1459 results about "Reaction timing" patented technology

An automatic playback overshoot correction system predicts the position in the program material where the user expects to be when the user stops the fast forward or reverse progression of the program material. The invention determines the position where the program material was stopped. The media controller transitions to the new mode that the user selected, starting at the stopped position with an overshoot correction factor added or subtracted from it. The invention adapts to the user by remembering how much the user corrects after he stops the fast forward or reverse mode. Correction factors are calculated using the user's corrections and adjusting the correction factors if the user continues to make corrections. The invention also uses a prediction method to correctly place the user within the program upon transition out of either mode and determines if the speed of the fast forward or reverse modes and then automatically subtracts or adds, respectively, a time multiple to the frame where the transition was detected and positions the user at the correct frame. The time multiple is fine tuned if the user is consistently correcting after the fast forward or rewind mode stops. Another method initially tests the user's reaction time using a test video and asks the user to press the fast forward or reverse button on his control device during the test video and then asks the user to position the video to the place that he expected the system to have been. This time span is then used whenever the user uses the fast forward or reverse modes and is adjusted with a multiple for each speed. A final method allows the user to simply set a sensitivity setting that the system will use as a correction factor and a multiple is subtracted or added to the release frame whenever the user uses the fast forward or reverse modes, respectively.

Disclosed herein is a dissolvable downhole tool. The tool includes, a dissolvable body constructed of at least two materials and at least one of the at least two materials is a reactive material, and a first material of the at least two materials being configured to substantially dissolve the dissolvable body and a second material configured to control reaction timing of the first material.

Methods and systems for the production of ethyl acetate are described herein. The methods and systems incorporate the novel use of a high shear device to promote dispersion and mixing of a carbonyl co-reactant (e.g. acetic acid, acetaldehyde) with ethanol. The high shear device may allow for lower reaction temperatures and pressures and may also reduce reaction time with existing catalysts.

In reagent reaction experiments using microplates, a desired period of time can be set for determining the time to introduce a reaction stop solution after introduction of a reagent. The set time is measured starting from the introduction of the reagent and the reaction stop solution is introduced immediately after expiration of the set time. A control device for an automatic liquid handling system having the above-described reaction time managing feature is also provided with a self-diagnosing function that is capable of determining whether scheduled processes are executable or not during the time set before execution of the processes and informing an operator of the results of determination.

The invention discloses a modulating method of LiFePO4 particle shape, which comprises the following steps: blending one or more composition with lithium ion, ferric ion and phosphate radical ion; adding solvent and certain quantity of crystal growing inhibitor; proceeding solvent heat reaction under certain temperature; washing; filtering; drying; sintering to improve crystallizing property; obtaining the product with regular shape and size.

A method for manufacturing 3-hydroxy-3-methylbutanoic acid (HMB) in commercially viable amounts is disclosed. The reaction mixture cycles through an external heat exchanger while the primary reactant is added in a warmer so as to control and maintain a low temperature for the reaction mixture. The manufacturing process herein disclosed increases yield while decreasing reaction time from the synthetic processes currently practiced.

A method for producing a cross-linked hyaluronic acid in accordance with the present invention comprises: (a) cross-linking at least one polymer at a temperature, from about 35° C. to about 60° C., for a reaction time of from about 0.1 hour to about 72 hours with a cross-linking agent; and (b) lowering the temperature in step (a) to form about 10° C. to about 30° C. for a reaction time of from about 48 hours to about 28 days to obtain the cross-linked hyaluronic acid, whereby, a cross-linking agent content in a product of the method can be decreased so the product does not require purification.

