• Bulletin of the Korean Chemical Society
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• 제35권3호
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• pp.793-797
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• 2014

To develop a methodology for absolute determination of the surface areal density of functional groups on organic and bio thin films, medium energy ion scattering (MEIS) spectroscopy was utilized to provide references for calibration of X-ray photoelectron spectroscopy (XPS) or Fourier transformation-infrared (FT-IR) intensities. By using the MEIS, XPS, and FT-IR techniques, we were able to analyze the organic thin film of a Ru dye compound ($C_{58}H_{86}O_8N_8S_2Ru$), which consists of one Ru atom and various stoichiometric functional groups. From the MEIS analysis, the absolute surface areal density of Ru atoms (or Ru dye molecules) was determined. The surface areal densities of stoichiometric functional groups in the Ru dye compound were used as references for the calibration of XPS and FT-IR intensities for each functional group. The complementary use of MEIS, XPS, and FT-IR to determine the absolute surface areal density of functional groups on organic and bio thin films will be useful for more reliable development of applications based on organic thin films in areas such as flexible displays, solar cells, organic sensors, biomaterials, and biochips.

• Journal of Plant Biotechnology
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• 제33권4호
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• pp.277-281
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• 2006

Fourier transform - infrared spectroscopy (FT-IR) provides biochemical profiles containing overlapping signals from a majority of the compounds that are present when whole cell extracts are analyzed. We attempted to determine the ripeness of strawberry fruit flesh by FT-IR. Fruit ripeness was divided into four developmental stages based on fruit skin color: 'yellow-green', 'pink-green', 'pink', and 'red' stages. Principal component analysis of FT-IR data of inside fruit flesh extracts clustered samples of four different developmental stages into three discrete groups: (1) 'yellow-green' group, (2) 'pink-green' group, and (3) 'pink' and 'red' group. The most remarkable difference between four different developmental stages was found in the carbohydrate fingerprint region $(1,000-1,100cm^{-1})$ of the FT-IR spectrum, indicating that differences in carbohydrate compounds represented the ripeness of strawberry fruit. Overall results indicate that FT-IR in combination with PCA enables discrimination of the ripeness of strawberry fruit flesh.

• 유기물자원화
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• 제22권2호
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• pp.17-26
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• 2014

본 연구에서는 벤토나이트를 이용하여 수용액상에서 혼합 중금속의 흡착 특성을 평가하였다. 벤토나이트는 SEM과 FT-IR에 의해 물리 화학적 성상을 분석하였고, 중금속 흡착 특성은 Freundlich 및 Langmuir 방정식을 이용하여 해석하였다. 평형흡착 실험결과는 Langmuir 모델에 잘 부합되었으며, $Pb^{2+}$ > $Cu^{2+}$ > $Cd^{2+}$ > $$Zn^{2+}{\sim_=}Ni^{2+}$$순으로 평형 흡착량이 높았다. 용액의 pH가 6에서 10으로 증가함에 따라 흡착량은 증가하는 경향을 나타내었다. SEM과 FT-IR에 의한 벤토나이트의 표면 관찰결과에서 주 관능기는 Si-O 및 Si-O-Al 로 나타났다. 이러한 결과로부터 중금속 흡착 메카니즘은 표면흡착과 이온교환뿐만 아니라 표면 침전이다. 본 연구 결과를 통해 벤토나이트는 수용액 내 중금속을 효율적으로 제거할 수 있는 흡착제로 판단된다.

• 한국염색가공학회지
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• 제16권1호
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• pp.59-64
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• 2004

As a simulation of solvent-assisted dyeing, the solvent effects on the structure of polyethylene terephthalate(PET) film treated by dimethylformamide(DMF) were investigated. The effects were evaluated by the atomic force microscopy(AFM) topographical changes and FT-IR spectrum analysis. PET films treated with DMF at $70^{\circ}C$ for several different treatment time(20, 40, and 60 min). AFM topography showed that, with increasing treatment time by DMF, PET surfaces became smooth due to the swelling phenomenon and the rigid structure changed into flexible state which was contributed to increase the surface area of PET films. FT-IR spectrum analysis showed that DMF and molecular chains of PET interacted each other via their polar carbonyl groups and that DMF also affected the out-of-plane bending vibration mode of phenyl ring of PET.

