• 대한화학회지
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• 제45권1호
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• pp.7-13
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• 2001

양이온 계면활성제인 TTAB(tetradecyltrimethylammonium bromide)의 수용액에서 benzenesulfonate 음이온과 유도체($C_6H_5SO_3^-, p-$CH_3C_6H_4SO_3^- 및 $p-C_2H_5C_6H_4SO_3^-$)들의 가용화 현상을 UV/Vis 분광광도법을 이용하여 연구하였다. 온도의 변화에 따른 가용화상수($K_s$)의 변화를 측정하고 분석하였으며, 또한 가용화에 영향을 미치는 n-펜탄올과 NaBr의 효과에 대하여 조사하였다. 이러한 첨가제는 $K_s$와 CMC 값을 동시에 큰 폭으로 감소시키는 경향을 나타내었으며, 측정한 In$K_s$ 값은 InCMC 값에 대하여 일차함수의 관계를 나타내었다. 그리고 열역학적 고찰을 위하여 온도에 따른 $K_s$ 값의 변화로부터 여러 가지 열역학 함수값(${\Delta}G^0_s$, ${\Delta}H^0_s$ 및 ${\Delta}S^0_s$)을 계산하고 분석하였다.

• 대한화학회지
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• 제44권3호
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• pp.177-183
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• 2000

CTAB/TTAB 혼합계면활성제 용액에서 Phenoxide 음이온의 가용화를 UV/Vis분광광도법을 이용하여 연구하였으며, 혼합계면활성제의 몰분율조성($$\alpha_{CTAB}$)에 따른 가용화상수(Ks)와 임계마이셀농도(CMC)의 변화를 측정하고 분석하였다. 또한 Phenoxide 음이온의 가용화에 영향을 미치는 n-펜탄을과 NaBr의 효과에 대하여 조사하였으며, 이러한 첨가제는 $K_s$와 CMC 값을 큰 폭으로 감소시키는 경향을 나타내었다·열역학적 고찰을 위하여 $K_s$ 값의 온도에 따른 변화를 측정하였으며, 온도에 따른 $K_s$ 값의 변화로부터 Phenoxide 음이온의 가용화에 대한 열역학 함수값(${\Delta}G^0_s$, ${\Delta}H^0_s$ 및 ${\Delta}S^0_s$)을 계산하였다·그 결과 ${\Delta}G^0_s$와 ${\Delta}H^0_s$은 측정한 범위 내에서 모두 음의 값을 그리고 ${\Delta}S^0_s$ 은 모두 양의 값을 나타내었다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제15권1호
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• pp.66-72
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• 2010

The partitioning tracer method is to estimate the residual saturation of nonaqueous phase liquid (NAPL) in soils by analyzing tracer's retardation induced by the reversible partitioning of tracer with NAPL. This study is to estimate the residual diesel saturation in soils using the partitioning tracer method. Two-dimensional soil box was used to represent the 2-dimensional flows of groundwater and tracer solution in the saturated aquifer, and the soil box was filled with soil and then saturated with water. The residual diesel saturation was induced in saturated soil, and the partitioning tracer method was applied. The results from batch-partitioning experiment indicated that the diesel-water partitioning was linear with respect to tracer's concentration, and the partition coefficient of tracer between diesel and water was measured by their linearities. The groundwater flow in the saturated aquifer was simulated in the 2-dimensional soil box, and the residual diesel contamination was visually identified. The results from the partitioning tracer method with or without diesel in soils confirmed that 4-methyl-2-pentanol, 2-ethyl-1-butanol and 1-hexanol, can be used as a detecting method for diesel contamination. By the accuracies of estimations for diesel contamination using the partitioning tracer method, 2-ethyl-1- butanol showed the highest accuracy with 83%.

• 대한화학회지
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• 제41권6호
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• pp.284-291
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• 1997

양이온성 계면활성제인 Cetylpyridinium Chloride(CPC)와 비이온성 계면활성제인 Triton X-100(TX-100)의 혼합계면활성제가 n-알코올(메탄올, 에탄올, 1-프로판올, 1-부탄올 및 1-펜탄올) 수용액에서 나타내는 임계미셀농도값($CMC^*$)을 25$^{\circ}C$에서 UV 분광광도법으로 측정하였다. 이들 $CMC^*$ 값들로부터 여러 가지 열역학 함수값들을 유사상태분리모델(pseudo-phase separation model)을 이용한 식에 의해 계산하였으며 그 값들을 상호 비교하였다. 그 결과 n-알코올들을 첨가한 CPC/TX-100 혼합계면활성제의 미셀화는 비이상적 혼합미셀모델과 잘 일치하였으며, 이상적 혼합미셀모델과는 음의 벗어남을 보였다.

