41 results about "High activation" patented technology

The invention provides a calcium carbonate modified polypropylene composite material and a preparation method thereof.The preparation method comprises the steps that calcium carbonate powder and a surfactant containing double bonds are mixed and stirred at the high temperature for preset time, and surface modified calcium carbonate is obtained; and mixing the surface modified calcium carbonate with polypropylene and an initiator, stirring for a preset time, and carrying out melt extrusion at 170-210 DEG C to obtain the calcium carbonate modified polypropylene composite material. The preparation method provided by the invention has the advantages of rapid activation and simple process, and the prepared surface modified calcium carbonate powder has the advantages of concentrated size distribution, uniform particle size and high activation degree, has good compatibility with polyolefin materials, can enhance the tensile strength and other mechanical properties of a composite material when being filled into a polymer, and has good application prospects. And good economic benefits are achieved.

The invention relates to an easily-activated Ti-Fe-Y-Mn-Zr-Co-Zn-based hydrogen storage alloy and a preparation method thereof, belongs to the technical field of hydrogen storage alloy materials, and solves at least one of the problems of high activation difficulty, long activation period, poor hydrogen absorption and desorption dynamic performance and the like of a Ti-Fe-based hydrogen storage alloy in the prior art. The invention provides a Ti-Fe-Y-Mn-Zr-Co-Zn based hydrogen storage alloy easy to activate, the chemical formula of the hydrogen storage alloy is Ti 1.15, Fe 0.8, Y 0.03, Mn 0.35-x-y-z ZrxCoyZnz, x, y and z are atomic ratios, x is larger than or equal to 0.05 and smaller than or equal to 0.15, y is larger than or equal to 0.02 and smaller than or equal to 0.1, and z is larger than or equal to 0.02 and smaller than or equal to 0.1. The Ti-Fe-Y-Mn-Zr-Co-Zn based hydrogen storage alloy provided by the invention obtains good activation performance and hydrogen absorption and desorption performance by means of component design and preparation process improvement, can be activated at one time under the conditions of 30 DEG C and 3 MPa, and has the hydrogen storage capacity of more than or equal to 1.69 wt.%, the hydrogen absorption platform pressure of more than or equal to 0.39 MPa and the hydrogen desorption platform pressure of more than or equal to 0.3 MPa.

The invention relates to a rare earth modified AB2 type solid hydrogen storage alloy and a batch preparation method thereof, belongs to the technical field of hydrogen storage alloy materials, and solves the problems of high activation condition, long activation period, overhigh hydrogen absorption platform pressure, high batch preparation smelting difficulty, low yield, unstable product quality and the like of the traditional Ti-Mn series hydrogen storage alloy in the prior art. The specific composition of the hydrogen storage alloy is Ti < 1.1-x-y > Y < x > Zr < y > Mn < 2.0-y-z-m > Cr < z > Ni < m > Co < n >, x, y, z, m and n in the formula are atomic ratios, x is larger than or equal to 0.01 and smaller than or equal to 0.04, y is larger than or equal to 0.10 and smaller than or equal to 0.35, z is larger than or equal to 0.45 and smaller than or equal to 0.70, m is larger than or equal to 0.1 and smaller than or equal to 0.2, and n is larger than or equal to 0.05 and smaller than or equal to 0.15. The hydrogen storage alloy has good activation performance and hydrogen absorption and desorption performance, the hydrogen storage capacity is larger than or equal to 1.86 wt.%, and the hydrogen absorption and desorption platform pressure can be adjusted according to application requirements; under the conditions that the temperature is 20 DEG C and the initial hydrogen pressure is 3 MPa, activation can be completed through one-time hydrogen absorption and desorption circulation; after 200 times of hydrogen absorption and desorption cycles, the capacity retention ratio of the alloy is gt; and 98%. The invention further provides a preparation method of the hydrogen storage alloy, the method has the advantages of being simple and easy to operate, high in yield, stable in product quality and the like, and the problem of component segregation of a casting process is fundamentally solved.

