이 연구는 유기농 식물성 계면활성제의 화장품 가용화력에 관한 연구이다. 유기농으로 인증된 원료를 사용하여 고순도의 폴리글리세릴-10올리에이트와 폴리글리세릴-10스테아레이트를 합성하여 우수한 가용화력을 가진 계면활성제를 개발하였다. 이 혼합원료의 이름을 Solubil ORG-1300으로 칭하였다. 이 원료의 외관은 엷은 노란색의 페이스트이었고, 특이한 고유의 냄새를 가지고 있었다. 비중은 1.15, 산가는 0.072±0.1로 순도가 높았다. 이 계면활성제의 HLB값은 평균값=15.1로 Griffin식을 사용 하여 계산하였다. 유기농 가용화제가 향과 오일을 어떻게 가용화되는가를 메커니즘적으로 해석하였다. 가용화 실험은 두 가지 오일에 대하여 성능실험을 통하여 육안으로 판별하고 UV분광광도계로 890nm에서 투과도를 측정하여 투명도를 평가하였다. 이 결과 베르가못오일을 가용화하는데 필요한 계면활성제의 농도는 약 2배정도가 필요한 것으로 나타났다. 또한 토코페릴아세테이트를 가용화하는데 필요한 계면활성제의 농도는 약 8배정도가 필요한 것으로 나타났다. pH변화에 따른 가용화력을 실험한 결과 pH=3.5의 산성영역, pH=7.2의 중성영역, pH=11.5의 알칼리성영역에서도 안정화된 가용화력을 보였다. 화장품의 응용분야로써 보습스킨토너 처방을 성공적으로 개발하였다. 이러한 결과를 바탕으로 스킨케어, 베이비 로션, 민감성 혹은 아토피 피부용 화장품에 폭넓게 응용이 가능할 것으로 기대한다.

양이온 에스테르형 계면활성제인 N-2-hydroxy-3-(2-hydroxyacetoxy)proply-N,N-dimethyl dodecylaminium chloride (HPDA)를 합성하였고, FT-IR 과 ¹H-NMR 분석으로 확인하였다. 합성화합물의 묽은 수용액에 대하여 표면장력을 측정하고, 임계미셀농도를 산정하였다. 표면장력은 10-³∼10-² mol/L 농도 범위에서 33～34 dyne/cm 이었고, 표면장력법에 의해 산정한 임계미셀농도는 8.5 ×10-³ mol/L 이었다. 합성 계면활성제인 HPDA와 SLS, TTAB의 유화특성을 시험하였다. 그 결과 HPDA가 우수한 유화제로 확인되었다. 그리고 Ross-Miles 방법으로 기포력과 기포안정성도 측정하였다.

이 연구는 글리시딜 숙시네이트 양이온 제미니 계면활성제의 합성에 관한 것이다. 제미니 계면활성제는 2-메틸 디소디움 숙시네이트와 에피클로로히드린, N, N-디메틸 도데실 아민을 사용하여 합성하였다. FT-IR과 1H-NMR을 통해 물성을 확인하였다. 표면장력과 cmc 측정, 유화력 및 기포력을 각각 주어진 조건을 이용하여 측정하였다. 제미니 계면활성제의 표면장력은 33~34 dyne/cm이며 cmc 값은 10-4~10-3mol/L 였다. 제미니 계면활성제의 유화력은 유기용매에서 더 우수하였고 기포력이 안정한 것을 확인하였다.

Core-Shell polymers of silicone dioxide-styrene system were prepared by sequential emulsion polymerization. In inorganic/organic Core-Shell composite particle polymerization, silicone dioxide adsorbed by surfactant sodium dioctyl sulfosuccinate (EU-DO133L) was prepared initially and then core silicone dioxide was encapsulated emulsion by sequential emulsion polymerization using styrene at the addition of potassium persulfate (KPS) as an initiator. We found that SiO2 core shell of SiO2/styrene structure was formed when polymerization of styrene was conducted on the surface of SiO2 particles, and the concentration sodium dioctyl sulfosuccinate (EU-DO133L) was 0.5~2.0g. The structure of core-shell polymer were investigated by measuring to the thermal decomposition of polymer composite using thermogravimetric analyzer and morphology of latex by scanning electron microscope(SEM).

