Abstract: There is provided a platy zinc oxide sintered compact containing 0.80 wt % or less at least one first dopant element selected from the group consisting of Al, Ga and In, the balance consisting essentially of ZnO and optionally at least one second dopant element selected from the group consisting of Br, Cl, F, Sn, Y, Pr, Ge, B, Sc, Si, Ti, Zr, Hf, Mn, Ta, W, Cu, Ni, Cr, La, Gd, Bi, Ce, Sr and Ba, the second dopant element being optional component, wherein the (002)-plane orientation in the plate surface is 60% or more. The zinc oxide sintered compact of the present invention has excellent properties such as high orientation in addition to transparency and conductivity.

Abstract: Provided in one implementation is a method of manufacturing a three-dimensional object. The method can include depositing a substantially uniform layer of raw material onto a substrate. The raw material can include ceramic particles. The method can include selectively fusing particles of the raw material to form a first layer of the object. The method can include clearing non-fused particles of the raw material from the first layer of the object. The method can include repeating the steps of depositing a raw material, selectively fusing particles of the raw material, and clearing non-fused particles of the raw material to form additional layers of the object above the first layer.

Abstract: There is herein described a method for forming a ceramic wavelength converter assembly which achieves a direct bonding of an alumina-based ceramic wavelength converter to an alumina-based ceramic substrate such as polycrystalline or sapphire. The method comprises applying a silica-containing layer between the converter and the substrate and then applying heat to bond the converter to the substrate to form the ceramic wavelength converter assembly. Because direct bonding is achieved, the ceramic wavelength converter may operate at much higher incident light powers than conventional silicone glue-bonded converters.

Abstract: A method of treating a ceramic surface containing zirconia, whereby the ceramic surface is ablated by directing a laser beam with a diameter of 200-400 ?m produced by a CO2 laser with a pulse frequency of 1200-1800 Hz onto the ceramic surface, and a N2 assist gas is concurrently applied with a pressure of 550-650 KPa co-axially with the laser beam to form an ablated ceramic surface comprising microgrooves with ZrN present on a surface of the microgrooves, wherein the ablated ceramic surface has a higher surface hydrophobicity than the ceramic surface prior to the ablating.

Abstract: The invention relates to a method for recovery of urea dust and ammonia from a gas stream by contacting said gas stream with an aqueous sulphuric acid solution, thus forming an acid solution of ammonium sulphate and urea, characterized in that the acid solution is concentrated to a melt comprising less than 5 wt % of water, which melt is subsequently transferred into solid particles comprising urea and ammonium sulphate.

Abstract: The invention concerns a method for treating a mixture of wastes (4) comprising biodegradable wastes, the method being characterized in that it includes the following successive steps: Step A: the mixture of wastes (4) is subjected to a first composting cycle so as to obtain a mixture of pre-composted wastes (4), Step B: the mixture of pre-composted wastes (4) is subjected to a drying so as to obtain a mixture of dried wastes (4), Step C: the mixture of dried wastes (4) is separated into at least a portion of heavy wastes (14) and a portion of light wastes (13), Step D: the portion of light wastes (13) is subjected to a second composting cycle to so as to obtain a mixture (4) of refined wastes (20). Treatment of biodegradable wastes.

Abstract: A method is provided for producing a biochar solution. The method comprises the steps of collecting biochar particles, dispersing the biochar particles in a liquid solution and adding a stabilizing agent to keep the biochar in flowable suspension. The stabilizing agent may be added to the liquid solution or to the biochar prior to placing the biochar in solution.

Abstract: A method for forming a pelletised evaporite mineral product, the method comprising: forming a material comprising a liquid and at least 50% by mass of an evaporite mineral powder; and processing the material using a pan pelletiser to form pellets comprising the material, the pan pelletiser being configured so that the mean dwell time of the material in the pan of the pelletiser is in the range from 60 to 120 seconds and the mean diameter of the pellets formed by the pelletiser is in the range from 1 to 8 mm.

