43 results about "Carbon Chloride" patented technology

The invention relates to a method for continuously producing 1, 1, 1, 3-tetrachloropropane, which comprises the following steps: adopting a loop reactor in which a beam pipe is arranged in the reactor, mixing reaction raw materials ethylene and carbon tetrachloride at a Venturi nozzle at the lower part of the reactor through a gas circulation loop and a liquid circulation loop outside the reactor, and spraying into the reactor filled with a main catalyst. A cocatalyst and a chelating agent are added into a carbon tetrachloride raw material in advance, are pumped into a liquid loop by a feeding pump and then enter a reactor. Reaction raw materials are circularly stirred under the action of a beam pipe in the reactor, so that solid, liquid and gas phases are fully mixed. By adopting the method disclosed by the invention, the selectivity and the production efficiency of the 1, 1, 1, 3-tetrachloropropane can be greatly improved, and the method also has the advantages of simplicity in operation, environment friendliness, long service life of the catalyst and low cost.

The invention relates to a preparation method of a hydrophobic manganese-based low-temperature denitration catalyst. According to the catalyst, a composite oxide of CeO2 and MnO2 is used as an active component, and polyacrylonitrile submicron fibers are used as a carrier; a mixed solution of carbon tetrachloride and gamma-aminopropyltriethoxysilane is used as a hydrothermal solution substrate, a mixed solution of ethyl acetate and gamma-aminopropyltriethoxysilane is used as a hydrothermal solution supernatant, and a hydrothermal-electrostatic spinning method is adopted for preparation; on the basis of the mass of the polyacrylonitrile submicron fiber carrier, the mass percentage of the active component is 10-20%, and the mass ratio of CeO2 to MnO2 in the active component is 1: (1-2). The catalyst not only can be used for catalytically reducing NO into N2 at low temperature, but also can be used for filtering particles in flue gas, has excellent water and sulfur poisoning resistance, and has relatively high economic value and wide market application prospect.

The invention relates to the technical field of chemical recovery, and particularly discloses a carbon tetrachloride removal system and process, the system comprises a washing tower and a carbon tetrachloride removal assembly, the washing tower is used for introducing a solvent and a phosgene material; the tower top of the washing tower is used for outputting treated substances; a tower kettle of the washing tower is communicated with the carbon tetrachloride removal assembly, and the carbon tetrachloride removal assembly is used for removing carbon tetrachloride in materials from the washing tower. The solvent is introduced into the washing tower to wash the phosgene material, and after the solvent is introduced, the washing tower is not pure phosgene equipment, so that the safety performance is improved; and compared with the prior art that carbon tetrachloride is removed by utilizing a phosgene rectifying tower and a solvent refining tower, the combination of the washing tower and the carbon tetrachloride removal assembly is beneficial to reducing the energy consumption.

The invention relates to a preparation method of 1, 1, 1, 3, 3-pentachloropropane and a catalyst, in the presence of a loaded zero-valent bimetallic nanoparticle catalyst and a cocatalyst, carbon tetrachloride and vinyl chloride are subjected to an addition reaction to obtain 1, 1, 1, 3, 3-pentachloropropane, the zero-valent bimetallic nanoparticle loaded catalyst comprises a carrier and an active component loaded on the carrier; the active component is prepared from zero-valent Pd-Fe nano particles or Cu-Fe nano particles; the cocatalyst comprises boric acid ester or acetyl citrate. The preparation method of 1, 1, 1, 3, 3-pentachloropropane can effectively avoid easy agglomeration when only Fe powder is used as a catalyst, the specific surface area of the iron powder is increased, the reaction is promoted, meanwhile, the used cocatalyst is a nitrogen-free and phosphorus-free catalyst, emission of three wastes containing nitrogen and phosphorus is avoided, and the preparation method is environment-friendly.

