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35 results about "Benzene" patented technology

Benzene is an organic chemical compound with the chemical formula C₆H₆. The benzene molecule is composed of six carbon atoms joined in a ring with one hydrogen atom attached to each. As it contains only carbon and hydrogen atoms, benzene is classed as a hydrocarbon.

Method for synthesizing citric acid ester type compound

The invention discloses a method for synthesizing a citric acid ester type compound, which belongs to the technical field of chemical synthesis. The method comprises the following steps of: using citric acid and fatty alcohol as main raw materials, and using benzene sulfonic acid or amino benzene sulfonic acid as a catalyst; and performing esterification and the purification processes of acetylation, neutralization, washing, drying, distillation and the like. The catalyst has rich sources, a low cost and high activity, can be separated from an esterification liquid easily after the neutralization, is coke-free during the distillation, has less corrosion to equipment, and is safe and environment-friendly; the water generated by the esterification is separated out by adopting a binary heterogeneous separation technique, and no water separating agent is additionally added; and acetyl citric acid ester is produced by adopting an esterification-acetylation continuous synthesis method, the flow is greatly simplified, and a synthesis process is shortened. The citric acid ester prepared by the method has the advantages of high quality, high purity, low degree of color and wide applicationrange.
Owner:NORTHWEST NORMAL UNIVERSITY

Method for preparing 2-iodine amyl -2-ene-1,4-diketone derivative by adopting visible light catalysis

The invention discloses a method for preparing a 2-iodine amyl -2-ene-1,4-diketone derivative by adopting visible light catalysis. The method comprises the steps of adding allene, perfluorobutyl iodide, an additive and a photocatalyst as shown in a formula (I) to an organic solvent at the molar ratio of 1:(1-2):(1-2):(0.005-0.1), stirring under the conditions of an oxygen atmosphere, visible light illumination, room temperature and ordinary pressure for 10-20h, carrying out post-treatment on a reaction liquid to obtain a 2-iodine amyl -2-ene-1,4-diketone derivative as shown in a formula (II), wherein the additive is NaI, NH4I or KI; the organic solvent is ethanol, dichloromethane, benzene, methylbenzene, tetrahydrofuran or acetonitrile; the photocatalyst is selected from one of the following components: Ir(ppy)3, Eosin Y, Rose Bengal, [Ir(dF-CF3-ppy)2(dtbbpy)]PF6, [Ir(ppy)2(tbbpy)]PF6, Ru(bpy)3(BF4)2. The method is mild in reaction condition, simple in operation, high in selectivity and good in yield; a substituent group can be expanded; and visible light catalysis is adopted, so that the method has the characteristics of being free of pollution and environment-friendly. The formulas are as shown in the specification.
Owner:ZHEJIANG UNIV OF TECH

Method for producing coating ultra-sense paper

InactiveCN101250835AProcessing into excellent performanceEasy to processSpecial visual effect coatingsCoatings with pigmentsFiberBenzene
The invention relates to a method for preparing a coating hypersensitive paper, which comprises the following steps: firstly, adopting fiber 100% as raw material, beating, dispensing, drawing the vibrator for fixation, modeling, drying, gluing and drying to produce the hypersensitive base stock which is provided with natural and native texture. The hypersensitive base stock is coated and manufactured through a 1760mm coater which velocity is 150 / min and the coating quantity area is 15g / m2. The coating paint comprises dye and latex adhesive, wherein the dye is selected from specially processed titanium oxide and kaolin, the particle size of titanium oxide and kaolin is less than 2 mum. The latex adhesive adopts benzene latex and starch to blend together. The hypersensitive base stock surface of the invention forms a natural and native texture dull base stock on the net without pressing, polishing and dressing. The prepared coating hypersensitive paper has the advantages of reducing manufacturing procedure, increasing natural and native texture of the paper and stereo aesthetics, reducing reflection light, which is non-excited in eyes, soft and comfortable in scene, easy in preparation and low in preparation cost.
Owner:SHANDONG KAILI SPECIAL PAPER

Method for removing phenol in phenol contained wastewater by using hollow fiber membrane

