• 제목/요약/키워드: Infrared(IR)

검색결과 1,561건 처리시간 0.029초

Synthesis of Polyamine Grafted Chitosan Copolymer and Evaluation of Its Corrosion Inhibition Performance

  • Li, Heping;Li, Hui;Liu, Yi;Huang, Xiaohua
    • 대한화학회지
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    • 제59권2호
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    • pp.142-147
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    • 2015
  • Two new chitosan derivatives, polyamine grafted chitosan copolymers have been synthesized for corrosion protection of carbon steel in acidic medium. First, methyl acrylate graft chitosan copolymer (CS-MAA) was prepared by the reaction of chitosan (CS) and methyl acrylate (MAA) via the Michael addition reaction. Then, CS-MAA was reacted with ethylene diamine (EN) and triethylene tetramine (TN) respectively to synthesize ethylene diamine grafted chitosan copolymer (CS-MAA-EN) and triethylene tetramine grafted chitosan copolymer (CS-MAA-TN), and the structures were characterized by Fourier-transform infrared spectroscopy (FT-IR). At last, the corrosion inhibition activities on Q235 carbon steel were investigated by using gravimetric measurements, metallographic microscope, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) measurements. The compounds CS-MAA-EN and CS-MAA-TN show an appreciable corrosion inhibition property against corrosion of Q235 carbon steel in 5% HCl solution at $25^{\circ}C$. It has been observed that CS-MAA-EN shows greater corrosion inhibition efficiency than CS-MAA-TN. The inhibition efficiency of CS-MAA-EN was close to 90% when the mass fraction concentration was 0.2%~0.3%; the inhibition efficiency of CS-MAA-TN was close to 85% when the mass fraction concentration was 0.02%. The present work provided very promising results in the preparation of green corrosion inhibitors.

The Influence of Hydrotalcite Intercalated with Benzoate on UV Stability of Acrylic Coating

  • Nguyen, Thuy Duong;Nguyen, Anh Son;Thai, Thu Thuy;Pham, Gia Vu;To, Thi Xuan Hang;Olivier, Marie-Georges
    • Corrosion Science and Technology
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    • 제19권1호
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    • pp.16-22
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    • 2020
  • It is important to realize that benzoate was intercalated into hydrotalcite (HTC-Bz) by the co-precipitation method. In this case, acrylic coating with 0.5 wt% HTC-Bz was deposited on carbon steel using the spin coating method. Next, the HTC-Bz structure was characterized by Field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR). In fact, an ultraviolet vision spectroscopy (UV-Vis) was used to determine the benzoate content in HTC-Bz, and the UV absorption ability of HTC-Bz. Using electrochemical techniques, water contact angle measurement, and thermal-gravimetric analysis, we compared the protective properties before and after QUV test, hydrophobicity and the thermal stability of acrylic coating containing HTC-Bz. The obtained results showed that HTC-Bz with a plate-like structure was successfully synthesized; benzoate was intercalated into the interlayer of hydrotalcite with a concentration of 28 wt%. Additionally, it was noted that HTC-Bz has an UV absorption peak at 225 nm. In conclusion, the addition of HTC-Bz enhanced the UV stability, hydrophobicity and the thermal stability of acrylic coating.

C2-Symmetric Dichloro[rac-ethylenebisindenyl] zirconium(IV)/Methylaluminoxane 시스템을 이용한 배위 중합에 관한 연구 (A Study on the Coordination Polymerization Using C2-Symmetric Dichloro[rac-ethylenebisindenyl] zirconium(IV)/Methylaluminoxane System)

