• Applied Biological Chemistry
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• 제37권3호
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• pp.189-193
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• 1994

이온성 계면활성제인 sodium laurylsulfate(NaLs)와 cetyltrimethylammonium bromide(CTABr)의 존재하에서 항균성 N-[1-(benzotriazol-1-yl)benzyl]aniline(BBA)분자의 가수 분해 반응에 미치는 미셀효과를 검토한 바, NaLs가 존재하는 높은 pH에서 미셀 촉매효과가 나타났으며 결합상수(Ks)는 $1.45{\times}10^4M^{-1}$이었다. 이와 같은 미셀 촉매효과는 (BBA)의 소수성(${\pi}$: 4.93)보다 전이상태에서 생성되는 carbocation이 음이온성 미셀에 의한 정전기적 안정화에 기인한 결과로 보여진다.

• 전기화학회지
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• 제13권3호
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• pp.163-168
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• 2010

본 연구에서는 양극 산화를 통해 얻어지는 다공성 니오븀 산화물 제조에 양이온 계면활성제인 Cetyl Trimethyl Ammonium Bromide (CTAB)와 음이온 계면활성제인 Sodium Dodecyl Sulfate (SDS)의 영향을 비교 관찰하였다. SDS가 전해질에 첨가되어 제조된 다공성 니오븀 산화 막은 표면에 장시간 용출이 발생하지 않았고, 계면활성제가 첨가되지 않고 제조된 다공성 니오븀 산화막의 두께와 비교 하였을 때 두께가 두 배 이상 증가된 값을 얻을 수 있었다. 하지만 CTAB가 전해질에 첨가되어 제조된 다공성 니오븀 산화물의 표면에는 용출이 일어났다. 이러한 차이점을 양성으로 대전된 니오븀산화물과 음이온/또는 양이온 계면활성제 사이의 상호작용에 근거하여 설명하였다.

• 대한화학회지
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• 제17권6호
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• pp.411-415
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• 1973

Cyanide ion과 triphenylmethane dye와의 반응은 cetyltrimethyl ammonium bromide(CTABr)의 cationic micelle에 의하여 현저히 반응속도가 빨라지며 sodium lauryl sulfate(NaLS)의 anionic micelle에 의하여 반응속도가 늦어진다. 또한 CTABr존재하의 반응은 inorganic anion에 의하여 inhibition, 되며 NaLS존재하의 반응은 inorganic cation중의 몇가지, 특히 $Zn^{++},\;Cd^{++}$등에 의하여 현저하게 반응이 빨라지는 salt effect를 나타낸다. 물과 잘 혼합되는 몇가지 유기용매의 micelle catalysis에 대한 영향은 대체로 수용액 일때보다 작게 나타나서 반응속도가 늦어지거나 malachite green과의 반응에서 methanol은 수용액일때보다 반응속도가 빨라지는 특이한 solvent effect를 나타내었다.

• 한국환경보건학회지
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• 제44권3호
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• pp.244-249
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• 2018

Objectives: The purpose of this study was the investigation of bromide and bromate in drinking water of water supply plants, mineral springs and small water supply system located in northern area of Gyeonggi province. Methods: Analytical method was based on EPA 326.0 to use Postcolumn reaction (PCR). The instrument was 887 professional UV/VIS detector IC manufactured in Metrohm. Results: Bromate was detected at $0.5{\sim}2.4{\mu}g/L$ in tap water from 5 water supply plants. These plants were used as disinfection method for sodium hypochlorite and on-site chlorine that causes generate bromate as a by products even if not used ozone. Conclusions: The bromate was detected up to $2.5{\mu}g/Lin$ drinking water in northern Gyeonggi area that showed within $10{\mu}g/L$ for standard of tap water. However, the continuous monitoring of bromate is necessary in drinking water.

