• Journal of Applied Biological Chemistry
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• 제57권3호
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• pp.197-203
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• 2014

Various parameters such as solvent selection, concentration, solid/liquid ratio, soaking time, temperature, stationary, shaking conditions, and repeated extractions were investigated in order to determine the optimum extraction conditions of ${\beta}$-glucosidase from bagasse fermented by mixed culture of Aspergillus niger NRC 7A and Aspergillus oryzae NRRL 447. Among various solvents tested, non ionic detergents gave the best results than the inorganic or organic salt solutions and distilled water. The optimum conditions for extraction of ${\beta}$-glucosidase were 30 min soaking time at $40^{\circ}C$ under shaking condition at 150 rpm, with solid/liquid ratio 1:15 (w/v), which yielded $2882.74{\pm}95.52U/g$ fermented culture (g fc) of enzyme activity. With repeated washes under the above optimum conditions, the results showed that enzyme extracted in the $1^{st}$ and $2^{nd}$ washes represents about 90% of the total activity.

• 공업화학
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• 제31권3호
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• pp.317-322
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• 2020

수산화암모늄나이트레이트(HAN; NH₃OHNO₃)는 낮은 용융점과 증기압의 특성을 가지고 있고, 상대적으로 높은 산소균형을 이루고 있는 이온성 화합물이다. 본 연구에서는 높은 함량의 액상추진제를 제조하기 위한 산화제로 활용하기 위하여 이중용매를 적용하여 고체입자상으로 얻었다. 감압 하에서 액상의 HAN으로부터 수분을 증발시킨 후, 반용매로서 아세톤과 에탄올을 적용하여 추출한 입자상의 HAN에는 13.8 wt%의 수분이 포함되어 있었다. 아세톤을 단독으로 적용하였을 때, 합성수율은 질량기준으로 최대 88%이었고, TGA로 측정된 최대 함량은 86.2%, 분해온도는 160~205℃ 범위로 나타났다.

• 한국식품과학회지
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• 제35권5호
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• pp.951-958
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• 2003

국내 외에서 수집 재배한 24품종 유색미를 순차적인 유기용매 처리에 의해서 지용성 분획과 색소를 함유하는 분획, 색소성분 만의 분획을 얻었고 각 분획이 가지는 항산화성 및 항변이원성을 검정하였다. 유기용매 추출이 진행되어 분획성분의 조성이 간단해질수록 품종마다 차이는 없지만 항산화성은 오히려 약화되는 경향이 있었는데. 특히 LK 1-3-6-12-1-1과 길림흑미의 항산화 활성이 상당히 낮았다. 70%에탄올 추출물에서는 항변이원성을 나타내던 유색미 품종들도 색소분획을 포함하는 분획들에서는 모든 품종에서 오히려 변이원생을 나타내고 있었으며, 특히 wx 124-153-45-7-1-1-1 및 LK 1B-2-1-1 등에서 강한 변이원성이 관찰되었다. 유색미 품종별 색소의 함량은 IR 17491-5-4-3-3>LK 1-3-6-12-1-1>LK ID-2-12-1>RGS No336. Elwee 등의 순서로 나타난다. 유기용매에 의해서 분획되는 성분들의 조성 및 함량이 유색미 품종들과 일반미 품종간에는 상당히 차이가 있음을 알 수 있었으며, 일반미 품종에 비교하면 유색미 품종들의 유기용매에 의해서 용출되는 수된 성분 분사들은 긴 탄화수소를 가진 성분들이었다.

• 한국응용과학기술학회지
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• 제8권1호
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• pp.79-83
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• 1991

The extracts of Quercisemen(Quereus acutissima Carruthers seed) powder was obtained by the extraction with distilled water, water : acetonet(1:1, v/v), ethanol and ethyl ether, respectively. As a result this experiment, the antioxidative activity of each solvent extracts on linoleic acid were examined as follows: 1. Each fraction extracted by the acetone : water(1:1, v/v), water and ethanol respectively showed high antioxidative activity. 2. A fraction of the tannin extracted from the solvent, acetone, water(1:1, v/v) showed even more antioxidative activity than that of the ${\alpha}$-tocopherol or BHT. 3. Acceleration of peroxide reaction by $Fe^{++}$ and $Cu^{++}$ on the linoleic acid was strongly inhibited by adding the tannin, 4. Organic acid, such as malic acid, citiric acid and tartaric acid with the tannin were showed the synergistic effect fo the antioxidation reaction.

