Academic literature on the topic 'FT'

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Journal articles on the topic "FT"

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OZAKI, YUKIHIRO. "Rheooptical FT-IR,FT-NIR,FT - Raman spectroscopy of polymers." Journal of the Spectroscopical Society of Japan 44, no. 1 (1995): 31–32. http://dx.doi.org/10.5111/bunkou.44.31.

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Güllüoğlu, M. T., Y. Erdogdu, J. Karpagam, N. Sundaraganesan, and Ş. Yurdakul. "DFT, FT-Raman, FT-IR and FT-NMR studies of 4-phenylimidazole." Journal of Molecular Structure 990, no. 1-3 (March 2011): 14–20. http://dx.doi.org/10.1016/j.molstruc.2011.01.001.

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Jose, Sujin P., and S. Mohan. "FT-IR and FT-RAMAN investigations of nicotinaldehyde." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 64, no. 1 (May 2006): 205–9. http://dx.doi.org/10.1016/j.saa.2005.06.040.

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Panicker, C. Yohannan, Hema Tresa Varghese, Annamma John, Daizy Philip, Krisztina Istvan, and Gabor Keresztury. "FT-IR, FT-Raman and FT-SERS spectra of 4-aminosalicylic acid sodium salt dihydrate." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 58, no. 2 (January 2002): 281–87. http://dx.doi.org/10.1016/s1386-1425(01)00541-8.

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Ahn, Myong-Ku. "A comparison of FT NMR and FT IR techniques." Journal of Chemical Education 66, no. 10 (October 1989): 802. http://dx.doi.org/10.1021/ed066p802.

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Naumann, Dieter. "FT-INFRARED AND FT-RAMAN SPECTROSCOPY IN BIOMEDICAL RESEARCH." Applied Spectroscopy Reviews 36, no. 2-3 (June 30, 2001): 239–98. http://dx.doi.org/10.1081/asr-100106157.

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Mylrajan, M. "SERS, FT-Raman and FT-IR studies of dithiocarbamates." Journal of Molecular Structure 348 (March 1995): 257–60. http://dx.doi.org/10.1016/0022-2860(95)08637-b.

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VARGHESE, HEMA TRESA, J. B. BHAGYSREE, RAJEEV T. ULAHANNAN, R. RENJITH, and C. YOHANNAN PANICKER. "FT-IR, FT-Raman and Computational study of Phenylurea." Oriental Journal Of Chemistry 29, no. 1 (March 5, 2013): 361–67. http://dx.doi.org/10.13005/ojc/290158.

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Gärd, Rune, Zhong-Xi Sun, and Willis Forsling. "FT-IR and FT-Raman Studies of Colloidal ZnS." Journal of Colloid and Interface Science 169, no. 2 (February 1995): 393–99. http://dx.doi.org/10.1006/jcis.1995.1048.

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Erdogdu, Yusuf. "Investigations of FT-IR, FT-Raman, FT-NMR spectra and quantum chemical computations of Esculetin molecule." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 106 (April 2013): 25–33. http://dx.doi.org/10.1016/j.saa.2012.12.043.

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Dissertations / Theses on the topic "FT"

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Gärd, Rune. "FT-IR and FT-Raman studies of colloidal ZnS." Licentiate thesis, Luleå tekniska universitet, 1995. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-26295.

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Chen, De. "Examination of Fat Oxidation Products by FT-NMR & FT-IR." TopSCHOLAR®, 1993. https://digitalcommons.wku.edu/theses/2213.