Abstract: Reaction products and methods for making and using the same are provided. The reaction products particularly may include adducts of two or more reactants. The adducts particularly can incorporate a nitrification inhibitor, such as DCD. In particular embodiments, reaction products may be formed from the reaction of formaldehyde, DCD, urea, and an ammonia source. The adducts may be included in agricultural products, including fertilizer compositions and nitrification inhibitor systems. Fertilizer compositions including the adducts can be beneficial for reducing leaching of nitrification inhibitors applied to soil.

Abstract: Reaction products and methods for making and using such reaction products are provided. For example, a reaction product comprising an adduct formed from urea, formaldehyde, and a urease inhibitor is described, which can be provided in various forms. For example, such a reaction product can be in the form of a solid or solution. Such a reaction product can also be combined with one or more additional components, including but not limited to, additional urease inhibitor and/or a nitrogen-based fertilizer composition.

Abstract: A method for obtaining the explosive charge in dry granular form as well as a device suitable for implementing the method. The method includes: filtering the suspension, by passing same through a static filter in order to obtain a cake containing the granular explosive charge agglomerated by residual liquid; dewatering the cake by subjecting the cake to pressurized gas; splitting the dewatered cake and obtaining a fluidized bed of the desired explosive charge by exposing the dewatered cake to at least one stream of gas; at least one stream of gas being injected, under the dewatered cake to impinge said dewatered cake, according to two consecutive modes and the gas having a humidity height below that of the dewatered cake and a dew point temperature higher than the injection temperature thereof; and stopping at least one stream of gas and recovering the explosive charge in dry, granular form.

Abstract: Energetic compositions and methods of forming components from the compositions are provided. In one embodiment, a composition includes aluminum, molybdenum trioxide, potassium perchlorate, and a binder. In one embodiment, the binder may include a silicone material. The materials may be mixed with a solvent, such as xylene, de-aired, shaped and cured to provide a self-supporting structure. In one embodiment, one or more reinforcement members may be added to provide additional strength to the structure. For example, a weave or mat of carbon fiber material may be added to the mixture prior to curing. In one embodiment, blade casting techniques may be used to form a structure. In another embodiment, a structure may be formed using 3-dimensional printing techniques.

Abstract: Propellants for rockets, space transportation vehicles, launch vehicles and systems, crew escape vehicles and systems, launch escape towers, and space vehicle systems are disclosed. Some embodiments provide a rocket propellant comprising a mixture of a small chain alkane from 1 to 4 carbons and a small chain alkene from 3 to 4 carbons. The mixture of the small chain alkane and small chain alkene is in a proportion that lowers the melting of the mixture below the melting point of both the small chain alkane and small chain alkene.

Abstract: The present invention relates to a pyrotechnic igniting agent which contains basic salts of 5,5?-azotetrazole having the general empirical formula: Mm+n(C2N102?)p(CO32?)q(OH?)r, wherein: M is an element of the 3rd to 12th group of the periodic table having an atomic number in the range from 21 to 80, (C2N102?) is azotetrazolate dianion having the structure (AA), m is the valence of the cation, n is an integer from 1 to 6, p is an integer from 1 to 4, q is an integer from 0 to 8, r is an integer from 0 to 4 and q+r?0, wherein the proportion of the basic azotetrazolate component is 30 to 100 wt %, and 0 to 70 wt % of an additive or mixtures of a plurality of additives is contained.

Abstract: An in-situ process for synthesizing highly pyrophoric foam materials using metal and carbon precursors wherein the precursors serve as foaming and activating agents to disperse and lock nano-sized metal particles within a rigid porous carbon matrix. The resulting carbon matrix is also pyrophoric.

Abstract: The present invention relates to a process for producing an organic compound comprising an 18F atom. The compounds comprising an 18F can be useful as PET ligands for use in diagnostics and/or scanning. The process of the invention comprises treating an organoboron compound, which organoboron compound comprises a boron atom bonded to an sp2 hybridised carbon atom, with (i) 18F— and (ii) a copper compound. The invention also provides the use of an organoboron compound, which organoboron compound comprises a boron atom bonded to an sp2 hybridised carbon atom, in a process for producing an organic compound comprising an 18F atom, which process comprises treating the organoboron compound with (i)18F— and (ii) a copper compound.

