Abstract:
PURPOSE: A method for manufacturing soda lime-based glass using coal wastes is provided to produce glass-based secondary products with various colors and the superior heat resistance characteristic by mixing soda ash, calcium carbonate, magnesium sulfate, silica, and cullet into the coal wastes. CONSTITUTION: A method for manufacturing soda lime-based glass includes the following: 5 to 70 weight% of coal wastes, 5 to 30 weight% of soda ash, 5 to 20 weight% of calcium carbonate, 0 to 10 weight% of magnesium sulfate, 5 to 15 weight% of silica, and 10 to 80 weight% of cullet are mixed to obtain a mixture. The mixture is melted at temperature between 1300 and 1700 degrees Celsius for 0.5 to 5 hours. The melted mixture is molded. The molded mixture is annealed.
Abstract:
본 발명은 퓨란 유도체와 금 및 은 촉매를 이용한 이의 제조방법에 관한 것으로, 보다 상세하게는 인아인-1,6-다이올 유도체를 금(Au) 및 은(Ag) 촉매 조건에서 산소-탄소간의 선택적인 분자내 고리화 반응을 수행하여 제조된 신규 구조의 하기 화학식 1로 표시되는 퓨란 유도체와 이의 제조방법에 관한 것이다.
상기 화학식 1에서, A는 C 1 -C 6 알킬기; C 5 -C 8 사이클로알킬기; 또는 할로겐, 하이드록실, C 1 -C 4 알킬, C 1 -C 4 알콕시, C 2 -C 4 알카노에이트 중에서 선택된 치환체가 하나 이상 치환 또는 비치환된 페닐기를 나타낸다. 금촉매, 은촉매, 인아인-1,6-다이올, 분자내 고리화반응, 퓨란
Abstract:
본 발명은 하기 화학식 1로 표시되는 인아인-1,6-다이올(Enyne-1,6-diol) 유도체와 이의 제조방법에 관한 것으로, 보다 상세하게는, 인듐(In)과 알릴 할라이드 화합물의 반응으로부터 얻어지는 알릴 인듐 유도체를 알리나인-1,6-다이올 화합물과의 반응을 통해 알릴 그룹이 알리나인-1,6-다이올의 알렌그룹에 선택적으로 첨가되어 제조된 인아인-1,6-다이올(Enyne-1,6-diol) 유도체 및 이의 제조방법에 관한 것이다.
상기 화학식 1에서, A는 C 1 -C 6 알킬기; C 5 -C 8 사이클로알킬기; 할로겐, 하이드록실, C 1 -C 4 알킬, C 1 -C 4 알콕시, C 2 -C 4 알카노에이트 중에서 선택된 치환체가 하나 이상 치환 또는 비치환된 페닐기; 또는 퓨릴기를 나타내고, B는 수소, C 1 -C 6 알킬기 또는 페닐기를 나타낸다. 인듐, 인아인-1,6-다이올, 알리나인-1,6-다이올, 알릴 인듐 유도체
Abstract:
PURPOSE: A method for preparing 2-aryl allenoate derivatives is provided to obtain 2-aryl allenoate derivatives with high yield through a cross coupling reaction of an organic indium reagent in the presence of an arene derivative and palladium catalyst, wherein the organic indium reagent is obtained in in-situ from the reaction of indium with 4-bromo-2-butenoate. CONSTITUTION: A method for preparing 2-aryl allenoate derivatives is represented by chemical formula 1. In chemical formula 1, R^1 and R^5 are hydrogen, (C1~C7) alkyl, halogen, (C6~C20) aryl or (C1~C7) alkoxycarbonyl; R^2 and R^4 are hydrogen, (C1~C7) alkoxy or nitro; R^3 is hydrogen, (C1~C7) alkyl, (C6~C20) aryl, halogen, formyl, acetyl, alkoxycarbonyl or (C6~C20) aryl (C1~C7) alkylcarbamoyl aryl; R^6 is hydrogen or (C1~C7) alkyl; and R^7 is (C1~C7) alkyl or (C6~C20) aryl.