The invention discloses a preparation method of a novel hyperbranched triazine char forming agent, which comprises the following steps: adding a dissolved diamine solution at 0-10 DEG C, gradually and dropwisely adding a dispersed cyanuric chloride solution, and reacting for 1-4 hours; heating to 30-70 DEG C, adding an acid-binding agent, and reacting for 3-8 hours; heating to 90-150 DEG C, and reacting for 6-10 hours; and stopping stirring, carrying out vacuum filtration, washing with water, and drying to obtain the triazine hyperbranched char forming agent. Compared with the prior art, the invention has the advantages of continuous reaction process, short reaction time, cheap raw materials, low solvent consumption, no addition of any blocking agent in the reaction process, simplified synthesis technique, high heat stability and high char forming ratio.

The invention relates to a method for making a chitosan derivative. The method is characterized in that: firstly, the purified chitosan is activated by a strong base to form a hydroxyl-K type chitosan; secondly, a 1, 2-butyl oxide linkage is taken as an etherifying agent, an isopropanol is taken as a disperse phase, the reaction lasts 2 to 4 days moderately at room temperature; after the reaction is finished, 8 to 10 times volume of acetone is precipitated and washed to be neutral as well as is dried in vacuum at a temperature of 50 DEG C to obtain the white powder. The hydroxybutyl chitosan with different degrees of substitution is obtained by controlling the proportion of the chitosan and the 1, 2-butyl oxide linkage and the reaction time. The method has the advantages of good water-solubility and the existence of the temperature sensitivity at a physiological temperature.

The invention discloses a covalent organic framework material and a preparation method thereof and belongs to the technical field of preparation of covalent organic framework materials. Multiple covalent organic framework materials are quickly synthesized under a room temperature and an open system by utilizing ionothermal reaction, and include a Schiff-base type covalent organic framework material and a boric-acid type covalent organic framework material, and also include covalent organic framework materials with two-dimensional and three-dimensional structures. The synthetic method has the advantages of short reaction time, low energy consumption, no pollution of volatile organic matters, no additive, simple operation and the like. Ironic liquid can be reused for at least three times after being simply filtered and separated. The covalent organic framework material synthesized by the method has potential application in the aspects of gas storage and separation and the like because ofloading the ironic liquid.

The present invention discloses a three-phase ultrasonic photo-catalyzed reaction device and a CO₂ reducing method with the device. With the device, a photo-catalyst is placed in a photo-reactor, and the reactor is placed in a water bath of an ultrasonic generator. A light source is arranged above the photo-reactor. The method is that the CO₂ gas to be reduced is mixed evenly with the photo-catalyst and a sodium hydroxide solution in the photo-reactor under the ultrasonic action, and reacts for 3-20 hours with radiation of the light source. Then the CO₂ gas is reduced. The photo-catalyst is made from titanium dioxide or silicon dioxide and metal phthalocyanine. Metal phthalocyanine is supported on the surface of titanium dioxide in the way of in-situ synthesis, sol-gel, and immersion. The present invention promotes the photo-catalysis efficiency, reduces the reaction time, and saves the energy. Visible light can be used for reducing. Moreover, the phot-catalyst can be recycled, which reduces the pollution and the cost, sot the present invention is quite applicable for the three-phase ultrasonic photo-catalyzed reaction device and photo-catalyzed CO₂ reducing.

The invention discloses a method for hydrolyzing lignocellulose. Lignocellulose is pulverized into particles, and the particles are mixed with water to form even seriflux; the seriflux is preheated to60-150 DEG C by using ultrasonic waves or microwaves; the preheated even seriflux is quickly heated to 120-300 DEG C, solid acid is added and used as a catalyst, and stirring and catalytic reaction are simultaneously carried out for 15-300 minutes. The use of the ultrasonic waves or microwaves radiation in synergism with solid alkali for catalyzing and hydrolyzing the lignocellulose can greatly reduce the reaction time as well as energy consumption. The solid acid catalyst can be repeatedly used, is easily separated, and has the advantages of high mechanical strength, high durability, certainselectivity, relative singularity of catalytic hydrolyzate, high hydrolyzing efficiency and good market application prospect.