• 분석과학
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• 제16권1호
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• pp.25-31
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• 2003

Cr(III) picolinate는 생체이용성 물질로 동물이나 사람에게 필수 미네랄 크롬을 공급하는 물질로 알려져 있다. 본 연구에서는 두 가지 방법으로 Cr(III)- picolinate를 합성하고 원소분석, FT-IR, 고성능액체크로마토그래피 및 MALDI-MS 등으로 생성물 및 부산물의 순도와 구조를 확인하였다.

• Elastomers and Composites
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• 제51권1호
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• pp.1-9
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• 2016

Characterization of the UV oxidation for raw natural rubber (NR) was investigated in controlled conditions through image and FT-IR analysis. The UV oxidation was performed on a thin film of natural rubber coated on a KBr window at 254 nm and room temperature to exclude the thermal oxidation. Before or after exposure to UV light, image of the NR thin film was observed at a right or tilted angle. FT-IR absorption spectra were measured in transmission mode with the UV irradiation time. The UV oxidation of NR was examined by the changes of absorption peaks at 3425, 1717, 1084, 1477, 1377, and $833cm^{-1}$ which were assigned to hydroxyl group (-OH), carbonyl group (-C=O), carbon-oxygen bond (-C-O), methylene group $(-CH_2-)$, methyl group $(-CH_3)$, and cis-methine group $(cis-CCH_3=CH-)$, respectively. During the initial exposure period, the results indicated that the appearance of carbonyl group was directly related to the reduction of cis-methine group containing carbon-carbon double bond (-C=C-). Most of aldehydes or ketones from carbon-carbon double bonds were formed very fast by chain scission. A lot of long wide cracks with one orientation at regular intervals which resulted in consecutive chain scission were observed by image analysis. During all exposure periods, on the other hand, it was considered that the continuous increment of hydroxyl and carbonyl group was closely related to the decrement of methylene and methyl group in the allylic position. Therefore, two possible mechanisms for the UV oxidation of NR were suggested.

• Elastomers and Composites
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• 제55권1호
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• pp.51-58
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• 2020

In this study, the thermal oxidation of raw natural rubber (NR) was investigated under controlled conditions by optical image and fourier transform infrared (FT-IR) analysis. The thermal oxidation was performed on a transparent thin film of raw NR coated on a KBr window in a dark chamber at 80℃ under low humidity conditions to completely exclude moisture and restrict light oxidation. Images of the thin film of raw NR were obtained before and after thermal oxidation. FT-IR absorption spectra were measured in the transmission mode at different thermal exposure times. The thermal oxidation of NR was examined by the changes in the absorption peaks at 3449, 1736, 1447, 1377, 1242, 1072, and 833 cm^-1, which corresponded to a hydroxyl group (-OH), a carbonyl group (-C=O) from an aldehyde and a ketone, a methylene group (-CH₂-), a methyl group (-CH₃), a carbon-oxygen single bond (-C-O) from an epoxide, a carbon-oxygen bond (-C-O) from an ether, an alcohol, a peroxide, or a cyclic peroxide, and a cis-methine group (cis-CCH₃=CH-), respectively. In the initial stage of thermal oxidation, two different types of free radicals were produced quickly and randomly by the homolytic cleavage of a double bond and allylic hydrogen abstraction. Aldehydes and ketones were formed from chain scissions of the double bonds and alcohols were produced from allylic hydrogen abstraction at the methylene or methyl groups. Two reactions seemed to proceed competitively with each other. At a later stage, oxidative crosslinks seemed to dominate through the combination of free radicals such as an allyl radical (CH=CHCH₂·), alkoxy radical (RO·), and peroxy radical (ROO·) and the reaction of a hydroperoxide (-ROOH) with a double bond. The image obtained after thermal oxidation showed hardening without cracks. Based on these observations, a plausible two-step mechanism was suggested for chain hardening caused by the thermal oxidation.

