Relevant bibliographies by topics / FTIR

Academic literature on the topic 'FTIR'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 May 2024

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Journal articles on the topic "FTIR"

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Norton, Kelly L., Andrew J. Lange, and Peter R. Griffiths. "A unified approach to the chromatography-FTIR interface: GC-FTIR, SFC-FTIR, and HPLC-FTIR with subnanogram detection limits." Journal of High Resolution Chromatography 14, no. 4 (April 1991): 225–29. http://dx.doi.org/10.1002/jhrc.1240140403.

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Jaiswal, A. K., N. G. Giri, Anil Kumar Jaiswal, Nilima Samal, P. Sharma, T. Millo, and S. K. Gupta. "Forensic Applications of IR/FTIR." Journal of Forensic Chemistry and Toxicology 3, no. 1 (June 15, 2017): 39–68. http://dx.doi.org/10.21088/jfct.2454.9363.3117.5.

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Infra-Red spectroscopy plays important role for analysis of several compounds, metals etc. Its use is readily understood from breadth of its applications. The range of material that can be analyzed by IR/FTIR is essentially unlimited. Applications are found in diverse fields such as forensic science, pharmaceuticals, food and agriculture, biological and clinical chemistry, environmental chemistry and many others.
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Woods, Ron, and Giles Henderson. "FTIR rotational spectroscopy." Journal of Chemical Education 64, no. 11 (November 1987): 921. http://dx.doi.org/10.1021/ed064p921.

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Genvert, Klaus, and Georg Souvignier. "Zeitaufgelöste FTIR-Differenzspektroskopie." Nachrichten aus Chemie, Technik und Laboratorium 41, no. 9 (September 1993): 950–56. http://dx.doi.org/10.1002/nadc.19930410905.

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Della Ventura, G., A. Marcelli, and F. Bellatreccia. "SR-FTIR Microscopy and FTIR Imaging in the Earth Sciences." Reviews in Mineralogy and Geochemistry 78, no. 1 (January 1, 2014): 447–79. http://dx.doi.org/10.2138/rmg.2014.78.11.

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Chen, Yanyan, Agnieszka Furmann, Maria Mastalerz, and Arndt Schimmelmann. "Quantitative analysis of shales by KBr-FTIR and micro-FTIR." Fuel 116 (January 2014): 538–49. http://dx.doi.org/10.1016/j.fuel.2013.08.052.

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Karamancheva, I., V. Stefov, B. Šoptrajanov, G. Danev, E. Spasova, and J. Assa. "FTIR spectroscopy and FTIR microscopy of vacuum-evaporated polyimide thin films." Vibrational Spectroscopy 19, no. 2 (April 1999): 369–74. http://dx.doi.org/10.1016/s0924-2031(99)00011-9.

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Gaillard, F., I. Linossier, M. Sweeney, J. A. Reffner, and M. Romand. "Grazing-angle micro-FTIR spectroscopy (GAM-FTIR): applications to adhesion studies." Surface and Interface Analysis 27, no. 9 (September 1999): 865–70. http://dx.doi.org/10.1002/(sici)1096-9918(199909)27:9<865::aid-sia652>3.0.co;2-p.

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Barraza-Garza, Guillermo, Hiram Castillo-Michel, Laura A. de la Rosa, Alejandro Martinez-Martinez, Jorge A. Pérez-León, Marine Cotte, and Emilio Alvarez-Parrilla. "Infrared Spectroscopy as a Tool to Study the Antioxidant Activity of Polyphenolic Compounds in Isolated Rat Enterocytes." Oxidative Medicine and Cellular Longevity 2016 (2016): 1–10. http://dx.doi.org/10.1155/2016/9245150.

