• 제목/요약/키워드: Acid-Base Reaction

검색결과 227건 처리시간 0.031초

A Newly Synthesized Schiff Base Derived from Condensation Reaction of 2,5-dichloroaniline and benzaldehyde: Its Applicability through Molecular Interaction on Mild Steel as an Acidic Corrosion Inhibitor by Using Electrochemical Techniques

  • Ozkir, Demet
    • Journal of Electrochemical Science and Technology
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    • 제10권1호
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    • pp.37-54
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    • 2019
  • A new organic Schiff base compound N-benzylidene-2,5-dichloroaniline (BDC) was synthesized and the structure of the Schiff base is illuminated by some spectroscopic techniques. In addition, whether it is an applicable inhibitor in the industrial field was examined by conventional methods such as linear polarization resistance (LPR), electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization for different concentrations. The BDC concentration and temperature effects were surveyed for elucidating the inhibitive mechanism. The BDC molecules are adsorbed to surface of mild steel via the Langmuir isotherm. Atomic force (AFM) and scanning electron microscope (SEM) techniques were utilized to give insight into surface characterization.

새로운 술폰아미드계의 촉매의 합성 (Synthesis of Indoline tri-isopropyl benzene sulfonamide as a potential new asymmetric catalyst)

  • 윤인권;김환철
    • 자연과학논문집
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    • 제7권
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    • pp.47-51
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    • 1995
  • 입체 이성질체를 합성하는 방법으로 최근에 알려진 입체선택성 촉매를 이용한 유기반응을 연구 하기 위하여 비천연 아미노산인 인돌린-2- 카르본산으로 부터카르본산그룹의 환원,2차아민기의 보호화,메실화,아지도치환,환원에 의한 아민기로의 전환, 술폰화, 보호기제거등의 총 5단계의 합성과정을 거쳐 목적하는 술폰아미드를 합성하였다. 각 생성물은 관 크로마토그래피에 의하여 분리 정제후 핵자기공명스펙트럼($^1H,^13C $ NMR) 적외선 스펙트럼 등에 의하여 구조를 확인 하였다.

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신남산 유도체 I, Cinnamanilide 유도체의 가수분해 메카니즘과 반응속도론적 연구 (Cinnamic Acid Derivatives I, The Kinetics and Mechanism of the Hydrolysis and Synthesis of Cinnamanilide Derivatives)

  • 이기창;황용현;이광일;정택서;박광하
    • 한국응용과학기술학회지
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    • 제6권2호
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    • pp.59-65
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    • 1989
  • The rate constants of the hydrolysis of cinnamanilide derivatives were determined UV spectrometry in $H_2SO_4\;(5{\sim}20N)$, NaOH($5{\sim}11N)\;at\;50{\sim}110^{\circ}C$ and rate equation could be applied over a strong acid and strong base were obtained. Final product of the hydrolysis was a cinnamic acid. The ${\rho}$ values obtained from the slope of linear plots of log $k_{abs}$ vs. Hammet $t{\sigma}$ constants were slightly negatives, Substituents on cinnamanilide showed a relatively small effect, with hydrolysis facilitated be electron donating group. Activation energy(Ea)was also calculated for the hydrolysis of the cinnamanilide. From this reaction rate equation, substituent effect and experimental of rate constants, that the hydrolysis of cinnamanillde was Initiated by the netural molecule of $H_2O$ which do not dissociate at strong acid, and proceeded by hydroxide ion at strong base.

Synthesis and Characterization of Poly(arylene ether)s Containing Benzoxazole Pendants from Novel Aromatic Difluoride Monomer

  • 김지형;방상우;김영준
    • Bulletin of the Korean Chemical Society
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    • 제21권9호
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    • pp.896-900
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    • 2000
  • A study was done on the synthesis of new poly(arylene ether)s and poly(arylenesulfide) with rigid benzoxazole pendants using nucleophilic aromatic substitution reaction. As a new aromatic monomer, 1,4-bis(2-benzox-azolyl)-2,5-difluorobenzene [I] w as synthesized in three steps starting from 1,4-dibromo-2,5-difluorobenzene. A model reaction of difluoro monomer [I] with two equivalents of m-cresol or thiophenol in a typical ether con-densation reaction conditions gave very high yields ( > 93%) of the desired disubstituted product, suggesting the feasibility of polymer formation in these reaction system. Monomer[I] was polymerized with bisphenols and bisbenzenethiol in NMP using K2CO3 as base. The molecular weight of the resulting polymers, however,seemed relatively low according to their solution viscosity values ( ηinh = 0.15-0.29 dL/g). The poly(arylene ether)s were soluble in several common organic solvents including chloroform, pyridine and N,N'-dimethylfor-mamide. The poly(arylene sulfide) was, however, ony soluble in strong acids like sulfuric acid and trifluoro-acetic acid. The glass transition temperatures were found to be 175-215 $^{\circ}C.$ These polymers were stable up to 380-420 $^{\circ}C$ in both nitrogen and air, as determined by the temperature that a significant weight loss began to appear on TGA.

