• 제목/요약/키워드: dicarboxylic acid

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폴리우레탄-실리카 복합 발포체의 합성 및 물성에 관한 연구 (Synthesis and Characterization of Polyurethane-silica Composite Foam)

  • 강현석;김상범
    • 공업화학
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    • 제31권1호
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    • pp.30-35
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    • 2020
  • 본 연구에서는 폴리우레탄-실리카 복합 발포체를 합성하여 복합 발포체의 단열 특성 및 기계적 물성을 분석하였다. 폴리우레탄-실리카 복합 발포체를 합성하기 위해 폴리에스테르-실리카 복합 폴리올을 합성하였다. 폴리에스테르-실리카 복합 폴리올은 실리카 졸과 모노머 상태의 다이카복실산(dicarboxylic acid), 글리콜(glycol)과의 중합 반응을 통해 합성하였다. 합성된 복합 폴리올을 이용하여 폴리우레탄-실리카 복합 발포체를 합성하여 물성을 분석하였다. 폴리우레탄-실리카 복합 발포체의 열전도도는 HPUF0, HPUF1, HPUF3, HPUF5 모두 큰 차이가 없는 것을 확인하였다. 압축강도는 실리카 함량이 증가함에 따라 HPUF0보다 증가하였으며 HPUF0보다 HPUF5가 약 25% 정도 기계적 물성이 향상되는 것을 확인하였다.

2차원 Manganese-Imidazoledicarboxylate 배위 고분자:aqua(imidazole-4,5-dicarboxylateo)manganese(II), [Mn(IDC)($H_2O$)]의 합성 및 구조 (2-Dimensional Manganese-Imidazoledicarboxylate Coordination Polymer:Preparation and Structure of aqua(imidazole-4,5-dicarboxylateo)manganese(II), [Mn(IDC)($H_2O$)])

  • 민동원;이순원
    • 한국결정학회지
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    • 제12권4호
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    • pp.212-215
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    • 2001
  • NaOAC·3H₂O 존재 하에서, manganese nitrate(Mn(NO₃)₂·H₂O )와 imidzole-4,5-dicarboxylic acid(IDCH₂)가 수열반응하여, 실험식 [Mn(IDC)(H₂O)]을 가지는 2차원 배위고분자 합성되었다. 화합물 1의 구조가 분광학적 방법(IR) 및 X-ray 회절법으로 규명되었다. 화합물의 1의 결정학적 자료: 사방정계 공간군 Pbca, a=7.257(5) Å b=13.687(5)Å, c=14.332(6)Å Z=8, R(wR₂)=0.0498(0.0999).

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Structure and Properties of Polynorbornene Derivatives: Poly(norbornene dicarboxylic acid dialkyl ester)s and Poly(norbornene dimethyl dicarboxylate)s

  • Shin, Boo-Gyo;Cho, Tai-Yon;Yoon, Do-Y.;Liu, Binyuan
    • Macromolecular Research
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    • 제15권2호
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    • pp.185-190
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    • 2007
  • Poly(norbornene dimethyl dicarboxylate)s, (PNDMD)s, were prepared by addition polymerization with palladium(II) catalyst from pure exo-monomers, and their structure and properties were compared with those of poly(norbornene dicarboxylic acid dialkyl ester)s, (PNDADA)s. Both polymer series exhibited good solubility in general organic solvents and excellent thermal stability up to $330^{\circ}C$. Wide-angle X-ray scattering (WAXS) study indicated the presence of nano-scale layer-like order in amorphous PNDADAs, while PNDMDs showed random amorphous structure. The glass transition temperatures and dielectric constants of solid polymers were found to decrease as the alkyl side-chain length increases for both polymer series. However, PNDMDs showed lower glass transition temperatures and higher dielectric constants, as compared with those of PNDADAs containing the same alkyl substituents. This difference, caused by the higher side-group mobility of PNDMDs, may be closely related to the nano-scale order in amorphous PNDADAs and its absence in PNDMDs.

