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Journal articles on the topic 'Fluorinated Hydrocarbons'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Chen, Kuo-Hsiang, Jenn-Huei Lii, Gerald A. Walker, Yaoming Xie, Henry F. Schaefer, and Norman L. Allinger. "Molecular Mechanics (MM4) Study of Fluorinated Hydrocarbons." Journal of Physical Chemistry A 110, no. 22 (2006): 7202–27. http://dx.doi.org/10.1021/jp060430x.

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2

Schmidt, I., F. Hentschel, and C. Benndorf. "Low temperature diamond growth using fluorinated hydrocarbons." Diamond and Related Materials 5, no. 11 (1996): 1318–22. http://dx.doi.org/10.1016/0925-9635(96)00542-0.

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3

Hort, Norbert, Börn Wiese, Hajo Dieringa, and Karl Ulrich Kainer. "Magnesium Melt Protection." Materials Science Forum 828-829 (August 2015): 78–81. http://dx.doi.org/10.4028/www.scientific.net/msf.828-829.78.

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Mg especially in the molten state is well known for its high affinity to O2. When O2 content of the atmosphere is larger than 4%, molten Mg will burn! To avoid this, melt protection is necessary. At present mostly SF6 is used during primary production and processing of Mg and its alloys. Unfortunately SF6 is a very potent greenhouse gas that is > 23,000 times more effective than CO2. This also affects life cycle considerations e.g. for the use of Mg alloys in transportation. However, other protective gases like SO2 or fluorinated hydrocarbons like HFC134a, Novec 612, or AMCover (=HFC134a) h

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4

Bedekar, Ashutosh V., Anju R. Chaudhary, M. Shyam Sundar, and Murali Rajappa. "Expeditious synthesis of fluorinated styrylbenzenes and polyaromatic hydrocarbons." Tetrahedron Letters 54, no. 5 (2013): 392–96. http://dx.doi.org/10.1016/j.tetlet.2012.11.022.

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5

Chen, K. H., G. A. Walker, and N. L. Allinger. "A molecular mechanics (MM3) study of fluorinated hydrocarbons." Journal of Molecular Structure: THEOCHEM 490, no. 1-3 (1999): 87–107. http://dx.doi.org/10.1016/s0166-1280(99)00079-2.

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6

Antti-Poika, M., J. Heikkila, and L. Saarinen. "Cardiac arrhythmias during occupational exposure to fluorinated hydrocarbons." Occupational and Environmental Medicine 47, no. 2 (1990): 138–40. http://dx.doi.org/10.1136/oem.47.2.138.

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7

Burgess, D. R., M. R. Zachariah, W. Tsang, and P. R. Westmoreland. "Thermochemical and chemical kinetic data for fluorinated hydrocarbons." Progress in Energy and Combustion Science 21, no. 6 (1995): 453–529. http://dx.doi.org/10.1016/0360-1285(95)00009-7.

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8

Chekryshkin, Yu S., T. A. Rozdyalovskaya, Z. R. Ismagilov, M. A. Kerzhentsev, O. A. Tetenova, and A. A. Fedorov. "Deep Oxidation of Fluorinated Hydrocarbons in Molten Catalysts." Eurasian Chemico-Technological Journal 5, no. 2 (2016): 137. http://dx.doi.org/10.18321/ectj293.

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<p>The oxidation of fluorine-containing organic substances: fluorocarbon liquid M-1, fluorinated alcohol H(CF<sub>2</sub>)<sub>8</sub>CH<sub>2</sub>OH, and powder polytetrafluoroethylene with air has been studied in melts: NaOH; 43 mol.% LiCl - 33 mol.% NaCl - 24 mol.% KCl (eutectic mixture); (LiCl-NaCl-KCl)eutec. + 10 mass.% V<sub>2</sub>O<sub>5</sub>; (LiCl-NaCl-KCl) eutec. + 15 mass.% V<sub>2</sub>O<sub>5</sub>; 56 mol.% Na<sub>2</sub>CO<sub>3</sub> - 44 mol.% K<sub>2</

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9

ROBBINS, BENJAMIN H. "Preliminary Studies of the Anesthetic Activity of Fluorinated Hydrocarbons." Survey of Anesthesiology 30, no. 3 (1986): 173???178. http://dx.doi.org/10.1097/00132586-198606000-00053.

