PVDF Chemical Resistance Guide
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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. -
Poly[4(5)-Vinylimidazole]/Polyvinylidene Fluoride Composites As Proton Exchange Membranes Jingjing Pan
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by RIT Scholar Works Rochester Institute of Technology RIT Scholar Works Theses Thesis/Dissertation Collections 4-1-2009 Poly[4(5)-vinylimidazole]/polyvinylidene fluoride composites as proton exchange membranes Jingjing Pan Follow this and additional works at: http://scholarworks.rit.edu/theses Recommended Citation Pan, Jingjing, "Poly[4(5)-vinylimidazole]/polyvinylidene fluoride composites as proton exchange membranes" (2009). Thesis. Rochester Institute of Technology. Accessed from This Thesis is brought to you for free and open access by the Thesis/Dissertation Collections at RIT Scholar Works. It has been accepted for inclusion in Theses by an authorized administrator of RIT Scholar Works. For more information, please contact [email protected]. Poly[4(5)-Vinylimidazole]/Polyvinylidene Fluoride Composites as Proton Exchange Membranes Jingjing Pan April 2009 Thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Chemistry. Approved: _______________________________________ Thomas W. Smith (Advisor) ______________________________ Paul Rosenberg (Department Head) Department of Chemistry Rochester Institute of Technology Rochester, New York 14623-5603 Copyright Release Form: INVESTIGATION OF POLY[4(5)-VINYLIMIDAZOLE] COMPOSITES AND THEIR POTENTIAL AS PROTON CONDUCTIVE MEMBRANES I, Jingjing Pan, hereby grant permission to the Wallace Memorial Library of Rochester Institute of Technology to reproduce my thesis in whole or in part. Any reproduction will not be for commercial use or profit. Jingjing Pan April, 2009 i Abstract In the present research, the morphology and thermal chemical characteristics of composite films comprised of poly(vinylidene fluoride) (PVF2) and poly[4(5)-vinylimidazole/vinylimidazolium trifluoromethylsulfonylimide] (PVIm/VIm+TFSI-]) were studied. -
1,1,1,2-Tetrafluoroethane
This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the United Nations Environment Programme, the International Labour Organisation, or the World Health Organization. Concise International Chemical Assessment Document 11 1,1,1,2-Tetrafluoroethane First draft prepared by Mrs P. Barker and Mr R. Cary, Health and Safety Executive, Liverpool, United Kingdom, and Dr S. Dobson, Institute of Terrestrial Ecology, Huntingdon, United Kingdom Please not that the layout and pagination of this pdf file are not identical to the printed CICAD Published under the joint sponsorship of the United Nations Environment Programme, the International Labour Organisation, and the World Health Organization, and produced within the framework of the Inter-Organization Programme for the Sound Management of Chemicals. World Health Organization Geneva, 1998 The International Programme on Chemical Safety (IPCS), established in 1980, is a joint venture of the United Nations Environment Programme (UNEP), the International Labour Organisation (ILO), and the World Health Organization (WHO). The overall objectives of the IPCS are to establish the scientific basis for assessment of the risk to human health and the environment from exposure to chemicals, through international peer review processes, as a prerequisite for the promotion of chemical safety, and to provide technical assistance in strengthening national capacities for the sound management of chemicals. The Inter-Organization -
Piezoelectricity in PVDF and PVDF Based Piezoelectric Nanogenerator: a Concept