옥시캄 계열의 1,2-벤조티아진 유도체의 합성 (Synthesis of 1,2-Benzothiazine Derivatives as Oxicam Family)

  • 박명숙
    • 약학회지
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    • 제44권6호
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    • pp.494-498
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    • 2000
  • Noble 7,7'-substituted (or unsubstituted) 4-oxo-1,1',2,2'-dibenzothiazine-3,3'-dicarboxylic acid methyl ester 1,1,1',1'-tetraoxide 3,4'-yl ethers 2a-h were synthesized through the dehydration of 7-substituted (or unsubstituted) 4-hydroxy-1,2-benzothiazine-3-carboxylic acid methyl ester 1,1-dioxides 1a-h using silver(I) oxide for the development of new nonsteroidal antiinflammatory drugs (NSAIDs). Optimal reaction was proceeded through stirring of distilled acetone using 100 mol% of silver(I) oxide at room temperature for 24-68 hrs.

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당질과 아미노산이 Ascorbic Acid 의 안정도에 미치는 영향 (Stability of Ascorbic Acid in the Solutions of Sugars and Amino Acids)

  • 황희자
    • Journal of Nutrition and Health
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    • 제15권1호
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    • pp.22-29
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    • 1982
  • As sugar and amino acid were added to the ascorbic acid solution the content of ascorbic acid was quantitatively determined by 2, 4-dinitrophenyl hydrazine method. The residual ascorbic acid was shown to increase slightly when sorbose, rhamnose or mannose was added to the ascorbic acid solution whereas residual ascorbic acid was shown to decrease in time to the addition of other sugars. The effects of amino acid to the ascorbic acid solution were found that monoamino-mono, or dicarboxylic acids and aromatic amino acids increased the residual ascorbic acidity whereas diamino-monocarboxylic acids and sulfur containing amino acids decreased the residual ascorbic acidity.

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기체크로마토그래피법에 의한 타액내 유기산의 신속한 스크리닝 (Rapid Gas Chromatographic Screening of Saliva Samples for Organic Acids)

  • 김경례;김정한;박영준;김정옥
    • 약학회지
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    • 제39권3호
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    • pp.283-288
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    • 1995
  • Rapid gas chromatographic profiling method was applied to saliva from healthy subjects for the analysis of free organic acids. Saliva samples were first saturated with NaHCO$_{3}$ and extracted with diethyl ether. The aqueous phase was solid-phase extracted using Chromosorb P as the adsorbent and diethyl ether as the eluent after the acidification and NaCl saturation, followed by triethylamine treatment. The resulting tiiethylammonium salts of acids were directly converted into stable tert.-butyl-dimethylsflyl derivatives, with subsequent analysis by dual-capiuary column gas chromatography and gas chromatograpy -mass spectrometry. From the ten saliva samples studied, twenty eight free organic acids including various fatty acids, hydroxy acids, dicarboxylic acids, md aromatic acids were tentatively identified. Among the acids identified , the concentration of lactic acid was highest for five saliva samples while $\alpha$-hydroxyisocaproic acid was most abundant for me sample, and succinic acid and glycolic acid for two samples. respectively. When the GC profiles were simplified to the corresponding acid retention index spectra of bar graphical form, they presented characteristic patterns for each individual.

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가교 반응이 가능한 말단 무수물을 이용한 무색투명한 폴리이미드 필름 (Colorless and Transparent Polyimide Films from Poly(amic acid)s with Cross-linkable Anhydride End)

  • 민웅기;장진해
    • 폴리머
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    • 제34권6호
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    • pp.495-500
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    • 2010
  • 4,4'-(Hexafluoroisopropylidene)diphthalic anhydride(6FDA)와 bis[4-(3-amino phenoxy)phenyl] sulfone(BAPS)의 조성에 cis-4-cyclohexene-1,2-dicarboxylic anhydride(CDBA)를 다양한 몰%로 사용하여 사슬 말단에 가교 반응이 된 폴리이미드(PI)를 얻었다. Grubbs 촉매 0.1 wt%를 사용하여 가교된 폴리아믹산(poly(amic acid), PAA)을 합성한 후에 PAA를 다양한 온도에서 열처리를 통해 가교된 PI 필름을 합성하였다. 제조된 필름의 열적-기계적 성질은 퓨리에 변환 적외선 분광기(FTIR), 시차주사 열량계(DSC), 열중량 분석기(TGA), 열기계 분석기(TMA), 만능인장 시험기(UTM) 등을 사용하여 측정하였고, 색차계(spectrophotometer)와 자외선-가시광선 흡광도기(UV-Vis. spectrometer)를 이용하여 광학적 특성을 확인하였다. CDBA의 몰%가 증가함에 따라 열적 기계적 성질은 증가하였지만 광학적 투명도는 이와는 반대로 감소하였다.