  • 양동진;김현기;박노형;이준철;김동현
    • Elastomers and Composites
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    • 제48권1호
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    • pp.2-9
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    • 2013
  • rac-$Et(Ind)_2ZrCl_2$ 메탈로센 촉매와 메틸알루미늄옥산 공촉매를 이용하여 polyethylene, poly(ethylene-co-1-decene), poly(ethylene-co-p-methylstyrene) 및 poly(ethylene-ter-1-decene-ter-p-methystyrene)를 합성하였다. $^{13}C$ NMR과 $^1H$ NMR 및 FT-IR을 이용하여 삼원공중합체의 특성을 분석하였다. 삼원공중합의 최적조건을 확립하기 위해 동일한 중합조건을 유지한 채 촉매량, 공촉매/촉매 몰비, 중합 시간 및 중합 온도를 변경하여 실험하였다. 촉매량이 증가할수록 삼원공중합체의 촉매활성도 및 중량평균분자량은 증가하였으나, 중합시간이 30분을 초과하자 촉매활성도는 감소하였다. 공촉매/촉매 몰비를 증가시킨 결과 중량평균분자량은 감소하였고, 촉매활성도는 어느 정도 증가하였다. 촉매활성도는 중합온도가 증가함에 따라 상승하였으나 중량평균 분자량은 감소하였다.

실리콘 이온이 첨가된 biphasic calcium phosphate의 합성 및 특성평가 (Synthesis and characterization of silicon ion substituted biphasic calcium phosphate)

  • 송창원;김태완;김동현;박홍채;윤석영
    • 한국결정성장학회지
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    • 제20권5호
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    • pp.243-248
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    • 2010
  • Si-BCP(si-substituted biphasic calcium phosphate)를 제조하기 위하여 $Ca(NO_3)_2{\cdot}4H_2O$, $(NH_4)_2HPO_4$, $Si(OC_2H_5)_4$을 출발 물질로 공침법(co-precipitation process)을 이용하여 합성하였다. 합성된 분말의 HAp/${\beta}$-TCP 결정상 비율 및 Si-P 치환 거동은 X-선 회절 상 분석을 이용하여 측정하였고, silicon ion 첨가 시 나타나는 BCP의 화학적 결합거동을 측정하기 위하여 FT-IR를 사용하여 분석하였다. 또한 Si-BCP 분말의 in-vitro 생분해거동 및 생체활성도를 측정하기 위하여 제조된 분말을 SBF(simulated body fluid) solution에 침적시킨 뒤 분말의 형상과 구성 성분은 SEM과 EDS를 통하여 확인하였다.

티오프로피온 아미드의 수소 결합 능력에 대한 근 적외선 분광학 연구 (The Near Infrared Spectroscopic Studies on the Hydrogen Bonding Ability of Thiopropionamide)

  • 주설아;박정희;윤창주;최영상
    • 대한화학회지
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    • 제39권11호
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    • pp.837-841
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    • 1995
  • 사염화탄소 속에서 티오프로피온아미드(TPA)와 triethylphosphine oxide(TEPO), triethylphosphine oxide(TPPO), trimethylphosphate(TMP), 그리고 tributyl phosphate(TBP)간의 수소 결합에 대한 열역학적 상수들을 근적외선 분광법을 이용하여 구하였다. TPA의 .nu./.alpha./+amide 2 조합띠는 TPA 단위체 및 수소 결합을 이룬 TPA의 띠로 이루어져 있음이 확인되어 이 띠를 두 개의 Lorentzian-Gaussian 곱함수의 띠로 분해하였다. 온도 및 농도의 변화에 따른 이 조합띠의 변화기로부터 TPA와 TEPO, TPPO, TMP, TBP의 수소 결합 엔탈피는 각각 -21.4, -16.8, -12.8, -12.9kJ/mol이었다. 이 결과는 치환기의 inductive effect 및 steric effect로 설명할 수 있다.

