329 results about "Straw" patented technology

The invention relates to a straw biology organic fertilizer and the manufacture method that could effectively solves the fully use of straw, fertilizing, and good harvest problem. The method is mixing straw powder, dejection, shale powder, fused calcium magnesium phosphate, mixed cake, bran powder, urea, and other assistant material and compounding enzyme nutrient solution. The method is that adding dejection, shale powder, fused calcium magnesium phosphate, mixed cake, bran powder, urea, and assistant material to the smashed straw, mixing with enzyme nutrient solution taking fermenting, deodorizing, detoxicating, graining, drying, filtering, and packaging. The invention has good effect, easy method, plenty resource, wide application, and has great prospect.

The invention discloses a vaginitis test kit which comprises a reaction device, a sampling test tube, a straw, joint test diluent, joint test chromogenic reagent, joint test stop solution, a user manual and a joint test colourimetric card, wherein a hydrogen peroxide reaction hole, a leukocyte esterase reaction hole, a sialic acid glucoside enzyme reaction hole, a beta- glucuronic acid enzyme reaction hole, a P glucosidase reation hole and a pH value hole; relevant reaction bases are arranged in the reaction holes; reach reaction base comprises a corresponding reaction substrate curing layer,a chromogenic promotional layer and a chemical inert carrier layer. The invention also provides a preparation method of the test kit and the preparation method of a novel chemical carrier. The test kit can be used for distinguishing bacterial vaginosis and vaginitis, and can further identify aerobic/anaerobic bacteria, facultative anaerobic bacteria and other flora in vaginal secretion. The method is simple and quick to operate, has high accuracy, and is applicable to clinical practice, particularly hospital outpatient practice.

The invention relates to a large-scale anaerobic fermentation technique of straws and a device thereof. The fermentation technique includes biological pretreatment, anaerobic fermentation and anaerobic bacteria separation of the straws for separating an anaerobic bacteria liquid used for another circulation. The anaerobic fermentation device for implementing the method is composed of a feed device, an anaerobic generator and an anaerobic bacteria separator. The technique and the device do not need nitrogen source during the fermentation process of the straws and realize continuous feed and discharge during the anaerobic process of the straws; the molecular structure of the straws is changed through the mode of biochemistry; a large amount of straw lignin hard to be anaerobically digested is converted into a carbon source which is easily biodegraded; and a waxiness component for protecting the straws is decomposed, thus being capable of leading the anaerobic bacteria to successfully enter the inside of the straws, improving the speed of the degraded straws and being capable of realizing the production with low cost and large scale.

The invention discloses a method for culturing biofloc and a method for applying the biofloc to aquaculture, and belongs to the technical field of aquaculture. Straw is crushed, and evenly mixed with corn starch and water, the mixture is cut up to solid particles of 0.45 mm to 0.55 mm after being puffed, and the solid particles and aquaculture water are mixed according to the volume ratio of (1-1.2):1; bacillus is added to the aquaculture water, so that the viable count is (2-5)*1,010 cfu/L; suspended solids in a culturing unit are collected, and the biofloc is obtained; when aquaculture is carried out, 0.3-0.5 kg of biofloc is added to each stere of culture pond water, the biofloc is sprayed into the aquaculture water, and the volume ratio of the biofloc to water in a culture pond is kept to range from 10% to 15% in the culture period. A carbon source is obtained through biochemical treatment on the straw, the culturing cost of the biofloc is reduced, the biofloc is promoted to fast grow, and the biofloc with the grain size of 500 micrometers to 1,000 micrometers is obtained. The quality of the aquaculture water is adjusted, and the utilization rate of bait is increased.

