30 results about "Autocatalytic reaction" patented technology

There is disclosed a method of making unsupported particles of a base metal selected from the group consisting of iron, cobalt, and nickel, which comprises combining an aqueous solution or suspension of a base metal salt, a strong base so that the resulting combination has an effective hydroxide ion concentration, and a reducing agent, which is then subjected to an autocatalytic reaction at about atmospheric pressure to form a precipitate of the metal. The unsupported base metal particles exhibit an anisometric morphology, generally platetlet or disk-shaped, and have a relatively high aspect or width to thickness ratio, which is preferably three or greater, exhibit ferromagnetic properties, and one or more of these base metals may be formed to exhibit a single magnetic domain. The resulting precipitate of metal particles may be formed as an agglomerate as by subjecting the precipitate to aging or to external means.

Radiation-activated catalysts (RACs), autocatalytic reactions, and protective groups are employed to achieve a. highly sensitive, high resolution, radiation directed combinatorial synthesis of pattern arrays of diverse polymers. When irradiated, RACs produce catalysts that can react with enhancers, such as those involved in autocatalytic reactions. The autocatalytic reactions produce at least one product that removes protecting groups from synthesis intermediates. This invention has a wide variety of applications and is particularly useful for the solid phase combinatorial synthesis of polymers.

The invention discloses a method and a system for treating alkaline chemical nickel plating wastewater. The method and the system can reduce the treatment cost of nickel-containing wastewater, improvethe cyclic utilization rate of nickel resources and enable nickel in the alkaline chemical nickel plating wastewater to reach the standard. The method comprises the following steps: 1) pumping wastewater with the pH value of 8.0-10 into a collecting tank; 2) heating the wastewater to 80-90 DEG C; 3) carrying out an electrolytic reaction by adopting an electro-deposition reactor; and 4) carrying out an autocatalytic reaction on nickel ions released after anodic oxidation in the nickel-containing complex state by taking metallic nickel, generated by reduction on a cathode, as an initiator to quickly reduce the nickel ions into elemental metal nickel on the cathode. The system adopts a multistage reaction device, so that the alkaline chemical nickel plating wastewater with high nickel and high phosphorus content can be quickly treated, the treated wastewater reaches the discharge standard specified by national standards, the nickel content of the treated wastewater is less than 0.1 ppm,and the TP value of the treated wasteater is less than 0.5 ppm. The method can replace the existing processes such as a chemical precipitation method, an ion exchange resin method, a membrane separation technology and the like.

The invention relates to a preparation method of lithium vanadium phosphate of lithium ion batteries cathode materials, which comprises the following steps: weighing a vanadium-containing compound, a lithium-containing compound and phosphate according to mol ratio of 1:(2.8-3.2):3; weighing citric acid which accounts for 30%-60% of mass of raw material, adding distilled water to prepare a 20%-50% of solution, uniformly mixing the vanadium-containing compound, the lithium-containing compound and phosphate, adding 15-45% of deionized water and reacting for 0.5-2 hours; adding a citric acid solution in the reactive raw material and heating to obtain a solid phase, drying, performing ball milling, putting into an inert atmosphere furnace and heating to the temperature of 300-1000 DEG C, and keeping the temperature for 2-24 hours to prepare lithium vanadium phosphate. The preparation method provided by the invention uses an autocatalytic reaction to uniformly mix the raw material, and is good for providing primary particles with small size to lithium vanadium phosphate.

The invention provides polyimide precursor resin as well as a preparation method and application thereof. The polyimide precursor resin is obtained through polycondensation of a diamine monomer and aromatic tetracarboxylic dianhydride. The diamine monomer comprises at least one compound with a structure as shown in a formula I and is a diamine monomer containing an aza-aromatic ring, the diamine monomer with the structure can be subjected to an autocatalytic reaction in a heated and cured polyimide precursor resin, the imidization reaction process is accelerated, and the reaction time is shortened. The imidization rate of the polyimide precursor resin at low temperature is obviously improved. The polyimide precursor resin can be cured at low temperature to obtain a polyimide film with excellent mechanical property and thermal stability, so that high stress residue caused by high-temperature curing is effectively avoided; therefore, the application requirements of the polyimide precursor resin in low-temperature processing environments such as microelectronic chip materials, packaging materials and interlayer dielectric layers are fully met.

