• 제목/요약/키워드: Terephthalic acid

검색결과 73건 처리시간 0.035초

오존산화에 의한 염색체수의 색도 제거에 관한 연구 (A Study on Removal of Color in Dyeing Wastewater by Ozone Oxidation)

  • 정순형;최준호
    • 환경위생공학
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    • 제18권4호
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    • pp.45-51
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    • 2003
  • This study was conducted to remove the color in dyeing wastewater by ozone oxidation process, and the results were summarized as follows ; The 18.3% of BOD and 56.3% TOC were removed as decreasing with pH 1 in dyeing wastewater, containing the polyester reducing process. It showed that terephthalic acid was precipitated at low pH. The color of dyeing wastewater was removed by the first order reaction, and the reaction rate constants at pH 3, 7, 12 were investigated $0.234{\;}min^{-1},{\;}0.215{\;}min^{-1}{\;}and{\;}0.201{\;}min^{-1}$ respectively. It showed that color was more effectively removed with direct reaction of ozone than radical reaction(non-direct reaction). As increasing of the water temperature, the reaction rate constants were increased slightly. It indicated that activity of ozone was improved at high water temperature.

Synthesis and Characterization of Poly(trimethylene terephthalate) via TPA Process Using Titanium Catalyst

  • Kim, Kap-Jin;Park, Jung-Il;Pio Sifuentes;Lee, Jong-Soon
    • 한국섬유공학회:학술대회논문집
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    • 한국섬유공학회 2003년도 The Korea-Japan Joint Symposium
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    • pp.92-92
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    • 2003
  • poly(trimethylene terephthalate) (PTT) was synthesized via condensation polymerization using different molar ratios of 1,3-propane diol (PDO)/terephthalic acid (TPA) in the presence of tetraisopropyl titanate (TiPT) as a polyesterifi-cation catalyst. The effect of reaction conditions on the characteristics of as-polymerized PTT was investigated.

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Ag-modified BiOX (X=Cl, Br and I) Plates for Photocatalytic Dye Removal

  • 이승원;최영인;이주헌;박요한;손영구
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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    • pp.424.2-424.2
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    • 2014
  • Ag-modified BiOX (X=Cl, Br and I) nanoplates were synthesized by an ion-exchange reaction. We examined the fundamental properties by scanning electron microscopy (SEM), electron transmission microscopy (TEM), X-ray diffraction, UV-visible absorption, Fourier-transform infrared and photoluminescence spectroscopy. The adsorption and photocatalytic performances of the catalysts were tested with dyes under UV and visible light. A chemical scavenger method was employed to test the roles of active species (${\cdot}OH$, ${\cdot}O2-$ and h+) and understand photodegradation mechanism. Photoluminescence spectroscopy was used to examine ${\cdot}OH$ radical formation using terephthalic acid during photoirradiation.

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Interchange Reaction Kinetics and Sequence Distribution of Liquid Crystalline Poly(ethylene terephthalate-co-2(3)-chloro-1,4-phenylene terephthalate)

  • Rhee, Do-Mook;Ha, Wan-Shik;Youk, Ji-Ho;Yoo, Dong-Il
    • Fibers and Polymers
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    • 제2권2호
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    • pp.86-91
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    • 2001
  • Liquid crystalline (LC) poly(ethylene terephthalate-co-2(3)-chloro-1,4-phenylene terephthalate) [copoly(ET/CPT)] was prepared using poly(ethylene terephthalate) (PET) as a flexible spacer, terephthalic acid (TPA), and chlorohydroquinone diacetate (CHQDA). All reactions involved in the copolymerization were investigated using some model compounds: TAP was used for acidolysis, diphenylethyl terephthalate (DPET) for interchange reaction between PET chains, and 야-o-chlorophenyl terephthalate (DOCT) and di-m-chlorophenyl terephthalate (DMCT) for interchange reaction between PET and rigid rodlike segments. Activation energies obtained for the acidolysis of PET with TPA and for interchange reaction of PET with DPET, DOCT, and DMCT were 19.8 kcal/mol, 26.5 kcal/mole, and 45.9 kcal/mole, respectively. This result supports that the copolymerization proceeds through the acidolysis of PET with TPA first and subsequent polycondensation between carboxyl end group and CHQDA or acetyl end group, which is formed from the reaction of CHQDA and TPA. Also, it was found that ester-interchange reaction can be influenced by the steric hindrance. Copoly(ET/CPT)s obtained has ethylene acetate end groups formed from acetic acid hydroxy ethylene end groups and showed almost the random sequence distribution for all compositions.

