Academic literature on the topic 'Fluorocarbons'

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Journal articles on the topic "Fluorocarbons"

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FAITHFULL, N. S. "Fluorocarbons." Anaesthesia 42, no. 3 (March 1987): 234–42. http://dx.doi.org/10.1111/j.1365-2044.1987.tb03033.x.

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Morita, Yoshinori, and Toshikazu Shiratori. "Key Drivers behind the Development of Fluorocarbons Destruction Infrastructure: A Case Study of Japan." Journal of Sustainable Development 14, no. 2 (February 5, 2021): 27. http://dx.doi.org/10.5539/jsd.v14n2p27.

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The Montreal Protocol has been ratified to progress phase-out of CFCs and HCFCs globally. HFCs have come into wide use as alternatives to CFCs and HCFCs, but as we know today, it was found that HFCs have a huge negative influence on global warming, and the Kigali Amendment to the Montreal Protocol entered into force to promote phase-down of HFCs. Since the enforcement of the Fluorocarbons Recovery and Destruction Law (F-gas law) in 2002, Japan has been undertaking fluorocarbons collection and destruction by environmentally-sound manners. However, no study has been reported investigates on how the Japanese fluorocarbons destruction infrastructure has been developed over the past several years. To analyze the development, we studied key drivers that contributed to encourage fluorocarbons collection from end of life electric appliances and to promote fluorocarbons destruction by environmentally and commercially sustainable technologies. We showed that recycling laws and the F-gas law have made progress in encourage fluorocarbons collection and destruction by making relevant stakeholders take physical and financial responsibilities for proper fluorocarbons disposal. This study also researched fluorocarbons destruction technologies that destruction operators used as of 2004 and 2019, and found that three specific destruction technologies have long been used practically in Japan. Finally, we discussed influencing factors that have made these technologies accepted, installed and practically used by fluorocarbons destruction operators. In conclusion, we identified that existence of political frameworks as well as application of fluorocarbons destruction technologies that are commercially sustainable and socially acceptable were key drivers behind the development of fluorocarbons destruction infrastructure in Japan.
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Rauf, Farooq, Muhammad Umair, Khubab Shaker, Yasir Nawab, Tehseen Ullah, and Sheraz Ahmad. "Investigation of Chemical Treatments to Enhance the Mechanical Properties of Natural Fiber Composites." International Journal of Polymer Science 2023 (July 14, 2023): 1–13. http://dx.doi.org/10.1155/2023/4719481.

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A sustainable approach to composites is leading to the use of natural fibers rather than synthetic materials, like carbon or glass, for reinforcement. However, the higher moisture absorption of natural fibers impairs the composite’s mechanical properties. Therefore, to improve the mechanical properties, some chemical treatments like silane and fluorocarbon can be performed to reduce the moisture absorption of natural fibers. In this study, flax was used as reinforcement, and epoxy was used as a matrix. In the first part of the study, flax reinforcement was treated with different concentrations of silane (20, 40, and 60 g/L) and fluorocarbons (80, 100, and 120 g/L). Moisture regains (MRs), absorbency, and tensile strength were measured at reinforcement levels. According to the results, reinforcements treated with 60 g/L silane (S3) and 120 g/L fluorocarbons (F3) exhibited the lowest MR values of 7.09% and 3.06%, respectively, whereas water absorbency was significantly reduced. The sample treated with 120 g/L fluorocarbons required 300 seconds extra time to absorb the water as compared with the untreated sample, whereas samples S3 and F3 showed an increase in tensile strength by 20.16% and 34.80% when compared with untreated reinforcement flax reinforcement. In the second part of the study, untreated and treated flax reinforcements were combined with an epoxy matrix for composite fabrication. MR and mechanical tests (tensile, flexural, and Charpy impact tests) were performed. Results revealed that treated flax-reinforced composites exhibited lower MR values 0.86% for F3 and 0.42% for S3, respectively. The tensile, flexural, and pendulum impact strengths of silane-treated reinforced composite sample C.S3 were increased by 15.07%, 117%, and 20.01%, respectively, compared with untreated reinforced composite samples. Consequently, both chemical treatments improve composite mechanical performance as well as service life.
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Kivevele, Thomas. "Propane (HC – 290) as an Alternative Refrigerant in the Food Transport Refrigeration Sector in Southern Africa – a Review." Automotive Experiences 5, no. 1 (January 1, 2022): 75–89. http://dx.doi.org/10.31603/ae.5994.

