66 results about "Periodic table" patented technology

Naphtha reforming catalysts are described. The catalyst includes a support comprising a solid solution or a homogenous mixture of atoms in solid state having a single crystal structure comprising AI2O3, and / or 0.01 to 3 wt% of a first metal of Group 2 or Group 15 of the Periodic Table, or a combination thereof. It also includes 0.05 to 5.0 wt% Pt and 0.05 to 5.0 wt% Re; 0.01 to 2 wt% of at least one additional metal from Groups 1, 2, 3, 9, or 15 of the Periodic Table, or combinations thereof; 0.03 to 1.0 wt% S; and 0.5 to 2 wt% of a halogen. The catalyst has an average bulk density in a range of 0.25 - 1.50 g / cc and a surface area in a range of 50-300 m2 / g. Catalytic reforming processes are also described.

The present invention addresses the problem of providing a metal carbide sintered body in which the occurrence of cracks is suppressed. Also provided is a method for producing a metal carbide sintered compact in which the occurrence of cracks is suppressed. This problem is solved by a metal carbide sintered body of at least one metal selected from the group consisting of Group 4 and Group 5 elements of the periodic table, the average particle diameter of the particles in the first region being 3.5-9.5 [mu] m, and the average particle diameter of the particles in the second region being 3.5-9.5 [mu] m. The ratio of the average particle diameter of the particles in the second region to the average particle diameter of the particles in the first region is from 0.75 to 1.0 (inclusive). Furthermore, this problem is solved by a method for producing a sintered carbide, the method comprising: a step for adding a carbon powder to a mixed powder of a SiO2 powder and a metal carbide of at least one metal selected from the group consisting of Group 4 and Group 5 elements of the periodic table; and a step for sintering the mixture to which the carbon powder has been added, the amount of the carbon powder added being 0.30-3.00 parts by mass (inclusive) per 100 parts by mass of the mixed powder.

The invention discloses a processing method for manufacturing a novel powder material through controlled atom spraying. In the method, the material (target) to be deposited may be selected from any element in the periodic table of elements or from a combination of at least two elements. The material to be deposited is referred to as a base material or substrate, which may be selected from polymers, metals, semiconductors, ceramics, molecular sieves, perovskite, MOFs, carbonaceous materials, or any type or class of powder material having a vapor pressure of less than 10 <-1 > mbar. The processing method taught in the invention describes a means of planning and implementing different coating structures on a substrate (substrate) by defining and controlling the production process. As a result, a plurality of novel materials having a plurality of novel properties and predetermined properties can be obtained.

This invention relates to a thermoplastic composition comprising: a) 20 to 90 wt% of a thermoplastic resin, b) a laser-direct structuring additive, c) optionally, ceramic filler particles without laser-direct structuring additive function, and d) 0.1 to 5.0 wt% of an acid-modified polymer, wherein b) comprises b1) a conductive metal oxide, wherein the conductive oxide has a maximum of 5 x 10⁻⁶ ppm. 3 The resistivity is Ω·cm, and it contains at least a metal of Group n and Group (n+1) of the periodic table, where n is an integer from 3 to 13, and / or b2) calcium copper titanate.

A catalyst used for converting a heavy hydrocarbon, wherein the catalyst includes an extrudate having a co-mulled mixture of an inorganic oxide; and at least one metal from Group VIB and at least one metal from Group VIII of the Periodic Table of Elements. An atomic ratio of the at least one metal from Group VIII to the at least one metal from Group VIB is in the range of from 0.0 to 0.3, and the catalyst has a pore structure such that 15 vol.% to 25 vol.% of the total pore volume is present in pores of a diameter greater than 1,000 A and a surface area of that is greater than 150 square meters (m2) / gram (g) and less than 240 m2 / g.

ELECTROLYTIC HYDROGEN PURIFICATION The present invention relates to a method for purifying a hydrogen stream contaminated by water, oxygen, and optionally nitrogen. The method comprises contacting the hydrogen stream to be purified with a zeolitic adsorbent material comprising at least one metal selected from the metals of columns 3 to 12 of the Periodic Table of Elements, in its zero-valence metallic form, or in its oxidized or reduced form, and recovering the purified hydrogen stream. The invention also relates to the use of a zeolitic adsorbent material comprising at least one metal from columns 3 to 12 of the Periodic Table of Elements for hydrogen purification, as well as the use of hydrogen thus purified in industrial processes. Fig.: None

The embodiment of the present application provides a kind of phase change material and its manufacturing method, phase change memory and its manufacturing method, wherein the phase change material includes: first doped element, second doped element and phase change bulk material;Wherein, the first doped element and the second doped element can form chemical bond with the element in the phase change bulk material;The bond energy of the chemical bond formed is greater than the bond energy of the chemical bond between elements in the phase change bulk material;The first doped element and the second doped element belong to the elements of different groups in periodic table.The embodiment of the present application can improve the amorphous thermal stability and data retention of phase change material, so as to improve the electrical performance of phase change memory.

