Abstract: Provided is an alkali-free glass substrate having a high strain point and excellent bubble count, and a method for manufacturing the alkali-free glass substrate. The method includes: a batch preparing process of preparing a raw material batch so as to obtain alkali-free glass containing, in mass %, 50 to 80% of SiO2, 15 to 30% of Al2O3, 0 to 4.5% of B2O3, 0 to 10% of MgO, 0 to 15% of CaO, 0 to 10% of SrO, 0 to 15% of BaO, 0 to 5% of ZnO, 0 to 5% of ZrO2, 0 to 5% of TiO2, 0 to 15% of P2O5 and 0 to 0.5% of SnO2 as a glass composition; a melting process of melting the prepared raw material batch; a fining process of fining the molten glass; and a forming process of forming the fined glass into a sheet shape. The raw material batch is melted such that a bubble enlarging temperature of the obtained glass is lower than a maximum temperature of the fining process.

Abstract: A chemically toughenable or toughened glass is provided. The glass has, before chemical toughening, a thickness of at most 500 ?m. The glass, after chemical toughening, has a BACT (bendability and chemical toughenability) calculated as BACT=(CS*DoL)/(t*E) which is greater than 0.00050 and/or a NS (normalized stiffness) calculated as NS=CS/E which is greater than 0.0085, where CS is a compressive stress in MPa measured at one side of the glass after chemical toughening, DoL is a total depth of all ion-exchanged layers in ?m on one side of the glass after chemical toughening, t is a thickness of the glass in ?m after chemical toughening, and E is a E-modulus in MPa after chemical toughening.

Abstract: Systems and methods are disclosed for vaporization suppression. Vaporization suppression may include, for example, evaporation control and/or odor control. A layer of foam glass aggregates may be placed on a body of water. Bodies of water may include natural and man-made aqueous bodies (such as, for example, ponds, lakes, lagoons, reservoirs, tanks, pools, runoff areas, etc.). Water may include clean water, natural water, rainwater, runoff, industrial output, manure slurries, leachates, treatment effuse, etc.). When placed, the foam glass aggregates in contact with the water may have a first moisture constant. At equilibrium, the foam glass aggregates in contact with the water may have a second moisture content. The second moisture content may be greater than the first moisture content. The foam glass aggregates in contact with the water may have a bulk density at the second moisture content that is sufficient to maintain buoyancy at the surface of the body of water.

Abstract: Provided is a glass composition for glass fiber having a low dielectric constant and a low dielectric loss tangent, suppressing occurrence of phase separation, and reducing viscosity at high temperatures. The glass composition for glass fiber includes: SiO2 in the range of 52.0 to 59.5% by mass; B2O3 in the range of 17.5 to 25.5% by mass; Al2O3 in the range of 9.0 to 14.0% by mass; SrO in the range of 0.5 to 6.0% by mass; MgO in the range of 1.0 to 5.0% by mass; and CaO in the range of 1.0 to 5.0% by mass, and includes F2 and Cl2 in the range of 0.1 to 2.5% by mass in total, with respect to the total amount.

Abstract: The present invention relates to coating glass for architectural or automotive use, either monolithic or laminated, having solar control properties. The coating consists of several layers of different metal oxide semiconductors (TiO2, ZnO, ZrO2, SnO2, AlOx) and a layer of metallic nanoparticles, which when superimposed on a pre-established order give the glass solar control properties. In particular the use of protective layers of n-type semiconductors around the metallic nanoparticles layer. It also relates to the method for obtaining the coating by means of the aerosol-assisted chemical vapor deposition technique, using precursor solutions containing an organic or inorganic salt (acetates, acetylacetonates, halides, nitrates) of the applicable elements and an appropriate solvent (water, alcohol, acetone, acetylacetone, etc.). The synthesis is performed at a temperature between 100 and 600° C. depending on the material to be deposited.

Abstract: An article includes a glass substrate including two main faces defining two main surfaces separated by edges and a temporary protective layer comprising an organic polymer matrix deposited on at least one portion of a main surface of the glass substrate, wherein the temporary protective layer has a rough surface defined by a surface roughness parameter Sa, corresponding to the arithmetic mean height of the profile of the surface, of greater than 0.2 ?m.