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Most of the food transport trucks in Sothern Africa are equipped with refrigeration and air conditioning systems filled with fluorocarbon refrigerants such as R404A to facilitate the heat transfer process. These refrigerants are synthetic chemicals and have high potential to cause global warming and damage to the ozone layer. Currently, natural refrigerants are considered as alternatives to these man-made refrigerants to mitigate some of the environmental risks. The natural refrigerants are the substances that occur in nature such as hydrocarbons (HC), ammonia, and carbon dioxide. These type of refrigerants have been in the market for many years, but in some applications such as domestic refrigerators, heat pumps, chillers, and air conditioners, whereas fluorocarbons are the mostly used in the food transport refrigeration systems. Natural refrigerants such as propane (HC – 290) are now penetrating the market in food transport refrigeration systems where previously fluorocarbons were the favoured option. Therefore, this work reports the possibilities of using non-fluorinated hydrocarbon/natural refrigerant (propane – R290) in the food transport refrigerated systems in Southern Africa; a case study of South Africa. R290 has the potential to lower greenhouse gases emissions compared to hydrofluorocarbons (HFCs) which are widely used in most of the existing food transport refrigeration systems in South Africa. R290 has negligible Global Warming Potential (GWP) of 3 which is well below the global threshold value of 150. The review revealed that refrigeration capacity of R290 is in the average of 10 – 30% higher than commonly used fluorocarbon refrigerants such as R404A and R134A. Since R290 is labeled as a flammable refrigerant, the present study also reviews its flammability safety measures.
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Solé-Violan, Luis, and Bernard Devallez. "Excess thermodynamic functions of mixtures of fluorocarbons with fluorocarbon-hydrocarbon compounds." New J. Chem. 28, no. 12 (2004): 1526–30. http://dx.doi.org/10.1039/b405395h.

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Schack, Carl J., and Karl O. Christe. "Bis-pentafluorotelluriumoxide fluorocarbons." Journal of Fluorine Chemistry 27, no. 1 (January 1985): 53–60. http://dx.doi.org/10.1016/s0022-1139(00)80897-0.

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Erdmann, W., and N. S. Faithfull. "Introduction to Fluorocarbons." Journal of the World Association for Emergency and Disaster Medicine 3, no. 2 (1987): 46–52. http://dx.doi.org/10.1017/s1049023x00029058.

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Fluorocarbons, which strictly speaking should perhaps be termed perfluorocarbons or perfluorochemicals (PFCs), are organic compounds produced by extensive fluorination of relatively simple alphatic and aromatic chemicals. They have, over the last thirty or forty years, been used for a wide variety of purposes in both industrial and domestic fields. As a consequence of one of their physical properties, namely their high solubility for respiratory gases, they are being developed as constituents of oxygen transporting plasma substitutes. Preliminary trials are being carried out in Japan and the United States and PFCs may well be on the verge of entering routine clinical medicine.
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CLARK, LELAND C. "Introduction to Fluorocarbons." International Anesthesiology Clinics 23, no. 1 (1985): 1–10. http://dx.doi.org/10.1097/00004311-198502310-00005.

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Lentz, Dieter, and Heike Michael. "Clusters containing fluorocarbons." Journal of Organometallic Chemistry 372, no. 1 (August 1989): 109–15. http://dx.doi.org/10.1016/0022-328x(89)87081-0.

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Kabalnov, A. S., K. N. Makarov, and O. V. Sheherbakova. "Solubility fluorocarbons in water as a key parameter for fluorocarbon emulsions stability." Journal of Fluorine Chemistry 45, no. 1 (October 1989): 207. http://dx.doi.org/10.1016/s0022-1139(00)84577-7.

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Dissertations / Theses on the topic "Fluorocarbons"

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Niyogi, Sandip. "Synthesis and characterization of molecules to study the conformational barriers of fluorocarbon chains." Thesis, University of North Texas, 2000. https://digital.library.unt.edu/ark:/67531/metadc2511/.

