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164 results about "Liter" patented technology

The litre (international spelling) or liter (American spelling) (SI symbols L and l, other symbol used: ℓ) is a metric system unit of volume which is a non-SI unit mentioned in the SI. It is equal to 1 cubic decimetre (dm³), 1,000 cubic centimetres (cm³) or 1/1,000 cubic metre. A cubic decimetre (or litre) occupies a volume of 10 cm × 10 cm × 10 cm (see figure) and is thus equal to one-thousandth of a cubic metre.

Rhodamine 6G hydrazide salicylaldehyde azomethine, synthesizing process and application in measuring content of copper ion

The present invention relates to rhodamine 6G hydrazide salicylal azomethine, a synthesization method and an application in the content determination of cupric ions, which belong to the field of the analysis and determination of cupric ions in water sample. The molecular structural formula of the rhodamine 6G hydrazide salicylal azomethine is shown on the right, and the present invention discloses the synthesization method of the rhodamine 6G hydrazide salicylal azomethine and rhodamine 6G hydrazide salicylal azomethine solution used for the content determination of a small amount of cupric ions in water sample: 0 percent to 98.99 percent of ethanol, 99.99 percent to 1 percent of acetic acid / sodium acetate buffer solution with the pH value of 5 to 9, in which the total concentration of acetic acid is 1 to 100 millimoles per litre, 0.01 percent of N, N-dimethylformamide and 1ppm to 100ppm of rhodamine 6G hydrazide salicylal azomethine, all measured in mass percentage. By a spectrophotometer, the solution can be used for the accurate quantitative determination of 0.005ppm to 0.256ppm of cupric ions in water sample as well as the semiquantitative determination of no less than 0.075ppm of cupric ions in water sample by direct naked-eye observation on the change of colors.
Owner:TSINGHUA UNIV

Cultivation method for north America rhododendron

Disclosed is a method for tissue culture of rhododendron. The tissue culture method comprises the steps that: step 1: rhododendron explant material is collected, and placed on a supper-clean bench after being treated; the rhododendron explant material is disinfected by alcohol with a concentration of 75 percent for 6 to 8 seconds, washed by sterile water for three times, disinfected by 0.001 litre of mercury for 6 to 8 minutes, and washed by sterile water for three times in order; step 2: the material after being disinfected and cut is implanted into bud induce culture medium for thirty days; 30 days later, the obtained material is then implanted into proliferation culture medium for 60 days; step 3: healthy and strong rhododendron seedlings cut with 2 to 3cm by height are implanted into a rooting culture medium for 45 days; step 4: after the newborn root of rhododendron is about 0.5 cm long, the culture medium attached to the root is cleaned and newborn root is moved into sterile thick sand, the air humidity of which is kept ranging from 75 percent to 85 percent; one week later, the newborn root is moved into the mixed material of turfy soil and perlite; 45 days later, the treated root is moved into the field where the root is under the shade for one week. The method can realize industrial culture of seedling within 6 to 7 mouths and mass production of shipshape nursery stock of rhododendron.
Owner:CHINA PAULOWNIA RES CENT

Method for curing soil by using carbonate mineralized bacterium

The invention discloses a soil curing method through carbonate-mineralization microbes, including the following steps: first, preparing high concentration microbe liquid: inoculating Bacillus pasteurii strain into the culture fluid of beef extract and peptone; wherein each litre of culture fluid contains 4-6g peptone and 2-4g beef extract; cultivating for16-24h under30DEG C with the pH value controlled at 6-8, then getting out the mixture and centrifuging for 5-8min under the speed of 5000-8000rpm, thus getting high-concentration microbe liquid at concentration of 2 X 10<9>-2 X 10<11>cell/ml; second, mixing the soil: mixing the high-concentration microbe liquid prepared in the first step and the newly prepared culture fluid into the dried soil sample through lime(3%-7% the weight of the dry soil) and carbamide(2%-6% the weight of the dry soil) according the proportioning of 100g dry soil per 2-3mL high-concentration microbe liquid and 0-50mL newly prepared culture fluid, blending to be even and then cultivating for 0.5-8days; third; molding through a die: molding the soil mixture cultivated in second step in a die when the mixture reaches the optimal water ratio, then demoulding and conserving in constant temperature of 20 DEG C. Seven days later, the soil will be cured, with the compressive resistance reaching above 1.0MPa, up by 38% as compared with pure soil.
Owner:SOUTHEAST UNIV

