Silicone dioxide absorbed polyoxyethylene alkylether sulfate (EU-S133D) surfactant was prepared. Core-shell polymers of inorganic/organic pair, which have both core and shell component, were synthesized by sequential emulsion polymerization using Acrylate as a shell monomer and potassium persulfate (KPS) as an initiator. We found that when Acrylate core prepared by adding 2.0 wt% EU-S133D, silicone dioxide/Acrylate core-shell polymerization was carried out on the surface of silicone dioxide particle without forming the new silicone dioxide particle during acrylate shell polymerization in the inorganic/organic core-shell polymer preparation. 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).

본 연구에서는 용매로 N-methyl-2-pyrrollidone을 사용하여, 상전환 방법으로 carboxylic acid를 함유한 음이온성 한외여과막을 제조하였다. 첨가제, 제막조건 및 운전조건에 따른 투과 특성을 알아보았다. Bovin serum albumin (BSA) 수용액의 pH에 따른 상대투과유속을 측정하여 fouling형성에 따른 투과 특성의 변화를 살펴보았다. 투과 특성은 막 제조환경과 투과 공정에 영향을 받았다. 이온교환용량과 측정 온도가 증가할수록, 그리고 BSA의 등전점으로부터 수용액의 pH값이 멀어질수록 상대투과유속이 증가하였다.

The inorganic-organic composite particles with core-shell structure were polymerized by using styrene and potassium persulfate (KPS) as a shell monomer and an initiator, respectively. We studied the effect of surfactants on the core-shell structure of silicone dioxide/styrene composite particles polymerized in the presence of sodium dodecyl sulfate(SDS), polyoxyethylene alkylether sulfate (EU-S133D), and at none surfactant condition. We found that SiO2 core / polystyrene(PS) shell structure was formed when polymerization of styrene was conducted on the surface of SiO2 particles, and the concentration SDS and EU-Sl33D was 8.34×10-2mole/L. The core-shell structure was confirmed by measuring the thermal decomposition of the polymer composite using thermogravimetric analyzer (TGA), and the morphology of the composite particles was characterized by transmission electron microscope (TEM).

The core-shell composite particles 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 core-shell structure of silicone dioxide/styrene in the presence of an anionic surfactant sodium lauryl sulfate (SLS) and polyoxyethylene alky lether sulfate (EU-S133D). We found that when SiO2 core/PSt shell polymerization was prepared on the surface SiO2 particle, to minimize the coagulation during the shell polymerization, the optimum conditions were at concentration of 2.56×10-2mole/L SLS. The structure of core-shell polymer was confirmed by measuring the thermal decomposition of polymer composite using thermogravimetric analyzer and morphology of core-shell polymer particles by transmission electron microscope (TEM).

지하수나 폐수 등에 포함된 독성을 가진 음이온류나 양이온류 등의 유독물질을 경제적으로 처리하는데 탁월한 분리기능을 가진 것으로 알려진 전기투석공정에 사용하기 위해 음이온 교환 복합막을 제조하여 그 전기화학적인 특성을 조사하였다. 다양한 조성의 vinylbenzylchloride (VBC)와 divinylbenzene (DVB) 그리고 α,α-azobis(isobutyronitrile) (AIBN)으로 이루어진 단량체 용액에 다공성 지지체인 poly(ethylene) (PE)을 함침한 후 열중합 가교시켜 poly(VBC-DVB)/PE 복합막을 생성한 다음 trimethylamine(TMA)과 acetone을 이용해 음이온 교환기(-N + (CH3)3)를 함유하는 복합막을 제조하였다. 음이온 교환막 제조시 VBC/DVB의 비율과 TMA/Acetone의 비율에 따른 막의 함수율, 이온교환용량(IEC) 및 전기저항을 조사하였다. 그 결과 제조된 막들은 사용된 PE지지체의 얇은 막두께에 기인하여 아스톰사의 상용화 음이온 교환막(AMX)보다 높은 IEC와 낮은 전기저항 및 낮은 함수율 등을 나타내는 것을 확인할 수 있었다. 본 실험에서 제조된 복합막은 저렴한 제조비용과 우수한 전기화학적 특성으로 정수 및 폐수처리를 위한 전기투석공정에 충분히 적용될 수 있음을 알 수 있었다.

