{"id":4320,"date":"2016-04-22T08:00:55","date_gmt":"2016-04-22T14:00:55","guid":{"rendered":"https:\/\/www.ulprospector.com\/knowledge\/?p=4320"},"modified":"2019-01-07T16:05:08","modified_gmt":"2019-01-07T22:05:08","slug":"pc-acrylic-resin-fundamentals","status":"publish","type":"post","link":"https:\/\/ulprospector.ul.com\/4320\/pc-acrylic-resin-fundamentals\/","title":{"rendered":"Acrylic Resin Fundamentals"},"content":{"rendered":"<p>Coatings utilizing <a href=\"https:\/\/www.ulprospector.com\/en\/na\/Coatings\/Product\/search?k=acrylic+resin&amp;st=31\" target=\"_blank\" rel=\"noopener\">acrylic resins<\/a> are the leading polymer technology in the coatings industry. Historically <a href=\"https:\/\/www.ulprospector.com\/en\/na\/Coatings\/Product\/search?k=alkyd&amp;st=31\" target=\"_blank\" rel=\"noopener\">alkyd<\/a> finishes have held the leading position in coatings for decades. Acrylics are utilized in architectural coatings, product finishes for original equipment manufacture including automotive (OEM) and refinish, as well as special-purpose coatings.<\/p>\n<p>Acrylic resins are primarily based on<a href=\"https:\/\/www.ulprospector.com\/en\/na\/Coatings\/Product\/search?k=acrylate&amp;st=31\" target=\"_blank\" rel=\"noopener\"> acrylate<\/a> and <a href=\"https:\/\/www.ulprospector.com\/en\/na\/Coatings\/search?k=methacrylate&amp;st=31\" target=\"_blank\" rel=\"noopener\">methacrylate <\/a>monomers and provide good weather resistance, resistance to hydrolysis, gloss and color retention in exterior applications. Due to their versatility and performance, acrylic coatings account for over 25% of all coatings and global sales approaching $25 billion. Acrylic resins can be thermoplastic or thermosett and are used in organic solvent born, waterborne, powder and radiation-curable coatings<\/p>\n<figure id=\"attachment_4327\" class=\"thumbnail wp-caption alignleft\" style=\"width: 387px\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/ulprospector.ul.com\/media\/2016\/04\/acrylics_table_1-1.jpg\" alt=\"Table I \u2013 Tg of Nonfunctional Homopolymers. Learn about the function of acrylic resin in coatings in the Prospector Knowledge Center. \" width=\"387\" height=\"329\" \/><figcaption class=\"caption wp-caption-text\">Table I \u2013 Tg of Nonfunctional Homopolymers<\/figcaption><\/figure>\n<p>Three broad classes of liquid coatings utilizing acrylic resins include <strong><em>thermoplastic, thermoset and waterborne<\/em><\/strong>. Many acrylic resins may also include other vinyl monomers such as<a href=\"https:\/\/www.ulprospector.com\/en\/na\/Coatings\/Product\/search?k=styrene&amp;st=31\" target=\"_blank\" rel=\"noopener\"> styrene<\/a> or <a href=\"https:\/\/www.ulprospector.com\/en\/na\/Coatings\/Product\/search?k=vinyl+acetate&amp;st=31\" target=\"_blank\" rel=\"noopener\">vinyl acetate<\/a> primarily to reduce cost. Acrylic monomers have a lower Tg than their analogous methacrylate monomers (for example compare the Tg for n-butyl acrylate versus n-butyl methacrylate see Table I and Table II). As Table II suggests, the glass transition temperature of the monomers selected for synthesis of a resin can be selected to enhance multiple properties that may include weather resistance, moisture resistance, oxygen permeability, flexibility reactivity, cure and hardness. In addition, acrylics can be functionalized with a variety of monomers to provide improved adhesion to metal, or to react for example with aminoplast or isocyanate crosslinkers.<\/p>\n<figure id=\"attachment_4325\" class=\"thumbnail wp-caption alignleft\" style=\"width: 395px\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/ulprospector.ul.com\/media\/2016\/04\/acrylics_table_2.jpg\" alt=\"Table: Relationship of Tg to Physical Properties. Learn about the function of acrylic resin in coatings in the Prospector Knowledge Center.\" width=\"395\" height=\"200\" \/><figcaption class=\"caption wp-caption-text\">Table II Relationship of Tg to Physical Properties<\/figcaption><\/figure>\n<p><strong><em>Thermoplastic acrylic polymers<\/em><\/strong> (TPA) in general have excellent properties including exterior durability. Such resins were widely used in automotive OEM and Refinish topcoats from the 50\u2019s to the 70\u2019s, but their use has dramatically declined due to the high molecular weight necessary to provide properties, they require a high amount of organic solvent to enable air atomized spray application. Accordingly these paints apply at about 20% weight solids. Thermoplastic resins typically use a high level of methyl methacrylate in their<a href=\"https:\/\/www.ulprospector.com\/en\/na\/Coatings\/search?k=polymer&amp;st=31\" target=\"_blank\" rel=\"noopener\"> polymer <\/a>backbone to provide excellent hardness and exterior durability.