5315 results about "Amide" patented technology

The invention discloses a high-bonding-strength flame-retardant composite current collector base film and a preparation method thereof. The high-bonding-strength flame-retardant composite current collector base film is prepared from the following raw materials in parts by weight: 100 parts of PP resin, 1.5 parts of a lubricant, 0.8 part of an antioxidant and 16 parts of reinforced flame-retardant composite particles, the reinforced flame-retardant composite particles are prepared by the following steps: S1, preparing amidated porous carbon microspheres; s2, compounding the amidated porous carbon microspheres with mica powder to prepare a composite carrier; s3, loading a flame retardant to prepare a flame-retardant compound; s4, in-situ grafting of maleic anhydride grafted polypropylene is carried out, and the reinforced flame-retardant composite particles are obtained. By adding the reinforced flame-retardant composite particles into the PP resin, the flame retardance and mechanical strength of the PP-based composite current collector base film and the interface bonding force between the PP base film and the metal conductive layer can be comprehensively improved.

The invention belongs to the technical field of pharmaceutical chemical processes, and particularly relates to a preparation method of a penem antibiotic intermediate 4-BMA, which comprises the following steps: adding Zn powder, chlorosilane, aliphatic tertiary amine, zinc salt and 4-AA in a formula (I) into THF (tetrahydrofuran), uniformly stirring, dropwise adding a THF solution of alpha-haloamide with an induction group in a formula (II) for reaction, filtering the reaction solution, removing the zinc powder, and drying to obtain the penem antibiotic intermediate 4-BMA. Extracting the filtrate to obtain a THF phase, washing with an aqueous solution of potassium oxalate, and recovering THF to obtain a formula (III); and carrying out oxidative hydrolysis, sulfur dioxide quenching, sulfur dioxide acid regulation crystallization and recrystallization on the formula (III) to obtain the intermediate 4-BMA. According to the preparation method disclosed by the invention, a zinc salt is used as a catalyst during preparation of the formula (III), potassium oxalate is used for removing residual Zn (II) in a THF phase, SO2 is used for quenching hydrogen peroxide and acid regulation and crystallization of 4-BMA, the oxygenolysis problem of 4-BMA is solved, and the preparation method has the characteristics of greenness, safety and high efficiency, is strong in product competitive advantage and is suitable for industrial production.

The invention belongs to the field of skin care products, and particularly relates to an anti-wrinkle and anti-aging composition as well as a preparation method and application thereof, and the anti-wrinkle and anti-aging composition comprises neurotransmitter inhibition peptide, signal peptide, madecassoside, inositol and glycosylglycerol. The neurotransmitter inhibition type peptide is at least three of acetyl hexapeptide-8, arginine / lysine polypeptide, dipeptide diaminobutyrylbenzylamide diacetate and acetyl octapeptide-3, and the signal type peptide is at least two of palmitoyl pentapeptide-4, decapeptide-4 and acetyl tetrapeptide-9. Compared with the prior art, all the components of the anti-wrinkle and anti-aging composition act on different anti-aging pathways and can be matched with one another from multiple aspects of oxidation resistance, inflammation resistance, moisturizing, cell viability enhancement, wrinkle reduction and the like, a more comprehensive and better anti-aging effect is provided, skin aging is comprehensively resisted, the skin is in a more young state, and the anti-wrinkle and anti-aging composition has the advantages that the anti-wrinkle and anti-aging effects are achieved. And the anti-wrinkle and anti-aging composition is small in irritation and good in stability.

The invention discloses a full D-type antibacterial peptide with high enzymolysis stability and broad-spectrum antibacterial activity and application thereof. The antibacterial peptide is obtained by sequentially and repeatedly arranging D-type tryptophan, D-type arginine and D-type lysine for four times and carrying out C-terminal amidation; the amino acid sequence of the gene is (D-Trp)-(D-Arg)-(D-Lys)-(D-Trp)-(D-Arg)-(D-Lys)-(D-Trp)-(D-Arg)-(D-Lys)-(D-Trp)-(D-Arg)-(D-Lys)-(D-Trp)-(D-Arg)-(D-Lys)-NH2, and is marked as DWRK-12. The antibacterial peptide shows broad-spectrum antibacterial activity and excellent stability, can effectively resist clinically separated multidrug resistant strains, and keeps high cell selectivity at the same time. Due to the characteristics, the antibacterial peptide has important application value in the aspect of developing novel antibacterial drugs, especially in the field of treatment of infection of multiple drug-resistant bacteria.