Abstract: Multiphase separators, processes and systems for converting an oxygenate and/or olefin feedstock to a hydrocarbon product are described herein.

Abstract: A process for the preparation of a compound of formula (V): comprising at least the step of reacting a compound of formula (VI) ?with a compound (VII) wherein; R2 is hydrogen or a C1-C20 hydrocarbyl radical provided that at least one R2 is not hydrogen; R5 is hydrogen or a C1-20 hydrocarbyl group optionally containing one or more heteroatoms from groups 14-16; R6 is hydrogen or a C1-20 hydrocarbyl group optionally containing one or more heteroatoms from groups 14-16; n is 1, 2 or 3; each R8 is a C1-20 hydrocarbyl group; and Hal is a halide; in the presence of a nickel imidazolidin-2-ylidene compound.

Abstract: An energy storage system is provided. The energy storage system includes a vessel made of a refractory material and containing a phase change material, a thermally insulating cover at least partially surrounding the vessel, an emitter, made of a refractory material, having a first side arranged to be heated by the phase change material and a second side intended to radiate thermal power, at least one photovoltaic cell arranged to receive the thermal power emitted by the second side of the emitter, and electric means for heating the phase change material.

Abstract: A system (1, 1A) for manufacturing an aromatic compound according to the present invention includes: a first manufacturing device (2) that synthesizes a target substance from natural gas; a second manufacturing device that synthesizes an aromatic compound by a catalytic reaction from the natural gas and supplies a mixed gas mainly including unreacted methane and by-product hydrogen to the first manufacturing device (2) to manufacture the target substance; and a hydrogen separation device (3, 3A) that separates hydrogen from purge gas generated from the first manufacturing device (2) and supplies the same to the second manufacturing device (4, 4A) to regenerate the catalyst used for the catalytic reaction.

Abstract: A process includes hydrogenating, in a reaction zone, a highly unsaturated hydrocarbon received from a hydrocarbon stream to yield a product having an unsaturated hydrocarbon, the hydrogenating step occurring in the presence of a hydrogenation catalyst which has a selectivity for conversion of the highly unsaturated hydrocarbon to the unsaturated hydrocarbon of about 90 mol % or greater based on the moles of the highly unsaturated hydrocarbon which are converted to the product, the hydrogenating step occurring in a reaction zone under conditions which include a flow index (IF) in a range of about 0.09 to about 35, wherein the IF is defined as: I F = F × [ CO ] V , wherein F is the flow rate of the hydrocarbon stream into the reaction zone in units of kg/h, [CO] is the concentration of carbon monoxide in the hydrocarbon stream in units of mol %, and V is the volume of the reaction zone in units of ft3.

Abstract: The invention relates to a process of the oxidative dehydrogenation of an alkane containing 2 to 6 carbon atoms and/or the oxidation of an alkene containing 2 to 6 carbon atoms, comprising contacting a first gas stream comprising oxygen and the alkane containing 2 to 6 carbon atoms and/or the alkene containing 2 to 6 carbon atoms with a mixed metal oxide catalyst containing molybdenum, vanadium, niobium and optionally tellurium; followed by contacting a second gas stream comprising methane, an inert gas or oxygen or any combination of two or more of these with the catalyst, wherein the second gas stream comprises 0 to 25 vol. % of the alkane containing 2 to 6 carbon atoms and/or alkene containing 2 to 6 carbon atoms.

Abstract: The invention relates to a process of the oxidative dehydrogenation of an alkane containing 2 to 6 carbon atoms and/or the oxidation of an alkene containing 2 to 6 carbon atoms, comprising contacting a first gas stream comprising methane, an inert gas or oxygen or any combination of two or more of these, wherein the first gas stream comprises 0 to 2 vol. % of the alkane containing 2 to 6 carbon atoms and/or alkene containing 2 to 6 carbon atoms, with a mixed metal oxide catalyst containing molybdenum, vanadium, niobium and optionally tellurium; followed by contacting a second gas stream comprising oxygen and the alkane containing 2 to 6 carbon atoms and/or the alkene containing 2 to 6 carbon atoms with the catalyst.