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Edible oils are easily oxidized when used for frying. Oxidation originates with double bonds present in unsaturated fatty acids. A new NMR method is presented which offers potential for determining the products of oil oxidation. High resolution fourier transform nuclear magnetic resonance (FT-NMR) and fourier transform infrared (FT-IR) spectroscopy have found increasing use in biochemistry. One pure fat, trioleoylglycerol, was heated at 160°C in the presence of air Samples were taken for FT-NMR and FT-IR analyses at 4, 10. 20. 25, 35, 50, 70 and 100 hours. Proton, Carbon-13 and several types of two-dimensional FT-NMR spectra were obtained using a JEOL 270 Mhz instrument. The spectra suggest initial oxidation occurs by an allyl free radical mechanism facilitating the formation of epoxide and peroxide products.
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Sanches, Natália Beck. "Caracterização de proteções térmicas de EPDM POR PIR-G/FT-IR E TG/FT-IR." Instituto Tecnológico de Aeronáutica, 2015. http://www.bd.bibl.ita.br/tde_busca/arquivo.php?codArquivo=3206.

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A borracha de EPDM vem sendo empregada com sucesso como proteção térmica flexível de motor foguete. Entretanto, sendo essa aplicação ainda recente em nosso país, existe a necessidade do desenvolvimento de metodologias de caracterização para o melhor entendimento de seus mecanismos de degradação e otimização de suas formulações. As metodologias existentes para análise de aditivos desse material envolvem etapa de extração, aumentando o tempo de análise. Sendo assim, nesta tese de doutorado, a borracha de EPDM crua e vulcanizada, bem como seus aditivos, foram investigados, sem extração, por pirólise gasosa aliada à espectroscopia no infravermelho com transformada de Fourier (PIR-G/FT-IR) e pelo acoplamento das técnicas termogravimetria (TG) e espectroscopia no infravermelho com transformada de Fourier (TG/FT-IR). Foi realizada também uma comparação entre os dados obtidos com as duas metodologias. Os resultados demonstraram que grupos funcionais dos aditivos podem ser detectados nas borrachas crua e vulcanizada, sem extração prévia. Os aditivos sulfurados TMTM e MBT, em teores tão baixos quanto 0,7 phr (0,63%), foram detectados por ambas as metodologias. Contudo, outros aditivos como óleo parafínico, ácido esteárico e TMQ não puderam ser identificados na borracha formulada. Individualmente, todos os aditivos analisados apresentaram espectros FT-IR distintos e foram identificados de forma inequívoca pelas metodologias PIR-G/FT-IR e TG/FT-IR.
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Rossell, Colleen A. "Authentication of Andean Flours using a Benchtop FT-IR System and a Portable FT-IR Spectrometer." The Ohio State University, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=osu1366303651.

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Chen, Fu-Tseng Andy. "Molecular Dynamics in the Liquid Phase by FT-NMR, FT-IR and Laser Raman Lineshape Analysis." Thesis, University of North Texas, 1988. https://digital.library.unt.edu/ark:/67531/metadc330608/.

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Nuclear magnetic resonance (NMR) provides a convenient probe for the study of molecular reorientation in liquids because nuclear spin-lattice relaxation times are dependent upon the details of molecular motion. The combined application of Raman and Infrared (IR) lineshape analysis can furnish more complete information to characterize the anisotropic rotation of molecules. Presented here are the studies of NMR relaxation times, together with Raman/IR Mneshape analysis of the solvent and temperature dependence of rotational diffusion in 1,3,5-tribromobenzene and 1,3,5-trifluorobenzene. In these experiments, it was found that the rotational diffusion constants calculated from Perrin's stick model were two to three times smaller than the measured values of D, and D,,. Similarly, rotational diffusion constants predicted by the Hu-Zwanzig slip model were too large by a factor of 2. Application of the newer Hynes-Kapral-Weinberg model furnished rotational diffusion constants that were in reasonable agreement with the experimental results. The vibrational peak frequencies and relaxation times of the isotropic Raman spectra of the υ1 modes of CD2Br2 and CHBr3 were studied in solution. The frequency shifts in non-interactive solvents were explained well on the basis of solution variations in the dispersion energy. In Lewis bases, the displacements were in some, but not all, cases greater than predicted. On the other hand, it was found that the vibrational relaxation times of the C-H/C-D modes decreased dramatically in all Lewis base solvents. Therefore, it was concluded that relaxation times of the υ1 modes, rather than frequency shifts, furnish a more reliable measure of hydrogen bonding interactions of halomethanes in solution.
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Ingvordsen, Mette. "Anvendelse af semikvantitative ELISA progesterontest til bestemmelse af ovulationstidspunktet hos tæven = The use of semi-quantitative ELISA progesterone assay for determination the ovulation time in the bitch." [København] : Den kgl. Veterinær- og Landbohøjskole, Institut for Produktionsdyr og Heste, 2006. http://dvjb03.life.ku.dk/ft/SPECIALE%20METTE%20INGVORDSEN.pdf.