Abstract: Methods for chemically strengthening a cover for an electronic are disclosed. The methods include removing material from a mounting surface of the cover to counteract warping of the mounting surface due to ion exchange. The chemically strengthened covers have a high bend strength and allow a strong seal to be formed between the cover and an enclosure component.

Abstract: Embodiments of a glass-based article including a first surface and a second surface opposing the first surface defining a thickness (t) of about 3 millimeters or less (e.g., about 1 millimeter or less), and a stress profile, wherein all points of the stress profile between a thickness range from about 0·t up to 0.3·t and from greater than about 0.7·t up to t, comprise a tangent with a slope having an absolute value greater than about 0.1 MPa/micrometer, are disclosed. In some embodiments, the glass-based article includes a non-zero metal oxide concentration that varies along at least a portion of the thickness (e.g., 0·t to about 0.3·t) and a maximum central tension in the range from about 80 MPa to about 100 MPa. In some embodiments, the concentration of metal oxide or alkali metal oxide decreases from the first surface to a value at a point between the first surface and the second surface and increases from the value to the second surface. The concentration of the metal oxide may be about 0.

Abstract: The present invention relates to a cover member (1) made of chemically strengthened glass for protecting an object to be protected, the cover member (1) being characterized by: at least one recessed part (7) being provided on at least one of a first main surface (3) and a second main surface (5) of the cover member (1); the cover member (1) integrally comprising a thin part (13) formed by the recessed part and a thick part (17) connecting with the thin part (13); and, defining tensile stress as positive and compressive stress as negative, the integral value S for main stress difference in the through-thickness direction of the thin part (13) at the position of the center of gravity of the thin part being less than 0 MPa.

Abstract: The present invention relates to a mineral wool product comprising mineral fibres bound by a cured formaldehyde-free binder, wherein the binder in its uncured state comprises carbohydrate in a content of 70 to 97 wt. % of the total binder component solids; the mineral wool product has an unaged delamination strength of 20 kPa or more; the mineral wool product has a ratio between the aged delamination strength and the unaged delamination strength of more than 40%.

Abstract: A binding compound for mineral or organic fibres, includes from 40 to 95 wt % of furan resin, and from 5 to 60 wt % of at least one reducing sugar and/or of at least one non-reducing sugar, relative to the total dry weight of the composition, the binding composition having a dry matter content between 0.5 to 50 wt %.

Abstract: Provided is an amphoteric composite hydrogel, including: a polymer having a structure of formula I, wherein m, n, p and q are each an integer of 0 to 1000, m+n>100, p+q>100, R is R1 is H or an alkali metal element, and R2 is H or CH3; and a pozzolanic material incorporated into the structure of formula 1. Also provided are a cement mortar composition and a concrete composition each comprising the amphoteric composite hydrogel and a method of preparing the amphoteric composite hydrogel.

Abstract: A nonvolatile cold modified asphalt binder and a nonvolatile cold recycled asphalt mixture using the same are manufactured by optimally mixing a petroleum asphalt, a native asphalt, a polymer modifier, process oil, and an adhesive strength enhancer. The nonvolatile cold modified asphalt binder includes at least one petroleum asphalt selected from a straight asphalt or a blown asphalt; at least one native asphalt selected from gilsonite, glance pitch, and grahamite; a rubber-modified-compound (RMC) polymer modifier which is a vinyl aromatic hydrocarbon-conjugated diene block copolymer including at least one of a styrene-butadiene block copolymer (SBS), a styrene-isoprene block copolymer (SIS), and a styrene-ethylene-butylene block copolymer (SEBS); at least one process oil selected from paraffin oil, naphthenic oil, aromatic oil, natural oil, and mineral oil; and at least one adhesive strength enhancer selected from rosin esters, modified acryls, modified silicones, polyvinyl esters, and silicone resins.

Abstract: An asphalt composition comprising 0.1 to 10.0 wt.-% based on the total weight of the composition of a thermosetting reactive compound selected from the group consisting of polymeric MDI, epoxy resins and melamine formaldehyde resins, wherein at least 18% by weight based on the total weight of the composition are particles with a sedimentation coefficient above 5000 Sved in a white spirit solvent.