The invention relates to a Ti-Fe-Ce-Mn-Zr-Al-Co-based hydrogen storage alloy and a preparation method thereof, belongs to the technical field of hydrogen storage alloy materials, and solves at least one of the problems of high activation condition, long activation period, poor hydrogen absorption and desorption performance and the like of the traditional TiFe hydrogen storage alloy in the prior art. The invention provides a Ti-Fe-Ce-Mn-Zr-Al-Co-based hydrogen storage alloy which is characterized in that the specific composition of the alloy is Ti < 1.05 > Ce < 0.05 > Fe < 1.15-x-y-z-m > Mn < x > Zr < y > Al < z > Com, x, y, z and m are atomic ratios, x is larger than or equal to 0.1 and smaller than or equal to 0.25, y is larger than or equal to 0.05 and smaller than or equal to 0.2, z is larger than or equal to 0.02 and smaller than or equal to 0.1, and m is larger than or equal to 0.02 and smaller than or equal to 0.1. The hydrogen storage alloy has good activation performance and hydrogen absorption and desorption performance, the hydrogen storage capacity is larger than or equal to 1.70 wt.%, the hydrogen absorption plateau pressure is larger than or equal to 0.41 MPa, and the hydrogen desorption plateau pressure is larger than or equal to 0.31 MPa; activation can be completed at a time under the conditions that the temperature is 30 DEG C and the initial hydrogen pressure is 3 MPa, and the solid hydrogen storage material can be widely applied to hydrogen fuel cells and other scenes as a solid hydrogen storage material.

The problem addressed by the present invention is that of achieving a higher activation effect than conventional non-power generation methods at a lower cost than conventional power generation methods. In order to solve the problem, the fuel cell activation device of the present invention activates the fuel cell cells. A fuel cell is provided with an anode layer, an electrolyte membrane, and a cathode layer in this order from one side. Platinum is contained as a catalyst in the anode layer and the cathode layer. A fuel cell activation device is provided with an anode-side gas supply device, a cathode-side gas supply device, and a potential scanning circuit. In a fuel cell activation device, fuel cells are activated by supplying a fuel gas to an anode layer by means of an anode-side gas supply device, supplying a low-oxygen gas to a cathode layer by means of a cathode-side gas supply device, and controlling the potential of the cathode layer by means of a potential scanning circuit.

The present invention relates to the technical field of modified calcium carbonate, particularly to the field of IPC C08K, and more specifically to a method for preparing and applying ultrafine modified calcium carbonate. By selecting a specific modifier and combining it with a preparation method, the present invention controls the amount of added additives to below 1.5 wt%, thereby reducing production costs and achieving optimal cost-performance. Furthermore, the prepared calcium carbonate has low oil absorption, high activation rate, and excellent dispersion properties, making it highly suitable for use as a filler modifier for polypropylene, nylon, and ABS plastics.

The application provides a high-purity germanium detector molecular sieve activation device and activation method under vacuum sealing conditions, and is used for solving the technical problems of low efficiency, complicated operation and difficult process guarantee of the existing molecular sieve activation method, unstable adsorption performance and quality of the molecular sieve, poor adsorption effect and poor economy. The high-purity germanium detector molecular sieve activation device under vacuum sealing conditions comprises an automatic control unit formed by an alternating current contactor, a temperature controller and a starting button, and the automatic control unit is matched with a temperature sensor and a heating pipe respectively, so that the molecular sieve activation device has a temperature monitoring function, and automatic stopping and automatic heating of the molecular sieve heating activation are realized through temperature monitoring. The application has the advantages of simple structure, convenient control, molecular sieve activation and vacuum preservation functions, cost saving, activation efficiency improvement, high vacuum high-temperature baking and degassing functions of the vacuum assembly, and the like.

