• 제목/요약/키워드: chemical product

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Influence of "Historical Effects" on the Rheological Properties of a Polyacrylonitrile Copolymer Solution

  • Cheng, Yumin;Zhang, Huibo;Zhang, Shuangkun;Liu, Weiwei;Wang, Jing;Cheng, Run;Ryu, SeungKon;Jin, Riguang
    • Carbon letters
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    • 제14권1호
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    • pp.45-50
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    • 2013
  • Polyacrylonitrile (PAN) copolymers of different molecular weights were synthesized by a suspension polymerization and precipitation polymerization method. The rheology behaviors of the synthesized PAN copolymers were investigated in relation to their molecular weight, solid content and melting temperature. The influence of "historical effects" on the spinning solution of PAN was studied by analyzing the laws of viscosity considering the diversification time and temperature. The viscosity disciplines of each spinning solution conformed well to the rheological universal laws in a comparison of the suspension polymerization product with that of precipitation polymerization. Viscosity changes in the swelling process of dissolution were gentler in the suspension polymerization product; a small amount of water will quickly debase the solution viscosity, and high-speed mixing can greatly shorten the time required by the spinning solution to reach the final viscosity.

메탄올을 이용한 올레핀 생산 분리공정의 기술 및 경제성 분석 (Techno-Economic Analysis of Methanol to Olefins Separation Processes)

  • 박종현;정영민;한명완
    • Korean Chemical Engineering Research
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    • 제58권1호
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    • pp.69-83
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    • 2020
  • 경질 올레핀은 중요한 석유화학제품일 뿐 아니라 다양한 화학 중간체들을 위한 기본 구성체이다. 최근 에틸렌이 생산 제품의 대부분을 차지하는 Ethane Cracking Center (ECC) 공정이 크게 늘어남에 따라 프로필렌 공급이 매년 꾸준히 증가하는 프로필렌 수요를 따라잡지 못하고 있다. 이에 따라 프로필렌의 수요를 따라잡기 위하여 메탄올로부터 올레핀으로 전환하는 기술이 보다 중요하게 되었다. Methanol to olefins (MTO) 공정은 합성가스를 통해 메탄올을 생산하고 메탄올로부터 프로필렌 등 올레핀을 생산한다. 메탄올을 올레핀으로 전환하는 반응은 사용되는 촉매에 따라 다른 반응생성물 조성을 갖기 때문에 생성물에 따른 적절한 분리 방법이 고려되어야 한다. 따라서 네 가지의 대표적인 반응 생성물 조성들에 대하여 네 가지의 분리공정 대안들을 Aspen plus를 이용하여 모사하였다. 또한 모사 결과를 바탕으로 기술적 경제적 분석을 통하여 MTO 공정의 반응 생성물 조성에 대한 각 분리공정의 성능을 평가하였으며, 이를 통해 MTO 공정의 반응기에서 생산되는 생성물 조성에 따라 적합한 분리공정 선정을 위한 지침을 제시하였다.

광학패턴 가공방법에 따른 LGP 금형 및 성형품의 표면특성 연구 : Laser Ablation, Chemical Etching, LiGA-Reflow 방식 (A Study on the surface characteristics of LGP mold and product depending on different fabrication methods of optical pattern)

  • 도영수;김종선;고영배;김종덕;윤경환;황철진
    • 한국소성가공학회:학술대회논문집
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    • 한국소성가공학회 2007년도 춘계학술대회 논문집
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    • pp.213-216
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    • 2007
  • LGP (light guide plate) of LCD-BLU (Liquid Crystal Display - Back Light Unit) is one of the major components which affects the product quality of LCD. In the present study, the optical patterns of LGP(2.2") are manufactured by three different methods, namely, laser ablation, chemical etching and LiGA - reflow, respectively. The pattern surface images and roughness of mold and product were compared to check the optical characteristics. From the results of measurement the optical patterns fabricated by LiGA - reflow method showed the best geometric structure as intended in design and the lowest roughness among those.

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An advanced single-particle model for C3S hydration - validating the statistical independence of model parameters

  • Biernacki, Joseph J.;Gottapu, Manohar
    • Computers and Concrete
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    • 제15권6호
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    • pp.989-999
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    • 2015
  • An advanced continuum-based multi-physical single particle model was recently introduce for the hydration of tricalcium silicate ($C_3S$). In this model, the dissolution and the precipitation events are modeled as two different yet simultaneous chemical reactions. Product precipitation involves a nucleation and growth mechanism wherein nucleation is assumed to happen only at the surface of the unreacted core and product growth is characterized via a two-step densification mechanism having rapid growth of a low density initial product followed by slow densification. Although this modeling strategy has been shown to nicely mimic all stages of $C_3S$ hydration - dissolution, dormancy (induction), the onset of rapid hydration, the transition to slow hydration and prolonged reaction - the major criticism is that many adjustable parameters are required. If formulated correctly, however, the model parameters are shown here to be statistically independent and significant.

Total Synthesis of Fosfazinomycin A

  • Ik Joong Kang;Suk In Hong;Yong Joon Kim
    • Bulletin of the Korean Chemical Society
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    • 제12권2호
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    • pp.127-130
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    • 1991
  • Fosfazinomycin A(1), methyl valylarginylmethylhydrazinohydroxyphosphonohydro xyacetate, has been synthesized. N-Carbobenzyloxyvalylnitroarginine(6) was reacted with methyl methylhydrazinobenzyloxyphosphonobenzyloxyacet ate(10) which has carbon-phosphorus bond, to give a coupled product of methyl N-Carbobenzyloxyvalylnitroarginylmethylhydrazinob enzyloxyphosphonobenzyloxyacetate(11). The deprotection of (11) by hydrogenation yielded Fosfazinomycin A(1).

Chemical Genomics with Natural Products

  • Jung, Hye-Jin;Ho, Jeong-Kwon
    • Journal of Microbiology and Biotechnology
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    • 제16권5호
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    • pp.651-660
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    • 2006
  • Natural products are a rich source of biologically active small molecules and a fertile area for lead discovery of new drugs [10, 52]. For instance, 5% of the 1,031 new chemical entities approved as drugs by the US Food and Drug Administration (FDA) were natural products between 1981 and 2002, and another 23% were natural product-derived molecules [53]. These molecules have evolved through millions of years of natural selection to interact with biomolecules in the cells or organisms and offer unrivaled chemical and structural diversity [14, 37]. Nonetheless, a large percentage of nature remains unexplored, in particular, in the marine and microbial environments. Therefore, natural products are still major valuable sources of innovative therapeutic agents for human diseases. However, even when a natural product is found to exhibit biological activity, the cellular target and mode of action of the compound are mostly mysterious. This is also true of many natural products that are currently under clinical trials or have already been approved as clinical drugs [11]. The lack of information on a definitive cellular target for a biologically active natural product prevents the rational design and development of more potent therapeutics. Therefore, there is a great need for new techniques to expedite the rapid identification and validation of cellular targets for biologically active natural products. Chemical genomics is a new integrated research engine toward functional studies of genome and drug discovery [40, 69]. The identification and validation of cellular receptors of biologically active small molecules is one of the key goals of the discipline. This eventually facilitates subsequent rational drug design, and provides valuable information on the receptors in cellular processes. Indeed, several biologically crucial proteins have already been identified as targets for natural products using chemical genomics approach (Table 1). Herein, the representative case studies of chemical genomics using natural products derived from microbes, marine sources, and plants will be introduced.