Characteristics of Thermoplastics for Ultrasonic Assembly Applications

Total Page:16

File Type:pdf, Size:1020Kb

Characteristics of Thermoplastics for Ultrasonic Assembly Applications Characteristics of Thermoplastics for Ultrasonic Assembly Applications Basic Principles Near-Field / Far-Field Welding The basic principle of ultrasonic assembly involves conversion Before discussing welding characteristics, the difference be - of high-frequency electrical energy to high-frequency me - tween near-field and far-field welding must be understood. chanical energy in the form of reciprocating vertical motion, Near-field welding refers to welding a joint located 1/4 inch which, when applied to a thermoplastic, can generate frictional (6 mm) or less from the area of horn contact; while far-field heat at the plastic/plastic or plastic/metal interface. In ultra - welding refers to welding a joint located more that 1/4 inch sonic welding, this frictional heat melts the plastic, allowing (6 mm) from the horn contact area. The greater the distance the two surfaces to fuse together; in ultrasonic staking, form - from the point of horn contact to the joint, the more difficult it ing or insertion, the controlled flow of the molten plastic is used will be for the vibration to travel through the material, and for to capture or retain another component in place (staking/form - the welding process to take place. ing) or encapsulate a metal insert (insertion). The differential, if any, in the melt temperature of the materials Thermoplastics can be ultrasonically assembled because they being welded should not exceed 30 degrees F (17 degrees C), melt within a specific temperature range, whereas thermoset - and the materials’ molecular structure should be compatible; ting materials, which degrade when heated are unsuitable for i.e.: blends, alloys, copolymers, and terpolymers. Moisture ultrasonic assembly. content, mold release agents, lubricants, plasticizers, fillers, reinforcing agents, regrinds, pigments, flame retardants, and Weldability of any thermoplastic depends on its stiffness or resin grade are all variables that can influence weldability. modulus of elasticity, density, coefficient of friction, thermal conductivity, specific heat and T or T . m g Variables Influencing Weldability Rigid plastics exhibit excellent welding properties because they readily transmit vibratory energy. Soft plastics, having a The moisture content of parts molded from resins that are hy - low modulus of elasticity, attenuate the ultrasonic vibrations, groscopic (moisture absorbent) can be problematical. Nylon and as such are more difficult to weld. In staking, forming or (and to a lesser degree polycarbonate and polysulfone) pres - spot welding, the opposite is true. Generally, the softer the ent most of the problem, and parts molded in these resins plastic, the easier it is to stake, form or spot weld. should be stored in sealed polyethylene bags with an appro - priate dessicant immediately after molding. If moist parts are Resins welded, the escaping vapors may cause voids and fissures in the molten material resulting in a weld of poor integrity. Resins are classified as amorphous or crystalline. Mold release agents such as zinc stearate, aluminum stearate, Ultrasonic energy is easily transmitted through amorphous fluorocarbons and silicones are not compatible with ultrasonic resins and as such, these resins lend themselves readily to ul - welding. If it is necessary to use a mold release agent, the trasonic welding. Amorphous resins are characterized by ran - paintable/printable grades that permit painting and silk screen - dom molecular arrangements, and a broad melting ing should be considered. Other release agents should be re - temperature range that allows the material to soften gradually moved with either TF Freon for crystalline resins or a 50/50 before melting and flow without prematurely solidifying. solution of water and liquid detergent. Because the molecular structure in the crystalline resins at - Lubricants, whether waxes, stearates