• 제목/요약/키워드: Chromatogram

검색결과 317건 처리시간 0.029초

전기 자동차용 폴리올 에스테르계 냉동기유의 R-1234yf 냉매와의 적합성 연구 (Study on Chemical Stabilities with R-1234yf Refrigerant of Polyol Ester Refrigerant Oil for Electric Vehicles)

  • 홍지수;정근우;김남균;신지훈;김영운;이은호;고봉성;황승용
    • Tribology and Lubricants
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    • 제36권3호
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    • pp.139-146
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    • 2020
  • Global warming has led to an increase in demand of eco-friendly vehicles, such as electric cars, for reducing greenhouse gas emissions, and especially, regulating carbon dioxide generation. In addition, electric vehicles are equipped with an electric drive-type hermetic scroll compressor and a refrigerant, which exhibit current and future trends of using environmentally friendly refrigerants, including R-1234yf. In this study, polyol ester-based refrigeration oils are prepared via condensation esterification of polyol and fatty acids. The oils can be combined with R-1234yf refrigerant for applications in air conditioning and cooling systems of electric vehicles. The structure of synthetic polyol esters is confirmed via 1H-NMR and FT-IR spectrum analysis, and the composition of the polyol ester is analyzed via gas chromatogram analysis. Furthermore, kinematic viscosity, viscosity index, total acid value, pour point, and color are analyzed as fundamental physical properties of the synthetic polyol esters. The compatibility and chemical stability of the synthetic polyol ester combined with the R-1234yf refrigerant are obtained via high temperature and high pressure oil-resistant refrigerant tests. The changes in the oil color and catalyst activity are observed before and after the experiment to determine whether it is suitable as a refrigerator oil.

황금(黃芩)의 엽조직(葉組織) 배양(培養)에 의한 식물체(植物體) 재분화(再分化)와 주요(主要) 성분(成分) (Plant Regeneration from Leaf Tissue Culture and Some Effective Substances in Scutellaria baicalensis G.)

  • 이만상;김귀호;오기홍
    • 한국약용작물학회지
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    • 제1권1호
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    • pp.43-48
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    • 1993
  • 황금(黃芩)(Scutellaria baicalensis)의 엽조직(葉組織)을 배양(培養)하여 기내(器內) 종묘(種苗)를 대양증식(大量增殖)시키고 유기(誘起)된 Callus 내(內)의 약효성분(藥效成分)을 검정(檢定)하여 2차(次) 산물(産物)의 효율적(效率的)인 이용(利用)을 도모하기 위하여 식물생장조절제(植物生長調節劑)가 캘러스유기 및 기관분화에 미치는 영향을 조사(調査)하였다. 엽(葉)으로부터 캘러스 유기(誘起)는 NAA $0.5mg\;/\;{\ell}$ 의 단독처리(單獨處理)에서 양호(良好)했으며, 혼합처리(混合處理)에서는 NAA $0.5mg\;/\;{\ell}\;와\; zeatin\;0.5mg\;/{\ell}$ 의 처리구(處理區)에서 양호(良好)하였다. 캘러스로부터 식물체(植物體) 재분화(再分化)를 위해서는 BAP $1.0mg\;/\;{\ell}\;+\;NAA\;0.5mg\;/\;{\ell}\;와\;zeatin\;1.0mg\;/\;{\ell}\;+\;NAA\;0.5,\;1.0mg\;/\;L$ 혼합처리구(混合處理區)에서 가장 효과적(效果的)이었다. 2차(次) 산물(産物)의 이용(利用)을 위해 캘러스를 TLC법(法)에 의해 성분분석(成分分析)한 결과(結果) baicalin의 존재(存在)를 확인하였다.

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Lactobacillus plantarum 발효에 의한 갈근탕의 생물 전환 성분 연구 (Bioconversion Constituents of Galgeun-tang Fermented by Lactobacillus plantarum)

