561 results about "Order structure" patented technology

Systems and methods for relative ordering circuit synthesis are provided herein. One aspect provides for generating at least one circuit design via at least one processor accessible by a computing device; wherein generating at least one circuit design comprises: generating at least one relative order structure based on at least one circuit design layout, the at least one relative order structure comprising at least one placement constraint associated with at least one circuit element; placing the at least one circuit element associated with the at least one placement constraint within a circuit design according to the at least one placement constraint; and placing circuit elements not associated with the at least one placement constraint within the circuit design. Other embodiments and aspects are also described herein.

The invention relates to a method to construct ordered structure on base, and the application of using the base to construct metal ordered structure. The method includes the following steps: adopting inorganic base or polymer base, taking base surface process to make it could conduct electricity, construct ordered microstructure of different functional group or macromolecule barrier layer; assembling the metal nanometer particle into the ordered structure to gain metal nanometer ordered structure. The invention could be widely used in making high sensitive metal sensor and detector.

A method for modeling optical scattering includes an initial step of defining a zero-th order structure (an idealized representation) for a subject including a perturbation domain and a background material. A Green's function and a zero-th order wave function are obtained for the zero-th order structure using rigorous coupled wave analysis (RCWA). A Lippmann-Schwinger equation is constructed including the Green's function, zero-th order wave function and a perturbation function. The Lippmann-Schwinger equation is then evaluated over a selected set of mesh points within the perturbation domain. The resulting linear equations are solved to compute one or more reflection coefficients for the subject.

The invention provides a method for preparing a polymer superhydrophobic surface by using nano-particles for assisting micromolding. The method firstly uses a PDMS as a raw material for copying a micro-structure on the surface of a fresh lotus leaf to be used as a soft template, then casts or hot presses the modified nano particles and a polymer on the surface of the PDMS soft template and strips after molding, thereby obtaining the polymer superhydrophobic surface which contains a micro / nano second-order structure on the surface and has a certain function. The method has simple operation process, high efficiency and good controllability and repeatability; as the obtained surface contains the functional nano-particles, the method not only gives the superhydrophobic property to the polymer surface, but also gives a certain function to the superhydrophobic surface, thereby providing a simple and effective way for preparing the superhydrophobic surface and having wide application value and broad market prospect.

The invention provides a block poly-carboxylic acid concrete high-efficiency water reducing agent with an ordered structure and a preparation method thereof. The block poly-carboxylic acid is prepared by using atom transfer radical polymerization, the structural regularity and the molecular weight distribution of the poly-carboxylic acid are controlled effectively, and the water reducing agent is used in a cement dispersing process. By adoption of the block poly-carboxylic acid concrete high-efficiency water reducing agent and the preparation method thereof, the problems of uncontrollable molecular weight of the poly-carboxylic acid, wider molecular weight distribution, un-designable molecular structure and the like are solved.

A device for removing substances from blood or other body fluids, comprising a bundle of semi-permeable hollow fibers, the ends of which are embedded and held in a pottant, and a tubular casing surrounding the hollow fiber bundle. At the ends of the casing, inlet and outlet pipes are connected with partitioned fluid chambers formed in the casing. Different aspects are provided to improve the flow properties, for increasing the filtering efficiency, such as varying packing density along the length of the fiber bundle, a distributor disc within a cap, apertures on the circumference of the pottant and an ordered structure of the rippling of the hollow fibers.

