301 results about "Phenol" patented technology

The application provides a synthesis method of p-benzoquinone dioxime. The synthesis method comprises the following steps: (1) adding solid acid into an ethanol solution of phenol to obtain a mixed solution A, then vacuumizing and filling with inert gas; dissolving nitrite into ethanol, uniformly mixing to obtain an ethanol solution of nitrite, then vacuumizing and filling with inert gas; in an inert gas atmosphere, adding the ethanol solution of nitrite into the mixed solution A dropwise to perform nitrosation reaction, to obtain a reaction liquid B; in the inert gas atmosphere, adding an ethanol solution of hydroxylamine into the obtained reaction liquid B to perform oximation reaction; after the reaction is completed, filtering the obtained reaction liquid C, performing reduced pressure distillation on the obtained filtrate, and performing washing, filtering and drying on the obtained residual liquid of the reduced pressure distillation, to obtain p-benzoquinone dioxime. The method provided by the application reduces the occurrence of side reactions, improves the conversion rate of the reaction, and improves the yield and purity of p-benzoquinone dioxime.

This application proposes methods for synthesizing aromatic compounds using ionizing radiation based on N₂O, and methods for synthesizing aromatic compounds using industrial waste gas. The method includes: placing benzene and a combined gas containing N₂O in a sealed container, and adjusting the volume of the combined gas to bring the benzene in the sealed container to its saturated vapor pressure; irradiating the sealed container with radiation to cause the benzene to react and yield the aromatic compounds, wherein the radiation includes X-rays, gamma rays, or electron beams, the energy range of which is 0.0110 MeV, and the absorbed dose rate is 0.1 Gy / min to 1000 kGy / min. This method can synthesize aromatic compounds such as phenol in one step using ionizing radiation based on N₂O without the use of a catalyst, achieving precise and high-value utilization of N₂O.

Disclosed herein are aspects of a compound according to Formula (I). tHe compounds are useful as surfactants and can be used in applications for which a surfactant is indicated. The disclosed compounds are biodegradable and do not form toxic by-products when degraded. As such, the disclosed compounds can be used as replacements for current surfactants, such as current octylphenol ethoxylates (OPEs) and nonylphenol ethoxylates (NPEs) that have toxic effects when degraded. Also disclosed are aspects of a method for making the compounds and methods for using the compounds in cell assays.

This invention discloses a method for treating high-COD benzene-containing wastewater from phenol and acetone production, comprising sequential pretreatment and biological treatment. The pretreatment includes a single-effect falling film evaporator, a first-effect evaporator, a second-effect evaporator, and a third-effect evaporator. The biological treatment includes an acidification hydrolysis tank, an oxidation ditch, a primary aerobic tank, a secondary aerobic tank, a primary sedimentation tank, a secondary sedimentation tank, and a sludge thickening tank. This invention achieves chain-breaking degradation and carbon reduction, effectively treating the wastewater and ensuring that the final effluent meets the prescribed discharge requirements.

The present application relates to a kind of phenol and methanol directly prepared (methyl) anisole mode, the method includes the following steps: under the action of composite catalyst, phenol and methanol are catalytically generated methyl anisole, the composite catalyst is Ho / β molecular sieve catalyst and Ti / UiO-66 with mass ratio Ho / β:Ti / UiO-66 0.3-0.6:1 Mixed composite catalyst.The process reaction step is simple, and synthesis is realized in one step, and the total selectivity of methyl anisole is as high as 76% or more, and can be continuously and stably operated for 3000h.

This invention discloses an extraction solvent recovery device for reducing the unit consumption of dichlorophenol (oxadiazon), belonging to the field of chemical equipment. The device includes: an extraction vessel, rotatably connected to a stirring shaft, with a partition plate attached to the inner wall of the extraction vessel. The partition plate has several evenly distributed sedimentation ports. A lifting frame is slidably connected to the stirring shaft, with sealing plates corresponding to each sedimentation port. A lifting assembly is connected to the partition plate, and the lifting assembly is driven by a drive mechanism. This assembly moves the lifting frame and the sealing plates, sealing the sedimentation ports and thus isolating the upper and lower layers of liquid within the extraction vessel, allowing for the extraction of the upper layer. Simultaneously, by isolating the upper and lower solutions within the extraction vessel, the device effectively improves the convenience and efficiency of phenol recovery, solving the problem of high unit consumption of dichlorophenol in existing solutions.