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Fox, Brigitte S. "FT-ICR studies of solvated ions." [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=964184176.

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Anderson, Todd Sterling. "Isotope edited FT-IR of peptides." Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/11213.

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Weidt, Stefan K. "FT-ICR mass spectrometry of metalloproteins." Thesis, University of Edinburgh, 2008. http://hdl.handle.net/1842/12146.

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Fourier transform ion cyclotron mass spectrometry (FT-ICR MS) has been used to study a number of metalloproteins. The combination of high-resolution and mass-accuracy, along with fragmentation techniques such as CID, IRMPD and ECD, is shown to be a powerful method to probe metalloproteins and metallodrug interactions. The inherent high resolving power and mass measurement accuracy of the FT-ICR MS also enables the oxidation state of the metal present in a metalloprotein to be identified from the isotopically resolved spectra. Carbonic anhydrase II (29 kDa) is an enzyme that catalyses the reversible hydration of carbon dioxide and contains one Zn2+ ion. To investigate non-covalent protein-drug interactions, the inhibitor acetazolamide was added to a sample of carbonic anhydrase II. Nozzle-skimmer CID, IRMPD and titration methods were used to probe the strength of interaction of the carbonic anhydrase-acetazolamide complex. It was found that lower charge-states bind more strongly than higher charge-states suggesting that the protein unfolds when more protons are bound. FT-ICR MS was used to investigate the nature of adducts between the platinum anti-cancer drug cisplatin, and SOD. The structure showed a cisplatin adduct at His19 of beSOD, which had retained the chloride ligands; these are usually lost in aqueous conditions. After incubation with cisplatin, the mono-platinated species was the most prominent adduct observed. The use of 15N-labelled cisplatin led to unambiguous assignment of the two ammonia ligands being retained after binding to beSOD, supporting established cisplatin solution behaviour. Mass spectra of heSOD were more complex than those for beSOD due to phosphate buffer adducts and the loss or substitution of the chloride ligands. ECD fragmentation spectra of the isolated mono-platinum adduct of beSOD were used in order to localise the site of modification.
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Carneiro, Helena Silva Pereira. "Determinação de adulteração de etanol combustível com metanol através de análise multivariada no FT-MIR e FT-NIR." reponame:Repositório Institucional da UnB, 2008. http://repositorio.unb.br/handle/10482/2149.