Provided is a polyamide resin, which is a copolymer of a biodegradable polyamide, such as polyamide 2 to polyamide 4, and another polyamide, the polyamide resin having enhanced biodegradability. The polyamide resin contains a structural unit represented by Formula (1) and another polyamide structural unit, and a difference between a degree of randomness determined based on a proportion of each structural unit as determined by 1H-NMR measurement when structural units are assumed to have an ideal random sequence and a degree of randomness determined based on a proportion of carbonyl carbon of an amide group linking different structural units with respect to a total peak integrated value for carbonyl carbon as determined by 13C-NMR measurement is 0.10 or less, where in Formula (1), x is an integer of 1 or greater and 3 or less.

In order to solve the problems of poor high-temperature and low-temperature cycle performance and poor safety performance of a lithium ion battery in the prior art, the invention provides a lithium ion battery, which comprises a positive electrode, a negative electrode, a diaphragm and an electrolyte, the positive electrode comprises a positive electrode active material layer, the positive electrode active material layer comprises a positive electrode active material and an oxide solid electrolyte, the surface of at least one side of the diaphragm is coated with an oxide solid electrolyte coating, the electrolyte comprises a first additive and a second additive, the first additive comprises a fluorosulfonyl amide compound, and the second additive comprises mannitol carbonate sulfate; the lithium ion battery meets the following relational expressions: (H + X) / P is more than or equal to 0.8 and less than or equal to 8; formula 2: 0.75 < = (A + B) / (H + X) < = 20; formula 3: 0.16 < = H / X < = 6.43; formula 4: 1.25 < = A / B < = 36.

Stable and bioavailable formulations and dosage forms comprising a dispersion (e.g., spray-dried dispersion) of solid amorphous 6-(cyclopropancamido)-4-((2-methoxy-3-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)amino)-N-(methyl-d3)pyridazine-3-carboxamide (Formula (I): BMS-986165) in a solid polymer matrix are provided for the treatment of auto-immune and auto-inflammatory diseases such as an inflammatory bowel disease (IBD) and psoriasis.

The lithium secondary battery comprises a positive electrode, a negative electrode, a diaphragm and a polymer electrolyte, the polymer electrolyte contains the flame-retardant microcapsule, the flame-retardant microcapsule has a core-shell structure, a copolymer material containing one or more of an amide group, an ester group and an ether group is taken as a shell layer, and a flame retardant is taken as a core; the rupture collapse temperature of the flame-retardant microcapsule shell material is 60-120 DEG C, the melting point of the flame retardant is 20-120 DEG C, and the rupture collapse temperature of the copolymer material is higher than the melting point of the flame retardant. The lithium secondary battery disclosed by the invention has excellent flame retardance, the flame-retardant microcapsule added in the lithium secondary battery can be broken and collapsed when the battery is in thermal runaway, and the flame retardant is quickly released, so that the thermal runaway is actively defended in advance from the interior of the battery, and the electrochemical performance of the battery is not reduced.

The invention discloses an omariglitazone intermediate as well as a synthesis method and application thereof, and belongs to the technical field of pharmaceutical chemistry synthesis. The invention provides a synthesis method of an omarigliflozin intermediate and application of the intermediate in synthesis of omarigliflozin. The key of the synthesis method provided by the invention lies in the deprotection process of polycyclic indole amide, nitrile groups are not hydrolyzed, indole carboxylic acid is generated with high selectivity, molecular lactamization is avoided in the condensation process with polycyclic imine B, and expensive amidation reagents such as HATU are not needed in the process, so that the synthesis method is simple and easy to implement. And the purpose of preparing omariglitazone with low cost and high yield is achieved. The synthesis method has the advantages of easily available raw materials, mild reaction conditions, small side reaction influence, simplicity and convenience in operation and high yield, improves the yield, is easy to purify, and is suitable for industrial production of omariglitazone.