This invention provides a semiconductor device with a high activation rate for p-type impurities. [Solution] The method for manufacturing a semiconductor device comprises: a p-type layer formation step of forming a p-type layer 12 made of a group III nitride semiconductor doped with p-type impurities by MOCVD; an annealing step of performing an annealing treatment on the surface of the p-type layer 12 with at least a region contributing to the device operation exposed to activate the p-type impurities of the p-type layer 12; and an n-type layer formation step of forming an n-type layer (second n-type layer 13) made of an n-type group III nitride semiconductor on the p-type layer 12 by a formation method using materials that do not contain hydrogen in the raw materials and carrier gas.

This application relates to the field of memory, providing a refresh control circuit, a memory, and a refresh control method. The refresh control circuit includes a page table, a first comparison circuit, and a second comparison circuit. The page table is configured to store multiple row addresses and their activation counts. The first comparison circuit, connected to the page table, is configured to receive the currently active row address and its activation count, and compare the currently active row address and its activation count with the multiple row addresses and their activation counts stored in the page table. When a first preset condition is met, the currently active row address and its activation count are stored in the page table. The second comparison circuit, connected to the page table, is configured to compare the activation counts of the multiple row addresses in the page table and output the row address with the highest activation count as a candidate row address.

This invention relates to a Ti-Fe-Ce-Mn-Zr-Al-Co based hydrogen storage alloy and its preparation method, belonging to the technical field of hydrogen storage alloy materials. It solves at least one of the problems of high activation conditions, long activation cycles, and poor hydrogen absorption / desorption performance in existing TiFe hydrogen storage alloys. This invention provides a Ti-Fe-Ce-Mn-Zr-Al-Co based hydrogen storage alloy, characterized in that: the alloy's specific composition is Ti... 1.05 Ce 0.05 Fe 1.15‑x‑y‑z‑m Mn x Zr y Al z Co m Where x, y, z, and m are atomic ratios, and 0.1≤x≤0.25, 0.05≤y≤0.2, 0.02≤z≤0.1, 0.02≤m≤0.1. The hydrogen storage alloy exhibits excellent activation and hydrogen absorption / desorption properties, with a hydrogen storage capacity ≥1.70 wt.%, a hydrogen absorption plateau pressure ≥0.41 MPa, and a hydrogen desorption plateau pressure ≥0.31 MPa. It can be activated in a single step at 30°C and an initial hydrogen pressure of 3 MPa, making it suitable for widespread application as a solid-state hydrogen storage material in hydrogen fuel cells and other scenarios.

The invention discloses a vanadium-based hydrogen storage alloy capable of being activated at room temperature, a preparation method of the vanadium-based hydrogen storage alloy and application of Sm, belongs to the technical field of hydrogen storage materials, and aims at solving the technical problems that an existing vanadium-based hydrogen storage alloy is high in activation temperature and long in activation time. The vanadium-based hydrogen storage alloy capable of being activated at room temperature provided by the invention has a general formula of V < x > Ti < y > Cr < z > Fe < a + b wt% S < m >, x + y + z + a = 10, 7 < = x < = 8, 0.7 < = y < = 1.4, 1.0 < = z < = 1.6, 0.2 < = a < = 0.3, 0.005 < = b < = 0.010; wherein x, y, z and a are atomic ratios, and b is the mass percent of Sm in the vanadium-based hydrogen storage alloy. After the vanadium-based hydrogen storage alloy is vacuumized at the temperature of 40 DEG C for 3000 seconds, the vanadium-based hydrogen storage alloy absorbs hydrogen once under the hydrogen conditions of 40 DEG C and 8 MPa, and the vanadium-based hydrogen storage alloy can be completely activated.

The invention discloses a redundant structure backdoor detection method based on a branch activation statistical mechanism, electronic equipment and a storage medium, branch channel function packaging is carried out on a suspicious model, and a dynamic counter is used for counting the calling times and activation proportions of branches, so that potential redundant backdoor branches existing in the model are effectively identified. In an application scene of a complex multi-branch network, no matter whether the model is affected by structure poisoning, the activation behavior characteristics of each branch of the model can be accurately captured, and the redundancy condition of the model is comprehensively evaluated. When a certain branch of the multi-branch neural network presents an extremely high activation frequency under specific input and the activation contribution degree is significantly low during normal input, the branch is judged as a backdoor attack redundant branch of a specific task. According to the method, the potential threat of the structure backdoor attack to the deep model can be effectively reduced, the robustness and the practical application value of the model are remarkably improved, and a brand new technical means is provided for the field of intelligent model security.