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Dissertação (mestrado)—Universidade de Brasília, Instituto de Química, 2008.
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Os primeiros relatos a respeito do álcool no Brasil datam do início da década de 1920 quando, numa tentativa de auxiliar o mercado açucareiro que se encontrava em crise acentuada desde 1923, o governo Brasileiro adotou uma série de medidas para estimular a produção desse combustível. Porém, o uso do álcool teve início realmente apenas mais tarde, em 1975, com o lançamento do Programa Nacional do Álcool, o Proálcool, como forma de conter a crise de desabastecimento dos combustíveis causada pelo 1° choque do petróleo em 1973. Visava-se com o Proálcool proteger a economia do País e garantir a disponibilidade de combustível e energia. Atualmente, o uso do etanol combustível está se tornando mundial e o Brasil é o maior consumidor de etanol combustível na forma de Álcool Etílico Hidratado Combustível (AEHC). Devido às similaridades de propriedades físicoquímicas entre o etanol e o metanol, o etanol está sendo adulterado com metanol. Nessa dissertação de mestrado é proposto o uso de modelos de calibração por mínimos quadrados parciais (PLS) baseados em medidas no infravermelho médio por transformada de Fourier (FT-MIR) e no infravermelho próximo por transformada de Fourier (FT-NIR) como um método rápido, preciso, e exato para avaliar a qualidade do AEHC, bem como detectar a sua adulteração por metanol. Foram preparados oitenta padrões da mistura etanol/metanol/água. Sessenta desses padrões foram usados para a calibração e vinte para a validação dos modelos. As amostras de validação também foram analisadas por cromatografia gasosa com detector por ionização de chama (CG-FID) para determinar a quantidade de etanol e metanol. Os resultados mostram que dentre as técnicas espectroscópicas investigadas, o modelo PLS/FT-NIR apresentou o melhor desempenho para a detecção de metanol com um erro quadrado médio aleatório de predição (RMSEP, % m/m) de 0,15 comparado com 0,54 obtido pelo modelo PLS/FT-MIR, enquanto os resultados do CG-FID apresentaram um RMSEP de 0,52 (% m/m). A concentração mínima de metanol detectada com o modelo PLS/FT-NIR foi de 0,51 (% m/m). _______________________________________________________________________________________ ABSTRACT
The first reports related to ethanol in Brazil date from 1920’s when, in an attempt of helping the sugar market that was in crisis since 1923, the Brazilian Government adopted a series of means to estimulate the production of this fuel. Although, the use of ethanol really began later, in 1975, with the launch of the Ethanol National Program, called Proálcool, as a form of contain the crisis of nonsupply of fuels caused by the 1° petroleum chock in 1973, protect the country economy and assure the availability of fuel and energy. Nowadays, the use of ethanol fuel is becoming worldwide and Brazil is the largest consumer of ethanol fuel as hydrated ethyl alcohol fuel (AEHC). Due to the similarities of the physical-chemical properties of ethanol and methanol, ethanol fuel is being adulterated with methanol. In the present work, we propose the use of partial least squares regression (PLS) calibration models based on Fourier transform mid-infrared (FT-MIR) and Fourier transform near-infrared (FT-NIR) measurements as a fast, precise, and accurate method to evaluate the quality of AEHC as well as to detect its adulteration with methanol. Eighty mixtures of methanol/ethanol/water standards were prepared. Sixty were used for calibration, and twenty, for validation. The validation samples were also analyzed by gas chromatography flame ionization detection (GC-FID) to determine the ethanol and methanol content. The results have shown that among the two investigated spectroscopic techniques, PLS/FT-NIR presented the best performance for the detection of methanol with a root-mean-square error of prediction (RMSEP % w/w) of 0.15 as compared to the value of 0.54 obtained by the FT-MIR model, while the GC-FID results presented a RMSEP of 0.52 (% w/w). The minimum detected net concentration of MeOH with the FT-NIR model was 0.51 (% w/w).
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Books on the topic "FT"

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Buback, Michael. FT-NIR atlas. Weinheim: VCH, 1993.

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R, Pachler Klaus G., Matlok Franz, Gremlich Hans-Ulrich, E. Merck (Firm), and Bruker Analytische Messtechnik GmbH, eds. Merck FT-IR Atlas: Eine Sammlung von FT-IR Spektren = a collection of FT-IR spectra. Weinheim (Federal Republic of Germany): VCH, 1988.

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Sierra Club. Dallas Regional Group. Dallas/Ft. Worth outdoors. [Dallas, Tex.]: Dallas Regional Group, Sierra Club, 1987.

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ABCs of FT-NMR. Sausalito, CA: University Science Books, 2000.

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Roberts, John D. ABCs of FT-NMR. Sausalito, Calif: University Science Books, 2000.

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Medawar, Mardi Oakley. The Ft. Larned incident. New York: St. Martin's Minotaur, 2000.

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Ft Guides Pack (FT). Financial Times Prentice Hall, 1995.

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Birley, Sue. FT Mastering Enterprise (FT Mastering). Financial Times/Prentice Hall, 2001.

