340results about How to "Effective compound" patented technology

Disclosed is a process for the treatment of a plant fluid effluent containing odor compounds including an alkyl mercaptan or an alkyl thiol, an amine compound, ammonia, hydrogen sulfide and mixtures thereof by contacting the plant effluent in either a counterflow or cocurrent flow process. In the process, the effluent is contacted with an aqueous solution comprising a peracid compound. When contacted with the peracid, odor compounds in the effluent are oxidized and converted from the gaseous phase into a chemically modified highly aqueous soluble phase in the aqueous treatment. In this way, odor removal from the gas is preferred and odor compounds are efficiently transferred into the aqueous treatment solution. The use of such a process produces a significant improvement in odor quality index as measured by a conventional process using an expert panel when compared to conventional treatment methods.

On a surface of a GaAs substrate, layers to be a top cell are formed by epitaxial growth. On the top cell, layers to be a bottom cell are formed. Thereafter, on a surface of the bottom cell, a back surface electrode is formed. Thereafter, a glass plate is adhered to the back surface electrode by wax. Then, the GaAs substrate supported by the glass plate is dipped in an alkali solution, whereby the GaAs substrate is removed. Thereafter, a surface electrode is formed on the top cell. Finally the glass plate is separated from the back surface electrode. In this manner, a compound solar battery that improves efficiency of conversion to electric energy can be obtained.

The invention relates to a preparation method for a polyimide/oxidized graphene nanocomposite film, and belongs to the technical field of preparation of functional polymer materials. The preparation method comprises the following steps: performing ultrasonic even dispersion on the oxidized graphene in an organic solvent to obtain an oxidized graphene sheet suspension, wherein per ml of the oxidized graphene sheet suspension contains 1.3*10<-5>-1.3*10<-4>g oxidized graphene sheets; introducing nitrogen for carrying out deoxidization protection, adding diamine monomers into the suspension, mechanically stirring until full dissolution is achieved, adding dianhydride monomers, the moles of which are equal to that of the diamine monomers, in batches, and mixing for one to six hours under the ice bath conditions, so as to obtain polyamide acid/oxidized graphene composite solution; pouring the polyamide acid/oxidized graphene composite solution onto a die, removing the organic solvent, performing gradient temperature rise within 100-300DEG C, and carrying out thermal imidization to obtain the polyimide/oxidized graphene nanocomposite film.

Compositions and methods are disclosed in embodiments relating to induction of cell death such as in cancer cells. Compounds and related methods for synthesis and use thereof, including the use of compounds in therapy for the treatment of cancer and selective induction of apoptosis in cells are disclosed. Compounds are disclosed that have lower neurotoxicity effects than other compounds.

The invention relates to a lithium ion battery composite cathode material and a preparation method thereof, which belongs to the technical field of lithium ion battery. The invention aims at improving the cycle performance of silicon cathode material at the same time when keeping the high ratio volume of lithium ion battery silicon cathode material. The proposal of the invention is that silica-based material coated by disordered carbon is treated with surface modification processing by utilizing lithium salt, namely, the lithium salt is coated on the surface of Si/G/DC (silicon/graphite/disordered carbon) to be prepared into the composite cathode material, therefore, the lithium-embedding and removing depth of the silicon can be effectively controlled, and the material is the lithium ion battery composite cathode material which has high specific capacity and good cyclical stability; furthermore, the material is safe and pollution-free, and presents higher thermal stability in various lithium salt electrolytes and solvents.

The invention relates to a method of improving the bacterinertness of a silk fibroin solution. Silk fibroin material has favorable prospects when applied in biomedicine aspect, and thus the search of a method of improving the bacterinertness of silk material is meaningful. The invention comprises a silk fibroin solution preparing working procedure which adopts silk fibroin to prepare the silk fibroin solution and is characterized by also comprising a nanometer noble metal feeding working procedure by selecting nanometer noble metal with the grain diameter between 5 nanometers to 100 nanometers. When a temperature is between 0 DEG C to 50 DEG C, the nanometer noble metal is fed to a stand-by silk fibroin solution and is stirred at a rotating speed of 100-400 round/min to obtain the silk fibroin solution comprising the nanometer noble metal; the concentration of the silk fibroin is 0.5-15w/v percent, and the concentration of the nanometer noble metal is 0.005-0.2w/v percent. The invention can favorably improve the antibiotic performance of the silk fibroin solution so that the silk fibroin can be more widely applied to biological material.

α-Galactosylceramides and glycosylceramides (“ceramide-like glycolipids”) that modulate NK T cells. The ceramide-like glycolipids vary in the cytokines induced in NK T cells and vary in the antigen-presenting cells that are capable of efficiently presenting the compounds to NK T cells. Pharmaceutical compositions of the ceramide-like glycolipids are provided, as are pharmaceutical compositions of the ceramide-like glycolipids combined with dendritic cells. Methods utilizing the ceramide-like glycolipids in vaccines, to activate NK T cells, to stimulate the immune system, and to treat mammals are also provided. The invention also provides methods of evaluating a compound for its ability to activate an NK T cell in the presence of a cell expressing a CD1d protein.

The invention belongs to the technical field of transitional metal sulfide-carbon materials, and particularly relates to a tungsten disulfide/carbon nanofiber/graphene composite material and a preparation method thereof. The preparation method comprises the following steps: preparing a polyacrylonitrile nanofiber membrane in an electrostatic spinning manner; wrapping a polyacrylonitrile nanofiber with a graphene oxide through a solution immersion method; preparing a carbon nanofiber/graphene composite membrane through a high-temperature carbonization; and finally growing a tungsten disulfide nanosheet on the carbon nanofiber/graphene in situ through a one-step solvothermal method. The prepared tungsten disulfide/carbon nanofiber/graphene composite material has the advantages of stable chemical property, good conductivity, excellent mechanical property and the like, and can be used as an ideal high-performance electric catalytic material and an electrode material for new energy devices of a lithium-ion battery, a solar battery and the like.