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The protective effect of different polyphenols, catechin (Cat), quercetin (Qc) (flavonoids), gallic acid (GA), caffeic acid (CfA), chlorogenic acid (ChA) (phenolic acids), and capsaicin (Cap), against H2O2-induced oxidative stress was evaluated in rat enterocytes using Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) Spectroscopy and Fourier Transform Infrared Microspectroscopy (FTIRM), and results were compared to standard lipid peroxidation techniques: conjugated dienes (CD) and Thiobarbituric Acid Reactive Substances (TBARS). Analysis of ATR-FTIR and FTIRM spectral data allowed the simultaneous evaluation of the effects of H2O2and polyphenols on lipid and protein oxidation. All polyphenols showed a protective effect against H2O2-induced oxidative stress in enterocytes, when administered before or after H2O2. Cat and capsaicin showed the highest protective effect, while phenolic acids had weaker effects and Qc presented a mild prooxidative effect (IR spectral profile of biomolecules between control and H2O2-treated cells) according to FTIR analyses. These results demonstrated the viability to use infrared spectroscopy to evaluate the oxidant and antioxidant effect of molecules in cell systems assays.
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Mališová, Miroslava, Michal Horňáček, Jozef Mikulec, Pavol Hudec, and Vladimír Jorík. "FTIR study of hydrotalcite." Acta Chimica Slovaca 11, no. 2 (October 1, 2018): 147–56. http://dx.doi.org/10.2478/acs-2018-0021.

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Abstract The aim of the research was the study of aluminium-magnesium hydrotalcite by FTIR analysis and detection of differences in structure due to calcination. Three types of samples were analysed. In the first two samples, cobalt was added into the structure and the third sample contained nickel and zinc. Hydrotalcite was prepared by one of the most common methods of hydrotalcite preparation, co-precipitation. After preparation, the samples were calcined at temperatures from 150 °C to 750 °C. Samples were compared in terms of calcination temperature; but in case of samples containing cobalt, two samples to each other. The most significant changes were noticed in the 500–700 cm−1 region, where a spinel structure was formed at higher calcination temperatures.
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Dissertations / Theses on the topic "FTIR"

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Nybacka, Louise. "FTIR spectroscopy of glucose." Thesis, Uppsala universitet, Fasta tillståndets elektronik, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-306952.

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Approximately 450 000 people have diabetes in Sweden today, and the number of diabetics only rises. Monitoring blood sugar several times a day is a fundamental part of managing the disease, and reducing the risks of complications. Today’s glucose monitoring devices are invasive and require small needle sticks for a measurement. Providing a painless method of monitoring the blood sugar level would relieve the lives of diabetics world-wide.   The objective of this project was to investigate the absorption spectra of aqueous glucose concentrations (100 to 5000 mg/dl) in the mid infrared region with Fourier Transform spectroscopy (FTIR), and finally implementing a hand-held monochromatic spectrometer to demonstrate a non-invasive concept. The method chosen for implementing the hand-held demo is due to the commercial availability of diodes and detectors at those wavelengths.   The results from the FTIR showed a trend among concentrations in all wavelengths, in between 1180 to 980 cm-1, specifically at 1035 cm-1, but also in the region 2920 to 2850 cm-1. The hand-held spectrometer did not register any transmittance of the glucose samples. For future implementations, 1035 cm-1 should be investigated more in-depth for a hand-held device.
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Oliveira, Jefferson Saraiva de. "Avaliação da qualidade de biodiesel por espectroscopias ftir e ftnir associadas à quimiometria." reponame:Repositório Institucional da UnB, 2007. http://repositorio.unb.br/handle/10482/2952.