Silicone dioxide absorbed polyoxyethylene alkylether sulfate (EU-S75D) surfactant was prepared. The core-shell composite of inorganic/organic were polymerized by using styrene(St) as a shell monomer and potassium persulfate(KPS) as an initiator. We studied the effect of surfactants on the core-shell structure of silicone dioxide/styrene in the presence of an anionic surfactant lauryl sulfate(SLS). The structure of core-shell polymer were investigated by measuring to the thermal decomposition of polymer composite using thermogravimetric analyzer(TGA) and morphology of latex by scanning electron microscope(SEM).

Silicone surfactants are widely used in many industrial area because of its thermal stability and lower foaming property. But it has limitation to expand the application because of migration and bubble generation issues when it is mixed with organic surfactant. In this study, epoxy functionalized fluoro-silicone surfactant, perfluoro glycidoxypropyl polyether siloxane(PFGES), was synthesized using hydrosilylation reaction among perfluoro methyl hydrogen siloxane, allyl glycidyl ether, and allyl ployether in order to get lower surface tension, better thermal stability than conventional silicone surfactant, and reactivity with anhydride function.

The hydrosilylation is an addition reaction of Si-H bond to unsaturated double bonds, which provides a convenient mechanism to synthesize poly(dimethylsiloxane-co-methylsiloxane)copolymer having siloxy units in polymer backbone. In this study, Poly(dimethylsiloxane-co-methylsiloxane) copolymer was synthesized through the polymerization reaction of cyclopentasiloxane with poly(methyl-hydrogen) siloxane. Silicone-hydrogen functional group of the poly(dimethylsiloxane-co-methylsiloxane) copolymer was substituted to the alkyl groups by hydrosilylation. And their structure was analyzed with FT-IR, H-NMR and GPC instruments, respectively. Surface tension of the synthetic compounds is increased from 22dyne/cm to 25dyne/cm according to increase additional EO moles. The cmc which was evaluated by surface tension was ranged 10-5 to 10-4mol/L and it was decreased according to increase of dimethyl siloxyl content. HLB number of these surfactants was evaluated 9.5 to 11.5 range. These silicone surfactants is applied to self-emulsifier defoamer and personal care products as surface tension depressant, emulsifier, foam control agent.

These N-acyl amino acid surfactants is normally produced by reaction of acid anhydride with sodium l-glutamate hydrolysates under Schotten-Baumann condition i.e., in alkaline aqueous medium. To avoid using fatty acid chlorides, acylations were also carried out with the fatty acids themselves or with their methyl esters, but unfortunately these methods cannot be used in practice, dodecenyl succinic anhydride, was to be studied for their suitability as acylating agents the production if acylated glutamine hydrolysates. The surface activities including surface tension forming power, forming stability and emulsifying power were measured. The experimental results revealed that the products have a good emulsifying power. Thus, there derivatives will be expected to be used an emulsifying agent for O/W type cosmetic emulsion.

Fluorescent anionic oligo surfactants were synthesized by the condensing products of long chain alkylvinylether-maleic anhydride cooligomers and resorcinol including dye structures. Their various surface activities and dispersing action were studied on the aqueous solution. These oligo surfactants exhibited a remarkable surface tension lowering property, lower foaming and a large dispersing action for the particles of α-copper phthalocyanine blue. Further it was ascertained that the binding of oligo surfactant onto the pigment surface caused the deviation towards lower wavelengths at the maximum fluorescent intensity as compared with aqueous oligo surfactant solutions, These surface active properties of the oligo surfactants may be attributed to rigid and hydrophobic structure of dye groups, besides surface-active groups of alkylether groups and carboxylic group of the anionic oligo surfactants.

미셀반응, 유화중합, 상간이동촉매반응 등에 이용되는 계면활성제가 갖고 있는 문제점을 해결하기 위하여 반응 후 분해되는 분해성 계면활성제를 합성하였다. 케탈이나 아세탈반응에 의하여 이루워진 1,3-디옥솔란 고리가 산수용액 중에서 불안정해 쉽게 가수분해로 계면활성을 띠지 않는 분해성 계면활성제를 합성하였다. 합성된 화합물은 백색결정상태로 얻었으며 수율은 90% 이상이었다. 그리고 이 화합물과 중간생성물은 얇은막 크로마토그래피와 컬럼 크로마토그래피로 분리하여 적외선과 수소핵자기공명 및 원소분석 스텍트라로 그 화합물들의 구조를 확인하였다.