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10

Gjølstad, Merete, Dag G. Ellingsen, Oscar Espeland, et al. "Occupational exposure to fluorinated hydrocarbons during refrigeration repair work." Journal of Environmental Monitoring 5, no. 2 (2003): 236–40. http://dx.doi.org/10.1039/b212612e.

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11

Thanh, Nguyen Van, and Nguyen Anh Tuan. "Towards Design of High Spin Metal-free Materials." Communications in Physics 23, no. 4 (2014): 321. http://dx.doi.org/10.15625/0868-3166/23/4/3665.

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In this paper, in order to explore high-spin carbon-based magnetic materials with strong ferromagnetic coupling, geometric structure, electronic structure and magnetic properties of alternating stacks of \(\pi \)-radical-halogenated-hydrocarbons and diamagnetic molecules have been investigated based on density-functional theory with dispersion correction. These alternating stacks are predicted to avoid the typical antiferromagnetic spin-exchange of indentical face-to-face radicals via spin polarization of a diamagnetic molecule in between. Our results show that \(\pi\)-radical-halogenated-hydr

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12

Mayele, M., S. Neutzler, and L. R. Oellrich. "Investigation on the diffusivity of partly fluorinated hydrocarbons in polymers." Magnetic Resonance Imaging 21, no. 3-4 (2003): 409–10. http://dx.doi.org/10.1016/s0730-725x(03)00152-8.

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13

Bedekar, Ashutosh V., Anju R. Chaudhary, M. Shyam Sundar, and Murali Rajappa. "ChemInform Abstract: Expeditious Synthesis of Fluorinated Styrylbenzenes and Polyaromatic Hydrocarbons." ChemInform 44, no. 22 (2013): no. http://dx.doi.org/10.1002/chin.201322089.

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14

Weis, Uwe, and Jan T. Andersson. "Synthesis of Fluorinated Polycyclic Aromatic Hydrocarbons Through a Photochemical Cyclization." Polycyclic Aromatic Compounds 22, no. 1 (2002): 71–85. http://dx.doi.org/10.1080/10406630210376.

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15

Lyons, R. A. "Investigation of an acute chemical incident: exposure to fluorinated hydrocarbons." Occupational and Environmental Medicine 57, no. 9 (2000): 577–81. http://dx.doi.org/10.1136/oem.57.9.577.

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16

Neutzler, S., and L. R. Oellrich. "NMR Methods Investigating the Mobility of Partly Fluorinated Hydrocarbons in Polymers." Chemical Engineering & Technology 29, no. 7 (2006): 840–46. http://dx.doi.org/10.1002/ceat.200600119.

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17

Kuzmenko, N. Ya, S. N. Kuzmenko, O. V. Skrinnik, and V. V. Bugrym. "SYNTHESIS AND PROPERTIES OF INTERACTION PRODUCTS OF TRIS[TRI(BUTOXY)TITANATE]BORON AND ALIPHATIC FLUORINATED ALCOHOLS." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 59, no. 1 (2018): 75. http://dx.doi.org/10.6060/tcct.20165901.5244.

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Synthesis and properties of products based on tris[[tri(butoxy)titanate]boron with complete or partial substitution of butoxy groups linked with titanium by fluorinated alkoxy group were described. Extracted products were liquid or solid substances which are high soluble in aliphatic-, aromatic- chloraromatic- and chlorinated hydrocarbons, low alcohols, and ketone. Their structure was confirmed by elemental analysis, determination of molecular mass, IR and 1H NMR spectroscopy.