오메가 3 지방산을 함유한 Sucrose Ester의 합성 (The Base Catalyzed Synthesis of Sucrose Ester Containing Omega-3 Fatty Acids)

  • 신정아;장지선;홍장환;이기택
    • 한국식품영양과학회지
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    • 제35권9호
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    • pp.1224-1231
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    • 2006
  • 고급불포화지방산인 docosahexaenoic acid ethylester (DHAEE)와 sucrose를 transesterification반응을 하여 sucrose ester를 기질 및 촉매의 비율, 반응시간, 용매사용 및 기압 등을 달리하여 합성하고, 합성율을 살펴보았고, 특히, 섭취 시 인체 내에서 이용 가능한 DHA를 함유하고 있으며, hydrophilic한 유화제로써 sucrose fatty acid mono ester의 합성율을 높이는 합성조건을 연구하였다. 무용매 상태에서의 sucrose ester의 합성율이 낮았기 때문에 반응용매로써 dimethyl sulfoxide(DMSO)를 사용하여 몰비율과 반응시간에 따른 합성을 실시하였다. 여러 반응조건 중 DHAEE의 전환율(%)은 sucrose:DHAEE의 몰비율이 1:0.98, 1:0.60, 1:0.40, 1:0.20인 SE#4, SE#5, SE#6, SE#7에서 모두 96% 이상을 나타내었다. 특히, SE#6(1:0.4 mole)에서 반응시간에 따른 전환율과 sucrose ester의 조성변화를 살펴본 결과, 반응시간 1시간일 때 55.3%의 전환율(mono ester 91.6%)을 보였고, 이후 반응 3.5시간일 때에는 97.1%(mono ester 66%)의 전환율을 보였다. 따라서 반응초기에 대부분의 sucrose ester가 합성되며, 특히 반응시간이 길어짐에 따라 mono ester에서 di-, tri- 및 polyester로 그 조성이 점차 변화됨을 확인하였고, 기질 중 DHAEE의 비율이 증가할수록 sucrose mono ester의 생성은 감소한 반면에, sucrose di-, tri- 및 polyester의 생성은 증가함을 확인하였다. 연구된 합성조건 중 sucrose mono ester의 합성은 1:0.2(sucrose:DHAEE)의 몰비율로 2.5시간동안 반응(SE#7)하였을 때 98.5%의 높은 전환율을 보이면서 그 조성은 87.3%로 가장 높게 합성되었다.

2009·2015 개정 교육과정 화학 I 및 화학 II 교과서 및 교사용 지도서에 제시된 산·염기 모델 내용에 대한 '이그노런스' 분석 (Analysis of 'Ignorance' in Acid-base Models Contents of Chemistry I and Chemistry II Textbooks & Teacher's Guides in 2009 & 2015 Revised Curriculum)

  • 류은주;백성혜
    • 대한화학회지
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    • 제64권3호
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    • pp.175-188
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    • 2020
  • 이 연구에서는 모델의 중요한 특징 중 하나인 '이그노런스'의 관점으로 화학 교과서 및 교사용 지도서의 내용을 분석하였다. 이는 2015 개정 교육과정에서 학생들의 모델링 역량을 기르는 것을 강조하고 있기 때문이다. 화학 교육과정에서 중요하게 다루는 내용인 산과 염기의 중화반응에 관련된 모델로 Arrhenius 모델과 Brønsted-Lowry 모델을 선정하고, 이에 관련된 '이그노런스'를 다룬 선행 연구와 대학 일반화학 교재 4종을 분석하여 연구의 분석 기준을 추출하였다. 추출한 분석 기준으로 2015 개정 교육과정의 화학 I 교과서 및 교사용 지도서 9종과 화학 II 교과서 및 교사용 지도서 6종을 분석하였다. 또한 개정 교육과정에 따른 내용의 차이를 비교하기 위해 2009 개정 교육과정의 화학 I 교과서 및 교사용 지도서 4종 그리고 화학 II 교과서 및 교사용 지도서 3종도 분석하였다. '중화 반응' 개념, '중성' 개념, '중화 반응의 양적 관계', '이온화도', '이온화 상수'에 관련된 내용을 중심으로 분석하였다. 연구 결과를 토대로, 모델의 '이그노런스'를 화학 교사들이 이해하고 학생들의 모델링 역량을 길러줄 수 있도록 교사용 지도서에 이와 관련된 내용을 제시하는 방안을 제안하였다.

