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50results about How to "High industrial production value" patented technology

Honeycomb-shaped wet-method black-silicon texturing structure and preparing method thereof and black-silicon cell and preparing method thereof

The invention provides a honeycomb-shaped wet-method black-silicon texturing structure and a preparing method thereof and a black-silicon cell and a preparing method thereof, and relates to the technical field of black-silicon cell preparing. The preparing method of the honeycomb-shaped wet-method black-silicon texturing structure includes the steps that a diamond-wire polycrystalline silicon slice is subjected to hole digging operation through a wet-method black-silicon-tank hole digging device; products after hole digging operation is completed are subjected to hole expanding operation through a RENA chain-type device, NH3.H2O and H2O2 are added into alkaline wash liquid in an alkaline wash tank of the RENA chain-type device, and H2O2 is added into acid wash liquid of an acid wash tank.The ideal honeycomb-shaped wet-method black-silicon texturing structure with the excellent quality can be prepared, existing polycrystal production devices are fully used, and the device procurement / improvement costs are effectively reduced. The black-silicon cell prepared with the method is good in appearance performance and excellent in electric performance and has the large market popularization value.
Owner:江西瑞安新能源有限公司

Method for reducing and/or removing default peptide in solid phase synthesis of polypeptide

The invention relates to the field of polypeptide synthesis and particularly relates to a method for reducing and / or removing a default peptide in solid phase synthesis of a polypeptide. The method adopts an all-protected peptide fragment comprising a default amino acid and an amino acid (C-N) in front of default amino acid in the solid phase synthesis of the polypeptide, the problems of default of the amino acid caused by incomplete removal of Fmoc and incomplete condensation reaction are solved at the same time, and the impurity of the default peptide is reduced to lower than the qualification threshold in the synthesis stage. For the specific performance, the Ala2 default impurity and the Thr5 default impurity in liraglutide are respectively reduced from more than 1% to the nesiritide amount and lower than 0.15%, and the Ser19 default peptide impurity in nesiritide is reduced to the undetectable amount.
Owner:HYBIO PHARMA

Preparation method of aluminum hydroxide surface modified expansible graphite flame retardant and method for preparing flame-retardant polyurethane foam plastic by using the same

The invention discloses a preparation method of an aluminum hydroxide surface modified expansible graphite flame retardant and a method for preparing flame-retardant polyurethane foam plastic by using the same, belongs to the field of flame-retardant materials, and particularly relates to a preparation method of a modified expansible graphite flame retardant and a method for preparing flame-retardant polyurethane foam plastic by using the modified expansible graphite flame retardant. The invention aims to solve the problems that the existing aluminum hydroxide flame retardants are more uniformly dispersed in polyurethane foam, and the mechanical property of the existing polyurethane foam plastic is poorer. According to the preparation method, sodium hydroxide, aluminum hydroxide and expandable graphite are used as raw materials, and a hydrothermal method is adopted. The method for preparing the flame-retardant polyurethane foam plastic comprises the following steps: 1, weighing; 2, mixing; and 3, curing. The method has the advantages that the limit oxygen index can be increased to 28.5%; the compression strength is improved to 0.162 MPa, and the percentage of closed area is improved. The methods are mainly used for preparing the aluminum hydroxide surface modified expandable graphite flame retardant and flame-retardant polyurethane foam plastic.
Owner:HARBIN ENG UNIV

Multi-stage sewage treatment device and sewage purification system

The invention provides a multistage sewage treatment device and a sewage purification system and relates to the field of sewage purification. The multistage sewage treatment device comprises a device body, an oxygen supply device, a dissolved oxygen measurement device and a control system, wherein a sewage inlet and a purified water outlet is arranged on the device body; the device body further includes a settling section, a swirling oil-gas separation section, a large particulate matter filtration section, and a fine-particle filtration section which are sequentially arranged from top to bottom; the sewage inlet is arranged on the settling section and the purified water outlet is arranged on the fine-particle filtration section; the oxygen supply device is connected to the swirling oil-gas separation section through an oxygen supply pipe; the dissolved oxygen measurement device comprises a dissolved oxygen electrode which is arranged in the swirling oil-gas separation section and a dissolved oxygen meter which is electrically connected with the dissolved oxygen electrode and is arranged outside the device body; the dissolved oxygen meter and the oxygen supply device are electrically connected to the control system. The multi-stage sewage treatment device has the advantages that usage is simple, automation degree is high, sewage treatment effect is good, industrial production value is greater.
Owner:YANCHENG INST OF TECH

