Knowledge (XXG)

Ionomer

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physical properties of the ionomer; the most commonly used metal cations (at least in academic research) are zinc, sodium, and magnesium. Neutralization or ionomerization, can also be accomplished in two ways: the acid copolymer can be melt-mixed with a basic metal or neutralization can be achieved through solution processes. The former method is preferred commercially. However, as commercial manufacturers are reluctant to share their procedures, little is known about the exact conditions of the melt-mixing neutralization process other than that hydroxides are generally used to provide the metal cation. The latter solution neutralization process is generally used in academic settings. The acid copolymer is dissolved and a basic salt with the appropriate metal cation is added to this solution. Where dissolution of the acid copolymer is difficult, simply swelling the polymer in the solvent is sufficient, though dissolving is always preferred. Because basic salts are polar and are not soluble in the non-polar solvents used to dissolve most polymers, mixed solvents (e.g. 90:10 toluene/alcohol) are often used.
262:: In the packaging industry, ionomers are prized for their combination of optical clarity, toughness, and sealing properties. They can form strong, heat-sealable bonds. This makes them ideal for food packaging films. Both durability and transparency are important for these films. The films can protect the contents from external contaminants. They also provide a clear view of the product, enhancing consumer appeal. Additionally, ionomers are resistant to punctures and tears. This ensures that the packaging remains intact during transportation and handling. Furthermore, ionomers are resistant to oils and fats. This makes them particularly useful in packaging greasy or oily foods. The packaging maintains its integrity without degradation. 304:: Ionomers have potential applications in the biomedical field. They can be used in drug delivery systems and medical implants. Ionomers are biocompatible. They can interact with biological tissues. This makes them suitable for devices that require controlled release of drugs. They are also suitable for devices that need to integrate with living tissue. Research is ongoing to explore the use of ionomers in innovative medical applications. Their unique properties could offer new solutions for healthcare challenges. For example, ionomer-based drug delivery systems can provide targeted therapy. They can control the release rate of medications. This can improve the efficacy and reduce the side effects of treatments. 292:(TPEs). Their elasticity and ability to be remolded without significant degradation are advantageous. These materials can be stretched and deformed. They can return to their original shape when the stress is released. This makes them useful in applications requiring both flexibility and strength. TPEs based on ionomers are found in a wide range of products. These include footwear and medical devices. In these products, comfort, durability, and resilience are critical. Moreover, their resistance to chemical and UV degradation makes them ideal for outdoor applications. Long-term exposure to the elements is a concern in these applications. 298:: Ionomers are used in coatings and paints. Their adhesion properties and resistance to environmental damage make surfaces more durable. In automotive and industrial coatings, ionomers create protective layers. These layers resist corrosion, abrasion, and chemical exposure. Ionomers can form smooth, uniform coatings. This makes them suitable for applications needing both aesthetic and functional surface protection. Additionally, ionomer-based coatings have self-healing properties. Small scratches can be repaired through thermal treatment. This extends the lifespan of coated products and reduces maintenance costs. 256:: Ionomers are widely used to make golf ball covers. They are essential for these covers because they have impact resistance, toughness, and durability. The ionic crosslinks in the polymer structure allow the material to withstand the high forces of a golf swing. It keeps its shape and performance over time. The resilience from the ionic clusters helps the ball maintain its flight characteristics. This ensures the ball has a longer lifespan. Additionally, the material's excellent abrasion resistance reduces surface wear. This allows for consistent performance across many rounds of play. 282:: Ionomers have strong adhesive properties and are flexible. That's why they are used in adhesives and sealants. Ionomers can form strong bonds with different materials like metals, plastics, and glass. This makes them suitable for use in automotive, construction, and consumer goods. In sealants, ionomers provide excellent resistance to environmental factors like moisture and temperature changes. This ensures long-lasting performance even in harsh conditions. Ionomers maintain their flexibility, which is important in applications where materials expand or have mechanical stress. 310:: Ionomers are used to make ion-exchange resins. These resins are important for water treatment and purification. The resins are made from ionomer materials. The resins can selectively exchange ions in a solution. This allows them to remove unwanted contaminants like heavy metals. They can also soften water by exchanging calcium and magnesium ions with sodium or potassium ions. Ionomer-based resins are stable and durable. This makes them suitable for repeated use in industrial and household water treatment systems. 276:. This selective ion transport is crucial for the efficiency and effectiveness of these devices. It allows for controlled chemical reactions and energy production. In water purification, ionomer-based membranes can selectively remove contaminants. They allow pure water to pass through. This contributes to safe and efficient filtration processes. 268:: Ionomers are used to make semipermeable membranes. These membranes are used in applications that require selective ion transport. This includes fuel cells and water purification systems. The ionic domains in the ionomer structure allow ions to pass through selectively. They block other molecules. This makes ionomers ideal for use in 215:
In most cases, the acid form of the copolymer is synthesized (i.e. 100% of the carboxylic acid groups are neutralized by hydrogen cations) and the ionomer is formed through subsequent neutralization by the appropriate metal cation. The identity of the neutralizing metal cation has an effect on the
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Usually ionomer synthesis consists of two steps – the introduction of acid groups to the polymer backbone and the neutralization of some of the acid groups by a metal cation. In very rare cases, the groups introduced are already neutralized by a metal cation. The first step (introduction of acid
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Neutralization level must be determined after an ionomer is synthesized as varying the neutralization level varies the morphological and physical properties of the ionomer. One method used to do this is to examine the peak heights of infrared vibrations of the acid form. However, there may be
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devices, ionomers play a crucial role as solid electrolytes. Ionomers can conduct ions while acting as an insulating barrier for electrons. This makes them ideal for use in batteries, supercapacitors, and fuel cells. The ionomers' stability under electrochemical conditions ensures long-term
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groups) can be done in two ways; a neutral non-ionic monomer can be copolymerized with a monomer that contains pendant acid groups or acid groups can be added to a non-ionic polymer through post-reaction modifications. For example, ethylene-methacrylic acid and sulfonated
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substantial error in determining peak height, especially since small amounts of water appear in the same wavenumber range. Titration of the acid groups is another method that can be used, though this is not possible in some systems.
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are polymers where ionic groups are part of the actual polymer backbone. These two classes of ionic-group-containing polymers have vastly different morphological and physical properties and are therefore not considered ionomers.
120:). Ionomers also have unique morphological properties as the non-polar polymer backbone is energetically incompatible with the polar ionic groups. As a result, the ionic groups in most ionomers will undergo 778:
Spencer, M.W., M.D. Wetzel, C. Troeltzsch, and D.R. Paul. "Effects of Acid Neutralization on the Properties of K and Na Poly(ethylene-co-methacrylic Acid) Ionomers." Polymer 53 (2011): 569-80. Print.
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The classification of a polymer as an ionomer depends on the level of substitution of ionic groups as well as how the ionic groups are incorporated into the polymer structure. For example,
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Grady, Brian P. "Review and Critical Analysis of the Morphology of Random Ionomers Across Many Length Scales." Polymer Engineering and Science 48 (2008): 1029-051. Print.
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also have ionic groups covalently bonded to the polymer backbone, but have a much higher ionic group molar substitution level (usually greater than 80%);
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Lundberg, R. D. (1987), "Ionomer Applications Including Ionic Elastomers and Polymer/Fluid Additives", in Pineri, Michel; Eisenberg, Adi (eds.),
423: 365: 759: 731: 700: 325:(MEA). In the MEA, ionomers facilitate the transport of protons from the anode to the cathode. This enables the generation of electricity. 640:
Xu, Wu; Scott, Keith (2010-11-01). "The effects of ionomer content on PEM water electrolyser membrane electrode assembly performance".
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Zhang, Longhe; Brostowitz, Nicole R.; Cavicchi, Kevin A.; Weiss, R. A. (2014-02-01). "Perspective: Ionomer Research and Applications".
212:(Nafion) are synthesized through copolymerization while polystyrene sulfonate is synthesized through post-reaction modifications. 322: 431: 373: 796: 269: 811: 289: 136: 109: 244:, yielding the sodium salt. Crystals of ethylene-methacrylic acid ionomers exhibit dual melting behavior. 132: 140: 121: 649: 801: 456: 398: 448: 390: 117: 791: 755: 727: 721: 696: 665: 619: 749: 561: 688: 657: 611: 440: 382: 241: 237: 86: 26: 148: 317: 209: 97: 75: 653: 806: 785: 321:
performance and efficiency in these devices. In fuel cells, ionomers are used in the
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used as a coating and packaging material. DuPont neutralizes the acid with
116:—increase in ionomer solution viscosity with increasing temperatures (see 113: 424:"Glossary of basic terms in polymer science (IUPAC Recommendations 1996)" 366:"Glossary of basic terms in polymer science (IUPAC Recommendations 1996)" 345: 233: 101: 422:
Jenkins, A. D.; Kratochvíl, P.; Stepto, R. F. T.; Suter, U. W. (1996).
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Jenkins, A. D.; Kratochvíl, P.; Stepto, R. F. T.; Suter, U. W. (1996).
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Martin R. Tant; K. A. Mauritz; Garth L. Wilkes (31 January 1997).
