Blends of Polyimides with Poly(Ether Ether Ketone) and PEEK Derivatives/ Robert J
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Development of Polysulfone Hollow Fiber Porous Supports for High Flux Composite Membranes: Air Plasma and Piranha Etching
fibers Article Development of Polysulfone Hollow Fiber Porous Supports for High Flux Composite Membranes: Air Plasma and Piranha Etching Ilya Borisov 1,*, Anna Ovcharova 1,*, Danila Bakhtin 1, Stepan Bazhenov 1, Alexey Volkov 1, Rustem Ibragimov 2, Rustem Gallyamov 2, Galina Bondarenko 1, Rais Mozhchil 3, Alexandr Bildyukevich 4 and Vladimir Volkov 1 1 A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow 119991, Russia; [email protected] (D.B.); [email protected] (S.B.); [email protected] (A.V.); [email protected] (G.B.); [email protected] (V.V.) 2 Kazan National Research Technological University, Kazan 420015, Russia; [email protected] (R.I.); [email protected] (R.G.) 3 National Research Nuclear University “MEPhI”, Moscow 115409, Russia; [email protected] 4 Institute of Physical Organic Chemistry, National Academy of Sciences of Belarus, Minsk 220072, Belarus; [email protected] * Correspondence: [email protected] (I.B.); [email protected] (A.O.); Tel.: +7-495-955-4893 (I.B.); +7-495-647-59-27 (A.O.) Academic Editors: Alberto Figoli and Tao He Received: 30 December 2016; Accepted: 4 February 2017; Published: 13 February 2017 Abstract: For the development of high efficiency porous supports for composite membrane preparation, polysulfone (PSf) hollow fiber membranes (outer diameter 1.57 mm, inner diameter 1.12 mm) were modified by air plasma using the low temperature plasma treatment pilot plant which is easily scalable to industrial level and the Piranha etch (H2O2 + H2SO4). Chemical and plasma modification affected only surface layers and did not cause PSf chemical structure change. -
II. Plasticizer-Free Polyvinyl Chloride, Plasticizer-Free Copolymers of Vinyl
This is an unofficial translation. Only the German version is binding. II. Plasticizer-free Polyvinyl Chloride, Plasticizer-free Copolymers of Vinyl Chlo- ride and Mixtures of these Polymers with other Copolymers and Chlorinated Polyolefins Containing Mainly Vinyl Chloride in the Total Mixture As of 01.01.2012 The monomers and other starting substances as well as additives used in the production of plasticizer-free polyvinyl chloride, plasticizer-free copolymers of vinyl chloride containing mainly vinyl chloride, mixtures of these polymers with other copolymers, and chlorinated polyolefins containing mainly vinyl chloride in the total mixture are subject to the requirements of the Commission Regulation (EU) No 10/2011. Otherwise, there are no objections to the use of these plastics for commodities in the sense of § 2, Para. 6, No 1 of the Food and Feed Code (Lebensmittel- und Futtermittelgesetzbuch), pro- vided they are suitable for their intended purpose and comply with the following conditions: 1. The use of monomers and other starting materials for polyethylene is subject to the stipula- tions of the Commission Regulation (EU) No 10/2011. The evaluation presented in the following refers to polymers from the following monomeric starting substances: a) Vinyl chloride b) Vinylidene chloride c) Trans-dichloroethylene d) Vinylesters of aliphatic carbonic acids C2-C18, in so far as covered by the positive list of the Commission Regulation (EU) No 10/2011 e) Esters of acrylic acid, methacrylic acid and/or maleic acid or fumaric acid with -
Radel® PPSU, Udel® PSU, Veradel® PESU & Acudel® Modified PPSU
Radel ® | Udel ® | Veradel ® | Acudel ® Radel® PPSU, Udel® PSU, Veradel® PESU & Acudel® modified PPSU Processing Guide SPECIALT Y POLYMERS 2 \ Sulfone Polymers Processing Guide Table of Contents Introduction ............................. 5 Part Ejection . 14 Draft . 14 Ejector pins and/or stripper plates . 14 Sulfone Polymers........................ 5 Udel® Polysulfone (PPSU) . 5 Injection Molding Equipment ............. 15 ® Veradel Polyethersulfone (PESU) . 5 Controls . 15 ® Radel Polyphenylsulfone (PPSU) . 5 Clamp . 15 ® Acudel modified PPSU . 5 Barrel Capacity . 15 Press Maintenance . 15 Resin Drying . .6 Screw Design . 15 Rheology................................ 8 Screw Tips and Check Valves . 15 Viscosity-Shear Rate ..................... 