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18

Prasher, V. P., and J. A. Corbett. "Aerosol Addiction." British Journal of Psychiatry 157, no. 6 (1990): 922–24. http://dx.doi.org/10.1192/bjp.157.6.922.

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A case of dependency on prescribed pressurised aerosols in a patient with asthma and mild mental handicap is reported. The majority of reported cases involve young asthmatics, abuse being reported mainly using salbutamol inhalers although other inhalers have also given cause for concern. The agent of addiction is uncertain although it may be the fluorinated hydrocarbons used as propellents, rather than the active substance itself.

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19

Kim, Min-Jae, Yeonjin Kim, Jae-Rang Youn, et al. "Effects of Sulfuric Acid Treatment on the Performance of Ga-Al2O3 for the Hydrolytic Decomposition of 1,1,1,2-Tetrafluoroethane (HFC-134a)." Catalysts 10, no. 7 (2020): 766. http://dx.doi.org/10.3390/catal10070766.

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HFC-134a, one of the representative hydrofluorocarbons (HFCs) used as a coolant gas, is a known greenhouse gas with high global warming potential. Catalytic decomposition is considered a promising technology for the removal of fluorinated hydrocarbons. However, systematic studies on the catalytic decomposition of HFC-134a are rare compared to those for other fluorinated hydrocarbon gases. In this study, Ga-Al2O3 and S/Ga-Al2O3 catalysts were prepared and the change in their properties post-acid treatment was investigated by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), temperature-pro

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20

Saner, B., Y. Z. Menceloglu, and N. Bilgin Oncu. "Branched Pentablock Poly(L-lactide-co-∊-caprolactone) Synthesis in scCO2." High Performance Polymers 19, no. 5-6 (2007): 649–64. http://dx.doi.org/10.1177/0954008307081209.

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Pentablock poly(L-lactide-co-∊-caprolactone) (PLLA/PCL), with a central fluorinated segment and four PLLA/PCL side chains was synthesized by sequential ring-opening polymerization (ROP) with stannous octoate catalyst in an environmentally benign and clean medium, scCO2. Copolymers of PLLA and PCL are extensively researched for biomedical applications. Fluorinated hydrocarbons are similarly promising for biomedicine, and especially for oxygen-carrying substitute applications. Initially, a fluorinated reactive triblock stabilizer (prepolymer, PCL-FLKT-PCL) with inner fluorinated segment and PCL

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21

Ponduru, Tharun T., Changling Qiu, James X. Mao, et al. "Copper(i)-based oxidation of polycyclic aromatic hydrocarbons and product elucidation using vacuum ultraviolet spectroscopy and theoretical spectral calculations." New Journal of Chemistry 42, no. 24 (2018): 19442–49. http://dx.doi.org/10.1039/c8nj04740e.

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22

Giesy, John P., Kurunthachalam Kannan, and Paul D. Jones. "Global Biomonitoring of Perfluorinated Organics." Scientific World JOURNAL 1 (2001): 627–29. http://dx.doi.org/10.1100/tsw.2001.342.

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The environmental distribution of fluorinated organic compounds (FOCs) has been less well described than the other halogenated hydrocarbons such as chlorinated and brominated compounds. This is despite the fact that FOCs have been used in a wide variety of products and applications for more than 50 years. FOCs are resistant to hydrolysis, photolysis, microbial degradation, or metabolism by vertebrates due to the high energy of carbon–fluorine bond. In particular, perfluorinated (fully fluorinated) compounds (PFCs) have the potential to persist in the environment. But, until recently, the exten

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23

GANCET, C., C. GUIGNARD, and P. FOURMENTRAUX. "Catalysis by a Lipase-bearing Rhizopus arrhizus Mycelium in (Halogeno) Fluorinated Hydrocarbons." Annals of the New York Academy of Sciences 542, no. 1 Enzyme Engine (1988): 213–18. http://dx.doi.org/10.1111/j.1749-6632.1988.tb25831.x.

