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100results about How to "Reduce polymerization" patented technology

Compositions and methods for treatment of viral diseases

InactiveUS20100009970A1Slow and stop replicationReduce loadBiocideNervous disorderSingle-Stranded RNADisease
The present invention features compositions, methods, and kits useful in the treatment of viral diseases. In certain embodiments, the viral disease is caused by a single stranded RNA virus, a flaviviridae virus, or a hepatic virus. In particular embodiments, the viral disease is viral hepatitis (e.g., hepatitis A, hepatitis B, hepatitis C, hepatitis D, hepatitis E) and the agent or combination of agents includes sertraline, a sertraline analog, UK-416244, or a UK-416244 analog. Also featured are screening methods for identification of novel compounds that may be used to treat a viral disease.
Owner:EXCRX SINGAPORE PTE +1

Multi-Solution Bone Cements and Methods of Making the Same

InactiveUS20080039586A1Improve mechanical propertiesAdvantageous for clinical performanceCosmetic preparationsImpression capsDouble bondMonomer
The present invention relates to bone cements and, more particularly, to multi-solution bone cements and methods for making the same. An embodiment of the present invention provides multi-solution bone cements which include cross-linked PMMA beads, thereby providing for a significant increase in the polymer-to-monomer (P:M) ratio. Another embodiment of the present invention provides cross-linked PMMA beads which are surface modified with unsaturated carbon double bonds. A further embodiment of the present invention provides multi-solution bone cements made with PMMA-PMMA spherical brush polymers.
Owner:SYRACUSE UNIVERSITY

Selective hydrosilylation method using hydrido (hydrocarbonoxy) silane

A method for hydrosilylating a vinyl-substituted aromatic compound comprising reacting a hydrido (hydrocarbonoxy)silane compound with the vinyl-substituted aromatic compound in the presence of a platinum or platinum compound catalyst and a carboxylic acid. The presence of the carboxylic acid increases the positional selectivity of addition in the hydrosilylation reaction and reduces the polymerization of vinyl groups even in the case of a high-temperature or long-term hydrosilylation reaction.
Owner:DOW CORNING ASIA

Method for widening catalytic reforming feedstock

ActiveCN102041092AExpand sourceSlow down olefin polymerizationTreatment with hydrotreatment processesChemistryNaphtha
The invention relates to method for widening catalytic reforming feedstock. The comprises the following steps: mixing FCC (fluid catalytic cracking) stabilized gasoline and straight-run naphtha in a ratio of (50:50) to (70:30), filtering the obtained mixture by a feedstock filter so as to remove impurities in the mixture, and then removing the water carried in the mixed naphtha by a coalescer; mixing the mixed naphtha with hydrogen, and heating the obtained mixture to a reaction temperature by a heating furnace, then feeding the obtained mixture into a hydrogenation reactor to contact with a hydrogenation catalyst so as to be subject to olefin saturation, desulphurization and denitrification reactions; and condensating and cooling the obtained hydrogenation effluent, then separating the obtained product so as to obtain hydrogen-rich gas and hydrogenated gasoline, recycling the hydrogen-rich gas, and feeding the hydrogenated gasoline into an evaporation tower to be subject to strippingfractionation, thereby obtaining a refined naphtha meeting the reforming feeding requirements. By utilizing the method provided by the invention, the mixed naphtha containing more than 50 percent of the FCC stabilized gasoline can be subject to hydroprocessing so as to obtain the refined naphtha, wherein the content of the impurities in the refined naphtha satisfies the reforming feeding requirements, thereby solving the shortage problem of the reforming feedstock, and widening the source of the reforming feedstock.
Owner:PETROCHINA CO LTD +1

Method for preparing high-purity dicyclopentadiene

The invention discloses a method for preparing high-purity dicyclopentadiene (DCPD). The method comprises the steps of adding a diluting agent into crude dicyclopentadiene serving as a raw material during depolymerization, mixing dicyclopentadiene with the diluting agent in a ratio of 0.5-5, and then putting the mixture into a depolymerization rectifying tower, wherein at a normal pressure, the depolymerization temperature is 160-200 DEG C, the reflux ratio is 0.5-5, and the depolymerization time is 1-3 hours; obtaining high-purity cyclopentadiene (CPD) from the top of the tower, putting the cyclopentadiene into a tubular reactor to finally obtain dicyclopentadiene of which the purity is more than 99%, wherein the reaction temperature is 40-120 DEG C, the reaction pressure is 0.1-1.5MPa, and the residence time is 4-10 hours. The method disclosed by the invention has obvious beneficial effects, can reduce polymerization reaction of the crude dicyclopentadiene during depolymerization, and can improve the yield of the dicyclopentadiene; meanwhile, the diluting agent can ensure that impurities including isopropenyl norbornene and the like can be depolymerized, and the purity of dicyclopentadiene is improved, so that the method is particularly suitable for preparing high-purity dicyclopentadiene from the raw material of crude dicyclopentadiene which is obtained through pyrolysis C5 thermal dimerization separation.
Owner:CHINA PETROLEUM & CHEM CORP +1

