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44 results about "M-toluidine" patented technology

Environment-friendly type lubricating oil additive

An environment-friendly type lubricating oil additive is composed of the following raw materials in parts by weight: 7 to 12 parts of castor oil polyoxyethylene ether, 3 to 6 parts of molybdenum disulfide colloid, 2 to 7 parts of n-octadecanoic acid, 4 to 8 parts of critic acid, 6 to 13 parts of molybdenum dialkyldithiophosphate, 4 to 8 parts of butyl oleate, 3 to 6 parts of tackifier, 5 to 8 parts of o-toluidine / m-toluidine, 6 to 8 parts of methyl citrate, 4 to 7 parts of triphenyl phosphorothionate, 6 to 12 parts of sulfurized isobutylene, 5 to 8 parts of benzotriazole amine, 2 to 6 parts of n-butyl acetate, 1 to 4 parts of p-methoxyl styrene, 8 to 16 parts of linoleic acid, 4 to 6 parts of methanol, 7 to 13 parts of polyethylene glycol monomethyl ether, 4 to 7 parts of magnesium silicate, and 4 to 6 parts of fluorine surfactant. The provided environment-friendly type lubricating oil additive can improve the wear-resistant performance, extreme pressure resistant performance, and oxidation resistant performance of lubricating oil, has the advantages of convenient operation and environment-friendliness, and is according with the green and environment-protection requirements.
Owner:QINGDAO WENSHENG AUTOMOBILE COMPONENTS & PARTS

Preparation method for disperse red 343:1 dye

The invention discloses a preparation method for disperse red 343:1 dye. The preparation method comprises the following steps: 1) diazotization, to be specific, adding water into a reaction kettle, cooling with cooling water, adding sulfuric acid, and then, dropwise adding nitrosyl sulfuric acid; after completing adding the nitrosyl sulfuric acid, adding 2-amino-5, 6-dichloro benzothiazole, stirring, and performing standing to obtain diazonium salt; 2) coupling, to be specific, adding water, glacial acetic acid, sulfamic acid and peregal into a coupling bucket, adding N-ethyl-N-benzoyloxy ethyl m-toluidine, adding ice for cooling, pressing-in the diazonium salt, and coupling; 3) after completing the coupling, and adding water for heating; 4) performing press-filtering, and washing, so as to obtain dye filter cakes; 5) mixing the dye filter cakes and an auxiliary agent, so as to obtain the disperse red 343:1 dye. According to the invention, the disperse red 343:1 dye serves as a substitute object of disperse red 343, the preparation technology is simple, only one-time coupling reaction is performed, the process route is shortened, the waste water discharge is greatly reduced, the yield is increased, the cyanation reaction adopting plenty of virulent cyanide is avoided, the possibility for harming human beings and the environment is reduced, and the finally prepared disperse red 343:1 dye is high in light fastness and can meet the use requirements of textiles on high-solarization dye.
Owner:ZHEJIANG HUADIE CHEM

Trisazo carmoisine and preparation method thereof

The invention discloses a trisazo carmoisine, and also discloses a preparation method thereof. The preparation method comprises the following steps: diaminoazobenzene, hydrochloric acid and a sodium nitrite solution react in water, and residual nitrous acid is eliminated after the reaction to obtain a diazonium salt solution; and reaction raw materials react with the diazonium salt solution to finally obtain the corresponding trisazo carmoisine, wherein the reaction raw materials are N-ethyl-N-benzyl aniline-3'-sulfonic acid and N-ethyl-N-benzyl m-toluene-3'-sulfonic acid. The trisazo carmoisine disclosed by the invention does not contain carcinogenic dye or heavy metal dye, and belongs to safe and environment-friendly dye. The dye composition has good water solubility, is gentle in dyeingin a dyeing system and good in leveling property, can be efficiently combined with protein and polyamide fibers, is high in dyeing rate, enables dyed fibers to have excellent color fastness, and is an ideal substitute for metal complex dyes.
Owner:JINHUA SHUANGHONG CHEM CO LTD

Catalyst for m-toluidine prepared from m-nitrotoluene through gas phase hydrogenation, preparation method and regeneration method thereof

The invention discloses a catalyst for m-toluidine prepared from m-nitrotoluene through gas phase hydrogenation, a preparation method and a regeneration method thereof. In the catalyst, SiO2 is used as a carrier and copper is used as a main active ingredient; and based on the weight of the catalyst, Cu accounts for 10 to 30 percent and the balance is SiO2. The method for preparing the catalyst comprises the following steps: weighing copper nitrate and silica gel; adding distilled water into the copper nitrate until the copper nitrate is fully dissolved; adding solution of ammonia water into the mixture until no precipitate is generated in the solution; adjusting the pH value; adding the silica gel into the prepared solution and stirring the solution; filtering and washing the obtained solution until the filtrate becomes colorless; and finally drying and baking the filtrate to obtain the catalyst. The catalyst after being inactivated can be regenerated through an air oxidizing roasting method. The catalyst has the advantages of long service life, excellent catalytic activity, high selectivity, simple preparation and regeneration methods and low cost, and wide application.
Owner:NANJING UNIV OF SCI & TECH

Method for detecting impurities, namely meta-methylnitrobenzene and m-toluidine, in m-cresol simultaneously