The invention discloses a metal powder injection molding process based on a thermal degreasing adhesive, and belongs to the technical field of metal powder metallurgy molding, and the metal powder injection molding process comprises the following steps: weighing raw materials, preheating and activating to obtain a premixture, melting and mixing to obtain an adhesive, extruding and granulating, obtaining feeding particles, carrying out injection molding to obtain a product green body, sintering and thermally degreasing, and cooling. A pure thermal degreasing process is adopted, dangerous chemical reagents such as nitric acid and oxalic acid do not need to be used, solvents such as n-pentane and carbon tetrachloride do not need to be depended on, in actual production, potential safety hazards in the production link can be greatly reduced, damage to the ecological environment is reduced, meanwhile, the body health of operators is guaranteed, and the production cost is reduced. The core requirements of modern industry on safe and environment-friendly production are met.

The present application discloses a full-process continuous process for synthesizing 1,1,1,3,3-pentafluoropropane, including a telomerization reaction: vinyl chloride, carbon tetrachloride, catalyst 1 and a cocatalyst are added to a pre-reactor mixer for premixing to obtain mixture 1, mixture 1 is pumped into a reactor system for telomerization reaction to obtain the material of the telomerization reaction, the material of the telomerization reaction is continuously pumped out and separated to obtain R240fa, and the separated vinyl chloride, carbon tetrachloride, catalyst 1, cocatalyst and unseparated R240fa are returned to the pre-reactor mixer for continuous reaction; a fluorination reaction: the R240fa, chlorine gas and anhydrous hydrogen fluoride obtained from the telomerization reaction are continuously introduced into a fluorination reaction kettle containing activated catalyst 2 for fluorination reaction to obtain a fluorination reaction product, the fluorination reaction product is separated to obtain 1,1,1,3,3-pentafluoropropane, and the remaining product after separating 1,1,1,3,3-pentafluoropropane is returned to the fluorination reaction kettle for continuous reaction.

The application discloses a preparation method and application of a catalyst for cracking 1,2-dichloroethane to produce vinyl chloride, and comprises the following steps: 1) a neodymium ore is leached with hydrochloric acid, and after filtering a leaching solution, potassium chloride is added to form a doped precursor K2[NdCl3]; 2) an active metal oxide is dissolved in hydrochloric acid, and then added into the doped precursor K2[NdCl3] solution, and co-precipitation is carried out by adding alkali to obtain an emulsion of a doped active component; the active metal oxide is at least one of oxides of vanadium, manganese, titanium and scandium; 3) the emulsion of the doped active component is mixed with a liquid carrier to obtain the catalyst; the liquid carrier is one or more of chloroform, carbon tetrachloride, 1,1,2-trichloroethane and chlorobenzene.

This invention discloses an apparatus for producing hydrogen chloride from carbon tetrachloride, belonging to the field of hydrogen chloride process technology. It aims to solve the problem in existing technologies where the reaction of carbon tetrachloride with water produces toxic phosgene if too little water is used, and hydrogen chloride and carbon dioxide gases are produced if too much water is used. Since the boiling points of these two gases are very close at atmospheric pressure, separation is difficult. The apparatus includes a carbon tetrachloride storage tank and a pure water tank, each equipped with a heater. A first valve is installed on the carbon tetrachloride storage tank, and a second valve is installed on the pure water tank. The carbon tetrachloride storage tank is connected to a first heat exchanger, which is connected to a first gas pump. The pure water tank is connected to a second heat exchanger, which is connected to a second gas pump. The second and first gas pumps are connected to a mixing mechanism, which is connected to a tubular hydrolysis reactor. A concentrated sulfuric acid contact tower is connected to the tubular hydrolysis reactor.

The present invention discloses a method for reducing dechlorinated chlorohydrocarbons by coupling a compound surfactant with a sulfide micron zero-valent iron system, and belongs to the technical field of in-situ chemical remediation of water bodies. The present invention uses a compound surfactant HTAB and Tween80 coupled with a sulfide micron zero-valent iron material as a reducing agent to reduce chlorinated hydrocarbons in water bodies. Under the effective regulation of the compound surfactant, the sulfide micron zero-valent iron is promoted to efficiently reduce carbon tetrachloride. The compound surfactant coupled with the sulfide micron zero-valent iron is superior in reusability to the HTAB coupled with the sulfide micron zero-valent iron system, and has a higher removal rate for chlorinated hydrocarbons (carbon tetrachloride). The surfactant compound system reduces the amount and cost of the cationic surfactant HTAB without causing secondary pollution to the environment. In addition, the method provided by the present invention has a simple preparation process, a fast reaction rate, a strong ability to remove a variety of chlorinated hydrocarbon pollutants, a wide applicable pH range, and is more suitable for practical applications.

