• 제목/요약/키워드: purity

검색결과 2,390건 처리시간 0.046초

접촉분해경유 중의 2,6-dimethylnaphthalene (2,6-DMN)의 고순도 정제 - 결정화에 의한 DMN 이성체 농축액 중의 2,6-DMN의 정제 - (High-Purity Purification of 2,6-Dimethylnaphthalene (2,6-DMN) in Light Cycle Oil - Purification of 2,6-DMN from Concentrate of DMN Isomers by Crystallization -)

  • 김수진;정화진
    • 공업화학
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    • 제19권1호
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    • pp.105-110
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    • 2008
  • 증류-추출의 조합에 의해 접촉분해경유(LCO)로부터 회수한 dimethylnaphthalene (DMN) 이성체 농축액을 원료로 사용하여 결정화조작을 행해 2,6-DMN의 정제를 검토했다. 2,6-DMN의 정제에 적합한 용매의 선정을 위해 13종의 용매(acetone, cyclohexanone, ethanol, ethyl ether, ethyl acetate, isopropyl ether, methanol, n-hexane, n-heptane, pyridine, THF, toluene, methanol과 acetone의 혼합용매)를 사용하여 결정화조작을 행한 결과, 60 vol% methanol과 40 vol% acetone의 혼합용매(M/A = 1.5)가 2,6-DMN의 순도 및 수율의 측면에서 우수한 정제성능을 보였다. 결정화 온도의 상승 및 용매(M/A = 1.5)/원료(농축액)의 체적비의 증가는 2,6-DMN의 순도를 향상시켰으나, 역으로 수율의 저하를 초래시켰다. DMN 이성체 농축액을 원료(10.43 wt% 2,6-DMN)로 사용한 결정화를 통해 회수한 결정(76 wt% 2,6-DMN)을 원료로 사용하여 재차 결정화조작을 행한 결과, 40%의 수율로 99.7 wt% 2,6-DMN의 결정을 얻을 수 있었다.

Development of analytical method for the isotope purity of pure D2 gas using high-precision magnetic sector mass spectrometer

  • Chang, Jinwoo;Lee, Jin Bok;Kim, Jin Seog;Lee, Jin-Hong;Hong, Kiryong
    • 분석과학
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    • 제35권5호
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    • pp.205-211
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    • 2022
  • Deuterium (D) is an isotope with one more neutron number than hydrogen (H). Heavy elements rarely change their chemical properties with little effect even if the number of neutrons increases, but low-mass elements change their vibration energy, diffusion rate, and reaction rate because the effect cannot be ignored, which is called an isotope effect. Recently, in the semiconductor and display industries, there is a trend to replace hydrogen gas (H2) with deuterium gas (D2) in order to improve process stability and product quality by using the isotope effect. In addition, as the demand for D2 in industries increases, domestic gas producers are making efforts to produce and supply D2 on their own. In the case of high purity D2, most of them are produced by electrolysis of heavy water (D2O), and among D2, hydrogen deuteride (HD) molecules are present as isotope impurities. Therefore, in order to maximize the isotope effect of hydrogen in the electronic industry, HD, which is an isotope impurity of D2 used in the process, should be small amount. To this end, purity analysis of D2 for industrial processing is essential. In this study, HD quantitative analysis of D2 for high purity D2 purity analysis was established and hydrogen isotope RM (Reference material) was developed. Since hydrogen isotopes are difficult to analyze with general gas analysis instrument, they were analyzed using a high-precision mass spectrometer (Gas/MS, Finnigan MAT271). High purity HD gas was injected into Gas/MS, sensitivity was determined by a signal according to pressure, and HD concentrations in two bottles of D2 were quantified using the corresponding sensitivity. The amount fraction of HD in each D2 was (4518 ± 275) μmol/mol, (2282 ± 144) μmol/mol. D2, which quantifies HD amount using the developed quantitative analysis method, will be manufactured with hydrogen isotope RM and distributed for quality management and maintenance of electronic industries and gas producers in the future.