or fatty esters, reduce tenuate a great amount of energy, crystalline resins do not intermolecular friction within the polymer and inhibit the ultra - readily transmit ultrasonic energy, and they require higher en - sonic assembly process. However, since they are generally dis - ergy levels than amorphous resins. These resins are charac - persed internally, their effect is usually negligible. terized by a high, sharply defined melting point that causes Plasticizers, which usually impart flexibility and softness to a melting and resolidification to occur rapidly. For these reasons, resin can interfere with a resin’s ability to transmit vibratory when welding crystalline resins, higher amplitude and energy energy. FDA-approved plasticizers do not present as much of levels should be used, and special consideration should be a problem as metallic plasticizers, but experimentation is given to joint design. recommended. 1 Although fillers and reinforcing agents such as glass and talc tic has not been degraded. Regrind limitations suggested by can increase the ultrasonic weldability of soft thermoplastics the resin suppliers should be observed. considerably, they should be judiciously used. When additive Although most pigments do not interfere with the ultrasonic content exceeds 10%, premature horn wear may result, and process, some oil-based colorants can adversely influence specially treated steel or carbide-faced titanium horns might weldability. Non-oil based pigments should be used. be required. When filler content approaches 35%, there may be insufficient resin at the surface to attain hermetic seals; and Flame retardants greatly affect the weldability of thermoplas - when filler content exceeds 40%, insufficient plastic is present tics and the effects of these various additives should be in - at the interface to form a positive bond. Reinforcement com - vestigated experimentally prior to resin selection. The grade of posed of long glass fibers are always more problematical than resin can have a significant influence on weldability. There is a reinforcement composed of short glass fibers. great difference between injection/extrusion grades and cast grades. Their molecular weight, melt temperature and modu - Ultrasonic assembly is one of the few methods that permits lus of elasticity are quite different. Injection/extrusion grades regrinding of parts, since no foreign substance is introduced should only be used with injection/extrusion grades, and cast into the resin. Ultrasonically assembling parts which have been grades should only be used with cast grades. manufactured from regrind parts presents no problem provided that the percentage of regrind is not excessive, and the plas - . 2 Chart I Characteristics of Thermoplastics FIELD OF WELDING SPOT STAKING MATERIAL WELDING SWAGING INSERTING NEAR FAR AMORPHOUS: ABS EEEEG ABS/POLYCARBONATE GGGGF ABS/PVC GGFGF ACRYLIC GFGGF ACRYLIC MULTI-POLYMER-XT POLYMER GGGGF ACRYLIC/PVC GGFGF ACRYLIC – IMPACT MODIFIED FFPFP BUTADIENE – STYRENE (BDS) GGGGF CELLULOSICS – CA, CAB, CAP PGEP – MODIFIED PHENYLENE OXIDE EEEEG POLYARYLATE FFGGF POLYCARBONATE GFGGF POLYETHERIMIDE GGE EG POLYSTYRENE, G.P. FFGEE POLYSTYRENE, IMPACT MODIFIED FFGGP PVC – RIGID FGEPP PVC – FLEXIBLE P––P– SAN – NAS – ASA FFGEE STYRENE-MALEIC-ANHYDRIDE EEEEG SULFONE POLYMERS FFGGF CRYSTALLINE: ACETAL COPOLYMER FFGGF ACETAL HOMOPOLYMERS FFGGF FLUOROPOLYMERS –––P– NYLON FFGGF PC-PET GGE EG POLYESTER – PBT FFGGF POLYESTER – PET FFGGF POLYETHERETHERKETONE GGE EG POLYETHYLENE (LDPE, HDPE) GFGPP POLYETHYLENE (UHMW) ––––– POLYMETHYLPENTENE GFEFP POLYPHENYLENE SULFIDE FPGGF POLYPROPYLENE EEGF-P P E - Excellent G - Good F - Fair P - Poor – Not Suitable for Ultrasonic Assembly . 