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are ionized. The ionized units are often carboxylic acid groups.
481:"An Ionomer Resin Providing Clarity, Toughness, and Versatility" 79: 50: 38: 751:
Ionomers: Synthesis, Structure, Properties, and Applications
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Polymer containing many ionic or ionizable functional groups
687:, NATO ASI Series, Springer Netherlands, pp. 429–438, 44: 32: 228:
Surlyn is the brand name of an ionomer resin created by
195:: Some protein molecules may be classified as ionomer 524:"Structure and Properties of Crystallizable Ionomers" 41: 29: 108:Ionomers have unique physical properties including 82:units covalently bonded to the polymer backbone as 47: 35: 644:. VIII symposium of the Mexican Hydrogen Society. 160: 127:Commercial applications for ionomers include 8: 642:International Journal of Hydrogen Energy 505:. The University of Southern Mississippi 356: 139:. Common examples of ionomers include 7: 723:Structure and Properties of Ionomers 685:Structure and Properties of Ionomers 635: 633: 597: 595: 593: 591: 589: 587: 585: 583: 581: 556: 554: 552: 550: 548: 546: 544: 542: 540: 604:Macromolecular Reaction Engineering 14: 74:composed of repeat units of both 483:. du Pont de Nemours and Company 25: 712:Eisenberg, A. and Kim, J.-S., 662:10.1016/j.ijhydene.2010.08.055 183:significant proportion of the 1: 720:Michel Pineri (31 May 1987). 693:10.1007/978-94-009-3829-8_35 346:Ionomer primer with examples 124:to form ionic-rich domains. 78:neutral repeating units and 323:membrane electrode assembly 89:. Usually no more than 15 828: 432:Pure and Applied Chemistry 374:Pure and Applied Chemistry 189:or ionic groups, or both. 270:proton exchange membranes 754:. Springer. p. 16. 716:, New York: Wiley, 1998. 714:Introduction to Ionomers 562:"Properties of Ionomers" 290:thermoplastic elastomers 286:Thermoplastic Elastomers 165:: A polymer composed of 137:thermoplastic elastomers 445:10.1351/pac199668122287 387:10.1351/pac199668122287 314:Electrochemical Devices 302:Biomedical Applications 288:: Ionomers are used as 266:Semipermeable Membranes 133:semipermeable membranes 110:electrical conductivity 616:10.1002/mren.201300181 526:. Princeton University 280:Adhesives and Sealants 199: 141:polystyrene sulfonate 122:microphase separation 185:constitutional units 181:in which a small but 654:2010IJHE...3512029X 648:(21): 12029–12037. 566:polymerdatabase.com 501:Greg Brust (2005). 308:Ion-Exchange Resins 296:Coatings and Paints 135:, sealing tape and 118:conducting polymer 761:978-0-7514-0392-3 733:978-90-277-2458-8 702:978-94-009-3829-8 439:(12): 2287–2311. 381:(12): 2287–2311. 232:, a copolymer of 167:ionomer molecules 819: 797:Polyelectrolytes 772: 770: 768: 744: 742: 740: 706: 705: 680: 674: 673: 637: 628: 627: 599: 576: 575: 573: 572: 558: 535: 534: 532: 531: 520: 514: 513: 511: 510: 498: 492: 491: 489: 488: 477: 471: 470: 468: 467: 461: 455:. Archived from 428: 419: 413: 412: 410: 409: 403: 397:. Archived from 370: 361: 254:Golf Ball Covers 238:methacrylic acid 173:Ionomer molecule 98:polyelectrolytes 57: 56: 53: 52: 49: 46: 43: 40: 37: 34: 31: 827: 826: 822: 821: 820: 818: 817: 816: 782: 781: 766: 764: 762: 747: 738: 736: 734: 719: 709: 703: 682: 681: 677: 639: 638: 631: 601: 600: 579: 570: 568: 560: 559: 538: 529: 527: 522: 521: 517: 508: 506: 500: 499: 495: 486: 484: 479: 478: 474: 465: 463: 459: 426: 421: 420: 416: 407: 405: 401: 368: 363: 362: 358: 354: 342: 332: 318:electrochemical 260:Packaging