47 results about "Withdrawal time" patented technology

A list of products is created that includes one or more products to be introduced within a future time interval and for zero or more products to be withdrawn within a future time interval, an indication of a withdrawal time. For multiple products of the list of products, a list of parts used by those products is generated. From that list of parts, information is obtained to manage parts of products. This information includes an indication of those parts that are unique, and thus, may be replaced by common parts.

The invention discloses a differential withdrawal method based on user classification in a 5G large-connection IOT. The differential withdrawal method comprises the steps that: (1), the coverage class, which a user terminal belongs to, is judged according to channel fading information of the user terminal; (2), a base station sends the coverage class, which the user terminal belongs to, to the user terminal through a downlink control channel; (3), the user terminal initiates a random access request; when being not accessed, the user terminal generates withdrawal time; after the withdrawal time, the user terminal re-initiates the random access request; when the user terminal is accessed, differential withdrawal based on user classification in the 5G large-connection IOT is completed; and otherwise, it turns to the step (4); and (4), when the time that the user terminal initiates the random access request is less than the pre-set maximum withdrawal time, it turns to the step (3); and otherwise, when the next service period is waited, it turns to the step (3). By means of the method, the system capacity can be effectively increased; and the system access failure probability can be reduced.

The invention discloses an eprinomectin transdermal agent, a preparation method and application. The eprinomectin transdermal agent is composed of azone, oleic acid, propylene glycol, dimethyl sulfoxide and alcohole with a certain weight amount. The preparation method comprises: A, performing sample preparation, namely, setting five levels for each transdermal promoting agent, and adding alcohol for preparing samples; B, performing in-vitro transdermal experiments, fixedly disposing skin of a white mouse between a dispersion pool and a receiving pool of a YB-P6 intelligent transdermal tester, enabling the inner layer surface of skin to face to the receiving pool, enabling the whole dispersion pool to be full with the eprinomectin transdermal-agent formula sample, and adding acetonitrile to fill the receiving pool as a receiving solution; C, detecting the receiving solution obtained in the step B by using high performance liquid chromatographic instrument, and selecting a formula through visual analysis and variance analysis on an orthogonal experiment result; D, preparing the formula and verifying according to the front steps; and E, preparing a final product, and preparing a transdermal agent containing 0.025-0.1 g of eprinomectin. The formula is reasonable, convenient to use and capable of continuously expelling parasites without needing withdrawal time, and has the expelling rate of 90% or more on nematode and ectoparasites.

The invention relates to a pesticide for plants. The pesticide is characterized by comprising the following components in parts by mass: 15.4-26.6 parts of garlic, 29.4-39.7 parts of onion, 2.4-2.6 parts of rheum officinale, 2.8-3.2 parts of radix sophorae flavescentis, 2-3 parts of sulphur, 2-3 parts of calamine, and 3.8-9.9 parts of 40% ethyl alcohol. The pesticide is easy to prepare and convenient to use; edible plants are used as the raw materials, so that the pesticide integrates insect prevention and control and plant nutrition supplementation and is pollution-free, residue-free and high in efficiency; the using amount of the plant pesticide is small, and the withdrawal time is not needed.

The invention provides a raw material prescription of traditional Chinese medicine fruit and vegetable juice drink product for quitting smoking (sugar-free) and a production method thereof; and according to traditional Chinese medicine theory, the product is prepared by using fruits, vegetables, sea foods and edible and medicinal Chinese medicine in combination with methods of pharmaceutical preparation and food preparation. The product for quitting smoking according to the prescription and the production method thereof have the following characteristics: (1) the prescription is reasonable; the effect for quitting smoking is distinct; the product is convenient to take; the product can be taken at any time and with any amount according to the extent of addiction and the withdrawal time whenthe addiction works; and the addiction can be quit within 10-30 days; (2) as the prescription medicine is made from fruits, vegetables, sea foods and edible and medicinal Chinese medicine without toxicity and side effects, the achievement transformation is easy to operate; (3) the product is sugar-free so that the diabetes can take the product at ease; and (4) the product is easily acceptable because of cool and mellow taste, and the product is suitable for all ages without gender and religion constraints. The product made by the prescription and the production method stand head and shouldersabove all others because of the characteristics such as exact effect, convenient taking and carrying, fashion and the like.

The invention discloses an artificial immunization-based MANET network attack detection method, which achieves low error judgment rate and high detection speed. The method comprises five parts, namely recording of a node transmission frame counting sequence, recording of a channel transmission frame counting sequence, a double-element accumulation sliding window detection method, a residual sliding window threshold judgment method and a gene matching detection method. When the transmission frame counting sequence at intervals of delta t time aiming at a hostile attack recording channel is used as a characteristic sequence, the double-element accumulation sliding window detection method id adopted; the private attack detection is divided into two conditions, namely when the detection node is in a saturated state, the transmission frame counting sequence of each node t intervals of delta t time is recorded, initial detection is performed by adopting the residual sliding window threshold judgment method, and the withdrawal time sequence of the private node is recorded, coded and geneticized and then used as a gene detection body; and when the detection node is in an unsaturated state, the gene matching detection method is adopted. The method is suitable for comprehensive detection of MAC layer attack of an MANET network.