8 Nozzles . 16 Molding Process . 16 Resin Flow Characteristics . 9 Melt flow index . 9 Polymer Injection or Mold Filling . 16 Spiral flow . 9 Packing and Holding . 17 Injection Molding . .10 Cooling . 17 Molds and Mold Design .................. 10 Machine Settings ....................... 17 Tool Steels . 10 Barrel Temperatures . 17 Mold Dimensions . 10 Mold Temperature . 18 Mold Polishing . 10 Residence Time in the Barrel . 18 Mold Plating and Surface Treatments . 10 Injection Rate . 18 Tool Wear . 10 Back Pressure . 18 Mold Temperature Control . 10 Screw Speed . 18 Mold Types . 11 Shrinkage . 18 Two-plate molds . 11 Three-plate molds . 11 Regrind ............................... 19 Hot runner molds . 11 Cavity Layout . 12 Measuring Residual Stress ............... 19 Runner Systems . 12 Extrusion............................... 22 Gating . 12 Sprue gating . 12 Edge gates . 13 Predrying ............................. 22 Diaphragm gates . 13 Tunnel or submarine gates . 13 Extrusion Temperatures ................. 22 Pin gates . 13 Screw Design Recommendations . 22 Gate location . 13 Venting . 14 Sulfone Polymers Processing Guide / 3 Die Design ............................. 22 Extruded Product Types . 23 Wire . 23 Film . 23 Sheet . 23 Piping and tubing . 23 Start-Up, Shut-Down, and Purging ....... -
Biocompatibility of Polyimides: a Mini-Review
materials Review Biocompatibility of Polyimides: A Mini-Review Catalin P. Constantin 1 , Magdalena Aflori 1 , Radu F. Damian 2 and Radu D. Rusu 1,* 1 “Petru Poni” Institute of Macromolecular Chemistry, Romanian Academy, Aleea Grigore Ghica Voda 41A, Iasi-700487, Romania; [email protected] (C.P.C.); mafl[email protected] (M.A.) 2 SC Intelectro Iasi SRL, Str. Iancu Bacalu, nr.3, Iasi-700029, Romania; [email protected] * Correspondence: [email protected]; Tel.: +40-232-217454 Received: 14 August 2019; Accepted: 25 September 2019; Published: 27 September 2019 Abstract: Polyimides (PIs) represent a benchmark for high-performance polymers on the basis of a remarkable collection of valuable traits and accessible production pathways and therefore have incited serious attention from the ever-demanding medical field. Their characteristics make them suitable for service in hostile environments and purification or sterilization by robust methods, as requested by most biomedical applications. Even if PIs are generally regarded as “biocompatible”, proper analysis and understanding of their biocompatibility and safe use in biological systems deeply needed. This mini-review is designed to encompass some of the most robust available research on the biocompatibility of various commercial or noncommercial PIs and to comprehend their potential in the biomedical area. Therefore, it considers (i) the newest concepts in the field, (ii) the chemical, (iii) physical, or (iv) manufacturing elements of PIs that could affect the subsequent biocompatibility, and, last but not least, (v) in vitro and in vivo biocompatibility assessment and (vi) reachable clinical trials involving defined polyimide structures. The main conclusion is that various PIs have the capacity to accommodate in vivo conditions in which they are able to function for a long time and can be judiciously certified as biocompatible. -
Technical Datasheet: Udel® P-1700
Udel® P-1700 Polysulfone Solvay Specialty Polymers www.ulprospector.com Technical Data Product Description Udel® P-1700 polysulfone (PSU) is a tough, rigid, high-strength thermoplastics suitable for continuous use up to 300°F (149°C). It is resistant to oxidation and hydrolysis and withstand prolonged exposure to high temperatures and repeated sterilization. Udel® P-1700 polysulfone is highly resistant to mineral acids, alkali and salt solutions. Resistance to detergents and hydrocarbon oils is good, but the resin may be attacked by polar solvents such as ketones, chlorinated hydrocarbons and aromatic hydrocarbons. These resins are also highly resistant to degradation by gamma or electron beam radiation. Electrical properties of Udel® P-1700 polysulfones are stable over a wide temperature range and after immersion in water or exposure to high humidity. The resins comply with FDA 21 CFR 177.1655 and may be used in articles intended for repeated use in contact with foods. Additionally, they are approved by the NSF, by the Department of Agriculture for contact with meat and poultry and by the 3-A Sanitary Standards of the Dairy Association. • Transparent: Udel® P-1700 CL 2611 CMP • Transparent: Udel® P-1700 NT 06 • Transparent: Udel® P-1700 NT 11 • Opaque Black : Udel® P-1700 BK 937 • Opaque White: Udel® P-1700 WH 6417 • Opaque White: Udel® P-1700 WH 7407 • Opaque Gray: Udel® P-1700 GY 8057 General Material Status • Commercial: Active Literature 1 • Technical Datasheet UL Yellow Card 2 • E36098-231084 • Solvay Specialty Polymers Search for -
