Naphthoquinone-1,2-diazide-5-sulfonyl[NDAS] derivatives members of quinone diazide compound that are utilizable as photosensitive polymer material were synthesized, and photoresist were prepared by mixing these derivatives with m-cresol novolak(a matrix resin) at various weight ratios. Photosensitive characteristics of photoresist were studied by examining UV and IR, relative sensitivity using a Gray scale method, and SEM to analyze if they can be used as photosensitive material in printing process. Experimental results showed that, by UV, NDAS derivatives were photoconverted and developer-soluble photoresist were produced. The mixing ratio of 1:4(by mass) of NDAS+p-ydroxybenzophenone+sensitizer and m-cresol novolak gave rise to the highest dissolution rate. In addition, photoresist obtained at this condition resulted in the most superior sensitivity and contrast.

Furfurylidene acetophenone derivatives were synthesis, it was measured that hydrolysis made use of UV at a wide pH 1.0~13.0 range in 30% dioxane-H2O solution, 25±1℃. On the basis of general base catalysis, substitutent effect, confirmation of hydrolysis products, it was measured the reaction rate of furfurylidene acetophenone derivatives for the pH change. It maybe concluded that a part was unrelated to pH and another part was in proportion to concentration of hydroxide ion : Above pH 10.0, It was in proportion to concentration of hydroxide ion, a part having no concern with pH was added to the neutral H2O molecule. From the result of measurement the reaction rate, hydrolysis of furfurylidene acetophenone derivatives confirmed to the irreversible first order. Through measurement the substituent effect, It found that reaction rate was accelerated by electron attracting group. Also, From the result of final product, There were furfural and acetophenone. On the basis of these findings, Hydrolysis for the furfurylidene acetophenone derivative was proposed a fitting mechanisms.

Benzoyl styrene derivatives were synthesized by Claisen-Schmidt condensation. It was measured that nucleophilic addition of thiourea for benzoyl styrene made use of ultraviolet spectrophotometery at a wide pH 1.0~13.0 range in 5% dioxane-H2O at 40℃. On the basis of general base catalysis, substitutent effect, and confirmation of addtion reaction product, the nucleophilic addtion kinetics of thiourea for benzoylstyrene derivatives were measured by pH change. It maybe concluded that a part was unrelated to pH and another part was in proportion to concentration of hydroxide ion : Above pH 10.0. It was in propotion to concentration of hydroxide ion, a part having no concern with pH was added to the neutral thiourea molecule. From the results of measurement the reaction rate and there findings, nucleophilic addition of thiourea to benzoylstyrene derivative was proposed a fitting mechanism.

Phenylvinylsulfone derivatives were synthesized by Kirners condition. The structure of these compounds were ascertained by means of ultraviolet, melting point, IR and 1H-NMR spectra. The nucleophilic addtion reaction kinetics of L-cysteiene for phenylvinylsulfone was investigated by ultraviolet spectrophotometery in 40% EtOH-H2O at 25℃. The rate equations which were applied over a wide pH 1.0~13.0 range. On the basis of general base catalysis and confirmation of addtion reaction product, the nucleophilic addtion reaction kinetics of L-cysteiene for phenylvinylsulfone were measured by the pH change. From the result of the above caption, a plausible nucleophilic addtion reaction mechanism of L-cysteiene for phenylvinylsulfone was proposed. These compounds may by used ad the starting materials for the preparation of the engineering plastics or the germicide.

The Hydrolysis kinetics of Benzoyl Styrene Derivatives[I]~[IV] was investigated by ultraviolet spectrophotometery in 5% dioxane-H2O at 40℃. The structure of these compounds were ascertained by means of ultraviolet, melting point, IR and NMR spectra. The rate equations which were applied over a wide pH range (pH 1.0~13.0) were obtained. The substituent effects on Benzoyl styrene derivatives[I]~[IV] were studied, and the hydrolysis were facilitated by electron attracting groups. On the basis of the rate equation and substitutent effect and final product, the plausible hydrolysis reaction mechanism was proposed: At pH 1.0~pH 9.0, not relevant to the hydrogenl ion concentration, neutral H2O molecule competitively attacked on the double bond. By contrary. Above pH 9.0, It was proportional to concentration of hydroxidel ion.

The kinetics of the addition of 1-benzylindole-3-(p-substituted) acetophenone derivatives was investigated by ultraviolet spectrophotometery in 30% dioxane -H2O at 25℃. A rate equation which can be applied over wide pH range was obtained. The Substituent effects on 1-benzylindole-3-(p-substituted) acetophenone derivatives were studied, and addition were facilitated by electron attracting groups. On the base of the rate equation, substituent effect, and general base effect the plausible addition mechanism was proposed : Below pH 3.0, only neutral thiourea molecule was added to the carbon-carbon double bond, and in the range of pH 0.0~14.0, netural thiourea molecule and thiourea anion competitively attacted the double bond. By contrast, above pH 10.0, the reaction was dependent upon only the addition of thiourea anion.

본 연구에서는 효율적인 와류형 미필터 비점오염저감장치를 개발하고 검증하였다. 저감장치의 검증을 위해 오염물질을 이용하여 총 12개 형태(3개 강우강도×2개 상태×2개 단계)의 실험을 진행하였다. 실험은 (1) 모의유입량 산정(강우강도 2.5 mm/hr: 0.00152 m3/s, 강우강도 3.395mm/hr: 0.00206 m3/s, 강우강도 6.870 mm/hr: 0.00326 m3/s); (2) 오염물질 채취 및 투입(4개 입경 사이즈의 25%씩 혼합); (3) 오염물질 제거효율 측정으로 구성하였고, 장치 초기상태와 운영상태로 구분하여 수행되었다. 강우강도별로 분석한 결과, 모든 강우강도에서 초기상태 및 운영상태 모두 오염물질 농도가 감소하였으며, 유입수 대비 유출수 오염물질 제거효율에서도 오염물질을 환경부 기준 80% 이상 제거하는 결과를 보였다. 특히 제거효율이 시간이 지남에 따라 서서히 증가하여 약 90%를 상회하였으며, 초기상태보다 운영상태에서 오염물질 제거효율이 더 높은 것으로 나타났다. 따라서 본 연구에서 개발한 와류형 미필터 비점오염저감장치로 효율적인 비점오염원을 제거할 수 있음을 증명하였다.