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Relevant bibliographies by topics / Fluoropolymere

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Academic literature on the topic 'Fluoropolymere'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Fluoropolymere"

1

Gardiner, James. "Fluoropolymers: Origin, Production, and Industrial and Commercial Applications." Australian Journal of Chemistry 68, no. 1 (2015): 13. http://dx.doi.org/10.1071/ch14165.

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Fluoropolymers have had a profound effect on all aspects of industry since their discovery during the 1930s. This review briefly describes the historical development of the fluoropolymer industry, with a focus on traditional fluoroplastics, and lists the major industrial and commercial materials currently in use. These include polytetrafluoroethylene (PTFE, Teflon), polychlorotrifluoroethylene (PCTFE), fluorinated ethylene propylene (FEP), the ethylene copolymer of tetrafluoroethylene (ETFE), the ethylene copolymer of chlorotrifluoroethylene (ECTFE), perfluoroalkoxy (PFA), polyvinylfluoride (PVF), polyvinyldifluoride (PVDF), Nafion, fluoroethylenevinylether (FEVE), a semicrystalline three component terpolymer of tetrafluoroethylene, hexafluoropropylene, and vinylidene fluoride (THV), Teflon-AF, Cytop, and Hyflon. The production, processing, and properties of these fluoropolymers are discussed, together with examples of the specific uses in chemical industry, manufacturing, electronics, architecture, energy, health and domestic sectors. Other related fluoropolymers such as fluoroelastomers, perfluoropolyethers, and fluorosurfactants are briefly mentioned. Environmental aspects of fluoropolymers are considered as is the current state of the fluoropolymer industry.

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Wu, Hao, Hao Li, Ahmad Umar, Yao Wang, and Guofu Zhou. "Bifunction-Integrated Dielectric Nanolayers of Fluoropolymers with Electrowetting Effects." Materials 11, no. 12 (December 5, 2018): 2474. http://dx.doi.org/10.3390/ma11122474.

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Fluoropolymers play an essential role in electrowetting (EW) systems. However, no fluoropolymer possesses the desirable properties of both hydrophobicity and dielectric strength. In this study, for the first time, we report the integration of two representative fluoropolymers—namely, Teflon AF (AF 1600X) and Cytop (Cytop 809A)—into one bifunctionalized dielectric nanolayer. Within this nanolayer, both the superior hydrophobicity of Teflon AF and the excellent dielectric strength of Cytop were able to be retained. Each composed of a 0.5 μm Cytop bottom layer and a 0.06 μm Teflon AF top layer, the fabricated composite nanolayers showed a high withstand voltage of ~70 V (a dielectric strength of 125 V/μm) and a high water contact angle of ~120°. The electrowetting and dielectric properties of various film thicknesses were also systemically investigated. Through detailed study, it was observed that the thicker Teflon AF top layers produced no obvious enhancement of the Cytop/Teflon AF stack.

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Leis, Andrew P., Sven Schlicher, Hilmar Franke, and Martin Strathmann. "Optically Transparent Porous Medium for Nondestructive Studies of Microbial Biofilm Architecture and Transport Dynamics." Applied and Environmental Microbiology 71, no. 8 (August 2005): 4801–8. http://dx.doi.org/10.1128/aem.71.8.4801-4808.2005.

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ABSTRACT We describe a novel and noninvasive, microscopy-based method for visualizing the structure and dynamics of microbial biofilms, individual fluorescent microbial cells, and inorganic colloids within a model porous medium. Biofilms growing in flow cells packed with granules of an amorphous fluoropolymer could be visualized as a consequence of refractive index matching between the solid fluoropolymer grains and the aqueous immersion medium. In conjunction with the capabilities of confocal microscopy for nondestructive optical sectioning, the use of amorphous fluoropolymers as a solid matrix permits observation of organisms and dynamic processes to a depth of 2 to 3 mm, whereas sediment biofilms growing in sand-filled flow cells can only be visualized in the region adjacent to the flow cell wall. This method differs fundamentally from other refractive index-matching applications in that optical transparency was achieved by matching a solid phase to water (and not vice versa), thereby permitting real-time microscopic studies of particulate-containing, low-refractive-index media such as biological and chromatographic systems.