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Intermolecular Hydrogen Bonding and Vibrational Analysis of N,N-Dimethylformamide Hexamer Cluster

  • Park, Sun-Kyung;Min, Kyung-Chul;Lee, Choong-Keun;Hong, Soon-Kang;Kim, Yun-Soo;Lee, Nam-Soo
    • Bulletin of the Korean Chemical Society
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    • 제30권11호
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    • pp.2595-2602
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    • 2009
  • Hexamer cluster of N,N-dimethylformamide(DMF) based on the crystal structure was investigated for the equilibrium structure, the stabilization energies, and the vibrational properties in the density functional force field. The geometry (point group $C_i$) of fully optimized hexamer clustered DMF shows quite close similarity to the crystal structure weakly intermolecular hydrogen bonded each other. Stretching force constants for intermolecular hydrogen bonded methyl and formyl hydrogen atoms with nearby oxygen atom, methyl C–H${\cdots}$O and formyl C–H${\cdots}$O, were obtained in 0.055 $\sim$ 0.11 and $\sim$ 0.081 mdyn/$\AA$, respectively. In-plane bending force constants for hydrogen bonded methyl hydrogen atoms were in 0.25 $\sim$ 0.33, and for formyl hydrogen $\sim$ 0.55 mdynÅ. Torsion force constants through hydrogen bonding for methyl hydrogen atoms were in 0.038 $\sim$ 0.089, and for formyl hydrogen atom $\sim$ 0.095 mdynÅ. Calculated Raman and infrared spectral features of single and hexamer cluster represent well the experimental spectra of DMF obtained in the liquid state. Noncoincidence between IR and Raman frequency positions of stretching C=O, formyl C–H and other several modes was interpreted in terms of the intermolecular vibrational coupling in the condensed phase.

Synthesis and Characterization of Magnetic Nanoparticles and Its Application in Lipase Immobilization

  • Xu, Jiakun;Ju, Caixia;Sheng, Jun;Wang, Fang;Zhang, Quan;Sun, Guolong;Sun, Mi
    • Bulletin of the Korean Chemical Society
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    • 제34권8호
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    • pp.2408-2412
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    • 2013
  • We demonstrate herein the synthesis and modification of magnetic nanoparticles and its use in the immobilization of the lipase. Magnetic $Fe_3O_4$ nanoparticles (MNPs) were prepared by simple co-precipitation method in aqueous medium and then subsequently modified with tetraethyl orthosilicate (TEOS) and 3-aminopropyl triethylenesilane (APTES). Silanization magnetic nanoparticles (SMNP) and amino magnetic nanomicrosphere (AMNP) were synthesized successfully. The morphology, structure, magnetic property and chemical composition of the synthetic MNP and its derivatives were characterized using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) analysis, X-ray diffraction, superconducting quantum interference device (SQUID) and thermogravimetric analyses (TGA). All of these three nanoparticles exhibited good crystallization performance, apparent superparamagnetism, and the saturation magnetization of MNP, SMNP, AMNP were 47.9 emu/g, 33.0 emu/g and 19.5 emu/g, respectively. The amino content was 5.66%. The AMNP was used to immobilize lipase, and the maximum adsorption capacity of the protein was 26.3 mg/g. The maximum maintained activity (88 percent) was achieved while the amount of immobilized lipase was 23.7 mg $g^{-1}$. Immobilization of enzyme on the magnetic nanoparticles can facilitate the isolation of reaction products from reaction mixture and thus lowers the cost of enzyme application.