A bottle (10), container or beverage glass for containing a hops based beverage, in particular beer, includes a concentration between 10 [mu]g/l and 10 mg/l of Riboflavin. The bottle, container or beverage glass are at least partially transparent or translucent to visible light and have an optical filter characteristic preventing light transmission of wavelengths between 200 nm and 510 nm to a level preventing generation of more than a tasteable concentration of MBT in the beverage through photochemical reactions and photochemically initiated auto-catalytic reactions involving the Riboflavin. The tasteable concentration is between 1 ng/l and 35 ng/l, preferably between 5 ng/l and 25 ng/l, and more preferably 10 ng/l.

The invention discloses a process for manufacturing a metallized coating under a wafer bump and a coating structure thereof. A substrate in the process is a silicon or silicon carbide semiconductor; wherein a conductive circuit area and a non-conductive area are arranged on the surface of the substrate, and the conductive circuit area on the surface of the substrate sinks downwards to form an inverted wafer bump. The coating obtained through a chemical tin alloy plating process is a chemical replacement type coating, electrification is not needed, a traditional chemical auto-catalytic reactionis not needed, and only a replacement reaction is needed. The under bump metallization (UBM) and the redistribution line (RDL) obtained by the method provided by the invention not only can have binding property, but also have good weldability.

The invention discloses a method for treating chemical nickel-plating waste liquid by utilizing an autocatalytic reaction. The method comprises the following steps: (1) adjusting the pH value of to-be-treated chemical nickel-plating waste liquid to be 10-11; (2) adding a treatment preparation into the to-be-treated chemical nickel-plating waste liquid subjected to ultrasonic dispersion; (3) standing and layering the reaction liquid; (4) adding halogen powder into the solution obtained in the step (3); (5) putting the solution filtered in the step (4) into a cathode chamber of an electrolytic cell for electrolysis; and (6) adding a calcium chloride solution into the solution obtained after electrolysis. According to the method, the mechanism of the chemical nickel autocatalytic reaction isutilized, various elements are recycled at a time, the cost is low, the process is short, the efficiency is high, operation is easy and convenient, and recycling and reusing of nickel resources are facilitated.

The present invention relates to a three-phase reactor for the reaction of a hydrocarbon feedstock with hydrogen and to a hydroconversion process, for example of H-Oil™ type, employing it, comprising a chamber with an upper end and a gas/liquid separation device comprising:

• • a recycle cup, above the catalytic reaction zone and delimiting, with the upper end, a recycle zone, comprising a cylindrical upper part extended by a lower part of decreasing section and of variable angle of inclination, provided with vertical pipes for the passage of a gas/liquid mixture originating from a catalytic reaction zone, and having a fixed angle of inclination β of between 50° and 85° with respect to the axis of the cylindrical part,
  • a pipe for recycle of the liquid at the apex of the lower part, in fluidic communication with the lower end of the chamber by recirculation means.

The invention relates to phytosterol isostearate and a preparation method thereof. The preparation method comprises the steps of preparation of a mixture solution, preparation of a membrane casting solution, coating, soaking, autocatalytic reaction of phytosterol isostearate, concentration of eluent and the like. Compared with the prior art, the preparation method of the phytosterol isostearate has the advantages of high conversion rate and simple production technology. The preparation method does not need high temperature, and the phytosterol isostearate molecularly imprinted membrane can specifically separate a product from a reaction system; and the purity of the product can reach 99.9% or above by weight, and the product is good in color and does not need to be decolored.

The invention discloses an online resourceful treatment method for chemical copper plating waste liquid. A copper-based catalyst is employed and used for carrying out an autocatalytic reaction on thechemical copper plating waste liquid in an autocatalytic reactor; copper ions in the waste liquid are reduced into elemental copper and are recycled; the treated waste liquid enters a three-dimensional electrolysis device; organic substances such as a reducing agent and a complexing agent in the waste liquid are efficiently oxidized; then, the method includes further flocculating and precipitatingthe waste liquid by adopting a chemical precipitation method to remove ammonia nitrogen and macromolecular substances in the water; and finally, membrane filtration equipment is adopted for purification treatment and is used for further intercepting residual copper ions in the wastewater and returning the residual copper ions to the autocatalytic reactor for circular treatment, so that the copperions in the waste liquid can be recycled to the greatest extent.