The invention discloses a preparation method of nano calcium carbonate with high dispersity and high activation degree. In the initial stage of the aging process, polyepoxysuccinic acid is adopted as a dispersing agent, and in the modification process, gamma-glycidyl ether oxypropyl trimethoxy silane / XH-CS05 / stearic acid is used for composite modification, so that the surface performance is greatly optimized, the hydrophilic performance is reduced, the closest distance between calcium carbonate particles is effectively increased, and the service life of the calcium carbonate particles is prolonged. Meanwhile, gaps among the particles are filled, mutual agglomeration of the calcium carbonate particles is successfully prevented, and the dispersity among the particles is improved. According to the prepared nano calcium carbonate with high dispersity and high activation degree, the activation degree is as high as 100%, the oil absorption value is 28g / 100g, the specific surface area BET value is 37.3668 m / g, and the nano calcium carbonate has the characteristics of high activation degree, low oil absorption value and relatively high specific surface area. The nano calcium carbonate modified by the method has the advantages of high activation degree, good dispersibility, simple process, convenient operation, easily available raw materials and the like, is easy to realize industrial production, and can be better applied to downstream products.

The invention discloses a coal gangue microwave-chemical synergistic activation method and activated coal gangue, the coal gangue microwave-chemical synergistic activation method comprises the following steps: (1) crushing coal gangue to obtain a crushed product; (2) mixing the crushed product with a composite activator, and performing microwave treatment to obtain an activated product; the composite activating agent comprises waste alkali liquor, fly ash aluminum extraction residues and water glass; and (3) drying, cooling and grinding the activated product to obtain the activated coal gangue. The microwave-chemical synergistic activation method for the coal gangue is high in activation efficiency, efficient destruction of crystal lattices of coal gangue minerals is achieved through the synergistic effect of microwaves and the composite activating agent, the activation time is shortened, the silicon-aluminum dissolution rate is increased, the silicon dissolution rate reaches 80% or above, the aluminum dissolution rate reaches 70% or above, the problem that single chemical activation is low in efficiency is solved, and the method is suitable for industrial production. And the obtained activated coal gangue product has high activity.

The application relates to an easily-activated Ti-Fe-Y-Mn-Zr-Co-Zn-based hydrogen storage alloy and a preparation method thereof, and belongs to the technical field of hydrogen storage alloy materials. At least one of the problems in the prior art, such as high activation difficulty, long activation period, poor hydrogen absorption and desorption kinetic performance and the like of a Ti-Fe-based hydrogen storage alloy, is solved. The application provides an easily-activated Ti-Fe-Y-Mn-Zr-Co-Zn-based hydrogen storage alloy, and the chemical formula of the hydrogen storage alloy is Ti 1.15 Fe 0.8 Y 0.03 Mn 0.35‑x‑y‑ z Zr x Co y Zn z , wherein x, y and z are atomic ratios, and 0.05<=x<=0.15, 0.02<=y<=0.1 and 0.02<=z<=0.1. The Ti-Fe-Y-Mn-Zr-Co-Zn-based hydrogen storage alloy provided by the application has good activation performance and hydrogen absorption and desorption performance through component design and preparation process improvement, and can be activated at one time under the condition of 30 DEG C and 3 MPa, the hydrogen storage capacity is greater than or equal to 1.69 wt.%, the hydrogen absorption plateau pressure is greater than or equal to 0.39 MPa, and the hydrogen desorption plateau pressure is greater than or equal to 0.3 MPa.