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24

Adonin, Nicolai Yu, and Vladimir F. Starichenko. "Hydrogenolysis of CF bonds in fluorinated aromatic hydrocarbons catalysed by nickel complexes." Mendeleev Communications 10, no. 2 (2000): 60–61. http://dx.doi.org/10.1070/mc2000v010n02abeh001171.

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25

Lindström, Irmeli, Anna‐Mari Ryhänen, Soile Jungewelter, Hille Suojalehto, and Katri Suuronen. "Asthma onset after exposure to fluorinated hydrocarbons in the presence of combustion." American Journal of Industrial Medicine 63, no. 11 (2020): 1054–58. http://dx.doi.org/10.1002/ajim.23181.

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26

Chai Kao, C. P., M. E. Paulaitis, G. A. Sweany, and M. Yokozeki. "An equation of state/chemical association model for fluorinated hydrocarbons and HF." Fluid Phase Equilibria 108, no. 1-2 (1995): 27–46. http://dx.doi.org/10.1016/0378-3812(95)02701-f.

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27

Futamura, Shigeru, and Annadurai Gurusamy. "Synergy of nonthermal plasma and catalysts in the decomposition of fluorinated hydrocarbons." Journal of Electrostatics 63, no. 6-10 (2005): 949–54. http://dx.doi.org/10.1016/j.elstat.2005.03.067.

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28

Dutt, N. V. K., and D. Venugopal. "Prediction of liquid viscosities of fluorinated hydrocarbons by the extended Thomas' method." Chemical Engineering Journal 44, no. 3 (1990): 173–75. http://dx.doi.org/10.1016/0300-9467(90)80074-m.

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29

Yamamoto, Fumiko M., and Souji Rokushika. "Retention properties of the fluorinated bonded phase on liquid chromatography of aromatic hydrocarbons." Journal of Chromatography A 898, no. 2 (2000): 141–51. http://dx.doi.org/10.1016/s0021-9673(00)00866-9.

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30

Samojłowicz, Cezary, Etienne Borré, Marc Mauduit, and Karol Grela. "Microwave-Assisted Ruthenium-Catalysed Olefin Metathesis in Fluorinated Aromatic Hydrocarbons: A Beneficial Combination." Advanced Synthesis & Catalysis 353, no. 11-12 (2011): 1993–2002. http://dx.doi.org/10.1002/adsc.201100053.

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31

Шебеко, Алексей Юрьевич, and Юрий Николаевич Шебеко. "On a composition of combustion products at a burning of methane-fluorinated hydrocarbon mixtures in air." Pozharnaia bezopasnost`, no. 3(100) (September 28, 2020): 44–49. http://dx.doi.org/10.37657/vniipo.pb.2020.43.68.005.

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Выполнена расчетная оценка равновесного состава продуктов горения околостехиометрических смесей вида метан - фторированный углеводород - воздух с использованием как программного комплекса Chemical Workbench, так и предложенной в настоящей работе упрощенной методики. Найдено, что основными продуктами горения являются CO, HO, CO, HF. При этом концентрации прочих продуктов горения имеют существенно более низкие значения. С помощью программного комплекса FDS выполнен расчет динамики концентраций опасных продуктов (СО, HF) в атмосфере модельного помещения объемом 12,6 м. Найдено, что для указанного

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32

Kannan, Kurunthachalam, John Newsted, Richard S. Halbrook, and John P. Giesy. "Perfluorooctanesulfonate and Related Fluorinated Hydrocarbons in Mink and River Otters from the United States." Environmental Science & Technology 36, no. 12 (2002): 2566–71. http://dx.doi.org/10.1021/es0205028.

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33

Kannan, Kurunthachalam, John Newsted, Richard S. Halbrook, and John P. Giesy. "Perfluorooctanesulfonate and Related Fluorinated Hydrocarbons in Mink and River Otters from the United States." Environmental Science & Technology 38, no. 4 (2004): 1264. http://dx.doi.org/10.1021/es0354061.

