• 제목/요약/키워드: quaternary amines

검색결과 13건 처리시간 0.016초

수용성고분자와 아민을 이용한 내구성 대전방지제 개발에 관한 연구 (A Study on the Synthesis of Durable Antistatic Agent Using Water Soluble Polymers and Amines)

  • 박성우;이석영;서말용;서장혁;신용섭;구강
    • 한국염색가공학회지
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    • 제13권6호
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    • pp.413-427
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    • 2001
  • In this studs, we synthesized durable antistatic agents with acrylic monomers for preventing the electrification of static electricity which is one of defects of polyester fabrics. Also we synthesized quaternary ammonium salts which give antistatic property and crosslinking agents which make antistatic agents adhere to fiber. The treatment of synthesized antistatic agents on polyester fabric carried out at the condition of various concentrations, treatment times and temperatures. The antistatic property, handle characteristics and other properties of treated and untreated polyester fabrics were also investigated.

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수용성고분자와 아민을 이용한 내구성 대전방지제 개발에 관한 연구 (A Study on the Synthesis of Durable Antistatic Agent Using Water Soluble Polymers and Amines)

  • 박성우;이석영;서말용;서장혁;신용섭;구강
    • 한국염색가공학회지
    • /
    • 제13권6호
    • /
    • pp.55-55
    • /
    • 2001
  • In this study, we synthesized durable antistatic agents with acrylic monomers for preventing the electrification of static electricity which is one of defects of polyester fabrics. Also we synthesized quaternary ammonium salts which give antistatic property and crosslinking agents which make antistatic agents adhere to fiber. The treatment of synthesized antistatic agents on polyester fabric carried out at the condition of various concentrations, treatment times and temperatures. The antistatic property, handle characteristics and other properties of treated and untreated polyester fabrics were also investigated.

Development of Novel Pyrrolidine Organocatalyst

  • 임설희;강성호
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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    • pp.198-198
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    • 2011
  • Organocatalysis is a relatively new and popular area within the field of chiral molecule synthesis. It is one of the main branches of enantioselective synthesis with enzymatic and organometallic catalysis. In recent years, immense high quality studies on catalysis by chiral secondary amines were reported. These progresses instantly led to different organocatalytic activation concepts, so thousands of researchers from academia and the chemical industry are currently involved in this field and new ideas, new approaches, and creative thinking have been rapidly emerged. Organocatalysts, some of which are natural products, appear to solve the problems of metal catalysts. Compared to metal-based catalysis, they have many advantages including savings in cost, time, and energy, easier experimental procedure, and reduction of chemical waste. These benefits originate from the following factors. First, organocatalysts are generally stable in oxygen and water in the atmosphere, there is no need for special equipments or experimental techniques to operate under anhydrous or anaerobic conditions. Second, organic reagents are naturally available from biological materials as single enantiomers that they are easy and cheap to prepare which makes them suitable for small-scale to industrial-scale reactions. Third, in terms of safety related catalysis, small organic molecules are non-toxic and environmentally friendly. Therefore, the purpose of this research is to develop novel synthetic methods and design for various organocatalyst. Furthermore, it is expected that these organocatalysts can be applied to a variety of asymmetric reactions and study the transition state of these reactions using a metal sulface. Here, we report the synthesis of unprecedented organocatalysts, proline and pyrrolidine derivatives with quaternary carbon center.

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