• 제목/요약/키워드: Product selectivity

검색결과 137건 처리시간 0.031초

더블허들 모형을 이용한 전통시장 재방문객의 농산물 구입결정 요인에 관한 연구 (A Study on Purchasing Agricultural Products of Re-visitors In Traditional Market Using Double Hurdle Model)

  • 이향미
    • 농촌계획
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    • 제21권2호
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    • pp.137-147
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    • 2015
  • In this study, consumers who have experience of visiting Jeongsun Arirang Market has been selected as samples to understand the characteristics of agricultural products purchase. For this, double hurdle model was used in order to resolve sample selection problem and obtain consistent estimator. The key points are the following. First, as the age increases(up to 59.8 years), chances of purchasing the products at traditional market increase as income increases. Second, when the residence area is outside of Gangwon-province, the purchase amount of the products increased compared to those from visitors within the Gangwon province. Also, visitors who use public transportations purchase less products compared to those who use their own car. Third, probability of agricultural products increase as the visitors consider positive effect the product purchase leads to the local farmers. Fourth, if the visitors consider the quality of the agricultural products, probability of purchasing agricultural product at the site increases. However, if the visitors consider the freshness of the agricultural products, the purchase amount rather drops. Fifth, the probability of purchase increases as visitors consider the brand of traditional market.

아크젯 플라즈마에서의 메탄개질의 최적화 (PROCESS OPTIMIZATION OF METHANE REFORMING IN ARC JET)

  • 황나경;이대훈;송영훈
    • 한국연소학회:학술대회논문집
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    • 한국연소학회 2006년도 제33회 KOSCO SYMPOSIUM 논문집
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    • pp.266-271
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    • 2006
  • Characteristic of partial oxidation of methane using arc-jet plasma by AC power is investigated. Arc-jet reactor used in this work is slightly modified from typical arc jet reactor so that it can make and sustain stable state of plasma. Methane conversion, selectivity of chemicals such as hydrogen and hydrocarbon materials in the product are analyzed. Parametric approach on the performance of the reactor or detail on the partial oxidation process is carried with $O_2/C$ ratio as parameter. In addition to the results, SED and arc length is changed to understand the effect of current-voltage correlation on the reforming performance and relative role of thermal process.

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Correlation of the Rates of Solvolyses of 4-Methylthiophene-2-carbonyl Chloride Using the Extended Grunwald-Winstein Equation

  • Choi, Ho-June;Koo, In-Sun
    • Bulletin of the Korean Chemical Society
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    • 제33권2호
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    • pp.499-504
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    • 2012
  • The specific rates of sovolysis of 4-methylthiophene-2-carbonyl chloride (1) have been determined in 26 pure and binary solvents at $25.0^{\circ}C$. Product selectivities are reported for solvolyses of 1 in aqueous ethanol and methanol binary mixtures. Comparison of the specific rates of solvolyses of 1 with those for p-methoxybenzoyl chloride (2) in terms of linear free energy relationships (LFER) are helpful in mechanistic considerations, as is also treatment in terms of the extended Grunwald-Winstein equation. It is proposed that the solvolyses of 1 in binary aqueous solvent mixtures proceed through an SN1 and/or ionization (I) pathway rather than through an associative $S_N2$ and/or addition-elimination (A-E) pathway.

Improvement in Catalytic Activity of Ag Catalyst via Simple Mixing with Carbon

  • Choun, Myounghoon;Baek, Ji Yun;Eom, Taehyoung
    • KEPCO Journal on Electric Power and Energy
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    • 제5권4호
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    • pp.331-335
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    • 2019
  • In this study we investigate catalytic activity and selectivity of mixture of Ag and ketjenblack according to their ratios by product analysis and electrochemical experiments, such as cyclic voltammetry, linear sweep voltammetry and chronoamperometry. We reveal that catalytic activity toward CO2 reduction to CO is improved by simple mixing Ag nanoparticle and ketjenblack because addition of ketjenblack suppresses aggregation of Ag nanoparticles and brings increase in electrochemical active surface area. However, excess amount of ketjenblack rather inhibit the CO2 reduction to CO. These observations provide clues to develop highly active Ag catalyst or electrode toward electrochemical reduction of CO2.

아크릴로니트릴 제조공정에서 아세토니트릴 회수에 관한 연구 (A Study on the Recovery of Acetonitrile in the Process of Manufacturing Acrylonitrile)

  • 박동원;최성욱;김영일
    • 자원리싸이클링
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    • 제8권3호
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    • pp.31-36
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    • 1999
  • 아크릴로니트릴 제조공정 중 부산물로 생성되는 물과 아세토니트릴 공비혼합물을 분비, 회수하기 위하여 혼합용매로서 toluene-ethylacetate를 선택하여 $25^{\circ}C$에서 4성분계 toluene(1)-water(2)-acetonitrile(3)-ethylacetate(4)에 대한 액-액평형 데이터를 구하였다. Tie-line 계산치를 예측하기 위하여 실험치를 UNIFA 모델식의 파라미터와 상호연관시켜 비교하였다. 또한 용매의 성능을 비교하기 위하여 분배계수 및 선택도를 고찰하였다.