난의 종류별로 심비디움, 심비디움 교배종, 덴팔레, 온시디움, 호접란, 그리고 나도풍란의 음이온 발생량을 조사하였으며, 심비디움 20, 40, 60, 80%와 심비디움 교배종 25, 50, 75, 100%의 투입율에 따른 음이온 발생량의 변화를 조사하였다. 그 결과 심비디움 332개 /cm3, 심비디움 교배종 323개/cm3로 심비디움 속이 가 장 발생량이 많았으며, 그 다음이 덴팔레 250개/cm3, 온시디움 203개/cm3, 나도풍란 119개/cm3, 호접란이 77개/cm3 순이었다. 투입율 증가에 따라 심비디움은 40%, 심비디움 교배종은 75%까지는 음이온 발생량이 증가하였으나, 그 이상 투입율에서는 다소 감소하는 경 향이었다. 따라서 식물 종류별로 음이온 발생량을 상호 비교하기 위해서는 식물 투입율이 40% 이하가 적절하 며, 상대습도 등을 감안할 경우 약 30% 정도가 가장 적절한 것으로 보인다.

The core-shell latex particles were prepared by sequential emulsion polymerization using alkyl methacrylate as a shell monomer and potassium persulfate (KPS) as an initiator. We study the effects of core-shell structure of calcium carbonate/alkyl methacrlyate in the presence of an anionic surfactant sodium lauryl sulfate (SLS) and polyoxyethylene alkyl ether sulfate (EU-S133D)). 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 transmission electron microscope (TEM).

The rheological properties and surface tensions of polymer solutions and polymer-surfactant mixed solutions were investigated. The polymers used in this study were a homopolymer of acrylic acid crosslinked with an allyl ether of pentaerythritol, an allyl ether of sucrose, or an allyl ether of propylene (CARBOMER), acylate/C10-30 alkyl acylate crosspolymer (AAAC), and ammonium acryloydimethyltaurate/VP copolymer (ADTV). A solubilizing agent PEG-40 hydrogenated castor oil (HCO-40) and an emulsifying agent polyoxyethylene (20) sorbitan monostearate (POLYSORBATE 60) made the micelles intervening between AAAC polymers, resulting in the increase of viscosity. However, HCO-40 made this behavior over the wider range of surfactant concentration than POLYSORBATE 60. From the view point of surface tensions in the same range of surfactant concentration, AAAC/HCO-40 solution showed the area of increasing surface tension with surfactant concentration in contrast to the AAAC/POLYSORBATE 60 solution showing no increasing area.

Ozone has become a significant pollutant not only outdoors but also indoors. The ozone emission test was conducted for the sum of forty five air cleaners selected in the online shops and department stores. Negative ion emission test was also conducted for the selected fifteen ones which had the function to generate negative ions. Filter-type and complex type air cleaners emitted ozone less than 0.05 ppm, the standard of indoor ozone emission of air cleaner. Wet type ones emitted no ozone. In the case of ionizer type, 66.7% in the nine ones emitted ozone about 1.4~10 times larger than 0.05ppm. Most of air cleaners used a pin corona discharge emitted large amount of ozone. Those which used carbon fiber emitted little ozone in spite of generating a lot of negative ions.

Cs 이온에 대해 선택성을 갖는 ferrocyanide-음이온 교환수지를 제조하여 모의 제 염폐액 내에 존재하는 Cs 이온에 대한 흡착실험을 수행하였다. 제조된 이온교환 수지가 citric acid를 주제염제로 하는 제염폐액 내에 존재하는 Cs+ 이온에 대한 흡착능력은 상용 양이온교환수지에 비해 4배 이상 효과적인 것으로 나타났다. 모의 제염폐액과 선택성 이온교환수지를 접촉시킨 후 360분이 경과하면 금속이온에 대한 흡착반웅이 평형에 도달하였다. 본 연구범위에서 Co 이온농도가 필요이상 증가하게 되면 Cs 이온의 흡착율은 감소하였다. 과산화수소와 히드라진을 사용한 선택성 폐 이온교환수지의 재생실험 결과 전기중성화조건을 만족시키기 위해 Cs 이온이 수지로부터 용출됨을 확인하였고 열화없이 재 사용가능성을 확인하였다.

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.

The interaction between anion and zwitterionic surfactants was investigated by means of surface tension, NMR spectroscopy, and fluorescence studies. These systems are N-tetradecyloxymethyl-N,N-dimethyl betaine (C14, TDB), N-octadecyloxymethyl-N,Ndimethyl betaine (C18, ODB), and sodium dodecylethoxy sulfate (SDE). These systems show a composition dependency in micellar properties. When the molar fraction of TDB and ODB was about 0.6, the cmc values of these systems showed minima, whereas the solubilized amount of a water insoluble dye, NMR line width showed maxima. These changes comes from the intramolecular complexes formed in the mixed micelles. The complexes are due to the electrostatic interaction of oppositely charged head groups of betaine and sodium dodecylethoxy sulfate. A comparison of betaine and SDE alkyl methylene group line widths to those of n-methyl group indicates that the interior of the micelle in the restricted region is more immobile than the head group.