The invention relates to a preparation method for a plant pesticide. The preparation method comprises the following steps of cutting 15.4-26.6 parts of garlic into small granules, turning the small garlic granules over in air for 15-20 minutes, adding 6.8-9.9 parts of edible alcohol, and grinding the mixture into mashed alcohol garlic; cutting 29.4-39.7 parts of onions into small blocks, grinding the small onion blocks into slurry, and uniformly mixing the onion slurry and the mashed alcohol garlic; crushing 2.4-4.6 parts of rheum officinale, extracting the rheum officinale in water for 2-5 hours, and filtering slag to obtain an extracting solution; adding the extracting solution into the onion garlic alcohol slurry for uniform stirring, standing the mixture for 15-20 days, and filtering slag to obtain the plant pesticides. According to the preparation method, edible plants are used as the raw materials, so that the plant pesticide integrates disease and insect prevention and control and plant nutrition supplementation and is pollution-free, residue-free and high in efficiency; the using amount of the plant pesticide is small, and the withdrawal time is not needed.

The invention discloses a compound traditional Chinese medicine perfusion agent used for treating endometritis of a dairy cow. The compound traditional Chinese medicine perfusion agent used for treating the endometritis of the dairy cow is prepared from the following medicinal materials: 5-9 parts of Chinese angelica, 5-8 parts of radix paeoniae alba, 4-7 parts of szechwan Chinaberry fruit, 4-7 parts of motherwort, 3-6 parts of peach kernel, 3-6 parts of ligusticum wallichii, 2-5 parts of rhizoma cyperi, 2-5 parts of cortex lycii radicis, 1-3 parts of radix bupleuri and 1-3 parts of mint. The invention provides a traditional Chinese medicine veterinary drug perfusion agent mainly used for preventing and treating the endometritis of the dairy cow and has the characteristics of quick effect, real curative effect, no drug residue and no need for withdrawal time.

The invention discloses a nanometer povidone iodine oral liquid for protecting pig stomach intestines and a preparation method for the nanometer povidone iodine oral liquid. The nanometer povidone iodine oral liquid is prepared from the following raw materials in percentage by weight: 20-25 percent of povidone, 4.5-5.6 percent of iodine, 1.3-2.5 percent of edible glycerin, 2.1-3.1 percent of haw slice, 2.7-3.6 percent of potassium iodide and 65-80 percent of deionized water. The invention relates to the technical field of veterinary drugs and pharmacy. For the nanometer povidone iodine oral liquid for protecting the pig stomach intestines and the preparation method, proteins in the bacteria are directly denatured and precipitated by releasing effective iodine by povidone iodine of nano-scale particles, so that pathogenic microorganisms die, efficient disinfection and sterilization are realized, the protection effect to the pig stomach intestines is exerted, the resistance and the immunity of a pig are improved, and the death rate is lowered; the production process is simple and scientific, soaking, reaction, stirring, drying, grinding, extraction, heating, complexing, dilution, filling are accomplished at a stretch, less power is consumed, and the labor is saved; and The nanometer povidone iodine oral liquid for protecting the pig stomach intestines is environmentally friendlywithout any residue, is zero to the withdrawal time and large in market space, is directly diluted and used and is simple and quick to operate for a user.

The invention discloses an endocrine hydrops withdrawal device, comprising a controller, a micro motor, a hydrops withdrawal pump, a fixing piece, a support, a hydrops discharging tube, a switch, a hydrops storage box, scales, a connecting tube and a needle, wherein the controller is arranged behind the micro motor; the micro motor is arranged behind the hydrops storage box; the hydrops withdrawal pump is arranged in the fixing piece; the fixing piece is arranged on the upper end of the hydrops storage box; the support is arranged below the micro motor and the controller; the hydrops discharging tube is arranged below the hydrops storage box; the switch is arranged on the lower end of the hydrops discharging tube; the hydrops storage box is arranged ahead of the micro motor; the scales are formed in the surface of the hydrops storage box; the connecting tube is connected onto the upper face of the hydrops storage box; the needle is connected onto the upper face of the connecting tube. By applying the endocrine hydrops withdrawal device, the precision of withdrawal time and weight is realized; the artificial operation is replaced; the withdrawal efficiency is improved; the labor is saved.

