3467results about "Products" patented technology

One aspect is a method for producing a first intermediate product. A feedstock is provided that comprises a first polyester. The feedstock is contacted with a first amount of a first organic compound in a volume section V1 to obtain a first initial mixture. The first amount is in the form of a liquid. The first polyester is transported, and at least a fraction of the first amount of the first organic compound, from the volume section V1 to a volume section V2. The volume section V2 is at least partially filled with the first organic compound. A level of the first organic compound in the volume section V1 is at a height H1 from a floor, and a level of the first organic compound in the volume section V2 is at a height H2 from the floor. The first polyester is contacted with a further organic compound in a volume section V3, to obtain a further initial mixture. A weight average molar mass of the first polyester is reduced in the volume section V3, to obtain a first intermediate mixture. The first intermediate mixture comprisesa first intermediate product,the further organic compound.H1<H2.

One aspect is a method for producing a first intermediate product. A feedstock is provided that comprises a first polyester. The first polyester is contacted with a further organic compound in a volume section V3 to obtain a further initial mixture. A weight average molar mass of the first polyester is reduced in the volume section V3 to obtain a first intermediate mixture. The first intermediate mixture comprises a first intermediate product and, the further organic compound. A b value of the Hunter Lab colour coordinates of the first intermediate mixture is adjusted in a volume section V5. The b value of the Hunter Lab colour coordinates of the first intermediate mixture is adjusted so that b≤0.

One aspect is a method for producing a first intermediate product. A feedstock is provided that comprises a first polyester. The feedstock is separated into a least a first feedstock amount and a further feedstock amount. The first feedstock amount and the further feedstock amount comprise the first polyester.The first feedstock amount is transported into a first reaction line, and the further feedstock amount is transported into a further reaction line.In a reaction line the first polyester is contacted with a further amount of a first organic compound, a weight average molar mass of the first polyester is reduced, the first polyester is contacted with a further organic compound to obtain a further initial mixture; a weight average molar mass of the first polyester is reduced to obtain a first intermediate mixture. The first intermediate mixture comprisesa first intermediate product andthe further organic compound.At least one process parameter varies by at least 10%, between the first reaction line and the further reaction line.

One aspect is a method for producing a first intermediate product. A feedstock is provided that comprises a first polyester. The feedstock is contacted with a first amount of a first organic compound in a volume section V1 to obtain a first initial mixture. The first amount is in the form of a liquid. The first polyester is contacted with a further organic compound to obtain a further initial mixture. A weight average molar mass of the first polyester is reduced to obtain a first intermediate mixture. The first intermediate mixture has a first intermediate product, the further organic compound. A mass ratio of the feedstock to the first organic compound in the volume section V1 is in the range of 0.02 to 3.

A method for pyrolysis of a mass of waste material, includes: providing a screw arrangement adapted to supply heat to the mass by mechanical shear; providing a reactor after the screw arrangement, adapted to supply heat to the mass in the absence of oxygen by heating the reactor wall; heating the mass to an exit temperature and increasing the pressure to an exit pressure in the screw arrangement; thermally degrading the mass in the reactor. The mass is brought into an extreme condition at the exit temperature and exit pressure by the screw arrangement, such that during the pressure drop pyrolysis occurs, thereby forming gaseous hydrocarbons within the connecting element.

Chemical recycling facilities for processing mixed plastic waste are provided herein. Such facilities have the capability of processing mixed plastic waste streams and utilize a variety of recycling facilities, such as, for example, solvolysis facility, a pyrolysis facility, a cracker facility, a partial oxidation gasification facility, an energy generation / energy production facility, and a solidification facility. Streams from one or more of these individual facilities may be used as feed to one or more of the other facilities, thereby maximizing recovery of valuable chemical components and minimizing unusable waste streams.

The present application relates to hydrogen production technology field, especially to a kind of methanol hydrogen production method, comprising the following steps: S10: methanol water is heated and vaporized to obtain methanol water vapor;S20: methanol reforming reaction obtains hydrogen mixture gas;S30: after cooling treatment to hydrogen mixture gas, through water washing tower absorption unreacted methanol water, then, adjust the relative humidity and temperature of hydrogen mixture gas;S40: hydrogen mixture gas is input into carbon dioxide absorption tower to remove carbon dioxide;S50: after removing carbon dioxide, product hydrogen is obtained and input hydrogen tank storage to supply user end.The above-mentioned methanol hydrogen production method, by methanol water vapor reforming hydrogen treatment, obtains hydrogen mixture gas.Again, hydrogen mixture gas is purified to obtain product hydrogen with very low carbon monoxide content, with raw material easy to transport, the hydrogen purity of output is high, equipment construction cost is low, and energy consumption is low and the like advantages, reach the purpose of expanding hydrogen application range.