3 Chart II Compatibility of Thermoplastics E D I R R E D E Y N H E M O T T Y N L A E A - N O K E E E C P R O I T T T I D N E E E B I A B E T E E L H N R S L E P P N M L I T A N - - E A T C U Y O I L E R R R R A C M S P B S M E E Y - R L E E S Y E R O E T T O Y Y L H H H C C C N A I I L R T L S S T T T N R T O V N L L O C E E E E E P S A E U A E P P O Y Y T / / O F L Y Y Y Y Y Y Y Y Y R P P L L L L L L L L L S R E R L / L L S S S N C Y P E Y D B C C C B B C O O O O O O O O O V A U T A A A A C A A B M N P P P P P P P P P P P S A S ABS I G I GGG GI ACRYLIC MULTI POLYMER G I GGG G ACETAL I ACRYLICS I G I GG GI CELLULOSICS I ABS/POLYCARBONATE GG G I GG G ABS/PVC GG G GI GG BDS G I GG MPPO I G NYLON I PC/PET I GG POLYARYLATE I POLYCARBONATE GGI G POLYESTER-PBT I POLYESTER-PET G I POLYETHERTHERKETONE I POLYETHERIMIDE I POLYETHYLENE I POLYPROPYLENE I POLYSTYRENE GG I GG PVC G I SAN GG G G I G ATYRENE-MALEIC-ANHYDRIDE IIGGG G G GI SULFONES I I Denotes compatibility G Denotes some compatibility, but not all grades and compositions are compatible. © 2016 Sonics & Materials, Inc. Specifications subject to change without notice. Not responsible for 10000819 ISO 9001 Corporate Headquarters 53 Church Hill Road, Newtown, CT 06470 USA typographical errors. 203.270.4600 800.745.1105 203.270.4610 fax [email protected] Printed in U.S.A. 1C/06/16 Sonics & Materials, Inc..
Recommended publications
  • Chlorine Dioxide Compatibility Assessment
    Chlorine Dioxide Compatibility Assessment DRF3366 - TECH-COMM-001 Created by: Tristel Solutions Limited, Lynx Business Park, Cambs, UK, CB8 7NY Copyright © Tristel Solutions T +44 (0) 1638 721500 – E [email protected] – W www.tristel.com January 2018 Key - Excellent - no change at all in the device - Good - slight cosmetic change/ decolourisation – material/device still fully functional - Fair – slight damage is observed– material/device still fully functional - Poor – visible pitting, breaking, brittle METALS Materials of construction 1 2 3 4 (Excellent) (Good) (Fair) (Poor) Stainless Steel 317 (Pure) X Stainless Steel 316 (pure, fully X austenitic with no ferric content) Stainless Steel 304 X (High grade, low ferric content) Hastelloy X Titanium X Aluminium X Aluminium (Anodised) X Brass X Copper X Chrome X Mild Steel X DRF3366 - TECH-COMM-001 Created by: Tristel Solutions Limited, Lynx Business Park, Cambs, UK, CB8 7NY Copyright © Tristel Solutions T +44 (0) 1638 721500 – E [email protected] – W www.tristel.com January 2018 PLASTICS Materials of construction 1 2 3 4 (Excellent) (Good) (Fair) (Poor) Perfluoroelastomer X PEEK X X Polypropylene X PVDF X X Polycarbonate X Polysulphone (natural) X Polysulphone (white) X PET-P X PMMA X Polyamide X Polyethylene X Polyoxymethylene X Acetal X ABS X Polymethylpentene (TPX) (PMP) X DRF3366 - TECH-COMM-001 Created by: Tristel Solutions Limited, Lynx Business Park, Cambs, UK, CB8 7NY Copyright © Tristel Solutions T +44 (0) 1638 721500 – E [email protected] – W www.tristel.com January 2018 PLASTICS
    [Show full text]
  • TPX® Datasheet
    Metals & Materials for Research and Industry TPX® Datasheet GOODFELLOW & MITSUI & CO. EUROPE PLC TPX® Polymethylpentene (PMP) TPX®, a 4-methylpentene-1 based polyolefin manufactured solely by Mitsui Chemicals, Inc. is now available in small order lots from Goodfellow. This lightweight, functional polymer displays a unique combination of physical properties and characteristics due to its distinctive molecular structure. Because of its superb chemical resistance and optical clarity TPX® is an ideal choice when replacing polycarbonate or acrylic in some chemically demanding environments. • High heat resistance (melt temperature 236°C) • Lowest specific gravity of any known polymer (0.833 g/cc) CH CH2 CH CH2 • Superior steam sterilisation capabilities • Superior transparency to visible light CH CH • Excellent UV transmission characteristics 2 2 • Lower refractive index than other transparent resins CH CH • Excellent acoustic properties • Excellent chemical resistance H C CH H C CH • High gas and moisture permeability 3 3 3 3 • Outstanding dielectric properties The properties of TPX® make it ideal for extruding items such as film and paper coating, injection moulded items and blow moulded components, and we list some of the possible applications below: • Release film • Release paper for synthetic leather • LED moulds • Mandrels and sheaths for hose and cable use • Cosmetic caps and tubes • Heat resistant non-woven fabric and fibres • Chemical tubes • Animal cages • Sterilisation containers Goodfellow Cambridge Ltd [email protected] Ermine