WHAT MAKES A RADIO-AGN TICK? TRIGGERING AND FEEDING OF ACTIVE GALAXIES WITH STRONG RADIO JETS

  • KAROUZOS, MARIOS;IM, MYUNGSHIN;KIM, JAE-WOO;LEE, SEONG-KOOK;CHAPMAN, SCOTT
    • 천문학논총
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    • 제30권2호
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    • pp.447-449
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    • 2015
  • Although the link between activity in the nuclei of galaxy and galactic mergers has been under scrutiny for several years, it is still unclear to what extent and for which populations of active galaxies merger-triggered activity is relevant. The environments of AGN allow an indirect probe of the past merger history and future merger probability of these systems, suffering less from sensitivity issues when extended to higher redshifts than traditional morphological studies of AGN host galaxies. Here we present results from our investigation of the environment of radio selected sources out to a redshift z=2. We employ the first data release J-band catalog of the new near-IR Infrared Medium-Deep Survey (IMS), 1.4 GHz radio data from the Faint Images of the Radio Sky at Twenty-cm (FIRST) survey and a deep dedicated VLA survey of the VIMOS field, covering a combined total of 20 sq. degrees. At a flux limit of the combined radio catalog of 0.1 mJy, we probe over 8 orders of magnitude of radio luminosity. Using the second closest neighbor density parameters, we test whether active galaxies inhabit denser environments. We find evidence for a sub-population of radio-selected AGN that reside in significantly overdense environments at small scales, although we do not find significant overdensities for the bulk of our sample. We show that radio-AGN in the most underdense environments have vigorous ongoing star formation. We interpret these results in terms of the triggering and fuelling mechanism of radio-AGN.

팔라듐 촉매화 비닐 치환 반응을 이용한 Conjugated Dienals의 합성 (Synthesis of Conjugated Dienals by Palladium-Catalyzed Vinyl Substitution Reaction)

  • 이종태;김진일
    • 대한화학회지
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    • 제28권5호
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    • pp.335-341
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    • 1984
  • ${\alpha},{\beta}$-불포화 알데히드의 아세탈은 브롬화 방향족화합물들과 팔라듐 촉매와 트리에틸아민 존재하에서 쉽게 반응하여 방향족의 conjugated enals을 생성하였다. 불포화 아세탈로서 acrolein diethyl acetal과 methacrolein diethyl acetal을 사용하여 이들을 메틸기와 이소프로필기로 치환된 브롬화 방향족화합물들과 $100^{\circ}C$에서 반응시킨 뒤 생성물들을 옥살산 수용액으로 처리하여 방향족의 conjugated enals를 합성하였다. o-bromotoluene과 methacrolein diethyl acetal과의 반응을 제외하고는 모두 60% 이상의 좋은 수득율을 얻을 수 있었으며 생성물의 구조는 proton NMR과 IR스펙트럼으로 확인하였다. 3-bromopropenal dimethyl acetal 및 (E)-3-bromo-2-methylpropenal diethyl acetal을 할로겐화 비닐화합물의 반응 부위로 하고 1-알켄과 ethyl acrylate등을 올레핀 반응 부위로 하는 반응물들의 역조합(reverse combination)에 의하여 지방족의 2,4-dienals를 50% 이상의 수득율로 합성 할 수 있다.

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플라즈마 중합법에 의한 스티렌 박막의 분자 구조 및 분자량 제어에 관한 연구 (A Study on the molecular structure and molecular weight control of styrene films by plasma polymerization)

  • 김종택;최충양;박종관;박응춘;이덕출
    • 한국진공학회지
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    • 제6권3호
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    • pp.213-219
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    • 1997
  • 본 연구에서는 내전극 정전결합 유동가스형 반응장치를 이용하여 플라즈마 중합 스 티렌 박막을 제작하고 적외선분광스펙트럼, 열분해가tm크로마토그래피, 시차주사열량계 및 겔투과성 크로마토그래피의 분석을 통하여 중합조건이 분자구조 및 분자량 분포에 미치는 영향을 조사하였다. 위의 결과로부터 개시 모노머의 화학적 특성과는 다른 고도로 가교된 박막이 생성되었으며, 방전압력, 방전전력 및 가스의 유량 등의 중합조건 조절에 의해 분자 구조, 가교도, 분자량 분포 등의 제어가 가능함이 판명되었다. 따라서 내전극 정전결합 유동 가스형 반응장치에 의해 수행된 플라즈마중합법은 중합조건의 조절에 의해 센서의 감지막, 광도전성 소자 및 포토 레지스트 등에 응용가능한 기능성 유기박막의 제작에 좋은 특성을 나타내는 것을 알 수 있었다.

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