CABLE MANUFACTURER A E R I A L D R O P C A B L E J A C K E T • Pass clamp test requested by end customer • Strong UV resistance & mechanical performance • Excellent processing • Good fire performance to pass CPR class Cca / Dca • Low shrinkage (< 1%) • Exceeded material fire performance requirements and met all other performance criteria • Simplified supply chain with local manufacture in Europe • Enabled customer to run material at optimum processing conditions by providing support with machine set up ECCOH™ 5978 UV Formulation KEY REQUIREMENTS WHY AVIENT? https://www.avient.com/products/engineered-polymer-formulations/eco-conscious-formulations/eccoh-low-smoke-and-fume-non-halogen-formulations Cable manufacturer

OFF-ROAD VEHICLE MANUFACTURER C A R G O R A C K • Design freedom • Improve process efficiency to reduce cost • High strength-to-weight ratio • Aesthetic appeal • Weather and chemical resistance • Replaced metal with a injection-moldable thermoplastic plus TPE overmold to meet performance demands and maintain premium brand quality • Provided technical support to help expand the design and function of the cargo rack • Reduced manufacturing costs by eliminating the painting step from the process Versalloy™ TPE and thermoplastic substrate KEY REQUIREMENTS WHY AVIENT? https://www.polyone.com/products/thermoplastic-elastomers/versalloy-thermoplastic-elastomers off-road vehicle Manufacturer

TIER 2 SUPPLIERS P A N E L S F O R O F F - R O A D V E H I C L E S • Transfer OEM-approved materials from North America to manufacturers in Europe • Help manufacturers avoid cash flow issues on small lot orders • Managed REACH qualification for 10 OEM- approved materials • Optimized logistics so manufacturers could purchase small lots 10 engineered material and Masterbatch solutions KEY REQUIREMENTS WHY AVIENT?

SILICONE PRODUCT MANUFACTURER M E N S T R U A L C U P S • Biocompatible silicone pigment dispersion that meets healthcare industry material requirements • Custom-colored silicone paste colorant dispersion for liquid silicone rubber (LSR) • Offered a USP Class VI certified, biocompatible silicone colorant dispersion with necessary regulatory support to meet the stringent demands of healthcare product manufacturing • Provided color customization options through personalized communication and high-level technical support Stan-Tone HC Plus Silicone Dispersions for Healthcare KEY REQUIREMENTS WHY AVIENT? https://www.avient.com/products/polymer-colorants/colorant-dispersions/stan-tone-hc-plus-silicone-dispersions-healthcare Slide 1: Silicone product manufacturer

ECCOH™ Specialty Solutions Helping Cable Manufacturers Meet CPR Standards PRODUCT BULLETIN ECCOH™ Low Smoke and Fume Non-Halogen (LSFOH) formulations offer a range of non- halogen, flame retardant solutions that enable manufacturers to meet the Construction Products Regulation (CPR) standards set out by the harmonized European Standard, EN13501. SELECTING THE RIGHT ECCOH SOLUTION Avient provides additional technical services to help cable manufacturers find the right CPR compliant cable solutions. The cable design, other materials used in the cable, and the cable manufacturing process can all influence CPR test results.

ECCOH™ Specialty Solutions Helping Cable Manufacturers Meet CPR Standards PRODUCT BULLETIN ECCOH™ Low Smoke and Fume Non-Halogen (LSFOH) formulations offer a range of non- halogen, flame retardant solutions that enable manufacturers to meet the Construction Products Regulation (CPR) standards set out by the harmonized European Standard, EN13501. SELECTING THE RIGHT ECCOH SOLUTION Avient provides additional technical services to help cable manufacturers find the right CPR compliant cable solutions. The cable design, other materials used in the cable, and the cable manufacturing process can all influence CPR test results.

CUSTOM FORMULATION IMPROVES PRODUCTIVITY AND MANUFACTURING EFFICIENCY CASE STUDY: TRILLIANT™ HC SPECIALTY ENGINEERED MATERIALS Challe nge Accepted. THE CHALLENGE A manufacturer of high-quality laboratory research products was eager to expand into the conductive pipette tip market. Total Manufacturing Cost Savings: Despite an increase I price per pound over the competition, the manufacturer’s total cash costs were reduced by over $45,000 on an annualized basis as a result of the proven, quantified savings in cycle time, productivity and scrap.