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Fluorocarbons are known to be stiffer than their hydrocarbon analogues, a property that underlines the extensive industrial application of fluorocarbon materials. Although there has been previous studies on the rotational barrier of molecules having fluorocarbon centers, a detailed systematic study is necessary to quantify flurocarbon stiffness. The molecules, Pyrene-(CF2)n-Pyrene, Pyrene-(CF2)n-F, Pyrene-(CH2)n-Pyrene and Pyrene-(CH2)n-H were therefore synthesized to enable the determination of the barrier to rotation of the carbon backbone in fluorocarbons. Conformational studies will be completed with steady-state and time-dependent emission spectroscopy.
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Ma, Ruowei. "Quantification and partition of perfluorochemicals in Hong Kong wastewater sludge." Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B43223862.

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Lindup, Richard J. "Metal-mediated borylation of fluorocarbons." Thesis, University of York, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.434017.

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Tang, Yi. "Atmospheric fate of various fluorocarbons." Thesis, Massachusetts Institute of Technology, 1993. http://hdl.handle.net/1721.1/10598.

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Wang, Fei, and 王飞. "Behavior of perfluorochemicals on solid surfaces: sorption and mineralization processes." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hub.hku.hk/bib/B50899892.

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The study evaluated the sorption behavior of PFOS and PFOA on γ-alumina and boehmite. The results of adsorption kinetics on γ-alumina and boehmite show that it takes 48 h to reach equilibrium. The adsorption isotherms reveal the maximum adsorption capacities of PFOS and PFOA are different due to their different functional groups. An increase in pH leads to a decrease in PFOS and PFOA adsorption on alumina, which may be attributed to the reduction in electrostatic interaction. The adsorption of both PFOS and PFOA decreases with an increase in ionic strength due to the compression of the electrical double layer. The different sorption level of PFC on γ-alumina and boehmite indicated that the crystal phase of mineral also affected the sorption process. The sorption of PFOS and PFBuS on boehmite was significantly retarded by the competitive sorption of humic acid (HA), implying that PFOS and PFBuS are likely more mobile in water and groundwater systems enriched with HA. The sorption behavior of PFOS and PFBuS on the HA-modified boehmite surface was also found to differ due to their different chain lengths. In addition, the results revealed that the sorption of PFOS and PFBuS on HA-modified boehmite is pH-dependent. The isotherm study of FOSA on three types of microplastics indicated that hydrophobic interaction plays a dominant role in the sorption process and the molecule structure of different microplastics can affect its sorption level. The PFOS sorption isotherm indicated that electrostatic interaction plays an important role in the PFOS sorption process on PE and PS while its sorption on PVC was electrostatic interaction independent. The effects of pH and ionic strength indicated that electrostatic interaction plays an important role in PFOS sorption process. The kinetic study showed that the PCMAs had a rapid sorption towards PFAS species and the isotherm study indicated that hydrophobic interaction played an important role in the sorption process. The sorption of PFOS by the PCMAs was not significantly affected by the pH and slightly decreased with an increase in ionic strength. Moreover, the sorbent had showed excellent regeneration performance. Two main fluorine mineralization mechanisms leading to the substantial formation of CaF2 and Ca5(PO4)3F phases were observed. They had a close relationship with the thermal treatment condition and the PFOS content of the sludge. At low temperatures (300C -600C), CaF2 dominated in the product and increases in treatment time and temperature generally enhanced the fluorine transformation. However, at higher temperatures (700C -900C), increases in treatment time and temperature had a negative effect on the overall efficiency of the fluorine crystallization. The results suggest that in the high temperature environment there were greater losses of gaseous products such as HF and SiF4 in the transformation of CaF2 to Ca5(PO4)3F, the hydrolysis of CaF2, and the reaction with SiO2. The quantitative analysis also showed that when treating sludge with low PFOS content at high temperatures, the formation of Ca5(PO4)3F may be the primary mechanism for the mineralization of the fluorine in PFOS.
published_or_final_version
Civil Engineering
Doctoral
Doctor of Philosophy
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Jones, S. L. "Functional fluorocarbons via free radical additions to hexafluoropropene." Thesis, Durham University, 1987. http://etheses.dur.ac.uk/6781/.

