69results about How to "Shorten the compositing time" patented technology

A template for a logic synthesis command script is broken into smaller and functionally independent templates termed "micro-templates." Using micro-templates, logic synthesis time may be significantly reduced. Each micro-template may correspond to a particular synthesis operation and may be enabled or disabled. Where synthesis of a particular set of synthesis operations is desired, the micro-templates corresponding to those synthesis operations are enabled.

A method for producing zeolite films or membranes at essentially ambient pressure, which includes preparing a synthesis mixture comprising an ionic liquid solvent and an aluminum and/or silicon and/or phosphate source and converting the synthesis mixture to form a continuous zeolite layer. In addition, a method of synthesizing zeolite nanocrystals, which includes preparing a synthesis mixture, the synthesis mixture having a silica or a silica and alumina source, and a template; and synthesizing the synthesis mixture to form zeolite nanocrystals.

Improved synthesis of seco(−)CBI (5-hydroxy-3-amino-1-[S]-(chloromethyl)-1,2-dihydro-3H-benz(e)indole):

and improved syntheses therefrom of a wide variety of CC-1065 analogs that comprise a cyclopropabenzidole (CBI) alkylating moiety, and which are collectively DC1 and its derivatives, for the synthesis of cell-targeted therapeutic agents.

An imaging apparatus, includes: an imaging optical system; an image pickup device; and a control device which is configured to control the image pickup device, wherein the control device is configured to preliminarily decide an exposure order of a relatively short time exposure in a prescribed image size; an exposure with almost the same exposure time as the relatively short time in a smaller image size than the prescribed image size, and a relatively long time exposure in the prescribed image size, and to perform an imaging operation once by exposing the image pickup device by the decided exposure order.

The invention provides a process for producing a sulfide-based solid electrolyte, the process having: a raw material composition preparation step for preparing a raw material composition containing at least sulfur (S), an adhesion inhibitor addition step for adding to the raw material composition an adhesion inhibitor that inhibits formation of adhered substances including the unreacted raw material composition, on the inner surface of a milling pot during mechanical milling, and a vitrification step for synthesizing sulfide-based glass by carrying out mechanical milling on the raw material composition to which the adhesion inhibitor has been added.

The present invention provides a method for producing catalyst for wastewater treatment, which comprising mixing polymers and additives, reacting with a titanate precursor, and then subjecting the resultant product to hydrolysis and condensation to form catalyst slurry. Due to using the titanate as a source of metal ions and the polymer compound as a dispersant and stabilizer, the aggregation between particles can be habited, and due to using additives as chelating agent and catalyst, it can improve solution stability and inhibit the oxidation of the metal, thereby facilitate the condensation and hydrolysis and shorten the reaction time. The catalyst slurry prepared by the method of the present invention exhibits excellent dispersibility to effectively contact with and decompose organics, such as those containing in wastewater and thus is suitable for wastewater treatment. In addition, the resultant catalyst slurry can be processed in the form of powder or film for using in industrial wastewater treatment.

Disclosed is a method for the preparation of norbornene and substituted norbornene compounds via a Diels-Alder reaction, in which a cyclic diene is reacted with an olefinic compound in order to prepare a norbornene compound. According to the invention a cyclic diene is gradually added to react with an olefinic compound, in order to keep the concentration of the cyclic diene in the reaction mixture as low as possible during the reaction. It is possible to obtain a very pure product, high yield, short reaction time and high concentrations of the exo diastereomer with the method of the invention.

The invention provides a method for rapidly preparing AlON ceramic powder by means of carbon thermal reduction. The method takes low-cost gamma-Al2O3 powder and a carbon source, uniformly mixing the raw materials by means of wet-process ball milling, then drying and putting the raw materials in a zirconium oxide crucible, conducting a high-temperature carbon thermal reduction nitridation reaction at the high-pressure nitrogen atmosphere of 0.1-1MPa, quickly synthesizing the AlON powder, and then removing carbon at the low temperature of 500-900 DEG C to obtain the superfine, high-purity and uniformly dispersed single-phase AlON powder. Compared with the prior art, rapid sintering and carbon thermal reduction are combined under the condition of high nitrogen pressure, so that the activity of the AlON powder is improved, the preparation process is simplified, the preparation cost is lowered, and the method has an excellent industrialized application prospect.

A process for synthesizing the meso-porous molecular sieve SBA-15 features that the tri-block copolymer 'polyepoxyethene-polyepoxypropane-polyepoxyethene' is used as template, the non-fluorine anionic salt as inducing agent, and the heteropoly acid as promoter and acidity regulator. Its advantages are short time and low environmental pollution and cost.

The invention discloses a monodisperse platinum-based two-dimensional metal hydroxide, and an in situ synthesis method and an application thereof in the purification of volatile oxygen-containing hydrocarbons. A triblock copolymer poly(ethylene oxide)-polypropylene oxide-poly(ethylene oxide) is dissolved into deionized water, so taht a transparent and clear solution can be formed through stirring;hexamethylene tetramine is added, and then cerium or cobalt salts are added after uniform stirring; glycol is added after uniform stirring; a chloroplatinic acid hexahydrate-glycol solution is addedafter uniform stirring, so that a mixed solution can be obtained after uniform stirring; and heating reflux reaction is performed on the mixed solution in a microwave generator, and centrifugation androasting are performed after complete reaction, so that the monodisperse platinum-based two-dimensional metal hydroxide can be obtained. The prepared catalytic material has atomic-scale dispersed platinum active sites and shows excellent low temperature purifying capabilities of volatile oxygen-containing hydrocarbons; and the related catalyst synthetic method is simple and low in raw material price, and has good industrial application prospects.