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34

Fuchibe, Kohei, Kento Shigeno, Nan Zhao, et al. "Pinpoint-fluorinated polycyclic aromatic hydrocarbons (F-PAHs): Syntheses of difluorinated subfamily and their properties." Journal of Fluorine Chemistry 203 (November 2017): 173–84. http://dx.doi.org/10.1016/j.jfluchem.2017.09.002.

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35

Ivanitskii, G. R., F. F. Beloyartsev, V. I. Islamov, et al. "Effect of an emulsion of fluorinated hydrocarbons on the protective properties of cardioplegic solutions." Bulletin of Experimental Biology and Medicine 102, no. 2 (1986): 1078–80. http://dx.doi.org/10.1007/bf00836201.

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36

Wang, Heng, Álvaro Castillo, and Joseph W. Bozzelli. "Thermochemical Properties Enthalpy, Entropy, and Heat Capacity of C1–C4 Fluorinated Hydrocarbons: Fluorocarbon Group Additivity." Journal of Physical Chemistry A 119, no. 29 (2015): 8202–15. http://dx.doi.org/10.1021/acs.jpca.5b03912.

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37

Shebeko, Yu N., V. V. Azatyan, I. A. Bolodian, et al. "The influence of fluorinated hydrocarbons on the combustion of gaseous mixtures in a closed vessel." Combustion and Flame 121, no. 3 (2000): 542–47. http://dx.doi.org/10.1016/s0010-2180(99)00168-6.

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38

Adonin, Nicolai Yu, and Vladimir F. Starichenko. "ChemInform Abstract: Hydrogenolysis of C-F Bonds in Fluorinated Aromatic Hydrocarbons Catalyzed by Nickel Complexes." ChemInform 31, no. 30 (2010): no. http://dx.doi.org/10.1002/chin.200030061.

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39

Radilov, A. S., I. E. Shkayeva, S. A. Solntseva, V. A. Kondrashov, N. M. Menshikov, and O. S. Nikulin. "EXPERIMENTAL STUDIES OF THE TOXIC PROPERTIES OF HALOGEN-DERIVATIVES OF SATURATED HYDROCARBONS (CHLADONS)." Toxicological Review, no. 6 (December 28, 2017): 35–41. http://dx.doi.org/10.36946/0869-7922-2017-6-35-41.

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A study was made on toxicity and hazards of 16 chladons which are representatives of various halogen derivatives of saturated hydrocarbons (fluorine derivatives of methane, ethane, propane, butane). It is shown that in terms of acute toxicity parameters, the studied chladons refer to low-toxic and low-risk substances (hazard class 4 according to GOST 12.1.007). The least toxic are fully fluorinated hydrocarbons: tetrafluoromethane, hexafluoroethane, octafluoropropane, decafluorobutane.` In the clinical picture of acute poisoning, signs of a narcotic effect prevail. Limit values Limac were dete

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40

Yang, Hong Wei, Shi Liang Yang, Chao Wu, Yi Wei Fei, and Xian Yong Wei. "The Applications of Direct Fluorinated HDPE in Oil & Gas Storage and Transportation." Advanced Materials Research 328-330 (September 2011): 2436–39. http://dx.doi.org/10.4028/www.scientific.net/amr.328-330.2436.

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Characteristics of elemental fluorine and carbon-fluorine bonds were analyzed. The barrier and oil-resistance properties of direct fluorination of HDOE were unveiled from molecule structure. The HDPE surface fluorination results in the increase of surface energy, cross link to some extent and shrinkage of polymer free volume.The application of direct fluorination of HDPE in oil in oil ＆ gas storage and transportation fields were reviewed, including oil and gas pipe,plastic petrol-tanks and HDPE impermeable membrane applied in oil tank foundation. After direct fluorination processing, the anti-

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41

Hoyt, Andrea E., Antonio J. Ricco, Huey C. Yang, and Richard M. Crooks. "Speciation of linear and branched hydrocarbons by a fluorinated polyimide film based surface acoustic wave sensor." Journal of the American Chemical Society 117, no. 33 (1995): 8672–73. http://dx.doi.org/10.1021/ja00138a026.

