Na2CO3. Sodium orthosilicate (Na-OSi), Tetronix T-701 (T-701), Na-dioctyl sulfosuccinate (303C), Newpol PE-68 (PE-68), MJU-100A, and tetrasodium pyrophosphate were blended to prepare high performance alkaline cleaning agents (ACASs). The results of cleaning test with steel specimen showed that ACAS-6 (Na2CO3 50g/Na-OSi 35g/T-701 20g/303C 18g/PE-68 17g/MJU-100A 10g/TSPP 20g/ water 180g mixture) had a good cleaning power. The cleaning power for press-rust preventing oil was 98% and 99% degreasing at 4wt%, 70℃ and 90℃, respectively ; for quenching oil, the cleaning power of ACAS-6 was 91% degreasing at 4wt% and 70℃. The foam heights measured immediately after foaming by Ross & Miles method and Ross & Clark method at 6wt%, 60℃ were 18mm and 65mm, respectively. It was concluded that ACAS-6 had a good low foaming cleaning agent.

Chlorine-containing modified polyester polyols were synthesized by two-step condensation reactions. Intermediate was synthesized by the esterification of monochloroacetic acid with trimethylolpropane in the first step. Polycondensation of the intermediate (MCAOs), 1,4-butanediol, and trimethylolpropane with adipic acid was carried out. Two-component polyurethane (PU) coatings were prepared by blending MCAOs and IPDI-isocyanurate. There new flame-retardant coatings showed various properties comparable to other non-flame-retardant coatings. They were superior to flammable coatings from the experimental results showing rapid and 10 to 13 hours of pot-life. Coatings with 30wt% monochloroacetic acid was not flammable by the vertical flame retardancy test.

Ag powder was prepared from by wet chemical reduction method using various reduction agent system involving , (AgCl) and Ag complex ion aqueous solution. The pure Ag powder could be prepared regardless of reaction system but the particle shape and distribution were affected very much according to the kind of reduction agents and reaction systems. The optimum reaction system for the preparation of the silver powder having the uniform particle shape and size distribution was Ag complex ion aqueous solution-reduction agent system and in particular, and as a reduction agent leaded the more uniform particle shape and size distribution

꼬막, 참굴, 바윗굴 및 가리비 등 폐기되는 몇 종의 패각류를 이용하여 칼슘 보강용 식품 첨가제의 원료로써 사용 할 수 있는 고순도의 탄산칼슘을 제조하고자 하였다. 꼬막 패각을 900℃에서 5시간 회화한 회화분의 칼슘 함량이 64.9%로 가장 높게 나타났으며, 가리비 62.5%, 참굴 62.4%, 바윗굴 61.5% 순이었다. 백색도는 가리비 패각 회화분의 경우 81.6-85.8로서 패각류 중 가장 높았다. 꼬막 패각 회화분(Ca 39.92%)에 ammonium chloride process(ACP)와 ammonium nitrate process(ANP)법을 적용하여 제조한 CaCO₃의 Ca 함량은 40.03-40.04%로 높아졌고, ANP법에 의해 제조한 pH조정 시료의 경우가 40.04%로서 가장 높았으며, 이 방법들에 의해 불순물이 거의 대부분 제거되는 것으로 나타났다. ACP법과 ANP법에 의해 제조한 CaCO₃의 백색도는 101.0-101.5로 매우 우수하였으며, 칼슘보강용 식품첨가제로서 사용될 가능성이 충분하다고 판단된다.

The preparation of CaSO4 nanoparticle by vesicles formed spontaneously in cationic OTAC and anionic ADS mixed surfactant solution whose ratio is 0.3/0.7 is investigated. Added electrolytes for preparing nanoparticles reduce vesicle size about 200-300 nm comparing with that of pure vesicle whose size is 700-800 nm by DLS. The core of vesicles has 200 nm size and acts as nanoreactors which same size of monodisperse CaSO4 nanopaticles are formed. Although CaSO4 particles are formed at the outer of vesicles, they are very large and amorphous. The formed particles are identified with XRD analysis after separation due to coinciding with CaSO4 particles.

Highly crosslinked micron-size monodispersed PMMA/PDVB and PS/PDVB particles were prepared using seeded multi-stage emulsion polymerization. PMMA and PS seed particles were synthesized by seeded multi-stage emulsion polymerization and soap-free emulsion polymerization. Then PMMA/PDVB and PS/PDVB particles were obtained using semi-batch type emulsion polymerized using divinyl benzene as a cross-linkable monomer in the presence of seed particles. PMMA particles with size of ca. 730 nm and polydispersity of 1.03 were successfully prepared in this experiment. PS particles with size of ca. 1.5 μm and polydispersity of 1.01 were prepared in this experiment. Highly crosslinked PS/PDVB particles with size of ca. 1.3 μm and polydispersity of 1.00 were obtained.

Reaction conditions and catalysts were investigated for direct CF3I synthesis. Optimum reaction temperature was determined by pyrolysis of CF3H and catalytic reactions. Reactions with changing oxygen concentration were performed. As a result, yield of CF3I increased with decreasing oxygen concentration. Catalytic activity was changed with the weight ratio of the used metal salts. This result was stemmed from the change in the pore size of activated carbon by the metal salts. The optimum reaction conditions were: 600℃, space velocity of 45hr-1, and with 7wt% KF/AC catalyst.