Drying method

The invention provides a method for the drying of a wet substrate, the method comprising treating the substrate with a solid particulate material at ambient or elevated temperature, the treatment being carried out in an apparatus comprising a drum comprising perforated side walls, wherein the drum comprising perforated side walls is rotated so as to facilitate increased mechanical action between the substrate and the particulate material. Preferably, the drum comprising perforated side walls has a capacity of between 5 and 50 litres for each kg of fabric in the load and is rotated at a speed which generates G forces in the range of from 0.05 to 0.99 G, and the method is carried out at a temperature of between 5° and 120° C. Preferably, the solid particulate material comprises a multiplicity of particles at a particle to fabric addition level of 0.1:1-10:1 by mass, wherein the particles comprise polymeric particles, non-polymeric particles, or mixtures of polymeric and non-polymeric particles. All particles may be solid or hollow in their structure, have smooth or irregular surface features, and are of such a shape and size as to allow for good flowability and intimate contact with the wet substrate. The invention provides optimum drying performance as a result of improved mechanical interaction between substrate and particulate media and is preferably used for the drying of textile fabrics. The method allows for significant reduction in the consumption of energy when compared with the conventional tumble drying of textile fabrics, and also facilitates reduced textile fabric damage.
Owner:XEROS LTD

Production method of polishing powder for liquid crystal display device

The invention relates to a method for producing polishing powder used for a liquid crystal display device. The method comprises the following steps: at the room temperature, 30 to 40 percent of fluorosilicic acid is added into rare earth chloride solution with REO of between 80 and 100 gram/litre and CeO2/REO of more than or equal to 70 percent under the stirring; after five minutes, an additive A is added into the mixture, is heated to the temperature of between 70 and 80 DEG C, is kept at the temperature and is added with mixed precipitant solution till the reaction ends; the PH value of the mixture is 7; the mixture is stirred for 10 minutes, is kept stand for 3 to 5 hours and supernatant fluid of the mixture is removed through siphonage; under the stirring, cold water is added to nearly fill a groove fully; before the stirring is stopped, flocculant solution is added till appearing the flocculating effect; the mixture is kept stand, is deposited and the supernatant fluid of the mixture is removed through siphonage for three times; the mixture is washed, is heated up to 98 DEG C, is kept at the temperature for 10 minutes and is discharged to a stainless steel sieve with 120 meshes; the mixture is subjected to solid-liquid separation, vacuum extraction and filtering and dewatering by a centrifuge; a filter cake is transferred to a quartz material sagger; the charging thickness is less than or equal to 9 centimeters; the filter cake is transported to a muffle tunnel kiln at the temperature of 900 DEG C, is subjected to dehydration in a preheating section and decomposition and transformation at certain degree, is roasted for 3 to 4 hours at high temperature of 900 DEG C, is cooled to the temperature of less than 400 DEG C in a cooling section and comes out from the kiln; a roasted material is cooled to the room temperature and is subjected to stage treatment; and a quality part is the product.
Owner:SHANGHAI JIELONG RARE EARTCH FINE ABRASIVE MATERIAL

Mulberry leaf tea beverage and preparation method thereof

InactiveCN101558798ASolve the problem of bad taste and difficult to be accepted by the publicChange the single agricultural production modelPre-extraction tea treatmentFood preparationAcute hyperglycaemiaSodium Bentonite
The invention relates to a mulberry leaf tea beverage and a preparation method thereof. Each litre of the mulberry leaf tea beverage comprises the following compositions: 4 to 6 grams of mulberry leaf powders, 0.4 to 0.6 gram of tea powders, 0.14 to 0.18 gram of AK sugar, 0.14 to 0.18 gram of aspartame, 2.0 to 2.2 grams of citric acid, 0.5 to 0.7 gram of sodium citrate, 0.06 to 0.1 gram of sodium erythorbate, 0.15 to 0.25 gram of salt, 0.15 to 0.25 milliliter of citric acid black tea flavor and 0.15 to 0.25 milliliter of black tea flavor. The preparation method comprises the following steps that: the mulberry leaf powders are extracted by 95 percent ethanol; the residue is extracted by water; an extraction solution is subjected to vacuum condensation at a temperature of 60 DEG C; each litre of the extraction solution is subjected to adsorption treatment by 0.2 gram of bentonite; mulberry leaf juice and tea juice are mixed in volume ratio of 10:1, added with an auxiliary material and homogenized; and the mixture is subjected to short-time sterilization for 4 seconds at high temperature of 105 DEG C and heat exchange to quickly cool to a temperature of 65 DEG C, and canned. The test proves that the beverage taking mulberry leaf as a main material can effectively prevent hyperglycemia and hyperlipemia and has safe edibility and good mouthfeel.
Owner:ZHEJIANG GONGSHANG UNIVERSITY

