1214 results about "Surface chemical" patented technology

The invention is directed to a novel approach to thin film synthesis that is described as high vacuum plasma-assisted chemical vapor deposition (HVP-CVD). In one application of HVP-CVD, atomic oxygen and organometallic precursors are simultaneously introduced into a high vacuum chamber. Gas-phase chemistry is eliminated or substantially eliminated in the collisionless or substantially collisionless environment, allowing the surface chemistry between atomic oxygen and the precursor(s) to be interrogated directly. In preliminary work it has been observed that the presence of atomic oxygen greatly accelerates the desorption of organic ligands, facilitating oxide formation. The prominent advantages of the HVP-CVD include reduced substrate temperature, significant rates, inherent uniformity, facilitated doping, and the ability to directly study these processes in-situ with high vacuum diagnostics that are not compatible with conventional CVD technologies.

Nanoparticles that activate complement in the absence of biological molecules are described. The nanoparticles are shown to specifically target antigen presenting cells in specifically in lymph nodes, without the use of a biological molecule for targeting. These particles are useful vehicles for delivering immunotherapeutics. Surface chemistries and chemical formulations for the nanoparticles are described.

A highly specific and versatile surface chemistry for immobilization of amine-terminated probes is disclosed. A bi-layered polymer thin film serves as the platform for coupling the probes, which are preferably oligonucleotides. The process involves sequentially coating a substrate with polyamine and polyacid anhydride. Hydrolyzed polyacid anhydride groups may be converted to non-hydrolyzed groups at about 100° C. prior to probe attachment. The process of coating the substrate requires no harsh chemical pretreatment of substrates such as RCA or Piranha cleaning. In addition, simple thermal activation of the anhydride groups has a low requirement for storage, leading to a long shelf life of modified surfaces. The disclosed surface chemistry is especially compatible with microfabrication processes, and its effective application to magnetic biosensors is demonstrated.

The specification describes a contact printing technique for forming patterns of thin films with nanometer resolution over large areas. The procedure, termed here “nanotransfer printing (nTP)”, relies on tailored surface chemistries for transferring thin films, typically metal films, from the raised regions of a stamp to a substrate when these two elements are brought into intimate physical contact. This technique is purely additive, it is fast (<15 s contact times), and the printing occurs in a single processing step at room temperature in open air. nTP is capable of producing patterns with a wide range of features with sizes down to ˜100 nm, and edge resolution better than 25 nm. Electrical contacts and interconnects have been fabricated for high performance organic thin film transistors (TFTs) and complementary inverter circuits, to demonstrate one of the many potential applications for nTP.

The large-area untrathin nano carbon tube film with well feature in microcosmic level comprises nano carbon tubes with centimeter-level length and more then 90wt% purity. Wherein, the least thickness of single-layer film can achieve 20nm with near transparent color and more then 10cm2 film area; there are multiple functional groups on tube surface. It also discloses the opposite preparation technique: with the macroscopic body of nano carbon tube, oxidating the macroscopic body in air; then, dipping into hydroperoxide; adding strong acid to poach till the liquid shows neutrality; finally, adding alcohol or acetone into the liquid to float the tube and form the film.

The invention belongs to the technical field of the preparation of graphene quantum dots (GQDs), and particularly relates to a method for preparing fluorescent graphene quantum dots with controllable oxidation degree and fluorescence by a solvothermal method. According to the technical scheme, the method comprises the following steps of: 1, preparing graphene oxide; 2, preparing green fluorescent graphene quantum dots by a single-step method starting from the graphene oxide; and 3, preparing the fluorescent graphene quantum dots with the controllable oxidation degree by a column chromatographic separation method. According to the method, the sizes and surface oxidation degree of the graphene quantum dots can be controlled under the synthetic condition, so that the fluorescent properties and surface chemical characteristics of the graphene quantum dots are controlled. The prepared graphene quantum dots are high in chemical stability and biocompatibility, low in biotoxicity, and high in property of applicable upconversion fluorescence, matt and the like and bleaching performance. By the excellent properties, the graphene quantum dots have a wide application range in aspects of biological imaging, photovoltaic devices and sensors, and are novel promising fluorescent nano materials.

The invention relates to a microfluidic chip and a manufacturing method thereof. The microfluidic chip comprises an upper chip unit and a lower chip unit; the surfaces of the chip units are respectively provided with a liquid storing hole, a liquid channel communicated with the liquid storing holes and a microchannel communicated with the liquid channel; the upper chip unit and the lower chip unit are attached to each other and the microchannel is sealed between the two chip units; the microfluidic chip also comprises a micro valve, wherein the micro-valve main body is one of the following structures: a three-dimensional micrometer and three-dimensional nanometer hierarchical structure of polymers formed on the microchannel in array arrangement, a three-dimensional micrometer structure ofpolymers formed on the microchannel in array arrangement or a three-dimensional nanometer structure of polymers formed on the microchannel in array arrangement; the polymers can generate specific responses to an external field under the action of the external field; and the specific responses are reversibility transformation of one or more of surface chemical compositions of the polymers, the above structures and surface properties, thus realizing controllable operations for the flow state of a microfluid in the microchannel. The micro valve in the microfluidic chip is manufactured in situ and miniaturized on the microfluidic chip, thus realizing switch gradient control for the flow of the microfluid and fast switch reversibility transformation.