Method for producing hexamethylenediamine key intermediate 6-aminocapronitrile by continuous gas-phase two-step method

The invention provides a method for producing a hexamethylenediamine key intermediate 6-aminocapronitrile by a continuous gas-phase two-step method. The method comprises the following steps: S1, mixing caprolactam and water in a gas phase state to carry out continuous hydrolysis or mixing caprolactam and ammonia water in a gas phase state to carry out continuous hydrolysis ammoniation reaction toobtain a first product system containing 6-aminocaproic acid, 6-aminocaproic acid ammonium salt and/or 6-aminocaproamide; and S2, carrying out continuous gas-phase catalytic ammoniation and dehydration reaction on the first product system and ammonia gas to obtain a second product system containing 6-aminocapronitrile. According to the patent of the invention, the problem that water generated by reaction in a one-step process promotes polymerization reaction of the raw material caprolactam is reduced from the source, and the selectivity of aminocapronitrile is improved; and the problems of catalyst deactivation and pressure drop rise caused by polymerization and coking of caprolactam in the reactor are effectively reduced, the stability of the device is improved, and the service life of the catalyst is prolonged.
Owner:JIANGSU YANGNONG CHEM GROUP +2

Method for separating and cracking cyclopentadienyl from carbon 5 fraction

The invention discloses a method for separating and cracking cyclopentadiene in C5 distillate. The method belongs to the technical field of C5 separation. In order to solve the problems that the industry requires the dimerization reaction of cyclopentadiene as much as possible; and the industry also requires the higher quality of a dicyclopentadiene product and little loss of isoprene, the invention provides the method which comprises the following steps: setting a suspension type dimerization reactor on the body of a C5 mixture rectification tower, leading liquid phase material stream from a tower plate of the rectification tower and pumping the liquid phase material stream into the dimerization reactor, making the cyclopentadiene in the material stream to have a liquid phase dimerization reaction in the suspension type dimerization reactor, and then returning the material stream back to the rectification tower from the suspension type dimerization reactor. The method can be applied to the prior industrial C5 production device and the process of one-section extraction separation and cracking of C5 distillate. The method can reduce polyreaction besides the self-dimerization of cyclopentadiene, improve the quality of the dicyclopentadiene product, reduce the loss rate of isoprene, and reduce the cyclopentadiene content in the materials as much as possible.
Owner:CHINA PETROLEUM & CHEM CORP +1

Oil slurry scale inhibitor

The invention discloses an oil slurry scale inhibitor. The oil slurry scale inhibitor is prepared from the following components in percentage by mass: 25 to 40 percent of a detergent dispersant, 6 to12 percent of a phenol-amine type antioxidant, 5 to 10 percent of a corrosion inhibitor, 0.5 to 3 percent of a detergent, 0.4 to 0.5 percent of a metal passivating agent and the balance of a solvent,wherein the detergent dispersant is polyisobutylene succinimide and / or polybutadiene mercaptohexanediol phosphate. The oil slurry scale inhibitor disclosed by the invention has a low freezing point (less than or equal to -15 DEG C), small viscosity (the kinematic viscosity is less than or equal to 50 mm<2> / s at 20 DEG C), a strong anti-oxidization capability and good thermal stability; propertiesand utilization performance of the oil slurry scale inhibitor are not influenced at relatively high temperature of 350 to 400 DEG C and the oil slurry scale inhibitor is suitable for scale inhibitionand descaling in an oil slurry system in a catalytic cracking device; the adding amount of the oil slurry scale inhibitor in oil slurry is 30 to 100 ppm; the oil slurry scale inhibitor can be used foreffectively inhibiting equipment including the oil slurry system, a pipeline, a heat exchanger and the like from being coked; the scale inhibition rate can reach 90 percent and safe and stable operation of a device is ensured.
Owner:JIANGSU KECHUANG PETROCHEM

Method for producing polyalkylene glycol derivative having amino group at end

A method simply produces a narrowly distributed and high-purity polyalkylene glycol derivative having an amino group at an end without using a heavy metal catalyst. A method for producing a polyalkylene glycol derivative having an amino group at the end by reacting a compound represented by the general formula (V) with an alkylene oxide, then reacting a reaction product with an electrophile represented by the general formula (I), and deprotecting the obtained product without using a heavy metal:RA3O(RA4O)k-1RA4O−M+  (V)wherein RA3 represents a linear; branched, or cyclic hydrocarbon group having 1 to 20 carbon atoms; RA4 represents an alkylene group having 2 to 8 carbon atoms; k represents an integer of 2 to 5; and M represents an alkali metal;wherein RA1a and RA1b each independently represent a protective group of the amino group, or one of RA1a and RA1b represents H and the other represents a protective group of the amino group, or RA1a and RA1b bind to each other to form a cyclic protective group, and the protective group is deprotectable without using a heavy metal; RA2 represents a linear, branched, or cyclic hydrocarbon group having 1 to 6 carbon atoms; and X represents a leaving group.
Owner:SHIN ETSU CHEM IND CO LTD
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