• 자원리싸이클링
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• 제27권6호
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• pp.53-58
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• 2018

염산농도가 낮은 용액에서 TBP/MIBK와 다른 중성추출제(Cyanex 923, TOPO, TOP)의 혼합용매에 의한 리튬(I)의 용매추출실험을 수행했다. 0.1 M의 $FeCl_3$가 추출된 TBP/MIBK는 염산농도를 1에서 9 M로 변화시켜 준비하였다. 약한 염산용액에서 리튬(I)의 추출은 유기상에서 $FeCl_3$의 안정도와 관계된다. $FeCl_3$가 추출된 TBP를 진한 염산용액에서 제조하는 경우, 추출시 철의 탈거율이 작아 리튬(I)이 수소이온과의 교환반응에 의해 추출되었다. 혼합용매에서 TBP의 농도도 $FeCl_3$의 안정에 영향을 미쳤다. TBP에 비해 $FeCl_3$는 MIBK로부터 쉽게 탈거되어 리튬(I)을 추출하지 못했다. TBP/MIBK와 혼합용매로 첨가된 중성추출제의 종류는 리튬(I)의 추출과 철의 탈거에 영향을 미치지 않았다.

• Bulletin of the Korean Chemical Society
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• 제34권11호
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• pp.3444-3450
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• 2013

Three phase hollow fiber-liquid phase microextraction (HF-LPME), which is faster, simpler and uses a more environmentally friendly sample-preparation technique, was developed for the analysis of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) in human urine. For the effective simultaneous extraction/concentration of NSAIDs by three phase HF-LPME, parameters (such as extraction organic solvent, pH of donor/acceptor phase, stirring speed, salting-out effect, sample temperature, and extraction time) which influence the extraction efficiency were optimized. NSAIDs were extracted and concentrated from 4 mL of aqueous solution at pH 3 (donor phase) into dihexyl ether immobilized in the wall pores of a porous hollow fiber, and then extracted into the acceptor phase at pH 13 located in the lumen of the hollow fiber. After the extraction, 5 ${\mu}L$ of the acceptor phase was directly injected into the HPLC/UV system. Simultaneous chromatographic separation of seven NSAIDs was achieved on an Eclipse XDB-C18 (4.6 mm i.d. ${\times}$ 150 mm length, 5 ${\mu}m$ particle size) column using isocratic elution with 0.1% formic acid and methanol (30:70) at a HPLC-UV/Vis system. Under optimized conditions (extraction solvent, dihexyl ether; $pH_{donor}$, 3; $pH_{acceptor}$, 13; stirring speed, 1500 rpm; NaCl salt, 10%; sample temperature, $60^{\circ}C$; and extraction time, 45 min), enrichment factors (EF) were between 59 and 260. The limit of detection (LOD) and limit of quantitation (LOQ) in the spiked urine matrix were in the concentration range of 5-15 ng/mL and 15-45 ng/mL, respectively. The relative recovery and precision obtained were between 58 and 136% and below 15.7% RSD, respectively. The calibration curve was linear within the range of 0.015-0.96 ng/mL with the square of the correlation coefficient being more than 0.997. The established method can be used to analyse of NSAIDs of low concentration (ng/mL) in urine.

• 분석과학
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• 제33권1호
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• pp.11-22
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• 2020

When extracting semi-volatile components of herbal medicines using hot water vapor, some substances may react with water vapor or oxygen, and some volatile substances may be lost, when using an organic solvent extraction method has the disadvantage that it may contain a non-volatile material and residual organic solvent. In addition, it is inefficient to separate semi-volatile substances from herbal medicines into each single component and conduct biological activity research for each component to determine the effective ingredient, and some components may be lost in the separation process. In this study, semi-volatile substances evaporated under two pressure-reduced conditions in Chinese herbal medicines such as Cnidii Rhizoma, Aucklandiae Radix and Amomum Fructus were separated by cooling with liquid nitrogen. Those were analyzed by gas chromatography-mass spectrometry (GC-MS) to identify the components, and this method may be used to study biological activities at the cellular level. The substances separated under reduced pressure, essential oil obtained by simultaneous distillation extraction (SDE) method and substances by using solid phase micro-extraction (SPME) from Cnidii Rhizoma, Aucklandiae Radix and Amomum Fructus were analyzed by GC-MS. In the case of Cnidii Rhizoma and Aucklandiae Radix, there were some differences among the essential oil components obtained by SDE and those identified by low temperature capture (CT) and SPME method, these were believed to be produced by some volatiles reacting with water or oxygen at the boiling point temperature of water.

• 자원리싸이클링
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• 제1권1호
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• pp.58-68
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• 1992

아연을 함유하고 있는 산업폐기물로부터 첨단산업의 소재원료인 미립의 고순도 ZnO 분말을 아연제련의 용매추출 공정에서 직접 합성할 수 있는 방법을 개발하고자 하였다. 아연 함량이 55%인 선재산업의 폐기물을 황산으로 침출하여 아연을 추출하였다. 함아연 용액에서 철분을 침전시켜 제거한 후 D2EHPA를 추출제로 사용하는 용매추출에 의해 아연이온을 유기상으로 추출하여 정제한 뒤 oxalic acid와 같은 침전제를 사용하여 유기상의 아연 이온을 precipitation stripping 법으로 탈거, 침전시켜 $ZnC_2O_4$ 분말을 합성하였으며 이를 해소하여 99.9% 이상의 ZnO 분말을 제조하였다. 황산농도, 침출시간, 황액농도가 아연의 침출율에 미치는 영향과 용매추출시 용액의 산도에 따른 아연과 불순물의 추출거동을 조사하여 최적정제조건을 얻었다. 또한 oxalic acid의 농도, 온도, 계면활성제의첨가, 침전시간 등이 생성된 $ZnC_2O_4$ 분말의 형상과 입자크기 및 분포에 미치는 영향에 대해 조사하였다.