A method for effecting a superficial chemical skin peel is provided wherein a concentrated solution of salicylic acid in a dermatologically acceptable solvent is applied to be treated. The concentrated salicylic acid solution contains at least 15 wt % salicylic acid and preferably at least about 20 wt % salicylic acid, The composition and method are useful in the treatment of skin disorders such as photodamaged skin, hyperpigmentation, acne vulgaris, and the like.

A method and porous multi-component material for the capture, separation or chemical reaction of a species of interest is disclosed. The porous multi-component material includes a substrate and a composite thin film. The composite thin film is formed by combining a porous polymer with a nanostructured material. The nanostructured material may include a surface chemistry for the capture of chemicals or particles. The composite thin film is coupled to the support or device surface. The method and material provides a simple, fast, and chemically and physically benign way to integrate nanostructured materials into devices while preserving their chemical activity.

The present invention provides process of organizing the surface to modify inorganic powder, and during the process, inorganic superfine particles are dispersed homogeneously in non-polar organic solvent and have the surfaces well organization modified. The process includes preparing water solution for dispersing inorganic powder, dissolving organic surface modifier, organic surface modifying, solid-liquid separating and washing, and post-treatment. The process features that oil-water interface and phase transfer are utilized for organic surface modification of inorganic superfine powder in non-polar organic solvent.

The invention discloses a method for conducting surface chemical copper plating on inorganic particles through dopamine. The method comprises the steps that poly-dopamine layers are made to subside on the surfaces of the inorganic particles in an alkaline solution through the oxidative polymerization effect of the dopamine, then by utilizing functional groups of the poly-dopamine layers, and meanwhile under the effect of an additional auxiliary reducing agent of dimethylamine broane (DMAB), copper ions are reduced to pure copper on the surfaces of the inorganic particles, and a continuous and compact metal copper layer is formed. The method is simple to operate, low in equipment requirement and low in cost; the prepared copper-plated inorganic particles have the characteristics of being low in density, good in conductivity and the like; the method can be used for preparing electricity and thermal conductive coatings, electromagnetic shielding paint, wave-absorbing materials and the like.

The invention relates to a preparation method for a light metal superhydrophobic surface, in particular to a light metal surface with a superhydrophobic property and corrosion and wear resistance. The preparation method comprises the following steps: a layer of porous oxidation film is formed on the surface through anodic oxidation of the light metal surface first; the surface is modified by a low-temperature plasma treatment technique; and at last, the superhydrophobic surface is formed on the surface of the oxidation film through chemical modification. The method does not require complex and expense equipment and has a simple process, good repetitiveness, a contact angle of the surface and water up to 153 to 170 degrees as well as good corrosion and wear resistance.

The disclosed surface chemical thermal treatment technique for a high-C-Cr bearing comprises: setting parameters, front cleaning, pre-oxidizing, heating, carbonitriding, cooling to diffuse, quenching, and tempering. This invention uses the treatment device in vehicle and motor cycle gear process to form one layer with special tissue and improve contact fatigue strength and surface hardness.

The invention belongs to the technical field of preparation of self-repairing coatings, and relates to a method for preparing a polyelectrolyte coating having self-repairing capability based on a layer-by-layer assembly technology. The prepared polyelectrolyte coating has high strength in the air and high mobility when the coating is immersed in water or the water is sprayed on the coating, so huge scratches caused by mechanical damage on the coating can be spontaneously repaired. The self-repairing polyelectrolyte coating has the advantages that: a repair means is easy to implement, the sameposition can be repeatedly and spontaneously repaired, and the preparation of the coating is free from the limitation of a substrate. Moreover, the method for preparing the self-repairing polyelectrolyte coating is simple, and the used raw materials are non-toxic and harmless. The method for preparing the self-repairing coating is believed to contribute to research of aspects comprising material science, surface chemistry, polymer science and the like, and the self-repairing polyelectrolyte coating is expected to be widely applied in aspects of preparation of protective coatings, biological material coatings, display equipment and the like.

A method of making a printing plate in which the uncoated surface of a substrate is treated with a pre-treatment solution prior to the deposition of ink on the surface. The pre-treatment liquid comprises a polyvalent metal salt, and at least one of an organic swelling reagent and/or a coalescence reagent. The pre-treatment liquid is applied to form a thin, homogenous layer of approximately 4 μm to the entire upper surface of the recording plate. The swelling reagent and/or the coalescence reagent and the polyvalent metal cations are physically well localized in the porous structure of the plate's surface. After partial drying of the pretreated anodized aluminum plate, CTP liquid is deposited onto the surface to form an image. The CTP liquid solids react with the pre-treatment liquid and are, therefore, chemically bound to the surface. This allows all data to be deposited in a single pass of the inkjet head without the problem of clustering.