Abstract: Disclosed are methods and systems for removing a highly reactive polymer precursor such as carbonyls from a liquid hydrocarbon stream. Embodiments may disclose a method for removal of carbonyls from a liquid hydrocarbon stream comprising the steps of providing a liquid hydrocarbon stream containing carbonyls, providing a liquid bisulfite stream comprising an alkali metal bisulfite, and contacting the liquid hydrocarbon stream and the liquid bisulfite stream in a mass transfer device wherein at least a portion of the carbonyl reacts with the alkali metal bisulfite to form a solid adduct that is soluble in the bisulfite solution.

Abstract: Asymmetric membrane structures are provided that are suitable for hydrocarbon reverse osmosis of small hydrocarbons. Separation of para-xylene from ortho- and meta-xylene is an example of a separation that can be performed using hydrocarbon reverse osmosis. Hydrocarbon reverse osmosis separations can be incorporated into a para-xylene isomerization and recovery system in a variety of manners.

Abstract: In an oxychlorination process of the type where ethylene is converted to 1,2-dichloroethane in the presence of a supported copper catalyst, the improvement comprising: the use of a supported catalyst prepared by (i) impregnating, within a first step, an alumina support with a first aqueous solution including copper, to thereby form a first catalyst component; and (ii) impregnating, within a subsequent step, the first catalyst component with a second aqueous solution including copper and alkaline earth metal, to thereby form the supported catalyst.

Abstract: The present invention discloses a manufacturing process to produce high purity 1234yf from 245eb, which preferably includes the removal of impurities present in 245eb raw material, the dehydrofluorination of 245eb, and the removal of impurities present in final crude product. The disclosed manufacturing process allows the production of a 1234yf product with lower the levels of 1225ye and/or trifluoropropene, preferably in amounts of less than about 500, and 50 ppm, respectively.

Abstract: Disclosed is a process for the formation of a mixture of the compounds 2,3,3,3-tetrafluoropropene (1234yf) and vinylidine fluoride, comprising pyrolyzing 1,1,2-trifluoro-2-trifluoro-methyl-cyclobutane under conditions effective to produce a reaction product comprising 1234yf and vinylidine fluoride in a 1234yf:vinylidine fluoride molar ratio of from about 0.5 to about 1.2.

Abstract: A process for the preparation of ethylene glycol comprising the steps of pyrolysing a monosaccharide and hydrogenating the product composition in the presence of a catalyst and a solvent, wherein the pressure of the hydrogenation reaction is 40 bar or greater.

Abstract: A method for producing olefins and methanol comprising introducing a first reactant mixture comprising CH4 and O2 to a first reaction zone; allowing the first reactant mixture to react via an OCM reaction to form a first product mixture characterized by a first H2/CO molar ratio; introducing a second reactant mixture comprising the first product mixture and an ethane stream to a second reaction zone, wherein ethane of the second reactant mixture undergoes a cracking reaction to produce ethylene; recovering a second product mixture from the second reaction zone, wherein the second product mixture is characterized by a second H2/CO molar ratio, and wherein the second H2/CO molar ratio is greater than the first H2/CO molar ratio; recovering from the second product mixture a methanol production feed stream comprising methane, H2 and CO; and introducing the methanol production feed stream to a third reaction zone to produce methanol.

Abstract: A process of preparing an alkoxylation catalyst wherein a catalyst precursor which is formed from an alkoxylated alcohol, calcium hydroxide, carboxylic acid, inorganic acid, and propylene oxide, is mixed with an antioxidant, preferably butylated hydroxyl toluene. A process of alkoxylation using the catalyst of the present invention.

Abstract: The present invention relates to a method for preparing dimethyl ether from methanol which is carried out in a reaction device arranged with a plurality of catalyst bed layers connected in series, and comprises: dividing the reactant stream that contains methanol into n substreams, and feeding these different substreams into the reaction device through top feed ports or side feed ports between the catalyst bed layers of the reaction device for methanol-to-dimethyl ether reaction; wherein, the temperature T1 of the substream fed into the first catalyst bed layer is controlled within the following range: 290?50K1?T1?150K12?271K1+397.5; where, 1>K1?0.5, and T1 is in unit of ° C.