The invention discloses a method for preparing magnetic biochar by a one-step method. The method comprises the following steps: S1, straw pretreatment: drying and crushing plant straws, and screeningparticles with the particle size of 60-30 meshes for later use; S2, iron salt dipping: adding an iron salt solution into the straw particles in the step S1 for dipping, adjusting the pH value to 10-11with an alkali solution, and then carrying out heat preservation dipping; S3, high-temperature pyrolysis: performing suction filtration on the impregnated particles in the step S2, drying, and transferring into an atmosphere furnace for high-temperature pyrolysis to obtain a magnetic biochar crude product; and S4, post-treatment: carrying out suction filtration, cleaning and drying on the magnetic biochar crude product obtained by pyrolysis in S3 to obtain a magnetic activated carbon finished product. According to the method for preparing the magnetic biochar through the one-step method, plant straw serves as a raw material, pyrolysis and magnetization can be achieved through one step to prepare the magnetic activated carbon, the method is simple, and large-scale production is easy to achieve.

The invention belongs to the technical field of biochar, and provides an integrated device for preparing biochar through co-pyrolysis of sludge and straw, which comprises a crushing device and a carbonizing device, the crushing device comprises a crushing bin, a feeding storage bin, a crushing mechanism and a first sieve plate; and the carbonizing device comprises a carbonizing bin and a stirringmechanism. According to the device, preparation steps and preparation equipment for preparing the biochar through sludge and straw heat supply are simplified, the time for connecting all procedures isshortened, and the working efficiency is improved.

The invention discloses a method for preparing feed from organic perishable wastes to breed black soldier flies. According to the method, the organic perishable wastes are adopted as a feed raw material, and together with multiple optimally designed auxiliary materials and composite bacteria, efficient breeding of the black soldier flies is achieved. By adopting the breeding method disclosed by the invention, requirements of black soldier fly breeding can be met, the food taking efficiency of black soldier fly larvae can be improved, the survival rate of the black soldier fly larvae can be increased, nutrient components in the organic perishable wastes are sufficiently utilized, and rapid conversion and utilization can be achieved. The method reuses waste resources such as the organic perishable wastes, straw and bean dregs and is simple to operate, low in cost, low in carbon, good in environment protection and high in economic value, and a basic scheme is provided for on-scale and industrial breeding of the black soldier flies.

The invention provides Trichoderma afroharzianum Ta97 and application thereof in straw returning. The strain is classified and named as Trichoderma afroharzianum in Latin, the strain is preserved in China General Microbiological Culture Collection Center on July 14th, 2020, the preservation unit is called CGMCC for short, the address is Courtyard 1, Beichen West Road, Chaoyang District, Beijing City, and the preservation number is CGMCC No.19930. The invention further discloses the application of the Trichoderma afroharzianum Ta97 in the straw returning. The Trichoderma afroharzianum Ta97 is applied to the straw returning, in a laboratory test, the average weight loss rate of straw reaches 80.40% within 30 days, and in a field test, the straw can be fully degraded within 30 days to reach the fourth level of decomposition, nutrition is provided for growth of next-stubble crops, and the purposes of straw returning cyclic utilization and fertilizer cost saving are achieved.

The invention discloses a lowline embryo freezing liquid, a freezing method and an unfreezing method and belongs to the technical field of bioengineering and embryonic heredity. The lowline embryo freezing liqui comprises ethanediol, cane sugar and DMSO. The freezing method comprises the following steps: freezing an obtained embryo for pre-treating, putting the embryo in a tube and freezing the embryo. The unfreezing method comprises the following steps: retaining a straw in air for 5-10 seconds, putting the straw in water bath at the temperature of 35-38 DEG C for 10-15 seconds, detecting the embryo, transferring the embryo in WM1 liquid drops, transferring into another hole liquid drops containing the same solution, then respectively transferring to WM2 and liquid drop containing HM with the concentration being 800 microliter per hole and retaining for 5 minutes each time; and washing the embryo by a culture solution for three times, continuously observing the development condition of the embryo in the culture solution or transplanting the embryo to a receptor cow after being subjected to estrus synchronization. The freezing liquid, the freezing method and the unfreezing method have the good freezing effect, are strong in operability, convenient to operate and suitable for popularization and application.

