저 분자량(Mw=1970)의 poly(styrene)(PS)와 poly(vinylmethylether)(PVME)의 블렌드를 열 산화시킬 때 저 분자량의 PS의 첨가량이 증가할수록 유도기간이 증가하며 열 산화속도는 감소함을 알 수 있었다. 열 산화과정 동안 저 분자량 PS와 PVME 블렌드는 상 분리를 보이지 않았다. 저 분자량을 갖는 PS와 PVME 블렌드에서 PVME의 산화 속도는 높은 분자량을 갖는 PS와 PVME 블렌드에서 PVME의 열 산화 속도보다 훨씬 느려짐을 보였다.

Cinnamoyl ester(PGEFC) of poly(phloroglucinol-formaldehyde) glycidyl ether which has photosensitive functional group was prepared to apply to photoresist. Photosensitivity of PGEFC was estimated by the solubility difference in organic solvent before and after exposure to light. The yield of residual film was calculated by immersing the sample-coated quartz plates in the solvent which was used in coating. The yield of the residual film which was closely related to the sensitivity of the film, was affected by the degree of polymerization of the backbone resin, sensitizers and their concentration. The sensitivity was depended upon the degree of polymerization. Most of effective sensitizer for PGEFC among the sensitizers was 2, 6-dichloro-4-nitroaniline.

Durable softening water repellents such as PODCWs were prepared by blending cationized compound of poly(octadecyl methacrylate-co-2-diethylaminoethyl methacrylate), of which synthetic methods were reported in the previous paper, activated polythylene, waxes, and emulsifiers. Water repellency of prepared PODCWs was measured by performing water repellent finish to various fabrics, PODCWs showed a good water repellency for P/C blended fabrics and their repelling tendency was in the order of P/C blended fabrics〉cotton fabrics〉nylon taffeta. The initial water repellencies of PODCW-1 and PODCW-2 were 100 and 100- points, respectively, for P/C blended fabrics. And also, PODCW-1 and PODCW-2 were confirmed as durable water repellents with the results of making little difference of water repellency as ±5 point after and before washing.

In this study, sensitizing dye was prepared by the reaction of 2-methyl-3-sulfopropyl-4, 5-naphthothiazolium(inner salt) with triethyl orthoformate in the presence of triethylamine. The product was identified by using various analytical tools such as Elemental analyzer, IR spectrophotometer, UV-Vis spectrophotometer, 1H-NMR spectrometer, TGA and DSC. Therefore, it was concluded that naphthothiazolo carbocyanine dye can be used as red-sensitizing dye for the spectral sensitization of photographic emulsion.