Abstract: Disclosed herein are compositions and methods related to the hydroformylation of cyclododecatriene to form cyclododecatriene trialdehyde, and the conversion of the trialdehyde to the polyphenols of Formula 1: where R, m p and Q are as defined herein. Curable compositions comprising compounds of Formula 1, including powder coating compositions, and methods of curing the compositions are also disclosed.

Abstract: The invention discloses a method for the preparation of 4-alkoxy-1,1,1-trifluorobut-3-en-2-ones from 1,1,1-trifluoroacetone.

Abstract: The present invention is in the field of nanostructure synthesis. The present invention is directed to methods for producing nanostructures, particularly Group III-V semiconductor nanostructures. The present invention is also directed to preparing Group III inorganic compounds that can be used as precursors for nanostructure synthesis.

Abstract: Process for producing acetic acid are disclosed in which a vapor sidedraw is withdrawn from the second column in the primary purification train. The vapor sidedraw comprises acetic acid and lithium-containing compounds at a concentration of no more than 100 wppb. A bottoms stream that is enriched in lithium-containing compounds, such as lithium acetate, or lithium acetate dihydrate, is also withdrawn from the second column. Advantageously, the vapor sidedraw, or a condensed portion thereof, is directly fed to a metal-exchanged ion exchange resin having acid cation exchange sites to produce purified acetic acid. This prevents displacement of the metals in the ion exchange resin.

Abstract: Disclosed are methods for synthesizing an ester or a carboxylic acid from an organic alcohol. To form the ester one reacts, in the presence of oxygen gas, the alcohol with methanol or ethanol. This reaction occurs in the presence of a catalyst comprising palladium and a co-catalyst comprising bismuth, tellurium, lead, cerium, titanium, zinc and/or niobium (most preferably at least bismuth and tellurium). Alternatively that catalyst can be used to generate an acid from that alcohol, when water is also added to the reaction mix.

Abstract: The present invention relates to selective catalytic dehydroxylation method of aldaric acids for producing muconic acid and furan chemicals, which can be used directly in fine chemical and polymer applications (FCA/FDCA) and as intermediates in the preparation of industrially significant chemicals, such as terephthalic acid, adipic acid, caprolactone, caprolactam, nylon 6.6, 1,6-hexanediol and multiple pharmaceutical building blocks (MA/MAME).

Abstract: Processes for purifying acetic acid by distilling a process in a column in which acetic anhydride is formed in the lower portion of the column. The product stream withdrawn from the column comprises acetic acid, water at a concentration of no more than 0.2 wt. %, and acetic anhydride at a concentration of no more than 600 wppm. The process further comprises hydrating the acetic anhydride in the product stream to form a purified acetic acid product comprising acetic anhydride at a concentration of no more than 50 wppm.

Abstract: In one aspect, the invention provides a method for synthesizing a fatty olefin derivative. The method includes: a) contacting an olefin according to Formula I with a metathesis reaction partner according to Formula IIb in the presence of a metathesis catalyst under conditions sufficient to form a metathesis product according to Formula IIIb: and b) converting the metathesis product to the fatty olefin derivative. Each R1 is independently selected from H, C1-18 alkyl, and C2-18 alkenyl; R2b is C1-8 alkyl; subscript y is an integer ranging from 0 to 17; and subscript z is an integer ranging from 0 to 17. In certain embodiments, the metathesis catalyst is a tungsten catalyst or a molybdenum catalyst. In various embodiments, the fatty olefin derivative is a pheromone. Pheromone compositions and methods of using them are also described.

Abstract: The invention provides polyglycerol partial esters based on mono- and dicarboxylic acids and their use as solubilizers, particularly in cosmetics, for example for perfume oils and essential oils in aqueous systems.

Abstract: The present invention relates to a process for preparing di- and polyamines of the diphenylmethane series (MDA), a system for producing MDA and a process for operating a system for preparing MDA. The invention enables optimization of production standstills during operation of the MDA process with respect to time expenditure and optionally also with respect to energy and material consumption by means of a so-called recirculation mode for individual system components. During interruption of the process or interruption of the operation of individual system components, formaldehyde is not introduced into the reaction and the system components that are not affected by a revision, repair, or cleaning measure are operated in so-called recirculation mode.

