• 청정기술
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• 제23권4호
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• pp.393-400
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• 2017

본 연구에서는 염화제이철의 재생공정으로 기존 용매추출법에서 사용하고 있는 용매인 TBP 및 Alamine336 대신에 새로운 용매를 통해 용액 내에 존재하는 Ni과 Fe를 분리 및 회수하는 공정을 개발하였다. Lab 실험을 통하여 실험조건을 최적화하였으며, 이를 바탕으로 상업화를 위한 $10L\;h^{-1}$급 파일럿 설비를 구축하였다. 또한 파일럿 실험을 통하여 양산을 위한 공정 데이터를 확보하였으며, 제조된 염화제이철의 부식실험을 통하여 사용할 수 있는 제품 품질에 문제없음을 확인하였다.

• Journal of Ginseng Research
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• 제41권3호
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• pp.428-433
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• 2017

Background: In this study, the fermentation of ginseng seeds was hypothesized to produce useful physiologically-active substances, similar to that observed for fermented ginseng root. Ginseng seed was fermented using Bacillus, Pediococcus, and Lactobacillus strains to extract ginseng seed oil, and the extraction yield, color, and quantity of phenolic compounds, fatty acids, and phytosterol were then analyzed. Methods: The ginseng seed was fermented inoculating 1% of each strain on sterilized ginseng seeds and incubating the seeds at $30^{\circ}C$ for 24 h. Oil was extracted from the fermented ginseng seeds using compression extraction, solvent extraction, and supercritical fluid extraction. Results and Conclusion: The color of the fermented ginseng seed oil did not differ greatly according to the fermentation or extraction method. The highest phenolic compound content recovered with the use of supercritical fluid extraction combined with fermentation using the Bacillus subtilis Korea Food Research Institute (KFRI) 1127 strain. The fatty acid composition did not differ greatly according to fermentation strain and extraction method. The phytosterol content of ginseng seed oil fermented with Bacillus subtilis KFRI 1127 and extracted using the supercritical fluid method was highest at 983.58 mg/100 g. Therefore, our results suggested that the ginseng seed oil fermented with Bacillus subtilis KFRI 1127 and extracted using the supercritical fluid method can yield a higher content of bioactive ingredients, such as phenolics, and phytosterols, without impacting the color or fatty acid composition of the product.

• 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.

• Journal of Microbiology and Biotechnology
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• 제17권5호
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• pp.847-852
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• 2007

This study investigated an efficient method for the extraction of astaxanthin from the red yeast Xanthophyllomyces dendrorhous. The extraction process comprised three steps: 1) cultivating the yeast; 2) treating the yeast culture suspension with microwaves to destroy the cell walls and microbodies; and 3) drying the yeast and extracting the astaxanthin pigment using ethanol, methanol, acetone, or a mixture of the three as the extraction solvent. Ultimately, various treatment tests were performed to determine the conditions for optimal pigment extraction, and the total carotenoid and astaxanthin contents were quantified. A frequency of 2,450 MHz, an output of 500 watts, and irradiation time of 60 s were the most optimum conditions for yeast cell wall destruction. Furthermore, optimal pigment extraction occurred when using a cell density of 10g/l at $30^{\circ}C$ over 24 h, with a 10% volume of ethanol.

• 한국수산과학회지
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• 제10권4호
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• pp.189-197
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• 1977