IOSR Journal of Applied Physics (IOSR-JAP) e-ISSN: 2278-4861.Volume 9, Issue 3 Ver. I (May. – June. 2017), PP 95-99 www.iosrjournals.org Piezoelectricity in PVDF and PVDF Based Piezoelectric Nanogenerator: A Concept Binoy Bera1,*, Madhumita Das Sarkar2 1,2Department of computer science and engineering, West Bengal University of Technology, Kolkata – 700064, India Abstract: Polyvinylidene fluoride or simply PVDF is one of the most important semicrystalline polymers which generate piezoelectricity when a pressure or mechanical force applied on it. It has four crystalline phases α, β, ɣ and δ depending on the chain conformation structure. Among them α is non polar phase and β and ɣ are polar phase. Piezoelectricity in PVDF arises due to the β and ɣ phase formation. Several materials have been introduced for the preparation of nanogenerator. Among them PVDF (polyvinylidene fluoride) is most interesting material used in nanogenerator preparation due to its flexibility, bio- compatiable, nontoxic in nature. It is used in nanogenerator application due to its good ferroelectric, piezoelectric and pyroelectric properties. In this article we describe little bit concept about PVDF, its piezoelectricity and PVDF based nanogenerator. Application of piezoelectric nanogenerator is also briefly described here. Keywords: PVDF, nanogenerator, piezoelectricity, β phase, electrospinning, electroactive phase, Poling process. I. Introduction Polyvinylidene fluoride, or polyvinylidene difluoride, (PVDF) is a highly non- reactive thermoplastic fluoropolymer produced by the polymerization of vinylidene difluoride. PVDF has four crystalline phases α, β, ɣ and δ depending on the chain conformation. Among them α is thermodynamically most stable and non polar in nature. β and ɣ are polar phase. -
A Study of the Decomposition of Some Aromatic Diazonium Hexafluorophosphate Salts
University of Windsor Scholarship at UWindsor Electronic Theses and Dissertations Theses, Dissertations, and Major Papers 1-1-1964 A study of the decomposition of some aromatic diazonium hexafluorophosphate salts. William A. Redmond University of Windsor Follow this and additional works at: https://scholar.uwindsor.ca/etd Recommended Citation Redmond, William A., "A study of the decomposition of some aromatic diazonium hexafluorophosphate salts." (1964). Electronic Theses and Dissertations. 6038. https://scholar.uwindsor.ca/etd/6038 This online database contains the full-text of PhD dissertations and Masters’ theses of University of Windsor students from 1954 forward. These documents are made available for personal study and research purposes only, in accordance with the Canadian Copyright Act and the Creative Commons license—CC BY-NC-ND (Attribution, Non-Commercial, No Derivative Works). Under this license, works must always be attributed to the copyright holder (original author), cannot be used for any commercial purposes, and may not be altered. Any other use would require the permission of the copyright holder. Students may inquire about withdrawing their dissertation and/or thesis from this database. For additional inquiries, please contact the repository administrator via email ([email protected]) or by telephone at 519-253-3000ext. 3208. A STUDY OF THE DECOMPOSITION OF SOME AROMATIC DIAZONIUM HEXAFLUOROPHOSPHATE SALTS BY WILLIAM A. REDMOND A Thesis Submitted to the Faculty of Graduate Studies through' the Department of Chemistry in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy at the University of Windsor Windsor, Ontario 1964 Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. -
Functionalization of Heterocycles: a Metal Catalyzed Approach Via
FUNCTIONALIZATION OF HETEROCYCLES: A METAL CATALYZED APPROACH VIA ALLYLATION AND C-H ACTIVATION A Dissertation Submitted to the Graduate Faculty of the North Dakota State University of Agriculture and Applied Science By Sandeepreddy Vemula In Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY Major Department: Chemistry and Biochemistry October 2018 Fargo, North Dakota North Dakota State University Graduate School Title FUNCTIONALIZATION OF HETEROCYCLES: A METAL CATALYZED APPROACH VIA ALLYLATION AND C-H ACTIVATION By Sandeepreddy Vemula The Supervisory Committee certifies that this disquisition complies with North Dakota State University’s regulations and meets the accepted standards for the degree of