The invention relates to the field of fine chemical engineering, and discloses a green process for preparing chloramine T by a continuous flow reactor. The method comprises the following steps: respectively pumping p-toluenesulfonamide, a sodium hydroxide solution and a sodium hypochlorite solution into a micro-channel mixer for instantaneous mixing, and carrying out chlorination reaction in a multi-stage temperature control tubular reaction unit; the concentration of free chlorine is detected on line at an outlet, and the flow rate of a chlorine source is dynamically adjusted through a PID algorithm, so that closed-loop control is realized; the reaction liquid is directly crystallized and separated to obtain the product without alkali wash. The system comprises a base solution and chlorine source conveying subsystem, a micro-channel mixer, a multi-stage reaction unit, an online monitoring module, a central controller and a crystallization unit. The side reaction is inhibited from the source, so that the free chlorine is less than or equal to 0.5 mg / L, the alkali washing step is omitted, the COD (Chemical Oxygen Demand) of the wastewater is reduced by more than 80%, the product purity is more than or equal to 99.5%, and the productivity is improved by 3 times.

The invention discloses a preparation method of 5-hydroxy-3-iminopyridine-2, 6-diketone, and relates to the technical field of compound preparation. The invention provides a preparation method of 5-hydroxy-3-iminopyridine-2, 6-diketone, which comprises the following steps: uniformly mixing observation blue with at least one oxidant of sodium hypochlorite, potassium permanganate and hydrogen peroxide according to a molar ratio of 1: (0.5-1.5) under a solution condition, reacting for 5-120 minutes, and adding a reducing agent to finish the reaction, thereby obtaining a target product. According to the preparation method provided by the invention, on the basis of the amide structure of the ornamental blue, 'endogenous catalysis' of the reaction can be realized, no additional catalyst needs to be introduced, and the 5-hydroxy-3-iminopyridine-2, 6-diketone with the yield of more than 60.53% and the purity of more than 60.2% can be prepared through a simple and convenient one-step reaction.

The invention provides a battery and an electric device. A positive plate comprises a positive active material, and the positive active material is doped and / or coated with a lanthanum element; the surface of the diaphragm is coated with a ceramic coating; the electrolyte comprises a first solvent, a second solvent, a first additive and a second additive; the first solvent comprises a cyclic carbonate compound, the second solvent comprises a chain fluorosulfonamide compound, the first additive comprises mannitol carbonate sulfate, and the second additive comprises succinonitrile; the lanthanum element is doped / coated on the positive active material, so that the release of lattice oxygen at high voltage or high temperature can be effectively inhibited, and the exothermic reaction activity at the thermal runaway initial temperature is reduced; the first additive and the second additive in the electrolyte respectively form a compact CEI film and an SEI film with high thermal stability on the surfaces of the positive electrode and the negative electrode; the diaphragm ceramic coating provides a physical barrier, the thermal shrinkage temperature of the diaphragm is increased, and internal short circuit is prevented.

The invention discloses a composition for improving the stability of oleuropein in a solution as well as a preparation method and application of the composition. The composition comprises oleuropein and at least one stabilizer, and the stabilizer is selected from the group consisting of anisic acid, lactobionic acid, glycyrrhizic acid, 3, 3-thiodipropionic acid, N-acetyl-L-glutamine, propyl-cysteine and lauramidopropyl betaine; and the pH value of the aqueous solution of the composition is 4.0-8.0. The preparation method comprises the following steps: dissolving oleuropein in water, adding the stabilizer, and uniformly mixing. Through simple physical mixing, by utilizing the synergistic effect of the specific stabilizer and the oleuropein, the degradation and discoloration of the oleuropein in the storage process are remarkably inhibited. Experiments show that after the preferable composition is preserved for 30 days in an open manner, the retention rate of the oleuropein still reaches up to 80% or above, and is far superior to that of blank control and a traditional liposome wrapping method. The composition is simple and convenient in preparation process and low in cost, and provides reliable technical support for wide application of oleuropein in liquid products such as food, medicine and cosmetics.

