• 제목/요약/키워드: 1M ammonium acetate

검색결과 73건 처리시간 0.027초

4-biphenyl acetate 수용액에서 Cetyltrimethyl Ammonium Bromide의 미셀화에 관한 연구 (Study on the micellization of cetyltrimethyl ammonium bromide in 4-biphenyl acetate solution)

  • 오정희
    • 분석과학
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    • 제8권2호
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    • pp.107-116
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    • 1995
  • 양이온 계면활성제인 cetyltrimethyl ammonium bromide(CTAB)를 첨가함에 따라 4-biphenyl acetate ($BPA^-$) 음이온의 202nm band의 흡광도 변화를 측정하여 CTAB의 CMC를 구하였다. 또한 $30^{\circ}C{\sim}70^{\circ}C$의 온도범위에서 CTAB의 미셀화 과정에 수반되는 열역학적 파라미터를 구하였다. 이 온도범위에서 CTAB의 미셀화 자유에너지는 음의 값을 나타내며 미셀화 엔트로피(${\Delta}S^{\circ}m$)는 큰 양의 값을 나타내고 있다. CTAB의 미셀화 과정은 자발적인 상전이(phase transition) 현상임을 알 수 있었다. $300MHz\;H^1-NMR$ 자료로부터 $BPA^-$ 음이온의 CTAB 미셀내의 배향을 알 수 있었다. $BPA^-$ 음이온의 방향족 기가 CTAB 미셀내의 palisade layer까지 침투하여 혼합 미셀을 형성함을 알 수 있었다.

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Cation Exchange Capacity in Korean Soils Determined by the Copper(II) Acetate Spectrophotometry Method

  • Park, Won-Pyo;Chang, Kong-Man;Koo, Bon-Jun;Hyun, Hae-Nam
    • 한국토양비료학회지
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    • 제50권6호
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    • pp.653-662
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    • 2017
  • Copper(II) acetate spectrophotometry method (CASM) was used for the rapid and convenient determination of cation exchange capacity (CEC) in soils. This method is composed of a single-step exchange reaction that adsorbs copper and is measured through spectrophotometry. The CEC of 16 Korean soils were measured using 1M ammonium acetate method (AAM) and the CASM. The CEC values determined by CASM and AAM were not significantly different, and were highly correlated ($r=0.966^{**}$). Due to the convenience, cost effectiveness, and time saving analysis of CASM, this method is recommended for most soil laboratories to measure CEC in Korean soils. However, CASM may not be applicable for soils that have a much higher CEC (greater than $20cmol_c\;kg^{-1}$).

Ammonium Acetate Supplement Strategy for Enhancement of Chaetominine Production in Liquid Culture of Marine-Derived Aspergillus fumigatus CY018

  • Liu, Chang-Qing;Wei, Xing-Chen;An, Fa-Liang;Lu, Yan-Hua
    • Journal of Microbiology and Biotechnology
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    • 제29권4호
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    • pp.587-595
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    • 2019
  • Pharmacological research on (CHA), a marine-derived quinazolinone alkaloid with significant cytotoxic activity, is restricted by low yields and is a problem that needs to be settled urgently. In this work, the selection of additional nitrogen sources and the optimization of additional concentrations and longer fermentation times using ammonium acetate, were investigated. CHA production was optimized to 62.1 mg/l with the addition of 50 mM ammonium acetate at 120 h of the fermentation in the shaker flask. This feeding strategy significantly increased 3-deoxy-arabino-heptulosonate-7-phosphate synthase activity and transcript levels of critical genes (laeA, dahp, and trpC) in the shikimate pathway compared with the non-treatment group. In addition, the selection of the feeding rate (0.01 and $0.03g/l{\cdot}h$) was investigated in a 5-L bioreactor. As a result, CHA production was increased by 57.9 mg/l with a $0.01g/l{\cdot}h$ ammonium acetate feeding rate. This work shows that the strategy of ammonium acetate supplementation had an effective role in improving CHA production by Aspergillus fumigatus CY018. It also shows that this strategy could serve as an important example of large-scale fermentation of a marine fungus in submerged culture.

Synthesis of Some new 4-Substituted Antipyrines as Potential Antipyretic Analgesics

  • Hammouda, M.
    • Archives of Pharmacal Research
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    • 제15권1호
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    • pp.1-4
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    • 1992
  • 4-Acetylantipyrine 1 underwent condensation with 4-formyl-antipyrine 2 to give 3. Condensation of either 3 with 1 or 1 with 2 in a molar ratio of (2 :1) afforded 4. Cyclization of 4 in the presence of PPA and ammonium acetate or 4-aminoantipyrine in the presence of glacial acetic acid gave 5-6 respectively. Claisen condensation of 1 with ethyl acetate and diethyl oxalate afforded compounds 8-10. The reaction of 1 and 2 with indole in ethanol/conc. hyddrochloric acid was also investigated.