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Dissertação (mestrado)—Universidade de Brasília, Instituto de Química, 2007.
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Após a introdução do biodiesel na matriz energética Brasileira, se tornou necessária a avaliação da qualidade deste tipo de combustível seguindo normas estabelecidas pela Agência Nacional do Petróleo (ANP). A possibilidade do uso de diferentes fontes de óleos vegetais na produção do biodiesel gera problemas relacionados à produção e qualidade deste combustível, abrindo precedentes para fraudes fiscais. Considerando esta demanda socioeconômica, a proposta é o uso de técnicas espectroscópicas combinadas com ferramentas quimiométricas como métodos para determinar o teor de ésteres metílicos (biodiesel) nas misturas diesel/biodiesel. Neste trabalho as técnicas espectroscópicas FTIR-ATR (Infravermelho com transformada de Fourier - reflectância total atenuada) e FTNIR (Infravermelho Próximo com transformada de Fourier) combinadas com a análise de PLS (Regressão por Mínimos Quadrados Parciais) e de ANN (rede neural artificial) foram empregadas. Os ésteres metílicos usados para preparar as amostras da calibração foram obtidos pela metanólise dos óleos de soja, babaçu, dendê e de óleo de soja usado em frituras. Sua pureza foi avaliada por cromatografia gasosa (GC-FID). As amostras foram separadas em dois grupos: Grupo I, misturas binárias (diesel + um tipo de éster metílico), correspondendo a 96 misturas do biodiesel (0-100%, m/m), e Grupo II, misturas quaternárias (diesel + três tipos de ésteres metílicos), correspondendo a 60 misturas do biodiesel (0-100%, m/m). Os resultados de PLS mostraram que o modelo de FTNIR para o Grupo I é mais preciso e exato (± 0,02 e ± 0,06%, m/m). No caso do Grupo II, os modelos de PLS (FTIR-ATR e FTNIR) apresentaram as mesmas exatidões, enquanto os modelos de ANN/FTNIR apresentaram melhor desempenho do que os modelos de ANN/FTIR-ATR. A melhor exatidão foi obtida pelo modelo de ANN/FTNIR para a determinação diesel (0,14%, m/m), já o modelo de ANN/FTIR-ATR para o dendê (0,6%, m/m) apresentou um desempenho inferior. As precisões na análise do Grupo II variaram de 0,06 a 0,53% (m/m) e os coeficientes de variação foram melhores que 3%, indicando que estes modelos são apropriados para a determinação das misturas diesel-biodiesel compostas por ésteres metílicos derivados de diferentes óleos vegetais. __________________________________________________________________________________________ ABSTRACT
After the introduction of biodiesel in the Brazilian energetic matrix it became necessary the evaluation of the quality of this kind of fuel following norms as established by the ANP (Brazilian Agency for Petroleum, Gas, and Biofuels). One of the problems that is concerned to the biodiesel production and quality is the use of different sources of vegetable oils in the biodiesel production, opening the possibility for fiscal frauds. Considering this socioeconomical demand it is proposed in this work the use of spectroscopic techniques combined to chemometric tools as methods to determine the content of methylseters (biodiesel) in diesel/biodiesel blends. The methods presented in this work have made use of spectroscopic techniques such as FTIR-ATR (attenuated total reflectance-Fourier transform infrared) and FTNIR (Fourier transform nearinfrared) combined to chemometric tools like PLS (partial least square regression analysis) and ANN (artificial neural network) analysis. The methyl esters used to prepare the calibration samples were obtained by the methanolysis of soybean, babassu, dende, and soybean fried oils. Their purity was evaluated by gas-chromatography (GC-FID). The samples were separated in two sets: Group I, binary mixtures (diesel + one kind of methyl ester), corresponding to 96 biodiesel blends (0–100%, w/w), and Group II, quaternary mixtures (diesel + three types of methyl esters), corresponding to 60 biodiesel blends (0–100%, w/w). The PLS results have shown that the FTNIR model for Group I is more precise and accurate (±0.02 and ±0.06%, w/w). In the case of Group II the PLS models (FTIR-ATR and FTNIR) have shown the same accuracies, while the ANN/FTNIR models has presented better performance than the ANN/FTIR-ATR models. The best accuracy was achieved by the ANN/FTNIR model for diesel determination (0.14%, w/w) while the worthiest was that of dende ANN/FTIR-ATR model (0.6%, w/w). Precisions in Group II analysis ranged from 0.06 to 0.53% (w/w) and coefficients of variation were better than 3% indicating that these models are suitable for the determination of diesel–biodiesel blends composed of methyl esters derived from different vegetable oils.
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Few, Julian William. "FTIR studies of chemical processes." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:b7dbc587-fb9e-46de-8f04-44892fde0bf4.