<\/p>\n<figure id=\"attachment_4355\" class=\"thumbnail wp-caption aligncenter\" style=\"width: 580px\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/ulprospector.ul.com\/media\/2016\/04\/figure-1-revised.jpg\" alt=\"Figure I \u2013 Structure of poly MMA and poly MA. Learn the basics of acrylic resin in coatings in the Prospector Knowledge Center.\" width=\"580\" height=\"272\" \/><figcaption class=\"caption wp-caption-text\">Figure I \u2013 Structure of poly MMA and poly MA<\/figcaption><\/figure>\n<p><strong><em>Thermosetting acrylic resins (TSA) <\/em><\/strong>are designed with functional monomers to either react with themselves when exposed to heat or moisture, or with that of a cross-linker to form a cross-linked film. Thermoset resins as a group are lower molecular weight and thus have higher application solids. Once cross-linked, as a class they offer films with excellent resistance to organic solvents, moisture and UV light and do not soften appreciably when exposed to moderately high temperatures as thermoplastics do.\u00a0 An example of acrylic monomers with functional groups that can be used to functionalize acrylic polymers to provide properties such as crosslinking, self-crosslinking, improved adhesion or pigment wetting are provided in Table III.<\/p>\n<figure id=\"attachment_4326\" class=\"thumbnail wp-caption alignleft\" style=\"width: 465px\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/ulprospector.ul.com\/media\/2016\/04\/acrylics_figure_2.jpg\" alt=\"Table III \u2013 Functional Acrylic Monomers. Learn about the function of acrylic resin in coatings in the Prospector Knowledge Center.\" width=\"465\" height=\"274\" \/><figcaption class=\"caption wp-caption-text\">Table III \u2013 Functional Acrylic Monomers<\/figcaption><\/figure>\n<p>Being able to functionalize an acrylic resin with a wide range of reactive moieties provides the ability to tailor the performance of the resin backbone to provide improved adhesion over a variety of substrates, improved pigment wetting and\/or the ability to provide crosslinking or self-crosslinking. Other acrylic monomers are also available to impart sulfonic acid, or phosphoric acid functionality to the acrylic resin.<\/p>\n<p>Being able to functionalize an acrylic resin with a wide range of reactive moieties provides the ability to tailor the performance of the resin backbone to provide improved adhesion over a variety of substrates, improved pigment wetting and\/or the ability to provide crosslinking or self-crosslinking. Other <a href=\"https:\/\/www.ulprospector.com\/en\/na\/Coatings\/search?k=acrylic+monomer&amp;st=31\" target=\"_blank\" rel=\"noopener\">acrylic monomers<\/a> are also available to impart sulfonic acid, or phosphoric acid functionality to the acrylic resin.<\/p>\n<hr \/>\n<h3>Looking for acrylic resins for your coatings formulations?<\/h3>\n<p>Prospector has over a thousand listings for acrylic resin materials. View product data sheets, request samples and more now&#8230;<\/p>\n<h3><a role=\"button\" href=\"https:\/\/www.ulprospector.com\/en\/na\/Coatings\/Product\/search?k=acrylic+resin&amp;st=31\" target=\"_blank\" rel=\"noopener\"><br \/>\nSearch Acrylic Resins<br \/>\n<\/a><\/h3>\n<hr \/>\n<p>Carbamate functional acrylics can also be made for example by reacting an isocyanate functional acrylic with hydroxypropyl carbamate. Many of the acrylics in the category of functionalized acrylic resins are used in automotive OEM and refinish clearcoats to provide an excellent combination of mar resistance, chemical resistance and light stability.<\/p>\n<p>Acrylic polymers are also used extensively to make <strong><em>water reducible and emulsion resins<\/em><\/strong>.\u00a0 <strong><em>Water reducible acrylic<\/em><\/strong> resins typically have acid numbers of 40 to 60. An example of a water reducible TSA would have a resin composition comprised of MMA\/STY\/BA\/HEMA\/AA in a weight ratio of 40\/20\/22\/10\/ 8 prepared by free radical polymerization in a water reducible solvent such as a glycol ether solvent like 2-butoxy ethanol with butyl alcohol. To begin the process of making paint, a suitable amine is used to neutralize the acrylic acid in the resin backbone to provide an acid salt. The amine is used at less than the theoretical level of neutralization using for example 2-(dimethyl amino) ethanol (DMEA) or 2-Amino-2-methyl-1-propanol (AMP).\u00a0 The next step in the paint making process involves the addition of water. Please refer to a previous Prospector article concerning\u00a0 waterborne resins: <a href=\"https:\/\/ulprospector.ul.com\/3069\/pc-fundamentals-waterborne-resin-technology\/\">https:\/\/ulprospector.ul.com\/3069\/pc-fundamentals-waterborne-resin-technology\/<\/a> as well as additional information on viscosity versus reduction characteristics of waterborne resins: <a href=\"https:\/\/ulprospector.ul.com\/639\/flow-leveling-viscosity-control-water-born-coatings\/\">https:\/\/ulprospector.ul.com\/639\/flow-leveling-viscosity-control-water-born-coatings\/<\/a>.