• 대한약리학회지
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• 제29권1호
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• pp.157-163
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• 1993

n-Alkanols의 분자적 약리작용기전 탐구에 기초자료를 제공하기 위하여 소의 신선한 대뇌피질로부터 분리한 synaptosomal plasma membrane vesicles (SPMV) 지질 이중층의 측방확산운동에 미치는 n-alkanols의 영향을 형광 probe법으로 검색하였다. n-Alkanols는 SPMV 지질 이중층의 측방확산운동 범위와 속도를 농도 의존적으로 증가시켰고 1-nonanol까지는 탄소수가 두개 증가될 때마다 그 효력은 약 10배 가량 증가되었으나 탄소수 10개인 1-decanol의 효력은 오히려 감소되는 경향을 나타내었다.

• 한국지반공학회:학술대회논문집
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• 한국지반공학회 2009년도 세계 도시지반공학 심포지엄
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• pp.1372-1377
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• 2009

For the remediation of the subsurface contaminated by nonaqueous phase liquids(NAPLs), it is important to characterize the NAPL zone properly. Conventional characterization methods provide data at discrete points. To overcome the weak points of conventional characterization methods, the partitioning tracer method has been developed and studied. The average saturation of NAPL($S_n$), which is the representative and continuous saturation value within contaminated site, can be calculated by comparing the transport of the partitioning tracers to that of the conservative tracer in the partitioning tracer method. In this study, the application of the partitioning tracer method in heterogeneous media was investigated. To represent the heterogeneous condition of subsurface, a two-dimensional soil box was divided into four layers and each layer contained different sized soils. Soils in the soil box were contaminated by the mixture of kerosene and diesel, and partitioning tracer tests were conducted before and after the contamination using methanol as conservative tracer and 4-methyl-2-pentanol, 2-ethyl-1-butanol, and hexanol as partitioning tracers. The response curves of partitioning tracers from contaminated soils were separated and retarded in comparison with those from non-contaminated soils. The contamination of soils by NAPLs, therefore, can be detected by partitioning tracer method considering these retardations of tracers. From our experiment condition, the average saturation of NAPLs calculated by partitioning tracer method using the methanol as conservative tracer and hexanol as partitioning tracer showed the highest accuracy, though all results were underestimated. Further studies, therefore, were needed for improving the accuracy using the partitioning tracer test in heterogeneous media.

• 대한화학회지
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• 제42권4호
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• pp.383-390
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• 1998

몇 가지 양이온 계면활성제(DTAB, TTAB, CTAB, CDEAB 및 CTAC)의 마이셀과 Phenoxide 음이온과의 상호작용을 연구하기 위하여 UV/Vis분광광도법을 이용하였다. Phenoxide 음이온의 용액에 양이온 게면활성제를 녹였을 때 일어나는 흡광도의 변화로부터 Phenoxide 음이온의 가용화상수($K_s$)와 양이온 계면활성제의 임계마이셀농도(CMC)값을 함께 측정하였다. 각 양이온 계면활성제의 수용액에서 Phenoxide 음이온의 가용화상수값($K_s$)은 다음의 순서로 변하였다: $K_s(CTAC)>K_s(CDEAB)>K_s(CTAB)>K_s(TTAB)>K_s(DTAB).$ 또한 Phenoxide 음이온의 가용화에 미치는 염(NaCl 및 NaBr)과 n-알코올(부탄올, 펜탄올 및 헥산올)의 효과에 대하여 조사하였으며, 그 결과 염과 n-알코올의 첨가로 Ks와 CMC값은 크게 감소하는 경향을 보였다. 그리고 온도에 다른 Ks값의 변화로부터 Phenoxide 음이온의 가용화에 대한 표준자유에너지, 엔탈피, 및 엔트로피의 변화를 계산하고 분석하였다.

• Bulletin of the Korean Chemical Society
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• 제15권10호
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• pp.881-888
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• 1994

The approximate rates and stoichiometry of the reaction of excess sodium tris(diethylamino)aluminum hydride (ST-DEA) with selected organic compounds containing representative functional groups under standardized conditions(tetrahydrofuran, $0{\circ}$) were studied in order to characterize the reducing characteristics of the reagent for selective reductions. The reducing ability of STDEA was also compared with those of the parent sodium aluminum hydride (SAH) and lithium tris(diethylamino)aluminum hydride (LTDEA). The reagent appears to be milder than LTDEA. Nevertheless, the reducing action of STDEA is very similar to that observed previously for LTDEA, as is the case of the corresponding parent sodium and lithium aluminum hydrides. STDEA shows a unique reducing characteristics. Thus, benzyl alcohol, phenol and 1-hexanol evolved hydrogen slowly, whereas 3-hexanol and 3-ethyl-3-pentanol, secondary and tertiary alcohols, were essentially inert to STDEA. Primary amine, such as n-hexylamine, evolved only 1 equivalent of hydrogen slowly. On the other hand, thiols examined were absolutely stable. STDEA reduced aidehydes and ketones rapidly to the corresponding alcohols. The stereoselectivity in the reduction of cyclic ketones by STDEA was similar to that by LTDEA. Quinones, such as p-benzoquinone and anthraquinone, were reduced to the corresponding 1,4-dihydroxycyclohexadienes without evolution of hydrogen. Carboxylic acids and anhydrides were reduced very slowly, whereas acid chlorides were reduced to the corresponding alcohols readily. Esters and epoxides were also reduced readily. Primary carboxamides consumed hydrides for reduction slowly with concurrent hydrogen evolution, but tertiary amides were readily reduced to the corresponding tertiary amines. The rate of reduction of aromatic nitriles was much faster than that of aliphatic nitriles. Nitrogen compounds examined were also reduced slowly. Finally, disulfide, sulfoxide, sulfone, and cyclohexyl tosylate were readily reduced without evolution of hydrogen. In addition to that, the reagent appears to be an excellent partial reducing agent: like LTDEA, STDEA converted ester and primary carboxamides to the corresponding aldehydes in good yields. Furthermore, the reagent reduced aromatic nitriles to the corresponding aldehydes chemoselectively in the presence of aliphatic nitriles. Consequently, STDEA can replace LTDEA effectively, with a higher selectivity, in most organic reductions.