The present disclosure relates to metallocene complexes of formula (I) wherein Mt is Zr or Hf; x is a sigma ligand; r < 1 >, each independently, equal to or different from each other, is a C1-C20 hydrocarbon group, optionally containing up to two heteroatoms of groups 14-16 of the periodic table, or forming together with the Si atom to which they are attached a C4-C8 ring; r1 and R2'are each independently, equal to or different from each other, a C1-C10-hydrocarbyl group, n are each independently an integer from 1 to 5, R3 and R4 are each independently H, a C1-C10-hydrocarbyl group, or an-OR31,-SR31 or-NR312 group, where R31 is a C1-C10-hydrocarbyl group, where at least one R3 of each phenyl group is not hydrogen and at least one R4 is not hydrogen, R51 'is a C1-C10-hydrocarbyl group, and R6' is C (R61) 3, where R61 is a linear or branched C1-C6-alkyl group.

The invention relates to a cutting tool comprising a support body and a cBN or PCD cutting edge tip, wherein the cBN or PCD cutting edge tip is connected to the support body by a brazing joint of 5-150 pm thickness, the support body is a cemented carbide comprising 3-25 wt% of a metallic binder, optionally up to 25 wt% of a carbide or carbonitride of one or more elements of group 4, 5 or 6 of the periodic table, and the remainder WC, wherein the metallic binder comprises at least 40 wt% of Ni, and wherein the brazing joint comprises in order from the support body: a first layer of TiC, immediately adjacent to the support body, having an average thickness of 10-400 nm; a second layer having an average thickness of 0.5-8 pm comprising on average at least 5 wt% of the metal Ni, on average 25-60 wt% of the metal Cu and on average 15-45 wt% of the metal Ti; and a third layer having an average thickness of 4-145 pm comprising the metal Ag and the metal Cu.

A sintered cemented carbide is composed of: a hard phase having NbC as a main component, the hard phase including a first hard phase composed of a carbide containing at least one element selected from group 4 to 6 elements in the periodic table (provided that Nb is an essential component); and a second hard phase composed of a boride containing at least one element selected from Group 4 to 6 elements in the periodic table; and a binder phase containing at least one element selected from the group consisting of Ni, Co and Fe, in which the sintered cemented carbide contains at least one element (excluding Nb) selected from the group consisting of Group 4 to 6 elements in the periodic table in an amount of 3 to 30 vol% (calculated as carbide) based on the total amount of the hard phase, at least one member selected from the group consisting of Ni, Co, and Fe is contained in an amount of 4-40 vol% as a binder phase component, and B is contained in a mass ratio of 0.3-8% based on the binder phase component.

To provide a novel light-emitting device that offers superior convenience, usefulness, or reliability. [Solution] The present invention provides a light-emitting device having an anode sandwiched between an EL layer on the cathode, the EL layer comprising at least a light-emitting layer and an oxidation-resistant layer on the light-emitting layer, the EL layer having sides, and a block layer in contact with the top surface and sides of the EL layer, the cathode in contact with the sides of the EL layer via the block layer, and the block layer comprising a heterocyclic compound. In the light-emitting device of the above configuration, the oxidation-resistant layer may comprise one or more selected from oxides of metals belonging to groups 4 to 8 of the periodic table and organic compounds having electron-withdrawing groups.

The invention relates to a metallised film (1) comprising a substrate film (2) and a metallic layer (3) located on the substrate film (2), wherein the substrate film (2) has a first main surface and a second main surface, and the metallic layer (3) is applied in a metallisation region (3a) of the substrate film (2) located on the first main surface, wherein the metallisation region (3a) covers at least 90%, in particular 100%, of the first main surface (3a), wherein the metallic layer (3) completely and uniformly covers the entire metallisation region, and wherein the metallic layer (3), at every point on its surface, when viewed in plan view from the side of the first main surface (3a), exhibits the same visual appearance irrespective of viewing angle, characterised in that the metallic layer (3) is made from at least one metal from Group 6, 10, 11, 12 or 14 of the periodic table and / or from two or more of these metals.