Pond polyculture method for Yangtze-river two-year-old coilia ectenes fingerlings and scatophagus argus

The invention discloses a pond polyculture method for Yangtze-river two-year-old coilia ectenes fingerlings and scatophagus argus. The method is characterized by comprising the following steps: firstly, an estuary-area pond and natural brackish water with an inflow salinity of 0.5-1.5% are chosen, and food organism is inoculated in the pond; secondly, fingerlings are put in the pond in winter or in early spring, wherein the stocking size of Yangtze-river two-year-old coilia ectenes fingerlings is a total length of 10 to 12 cm, and the stocking density thereof is 500 to 600 fishes per mu; thirdly, the scatophagus argus is put in the pond from the end of April to the beginning of May, wherein the stocking density is 150 to 250 fishes per mu,and the stocking size is 20 to 30 gram per fish; fourthly, 1 / 3 of water is changed each month from January to June, 1 / 3 of water is changed each half month from July to September, and 1 / 3 of water is changed each month from October to December; fifthly, food organism is supplemented timely when the density of the food organism is lower than 1 per litre; sixthly, during a cultivation period, artificial pellet feed is supplemented as the feed for the scatophagus argus, opossum shrimp and crustacean 1 to 2 jin per mu and 1 time per day; finally, fishes are captured with nets in early winter, wherein the specification of captured coilia ectenes is 16 to 20 gram per fish while the specification of the scatophagus argus is 110 to 130 gram per fish.
Owner:上海市水产研究所(上海市水产技术推广站)

Casing preservation method

The invention relates to a casing preservation method and a preparation method for a fresh-retaining solution. The method solves difficult problems of a conventional casing preservation method is high in casing breakage ratio and wastes water source because of requiring a great amount of water to wash before use, and the casing is poor in elasticity and toughness. The method comprises the steps of preparing the fresh-retaining solution according to the following components: 0.05% of nisin : 0.03% of natamycin : 1% of ascorbic acid : 3.5% of a phosphate combination (including 29% of sodium tripolyphosphate, 55% of sodium metaphosphate, 3% of sodium pyrophosphate, 13% of sodium dihydrogen phosphate) : 95.42% of oxygen-enriched water; immsersing the casing in the fresh-retaining solution for 6 hours according to a proportion of 200 per litre; fishing the casing out, draining off and packaging for use, or immersing the fresh-retaining solution in the casing for a long time, or immersing the fresh-retaining solution in the casing for a long time; and keeping the casing in a sealed container in a normal temperature. The casing preservation method is advantageous in that the fresh-retaining solution and the preservation method which are prepared by the invention, can be preserved for six months without deteriorating or decoloring and can be preserved for 24 months to the longest; the fresh-retaining solution is natural and non-toxic and has high security of biological preservation; breakage rate of the casing is zero; a processing process of washing with a great amount of water; no water resource is wasted; and elasticity and toughness of the casing are increased.
Owner:山东省蓝源生物工程有限公司

Method for treating diseases associated with changes of qualitative and/quantitative composition of blood extracellular dna

The invention relates to medicine and veterinary science and can be used for treating diseases associated with changes of the qualitative and/quantitative composition of blood extracellular DNA, namely generalised infection diseases provoked by bacteria, diseases provoked by fungi and protozoa, atherosclerosis, pancreatic diabetes, allergic diseases associated with delayed response hypersensitivity and diseases due to somatic cell gene mutations. The inventive method for treating diseases associated with modifications of the qualitative and/or quantitative composition of blood extracellular DNA, namely generalised infection diseases provoked by bacteria, diseases provoked by fungi and protozoa, atherosclerosis, pancreatic diabetes, allergic diseases associated with delayed response hypersensitivity and diseases due to somatic cell gene mutations consists in injecting an agent destroying blood extracellular DNA. DNAse enzyme injected into a systemic blood circulation in doses which modify the electrophoretic profile of the blood extracellular DNA definable by pulse-electrophoresis can be used in the form of an agent destroying said blood extracellular DNA. Said DNAse enzyme can be injected in doses and at regimes ensuring the level of a blood plasma DNA-hydrolytic activity which is measured in the blood plasma and is higher than 150 Kunz units per litre of plasma during a total time higher than 12 hours a day. The inventive method makes it possible to develop a high-efficient and low-toxic method for treating diseases associated with modifications of qualitative and/or quantitative composition of blood extracellular DNA individually or in combination thereof.
Owner:CLS THERAPEUTICS
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