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CDP 섬유의 염색성(III) -극세 CDP섬유의 염색성, Solvent wicking성 및 물성- (Dyeing Properties of CDP Fiber(III) - Dyeing and Solvent Wicking and Physical Properties of Micro CDP Fiber -)

  • 김영희;정동석;이문철
    • 한국염색가공학회지
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    • 제17권5호
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    • pp.1-12
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    • 2005
  • Polyester fibers can be modified into cationic dyeable polyester fibers(CDP) by the copolymerization of terephthalic acid and 5-sodium sulphoisophthalic acid with ethylene glycol. The advantage of CDP on most cationic dyes is the conspicuous brilliance due to a narrow steep absorption band and the wash fastness and etc. Weight reduction by alkali hydrolysis, dyeing and solvent wicking properties of fabrics with cationic dyes, and change of fine structure were investigated. To obtain optimum splitting process parameters for dyeing and physical properties of micro CDP fiber, splitting method under various conditions was carried out. By means of SEM, it was confirmed that the splitting process of the micro CDP fiber be achieved at the weight reduction. A comparatively greater quantity of dye is necessary to dye microfiber than conventional fiber. The fastness and solvent wicking of regular CDP fiber is higher than that of micro CDP fiber.

1,2-Bis(4-trimellitimidophenoxy)benzene으로 부터 유도된 신규 방향족 폴리아미드이미드 (Noble Aromatic Poly(amide-imide)s Derived from 1,2-Bis(4-trimellitimidophenoxy)benzene)

  • 정화진
    • 한국응용과학기술학회지
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    • 제27권2호
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    • pp.129-136
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    • 2010
  • A series of noble poly(amide-imide)s and copoly(amide-imide)s bearing 1,2-bis(4-phenoxy)benzene units were synthesized by the direct polycondensation of 1,2-bis(4-trimellitimidophenoxy)benzene[1,2-PTPB] with a combination of commercially available aromatic diamines and diacids such as m-phenylene diamine, p-phenylene diamine(PPD), isophthalic acid and terephthalic acid(TA) in N-methyl-2-pyrrolidone(NMP) using triphenyl phosphite and pyridine as a condensing agent in the presence of dehydrating agent ($CaCl_2$). The resulting polymers had inherent viscosities in the range of 0.37~0.78 dL/g and most of them were soluble m common organic solvents including NMP, dimethylacetamide, dimethylsulfoxide, dimethylformamide, and m-cresol. Wide-angle X-ray diffractograms revealed that the copoly(amide-imide) derived from PPD with mixed acids of 1,2-BTPB and TA, showed crystalline nature, whereas all of the other polymers were found to be amorphous. The glass transition temperatures of the polymers occurred over the temperature range of $270{\sim}323^{\circ}C$ in their differential scanning calorimetry curves and their 10% weight loss temperature, determined by thermogravimetric analysis in air and nitrogen atmosphere, were in the range $465{\sim}535^{\circ}C$, $500{\sim}550^{\circ}C$, respectively, indicating their good thermal stability.

비페닐렌구조가 액정중합체의 성질에 미치는 영향 (Effects of Biphenylene Structure on the Properties of Liquid Crystalline Polymer)

  • 육경창;신대윤;신홍철;김완영
    • 공업화학
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    • 제3권2호
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    • pp.280-287
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    • 1992
  • 테레프탈산, 비페닐 디카르복시산과 히드로퀴논을 용액중합하여 전방향족 액정 폴리에스테르를 합성하고 테레프탈산과 비페닐 디카복시산의 몰비가 액정중합체의 열적성질, 열안정성 및 메소상의 구조에 미치는 영향을 DSC, TGA, 편광현미경 및 X선회절기로 조사하였다. 본 연구에서 합성한 중합체는 모두 열방성 액정중합체였고 네마틱 액정상을 나타내었으며, 용융온도 및 등방화온도는 중합체중의 비페닐렌구조가 증가함에 따라 약간씩 증가하였다. 또한 중합체의 열안정성은 중합체중의 비페닐렌구조가 증가함에 따라 개선되었으며, 비페닐렌구조를 가지는 중합체의 결정도는 상당히 높아서 약 33%정도로 나타났다.