  • 양민철;김동선;정상원;마진열
    • 한국약용작물학회지
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    • 제19권6호
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    • pp.446-455
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    • 2011
  • Galgeun-tang (GGT) is a traditional medicinal formula that is widely prescribed to treat cold, asthma, and hives in Korea. Fermented herbal medicines can be made more effective than normal herbal medicines by increasing the absorption and bioavailability of the active compounds. In this study, we fermented Galgeun-tang to produce bioconversion constituents using Lactobacillus plantarum (GGT144), and found that four peaks were decreased, three peaks were increased and two new peaks appeared in the HPLC-DAD chromatogram. After HPLC-DAD-guided fractionation of the newly-appearing compounds (1 and 5) and the increased (6, 7, and 9) compounds, the structure of the compounds was determined using NMR and MS. Using this approach the compounds were identified to be pyrogallol (1), daidzein (5), liquiritigenin (6), cinnamyl alcohol (7), and formononetin (9), respectively. In addition, the decreased compounds were identified to be daidzin (2), liquiritin (3), ononin (4), and cinnam aldehyde (8) using HPLC-DAD analysis with standard compounds. The high performance liquid chromatography method was used to quantify the nine constituents in GGT and GGT144. All calibration curves of the standard compounds displayed excellent linearity with a $R^2$ > 0.9968.

의이인(薏苡仁)(Coicis Semen)의 의약품개발(醫藥品開發)에 관(關)한 연구(硏究)(I) -아미노산(酸)의 함량(含量)에 대하여- (Studies on the Drug Development of Coicis Semen(I) -Aminoacid Contents in Coicis Semen-)

  • 용재익
    • Journal of Pharmaceutical Investigation
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    • 제7권1_4호
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    • pp.1-12
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    • 1977
  • Free amino acid in ethanol extracts and total amino acid hydrolysates of Coicis semen were analyzed by amino acid autoanalyzer. The sample A (unpolished Coicis Semen) and sample B(polished Coicis Semen) are used in this experiments. The results obtained from this study are as follows: 1) 17 kinds of free amino acid (Asp, Thr, Ser, Glu, Pro, Gly, Ala, Val, Cys, Met, Ileu, Lew, Try, Phe, Lys, His, Arg,) including 7 kinds of essential amino acid (Val, Lew, Ileu, Thr, Lys, Met, Phe,) as human nutrition were identified and quantified but tryptophan. 2) Total free amino acids of sample A is more than about 3 folds that of sample B. 3) The distribution of free amino acids contained in sample A, threonine is the richiest and then comes Ala, Glu, Asp, and Pro, in that order. In sample B, glutamic acid is the richiest and then comes Thr, Asp, Ala, and Gly, in that order. 4) 17 kinds of total amino acid (Asp, Thr, Ser, Glu, Pro, Gly, Ala, Val, Cys, Met, Ileu, Lew, Tyr, Pher, Lys, including 7 kinds of essential amino acid (Val, Leu, Ileu, Thr, Lys, Met, Phe,) in human nutrition except tryptophan were identified and quanified. 5) Total amino acid content of sample A is more than about 1.06 folds that of sample B. 6) Total amino acid content of sample A in acid hydrolysates is more than about 1.06 folds that of sample B in acid hydrolysates. 7) Unknown chromatogram of ethanol extracts and acid hydrolysates of Coicis Semen were identified as Ornitine.

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Enzymatic Properties of Cytochrome Oxidase from Bovine Heart and Rat Tissues

  • Lee, Jae-Yang;Lee, Sang-Jik
    • BMB Reports
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    • 제28권3호
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    • pp.254-260
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    • 1995
  • Cytochrome oxidase was purified from bovine-heart mitochondria and its enzymatic properties were examined. The purified cytochrome oxidase was identified by its absorption spectrum and chromatogram through gel filtration. The specific activity, purification degree and yield of purified cytochrome oxidase were 18 nmol/mg/ml/min, 24.83 fold and 0.93%, respectively. The activity of the enzyme assayed by a ferrocytochrome $c-O_2$ system was optimized at $25^{\circ}C$ and pH 6.5. Examining the effect of nonionic detergents established that cytochrome oxidase was deactivated by Triton X-100. The oxidase was activated by Tween 80 and deactivated by Tween 20. The Michaelis constant and maximum velocity of the oxidase for ferrocytochrome c were 0.032~0.044 mM and 0.019~0.021 mM/min, respectively. After adaption to basal diet for a week, experimental diets containing 6 mg Cu/kg, or zero mg Cu/kg, or 12 mg Cu/kg were fed to a control group, a copper-free group and a copper-rich group of Sprague-Dawley rats, respectively, for 4 weeks. The specific activities assayed for the ferrocytochrome $c-O_2$ system of isolated cytochrome oxidase from the rat liver of control, copper-free, and copper-rich group were 1.00, 1.19, and 0.878 nmol/mg/ml/min, respectively. Their degrees of purification were 11.38, 10.82 and 8.78 fold, respectively. The specific activities for liver and heart mitochondrial cytochrome oxidase of copper-free/copper-rich groups assayed using the ferrocytochrome $c-O_2$ system were 81.4% and 96.4%/64.1% and 61.1%, respectively, compared with those of the control.