<\/p>\n<p><strong><em>Acrylic emulsion polymerization<\/em><\/strong> is carried out in water with monomers, a water soluble initiator and surfactants. Many of the same monomers are used in emulsion polymerization as that in solution polymerization, however the properties of the latex can be greatly affected by changes in the: polymerization conditions, monomer structure and solubility, monomer concentration, surfactant type and level, temperature, initiator type and initiator concentration are all variables that can effect the emulsion particle size, structure and molecular weight of the final polymer. A detailed examination of latex polymerization is a significantly large subject and is thus out of scope for this article. Acrylic polymers are also used in powder coatings along with acrylate functional acrylic resins for radiation cure coatings. The fundamental influence of monomer Tg, molecular weight and functional monomers remain the same for all the applications described herein.<\/p>\n<p>In summary it is the goal of this article to provide a heightened understanding of acrylic resin technology and its ramifications on paint performance characteristics and mechanical properties.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Coatings utilizing acrylic resins are the leading polymer technology in the coatings industry. Historically alkyd finishes have held the leading position in coatings for decades. Acrylics are utilized in architectural coatings, product finishes for original equipment manufacture including automotive (OEM) &hellip; <a href=\"https:\/\/ulprospector.ul.com\/4320\/pc-acrylic-resin-fundamentals\/\">Continued<\/a><\/p>\n","protected":false},"author":12,"featured_media":4321,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"episode_type":"","audio_file":"","podmotor_file_id":"","podmotor_episode_id":"","cover_image":"","cover_image_id":"","duration":"","filesize":"","filesize_raw":"","date_recorded":"","explicit":"","block":"","itunes_episode_number":"","itunes_title":"","itunes_season_number":"","itunes_episode_type":"","footnotes":""},"categories":[16],"tags":[],"ppma_author":[1249],"class_list":{"0":"post-4320","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-paint-coatings","8":"entry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Acrylic resin fundamentals: Coating functions and benefits<\/title>\n<meta name=\"description\" content=\"Coatings that include an acrylic resin are used in a variety of applications. 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Lewarchik, President and CEO of Chemical Dynamics, LLC, brings 40 years of paint and coatings industry expertise to his role as a contributing author with the Prospector Knowledge Center. As a contributing writer, Ron pens articles on topics relevant to formulators in the coatings industry. He also serves as a consultant for the Prospector materials search engine, advising on issues related to optimization and organization materials within the database. Ron's company, Chemical Dynamics, LLC (www.chemicaldynamics.net), is a full-service paint and coatings firm specializing in consulting and product development based in Plymouth, Michigan. Since 2004, he has provided consulting, product development, contract research, feasibility studies, failure mode analysis and more for a wide range of clients, as well as their suppliers, customers and coaters. He has also served as an Adjunct Research Professor at the Coatings Research Institute of Eastern Michigan University. As such, Ron was awarded a sub-grant from the Department of Energy to develop energy-saving coating technology for architectural applications, as well as grants from private industry to develop low energy cure, low VOC compliant coatings. He taught courses on color and application of automotive top coats, cathodic electro-coat and surface treatment. His experience includes coatings for automotive, coil, architectural, industrial and product finishing. Previously, Ron was the Vice President of Industrial Research and Technology, as well as the Global Director of Coil Coating Technology for BASF (Morton International). During his fourteen-year tenure with the company, he developed innovative coil coating commercial products primarily for roofing, residential, commercial and industrial building, as well as industrial and automotive applications. He was awarded fifteen patents for new resin and coating formulas. From 1974 to 1990, Ron