The present invention is directed to the creation of macroscopic materials and objects comprising aligned nanotube segments. The invention entails aligning single-wall carbon nanotube (SWNT) segments that are suspended in a fluid medium and then removing the aligned segments from suspension in a way that macroscopic, ordered assemblies of SWNT are formed. The invention is further directed to controlling the natural proclivity or nanotube segments to self assemble into or ordered structures by modifying the environment of the nanotubes and the history of that environment prior to and during the process. The materials and objects are “macroscopic” in that they are large enough to be seen without the aid of a microscope or of the dimensions of such objects. These macroscopic ordered SWNT materials and objects have the remarkable physical, electrical, and chemical properties that SWNT exhibit on the microscopic scale because they are comprised of nanotubes, each of which is aligned in the same direction and in contact with its nearest neighbors. An ordered assembly of closest SWNT also serves as a template for growth of more and larger ordered assemblies. An ordered assembly further serves as a foundation for post processing treatments that modify the assembly internally to specifically enhance selected material properties such as shear strength, tensile strength, compressive strength, toughness, electrical conductivity, and thermal conductivity.

The invention relates to biodegradable Mg-Gd-Zn-Ag-Zr series magnesium alloy and a preparation method thereof in the technical field of medical alloy. The alloy consists of Gd, Zn, Ag, Zr and Mg in percentage by weight: 5-10 percent of Gd, 0.5-3 percent of Zn, 0.1-1 percent of Ag, 0.1-1 percent of Zr and the balance of Mg. Through reasonably designing the alloy elements, a long-period stacking order structure (LPSO structure) is formed in an alloy structure; and with the adoption of the structure, the alloy can be strengthened and toughened, and the corrosion resistance and the local corrosion resistance of the alloy can be improved. Through deformation processing and heat treatment, the strong toughness and the corrosion resistance of the magnesium alloy can be further improved. The magnesium alloy provided by the invention is uniformly corroded in simulated body fluid, so that the overall failure of an implant material due to local corrosion is avoided, and no remarkable cytotoxicity exists; and the magnesium alloy can be used as a fixed implant material in the department of orthopedics. After solid solution treatment, the biodegradable Mg-Gd-Zn-Ag-Zr series magnesium alloy has good secondary shaping capability and can be used as an implant material in a blood vessel.

The invention provides a low-expansion antioxidative Ni-Fe-Cr-based high temperature alloy and a preparation method thereof. The alloy comprises 20 to 25% of Fe, 14 to 18% of Cr, 1.5 to 2.0% of Al, 1.5 to 2.5% of Ti, 0.5 to 2.0% of Nb, 0.3 to 2.0% of Mo, 0.5 to 2.0% of W, no more than 1.0% of Si, no more than 1.0% of Mn, no more than 0.5% of Cu, no more than 0.1% of C, no more than 0.01% of B, no more than 0.05% of Zr, no more than 0.05% of P and no more than 0.20% of a rare earth element, with the balance being Ni. The alloy is of a double-phase structure, wherein a substrate is an austenite (gamma) phase with a disordered face-centered structure, and a gamma' [Ni3(Al,Ti)] phase with an ordered structure is dispersed in the austenite. According to the invention, on the basis that structural stability, corrosion resistance and high temperature strength of the alloy are not influenced, the content of Fe is increased as much as possible to improve hot workability of the alloy and reduce cost. Compared with the prior art, the alloy provided by the invention has the advantages of low material cost, a low thermal expansion coefficient, excellent high temperature strength, hot-working performance and anti-oxidation corrosion and in particular, better cost performance when used under the conditions of high temperature, high pressure and supercritical water vapor.

The invention relates to a cathode material which has a tubular ordered structure and is applied in lithium ion batteries and a preparation method thereof, belonging to the fields of nano-material preparation technology and green energy. The cathode material is of a Li-rich layered structure and has a chemical molecular formula of xLi2MnO3.(1-x)Li[Ni1 / 3Mn1 / 3Co1 / 3]O2, wherein, x is more than 0 and less than 1. According to the invention, a natural biomaterial is used as a template for the cathode material, an internally uniform and dispersive cathode material precursor of the template is prepared by using the sol-gel method, and the template is removed by high temperature calcination so as to obtain a final product. Since a transition metal layer of the cathode material contains a certain amount of lithium, reversible and deintercalated lithium ions in actual discharge can be increased, and therefore, the discharge capacity of the cathode material is improved. The preparation method is capable of synthesizing tubular cathode materials, which enables the migration path of lithium ions in an electrode material to be shortened and the deintercalation rate of lithium ions to be enhanced.