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This thesis presents the study of a selection of gas phase chemical processes using time-resolved Fourier transform infrared (FTIR) emission spectroscopy. Such processes include molecular energy transfer, chemical reaction and photodissociation. The major focus of this thesis was the investigation of collisional energy transfer from the electronically excited states of NO and OH, with particular attention paid to the fate of the electronic energy. NO A2Σ+(v = 0) is prepared by laser excitation, pumping the overlapped Q1 and P21 band heads of the NO A-X (0,0) transition at 226.257 nm. The quenching of this state by O2 and CO2 was studied. Experiments were performed to investigate what channels contribute to the quenching process, the branching ratio of these different channels and the partitioning of energy among the various products. Quenching by O2 was found to proceed mostly through non-reactive channels. High vibrational excitation of NO X 2Π was observed, with population detected in v = 22, representing 79% of the available energy. The O2 product was found to be formed in more than one electronic state: the ground state, X 3Σ-g, and a high-lying electronically excited state, such as the A 3Σ+u, A' 3Δu or c 1Σ-u states. A reactive channel producing vibrationally excited NO2 was observed, but was found to be a minor process with an upper limit of 18% for the branching ratio. In contrast the quenching of NO A 2Σ+(v = 0) by CO2 was found to proceed predominately by reaction, with a branching ratio of 76 %. While emission from NO2 was observed, it was weak, and therefore it was concluded that the main reaction products were CO, O(3P) and NO X 2Π(v = 0). The nascent strong CO2 v3 emission band from the non-reactive channel exhibited a large red-shift from its fundamental position. This indicates that the CO2 vibrational distribution is significantly hotter than statistical. Investigations were then performed studying the quenching of NO A 2Σ+(v = 1) by NO and CO2, with both systems exhibiting similar characteristics to the quenching of the ground vibrational level of NO A 2Σ+. From comparison of the emission intensity of the CO fundamental and CO2 v3 mode following quenching of the v = 0 and 1 levels of the NO A 2Σ+ state, it was concluded that the branching ratio for reactive quenching was larger in the latter case. Secondly, experiments were performed to measure the rate constants for the quenching of NO A 2Σ+(v = 0) by the noble gases. The noble gases are inefficient quenchers of electronically excited NO and therefore careful experimental design was required to minimise the influence of impurities on the results. All the rate constants were found to be of the order of 10-14 cm3 molecule-1 s-1. The value for Xe was 50 times smaller than reported previously in the literature. In light of this new measurement, a re-analysis of experiments, performed previously in the group, on the electronic quenching of NO A 2Σ+(v = 0) by Xe was performed. A very hot vibrational distribution of NO X 2Π was obtained. Next, the collisional quenching of OH A 2Σ+(v = 0) by H2 was investigated. OH radicals were generated in situ by the photolysis of HNO3 at 193 nm, which were excited to the A 2Σ+(v = 0) state on the overlapped Q1(1) and P21(1) rotational lines at 307.935 nm. Reactive quenching was found to be the major pathway, in agreement with the literature. Copious emission from vibrationally excited water was observed. Comparison of this emission with theoretical calculations revealed a hotter distribution than predicted. It was concluded that the energy channelled into the vibrational modes of H2O is in excess of 60% of the available energy. Experiments performed with D2 allowed the non-reactive channel to be studied; a cold vibrational distribution of the OH X 2Π was observed. Finally the reaction between CN radicals and cyclohexane was studied. CN was generated by the photolysis of ICN at 266 nm. Prompt emission from HCN in the C-H stretching region was observed meaning the new bond was formed in a vibrationally excited state. Analysis of the emission revealed HCN was populated up to v3 = 2. Excellent agreement with the results of a theoretical study of the system was found.
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Becker, Edo. "FTIR-Emissionsspektroskopische Untersuchungen der arktischen Atmosphäre = Investigations of the arctic atmosphere by FTIR-Emission spectroscopy /." Bremerhaven : Alfred-Wegener-Inst. für Polar- und Meeresforschung, 1998. http://www.gbv.de/dms/bs/toc/247022616.pdf.