Films 250: 226: 210:perfluorocarbon 205: 200: 196: 188: 182: 159: 28: 24: 17: 12: 11: 5: 825: 823: 815: 814: 812:Thermoplastics 809: 804: 799: 794: 784: 783: 780: 779: 776: 773: 760: 745: 732: 717: 708: 707: 701: 675: 629: 577: 536: 515: 493: 472: 414: 355: 353: 350: 349: 348: 341: 340:External links 338: 331: 328: 327: 326: 311: 305: 299: 293: 283: 277: 263: 257: 249: 246: 225: 222: 204: 201: 187:have ionizable 154: 153: 15: 13: 10: 9: 6: 4: 3: 2: 824: 813: 810: 808: 805: 803: 800: 798: 795: 793: 790: 789: 787: 777: 774: 763: 757: 753: 752: 746: 735: 729: 725: 724: 718: 715: 711: 710: 704: 698: 694: 690: 686: 679: 676: 671: 667: 663: 659: 655: 651: 647: 643: 636: 634: 630: 625: 621: 617: 613: 609: 605: 598: 596: 594: 592: 590: 588: 586: 584: 582: 578: 567: 563: 557: 555: 553: 551: 549: 547: 545: 543: 541: 537: 525: 519: 516: 504: 497: 494: 482: 476: 473: 462:on 2016-03-04 458: 454: 450: 446: 442: 438: 434: 433: 425: 418: 415: 404:on 2016-03-04 400: 396: 392: 388: 384: 380: 376: 375: 367: 360: 357: 351: 347: 344: 343: 339: 337: 336: 329: 324: 319: 315: 312: 309: 306: 303: 300: 297: 294: 291: 287: 284: 281: 278: 275: 271: 267: 264: 261: 258: 255: 252: 251: 247: 245: 243: 239: 235: 231: 223: 221: 217: 213: 211: 202: 198: 194: 190: 186: 180: 179: 178:macromolecule 174: 170: 168: 164: 157: 152: 150: 146: 142: 138: 134: 130: 125: 123: 119: 115: 111: 106: 103: 99: 94: 92: 88: 85: 84:pendant group 81: 77: 73: 69: 68: 63: 62: 55: 22: 765:. Retrieved 750: 737:. Retrieved 726:. Springer. 722: 713: 684: 678: 645: 641: 610:(2): 81–99. 607: 603: 569:. Retrieved 565: 528:. Retrieved 518: 507:. Retrieved 496: 485:. Retrieved 475: 464:. Retrieved 457:the original 436: 430: 417: 406:. Retrieved 399:the original 378: 372: 359: 333: 313: 307: 301: 295: 285: 279: 265: 259: 253: 227: 218: 214: 206: 192: 191: 184: 176: 172: 171: 166: 162: 161: 126: 107: 95: 91:mole percent 76:electrically 65: 59: 20: 18: 248:Application 197:molecules. 802:Copolymers 786:Categories 571:2019-12-10 530:2014-12-24 509:2014-12-24 503:"Ionomers" 487:2014-12-24 466:2013-07-24 408:2013-07-24 352:References 274:fuel cells 272:(PEMs) in 158:definition 670:0360-3199 624:1862-8338 203:Synthesis 129:golf ball 114:viscosity 792:Plastics 453:98774337 395:98774337 330:See also 234:ethylene 131:covers, 87:moieties 767:30 June 739:30 June 650:Bibcode 163:Ionomer 102:ionenes 80:ionized 72:polymer 70:) is a 21:ionomer 758:  730:  699:  668:  622:  451:  393:  335:Nafion 230:DuPont 224:Surlyn 145:Nafion 807:Salts 460:(PDF) 449:S2CID 427:(PDF) 402:(PDF) 391:S2CID 369:(PDF) 316:: In 156:IUPAC 149:Hycar 61:iono- 769:2012 756:ISBN 741:2012 728:ISBN 697:ISBN 666:ISSN 620:ISSN 242:NaOH 236:and 193:Note 175:: A 147:and 112:and 67:-mer 689:doi 658:doi 612:doi 441:doi 383:doi 58:) ( 19:An 788:: 695:, 664:. 656:. 646:35 632:^ 618:. 606:. 580:^ 564:. 539:^ 447:. 437:68 435:. 429:. 389:. 379:68 377:. 371:. 169:. 151:. 143:, 64:+ 51:ər 39:ɑː 33:aɪ 771:. 743:. 691:: 672:. 660:: 652:: 626:. 614:: 608:8 574:. 533:. 512:. 490:. 469:. 443:: 411:. 385:: 54:/ 48:m 45:ə 42:n 36:ˈ 30:ˌ 27:/ 23:(

Index

/ˌˈɑːnəmər/
iono-
-mer
polymer
electrically
ionized
pendant group
moieties
mole percent
polyelectrolytes
ionenes
electrical conductivity
viscosity
conducting polymer
microphase separation
golf ball
semipermeable membranes
thermoplastic elastomers
polystyrene sulfonate
Nafion
Hycar
IUPAC
macromolecule
perfluorocarbon
DuPont
ethylene
methacrylic acid
NaOH
proton exchange membranes
fuel cells

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