Provided is a method for preparing a defect-free DDR molecular sieve membrane. Sigma-1 molecular sieve is used as an inducing seed crystal to prepare and obtain a continuous and compact DDR molecular sieve membrane on the surface of a porous ceramic support. An ozone atmosphere or an external field assisted technology is used to remove a template in the pores of the molecular sieve membrane at a low temperature. The invention avoids the formation of intercrystal defects and cracks, an activated DDR molecular sieve membrane has a good selectivity for separating CO2, and the membrane preparation time is significantly reduced.

Disclosed is a method and device for simply and safely preparing, using a direct synthesis process at room temperature, a radioactive methyl iodine (CH₃¹³¹I) tracer for use in evaluating the ability of impregnated activated carbon to adsorb radioactive organic iodine according to ASTM D 3803 (Standard Test Method for Nuclear-Grade Activated Carbon), in which the tracer can be directly synthesized by mixing radioactive sodium iodide (Na¹³¹I) with methyl iodine (CH₃I) at room temperature under reduced pressure, thus shortening excessive synthesis time and decreasing the probability of radiation exposure due to leakage of volatile material during the distillation.

This invention relates to catalyst compounds and the synthesis and applications useful in olefin metathesis reactions. The catalyst compounds of the invention are represented by the formula (I): wherein M is a Group 8 metal; X¹ and X² are anionic ligands; L¹ and L² are neutral two electron donor ligands. The present invention also relates to an easy applicable catalyst synthesis and the application in different olefin metathesis processes, e.g. Reaction Injection Molding (RIM), process to make α-olefins from fatty acid ester, e.g. methyl oleate.

The invention relates to the technical field of thermocatalysis, in particular to a preparation method and application of a small-pore molecular sieve-loading noble metal material prepared by one-potreaction. The small-pore molecular sieve-loading noble metal material provided by the invention comprises a small-pore molecular sieve SSZ-13 and a noble metal Pd species dispersed in the small-pore molecular sieve. The one-pot reaction for preparing the small-pore molecular sieve-loading noble metal material can effectively reduce the synthesis steps and shorten the preparation time of a catalytic material. The method can uniformly disperse noble metal in the molecular sieve, prevent agglomeration of the noble metal species, and provide more NOx adsorption sites. The small-pore molecular sieve-loading noble metal material disclosed by the invention is applied to the field of low-temperature NOx adsorption and high-temperature NOx desorption, the adsorption efficiency of the small-pore molecular sieve-loading noble metal material prepared by the one-pot reaction on NOx under a low-temperature condition is remarkably improved, so that NOx removal at a low temperature can be effectivelyrealized, and the small-pore molecular sieve-loading noble metal material can be applied to the field of atmospheric pollution treatment.

The invention relates to the field of building materials, and particularly discloses a polycarboxylate superplasticizer catalyzing production technology without high temperature. The polycarboxylate superplasticizer catalyzing production technology comprises the following steps: (1) sequentially adding tap water, methyl polyoxyethylene alkenyl ether, sodium persulfate and azo diisopropyl imidazoline hydrochloride into an agitation tank to be uniformly stirred; (2) adding 30-40 kg of sodium bisulfite and 150 kg of tap water into a measuring tank, fully stirring to enable the sodium bisulfite to be completely dissolved to prepare a sodium bisulfite aqueous solution; (3) sequentially adding 420 kg of water, 140 kg of acrylic acid and the sodium bisulfite aqueous solution into an overhead tank to be uniformly stirred to obtain a mixed solution; (4) opening a valve of the overhead tank to enable the mixed solution to be dropwise added into the agitation tank, performing dripping and stirring at the same time, allowing the dripping to be completed within 1 hour, and obtaining the polycarboxylate superplasticizer after discharging. The production technology has the benefits that the production efficiency is improved, the synthesis reaction temperature is reduced, the synthesis time is shortened, the production cost is greatly reduced, and environmental pollution is reduced.

The invention relates to a preparation method of a lithium iron phosphate positive electrode material precursor and belongs to the technical field of preparation of positive electrode materials for lithium-ion batteries. The method comprises the steps of carrying out combination reaction and ageing on an iron source and a phosphorus source, obtaining iron phosphate precipitates, washing the iron phosphate precipitates until the pH value of filtered water is 7-8 and drying to obtain iron phosphate powder; preparing a lithium source solution from a lithium source according to the molar ratio ofLi to Fe to P in the lithium source, the iron source and the phosphorus source being (0.95-1.10):1:1; dissolving a conductive additive into an additive solution; and adding the lithium source solutionand the additive solution to the iron phosphate powder, stirring evenly and then drying to obtain the lithium iron phosphate positive electrode material precursor. According to the method, various raw materials are dissolved into the solution, so that mixing at the atomic or molecular level is achieved; ball-milling and ultrafine grinding are not needed, the used raw materials are primary raw materials and iron phosphate, and the procedures, such as drying and packaging are not needed, so that the production cost can be reduced.

The invention relates to the field of nanoscale biomedical materials, in particular to a nanometer material as well as a preparation method and application thereof. The nanometer material comprises BSA: RE1, an RE2 inner core, a PDA shell layer covering the surfaces of the BSA: RE1 and the RE2 inner core, and FA on the surface of PDA, where RE1 and RE2 are different. The nanometer material has good dispersibility, is easy to prepare, has excellent biocompatibility and safety, can accurately perform multimodal MRI/CT imaging on tumors, and has a good photothermal treatment effect on the tumors.