• 분석과학
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• 제11권6호
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• pp.413-420
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• 1998

물-메탄올 혼합 용액과 계면활성제 용액에서 1-나프탈렌아세트산 나트륨염, 1-나프탈렌말론산 나트륨염, 2-나프탈렌아세트산 나트륨염과 2-나프탈렌프로피온산 나트륨염과 같은 나프탈렌 나트륨 유도체들의 소수성 상호작용에 대해서 연구하였다. 물-메탄올 혼합 용액에서 소수성 상호작용을 측정하였고, 방출선은 red shift가 일어났다. 양이온 계면활성제인 세틸트리메틸암모늄 브롬화 용액에서도 흡수, 방출선은 red shift됨을 보여주었다.

• Archives of Pharmacal Research
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• 제29권10호
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• pp.840-844
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• 2006

For the exploration of pharmacophoric moiety of malloapelta B (1) possessing the inhibitory activity of $NF-{\kappa}B$ activation, structural variation of ${\alpha},{\beta}-unsaturated$ carbonyl motif was attempted. 1 was reduced by catalytic hydrogenation, sodium borohydride, and lithium aluminumhydride. Catalytic hydrogenation with 30 psi or 15 psi of $H_2$ gas of 1 generated 8-butyl-5,7-dimethoxy-2,2-dimethylchroman (2) and 1-(5,7-dimethoxy-2,2-dimethylchroman-8-yl)butan-1-one (3), respectively. Reduction with sodium borohydride occurred at the double bond of ${\alpha},{\beta}-unsaturated$ ketone of 1 to give 1-(5,7-dimethoxy-2,2-dimethyl-2H-chromen-8-yl)butan-1-one (4). Reduction of 1 with lithium aluminumhydride and then quenched with methanol and water produced unexpected products, 1-(5,7-dimethoxy-2,2-dimethyl-2H-chromen-8-yl)-3-methoxy-1-butene (5) and 1-(5,7-dimethoxy-2,2-dimethyl-2H-chromen-8-yl)-3-hydroxy-1-butene (6). These are formed from the isomerization of initial product 9 through the continuous conjugate carbocation intermediate 11. Addition of ethylmagnesium bromide and dimethyl malonate anion to 1 gave the conjugate adducts 7 and 8. Ethylmagesium bromide and sodium borohydride reduction unusually gave the conjugate addition due to steric congestion around carbonyl group of 1. Compound 2 exhibits the reduced inhibitory activity against $NF-{\kappa}B$ activation and the others do not show the activity. Therefore ${\alpha},{\beta}-unsaturated$ carbonyl group of 1 should be important for its inhibitory activity.

• Korean Journal of Chemical Engineering
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• 제35권11호
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• pp.2269-2282
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• 2018

Mixed micelle formation behavior of cationic surfactant-cetyltrimethylammonium bromide (CTAB) and anionic surfactant sodium dodecyl sulfate (SDS) in aqueous as well as in urea medium from 303.15 K to 323.15 K at 5 K interval was carried out by conductometric method. The differences between the experimental values of critical micelle concentrations (cmc) and ideal critical micelle concentrations ($cmc^{id}$) illustrate the interaction between the amphiphiles studied. The values of micellar mole fraction ($X_1^{Rub}$ (Rubingh), $X_1^M$ (Motomura), $X_1^{Rod}$ (Rodenas) and $X_1^{id}$(ideal) of surfactant CTAB determined by different proposed models and outcome indicate high involvement of CTAB in SDS-CTAB mixed micellization, which enhance by means of the augment of mole fraction of CTAB. The negative value of interaction parameter (${\beta}$) showed an attractive interaction involving CTAB and SDS. Activity coefficients were less than unity in all case, which also reveals the presence of interaction between CTAB & SDS. The negative ${\Delta}G^0_m$ values imply the spontaneous mixed micellization phenomenon. The attained values of ${\Delta}H^0_m$ were positive at inferior temperature, while negative at superior temperature. The negative ${\Delta}H^0_m$ values in urea ($NH_2CONH_2$) medium illustrate exothermic micellization process. The magnitudes of ${\Delta}S^0_m$ were positive in almost all cases. The excess free energy of mixed micelle formation (${\Delta}G_{ex}$) was found to be negative, which indicates the stability of mixed micelle as compared to the individual's components micelles.