DOCTOR OF PHILOSOPHY SUPERVISORY COMMITTEE: Prof. Gregory R. Cook Chair Prof. Mukund P. Sibi Prof. Pinjing Zhao Prof. Dean Webster Approved: November 16, 2018 Prof. Gregory R. Cook Date Department Chair ABSTRACT The central core of many biologically active natural products and pharmaceuticals contain N-heterocycles, the installation of simple/complex functional groups using C-H/N-H functionalization methodologies has the potential to dramatically increase the efficiency of synthesis with respect to resources, time and overall steps to key intermediate/products. Transition metal-catalyzed functionalization of N-heterocycles proved as a powerful tool for the construction of C-C and C-heteroatom bonds. The work in this dissertation describes the development of palladium catalyzed allylation, and the transition metal catalyzed C-H activation for selective functionalization of electron deficient N-heterocycles. Chapter 1 A thorough study highlighting the important developments made in transition metal catalyzed approaches for C-C and C-X bond forming reactions is discussed with a focus on allylation, directed indole C-2 substitution and vinylic C-H activation. -
Gasket Chemical Services Guide
Gasket Chemical Services Guide Revision: GSG-100 6490 Rev.(AA) • The information contained herein is general in nature and recommendations are valid only for Victaulic compounds. • Gasket compatibility is dependent upon a number of factors. Suitability for a particular application must be determined by a competent individual familiar with system-specific conditions. • Victaulic offers no warranties, expressed or implied, of a product in any application. Contact your Victaulic sales representative to ensure the best gasket is selected for a particular service. Failure to follow these instructions could cause system failure, resulting in serious personal injury and property damage. Rating Code Key 1 Most Applications 2 Limited Applications 3 Restricted Applications (Nitrile) (EPDM) Grade E (Silicone) GRADE L GRADE T GRADE A GRADE V GRADE O GRADE M (Neoprene) GRADE M2 --- Insufficient Data (White Nitrile) GRADE CHP-2 (Epichlorohydrin) (Fluoroelastomer) (Fluoroelastomer) (Halogenated Butyl) (Hydrogenated Nitrile) Chemical GRADE ST / H Abietic Acid --- --- --- --- --- --- --- --- --- --- Acetaldehyde 2 3 3 3 3 --- --- 2 --- 3 Acetamide 1 1 1 1 2 --- --- 2 --- 3 Acetanilide 1 3 3 3 1 --- --- 2 --- 3 Acetic Acid, 30% 1 2 2 2 1 --- 2 1 2 3 Acetic Acid, 5% 1 2 2 2 1 --- 2 1 1 3 Acetic Acid, Glacial 1 3 3 3 3 --- 3 2 3 3 Acetic Acid, Hot, High Pressure 3 3 3 3 3 --- 3 3 3 3 Acetic Anhydride 2 3 3 3 2 --- 3 3 --- 3 Acetoacetic Acid 1 3 3 3 1 --- --- 2 --- 3 Acetone 1 3 3 3 3 --- 3 3 3 3 Acetone Cyanohydrin 1 3 3 3 1 --- --- 2 --- 3 Acetonitrile 1 3 3 3 1 --- --- --- --- 3 Acetophenetidine 3 2 2 2 3 --- --- --- --- 1 Acetophenone 1 3 3 3 3 --- 3 3 --- 3 Acetotoluidide 3 2 2 2 3 --- --- --- --- 1 Acetyl Acetone 1 3 3 3 3 --- 3 3 --- 3 The data and recommendations presented are based upon the best information available resulting from a combination of Victaulic's field experience, laboratory testing and recommendations supplied by prime producers of basic copolymer materials. -
Microflex Gloves Chemical Compatibility Chart
1 1 1 2 2 3 1 CAUTION (LATEX): This product contains natural rubber 2 CAUTION (NITRILE: MEDICAL GRADE): Components used 3 CAUTION (NITRILE: NON-MEDICAL GRADE)): These latex (latex) which may cause allergic reactions. Safe use in making these gloves may cause allergic reactions in gloves are for non-medical use only. They may NOT be of this glove by or on latex sensitized individuals has not some users. Follow your institution’s policies for use. worn for barrier protection in medical or healthcare been established. applications. Please select other gloves for these applications. Components used in making these gloves may cause allergic reactions in some users. Follow your institution’s policies for use. For single use only. NeoPro® Chemicals NeoPro®EC Ethanol ■NBT