Abstract: A method for forming a self-healing ceramic matrix composite (CMC) component includes depositing a first self-healing particulate material in a first region of a CMC preform of the CMC component and depositing a second self-healing particulate material having a different chemical composition than the first self-healing particulate material in a second region of the CMC preform distinct from the first region.

Abstract: An article may include a substrate and a coating system on the substrate. The coating system may include a thermal and/or environmental barrier coating (T/EBC) layer, wherein the T/EBC layer includes a silicate phase including more than one metal cation.

Abstract: Provided is a method including obtaining ceramic matrix composite (CMC) with a first matrix portion including a silicon carbide and silicon phase dispersed therewithin, disposing a coating thereupon to form a sealed part, and forming thereupon another segment comprising a CMC, which may be another matrix portion including a silicon carbide and a silicon phase dispersed within therewithin. Also provided is a gas turbine component with a CMC segment including a matrix portion including a silicon carbide and a silicon phase dispersed therewithin, a sealing layer including silicon carbide enclosing the first segment, and a second segment on the sealing layer, wherein the second segment includes a melt-infiltrated CMC having a matrix portion including a silicon carbide and a silicon phase dispersed therewithin.

Abstract: One aspect is a logic power module, with at least one logic component, at least one power component and a substrate. The logic element and the power component are provided in separate areas on the substrate. The logic component on the substrate is provided by thick printed copper; and the power component is provided by a metal-containing thick-film layer, and, provided thereon, a metal foil.

Abstract: Compositions and methods are presented that selectively dissolve calcium from a variety of cementitious materials without dissolving or otherwise degrading calcium silica hydrate (CSH). Preferably, contemplated compositions comprise guanidine bisulfate hydrochloride, which can be prepared from a reaction of urea, hydrochloric acid, and sulfamic acid. Therefore, it is especially contemplated that the compositions contemplated herein are particularly suitable to clean or otherwise condition surfaces of cured concrete, Portland cement-based material, or an aggregate containing CSH.

Abstract: A coated component, along with methods of its formation and use, is provided. The coated component includes a ceramic matrix composite (CMC) substrate comprising silicon carbide and having a mullite bondcoat on its surface. The mullite bondcoat includes an oxygen getter phase contained within a mullite phase. For example, the mullite bondcoat may include 60% to 98% by volume of the mullite phase. An environmental barrier coating is on the mullite bondcoat.

Abstract: A coated component, along with methods of making and using the same, is provided. The coated component includes a ceramic matrix composite (CMC) substrate comprising silicon carbide and having a surface; a mullite/NOSC bondcoat on the surface of the substrate; and an environmental barrier coating on the mullite/NOSC bondcoat. The mullite/NOSC bondcoat comprises a non-oxide silicon ceramic (NOSC) phase contained within a mullite phase, with the mullite/NOSC bondcoat comprising 60% to 95% by volume of the mullite phase, such as 65% to 93% by volume of the mullite phase.

Abstract: The disclosure describes a method for forming a surface layer of a ceramic matrix composite (CMC) article. The technique includes depositing a slurry on a surface of an infiltrated CMC. The slurry includes a carrier material, a binder, a plasticizer, and solid particles. The solid particles include a plurality of fine ceramic particles defining a fine particle average size less than about 5 micrometers. The method further includes drying the slurry to form an article having an outer surface layer that includes the solid particles on the infiltrated CMC. The method further includes machining at least a portion of the outer surface layer of the article. The method further includes infiltrating the article with a molten infiltrant to form a composite article.

Abstract: A particulate fertilizer coating composition or a coated fertilizer containing a solid acidic particulate material and a solid basic particulate material. The coating composition and coated fertilizer are each stable, chemical compatible with other fertilizers, and/or are abrasion resistant.

Abstract: This disclosure relates to a semi-humic material, and compositions comprising the same, obtained from leonardite ore and a non-humic organic carbon source and a process for obtaining the same. Also described are methods for maintaining more available nitrogen and phosphorus in the plant root zone and minimizing premature leaching and loss of the nitrogen and/or phosphorus into the atmosphere, surface waters and/or subsurface ground water.