This invention discloses a ternary composite adsorbent based on iron-catechol-boric acid, its preparation method, and its application, belonging to the field of dyeing and printing wastewater treatment. The adsorbent of this invention uses tannic acid with a surface rich in catechol groups as a substrate. A stable metal-phenolic network is formed through the coordination of trivalent iron with catechol groups, efficiently capturing anions using metal bridging and electrostatic attraction to form the adsorption core. Boric acid groups are further introduced as specific recognition units, forming specific dynamic covalent bonds with the catechol groups of anionic dyes. Compared with traditional adsorbents, the adsorbent of this invention provides ultra-high adsorption capacity and selectivity through the synergistic effect of multiple mechanisms, including electrostatic adsorption, coordination complexation, hydrogen bonding, and reversible covalent bonding of borate ester bonds. It can achieve efficient desorption of dyes and recycling of materials, and efficiently and rapidly remove anionic dyes from water.

The present invention provides means with which bile acids, phenols, indoles and organic acids contained in a sample can be stably preserved without cryopreservation of the sample. A sample preservation solution of the present invention is a sample preservation solution used for analyzing at least one component selected from the group consisting of bile acids, phenols, indoles and organic acids contained in a biological or environmental sample, containing at least the following (A) and (B): (A) condensed phosphate or polyoxyethylene sorbitan alkylate; and (B) guanidinium thiocyanate, Tris-HCl (pH 7 to 9), and EDTA.

This invention discloses a weather-resistant, high-hardness composite anti-corrosion coating and its preparation method, belonging to the field of anti-corrosion coating technology. The preparation method includes: firstly, synthesizing an epoxy resin containing dynamic disulfide bonds by reacting dithiodibenzoic acid and epichlorohydrin in an alkaline aqueous phase; secondly, constructing a low surface energy siloxane network using hydroxyl-terminated polydimethylsiloxane and methyltriethoxysilane; subsequently, introducing chlorzoxazone and N-acetyl-p-aminophenol as composite organic corrosion inhibitors, blending them with the resin to obtain a composite base material; finally, adding graphene, carbon nanotubes, and inorganic anti-corrosion fillers, and cross-linking and curing to form a film using a polyamine curing agent. This invention suppresses microcracks through the dynamic stress relief of disulfide bonds, combined with the weather-resistant barrier of the siloxane network, the active interface passivation of the heteroatom corrosion inhibitor, and the three-dimensional synergistic mechanical bonding of carbon-based nanomaterials, achieving a perfect unity of ultra-strong corrosion resistance, excellent weather resistance, and high mechanical hardness in the coating.

The present disclosure relates to solid state forms of Compound (1) freebase. The present disclosure also relates to processes for the preparation of the solid state forms, the pharmaceutical compositions comprising the forms, and the use thereof, e.g., in the treatment and prevention of disorders in which NLRP3 activity is implicated.

This invention relates to the field of energy conservation and consumption reduction in chemical plants, specifically to a method for the combined utilization of low-temperature waste heat from a CHPPO unit and a phenol-acetone unit. The method involves setting up multiple circulating branches connecting different heat sources and heat traps within the CHPPO and phenol-acetone units. The large amount of low-temperature waste heat generated by each heat source within the units is recovered and enriched through a heat transfer medium (water) for heating low-temperature materials within the units. This replaces the low-pressure steam originally required for heating the heat traps, improving the plant's energy efficiency and reducing energy consumption and heating costs in production. Based on the different operating conditions of the units at the initial and final stages, each heat exchange component of each branch is controlled and adjusted holistically, rationally planning and utilizing the low-temperature waste heat of each unit, reducing heat loss directly discharged into the environment, and achieving the overall goal of energy conservation, consumption reduction, cost reduction, and efficiency improvement in the production unit.

The invention is directed to a crosslinkable polyethylene composition comprising an additive composition consisting of polyethylene glycol and a mixture of 4,4′-thiobis (2-tertbutyl-5-methylphenol) plus thiodiethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate].

The application belongs to the field of organic synthesis, and discloses a method for preparing chiral 2-(1,3-diarylallyl)malonate by using a Pd / phosphine oxygen bidentate phosphine phenol ligand catalysis, which comprises the following steps: under a protective atmosphere, mixing P, O-bidentate phosphine phenol ligand, a palladium catalyst, N, O-bis(trimethylsilyl)acetamide, a malonate nucleophilic reagent and an allyl acetate electrophilic reagent in dichloromethane, and reacting to obtain chiral 2-(1,3-diarylallyl)malonate product. The system has the advantages of high enantioselectivity, high catalytic efficiency, wide substrate application range and mild conditions.