InactiveCN103304005AImprove stabilityImprove mass transfer efficiencyWater contaminantsWater/sewage treatment bu osmosis/dialysisHollow fibre membraneBenzene
The invention discloses a method for removing phenol in phenol contained wastewater by using a hollow fiber membrane. The method comprises the following steps of: mixing a carrier and a diluent to prepare an extractant, wherein the adopted extractant carrier is tributyl phosphate, and the adopted diluent is coal oil or benzene; stirring and fully mixing the extractant and a stripping agent to prepare treating fluid; removing the phenol out of the phenol contained wastewater by using a hollow fiber membrane device; and after pretreating the hollow fiber membrane device, injecting the treating fluid into a tube pass of a membrane component, and injecting the phenol contained wastewater into a shell pass of the hollow fiber membrane component, wherein the wastewater can be treated through the same membrane component or a plurality of serial membrane components in a circular manner for many times; after the wastewater is subjected to two-stage treatment, the phenol concentration is less than 100mg/L; and after the wastewater is subjected to five-stage treatment, the phenol concentration is less than 5mg/L, the removal rate reaches up to 99.8 percent, and the wastewater reaches the national emission standard.
Owner:BEIJING UNIV OF CHEM TECH

High-strength marine rubber fender

InactiveCN103012863AImprove tensile strength at breakRubber materialSulfide
The invention relates to a high-strength marine rubber fender. Rubber raw materials consist of the following components in parts by weight: 70-90 parts of natural rubber 1#, 30-50 parts of chloroprene rubber 21, 2-3 parts of stearic acid, 1-2 parts of paraffin, 15-25 parts of hard carbon black, 2-3 parts of anti-aging agent DTPD, 2-4 parts of vulcanizing agent TRA, 20-30 parts of calcium carbonate, 3-5 parts of zinc oxide, 4-5 parts of magnesium oxide, 2-5 parts of Vaseline, 0.3-0.5 part of accelerant DM, 1.1-1.3 parts of accelerant TT, 0.9-1.1 parts of anti-aging agent 4010 and 0.9-1 part of anti-aging agent D, wherein the anti-aging agent DTPD is domestically called an anti-aging agent 3100 which has the Chinese name of N,N'-xylyl-p-phenylenediamine mixture, the vulcanizing agent TRA is also called DPTT which has the Chinese name of tetra-sulfide bis(pentamethylene) thiuram and the molecular formula of C12H20N2S4, the accelerant DM has the Chinese name of 2,2'-dithio-dibenzothiazole and the molecular formula of C14H8N2S4, the accelerant TT has the Chinese name of disulfide tetramethyl thiuram and the molecular formula of C6H12N2S4, the anti-aging agent 4010 has the Chinese name of N-isopropylbenzene-N-phenylene-p-phenylenediamine, and the anti-aging agent D has the Chinese name of N-phenyl-2-naphthylamine and the molecular formula of C16H13N. According to the high-strength marine rubber fender, the tensile breaking strength of the rubber fender is improved through changing the proportions of a rubber material, a polar material and polysulfur bonds.
Owner:XIAN ZHITAI RUBBER & PLASTIC IND

Preparation method of non-woven fabric

InactiveCN108517621AImprove toughnessImprove wear resistanceBiochemical fibre treatmentNon-woven fabricsCardingPyrophosphate
The invention discloses a preparation method of a non-woven fabric, and belongs to the field of spinning. Sodium pyrophosphate, glucose, sodium hydroxide, ferrous sulfate and water are sampled, nitrogen protection is adopted, heating and stirring are performed, and then cumyl hydroperoxide and polybutadiene are added and stirred and mixed; a stirring mixture, allyl benzene, methyl methacrylate, epoxypropyl methacrylate and dibenzyl phthalate are obtained to be added into magnesium sulfate, stirring, mixing and drying are performed, a drying object is obtained to be added into polylactic acid to be mixed, and a mixed matrix is obtained; folium eriohotryae and aloe are obtained to be mixed and homogenized, deionized water is added for digestion and suction filtration, a filtrate is obtainedfor centrifuging, a supernate is obtained to be added into a copper nitrate solution to be mixed, and an antibiotic finish solution is obtained; processed linen fiber, a dispersing solution and the antibiotic finish solution are obtained to be soaked and filtered, the linen fiber is taken to be cleaned with deionized water, and linen fiber is obtained; linen fiber, the mixed matrix, polypropyleneand sodium alginate are obtained to be mixed for opening, carding and lapping, the mixture is placed into a needle machine for needling treatment, and hot rolling is performed to obtain the non-wovenfabric.
Owner:徐冬