The invention relates to the technical field of ordered porous materials, in particular to a highly ordered porous silica and a porous silicon carbonitride material and a preparation method and application thereof. Under a certain temperature, egg white adopted as template and structure-directing agent is stirred and then hydrolytically polycondensed through oil-soluble silicon source capable of controlling hydrolysis, and the template is removed from the obtained mixture under different roasting conditions, so that the ordered porous silica and the ordered porous silicon carbonitride material can be respectively obtained. The two materials have the unique ordered structure of the egg white, and have a specific surface area and good heat stability. Compared with the conventional method, the invention has the advantages of low cost, simple preparation technique, environment-friendliness and the like, and the obtained materials have a broad application prospect in fields such as the controlled release, separation, adsorption and catalysis of large biological molecules and proteins.

A process for depositing anti-microbial materials into or onto the surface of a substrate using ionic plasma deposition. The process includes the steps of providing a cathode of target material having anti-microbial potential which is disposed within a partial vacuum, powering the cathode to generate a plasma discharge for ionizing the target material into a plasma of constituent particles. The plasma particles are reacted with ionized gas, and are selected, controlled and directed toward the substrate by electromagnetic fields generated by at least one first anode adjacent to the cathode and at least one second anode positioned adjacent the first anode. Additional anode structures and charged screens provide further control of the plasma constituents. The plasma constituents, comprising the anti-microbial materials, are deposited on the substrate as dispersed ordered structures which form an anti-microbial surface into and onto the substrate.

Semiconductor micro- and nanotubes allow the incorporation of ordered structures such as quantum wells and quantum dots into them providing the potential for ultralow threshold micro- and nanoscale lasers for use in applications such as future ultrahigh-speed photonic systems as well as quantum information processing. According to the invention a means of manufacturing these with high reproducibility, low processing complexity, and at high densities is provided. Also provided is a means of releasing these micro- and nanotubes with low stress and a method of “pick-and-place” allowing micro- and nanotubes to be exploited in devices integrated on substrates that are either incompatible with the manufacturing technique or where the area of substrate required to manufacture them is detrimental to the cost or performance of the circuit.

The method imposes external electric field on microball cladded in microcapsule between two parallel electrode panel and the microballs are directional-moved and order-arranged under the action of the external electric field because of electric charge of itself so colour display can be obtained by totally reflecting light mating to the wavelength. Since the present invention applies method of varying external electric field i.e voltage to adjust ball arrangement state i.e ordering structure period of photon crystal, the aim of colour display can be achieved by generating different, reflection light.

One embodiment is a nanostructured arrangement having a base and pyramidal features formed on the base. Each pyramidal feature includes sloping sides converging at a vertex. The nanostructured arrangement further includes a nanostructured surface formed on at least one of the sloping sides of at least one of the pyramidal features. The nanostructured surface has a quasi-periodic, anisotropic array of elongated ridge elements having a wave-ordered structure pattern. Each ridge element has a wavelike cross-section and oriented substantially in a first direction.

The invention discloses a preparation method of a polyimide porous film. According to the invention, silica colloid ball is used as a template; uniformly dispersed polyamide acids (PAA) / SiO2 colloidal solution is dried to obtain a PAA / SiO2 composite film with an ordered structure; the composite film is treated with thermal imidization, etched by a hydrofluoric acid solution to remove the SiO2 colloid ball, washed and dried in vacuum to obtain the polyimide porous film with an ordered structure. The invention is simply operated, at low cost and easy for industrialized production; the prepared polyimide porous material has advantages of ordered structure, ordered aperture, large strength and heat resistance, etc.