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Marshall, Jean E., Anna Zhenova, Samuel Roberts, Tabitha Petchey, Pengcheng Zhu, Claire E. J. Dancer, Con R. McElroy, Emma Kendrick, and Vannessa Goodship. "On the Solubility and Stability of Polyvinylidene Fluoride." Polymers 13, no. 9 (April 21, 2021): 1354. http://dx.doi.org/10.3390/polym13091354.

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This literature review covers the solubility and processability of fluoropolymer polyvinylidine fluoride (PVDF). Fluoropolymers consist of a carbon backbone chain with multiple connected C–F bonds; they are typically nonreactive and nontoxic and have good thermal stability. Their processing, recycling and reuse are rapidly becoming more important to the circular economy as fluoropolymers find widespread application in diverse sectors including construction, automotive engineering and electronics. The partially fluorinated polymer PVDF is in strong demand in all of these areas; in addition to its desirable inertness, which is typical of most fluoropolymers, it also has a high dielectric constant and can be ferroelectric in some of its crystal phases. However, processing and reusing PVDF is a challenging task, and this is partly due to its limited solubility. This review begins with a discussion on the useful properties and applications of PVDF, followed by a discussion on the known solvents and diluents of PVDF and how it can be formed into membranes. Finally, we explore the limitations of PVDF’s chemical and thermal stability, with a discussion on conditions under which it can degrade. Our aim is to provide a condensed overview that will be of use to both chemists and engineers who need to work with PVDF.

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Pugachev, A. K. "Analysis of development of Russian fluoropolymer chemistry, production and fields of fluoropolymes application: Some aspects of the history of creating Russian fluoropolymers." Russian Journal of General Chemistry 79, no. 3 (March 2009): 517–19. http://dx.doi.org/10.1134/s1070363209030323.

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Baxter, Chance, Jena McCollum, and Scott Iacono. "Preparation and Thermal Analysis of Blended Nanoaluminum/Fluorinated Polyether-Segmented Urethane Composites." Journal of Composites Science 3, no. 1 (March 7, 2019): 25. http://dx.doi.org/10.3390/jcs3010025.

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The thermally induced reaction of aluminum fuel and a fluoropolymer oxidizer such as polytetrafluoroethylene (via C-F activation) has been a well-studied thermite event for slow-burning pyrolants among a multitude of energetic applications. Generally, most metallized thermoplastic fluoropolymers suffer from manufacturing limitations using common melt or solvent processing techniques due to the inherent low surface energy and high crystallinity of fluoropolymers. In this report, we prepared an energetic composite utilizing the versatility of urethane-based polymers and provide a comparative thermal characterization study. Specifically, a thermite formulation comprising of nanometer-sized aluminum (nAl) fuel coated with perfluoropolyether (PFPE) oxidizer was solvent-blended with either a polyethylene glycol (PEG) or PFPE-segmented urethane copolymer. Thermal data were collected with calorimetric and thermogravimetric techniques to determine glass transition temperature and decomposition temperature, which showed modest effects upon various loadings of PFPE-coated nAl in the urethane matrix. While our application focus was for energetics, this study also demonstrates the potential to expand the ability to broadly manufacture structural metallized composites to their consideration as coatings, foams, or fibers.

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Banpurkar, Arun G., Yogesh Sawane, Sandip M. Wadhai, C. U. Murade, Igor Siretanu, D. van den Ende, and F. Mugele. "Spontaneous electrification of fluoropolymer–water interfaces probed by electrowetting." Faraday Discussions 199 (2017): 29–47. http://dx.doi.org/10.1039/c6fd00245e.

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Fluoropolymers are widely used as coatings for their robustness, water-repellence, and chemical inertness. In contact with water, they are known to assume a negative surface charge, which is commonly attributed to adsorbed hydroxyl ions. Here, we demonstrate that a small fraction of these ions permanently sticks to surfaces of Teflon AF and Cytop, two of the most common fluoropolymer materials, upon prolonged exposure to water. Electrowetting measurements carried out after aging in water are used to quantify the density of ‘trapped’ charge. Values up to −0.07 and −0.2 mC m⁻²are found for Teflon AF and for Cytop, respectively, at elevated pH. A similar charge trapping process is also observed upon aging in various non-aqueous polar liquids and in humid air. A careful analysis highlights the complementary nature of electrowetting and streaming potential measurements in quantifying interfacial energy and charge density. We discuss the possible mechanism of charge trapping and highlight the relevance of molecular scale processes for the long term stability and performance of fluoropolymer materials for applications in electrowetting and elsewhere.

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Sánchez-Urbano, Francisco, Guillermo Paz-Gómez, Óscar Rodríguez-Alabanda, Pablo Romero, Miguel Cabrerizo-Vílchez, Miguel Rodríguez-Valverde, and Guillermo Guerrero-Vaca. "Non-Stick Coatings in Aluminium Molds for the Production of Polyurethane Foam." Coatings 8, no. 9 (August 27, 2018): 301. http://dx.doi.org/10.3390/coatings8090301.

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The manufacturing of polyurethane foam is a process of great industrial importance in the automotive and furniture sector. The operation of demolding is the most delicate, since the foam sticks firmly to the walls of the mold onto which it has spread. In order to avoid the use of demolding agents, the proposal is to coat the inside of the molds with non-stick coatings. In this work, three types of different coatings were studied: fluoropolymers, ceramics, and elastomers. After carrying out different tests in the laboratory, two fluoropolymer coatings (PFA (perfluoroalkoxy) and PTFE (polytetrafluoroethylene)) were selected for a test at the industrial level and, after 1500 cycles of demolding, it was experimentally proven that the PFA coating is the most adequate for the use studied.

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Kredel, Julia, and Markus Gallei. "Compression-Responsive Photonic Crystals Based on Fluorine-Containing Polymers." Polymers 11, no. 12 (December 16, 2019): 2114. http://dx.doi.org/10.3390/polym11122114.

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Fluoropolymers represent a unique class of functional polymers due to their various interesting and important properties such as thermal stability, resistance toward chemicals, repellent behaviors, and their low refractive indices in comparison to other polymeric materials. Based on the latter optical property, fluoropolymers are particularly of interest for the preparation of photonic crystals for optical sensing application. Within the present study, photonic crystals were prepared based on core-interlayer-shell particles focusing on fluoropolymers. For particle assembly, the melt-shear organization technique was applied. The high order and refractive index contrast of the individual components of the colloidal crystal structure lead to remarkable reflection colors according to Bragg’s law of diffraction. Due to the special architecture of the particles, consisting of a soft core, a comparably hard interlayer, and again a soft shell, the resulting opal films were capable of changing their shape and domain sizes upon applied pressure, which was accompanied with a (reversible) change of the observed reflection colors as well. By the incorporation of adjustable amounts of UV cross-linking agents into the opal film and subsequent treatment with different UV irradiation times, stable and pressure-sensitive opal films were obtained. It is shown that the present strategy led to (i) pressure-sensitive opal films featuring reversibly switchable reflection colors and (ii) that opal films can be prepared, for which the written pattern—resulting from the compressed particles—could be fixed upon subsequent irradiation with UV light. The herein described novel fluoropolymer-containing photonic crystals, with their pressure-tunable reflection color, are promising candidates in the field of sensing devices and as potential candidates for anti-counterfeiting materials.

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Zhen, Zhao Xiang. "Long lived fluoropolymeric radicals in irradiated fluoropolymer powders at room temperature." International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry 35, no. 1-3 (January 1990): 194–98. http://dx.doi.org/10.1016/1359-0197(90)90084-u.

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Dissertations / Theses on the topic "Fluoropolymere"

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Aymes-Chodur, Caroline. "Radiogreffage de fluoropolymères en vue de l'obtention de surfaces hémocompatibles : étude comparative de l'influence des ions lourds rapides (E>1 MeV/uma) et des rayonnements gamma." Bordeaux 2, 1998. http://www.theses.fr/1998BOR28595.

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Durrieu-Porte, Marie-Christine. "Améliorations de l'hémocompatibilité de matériaux en vue de l'obtention : de surfaces antithrombotiques par radiogreffage de groupements sulfonamides sur des fluoropolymères ; de surfaces endothélialisables par greffage chimique de peptides sur une surface modèle : la silice." Bordeaux 2, 1998. http://www.theses.fr/1998BOR28598.

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Lousenberg, Robert Daniel. "Synthesis of novel fluoropolymers." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0019/NQ53677.pdf.

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Mukherjee, Tamal. "Investigation of Post-Plasma Etch Fluorocarbon Residue Characterization, Removal and Plasma-Induced Low-K Damage for Advanced Interconnect Applications." Thesis, University of North Texas, 2016. https://digital.library.unt.edu/ark:/67531/metadc849649/.

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Modern three-dimensional integrated circuit design is rapidly evolving to more complex architecture. With continuous downscaling of devices, there is a pressing need for metrology tool development for rapid but efficient process and material characterization. In this dissertation work, application of a novel multiple internal reflection infrared spectroscopy metrology is discussed in various semiconductor fabrication process development. Firstly, chemical bonding structure of thin fluorocarbon polymer film deposited on patterned nanostructures was elucidated. Different functional groups were identified by specific derivatization reactions and model bonding configuration was proposed for the first time. In a continued effort, wet removal of these fluorocarbon polymer was investigated in presence of UV light. Mechanistic hypothesis for UV-assisted enhanced polymer cleaning efficiency was put forward supported by detailed theoretical consideration and experimental evidence. In another endeavor, plasma-induced damage to porous low-dielectric constant interlayer dielectric material was studied. Both qualitative and quantitative analyses of dielectric degradation in terms of increased silanol content and carbon depletion provided directions towards less aggressive plasma etch and strip process development. Infrared spectroscopy metrology was also utilized in surface functionalization evaluation of very thin organic films deposited by wet and dry chemistries. Palladium binding by surface amine groups was examined in plasma-polymerized amorphous hydrocarbon films and in self-assembled aminosilane thin films. Comparison of amine concentration under different deposition conditions guided effective process optimization. A time- and cost-effective method such as current FTIR metrology that provides in-depth chemical information about thin films, surfaces, interfaces and bulk layers can be increasingly valuable as critical dimensions continue to scale down and subtle process variances begin to have a significant impact on device performance.

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Li, Xiaohong. "Advanced NMR Studies of Fluoropolymers." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1310482724.

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Ho, Kingsley Kin Chee. "High performance fibre reinforced fluoropolymers." Thesis, Imperial College London, 2009. http://hdl.handle.net/10044/1/11259.

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Blackmore, Patrique Michelle. "Synthesis and properties of stereoregular fluoropolymers." Thesis, Durham University, 1986. http://etheses.dur.ac.uk/6795/.

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The work described in this thesis was concerned with the synthesis and metathesis ring .opening polymerization of some fluorinated norbornenes and norbornadienes. The objectives of the work were to synthesise some new stereoregular fluoropolymers.This thesis is divided into five chapters. In the first chapter the background of the olefin metathesis reaction is reviewed. Chapter Two gives details of the synthesis of some fluorinated norbornenes and norbornadienes. The third chapter discusses the ring opening metathesis polymerization of a series of relatively simple monomers, and the characterization of the polymers produced, by (^13)C n.m.r. and infrared spectroscopy. In the fourth chapter the polymerization of a series of more complicated monomers is described. The final chapter details some of the physical properties of the polymers.

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Lee, Sangwha. "Transient sorption and permeation in fluoropolymers /." The Ohio State University, 1995. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487862399448826.

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Mathieson, Isla. "Pretreatments of fluoropolymers to enhance adhesion." Thesis, Loughborough University, 1995. https://dspace.lboro.ac.uk/2134/19465.

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The aim of the project was to gain a better understanding of the factors that affect adhesion of fluoropolymers. This was achieved by employing various analytical techniques to the treated and untreated polymers. The effects of novel pretreatments, and established treatments, on Polytetrafluoroethylene, PTFE, Poly (vinyl fluoride), PVF, and poly (vinylidene fluoride) PVdF, were characterised using: adhesion tests, X-ray photoelectron spectroscopy (XPS), including derivatisation reactions, Fourier Transform Infrared (FTIR), contact angles and scanning electron microscopy (SEM) For untreated PVF and PTFE it was found that a certain degree of adhesion improvement was achievable without any chemical modification of the surfaces. This was observed when the substrates were repeatedly bonded. It is proposed that weakly cohesive material was present in the polymers and these acted as weak boundary layers when bonded. Removal of weak boundary layers alone was found to be insufficient to obtain high adhesion with PTFE. Surface functionality, increased wettabiIity and favourable topography all contributed to the high bond strengths observed with 'Tetra-Etch' treated PTFE. 'Tetra-Etch' treatment is used commercially on PTFE but prior to this programme was unreported on PVF and PVdF. The treatment was effective at promoting adhesion for PVF though at a much slower rate than for PTFE. Additional mechanisms to that for PTFE (Le. electron transfer) are proposed for the action of 'Tetra-Etch' on PVF. These are dehydrohalogenation through electron transfer and an elimination reaction. The same mechanisms are proposed for PV dF. Flame and low pressure plasma treatments were carried out on PVF and PTFE. Flame was found to be ineffective for PTFE but with PVF chemical modification (oxidation) occurred at the carbon/hydrogen sites. No defluorination was observed; this was in contrast to the mechanism of oxidation via plasmas on PVF, where defluorination, oxidation, ablation, and crosslinking may have all contributed to the high bond strength obtained. Certain plasma treatments were effective at improving the adhesion of PTFE but were slower and caused less modification. Removal of weak boundary layers was proposed as the major factor since oxidation was often slight. Reaction with solutions of potassium hydroxide (KOH), sodium hydroxide (NaOH) and lithium hydroxide (LiOH) were effective as adhesion pretreatments for PVF and PVdF but not for PTFE. For PVF and PVdF rates of reaction and chemical modification varied with time, temperature, molarity of solution and the nature of the solution i.e. aqueous or alcoholic. The greatest improvement in rate and effectiveness of the treatment for adhesion improvement was on the addition of a phase transfer catalyst to the aqueous solution. It was found for PVF that substantial surface oxidation could be achieved without improving the adhesion. It was suggested that oxidation occurred at sites present in a weakly cohesive layer. Mechanisms of the reactions were considered in terms of neucloephilic substitution and elimination; for PVF and PV dF both are likely. The mechanism of the phase transfer catalyst was investigated and found to be complex. It was found not to be simply a wetting agent but had inherent reactivity on its own. A combination of mechanisms was proposed.

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Grobler, Johannes Marthinus. "Fluoropolymer-based 3D printable pyrotechnic compositions." Diss., University of Pretoria, 2017. http://hdl.handle.net/2263/66199.

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The work herein covers the complete process for development, production and testing of a melt processable pyrotechnic composition, with the goal of using the composition as a printing material in a fused deposition modelling (FDM) type 3D printer. 3D printing is fast becoming an area of interest for energetic materials research. This is due to the role that geometry can play in combustion performance of a composition and 3D printing’s ability to produce a variety of complex designs. Melt processable fluoropolymers were selected as oxidisers. The polymers selected for the study were FK-800® and Dyneon 31508®. Both are co-polymers of vinylidene fluoride (VDF) and chlorotrifluoroethylene (CTFE). Aluminium was the choice fuel in this instance as it had better energetic performance than the alternatives investigated. It was also deemed to be a safer fuel when considering the combustion products. Hazardous combustion products like hydrofluoric and hydrochloric acid could be suppressed by increasing the fuel loading to 30 wt.%, thereby reducing the risks associated with burning the composition. Preliminary differential thermal analysis (DTA) analysis indicated that the compositions would only ignite above 400 °C which was well above the suggested processing temperature of 230 °C as determined from thermogravimetric (TGA) analysis. These thermal analysis techniques indicated that the reactions were most likely a gas-solid reactions due to ignition temperatures being significantly lower than those associated with phase changes occurring in the fuels tested, yet above the decomposition temperatures for the oxidisers. ii Extrusion of the compositions proceeded with addition of LFC-1® liquid fluoroelastomer. This addition was made in order to order to lower the melt viscosity, thereby improving the quality of the filament produced. Compositions were extruded with an aluminium loading of 30 wt.%. Oxidiser and LFC-1® made up the rest of the mass with the LFC-1® contributions being either 7 wt.% or 14 wt.%. Burn rates, temperatures and ignition delays were all influenced by the addition of LFC-1® to the system. FK-800® was found to be a better oxidiser in this instance since its burn rates were consistent especially when compared to erratic nature of the Dyneon 31508® burns. Linear burn rates for the FK-800® increased from 15.9 mm·s−1 to 18.9 mm·s−1 with the increase in LFC-1® loading. Combustion temperature also increased by approximately 180 °C from 794 °C. Printing with the material was achieved only after significant alterations were made to the hot end used. Printing proceeded in a staged, start-stop manner. After each new layer of material was deposited the printer was cleared of material and the hot end was allowed to cool. If this procedure was not followed it led to significant preheating of the material within the feeding section of the extruder. This premature heating caused feeding problems due to softening and swelling of the material within the cold side of the hot end which led to blockages, leading to the conclusion that the composition was not compatible with the off-the-shelf hot end used in this study. Low quality printing could be achieved with both FK-800® and Dyneon 31508® compositions. This would suggest that slight compositional changes paired with the alterations made to the hot end could improve the quality of the prints to an extent that would be comparable to that of more commonplace printing materials.
Dissertation (MEng)--University of Pretoria, 2017.
Chemical Engineering
MEng
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Books on the topic "Fluoropolymere"

1

Hougham, Gareth. Fluoropolymers: Properties. New York: Kluwer Academic, 2002.

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Hougham, Gareth, Patrick E. Cassidy, Ken Johns, and Theodore Davidson, eds. Fluoropolymers 2. Boston: Kluwer Academic Publishers, 2002. http://dx.doi.org/10.1007/b114560.

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Drobny, Jiri George. Technology of fluoropolymers. 2nd ed. Boca Raton: Taylor & Francis, 2009.

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Technology of fluoropolymers. Boca Raton: CRC Press, 2001.

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Hougham, Gareth, Patrick E. Cassidy, Ken Johns, and Theodore Davidson, eds. Fluoropolymers 1: Synthesis. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/b114559.

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Smith, Dennis W., Scott T. Iacono, and Suresh S. Iyer, eds. Handbook of Fluoropolymer Science and Technology. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118850220.

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Xingyu, Liang, and Cai Hongzhi, eds. Fu xiang jiao ying yong ji shu. Beijing: Hua xue gong ye chu ban she, 2009.

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Hong, Li, and Zhang Heng, eds. Han fu gong neng cai liao: Hanfu gongneng cailiao. Beijing Shi: Hua xue gong ye chu ban she, 2008.

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Bernard, Boutevin, ed. Well-architectured fluoropolymers: Synthesis, properties and applications. Amsterdam: Elsevier, 2004.

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ETFE: Technology and design. Basel: Birkhäuser, 2008.

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Book chapters on the topic "Fluoropolymere"

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Gooch, Jan W. "Fluoropolymers." In Encyclopedic Dictionary of Polymers, 319. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_5170.

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Saunders, K. J. "Fluoropolymers." In Organic Polymer Chemistry, 149–66. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1195-6_7.

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Yagüe, Jose L. "CVD Fluoropolymers." In CVD Polymers, 219–32. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527690275.ch10.

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Avataneo, Marco. "Amorphous Fluoropolymers." In Encyclopedia of Membranes, 64–65. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-44324-8_1768.

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Avataneo, Marco. "Amorphous Fluoropolymers." In Encyclopedia of Membranes, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-40872-4_1768-3.