Synthesis of Azo Bonded Immunoregulatory Compounds

ActiveUS20080033153A1Organic chemistryCoupling reaction in azo dyesMetaboliteNitrobenzene
Methods are disclosed for preparing compounds of Formula I: where R1, R3, and R4are independently hydrogen or C1 to C4 alkyl, and R2 is: where R5 is selected from the group consisting of hydrogen and C1 to C4 alkyl, or where R6, R7 and R8 are independently hydrogen or C1 to C4 alkyl; or the esters or pharmacologically acceptable salts thereof. The methods can involve converting a suitably functionalized aniline compound to a diazonium salt (which aniline compound can be first formed by reduction of a nitrobenzene) and coupling the diazonium salt with a suitably functionalized benzene compound. The suitably functionalized aniline compound either includes a primary alcohol or aldehyde group, which is then oxidized to a carboxylic acid group, or includes a nitrile or amide group, which is hydrolyzed to a carboxylic acid group. The methods can also involve the direct coupling (via reduction of nitro groups to form an azo linkage) of suitably functionalized nitrobenzenes. The compounds and or their metabolites can be used to treat or prevent various diseases, particularly inflammatory conditions of the GI tract.
Owner:BIOCON LTD

Production method of 2,2'-dimethyl[1,1'-biphenyl]-4,4'-diamine

ActiveCN110590596AHigh selectivityHydrazine preparationOrganic-compounds/hydrides/coordination-complexes catalystsBenzeneHydroxyanthraquinone
The invention discloses a production method of 2,2'-dimethyl[1,1'-biphenyl]-4,4'-diamine. According to the production method of the 2,2'-dimethyl[1,1'-biphenyl]-4,4'-diamine, with 3-nitrotoluene as aninitial raw material, reduction is conducted at first to obtain 3,3'-dimethylhydrazo-benzene, and then rearrangement is conducted to obtain the 2,2'-dimethyl[1,1'-biphenyl]-4,4'-diamine; reduction isconducted with Pd/C as a main catalyst and an anthraquinone compound plus sodium di(2-ethyl-hexyl)sulfosuccinate as cocatalysts; and the anthraquinone compound is one or two of 1,4-dihydroxyanthraquinone, 2-hydroxyanthraquinone and 2,6-dihydroxyanthraquinone. According to the production method of the 2,2'-dimethyl[1,1'-biphenyl]-4,4'-diamine, through a large number of experiments, it is found that by combining the sodium di(2-ethyl-hexyl)sulfosuccinate and the anthraquinone compound as the cocatalysts, the reaction selectivity of production of the 3,3'-dimethylhydrazo-benzene through reduction of the 3-nitrotoluene can be greatly improved, and the reaction yield which is 70% or above can be obtained finally, so that conditions are created for mass application of the 2,2'-dimethyl[1,1'-biphenyl]-4,4'-diamine on the aspect of production of special materials.
Owner:CHANGZHOU SUNLIGHT PHARMA

Anti-cracking epoxy ceramic paint and preparation method thereof

The invention provides anti-cracking epoxy ceramic paint, which is prepared from the following raw materials in parts by weight: diatomite, silicon carbide powder, corn starch, coconut oil acid diethanolamide, aluminum oxide, C12 alcohol ester, triphenyl phosphate, diethylene glycol monobutyl ether, expanded vermiculite, nanometer silicon dioxide, barium sulfate, styrene-acrylate emulsion, tri(dodecyl benzene sulfonyl) titanium isopropoxide, carbon fiber, epoxy resin E-44, diluents 660A, triglycidyl p-aminophenol, bisoxaldihydrazone, water glass, hydroxypropyl methyl cellulose and a proper amount of deionized water. The prepared epoxy ceramic paint has excellent characteristics that the coating is compact and smooth, and is firm as ceramics; the bonding is firm; the thickness is uniform; the water-resistant, anti-corrosion and electric insulation performance is excellent, and the like.
Owner:黄春梅