• 한국응용과학기술학회지
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• 제28권2호
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• pp.140-145
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• 2011

Cationic gemini-surfactant, namely 1,4-butane-bis(N-alkanoyloxyethyl-N,Ndimethyl)-diammonium bromide was synthesized and their inhibition effect on corrosion of mild steel in 1 M HCl solution was tested by weight loss method. The synthesized product was confirmed by FT-IR and $^1H-NMR$ spectroscopy. Surface tensions were measured by surface tensiometer Sigma 70. Their c.m.c. values evaluated by surface tension method was $4.1{\times}10^{-5}{\sim}5.4{\times}10^{-5}$ mol/L. The Krafft point of the these surfactants were <0~$10.7^{\circ}C$. The emulsifying properties of synthesized cationic gemini surfactants and sodium dodecyl sulfate (SDS), tetradecyl trimethyl ammonium bromide (TTAB) was investigated. Of these, 1,4-butane-bis(N-lauroyloxyethyl-N,N-dimethyl)- diammonium bromide, CGL 14-4-14 has been confirmed as a good emulsifier. The inhibition efficiency increases by increasing cationic gemini surfactant concentration. As a result, these surfactants are expected to be applied as corrosion inhibitors.

• 한국응용과학기술학회지
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• 제31권1호
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• pp.1-6
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• 2014

Gemini type of cationic surfactant, namely ${\alpha},{\omega}$-alkane-bis(N-lauroyloxyethyl-N,N-dimethyl)-diammonium bromide was synthesized and confirmed by FT-IR and $^1H$-NMR spectroscopy. Their inhibition effect on corrosion of mild steel in 1 M HCl solution was tested by weight loss method. Surface tensions were measured by surface tensiometer Sigma 70. Their c.m.c. values evaluated by surface tension method was $4.01{\times}10^{-5}{\sim}4.99{\times}10^{-5}mol/L$. The Krafft point of the these surfactants were < $0^{\circ}C$. The emulsifying properties of synthesized cationic gemini surfactants and sodium dodecyl sulfate (SDS), tetradecyl trimethyl ammonium bromide (TTAB) was investigated. Of these, ${\alpha},{\omega}$-alkane-bis(N-lauroyloxyethyl-N,N-dimethyl)-diammonium bromide has been confirmed as a good emulsifier. The inhibition efficiency increases by increasing cationic gemini surfactant concentration. As a result, these surfactants are expected to be applied as corrosion inhibitors.

• 한국응용과학기술학회지
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• 제6권2호
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• pp.29-37
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• 1989

Using the quarternary ammonium salts as phase transfer catalyst, the nucleophilic substitution reaction of 1-chlorooctane with sodium-cyanide was investigate kinetically with respect to the formation of octanenitrile. The product was analyzed with gas chromatograph, and quantity of octanenitrile was measured. The reaction condition was considered by the effect of the reaction temperature, of the species and the amount of catalyst, of the speed of strirring, and of the concentration of reactants. The reaction was carried out in the first order on the concentration of 1-chlorooctane and sodium cyanide, respectively. The over-all order was 2nd. The activation energies for the nucleophilic substitution reaction of 1-chlorooctane and 1-bromooctane under tetrabutylammonium hydrogen-sulfate were calculated as 2.05 and 10.08kcal/mol, respectively. The effect of various caltalysts was decreased in the order of tetrabutylammonium bromide, terabutylammonium, tetrabutylammonium hydrogensulfate, and tetrabutylammonium iodide. The reaction rate was dependent on the concentration of sodium-cyanide dissolved in the aqueous phase, and the good result was shown when the mol ratio between 1-chlorooctane and sodium cyanide was one per three.