Disclosed herein are methods for pyrolysis of plastic feedstock comprising post-consumer and / or post-industrial plastics. In various implementations, the methods include directing the plastic feedstock into an internal volume of a reactor vessel, and pyrolyzing the plastic feedstock in the internal volume of the reactor vessel.

Chemical recycling facilities for processing mixed plastic waste are provided herein. Such facilities have the capability of processing mixed plastic waste streams and utilize a variety of recycling facilities, such as, for example, solvolysis facility, a pyrolysis facility, a cracker facility, a partial oxidation gasification facility, an energy generation / energy production facility, and a solidification facility. Streams from one or more of these individual facilities may be used as feed to one or more of the other facilities, thereby maximizing recovery of valuable chemical components and minimizing unusable waste streams.

The invention provides a leakage point pressure difference response high-strength blocking agent based on iron ion dynamic cross-linked latex and a preparation method thereof, and the raw materials comprise the following components in parts: 60-120 parts of latex, 60-120 parts of deionized water, 5-15 parts of an activator, 5-10 parts of a defoamer, 100 parts of a terminator, 100 parts of a stabilizer, 10 parts of a 20% ferric chloride solution, and the balance of water. Rubber particles are dynamically crosslinked through ferric ions, and the plugging strength is remarkably improved. Compared with a traditional differential pressure plugging agent, the plugging strength for small holes with the diameter of 0.5 mm reaches 35.67 MPa and is improved by about 238%, and the plugging strength for large holes with the diameter of 1 mm reaches 9.68 MPa and is improved by about 428%. And the plugging device is suitable for plugging conditions with higher leakage point pressure difference. In addition, the plugging agent can realize rapid and high-strength plugging of an underground pipe column, and provides a more efficient and more reliable solution for well site construction.

Disclosed herein are reactors for pyrolysis of plastic feedstock comprising post-consumer and / or post-industrial plastics. In various implementations, the reactors include a reactor vessel, and one or more heaters configured for heating the feedstock in the reactor vessel's internal volume.

Disclosed herein are reactors for pyrolysis of plastic feedstock comprising post-consumer and / or post-industrial plastics. In various implementations, the reactors include a reactor vessel, and one or more heaters configured for heating the feedstock in the reactor vessel's internal volume.

Disclosed herein are reactors for pyrolysis of plastic feedstock comprising post-consumer and / or post-industrial plastics. In various implementations, the reactors include a reactor vessel for receiving and pyrolyzing the plastic feedstock, and one or more heaters for heating the feedstock in the reactor vessel's internal volume.

Disclosed herein are methods for pyrolysis of plastic feedstock comprising post-consumer and / or post-industrial plastics. In various implementations, the methods include directing the plastic feedstock into an internal volume of a reactor vessel, and pyrolyzing the plastic feedstock in the internal volume of the reactor vessel.

The invention relates to a plugging agent suitable for a malignant leakage formation and a preparation method and application thereof, and belongs to the technical field of petroleum and natural gas drilling engineering. According to the invention, through compounding of the skeleton particles, the intelligent response adhesive and the impact-resistant reinforcing component and cooperation of the skeleton particles and the intelligent response adhesive, a mechanical barrier can be rapidly formed at a crack inlet and a crack is dynamically filled, so that the plugging efficiency and the anti-scouring capability are improved, the compressive strength of a plugging layer is greater than or equal to 20MPa, and the anti-scouring time is prolonged to more than 48 hours; the intelligent response adhesive enables the plugging agent to have good intelligent response characteristics and reservoir protectiveness, self-adaptive adjustment in the plugging process is ensured through a temperature and pH dual mechanism, the biodegradation rate is larger than or equal to 70%, the reservoir pollution risk is remarkably reduced, the compressive strength of a plugging layer formed at high temperature and high pressure is larger than or equal to 20 MPa and is improved by 100% or above compared with that of a traditional plugging agent, and the plugging agent has good application prospects. The biodegradation rate is greater than or equal to 70%, and the plugging problem of the ultra-deep malignant leakage stratum is effectively solved.

