93results about How to "Short activation time" patented technology

A multi-part kit system comprising a solid part A which comprises at least one acetyl donor, a liquid part B in the form of an aqueous composition which comprises 3 to 35 wt. % of hydrogen peroxide and one or more parts C, wherein the solid part A and/or the part(s) C comprise at least one surfactant selected from the group consisting of anionic surfactants, amphoteric surfactants and nonionic surfactants, wherein the composition of the parts of the multi-part kit system is such, that directly after being mixed with each other and water in a specified ratio the pH of the mixture is in the range of 5.5 to 8.

The invention relates to a detection agent for hemostasis and thrombus belonging to medical clinical detection technical field, in particular to a detection agent for measuring activation partial thromboplastin time (APTT) of blood plasma. The invention is characterized in that the agent is prepared from 0.05-0.5g/L agent solid activator, 20-200mg/L phosphatide, 0.1-10mmol/L divalent metal ion salt, 0.1-0.5g/L stabilizer, 0.1-10g/L polyethylene glycol PEG, 0.05-4.0g/L buffer agent, 2.0-5.0g/L revival agent, while the left is water. The invention provides a high-stability standard agent for meeting APTT measurement, with simple operation, suitable price, short activation time and high sensitivity.

The invention relates to a method for preparing activated carbon with a large specific surface area through rapid activation. The activated carbon with a large specific surface area is prepared through rapidly activating high-carbon raw materials, such as anthracite, petroleum coke and the like, by auxiliaries and alkali together. The method comprises the steps of uniformly mixing the high-carbon raw materials, the activating auxiliaries and KOH, so as to obtain an alkali-carbon mixture, and heating the alkali-carbon mixture under the protection of an inert atmosphere, so as to obtain an activation product; quickly cooling the activation product to room temperature under the protection of the inert atmosphere; washing the activation product with water, and drying, thereby preparing the activated carbon with a large specific surface area. According to the method, the activation temperature is low, the activation time is short, a relatively high yield of activated carbon with a large specific surface area is obtained under the condition of a lower alkali/carbon ratio, the utilization ratio of alkali, carbon and energy is increased, the production cost is reduced, and the pollution is reduced.

The invention relates to an activate method of membrane electrode of fuel battery, wherein the fuel battery comprises baffle plates, an anode room 4, a cathode room 5, and a membrane electrode. The membrane electrode is between the baffles, the membrane electrode comprises an anode 1, a cathode 2, and an atom exchange membrane 3 between the anode 1 and the cathode 2, the anode room 4 is between the anode 1 and the baffle plates, and the cathode room 5 is between the cathode 2 and the baffle plates. The method comprises that connecting the anode and cathode of a power supply respectively with the anode 2 and the cathode 2 of fuel battery, adding one external power on the fuel battery, filling fuel into the anode room 4 before closing the power supply, and filling water into the cathode room 5. The active area of membrane electrode activated by the invention is significantly improved, and therefore, the power of fuel battery is improved. The inventive activate method ha simple operation, short activate time, and better repeatability.

The invention provides petroleum coke based activated carbon, a preparation method therefor and use thereof. The petroleum coke based activated carbon has the following characteristics that the specific surface area calculated by the BET method is 1,700-2,500m<2>/g, the ratio of mesopores with the pore size of 2-50nm accounts for 20-40% of whole pores, the average particle diameter is 5-20 microns, the total content of surface oxygen-containing functional groups tested by the Boehm titration method is lower than 0.1mmol/g, the content of contained total heavy-metal impurities is lower than 100ppm, and the content of anions is lower than 50ppm. The petroleum coke based activated carbon has a high specific surface area, reasonable pore size distribution, low impurity content and high specific capacity and can be applied to supercapacitors.

A method to limit overheating of a brake equipped with an electromechanically actuable parking brake including the steps of: driving a threaded spindle by an electric motor until a power drain (I_max), corresponding to a brake application force (F), is reached; detection of a travel distance (x₀) of the piston corresponding to the brake application force (F) of the brake caliper in a locked state; determination of a second travel distance (x₁) by adding a further travel distance value (x₁₁), which corresponds to the desired clearance value, to form (x₀); driving of the electric motor until the second travel distance (x₁) has been covered by the brake piston; and comparing the vehicle speed with a predefined first speed value, at the upward transgression of which the electric motor is driven once more in the release direction until a further, previously defined travel distance (x₁₂) has been covered.

An image heating apparatus has a first rotatable member contacting a second rotatable member, wherein the recording material bearing the image passes through a nip portion formed at a position between the first rotatable member and the second rotatable member; a heater for heating the first rotatable member, the heater having a third rotatable member that is flexible and a temperature detecting element, wherein the third rotatable member contacts an outer peripheral surface of the first rotatable member and the temperature detecting element is provided in an area of an inside surface said third rotatable member, wherein the first rotatable member and the third rotatable member contact; and a controller for controlling the heater based on detecting the temperature of said temperature detecting element.

The invention relates to a method for carrying out surface activating treatment on the surface of titanium alloy. The method includes the following steps: 1. oil and rust removing is first carried out on a titanium alloy base material part; 2. etching treatment is carried out on the part; 3. surface activating treatment is carried out on the part, wherein activating solution of the surface activating treatment is a mixture of glycol, acidic ammonium fluoride, nickel chloride, boric acid, lactic acid and acetic acid, the temperature of the surface activating treatment is within 40 to 60 DEG C, and the time of the surface activating treatment is within 30 to 40min; 4. drying and after-treatment procedures are carried out. Compared with the prior art, the method has the following characteristics: the activating time is short, the activating effect is good, no corrosion is incurred on the part, the risk of corrosion on the part is basically eliminated, and the environmental pollution is mild; with high stability and quick deposition, the activating solution that the method adopts can form a coating with good corrosion/wear resisting properties and good metallurgical combination with a matrix on the surface of the titanium alloy, thereby preventing contact corrosion between the titanium alloy part and aeronautical materials such as aluminum alloy, high-temperature alloy and the like.