The utility model discloses an efficient carbonized material activating device which comprises a microwave activating oven, a feeding hopper is fixedly communicated with the left side of the top of the microwave activating oven, vibration motors are symmetrically erected on the lower portion of the left side of the feeding hopper in a front-back mode, and a plurality of damping dampers are fixedly arranged between the vibration motors and the microwave activating oven in an annular array mode. The bottom output end of the vibration motor slidably extends into the microwave activation furnace and is fixedly connected with a frame plate, the bottom of the frame plate is fixedly connected with a fan-shaped screen, a through hole is formed in the center of the top of the fan-shaped screen, and carbonization materials and metal particle catalysts falling in a concentrated mode are continuously oscillated and scattered. And meanwhile, the vibration motor can improve the activity of the carbonized material and the metal particle catalyst on the fan-shaped screen and increase the interaction strength of the carbonized material and the metal particle catalyst, so that the activation rate of the carbonized material is increased, and the activation quality is improved.

The invention discloses a thermal battery with high integration, temperature self-adaption and high activation time precision in the technical field of power supply systems, and the thermal battery comprises one or more unit thermal batteries and a micro-miniature control system, the micro-miniature control system is mechanically connected with the thermal battery, and the micro-miniature control system is electrically connected with the thermal battery. According to the scheme, the thermal battery with high integration, temperature self-adaption and high activation time precision is provided, and the problem that the activation time of the thermal battery is influenced by the temperature and the size of the battery is solved.

The invention discloses a cathode material for electrocatalytic degradation of tetracycline, and a preparation method and application thereof, wherein the cathode material is high in activation efficiency, reusable and small in secondary pollution. The preparation method of the cathode material for electrocatalytic degradation of tetracycline comprises the following steps: preparing a reaction solution, wherein the reaction solution contains zinc ions, iron ions, manganese ions, urea and ammonium fluoride; obtaining a carrier, wherein the carrier has a three-dimensional network structure; performing high-pressure heat treatment on the mixture of the carrier and the reaction liquid to generate a precursor containing the carrier; and calcining the precursor to obtain the cathode material containing the carrier. The cathode material for electrocatalytic degradation of tetracycline is prepared by the preparation method. The purification method of tetracycline in water adopts the cathode material prepared by the preparation method to perform electrocatalytic degradation treatment on a to-be-treated water body containing tetracycline.

The invention belongs to the technical field of silicon micro-powder, and provides a preparation method of high-activation-degree crystalline silicon micro-powder. The preparation method comprises the following steps: mixing crystalline silicon micro-powder with an alkaline solution to obtain alkali-modified crystalline silicon micro-powder; and mixing the alkali-modified crystalline silicon micro-powder, a silane coupling agent and absolute ethyl alcohol, and carrying out surface modification to obtain the crystalline silicon micro-powder with high activation degree. The number of hydroxyl groups on the surface of the alkali-modified crystalline silicon micro-powder is remarkably increased, more reaction sites are provided for subsequent silane coupling agent modification, and the activation degree of the crystalline silicon micro-powder is remarkably improved and reaches up to 90.5%; according to the invention, the crystalline silicon micro-powder is subjected to surface modification by adopting a post-synthesis modification technology, functional groups on the surface of the crystalline silicon micro-powder are constructed from the molecular level, and the compatibility and dispersity among the crystalline silicon micro-powder, a silane coupling agent, a polymer substrate and the like are improved, so that the crystalline silicon micro-powder can meet the requirements in the fields of high-end copper-clad plates, chip packaging and the like.

This invention belongs to the field of hydrogen storage alloy technology, and discloses a vanadium-based solid solution hydrogen storage alloy with high activation performance and its preparation method. The general formula for hydrogen storage alloys is Ti. a Cr b V c Al1Si 0.5 A d In the formula, A represents a rare earth element, and a, b, c, and d represent weight percentages with the following numerical ranges: 11≤a≤18, 19≤b≤33, 40≤c≤60, and 6≤d≤13. The thickness of the metal oxide layer on the surface of the hydrogen storage alloy is 1-10 nm. The hydrogen storage alloy is prepared using a stepwise addition method of rare earth raw materials. The resulting vanadium-based solid solution hydrogen storage alloy can be activated at room temperature and possesses excellent hydrogen storage performance.