To provide a method for fixing carbon dioxide by which bubbles of carbon dioxide introduced into a solution can be made fine without increasing energy consumption.SOLUTION: A carbon dioxide fixation method comprising a precipitation step of introducing a gas containing carbon dioxide into a carbon dioxide fixation solution in which calcium ions are eluted to generate bubbles of the gas containing carbon dioxide in the carbon dioxide fixation solution, thereby reacting the calcium ions eluted in the carbon dioxide fixation solution with carbon dioxide to precipitate calcium carbonate, wherein the carbon dioxide fixation solution is an aqueous solution in which calcium ions are eluted in an aqueous solution of methylparaben.SELECTED DRAWING: Figure 1

The utility model discloses an atomization rotational flow crystallization device for CO2 resource recovery, which relates to the technical field of recovery of CO2 in combustion flue gas and comprises a spray gas inlet device, a spherical cyclone and a condensation crystallization device. According to the utility model, the atomization rotational flow crystallization device is adopted to realize CO2 resource recovery of flue gas, the flue gas is firstly in full contact with atomization absorption liquid sprayed by the multi-point spraying array assembly to form a flue gas absorption liquid mixture, the flue gas absorption liquid mixture is in a rotational flow state after entering the spherical hydrocyclone, and gas-liquid phase separation is carried out, so that the CO2 resource recovery is realized. The liquid phase is condensed under the condensation action of the condensation crystallization device to obtain a solid-phase product sodium bicarbonate and a liquid-phase absorption liquid, and the liquid-phase absorption liquid is subjected to temperature control adjustment and atomization again to provide an absorption liquid for the multi-point spray array assembly; and the method can also be used for large-scale CO2 resource recovery scenes such as thermal power plants and the like, the process and equipment are stable and reliable, the operation is flexible, and the CO2 absorption conversion rate is high.

The production device comprises a base, a reaction barrel is fixedly arranged on the base, a mounting frame is fixedly arranged on the outer side of the reaction barrel, a motor is fixedly connected to the top end of the mounting frame, and a stirring device for stirring basic zirconium sulfate and tartaric acid is arranged in the reaction barrel. The feeding parts are sequentially added into the reaction barrel, and a discharging part for discharging reacted liquid is arranged in the reaction barrel; through the staggered and periodic coincidence design of discharging grooves of the inner barrel and the outer barrel in the feeding part, the rotating rod is matched to drive the outer barrel to spirally move downwards, accurate and quantitative adding of the basic zirconium sulfate solution is achieved, meanwhile, the adding time and flow of the tartaric acid solution are automatically controlled through magnetic ring adsorption of the upper barrel and the outer barrel and stored energy release of the first spring, and the feeding efficiency is improved. Manual intervention is reduced, efficiency loss caused by step-by-step feeding is avoided, and the preparation efficiency of the water repellent agent is remarkably improved.

The invention provides a temperature-resistant and salt-resistant wall-fixing agent for a water-based drilling fluid for a myriameter deep well as well as a preparation method and application of the wall-fixing agent, and belongs to the technical field of drilling. The preparation method of the wall fixing agent comprises the following steps: adding acrylic acid into deionized water, adjusting the pH value of a system to 7.0, then sequentially adding N-hydroxymethyl acrylamide, N-[2-(3, 4-dihydroxyphenyl) ethyl]-2-acrylamide, an emulsifier, octadecyl vinyl ether and a complexing agent into the system, and shearing to obtain a monomer solution; adding an initiator into the monomer solution, and reacting; and after the reaction is completed, washing, drying and crushing to obtain the wall fixing agent. The wall fixing agent can resist the temperature of 200 DEG C, can resist the salt to be saturated, has strong adsorbability and high cohesion, and can effectively adsorb, block and bond micropores and micro cracks of rocks, so that the rocks are solidified, the well wall stability is effectively enhanced, drilling fluid leakage is prevented, and a technical guarantee is provided for safe and efficient drilling of deep wells.

The application provides a temperature-resistant and salt-resistant wall stabilizer for a ten-thousand-meter deep well water-based drilling fluid and a preparation method and application thereof, and belongs to the technical field of drilling. The preparation method of the wall stabilizer comprises the following steps: acrylic acid is added into deionized water, the pH of the system is adjusted to 7.0, then N-hydroxymethyl acrylamide, N-[2-(3,4-dihydroxyphenyl)ethyl]-2-acrylamide, an emulsifier, octadecyl vinyl ether and a complexing agent are sequentially added into the system, shearing is performed, a monomer solution is obtained, an initiator is added into the monomer solution, and reaction is performed; after the reaction is completed, washing, drying and crushing are performed, and the wall stabilizer is obtained. The wall stabilizer has a temperature resistance of 200 DEG C and a salt resistance of saturation, has strong adsorption and high cohesion, can effectively adsorb, plug and cement micro-pores and micro-cracks of rocks, thereby consolidating the rocks, effectively enhancing the well wall stability, preventing drilling fluid leakage and providing technical support for safe and efficient drilling of deep wells.