• Bulletin of the Korean Chemical Society
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• 제14권4호
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• pp.469-475
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• 1993

The approximate rates and stoichiometry of the reaction of excess lithium tris(diethylamino)aluminum hydride (LTDEA) with selected organic compounds containing representative functional groups under standardized condition (tetrahydrofuran, 0$^{\circ}C$) were examined in order to define the characteristics of the reagent for selective reductions. The reducing ability of LTDEA was also compared with those of the parent lithium aluminum hydride (LAH) and lithium tris(dibutylamino)aluminum hydride (LTDBA). In general, the reactivity toward organic functionalities is in order of LAH${\gg}$LTDEA${\geq}$LTDBA. LTDEA shows a unique reducing characteristics. Thus, benzyl alcohol and phenol evolve hydrogen slowly. The rate of hydrogen evolution of primary, secondary, and tertiary alcohols is distinctive: 1-hexanol evolves hydrogen completely in 6 h, whereas 3-hexanol evolves hydrogen very slowly. However, 3-ethyl-3-pentanol does not evolve any hydrogen under these reaction conditions. Primary amine, such as n-hexylamine, evolves only 1 equivalent of hydrogen. On the other hand, thiols examined are absolutely inert to this reagent. LTDEA reduces aldehydes, ketones, esters, acid chlorides, and epoxides readily to the corresponding alcohols. Quinones, such as p-benzoquinone and anthraquinone, are reduced to the corresponding diols without hydrogen evolution. However, carboxylic acids, anhydrides, nitriles, and primary amides are reduced slowly, where as tertiary amides are readily reduced. Finally, sulfides and sulfoxides are reduced to thiols and sulfides, respectively, without evolution of hydrogen. In addition to that, the reagent appears to be an excellent partial reducing agent to convert esters, primary carboxamides, and aromatic nitriles into the corresponding aldehydes. Free carboxylic acids are also converted into aldehydes through treatment of acyloxy-9-BBN with this reagent in excellent yields.

• 한국식품과학회지
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• 제29권3호
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• pp.563-570
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• 1997

GC와 GC-MS를 사용하여 발효 16일 후 탁주술덧의 휘발성 향기성분으로 alcohol 20종, ester 26종, acid 10종, aldehyde 10종, 기타 6종 등 모두 72종이 검출되었다. Aspergillus oryzae구는 68종으로 가장 많았고 재래누룩구의 술덧은 60종으로 적었다. 72종의 휘발성 향기성분 중 54종의 향기성분이 모든 시험 구에서 공통으로 검출되었다. 휘발성 향기성분의 면적비율은 alcohol류 $71.28{\sim}90.23%$, ester류 $0.66{\sim}9.05%$, acid류 $0.20{\sim}0.60%$, aldehyde류 $0.02{\sim}0.09%$순으로 나타났다. 시험구에 따라 차이가 있으나 ethanol, 2-methyl-1-propanol, 3-methyl-1-butanol, 1-hexanol, 2.3-butadienol(D,L), benzeneethanol, acetic acid ethyl ester, succinic acid diethyl ester, butanoic acid monoethyl ester, acetic acid 그리고 benzene acetic acid 4-acetyloxy-3-methyl ethyl ester 등의 면적 비율이 높아 본 실험 탁주 술덧의 휘발성 향기 주성분으로 나타났다. 재래 누룩구는 1-pentanol, hexanoic acid ethyl ester의 면적비율이 다른 시험구보다 높았고, Mucor racemosus 누룩구는 1-hexanol, 1-dodecanol, 1,2-benzenedicarboxylic acid dipropenyl ester, acetic acid가, Rhizopus japonicus 누룩구는 2-methyl-1-propanol, 3-methyl-1-butanol, benzeneethanol, succinic acid diethyl ester, butanoic acid monoethyl ester, 4-methyl benzeneacetic acid phenyl ester, butanoic acid의 면적 비율이 타 시험구보다 각각 높았다. Aspergillus oryzae구는 acetic acid ethyl ester, 3-methyl butanoic acid, pentanoic acid가 높았으며 Aspergillus kawachii구에서는 1-butanol이 높았다.