A hydrotreating catalyst for a hydrocarbon oil is provided in which at least one metal selected from Group 6 metals in the periodic table and at least one metal selected from Group 9 and Group 10 metals in the periodic table are supported on a zinc / titanium-containing alumina carrier containing zinc and titanium.

The present invention relates to a metallic bipolar plate comprising a metal substrate and at least one layer of a non-hydrogenated transition metal-doped diamond-like carbon (DLC) provided on the metal substrate, wherein the non-hydrogenated DLC comprises at least one transition metal selected from groups 4d, 5d and 6d of the periodic table of elements and a part of the at least one transition metal is present in the form of carbide of the at least one transition metal in the non-hydrogenated DLC as a matrix. The non-hydrogenated transition metal-doped DLC has an indentation hardness of ≥35 GPa, preferably of ≥40 GPa. The metal-doped DLC used as a coating of metallic bipolar plates in fuel cells and electrolyzers exhibits high corrosion resistance and low interface contact resistance even for longer lifetimes (>10,000 hours) and harsh operational conditions. Therefore, the present invention also pertains to such uses, and also to fuel cells, in particular proton exchange membrane fuel cells, and electrolyzers comprising such coated metallic bipolar plates. Further, the present invention provides a cathodic arc discharge deposition method for depositing a coating of non-hydrogenated DLC comprising at least one of the above-mentioned transition metals, which is preferably the non-hydrogenated transition metal-doped DLC.

To provide an ionomer which is excellent in a balance among flowability, impact resistance, and adhesion to a dissimilar material having high polarity.SOLUTION: There is provided an ionomer, wherein in a copolymer (P) containing a structural unit (A) derived from ethylene and / or α-olefin having 3 to 20 carbon atoms, and a structural unit (B) derived from a monomer having a carboxyl group and / or a dicarboxylic acid anhydride group as essential components, and has a ratio of the structural unit (B) of 1-20 mol%, at least a part of the carboxyl group and / or the dicarboxylic acid anhydride is converted into metal-containing carboxylate containing at least one kind of metal ions selected from the group 2 in the periodic table by neutralization, (a) a phase angle δ at an absolute value G* of 0.1 MPa of a complex elastic modulus measured by a rotary type rheometer is 50-75 degrees, and (b) a degree of neutralization is 1-90 mol%.SELECTED DRAWING: None

The invention discloses a method and a system for predicting occurrence forms of heavy metal elements in waste residues, a medium and a terminal. The method comprises the following steps: acquiring physical and chemical attribute data in to-be-predicted waste residues, and performing data preprocessing to obtain characteristic data; wherein the physical and chemical attribute data comprises one or more of pH value, conductivity, element content, waste residue type, organic matter content, phase content and detection method; and inputting the feature data as input into the constructed and trained adaptive model for predicting the occurrence form of the target heavy metal for prediction, and outputting to obtain the occurrence form of the target heavy metal element. According to the method, similar element occurrence form data with similar physicochemical properties in the same family, the same period and the diagonal position of a target heavy metal element in the periodic table of elements are introduced, and a model for predicting the occurrence form of the heavy metal in the waste residues, which is high in prediction precision and strong in generalization ability, is successfully established through a transfer learning method.

Provided is a sputtering member comprising an alloy of Co, such as a Co-Nb alloy, and a group 5 element of the periodic table, said sputtering member being capable of reducing fine particles generated during sputtering. The sputtering member contains at least 1 at% and less than 25 at% of Nb, with the remainder comprising Co and unavoidable impurities, and has a relative density of 99.7% or more. The sputtering member contains at least 1 at% and less than 25 at% of one or more of V, Nb and Ta in total, with the balance being Co and unavoidable impurities, and has a relative density of 99.7% or more.