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The effect of substituents on the carbon-hydrogen bond reactivity in free radical additions to hexaf1uoropropene has been investegated. Ethers, amines, amides, isocyanates and silanes all give Free radical adducts. The order of reactivity has been compiled. The reactivity of cyclic ethers, amines and amides is discussed in terms of the stereoelectronic effect. The reactivity of tetrahydrofuran and N-methylpyrrolidine towards hexaf1uoropropene under uninitiated conditions has also been demonstrated. The ease of hydrogen abstraction from the substrates was estimated using a method based on the thermal decomposition of ditertiarybutylperoxide. A correlation between the ease of hydrogen abstraction and free radical reactivity is demonstrated, although the reactivity of aldehydes is not simply explained. The adducts of ethers and amines can be dehydrofluorinated to give a variety of alkenes. Further reactions of aldehyde and isocyanate adducts has given good synthetic routes to other functionally substituted fluorocarbons. The amide adducts are also a useful source o-f fluorinated amines which cannot be obtained directly. An amine 1:1 adduct has been fully fluorinated over cobalt trifluoride at 440 C in good yield, although higher adducts give lower yields. Remarkably high yields of perfluorinated alkanes are produced by successive reaction with sulphur tetrafluoride and cobalt trifluoride.
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Chatterjee, Ritwik 1974. "Evaluation of unsaturated fluorocarbons for dielectric Etch applications." Thesis, Massachusetts Institute of Technology, 2002. http://hdl.handle.net/1721.1/86859.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, February 2003.
Includes bibliographical references (p. 175-183).
The semiconductor industry is currently faced with the problem of the use and emissions of strong global warming compounds, known as perfluorocompounds (PFCs) for dielectric etch applications. The release of global warming compounds from this and other sources is suspected to result in changes in the earth's climate and weather patterns. Quantitative targets for emissions reduction set by the World Semiconductor Council (WSC) makes it urgent to find a solution to this issue. A long-term means of approaching this problem is to find and develop alternative chemistries that are more environmentally benign without sacrificing performance. Several classes of chemistries have been investigated to date, including hydrofluorocarbons (HFCs), iodofluorocarbons (IFCs), and NF3/hydrocarbons. One class of chemistries that have shown considerable promise is the unsaturated fluorocarbons (UFCs). The research documented herein uses the UFCs to assess etch process and emissions performance. Not only are these novel chemistries tested on conventional silicon dioxide films, but also on new low-k dielectrics that are likely candidates for future generation process flows. Emissions and process performance are reported for each of the different gases. The prospects for integration of some of these chemistries to next generation processes are good from both a process and emissions standpoint. The UFCs are not strong greenhouse gases as a result of their short atmospheric lifetimes (typically less than a day). Unlike many of the previous alternative chemistries studied, the emissions from UFCs are due to reformation of reactive products into strong global warming gases, specifically PFCs and HFCs, in the plasma environment. In this work, the formation of plasma effluents has been studied.
(cont.) In this work, the formation of plasma effluents has been studied. These reformation products are not only a result of the reformation of reactive species from the breakup of the feed gas, but also a result of the interaction of the plasma with surfaces in the etch chamber, including the wafer being etched. Process performance has been assessed by performing cross-sectional scanning electron microscopy (SEM). Emissions data have been collected using Fourier transform infrared spectroscopy (FTIR). In-situ process monitoring methods such as optical emission spectroscopy (OES) and residual gas analysis (RGA) have been used in some experiments. Ex-situ studies of fluorocarbon deposited films have been performed using X-ray photoelectron spectroscopy (XPS) and time of flight secondary ion mass spectrometry (TOF-SIMS). Screening experiments performed on an Applied Materials HDP high-density etch chamber showed that all of the UFCs in addition to a fluorinated ether were capable of process performance comparable to PFC based processes, such as C3F8. These studies showed that octafluorocyclopentene and hexafluoropropene processes result in greater than 70% emissions reduction compared to a C3F8-based reference process. Three isomers of C4F6 performed even better, with greater than 80% emissions reduction. Hexafluorobenzene based processes displayed the greatest silicon dioxide etch emissions reduction of 97% ...
by Ritwik Chatterjee.
Ph.D.
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Jackson, Philip R. "Thermodynamic studies of binary mixtures involving aromatic fluorocarbons." Thesis, University of Leicester, 1986. http://hdl.handle.net/2381/33750.