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Bacteria가 생산하는 Cysteinedesulfhydrase에 관한 연구(제이보) L-Cysteine 유도체의 효소적 합성에 관하여 (Studies on Cysteine desulfhydrase Produced by Bacteria(Part II) Enzymatic Preparation of L-Cysteine Derivatives by Cysteinedesulfhydrase from Aerobacter aerogenes.)

  • 최용진;양한철
    • 한국미생물·생명공학회지
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    • 제2권1호
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    • pp.45-50
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    • 1974
  • 1. L-cysteine을 pyruvate, sulfide 및 ammonia로 분해하는 반응을 촉매하는 효소인 cysteinedesulfhydrase의 촉매기능에 대해 연구해온 바 Aerobacter aerogenes로부터 유도생산한 cysteinedesulfhydrase를 사용하여 분해반응의 역반응에 의해 pyruvate, ammonia 및 sulfide로부터 cysteine의 유도체인 S-methyl-L-cysteine 및 S-ethyl-L-cysteine을 합성하였다. 2. 합성반응에 있어서 S-methyl-L-cysteine 및 S-ethyl-L-cysteine의 생성량은 반응시간과 효소량에 비예적인 관계를 나타내었고 반응의 최적 pH는 10.0이었다. 3. 효소적 합성법에 의해 생산된 S-methyl-L-cysteine 및 S-ethyl-L-cysteine을 반응액으로 부터 단리, 결정화해서 이들 합성산물에 대한 Ion exchange chromatogram, NMR spectrum, element analysis, molecular weight 및 melting point 측정 등의 분석시험을 행한 바 이들 화합물에 대한 이론치와 잘 일치되는 결과를 얻었다.

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출류(朮類) 대조 생약에 관한 연구 (Studies on the Crude Drugs of Atractylodis Species)

  • 김호현;전인주;강인호;함인혜;제금련;황완균;조형권
    • 생약학회지
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    • 제34권2호통권133호
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    • pp.123-127
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    • 2003
  • Atrartylodis Rhizoma(蒼朮)'s origin plants are Atratylodes lancea and A. Chinensis in Chinese, Japanese and Korean pharmacopoeia. A. Japonica is only indigenous in Korea, it is actually used as Atractylodis Rhizoma in Korean market. A. lancea is used in Hunan province, China and A. Chinensis is used in Hubei province, China. It is impossible to distinguish with species differency as macro- and micro-morphology. We tried to distinguish with species differency by HPLC and GC-Mass spectra. Atractylone(mw. 216) which is a marker compound in Atractylodis Rhizoma Alba(白朮) was detected in A. japonica. Atractylodin (mw.182) was detected in A. lancea and two eudesmadien derivatives (mw. 204) were detected in A. chinensis. HPLC chromatogram showed the same patterns. As a result, we propose that A. japonica will be added as Atractylodis Rhizoma (蒼朮)'s origin plant in Korean Pharmacopoeia. Atractylodis Rhizoma Alba(白朮)'s origin plants are A. macrocephala in China, and A. Japonica and A. ovata in Korea and Japan. In GC-Mass analysis, all samples showed same patterns and the main compound was atractylone.

작약(Paeonia lactiflora Pall.)에서 paeoniflorin 추출방법 및 HPLC 분석조건 (Extraction Methods and HPLC Analysis Conditions of Paeoniflorin in Peony, Paeonia lactiflora Pall.)

