Abstract: Disclosed is a device including a chamber configured as a tubular body, the chamber being connected to a ground power source; a power supply device disposed outside the chamber and configured to continuously apply voltage having a magnitude set as direct current or alternating current; an emitter configured as a hollow tubular body having a plurality of cusps formed on an outer surface thereof and configured to generate plasma, the emitter being disposed in the chamber, elongated in a direction parallel to a flow direction of the processing target gas, electrically connected to the power supply device, and configured to generate nonthermal plasma; a rod configured to electrically connect the emitter and the power supply device and support the emitter; and an insulator configured to electrically insulate the rod and the chamber and prevent arcing from occurring between the rod and the chamber.

Abstract: The present specification provides an electrolyte including a phthalate phosphine-type anion, an additive for a secondary battery including the electrolyte, and a secondary battery including the additive.

Abstract: The present specification relates to an additive for an electrochemical device including a compound having a silyloxy group, and an electrolyte, an electrode and an electrochemical device.

Abstract: The present specification relates to an additive for an electrochemical device including a compound having a silyloxy group, and an electrolyte, an electrode and an electrochemical device.

Abstract: The present specification provides an electrolyte including a phthalate phosphine-type anion, an additive for a secondary battery including the electrolyte, and a secondary battery including the additive.

Abstract: A non-aqueous electrolyte solution for a lithium secondary battery comprises a lithium salt and an organic solvent. The non-aqueous electrolyte solution further comprises a specific siloxane compound and a sulfonate compound. This non-aqueous electrolyte solution solves the capacity degradation phenomenon, which appears in a lithium secondary battery using a non-aqueous electrolyte solution containing only a specific siloxane compound when the lithium secondary battery is used for a long time, so this non-aqueous electrolyte solution is especially useful for high-capacity batteries.

Abstract: Disclosed is an electrolyte comprising a compound having both a sulfonate group and a cyclic carbonate group. The electrolyte forms a more stable and dense SEI layer on the surface of an anode, and thus improves the capacity maintenance characteristics and lifespan characteristics of a battery. Also, disclosed is a compound represented by the following Formula 1, and a method for preparing the same by reacting 4-(hydroxyalkyl)-1,3-dioxolan-2-one with a sulfonyl halide compound: wherein each of R1 and R2 independently represents a C1˜C6 alkylene group optionally containing a C1˜C6 alkyl group or C2˜C6 alkenyl group introduced thereto; R3 is selected from the group consisting of a hydrogen atom, C1˜C20 alkyl group, C3˜C8 cyclic alkyl group, C2˜C6 alkenyl group, halo-substituted alkyl group, phenyl group and benzyl group.

Abstract: A non-aqueous electrolyte solution for a lithium secondary battery comprises a lithium salt and an organic solvent. The non-aqueous electrolyte solution further comprises a specific siloxane compound and a sulfonate compound. This non-aqueous electrolyte solution solves the capacity degradation phenomenon, which appears in a lithium secondary battery using a non-aqueous electrolyte solution containing only a specific siloxane compound when the lithium secondary battery is used for a long time, so this non-aqueous electrolyte solution is especially useful for high-capacity batteries.

Abstract: Disclosed is an electrolyte comprising a compound having both a sulfonate group and a cyclic carbonate group. The electrolyte forms a more stable and dense SEI layer on the surface of an anode, and thus improves the capacity maintenance characteristics and lifespan characteristics of a battery. Also, disclosed is a compound represented by the following Formula 1, and a method for preparing the same by reacting 4-(hydroxyalkyl)-1,3-dioxolan-2-one with a sulfonyl halide compound: wherein each of R1 and R2 independently represents a C1˜C6 alkylene group optionally containing a C1˜C6 alkyl group or C2˜C6 alkenyl group introduced thereto; R3 is selected from the group consisting of a hydrogen atom, C1˜C20 alkyl group, C3˜C8 cyclic alkyl group, C2˜C6 alkenyl group, halo-substituted alkyl group, phenyl group and benzyl group.

Abstract: Provided are a vinyl chloride resin composition containing a vinyl chloride monomer and an organo-modified metal oxide nanoparticle which can be used in exterior construction materials due to markedly improved thermal stability and weather resistance, which are considered weaknesses of vinyl chloride resins, and a method of preparing the same.

Abstract: The present invention relates to a process for preparing a chiral ester according to the formula (100): by reacting (i) a racemic alcohol, (ii) a selected ruthenium complex to activate racemization of the racemic alcohol, (iii) a lipase to selectively acylate one enantiomer of the racemic alcohol, and (iv) an acyl donor compound to supply an acyl group to the lipase.

Abstract: The present invention relates to a method for preparing a chiral ester and more particularly, the method for preparing an optically pure chiral ester from an alkenyl ester at a high yield by mixing and reacting: an alkenyl ester; a ruthenium complex to activate reduction reaction of said alkenyl ester and racemization; a lipase to acylate selectively one of enantiomers of said alkenyl ester; and a reducing agent to supply a hydride to said ruthenium complex. Said optically pure chiral ester of the present invention can be prepared by one-step synthesis from various types of alkenyl esters at a high yield.

Abstract: The present invention relates to a method for preparing a chiral ester and more particularly, the method for preparing an optically pure chiral ester from an alkenyl ester at a high yield by mixing and reacting: