PTFE and PFA Similarities and Differences White Paper PTFE and PFA Similarities and Differences
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Fluorinated Polymers As Smart Materials for Advanced Biomedical Applications
polymers Review Fluorinated Polymers as Smart Materials for Advanced Biomedical Applications Vanessa F. Cardoso 1,2,* ID , Daniela M. Correia 3,4, Clarisse Ribeiro 1,5 ID , Margarida M. Fernandes 1,5 and Senentxu Lanceros-Méndez 4,6 1 Centro/Departamento de Física, Universidade do Minho, 4710-057 Braga, Portugal; cribeiro@fisica.uminho.pt (C.R.); margaridafernandes@fisica.uminho.pt (M.M.F.) 2 CMEMS-UMinho, Universidade do Minho, DEI, 4800-058 Guimaraes, Portugal 3 Departamento de Química e CQ-VR, Universidade de Trás-os-Montes e Alto Douro, 5001-801 Vila Real, Portugal; [email protected] 4 BCMaterials, Basque Center for Materials, Applications and Nanostructures, UPV/EHU Science Park, 48940 Leioa, Spain; [email protected] 5 CEB—Centre of Biological Engineering, University of Minho, 4710-057 Braga, Portugal 6 IKERBASQUE, Basque Foundation for Science, 48013 Bilbao, Spain * Correspondence: [email protected]; Tel.: +351-253-60-40-73 Received: 11 January 2018; Accepted: 6 February 2018; Published: 8 February 2018 Abstract: Fluorinated polymers constitute a unique class of materials that exhibit a combination of suitable properties for a wide range of applications, which mainly arise from their outstanding chemical resistance, thermal stability, low friction coefficients and electrical properties. Furthermore, those presenting stimuli-responsive properties have found widespread industrial and commercial applications, based on their ability to change in a controlled fashion one or more of their physicochemical properties, in response to single or multiple external stimuli such as light, temperature, electrical and magnetic fields, pH and/or biological signals. In particular, some fluorinated polymers have been intensively investigated and applied due to their piezoelectric, pyroelectric and ferroelectric properties in biomedical applications including controlled drug delivery systems, tissue engineering, microfluidic and artificial muscle actuators, among others. -
PVDF: a Fluoropolymer for Chemical Challenges
Electronically reprinted from August 2018 PVDF: A Fluoropolymer for Chemical Challenges When it comes to selecting materials of construction, keep in mind the favorable properties of fluoropolymers for corrosive service Averie Palovcak and Jason ince its commercialization in the Pomante, mid-1960s, polyvinylidene fluoride Arkema Inc. (PVDF) has been used across a Svariety of chemical process indus- tries (CPI) sectors due to its versatility and IN BRIEF broad attributes. With flagship applications PVDF AND THE in architectural coatings and the CPI, the FLUOROPOLYMER FAMILY breadth of industries where PVDF is utilized today is expansive. PVDF components (Fig- COPOLYMERS CHANGE ures 1 and 2) are utilized and installed where FLEXURAL PROPERTIES engineers are looking to maximize longevity PVDF COMPONENTS and reliability of process parts in many CPI sectors, including semiconductor, pharma- FIGURE 1. A variety of fluoropolymer components are shown ceutical, food and beverage, petrochemi- here cal, wire and cable, and general chemicals. change the performance properties. Fluo- PVDF and the fluoropolymer family ropolymers are divided into two main cat- PVDF is a high-performance plastic that falls egories: perfluorinated and partially fluori- into the family of materials called fluoropoly- nated [1]. The partially fluorinated polymers mers. Known for robust chemical resistance, contain hydrogen or other elements, while fluoropolymers are often utilized in areas the perfluorinated (fully fluorinated) poly- where high-temperature corrosion barriers mers are derivatives or copolymers of the are crucial. In addition to being chemically tetrafluoroethylene (C2F4) monomer. Com- resistant and non-rusting, this family of poly- monly used commercial fluoropolymers mers is also considered to have high purity, include polytetrafluoroethylene (PTFE), non-stick surfaces, good flame and smoke perfluoroalkoxy polymer (PFA), fluorinated resistance, excellent weathering and ultra- ethylene propylene (FEP), polyvinylidene violet (UV) stability. -
Teflon™ FEP Fluoropolymer Resins
Teflon™ FEP Fluoropolymer Resins Product and Properties Handbook Teflon™ FEP Fluoropolymer Resins Table of Contents Introduction . 3 Commercially Available Products . 3 Specifications . 3 General Properties of Teflon™ FEP . 3 Typical Properties of Teflon™ FEP . 3 Mechanical Properties . 3 Tensile Properties . 4 Flexural Modulus . 4 Compressive Stress . 5 Creep and Cold Flow . 5 Apparent Modulus of Elasticity . 5 Stress Relaxation . 5 Poisson’s Ratio . 9 Fatigue Resistance . 9 Impact Resistance . 9 Hardness . 10 Friction . 10 Thermal Properties . 10 Electrical Properties . 11. Chemical Resistance . 11 Absorption . 11 Permeability . 11 Weathering . 11 Cryogenic Service . .11 Mildew Resistance . 13 FDA Compliance . 13 Optical Properties . 13 Fabrication Techniques . 13 Forming and Fabrication . 14 Choose Correct Working Speeds . 14 Properly Shape and Use Tools . 14 Rules for Dimensioning and Finishing . 15 Closer Tolerances . 15 Measuring Tolerances . 15 Surface Finishes . 15 Safety Precautions . 15 2 Teflon™ FEP Fluoropolymer Resins Introduction Specifications Teflon™ FEP (fluorinated ethylene propylene) is The ASTM material specification covering Teflon™ FEP chemically a copolymer of hexafluoropropylene fluoropolymer resin is D2116. Teflon™ FEP fluoropolymer and tetrafluoroethylene. It differs from PTFE resin is also called out in various industrial and military (polytetrafluoroethylene) resins, in that it is melt- specifications for tubing, molded parts, and film, as well as processible using conventional injection molding and numerous -
Page 1 of 14 Green Chemistry
Green Chemistry Accepted Manuscript This is an Accepted Manuscript, which has been through the Royal Society of Chemistry peer review process and has been accepted for publication. Accepted Manuscripts are published online shortly after acceptance, before technical editing, formatting and proof reading. Using this free service, authors can make their results available to the community, in citable form, before we publish the edited article. We will replace this Accepted Manuscript with the edited and formatted Advance Article as soon as it is available. You can find more information about Accepted Manuscripts in the Information for Authors. Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content. The journal’s standard Terms & Conditions and the Ethical guidelines still apply. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains. www.rsc.org/greenchem Page 1 of 14 Green Chemistry Organofluorine Chemistry: Applications, sources and sustainability Antal Harsanyi and Graham Sandford* Department of Chemistry, Durham University, South Road, Durham, DH1 3LE, U.K. *Corresponding author E-mail: [email protected] Manuscript Abstract Fluorine is an essential element for life in the developed world that impacts hugely on the general public because many pharmaceuticals, agrochemicals, anaesthetics, materials and air conditioning materials owe their important properties to the presence of fluorine atoms within their structures. Accepted All fluorine atoms used in organic chemistry are ultimately sourced from a mined raw material, fluorspar (CaF 2), but, given current usage and global reserve estimates, there is only sufficient fluorspar available for a further 100 years. -
THE BECKMAN CENTER for the HISTORY of CHEMISTRY HERMAN E. SCHROEDER Transcript of Interviews Conducted by Raymond C. Ferguson In
THE BECKMAN CENTER FOR THE HISTORY OF CHEMISTRY HERMAN E. SCHROEDER Transcript of Interviews Conducted by Raymond C. Ferguson in Greenville, Delaware on 30 December 1986 and 12 January 1987 This interview has been designated as Free Access. One may view, quote from, cite, or reproduce the oral history with the permission of CHF. Please note: Users citing this interview for purposes of publication are obliged under the terms of the Chemical Heritage Foundation Oral History Program to credit CHF using the format below: Herman E. Schroeder, interview by Raymond C. Ferguson at Greenville, Delaware, 30 December 1986 and 12 January 1987 (Philadelphia: Chemical Heritage Foundation, Oral History Transcript # 0063). Chemical Heritage Foundation Oral History Program 315 Chestnut Street Philadelphia, Pennsylvania 19106 The Chemical Heritage Foundation (CHF) serves the community of the chemical and molecular sciences, and the wider public, by treasuring the past, educating the present, and inspiring the future. CHF maintains a world-class collection of materials that document the history and heritage of the chemical and molecular sciences, technologies, and industries; encourages research in CHF collections; and carries out a program of outreach and interpretation in order to advance an understanding of the role of the chemical and molecular sciences, technologies, and industries in shaping society. HERMAN E. SCHROEDER 1915 Born in Brooklyn, New York on 6 July Education 1936 A.B., chemistry, Harvard University 1937 A.M., chemistry, Harvard University -