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Inberg, R. Brandon. "Enhanced step mode FTIR position control." Thesis, Montana State University, 2005. http://etd.lib.montana.edu/etd/2005/inberg/InbergR1205.pdf.

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Finch, D. C. "FTIR spectroscopy of electron irradiated polymers." Thesis, Brunel University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381899.

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Morrell, Claire. "FTIR emission studies of chemical processes." Thesis, University of Oxford, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326026.

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Gowrie, Sarah. "FTIR emission studies of energy transfer." Thesis, University of Oxford, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.531817.

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Fuentes, A. Fernandez. "FTIR determination of sulphur isotope ratios." Thesis, University of Aberdeen, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334712.

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A new method for the determination of sulphur isotopic ratios by FTIR measuring the area or absorbance of individual lines, has been developed. The project could be divided into three parts: (i) In part one the infrared spectra of four sulphur gases SCO, H2S, SF6 and SO2, were collected and studied to evaluate which one would be the most appropriate to determine sulphur isotopic ratios. The synthesis of these gases was also assessed and performed in those cases where the means to carry them out were available. This part was designed to test the viability of these compounds as a means of extracting sulphur from natural samples. (ii) In part two, the methodology for the determination of sulphur isotopic ratios using the infrared spectrum of sulphur dioxide, gas chosen for this project, was performed. Different factors affecting the precision of the method, such as resolution, number of scans, etc., were evaluated and optimized. The UV/Vis spectrum of this gas was collected and the viability of using the L(1)-bound overdetermined Gaussian elimination method for assessing sulphur isotopic ratios over data obtained from this spectrum as well as from its infrared spectrum, was also tested. Both methods, integration of individual lines in the infrared spectrum of SO2, and use of the L(1)-bound overdetermined Gaussian elimination method over data also obtained from the infrared spectrum of sulphur dioxide, proved to be applicable when determining isotopic ratios in enriched samples. (iii) In part three, levels of sulphur-34 and nitrogen-15 in the biomass of four arable Scottish soils were determined. A slight enrichment in both isotopes was detected for one of the soils, being the first time such a measurement has been carried out. Sulphur and nitrogen deficiency in this soil are given as a possible explanation although the lack of sufficient number of data do not allow us to establish with certainty its cause.
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Hanh, Bui Duc, Ulrike Günther, Marcus Hartmann, Siegfried Wartewig, and Reinhard Neubert. "Drug penetration studied by FTIR methods." Universitätsbibliothek Leipzig, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-194960.

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Books on the topic "FTIR"

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Abidi, Noureddine. FTIR Microspectroscopy. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-84426-4.

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Al-Ghefaili, K. M. FTIR spectroscopic studies of zeolites. Manchester: UMIST, 1995.

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Becker, Edo. FTIR-Emissionsspektroskopische Untersuchungen der arktischen Atmosphäre =: Investigations of the arctic atmosphere by FTIR-emission spectroscopy. Bremerhaven: Alfred-Wegener-Institut für Polar- und Meeresforschung, 1998.

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Finch, Dudley Sean. FTIR spectroscopy of electron irradiated polymers. Uxbridge: Brunel University, 1988.

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1974-, Bhargava Rohit, ed. Liquid chromatography/FTIR microspectroscopy/microwave assisted synthesis. Berlin: Springer, 2003.

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Sigsby, John E. Evaluation of a FTIR mobile source measurement system. Research Triangle Park, NC: U.S. Environmental Protection Agency, Atmospheric Research and Exposure Assessment Laboratory, 1989.