Recycled content liquified pyrolysis gas (r-LPyG) is produced using a process and system that optimizes the production, separation, liquification, storage, loading, and / or transporting of gases generated from the pyrolysis of waste plastic. The r-LPyG can be utilized in a variety of end use applications, including as a raw material for other chemicals and chemical intermediates.

A carbon dioxide recovery device provided with a separation device that separates carbon dioxide from to-be-separated gas (for example, combustion exhaust gas) containing carbon dioxide, wherein: in order from the upstream side where the to-be-separated gas is supplied, the separation device and carbon dioxide sublimators, which sublimate (solidify) carbon dioxide that was separated in the separation device, are connected in series, refrigerant circuits in which a fluid having cold heat serves as the refrigerant, are connected to the carbon dioxide sublimators, and the refrigerant is used to sublimate (solidify) the carbon dioxide; and when the carbon dioxide is sublimated (solidified), the carbon dioxide sublimators are depressurized and set to negative pressure so as to draw in the carbon dioxide separated at the separation device.

The invention discloses a preparation device of pseudo-boehmite, which relates to the technical field of chemical equipment and comprises a reaction kettle, an electrode column, a grating and a stirring shaft. The invention also discloses a preparation method of the pseudo-boehmite preparation device. The preparation method comprises the following steps: material addition, colloid generation, aging, gibbsite conversion and repeated charging. The inner kettle and the outer kettle are arranged, a sodium aluminate solution and carbon dioxide are subjected to a neutralization reaction in the inner kettle to generate pseudo-boehmite colloid, part of gibbsite generated due to slow reduction of the pH value in the reaction process is precipitated at the bottom end of the inner kettle, and the pseudo-boehmite colloid can directly enter the outer kettle to be subjected to aging treatment after being generated; gibbsite can be heated at the bottom end of the inner-layer kettle to be converted into monohydrate gibbsite, and the monohydrate gibbsite can enter the outer-layer kettle along with subsequent pseudo-boehmite to be aged, so that the gibbsite can be directly converted and recycled in the preparation process of the pseudo-boehmite.

The utility model discloses a constant-temperature feeding assembly for preparing a PU (Poly Urethane) adhesive, relates to the technical field of adhesive preparation, and aims to solve the problem of slow feeding of raw materials in the preparation process of the PU adhesive, perform constant-temperature feeding and keep part of the raw materials which are greatly influenced by temperature stable, so that the product quality and the production efficiency are improved, and the production cost is reduced. According to the technical scheme, the constant-temperature feeding assembly for preparing the PU adhesive is characterized by comprising a reaction kettle and a constant-temperature feeding assembly body, the reaction kettle comprises a base, a kettle body, a support, a motor base, an explosion-proof motor, a direct feeding port and a discharging port, and the constant-temperature feeding assembly body comprises a heat preservation container, a heating part and a digital display part; the heat preservation container comprises a shell, a cover plate, a constant-temperature feeding port, a feeding pipe and a constant-temperature discharging port, the heating part comprises a constant-temperature controller, a semiconductor heating pipe, a temperature sensor and a temperature measuring rod, and the digital display part comprises a fixing base and a temperature display screen. The performance of the PU adhesive is prevented from being influenced by over-high temperature of the raw materials.

The present invention discloses a microwave continuous frequency modulation collaborative biomass directional depolymerization device and its usage method, belonging to the technical field of biomass resource utilization. The device includes a microwave continuous frequency modulation power supply, a microwave resonant cavity, a quartz tube reactor, and a product treatment device; a microwave feed port is provided on the microwave resonant cavity, and the microwave continuous frequency modulation power supply is connected to the microwave feed port; the quartz tube reactor is connected to an inert gas source, a biomass feed hopper is connected to the quartz tube reactor, a catalyst filling screen spacer is provided in the middle, an infrared thermal imager is provided above, and an infrared thermometer is provided at the catalyst filling screen spacer; the product treatment device includes a condensation system and a gas collection bag, the condensation system is arranged at the outlet of the quartz tube reactor, and the gas collection bag is arranged at the outlet of the condensation system. The present invention matches the microwave emission frequency with the intrinsic resonance frequencies of the three major components of biomass and the catalyst to achieve the goal of reducing the biomass cracking activation energy and realizing directional depolymerization.