The present invention provides an iron-carbon nanocomposite and a preparation method and application thereof. The preparation method comprises dissolving ferrous salt and aldose in an ethanol aqueous solution at a molar ratio of 1‑5:1‑10 to form a reactant solution, performing a hydrothermal reaction or a microwave heating reaction, and carbonizing to obtain the iron-carbon nanocomposite. The present invention also provides an iron-carbon nanocomposite obtained by the above preparation method. The present invention also provides the application of the above iron-carbon nanocomposite in treating halogenated hydrocarbon pollution. The preparation process of the iron-carbon nanocomposite provided by the present invention is simple, the raw materials used are cheap and easily available, and halogenated hydrocarbon organic pollutants such as carbon tetrachloride and trichloroethylene can be effectively removed from groundwater.

The invention relates to a continuous production method of carbon tetrachloride, which comprises the following steps: mixing and vaporizing perchlorinated hydrocarbon and chlorine, and carrying out chlorination reaction at the temperature of 200-500 DEG C under the pressure of 0.6-1 MPa to obtain a crude product; performing gas-liquid separation on the crude product, returning the gas to the mixed vaporization step for recycling, and rectifying the liquid to obtain a carbon tetrachloride product; and returning other products obtained by rectification to the mixed vaporization step for recycling. In the production process, the raw materials are perchloro and chlorine, no hydrogen element participates in the production process, the required temperature and pressure conditions are relatively low, the reaction conforms to the concept of green chemistry, and the utilization rate of chlorine atoms in the whole process is 95% or above.

The invention provides a viscosity reducer as well as a preparation method and application thereof. The invention provides a viscosity reducer which comprises the following raw materials in parts by weight: 10-50 parts of a non-polar component A, 10-60 parts of a polar component B and 30-50 parts of a surfactant C, the non-polar component A is selected from one or more of octane, petroleum ether, dotridecane, octacosane, carbon disulfide, carbon tetrachloride, ethane, cyclohexane, liquid paraffin, ethyl acetate and diethylene glycol monobutyl ether; the polar component B is prepared by reaction of styrene, maleic anhydride and acrylate; the surfactant C is prepared by reacting the polar component B, organic acid and polyamine. According to the viscosity reducer for the oil-based drilling fluid, provided by the invention, the viscosity and the shearing force of the oil-based drilling fluid can be remarkably reduced, the flowability of the oil-based drilling fluid is improved, and particularly, the viscosity and the shearing force of the polluted oil-based drilling fluid can be reduced.

The present application relates to stearic acid processing technical field, especially to a kind of stearic acid melting kettle with monitoring function, including kettle body, heating cavity is set in the inside of kettle body, heat-insulating cover is installed in the upper end of kettle body, heat-conducting block is embedded in the inner wall of kettle body, the heat transfer mechanism for heating is equipped in the bottom of kettle body, the outer wall of kettle body is equipped with the energy supply mechanism for heating and improving heating efficiency, the inside of kettle body is equipped with the mixing mechanism for improving melting speed and impurity removal mechanism.The advantages are that heating carbon tetrachloride will be vaporized, and carbon tetrachloride rising in bubble state will diffuse into upper water flow, so that the temperature of water flow is improved, and the bubble diffuses, the overall heat conduction is more uniform and fast, so that the melting of stearic acid is more unified and efficient, and the water temperature is lower, after heat transfer, the rising carbon tetrachloride is condensed, so as to sink after recovering liquid, so as to facilitate subsequent circulation diffusion heat exchange.