The invention provides a cellulose degradation strain with sewage ammonia nitrogen degradation capacity, and belongs to the technical field of microorganisms. The strain is Bacillus Velezensis strainNBL-B11010. The strain is preserved in China Center for Type Culture Collection on August 31, 2020, and the preservation number of the strain is CCTCC NO: M 2020458. The strain is obtained from a farmland rotten straw material through screening, purification, identification and other technologies, safety tests and fermentation conditions of the strain are studied, straw degradation efficiency andsewage ammonia nitrogen degradation efficiency are measured, it is shown that the strain is a beneficial strain with efficient cellulose degradation and sewage ammonia nitrogen degradation capacity, and has good practical application value.

Disclosed herein are methods for purification of RNA from a sample. The RNA can be total RNA or mRNA. The method involves preparing the sample in a solution of lysis buffer and depositing into a first end of a lysis straw such that the sample solution flows through the matrix of the lysis straw and is eluted from the opposite end of the lysis straw, and depositing the eluted material into a first end of a solid phase extraction (SPE) straw, such that the deposited solution flows through the matrix of the SPE straw towards the opposite end of the SPE straw, and eluting the RNA from the SPE straw by depositing a solution of elution buffer, into the first end of the SPE straw, such that the deposited solution flows through the matrix of the SPE straw and is eluted from the opposite end of the SPE straw, wherein purified RNA from the sample is present in the eluate of the SPE straw. When the RNA is total RNA, and the sample is a cell sample, and step b) requires adding a precipitating solution to the eluted material from step a), and depositing the solution into the first end of the SPE straw, wherein the straw comprises silica microspheres, such that the deposited solution flows through the matrix of the SPE straw toward the opposite end of the SPE straw. When the RNA is mRNA and step b) further comprises depositing the solution into the first end of the solid phase extraction (SPE) straw, wherein the straw comprises oligo-dT. Pressure (e.g., at least 10 psi pressure) and heat (e.g., about 60° C.) can be applied to the samples, and/or eluates and/or straws. Examples of lysis buffers, loading buffers and elution buffers are provided. Also disclosed are the specific straws and porous polymer monolith matrix components.

The invention discloses a preparation method of a porous biological carrier adsorption material and its application. The wheat straw powder a, attapulgite powder b and limonite powder c are uniformly mixed and then granulated by adding water, and the particle diameter is controlled at 6-6. 10mm, and then dried at 105°C to obtain pellets; the obtained pellets were placed in a high-temperature tube furnace, sintered at high temperature, and cooled to obtain a limonite-based Fe/C porous biological carrier adsorption material. The porous biological carrier adsorption material of the present invention can be used to treat the secondary effluent of the city, to COD, NH ₃ ‑N and total P have better adsorption removal effect.

The invention discloses a protective agent applied to frozen storage of livestock semen. The protective agent can remarkably improve the survival rate of livestock sperms, and the main substance of the protective agent is ganoderma lucidum polysaccharide. The preparation method is mainly characterized in that the ganoderma lucidum polysaccharide is used as the protective agent for long-term preservation of straw frozen semen of pigs, sheep and cattle, for artificial insemination, and for insemination after long-distance transportation of the semen subjected to ultralow temperature refrigeration for the first time at home and abroad. The survival rate, the acrosome integrity and plasma membrane integrity of sperms of pigs, sheep and cattle after freezing and thawing are notably improved.

The invention provides straw degrading bacteria and a separation and screening method, and belongs to the technical field of biology. The method comprises the following steps: screening microorganismsin soil with straw returned to the field for many years by taking lignin as a target to obtain lignin degrading single bacteria, and screening cellulose degrading single bacteria; and forming a floraby the screened cellulose degrading bacteria and lignin degrading bacteria with high straw degrading efficiency to obtain the flora with high degrading efficiency, mixing and fermenting strains to prepare a microbial agent, and screening a combination with high degrading efficiency in a field test.