    [Show full text]
  • Labware Chemical Resistance Table
    Labware Chemical Resistance Table Interpretation of Chemical Resistance The Chemical Resistance Chart that follows is a general guide only. Because so many factors can affect the chemical resistance of a given product, you should test under your own conditions. Effects of Chemicals on Plastics Chemicals can affect the strength, flexibility, surface appearance, color, dimensions or weight of plastics. The basic modes of interaction which cause these changes are: (1) chemical attack on the polymer chain, with resultant reduction in physical properties, including oxidation; reaction of functional groups in or on the chain; and depolymerization; (2) physical change, including absorption of solvents, resulting in softening and swelling of the plastic; permeation of solvent through the plastic; dissolution in a solvent; and (3) stress cracking from the interaction of a “stress cracking agent” with internal or external stresses. Mixing and/or dilution of certain chemicals can be potentially dangerous. The reactive combination of different chemicals or compounds of two or more classes may cause an undesirable chemical effect or result in an increased temperature, which can affect chemical resistance (as temperature increases, resistance to attack decreases). Other factors affecting chemical resistance include pressure and internal or external stresses (e.g. centrifugation), length of exposure, and concentra tion of the chemical. 608 www.thermoscientifi c.com appendix Environmental Stress Cracking Environmental stress cracking is the failure of a plastic material in the presence of certain types of chemicals. This failure is not a result of chemical attack. Simultaneous presence of three factors causes stress cracking: tensile stress, a stress cracking agent and the inherent susceptability of the plastic to stress cracking.
    [Show full text]
  • Adhesive Bonding of Polyolefin Edward M
    White Paper Adhesives | Sealants | Tapes Adhesive Bonding of Polyolefin Edward M. Petrie | Omnexus, June 2013 Introduction Polyolefin polymers are used extensively in producing plastics and elastomers due to their excellent chemical and physical properties as well as their low price and easy processing. However, they are also one of the most difficult materials to bond with adhesives because of the wax-like nature of their surface. Advances have been made in bonding polyolefin based materials through improved surface preparation processes and the introduction of new adhesives that are capable of bonding to the polyolefin substrate without any surface pre-treatment. Adhesion promoters for polyolefins are also available that can be applied to the part prior to bonding similar to a primer. Polyolefin parts can be assembled via many methods such as adhesive bonding, heat sealing, vibration welding, etc. However, adhesive bonding provides unique benefits in assembling polyolefin parts such as the ability to seal and provide a high degree of joint strength without heating the substrate. This article will review the reasons why polyolefin substrates are so difficult to bond and the various methods that can be used to make the task easier and more reliable. Polyolefins and their Surface Characteristics Polyolefins represent a large group of polymers that are extremely inert chemically. Because of their excellent chemical resistance, polyolefins are impossible to join by solvent cementing. Polyolefins also exhibit lower heat resistance than most other thermoplastics, and as a result thermal methods of assembly such as heat welding can result in distortion and other problems. The most well-known polyolefins are polyethylene and polypropylene, but there are other specialty types such as polymethylpentene (high temperature properties) and ethylene propylene diene monomer (elastomeric properties).