Working Towards a Global Emission Inventory of Pfass
WORKING TOWARDS A GLOBAL EMISSION INVENTORY OF PFASS: FOCUS ON PFCAS - STATUS QUO AND THE WAY FORWARD OECD Environment, Health and Safety Publications Series on Risk Management No. 30 WORKING TOWARDS A GLOBAL EMISSION INVENTORY OF PFASS: FOCUS ON PFCAS - STATUS QUO AND THE WAY FORWARD This publication is available electronically, at no charge. For this and many other Environment, Health and Safety publications, consult the OECD’s World Wide Web site (www.oecd.org/chemicalsafety/) or contact: OECD Environment Directorate, Environment, Health and Safety Division 2 rue André-Pascal 75775 Paris Cedex 16 France Fax: (33-1) 44 30 61 80 E-mail: [email protected] Environment Directorate ORGANISATION FOR ECONOMIC COOPERATION AND DEVELOPMENT Paris 2015 Also published in the Series on Risk Management: No. 1: Lead. Background and National Experience with Reducing Risk (1993) No. 2: Methylene Chloride. Background and National Experience with Reducing Risk (1994) No. 3: Selected Brominated Flame Retardants. Background and National Experience with Reducing Risk (1994) No. 4: Mercury. Background and National Experience with Reducing Risk (1994) No. 5: Cadmium. Background and National Experience with Reducing Risk (1994) No. 6: Methylene Chloride Information Exchange Programme: Survey Results (1996) No. 7: Proceedings of the OECD Workshop on Non-Regulatory Initiatives for Chemical Risk Management (1997) No. 8: Proceedings of the OECD Workshop on the Effective Recycling of Nickel-Cadmium Batteries, Lyon, France, 23-25 September 1997 (1999) No. 9: Proceedings of the OECD Workshop on the Integration of Socio-Economic Analysis in Chemical Risk Management Decision-making, London, 7-9 January, 1998 (1999) No. 10: Proceedings of the OECD Workshop on Sustainable Chemistry, Venice, 15-17 October 1998 (1999) No. -
Tribological, Mechanical and Thermal Properties of Fluorinated Ethylene Propylene Filled with Al-Cu-Cr Quasicrystals, Polytetraf
polymers Article Tribological, Mechanical and Thermal Properties of Fluorinated Ethylene Propylene Filled with Al-Cu-Cr Quasicrystals, Polytetrafluoroethylene, Synthetic Graphite and Carbon Black Leonid K. Olifirov, Andrey A. Stepashkin, Galal Sherif and Victor V. Tcherdyntsev * Laboratory of Functional Polymer Materials, National University of Science and Technology “MISIS”, Leninskii Prosp, 4, 119049 Moscow, Russia; [email protected] (L.K.O.); [email protected] (A.A.S.); [email protected] (G.S.) * Correspondence: [email protected]; Tel.: +7-9104002369 Abstract: Antifriction hybrid fluorinated ethylene propylene-based composites filled with quasicrys- talline Al73Cu11Cr16 powder, polytetrafluoroethylene, synthetic graphite and carbon black were elaborated and investigated. Composite samples were formed by high-energy ball milling of ini- tial powders mixture with subsequent consolidation by injection molding. Thermal, mechanical, and tribological properties of the obtained composites were studied. It was found that composite containing 5 wt.% of Al73Cu11Cr16 quasicrystals and 2 wt.% of nanosized polytetrafluoroethylene has 50 times better wear resistance and a 1.5 times lower coefficient of dry friction comparing with unfilled fluorinated ethylene propylene. Addition of 15 wt.% of synthetic graphite to the above men- tioned composition allows to achieve an increase in thermal conductivity in 2.5 times comparing with Citation: Olifirov, L.K.; Stepashkin, unfilled fluorinated ethylene propylene, at that this composite kept excellent tribological properties. A.A.; Sherif, G.; Tcherdyntsev, V.V. Tribological, Mechanical and Thermal Keywords: composites; fluoroplastic; quasicrystals; polytetrafluoroethylene; ball milling; injection Properties of Fluorinated Ethylene molding; wear resistance; coefficient of friction; thermal conductivity Propylene Filled with Al-Cu-Cr Quasicrystals, Polytetrafluoroethylene, Synthetic Graphite and Carbon Black. -
United States Patent (19) 11) Patent Number: 4,705,904 Bonfield Et Al