Effect of the Si-C Powder Prepared by Mechanical Alloying on the Densification of Silicon Carbide Powder

  • Yoon, Bola;Lee, Sea-Hoon;Lee, Heesoo;Hwang, Geumchan;Kim, Byungsook
    • 한국세라믹학회지
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    • 제53권1호
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    • pp.99-104
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    • 2016
  • High purity Si-C (99.999%) powder prepared by mechanical alloying was added to a commercial SiC powder as a sintering additive. Reaction bonded silicon carbide balls and jars with high purity (99.98%) were used for the mechanical alloying. As a result, the purity of the sintered Si-C was higher than 99.99%. When sintered at $2200^{\circ}C$ under 50 MPa pressure for 1 h, SiC containing 10 wt% of high purity Si-C showed a relative density of 95.3%, similar to the relative density of commercial SiC (95%). However, the relative density of SiC decreased to 90.6% without the additive when the applied pressure decreased to 40 MPa. In contrast, the relative density was nearly unaffected by the decrease of the pressure when using the Si-C additive. Therefore, the addition of Si-C powder promoted the densification of SiC above $2000^{\circ}C$ under 40 MPa pressure.

주석도금폐액으로부터 이온교환 및 사이클론 전해채취를 이용한 고순도 주석의 회수 (Recovery of High Purity Tin from Waste Solution of the Tin Plating by Ion-exchange and Cyclone-electrowinning)

  • 강용호;신기웅;안재우
    • 자원리싸이클링
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    • 제25권4호
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    • pp.42-48
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    • 2016
  • 주석도금폐액으로부터 고순도 주석 금속을 회수하는 연구를 실시하였다. 먼저 주석도금폐액을 Iminodiacetic 관능기를 가진 이온교환수지(Lewatit TP 207)를 사용하여 1차적으로 유기물 및 Fe, Zn, Na 등의 불순물을 제거하였고, 2차적으로 Ethylhexyl-phosphate의 관능기를 가진 이온교환수지(Lewatit VPOC 1026)를 사용하여 잔류하고 있는 불순물들을 모두 제거하여 고순도의 주석용액으로 회수하였다. 회수된 주석용액으로부터 고순도 금속주석으로 회수하기 위하여 사이클론식 전해방법을 사용하였으며, 전해채취 결과 약 99.98% 순도의 주석을 회수할 수 있었다.

키랄 크로마토그래피와 NMR 분광법에 의한 N-acetyl-1-naphthylethylamine의 광학순도 측정 (1Determination of optical purity of N-acetyl-1-naphthylethylamine by chiral chromatography and NMR spectroscopy)

  • 정영한;류재정
    • 분석과학
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    • 제23권1호
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    • pp.97-101
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    • 2010
  • (R)-N-3,5-dinitrobenzoyl (DNB) phenylglycinol로 부터 만들어진 키랄 선택제가 라세미 Nacylnaphthylalkylamines의 분리에 HPLC 키랄 정지상으로 이용된 바 있다. 본 연구에서는 (R)-phenylglycinol 유도체 키랄 선택제를 이용하여 키랄 크로마토그래피와 NMR 분광법에 의한 광학순도를 측정하였다. NMR과 HPLC 실험결과를 참값과 비교하여 각 광학순도 측정값의 정확도와 정밀도를 계산하였다. NMR 방법의 오차는 +2.2%, 평균 RSD는 4.54% 이었고, HPLC 방법의 오차는 -3.5%, 평균 상대표준편차는 3.23% 이었다.

Extrusion시킨 팽윤 전분을 기질로 한 새로운 Maltose 생산법 (A Novel Method for Production of Concentrated Purity Maltose Using Swollen Extruded Starch)

  • 이용현;김동선;신현동;박진서
    • 한국미생물·생명공학회지
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    • 제22권1호
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    • pp.106-113
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    • 1994
  • A novel method for production of concentrated purity maltose using swollen extruded corn starch was investigated. Degree of gelatinization of extruded starch suitable for maltose formation was found to be around 70%. The optimal amiunt of enzyme was 400 unit fungal $\alpha $-amylase per g of starch, and the reaction time was 12 hours. At extruded starch concentration of 300 g/l(w/v), maltose concentration and content were reached up to 220 g/l(w/v) and 77%(w/w), respectively. The maltose forming reaction was also successfully proceeded at high starch concentration of 700 g/l(w/v), however, the conversion yield and content were decreased. By the addition of extruded starch by fed-batch wise, the maltose concentration, purity, and conversion yield could be improved up to 465 g/l(w/v), 70%(w/w), and 0.63, respectively. The investigated maltose production process seems to have many potential advantages over the conventional process utilizing liquefied starch, and the feasibility for industrial application needs to be evaluated.

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