The invention belongs to the technical field of conversion process monitoring, and provides an on-line monitoring method for conversion of hydrochloric acid from carbon tetrachloride, which comprises the following steps: acquiring historical data of a conversion process in a steady state and operation under various preset abnormal working conditions, and constructing time sequence data including trichloromethane concentration and process parameters and a corresponding state label historical data set; performing statistical feature extraction on the historical data set, and establishing a correlation model between the statistical features of the trichloromethane concentration and the process parameter state based on a machine learning algorithm; the method comprises the following steps: detecting the concentration of trichloromethane in a reactor outlet product in real time through an online analysis instrument, calculating the real-time statistical characteristic of the real-time trichloromethane concentration as the input of a correlation model, and comparing the output process parameter monitoring combination with the currently activated process parameters to generate a control instruction. By monitoring a key reaction intermediate (trichloromethane), the number of monitored process parameters is optimized, and the preposition of abnormal early warning can also be realized.

A kind of urban sludge-containing sewage comprehensive treatment method and treatment system, solve the problems of low-cost high-efficiency sludge dewatering and sewage treatment, the treatment method is: sludge-containing sewage is stirred, mixed, precipitated with carbon tetrachloride liquid in displacement reaction tank, and forms water layer and carbon tetrachloride liquid and sludge mixed layer, overflowed water, carbon tetrachloride and sludge vaporization separation to remove organic water and dry sludge, carbon tetrachloride recycling is used.The treatment system scheme is: the system includes: displacement dewatering and organic matter processing part consisting of displacement reaction tank, water treatment part consisting of water intermediate tank and adsorption tower and displacement agent condensing tower consisting of displacement agent recovery part and heating station part.The beneficial effects of the present application are: simple process, safe and reliable, the treatment efficiency is increased by more than 10 times, the cost is reduced by 85%, the moisture content of sludge displacement dewatering is less than 5%, sludge displacement dewatering and sewage organic matter inactivation treatment are completed at the same time.

The invention is applicable to the technical field of gas detection, and provides a method and a system for detecting the carbon tetrachloride value of activated carbon, the system comprises a pretreatment module, a temperature and flow control module, a carbon tetrachloride bubbling module, two infrared detection modules and an activated carbon adsorption module, and the acquisition module is used for acquiring the concentration data of the carbon tetrachloride gas in the mixed gas before and after entering the activated carbon adsorption module, obtaining the adsorption efficiency of the activated carbon and obtaining the carbon tetrachloride value of the activated carbon based on the adsorption efficiency. The method has the advantage that the characteristic absorption peak of the carbon tetrachloride in the infrared spectrum can be accurately captured. By acquiring the concentration change of the carbon tetrachloride gas before and after the carbon tetrachloride gas is adsorbed by the activated carbon sample, the instrument can efficiently and accurately characterize the CTC value of the activated carbon. Compared with a traditional national standard weighing method, the method provided by the system has the advantages that the detection efficiency is remarkably improved, the operation process is simplified, and the measurement precision is improved.

The invention discloses a device for accurately controlling feeding of trace gas-phase carbon tetrachloride. The device comprises a constant-flux pump, a micro-channel evaporator, a constant-temperature unit and a CCl4 storage tank, the CCl4 storage tank is connected with the constant-flux pump through a pipeline, the constant-flux pump is connected with the micro-channel evaporator through a pipeline, and the constant-temperature unit is connected with the micro-channel evaporator through a pipeline to form a loop. Comprising the following steps: S1, setting the temperature of a constant temperature unit to be 90-120 DEG C, and starting the constant temperature unit; s2, the first valve and the third valve are in a closed state, and the second valve is in an open state; s3, setting the temperature of the first heating belt, the second heating belt, the third heating belt and the fourth heating belt to be 90-120 DEG C, and turning on a power supply of the heating belts; s4, the liquid level height of the CCl4 storage tank is checked and recorded; s5, when the actual temperature of the constant-temperature unit and the heating belt reaches the set temperature value, the flow of the constant-flux pump is set to be 0-20 mL / h, and the constant-flux pump and a third valve are opened; and S6, the constant-flux pump, the first heating belt and the second heating belt are sequentially closed, and the second valve is closed.