The application belongs to the technical field of circuit board production, and discloses a circuit board activation equipment and a circuit board production line. The circuit board activation equipment comprises an activation tank capable of containing activation liquid and a conveying mechanism for conveying the activated circuit board. In the conveying direction of the conveying mechanism, the middle section of the conveying mechanism extends to the bottom of the activation tank, so that the middle section of the conveying path of the circuit board conveyed by the conveying mechanism is below the liquid level of the activation liquid. The circuit board activation equipment and the circuit board production line provided by the application can make the liquid level of the activation liquid in the activation tank lower than the conveying surface of the whole equipment, ensure that the activation liquid in the activation tank is not easy to overflow, and thus it is not necessary to pump the activation liquid into the activation tank from the outside to maintain the liquid level height, the activation liquid in the activation tank can be maintained stable, compared with the prior art, the generation of bubbles in the activation liquid is effectively reduced, and the activation quality is improved.

The application discloses a non-target screening solid-phase extraction system and a screening method, and belongs to the technical field of pollutant treatment. The system comprises a plurality of solid-phase extraction columns and pH adjusting devices which are cross-connected. The pH adjusting devices are used for adjusting the pH value of the flowing water sample. The pH values adjusted by the plurality of pH adjusting devices are different. The types of the plurality of solid-phase extraction columns are different or the same. The application can meet the needs of non-target detection, and has the advantages of good enrichment effect, high enrichment efficiency, high activation and elution efficiency and the like.

The invention discloses a high-activation-performance vanadium-based solid solution hydrogen storage alloy, and relates to the field of hydrogen storage alloys, the hydrogen storage alloy has a gradient nanostructure, and comprises a core area: an isometric crystal structure with a grain size of 50-200 nm; the transition area is of a nanocrystalline structure with the grain size of 20-50 nm; and the surface layer area is an amorphous / nanocrystalline composite layer with the thickness of 2-8nm, by designing a gradient nanostructure and through the synergistic effect of the core area, the transition area and the surface layer area, the mechanical strength of the alloy is guaranteed, the surface activation performance is improved, and by means of the novel preparation technology combining ball milling with gradient sintering and accurately controlling technological parameters of all stages, the mechanical strength of the alloy is improved. And the optimized distribution of the additive and the controllable formation of the nano structure are realized.

The invention discloses a Wnt signal path adjusting system and a method for activating a Wnt signal path. The Wnt signal channel regulation system comprises a first regulator and a second regulator, each regulator comprises an I structural domain and an II structural domain, the first regulator comprises an I-1 structural domain and an II-1 structural domain which are respectively targeted to Wnt receptors Frizzled and LRP6, and the second regulator comprises an I-2 structural domain and an II-2 structural domain which are respectively targeted to Wnt receptors Frizzled and LRP6; the first regulator is different from the second regulator. The Wnt signal channel regulation system provided by the invention has the advantages of high activation capability, small toxic and side effects and selectivity in Wnt signal channel activation, and has a good application prospect.

The present application relates to the field of fuel cell, specifically to a kind of fuel cell quick activation method, comprising the following steps: S1, the anode and cathode of fuel cell are all connected into high humidity nitrogen and are purged;S2, activation procedure, including S21 and S22: S21, according to four from low to high activation current order in turn four activations are carried out in operating stack, each activation operation includes three "gas shortage-recovery" cycle and once manual stop stack test platform operation;S22, restart stack test platform, pull load to fourth activation current, according to the standard working condition of fourth activation current operation for a period of time, judge whether average single piece voltage fluctuation is ≤5mV, if yes, then execute step S3;S3, after activation procedure is completed, anode, cathode are connected into dry nitrogen and are purged.The present application shortens stack activation time under the premise of guaranteeing activation effect, reduces the complexity and energy consumption of activation operation, improves the large-scale production efficiency of fuel cell.