The invention provides a straw biological decomposition method by the adoption of a lactobacillus casei decomposition accelerator. The method comprises the step of adding the lactobacillus casei decomposition accelerator, the decomposition accelerator is composed of, by mass, 3-7 parts of complex microbial inoculants, 24-36 parts of radix ophiopogonis, 15-26 parts of rape flower pollen and 22-33 parts of scenedesmus quadricauda breb, according to the straw which is subjected to the decomposition treatment by means of the straw decomposition method, the cation exchange capacity is 70.4-72.6 cmol/kg, when the decomposition is finished, C/N is 14.23-15.15, T is 0.44-0.47, the germination index of seeds is 108.6-110.8%, and the germination rate of the seeds is 83.4-94.6%. The invention further provides the application of the method in recarburization and fertilization in saline-alkali soil, by means of the application, the soil salinity and soil pH can be reduced remarkably, the soil structure can be improved, the soil pores can be increased, the organic contents in the soil can be improved, and the soil fertility can be enhanced.

The invention provides a straw and mushroom matrix compression forming machine and belongs to the technical field of cultivation of edible mushrooms. The straw and mushroom matrix compression forming machine mainly comprises a bed, a discharging device, a compactor and a die. A raw material hopper and the discharging device part are arranged at the head part of one end of the bed. The compactor part is arranged at the tail part of the other end of the bed. The die capable of reciprocating is arranged at the middle part of the bed. The straw and mushroom matrix compression forming machine has simple and compact structure and is easy to operate. Straw culture materials can be compressed into one fifth of the original volume of the straw culture materials, so that the output in unit area is possibly improved for over five times; and compressed material blocks can be stacked and is developed toward the space and a mushroom bed does not need to be set up.

The invention provides a biological gas production system for filling straws in a mine goaf. The biological gas production system comprises a hot water entering well, a water returning well, a temperature monitoring well, an exogenous bacterium injection and bacterium colony monitoring well and a biological gas collection and conveying well which are formed above the mine goaf and are communicated with the ground, wherein heat insulation pipelines, which are made of stainless steel or an aluminum alloy material, are paved on the ground in the goaf in a crisscrossing manner; a residual heat water discharge pipe of a thermal power plant penetrates through the hot water entering well and stretches into the goaf to be connected with water inlets of the heat insulation pipelines; water outlets of the heat insulation pipelines are connected with a water returning pipe; the water returning pipe upward penetrates through the water returning well, and then is returned back to the thermal power plant; and the goaf is internally filled with crushed straws. The invention further discloses a gas production process of the biological gas production system for filling the straws in the mine goaf. According to the biological gas production system and the gas production process, provided by the invention, a good space advantage of the mine goaf is utilized, and the aim of green mining of mines is realized; and meanwhile, the straws are converted into a clean energy source by utilizing a biotechnology, and energy consumption and emission reduction are realized.

The invention relates to the field of biochar preparation methods, and particularly discloses a preparation method of high-activity straw biochar, which comprises the following steps: S1 to S2, activating straws, and S3, pyrolyzing the activated straws to obtain the high-activity straw biochar. The high-activity straw biochar prepared by the invention can improve the yield, specific surface area and porosity of a biochar product, and is a low-cost, ecological and environment-friendly preparation process.

The invention provides a microorganism, a microbial agent containing the microorganism, as well as a preparation method and application thereof. The microorganism is bacillus siamensis which is preserved in China General Microbiological Culture Collection Center, under the preservation number of CGMCC No. 18688, from October 15, 2019 on. The microorganism provided by the invention has relatively good ability to decompose cellulose, and can be effectively applied in straw composting so as to obviously accelerate temperature rise rate in an early stage of composting, raise fermentation temperature, increase straw weight loss rate after the composting, decrease C/N content and achieve high compost maturity; and thus, the microorganism is suitable for large-scale application.

A lid may include first and second openings disposed within a spout. The first opening may provide a first fluid pathway to a fluid disposed in an attached container and the second opening may provide a second fluid pathway to a fluid disposed in the container. The lid may also include a spout at least partially defined by an outer wall. First and second openings may be disposed within the spout and the openings may be at least partially defined by the outer wall of the spout. A conduit, such as a straw, may be coupled to an opening. If desired, a closure may be connected to the lid and the closure may selectively close one or more of the openings.