Provided is a method that makes it possible to produce a modified aluminosilicate more efficiently than conventional methods.　This method for producing a modified aluminosilicate comprises: a first step for obtaining an aluminosilicate (A-1) by bringing a gel-like or sol-like silica, zeolite, and an ammonium salt represented by formula (1) into contact with each other; a second step for treating the aluminosilicate (A-1) obtained in the first step with an acid; and a third step for bringing the product obtained in the second step into contact with a compound including at least one element selected from the group consisting of group-4 elements and group-5 elements in the periodic table, and then drying and sintering the same. (In formula (1), C represents a carbon atom, N+ represents a nitrogen cation, X- represents a halogen anion or a hydroxy anion, R and R1 each independently represent a hydrogen atom or a hydrocarbon group optionally having a heteroatom, m1 and m2 each independently represent an integer of 0-5, n1 and n2 each independently represent an integer of 0-5, the sum of n1 and n2 is 1-10, and R and R1 which are present in a quantity of more than one can bind to each other to form a ring structure.)

The application relates to a composite coating and a bipolar plate and a porous diffusion layer, the composite coating comprising a bottom layer arranged on the surface of a substrate, the material of the bottom layer comprising a non-noble metal element; and a composite material surface layer arranged on the surface of the bottom layer, the material of the composite material surface layer comprising a MAX material, a MXene material and a MAX-MXene material, the chemical formula of the MAX material being M-A-X, the chemical formula of the MXene material being M-X, and the MAX-MXene material having at least two crystal units sharing at least one M atom, wherein M comprises at least one of the elements in the ⅢB-ⅦB elements of the periodic table, A comprises at least one of the ⅦB-ⅥA elements in the second and third periods of the periodic table, and X comprises at least one of B, C and N, the composite material surface layer has pores, and the porosity of the composite material surface layer is 5%-50%. The composite coating can strengthen the corrosion resistance and stability of the substrate in a strong acid environment, effectively prolong the service life of a PEM electrolytic cell, and reduce the manufacturing cost of the PEM electrolytic cell.

M / M2+M4+ oxide catalysts have been developed for use in producing isobutanol in propanol-methanol, ethanol-methanol and propanol / ethanol mixture-methanol reactions. The catalysts can also be used in making n-butanol in ethanol-ethanol reactions. M may comprise one or more metals from Groups 3-12 of the Periodic Table. M2+ may comprise divalent magnesium, calcium, strontium, barium, or combinations thereof. M4+ may comprise tetravalent silicon, titanium, zirconium, or combinations thereof. Catalysts, and methods of using the catalysts are described.

A cubic boron nitride sintered material comprising cubic boron nitride grains and a binder, in which a content of the cubic boron nitride grains is no less than 30% by volume and no more than 80% by volume, the binder includes at least one selected from a second group consisting of a material made of a single element selected from a first group consisting of a group 4 element, a group 5 element and a group 6 element of the periodic table, aluminum, silicon, iron, cobalt and nickel, and an alloy and an intermetallic compound each composed of no less than two elements selected from the first group, and a content of a void in the cubic boron nitride sintered material is no less than 0.001% by volume and no more than 0.20% by volume.

The coated cutting tool of the present application has a substrate and at least one coating layer on the substrate. The coating layer contains cubic crystal which contains at least one element selected from among elements of Groups 4a, 5a, 6a of the periodic table, Al and Si; and at least one element selected from among C and N. The coating layer has a maximum value (I 1max ) of X-ray intensity in a measurement range of 0° or more and 90° or less in the X-ray intensity distribution of the alpha axis of the positive pole diagram with respect to the (111) plane of the cubic crystal, and an angle region (θ 1F ) in which the X-ray intensity is 85% or more of I 1max occupies 90% or more in a region of 30° or more and 90° or less.

A method for producing a Guerbet alcohol in which a starting material alcohol having 8-22 carbon atoms is reacted in the presence of a catalyst (A) containing a first component and a second component, the molar ratio of the second component to the first component, i.e., second component / first component, being 0.0001-0.005. A first component: copper; the second component is one element selected from the group consisting of Groups 9 to 13 belonging to cycles 4 to 6 of the periodic table and not copper.