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Raihane, Mustapha, and Bruno Ameduri. "Fluoropolymer Dielectrics." In Handbook of Fluoropolymer Science and Technology, 451–93. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118850220.ch20.

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Sawada, Hideo. "Fluoropolymer Nanocomposites." In Handbook of Fluoropolymer Science and Technology, 57–79. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118850220.ch4.

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Yamabe, Masaaki. "Fluoropolymer Coatings." In Organofluorine Chemistry, 397–401. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1202-2_18.

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Lin, Shiow-Ching, and Bradley Kent. "Flammability of Fluoropolymers." In ACS Symposium Series, 288–97. Washington, DC: American Chemical Society, 2009. http://dx.doi.org/10.1021/bk-2009-1013.ch017.

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Hintzer, Klaus, and Werner Schwertfeger. "Fluoropolymers-Environmental Aspects." In Handbook of Fluoropolymer Science and Technology, 495–520. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118850220.ch21.

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Conference papers on the topic "Fluoropolymere"

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Begolo, Stefano, Guillaume Colas, Laurent Malaquin, and Jean-Louis Viovy. "Production of Fluoropolymer Microchips for Droplet Microfluidics and DNA Amplification." In ASME 2010 8th International Conference on Nanochannels, Microchannels, and Minichannels collocated with 3rd Joint US-European Fluids Engineering Summer Meeting. ASMEDC, 2010. http://dx.doi.org/10.1115/fedsm-icnmm2010-30722.

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In this paper we present a novel fabrication technique for production of monolithic microfluidic chips made from a fluoropolymer (Dyneon THV). This material retains numerous properties of commonly used fluoropolymers (low surface energy and compatibility with chemicals such as organic solvents or fluorinated oil), and is easily processable at relatively low temperatures (lower than 180°C). We used hot embossing to mold microstructures on flat sheets of this polymer. The microchips are sealed through a combination of thermal and solvent bonding by applying uniform pressure with a flexible membrane. These closed channels can be used for the production and circulation of aqueous droplets in fluorinated oil. This droplet microfluidic configuration is suitable for DNA amplification since it avoids cross contamination between adjacent droplets.

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Clark, Karson P. "The Effects of Fluoropolymer Coated Fasteners on Nut Friction Factors." In ASME 2018 Pressure Vessels and Piping Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/pvp2018-84027.

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Fluoropolymer-industrial coatings containing PTFE, also referred to by the tradename Xylan® 1424, are applied in a thin film to provide both lubrication and corrosion resistance. Fluoropolymer coated fasteners are manufactured by a multitude of companies with varying manufacturing practices, procedures, and quality metrics. Fluoropolymer coated fasteners are being considered by major power producers to be used in natural gas transmission lines for their advertised and expected low coefficient of friction properties in place of standard carbon steel fasteners with manually applied lubrication. While some research exists for the nut friction factor of smaller diameter fluoropolymer coated fasteners, this paper will provide empirically obtained data and analysis of the nut friction factors for larger diameter fasteners, up to 2-1/4”, acquired from four different fluoropolymer coated fastener suppliers advertising equivalent fluoropolymer coating specifications and resulting performance. This study is a milestone to further understand the repeatability and quality of fluoropolymer coated fasteners as supplied from one manufacturer to another.

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Goldsberry, D. Roy. "Fuel Hose Permeation of Fluoropolymers." In International Congress & Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1993. http://dx.doi.org/10.4271/930992.

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Janesheski, Robert S., Lori J. Groven, and Steven Son. "Fluoropolymer and aluminum piezoelectric reactives." In SHOCK COMPRESSION OF CONDENSED MATTER - 2011: Proceedings of the Conference of the American Physical Society Topical Group on Shock Compression of Condensed Matter. AIP, 2012. http://dx.doi.org/10.1063/1.3686385.

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Brown, E. N., C. P. Trujillo, G. T. Gray, Mark Elert, Michael D. Furnish, William W. Anderson, William G. Proud, and William T. Butler. "DYNAMIC-TENSILE-EXTRUSION RESPONSE OF FLUOROPOLYMERS." In SHOCK COMPRESSION OF CONDENSED MATTER 2009: Proceedings of the American Physical Society Topical Group on Shock Compression of Condensed Matter. AIP, 2009. http://dx.doi.org/10.1063/1.3295027.