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Partners.com (FT). Financial Times Prentice Hall, 2001.

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FT 500. London: Financial Times Publishing, 1995.

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Book chapters on the topic "FT"

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Castano, Victor, and Igor Schagaev. "FT Models." In Resilient computer system design, 113–43. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15069-7_5.

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Krüger, Klaus-Eberhard, and Otto Mildenberger. "Fouriertransformation (FT)." In Transformationen, 116–65. Wiesbaden: Vieweg+Teubner Verlag, 2002. http://dx.doi.org/10.1007/978-3-322-88915-7_8.

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Richter, Lars. "FT-Control." In Robotized Transcranial Magnetic Stimulation, 85–101. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7360-2_5.

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Ulrich, Helmut, and Hubert Weber. "Fourier-Transformation (FT)." In Laplace-, Fourier- und z-Transformation, 16–28. Wiesbaden: Springer Fachmedien Wiesbaden, 2017. http://dx.doi.org/10.1007/978-3-658-03450-4_2.

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Davis, Burtron H., and Peter M. Maitlis. "Other FT Catalysts." In Greener Fischer-Tropsch Processes for Fuels and Feedstocks, 209–20. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527656837.ch10.

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Davis, Burtron H. "Cobalt FT Catalysts." In Greener Fischer-Tropsch Processes for Fuels and Feedstocks, 193–207. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527656837.ch9.

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Ulrich, Helmut, and Stephan Ulrich. "Fourier-Transformation (FT)." In Laplace-Transformation, Diskrete Fourier-Transformation und z-Transformation, 21–35. Wiesbaden: Springer Fachmedien Wiesbaden, 2022. http://dx.doi.org/10.1007/978-3-658-31877-2_2.

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Naumann, D. "FT-IR and FT Raman Spectroscopy in Medical Microbiology." In Spectroscopy of Biological Molecules: Modern Trends, 433–34. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5622-6_193.

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Chmielowski, Wojciech Z. "Free Optimisation Time, FT." In Management of Complex Multi-reservoir Water Distribution Systems using Advanced Control Theoretic Tools and Techniques, 45–68. Heidelberg: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-00239-2_5.

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Pogosian, Albert, Karine Hovhannisyan, and Arshak Isajanyan. "Polymer Friction Transfer (FT)." In Encyclopedia of Tribology, 2585–92. Boston, MA: Springer US, 2013. http://dx.doi.org/10.1007/978-0-387-92897-5_820.

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Conference papers on the topic "FT"

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Xie, Chenning, Zhijun Hao, and Haibo Chen. "X10-FT." In the 2013 International Workshop. New York, New York, USA: ACM Press, 2013. http://dx.doi.org/10.1145/2442992.2442994.

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McAndrew, Colin C. "On fT." In 2015 IEEE Bipolar/BiCMOS Circuits and Technology Meeting - BCTM. IEEE, 2015. http://dx.doi.org/10.1109/bctm.2015.7340573.

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Peña, Antonio J., Wesley Bland, and Pavan Balaji. "VOCL-FT." In SC15: The International Conference for High Performance Computing, Networking, Storage and Analysis. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/2807591.2807640.

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Li, Sihuan, Hongbo Li, Xin Liang, Jieyang Chen, Elisabeth Giem, Kaiming Ouyang, Kai Zhao, Sheng Di, Franck Cappello, and Zizhong Chen. "FT-iSort." In SC '19: The International Conference for High Performance Computing, Networking, Storage, and Analysis. New York, NY, USA: ACM, 2019. http://dx.doi.org/10.1145/3295500.3356195.

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Zhai, Yujia, Elisabeth Giem, Quan Fan, Kai Zhao, Jinyang Liu, and Zizhong Chen. "FT-BLAS." In ICS '21: 2021 International Conference on Supercomputing. New York, NY, USA: ACM, 2021. http://dx.doi.org/10.1145/3447818.3460364.

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Wu, Panruo, and Zizhong Chen. "FT-ScaLAPACK." In the 23rd international symposium. New York, New York, USA: ACM Press, 2014. http://dx.doi.org/10.1145/2600212.2600232.