  • 정명근;강광희
    • 한국작물학회지
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    • 제39권6호
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    • pp.542-547
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    • 1994
  • 경북 영천군 고경면 작약 재배농가의 정식 4년차인 의성품종(Paeonia lactiflora Pall.)을 1993년 6월 17일 수확하고, 굵기가 27mm 이상인 뿌리를 선별하여 paeoniflorin 추출방법 및 HPLC 분석조건에 대한 조사결과를 요약하면 다음과 같다. 1. 초음파추출 및 환류추출법에 의한 작약근 추출물의 HPLC chromatogram은 상호간의 차이가 없었으며, 두 추출법 모두에서 paeoniflorin retention time이 10.2분대에 peak가 존재하였다. 2. 환류추출법에 의한 paeoniflorin 추출은 60min., 1회로 충분하였다. 3. 초음파추출에서 추출시간이 1hr.∼2hr. 까지의 paeoniflorin함량은 동일시간의 환류추출보다 각각 0.28%, 0.32% 낮게 평가되었고 3hr.∼4hr.의 추출에서는 두 방법간에 차이가 없었다. 4. 초음파 추출법은 분석작업이 용이함으로 다수계통의 상대적 비교시에는 환류추출법보다 효과적이다. 5. 작약추출물 중 paeoniflorin, albiflorin을 HPLC를 이용하여 분석할 때 높은 감도를 보이는 가장 효과적인 UV Detector 파장은 각각 240nm, 254nm이고, 동시정량시에는 254nm가 비교적 안정적이었다.

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Identification of urinary metabolite(s) of CKD-712 by gas chromatography/mass spectrometry in rats

  • Jeon, Hee-Kyung;Park, Hae-Yeon;Kim, Youn-Jung;Kwon, Oh-Seung;Ryu, Jae-Chun
    • 한국환경독성학회:학술대회논문집
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    • 한국환경독성학회 2003년도 춘계학술대회
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    • pp.188-188
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    • 2003
  • Examination was made of the urinary metabolite(s) of CKD-712, which is a chiral compound, named S-YS49 derived from higenamine (one component of Aconite spp.) derivatives. First of all, to analyze the metabolite(s) of CKD-712, a simple and sensitive detection method for CKD-712 was developed by using gas chromatography-mass spectrometry GC/MS). Urine was collected from adult male Sprague-Dawley rats 250${\pm}$10g) in metabolic cage for 24hr after oral administration of 100 mg/kg of CKD-712. The recovery of CKD-712 after extraction and concentration with AD-2 resin column was above 90 % from rat urine. The detection limits of CKD-712 in urine was approximately 0.1 ng/mL. It has well been suggested that isoquinoline possessing catechol moiety such as CKD-712 should be subjected to the catechol-O-methyl kransferase activity in vivo. We detected three major peaks of presumed CKD-712 metabolites in the total ion chromatogram obtained from the rat urine sample after oral administration of CKD-712. From these results, it is assumed that the urinary metabolites are mono-methylation in the naphthyl moiety (metabolite I ), methylation at the C-6 or 7 hydroxy group in the isoquinoline moiety and hydroxylation at in the naphthyl moiety (metaboliteII), and methylation at the C-6 or 7 hydroxy group in the isoquinoline moiety (metaboliteIII).

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초임계 유체 크로마토그래피에서 새로운 분리방식인 변형제 조성 프로그래밍법 개발 (Development of New Separation Technique, Modifier Composition Programming in Supercritical Fluid Chromatography)

  • 김호현;표동진
    • 분석과학
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    • 제10권5호
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    • pp.350-356
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    • 1997
  • 초임계 유체 크로마토그래피(Supercritical Fluid Chromatography, SFC)는 종래의 크로마토그래피 방법으로 분석하기 어려운 물질을 분석해 내는 기술로서 발전이 되어 왔다. 그러나 초임계 유체 $CO_2$는 극성이 큰 시료들을 용출(elution)시키기가 어려워 초임계 $CO_2$에 극성을 지닌 변형제(modifier)를 섞어서 이동상으로 사용하였다. 기존의 간단하고 효과적인 방법으로는 변형제로 포화된 Silica Column을 사용하였는데, 이 방법의 가장 큰 단점을 변형제의 양을 조절할 수 없다는 것이다. 따라서 본 연구에서는 초임계 $CO_2$에 변형제를 지속적으로 첨가시키며, 변형제의 양을 조절할 수 있는 새로운 방법을 개발하였고, 첨가된 수분($H_2O$)의 양은 perfluorosulfonate ionomer (PFSI) film을 이용하여 만든 amperometric microsensor로서 측정하였다. 실제로 이 방법을 사용하여 PAH 혼합물을 변형제 조성 프로그래밍법으로 분리해 본 결과 좋은 크로마토그램을 얻었다.

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