The invention relates to the technical field of chemical industry and discloses a method for detecting impurities, namely meta-methylnitrobenzene and m-toluidine, in m-cresol simultaneously. The method comprises the following steps: diluting a to-be-detected m-cresol sample by using a mixed solvent of dimethyl sulfoxide, methanol and DMF to obtain a test sample solution, and taking the mixed solution of the meta-methylnitrobenzene and the m-toluidine as a control product solution; and performing sample introduction on the test sample solution and the control production solution by a headspace mode, performing gas chromatographic detection, and calculating the content of the impurities, namely the meta-methylnitrobenzene and the m-toluidine, in the m-cresol according to an external standard method and based on peak area. The sample is diluted by the mixed solvent of the dimethyl sulfoxide, the methanol and the DMF, sample instruction is conducted by the headspace mode, and chromatographic detection is conducted, so that the content of the minute amount of meta-methylnitrobenzene and m-toluidine in the product can be detected simultaneously and accurately, the detection sensitivity is greatly improved, and important practical value on production control of the product and quality control of the product is achieved.
Owner:HYBIO PHARMA

Clutch pump piston and preparation method thereof

The invention discloses a clutch pump piston and a preparation method thereof. The preparation method comprises the steps of 1) smashing sweet potato, putting the smashed sweet potato into a yeast solution for fermentation, then filtering and taking a filter cake, so as to obtain a modifier; 2) calcining bentonite and iron-ore slag, then putting the calcined bentonite and iron-ore slag in X-rays for activating treatment, so as to obtain an activator; 3) mixing makrolon, an ethylene-vinyl acetate copolymer, cellulose propionate, vinyl propionate, n-butyl alcohol, nanometer magnesia, a rare-earth oxide, a potassium titanate whisker, m-toluidine, anilmomethyl triethoxy silane, pyrimidine, p-benzoquinone, simethicone and the modifier with the activator, cooling, molding and pelleting to obtain a clutch pump piston material; 4) melting the clutch pump pulling bar material at 195 to 205 DEG C, and then the clutch pump piston is obtained by extrusion molding. The clutch pump piston prepared by the method has excellent mechanical property.
Owner:WUHU HENGKUN AUTO PARTS

High-strength polyimide, preparation method and production equipment

The invention discloses a preparation method of high-strength polyimide, which comprises the following steps: (1) preparing an organic solvent, and mixing transparent fibers in the organic solvent in a dispersed manner; (2) adding pyromellitic dianhydride and m-toluidine into an organic solvent, and polymerizing the pyromellitic dianhydride and the m-toluidine; (3) adding the biphenyl tetracarboxylic dianhydride, the oxydiphthalic anhydride or the benzophenone tetracarboxylic dianhydride into the organic solvent, and polymerizing the biphenyl tetracarboxylic dianhydride, the oxydiphthalic anhydride or the benzophenone tetracarboxylic dianhydride and the m-toluidine; and (4) carrying out imidization on the polyimide acid generated in the organic solvent. The invention also provides high-strength polyimide and production equipment. According to the present invention, the dispersed transparent fiber yarn is added in the organic solvent in advance, the transparent fiber yarn and the polyimide are subjected to composite molding after the polyimide is subjected to tape casting, and the transparent fiber yarn has the high strength, such that the prepared polyimide has the good strength;
Owner:苏州合尔达电子科技有限公司

Method for preparing CLT acid by taking m-toluidine as raw material

The invention discloses a method for preparing CLT acid by taking m-toluidine as a raw material, and belongs to the field of chemical synthesis. The method solves the problems that existing CLT acid production is low in yield, not environmentally friendly and the like. The method comprises: S01) an acylation step, namely a step of reacting m-toluidine and acetic anhydride to obtain acylation reaction solution; S02) a chlorination step, namely a step of adding acetic acid and concentrated hydrochloric acid into the acylation reaction solution, then adding hydrogen peroxide, and finally adding an aqueous solution containing sodium sulfite to obtain a chlorination reaction solution; S03) a hydrolyzing step to form salt, namely a step of adding concentrated sulfuric acid into the chlorinationreaction solution, and removing the solvent after reaction; S04) a transposition sulfonation step, namely a step of adding chlorobenzene into the solvent-removed reaction solution obtained in the stepS03, heating the mixture, adding dichlorobenzene, heating the mixture again, reacting the mixture for 7-10 hours with the temperature of the system being maintained at a temperature higher than 170 DEG C, and stopping heating; and S05) a step of post-treatment to obtain a finished product that is the CLT acid. The method has the advantages of environmental protection and the like.
Owner:ZHEJIANG UNIV OF TECH

Preparation method of 3-methyl-4-isopropylaniline

The invention relates to a preparation method of 3-methyl-4-isopropylaniline. The preparation method includes the following steps: (1) dissolving m-toluidine in sulfuric acid solution 50-98% in mass concentration as a component 1, then adding an isopropylation reagent into another container to serve as a component 2, simultaneously feeding the component 1 and the component 2 into a jet mixer with the flow rate of 5-10:1 to be mixed at the temperature of 10-35 DEG C, and then reacting at the temperature of 60-95 DEG C through a quartz reaction tube to obtain reaction solution for alkylation reaction; (2) subjecting the reaction solution obtained in the step (1) to separation and purification to obtain 3-methyl-4-isopropylaniline. The 3-methyl-4-isopropylaniline prepared through the method has the advantages of mild reaction condition, high yield, few by-products, less pollution and the like, and the problems of a lot of by-products, strict conditions and severe pollution in the preparation process of the 3-methyl-4-isopropylaniline in the prior art are solved effectively.
Owner:ZHEJIANG DINGLONG TECH +1
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