Chiral purification method of compound C

The invention provides a chiral purification method of a compound C. The compound C is a crude product (S,S)-8-benzyl-2,8-diazabicyclo[4.3.0]nonane with chiral purity ee of 90%-98%. The chiral purification method comprises the following steps: forming haloid salt from the compound C, and further crystallizing and purifying the compound C haloid salt to obtain a high-purity refined product haloid;carrying out alkali treatment and toluene extraction on the refined high-purity haloid acid salt to obtain the high-chiral-purity (S,S)-8-benzyl-2,8-diazabicyclo[4.3.0]nonane. According to the process, a relatively expensive optical resolving agent is prevented from being used for secondary resolution, and the whole process is simple to operate due to the fact that the refined product is insolublein water and an organic solvent is easy to extract; besides, the refining yield is greater than 90%, which is far higher than the yield of secondary resolution of the resolving agent, so that the method is easy to amplify and suitable for industrial production.
Owner:TAIAN HAVAY CHEM

Method for preparing 2,6-dichloro-alpha-(4-chlorphenyl)-4-nitro phenylacetonitrile

The invention discloses a method for preparing 2,6-dichloro-alpha-(4-chlorphenyl)-4-nitro phenylacetonitrile by condensation of 3,5-dichloro-4-fluronitrobenzene and p-chloro-phenylacetonitrile, wherein the used raw material 3,5-dichloro-4-fluronitrobenzene is derived from distillation residue of a production process for preparing 2,4-dichloro-3-fluronitrobenzene by nitrifying 2,6-dichlor fluorbenzene; and the residue contains 83.5-88.2% of 3,5-dichloro-4-fluronitrobenzene and 9.0-13.3% of 2,4-dichloro-3-fluronitrobenzene, and 3,5-dichloro-4-fluronitrobenzene with content more than 98% can be obtained by selective solvent extraction and once or twice recrystallization and is subjected to condensation with p-chloro-phenylacetonitrile to obtain 2,6-dichloro-alpha-(4-chlorphenyl)-4-nitro phenylacetonitrile with yield above 98%. Compared with the existing method for preparing 2,6-dichloro-alpha-(4-chlorphenyl)-4-nitro phenylacetonitrile, the method has the characteristics of inexpensive and easily available raw materials, sufficient utilization of resources, mild conditions, high yield, low wastewater discharge and the like, and is more suitable for industrial production.
Owner:江苏中丽新材料有限公司

Sphingosine monad and method for producing carotenoid with sphingosine monad

The invention provides sphingosine monad with the preservation number of CGMCC No.12394, a method for culturing carotenoid production strain, application of the carotenoid production strain to production of carotenoid, and application to industrial production of astaxanthin. According to the sphingosine monad generating nostoxanthin, the content of nostoxanthin can reach 3.98+ / -0.5 mg / g, accounting for at least 90% of total pigment. Bred colorless phytoene producing strain SP-Phy, red lycopene producing strain SP-Lyc and yellow zeaxanthine producing strain SP-Zea are subjected to at least five generations of continuous passage, the yield of phytoene, lycopene and zeaxanthine is stable, and the content of phytoene, the content of lycopene and the content of zeaxanthine reach 3.7+ / -0.5 mg / g, 3.9+ / -0.5 mg / g and 4.0+ / -0.5 mg / g respectively, accounting for at least 90% of total pigment. By introducing ketonized enzyme genes to the bred zeaxanthine producing strain SP-Zea, the zeaxanthine producing strain SP-Zea can be transformed into astaxanthin producing strain SPZ-AST, and the content of astaxanthin reaches 4.1+ / -0.5 mg / g, accounting for at least 90% of total pigment.
Owner:KUNMING INST OF BOTANY - CHINESE ACAD OF SCI