United States Patent (19) 11) Patent Number: 4,705,904 Bonfield et al. 45) Date of Patent: Nov. 10, 1987 54 VAPOR PHASE SYNTHESIS OF which comprises contacting in the vapor phase in a HEXAFLUOROSOBUTYLENE catalyst zone, B, of a reactor hexafluoropropylene oxide 75 Inventors: John H. Bonfield, Basking Ridge; with a fluorinated catalyst such as fluorinated silica Harry E. Ulmer, Morristown, both of alumina at a temperature of about 400-600 C. for a N.J. residence time sufficient to form a vapor stream com prising hexafluoroacetone which is thereafter directly 73) Assignee: Allied Corporation, Morris contacted in a heating zone of the reactor with a vapor Township, Morris County, N.J. stream comprising a keytone-generating compound 21 Appl. No.: 820,896 such as acetic anhydride at a temperature of about 500-700' C. for a residence time sufficient to form a 22 Filed: Jan. 17, 1986 stream comprising hexafluoroisobutylene, substantially free of perfluoroisobutylene and recovering the hexa Related U.S. Application Data fluoroisobutylene product is disclosed. A direct one 63 Continuation of Ser. No. 580,083, Feb. 14, 1984, aban reactor vapor phase synthesis of hexafluoroisobutylene doned. which comprises (a) contacting, in the vapor phase, 51) Int, Cl. .............................................. CO7C 17/26 hexafluoropropene with less than a stoichiometric 52 U.S. C. ..................................... 570/142; 570/153 amount of oxygen required to convert substantially all 58 Field of Search .................. 580/83; 570/153, 142; the hexafluoroisopropene into hexafluoropropylene 568/399, 407, 400, 384; 549/523 oxide in the presence of a fluorinated catalyst such as (56) References Cited fluorinated silica-alumina at a temperature of about 400-600 C. -
Catalytic Synthesis of Perfluorolyethers
J. Cent. South Univ. (2013) 20: 629-633 DOI: 10.1007/s1177101315285 Catalytic synthesis of perfluorolyethers YANG Weijun(阳卫军) 1, FANG Chao(方超) 1, ZHOU Jicang(周济苍) 2, GUO Cancheng(郭灿城) 1, WAN Wei(万伟) 2 1. College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China; 2. Hunan Nonferrous Fluorine Chemistry Corporation, Changsha 410063, China © Central South University Press and SpringerVerlag Berlin Heidelberg 2013 Abstract: Perfluorolyether is characterized by highly chemical inertness, oxidative stability, anticorrosion as well as radiation resistance. It can be used as lubricant especially in harsh environmental conditions. In this work, hexafluoropylene oxide was catalytically polymerized at low temperature using the methods of anionic polymerization, and perfluorolyethers were obtained with numberaverage degree of polymerization more than 15. CsF and RbF were used as catalysts and their catalytic activities were investigated. Experimental results show that perfluorolyethers with numberaverage molar masses up to 3 000 g/mol could be obtained using the two kinds of catalysts, respectively. As compared to CsF, the numberaverage degree of polymerization is higher and the relative molecular mass distribution interval is narrower when RbF is used as catalyst. The effect of factors such as impurities’ content, reaction temperature and reaction time on the numberaverage degree of polymerization was also investigated. It is found that low impurities’ content and low temperature are beneficial to the generation of high numberaverage degree of perfluorolyethers. The optimization reaction time is 24 h, and further increase of reaction time does not significantly affect the average relative molecular mass. -
2006 Dupont Data Book Contents Dupont Investor Relations
2006 DuPont Data Book Contents DuPont Investor Relations 1 2006 Summary 2 2006 At a Glance 4 Corporate Financial Data Corporate Highlights Carl Lukach Karen Fletcher Vice President Director Segment Information (302) 774-0001 (302) 774-1125 Consolidated Income Statements Consolidated Balance Sheets Consolidated Statements of Cash Flows Selected Additional Data 14 DuPont Core Values, Sustainability, and Six Sigma Laurie Conslato Jim Jacobson Pam Schools Manager Manager Investor Relations 15 Industries, Regions, and Ingredients (302) 774-6088 (302) 774-0017 Coordinator (302) 774-9870 16 DuPont Science & Technology 18 Business Segments DuPont Data Book has been prepared to assist financial analysts, portfolio managers Agriculture & Nutrition and others in understanding and evaluating the company. This book presents graphics, tabular, and other statistical data about the consolidated