This invention discloses a method and system for determining volatile halogenated hydrocarbons in dissolved gases of seawater, belonging to the field of analytical chemistry. The method employs direct gas injection combined with a six-way valve switching injection system, enabling the direct and simultaneous determination of seven volatile halogenated hydrocarbons in seawater: chloroform, carbon tetrachloride, trichloroethylene, bromodichloromethane, tetrachloroethylene, dibromochloromethane, and tribromomethane. This eliminates the need for organic solvents and complex pretreatment, filling a technological gap in this field. Validation shows a detection limit of 0.1–1.1 nmol / mol, a retention time RSD ≤ 0.20%, a concentration RSD ≤ 4.93%, and a relative error between -2.01% and 1.56%. The method exhibits advantages such as high sensitivity, good stability, simple operation, and environmental friendliness, and can be directly applied to fields such as marine environmental monitoring and seabed oil and gas resource exploration.

The invention relates to the technical field of nylon 6 and discloses a carbon nanotube grafted ABS modified nylon 6 composite material. Acylation reaction occurs between chlorinated carbon nanotubes and lysine, double bonds on ABS are combined with double bonds on maleic anhydride, anhydride modified ABS and amino modified carbon nanotubes undergo ring-opening reaction, carbon nanotubes are grafted onto ABS to avoid agglomeration of the carbon nanotubes, and when subjected to external force, the carbon nanotubes can form a uniform network structure, absorb a large amount of external force, and improve the toughness of a matrix. A large amount of carboxyl groups introduced into the surface of ABS plastic react with amide groups in a nylon 6 matrix to form a three-dimensional hydrogen bond network, thereby improving the compatibility and interface force between nylon 6 and carbon nanotube grafted ABS, enabling more uniform distribution and forming an island structure. When subjected to external force, more stress can be buffered, and the obtained composite material has excellent toughness.

The application discloses lattice copper and carbon vacancy co-modified zero-valent iron and a preparation method and application thereof in catalyzing dechlorination of carbon tetrachloride in water, and belongs to the technical field of functional catalysts and underground water pollution remediation. The application solves the technical problem of slow and incomplete dechlorination caused by inherent electron competition between carbon tetrachloride and water. Based on an in-situ sacrifice strategy of the iron oxide layer, the application utilizes consumption of the surface iron oxide layer, oxygen volatilization and carbon reduction in a high-temperature ball milling process to induce formation of carbon vacancies, promote lattice doping of copper in the core of the zero-valent iron, promote outward release of iron and inward migration of copper (lattice doping), and prepare the lattice copper and carbon vacancy co-modified zero-valent iron catalyst with a symbiotic structure. The catalyst can realize rapid and complete dechlorination of carbon tetrachloride, the product is a chlorine-free product (methane, carbon monoxide and formic acid), the product recovery rate is greater than 80%, and the dechlorination reaction can occur in a wide pH environment.

The invention provides a high-temperature-resistant PVC tile and a preparation method thereof, and belongs to the field of PVC materials, the high-temperature-resistant PVC tile is prepared from the following raw material components: 100 parts of PVC resin, 35-45 parts of calcium carbonate, 14-16 parts of a reinforcing agent, 2-3 parts of a plasticizer, 1-3 parts of a cross-linking agent, 0.5-1.5 parts of carbon black, 0.5-2 parts of zinc oxide and 0.4-0.6 part of an antioxidant, and then loading an acylating chlorination carbon nanotube on the surface. Through a unique formula and a preparation process, the heat stability of the PVC tile can be remarkably improved, the influence of high temperature on the performance of the material is effectively resisted, meanwhile, the binding force between the filler and a matrix is enhanced, the uniform dispersion capacity between the materials is improved, and it is guaranteed that the material has high mechanical strength under the condition of high filler content.