The invention relates to the technical field of medicine synthesis, in particular to an intermediate for synthesizing rilpivirine, a synthesis method of the intermediate and a synthesis method of the rilpivirine. The intermediate is synthesized according to the following synthesis route: wherein X is a halogen atom, and M is an acid. According to the method, the compound shown in the formula II can generate acid by itself, and then an acid environment is provided for the reaction, so that the compound shown in the formula I and the compound shown in the formula II can be directly subjected to autocatalytic reaction on the basis of not carrying out amino protection on the compound shown in the formula I; and the compound shown in the formula I and the compound shown in the formula II react to form the required intermediate, and the overall yield of the synthesized rilpivirine is increased.

The invention discloses a brush plating method for selective nickel plating in a groove. The brush plating method comprises the following steps: step 1, removing marks and dirt in the groove; step 2, surface preparation; 3, material detection preparation; 4, electrolytic decontamination in the to-be-plated bath: starting forward voltage, adding electrolyte into the to-be-plated bath, and brushing back and forth in the to-be-plated bath by using a nickel plating arc-shaped small brush handle along the same direction; 5, activating the metal surface of the to-be-plated bath: starting a reverse voltage, adding an activating solution into the to-be-plated bath, and brushing back and forth in the to-be-plated bath by using a nickel plating arc-shaped small brush in the same direction so as to activate the metal surface of the to-be-plated bath; and 6, nickel plating through autocatalytic reaction deposition, specifically, forward voltage is started, nickel plating liquid medicine is added into a liquid medicine pipe, meanwhile, brush plating is conducted back and forth above the groove opening face of the to-be-plated groove along with the nickel plating liquid medicine pipe in the same direction through a large plane brush, the nickel plating liquid medicine and the metal surface of the part are subjected to the autocatalytic reaction, and a nickel plating layer is formed. A plating layer can be uniform, natural and attractive, and the qualification rate of brush plating is high.

The invention relates to a trimethyl borate continuous esterification production process, which comprises the following steps: proportioning methanol and boric acid, carrying out pre-reaction in a pre-reactor, feeding into an esterification tower after pre-reaction, and continuing to carry out autocatalytic reaction; heat coupling of esterification and rectification is completed in the esterification tower, crude trimethyl borate is extracted from the tower top of the esterification tower, and water is extracted from the tower bottom of the esterification tower; a crude trimethyl borate gas phase extracted from the tower top of the esterification tower enters a refining tower, a qualified trimethyl borate product is extracted from the tower top of the refining tower, qualified recovered methanol is obtained from the tower bottom of the refining tower, and the methanol returns to a reaction system for recycling. According to the invention, no catalyst is added, and reactants are adopted for autocatalysis to complete esterification reaction; the esterification reaction operation and the rectification operation are coupled to be completed in one esterification reaction tower, so that the reaction conversion rate and the reaction yield can be improved; the esterification reaction is an exothermic reaction, the esterification reaction and the rectification operation are completed in the esterification reaction tower at the same time, the esterification reaction heat can be applied to the rectification operation, and the energy consumption of the system is greatly reduced.

The invention discloses a chemical nickel plating solution treatment device. The device mainly comprises an autocatalytic reaction tank, a filter tank, a concentration structure, a precipitation crystallization tank and a chemical precipitation tank, the autocatalytic reaction tank comprises a control mechanism, a catalysis mechanism and a steam box, the filter tank comprises a plurality of filtering pipes, a backwashing mechanism and a concentration structure, fiber filter elements are arranged in the filtering pipes, the concentration structure comprises a steam inlet pipe, a water inlet pipe, a condensate water outlet pipe and a concentrated solution outlet pipe, and the precipitation crystallization tank comprises a hydrogen peroxide inlet, a stirring mechanism and an adjuster; the chemical nickel plating solution treatment device is good in chemical nickel plating solution treatment effect, low in cost and suitable for wide popularization.

A metal surface treatment device, according to the present invention, is a metal surface treatment device which carries out surface treatment for a target metal heated at a temperature for which surface treatment is possible, the device comprising: a reaction chamber which has a shape corresponding to an outer shape of the target metal and is arranged within a certain interval from the outer side of the target metal, and which accommodates at least a part of the target metal; and a raw gas supply unit for supplying raw gas which is necessary for an autocatalytic reaction with the target metal accommodated within the reaction chamber. Furthermore, a metal surface treatment method using the same comprises the steps of: positioning a target metal within the reaction chamber, which has the shape corresponding to the outer form of the target metal and is arranged within a certain interval from the outer side of the target metal and which accommodates at least a part of the target metal; and forming a raw gas layer in the target metal through an autocatalytic reaction by supplying raw gas to the inside of the reaction chamber through the raw gas supply unit.