Abstract: The present application relates to systems and methods for processing organic material. The methods may include extraction of biochemical nutrients from organic material, such as food scraps. The method can include comminuting the organic material to form a slurry from components comprising liquid and organic material; combining the slurry with microorganisms, such as a yeast, under aerobic conditions to form a mixture of the slurry and yeast; aerating the mixture; and forming a biomass and a nutrient-rich broth, in which the biochemical nutrients are stabilized and anabolized. The systems may, in some embodiments, be configured to perform the methods of processing organic materials.

Abstract: Disclosed is a functionalized particle having at its core a porous particle that acts as a structured support element. This porous particle is surrounded by a protective sealant layer encasing the porous particle. The particle includes a plurality of pores holding a first beneficial agricultural component. The functionalized particle can also include a plurality of functionalized molecules embedded in the sealant layer. The functionalized molecules comprise a base material, comprising an active agricultural component or an inactive material, and an active second beneficial agricultural component. The functionalized molecules can all contain the same base material and the same active second beneficial agricultural component or a mixture of different base materials and a mixture of second beneficial agricultural components. The first and second beneficial agricultural components can either be single components or a mixture of components and may be the same or different from each other.

Abstract: A gastric tract acid (GTA) compound having the structure of formula I, as well as salts, esters, prodrugs, or labelled derivatives thereof, are provided. Such GTA compounds may be used for determining GTA levels of a sample, for diagnosing a subject as having or being at risk of developing colorectal cancer, or for raising antibodies. Antibodies, or fragments thereof, which specifically bind to the GTA of formula I are described, as well as uses of such antibodies or fragments for determining GTA levels in a sample, or for diagnosing a subject as having or being at risk of developing colorectal cancer. Kits comprising such GTA compounds and/or antibodies are also provided.

Abstract: The present disclosure relates to a catalyst composition for the oligomerization of ethylene comprising a zirconium-containing catalyst and an organoaluminum-containing co-catalyst. The disclosure also relates to a process for oligomerization of ethylene in the presence of the catalyst composition according to the disclosure. The disclosed process results in C4-C20 linear alpha olefins having improved linearity.

Abstract: A fluidized bed reactor for producing para-xylene and co-producing light olefins from benzene and methanol and/or dimethyl ether, including a first distributor and a second distributor. The first distributor is located at the bottom of the fluidized bed, and the second distributor is located at the downstream of the first distributor along a gas flow direction. Also, a method for producing para-xylene and co-producing light olefins, including the following steps: a material stream A enters a reaction zone of the fluidized bed reactor from the first gas distributor; a material stream B enters the reaction zone of the fluidized bed reactor from the second gas distributor; a reactant contacts a catalyst in the reaction zone to generate a gas phase stream comprising para-xylene and light olefins.

Abstract: The present disclosure provides processes to convert heavy hydrocarbons to light distillates. The present disclosure further provides compositions including light distillates. In an embodiment, a process for upgrading a hydrocarbon feed includes dehydrogenating a C3-C50 cyclic alkane and an C2-C50 acyclic alkane in the presence of a dehydrogenation catalyst to form a C3-C50 cyclic olefin and a C2-C50 acyclic olefin. The process includes reacting the C3-C50 cyclic olefin and the C2-C50 acyclic olefin in the presence of a group 6 or group 8 transition metal catalysts to form a C5-C200 olefin. The process further includes hydrogenating the C5-C200 olefin in the presence of a hydrogenation catalyst to form a C5-C200 hydrogenated product. Processes of the present disclosure may further include hydroisomerizing the C5-C200 hydrogenated product in the presence of a hydroisomerization catalyst to form a C5-C200 hydroisomerized product.

Abstract: The present disclosure provides processes to convert paraffins to corresponding olefins and or heavier hydrocarbons. In at least one embodiment, a process includes introducing, at a temperature of from about 50° C. to about 500° C., a hydrocarbon feed comprising paraffins to a first metal oxide comprising one or more group 1 to group 17 metal and one or more oxygen. The process includes obtaining a product mixture comprising one or more C3-C50 cyclic olefins, one or more C2-050 acyclic olefins, one or more C5-C200 hydrocarbons, such as one or more C5-C100 hydrocarbons, or a mixture thereof. In at least one embodiment, the product mixture is substantially free of H2 (e.g., <500 ppm). The introducing can reduce the first metal oxide to form a second metal oxide. Processes may include introducing the second metal oxide to an oxidizing agent to form the first metal oxide.

