1875 results about "Nanoscopic scale" patented technology

An electric-cigarette undertaking nanometer dimension fineness space heating pulverization to nicotine solution comprises a cigarette pole and a cigarette holder connected with the front end of the cigarette pole. The cigarette pole is a hollow rod shape cigarette pole welded with a plug at the back end. The intracavity of the cigarette pole is provided with a rechargeable battery, a liquid storage tank for storing nicotine solution, an imbibition liquid core arranged at the front end of the liquid storage tank and contacted with the nicotine solution, and a heater of space heating pulverization arranged inside the heating cavity positioned in the front part of the cigarette pole. The wall of the cigarette pole corresponding to the liquid storage tank is provided with a liquid inlet communicated with the liquid storage tank. Any place of the wall of the cigarette pole is provided with an electric heating switch. The center of the cigarette holder is provided with a hollow pipe which extends into the cigarette pole. The wall of front part of the cigarette holder is provided with a piezoelectric press sensor. The back end of the cigarette pole is provided with a recharging connection device which can charge the rechargeable battery through outer power. The piezoelectric press sensor is communicated with the rechargeable battery all the time. The electric heating switch, the piezoelectric press sensor and the rechargeable battery constitute a circuit loop. The invention has the advantages of convenient assembly and installation, easy carry, wide application and convenient use.

An improved method of and apparatus for real-time continual nanometer scale position measurement by beam probing as by laser beams and the like, both fixed and oscillating or scanning, over an atomic and other undulating surface such as gratings or the like, relatively moving with respect to the probing beams; and providing, where desired, increased detection speeds, improved positioning sensing response, freedom from or relaxed requirements of strict control on probing oscillation amplitude, and multi-dimensional position measurement with focused beam probes and the like.

Expandable surfaces made from sheet materials with slits distributed on the surface of sheet material where the surfaces expand by application of force along or/and across the surface of sheet material. The unexpanded surfaces are flat sheets, or closed surfaces like cylinders, spheres, tubes, or custom-designed organic shapes marked with pre-formed or post-formed slit designs. The expanded surfaces can be single units or modules which can be attached to one another through various means. The sheet materials range from hard surfaces like metals, to softer materials like papers and plastics, or pliable materials like fabrics, rubbers, synthetic surfaces or bio-surfaces. The slits are arranged in patterns ranging from periodic, non-periodic to irregular designs. The slits can be straight, bent, curved or irregularly shaped with even or uneven spacing. Slitting can be achieved by digital cutting or punching devices like laser-cutting, water-jet cutting, digital punching, automated dies, etc. or pre-formed when casting the sheet material. Force can be applied manually with tools or through the use of machines and special set-ups. Applications range from architectural surfaces, walls, ceilings, panel systems, structures and sculpture. On a smaller scale, applications include containers, packaging material, fabrics and human wear. On micro- to nano-scale, applications range from expandable surfaces for gauzes, band-aids, stent designs, skin grafts, semi-permeable membranes and micro-filters for various industries including purification of fluids and chemical substances.

An apparatus and method for performing nucleic acid (DNA and/or RNA) sequencing on a single molecule. The genetic sequence information is obtained by probing through a DNA or RNA molecule base by base at nanometer scale as though looking through a strip of movie film. This DNA sequencing nanotechnology has the theoretical capability of performing DNA sequencing at a maximal rate of about 1,000,000 bases per second. This enhanced performance is made possible by a series of innovations including: novel applications of a fine-tuned nanometer gap for passage of a single DNA or RNA molecule; thin layer microfluidics for sample loading and delivery; and programmable electric fields for precise control of DNA or RNA movement. Detection methods include nanoelectrode-gated tunneling current measurements, dielectric molecular characterization, and atomic force microscopy/electrostatic force microscopy (AFM/EFM) probing for nanoscale reading of the nucleic acid sequences.

A route to the fabrication of electronic devices is provided, in which the devices consist of two crossed wires sandwiching an electrically addressable molecular species. The approach is extremely simple and inexpensive to implement, and scales from wire dimensions of several micrometers down to nanometer-scale dimensions. The device of the present invention can be used to produce crossbar switch arrays, logic devices, memory devices, and communication and signal routing devices. The present invention enables construction of molecular electronic devices on a length scale than can range from micrometers to nanometers via a straightforward and inexpensive chemical assembly procedure. The device is either partially or completely chemically assembled, and the key to the scaling is that the location of the devices on the substrate are defined once the devices have been assembled, not prior to assembly.