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Wilcox, James R., Cormac Flanagan, and Stephen N. Freund. "V erified FT." In PPoPP '18: 23nd ACM SIGPLAN Symposium on Principles and Practice of Parallel Programming. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3178487.3178514.

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Vats, J. K., S. Soam, M. A. Palafox, P. Arora, H. P. Mittal, V. K. Rastogi, P. M. Champion, and L. D. Ziegler. "FT-IR and FT-Raman Spectra of 2, 6-Difluorobenzonitrile." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482734.

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Naumann, D. "FT-IR and FT-NIR Raman spectroscopy in biomedical research." In The eleventh international conference on fourier transform spectroscopy. AIP, 1998. http://dx.doi.org/10.1063/1.55827.

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Chen, Rong, Shangyuan Feng, Lina Liu, Wenqin Yang, and Shusen Xie. "FT-IR and FT-NIR Raman spectroscopy of human red cell." In Photonics Asia 2004, edited by Britton Chance, Mingzhe Chen, Arthur E. T. Chiou, and Qingming Luo. SPIE, 2005. http://dx.doi.org/10.1117/12.571233.

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Reports on the topic "FT"

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Visser, A., and J. Pathiyil. Design note of an air-cooled 2 ft x 2 ft x 10. 5 ft long muon spoiler. Office of Scientific and Technical Information (OSTI), January 1988. http://dx.doi.org/10.2172/5550635.

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Cardon, Jason. 8 Ft Vessel Refinishing Contract Introduction. Office of Scientific and Technical Information (OSTI), April 2022. http://dx.doi.org/10.2172/1863734.

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Brandner, R., L. Conroy, and R. Stastny. IANA Registration for Enumservice 'web' and 'ft'. RFC Editor, February 2005. http://dx.doi.org/10.17487/rfc4002.

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Romero, Christopher, Matthew Q. Johnson, Thomas Duffey, Edward A. Rodriguez, Richard K. Bingham, Kelly L. Bingham, and Steven Edward Dohleman. Current LANL SCE 3-ft Vessel Inspection Discussion. Office of Scientific and Technical Information (OSTI), March 2016. http://dx.doi.org/10.2172/1241643.

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ENTECH ENGINEERING INC READING PA. Ft. Detrick Boiler Plant Study (EEAP); Executive Summary. Fort Belvoir, VA: Defense Technical Information Center, December 1995. http://dx.doi.org/10.21236/ada330509.

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Mattie, David R., Teresa R. Sterner, Brian A. Wong, Darol E. Dodd, Debra K. Layko, Paul W. Ross, Elizabeth A. Gross, Gabrielle A. Willson, John P. Hinz, and Dean J. Wagner. 90-Day Inhalation Toxicity Study of FT Fuel. Fort Belvoir, VA: Defense Technical Information Center, August 2011. http://dx.doi.org/10.21236/ada557260.

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Williams, David, and Lawrence Carin. Summary of Progress on SIG Ft. Ord ESTCP DemVal. Fort Belvoir, VA: Defense Technical Information Center, April 2007. http://dx.doi.org/10.21236/ada631423.

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Lowry, Heard S., Mike S. Smith, William T. Bertrand, Fred Heltsley, and Daryl W. Sinclair. Integrated Optical Diagnostics for 16-ft Transonic Wind Tunnel. Fort Belvoir, VA: Defense Technical Information Center, February 2001. http://dx.doi.org/10.21236/ada387335.

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Wenski. E.G., R. E. Stinebaugh, and A. R. II York. Properties of 30 lb/ft{sup 3} rigid polyurethane foams. Office of Scientific and Technical Information (OSTI), March 1997. http://dx.doi.org/10.2172/469104.

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Culver, G. Feasibility study for aquaculture and space heating, Ft. Bidwell, California. Office of Scientific and Technical Information (OSTI), October 1985. http://dx.doi.org/10.2172/5060241.

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