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노루궁뎅이버섯(Hericium erinaceus)의 새로운 균사배양기의 조성 (Composition of a New Medium for Mycelial Growth of Hericium erinaceus)

  • 고한규;김동명;박원목
    • 한국균학회지
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    • 제25권4호통권83호
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    • pp.369-376
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    • 1997
  • 본 실험은 노루궁뎅이버섯(Hericium erinaceus isolate KU-1)의 균사생장에 관한 영양원 실험으로 대량의 균사체 수확을 위한 배양기 조성을 밝히기 위한 기초를 확립하고자 실시하였다. 최적온도는 $25^{\circ}C$이며 pH4에서 160.5 mg으로 가장 건물중이 높았고 탄소원 중 glucose, sucrose, galactose, mannose 순으로 균사생장 및 균사밀도가 우수하였다. 무기태질소원으로는 ammonium acetate 30 mM에서 균사생장이 가장 양호하였다. 아미노산 중 arginine 15 mM에서 우수하였다. C/N율 200에서 35.9 mm로 균사생장의 최대치를 보였다. 상술한 실험의 결과를 토대로 Table 1과 같은 새로운 합성배지를 조제할 수 있었고, 이를 Ko배지라 명명하였다. 이 Ko배지와 기존배지간의 한천배지상에서 균사생장 비교한 결과, Ko배지에 가장 우수한 균사생장과 균사밀도를 나타냈다. Ko배지의 조성은 glucose 18.02g, arginine 3.613g, ammonium acetate 2.313g, $CaCl_2\;0.33g$, $KH_2-PO_4\;8.5g$, $MgSO_4{\cdot}7H_2O\;2.0g$, $FeSO_4{\cdot}7H_2O\;0.02g$, $ZnSO_4{cdot}7H_2O\;0.02g$, $MnSO_4{\cdot}7H_2O\;0.02g$, water 1 liter이다.

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Simple Purification of Bromelain from Pineapple

  • Ko, Bo-Sung;Hwang, Yong-Il;Lee, Seung-Cheol
    • Preventive Nutrition and Food Science
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    • 제1권1호
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    • pp.106-110
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    • 1996
  • Bromelain(EC 3.4.22.4), the collective name for the proteolytic enzymes found in tissues of the plant family Bromeliaceae(pineapple), has been used as a tenderizing agent in food processing, and as an antiinflammatory agent in pharmaceuticals. In this paper, we describe the simple purification method of bromelain using Korean pineapple fruit. After removing contaminants at 30% saturation of ammonium sulfate, the supernatant obtained was treated again with ammonium sulfate to 80% saturation. Wit the above salt fractionation, partially purified bromelain could be obtained. To get highly purified bromelain, the previous 30% to 80% ammonium sulfate treated precipitate was dialyzed against 25mM sodium acetate buffer(pH 5.0) followed by passing through a CM- cellulose cation exchange column. Fruit bromelain was eluted as a major peak at 0.5~0.8M NaCI gradient. The present method is simpler with high wield than the traditional purification method-acetone treatment and several consecutive chromatographic processes.

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암모니아성 질소가 미생물연료전지에서 전류 발생에 미치는 영향 (Effect of ammonium on the current generation in the microbial fuel cell)

  • 장재경;최정은;유영선;이성현;김종구;강연구;김영화;이형모
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2011년도 춘계학술대회 초록집
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    • pp.219.1-219.1
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    • 2011
  • These studies carried out to know the effect of ammonium on the current generation in the microbial fuel cells (MFCs). MFCs used in the study were enriched with anaerobic digestion sludge and operated for 3 years using artificial wastewater (AWW). When the current was stably generated, ammonium ion with $27.0{\pm}0.0$, $51.5{\pm}0.0$, $103.5{\pm}0.0mg/L$ with acetate fed into the anode compartment. The current values under condition included ammonium were changed from its initial $6.30{\pm}0.06$ to $6.28{\pm}0.36$, $5.95{\pm}0.61$, $5.64{\pm}0.38mA$, respectively. The current value was slightly decreased to $5.64{\pm}0.38mA$ compared to $6.30{\pm}0.06mA$ generated from MFC without ammonium ion in the AWW. But After 3days operating under ammonium concentration with $103.5{\pm}0.0mg/L$, the current was unstably generated when artificial wastewater without ammonium was fed again. MFC enriched with AWW without ammonium ion was inhibited by high concentration of ammonium. At this time, the ammonium was removed 5.27~16.41 mg per day under all conditions.