Abstract:
The present invention relates to an E-glass fiber manufacturing method using coal waste and the E-glass fiber manufactured by using same. The present invention includes 1) a step for stirring and mixing E-glass fiber raw materials; 2) a step for forming molten glass through high-temperature melting of the mixed raw materials; and 3) a step for turning the molten glass into a fiber with a fiberizing device. Sandstone-based coal waste of silica-alumina with a relatively low carbon content is used and a waste input amount is changed so that bulk glass and fiber glass with the E-glass composition can be manufactured. The present invention can make a glass fiber satisfy thermal characteristics, optical characteristics, a thermal expansion coefficient, optical transparency, tensile strength, and the like. Accordingly, a high-efficiency glass fiber material can be manufactured with high efficiency and low costs. Also, resources recycling can be improved.
Abstract:
본 발명은 발포 유리 패널의 제조 방법 및 이에 의해 제조된 발포 유리 패널에 관한 것으로, 발포 유리 패널을 제조하기 위한 발포 과정에 있어 석탄폐석이 발포제로써 기능하도록 구성된 석탄폐석을 이용한 발포 유리 패널의 제조 방법과 이에 의해 제조된 발포 유리 패널을 제공하는 것에 목적이 있다. 상기 목적을 달성하기 위한 본 발명의 석탄폐석을 이용한 발포 유리 패널의 제조 방법은, 유리 원료, 규조토 및 적어도 일부의 석탄폐석이 포함된 발포제 혼합물을 형성하는 단계 및 상기 혼합물을 열처리하는 단계를 포함하여 구성된다.
Abstract:
PURPOSE: A method for manufacturing enyne-1,6-diol derivatives is provided to selectively synthesize enyne-1,6-diol derivatives by reacting an allyl indium reagent with an allenyn-1,6-diol compound through in-situ reaction without separate refining process. CONSTITUTION: A method for manufacturing enyne-1,6-diol derivatives comprises the steps of: reacting an allyl halide derivative represented by chemical formula 3 and indium to prepare an allyl indium reagent represented by chemical formula 4; and reacting an allylnyne-1,6-diol compound represented by chemical formula 2 to prepare an enyne-1,6-diol derivative represented by chemical formula 1.
Abstract:
A method for preparing an allyl allene derivative is provided to synthesize an allyl allene derivative at good yield by reacting an allyl indium reagent with a propargyl alcohol derivative without a separate refining process. A method for preparing an allyl allene derivative has a structure of chemical formula 1. In the chemical formula 1, R1 and R2 show C1-C6 alkyl group, or substituted or unsubstituted phenyl group, or R1 and R2 form 5-8-membered cycloalkyl ring; R3 and R4 show hydrogen atom, C1-C6 alkyl group, substituted or unsubstituted phenyl group, or phenyl-C1-C6 alkylene group. The substituted phenyl group is a phenyl group substituted with substituents selected from halide, hydroxyl, C1-C6 alkyl, C1-C6 alkoxy, ketone, ester, nitro, amide, aldehyde and amine.
Abstract:
A method for preparing a homoallenyl alcohol derivative is provided to selectively synthesize the homoallenyl alcohol derivative at high yield by reacting a synthesized organic indium reagent and an aldehyde compound. A method for preparing a homoallenyl alcohol derivative represented by chemical formula 1 comprises the steps of: reacting indium and propargyl chloride substituted with an ester group represented by chemical formula 2 to prepare an organic indium reagent; and adding an aldehyde compound represented by chemical formula 4. In chemical formula 1, 2 and 3, X is a halogen atom; R1 is a C1-C6 alkyl group; and R2 is a hydrogen atom, C1-C6 alkyl group, C3-C8 cycloalkyl group, phenyl group or phenyl-C1-C6 alkylene group. The benzene ring of phenyl or phenyl-C1-C6 alkylene group can be substituted or unsubstituted with 1-4 substituents selected from halogen, hydroxyl, nitro, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 acyl and C1-C6 alkoxycarbonyl.