The invention relates to a method for copper powder surface chemical plating silver, belonging to field of chemical silver plating. Said method comprises following steps: putting copper powder into diluted acid of 5-10% to remove oxide on surface of copper powder; adding disperser of 1-30% of copper powder by weight, stabilizer of 10-60% of copper powder by weight into deionized water to form reducing liquid, adding copper powder and stirring; adding silver nitrate into deionized water, adding ammonia, stirring and adding sodium-hydroxide and getting silver amine solvent; adding silver amine solvent into reducing liquid under stirring, finishing chemical silver plating of copper surface 10-50 minutes later; filtering, separating and washing, vacuum drying and getting silver-coated copper powder. The process is characterized by simple preparation and raw material, reduced silver-plated layer on container wall by adding silver amine solvent into reducing liquid, high silver converting rate. The electrical resistance of got copper powder is smaller than 2*10-4 omegacm.

A method is disclosed for coating substantially pure boron or highly boron-rich borides in a controlled manner. Such a method of coating of boron has a variety of applications, including surface chemical and wear protection, neutron absorption, prevention of impurity emission from heated filaments and ion beams, elimination of metal dust from vacuum systems, boridizing, boron cluster emission, and reactive chemistry. Borides with a boron-to-metal ratio of 20 or more are known to exist and may be used as a feedstock for substantially pure boron coatings for deposition processes requiring feedstock electrical conductivity, and/or enhanced reactivity. While most metal borides coincidentally produce significant metal vapor as a by-product, certain borides of yttrium, holmium, erbium, thulium, terbium, gadolinium, and lutetium have been identified as capable of producing substantially pure boron vapor.

The present invention provides a novel substrate for use in growing cells and for the study of mechanobiology. The membrane of the present invention comprises appropriate microtopography and surface chemical modifications to facilitate the production of adherent and oriented cells that phenotypically resemble cells in vivo.

The invention discloses a preparation method of a super-hydrophobic active carbon modified material. The material is prepared by applying a chemical liquid phase impregnation method, using trimethylchlorosilane as a modifier, using absolute methanol as a solvent, respectively using pre-processed coal columnar active carbon and coconut shell granulated active carbon as carriers, impregnating via liquid phase, drying in vacuum, and commonly blowing air and drying. The hydrophobic performance is respectively detected through a contact angle test and a liquid water adsorption experiment; and the adsorption is checked by using benzene adsorption experiment and an iodine value test. The invention has the advantages of simple preparation process, less material consumption and wild preparation condition; and the preparation method is carried out at room temperature. The prepared active carbon modified material has super-hydrophobic surface chemical performance and great pore volume, which makes up the shortcomings of easy absorption of moisture in the multi-pore carbon material with high humidity and small absorption capacity of the target organic matters; and the prepared active carbon modified material is easy to recycle and can be repeatedly recycled, so that the industrial cost is reduced and a foundation is further laid for the industrialized application.

The invention belongs to high molecular material technological field, concretely relates to a polymer shallow micro ball and its preparing method. The high molecular shallow micro ball links the surface chemical bond of the organic nm micro ball with a layer of polymer by micro latex synthesizing method, forming the micro ball with polymer inorganic nm compound core shell structure, then wash the inorganic material by strong acid to acquire the product, whose size is mm~nn. The invention has simple operation, high efficiency, average size of micro ball, and the shallow micro ball in the polymer made has outstanding heat stability and chemical stability, with bright future of application.

The invention relates to a method for preparing titania raw materials with high specific surface area used by denitration catalyst, which relates to the chemical product preparation technical field. The method comprises the following steps that: a metatitanic acid produced by adoption of the sulfuric acid method is processed by an organic surfactant and then modified so as to reduce the viscosity of the metatitanic acid; and loose titania products with high specific surface area and high surface chemical activity used by the denitration catalyst are prepared through filtration and calcination of the processed metatitanic acid. The method has a simple technique for processing the metatitanic acid and has low cost; and added organic substances are fully decomposed during the calcining stage, thereby impurities can not be brought into the final products and the environmental pollution can not be caused.

The invention provides a chemical regeneration method in the casting waste sand disposing process, relating to a process for performing surface chemical processing on various impurities which are attached on the surface of waste sand and are better not be reused in casting-form sand materials. During the chemical regeneration, chemical surface conditioning liquid I or/and chemical surface conditioning liquid II is or are used, and the disposing sand temperature is not more than 400 DEG C. The chemical regeneration method in the invention is carried out before or after the hot-method regeneration disposing or mechanical regeneration disposing of the casting waste sand disposing processing, and the chemical disposing technique is combined with the traditional hot-method regeneration and mechanical friction regeneration. The regeneration new sand formed in the method has better quality of the new sand, can better meet the application requirement on multi-form sand producing technique (hot core box, warm core box and cold core box) for recycling different casting waste sands (hot core box resin casting waste sand, warm core box resin casting waste sand, gas or/and organic fat hardening cold core box resin casting waste sand and profile damp die casting sand), and has better economical efficiency.