The invention belongs to the technical field of chemistry and chemical industry and functional materials, and relates to a method for preparing a metal mesh which has special wetting properties and is used for oil-water separation. The method adopts simple wet-method chemical etching technology, nano-scale microscopic bulges are prepared on the surface of a metal mesh with micron-grade pore diameters, and then a compound which does not contain fluorine and has low surface energy is modified on the surfaces of the microscopic bulges. For the surface of the prepared material, a contact angle of a water drop is more than 150 degrees, and a contact angle of oil is close to 0 degree. Due to the specific wetting properties, the material can allow the oil to pass through the metal mesh smoothly, but the water cannot permeate through the metal mesh completely, so that the property of effectively separating oil-water mixtures is realized. Particularly, the specific wetting properties of the surface of the material can keep stable in acid solution, alkali solution and salt solution, and thus the functional metal mesh can be excellently applied in aspects of metal corrosion prevention and the like. A mesh membrane does not contain the fluorine, and has the advantages of simple preparation method, high permeability of pore space and good oil-water separation effect, and corrosion resistance.

A stamp for use in transferring a pattern in nano-scale has a monomolecular antisticking layer. The anti-sticking layer comprises molecular chains, which are covalently bound to the surface of the stamp and which each comprise at least one fluorine-containing group. Each molecular chain contains a group Q, which comprises a bond which is weaker than the other bonds in the molecular chain as well as the covalent bond that binds the molecular chain to the surface of the stamp. Splitting of said bond in the group Q creates a group Q1, which is attached to the part of the molecular chain being left on the surface of the stamp and which is capable of reacting with a fluorine-containing compound to restore the antisticking layer. In a method of manufacturing a stamp for use in transferring a pattern in nanoscale, the stamp is provided with the above-mentioned molecular chain. In a method of repairing a damaged antisticking layer of the above-mentioned stamp, the stamp is treated with a repairing reagent, which has a coupling end, which is capable of reacting with the group Q1, and a fluorine-containing group located at the other end of the repairing reagent.

A method for controlling electric conduction on nanoscale wires is disclosed. The nanoscale wires are provided with controllable regions axially and/or radially distributed. Controlling those regions by means of microscale wires or additional nanoscale wires allows or prevents electric conduction on the controlled nanoscale wires. The controllable regions are of two different types. For example, a first type of controllable region can exhibit a different doping from a second type of controllable region. The method allows one or more of a set of nanoscale wires, packed at sublithographic pitch, to be independently selected.

This disclosure provides embodiments for the formation of vertical memory cell structures that may be implemented in RRAM devices. In one embodiment, memory cell area may be increased by varying word line height and/or word line interface surface characteristics to ensure the creation of a grain boundary that is suitable for formation of conductive pathways through an active layer of an RRAM memory cell. This may maintain continuum behavior while reducing random cell-to-cell variability that is often encountered at nanoscopic scales. In another embodiment, such vertical memory cell structures may be formed in multiple-tiers to define a three-dimensional RRAM memory array. Further embodiments also provide a spacer pitch-doubled RRAM memory array that integrates vertical memory cell structures.

Textured surface for increasing Leidenfrost temperature. The texture comprises of surface features over multiple length scales—from micro to nanoscale—wherein the features at each length scale have a size, aspect ratio, and spacing selected to increase the Leidenfrost temperature. The structure includes an array of microscale structures disposed on the surface, the structure having size, aspect ratio and spacing selected to increase Leidenfrost temperature. The microscale structures may also include nanoscale structures on their surface to create a hierarchical structure. The structures result in an increased Leidenfrost temperature.

The invention relates to a preparation method of a homogenized fine nano-cellulose fiber. The preparation method can solve the problems of uniform diameter distributor of biomass nano-cellulose prepared by the existing strong acid hydrolysis method and the high-strength mechanical shearing method, easy gathering among the nano-fiber and a narrow range of applications of the TEMPO catalytic oxidation method. The preparation method comprises the following steps: 1) extracting biomass fiber with benzyl alcohol solution; 2) carrying out treatment by using acidified sodium chlorite; 3) carrying out gradient treatment with alkaline liquor; 4) using TEMPO, sodium bromide and sodium hypochlorite for catalytic oxidation treatment; 5) using sodium chlorite for treatment; and 6) carrying out nano-scale processing by using the long-term stirring method, the ultrasonic method or the high-pressure homogenization method, drying, and then obtaining the homogenized fine nano-cellulose fiber. The fiber has the uniform diameter distribution, the diameter is 3-5nm, the length-diameter ratio is not less than 500, the fiber is mutually interwoven into a mesh snarling structure, and the method is applicable to preparing the nano-cellulose fiber by using wood pulp, paper-making pulp, wood, bamboo and crop straw.