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메탄올 자동차 배기가스 정화용 헤테로폴리산 촉매의 특성 (Characteristics of Heteropoly Acid Catalyst for Emission Gas Control in Methanol Fueled Vehicles)

  • 서성규;박남국;박훈수;김재승
    • 한국대기환경학회지
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    • 제11권1호
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    • pp.77-84
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    • 1995
  • To prevent or reduce air pollutant from methanol fueled vehicles, methanol oxidation reaction was carried out using a heteropoly acid catalysts. Catalytic activities of catalysts have been experimented at atmospheric pressure in a fixed bed flow reactor. Catalysts were characterized by XRD, IR, thermal analysis, N $H_{3}$-TPD and GC pulse technique. Acidities of catalysts were highly affected by poly-atoms. Methanol conversion was much higher on catalyst with W than on catalyst with Mo as a poly-atoms. With the increase of copper content(X) in C $u_{x}$ $H_{{3-2x}}$PMo catalyst, acidity was decreased and oxidation ability was increased. Methanol conversion and product distribution were affected by the acidity and oxidation ability of catalyst. Especially, supported PdSiW(1wt%) catalyst has a very good methanol conversion and C $O_{2}$ selectivity as high as a commertial 3-way catalyst.t.

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A Convenient HPLC/ELSD Method for the Quantitative Analysis of Betaine in Lycium chinense

  • Lee, Sang-Myung;Park, Chae-Kyu;Cho, Byung-Goo;Cho, Kyoung-Shim;Min, Byung-Sun;Bae, Ki-Hwan
    • Natural Product Sciences
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    • 제17권2호
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    • pp.104-107
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    • 2011
  • In order to facilitate the quality control of betaine from the fruits of Lycium chinense, we have developed a rapid and simple method for quantitative determination. Determination was achieved on a Discovery C18 column with an isocratic solvent system of 0.32% perfluoropentanoic acid aqueous-acetonitrile at a flow-rate of 0.5 mL/min and detected an ELSD. The method was reproducible with intra- and inter-day variations of less than 6% (R.S.D). The recoveries were in the range of 90.01~100.05%. The method turned out to be fast and simple, furthermore, to have a good selectivity and sensitivity for the quantity determination of betaine in the fruits of L.chinense.

isopropyl acetate을 이용한 페놀의 isopropylation 반응의 Al-MCM-48 분자체 촉매반응 특성 (Catalytic performance of Al-MCM-48 molecular sieves in the isopropylation of phenol with isopropyl acetate)

  • 칸단 벤카타찰람;푸시파라지 헤마라다;팽메이메이;장현태
    • 한국산학기술학회:학술대회논문집
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    • 한국산학기술학회 2011년도 춘계학술논문집 1부
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    • pp.144-146
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    • 2011
  • Al-MCM-48 molecular sieves (Si/Al = 25, 50, 75 and 100) were synthesized hydrothermally using cetyltrimethyl ammonium bromide as the structure directing template. The orderly arrangement of mesopores was evident from the low angle X-ray diffraction patterns and TEM images. The catalytic performance was evaluated in the vapour phase isopropylation of phenol with isopropyl acetate. Phenol conversion decreased with increase in the Si/Al ratio of the catalysts. The major reaction product was 4-isopropyl phenol (selectivity: 78%). Delocalization of phenolic oxygen electron pair over the aromatic ring promoted para-selective alkylation. Such delocalization could be aided by the hydrophilic surface of the molecular sieves. Though ester was used as the alkylating agent, phenyl isopropyl ether was not formed

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코발트 카르보닐을 촉매로한 할로겐화할로벤질의 선택적 모노-카르보닐화 (Ⅰ) (Cobalt Carbonyl Catalyzed Selective Mono-Carbonylation of Halobenzyl Halide (Ⅰ))

  • 심상철;도칠훈;윤영주;조찬식;우병원
    • 대한화학회지
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    • 제34권6호
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    • pp.658-662
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    • 1990
  • 할로벤질할라이드의 위치선택적 카르보닐화에 대한 방법을 검토하였다. 할로겐화 페닐아세트산 알킬은 상압의 일산화탄소 촉매량의 코발트카르보닐, 염기 및 알코올 존재하에서 할로겐화 할로벤질의 벤질 부분 할라이드를 카르보닐화 함으로써 쉽게 합성된다. 염기는 생성물의 선택성에 결정적인 역할을 하며, NEt$_3$가 사용된 염기 중에서 가장 좋았다.

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Cataytic Hydrogenation of o-Nitrochlorbenzene to 3,3'-Dichlorobenzidine

  • Shen, Kaihua;Li, Shude;Choi, Dong-Hoon
    • Bulletin of the Korean Chemical Society
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    • 제23권12호
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    • pp.1785-1789
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    • 2002
  • 2,2'-Dichlorohydroazobenzene was prepared by selective hydrogenation of o-nitrochlorobenzene with hydrogen in the presence of 0.8% and 5% Pd/C catalyst. O-Chloroaniline was a minor product in the catalytic hydrogenation of o-nitrochlorobenzene. The effects of base, Pd/C catalyst, and co-catalyst were discussed on catalytic hydrogenation. 2,2'-Dichlorohydroazobenzene, as an intermediate, was rearranged to 3,3'-dichlorobenzidine after reacting with HCl. It was shown that selectivity of catalytic hydrogenation of o-nitro-chlorobenzene is affected strongly by concentration of base, Pd/C catalyst, and co-catalyst. $^1Hand^{13}C$NMR spectroscopy confirmed the chemical structures of 2,2'-dichlorohydrazobenzene and 3,3'-dichlorobenzidine.