Using an Inhibitor to Prevent Plasticizer Migration from Polyurethane Matrix to EPDM Based Substrate Rezaei-Vahidian Hadi, Farajpour Tohid, Abdollahi Mahdi
Using an Inhibitor to Prevent Plasticizer Migration from Polyurethane Matrix to EPDM Based Substrate Rezaei-Vahidian Hadi, Farajpour Tohid, Abdollahi Mahdi Cite this article as: Rezaei-Vahidian Hadi, Farajpour Tohid, Abdollahi Mahdi. Using an Inhibitor to Prevent Plasticizer Migration from Polyurethane Matrix to EPDM Based Substrate[J]. Chinese J. Polym. Sci, 2019, 37(7): 681-686. doi: 10.1007/s10118-019-2251-y View online: https://doi.org/10.1007/s10118-019-2251-y Articles you may be interested in Antistatic PVC-graphene Composite through Plasticizer-mediated Exfoliation of Graphite Chinese J. Polym. Sci. 2018, 36(12): 1361 https://doi.org/10.1007/s10118-018-2160-5 SYNTHESIS OF POLYURETHANE MODIFIED BISMALEIMIDE (UBMI) AND POLYURETHANE-IMIDE ELASTOMER Chinese J. Polym. Sci. 2008, 26(1): 117 Synthesis and Properties of Reversible Disulfide Bond-based Self-healing Polyurethane with Triple Shape Memory Properties Chinese J. Polym. Sci. 2019, 37(11): 1119 https://doi.org/10.1007/s10118-019-2268-2 增塑剂对碱木质素/HDPE复合材料性能影响研究 The Effect of Plasticizer on the Properties of Alkali Lignin/HDPE Composites 高分子学报. 2014(2): 210 https://doi.org/10.3724/SP.J.1105.2014.13204 泊肃叶流中环形高分子的迁移行为及与线性高分子的差异 Migration of Ring Polymers in Poiseuille Flow and Comparison with Linear Polymers 高分子学报. 2019, 50(11): 1229 https://doi.org/10.11777/j.issn1000-3304.2019.19074 聚醚硅油表面迁移行为对聚苯乙烯表面极性的影响 THE IMPROVEMENT OF POLARITY OF POLYSTYRENE SURFACE BY THE SELECTIVE SURFACE MIGRATION OF POLYETHER SILICOME OIL 高分子学报. 2007(2): 165 Chinese Journal of POLYMER SCIENCE ARTICLE https://doi.org/10.1007/s10118-019-2251-y -
Recent Attempts in the Design of Efficient PVC Plasticizers With
materials Review Recent Attempts in the Design of Efficient PVC Plasticizers with Reduced Migration Joanna Czogała 1,2,3,* , Ewa Pankalla 2 and Roman Turczyn 1,* 1 Department of Physical Chemistry and Technology of Polymers, Silesian University of Technology, Strzody 9, 44-100 Gliwice, Poland 2 Research and Innovation Department, Grupa Azoty Zakłady Azotowe K˛edzierzynS.A., Mostowa 30A, 47-220 K˛edzierzyn-Ko´zle,Poland; [email protected] 3 Joint Doctoral School, Silesian University of Technology, Akademicka 2A, 44-100 Gliwice, Poland * Correspondence: [email protected] (J.C.); [email protected] (R.T.) Abstract: This paper reviews the current trends in replacing commonly used plasticizers in poly(vinyl chloride), PVC, formulations by new compounds with reduced migration, leading to the enhance- ment in mechanical properties and better plasticizing efficiency. Novel plasticizers have been divided into three groups depending on the replacement strategy, i.e., total replacement, partial replacement, and internal plasticizers. Chemical and physical properties of PVC formulations containing a wide range of plasticizers have been compared, allowing observance of the improvements in polymer per- formance in comparison to PVC plasticized with conventionally applied bis(2-ethylhexyl) phthalate, di-n-octyl phthalate, bis(2-ethylhexyl) terephthalate and di-n-octyl terephthalate. Among a variety of newly developed plasticizers, we have indicated those presenting excellent migration resistance and advantageous mechanical properties, as well as those derived from natural sources. A separate chapter has been dedicated to the description of a synergistic effect of a mixture of two plasticizers, primary and secondary, that benefits in migration suppression when secondary plasticizer is added to PVC blend. -
Studies on Radiation Crosslinking of Polysulfone