The invention discloses a preparation method for a triazine hyperbranched macromolecular carbon forming agent. The method is characterized by comprising the following steps: 1), mixing diamino or hydroxyl compound with non-protonic organic solvent, and adding catalyst in the atmosphere of inert gases; 2), dropwise adding cyanuric chloride non-protonic organic solution, and continuing the reaction at the temperature after finishing dropwise adding the cyanuric chloride non-protonic organic solution; 3), adding blocking agent, and carrying out reaction again; and 4), precipitating, filtering, cleaning the organic solvent, separating, and drying to obtain the triazine hyperbranched macromolecular carbon forming agent. Compared with the prior art, the invention has the advantages that the 'one-pot' method is adopted, the reaction process is continuous, the reaction time is short, the product has favorable heat stability, the carbon forming rate is high, and the processability is good.

The invention relates to a method for synthesizing methylethyl carbonate. According to the method, under ordinary pressure, dimethyl carbonate and ethanol which are used as raw materials are subjected to synthetic reaction of methylethyl carbonate at certain reaction temperature for some time by using an imidazole ionic liquid as a catalyst. The invention has the following advantages: the catalyst consumption is only 0.5-5 wt% of the dimethyl carbonate; the ionic liquid catalyst has high catalytic activity in the reaction process, the maximum yield of methylethyl carbonate is up to 71.22%, and the selectivity is up to 88.52%; and the catalyst can be recycled for cyclic utilization after being subjected to simple treatment after reaction, has the advantages of long service life and no pollution, and greatly lowers the preparation cost of methylethyl carbonate.

The invention discloses a preparing method of spinel lithium titanate as Li-secondary battery cathode material, which adopts titanium dioxide and inorganic Li salt as raw material to low-temperature fusing salt as synthetic dielectrics to generate the product through solid-phase reaction.

The invention relates to a reaction system for alkyl nitrite and a preparation method for the alkyl nitrite. The preparation method comprises the following steps that: a trickle-bed reactor is adopted and porcelain ring filler is filled into the trickle-bed reactor; liquid added into the reactor forms liquid membranes on the filler; alkyl alcohol is taken as a liquid-phase raw material and nitric monoxide, oxygen and nitrogen are taken as gas-phase raw materials; and gas and liquid phases are reacted in the trickle-bed reactor by means of co-current flow or countercurrent flow under the condition of nitrogen protection so as to generate the alkyl nitrite. The mol ratio of the alkyl alcohol to NO is between 2 to 1 and 7 to 1, and the mol ratio of the NO to O2 is between 4 to 1 and 8 to 1; the reaction temperature is between 40 and 100 DEG C, and the reaction pressure is between 0.1 and 1.0 MPa; and the retention time of continuous feeding of liquid-phase alkyl alcohol in the trickle-bed reactor is between 10 and 500 minutes, and the retention time of continuous feeding of gas phase in the trickle-bed reactor is between 0.02 and 1 minute. The reaction system and the preparation method have the advantages that: the operating condition is mild; the reaction time is short; the conversion rate of the raw materials, and the selectivity and the yield of products are high; and the whole reaction system is convenient for realizing continuous production, etc.

The invention relates to a rutile type titanium dioxide nanowire film and a preparation method and applications thereof. The preparation method of the film comprises the steps of directly growing rutile phase titanium dioxide nanowire array on a conductive glass substrate, and evenly distributing titanium dioxide nanowire clusters on the surface of the top end of the array; and regulating the proportion of various reactants, reaction time, temperature and other factors by taking sulfate radical-containing titanium slat as precursor for preparing the film. The invention further provides applications of the film, and the film can be used as anode materials to assemble a solar cell, or as photocatalyst to carry out water photolysis or organic matter degradation treatment. The method is simple, and has strong controllability, the problems that therutile phase is difficult to be prepared by using the sulfate radical-containing titanium slat and the titanium dioxide nanowire array grows on the conductive substrate in situ are solved, and the change on the diameter and length of the nanowire can be realized while the no change on crystallinity of a sample can be ensured through a calcination method.