing lixivium and a primary amine sulfate extraction agent for 3-6 stages of countercurrent centrifugal extraction separation to obtain an upper extracted organic phase;and (2) carrying out reverse extraction on the upper extracted organic phase with ammonia water to obtain white powder, and carrying out post-treatment on the obtained white powder to obtain ammoniummetavanadate. Based on the prior art, by means of an advantage of adopting the primary amine sulfate extraction agent combined with a centrifugal extractor, vanadium and chromium in the lixivium areseparated quickly and efficiently (3.6-7.2 min) by means of 3-6 stages of countercurrent centrifugal extraction; a two-step separation and purification coupling process is carried out by combining reverse extraction, so that the extraction rate of vanadium and the separating factors of vanadium and chromium are improved greatly to obtain high purity ammonium metavanadate compound white powder. Themethod provides a basic technical support for improving the cyclic utilization rate of the extractor and reducing the recycling cost of vanadium and chromium waste residues.

The invention discloses a fiber-modified antioxidant geogrid. The fiber-modified antioxidant geogrid comprises the following raw materials in parts by weight: 0.7 to 1 part of calcium fluoride, 3 to 4 parts of polyurethane, 10 to 17 parts of poly propyleneimine, 6 to 8 parts of tert-Butyl acrylate, 0.1 to 0.3 part of lithium aluminium hydride, 0.3 to 1 part of 4-dimethylamino pyridine, 0.4 to 1 part of an antioxidant 1010, 10 to 15 parts of multiwalled carbon nanotube, 0.6 to 1 part of an antioxidant 1680, 140 to 160 parts of high-density polyethylene, 2 to 3 parts of cellulose propionate, 1 to 2 parts of sodium carboxymethyl cellulose, 0.3 to 1 part of polydimethylsiloxane, 2 to 3 parts of ammonium zirconium hexafluoride, 0.1 to 0.2 part of pyromellitic dianhydride, 1 to 2 parts of tetrahydrofurfuryl alcohol, and 10 to 13 parts of calcined kaolin. According to the fiber-modified antioxidant geogrid, cellulose propionate and sodium carboxymethyl cellulose are added, so that the dispersity of fillers in a polymer can be effectively improved, and as a result, the intensity of a finished product can be improved.

The invention discloses a pressure-resistant and anti-oxidation geogrid, which is composed of the following raw materials in parts by weight: pentaerythritol 2-3, N-methylpyrrolidone 0.7-1, castor oil polyoxyethylene ether 0.1-0.2, Epoxidized soybean oil 4‑6, polypropylene imine 10‑17, tert-butyl acrylate 6‑8, lithium aluminum hydride 0.1‑0.3, 4‑dimethylaminopyridine 0.3‑1, antioxidant 10100.4‑1, multiwall Carbon nanotube 10‑15, antioxidant 1680.6‑1, high density polyethylene 140‑160, polyvinyl butyral 0.8‑1, polyamide wax micropowder 2‑4, silicon nitride 0.1‑0.3, wollastonite powder 10-15, 1,2-dimethylimidazole 0.6-1. The geogrid of the invention has good compression resistance, good weather resistance and long service life.

The invention discloses a casein anti-oxidation geogrid, which is composed of the following raw materials in parts by weight: 0.8-1 acetylated lanolin, 0.6-1 stannous octoate, 10-17 polypropylene imine, and acrylic acid Tert-butyl ester 6‑8, lithium aluminum hydride 0.1‑0.3, 4‑dimethylaminopyridine 0.3‑1, antioxidant 10100.4‑1, high density polyethylene 140‑160, bis-octylmethyl tertiary amine 0.5‑1 , casein 2‑3, N, N‑diethylaniline 0.1‑0.2, zinc cyanurate 0.3‑1, hexafluorobutyl acrylate 4‑6, sodium myristate soap 1‑2, fly ash 10‑14 , multi-walled carbon nanotubes 10-15, antioxidant 1680.6-1, dialkyl hydrodiphenol 0.7-1. Adding casein, acetylated lanolin and the like in the invention can effectively improve the dispersibility of the filler in the polymer and improve the stability and strength of the finished product.

The invention discloses a flame-retardant oxidation-resistant geogrid. The flame-retardant oxidation-resistant geogrid consists of the following raw materials in parts by weight: 1-2 parts of benzyltriphenylphosphonium chloride, 10-17 parts of polypropylenimine, 6-8 parts of tert-butyl acrylate, 0.1-0.3 part of lithium aluminium hydride, 0.3-1 part of 4-dimethylaminopyridine, 0.4-1 part of an antioxidant 1010, 10-15 parts of multi-walled carbon nano tubes, 0.6-1 part of an antioxidant 168, 140-160 parts of high density polyethylene, 2-4 parts of hydrous zinc borate, 5-7 parts of dibutyl maleate, 10-13 parts of fumed silica, 0.2-0.4 part of beta-hydroxyalkylamide, 1-2 parts of polyoxyethylene alkyl ether, 2-3 parts of ammonium polyphosphate, 1-2 parts of aluminium stearate, and 0.3-1 part of stearamide. The benzyltriphenylphosphonium chloride, the hydrous zinc borate and the like is added into the flame-retardant oxidation-resistant geogrid, and therefore, flame-retardant property of a finished product is improved effectively.