The invention discloses a system and a method for treatment and recovery of electronic electroplating wastewater. The system comprises a wastewater recovery and treatment unit and an RO (reverse osmosis) concentrate treatment unit. A grille, an adjusting tank, a coagulation reaction device, a settlement and membrane separation device, an ozone oxidation tank, an ozone digestion tank, a cartridge filter and an RO device are connected to the wastewater recovery and treatment unit sequentially. A hydrolytic acidification tank, a contact oxidation tank and a settling tank are connected to the RO concentrate treatment unit. The electronic electroplating wastewater is treated through the grille, the adjusting tank, the coagulation reaction device, the settlement and membrane separation device, the ozone oxidation tank, the ozone digestion device, the cartridge filter and the RO device. RO fresh water is then reused on an electronic electroplating line. RO condensed water is effectively treated through the hydrolytic acidification tank and the contact oxidation tank and stably meets the primary specification GB8978-1996 of integrated wastewater discharge standard, and discharge requirements DB4426-2001 of discharge limits of water pollutants of Guangdong.

The invention discloses a method and a system for injecting a hotfix into software of an embedded system, and relates to the technical field of software fixes for the embedded system. The method comprises the following steps: reserving a plurality of secondary jump table reserving zones in a software program, and reserving a plurality of tertiary jump table reserving zones in a fix file; distributing a nearest secondary jump instruction storage space for each original function, and distributing a nearest tertiary jump instruction storage space for each fix function; generating a secondary jump instruction sequence for each original function and storing each secondary jump instruction sequence into the corresponding secondary jump instruction storage space, and generating a tertiary jump instruction sequence for each fix function and storing each tertiary jump instruction sequence into the corresponding tertiary jump instruction storage space; finally, modifying the first instruction of each original function into a primary jump instruction. According to the method and the system, the operating of a system program is not influenced, and a compiler is not required to be modified; the memory space waste is low; the fix starting time is short.

When a content is playbacked via a network, if a transmission-sided terminal of the content is under stopping condition, then a lengthy time is required until the content is playbacked. When an activation time of a recorder is measured and contents are recorded on this recorder, a content corresponding to the activation time is copied to another recorder so as to be shared by the own recorder and another recorder. In the case that the content is playbacked via the network, the content held in the own recorder is firstly playbacked, and when the recorder holding the content is activated, so that the content can be transmitted, the own recorder directly receives the content from the recorder holding the content to playback the received content.

The invention discloses a preparation method of a sulfur, nitrogen and phosphorus codoped porous carbon material for a supercapacitor, and belongs to the technical field of a new energy source. Ginkgoleaves are used as a carbon source; deionized water is used for cleaning and removing surface impurities; after cleaning and drying, crushing is performed; the crushed ginkgo leaves and complex alkali metal hydroxide are uniformly mixed; in inert gas, the temperature is raised at a speed rate of 5 DEG C/min to reach activation temperature; heat insulation is performed for 2h to obtain an activated product; finally, the activated product is subjected to acid washing neutralization; deionized water is used for cleaning until a neutral state is reached; drying, grinding and sieving are performedto obtain the porous carbon material for the supercapacitor. The ginkgo leaves are used as raw materials for preparing the carbon material for the supercapacitor; the energy is saved; the environmentis protected; the process is simple; the cost is low; the sulfur, nitrogen and phosphorus self doping can be realized, so that the electrochemical active sites are increased; the wettability with electrolyte is enhanced; the porous carbon material has wide market application prospects when being used as a supercapacitor electrode material.

The invention provides a method for simultaneously producing activated carbon and medium heating value MHV fuel gas by using eupatorium adenophorum. The method comprises the following steps of: drying and heating up eupatorium adenophorum for carbonization; heating up and carrying out heat preservation after crushing, then heating up to 900-1000 DEG C, and feeding carbon dioxide to a furnace for activation, thereby obtaining crude products of the activated carbon and MHV fuel gas; and cooling the crude product of the activated carbon to room temperature under the protection of air isolation, and then drying to obtain the product of the activated carbon. The iodine adsorption capacity of the main quality index of the obtained activated carbon achieves the national primary standard, the adsorption property of the obtained activated carbon is good, and the prepared fuel gas has a heat value up to 11000-13000KJ/m<3>, includes main components C2H2, H2, CH4 and CO, belongs to the MHV fuel gas, and can be used as a gas fuel. According to the method for simultaneously producing activated carbon and medium heating value (MHV) fuel gas by using eupatorium adenophorum, the whole process is shorter in activation time, pollution-free in preparation process, high in comprehensive utilization of resources, and high in added value of the product; the materials are rich in source, and the eupatorium adenophorum resources can be fully converted into biomass energy products.

A drive circuit includes a circuit for feedback oscillation connected to a vibrator to form a feedback oscillation circuit and including a high-pass filter, an oscillation circuit that outputs a periodic signal, and a control circuit that controls whether or not the periodic signal output by the oscillation circuit is supplied to the circuit for feedback oscillation under a condition that the feedback oscillation circuit operates, and controls to bring a state between a first node as an output node and a second node grounded of the high-pass filter into a non-conduction state when the periodic signal is supplied to the circuit for feedback oscillation and bring the state between the first node and the second node into a conduction state when the periodic signal is not supplied to the circuit for feedback oscillation.