The invention discloses lattice copper and carbon vacancy co-modified zero-valent iron as well as a preparation method and application thereof in catalysis of dechlorination of carbon tetrachloride in a water body, and belongs to the technical field of functional catalysts and underground water pollution remediation thereof. According to the invention, the technical problem of slow and incomplete dechlorination caused by inherent electron competition between carbon tetrachloride and water in the prior art is solved. On the basis of an iron oxide layer in-situ sacrifice strategy, carbon vacancy formation is induced through consumption of a surface iron oxide layer, oxygen volatilization and carbon reduction in the high-temperature ball milling process, lattice doping of copper in a zero-valent iron core is promoted, outward release of iron and inward migration (lattice doping) of copper are promoted, and therefore the copper-containing zero-valent iron composite material is obtained. The lattice copper and carbon vacancy co-modified zero-valent iron catalyst with a symbiotic structure is prepared. The catalyst can realize rapid and complete dechlorination of carbon tetrachloride, the product is a chlorine-free product (methane, carbon monoxide and formic acid), the product recovery rate is greater than 80%, and the dechlorination reaction can be carried out in a wide pH environment.

The invention discloses an iron powder water purifying agent and a preparation method thereof, and the iron powder water purifying agent comprises the following components in parts by weight: 2.7 to 3.5 parts of dodecyl acrylate, 9.8 to 11.0 parts of dibenzoyl peroxide, and 0.23 to 0.35 part of hydrophobic association cationic PDMC flocculant. According to the iron powder water purifying agent and the preparation method thereof disclosed by the invention, the water purifying agent prepared by the method can repeatedly remove impurities entrained in sewage, can realize rapid sedimentation of the impurities and oil stains in the water, and can be separated from the impurities to form a relatively large flocculating constituent, so that rapid sedimentation can be realized; compared with the prior art, the device has the advantages that the treatment efficiency of pollutants difficult to degrade can be effectively improved, separated impurities can be conveniently recycled, the impurities cannot be damaged, the saturated oil absorption rate of carbon pentachloride is high, and the device can be used under severe conditions.

The invention provides a method for detecting the content of trichloromethane and carbon tetrachloride in a water body, which comprises the following steps: S1, pretreatment: collecting a to-be-detected water sample, placing the collected to-be-detected water sample in a headspace bottle, enabling the headspace bottle to enter a headspace automatic sampler, and heating at 60-70 DEG C for 15-25 minutes; s2, detecting and analyzing the water sample to be detected by using a gas chromatography-mass spectrometry analyzer; s3, substituting the obtained detection result into the standard curve to determine the content of trichloromethane and carbon tetrachloride in the water sample to be detected; a standard curve is drawn as follows: step 1, N, N-dimethylformamide and water are taken as diluents, trichloromethane and a carbon tetrachloride standard mother solution are diluted, and a standard use solution is obtained; respectively preparing standard working solutions with different concentrations by using the standard use solutions; and 2, detecting and analyzing the standard working solutions with different concentrations according to the sequence of S1 and S2, and drawing a standard curve according to obtained detection results. The method can realize accurate determination of trichloromethane and carbon tetrachloride in a water sample, and has a good application prospect.

This invention belongs to the field of organic synthesis technology, specifically relating to a method for preparing 1,1,3,3,3-pentafluoropropylene. This invention designs a perovskite-type catalyst doped with noble metals or synergistically constructs a supported metal catalyst. Through a collaborative mechanism where the support provides strong Lewis acidity and fluorination activity, while the noble metal provides dehydrogenation activity, the interfacial interactions and reaction matching of the catalytic system are precisely controlled. This allows for highly efficient catalysis of the integrated "telomerization-fluorination-dehydrogenation" reaction of vinyl chloride (CHCl=CH2), carbon tetrachloride (CCl4), and hydrogen fluoride (HF). The reaction can be carried out continuously in the same reactor and with the same synergistic catalyst system, without the need to change equipment or catalysts, resulting in outstanding production efficiency. Furthermore, the selectivity and controllability of the reaction conditions are significantly optimized, enabling high-selectivity and high-yield synthesis of the target product under mild conditions. Simultaneously, it achieves the resource utilization of industrial waste carbon tetrachloride, representing a major technological breakthrough in terms of raw material cost, process simplification, and environmental friendliness.