박과식물(科植物) 종실(種實)에는 총지질량(總脂質量)이 21.9~50.7%의 범위(範圍)로 비교적(比較的높았으며, 특(特)히 박, 하늘타리의 경우는 41.9%와 50.7%로 조사(調査)한 시료(試料)중에 제일 높았으며, 또 모든 시료(試料)가 약(約) 98% 이상(以上)의 중성지질(中性脂質)을 함유(含有)하고 있었다. 호박, 수세미오이, 수박, 참외, 오이 및 박종자(種子)의 총지질(總脂質)에는 리놀산(酸)의 함량(含量)이 제일(第一) 많아 56.8~84.0%이였으며, α-리놀레산(酸)의 함량(含量)은 0.0~0.6%로 매우 적었고, 올레산(酸)이 주성분(主成分)인 모노엔산(酸)과 팔미트산(酸)이 대부분(大部分)인 포화지방산(飽和脂肪酸)은 그 함량(含量)이 각각(各各) 5.7~22.2%와 9.9~20.6%로 시료(試料)에 따라 심한 차이(差異)를 보였다. 하늘타리 종자(種子)의 총지질(總脂質)에는 C18:2Ω6과 9c.11t.13c-C18:3(Punicic acid)이 40.5%와 34.9%로 주요(主要) 성분(成分)이였고, 그 다음으로 C18:1Ω9가 13.8% 함유(含有)되어 있었으며, 그러나 9c/11t.13t-C18:3(α-eleostearic acid)는 2.2%에 지나지 않았다. 한편 여주의 경우(境遇)에는 9c.11t.13c-C18:3이 66.9%로 제일(第一) 많았으며, 그 다음으로 C18:1Ω9와 C18:1Ω6이 17.7%, 10.4% 각각(各各) 함유(含有)되어 있었고, 하늘타리에 많이 함유(含有)되어 있는 9c.11t.13c-C18:3는 9t.11t.13c-C18:3(β-eleostearic acid)와 함께 1.1% 정도(程度)로 소량(少量) 포함(包含)되어 있었다. 9c.11t.13c-C18:3와 9c.11t.13t-C18:3와 같은 conugate trienoic acid는 여타시료(餘他試料)에서는 전연 검출(檢出)되지 않았다. 하늘타리와 여주의 종자유(種子油)의 극성지질(極性脂質)에는 이틀의 중성지질(中性脂質)에 다량(多量)으로 존재(存在)하는 conjugate trienoic acid가 극(極)히 소량(少量)밖에 존재(存在)하지 않는 것은 매우 특징적(特徵的)이며, 포화지방산(飽和脂肪酸)이 중성지질(中性脂質)(9.9~20.6%)에 비(比)하여 극성지질(極性脂質)(25.0~29.4%) 에 보다 많이 함유(含有)되어 있다는 사실(事實)을 나머지 시료(試料)에서 공통적(共通的)으로 찾아볼 수 있었다. 박과식물(科植物) 종자(種子)는 리놀산(酸)을 많이 함유(含有)하고 있는 군(群)과, 9c.11t.13c-C18:3 및 9c.11t.13t-C18:3와 같은 conjugate trienoic acid를 가진 군(群)으로 대별(大別)할 수 있었다.

The liposomes have been developed in many drugs and cosmetics fields. The liposomes prepared with main compounds of the intercellular lipids and lecithin. Amphiphile nonionic surfactants used for (PEG) n-sitosterol(n=5), diethanolamine cetylphosphate. The effect of gelation for liposomes have been on swelling reaction which have been mixed phospholipid with polyol-group at the high temperature. There were very good encapsulated properties of the active ingredients whether hydrophilic-group(magnesium ascorbyl phosphate, allantoin, sodium hyaluronate) and hydrophobic-group(vitamin-E acetate, vitamin-A palmitate). Optimum condition of liposomes were passed five times in the microfluidizer(700bar), wetting reaction temperature was at 95±5℃ for a hours. Particle size distribution of the vesicles should be within range 50-560nm(mean 200nm). The stability of liposomes for the course of time was stabilized for six months at 45℃. Application of the cosmetic was prepared moisturizing cream with liposomes of the phospholipid base.

We have prepared diamine-benzoquinone polymer which was known to excellent water proofing, high adhesion strength and good anti-corrosive effect, and have investigate with the possibility of application as a high performance resin for coatings. First of all, the reactivity of diamine-benzoquinone has been described an example of polymer reaction with research trend. The polymer reaction was divided into the polymerization with several diamine-benzoquinone and urethane group. The synthetic resin was shown a high solubility. In case of polymer containing urethane, water absorption content, water proofing and mechanical properties were controlled with the content, water proofing and mechanical properties were controlled with the content of quinone. It was shown that an use of choice was a possible result for various coatings. Diamine-quinone polymer can be used as a new resin for coatings. In addition, the polymer containing a functional group was shown a useful applicability as a high performance resin.