Compositions and methods for making robust pellets that contain a high percentage, by weight, of active drug agent, and which also contain additional components that enhance the absorption and solubility of the active drug agent within the gastrointestinal tract (GI tract) without diminishing the robust nature of the pellet, are disclosed.

There is provided a bleaching enzyme capable of generating a bleaching chemical and having a high binding affinity for stains present on fabrics. Furthermore, there is provided an enzymatic bleaching composition comprising the bleaching enzyme and a surfactant and a process for bleaching stains present of fabrics.

The invention discloses a nanometer tin diselenide/graphene composite material. The nanometer tin diselenide/graphene composite material is characterized in that tin diselenide particles with the average particle size of 3-10nm grow on the graphene surface. Nanometer tin diselenide and graphene have high binding strength, tin diselenide nanometer particles have good crystallization structures, graphene slice layers are disorderedly stacked to form a 3D skeleton, and nano-scale tunnels and a good charge transmission network are provided. The nanometer tin diselenide/graphene composite material is used as a cell cathode material and has good charge and discharge performances and stability. The invention also discloses a preparation method of the nanometer tin diselenide/graphene composite material. In synthesis, an ionic liquid is used and through improvement of binding strength of a metal sulfur nanometer structure and a carbon material, effective compounding of the carbon material and tin diselenide is realized and a high-performance lithium ion battery and sodion battery cathode material is obtained.

In a networked computer environment, a client is unencumbered from signature generating components, yet conversant to transmit signature-based documents in a signature-based metalanguage such as XML. The nonsigning client/user invokes a signature from a signature server to send a payload of data in a signed message format to a recipient also conversant in the metalanguage, according to the metalanguage format. The nonsigning client receives a signature block including a signature value from the server. The client identifies a payload for transmission according to the metalanguage. Employing the metalanguage interpreter in client, the client stores the payload data in the signature block without disrupting the signature and the data it covers in the signature block. The nonsigning client the sends the resulting signature message including the payload data and the signature value, in the metalanguage format, to the recipient destination conversant in the metalanguage. Accordingly, the nonsigning client employs signature-based messages without the encumbrance of cryptographic components.

The invention relates to codrugs having improved properties, methods for preparing and administering them, and methods of formulating and administering the codrugs as pharmaceutical preparations. In certain embodiments, the codrugs can be locally administered to deliver the constituent biologically active compound in a sustained-release fashion, reducing systemic concentrations of the biologically active compound.

The invention discloses a composite optical membrane which comprises protecting films, optical membrane layers and a shading double-side adhesive tape layer, and the surrounding of the shading double-side adhesive tape layer is an annular stickiness part with the middle forming a transparent part. The invention is characterized in that: the hierarchical structure of the composite optical membrane consists of a first protecting film, the shading double-side adhesive tape layer, a first optical membrane layer, a second optical membrane layer and a second protecting film which are orderly overlapped. The first optical membrane layer is larger than the transparent part but less than the second optical membrane layer; and the surrounding is jointed with the stickiness part. The second optical membrane layer is less than the shading double-side adhesive tape layer, and the surrounding part of the second optical membrane layer exceeding the first optical membrane layer is jointed with the stickiness part of the shading double-side adhesive tape layer. The invention uses the stickiness of the shading double-side adhesive tape layer to directly compound each layer of membrane together by an automatic processing device, which is different from prior complex production process, ensures the more reliable performance of a backlight module and improves the production efficiency.

The invention pertains to double phosphorescent dyes co-doped white organic light-emitting device and discloses the preparation method. The invention adopts sandwich structure and intermingles the two high-efficient phosphorescent dyes together in the wide band gap body; and also takes use of the energy difference between emission layer and its bilateral function layers to form a structure of energy sink type; restricts exaction within the structure completely, thereby realizing composite luminescence. The structure of the device is indium tin oxide (ITO)/metal oxide/hole-transporting layer/electron blocking layer/emission layer composed of the co-doped blue and orange light phosphorescent dyes/electron transporting(hole blocking)layer/metal cathode. The prepared devices are driven by direct voltage and obtain high-efficient white light emission. The maximum electroluminescence current efficiency is 52.8cd/A; the maximum electroluminescence (EL) power efficiency is 42.5lm/W; the maximum luminance is19500 cd/m2. The devices show simultaneous emission of complementary colors of orange and blue and stable spectrum when at work. The device has simple manufacturing process, low cost and excellent stability.

The invention discloses a bimetal composite pipe which comprises a base pipe and a lining pipe installed on the inner side of the base pipe in a sleeved mode. The lining pipe is shorter than the base pipe, the inner walls of the two ends of the base pipe are respectively provided with an annular groove, each annular groove is internally provided with a first surfacing layer in a welded mode, the internal diameter of each first surfacing layer is the same as that of the base pipe, a second surfacing layer is welded to the inner wall of each first surfacing layer and located at the end of the lining pipe, the ends of the second surfacing layers are flush with the end of the base pipe, and the internal diameter of each second surfacing layer is the same as that of the lining pipe. The invention further discloses a manufacturing process of the bimetal composite pipe. According to the bimetal composite pipe, the annular grooves are formed in the inner walls of the two ends of the base pipe and the first surfacing layers are welded to the annular grooves, the end of the base pipe and the end of the lining pipe can be compounded effectively, and it is ensured that the lining pipe of the bimetal composite pipe is not affected by the base pipe in the circular welding process.