All the activities and physical properties including surface tension' foaming power, foam stability, emulsifying power, dispersion effect of 3-(N, N-dimethyl N-alkylammonio)-2-hydroxyY-1-propane sulfonate (HSB)류와 3-CN-alkylamidopropyl-N,N-dimethylamm-onjo)-2-hydroxy-1-propane sulfonate (APSB) aquous solution were measured and critical micelle concentration was evaluated. Their cmc of hydroxy sulfobetaine derivatives evaluated by the surface tension method was 1.0×10-3~1.0×10-4 mol/l, and surface tension of the aquous solution was decreased to 27~38dyne/cm. The experimental results for foaming power, foam stability, emulsifying power in liquid paraffin showed a good surface active properties, especially, dispersion effect in ferric oxide exhibited some efficient surface active properties, and then it would be expected to application as detergent and dispersion agent.

In order to review industrial application of amphoteric surfactants, new types of hydroxy sulfobetaine, 3-(N, N-dimethyl N-dimethyl-N-alkylammonio)-2-hydroxy-1-propane sulfonate and 3-(N, N-dimethyl N-acylammonio)-2-hydroxy-1-propane sulfonate were prepared by the reaction of quaternized sodium 1-chloro-2-hydroxy-3-propane sulfonate with N, N-dimethyl-N-alkylamine and N, N-dimethyl N-acylamido propylamine that have a straight chain radical of 12, 18 carbon atoms respectively in the presence of alkali catalyst. All the reaction products could be separated by means of column and thin layer chromatography, and the yields of all products ranged in 85~90%, the structure of them could be confirmed from IR and 1H-NMR spectra.

Four novel amphoteric surfactants of N-alkoxyethylcarboxybetaine series were synthesized via Schotten-Baurnman reaction between four alkyl chlorides contaning 10, 12, 14 and 16 carbon atoms in their N-alkyl group and dimethylaminoethanol to give the intermediate products, alkoxyethyldimethylamine, Quaternization of these intermediates was permitted to form 2-(alkoxyethyldimethylarnmonio) acetates, whose structures were identified by elemental analysis. IR spectrophotometry and 1Hnmr spectrometry. The yield of the final products was shown in the range of 74~77% based on the yield of the intermediate products, Surface tension of the aqueous solution of the final products was measured. and the critical micelle concentrations(cmc) were shown in the range of 2.82×10-3~2.67×10-6mol/l, and the surface thension at erne was 35~43dyne/cm. Cmc was lowered gradually by the increase of carbon numbers in N-alkyl ether containing group. The isoelectric point was shown in the range of 4.08~6.03. It showed a tendency to lean toward the acidic site and its range was broadened as increase of the hydrophobic group length. A linear relationship between log erne and the number of carbon atoms(N) in the hydrophobic alkyl chain was shown in the relative equation of log cmc=2.49-0.50N.

N-alkyl carboxy pyridinium chlorides such as N-lauryl carboxy-pyridinium chloride, N-myristyl carboxy pyridinium chloride, N-cetyl carboxy pyridinium chloride and N-stearyl carboxy pyridinium chloride were synthesized by the reaction of nicotinic acid and isonicotinic acid with long chain alkyl chlorides, and N-alkyl pyrinium carboxylates such as N-lauryl pyridinium carboxylate, N-myristyl pyridinium carboxylate. N-cetyl pyridinium carboxylate and N-stearyl pyridinium carboxylate were prepared from N-alkyl carboxy pyridinium chlorides. These reaction products could be separated by both column chromatogrphy, and paper chromatography, and there dissociation constants of N-alkyl pyridinium carboxylates were found to pKa 1.0×1013~6,31×1014

Mesoporous silica was prepared from hydrothermal synthesis using gel mixture of tetraethylorthosilcate (TEOS) as silica source and cetyltrimethylammonium bromide (CTMABr) as a surfactant. In the optimum synthesis cause, molar ratio of template and silica changed. The surface and structure properties of mesoporous silica were determined by XRD, SEM, TEM and BET. Also, surface potential of mesoporous silica was measured using zeta potential. N2 adsorption isotherm characteristics, including the specific surface area (SBET), total pore volume (VT), and average pore diameter (DBJH), were determined by BET. As a result, SBET of 100 m² /g～1500 m² /g was determined from the N2 adsorption isotherm. Also, the average pore diameter was 2 nm∼4 nm. Mesoporous silica's surface potential of minus charge was determined from zeta potential.