The present invention discloses a self-degradable particle temporary plugging agent for fracturing and its preparation method and application, relating to the field of oilfield chemical technology. According to mass percentage, the temporary plugging agent is obtained by melt blending and crushing the materials including the following components: poly (3-hydroxybutyric acid-co-4-hydroxybutyrate), 70%-85%; auxiliary agent for auxiliary degradation, 2%~10%; nano silicon dioxide 10%~15%; sodium starch glycolate, 1%~7%. The temporary plugging agent of the present invention contains disintegrant sodium starch glycolate, which has a strong water absorption capacity and can quickly absorb water and expand its own volume by 250~300 times, so that the temporary plugging agent expands and cracks appear. On the one hand, in the early stage of plugging, the temporary plugging agent can reduce the gap between particles after absorbing water and expanding, thereby increasing the density of the entire plugging layer, thereby improving the plugging ability. On the other hand, cracks are generated on the surface of the temporary plugging agent after expansion, and water can penetrate into the interior of the temporary plugging agent particles from the cracks, which increases the contact area between the temporary plugging agent and water, thereby promoting its degradation and shortening the time of overall degradation.

Disclosed herein are systems for pyrolyzing plastic feedstock comprising post-consumer and / or post-industrial plastics. In various implementations, the systems include one or more energy transfer apparatuses configured for receiving the plastic feedstock and applying energy to the plastic feedstock.

The invention discloses a phosphorus trichloride production reaction kettle with a defoaming structure, and relates to the technical field of reaction kettles. According to the phosphorus trichloride production reaction kettle with the defoaming structure, through cooperation of the obliquely-installed sawtooth plates and the protruding strip rings, during rotation, the sawtooth plates drive foam on the liquid level to move towards the periphery, in the movement process, the foam on the liquid level is separated from the protruding strip rings, and the foam on the liquid level is removed. The sawteeth at the top of the sawtooth plate are in contact with accumulated foam, so that part of the foam is broken, the unbroken foam outwards impacts the inner wall of the convex strip ring under the action of centrifugal force, so that the foam is in contact with the convex strips uniformly arranged on the inner wall of the inner convex ring, and compared with a smooth inner wall of a traditional reaction kettle, the contact area is reduced when the convex strips of the inner convex ring are in contact with the foam; and the pressure during impact is increased, so that the foam is broken under higher pressure, and the defoaming effect is improved.

The present disclosure generally relates to systems and methods utilizing regenerative agriculture for the procurement, production, refinement and / or transformation of low carbon intensity transportation fuels, including low carbon intensity biodiesel and / or renewable diesel, low carbon intensity biogasoline, low carbon intensity aviation, marine and kerosene fuels as well as fuel oil blends, low carbon intensity ethanol, and low carbon intensity hydrogen, that may be beneficially commercialized directly to consumers. In further aspects, the systems and methods of the present disclosure advantageously generate low carbon intensity comestibles, including sustainably-sourced meal and / or feed. The disclosed systems and methods may be utilized and optimized such that the resulting fuels and foodstuffs are characterized by a reduction in greenhouse gas production and a diminution in the fertilizer, pesticide and water required for producing the associated crop feedstocks.

This invention provides a method for preparing monodisperse nano-calcium carbonate from calcium-containing industrial solid waste. The method comprises the following steps: S1: mixing calcium-containing solid waste and an ammonium salt solution, reacting the mixture, and filtering to obtain a calcium-containing filtrate; S2: mixing the calcium-containing filtrate, CO2 gas, and a crystal form control agent, reacting the mixture, and filtering to obtain nano-calcium carbonate; S3: mixing the nano-calcium carbonate with an aqueous solution containing a surfactant, reacting the mixture, centrifuging, washing, and drying to obtain monodisperse nano-calcium carbonate. This method improves the calcium leaching rate from calcium-containing solid waste, achieves explosive nucleation and rapid growth of calcium carbonate, enhances the reactivity and reaction time between the surfactant and the nano-calcium carbonate particles, and improves the dispersion and surface modification degree of the calcium carbonate nanoparticles.