The invention discloses an amino acid-amide-saccharide composite leaching agent and application thereof, and belongs to the technical field of industrial solid waste recycling and carbon dioxide capture and utilization, the composite leaching agent is formed by compounding a main leaching agent amino acid, an auxiliary leaching agent amide compound and an auxiliary chelating agent saccharide or a derivative thereof. According to the method, through the synergistic effect of the amino acid, the amide and the saccharide chelating agent, the calcium ions in the calcium-containing solid waste can be efficiently and highly selectively leached under the mild condition without additional acid. According to the composite system, through multiple coordination and spatial screening effects, the leaching selectivity of calcium ions can reach 99.5% or above, and dissolution of impurities is effectively inhibited; the zwitterionic characteristics of amino acid and the coordination of amide are utilized to realize proton self-sufficiency in the system and simplify the process; all the components have good biocompatibility and are green and environment-friendly; the composite system can also be used as a crystal modifier to induce high-purity calcium carbonate.

The invention relates to the technical field of polypropylene compositions and modified polymer materials thereof, and discloses a high-performance polypropylene-based green energy-saving cable insulation layer composition which comprises an isotactic polypropylene matrix, a maleic anhydride grafted polyolefin elastomer distributed in a dispersed phase and an amide nucleating agent distributed on a non-polar phase interface, an anchoring structure is constructed on a phase interface through hydrogen bond interaction, a matrix molecular chain is induced to grow to form a radial needle-shaped crystal cluster penetrating through the phase interface, and a three-dimensional interpenetrating crystal bridging network is constructed. Through the crystal bridging network, interface deep traps are converted into continuous shallow trap diversion channels, charges are guided to migrate orderly, space charge accumulation is inhibited, and the three-dimensional interpenetrating crystal bridging network is constructed. And the steric effect generated by the interface anchoring structure cooperatively restrains the thermal expansion of the dispersed phase, so that the high-temperature dimensional stability and dielectric property of the material are improved.

The invention discloses a method and a device for removing alcamines in NMP (N-Methyl Pyrrolidone), which comprises the following steps: reacting anhydride substances with NMP containing the alcamines substances to generate NMP containing amide substances; the NMP solution containing the amide substances is rectified to remove the amide substances, and NMP with the alcohol amine substances removed is obtained; the boiling point of the product is increased in a manner that anhydride substances react with alcohol amine substances in NMP to generate amide, so that the difference value between the reacted product and the boiling point of NMP is greater than the difference value between the alcohol amine substances and the boiling point of NMP, high-purity NMP is more easily separated in a subsequent rectifying tower, the energy consumption of the rectifying tower for separating the product and impurities can be reduced, and the production cost is reduced. In addition, due to the fact that different alcohol amine additives do not need to be added additionally, universality is improved, meanwhile, the anhydride reaction belongs to amidation reaction, reaction products are more stable, free amine cannot be decomposed in the high-temperature heating process, and therefore the purity of the separated NMP can be further improved.

The invention belongs to the technical field of antibacterial peptides, and particularly relates to an antibacterial peptide Mh-GC21 as well as a precursor and application thereof. The amino acid sequence of the antibacterial peptide Mh-GC21 provided by the invention is as shown in SEQ ID NO.1, and two cysteines are oxidized to form a pair of intermolecular disulfide bonds; the C tail end of the antibacterial peptide Mh-GC21 is subjected to amidation modification. The antibacterial peptide Mh-GC21 provided by the invention is from microhyla microcarpa, has broad-spectrum antibacterial activity, has relatively good antibacterial and bactericidal effects on standard strains of acinetobacter baumannii, escherichia coli and staphylococcus aureus and clinically sourced drug-resistant strains, and can be used for targeted destruction of cell membranes of bacteria, removal of biological membranes and inhibition of formation of the biological membranes. Moreover, the antibacterial peptide Mh-GC21 has the advantages of good stability, no hemolytic activity and cytotoxicity, and difficulty in inducing strains to generate drug resistance.