The ultraviolet blocking agents used to skincare are largely classified ultraviolet scattering agent and ultraviolet absorbent agents. There are UVC, UVB, and UBA in ultraviolet ray(UV) showing shorter wavelength than visible light. Both visible light and UVA give rise to 1st dark-skinned phenomena. On exposure of the skin to UV, phenomena of skin variation are termed sunburn or suntan. There are chronic and acute adverse reactions in skin response to UV. The latter is caused by UVB, which has mainly effects on the skin. But lately due to destruction of ozone layer, UVA has more serious irritation on the skin than UVB. In this paper spectrometric properties of UV absorbent agents such as PABA, octyl-PABA, Urocanic acid, and 2-hydroxy-4-methoxy benzophenone in vitro have been investigate. As results, it was found that the three fomer were more suitable than the last. UV scattering measurements on the sample used inorganic pigments showed that pigments containing titanium dioxide had a better scattering effects than the inorganic pigments such as Fe2O3, Al2O3, etc.

The influences of fluorophor, scatterer, absorber in turbid material by light scattering were interpreted for the scattered fluorescence intensity and wavelength, it has been studied the molecular properties by laser induced fluorescence spectroscopy. It has been found that the effects of optical properties in scattering media by the optical parameters(μs, μa, μt). The value of scattering coefficient μs is large by means of the increasing particles of scatterer, it has been found that the slope decays exponentially as a function of distance from laser source to detector. It may also aid in designing the best model for oil chemistry, laser medicine and application of medical engineering.

The Kinetics velocity for hydrolysis reaction of vanillylidene imine derivatives has been measured by ultra-violet ray spectrophotometer in 20wt% dioxane-H2O at 25℃. It was measured the reaction rate Constant of vanillylidene imine derivatives that can be applied widely following to pH-change at 25℃. Final products that hydrolyzed the vanillylidene imine certified in vanillin and aniline derivative, and the effect of substitution radical that has affected on hydrolysis reaction was largely promoted to reaction rate by electron attrating group in acidity and electron donoring group in basic. From the results of rate constant to hydrolysis reaction, substituent radical effect and final products. It has certified the hydrolysis reaction mechanism of vanillylidene imine derivatives.

Octadecyltrimethylammonium-TCNQ(1:1) complex was synthesized by the reaction of LiTCNQ with octadecyltrimethylammonium bromide and the reaction product was identified with FT-IR and UV/Vis spectroscopies. In order to prepare the LB films, π-A isotherm characteristics of octadecyltrimethylammonium-TCNQ(1:1) complex were investigated. The LB films of octadecyltrimethylammonium-TCNQ(1:1) complex were formed on various substrates and the formation of ultrathin films of octadecyltrimethylammonium-TCNQ(1:1) complex was confirmed by using FT-IR and UV-Vis spectroscopies.

Ultra-thin films of hexyltriphenylphosphonium-TCNQ(1:1) complex were formed on various substrates by Langmuir-Blodgett technique, where hexyltriphenylphosphonium-TCNQ(1:1) complex was synthesized by attaching hexyltriphenylphosphonium group to TCNQ. The reaction product was identified with FT-IR, and UV-Vis absorption spectroscopies. The formation of ultra-thin films of hexyltriphenylphosphonium-TCNQ(1:1) complex was confirmed also by FT-IR, and UV/Vis absorption spectroscopies.

This project has been worked out for isolation of EPA-producing bacteria from marine source of sea water, sea sediment and intestinal contents eviscerated from some red-muscle fish such as mackerel, horse-mackerel and spike fish. The samples were precultured on the media of PPES-II glucose broth and then pure-cultured on Nutrient agar and P-Y-M glucose. Lipids extracted from those bacterial mass collected by centrifugation were analysed in terms of lipid class and fatty acid composition. The results are resumed as follows : 1. 112 strains from sea water and 76 strains from sea sediment were tested for their EPA producing capability, but both strains of (SA-67 and SA-91) from the former and four strains(SS-35, 37, 51 and 71) from the latter have been proved to produce EPA above the level of 2% of total fatty acids. The strains such as GS-11, 29, 31, HM-9, 29, B-18, 33, 107, YL-129, 156, 203, 77, 104 and 256 which were isolated from fish intestinal contents, have also produced EPA at higher level than 2% of total fatty acids. 2. Contents of total lipids extracted from the cultures of these strains grown at 25℃, range from 2.8% to 6.9% (on dry weight %), and they are mainly composed of polar lipids(40.9~52.9%) such as phosphatidyl glycerol(+cardiolipin)(?) and phosphatidyl ethanolamine (33.8~40.0%), with smaller amount of free fatty acid (11.2~20.2%). 3. EPA was isolated from a mixture of fatty acid methyl esters obtained from the lipid of each strain by HPLC in silver-ion mode and was identified by GC-Mass spectrometry. 4. The strains of SW-91, GS-11, GS-29, HM-9, B-18 and YL-203 grown at 25℃ have a level of 5% EPA in their total fatty acids, and the GS-11 and HM-9 strains show a tendency of increase in the EPA level with an increase of growth temperature.