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Sigsby, John E. Evaluation of a FTIR mobile source measurement system. Research Triangle Park, NC: U.S. Environmental Protection Agency, Atmospheric Research and Exposure Assessment Laboratory, 1989.

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Analysis of surfactants: Atlas of FTIR spectra with interpretations. Munich: Hanser, 1996.

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Mattson, C. B. FTIR instrumentation to monitor vapors from shuttle tile waterproofing materials. [Washington, DC: National Aeronautics and Space Administration, 1995.

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Crowley, John N. A study of reaction mechanism by matrix isolation/FTIR spectroscopy. Norwich: University of East Anglia, 1987.

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Book chapters on the topic "FTIR"

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Abidi, Noureddine. "Biological Systems." In FTIR Microspectroscopy, 71–89. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-84426-4_5.

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Abidi, Noureddine. "Cancer." In FTIR Microspectroscopy, 57–70. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-84426-4_4.

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Abidi, Noureddine. "Cartilage, Bone, Collagen, and Biomaterials." In FTIR Microspectroscopy, 91–105. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-84426-4_6.

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Abidi, Noureddine. "Introduction to FTIR Microspectroscopy." In FTIR Microspectroscopy, 1–12. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-84426-4_1.

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Abidi, Noureddine. "Lipids and Proteins." In FTIR Microspectroscopy, 37–55. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-84426-4_3.

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Abidi, Noureddine. "Other Potential Applications." In FTIR Microspectroscopy, 107–23. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-84426-4_7.

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Abidi, Noureddine. "Plant and Biopolymers." In FTIR Microspectroscopy, 13–36. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-84426-4_2.

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Abidi, Noureddine. "Sample Preparation, Data Acquisition, Spectral Data Processing and Analysis." In FTIR Microspectroscopy, 125–28. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-84426-4_8.

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Schmitt, J., and H. C. Flemming. "FTIR Spectroscopy." In Microbially Influenced Corrosion of Materials, 143–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-80017-7_11.

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Fedelich, Nicolas. "TGA-FTIR." In Evolved Gas Analysis, 18–30. München: Carl Hanser Verlag GmbH & Co. KG, 2019. http://dx.doi.org/10.3139/9781569908105.003.

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Conference papers on the topic "FTIR"

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Moeller, Jon, and Andruid Kerne. "Scanning FTIR." In the fourth international conference. New York, New York, USA: ACM Press, 2010. http://dx.doi.org/10.1145/1709886.1709900.

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Echtler, Florian, Andreas Dippon, Marcus Tönnis, and Gudrun Klinker. "Inverted FTIR." In the ACM International Conference. New York, New York, USA: ACM Press, 2009. http://dx.doi.org/10.1145/1731903.1731909.

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Pesce-Rodriguez, Rose A., and Robert A. Fifer. "Characterization of plasticizers in solid propellant formulations by FTIR-microscopic, FTIR-photoacoustic, and GC-FTIR techniques." In Luebeck - DL tentative, edited by Herbert M. Heise, Ernst H. Korte, and Heinz W. Siesler. SPIE, 1992. http://dx.doi.org/10.1117/12.56420.

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Tonnisson, T. "Portable FTIR spectrometer." In International Biennial Baltic Electronics Conference. IEEE, 2006. http://dx.doi.org/10.1109/bec.2006.311089.

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Kumar, T., D. J. Johnson, and D. A. Compton. "FTIR And TGA/FTIR Characterization Of A Polyethylene Photodegradable Concentrate." In Intl Conf on Fourier and Computerized Infrared Spectroscopy, edited by David G. Cameron. SPIE, 1989. http://dx.doi.org/10.1117/12.969607.

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Compton, David A. C., Jay R. Powell, and Richard A. Crocombe. "TGA/FTIR and DSC/FTIR: combined approaches to solving problems." In Luebeck - DL tentative, edited by Herbert M. Heise, Ernst H. Korte, and Heinz W. Siesler. SPIE, 1992. http://dx.doi.org/10.1117/12.56310.