The invention provides a multi-shell-layer metal oxide hollow ball and a preparation method thereof. A hydrothermal method is used for preparing a carbon ball template; metal salts are dissolved in carbon ball suspension liquid, and the gradient distribution, the depth and the number of metal salts entering carbon balls are controlled through regulating adsorption conditions such as metal salt concentration, solution pH value, soaking temperature and time and the like; and the heat treatment is carried out on the carbon balls adsorbing metal ions, and the multi-shell-layer metal oxide hollow ball can be obtained. The shell-layer of the hollow ball prepared by the method is formed by accumulating nanometer crystal particles of metal oxides, the shell layer number can be regulated and changed from two to four, and both the size of the hollow ball and the thickness of the shell layers are controllable. The method provided by the invention is simple and is easy to implement, the controllability is high, the pollution is little, the cost is low, and in addition, the general applicability is realized. The prepared product has a hollow structure and the shell layers with the thickness inthe nanometer level, simultaneously, the internal space can be effectively utilized through the multilayer structure, and the multi-shell-layer metal oxide hollow ball is applied to gas sensitivity and photocatalysis and has the more excellent performance through being compared with the traditional nanometer material and a single-layer hollow ball.

The present invention is directed to micro- and nano-scale imprinting methods and the use of such methods to fabricate supported and/or free-standing 3-D micro- and/or nano-structures of polymeric, ceramic, and/or metallic materials. In some embodiments, a duo-mold approach is employed in the fabrication of these structures. In such methods, surface treatments are employed to impart differential surface energies to different molds and/or different parts of the mold(s). Such surface treatments permit the formation of three-dimensional (3-D) structures through imprinting and the transfer of such structures to a substrate. In some or other embodiments, such surface treatments and variation in glass transition temperature of the polymers used can facilitate separation of the 3-D structures from the molds to form free-standing micro- and/or nano-structures individually and/or in a film. In some or other embodiments, a “latch-on” assembly technique is utilized to form supported and/or free-standing stacked micro- and/or nano-structures that enable the assembly of polymers without a glass transition temperature and eliminate the heating required to assemble thermoplastic polymers.

The invention relates to a preparation method of a nano-ZSM-5 molecular sieve, which belongs to the field of preparation of zeolite molecular sieve catalysts. The preparation method can solve the problem that the existing synthesis technology has the defects of easy emergence of mixed crystal phase, high cost, environmental pollution and easy loss of features of nanomaterials. The method is as follows: adding pre-crystallized crystal seeds into a gel system of the template-free synthetic nano-ZSM-5 molecular sieve, carrying out crystallization for 24 hours at the temperature of 160-180 DEG C,cooling to room temperature, carrying out centrifugal filtration on products, washing, drying and baking. The prepared nano-ZSM-5 molecular sieve is highly concentrated nanoscale crystals without themixed crystal phase; and the method has the advantages of low cost and environmental protection.

The invention relates to a nano carbon material with a network structure consisting of polymer chains, in particular to a nano carbon sulfur composite material with a network structure suitable to be used in a secondary lithium sulfur battery anode and a preparation method thereof. The carbon sulfur composite material is formed by adopting the following steps of: introducing functional groups onto carbon particles by adopting the electric conductivity and the porosity of a carbon material and the reaction capacity of similar condensed aromatics of the carbon material and by means of an irreversible chemical reaction; introducing the polymer chains, wherein the polymer chains are stretched, bent and cross-linked on the surfaces of the carbon particles to form a cross-linked network structure; and compounding a sulfur element or a polysulfide (m is more than 2) containing -Sm- structure into the network structure to form the nano carbon sulfur composite material with the network structure. The carbon sulfur composite material has a rich cross-linked network structure, nano-scale network pores constrain the sulfur element or the polysulfide (m is more than 2) containing the -Sm- structure in the network, and the active substances are limited in a certain region to react, so that the composite material has predominant electrochemical performance.