Diazotization of 2-Amino-5-nitrophenol was Synthesized by the direct diazotization method. The diazonium salts are usually stabilized in the from of double salts. The double salts of zinc chloride are the Commonest, and the double salt method is Specially applicable to the yield-up of coupling. The azo dye(2-naphthol-1-(2'-diazo-5'-nitrophenol)) is Converted into a chromium Complex by heating(100℃) with chromic formate, and DMF. The removal of inorganic salts from dyestuffs was performed in DMF solvent. This effect was more pronounced. From these results, It was obtained to liquid dyestuffs of metal complex with High fastness and high adsorption.

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 rate constant of Nucleophilic addition of sodium thiophenoxide to nitrone were determined by UV Spectrophotometry and a rate equation which can be applied over wide pH range was obtained. Base on the rate equation, general base effect, substituent effect and final product, plausible mechanism of addition reaction have been proposed. Blow pH 3.0, the reaction was initiated of thiophenol, and in the range of pH 3.0~10.0, proceeded by the competitive addition of thiophenol and thiophenoxide anion. Above the pH 10.0, the reaction proceeded through the addition of a thiophenoxide anion.

The rate constant of the nucleophilic addition of 1-propanethiol to α-phenyl-N-iso-propylnitrone derivatives were determined at various pH and a rate equation which can be applied over wide pH range is obtained. Final product of the addition reaction was α-thiopropyl-p-phenylbenzylideneamine. Base on the rate equation, general base effect, substituent effect and final product, plausible mechanism of addition reaction have been proposed. Below pH 3.0, the reaction was initiated by the addition of 1-propanthiol, and in the range of pH 3.0-10.0, proceeded by the competitive addition of 1-propanethiol and propanethiolate. Above the pH 10.0, the reaction proceeded through the addition of propanethiolate.

1, 3-Di(2-dodecanoylaminoethyl)-2, 7-dioxy-1, 3, 6, 8-tetraazacyclodecane[DDTD] and sorbitan monostearate(SMS) were synthesized as a main component for softner. O/W type softner(DSA) was prepared by blending of DSA, SMS, polyoxyethylene(10) castor oil, glyceryl monooleate, and polyoxyethylene(7) stearyl ether. After treatment of DSA to all cotton fabrics, the physical properties such as tear strength, crease recovery, and flexing abrasion resistance were measured. As a result of the measurement, DSA was found to be durable softner with good softness.

1, 3-Di(dodecanoyl)-2, 7-dioxy-6, 8-di(2-hydroxyethyl)-1, 3, 6, 8-tetraazacyclodecane(DDDT) and pentaerythritol monostearate(PMS) were synthesized as a main component for softner. O/W type softner(DPSA) was prepared by blending DDDT and PMS with polyoxyethylene(10) castor oil, polyoxyethylene(20) oleyl ether, and polyoxyethylene(10) monolaurate. After treatment of DPSA to all cotton fabrics, the physical properties such as tear strength, crease recovery, and flexing abrasion resistance were measured. As a result of the measurement, DPSA was proved to be durable softner with good softness.