윤활유 첨가제에 따른 마멸분 화상해석

  • 서영백;이충엽;박홍식;전태옥
    • 한국윤활학회:학술대회논문집
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    • 한국윤활학회 1998년도 제27회 춘계학술대회
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    • pp.180-189
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    • 1998
  • This paper was undertaken to do shape analysis of wear debris on oiliness agent and extreme pressure agent. The lubricating wear test was performed under different experimental conditions using the wear test device was made in our laboratory and were- specimens of the pin on disk type was rubbed in paraffine series base oil by materials, varying applied load, sliding distance, oil additives such as stearine acid, DBDS, TCP. The four shape parameters (50% volumetric diameter, aspect, roundness and reflectivity) on a kind of the additives are different on applied load and sliding distance and Its are affected by absorbed film and reaction film. DBDS and TCP have a role of extreme pressure agent but a role of absorbed film of stearic acid decrease in high load. The maximum wear volume on applied load be in existence in three kinds of the specimens because of reaction characteristics of the additives.

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마이크로플루다이저를 사용한 MLV liposome 형성에 관한 연구 (A study on manufacturing formation of the MLV liposomes by the microfludizer)

  • 김인영;김중희
    • 대한화장품학회지
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    • 제21권1호
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    • pp.38-52
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    • 1995
  • Liposome은 의약과 화장품 분야에서 많은 발전을 하였다. 본 연구에서는 세포 간지질의 주요 성분인 cholesterol, palmitic acid, cholesterol ester와 lecithin을 사용하여 swelling반응에 의해 MLV liposome을 제조 하였다. 지질베이스와 마이크로플루다이저를 사용하여 MLV liposome 형성에 대한 특성들을 연구 하였다. MLV liposome은 multilamellar vesicle로서 형성되었다. MLV liposome의 gelation효과는 고온(90$\pm$5도씨)에서 polyol과 water phase에 지질을 혼합한 것에 스웰링 반응을 하였다. MLV liposome에 alpha hydroxy acid 성분들을 투입 제조하였다. MLV liposome의 최적 조건은 마이크로플루다이저에 3회 통과하였으며 vesicle의 입자크기는 150-350nm범위이고 이것을 freeze-fracture electron microscopy로 확인 하였다.

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자력에 의한 산성 광산 배수의 처리 - 철(Fe) 성분의 제거- (The Treatment of Acid Mine Drainage - The removal of Iron(Fe) component-)

  • 송근호;이광래
    • 산업기술연구
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    • 제32권A호
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    • pp.21-27
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    • 2012
  • The characteristics of floc formation of the iron(Fe) ions contained in the acid mine drainage was studied for developing the process treating the acid mine drainage. The iron(Fe) ions were formed into flocs by the acid-base reaction with the added $Ca(OH)_2$. The molal ratio of iron(Fe) vs $Ca(OH)_2$ was one of major control variables in treatment; pH change, iron(Fe) ions concentration in treated drainage, DO (dissolved oxygen content). In addition, the air gave much effect on the color of the $iron(Fe)-Ca(OH)_2$ flocs and the attachment to magnet. The attaching to the magnet of the flocs formed in the air was much less than the case without air.

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Optimization of biodiesel production via methyl acetate reaction from cerbera odollam

  • Dhillon, Sandip Singh;Tan, Kok Tat
    • Advances in Energy Research
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    • 제4권4호
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    • pp.325-337
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    • 2016
  • Cerbera Odollam (sea mango) is a proven promising feedstock for the production of biodiesel due to its high oil content. Fatty acid methyl esters (FAME) were produced as the final reaction product in the transesterification reflux condensation reaction of sea mango oil and methyl acetate (MA). Potassium methoxide was used as catalyst to study its reacting potential as a homogeneous base catalyst. The initial part of this project studied the optimum conditions to extract crude sea mango oil. It was found that the content of sea mango sea mango oil was 55%. This optimum amount was obtained by using 18 g of grinded sea mango seeds in 250 ml hexane. The extraction was carried out for 24 hours using solvent extraction method. Response surface methodology (RSM) was employed to determine the optimum conditions of the reaction. The three manipulated variables in this reaction were the reaction time, oil to solvent molar ratio, and catalyst wt%. The optimum condition for this reaction determined was 5 hours reaction time, 0.28 wt% of catalyst and 1:35 mol/mol of oil: solvent molar ratio. A series of test were conducted on the final FAME product of this study, namely the FTIR test, GC-FID, calorimeter bomb and viscometer test.