상전환 방법으로 제조된 음이온 성 Poly(his[4-(3-aminophenoxy)phenyl]sulfone pyromellite)imide(ACPI) 한외여과막의 순수 투과유속과 용질 배재도 측정치로 투과성능을 연구하였다. ACPI 한외여과막의 투과성능은 캐스팅 용액의 조성과 막 제조 및 측정조건에 영향을 받았다. Bovine serum albumin (BSA) 용액을 pH 2.5-9.0 상태에서 ACPI 한외여과 막의 상대투과유속과 membrane filtration index (MFI) 측정한 결과 BSA의 등전점에서 멀어 질수록 상대투과유속은 증가하고 막 오염정도를 나타내는 MFI는 감소하였다. 또한, 친수성인 ACPI 한외여과막의 이온교환용량(IEC)이 증가할수록 상대투과유속은 증가하고, MFI는 감소하였다.

피리디니움 (pyridunium) 그룹을 포함한 음이온교환막의 제조 및 전기화학적 특성 평가를 수행하였다. 실험 결과, 제조된 피리디니움 음이온교환막은 상용막과 대등한 전기저항 (3.0 Xicm2>, in 0.5 mol dm-3 NaCl) 및 높은 이온선택도 (Cl- 이온수송수 약 0.97)의 우수한 전기화학적 특성을 나타내었다. 또한 피리니디움 그룹을 함유한 음이온교환막에서의 물분해는 상용막 (AM-1, Tokuyama Corp., Japan)에 비해 동일한 전류밀도 하에서 약 100배 내지 1000배 가량 낮게 측정되었는데 이는 4차 아로마틱 피리디니움 그룹의 공명효과 (resonance effect)가 이온교환기의 분자구조적 안정성에 영향을 미쳤기 때문으로 사료되었다. 또한 피리디니움 음이온교환막의 전기투석 특성이 semi-pilot 스케일에서 평가되었다.

Oligomer type anionic surfactants(RmM-Na or RmD-Na were synthesized from C8~C16 long chain alkylvinylether and maleic anhydride (or maleic diethylether). And also their fluorescent anionic surfactants (RmF- Na) were obtained from alkali neutralization which opens the lactone ring of the condensing materials produced by maleic anhydride alkylvinylether copolymer and 3-aminophenol. The measurement results for the surface active properties of water soluble oligomer type anionic surfactants with fluorescent structure (RmF-Na) exhibited a remarkable surface tension lowing property, foam breaking property, and a ernulsing power.

A proposed method of determining the composition of mixed micelles in equilibrium with monomer of known composition is described. The systems were sodium α-sulfonated dodecanoyl ethyl esther (α-SR12Et) or sodium dodecyl sulfate(SDS)-polyoxyethylene 23 lauryl ether (Brij 35) un water and in 0.1M sodium chloride solution at 25℃. This technique applies the Gibbs-Duhem equation to the mixed micelles, which is treated as a pseudophase. This proposed methodology, which needs only critical micelle concentration data as a function of monomer composition, is applied to an anionic/nonionic surfactant pair. The calculated monomer-micelle equilibrium is found to be very similar to the much-used regular solution for nonideal systems.

Density, viscosity, conductance, dye solubility and carbon-13 nmr studies were performed in aqueous solution of three disodium 4-n-alkyl-3-sulfonatosuccinate anionic surfactant at 20℃. The cmc values were 0.14 mol/l for the disodium-4-n-octyl-3-sulfonatosuccinate(R8)S), 0.041mol/l for the disodium-4-n-decyl-3-sulfonatosuccinate(R10S), and 0.018mol/l for the disodium-n-dodecyl-3-sulfonatosuccinate 〈R12S). The aggregation numbers determined viscometrically and conductimetrically were 28 for R8S, 48 for R10S, and 67 for R12S. The volume changes upon micellization were 8.9cm3/mol for R8S, 9.5cm3/mol for R10S, and 10.1cm3/mol for R12S. Binding constants for the dye pada to the micelles and the fractions of unbound counter-ion were also obtained. The two polar heads with their carbon linkage were likely in an aqueous environment in the R8S micelles with the micelles themselves being spherical.