company and its business Coatings & Color Technologies segments. The information presented in this book is generally included in—or can be calculated from—previously issued press releases and published company reports on Electronic & Communication Technologies Forms 10K, 10Q, and 8K. In particular, segment data is consistent with the 8K furnished Performance Materials on April 4, 2007. Dollars are in millions except per share or where otherwise indicated. Most notes to financial statements are not included. This information is only a summary Safety & Protection and should be read in conjunction with the company’s audited consolidated financial Pharmaceuticals statements and “Management’s Discussion and Analysis,” which is located in the 2006 Form 10K filed with the Securities and Exchange Commission. Use of Non-GAAP Measures 39 Major Global Sites and Principal Products This data book presents certain non-GAAP (U.S. -
Comparison of PVDF and Fluoropolymer Coatings BEMO-FLON Vs
Comparison of PVDF and Fluoropolymer Coatings BEMO-FLON vs. PVDF In order to understand the comparability of these two systems we have to summarize the characteristic of these two ultra-durable polymers. PVDF stands for Polyvinylidene Fluorid which is based on a Kynar 500 or Hylar 5000 resin which has to be blended with 50 % for plain colors or 30 % for metallic colors with an acrylic powder. Developed 40 years ago, PVDF stands for long- term colour and gloss retention and resistance to chalking. PVDF coatings are always at least 2-coat systems (primer and top coat) for plain colors and 3 to 4 coat systems (primer, top coat, clear coat) for metallic colors. Due to the fact that PVDF is an emulsion, the direct adhesion to the substrate is insufficient and has to be guaranteed by a primer. The porosity caused by the blending of PVDF leads also to a lack of adhesion with metallic colors wherefore metallic colors always have to be protected by a clear coat. Fluoropolymer (FP) coatings have been developed in early 1980 basing on the good experiences made with PVDF and with the goal to improve it. The Fluoropolymer is a FEVE polymer (= Fluoroethylene Vinylether) which comes from the same family and therefore has a similar molecular structure as PTFE (Polytetrafluoroethylene). PTFE is better known under the brand name of Teflon and stands for a hard and very abrasion resistant material. Following picture shows the similarity of the molecular structure between Vernicron FP (=Fluoropolymer) and PTFE: Page 1 of 3 Comparison of PVDF and Fluoropolymer Coatings BEMO-FLON vs. -
Understanding Fluorotechnology
Fluoropolymers Product Group Understanding FluoroTechnology Per-and polyfluoroalkyl substances (PFASs) is a term that describes a wide and diverse array of chemistry containing fluorine and carbon. This class of chemistry is sometimes inaccurately called “PFCs.” Specific interest and concern from regulators, environmental groups, the media and other stakeholders is focused on a subset of PFAS chemistry: Long-chain perfluoroalkyl acids (PFAAs) and substances that may degrade to form them (known as “precursors”). It is often incorrect to make general statements about properties of the broad family of PFASs, particularly when discussing their safety and environmental impacts. This document explains some key FluoroTechnology terms and depicts those in an overview visual: Long-chain PFAAs Short-chain PFAAs Non-polymeric and Polymeric Fluorotelomer-based Products Fluoroplastics and Fluoropolymers LONG-CHAIN PFAAS SHORT-CHAIN PFAAS Long-chain PFAAs include: Short-chain PFAAs include: perfluoroalkane sulfonic acids (PFSAs) with PFSAs with carbon chain lengths of 5 and carbon chain lengths of 6 and higher, lower, including perfluorobutane sulfonic including perfluorohexane sulfonic acid acid (PFBS) (PFHxS) and perfluorooctane sulfonic acid PFCAs with carbon chain lengths of 7 and (PFOS). lower, including perfluorohexanoic acid perfluorocarboxylic acids (PFCAs) with (PFHxA). carbon chain lengths of 8 and higher, including perfluorooctanoic acid (PFOA). Precursors of these substances may be produced or present in products. Examples are short-chain Precursors of these substances may be produced perfluoroalkyl sulfonyl fluoride-based raw or present in products. Examples are long-chain materials and short-chain fluorotelomer-based perfluoroalkyl sulfonyl fluoride-based raw raw materials. materials and long-chain fluorotelomer-based raw materials.