The present invention discloses process of preparing selectively laser sintered inorganic nanometer particle reinforced nylon part. The process includes the following steps: surface organizing treatment of inorganic nanometer particle and ultrasonic treatment to disperse the inorganic nanometer particle homogeneously in mixed solvent to form inorganic nanometer particle suspension; heating the mixture of inorganic nanometer particle suspension, nylon resin and antioxidant inside a sealed container to dissolve the nylon resin in the solvent; cooling, decompression distilling to recover solvent, vacuum drying, ball milling and sieving to obtain composite nylon/inorganic nanometer particle composite material; and final selectively laser sintering to form. The selectively laser sintered inorganic nanometer particle reinforced nylon part has raised strength and high toughness.

The invention provides a high strength organic / inorganic nano composite film layer materials and method for preparation, wherein the composition comprises 10-13% of titanate, 7-17% of silicane coupling agent, 0-6% of silicate ester, 40-65% of alcohol solvent and 1-4% of water. The preparation of the composition consists of using inorganic acid as catalyst, co-hydrolyzing titanate, silicate and silane coupling agent in dimethyl carbinol, coating the obtained paint by rotary, dipping or spraying methods onto the surface of the appliances, finally solidifying 1-3 hours at 135- 150 deg. C.

The invention discloses a preparation method of colored zirconia ceramics, which belongs to the field of doped ceramic material preparation. The method comprises the following steps that: stabilizer and colorant are added into the suspension of zirconia powder by the mixture ratio of 850 to 980 parts of zirconia powder, 10 to 50 parts of stabilizer and 10 to 120 parts of colorant; by controlling the pH value of the solution or using various precipitant, the stabilizer and the colorant are precipitated on the surface of the zirconia powder; the solution is filtered and dried; the obtained powder is ground, screened, formed, degreased and sintered to obtain the colored zirconia ceramics. In nano-scale, the preparation method realizes the homogeneous compounding of the stabilizer, the colorant and the nano zirconia powder, can greatly reduce the volatilization of the colorant in the high-temperature sintering phase of the zirconia ceramics, has uniform sample color and good repeatability, and the colored zirconia ceramics prepared by the method can be widely applied to arts and crafts decoration, clocks and watches, mobile phone cases, jewelry and other fields.

The periodic stress and strain fields produced by a pure twist grain boundary between two single crystals bonded together in the form of a bicrystal are used to fabricate a two-dimensional surface topography with controllable, nanometer-scale feature spacings (e.g., from 50 nanometers down to 1.5 nanometers). The spacing of the features is controlled by the misorientation angle used during crystal bonding. One of the crystals is selected to be thin, on the order of 5-100 nanometers. A buried periodic array of screw dislocations is formed at the twist grain boundary. To bring the buried periodicity to the surface, the thin single crystal is etched to reveal an array of raised elements, such as pyramids, that have nanometer-scale dimensions. The process can be employed with numerous materials, such as gold, silicon and sapphire. In addition, the process can be used with different materials for each crystal such that a periodic array of misfit dislocations is formed at the interface between the two crystals.

The invention belongs to the technical field of preparation of phase-change microcapsules, in particular to a preparation method of a phase-change energy-storage microcapsule and the phase-change energy-storage microcapsule. A preparation technology of the phase-change energy-storage microcapsule provided by the invention comprises the following step of: coating a phase-change material inside micron and/or nano particles by adopting a melting and coaxial electronic injection method to form the phase-change energy-storage microcapsule with a core-shell structure. The phase-change energy-storage microcapsule provided by the invention has a core-shell structure constructed by a shell material and an organic phase-change core material packaged in the shell material; and the microcapsule has a phase-change energy-storage property. A melting and coaxial electronic injection preparation process provided by the invention has a simple process, and can be used for preparing a micron and/or nano-scale capsule; the capsule has high dispersity and a large specific surface area.

A storage device and a method of forming a storage device, includes depositing a metal layer on a substrate, and oxidizing the metal layer to form an oxide with a rutile structure on which a ferromagnetic material is selectively grown. The substrate may be substantially formed of either SiO2, Si3N4, or a compound of SiO2 and Si3N4. In another method, a method of forming a magnetic device, includes one of seeding a surface with one of Ti, Sn, and Ru islands having nanometer dimensions, and by exposing nanometer scale areas of the one of Ti, Sn, and Ru on a substrate, and coating the one of Ti, Sn, and Ru, with a ferromagnetic material. The surface may be substantially formed of either SiO2, Si3N4, or a compound of SiO2 and Si3N4. Similarly, the substrate may be substantially formed of either SiO2, Si3N4, or a compound of SiO2 and Si3N4.