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42

Smit, Martin F., Philippus D. R. van Heerden, Jakobus J. Pienaar, Ludwig Weissflog, Reto J. Strasser, and Gert H. J. Krüger. "Effect of trifluoroacetate, a persistent degradation product of fluorinated hydrocarbons, on Phaseolus vulgaris and Zea mays." Plant Physiology and Biochemistry 47, no. 7 (2009): 623–34. http://dx.doi.org/10.1016/j.plaphy.2009.02.003.

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43

Fuchibe, Kohei, Takeshi Fujita, and Junji Ichikawa. "Pinpoint-Fluorinated Polycyclic Aromatic Hydrocarbons (F-PAHs): Their Synthesis via Electrophilic Activation of Fluoroalkenes and Properties." Journal of Synthetic Organic Chemistry, Japan 76, no. 9 (2018): 938–53. http://dx.doi.org/10.5059/yukigoseikyokaishi.76.938.

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44

Ravishankar, S., David C. Tilotta, Kenneth W. Busch, and Marianna A. Busch. "An Element-Specific, Dual-Channel, Flame Infrared Emission, Gas Chromatography Detector for Chlorinated and Fluorinated Hydrocarbons." Applied Spectroscopy 44, no. 8 (1990): 1247–58. http://dx.doi.org/10.1366/000370290789619432.

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45

Evans, Meagan E., Catherine L. Burke, Sornanong Yaibuathes, Eric Clot, Odile Eisenstein, and William D. Jones. "Energetics of C−H Bond Activation of Fluorinated Aromatic Hydrocarbons Using a [Tp′Rh(CNneopentyl)] Complex." Journal of the American Chemical Society 131, no. 37 (2009): 13464–73. http://dx.doi.org/10.1021/ja905057w.

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46

Fuchibe, Kohei, Hisanori Imaoka, and Junji Ichikawa. "Synthesis of Pinpoint-Fluorinated Polycyclic Aromatic Hydrocarbons: Benzene Ring Extension Cycle Involving Microwave-Assisted SNAr Reaction." Chemistry - An Asian Journal 12, no. 18 (2017): 2359–63. http://dx.doi.org/10.1002/asia.201700870.

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47

Goodwin, A. R. H., and J. B. Mehl. "Measurement of the dipole moments of seven partially fluorinated hydrocarbons with a radiofrequency reentrant cavity resonator." International Journal of Thermophysics 18, no. 3 (1997): 795–806. http://dx.doi.org/10.1007/bf02575134.

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48

McCulloch, A. "Evidence for improvements in containment of fluorinated hydrocarbons during use: an analysis of reported European emissions." Environmental Science & Policy 12, no. 2 (2009): 149–56. http://dx.doi.org/10.1016/j.envsci.2008.12.003.

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49

Montagnolli, Renato Nallin, Paulo Renato Matos Lopes, and Ederio Dino Bidoia. "Fluorinated waste and firefighting activities: biodegradation of hydrocarbons from petrochemical refinery soil co-contaminated with halogenated foams." Environmental Science and Pollution Research 25, no. 36 (2018): 36002–13. http://dx.doi.org/10.1007/s11356-018-1593-2.

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50

Osuna, Reyes Malavé, Victor Hernández, Juan T. López Navarrete, Emiliana D’Oria, and Juan J. Novoa. "Theoretical evaluation of the nature and strength of the F···F intermolecular interactions present in fluorinated hydrocarbons." Theoretical Chemistry Accounts 128, no. 4-6 (2010): 541–53. http://dx.doi.org/10.1007/s00214-010-0830-7.

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