The application relates to the technical field of inks, and discloses a long-acting coagulation ink formula, a preparation method and application, the ink comprising a water-based polyurethane emulsion, pigments, a defoaming agent and a dispersing agent; the water-based polyurethane emulsion formula is polytetrahydrofuran glycol, glycerol monooleate, isophorone diisocyanate, a chain extender and a hindered phenol crosslinking agent; the hindered phenol crosslinking agent is prepared and introduced into a molecular chain segment of the water-based polyurethane binder, linear water-based polyurethane macromolecules are linked in the form of chemical bonds, a crosslinked network structure is formed, molecular chain movement is limited, aggregation is not easy, gel during storage can be reduced, and the hindered phenol is linked to the polyurethane molecular chain through chemical bonds, free radicals are captured by the hindered phenol groups, and the phenomenon of ink skinning, gelation and coagulation of the polyurethane ink caused by oxidation during storage and use is avoided; the ink has excellent stability, adhesion, skinning resistance, rubbing resistance and alcohol resistance.

Provided is a synthesis method for azoxystrobin, comprising: in a water-oil system of an organic solvent and an aqueous solution of trimethylamine, a compound represented by formula I reacts with 2-cyanophenol to obtain azoxystrobin, wherein the molar ratio of the compound represented by formula I to trimethylamine is 1:(0.96-2). The synthesis method has high reaction efficiency, does not produce CO2, avoids the risks of entrainment and overflow, reduces the generation of side reactions and solid waste emissions and is environmentally friendly. In addition, the method does not require the use of solid sodium carbonate or potassium carbonate, and the material reaction system is an oil-water reaction system, so that the reaction efficiency is greatly improved, and the yield can also be maintained at 95% or more, thereby taking both the efficiency (timeliness) and the yield into account and easily achieving continuous reaction, and thus providing technical support for intelligent and unmanned production. Moreover, since trimethylamine can be recycled, the use of one raw material is reduced, and further there is no need for complicated treatment for mixed salts and waste water thereof, thereby significantly reducing the energy consumption.

The present application relates to a kind of catalyst and its preparation method, the refining method of aniline, wherein the catalyst includes core and shell, the core includes acidic microporous-mesoporous composite molecular sieve and metal oxide loaded on the molecular sieve, the shell includes hydrophobic porous carrier layer and metal element loaded on the porous carrier layer.The catalyst of the present application can promote the conversion of cyclohexylamine and phenol in aniline into macromolecule, high-boiling substance, which can be quickly removed by simple rectification subsequently, finally realizing the synchronous efficient removal of phenol and cyclohexylamine, significantly improving the quality of aniline, while reducing the energy consumption of refining system and aniline loss, and no new impurities are introduced throughout.

This invention provides a biomass-derived phenol composition with suppressed acidic odor. [Solution] A phenol composition containing biomass-derived phenol (A), wherein the peak height percentage corresponding to propionic acid in total ion chromatography by GC-MS after pretreatment by 150°C headspace method is 0.35% or less.

The application discloses a silane-modified antioxidant with anti-precipitation and anti-migration, a preparation method and application thereof, and belongs to the technical field of polyethylene pipe materials. The antioxidant is obtained by optimizing and modifying a composite antioxidant, and three different types of antioxidants, namely, hindered phenol, aromatic amine and tocopherol, are chemically bonded to a molecular skeleton to form a composite and multi-mechanism antioxidant active end, so that the antioxidant has the advantages of excellent migration resistance and precipitation resistance, and the durability of the antioxidant is ensured. In addition, the modified antioxidant is applied to the preparation of a silane cross-linked polyethylene pipe material, has better compatibility, and is firmly fixed in a polymer network through covalent bond anchoring, so that the antioxidant molecule provides stable, durable and reliable antioxidant protection for the pipe material, the service life of the pipe material is greatly prolonged, and the total cost of replacement and maintenance is reduced.

This disclosure provides a method for preparing sulfidated alkylphenol salt products to achieve a high sulfidation ratio of sulfidated alkylphenol salt to unsulfidated alkylphenol salt / phenol in the context of neutralization and optional over-alkaliening additives. The sulfidated alkylphenol salt products are obtained by sulfidating alkylphenols with a sulfur chloride blend comprising about 40% to about 75% by weight of sulfur dichloride.