Process for synthesizing sex pheromone of pine caterpillar

The invention discloses a process for synthesizing sex pheromone of pine caterpillar, which employs 2-hexyne-1-alcohol as an initial raw material, three-bond positional transference is carried out under the effect of lithium and propane diamine to obtain 5-hexyne-1-alcohol; under acidic condition, 5-hexyne-1-alcohol is reacted with dihydropyran to obtain 1-THP-5-hexyne-1-alcohol protected by THP on hydroxyl, Under co-catalysis of metal palladium and cuprous iodide, 1-THP-5-hexyne-1-alcohol and trans-dichloroethylene are subjected to coupling reaction to generate conjugate enyne(7E)-1-THP-8-chlorine-5-alkyne-7-alkene-1-octanol; under the catalysis of metallic iron, (7E)-1-THP-8-chlorine-5-alkyne-7-alkene-1-octanol and a n-Butyl bromide grignard reagent are further subjected to coupling reaction to obtain (7E)-1-THP-5-alkyne-7-alkene-1-dodecanol, under the catalytic reduction of metal zinc, (5Z, 7E)-1-THP-dodecanol dienol; under the camphor sulfonic acid condition, (5Z, 7E)-1-THP-dodecanol dienol removes the THP protective group to obtain the final target product (5Z, 7E)-dodecanol dienol. The method of the invention has the advantages of easily available synthesis raw materials, low cost, mild reaction condition, easy operation, high yield and good stereoselectivity.
Owner:WENZHOU MEDICAL UNIV +1

A co-pyrolysis method of biomass and agricultural film based on double-barreled structure

The invention provides a method for co-pyrolysis of biomass and agricultural film. In the inner cylinder inside the outer cylinder, there is a gap between the inner cylinder and the outer cylinder, the inner cylinder can be rotated around the longitudinal axis, the outer wall of the inner cylinder and the inner wall of the outer cylinder are provided with a number of conical convex structures, and the sidewall of the outer cylinder There is a gas-phase product outlet, and a solid-phase product collection area is set at the bottom of the outer cylinder; the raw materials are heated to 550~650 °C in the gap and react for 40~50 minutes, and the inner cylinder is rotated, so that several conical protruding structures remain in the reaction process. Act on the raw material; the gas phase product is exported through the gas phase product outlet; the solid phase product enters the solid phase product collection area. The method of the invention effectively solves the problem of cracking the plastic melting layer wrapped on the biomass surface during co-pyrolysis, and at the same time can promote the advancement of raw materials and local stirring, the yield and quality of co-pyrolysis products are improved, and the overall performance is better. High industrial application value.
Owner:INST OF ENVIRONMENT & SUSTAINABLE DEV IN AGRI CHINESE ACADEMY OF AGRI SCI

A kind of three-dimensional porous nano-carbon composite lithium manganese oxide spherical positive electrode material and preparation method thereof

The invention discloses a three-dimensional porous nanocarbon composite lithium manganate spherical positive electrode material and a preparation method thereof. The preparation method comprises the following steps of adsorbing Mn<2+> ions onto a carbonyl (-COH-) group in a microgel three-dimensional macromolecular network by adopting poly(acrylamide, acrylic acid) microgel spheres as a template; increasing the pH value of the poly(acrylamide, acrylic acid) microgel spheres so as to in-situ hydrolyze the Mn<2+> ions to generate Mn(OH)2 crystal nucleus, depositing the Mn(OH)2 crystal nucleus into a space formed by the three-dimensional macromolecular network to form nano composite polymer microspheres; placing the obtained nano composite polymer microspheres into a tubular furnace to be calcined at a high temperature in an inert gas atmosphere to prepare the three-dimensional porous nanocarbon composite lithium manganate spherical positive electrode material. The positive electrode material has the advantages of excellent high-temperature cycling performance, large multiplying power charging-discharging performance and the like, and can be widely applied to the production of a lithium battery.
Owner:XIANGTAN UNIV
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