JP0050427 JAERI-Conf 2000-001 Studies on Radiation Crosslinking of Polysulfone Xiaoguang Zhong Jiazhen Sun Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun 130022, China Polysulfone is a kind of high temperature-resistance and radiation-resistance engineering plastic. The chemical structure is as follows: Brown (1), Lyon (2), Sasuga (3), et al have already studied its radiation effect. We studied CH3 radiation crosslinking effect of polysulfone by using of XPS, ESR, and CG methods and got some new results. Results and Discussions 1. Study radiation crosslinking of polysulfone by XPS method Because of conjugate system of benzene ring, polymer material which contains of benzene ring will appear shake-up peak in XPS spectra. Wanxi Zhang (4) shows that during radiation crosslinking of polystyrene increases with radiation dose and the intensity of shake-up peak decreases gradually with increase of radiation dose and crosslinking degree. This suggests that radiation crosslinking destroyed conjugate system of benzene ring. During radiation crosslinking of polysulfone, we find rules of shake-up peaks in the XPS spectra are different at different radiation crosslinking temperature. At lower temperature the intensity of shake-up peak decreases with the increase of radiation dose. This rule is similar to that of radiation crosslinking of polystyrene. The results are shown in Fig. 1. 183- JAERI-Conf 2000-001 Fig. 1. The spectra of radiation crosslinking of polysulfone at 70"C Comparing with radiation crosslinking at lower temperature, the intensity of shake-up peak increases with radiation dose when radiation crosslinking reaction takes place at temperature above glass transition temperature of polysulfone. -
Cross Linked Sulphonated Poly(Ether Ether Ketone) for the Development of Polymer Electrolyte Membrane Fuel Cell
Cross Linked Sulphonated Poly(ether ether ketone) for the Development of Polymer Electrolyte Membrane Fuel Cell Abdul Ghaffar Al Lafi, MSc. A Thesis Submitted for the Degree of Doctor of Philosophy The School of Metallurgy and Materials, The College of Engineering and Physical Sciences, The University of Birmingham, Birmingham, UK. September 2009 University of Birmingham Research Archive e-theses repository This unpublished thesis/dissertation is copyright of the author and/or third parties. The intellectual property rights of the author or third parties in respect of this work are as defined by The Copyright Designs and Patents Act 1988 or as modified by any successor legislation. Any use made of information contained in this thesis/dissertation must be in accordance with that legislation and must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the permission of the copyright holder. Synopsis Ion irradiation has been investigated as a route for the preparation of mechanically stable and highly durable cross linked sulphonated PEEK for fuel cell application. Ion irradiation was carried out using the University of Birmingham’s Scanditronix MC-40 Cyclotron operating at 11.7 MeV for H+ and 30 MeV for He2+ and the irradiated materials were characterized focusing on structural, thermal, morphological as well as dielectrical properties. Alterations produced in the molecular structure of amorphous PEEK by ion irradiation have been interpreted as due to chain scission and formation of cross links, as confirmed by sol-gel analysis in MSA using the well known Charlesby–Pinner equation. The thermal decomposition of irradiated PEEK was similar to that of untreated PEEK in that it occurred by a random chain scission process. -
Chapter 1 POLYIMIDES
Chapter 1 POLYIMIDES: chemistry & structure-property relationships – literature review 1.1 Introduction Polyimides are a class of thermally stable polymers that are often based on stiff aromatic backbones. The chemistry of polyimides is in itself a vast area with a large variety of monomers available and several methodologies available for synthesis. However, there has been considerable debate on the various reaction mechanisms involved in different synthesis methods. This review however, covers only the important fundamentals regarding the polyimide synthesis. The focus in this review will rest only on ‘aromatic’ polyimides as they constitute the major category of such materials. Secondly, the properties of polyimides can be dramatically altered by minor variations in the structure. The subtle variations in the structures of the dianhydride and diamine components have a tremendous effect on the properties of the final polyimide. This chapter reviews several such features that are important towards understanding these structure-property relationships. Specifically, the effects of changing the diamines, dianhydrides or the overall flexibility of the chain on the basic parameters like Tg and Tm are also examined. 