The utility model relates to the field of activated carbon activity testing, in particular to an activity testing device for carbon tetrachloride activated carbon, which comprises an air compressor, a waste gas tank, a first support, a second support and a carbon tetrachloride saturator. The carbon tetrachloride saturator comprises a water bath box and a mixing barrel, the mixing barrel is filled with carbon tetrachloride liquid, the water bath box heats the mixing barrel in a water bath mode, so that the carbon tetrachloride liquid in the mixing barrel is converted into gas to be mixed with the treated air, and the mixed air is heated through the water bath box. The top of the activated carbon sample plate is suspended at the bottom of the spring scale through the connecting belt, the spring scale can monitor the mass of the activated carbon sample plate in real time and display the mass on the display screen, the activated carbon sample plate does not need to be taken out for weighing, and the operation is more convenient and faster.

The application provides a viscosity reducer and a preparation method and application thereof. The application provides a viscosity reducer, which comprises the following raw materials in weight components: 10-50 parts of non-polar component A, 10-60 parts of polar component B and 30-50 parts of surfactant C; the non-polar component A is selected from one or more of octane, petroleum ether, dotriacontane, octacosane, carbon disulfide, carbon tetrachloride, ethane, cyclohexane, liquid paraffin, ethyl acetate and diethylene glycol butyl ether; the polar component B is prepared by the reaction of styrene, maleic anhydride and acrylate; and the surfactant C is prepared by the reaction of the polar component B, an organic acid and a polyamine. The viscosity reducer provided by the application can significantly reduce the viscosity and shear force of the oil-based drilling fluid, improve the flowability of the oil-based drilling fluid, and especially reduce the viscosity and shear force of the oil-based drilling fluid after pollution.

The invention belongs to the technical field of carbon dioxide adsorption separation materials, and particularly discloses a zeolite molecular sieve for adsorbing and separating carbon dioxide and a preparation method thereof. The method is used for solving the problem of how to improve the adsorption selectivity of the 5A zeolite molecular sieve on carbon dioxide. Comprising the following steps: adding 5-phosphonovaleric acid or 4-aminobutylphosphonic acid into a carbon tetrachloride solvent, then adding a 5A zeolite molecular sieve, and stirring, with the ratio of the organic phosphonic acid to the 5A zeolite molecular sieve being 0.0053-0.53 mmol: 1 g and the ratio of the carbon tetrachloride solvent to the 5A zeolite molecular sieve being 150-250 mL: 1 g; carrying out centrifugal separation, removing an upper solution, carrying out heat treatment, cooling to room temperature, and washing with a carbon tetrachloride solvent for multiple times; and finally, carrying out vacuum drying to prepare the surface modified 5A zeolite molecular sieve. The method is beneficial to improving the adsorption kinetic selectivity of carbon dioxide in propylene and propane gas.

The invention discloses a preparation method of dichloromolybdenum dioxide. The preparation method comprises the following steps: mixing molybdenum trioxide, carbon tetrachloride and a solvent; and in an inert atmosphere, heating to 180-240 DEG C for reaction to obtain the dichloro molybdenum dioxide. According to the preparation method, the reaction temperature is low, the reaction conditions are easy to control, the reaction selectivity is high, the purity of the obtained target product molybdenum dioxide is high, and the purity gt of the molybdenum dioxide is high; 99% of molybdenum metal ions gt; the purity is 99.9999%.

The invention discloses a methane chloride production process and device with adjustable product selectivity. According to the methane chloride production process with the adjustable product selectivity, the composition of a target product is adjusted by changing a chlorine feeding form into a gas, liquid or gas-liquid mixed state. The methane chloride production device with the product selectivity adjustable comprises a chlorine inlet, wherein the chlorine feeding form of the chlorine inlet can be gas, liquid or gas-liquid mixed state mutually switchable. The selectivity of dichloromethane, trichloromethane and carbon tetrachloride products can be flexibly regulated and controlled according to different feeding states, and market changes can be flexibly adapted.