Abstract: The present invention relates to a method for the purification of cadaverine from an aqueous cadaverine salt composition comprising one or more involatile impurities, the method comprising: (1) mixing the aqueous cadaverine salt composition with one or more bases selected from the group consisting of Ca(OH)2, Mg(OH)2, CaO and MgO to provide an aqueous cadaverine composition; and (2) distilling or evaporating the aqueous cadaverine composition to produce purified cadaverine; wherein one or more solvents are added to the evaporation/distillation system before the evaporation/distillation stops, and the one or more solvents comprise at least one or more high boiling point (HBP) solvents.

Abstract: One aspect of the invention relates to a method for the purification of cadaverine from an aqueous cadaverine composition comprising one or more involatile impurities, the method comprising: a) distilling or evaporating the aqueous cadaverine composition wherein one or more solvents are added to the evaporation/distillation system before the evaporation/distillation starts, during the evaporation/distillation and/or after the evaporation/distillation substantially stops when no more evaporation/distillation is observed to produce purified cadaverine, wherein the evaporation or distillation is done at a heating temperature of about 80° C. to about 180° C. and under a pressure of 1 atm or lower, and the one or more solvents comprise at least one or more high boiling point (HBP) solvents having a boiling point of at least about 185° C. (1 atm); and b) recovering the one or more HBP solvents.

Abstract: The invention relates to pharmaceutical salts comprised of a pharmaceutical active substance and of at least one sugar substitute, to medicaments containing these salts, and to the use of these salts for producing medicaments.

Abstract: The present invention provides arylalkylamine compounds as calcium sensing receptor modulators (CaSR). In particular, the compounds described herein are useful for treating, managing, and/or lessening the severity of diseases, disorders, syndromes and/or conditions associated with the modulation of calcium sensing receptors (CaSR). The invention also provides herein the pharmaceutical compositions thereof, and methods for treating, managing, and/or lessening the severity of diseases, disorders, syndromes and/or conditions associated with the modulation of CaSR. The invention also relates to process for the preparation of the compounds of the invention.

Abstract: The present invention aims to provide a medium-chain acyl basic amino acid derivative which, when blended in a liquid 5 cosmetic such as skin lotion, skin milk and the like, suppresses gelation while maintaining affinity to the skin and the like and can afford a stable preparation. The present invention relates to a compound represented by the formula (1) wherein each symbol is as described in the DESCRIPTION, or a salt thereof.

Abstract: Provided is a compound that thickens and/or gelatinizes a fluid organic substance to a desired viscosity, or uniformly stabilizes a composition containing the fluid organic substance. Also provided are: a thickening/stabilizing agent including the compound, a thickened/stabilized composition including the thickening/stabilizing agent and a fluid organic substance, and a method for producing the composition. The compound according to the present invention is represented by Formula (1): (R2—HNOC)4-n—R1—(CONH—R3)n??(1) where R1 is a group resulting from removing four hydrogen atoms from the structural formula of an aromatic hydrocarbon or cyclohexane; R2 is, independently in each occurrence, an aliphatic hydrocarbon group containing 1 to 4 carbon atoms; R3 is, independently in each occurrence, an aliphatic hydrocarbon group containing 6 or more carbon atoms; and n is an integer of 1 to 3.

Abstract: This invention provides novel 3-amino propanamide selective androgen receptor degrader (SARD) compounds, pharmaceutical compositions and uses thereof in treating prostate cancer, advanced prostate cancer, castration resistant prostate cancer, androgenic alopecia or other hyperandrogenic dermal diseases, Kennedy's disease, amyotrophic lateral sclerosis (ALS), and uterine fibroids, and to methods for reducing the levels of androgen receptor-full length (AR-FL) including pathogenic or resistance mutations, AR-splice variants (AR-SV), and pathogenic polyglutamine (polyQ) polymorphisms of AR in a subject.

Abstract: The present invention relates to a method of treating cataplexy in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of certain carbamate compounds.