The invention discloses high-purity oxamide with concentrated particle size and spherical morphology, a preparation method of the high-purity oxamide and application of the high-purity oxamide in preparation of a slow-release fertilizer, and belongs to the technical field of oxamide synthesis and application. The method comprises the following steps: mixing an ammonia-alcohol solution and an alcohol ester solution, conveying the mixed solution into a series tubular reactor for reaction, and then conveying the mixed solution into a parallel tubular reactor for reaction after pressure stabilization and flow equalization to obtain a reaction solution containing oxamide; performing flash evaporation on the reaction liquid to obtain flash evaporation liquid and flash evaporation gas, and performing solid-liquid separation on the flash evaporation liquid to obtain solid oxamide and filtrate; and drying the solid oxamide to obtain the oxamide. The method realizes high conversion rate and high purity, and the product has ultrafine particle size distribution. The purity of the prepared oxamide is greater than or equal to 99%, the D50 particle size is concentrated to 50 + / -15 microns, the spherical morphology is uniform, the release is stable, and the oxamide has a very good effect in preparation of long-acting slow-release fertilizers and combustion inhibitors and research on the nitrogen utilization rate.

The invention discloses a silane-crosslinked low-smoke halogen-free flame-retardant oil-resistant polyolefin cable material and a preparation method thereof. The method comprises the following steps: preparing a bio-based polyesteramide toughening phase which is pre-polymerized by castor oil-based polyamide and poly (butylene adipate-co-terephthalate) and is terminated by itaconic anhydride; the preparation method comprises the following steps: self-assembling phytic acid and melamine to wrap ammonium polyphosphate, so as to prepare supramolecular flame-retardant gel powder; the method comprises the following steps: grafting aramid pulp fibers by using a phosphorus-containing silane coupling agent to prepare a reactive liquid crystal reinforced phase; the preparation method comprises the following steps: blending and banburying the components with a hydrogenated styrene-isoprene-styrene block copolymer, an antioxidant and a peroxide cross-linking agent, carrying out dynamic vulcanization and interface bonding, and carrying out extrusion and electron beam irradiation to finally crosslink. An interpenetrating-topology network structure is formed in the prepared cable material, the crosslinking degree is larger than or equal to 82%, and the cable material is rapid in crosslinking, excellent in oil resistance, low in smoke and free of toxicity and is particularly suitable for super high-rise building hanging cables, deep sea exploration cables and new energy automobile liquid cooling cables.

Provided herein are compositions and methods for treating patients with Usher syndrome associated retinitis pigmentosa (UARP) comprising identifying that the subject has UARP and administering to the animal or human an effective amount of an N-acetylcysteine amide (NACA) sufficient to protect vision and inhibit degradation of Ellipsoid Zone (EZ) area and retinal sensitivity. In one example, the NACA formulation is doses at 50, 100, 200, 201, 210, 225, 250, 275, 300, 350, 400, 450, 500, 600, 700, 750, 800, 900, or 1,000 mg / day.

The invention belongs to the field of novel polyamide composite fiber materials, and particularly discloses a high-toughness polyamide fiber composite material and a preparation method thereof. The composite material is prepared from the following raw materials in parts by weight: 55-75 parts of long-chain polyamide PA610 resin, 10-25 parts of ultra-high molecular weight polyethylene fiber, 8-18 parts of polyether block amide elastomer, 1.5-4 parts of a compound nucleating agent, 0.8-2 parts of a titanate coupling agent and 0.3-1 part of a composite antioxidant. The preparation method is characterized by comprising the following steps: firstly, carrying out surface pretreatment on the ultra-high molecular weight polyethylene fiber by adopting a low-temperature plasma technology so as to improve the interfacial compatibility of the ultra-high molecular weight polyethylene fiber and a resin matrix; and then carrying out melt blending granulation on the pretreated fiber and other raw materials through a twin-screw extruder, wherein the fiber is added from a side feeding port to avoid excessive shearing and breaking. The obtained product has ultrahigh impact toughness, excellent rigidity, excellent low-temperature toughness and heat resistance, and is especially suitable for the fields of manufacturing automobile parts, sports protection equipment and the like with extremely high requirements on toughness and durability.