Highly ordered pure-silica MCM-41 materials possessing well-defined morphology have been successfully prepared with surfactant used as a template. The fabrication of mesoporous silica has received considerable attention due to the need to develop more efficient materials' for catalysis, separations, and chemical sensing. The surface modified MCM-41 was used as anadsorbent for biomolecules. Silica-supported organic groups and DNA adsorption on surface modified MCM-41 were investigated by FT-IR and UV-Vis spectrometer, respectively. The use of MCM-41 as the modification of electrode surfaces were investigated electrochemical properties of metal mediators with biomolecules. The modified ITO electrodes increased peak currents for a redox process of [Ru(bpy)3]2+ relative to the bare electrode. The electrochemical detection of DNA by cyclic voltammetry when the current is saturated in the presence of the mediator appeared more sensitive due to a higher catalytic current on the MCM-41 supported electrodes modified by carboxylic acid functional groups. The carboxyl or amine groups on the surface of MCM-41 interact and react with the -NH2 groups of guanine and backbone, respectively. Highly ordered mesoporous materials with organic groups could find applications as DNA sensors.

본 연구에서는 ionomer와 여러 가지의 유기화물로 처리된 MMT type의 clay를 이용하여 ionomer-clay 하이브리드 막을 용융삽입법으로 제조하였다. Twin extruder를 사용하여 clay를 ionomer에 분산시켰으며, 제조된 ionomer-clay 하이브리드에서 clay의 특성피크가 완전히 박리되거나 이동하는 XRD 결과로부터 clay의 층간거리가 넓어지는 고분자의 clay 층간삽입을 확인하였다. Clay의 종류에 따라서 제조된 ionomer-clay 하이브리드 막의 가스투과도, 기계적 물성 및 열적 성질을 측정하였다. ionomer-clay 하이브리드 막은 clay 자체의 도입과 층간거리의 확대로 기체분자의 tortuosity를 증가시켜서 가스투과도를 저하시키는 것을 확인하였다.

An acid cleaning agent (AACA) for aluminum was prepared by blending of sorbitol, n-octanoic acid, MJU-100A, Tetronix T-701, PPA-23, C8-83 and phosphoric acid. With the prepared AACA, degreasing, foam height, etching and derusting tests were carried out. As a result, AACA-4 and AACA-7 showed better cleaning ability than commercial acid cleaning agents.

In order to fabricate a high density sintered body of ITO, nano-sized ITO powders were synthesized by coprecipitation methods. Aqueous solutions of indium and tin salts were mixed and coprecipitated by changing their pH. Coprecipitated ITO powders possessed 20-30 nm crystallite size and a relatively high BET value however, aggregation of particles were occurred. Therefore, a novel recrystallization technique was applied in order to eliminate the aggregates. The recrystallized ITO material consists of a little bit larger needlelike crystals, , and it possesses a higher BET value compared to the plain coprecipitated material . Metastable phase formation and higher content of aggregated particles were observed in the coprecipitated materials. Densification was complete after 5 hour sintering at for the recrystallized powders while densities of the coprecipitated powders were below

Nano sized FeAl intermetallic particles were successfully synthesized by plasma arc discharge pro-cess. The synthesized powders shouted core-shell structures with the particle size of 10-20 nm. The core was metallic FeAl and shell was composed of amorphous Because of the difference of Fe and Al vapor pressure during synthesis, the Al contents in the nanoparticles depended on the Al contents of master alloy.

The bi-materials composed of and its composite reinforced with SiC particles were prepared by ball-milling and subsequent sintering process. The size of powder in Al-Mg/SiCp mixture decreased with increasing ball-milling time, it was saturated above 30 h when the ball and powder was in the ratio of 30 to 1. Both powders mixture and mixture were compacted under a pressure of 350MPa and were bonded by sintering at temperatures ranging from 873K to 1173K for 1-5h. At 873k, the sound bi-mate-rials could not be obtained. In contrast, the bi-materials with the macroscopically well-bonded interface were obtained at higher temperatures than 873K. The length of well-bonded interface became longer with increasing temperature and time, indicating the improved contact in the interface between unreinforced Al-Mg part and Al-Mg/SiCp composite part. The relative density in the bi-materials increased as the sintering temperature and time increased, and the bi-materials sintered at 1173K for 5h showed the highest density.

SPG (Shirasu porous glass) 관형 막이 설치된 회분식 막유화 장치를 사용하여 단분산 칼슘 알지네이트 미립자를 제조하기 위한 막유화 공정변수의 최적조건을 결정하였다. 막유화의 공정변수로는 연속상에 대한 분산상의 비율, 알지네이트 농도, 유화제의 종류와 농도, 안정제 농도, 가교제 농도, 교반속도, 막간 압력차 및 SPG 막의 세공크기로 설정하고, 이들 변수가 제조된 알지네이트 미립자의 입자 크기와 분포에 미치는 영향을 검토하였다. 막유화의 공정변수들 중에서 연속상에 대한 분산상의 비율, 막간 압력차 그리고 알지네이트 농도가 증가할수록 미립자의 크기가 증가하였다. 반면 유화제의 농도, 교반속도 그리고 가교제의 농도가 증가할수록 미립자의 크기가 감소하였다. 세공 크기 2.9mum인 SPG막을 사용한 경우 막유화의 공정변수 조절을 통해 최종적으로 평균 입자 크기 6mum, 크기 분산도 1.1인 단분산 알지네이트 미립자의 제조가 가능하였다.

An emulsion of octadecamidoethylaminoethyl dodecate (which provides softness) and an emulsion silicone oil KF-96 (which provides lubricity) were separately synthesized. Then PP finishing softeners (SSA-7) was prepared by blending of the synthesized emulsions with beef tallow hardened oil (a softness improving agent). PP finishing treatment was carried out with the prepared SSA-7 and PP finishing resin by a one bath method, and several physical properties were tested. As a result, crease recovery, tear strength, softness, lubricity, and bending resistance were all good, indicating that the prepared SSA-7 is a good PP finishing softener.