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화장품 중 수용성 고분자인 Xanthan gum 분석연구 (Sturdy of analysis of Xanthan gum as watersoluble-polymer in cosmetics)

  • 이용화;양재찬
    • 한국응용과학기술학회지
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    • 제30권4호
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    • pp.664-671
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    • 2013
  • 역상 HPLC 에 의한 화장품에 사용하는 수용성 고분자인 Xanthan gum의 간편하고 정확한 정량분석 방법을 개발하였다. 분석조건은 $C_{18}$분리관과 ELSD 검출기를 사용하였으며, 25mM ammonium acetate/acetonitrile의 기울기 용리에 의해 분리 되었다. 이때 검량선의 상관계수(correlation coefficient) $r^2=0.9993$, 정량범위 $50.3{\sim}604.1{\mu}g/ml$, 검출한계 $12.0{\mu}g/ml$ 및 정확성이 우수하였다. 이 방법은 화장품 중 Xanthan gum를 정확하고 간편하게 정량분석 가능함을 보여 주었다.

이온쌍-고성능 액체크로마토그래피에 의한 감기약 시럽에서 타르색소 첨가물의 동시분석 (Simultaneous Determination of Tar Color Additives in Cold Syrups by Ion Pair-high Performance Liquid Chromatography)

  • 김경옥;황호;이범규;이원재
    • KSBB Journal
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    • 제25권5호
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    • pp.459-465
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    • 2010
  • A simple and efficient analytical method for the simultaneous determination of seven tar color additives was developed using ion pair high performance liquid chromatography. The conditions for HPLC analysis were as follows: column, ${\mu}$-Bondapak C18 (10 ${\mu}m$, 300 ${\times}$ 3.9 mm i.d.); gradient mobile phase, 0.025 mol/L ammonium acetate (containing 0.01 mol/L tetrabutylammonium bromide)-acetonitrile-methanol (65:25:10) as a mobile for fraction A and 0.025 mol/L ammonium acetate (containing 0.01 mol/L tetrabutylammonium bromide)-acetonitrilemethanol (40:50:10) as a mobile for fraction B; flow rate, 1.0 mL/ min; detection wavelength, 254/520/620 nm. We could attain to the detection limits as 0.01~0.05 ${\mu}$g/mL (254 nm) and 0.005~0.01 ${\mu}$g/mL (520 nm) for six red tar color additives, and 0.05 ${\mu}$g/mL (254 nm) and 0.002 ${\mu}$g/mL (620 nm) for Fast green FCF. This analytical method was applicable to determine the tar color additives contained in several commercial cold syrups.

HPLC Method for the Determination of Nicorandil in Human Plasma

  • Park, Sun-Hee;Shin, In-Chul
    • Biomolecules & Therapeutics
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    • 제16권2호
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    • pp.168-172
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    • 2008
  • The present study is to determine of sensitive nicorandil analysis method using HPLC and measure the pharmacokinetics parameters (bioavailability, $C_{max}$, $T_{max}$, Ke, $T_{1/2}$) of nicorandil (5 mg, Tab; Choongwae Pharma Corporation). Plasma (500 ul) was mixed with furosemide (internal standard, 500 ug/ml). Detection wavelength was 256 nm. The mixture of 0.01 M ammonium acetate and acetonitrile 80:20 (v/v) was used mobile phase. The HPLC separation was accomplished on ODC reverse HPLC column. The nicorandil was analyzed by a HPLC system, which consists of CAPCELL PAK C18 column (5 ${\mu}$m, 4.6 × 150 mm) and a chromatography data analysis S/W, using a isocratic mobile phase (mixture of 0.01 M ammonium acetate and acetonitrile 80:20 ) at 1.0 ml/min. Its sensitivity, selectivity, accuracy and precision must be adequate for the bioavailabilty study of nicorandil, and the linearity ($r^2$ ≥ 0.9994) of nicorandil was also proved in the range of 0.05 ug/ml . 3 ug/ml. The pharmacokinetic parameters of nicorandil (5 mg) tablets were measured as the follow. AUC: 0.19 ug/ml·hr, $C_{max}$: 0.14 ug/ml, $t_{max}$: 0.58 hr, Ke: 0.11 hr., $t_{1/2\beta}$: 6.76 hrs. This method is simple and sensitive HPLC method using UV detector for determination of nicorandil in human plasma.