Abstract: An ionic liquid and a forward osmosis process employing the same are provided. The ionic liquid has a structure represented by Formula (I) ABn??Formula (I), wherein A is n is 1 or 2; m is 0, or an integer from 1 to 7; R1 and R2 are independently methyl or ethyl; k is an integer from 3 to 8; B is i is independently 1, 2, or 3; and j is 5, 6, or 7. The forward osmosis process employing the ionic liquid is used to desalinate a brine via a forward osmosis (FO) model.

Abstract: An ionic liquid and a forward osmosis process employing the same are provided. The ionic liquid has a structure represented by Formula (I) ABn ??Formula (I) , wherein A is n is 1 or 2; m is 0, or an integer from 1 to 7; R1 and R2 are independently methyl or ethyl; k is an integer from 3 to 8; B is i is independently 1, 2, or 3; and j is 5, 6, or 7. The forward osmosis process employing the ionic liquid is used to desalinate a brine via a forward osmosis (FO) model.

Abstract: An electrocatalyst is provided. The electrocatalyst includes Pd-containing metal nitride, wherein the metal is Co, Fe, Y, Lu, Sc, Ti, V, Cu, Ni, or a combination thereof. The molar ratio between the metal and Pd is greater than 0 and less than or equal to 0.8. A fuel cell utilizing the above electrocatalyst is further provided.

Abstract: An organic electroluminescent material is shown in General Formula (1), wherein R3 is a carboline group, R13 is a carbazole group or a carboline group, R1 to R2, R4 to R12 and R14 to R20 are each independently selected from the group consisting of a hydrogen atom, a fluorine atom, a cyano group, an alkyl group, a cycloalkyl group, an alkoxy group, a haloalkyl group, a thioalkyl group, a silyl group and an alkenyl group.

Abstract: An organic electroluminescent material is shown in General Formula (1), wherein R3 is a carboline group, R13 is a carbazole group or a carboline group, R1 to R2, R4 to R12 and R14 to R20 are each independently selected from the group consisting of a hydrogen atom, a fluorine atom, a cyano group, an alkyl group, a cycloalkyl group, an alkoxy group, a haloalkyl group, a thioalkyl group, a silyl group and an alkenyl group.

Abstract: An electrocatalyst is provided. The electrocatalyst includes Pd-containing metal nitride, wherein the metal is Co, Fe, Y, Lu, Sc, Ti, V, Cu, Ni, or a combination thereof. The molar ratio between the metal and Pd is greater than 0 and less than or equal to 0.8. A fuel cell utilizing the above electrocatalyst is further provided.

Abstract: A P-type metal oxide semiconductor material is provided. The P-type metal oxide semiconductor material has a formula of In(1?3)Ga(1?b)Zn(1+a+b)O4, wherein 0?a?0.1, 0?b?0.1, and 0<a+b?0.16. In particular, the P-type metal oxide semiconductor material has a hole carrier concentration of between 1×1011 cm?3 and 5×1018 cm?3.

Abstract: A P-type metal oxide semiconductor material is provided. The P-type metal oxide semiconductor material has a formula of In(1?3)Ga(1?b)Zn(1+a+b)O4, wherein 0?a?0.1, 0?b?0.1, and 0<a+b?0.16. In particular, the P-type metal oxide semiconductor material has a hole carrier concentration of between 1×1011 cm?3 and 5×1018 cm?3.

Abstract: The present invention relates to a new variant of the group 2 allergen from the house dust mite Dermatophagoides pteronyssinus, named Der p 2 variant, and uses thereof. The new variant exhibits cDNA and protein sequence diversity from other known Der p 2 variants.

Abstract: Disclosed is a trace detection device of a biological and chemical analyte, including a metal substrate, a periodic metal nanostructure on the metallic substrate, a dielectric layer on the periodic metal nanostructure, and a continuous metal film on the dielectric layer. Tuning the thickness of the dielectric layer and/or the continuous metal film to meet the laser wavelength can shift the absorption peak wavelength of the sensor, thereby further enhancing the Raman signals of the analyte molecules.

Abstract: The present invention relates to a new variant of the group 2 allergen from the house dust mite Dermatophagoides pteronyssinus, named Der p 2 variant, and uses thereof. The new variant exhibits cDNA and protein sequence diversity from other known Der p 2 variants.