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Solid-liquid phase diagrams have been determined for binary systems of hexafluorobenzene + naphthalene-type compounds, and indicate strong 1:1 congruently melting point complexes. Hexafluorobenzene + cis- and + trans-deca1in were found to give simple eutectic phase diagrams. Excess enthalpies, excess volumes and excess Gibbs functions have been measured for the same hexaf1uorobenzene + naphthalene-type compound mixtures and are large and negative, which is characteristic of systems where specific interactions take place. This contrasts with the large positive excess functions found with hexafluorobenzene + decalin systems, where only dispersion forces are assumed present. The excess Gibbs function for hexafluorobenzene + trans- and cis-decalin have been determined theoretically from freezing point data as well as directly from vapour pressure measurements. A batch calorimeter, besides being used for excess enthalpy measurememts, has been employed in determining heats of solution, which lead to a value for the enthalpy change for the process, solid + solid ? complex. The possibility of charge-transfer interactions occuring in hexafluorobenzene + naphthalene-type compound systems has been discussed in terms of HOMO/LUMO overlap considerations and is supported by the observation that pentafluorocyanobenzene forms stronger (higher melting point) complexes with 1- and 2-methylnaphthalene, than hexafluorobenzene does.
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Gilliam, Mary A. "A plasma polymerization investigation and low temperature cascade arc plasma for polymeric surface modification." Diss., Columbia, Mo. : University of Missouri-Columbia, 2006. http://hdl.handle.net/10355/4355.

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Thesis (Ph.D.)--University of Missouri-Columbia, 2006.
The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file viewed on (April 25, 2007) Vita. Includes bibliographical references.
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Ma, Ruowei, and 馬若為. "Quantification and partition of perfluorochemicals in Hong Kong wastewater sludge." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B43223862.

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Books on the topic "Fluorocarbons"

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Tebbutt, Andrew Alistair. Synthesis of chiral fluorocarbons. Birmingham: University of Birmingham, 1994.

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Baca, David R. Selected bibliography on ozone and fluorocarbons. Monticello, Ill., USA: Vance Bibliographies, 1989.

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Kenkyūjo, Mitsubishi Sōgō. Heisei 23-nendo chikyū ondanka taisaku no tame no furon-rui tō taisaku suishin ni kansuru kentō chōsa hōkokusho. [Tokyo]: Mitsubishi Sōgō Kenkyūjo, 2012.

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Pugachev, A. K. Pererabotka ftoroplastov v izdelii͡a︡: Tekhnologii͡a︡ i oborudovanie. Leningrad: "Khimii͡a︡," Leningradskoe otd-nie, 1987.

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Koroniak, Henryk. Reakcje termoizomeryzacji fluorowęglowodorów zawierających naprężone układy pierścieni trój-lub czteroczłonowych. Poznań: Wydawn. Nauk. Uniwersytetu im. Adama Mickiewicza w Poznaniu, 1986.

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S, Oremland R., and Geological Survey (U.S.), eds. Summary of research results on bacterial degradation of trifluoroacetate (TFA), November, 1994-May, 1995. Menlo Park, Calif: U.S. Dept. of the Interior, U.S. Geological Survey, 1995.

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J, Matheson Leah, Alternative Fluorocarbons Environmental Assessment Study, and Geological Survey (U.S.), eds. Summary of research results on bacterial degradation of trifluoroacetate (TFA), October, 1993 - October, 1995. Menlo Park, Calif: U.S. Geological Survey, 1996.

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Volkov, S. S. Svarka ftoroplastov. Moskva: "Khimii͡a︡", 1992.

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B, Watson Thomas, and Air Resources Laboratory (U.S.), eds. The perfluorocarbon tracer releases during the Big Bend regional aeorosol and visibility observational (BRAVO) study. Silver Spring, Md: U.S. Dept. of Commerce, National Oceanic and Atmospheric Administration, Oceanic and Atmospheric Research Laboratories, Air Resources Laboratory, 2000.

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Lagunov, V. S. Kompozit͡s︡ionnye tonkosloĭnye materialy na osnove ftoroplasta-4. Voronezh: Izd-vo Voronezhskogo universiteta, 1992.