The present invention provides a preparation method of high-strength bionic collagen membrane. The preparation method is by conducting gradient dialysis process on collagen to rearrange collagen molecules into an ordered structure, and endow the molecules with more consistent and more extensive collagen fiber orientation, thus improving the mechanical properties of the material. The collagen membrane prepared by using the method has similar appearance, structure and performance to natural dura and amnion of mammals, and good rehydration, and is free to bend and fold after water absorption; the bionic collagen membrane with high tensile strength can be stitched by using suture and can be used in clinical guided tissue regeneration or repair of various tissues.

The invention discloses a two-dimensional and double-cycle ordered structure array and a preparation method thereof. The array is an ordered porous film consisting of metals in a microparticle hole shape and a nanometer hole shape and arranged on a conductive substrate, the nanometer hole in the film is located in the microparticle hole and is in a stacking shape, or the nanometer hole is a single layer and is located at the bottom surface or the external surface of the microparticle hole or covers the internal surface and the external surface thereof, the diameter of the microparticle hole is 1,800-2,200 nm, and the diameter of the thenanometer hole is 180-220 nm. The method comprises the following steps of: firstly, self-assembling by using a polystyrene colloidal ball of one diameter in combination with a solution impregnating method or an electrodepositing method to obtain the ordered hole array of a bowl-shaped metal attached to the conductive substrate; and then self-assembling thereon by utilizing polystyrene colloidal of another diameter in combination with the electrodepositing method to prepare the two-dimensional and double-cycle ordered structure arrays in four structures. The product thereof has the characteristics of a macro-scale system, the preparation method has universality, and the two-dimensional double-cycle and ordered structure array consisting of other conductive materials can be prepared by the method.

The invention discloses a high-performance D type audio power amplifier adopting high-order multipath feedback structure, which comprises a prepositive variable gain amplifier, an integrator, a pulse width modulation (PWM) circuit, a three-state regulating circuit, a grid driving circuit and a power output stage. The integrator is in a two-order structure formed by cascade connection of two stages of integrators, and two paths of feedback are introduced to form a higher-order double-feedback loop, thereby effectively increasing the loop gain and the out-off-band attenuation, and obviously improving the suppression ratio of total harmonic distortion and noise to power sources and other main properties in the range of audio frequency band (22Hz-22KHz). By introducing two paths of voltage negative feedback and comprehensively considering the input dynamic range, the signal-to-noise ratio and stability factors, the ratio of two stages of feedback coefficients can be regulated by regulating the ratio of the input resistance and the feedback resistance of two stages of integrators, thereby ensuring the stability of a system. The D type audio power amplifier with the structure has the characteristics of high integration level and high performance and can be widely applied to the fields of portable equipment, consumer electronics and the like.

The invention provides a method for preparing a color-adjustable gel photonic crystal film. According to the method, by strictly controlling the concentration of PS (Polystyrene) microspheres and the volume ratio of PS microspheres to a precursor solution, the matching of the self-assembly rate of the PS microspheres and the polymerization rate of the precursor solution is adjusted and controlled at a low temperature, the PS microspheres are self-assembled into gel crystals having an ordered structure and meanwhile, hydrogel particles formed by polymerization of precursor solution are filled in gaps of the gel crystals so as to form a gel crystal-hydrogel compound structure, and after PS is removed, the color-adjustable gel photonic crystal film having a reverse opal structure is formed. The gel photonic crystal film having the inverse opal structure prepared by a co-deposition method has the characteristics of regular structure and three-dimensional ordered arrangement.

The invention discloses a tissue engineering fiber bundle structure body and a preparation method thereof. The invention provides a method A or B for preparing hydrogel fiber filaments containing cellular components. The method A comprises the following steps: 1) compositing a hydrogel material utilized as a matrix with cellular components to obtain a mixture containing cellular components; and 2) putting the mixture obtained in the step 1) into crosslinked fluid corresponding to the matrix to undergo crosslinking, thus obtaining the hydrogel fiber filaments containing cellular components. Experiments prove that the design can comprehensively meet the special bionic requirements of high-density cell composition, good vascularization development trend and achievement of directionally ordered structure in tissue engineering, so that the structure body is good in vascularization development prospect and can hopefully break through the development bottleneck that the tissue engineering can not become large and thick at present.