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Syntheses, Crystal Structures, and Spectral Properties of Two Coordination Compounds Based on 1,2-Bis(benzimidazolyl)benzene

  • Meng, Fa-Yan;Jiang, Bing-Li;Lin, Cui-Wu;Wang, Li;Tan, Xiao-He
    • Bulletin of the Korean Chemical Society
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    • 제32권3호
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    • pp.1017-1021
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    • 2011
  • Two new benzimidazolyl-containing complexes have been synthesized by reactions of $Cu^{II}$ salts and 1,2-bis(benzimidazolyl) benzene ($H_2bbbz$) with two different dicarboxylate ligands. When phthalate acid ($H_2pt$) was employed as secondary ligand, a 0D molecular complex Cu$(H_2bbbz)(pt){\cdot}(H_2pt)$ (1)was furnished and when the secondary ligand was instead by a linear bridging ligand of terephthalic acid ($H_2tp$) a 1D zipper-like coordination polymer $[Cu(H_2bbbz)(tp){\cdot}2(C_2H_5OH){\cdot}H_2O]_n$ (2) was obtained, suggesting the structure-direction effect of the secondary dicarbxylate ligand. The preliminary investigation on the spectral properties of the complexes was also presented.

형광분광법에 의한 Eu(Ⅲ)의 정량 (Determination of Eu(III) by Fluorescence Spectrometry)

  • 이상학;한종환;최상섭
    • 대한화학회지
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    • 제42권3호
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    • pp.285-291
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    • 1998
  • 리간드 증감 유발 형광을 이용한 형광 광도법으로 수용액 중의 Eu(Ⅲ) 이온을 Eu(Ⅲ)-terephthalic acid(TPA) 착이온의 방출 세기를 측정함으로써 정량하는 방법에 대하여 연구하였다. 들뜸 파장, pH, TPA의 농도 및 방출 파장의 방출 세기에 대한 영향을 조사하였다. Triton X-100에 용해시킨 Trioctylphosphine oxide(TOPO) 용액을 Eu(Ⅲ)-TPA 용액에 첨가하였을 때는 방출 세기가 현저히 증가함을 관찰하였다. Eu(Ⅲ) 이온검정 곡선의 직선 감응 범위와 검출 한계는 TOPO를 첨가하지 않았을 경우에는 들뜸 파장, pH 및 TOPO의 농도가 각각 284nm, 4.4 및 $1.0{\times}10^{-4}M$였을 때, 각각 $1.0{\times}10^{-6}M{\sim}4.0{\times}10^{-4}M$$1.0{\times}10^{-6}M$였다. TOPO를 첨가하였을 경우에는 들뜸 파장, pH, TPA의 농도 및 방출 파장이 각각 256nm, 5.6, $3.5{\times}10^{-4}M$ 및 615nm였을 때, 각각 $1.0{\times}10^{-7}M∼1.0{\times}10^{-7}M$였다. Eu(Ⅲ) 이온을 본 방법으로 정량할 때의 방해 이온 효과에 대해서도 조사하였다.

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폐플라스틱 필름의 열분해특성에 대한 연구 (Research on Pyrolysis Properties of Waste Plastic Films)

  • 김영민;이보람;한태욱;김승도;류태우;방병열;김종수;박영권
    • 공업화학
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    • 제28권1호
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    • pp.23-28
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    • 2017
  • 열중량 분석기와 파이롤라이저-가스크로마토그래피/질량분석기를 이용하여 폐플라스틱 필름의 열분해 특성연구를 수행하였다. 열중량 분석 결과, 최근 사용량이 증가된 녹말 첨가 바이오 플라스틱의 영향으로 폐플라스틱 필름의 열분해는 $200^{\circ}C$에서 $370^{\circ}C$ 사이의 녹말 분해구간과 $370^{\circ}C$에서 $510^{\circ}C$ 사이의 PS, PP, PE와 같은 플라스틱계열의 고분자 분해구간을 가지는 것을 확인할 수 있었다. Revised Ozawa method를 이용한 동역학 분석 결과 폐플라스틱 필름의 열분해 반응 활성화 에너지는 녹말과 플라스틱계열 고분자의 다른 분해 반응에 의해 급격하게 변화되었다. 파이롤라이저-가스크로마토그래피/질량분석 결과 폐플라스틱 필름에 포함된 각 고분자의 열분해 부산물인 levoglucosan (녹말), terephthalic acid (PET), styrene monomer/dimer/trimer (PS), methylated alkenes (PP), alkadiene/alkene/alkane으로 구성된 triplet 피크 (PE)가 나타남을 확인할 수 있었다. 또한 고분자 첨가제로 사용되는 프탈레이트 성분도 검출되었다.