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Book chapters on the topic "Fluorocarbons"

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Gooch, Jan W. "Fluorocarbons." In Encyclopedic Dictionary of Polymers, 318. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_5165.

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Poulos, Alfred. "Fluorocarbons." In The Secret Life of Chemicals, 143–55. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-80338-4_10.

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Faithfull, N. Simon. "Second Generation Fluorocarbons." In Oxygen Transport to Tissue XIV, 441–52. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3428-0_50.

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Mitkin, Valentin N. "Safe Synthesis of Superstoichiometric Mesoporous Fluorocarbons." In Efficient Preparations of Fluorine Compounds, 433–41. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118409466.ch66.

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Faithfull, N. S. "Microcirculatory and Other Applications of Fluorocarbons." In Update in Intensive Care and Emergency Medicine, 301–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82801-0_51.

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Motlagh, Safa, and John H. Moore. "Radicals from Electron Impact on Fluorocarbons." In Gaseous Dielectrics VIII, 15–21. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4899-7_2.

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Shiflett, Mark B., and A. Yokozeki. "Solubility of Fluorocarbons in Room Temperature Ionic Liquids." In ACS Symposium Series, 21–42. Washington DC: American Chemical Society, 2009. http://dx.doi.org/10.1021/bk-2009-1030.ch002.

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Zachariah, M. R., P. R. Westmoreland, D. R. F. Burgess, Wing Tsang, and C. F. Melius. "Theoretical Prediction of Thermochemical and Kinetic Properties of Fluorocarbons." In ACS Symposium Series, 358–73. Washington, DC: American Chemical Society, 1997. http://dx.doi.org/10.1021/bk-1995-0611.ch027.

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Stingele, R., B. Wagner, D. A. Wilson, R. C. Koehler, D. F. Hanley, and R. J. Traystman. "Simulation of the Oxygen Distribution in Brain Tissue Perfused with Fluorocarbons." In Advances in Experimental Medicine and Biology, 469–75. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-5399-1_66.

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Faithfull, N. S., M. Fennema, and W. Erdmann. "Haemodilution and Myocardial Ischaemia — Studies with Fluorocarbons and Dextran in Pigs." In Innovations in Physiological Anaesthesia and Monitoring, 151–58. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74114-2_12.

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Conference papers on the topic "Fluorocarbons"

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Tran-Quinn, Thuy, and Mark Lakritz. "Unsaturated Fluorocarbons in the Etching Process, Environmental Benefit, Technical Hurdles." In 2008 IEEE/SEMI Advanced Semiconductor Manufacturing Conference (ASMC). IEEE, 2008. http://dx.doi.org/10.1109/asmc.2008.4529003.

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Young, Justin, and Christopher Annesley. "FLUOROCARBONS IN SATELLITE PLUMES: THE PHOTOSYNTHESIS AND FLUORESCENCE FROM TRIFLUOROMETHYL RADICAL." In 73rd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.wh04.

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Yongsheng, Xu, and Luo Bing. "Calculation of Electric Field of Fluorocarbons in Gas-Liquid Mixed State." In 2022 IEEE International Conference on High Voltage Engineering and Applications (ICHVE). IEEE, 2022. http://dx.doi.org/10.1109/ichve53725.2022.9961432.

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Li, Kang, Weijun Xing, Guoqiang Zhang, Wenhao Niu, Xin Wang, and Yingying Wang. "Study on decomposition gas for faults diagnostic of electrical equipment using fluorocarbons." In 2010 International Conference on Power System Technology - (POWERCON 2010). IEEE, 2010. http://dx.doi.org/10.1109/powercon.2010.5666387.

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Kelleher, Matthew D., Robert Egger, Yogendra K. Joshi, and John R. Lloyd. "MODIFICATION OF THE NUCLEATE BOILING HYSTERESIS IN THE POOL BOILING OF FLUOROCARBONS." In International Heat Transfer Conference 10. Connecticut: Begellhouse, 1994. http://dx.doi.org/10.1615/ihtc10.4620.

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Lee, Kwangjoo, Steffen Jockusch, Nicholas J. Turro, Roger H. French, Robert C. Wheland, Michael F. Lemon, Andre M. Braun, Tatjana Widerschpan, and Paul Zimmerman. "157-nm pellicles for photolithography: mechanistic investigation of the deep-UV photolysis of fluorocarbons." In Microlithography 2004, edited by Bruce W. Smith. SPIE, 2004. http://dx.doi.org/10.1117/12.534381.