    [Show full text]
  • Thz Materials
    THz Materials Terahertz (THz) radiation is located in the spectral region ~0.1-10 THz (~3 mm - 30 µm, 3 cm-1 - 300 cm-1 ) between the microwave and mid infrared range of the electromagnetic spectrum. In comparison with visible or infrared waves, THz radiation can penetrate into organic materials such as skin, plastics, cloth, or paper products. Because of low photon energy involved, it does not cause any damage associated with ionizing radiation (e.g. X-rays). THz waves do not penetrate into metals. These properties can be used in process (e.g. drugs manufacturing) and quality control as well as in THz imaging. It is also of great current interest for such applications as safety control, packaging inspection, semiconductor characterization, chemical composition analysis, and biomedical investigations, with great promise for spectroscopy, defense imaging, and security applications. Fig. 2. The THz signals transmitted through air and HRFZ-Si.(*) Traditionally for THz applications we use High Resistivity Float Zone The complex dielectric permittivity of silicon depends on its Silicon (HRFZ-Si) as it is the most investigated substance for operating conductivity (i.e. free-carrier concentration). Figure 3 shows the within this range and has a good transmission performance. In parallel dielectric permittivity of silicon at 1 THz with different impurity with this material we have been investigating other materials which concentration. For low impurity concentration the dielectric also can be utilized in THz range. permittivity is almost a real value, which is approximately equal Below you can see transmission spectra and other characteristics of to the high frequency dielectric permittivity.
    [Show full text]
  • Iapd Thermoplastics Rectangle
    IAPD THERMOPLASTICS RECTANGLE IMIDIZED Key Characteristics Materials Very high cost per pound Polyimide (PI) High Cost Excellent physical properties above 400 degrees F Polyamide Imide (PAI) High Strength Excellent electrical properties Polybenzimidazole (PBI) High Temperature Excellent dimensional stability Low coefficient of friction (COF) AMORPHOUS HIGH PERFORMANCE THERMOPLASTICS SEMI-CRYSTALLINE HIGH PERFORMANCE THERMOPLASTICS Key Characteristics Materials Key Characteristics Materials High cost Polysulfone (PSU) High cost Polyvinylidene Fluoride (PVDF) High temperature Polyetherimide (PEI) High temperature Polytetrafluoroethylene (PTFE) High strength and good stiffness Polyethersulfone (PES) High strength Ethylene-Chlorotrifluoroethylene (ECTFE) Good chemical resistance Polyarylsulfone (PAS) Good chemical resistance Fluorinated Ethylene Propylene (FEP) Transparent Polyarylethersulfone (PAES) Good electrical properties Polychlorotrifluoroethylene (PCTFE) Hot water and steam resistance Low COF Perfluoroalkoxy (PFA) Good toughness Polyphenylene Sulfide (PPS) Polyetheretherketone (PEEK) AMORPHOUS ENGINEERING THERMOPLASTICS SEMI-CRYSTALLINE ENGINEERING THERMOPLASTICS Key Characteristics Materials Key Characteristics Materials Moderate cost Polycarbonate (PC) Moderate cost Nylon (PA) Moderate temperature resistance Polyphenylene Oxide (Mod PPO) Moderate temperature resistance Acetal (POM) Moderate strength Polyphenylene Ether (Mod PPE) Moderate strength Polyethylene Terephthalate (PET) Good to excellent impact resistance Thermoplastic
    [Show full text]
  • Chemical Compatibility Quick Reference Chart Chemical Resistance Classification Resin Codes E 30 Days of Constant Exposure Causes No Damage
    Chemical Compatibility Quick Reference Chart Chemical Resistance Classification Resin Codes E 30 days of constant exposure causes no damage. Plastic ECTFE Halar* ECTFE (ethylene-chlorotrifluoroethylene copolymer) ETFE Tefzel† ETFE (ethylene-tetrafluoroethylene) may even tolerate for years. FEP Teflon† FEP (fluorinated ethylene propylene) FLPE fluorinated high-density polyethylene G Little or no damage after 30 days of constant exposure FLPP fluorinated polypropylene to the reagent. HDPE high-density polyethylene LDPE low-density polyethylene F Some effect after 7 days of constant exposure to the PC polycarbonate PETG polyethylene terephthalate copolyester reagent. Depending on the