• 제목/요약/키워드: esterfication

검색결과 10건 처리시간 0.029초

Fine Line Lithography를 위한 Polymer Resist에 관한 연구 (Studies on Polymer Resist for Fine Line Lithography)

  • 박이순
    • 한국인쇄학회지
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    • 제11권1호
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    • pp.71-84
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    • 1993
  • Practically to put use high-photosensitive polymer, poly(vinyl cinnamoyl acetate), we investigated and confirmed UCHIDA`s synthesis, according to control solvent, which is the esterification of poly (vinyl alcohol) with monochloroacetic acid and can be freely conrolled the successive cinnamoyl acetoxyl esterfication of PVCiA, and intruducing photosensitizers,studied the photosensitivity of PVCiA.

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N-사이크로헥실말레아민산 이소부틸 에스테르의 제조 공정 개발 (Development of a Synthetic Process for N-Cyclohexylmaleiamic Acid Isobutyl Ester)

  • 문부현;주창식
    • Korean Chemical Engineering Research
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    • 제51권5호
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    • pp.545-549
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    • 2013
  • 높은 수율로 CHMI를 제조하는 공정을 개발하기 위한 연구의 일환으로, 공정 중간체 CHMAIE를 합성하는 실험적 연구를 수행하였다. CHMAIE 제조 공정의 중간체인 CHMA 생성반응은 무수 말레인산 용액에 사이크로헥실아민을 점적 투입한 후 반응액을 2시간 동안 숙성시키는 방법으로 완료하였으며, 생성된 CHMA를 $10^{\circ}C$ 이하에서 2.5시간 동안 석출시키면 98.2%의 수율을 얻을 수 있었다. CHMA로부터 CHMAIE를 제조하는 에스테르화 반응의 최적 온도는 $68^{\circ}C$ 이었으며, 이 최적 온도에서의 평형 전화율은 98.5%였다. 에스테르화 반응이 평형에 도달하는 시간은 온도에 따라 감소하며, 최적 온도에서의 평형도달 시간은 약 3시간 정도였다. 최종 생성물 중의 톨루엔은 진공 증류를 통하여 회수할 수 있었다. 톨루엔의 회수율은 증류 온도가 증가함에 따라 증가하였고, 증류 온도 $55^{\circ}C$에서의 톨루엔 회수율은 98%였다.

ASA 유화용 양성전분과 에스테르화전분의 특성 평가 (Characteristics of Cationic Starches and Esterified Starches for ASA Sizing)

  • 김종수;이학래
    • 펄프종이기술
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    • 제40권4호
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    • pp.16-26
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    • 2008
  • It is of great importance to decrease sheet break at the size press to enhance the runnability of today's high speed paper machines. To achieve this purpose it is required to control the penetration of the starch solutions at the size press. Use of ASA sizing system provides diverse advantages in improving machine runnability since it allows us to get rapid sizing development at the size press. Domestic paper industries, however, has not enjoyed these benefits of ASA sizing system mainly because of the poor efficiency of domestic corn starches used for ASA emulsification. To improve the emulsion stability and ASA sizing efficiency, it has been pointed out that new cationic starches are needed. In this study two methods of starch modifications, i.e. esterfication of cationic corn starch with OSA (Octenyl Succinic Anhydride), and acid hydrolysis by sulfuric acid were employed as methods to improve ASA sizing efficiency. The effect of these modification was compared with conventional cationic starches.

피혁 제조 공정 중 발생하는 폐돈지를 이용한 음이온성 계면활성제 제조 및 특성 (Preparation and Characteristics of Anionic Surfactant Using Waste Fleshing Scrap)

  • 신수범;민병욱;양승훈;박민석;원기천;백두현
    • 한국염색가공학회지
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    • 제18권6호
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    • pp.31-36
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    • 2006
  • Study has been made for producing anionic surfactant using waste fleshing scraps from the leather making process through refining, esterification, sulfonation and blending processes. As a most optimum lard oil refining method, refining was carried out for 4 hours under temperature of $120^{\circ}C$ and approximately 200 mbar vacuum, which gave a recovery of more than 80% lard oil. Refined lard oil obtained thus was undergone methlyl-esterification, then sulfonated to make a degreasing agent. By methyl-esterification using lard oil, more than 85% of fatty acid and $12{\sim}13%$ of glycerine were extracted from the oil. Sulfonation of the extracted fatty acid ester lard oil has shown most optimum at $15{\sim}20%$ chlorosulfonic acid content, and the content of bonding sulfate at this time was higher than 3.5%. Finally the followed anionic surfactant having degreasing force of 80% and higher could be made by blending process.

PTCA와 BTCA를 이용한 면셀룰로오스의 에스테르 가교화에 대한 pH 영향(I) (Effect of pH on the Ester-crosslinking of Cotton Cellulose with PTCA and BTCA(I))

  • Chan-Min, Lee;Chul-Ho, Choi
    • 한국염색가공학회지
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    • 제9권5호
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    • pp.30-41
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    • 1997
  • A purpose of this research is to prove unknown relation -ship between finish bath pH and crosslinking. In pursuit of these goals, we have treated 100% cotton broad cloth with PTCA and BTCA at different pH values. They were used with H$_{3}$PO$_{4}$, NaH$_{2}$PO$_{2}$, NaH$_{2}$PO$_{4}$, Na$_{2}$HPO$_{4}$, Na$_{3}$PO$_{4}$, catalysts to produce nonformaldehyde fabrics finishes. Treatments were applied to all cotton fabrics using a parletry-cure process. For the fully understood on the relationship of finish bath pH effect and cotton cellulose esterification, the relative concentrations of chemical species were calculated from ionization constants. The effect of pH on the cotton cellulose ester was investigated using Fourier transform infrared spectra, the surface area measurement by BET method and wrinkle recovery analysis. Results of differential FT-IR spectra and their relative concentration analysis were compared with those of catalyst treated controls. FT-IR and wrinkle recovery data indicated that the esterfication by polycarboxylic acids is pridependent. A similar phenomenon also occurred when a phosphate or hypophosphite was used. Therefore, it is necessary to choose the optimum pH range of a finishing bath in order to achieve the most effective esterification.