Abstract: The invention discloses a novel method for preparation of highly active and selective dehydrogenation catalyst, comprising of metal oxide of group VIB elements of periodic table, and at least one metal oxide from group IA and/or group VIII, supported on alumina or silica or mixture thereof, wherein the accessibility to active sites and dispersion of metal oxides is enhanced by the addition of carbonaceous material such as coke derived from coal or petroleum coke or any other form of carbon, during catalyst preparation and its combustion thereof during calcination.

Abstract: Implementations described herein generally relate to methods for purifying alpha-olefins. The alpha-olefins may be used to form drag reducing agents for improving flow of hydrocarbons through conduits, particularly pipelines. In one implementation, a method of increasing alpha-olefin content is provided. The method includes providing an olefin feedstock composition having an alpha-mono-olefin and at least one of a diolefin having an equal number of carbon atoms to the alpha-mono-olefin and/or a triolefin having an equal number of carbon atoms to the alpha-mono-olefin. The method further includes contacting the olefin feedstock composition with ethylene in the presence of a catalyst composition including an olefin metathesis catalyst. The method further includes reacting the olefin feedstock composition and ethylene at metathesis reaction conditions to produce an alpha-olefin product comprising the alpha-mono-olefin and alpha-olefins having fewer carbon atoms than the alpha-mono-olefin.

Abstract: A catalyst for synthesizing a conjugated diene from a raw material including an alcohol, which includes at least Ce and Zn as metal elements constituting the catalyst. An apparatus for producing a conjugated diene, including: a reaction tube (1) provided with the catalyst; a supply means for supplying a raw material gas containing the raw material into the reaction tube (1); and an outlet means for releasing a product from the reaction tube (1). A method for producing a conjugated diene, including contacting a raw material gas containing a raw material with the catalyst to obtain a conjugated diene. The amount of the raw material is preferably 10 to 50% by volume (in terms of gas volume) with respect to 100% by volume (in terms of gas volume) of the raw material gas.

Abstract: This method comprises passing a residual stream into a flash drum to form a gaseous overhead flow and liquid bottom flow, and feeding the bottom flow into a distillation column, It comprises cooling the overhead flow in a heat exchanger to form a cooled overhead flow. It comprises the extraction of a gaseous overhead stream at the head of the distillation column, and the formation of at least one effluent stream from the overhead stream and/or from the top stream. The separation of the cooled overhead flow flow comprises passing the cooled overhead flow into an absorber, and injecting a methane-rich stream into the absorber to place the cooled overhead flow in contact with the methane-rich stream.

Abstract: Processes to selectively crack alkyne compounds from a hydrocarbon stream including olefinic and di-olefinic compounds are described. The process includes contacting the hydrocarbon stream with a supported CuO catalyst under conditions sufficient to crack the alkynes to form a product stream that included cracked compounds and further separating the cracked organic compounds from the hydrocarbon stream.

Abstract: Described are methods and compositions for inhibiting polymerization of a monomer (e.g., styrene) composition using a hydroxylated quinone antipolymerant. The hydroxylated quinone antipolymerant can be used with little or no nitroxyl group containing antipolymerant yet still provide excellent antipolymerant activity in a monomer-containing composition.

Abstract: The present disclosure provides a process for producing trifluoroiodomethane (CF3I). The process may include providing a vapor-phase reactant stream comprising trifluoroacetic acid and iodine and reacting the reactant stream in the presence of a catalyst to produce a product stream comprising the trifluoroiodomethane. The catalyst includes silicon carbide.

Abstract: Provided is a method of manufacturing octafluorocyclopentene by bringing 1-chloroheptafluorocyclopentene into contact with an alkali metal fluoride. The manufacturing method includes a feedstock heating step of heating 1-chloroheptafluorocyclopentene to not lower than 40° C. and not higher than 55° C. and a fluorination step of maintaining a suspension containing a polar aprotic solvent and an alkali metal fluoride at 85° C. or higher while supplying heated 1-chloroheptafluorocyclopentene into the suspension and performing fluorination thereof to obtain octafluorocyclopentene.