plastic, the effect may be PFA Teflon† PFA (perfluoroalkoxy) crazing, cracking, loss of strength or discoloration. PMMA polymethyl methacrylate (acrylic) PMP polymethylpentene (“TPX”) Solvents may cause softening, swelling and permeation PP polypropylene losses with LDPE, HDPE, PP, PPCO and PMP. The PPCO polypropylene copolymer solvent effects on these five resins are normally PPO polyphenylene oxide PS polystyrene reversible; the part will usually return to its normal PSF polysulfone condition after evaporation. PUR polyurethane PVC polyvinyl chloride N Not recommended for continuous use. Immediate PVDF polyvinylidene fluoride ResMer ResMer™ Manufacturing Technology damage may occur. Depending on the plastic, the effect SAN styrene acrylonitrile will be a more severe crazing, cracking, loss of strength, TFE Teflon† TFE (tetrafluoroethylene) TPE thermoplastic
    [Show full text]
  • Solvent Compatibility-Plastic Resin.P65
    1022 Spruce Street PO Box 1502 Vineland, NJ 08362-1502 888-546-2531 HAI 508-893-8999 HAI 508-429-5732 Fax TECHNICAL INFORMATION (Courtesy Harvard Apparatus): [email protected] Solvent Compatibility – Plastic Resin www.harvardapparatus.com Plastic Resin Codes C (lMin) C (Max) º º Abbreviation Chemical Designation Temp Temp Autoclavable Microwavable Dry Heat Gas Gamma Disinfectants ABS Acryl-Butadienestyrene 100 -40 NO YES NO YES YES YES Acetal (Delrin®, Celcon®) 100 -40 NO YES NO YES YES YES LDPE Low Density Polyethylene 100 -80 NO YES NO YES YES YES HDPE High Density Polyethylene 120 -100 NO YES NO YES YES YES NYL Polyamide (Nylon®) 90 0 NO YES NO YES YES YES PCTFE Polychlorotrifluoroethylene (Kel-F®) 80 0 NO YES NO YES YES YES PC Polycarbonate 135 0 YES YES NO YES YES YES PP Polypropylene 135 0 YES YES NO YES NO YES PTFE Polytetrafluoroethylene (Teflon®) 250 -267 YES YES YES YES YES YES PVC Polyvinyl Chloride 70 -30 NO YES NO YES NO YES PVDF Kynar (polyvinyldene fluoride) 110 -62 YES YES NO YES NO YES E-CTFE Ethylene Chlortrifluoroethylene 150 -105 YES YES YES YES NO YES ETFE EthyleneTetrafluoroethylene (Tefzel®) 150 -105 YES YES YES YES NO YES PFA Perfluoroalkoxy (Teflon®) 260 -270 YES YES YES YES NO YES San Styrene 95 -20 NO YES NO YES YES YES PMP Polymethylpentene (TPX) 175 -70 YES YES NO YES YES YES PMMA Polymethylmetyacrylate (PMMP) 50 0 NO YES NO YES YES YES PS Polystyrene 90 -20 NO YES NO YES YES YES PEEK Polyetheretherketone 125 0 YES YES NO YES YES YES TFE Tetrafluoroethylene (Teflon®) 260 -267 YES YES YES YES YES YES PDF
    [Show full text]
  • Long Term Blood Oxygenation Membranes
    University of Kentucky UKnowledge Theses and Dissertations--Biomedical Engineering Biomedical Engineering 2015 Long Term Blood Oxygenation Membranes Joseph V. Alexander University of Kentucky, [email protected] Right click to open a feedback form in a new tab to let us know how this document benefits ou.y Recommended Citation Alexander, Joseph V., "Long Term Blood Oxygenation Membranes" (2015). Theses and Dissertations-- Biomedical Engineering. 28. https://uknowledge.uky.edu/cbme_etds/28 This Doctoral Dissertation is brought to you for free and open access by the Biomedical Engineering at UKnowledge. It has been accepted for inclusion in Theses and Dissertations--Biomedical Engineering by an authorized administrator of UKnowledge. For more information, please contact [email protected]. STUDENT AGREEMENT: I represent that my thesis or dissertation and abstract are my original work. Proper attribution has been given to all outside sources. I understand that I am solely responsible for obtaining any needed copyright permissions. I have obtained needed written permission statement(s) from the owner(s) of each third-party copyrighted matter to be included in my work, allowing electronic distribution (if such use is not permitted by the fair use doctrine) which will be submitted to UKnowledge as Additional File. I hereby grant to The University of Kentucky and its agents the irrevocable, non-exclusive, and royalty-free license to archive and make accessible my work in whole or in part in all forms of media, now or hereafter known. I agree that the document mentioned above may be made available immediately for worldwide access unless an embargo applies.