The invention relates to a health aquaculture technology for cultured fishes. Through developing immune diagnosis reagent kits and testing pathogen sensitive medicine, and through early diagnosis, the medicine can be targetedly used, the dosage can be reduced, and the medicine residual amount in a fish body can be reduced; through improving the water quality and optimizing the microelement additive, the disease-resistant ability of the fish body can be improved; and through clarifying the residual period of the medicine in the fish body, the medicine withdrawal time before fishing can be determined. In such a way, the influence of the residual medicine can be removed, and safe and green food can be obtained.

The invention discloses a drug composition for preventing and curing the diarrhea of a pig, comprising the following components according to the weight account: (1) polyporus frondosus polysaccharide 10 to 70 parts and ciprofloxacin 5 to 50 parts; (2) uniformly mixing the above components, making a drug composition for preventing and curing diarrhea of pig. The ciprofloxacin has fixation and adsorption function for the mycotoxin, virus, germ and the toxin produced by the germ in the alimentary canal; and has covering power for the mucosa of the alimentary canal, improving the defense function of the mucosa barrier against attack factor. The drug composition has the advantages of no withdrawal time, small poison and side effect, uneasy production of drug resistance, obvious effect for preventing and curing diarrhea of pig of the polyporus frondosus polysaccharide and ciprofloxacin, simple preparation technology, broad material source, convenient use for users to add the drug composition in the premix, and is a perfect premix for preventing and curing the diarrhea of pigs.

The invention belongs to the technical field of biomedical and particularly relates to a method for the quantum dot improvement and synchronous monitoring of antibacterial performance of ceftriaxone sodium. Cadmium telluride quantum dots serving as inorganic nano material are added in merchant ceftriaxone sodium to improve the antibacterial performance of the merchant ceftriaxone sodium. Antibacterial experiments performed by taking Escherichia coli as an example indicate that the cadmium telluride quantum dots have a remarkable coordination and improvement effect, which is far better than those achieved by the single use of the cadmium and telluride, on the antibacterial performance of the ceftriaxone sodium. Meanwhile, the number of bacteria and medicament antibacterial performance are synchronously monitored by using the change in the fluorescence intensity of the mixed solution of ceftriaxone sodium and the cadmium telluride quantum dots in an antibacterial process. Thus, a foundation is laid for the effective judgment of the treatment course and withdrawal time of a medicament.

The invention relates to a traditional Chinese medicine composition for treating avian infectious bronchitis and a preparation method thereof. The traditional Chinese medicine composition comprises the following components in parts by weight: 10-25 parts of liquorice root, 5-15 parts of white paeony root, 10-20 parts of largehead atractylodes rhizome, 5-10 parts of alum, 3-7 parts of honey and 3-7 parts of sesame oil. The traditional Chinese medicine composition has the beneficial effects that the components completely belong to traditional Chinese medicines; the traditional Chinese medicine composition is free of medicine residues, avoids withdrawal time after being taken, is convenient to use and is reasonable in price.

The invention relates to a traditional Chinese medicine composition capable of enhancing the disease resistance of wild pigs and reducing the fat content and a preparation method thereof. The traditional Chinese medicine composition comprises the following components in parts by weight: 20-30 parts of tuber fleeceflower root, 15-25 parts of oriental waterplantain rhizome, 20-28 parts of radix astragali, 18-25 parts of coptis root, 10-19 parts of cassia seed, 15-22 parts of largehead atractylodes rhizome, 10-16 parts of folium artemisiae argyi and 15-25 parts of hawthorn fruit. The traditional Chinese medicine composition has the beneficial effects that the components completely belong to traditional Chinese medicines; the traditional Chinese medicine composition is free of medicine residues, avoids withdrawal time after being taken, is convenient to use and is reasonable in price.

The invention discloses crucian bait for shortening withdrawal time. The bait is mainly composed of auxiliary materials, a bacteriostatic component and active components. The bacteriostatic componentis clindamycin; and the active components comprise, in parts by weight, 5 to 10 parts of malic acid, 2 to 20 parts of oligosaccharides, 10 to 30 parts of pokeberry roots, 3 to 20 parts of fourstamen stephania roots, 8 to 40 parts of corn stigmas, 5 to 30 parts of ginseng leaves and 1 to 3 parts of compound vitamins. The weight ratio of the auxiliary materials, the bacteriostatic component and active components is 100:2:(2-2.5). A preparation method comprises puffing the auxiliary materials, then mixing the puffed materials with the bacteriostatic component and the active components, and conducting granulation to obtain the bait. The bait can significantly reduce clindamycin residues in fish bodies, and increase the metabolism speed of the clindamycin in crucian bodies. After the auxiliarymaterials are puffed, the adsorption capacity of the auxiliary materials is improved, so that metabolism speed of antibiotics in the crucian bodies is further improved. The bait is targeted, and onlyapplicable to crucian breeding, has not seen significant results on other species of fishes yet, and is suitable for wide popularization and application to the crucian breeding industry.