Ethanolamine (99%) ■NBT Ether ■2 Ethidium bromide (1%) ■NBT Ethyl acetate ■1 Formaldehyde (37%) ■NBT Formamide ■NBT Gluteraldehyde (50%) ■NBT Test Method Description: The test method uses analytical Guanidine hydrochloride ■NBT equipment to determine the concentration of and the time at which (50% ■0 the challenge chemical permeates through the glove film. The Hydrochloric acid ) liquid challenge chemical is collected in a liquid miscible chemical Isopropanol ■NBT (collection media). Data is collected in three separate cells; each cell Methanol ■NBT is compared to a blank cell which uses the same collection media as both the challenge and Methyl ethyl ketone ■0 collection chemical. Methyl methacrylate (33%) ■0 Cautionary Information: These glove recommendations are offered as a guide and for reference Nitric acid (50%) ■NBT purposes only. The barrier properties of each glove type may be affected by differences in material Periodic acid (50%) ■NBT thickness, chemical concentration, temperature, and length of exposure to chemicals. -
(12) Patent Application Publication (10) Pub. No.: US 2011/005250.6 A1 Abel Et Al
US 2011 0052506A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2011/005250.6 A1 Abel et al. (43) Pub. Date: Mar. 3, 2011 (54) STABLE AEROSOL TOPICAL FOAMS Publication Classification COMPRISINGA HYPOCHLORITE SALT (51) Int. Cl. (75) Inventors: Douglas Abel, Sudbury, MA (US); st 94;O CR Ronald M. Gurge, Franklin, MA ( .01) (US); Mark W. Trumbore, A6IP3L/00 (2006.01) Westford, MA (US) (52) U.S. Cl. .......................................................... 424/45 (73) Assignee: Collegium Pharmaceutical, Inc., (57) ABSTRACT Cumberland, RI (US) Described herein are compositions useful in the treatment of atopic dermatitis and other skin conditions, which composi (21) Appl. No.: 12/872,566 tions exhibit enhanced stability. The compositions contain a 1-1. hypochlorite salt, useful for its antimicrobial properties, and (22) Filed: Aug. 31, 2010 are non-irritating when applied to the skin. The compositions O O also provide enhanced moisturizing properties. The compo Related U.S. Application Data sitions can be formulated into a topical aerosol foam with (60) Provisional application No. 61/238,439, filed on Aug. inert, non-flammable propellants, such as hydrofluoroal 31, 2009. kanes, and may be used in cosmetics or pharmaceuticals. US 2011/005250.6 A1 Mar. 3, 2011 STABLE AEROSOL TOPCAL FOAMS itch associated with atopic dermatitis; however, they can COMPRISINGA HYPOCHLORITE SALT cause sleepiness and may not help in all cases of atopic dermatitis. RELATED APPLICATION 0007 For mild cases of atopic dermatitis, an over-the counterformulation of coal taris often used. Coaltar has long 0001. This application claims benefit under 35 U.S.C. 119 been a treatment for a variety of skin conditions. -
Prepared by 3M
DRAFT ECOTOXICOLOGY AND ENVIRONMENTAL FATE TESTING OF SHORT CHAIN PERFLUOROALKYL COMPOUNDS RELATED TO 3M CHEMISTRIES XXX XX, 2008 Prepared by 3M Page 1 CONFIDENTIAL - SUBJECT TO A PROTECTIVE ORDER ENTERED IN 3M MN01537089 HENNEPIN COUNTY DISTRICT COURT, NO. 27-CV-10-28862 2231.0001 DRAFT TABLE OF CONTENTS Page Introduction (describes propose, goals, document organization .... ) 3 1) Degradation modes 4-27 Basic degradation pathways, Conversion routes from polymer to monomer & degradants or residual intermediates to degradants) 2) Degradants & Intermediates - Phys. Chem properties and test data by section & chapter i) Fluorinated Sulfonic acids and derivatives a) PFBS (PBSK) 28-42 b) PFBSI 43-44 ii) Fluorinated Carboxylates a) TFA 46-55 b) PFPA 56-59 c) PFBA (APFB) 60-65 d) MeFBSAA (MeFBSE Acid, M370) 66-68 iii) Fluorinated Non-ionics a) MeFBSE 70-74 b) MeFBSA 75-80 c) FBSE 81-84 d) FBSA 85-88 e) HxFBSA 89-91 iv) Fluorinated Inerts & volatiles a) PBSF 94-97 b) NFB, C4 hydride, CF3CF2CF2CF2-H 98-99 3) Assessments X Glossary 100-102 References/Endnotes 105- Page 2 CONFIDENTIAL - SUBJECT TO A PROTECTIVE ORDER ENTERED IN 3M MN01537090 HENNEPIN COUNTY DISTRICT COURT, NO. 