Preparation method of fiber mesh-compounded diatom ooze coating

InactiveCN112266631AGuaranteed flatnessImprove structural strengthCovering/liningsAntifouling/underwater paintsBenzeneFiber
The invention relates to the technical field of diatom ooze coatings, and discloses a preparation method of a fiber mesh-compounded diatom ooze coating. The preparation method comprises the followingstep: S1, preparing raw materials including a fiber mesh, 25-35 parts of deionized water, 15-25 parts of diatomite, 2-8 parts of a humectant, 15-25 parts of an odor-free pure benzene emulsion, 10-18 parts of a filler, 2-6 parts of quartz powder and 0.5-1 part of a dispersant. The invention further provides a construction method of the fiber mesh-compounded diatom ooze coating. The construction method comprises the following steps: S1, cleaning a wall surface, namely cleaning the wall surface to be constructed by using a tool; and S2, fixing the fiber mesh. According to the invention, the overall structural strength of a diatom ooze coating composite layer is improved, and the diatom ooze coating is distributed in meshes of the fiber mesh and bonded and compounded to the fiber mesh and a wall surface base layer, so the flexibility of the diatom ooze coating composite layer is improved, construction is convenient, formaldehyde, benzene and other organic matters can be effectively decomposed, and a good air purification effect is achieved.
Owner:佘丽辉

Preparation method of heterocyclic benzene compound

InactiveCN103012395AHigh reaction yieldReact SafeOrganic chemistryBenzeneCoupling reaction
The invention relates to a preparation method of a heterocyclic benzene compound. The preparation method comprises the step of carrying out coupled reaction between a compound as shown in formula I and the compound as shown in formula II under the effect of a catalyst A, so as to obtain the compound as shown in formula III; and the reaction is shown as follows, wherein Ar, R1, R2, X and A are identified as the specifications shown. According to the method of synthesizing the heterocyclic benzene compound, described in the technical scheme, the reaction yield is greatly increased; the 'one-pot' method is carried out, so that the reaction process is safe and simple; and the method is very suitable for industrial production.
Owner:NANJING YOKO PHARMA GRP CO LTD

Method for synthesizing 3-(methylthio) dibenzenamine by light/nickel concerted catalysis

ActiveCN108409618AMild reaction conditionsHigh coupling efficiencySulfide preparationNickel saltBenzene
The invention discloses a method for synthesizing 3-(methylthio) dibenzenamine by light / nickel concerted catalysis. According to the method, cheap 3-(methylthio) benzenamine and halogeno benzene are used as raw materials, a light / nickel concerted catalysis strategy is used for constructing C-N bonds for the first time, and pyridazines drug key intermediate 3-(methylthio) dibenzenamine is synthesized. The method has the advantages that 1) the use amount of a photocatalyst is low, and is 0.01-0.02% of the molar weight of the halogeno benzene; 2) nickel salt is directly used as a metal catalyst such as nickel bromide, and an external ligand is not required; 3) reaction conditions are gentle, and can be effectively carried out at the temperature of 40-50 DEG C; and 4) the product can be directly obtained by reduced pressure distillation and is easily separated. By the remarkable advantages, the method has good industrial application prospect.
Owner:SHAANXI NORMAL UNIV

Method for preparing magnesium sulfate from byproduct sulfuric acid of benzene sulfone chloride

PendingCN111977675AIncrease concentrationEasy to separateSulfur compoundsMagnesium sulfatesSulfonyl chlorideChlorosulfuric acid
The invention discloses a method for preparing magnesium sulfate from byproduct sulfuric acid of benzene sulfone chloride. The method comprises the following steps: (1) sulfonation reaction: chlorosulfonic acid and pure benzene are taken as raw materials; firstly, the chlorosulfonic acid is added into a reaction kettle; then, the reaction kettle is heated, and the reaction kettle is started; afterstarting, under the stirring state that the stirring rate is 100-150r / min, the pure benzene is dropwise added by employing a constant-pressure dropping funnel; and after being dropwise added, the pure benzene and the chlorosulfonic acid react for 2-3h to produce hydrogen chloride gas; then the produced hydrogen chloride gas is condensed and is absorbed by a secondary falling film to prepare a hydrochloric acid solution with mass concentration of 38%-45%; after the solution is obtained, 10-15g of sulfonation additive is added into the solution; then the reaction kettle is restarted for reaction; and after the reaction ends, cooling, hydrolyzing, crystallization, suction filtration, water washing and drying are performed to obtain the benzene sulfone chloride and by-products thereof; the sulfuric acid can be separated very conveniently, and the magnesium sulfate can be quickly prepared by using the sulfuric acid.
Owner:JIANGSU KANGXIANG GRP CORP +1
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