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Goldsberry, D. Roy, Sandra E. Chillous, and Rod R. Will. "Fluoropolymer Resins: Permeation of Automotive Fuels." In International Congress & Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1991. http://dx.doi.org/10.4271/910104.

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Ringler, Robin L., and Paul J. Butkevich. "Fluoropolymer Foam for Twisted Pair Cables." In SAE Aerospace Avionics Equipment and Integration Conference and Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1986. http://dx.doi.org/10.4271/860858.

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Toriumi, Minoru, Naomi Shida, Hiroyuki Watanabe, Tamio Yamazaki, Seiichi Ishikawa, and Toshiro Itani. "Fluoropolymer resists for 157-nm lithography." In SPIE's 27th Annual International Symposium on Microlithography, edited by Theodore H. Fedynyshyn. SPIE, 2002. http://dx.doi.org/10.1117/12.474218.

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Chow, Robert, Gary E. Loomis, and Edward F. Lindsey. "Optical multilayers with an amorphous fluoropolymer." In SPIE's 1994 International Symposium on Optics, Imaging, and Instrumentation, edited by James D. Rancourt. SPIE, 1994. http://dx.doi.org/10.1117/12.185797.

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Vohra, Vaishali R., Xiang-Qian Liu, Katsuji Douki, Christopher K. Ober, Will Conley, Paul Zimmerman, and Daniel Miller. "Fluoropolymer resists for 157 nm lithography." In Microlithography 2003, edited by Theodore H. Fedynyshyn. SPIE, 2003. http://dx.doi.org/10.1117/12.485097.

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Reports on the topic "Fluoropolymere"

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Feast, W. J. Synthesis of New Stereoregular Fluoropolymers. Fort Belvoir, VA: Defense Technical Information Center, August 1986. http://dx.doi.org/10.21236/ada174018.

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Orme, Chris A., Gautam Bordia, and Jim Lewicki. Phase changes in fluoropolymer binders. Office of Scientific and Technical Information (OSTI), January 2019. http://dx.doi.org/10.2172/1491962.

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Dooley, J. B. Cryogenic testing of fluoropolymer-coated stainless steel tubing. Office of Scientific and Technical Information (OSTI), November 1989. http://dx.doi.org/10.2172/7150572.

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LePort, F., A. Pocar, L. Bartoszek, R. DeVoe, P. Fierlinger, B. Flatt, G. Gratta, et al. A Liquid Xenon Ionization Chamber in an All-fluoropolymer Vessel. Office of Scientific and Technical Information (OSTI), February 2007. http://dx.doi.org/10.2172/900243.

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Mclntyre, J. F., R. K. Conrad, and A. Sheetz. Effectiveness of Thin Film Fluoropolymers as Protective Coatings in Marine Environments,. Fort Belvoir, VA: Defense Technical Information Center, June 1994. http://dx.doi.org/10.21236/ada331020.

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Creager, Stephen. Final Report for Project DE-FG02-05ER15718 Fluoropolymers, Electrolytes, Composites and Electrodes. Office of Scientific and Technical Information (OSTI), May 2017. http://dx.doi.org/10.2172/1358278.

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Orme, Chris, Gautam Bordia, and Jim Lewicki. Developing experimental methods to measure phase change in fluoropolymer binders (Progress Summary). Office of Scientific and Technical Information (OSTI), April 2019. http://dx.doi.org/10.2172/1544469.

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Mason, H. E. Progress Summary: Solid-state NMR experiments have been developed to probe crystallization behavior fluoropolymers. Office of Scientific and Technical Information (OSTI), July 2019. http://dx.doi.org/10.2172/1557035.

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Orme, Chris A. Progress Summary: Developing experimental methods to quantify the degree of crystallinity in fluoropolymer binders. Office of Scientific and Technical Information (OSTI), September 2018. http://dx.doi.org/10.2172/1476198.

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