27-CV-10-28862 2231.0002 DRAFT Introduction to Environmental White Papers on Perfluoroalkyl acids related to 3M chemistries Perfluorochemicals have been commonplace in chemical industry over 50 years but until recently there has been little information on environmental fate and effects avialble in open literature. The following chapters summarize the findings of"list specific C4 intermediates PFBS, PFBSI, PFBA, PFPA, MeFBSAA, TFA, MeFBSE, FBSA, HxFBSA, FBSE, PBSF, NFB " As background, 3M announced on May 16, 2000 the voluntary manufacturing phase out of perfluorooctanyl chemicals which included perfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), and PFOS-related chemistries. -
Systematic Review Protocol for the PFBA, Pfhxa, Pfhxs, PFNA, and PFDA (Anionic and Acid Forms) IRIS Assessments
EPA/635/R-20/131 IRIS Assessments Protocol www.epa.gov/iris Systematic Review Protocol for the PFBA, PFHxA, PFHxS, PFNA, and PFDA (anionic and acid forms) IRIS Assessments CASRN 335-76-2 (PFDA) CASRN 375-95-1 (PFNA) CASRN 307-24-4 (PFHxA) CASRN 355-46-4 (PFHxS) CASRN 375-22-4 (PFBA) Supplemental Information―Appendix A October 2019 Updated February 2020 (in response to public comments) This document was posted for public comment on November 8, 2019 (link to more information), and subsequently updated in response to those comments (updates are outlined in Section 12). It does not represent and should not be construed to represent any Agency determination or policy. Integrated Risk Information System Center for Public Health and Environmental Assessment Office of Research and Development U.S. Environmental Protection Agency Washington, DC Systematic Review Protocol for the PFBA, PFHxA, PFHxS, PFNA, and PFDA IRIS Assessments DISCLAIMER This document was posted for public comment on November 8, 2019 (link to more information), and subsequently updated in response to those comments (updates are outlined in Section 12). It does not represent and should not be construed to represent any Agency determination or policy. This document is a draft for review purposes only and does not constitute Agency policy. ii DRAFT―DO NOT CITE OR QUOTE Systematic Review Protocol for the PFBA, PFHxA, PFHxS, PFNA, and PFDA IRIS Assessments CONTENTS AUTHORS|CONTRIBUTORS|REVIEWERS ..................................................................................................... -
The Uses of Polyvinylidene Fluoride Based Resins in Chemical Handling Systems Denis K
INTERCORR2014_306 Copyright 2014, ABRACO Trabalho apresentado durante o INTERCORR 2014, em Fortaleza/CE no mês de maio de 2014. As informações e opiniões contidas neste trabalho são de exclusiva responsabilidade do(s) autor(es). The Uses of Polyvinylidene Fluoride based resins in Chemical Handling Systems Denis K. de Almeidaa, Fabio L. F. Paganinib, David Seilerc Abstract Polyvinylidene fluoride (PVDF) based polymer resins have been used for corrosive and chemically aggressive fluid containment since 1964. In the 1980’s copolymers of vinylidene fluoride and hexafluoropropylene (HFP) were introduced that complimented the very rigid PVDF product line with a more flexible version of PVDF. Recently, other new technologies have been introduced for PVDF where it has been functionalized which allows it to be bonded to lower cost structural polymers during processing. Additionally, recent development of special grades of PVDF allow for finely woven and non-woven chemical filtration products and the creation of reliable conductive versions. Due to special properties not found in other plastics or metals, PVDF is used extensively in the following industries: chlor-alkali containment, bromine, acid production & distribution, mining, metal preparation, petrochemical, pharmaceutical, food & beverage, semiconductor, pulp & paper, waste water treatment, and power generation. This paper will outline the use of PVDF, reactive PVDF and/or PVDF based copolymers in specific chemicals and the special corrosive conditions that can be associated with them.