분포량이 많고 식용되고 있는 중요해조인 둥근돌김, 잎파래, 구멍갈파래, 미역, 톳, 모자반, 셀만모자반, 누운청각의 식염가용성 및 알콜가용성 단백질 추출에 영향을 주는 제 요소 즉 추출용액의 농도, 용매량, 시간, 온도, pH의 영향을 검토하고 pH에 따른 TCA 침전단백질을 정량한 결과를 요약하면 다음과 같다. 1. 식염가용성 단백질에 있어서 미역, 톳, 돌김, 잎파래, 구멍갈파래는 0.25M의 식염용액에서, 모자, 셀만모자반, 누운청각은 1.0M에서 가장 좋은 추출성적을 얻었으며, 알콜가용성 단백징 전시료(미역, 모자반, 잎파래, 둥근돌김)가 $20\%$ 에타놀에서 가장 좋은 추출성적을 보였다. 2. 시료일추출용매비(w/v)는 식염가용성의 경우 1:30(w/v)에서 알콜 가용성 단백질은 건조시료 1g에 대하여 100ml을 가할 때 추출성적이 좋았다. 3. 3. 추출시간에 있어서 식염가용성 단백질은은 구멍 갈파래, 잎파래가 1시간, 둥근돌김, 누운청각이 2시간, 미역, 톳, 모자만, 셀만모자반은 3시간이 최적 추출시간이내, 추출성분이 좋았다. 4. 추출온도는 식염가용성일 경우, 잎파래, 구명 갈파래는 $40^{\circ}C$에서, 미역은 $50^{\circ}C$, 톳, 모자반, 셀만모자반, 누운청각은 $60^{\circ}C$서 최고의 추출성적을 보였고, 알콜가능성은 잎파래가 $30^{\circ}C$ 미역, 둥근돌김, 모자반이 $40^{\circ}C$에서 최고의 추출성적을 보였다. 5. pH의 영향은 각 시료마다 대동소이하며, 식염가용성 pH $8\~9$에서 알콜가용성은 pH $8\~9$에서 성적이 좋았다.

• 한국작물학회지
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• 제53권1호
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• pp.110-117
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• 2008

검정콩 품질평가의 한 기준이 되는 안토시아닌의 함량평가를 위한 분석기술 개발의 일환으로 검정콩 종피 함유 안토시아닌의 최적의 추출용매 및 추출방법을 확립하고, 주요재배 검정콩 종피 함유 안토시아닌의 함량을 정량적으로 평가한 결과를 요약하면 다음과 같다. 1. 검정콩 종피 함유 안토시아닌의 최적 추출용매를 검토한 결과 1% HCl - $H_2O$로부터 1% HCl - 80% MeOH용액까지 통계적 차이가 인정되지 않았으나, 산술적으로 1% HCl - 60% MeOH 용액으로 추출하였을 때 총 안토시아닌의 함량이 7.72 mg/g으로 가장 높은 양상을 나타내었으나, 추출용매에 메탄을 함량이 높아질수록 안토시아닌 피크의 분리도가 극히 불량한 결과를 나타내므로 종합적 견지에서 볼 때 1% HCl - 20% MeOH를 이용하여 안토시아닌을 추출하는 것이 가장 우수한 것으로 평가되었다. 2. 검정콩 종피 함유 안토시아닌의 최적 추출방법 및 추출시간을 검토한 결과 상온 12시간 추출이 가장 우수한 결과를 나타내었으며, 추출시간이 24시간 이상 지속될 경우 추출시간이 증대됨에 따라 안토시아닌의 함량이 소량 감소되는 양상을 확인할 수 있었다. 3. 국내외 주요 재배 검정콩 품종별 종피 함유 안토시아닌 색소의 함량을 비교한 결과 총 안토시아닌의 함량 범위는 1.58-10.62 mg/g으로 조사되었고, 조사된 품종 중 검정 올콩이 10.62 mg으로 가장 높은 양상을 나타내었으며, 가장 낮은 함량을 나타낸 흑청콩 대비 약 7배 높은 안토시아닌 함량을 나타내었다.