Abstract: An object of the present invention is to provide a method that can efficiently remove water contained in pentafluoropropane. Provided as a solution is a method comprising distilling a composition comprising pentafluoropropane and water to thereby extract pentafluoropropane with a water content higher than that of the composition as a first stream, and pentafluoropropane with a water content lower than that of the composition as a second stream.

Abstract: The present invention provides a process for preparing 4-methyl-5-nonanone of the following formula (3): the process comprising at least a step of subjecting 2-methylpentanoic anhydride of the following formula (1) and an n-butyl nucleophilic reagent of the following general formula (2) in which M represents Li, MgZ1, or ZnZ1, wherein Z1 represents a halogen atom or an n-butyl group, to a nucleophilic substitution. reaction Coproduce 4-methyl-5-nonanone (3), as well as a process for preparing 4-methyl-5-nonanol of the following formula (5), the process comprising at least steps of preparing 4-methyl-5-nonanone; and subjecting the obtained 4-methyl-5-nonanone and a reducing agent to a reduction reaction to produce 4-methyl-5-nonanol (5).

Abstract: The present invention provides a process for preparing 4-methyl-5-nonanone of the following formula (3), the process comprising at least a step of subjecting pentanoic anhydride of the following formula (1) and a 2-pentyl nucleophilic reagent of the following general formula (2), in which M represents Li, MgZ1, or ZnZ1, wherein Z1 represents a halogen atom or a 2-pentyl group, to a nucleophilic substitution reaction to produce 4-methyl-5-nonanone (3), as well as a process for preparing 4-methyl-5-nonanol of the following formula (7), the process comprising at least steps of preparing 4-methyl-5-nonanone and subjecting the obtained 4-methyl-5-nonanone and a reducing agent to a reduction reaction to produce 4-methyl-5-nonanol (7).

Abstract: A process for conducting exothermic equilibrium reactions, especially for the performance of methanol synthesis by heterogeneously catalysed conversion of synthesis gas, is proposed, which enables readjustment and hence optimization of the reaction conditions along the longitudinal coordinate of the reactor. For this purpose, in the process according to the invention, a reactor is used which is divided into a multitude of series-connected reaction cells, each of which comprises a preheating zone, a cooled reaction zone, one or more cooling zones and a deposition zone for condensable reaction products. In this way, the reaction conditions are adjustable to the respective, local composition of the reaction mixture and variable over the reactor length.

Abstract: The present disclosure relates to scalable processes for extracting, refining and fracationating extracts of natural products, such as plant material and for providing well controlled refined extracts.

Abstract: Disclosed herein are embodiments of a method for making cannabidiol. Also disclosed herein are embodiments of a composition comprising cannabidiol and one or more GRAS components. The method and composition embodiments described herein address the drawbacks associated with conventional methods for making and/or isolating cannabidiol.

Abstract: Methods for manufacturing phenoxyethanol from a reaction of a phenolate with a monohalohydrin. The phenolate is reacted with the monohalohydrin at a reaction temperature that is less than or equal to a boiling point of a reaction mixture to produce products that include the phenoxyethanol.

Abstract: Optionally substituted squarylium compounds, such as those depicted in Formula 1, may be useful in filters for display devices.

Abstract: A method for preparing methyl methacrylate from methacrolein and methanol. The method comprises contacting in a tubular reactor having at least four zones a mixture comprising methacrolein, methanol, oxygen and a base with a catalyst bed of heterogeneous catalyst comprising a support and a noble metal, wherein reaction zones comprising catalyst beds alternate with mixing zones not comprising catalyst beds.

Abstract: A process is provided for converting cyclic alkyleneureas into their corresponding alkyleneamines. The process includes reacting a feedstock comprising cyclic alkyleneureas in the liquid phase with water in an amount of from about 0.1 to about 20 mole water per mole urea moiety, at a temperature of at least 230° C., with removal of CO2. The process may allow the efficient conversion of alkyleneureas into the corresponding alkyleneamines. In certain embodiments, the process has a high yield and low side product production.

Abstract: A method of reducing color in an alkanolamine is described. The method includes contacting the alkanolamine with a color-reducing amount of a borane complex effective to provide a color-reduced alkanolamine composition having a Platinum-Cobalt Color Value, according to Test Method ASTM D1209, of less than 50.