The invention discloses an activation method and device for an NEG in an atomic clock air chamber, and relates to the technical field of atomic clocks.The activation method comprises the steps that a light beam control element is used for adjusting the light beam shape or the light beam output direction of laser emitted by a laser device, and a target laser beam is obtained; the target laser beam is controlled to be incident to the NEG in the atomic clock air chamber; collecting temperature data of the NEG under irradiation of the target laser beam; and monitoring the activation state of the NEG according to the temperature data so as to complete activation of the NEG. According to the method and the device provided by the invention, the NEG in the atomic clock air chamber is activated by adopting laser, so that the damage caused by punching and electricity leading on the atomic clock air chamber during electric activation is overcome, and the influence of baking activation on an air chamber shell is avoided. When the laser activates the NEG, the heat conduction direction in the air chamber of the atomic clock is from inside to outside, so that the NEG with higher activation temperature and stronger air suction capacity can be selected, and the vacuum degree in the air chamber can be better maintained.

The invention discloses a modeling method and system for a bicycle shock absorber, and belongs to the technical field of image modeling, and the method comprises the steps: obtaining shock absorber images of different types and different working states of the bicycle shock absorber; marking a key part of the shock absorber image, and processing the marked shock absorber image to obtain a preprocessed image data set; constructing an acting point activation analysis model based on a convolutional neural network, and inputting the preprocessed image data set into the acting point activation analysis model for calculation to obtain a shock absorber stress high activation area vector; and constructing a three-dimensional model of the bicycle shock absorber based on the shock absorber stress high activation area vector and the shock absorber parameters. According to the method, accurate position information can be provided through the stress point vectors obtained through the CNN, and the stress distribution conditions of the shock absorber under different conditions can be accurately known.

The invention discloses an activation processing control method and system based on image processing. The method comprises the following steps: when a target activation processing system executes high-temperature activation processing, obtaining a region image of an activation processing region; based on an image segmentation algorithm, determining a processed image and a processed image of the grenade shell in the regional image; according to the image during processing and the image after processing, determining an activation processing problem corresponding to the target activation processing system based on an image analysis algorithm; according to the activation processing problem, based on a preset instruction generation rule, generating an equipment control instruction corresponding to high-temperature processing equipment of the target activation processing system; the equipment control instruction is used for controlling the activation operation of the high-temperature treatment equipment on the lightning shell so as to solve the activation treatment problem. According to the invention, the working abnormity of the activation treatment system can be monitored and corrected more accurately and timely, the accuracy and efficiency of activation treatment are improved, and the product yield is improved.

The invention provides a formula of an AES and LAS compound concentrated detergent with high activation efficiency at low temperature, which comprises the following components in percentage by mass: 20-25% of fatty alcohol-polyoxyethylene ether sodium sulfate (AES); 18-22% of sodium linear alkyl benzene sulfonate (LAS); 5 to 8% of alkylphenol polyoxyethylene ether (AEO-9); 0.8 to 1.5 percent of sodium chloride (NaCl); and the balance of water. Wherein the mass ratio of AES to LAS is (1.1: 1)-(1.4: 1), and the total active matter content of the composition is greater than or equal to 40%; moreover, the composition does not contain a penetrant and a humectant. Through specific selection, accurate proportioning and synergistic effect of the components, the core technical problems of slow dissolution, easy gelation and poor decontamination efficiency of the concentrated detergent at low temperature are effectively solved, and high activation efficiency in low-temperature water is realized.

The present application relates to the field of wireless communication search and rescue, and particularly relates to a radio remote activation method, comprising the following steps: step 1, after a person is in distress, a distress device sends a distress alarm information, and enters a "sleep-work" mode; step 2, after the search device receives the distress alarm information, an activation instruction is sent to activate the distress device; step 3, the distress device receives the activation instruction, adjusts the working parameters of itself with the activation parameters in the activation instruction, and receives a communication instruction. The present application has higher activation efficiency and stronger universality by designing the remote activation instruction with multiple activation parameters; the corresponding activation parameters can be set by the user of the distress device and the user of the search device, and the search device can remotely and reliably activate the distress device; the activation instruction also has control parameters, which can increase the corresponding search and rescue command control ability.