Mixed Intramolecular Hydrogen Bonding in Dihydroxythiophene-based Units and Boron and Technetium Chelation

  • Ko, Sang-won;Park, Sang-Hyun;Gwon, Hui-Jeong;Lee, Jun-seong;Kim, Min-Jeong;Kwak, Yeon-ju;Do, Young-kyu;Churchill, David G.
    • Bulletin of the Korean Chemical Society
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    • 제27권2호
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    • pp.243-250
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    • 2006
  • Three novel potential metal ion chelating units have been synthesized and characterized: 5-hexylcarbamoyl-3,4-dihydroxythiophene-2-carboxylic acid methyl ester (5), 3-benzyloxy-4-hydroxythiophene-2,5-dicarboxylic acid bis-hexylamide (6), and 3,4-dihydroxythiophene-2,5-dicarboxylic acid bis-hexylamide (7). The crystal structure of 6 was obtained and suggests the presence of three distinct intramolecular hydrogen bonds, namely $[N_{amide}-H{\cdot}{\cdot}{\cdot}O]$ $[O-H{\cdot}{\cdot}{\cdot}O_{amide}]$ and $[N_{amide}-H{\cdot}{\cdot}{\cdot}S]$. Boron chelation with 5, 6 and 7 through the use of $BF_3, \;B(OH)_3 \;or \;B(OMe)_3$ was probed by $^1H$, $^{11}B$, and $^{13}C$ NMR spectroscopy. Technetium (I) chelation with 5, 6 and 7 was also studied via HPLC elutions using $[^{99m}Tc(CO)_3(OH_2)_3]^+$.

Polyesters Biosynthesis of Alcaligenes eutrophus H16(ATCC 17699) from Various Mono- and Dicarboxylic Acids and Diols

  • Song, Jae-Jun;Shin, Yong-Chul
    • Journal of Microbiology and Biotechnology
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    • 제3권2호
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    • pp.123-128
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    • 1993
  • The polyesters (polyhydroxyalkanoates; PHAs) production capability in a two-step cultivation of Alcaligenes eutrophus H16(ATCC 17699) was investigated by using various organic carbon sources. The carbon sources used included linear $C_2~C_10$ monocarboxylic acids, $C_3~C_10$ dicarboxylic acids, crotonic acid, and several linear vicinal and $\omega$-diols. The polyesters synthesized were characterized by 500 MHz $^1 H-NMR$ spectroscopy, intrinsic viscosity$[\eta]$ measurement in chloroform and differential scanning calorimetry (DSC). The PHAs synthesis data showed that the use of C-odd ($C_3, C_5, and C_7$) monocarboxylic acids resulted in poly(3-hydroxybutyrate-co-3-hydroxyvalerate)(P(3HB-co-3HV) (3HV content ranging 40 to 70 mol%) while the use of $C_9$ substrate gave the copolyester containing only 4 mol% of 3HV. All culture products obtained on $C_3$~C$_{10}$ dicarboxylic acids gave exclusively P(3HB). 500 MHz $^1 H-NMR$ analysis showed that all polyesters synthesized generally contained 1~2 mol% 3HV even for the unrelated substrates such as the carboxylic acids with even number of carbon. When $\alpha, \omega$-diols with even number of carbon were used as substrates, 4-hydroxybutyrate(4HB) was inserted into the polyester chain composed of P(3HB-co-4HB). Vicinal diols were generally not utilized by the bacterium for polyester production.n.

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