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Xing, Weijun, Kang Li, Guoqiang Zhang, Wenhao Niu, Xin Wang, and Yingying Wang. "Partial discharge performances under non- uniform electric field in gas mixtures with small fluorocarbons." In 2009 International Conference on Electrical Machines and Systems (ICEMS). IEEE, 2009. http://dx.doi.org/10.1109/icems.2009.5382639.

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van der Walt, I. J., J. T. Nel, J. L. Havenga, and J. Swanepoel. "The beneficiation of CaF2 to produce fluorocarbons and hf by means of hightemperature plasma processes." In 2009 IEEE 36th International Conference on Plasma Science (ICOPS). IEEE, 2009. http://dx.doi.org/10.1109/plasma.2009.5227765.

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Yoshida, H., V. Kmetik, H. Fujita, K. Yoshida, T. Yamanaka, and S. Nakai. "High performance of phase conjugated stimulated Brillouin scattering mirror based on high purity liquid heavy fluorocarbons." In Laser interaction and related plasma phenomena: 12th international conference. AIP, 1996. http://dx.doi.org/10.1063/1.50395.

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Liu, Yang, Xianglong Zhuge, Zhihua Wang, Bin Huang, and Xinpeng Le. "Case Study on Fluorocarbons Interior Coating for Anticorrosion and Wax-Deposition Inhibition in ASP Flooding Production." In SPE Annual Technical Conference and Exhibition. Society of Petroleum Engineers, 2018. http://dx.doi.org/10.2118/191656-ms.

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Reports on the topic "Fluorocarbons"

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Lemal, David M. Synthesis and Chemistry of Novel Cyclic Fluorocarbons. Fort Belvoir, VA: Defense Technical Information Center, May 1993. http://dx.doi.org/10.21236/ada267148.

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Walczak, M. The interaction of small oxygenated fluorocarbons and hydrocarbons with the Ru(001) surface. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6835384.

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Trowbridge, L. D. Estimation of Flammability Limits of Selected Fluorocarbons with F(sub 2) and CIF(sub3). Office of Scientific and Technical Information (OSTI), September 1999. http://dx.doi.org/10.2172/12455.

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Orkin, V. L., V. G. Khamaganov, A. G. Guschin, E. E. Kasimovskaya, and I. K. Larin. Development of atmospheric characteristics of chlorine-free alternative fluorocarbons. Report on R-134a and E-143a. Office of Scientific and Technical Information (OSTI), April 1993. http://dx.doi.org/10.2172/10141934.

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Julke, Timothy, and Hajimu Kawa. Durable Fluorocarbon-Based Coatings for Aircraft. Fort Belvoir, VA: Defense Technical Information Center, November 2000. http://dx.doi.org/10.21236/ada387686.

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Kaiser, R., C. E. Benson, E. S. Meyers, and V. C. A. Vaughen. Decontamination by cleaning with fluorocarbon surfactant solutions. Office of Scientific and Technical Information (OSTI), February 1994. http://dx.doi.org/10.2172/10128279.

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Kaiser, R., and O. K. Harling. Enhanced removal of radioactive particles by fluorocarbon surfactant solutions. Office of Scientific and Technical Information (OSTI), August 1993. http://dx.doi.org/10.2172/10184207.

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Gottlieb S. Oehrlein, H. Anderson, J. Cecchi, and D. Graves. Final report of ''Fundamental Surface Reaction Mechanisms in Fluorocarbon Plasma-Based Processing''. Office of Scientific and Technical Information (OSTI), September 2004. http://dx.doi.org/10.2172/831085.

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Kinsley, Karen M. Stress-Induced Cracking of Fluorocarbon Rubber MTL-0002 After Exposure to DS-2. Fort Belvoir, VA: Defense Technical Information Center, September 1993. http://dx.doi.org/10.21236/ada271753.

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Hogen-Esch, T. E. Synthesis and self-assembly of fluorocarbon- and hydrocarbon-modified hydrophilic polymers. Final report. Office of Scientific and Technical Information (OSTI), November 1996. http://dx.doi.org/10.2172/410387.

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