held positions with Desoto, Inc. and PPG Industries. He was the winner of two R&amp;D awards for coatings utilizing PVDF resins, developed the first commercial high solids automotive topcoat and was awarded 39 U.S. patents for a variety of novel technologies he developed. He holds a Masters in Physical Organic Chemistry from the University of Pittsburgh and subsequently studied Polymer Science at Carnegie Mellon University. Ron lives in Brighton, Michigan with his family. Contact Ron via email\u00a0or through his company\u2019s web site at www.chemicaldynamics.net to learn more about his consulting services\u2026\",\"sameAs\":[\"https:\\\/\\\/ulprospector.ul.com\"],\"url\":\"https:\\\/\\\/ulprospector.ul.com\\\/author\\\/ron-lewarchik\\\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Acrylic resin fundamentals: Coating functions and benefits","description":"Coatings that include an acrylic resin are used in a variety of applications. 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Lewarchik, President and CEO of Chemical Dynamics, LLC, brings 40 years of paint and coatings industry expertise to his role as a contributing author with the Prospector Knowledge Center. As a contributing writer, Ron pens articles on topics relevant to formulators in the coatings industry. He also serves as a consultant for the Prospector materials search engine, advising on issues related to optimization and organization materials within the database. Ron's company, Chemical Dynamics, LLC (www.chemicaldynamics.net), is a full-service paint and coatings firm specializing in consulting and product development based in Plymouth, Michigan. Since 2004, he has provided consulting, product development, contract research, feasibility studies, failure mode analysis and more for a wide range of clients, as well as their suppliers, customers and coaters. He has also served as an Adjunct Research Professor at the Coatings Research Institute of Eastern Michigan University. As such, Ron was awarded a sub-grant from the Department of Energy to develop energy-saving coating technology for architectural applications, as well as grants from private industry to develop low energy cure, low VOC compliant coatings. He taught courses on color and application of automotive top coats, cathodic electro-coat and surface treatment. His experience includes coatings for automotive, coil, architectural, industrial and product finishing. Previously, Ron was the Vice President of Industrial Research and Technology, as well as the Global Director of Coil Coating Technology for BASF (Morton International). During his fourteen-year tenure with the company, he developed innovative coil coating commercial products primarily for roofing, residential, commercial and industrial building, as well as industrial and automotive applications. He was awarded fifteen patents for new resin and coating formulas. From 1974 to 1990, Ron held positions with Desoto, Inc. and PPG Industries. He was the winner of two R&amp;D awards for coatings utilizing PVDF resins, developed the first commercial high solids automotive topcoat and was awarded 39 U.S. patents for a variety of novel technologies he developed. He holds a Masters in Physical Organic Chemistry from the University of Pittsburgh and subsequently studied Polymer Science at Carnegie Mellon University. Ron lives in Brighton, Michigan with his family. Contact Ron via email\u00a0or through his company\u2019s web site at www.chemicaldynamics.net to learn more about his consulting services\u2026","sameAs":["https:\/\/ulprospector.ul.com"],"url":"https:\/\/ulprospector.ul.com\/author\/ron-lewarchik\/"}]}},"authors":[{"term_id":1249,"user_id":12,"is_guest":0,"slug":"ron-lewarchik","display_name":"Ron Lewarchik","avatar_url":"https:\/\/ulprospector.ul.com\/media\/2014\/05\/Ron-Lewarchik_avatar_1399393591-96x96.png","0":null,"1":"","2":"","3":"","4":"","5":"","6":"","7":"","8":""}],"_links":{"self":[{"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/posts\/4320","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/users\/12"}],"replies":[{"embeddable":true,"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/comments?post=4320"}],"version-history":[{"count":0,"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/posts\/4320\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/media\/4321"}],"wp:attachment":[{"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/media?parent=4320"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/categories?post=4320"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/tags?post=4320"},{"taxonomy":"author","embeddable":true,"href":"https:\/\/ulprospector.ul.com\/wp-json\/wp\/v2\/ppma_author?post=4320"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}