The invention relates to the technical field of microelectronics, in particular to a unimolecular memristor based on a viologen derivative and a preparation method of the unimolecular memristor. The unimolecular memristor based on the viologen derivative comprises an electrode pair and an organic functional molecule, and the organic functional molecule is selected from the viologen derivative and assembled between the electrode pair through an amide condensation reaction. According to the organic functional molecule provided by the invention, functional modification is performed on the basis of a viologen molecular structure, so that an energy barrier of reversible oxidation-reduction reaction of a viologen unit is effectively reduced, and the performance of the single-molecule memristor is remarkably improved; meanwhile, the on-off ratio of the device is also improved by one order of magnitude. According to the preparation method provided by the invention, the stability and repeatability of a monomolecular device can be ensured, and the conductive stability and durability of the molecular junction of the organic functional molecule are effectively improved. The method is simple and convenient to operate, reaction conditions are easy to control, and large-scale production of molecular devices is facilitated.

The invention provides a method for constructing an axial halogen coordination iron-based catalyst and application of the axial halogen coordination iron-based catalyst, and belongs to the technical field of catalytic materials and environmental pollution control. The preparation method comprises the following steps: introducing amino to the surface of a multi-walled carbon nanotube to obtain a modified multi-walled carbon nanotube; iron tetracarboxyl phthalocyanine and the modified multi-walled carbon nanotubes are subjected to covalent grafting through an amidation reaction, and a precursor is obtained; mixing the precursor with a halogen-containing solid source and a nitrogen source, and carrying out temperature programming and segmented pyrolysis in an inert gas atmosphere to obtain a pyrolysis product; and carrying out acid pickling on the pyrolysis product. The core of the preparation method disclosed by the invention lies in a multi-step collaborative strategy of molecular isolation, interface bridging, gas phase migration, fixed-point capture and coordination regulation, so that ultrahigh monatomic dispersity is realized, and unification of high density and high dispersity is ensured; meanwhile, the electronic structure of the iron center is effectively optimized, and excellent intrinsic activity is shown.

The invention discloses a polyamide acid-resistant nanofiltration membrane and arsenic removal application thereof in hair dye preparation. According to the amide acid-resistant nanofiltration membrane, a polyamine monomer and trimesoyl chloride are subjected to an interface reaction on an ultrafiltration supporting bottom membrane, and the polyamide acid-resistant nanofiltration membrane containing the Telogen structure is obtained. According to the method for removing the arsenic in the hydroxyethyl diphosphoric acid, a polyamide acid-resistant nanofiltration membrane containing a Troger structure is adopted for at least one time of filtration treatment, the concentration of arsenate in the hydroxyethyl diphosphoric acid after secondary filtration treatment is reduced to 4.60 mg / kg from 480.02 mg / kg, and the arsenic content of the hair dye prepared from the hydroxyethyl diphosphoric acid is smaller than 0.07 mg / kg. According to the polyamide acid-resistant nanofiltration membrane containing the Troger structure, which is obtained by adopting a limited preparation method, the acid resistance is greatly improved, the separation selectivity is higher, arsenic in hydroxyethyl diphosphate can be effectively removed, and the arsenic content in a hair dye is greatly reduced.

Compounds of formula I (Formula I),where the substituents R1 through R5 are defined herein, and agrochemically acceptable salts, stereoisomers, enantiomers, tautomers and N-oxides of the compounds of Formula (I). In addition, methods and uses of compounds of Formula I as, for example, insecticides. Compositions having compounds of Formula (I) and their uses in controlling insects, particularly in crops of useful plants. Methods and intermediates related to the synthesis of compounds of Formula (I).

The invention belongs to the technical field of sulfonamide synthesis, and particularly relates to a green and environment-friendly sulfonamide amidation preparation method. Comprising the following steps: adding chlorosulfonic acid into a reactor, stirring, heating, adding o-nitrochlorobenzene, carrying out staged heat preservation, cooling, and adding thionyl chloride to obtain 2-nitro-4-chlorine sulfonate-chlorobenzene; the method comprises the following steps: separating and filtering 2-nitro-4-chlorine sulfonate-chlorobenzene, adding ammonia water, stirring, preserving heat, and carrying out filter pressing to obtain 2-nitro-4-amine sulfonate-chlorobenzene; the preparation method comprises the following steps: adding liquid caustic soda into 2-nitro-4-amine sulfonate-chlorobenzene, stirring, heating, and adjusting the pH value to obtain 2-nitro-4-amine sulfonate-phenol; the method comprises the following steps: adding water, a catalyst and hydrazine hydrate into 2-nitro-4-amine sulfonate-phenol, heating, stirring, and carrying out filter pressing to obtain 4-sulfonamide-2-amino-phenol. According to the preparation method of sulfonamide, generated tail gas is subjected to falling film absorption treatment, and the product prepared by the preparation method is high in purity.