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Amarie, Sergiu, Paul Zaslansky, Peter Fratzl, and Fritz Keilmann. "Nano-FTIR of biominerals." In 2011 36th International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz 2011). IEEE, 2011. http://dx.doi.org/10.1109/irmmw-thz.2011.6104769.

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Afanasyeva, Natalia I., Sergei F. Kolyakov, Vladilen S. Letokhov, Victor V. Sokolov, and George A. Frank. "Diagnostics of cancer by fiber optic evanescent wave FTIR (FEW-FTIR) spectroscopy." In BiOS Europe '96, edited by Nathan I. Croitoru, Martin Frenz, Terence A. King, Riccardo Pratesi, Anna M. Verga Scheggi, Stefan Seeger, and Otto S. Wolfbeis. SPIE, 1996. http://dx.doi.org/10.1117/12.259954.

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Griffith, D. W. T., I. M. Jamie, P. A. Beasley, O. T. Denmead, R. Leuning, I. E. Galbally, and C. P. Meyer. "FTIR in the Paddock: Trace gas soil flux measurements using FTIR spectroscopy." In The eleventh international conference on fourier transform spectroscopy. AIP, 1998. http://dx.doi.org/10.1063/1.55805.

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Juhari bin Mat Basri, M., Wong Yuen Yee, and B. Yeop Majlis. "Cleanroom contamination monitoring using FTIR." In 2004 IEEE International Conference on Semiconductor Electronics. IEEE, 2004. http://dx.doi.org/10.1109/smelec.2004.1620901.

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Reports on the topic "FTIR"

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Michaelian, K. H., and W. I. Friesen. Resolution enhancement of photoacoustic FTIR spectra. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1985. http://dx.doi.org/10.4095/304862.

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Friesen, W. I., and K. H. Michaelian. Fourier deconvolution of photoacoustic FTIR spectra. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1986. http://dx.doi.org/10.4095/304887.

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Maurer, M., A. Tooker, and S. Felix. Characterization of polyimide via FTIR analysis. Office of Scientific and Technical Information (OSTI), August 2014. http://dx.doi.org/10.2172/1165755.

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Zwinkels, J. C., J. C. Donini, and K. H. Michaelian. Photoacoustic and diffuse reflectance FTIR spectra of Kaolinite. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1985. http://dx.doi.org/10.4095/304863.

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Gamiles, D. S. Real Time Air Monitoring Using Open-Path FTIR. Office of Scientific and Technical Information (OSTI), September 1998. http://dx.doi.org/10.2172/1351.

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Mikhail, S. A., and P. E. King. The detection of SO3 gas by TG/FTIR. Natural Resources Canada/CMSS/Information Management, 1992. http://dx.doi.org/10.4095/328646.

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Gupta, P., A. C. Dillon, A. S. Bracker, and S. M. George. FTIR Studies of H2O and D2O Decomposition on Porous Silicon Surfaces. Fort Belvoir, VA: Defense Technical Information Center, July 1990. http://dx.doi.org/10.21236/ada226581.

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Herman, Matthew Joseph. FTIR analysis of X-ray irradiated Parylene-C using 2D correlation spectroscopy. Office of Scientific and Technical Information (OSTI), August 2015. http://dx.doi.org/10.2172/1213515.

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Rebagay, T. V., R. J. Cash, D. A. Dodd, L. L. Lockrem, J. E. Meacham, and W. D. Winkelman. Evaluation of FTIR-based analytical methods for the analysis of simulated wastes. Office of Scientific and Technical Information (OSTI), September 1994. http://dx.doi.org/10.2172/10189348.

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Wang, H., R. A. Palmer, D. K. Graff, and J. R. Schoonover. Dynamic opto-rheological study of estane copolymers using step-scan FTIR spectroscopy. Office of Scientific and Technical Information (OSTI), July 1998. http://dx.doi.org/10.2172/661440.

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