Versaflex™ TPE PORTABLE SPEAKER SOLUTIONS WATER AND DUST PROTECTION, DURABLE LOOK AND FEEL CE 3120-40 CE 3620 CE 3115 CE 3120-80 Application Gaskets Skins Skins Skins Product Aesthetics Tacky Translucent 42A 65A 65A 80A Special Characteristics Low compression set Low compression set High flow Abrasion resistance High strength Improved scratch/ mar, UV and abrasion Overmolding HOW VERSAFLEX TPEs MAKE THE DIFFERENCE IN PORTABLE SPEAKERS APPLICATIONS GASKETS Water and Dust Protection - Tight housing seals with no leakage over time Reduced Manufacturing Costs - Eliminates sourcing and assembly steps required of O-rings by overmolding directly onto the substrate; strong adhesion to PC & ABS - Faster cycle times than silicone or TPU Design Freedom - Injection molding TPEs in gaskets enables complex designs in which simple O-rings would be challenging to assemble SPEAKER SKINS Durable Look and Feel - Silky feel soft touch - Long lasting aesthetics with abrasion and UV resistance Reduced Manufacturing Costs - Eliminates sourcing and assembly steps required of silicone skins by overmolding directly onto the substrate; strong adhesion to PC & ABS - Faster cycle times than silicone or TPU Design Freedom - Overmolding TPE removes the need for mechanical interlocks and primers to get silicone materials to adhere to substrates To learn more about Versaflex TPEs for portable speakers, contact Avient at +1.844.4AVIENT. Today’s portable speaker manufacturers are searching for materials they can count on to protect against water and dust, but they also need durability and expanded design possibilities. Versaflex TPEs safely deliver on all of these requirements, while also accelerating production speed and reducing manufacturing cost.

Mevopur™ Healthcare Bio-based Polymer Solutions for Medical Devices and Pharmaceutical Packaging Manufacturers of medical devices and pharmaceutical packaging are increasingly faced with the challenge of integrating sustainability into the design of their products. KEY CHARACTERISTICS • Available for polyethylene, polypropylene, ABS, polycarbonate and styrenics • Bio-content of resin carrier varies from 70% to 100% depending on polymer—calculated to ASTM D6866 standard • Manufactured at four ISO 13485 certified sites, providing global consistency and security of supply • Documented change control beyond CAS number, reducing risk of change • Drop-in solutions that can be processed like fossil-based grades on common injection molding and extrusion machines • Can be provided as ready-to-use pre-colored or additive formulation REGULATORY SUPPORT • Raw materials tested to: - ISO 10993-1 - USP and (incl. class VI) - European Pharmacopeia, monograph 3.1.3/ 3.1.5 (polyolefin packaging materials) - USP (polyethylene) - Elemental impurities as per ICH Q3D • Registered Drug Master File (Type III) and/or Device Master File • Food contact according to US FDA and APPLICATION BULLETIN Sustainability Spotlight Bio-polymers Healthcare use limitations apply—see below. It is the responsibility of the medical device manufacturer and the person placing the medical device on the market to ensure compliance of the medical device with all applicable laws and regulations, including the suitability of all raw materials and components used for its manufacture.

The nucleating agents also foster constant process settings throughout part manufacturing with a higher crystallization temperature for improved crystallization speed. REGULATORY SUPPORT • Drug delivery devices • Pharmaceutical packaging • Medical equipment KEY CHARACTERISTICS • Manufactured at four ISO 13485 certified sites, providing global consistency and increased security of supply • Documented change control beyond CAS number level, reducing the risk of change • Allows crystallization in semi-crystalline polymers to begin faster and complete earlier REGULATORY SUPPORT • Raw materials tested to: - ISO 10993-1 and USP biological evaluation - European Pharmacopeia 3.1.3/3.1.5 (polyolefin) - USP (polyethylene) - ICH Q3D elemental impurities • Registered Drug Master File (Type III) and/or Device Master File • Food contact established with FDA/EU* APPLICATION BULLETIN * FDA/EU compliance information available upon request Healthcare use limitations apply—see below. It is the responsibility of the medical device manufacturer and the person placing the medical device on the market to ensure compliance of the medical device with all applicable laws and regulations, including the suitability of all raw materials and components used for its manufacture.