• 한국대기환경학회지
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• 제30권4호
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• pp.362-377
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• 2014

Polycyclic aromatic hydrocarbons (PAHs) have been of particular concern since they are present both in the vapor and particulate phases in ambient air. In this study, a simple method was applied to determine the vapor phase PAHs, and the performance of the new method was evaluated with a conventional method. The simple method was based on adsorption sampling and thermal desorption with GC/MS analysis, which is generally applied to the determination of volatile organic compounds (VOCs) in the air. A combination of Carbotrap (300 mg) and Carbotrap-C (100 mg) sorbents was used as the adsorbent. Target compounds included two rings PAHs such as naphthalene, acenaphthylene, and acenaphthene. Among them, naphthalene was listed as one of the main HAPs together with a number of VOCs in petroleum refining industries in the USA. For comparison purposes, a method based on adsorption sampling and solvent extraction with GC/MS analysis was adopted, which is in principle same as the NIOSH 5515 method. The performance of the adsorption sampling and thermal desorption method was evaluated with respect to repeatabilities, detection limits, linearities, and storage stabilities for target compounds. The analytical repeatabilities of standard samples are all within 20%. Lower detection limits was estimated to be less than 0.1 ppbv. In the results from comparison studies between two methods for real air samples. Although the correlation coefficients were more than 0.9, a systematic difference between the two groups was revealed by the paired t-test (${\alpha}$=0.05). Concentrations of two-rings PAHs determined by adsorption and thermal desorption method consistently higher than those by solvent extraction method. The difference was caused by not only the poor sampling efficiencies of XAD-2 for target PAHs and but also sample losses during the solvent extraction and concentration procedure. This implies that the levels of lower molecular PAHs tend to be underestimated when determined by a conventional PAH method utilizing XAD-2 (and/or PUF) sampling and solvent extraction method. The adsorption sampling and thermal desorption with GC analysis is very simple, rapid, and reliable for lower-molecular weight PAHs. In addition, the method can be used for the measurement of VOCs in the air simultaneously. Therefore, we recommend that the determination of naphthalene, the most volatile PAH, will be better when it is measured by a VOC method instead of a conventional PAH method from a viewpoint of accuracy.

• 자원리싸이클링
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• 제32권1호
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• pp.21-32
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• 2023

리튬이온 배터리(LIB) 제조를 위한 리튬의 사용이 점차 증가함에 따라 그에 따라 발생되는 리튬이온배터리 폐기가 증가될 것으로 사료된다. 이에 따라 폐배터리를 재활용을 하기위한 용매 추출을 통한 재활용에 대한 활발한 연구가 니켈, 코발트 및 망간과 같은 유가금속을 제거한 후 얻은 폐 용액에서 리튬의 회수가 중요하다. 본 연구에서는 폐이차전지 재활용공정 후 발생되는 폐액에서 리튬을 회수하기위해 추출제 Di-(2-ethylhexyl) hosphoricacid(D2EHPA)와 등유의 개질제 Tri-n-butyphosphate(TBP)를 선택적으로 혼합하여 추출조건을 최적화하였다. 폐액에는 리튬과 고농도의 나트륨(Li⁺ = 0.5% ~ 1%, Na⁺ = 3 ~ 6.5%)을 함유하고 있었으며, 리튬의 추출은 유기용매의 다른 구성에서 최종적으로 20% D2EHPA + 20% TBP + 60% 등유로 구성된 유기용매에서 효과적인 추출을 조건을 확립하였다. NaOH의 비누화를 이용한 SX 시스템에서는 평형 pH 4~4.5에서 유기 대 수성(O/A)이 5일 때 약 95% 이상의 리튬이 선택적으로 추출되는 것을 확인하였다. 적은 양의 나트륨으로 염화리튬에서 탄산리튬 분말을 얻기 위해 고순도 중탄산암모늄을 처리하였다. 최종적으로 처리된 탄산리튬에 여러번 세수를 통하여 미량의 나트륨을 제거하고 고순도 탄산리튬 분말(순도 99.2%)을 제조하였다. 따라서 본 연구를 통하여 폐이차전지 재활용공정에서 발생되는 폐액을 활용하여 탄산리튬의 효율적인 제조방법을 확인하였다.