1.2 Two step method for polyimide synthesis The most widely practiced procedure in polyimide synthesis is the two-step poly(amic acid) process. It involves reacting a dianhydride and a diamine at ambient conditions in a dipolar aprotic solvent such as N,N-dimethylacetamide (DMAc) or N- methylpyrrolidinone (NMP) to yield the corresponding poly(amic acid), which is then CHAPTER 1 3 cyclized into the final polyimide. This process involving a soluble polymer precursor was pioneered by workers at Dupont1 in 1950’s, and to this day, continues to be the primary route by which most polyimides are made. -
US3636140.Pdf
Jan. 18, 1972 A. F. INGULLI ETA 3,636,140 THERMOPLASTIC RESIN BLEND OF POLY SULFONE WITH ABS Filed Aug. 4, 1969 5. Sheets-Sheet, 2. R O /O 20 30 40 0 60 22 80 20 M22 (7, AOA. Yuo/MAOM/A /W AA S adze wa /MVA MV7 OAS Air 7- 4. a Zafa AA A. MM/G/ZZ / A/a. Mary A. at 7A air 2- 9% agew, Jan. 18, 1972 A. F. NGULL ET All- 3,636,140 "I HERMOPLASTIC RESIN BLEND OF POLYSULFONE WITH ABS Filed Aug. 4, 1969 5. Sheets-Sheet 3 S | | | | | | \ / | | | | |\ 1 \ | | | | | | | | \ | | | | | | | N TTTTTTTT O 3O 20 O SO 70 so 90 /OO 7. AozYuva /owa w Aaj azawo 2g z 7-5 MM/a M72A S. AAAAAA M. MMMGO/4 AM AyAAMA 1 A... a A. JAA larus 9.4 AG AW 7 Jan. 18, 1972 A. F. NGULL FT All- 3,636,140 TERMOPLASTIC RESIN BLEND OF POLYSULFONE WITH ABS Filed Aug. 4, 1969 5 Sheets-Sheet 4. 24.0 -- -T 22.ol | | | || 20.0 I Y Mas t SR I W. n w /4.0 | -- N - S v 2.0 HI N | n N S s S. v O /O 20 30 10 60 60 70 &0 70 /00 7./oz ruz/z/-owa //v4 as aza/v4 MM VAM/OA 27zz7 a AAAMAA A. MM6t/44/ A/AMMA)1 A. az Zafa 9ers /.4- a 47AM/7 Jan. 18, 1972 A. F. NGULL ET All- 3,636,140 THERMOPLASTIC RESIN BLEND OF POLYSULFONE WITH ABS Filed Aug. 4, 1969 5 Sheets-Sheet 5 JO J00 290 28 O 270 28 O 25 O 24 O 2.3 O O O 20 JO 40 50 60 70 8 O 3 O LOO % AOZyura/4 MoM2 //v 44, aza/V2 , , , . -
Preparation and Characterization of Polystyrene Hybrid Composites Reinforced with 2D and 3D Inorganic Fillers
micro Article Preparation and Characterization of Polystyrene Hybrid Composites Reinforced with 2D and 3D Inorganic Fillers Athanasios Ladavos 1,* , Aris E. Giannakas 2 , Panagiotis Xidas 3, Dimitrios J. Giliopoulos 3 , Maria Baikousi 4 , Dimitrios Gournis 4 , Michael A. Karakassides 4 and Konstantinos S. Triantafyllidis 3 1 Laboratory of Food Technology, Department of Business Administration of Food and Agricultural Enterprises, University of Patras, 30100 Agrinio, Greece 2 Department of Food Science and Technology, University of Patras, 30100 Agrinio, Greece; [email protected] 3 Department of Chemistry, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece; [email protected] (P.X.); [email protected] (D.J.G.); [email protected] (K.S.T.) 4 Department of Materials Science & Engineering, University of Ioannina, 45110 Ioannina, Greece; [email protected] (M.B.); [email protected] (D.G.); [email protected] (M.A.K.) * Correspondence: [email protected] Abstract: Polystyrene (PS)/silicate composites were prepared with the addition of two organoclays (orgMMT and orgZenith) and two mesoporous silicas (SBA-15 and MCF) via (i) solution casting and (ii) melt compounding methods. X-ray diffraction (XRD) analysis evidenced an intercalated structure for PS/organoclay nanocomposites. Thermogravimetric analysis indicated improvement in the thermal stability of PS-nanocomposites compared to the pristine polymer. This enhancement was more prevalent for the nanocomposites prepared with a lab-made organoclay (orgZenith). Citation: Ladavos, A.; Giannakas, Tensile measurement results indicated that elastic modulus increment was more prevalent (up to A.E.; Xidas, P.; Giliopoulos, D.J.; 50%) for microcomposites prepared using mesoporous silicas as filler. Organoclay addition led to Baikousi, M.; Gournis, D.; a decrease in oxygen transmission rate (OTR) values.