The invention relates to the technical field of feed processing, and discloses a lactating sow feed containing fermentation raw materials and a preparation method of the lactating sow feed. A three-layer microcapsule coating auxiliary material is prepared by taking a vitamin premix, an amino acid compound, a compound enzyme preparation and a probiotic agent as core materials through three-layer coating; the basic raw materials comprise corn, wheat, bran, a fermentation raw material, a mineral premix and grease, auxiliary material coating and basic raw material treatment are carried out in parallel in double lines during preparation, and finally, mixing granulation is carried out; the grafted copolymer formed by the amidation reaction of the sodium carboxymethyl cellulose and the chitosan oligosaccharide can cooperate with the sodium alginate to prevent the damage under acidic conditions, and the survival rate of viable bacteria is kept at 85-87% after treatment is carried out for 2 hours under the acidic condition with the pH value of 2.0-3.0; compared with a traditional fermentation raw material coating scheme, the dosage of coating raw materials is reduced by 70% or above; meanwhile, the vitamin premix and the amino acid compound in the auxiliary material can reduce the diarrhea rate by 6% and increase the lactation yield of the sow by 7-18%.

The invention belongs to the technical field of building materials, and particularly relates to fly ash concrete as well as a preparation method and application thereof. The invention provides fly ash concrete. Raw materials of the fly ash concrete comprise an in-situ polymerization material and a cementing material, the cementing material comprises the following components in parts by weight: 50-80 parts of fly ash and 20-50 parts of cement; the raw materials of the in-situ polymerization material comprise a monomer, an initiator, a cross-linking agent and an accelerator, the monomer includes an amide group and an alkali metal ion.

The invention provides a polyethylene glycol derivative-collagen cartilage repair gel which is characterized by being prepared from the following components in parts by weight: 8 to 12 parts of collagen (namely COL) solution, 0.5 to 2 parts of polydeoxyribonucleotide (namely PDRN), 4 to 8 parts of polyethylene glycol disuccinimide succinate (namely SS-PEG-SS) solution and 0.1 to 0.4 part of tannic acid (namely TA), and particularly discloses a preparation method and application of the polyethylene glycol derivative-collagen cartilage repair gel. In a word, the composite gel and the collagen are subjected to efficient amidation reaction through SS-PEG-SS to form a stable three-dimensional network, so that the structural support of the type I collagen, the tissue repair of PDRN and the anti-inflammatory and anti-oxidation characteristics of tannic acid are successfully integrated; therefore, the composite material has the comprehensive performance of good structural stability, high mechanical strength, good biocompatibility, controllable degradation period, excellent needle passing performance and the like, and shows the wide application prospects of clear repair effect, remarkable component synergistic effect, mature production process, outstanding cost effectiveness and the like.

The invention discloses a method for extracting ginsenoside based on a supercritical extraction method, and relates to the technical field of traditional Chinese medicine extraction. The ginsenoside is extracted through a supercritical extraction method, the extraction process is convenient and efficient, the purity of the ginsenoside is high, organic solvent residues are avoided, the method is green and environmentally friendly, carbon dioxide can be recycled, and the operation cost is low; through degreasing pretreatment, fat-soluble components in ginseng powder are removed, the extraction purity of saponin is increased, the solid loading capacity of supercritical extraction is reduced, the mass transfer resistance is reduced, and the extraction efficiency is improved; the ginsenoside is purified in a post-treatment mode of resin adsorption and elution, polar impurities can be further removed, glutamine is adopted for surface functionalization of the resin, acylamino and carboxyl are introduced to the surface of the resin and can form hydrogen bonds with phenolic hydroxyl groups in the ginsenoside, functional adsorption is achieved, meanwhile, impurities are removed, and the content of the ginsenoside is increased. Reaction conditions are simple and mild, and adsorption efficiency is high.