The invention discloses a low-VOC and low-migration polypropylene composite material and a preparation method thereof. The low-VOC and low-migration polypropylene composite material is prepared from 45 to 85 parts of polypropylene, 5 to 10 parts of polyethylene, 10 to 45 parts of inorganic filler, 0.05 to 0.1 part of vitamin E-type compound heat stabilizer and 0.05 to 0.1 part of titanium dioxide light stabilizer. The raw materials are mixed, extruded and granulated to be prepared into the low-VOC and low-migration polypropylene composite material. According to the low-VOC and low-migration polypropylene composite material disclosed by the invention, the green and environment-friendly aids of the vitamin E-type compound thermal stabilizer and the titanium dioxide light stabilizer are utilized to modify the polypropylene, and have small adding amount, good compatibility with a base material and no precipitation; thus, the prepared composite material has the characteristics of low VOC, low migration and the like, and can be applied to automotive trim materials of instrument boards, door boards, stand columns and the like of automobiles.

The invention provides a preparation method of a waxberry fruit wine, which has the advantages of accessible raw materials and simple operation, and is suitable for industrial production. The preparation method comprises the following steps of: (1) cleaning waxberries, and airing; (2) removing pits and juicing the aired waxberries to obtain waxberry juice, filtering for the first time through an ultrafiltration device, and sterilizing; (3) mixing the waxberry juice obtained in the step (2) with white sugar and grape yeast, and performing sealed fermentation at 20-25 DEG C for 75-90 days to obtain new waxberry wine; and (4) filtering and clarifying the new waxberry wine obtained in the step (3), and sequentially carrying out low-temperature aging, filling and sterilization on the filtrate to obtain the waxberry fruit wine. Cleaning water adopted in the method is deionized water for reducing dissolved oxygen in water through nitrogen purging, and oxidation of anthocyanin can be effectively reduced. The adopted clarifying agent is chitosan-bentonite, the clarifying time is short, and the effect is remarkable. After clarification, in order to improve the quality of the waxberry wine, acinnamic acid-D-sodium erythorbate composite additive is added for color protection. The waxberry wine prepared by the method is bright and clear in color, fine and mellow in taste, high in anthocyanin content and rich in nutritional value.

The invention discloses an antistatic high-cleanliness latex glove and a preparation method thereof. The anti-static waterproof coating is prepared from the following raw materials in parts by weight: 50 to 100 parts of latex, 20 to 40 parts of butyronitrile, 20 to 40 parts of polyvinyl chloride, 10 to 20 parts of sulfur, 10 to 20 parts of a conductive outer layer, 30 to 60 parts of a leather material, 10 to 20 parts of an anti-static PC (Polycarbonate) board, 20 to 40 parts of carbon black, 20 to 40 parts of mica powder, 5 to 10 parts of a de-foaming agent, 10 to 20 parts of wool fat, 10 to 20 parts of an accelerant, 10 to 20 parts of an anti-aging agent and 5 to 10 parts of a thickening agent. The preparation method comprises the following steps: S1, firstly, adding latex, butyronitrile, polyvinyl chloride, sulfur and a leather material into a stirrer, stirring and mixing according to fixed time, obtaining a first mixture after mixing is finished, meanwhile, putting the first mixture into a standing box, standing, and mixing, so as to obtain a second mixture; the antistatic high-cleanliness latex glove is good in antistatic capacity, long in service life, convenient to produce and convenient to popularize and use.

The invention discloses a preparation method of oriental cherry powder with activity of inhibiting generation of AGE. The method comprises low-temperature processes of cleaning, countercurrent extraction, filtration, concentration, sterilization, freeze drying, sieving and the like. Countercurrent extraction and low-temperature membrane treatment are combined for extraction of oriental cherry, and a low-temperature process is adopted in the whole process and totally-closed intensive continuous production is adopted. According to the method, the contents of total flavonoids, caffeoyl glucose (1-O-caffeoyl-beta-D-glucopyranoside) and quercetin glucoside (quercetin-3-O-beta-D-glucopyranoside) contained in the oriental cherry are fully reserved, separated and enriched, active ingredients are fully extracted, the transfer rate is high, the yield of the active ingredients of the prepared oriental cherry powder is high, and the prepared oriental cherry powder is suitable for industrial production. A green membrane material is adopted, the safety is high, and active ingredients are effectively enriched, so that the prepared oriental cherry powder has a remarkable effect of inhibiting the generation activity of AGEs, the generation inhibition rate of AGEs reaches 58% (when the concentration is 100 micrograms per milliliter), and IC50 reaches 67 micrograms per milliliter.