• 한국대기환경학회:학술대회논문집
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• 한국대기환경학회 2000년도 춘계학술대회 논문집
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• pp.321-322
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• 2000

대기중의 유해 유기오염물질의 배출농도를 규제하는 법규와 표준지침이 제정되어 있으나 시료채취와 분석까지 시간이 많이 걸려 빠른시간내 확인하기엔 어려운 실정이다. 특히 악취성 휘발성 유기물은 오염발생이 순간적으로 일어나 이를 신속하게 규명하지 않으면 원인 규명이 어려운 실정이다. 본 연구에서는 이동형 FT-IR을 사용하여 대기중에 존재하는 유해 유기오염물질의 신속하게 분석할 수 있는 분석법을 확립하고자 하였다. (중략)

• 한국진공학회:학술대회논문집
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• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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• pp.437-437
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• 2014

Various oxide particles are synthesized in an ambient condition using an electron beam irradiation system. The formation of oxide particles is confirmed by FT-IR spectra results and the X-ray photoelectron spectrum. It is also shown that the morphology and size of oxide particles are significantly influenced by the type and flowrate of dilution gas. The energy dispersive X-ray (EDX) analysis also confirms that various oxide particles are synthesized.

• Journal of Plant Biotechnology
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• 제42권1호
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• pp.60-70
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• 2015

본 연구의 목적은 적외선 분광스펙트럼 데이터를 이용하여 대두 종자내의 지방산 함량을 동시에 예측할 수 있는지 여부를 조사하기 위한 것이다. 총 153종의 대두(Glycine max Merrill) 종자로부터 적외선 분광스펙트럼 및 지방산의 함량을 기체크로마토그라피 분석을 통하여 확인하였다. 적외선 분광스펙트럼 조사결과 대두는 단백질이나 아미노산의 amide bond region ($1,700{\sim}1,500cm^{-1}$), 핵산이나 인지질의 phosphodiester groups ($1,500{\sim}1,300cm^{-1}$) 그리고 탄수화물 등 다당류의 sugar region ($1,200{\sim}1,000cm^{-1}$)에서 계통별로 큰 차이가 이루어짐을 알 수 있었다. 총 29라인의 대두 계통별 시료로부터 지방산 함량을 조사한 결과 총 지방산의 함량은 건조 시료 0.1 g 당 $185.57{\mu}g$에서 $325.9{\mu}g$으로 계통간에 차이가 있었음을 알 수 있었으며 평균 함량은 $244.48{\mu}g$이었다. PLS regression 분석을 이용하여 총 5개 지방산(팔미틱산, 스테아릭산, 올레익산, 리노레익산 그리고 리노레닉산) 함량 예측 calibration models의 실측 검증 결과, 팔미틱산($R^2=0.8002$), 올레익산($R^2=0.8909$) 그리고 리노레익산($R^2=0.815$)은 회귀분석 상관계수가 0.8 이상으로 정확도 높음을 알 수 있었다. 그러나 스테아릭산($R^2=0.4598$)과 리노레닉산($R^2=0.6868$)의 경우 상관계수가 0.7 이하로 상대적으로 예측정확도가 낮음을 알 수 있었다. 본 연구에서 확립된 기술은 지방산의 조성 변환을 통하여 새로운 대두 품종 개발을 위한 계통선발 과정에서 매우 효율적인 수단으로 활용이 가능할 것으로 사료된다. 더 나아가 본 기술은 대두는 물론 대두 유래 농산물이나 식품의 품질 검증 수단으로 활용이 가능할 것으로 기대된다.