    [Show full text]
  • Industry Acronyms
    INDUSTRY ACRONYMS AAS — Methacrylate-acrylic-styrene JIT — Just-in-time (delivery) PTFE — Polytetrafluoroethylene ABS — Acrylonitrile-butadiene-styrene LCD — Liquid crystal display PTMT — Polytetramethylene terephthalate AN — Acrylonitrile LCP — Liquid crystal polymer PUR — Polyurethane AO — Antioxidant L/D — Length:diameter ratio PVAC — Polyvinyl acetate APP — Atactic polypropylene LDPE — Low-density polyethylene PVAL — Polyvinyl alcohol AS — Antistatic LIM — Liquid injection molding PVC — Polyvinyl chloride ASA — Acrylonitrile-styrene-acrylate LLDPE — Linear low-density polyethylene PVCA — Polyvinyl chloride acetate ASTM — American Society for Testing & Materials LSM — Liquid silicone molding PVCC — Chlorinated polyvinyl chloride BMC — Bulk molding compound MAP — Modified atmosphere packaging PVDC — Polyvinylidene chloride BOPP — Biaxially oriented polypropylene MPC — Microprocessor-controlled PVDF — Polyvinylidene fluoride CAD — Computer-aided design MSDS — Material Safety Data Sheet PVF — Polyvinyl fluoride CAM — Computer-assisted manufacturing MDPE — Medium-density polyethylene QC — Quality control CAMM — Canadian Association of Mouldmakers MI — Melt index RAPRA — Rubber and Plastics Association (U.K.) CAP — Controlled atmosphere packaging mLLDPE — Metallocene linear low-density R&D — Research and development CFC — Chlorofluorocarbon polyethylene RFI — Radio frequency interference CIM — Computer-integrated manufacturing MMW — Medium molecular weight RFID — Radio frequency identification CM — Compression molding MRP — Materials requirement
    [Show full text]
  • Plastics Technology | Overview of Chemical Resistance
    Plastics technology | overview of chemical resistance EPDM Ethylene propylene diene monomer PA Polyamide PSU Polysulfone FEP Fluorinated ethylene-propylene (Tefl on, FEP) PC Polycarbonate PTFE Polytetrafl uoroethylene PETG Polyethyleneterephthalate PFA Perfl uoro-alkoxy (Tefl on, PFA) PVC Polyvinylchlorid FPM/FKM Fluoroelastomer (Viton) PMP Polymethylpentene (TPX) PVDF Polyvinylidenfl uoride HDPE High-density polyethylene PP Polypropylene SAN Styrene-acrylnitrile LDPE Low-densitiy polyethylene PS Polystyrene SI Silicone rubber Plastics Temperature Sterilization 5) Transparency Flexibility Specific Water abbreviations max. °C min °C steam 4) gas radiation chemical weight absorption 1) 2) 121°C ethyleneoxide 2.5 kGy formalin,ethanol g/cm3 % EPDM + 120° - 30° yes no yes yes transparent excellent 0.88 0.01 FEP + 205° - 255° yes yes no yes transparent very good 2.15 < 0.01 FPM + 200° - 20° no no no no black good 1.90 0.20 HDPE + 110° - 50° no yes yes