Techniques and methods of formation of ordered mixtures of particles by “clustering”. Clustering comprises local “structuring” consisting of a large “host” and smaller “guest” particles by various techniques. Small amounts of polymer are coated onto solid particles by various means. In one embodiment, an ordered mixture is created wherein the material that is of lesser quantity is of small particle size (the “B” particles) and the “A” particles are of larger size. The “B” particles are then coated onto a single A particle. By creating this ordered structure, each composite particle has the proper or stoichiometric amount of all ingredients. This dry composite material produced is appropriately used in various applications such as pharmaceutical formulations in the form of tablets, capsules, oral suspensions, inhalant, parenteral formulations and the like; energetics manufacture such as but not limited to explosives, propellants and pyrotechnics; agricultural products including but not limited to fertilizers, herbicides and pesticides; nutritional supplements and the like.

The invention discloses a synthesis method of graphitized ordered mesoporous carbon at low temperature. The method comprises the following steps: by a soft template path, introducing a metal precursor salt with a catalytic graphitizing effect in the organic-organic self assembly process of a carbon source and a surfactant, then carbonizing in an inert gas atmosphere, and carrying out one-step synthesis to obtain the graphitized ordered mesoporous carbon material. The method combines two independent steps of synthesis of the mesoporous carbon material and metal load into one step, greatly simplifies the synthesis steps, has simple and convenient operation, combines the carbonization process and the graphitizing conversion process, reduces the damage of high temperature to the ordered structure of the material, and greatly reduces the heat treatment temperature of graphitizing by utilizing the catalytic effect of metal. Compared with non-graphitized ordered mesoporous carbon material, the material serving as a catalyst carrier shows better electro-catalysis performance and provides a new choice for fuel-cell catalyst carriers.

A low-cost, efficient method of preparing hierarchically ordered structures by filling a minimold with a microsphere-containing latex suspension, forming an close-packed array of microspheres within the minimold and filling void space in the array with a self-assembling mixture of hydrolyzed inorganic species and amphiphilic block copolymers. A macroporous and mesoporous material can be produced by subsequent thermal removal of the microspheres and copolymers.

The invention discloses a preparation method of a surface-enhanced Raman scattering substrate. The preparation method comprises the following steps of: (1) preparing a flexible nano imprinting template with patterns and in a double-layer composite structure; (2) imprinting ordered nano structure patterns; (3) carrying out vacuum evaporation; and (4) eliminating a nano imprinting gel baffle layer. The preparation method can be applied to preparation of all surface-enhanced Raman scattering substrates; the defects that the substrate is strictly required in preparing the SERS (Surface-Enhanced Raman Scattering) substrate in the conventional nano imprinting mode, and metal ordered structure SERS substrates with high resolution are hard to be prepared on complex appearance and high-curvature surfaces are overcome; and moreover the method is simple in process, can be used for producing high-performance SERS substrates with large area, large scale and low cost, can solve the preparation requirements of the SERS substrates and can meet the present practical requirements well.

The present invention relates to new organic-inorganic hybrid silicates and metal-silicates called ECS, characterized by an X-ray powder diffraction pattern with reflections exclusively at angular values higher than 4.0° of 2θ, preferably at angular values higher than 4.7°, and an ordered structure containing structural units having formula (a) wherein R is an organic group: Formula (a) and possibly containing one or more elements T selected from groups III B, IV B, V B and transition metals, with a Si / (Si +T) molar ratio in said structure higher than 0.3 and lower than or equal to 1, wherein Si is the silicon contained in the structural unit (a). A process is also described, starting from disilanes, for the preparation of these materials, which does not include the use of templates or surfactants. These materials can be used as molecular sieves, adsorbents, in the field of catalysis, in the field of electronics, in the field of sensors, in the field of nanotechnologies.