Abstract:
본 발명은 (알콕시폴리옥시알킬렌글리콜)알킬 불포화카르복실산 디에스테르 화합물의 제조방법에 관한 것으로서, 더욱 상세하게는 시멘트, 모르타르 또는 콘크리트 조성물의 물성을 개선하기 위하여 첨가되는 폴리카르복실산계 혼화제의 원료물질로 사용되어지는 다음 화학식 1로 표시되는 (알콕시폴리옥시알킬렌글리콜)알킬 불포화카르복실산 디에스테르 화합물을 제조하는데 있어, 이중결합이 하나 이상 포함된 불포화 디카르복실산의 디알킬 에스테르를 산 촉매가 존재하는 조건에서 (폴리옥시알킬렌글리콜) 알킬 에테르와의 에스테르 교환 반응시켜 제조하는 방법에 관한 것이다.
상기 화학식 1에서, R 1 , R 2 , R 3 , R 4 및 n은 각각 발명의 상세한 설명에서 정의한 바와 같다. 에스테르 교환반응, 폴리카르복실산계 혼화제, (알콕시폴리옥시알킬렌글리콜)알킬 불포화카르복실산 디에스테르, 불포화 디카르복실산의 디알킬 에스테르
Abstract:
본 발명은 신규한 하이브리드형 고분자 전해질, 이를 포함하는 리튬이차전지 및 이들의 제조방법을 제공한다. 보다 구체적으로는, 본 발명은 1-3000 nm의 직경을 갖는 입자로 이루어진 초극세 섬유상 다공성 고분자 매트릭스와, 상기 매트릭스 내에 함입되는 고분자 및 리튬염이 용해된 유기 전해액을 포함하는 하이브리드형 고분자 전해질을 제공한다. 상기 하이브리드형 고분자 전해질은 전극과의 접합성, 기계적 강도, 저온 및 고온특성 그리고 리튬이차전지용 유기 전해액과의 호환성이 우수하므로, 리튬이차전지의 제조에 응용될 수 있다.
Abstract:
PURPOSE: Provided is a method for producing (alkoxy polyoxyalkylene glycol)alkyl unsaturated carboxylic acid diester compounds which have excellent thermal stability and shelf stability and thus are useful for starting materials of concrete admixture. CONSTITUTION: The method for producing an (alkoxy polyoxyalkylene glycol)alkyl unsaturated carboxylic acid diester compound represented by the following formula 1 comprises carrying out transesterification of a dialkyl ester of unsaturated dicarboxylic acid containing at least one double bond, represented by the following formula 2 with a (polyoxyalkyleneglycol)alkyl ether represented by the following formula 3 in the presence of an acid catalyst. In the above formulae 1-3, R1 is a C1-C6 unsaturated hydrocarbon group containing at least one double bond; R2 is a C2-C6 alkylene group; each of R3 and R4 is a C1-C6 alkyl group; and n is the number of added oxyalkylene group and represents an integer of 3-24.
Abstract:
PURPOSE: Provided is a process for producing 2,2,2-trifluoroethanol at a low reaction temperature for a short time in a high yield by using an imidazolium-based ionic solvent. CONSTITUTION: The 2,2,2-trifluoroethanol is produced by hydrolyzing 1-chloro-2,2,2-trifluoroethane in the presence of the imidazolium-based ionic solvent represented by the formula 1 and a base such a hydroxide salt of lithium, sodium and potassium, a carbonate, an acetate, and an organic acid salt. In the formula, R1 and R2 are independently C1-C8 alkyl or benzyl and X is PF6, BF4, NO3, NO2, CH3CO2, CF3CO2, or CF3SO3.
Abstract translation:目的:提供使用咪唑鎓系离子溶剂,在低反应温度下短时间高收率地制备2,2,2-三氟乙醇的方法。 构成:2,2,2-三氟乙醇是通过在由式1表示的基于咪唑鎓的离子溶剂存在下水解1-氯-2,2,2-三氟乙烷和碱如锂的氢氧化物盐, 钠和钾,碳酸盐,乙酸盐和有机酸盐。 在该式中,R 1和R 2独立地为C 1 -C 8烷基或苄基,X为PF 6,BF 4,NO 3,NO 2,CH 3 CO 2,CF 3 CO 2或CF 3 SO 3。
Abstract:
The present invention relates to a catalyst for producing 1,1-difluoroethane (HCFC-152a) and producing method thereof. More particularly, it is to provide the catalyst prepared by impregnating palladium on the active carbon pretreated with an aqueous hydrogen fluoride solution and an aqueous hydrogen chloride solution in series and its use in the production of 1,1-difluoroethane (HCFC-142b) by dehydrochlorinating 1,1-difluoro-1-chloroethane at 240-300° C. in the supplying molar ratio of 2-6 (H2/HCFC-142b) with maximizing a selectivity toward the product of HCFC-152a.
Abstract:
PURPOSE: A surface treatment method of forming a porous oxide coating film having superior biocompatibility with bone, chemical and physical stabilities, uniformed pore distribution, expanded pore size and smooth surface characteristics on the surface of implants comprising metallic titanium or titanium alloys is provided. CONSTITUTION: The electrochemical surface treatment method of implants comprising metallic titanium or titanium alloys comprises the processes of pre-treating the surface of implants comprising metallic titanium or titanium alloys; forming an oxide coating film on the surface of the implants by electrochemically oxidizing the pre-treated implants; and post-treating the formed oxide coating film with an acid or alkaline aqueous solution to obtain uniformed pore distribution, wherein the pre-treatment process comprises the steps of degreasing the implants using acetone or alcohol; water washing the implants taken out of the aqueous solution by taking the implants out of the aqueous solution after dipping the degreased implants into a NaOH aqueous solution or KOH aqueous solution having a concentration of 30 g/liter at 80 deg.C for 5 minutes, pickling the water washed implants in a solution comprising 15 mL of concentrate nitric acid having a concentration of 61 wt.%, 3 mL of hydrofluoric acid having a concentration of 49 wt.% and 82 mL of distilled water at an ordinary temperature for 5 minutes, and washing the implants with distilled water for 10 minutes.
Abstract:
PURPOSE: A guidance system and a guidance method of fiber filament are provided which can lead spun fiber filament without dispersion and damage. CONSTITUTION: The guidance system is comprised of: an adapter controlling direction and speed of flow being coagulating solution; and a pump circulating and feeding the coagulating solution. The guidance method is comprised of: (a)discharging the fed coagulating solution through a nozzle or a split to a spreading funnel; (b) leading the coagulating solution and the fiber filament to a leading funnel by the discharge; and then (c)discharging the leaded coagulating solution and the leaded fiber filament through the spreading funnel at the lower speed than the (a) step.
Abstract:
PURPOSE: A fluorine manufacturing method is provided to prevent the explosive recombination of the fluorine and the hydrogen and to improve the fluorine manufacture efficiency. CONSTITUTION: The fluorine manufacturing method is formed by the steps of: electrolyzing the anhydrous fluoric acid by using the fused alkali metal fluoric acid compound as an electrolytic solution; and leading the electrolytic solution to naturally convert to a specific direction by installing a few louver-typed horizontal gap only on the upper area of the whole area of a cathode(2) and by using a plate on the lower area.
Abstract:
The reactive catalyst for synthesizing 1,1,1,2-tetrafluoroethane(HFC-134a) is prepared by (1) reacting magnesium chromate(MgCrO4) or magnesium dichromate(MgCrO2) with hydrogen fluorine(HF) and ethanol, (2) filtering, drying and burning the reacted product. The produced catalyst remarkably lowers inactivation speed.