This invention discloses a cashew nut shell bisphenol and its preparation method and application. The preparation method of the bisphenol is as follows: First, cashew nut shell phenol, formaldehyde, and an alkaline catalyst are mixed and stirred evenly, and reacted at a certain temperature to obtain hydroxymethylated product A; product A is washed with water several times until the pH is neutral, and then centrifuged to remove water to obtain product B; product B is mixed with phenol and an acidic catalyst and stirred evenly, and reacted at a certain temperature to obtain product C after the phenol-alcohol reaction; product C is washed with water until neutral, and then distilled under reduced pressure to obtain the cashew nut shell bisphenol product. This invention utilizes the structural characteristics of cashew nut shell phenol, which has both a benzene ring and an alkane chain, to obtain a bisphenol structure that combines the rigidity of the benzene ring with the toughness of the long alkane chain on cashew nut shell phenol, while protecting the highly reactive phenolic hydroxyl group. Moreover, this bisphenol is green and low in toxicity, meeting the requirements of environmental protection and sustainable development. The epoxy coating prepared using this bisphenol has high crosslinking density, good corrosion resistance, and excellent mechanical properties.

This invention discloses a polyolefin-containing DCPD epoxy resin and a copper-clad laminate composition thereof, and its preparation method. The method is characterized by: polymerizing polyallyl phenol and catalyst A at high temperature to form polyallyl phenol; then reacting DCPD, polyallyl phenol, and catalyst B at high temperature to form a polyolefin-containing DCPD phenol resin; subsequently, epoxidizing the resin with epichlorohydrin and alkaline catalyst C to synthesize a polyolefin-containing DCPD epoxy resin; finally, mixing the resin with maleimide resin, phosphorus-containing phenolic resin, imidazole accelerator, inorganic filler, and solvent to obtain the polyolefin-containing DCPD epoxy resin composition for copper-clad laminates. The polyolefin-containing DCPD epoxy resin and copper-clad laminate composition prepared by this invention exhibits low dielectric constant, low dielectric loss, and high heat resistance, making it particularly suitable as a raw material for copper-clad laminates and highly practical.

The application discloses a high-elongation-strength anti-fatigue TPU blended material and a preparation method thereof, and relates to the field of polymer materials. In the preparation of the high-elongation-strength anti-fatigue TPU blended material, phosphorus chloride is reacted with 4'-vinyl-[1,1'-biphenyl]-4-alcohol and p-phenylphenol to obtain a phosphite antioxidant; nano-silicon dioxide is sequentially reacted with trimethoxysilane and the phosphite antioxidant to obtain modified silicon dioxide; a modified polyurethane elastomer is prepared by reacting hydroxyl-terminated polysiloxane, 1,4-butanediol, isophorone diisocyanate and adipic dihydrazide; polyether amide elastomer and the modified polyurethane elastomer are mixed, mixed with a compatilizer, modified silicon dioxide and antioxidant 1010, dried, mechanically mixed, and melt-blended to obtain the high-elongation-strength anti-fatigue TPU blended material. The high-elongation-strength anti-fatigue TPU blended material prepared by the application has the abilities of self-repairing, durability and flame resistance.

The application relates to the field of organic chemistry, in particular to a method for photocatalytic synthesis of silanol or silyl ether. The application provides a method for photocatalytic synthesis of silanol or silyl ether compound, in which, under the condition of existence of an iridium catalyst and an organic solvent, hydrosilane is reacted with any one of water, alcohol or phenol under light to obtain silanol or silyl ether. The synthesis method has high yield and selectivity, low catalyst consumption, mild reaction condition and high environmental protection and efficiency.

There is provided a resin composition including a resin having an alkyl group on a side chain of a molecule thereof, an inorganic filler and an antioxidant, wherein the antioxidant is either of a hydrazide-based antioxidant or a combination of a hindered phenol-based antioxidant and an organic metal chelate-based antioxidant.

A method for increasing the BEMT content in a composition comprising 2,4-bis[4-(2-ethylhexyloxy)-2-hydroxyphenol]-6-(4-methoxyphenol)-1,3,5-triazine (BEMT), the method comprising the steps of: a) providing a composition comprising BEMT and impurities; b) dissolving the composition in a solvent mixture at a first dissolution temperature to produce an unsaturated BEMT solution, wherein the solvent mixture comprises at least one polar solvent; c) lowering the temperature of the unsaturated BEMT solution to a saturation temperature, wherein the saturation temperature is below the first dissolution temperature, to produce a saturated BEMT solution; d) further lowering the temperature of the first saturated BEMT solution to a first crystallization temperature, wherein the first crystallization temperature is below the saturation temperature, thereby producing a supersaturated BEMT solution; e) during step d), adding BEMT seed crystals in an amount ranging from 0.00001 wt.-% to 20 wt.-% relative to the total weight of the composition to the supersaturated BEMT solution to produce a first BEMT suspension comprising BEMT particles; f) a) Heating the first BEMT suspension to a second dissolution temperature to produce a second BEMT suspension containing fewer BEMT particles than the first BEMT suspension, wherein the second dissolution temperature is higher than and lower than the first crystallization temperature; g) Cooling the second BEMT suspension to a second crystallization temperature to produce a final BEMT suspension containing BEMT particles larger than those in the first BEMT suspension; h) Separating these BEMT particles from the final BEMT suspension, wherein the second crystallization temperature is lower than the first crystallization temperature.

The present invention aims to provide a polyphenylene ether having excellent solubility in a general-purpose ketone-based solvent and a production method thereof. It also aims to provide a thermosetting composition, a prepreg, and a laminate each using the polyphenylene ether. The polyphenylene ether of the present invention is characterized by containing 5 to 85 mol% of repeating units derived from a phenol of formula (1) and 15 to 95 mol% of repeating units derived from a phenol of formula (2) relative to 100 mol% of the total of the repeating units derived from the phenol of formula (1) and the repeating units derived from the phenol of formula (2), and having a specific viscosity (ηsp / c) of 0.03 to 0.30 dL / g measured in a 0.5 g / dL concentration chloroform solution at 30°C.

Nanocomposites comprising nanoparticles, small molecules, and block copolymer (BCP)-based supramolecules are provided. The nanoparticles, small molecules, and BCP-based supramolecules self-assemble into a plurality of nanosheets that form a multilayer nanocomposite. The nanoparticles, small molecules, and BCP-based supramolecules can be Zr02, 3-pentadecylphenol (PDP), polystyrene-b-poly(4-vinylpyridine) block copolymer (PDP) 1, respectively. b A method of producing a nanocomposite by contacting nanoparticles, small molecules, and BCP-based supramolecules with a solvent and drying to remove the solvent to allow self-assembly is also provided. The nanocomposites provided herein can be used as a barrier material against volatile organic compounds, water, oxygen, or electrons, and can be used as a coating on various substrates and as a packaging material, or as an optical material.

The application discloses an acid-resistant non-noble metal catalyst and a preparation method and application thereof, and particularly relates to the field of acid-resistant metal catalysts, and the preparation method of the acid-resistant non-noble metal catalyst comprises the following steps: step 1, preparation of a carrier; step 2, modification of the carrier; step 3, preparation of an impregnation solution; step 4, preparation of an unactivated catalyst; step 5, activation of the catalyst; and step 6, functionalization of the catalyst. The acid-resistant non-noble metal catalyst prepared by the application can be applied to the synthesis of p-aminophenol from nitrobenzene. The catalyst has good acid resistance and stability, and when applied to the process of preparing p-aminophenol by rearrangement of nitrobenzene hydrogenation, the catalyst has high activity and high selectivity of p-aminophenol under relatively mild reaction conditions, the production conditions are improved, the production cost is reduced, and the product quality is improved.

The purpose of the present invention is to provide a production method with which it is possible to obtain a low-viscosity polyphenylene ether while controlling the reaction activity during polyphenylene ether production.　In order to solve the aforementioned problem, the present invention is characterized by comprising a step for introducing an oxygen-containing gas into a solution that contains a phenol represented by formula (1) and a phenol represented by formula (2) and performing oxidative polymerization, the moisture content of the oxygen-containing gas being 0.2-50 mg / L, and the reduced viscosity (ηsp / c) of the resulting polyphenylene ether measured by using a chloroform solution having a concentration of 0.5 g / dL at 30°C being 0.03-0.30 dL / g.

This invention relates to the field of polymer materials technology, specifically disclosing a high-adhesion, low-stress, room-temperature curing epoxy potting compound and its application. The high-adhesion, low-stress, room-temperature curing epoxy potting compound is composed of component A and component B; component A includes 100 parts by weight of epoxy resin and 50-200 parts by weight of filler; the filler is composed of D... 50 Spherical silicon with a particle size of 20-35 μm and D 50 The invention is formulated with aluminum hydroxide with a particle size ≤2μm; component B includes 30-45 parts by weight of an amine curing agent and 0.5-5 parts by weight of an accelerator; the amine curing agent is a compound of polyetheramine and 3,3'-dimethyl-4,4'-diaminodicyclohexylmethane; the accelerator is a compound of 2,4,6-tris(dimethylaminomethyl)phenol and salicylic acid. This invention can be cured at room temperature, avoiding the energy consumption and damage to heat-sensitive components caused by high-temperature curing, significantly improving production efficiency and reducing production costs.