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폴리카르복시 산 처리 면섬유의 DP가공에 관한 연구 (A Study on the Durable Press Finishing of Cotton Fiber Treated with Polycarboxylic Acid)

  • 이찬민;최철민
    • 한국염색가공학회지
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    • 제9권6호
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    • pp.58-67
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    • 1997
  • PTCA(1,2,3-propanetricarboxylic acid) and BTCA(1,2,3-butanetetracarboxylic acid) are selected as new nonformaldehyde agents for ester crosslinking of cotton cellulose to replace the traditional DMDHEU reagent. A goal of this research is to propose unknown ester mechanism of cotton cellulose by PTCA or BTCA using crystal structure model suggested by Meyer and Takahashi. In pursuit of these goals, we have treated 100% cotton broad cloth with PTCA or BTCA and different catalysts. They were used with $NaH_2PO_2,\;NaH_2PO_4,\;Na_2HPO_4,\;NaH_2PO_2,\;Na_3PO_4,$ catalysts to produce nonformaldehyde fabric finishes. Treatments were applied to all cotton fabrics using a pad-dry -cure process. The esterfication of cotton treated with BTCA or PTCA was investigated using Fourier transform infrared(FT-IR) spectra and the breaking strength, abrasion retention and discoloration properties were determined to prove the durable finished fabrics. Patterns with respect to abrasion resistance were more complex. Because PTCA and BTCA add-ons were comparable, the data suggest that the more effective catalysts, $NaH_2PO_2$ and mixed phosphate $NaH_2PO_2/NaH_2PO_4$) are effecting either a great number of crosslinks in the cotton or producing crosslinks that differ in actual structure.

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전분-구연산을 기반으로 한 생분해성 비산방지용 소재의 제조 및 특성 분석 (Manufacturing and Characteristics of Biodegradable Materials Based on Starch-Citric Acid for Anti-Particulate Scattering)

  • 이지성;이원규
    • Korean Chemical Engineering Research
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    • 제59권3호
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    • pp.443-449
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    • 2021
  • 전분과 구연산의 에스테르화 반응을 통한 가교화로 내수성 및 도포성이 우수한 생분해성 비산 방지용 박막소재를 제조하고 특성을 분석하였다. 이들 소재의 박막 형성 및 물성을 향상하기 위하여 PVA과 글리세린 등을 첨가하여 도포된 박막의 유연성을 확보하였다. 또한 원재료 및 첨가재의 농도, 온도 및 반응 시간에 따른 물에 대한 팽윤도 및 용해도와 같이 재료 기능성을 최적화하는 조건을 분석하였다. FT-IR 분석으로 전분과 구연산의 가교 반응을 확인하였으며, 이들 반응과정에서 단일 및 다중 에스테르화 반응이 동시에 일어남을 알 수 있었다. 가교된 전분-구연산 박막재료는 토양매립 후 12주가 지났을 때 95%가량 분해되었어 생분해성이 우수함을 알 수 있다.

1,5,3,7-Diazadiphosphocine-1,5-Dicarboxylic Acids의 합성과 반응 (Synthesis and Reaction of 1,5,3,7-Diazadiphosphocine-1,5-Dicarboxylic Acids)

  • 조승환;송주현;이도훈;이용균;박유미;최순규;한정태;정대일
    • 생명과학회지
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    • 제17권7호통권87호
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    • pp.910-914
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    • 2007
  • 본 연구는 MRI 조영제나 새로운 생리활성 물질을 개발키 위해 paraformaldehyde와 hypophosphorous acid를 아미노산인 glycine 혹은 glutamic acid와 함께 반응시켜 3,7-dihydroxy-3,7-dioxoperhydro-1,5,3,7-diazadiphos-phocme-1,5-diacetic acid 1 와 3,7-dihydrexy-3,7-dioxoperhydre-1,5,3,7-diazadiphos-phocme-1,5-di- (2-glutaric acid)3을 합성하였다. 그러나 aspartic acid에 의한 2-[5-(1,2-dicarboxy-ethyl)-3,7-dihydroxy-3,7-dioxo-315.715-[1,5,3,7]diazadiphosphocan-1-yl]-succinic acid 2는 얻지 못했다. 합성 된 3,7-dihydroxy-3,7-dioxoperhydro-1,5,3,7-dia-zadiphosphocine-1,5-diacetic acid 1을 산 촉매에 의한 에스테르화반응시켜 화합물 3,7-dihydroxy-3,7-dioxoper-hydro-1,5,3,7-diazadiphosphocine-1,5-diacetic acid methyl ester 4, 3,7-dihydroxy-3,7-dioxoperhydro-1,5,3,7-dia-zadiphosphocine-1,5-diacetic acid ethyl ester 5, 그리고 3,7-dihyoxy-3,74dioxoperhyo-1,5,3,7-diazadiphosphocine-1,5-diacetic acid propyl ester 6을 합성하였다. 계속해서 다양한 반응을 통해 새로운 화합물을 합성할 것이며 생리활성검색도 실시할 예정이다.