Abstract: Disclosed is a trace detection device of a biological and chemical analyte, including a metal substrate, a periodic metal nanostructure on the metallic substrate, a dielectric layer on the periodic metal nanostructure, and a continuous metal film on the dielectric layer. Tuning the thickness of the dielectric layer and/or the continuous metal film to meet the laser wavelength can shift the absorption peak wavelength of the sensor, thereby further enhancing the Raman signals of the analyte molecules.

Abstract: The present invention provides a methanation catalyst prepared by depositing Pt and Ru on a metal oxide carrier by incipient wetness impregnation or precipitation deposition, drying and calcining the deposited carrier to obtain a Pt—Ru/metal oxide catalyst. This catalyst can selectively catalyze methanation of CO, wherein hydrogen and CO in a hydrogen-rich reformate or synthesis gas are reacted to form methane and water, thereby the CO concentration in the hydrogen-rich reformate is reduced.

Abstract: The present invention provides a methanation catalyst prepared by depositing Pt and Ru on a metal oxide carrier by incipient wetness impregnation or precipitation deposition, drying and calcining the deposited carrier to obtain a Pt—Ru/metal oxide catalyst. This catalyst can selectively catalyze methanation of CO, wherein hydrogen and CO in a hydrogen-rich reformate or synthesis gas are reacted to form methane and water, thereby the CO concentration in the hydrogen-rich reformate is reduced.

Abstract: The present invention discloses a catalyst useful in converting carbon monoxide and water to hydrogen and carbon dioxide (water gas shift reaction), which includes a metal oxide carrier and 0.1-10% Pt and 0-5% Re supported on the carrier, based on the weight of the carrier. The carrier contains copper oxide, alumina, and a metal oxide selected from zinc oxide, chromium oxide and magnesium oxide. The present invention also discloses a method for reducing the content of carbon monoxide in a hydrogen-rich reformate gas.

Abstract: A method for producing maleimides. The method comprises reacting maleic anhydride and a primary amine at 100-180° C. in an organic solvent using a solid acidic catalyst, and purifying the maleimide produced therefrom by extraction and crystallization. The molar ratio of the primary amine to maleic anhydride is about 0.8-1.6. With the present invention, high production yield with high purity of maleimides can be achieved. In addition, the solid acidic catalyst can be easily separated and recycled for subsequent use. Thus, the present invention provides a number of distinct advantages, including substantially improved yield, conveniently reusable catalyst, reduced waste disposal and lower costs.

Abstract: The present invention discloses a catalyst useful in selective oxidation of carbon monoxide (CO) contained in a hydrogen-rich reformate gas. The catalyst is a zeolite carrying Pt, Ru or alloys thereof. Pt or Ru is deposited on the zeolite by incipient wetness impregnation with an aqueous solution. The reformate gas having a reduced CO concentration can be introduced to a fuel cell as a fuel.

Abstract: A method for producing maleimides. The method comprises reacting maleic anhydride and a primary amine at 100-180° C. in an organic solvent using a solid acidic catalyst, and purifying the maleimide produced therefrom by extraction and crystallization. The molar ratio of the primary amine to maleic anhydride is about 0.8-1.6. With the present invention, high production yield with high purity of maleimides can be achieved. In addition, the solid acidic catalyst can be easily separated and recycled for subsequent use. Thus, the present invention provides a number of distinct advantages, including substantially improved yield, conveniently reusable catalyst, reduced waste disposal and lower costs.

Abstract: An improved process for the esterification of carboxylic acid and alcohols into carboxylic ester is disclosed. It comprises the steps of: (a) charging the esterification reactants into a fixed bed reactor under a predetermined reaction condition; and (b) reacting the esterification reactants in the fixed bed reactor. The fixed bed reactor contains acidic catalysts that are present in a solid phase, and the reaction condition is controlled such that (i) the reactants and the products co-exist in a gas-liquid two-phase equilibrium in the fixed bed reactor and that (ii) at least one component of the reactants is present in one phase and at least one component of the products is present in another phase. Because a phase change is always taking place concurrently with the esterification reaction; the reaction stream is maintained at a relatively uniform temperature.