• 대한본초학회지
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• 제29권6호
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• pp.1-6
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• 2014

Objectives : This study was aimed to compare Gyejibokryeong-hwan (GBH) decoctions produced using different pressure levels for various extraction times to find the optimal extraction conditions through extraction yield, total soluble solids content (TSSC), hydrogen ion concentration (pH), and the contents of chemical compounds. Methods : Decoctions of GBH were prepared under the pressure levels of 0 or $1kgf/cm^2$ for 30-180 min using water as extraction solvent. The extraction yield, TSSC, and pH were measured, and the amounts of the chemical compounds were determined using high performance liquid chromatography-photodiode array detector. Results : The higher pressure and longer extraction time increased the values of TSSC and extraction yield, while decreased the pH value. The decoctions produced in 180 min by pressurized method and produced in 150 min by non-pressurized method showed maximum values of extraction yield and TSSC with minimum value of pH. The amounts of chemical compounds showed variations in pressurized and non-pressurized decoction during overall extraction times. The influences of pressure and extraction time on extraction yield, TSSC, pH, and the contents of chemical compounds were confirmed by regression analysis, which showed that all extraction values were significantly affected by at least one of two extraction factors, pressure and extraction time. Conclusions : This study suggests that the pressure and extraction time can significantly affect the extraction efficiency of components from GBH decoctions. However, optimal extraction conditions could not be chosen due to the variation of the amounts of chemical compounds.

• Journal of Ginseng Research
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• 제24권2호
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• pp.64-67
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• 2000

본 연구에서는 홍삼에 함유되어 있는 총 phenolic화합물을 정량하기 위하여 Folin-Denis방법을 사용하였으며, 이 때 정량에 방해를 줄 수 있는 물질에 대해서 조사하였고 홍삼분말로부터 phenolic 화합물 추출조건을 조사하였다. 아미노산중에서는 tyrosine, cystein 및 tryptophan이 영향을 미쳤고, 여러 가지 유기산, 당류 및 ginsenosides는 거의 영향을 미치지 않았다. 비타민 중에서는 vitimln B$_{12}$, d-biotin, D-pantothenic acid, niacinamide, nicotinic acid, vitamine A palmitate, vitamine D$_3$ 등을 제외한 비타민은 발색에 영향을 미쳤다. 홍삼으로부터 phenolic 화합물을 추출하기 위한 추출조건은 60% ethanol을 사용해서 80。C에서 1-2시간씩 3회 정도 추출이 적당하다고 판단된다.

• 한국물환경학회지
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• 제21권3호
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• pp.219-229
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• 2005

The analytical methods for dioxins in water sample from wastewater to tap water were reviewed. For extraction method, liquid-liquid extraction (LLE) has been widely used, however, this process needs too much time and man power. New approach including solid phase extraction (SPE) is now applicable to large volume of water sample with high extraction efficiency. Column clean up in classical analytical methods were very complex and time consuming procedures during decade. Modifications were tried to decrease solvent and reagents volume. Moreover, use of column connection method has been demonstrated in the environmental matrices. Instrumental configurations also have been improved, in which GC/MS/MS with large volume injection approach can analyze picogram levels. Absolute sensitivities of HRMS increased compared to old versions of double focusing sector type mass spectrometers. Based on these analytical evolutions during last 10 years, we tried to optimize the analytical method for dioxins in water sample from sample extraction to instrumental analysis.

• Bulletin of the Korean Chemical Society
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• 제32권5호
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• pp.1564-1568
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• 2011

A solvent extraction separation, preconcentration and determination of thorium with a new crown, 2-ethyl-N-benzyl-4,7,10,13,16-pentaoxa-1-azacyclooctadecane (MACE), is described in the study. The amount of thorium in the aqueous phase and organic phase was determined by Inductively Coupled Plasma-Optical Emission Spectroscopy and Ultraviolet-Visible, respectively. Thorium loaded organic phase was quantitatively stripped in a stage by using 1.0 M $HNO_3$. Thorium was effectively extracted with MACE in the pH range of 6-7 to produce a 3:2 complex ratio in the chloroform. A highly sensitive and rapid spectrophotometric method was described for determination of trace amounts of thorium with MACE. The effective molar absorption coefficient at 281 nm is $1.98{\times}10^3\;mol^{-1}cm^{-1}$, and the system complies with Beer's law in the range from 0.464 to 2.32 ${\mu}gm\;L^{-1}$ of thorium. Thorium was also determined in standard and environmental samples.