Abstract: Phosphor compositions having the formula (Ba,Sr,Ca)SiO4:Eu and light emitting devices including a semiconductor light source and the above phosphor. Also disclosed are blends of (Ba,Sr,Ca)SiO4:Eu and one or more additional phosphors and light emitting devices incorporating the same. Preferred blends include (Sr,Ba,Ca)2SiO4:Eu and at least one of (Sr,Mg,Ca,Ba,Zn)2P2O7:Eu,Mn; (Ca,Sr,Ba,Mg)5(PO4)3(Cl,F,OH):Eu,Mn; (Sr,Ba,Ca)MgAl10O17:Eu,Mn; and Mg4FGeO6:Mn4+; and one or more garnet phosphors having the general formula (Y,Gd,La,Lu,T,Pr,Sm)3(Al,Ga,In)5O12:Ce.

Abstract: A catalyst system comprising a catalyst and a reductant is disclosed. The catalyst comprises a metal oxide catalyst support, a catalytic metal oxide, and a promoting metal. The catalytic metal oxide comprises gallium oxide, indium oxide or a combination of the two. The promoting metal comprises at least one of silver, cobalt, vanadium, molybdenum, tungsten, zinc, tin and bismuth. The catalyst comprises about 5 to about 31 mol % catalytic metal oxide and about 0.5 to about 9 mol % promoting metal. The reductant comprises a fluid hydrocarbon having at least 4 carbon atoms. Also disclosed is a process for reducing NOx to N2 using the disclosed catalyst system by mixing NOx with a reductant and passing the mixture through a catalyst of the disclosed catalyst system.

Abstract: Phosphor compositions having the formula (Y1?x?y?zTbxGdyCez)3(M1M2)t(Al1?r?sGarIns)A?2tO12+D, where M1 is Mg or Zn, M2 is Si or Ge, 0<x+y<1, 0.01<z<0.1, 0.1<t<1.5, 0<r, s<0.5, 4.5<A<5.0, and ?1<D<1. Also disclosed are light emitting devices including a light source and at least one phosphor having the above formula. Such phosphors exhibit a deeper red emission when compared to conventional TAG phosphors, allowing the production of white light sources having improved properties.

Abstract: Aromatic compounds such as toluene and o-xylene are chlorinated in the presence of a catalyst combination prepared by combining (A) at least one salt comprising a metal selected from the group consisting of a Group 4-12 metal, a lanthanide and an actinide; and a counterion; and (B) at least one organic sulfur compound, preferably phenothiazine-N-carbonyl chloride. The catalyst combination may include reaction products of (A) and (B). Under these conditions, production of the p-chloro isomer is optimized. In some embodiments said counterion is an organic counterion derived from at least one acidic organic compound selected from the group consisting of those with an approximate pKa value relative to water of at least about 3.

Abstract: Propylene oxide is formed by reaction of hydrogen, oxygen, and propylene over a solid catalyst such as Pd on TS-1, the reaction being carried out in carbon dioxide solvent at conditions effective to provide a dense phase reaction mixture.

Abstract: A method for synthesizing hydrogen peroxide comprises the step of: mixing an analog of a secondary alcohol that is soluble with carbon dioxide with a free radical initiator and oxygen in carbon dioxide to generate hydrogen peroxide. Another method of synthesizing hydrogen peroxide comprises the step of: mixing hydrogen, oxygen and a CO2-philic catalyst in carbon dioxide phase. The CO2-philic catalyst is soluble or miscible in carbon dioxide and is suitable to catalyze the reaction of hydrogen and oxygen to produce hydrogen peroxide. The method also comprises the step of reacting the hydrogen and oxygen to produce hydrogen peroxide.

Abstract: A method for synthesizing hydrogen peroxide comprises the steps of: synthesizing an analog of anthraquinone that is miscible or soluble in carbon dioxide; reacting the analog of anthraquinone with hydrogen in carbon dioxide to produce a corresponding analog of tetrahydroquinone; and reacting the analog of tetrahydroquinone with oxygen to produce the hydrogen peroxide and regenerate the analog of anthraquinone. A chemical compound having the formula: wherein R1, R2, R3, R4, R5, R6, R7, and R8 are independently, the same or different, H, RC, or RSRC, wherein RS is a spacer group and RC is a fluoroalkyl group, a fluoroether group, a silicone group, an alkylene oxide group, a fluorinated acrylate group, or a phosphazine group, and wherein at least one of R1, R2, R3, R4, R5, R6, R7, and R8 is not H.

Abstract: Propylene oxide is formed by reaction of hydrogen, oxygen, and propylene over a solid catalyst such as Pd on TS-1, the reaction being carried out in carbon dioxide solvent at conditions effective to provide a dense phase reaction mixture.

Abstract: A method for synthesizing hydrogen peroxide comprises the steps of: synthesizing an analog of anthraquinone that is miscible or soluble in carbon dioxide; reacting the analog of anthraquinone with hydrogen in carbon dioxide to produce a corresponding analog of tetrahydroquinone; and reacting the analog of tetrahydroquinone with oxygen to produce the hydrogen peroxide and regenerate the analog of anthraquinone.

Abstract: The invention is a process for epoxidizing an olefin with hydrogen and oxygen in the presence of a catalyst comprising a noble metal and pretreated titanium zeolite. Titanium zeolite pretreatment comprises contacting the titanium zeolite with a leaching agent prior to use in epoxidation. Surprisingly, the process using the pretreated titanium zeolite shows decreased ring-opening to unwanted glycols and glycol ethers.

Abstract: The invention is a process for epoxidizing an olefin with hydrogen and oxygen in the presence of a modifier and a catalyst comprising a noble metal and titanium zeolite. The modifier is (a) calcium carbonate in the presence of carbon dioxide or (b) ammonium bicarbonate. The process results in increased catalyst activity, selectivity to epoxide, and increased catalyst life.

Abstract: A method for synthesizing hydrogen peroxide comprises the steps of: synthesizing an analog of anthraquinone that is miscible or soluble in carbon dioxide; reacting the analog of anthraquinone with hydrogen in carbon dioxide to produce a corresponding analog of tetrahydroquinone; and reacting the analog of tetrahydroquinone with oxygen to produce the hydrogen peroxide and regenerate the analog of anthraquinone. A chemical compound having the formula: wherein R1, R2, R3, R4, R5, R6, R7, and R8 are independently, the same or different, H, RC, or RSRC, wherein RS is a spacer group and RC is a fluoroalkyl group, a fluoroether group, a silicone group, an alkylene oxide group, a fluorinated acrylate group, or a phosphazine group, and wherein at least one of R1, R2, R3, R4, R5, R6, R7, and R8 is not H.

Abstract: A method for synthesizing hydrogen peroxide comprises the steps of: synthesizing an analog of anthraquinone that is miscible or soluble in carbon dioxide; reacting the analog of anthraquinone with hydrogen in carbon dioxide to produce a corresponding analog of tetrahydroquinone; and reacting the analog of tetrahydroquinone with oxygen to produce the hydrogen peroxide and regenerate the analog of anthraquinone.