yes transparent stiff 0.95 0.01 LDPE + 95° - 50° no yes yes yes transparent excellent 0.92 0.01 PA + 90° 0° no yes yes yes transparent stiff 1.13 1.30 PC + 135° - 135° yes yes yes yes clear rigid 1.20 0.35 PFA + 250° - 270° yes yes no yes transparent excellent 2.15 0.03 PMP + 175° - 150° yes yes yes yes glass-clear stiff 0.83 0.01 PP + 135° + 5° yes yes no yes transparent stiff 0.90 0.02 PS + 70° - 20° no no yes yes glass-clear stiff 1.05 0.05 PSU + 165° - 100° yes yes yes yes clear stiff 1.24 0.30 PTFE + 270° - 270° yes yes no yes white excellent 2.25 < 0.01 PVC + 70° - 30° no3) yes no yes clear stiff 1.35 0.06 PVDF + 160° - 40° yes yes yes yes transparent stiff 1.78 0.04 SAN + 95° - 40° no yes no yes glass-clear stiff 1.03 0.05 SI + 180° - 60° yes yes no yes transparent excellent 1.10 n/a PETG + 70° + 5° no yes yes yes glass-clear stiff 1.78 0.70 1) Even higher for short periods 5) Clean apparatus with distilled water fi rst (to avoid stress cracking corrosion).
    [Show full text]
  • ABS Acrylonitrile-Butadiene-Styrene ACM-V Vulcanized Acrylate Rubber
    ABS Acrylonitrile-Butadiene-Styrene ACM-V Vulcanized acrylate rubber ACS Acrylonitrile Chlorinated polyethylene Styrene AES or AEPDS Acrylonitrile EPDM Styrene ASA Acrylonitrile Styrene Acrylate BMC Bulk Moulding Compound BOPP Bi-axially Oriented PolyPropylene CA Cellulose Acetate CAB Cellulose AcetoButyrate CBT Cyclic polyButadiene Terephthalate CE Cyanate Ester CF Carbon Fibre CFC ChloroFluoroCarbon CM or CPE Chlorinated PolyEthylene COPE or TPEE COPolyEster TPE CP Cellulose Propionate CPE or CM Chlorinated PolyEthylene CPVC or PVC-C Chlorinated PVC Cy PolyCyanate DAP DiAllyl Phthalate DCPD Poly(DiCycloPentaDiene) DMC Dough Moulding Compound EBA, EGMA Ethylene-acid and ethylene-ester copolymers e.g. Ethylene-ButylAcrylate ECTFE, EEA, EMAH, EAA Ethylene monoChloroTriFluoroEthylene EMA Ethylene-MethAcrylate ionomers EMI ElectroMagnetic Interference EP EPoxy EPDM rubber Terpolymer ethylene propylene diene EPS Expandable (or Expanded) PolyStyrene ETFE Ethylene-TetraFluoroEthylene EVA E/VAC Ethylene-VinylAcetate copolymers EVAC /VAE/ EVM /EVOH Ethylene-Vinyl alcohol copolymers F-PVC Flexible PVC FEP Fluorinated Ethylene Propylene GFRP Glass Fibre Reinforced Plastic HDPE or PE HD High Density PolyEthylene HPGF High-Performance short Glass Fibre reinforced polypropylene HTPC Hybrid ThermoPlastic Composite LDPE or PE LD Low Density PolyEthylene LFRT Long Fibre Reinforced Thermoplastic LFT Long Fibre reinforced Thermoplastic LGF Long Glass Fibre LIM Liquid Injection Moulding LLDPE Linear Low Density PolyEthylene LSR Liquid Silicone Rubber LWRT
    [Show full text]