The present disclosure relates to metallocene complexes of formula (I): wherein Mt is Zr or Hf, preferably Zr; x is a sigma ligand; r < 1 >, each independently, equal to or different from each other, is a C1-C20-hydrocarbyl group, optionally containing up to two heteroatoms of groups 14-16 of the periodic table, or forming together with the Si atom to which they are attached a C4-C8-ring; r < 2 > is a linear C < 1 >-C < 20 >-hydrocarbyl group; r2'is an alpha-branched C3-C10-hydrocarbyl group or SiH (R21 ') 2 wherein each R21', independently, equal to or different from each other, is a C1-C10-hydrocarbyl group; n is each independently an integer from 1 to 5; r3 and R4, each independently, equal to or different from each other, are H, a C1-C10-hydrocarbyl group, or a-OR31,-SR31 or-NR312 group wherein R31 is a C1-C10-hydrocarbyl group wherein at least one R3 is not hydrogen and at least one R4 is not hydrogen; l is O or S; r51 and R51'are each independently, equal to or different from each other, and are C1-C10-hydrocarbyl groups; and R6 and R6'are each independently equal to or different from each other, C (R61) 3 or-OR61, where R61 is each independently equal to or different from each other, linear or branched C1-C6-alkyl, or adjacent LR51 and R6 and / or LR51 'and R6' together form a-O [C (R62) 2] mO-group, where each R62 is independently equal to or different from each other, H or linear or branched C1-C6-alkyl, where m is 1 to 3.

The invention relates to an evaporation boat for a metallization device. In one aspect, the present invention provides evaporation boats that, in some embodiments, exhibit resistance to corrosion and related performance degradation due to exposure to molten metals, including aluminum. Evaporation boats described herein include a body comprising a boron nitride (BN) component and a TiB2 component comprising a solid solution of TiB2 and one or more elements selected from the group consisting of silicon and metal elements of Groups IVB-VIIIB of the Periodic Table of Elements, and an evaporator surface.

A cubic boron nitride sintered body comprising 40% to 85% by volume of cubic boron nitride particles and 15% to 60% by volume of a binder, wherein the binder includes at least one element selected from the group consisting of Group 4, Group 5, Group 6 elements of the periodic table and aluminum, and at least one element selected from the group consisting of nitrogen, carbon, boron, and oxygen, and at least one solid solution derived from the compound, and the Raman spectrum of the cubic boron nitride sintered body is a Raman shift of 10⁴⁸ cm⁻¹. -1 The above is 1062cm. -1 The first peak is located below, and the Raman shift is 1076 cm. -1 Over 1090cm -1 This is a cubic boron nitride sintered body having one or both of the second peaks shown below.

A coated article includes a substrate and a coating applied over at least a portion of the substrate. The coating includes at least one metallic layer formed from one or more silver compounds doped with at least one metal selected from Groups 3 to 15 of the periodic table of the elements. Also disclosed are capsules that can absorb electromagnetic energy as well as a process of forming an antimony-doped tin oxide coating layer.

This cubic boron nitride sintered compact comprises 40-80 vol% of cubic boron nitride particles and 20-60 vol% of a binder phase. The average particle diameter d of the cubic boron nitride particles is 0.1-3 µm. The binder phase contains: at least one selected from a second group consisting of elementary substances of one element selected from a first group consisting of aluminum, group-4 elements, group-5 elements, and group-6 elements in the periodic table, alloys formed of two or more elements selected from the first group, and intermetallic compounds formed of two or more elements selected from the first group; or at least one selected from a fourth group consisting of first compounds formed of at least one element selected from the first group and at least one element selected from a third group consisting of nitrogen, carbon, boron, and oxygen, and solid solutions derived from the first compounds. In a cross section of the cubic boron nitride sintered compact, the coefficient of variation Z of area ratios of the cubic boron nitride particles is 0.25 or less. The coefficient of variation Z is obtained by: providing, in a binarized image of a backscattered electron image obtained by imaging the cross section of the cubic boron nitride sintered compact by using a scanning electron microscope at a magnification of 5000, a total of 260 unit regions each in a shape of a square in which the length of one side is two-fold of the average particle diameter d of the cubic boron nitride particles; calculating, on the basis of the total of 260 unit regions, the average of the area ratios and the standard deviation of the area ratios of the cubic boron nitride particles in each of the unit regions; and dividing the standard deviation by the average.

The present invention relates to a hybrid iron nanoparticle catalyst comprising: i) 1 to 50 wt. % nanoparticles comprising iron and at least one of a metal M selected from the group consisting of alkali metals, alkaline earth metals, transition metals of groups 3 to 7 and 9 to 11 of the Periodic Table of Elements, lanthanides and combinations of M thereof; and ii) 50 to 99 wt. % of an aluminosilicate or silicoaluminophosphate zeolite, based on the total weight of the catalyst, wherein said nanoparticle has a diameter of about 2 to 50 nm. The present invention also relates to a method of preparing the hybrid iron nanoparticle catalyst and a process for the production of light olefins using the hybrid iron nanoparticle catalyst.