In addition, after two years of extensive development and testing, the brand responsible for the world’s strongest fiber™ is again taking performance to new heights, offering brands and media an exclusive preview of its latest breakthrough technology: Dyneema® Woven Composites. Our expanding portfolio of offerings includes colorants, advanced composites, functional additives, engineered materials, and Dyneema®, the world’s strongest fiber™.

These new TPEs can help electronics brands and OEMs successfully and sustainably deliver on color, material, and finish trends without the fear of surface blooms.” This can occur due to improper injection molding conditions or the incompatibility of a TPE or vulcanized silicone material with certain additives. In addition, the materials’ outstanding mold release improves cycle times, reducing overall energy use to support manufacturers in reaching their sustainability goals.

In addition, resources like our Cycleworks™ Innovation Center for Plastic Recycling and Color Prediction Service are integral to strengthening our expertise and enabling our customers to meet their sustainability commitments. Avient has developed technologies to address these needs, including composites that are lightweight to decrease carbon emissions, functional additives that lightweight or improve the recycle content of plastic packaging, and biobased solutions that lower product carbon footprint.

In addition, some specialized products are produced in internally-certified sites operating under the same ISO13485 Standard Operating Procedures (SOP). To help customers manage their risk potential, dedicated facilities and systems govern the production of our medical colorants and performance masterbatches. Internal ISO13485 GMP is in operation at two additional specialist sites in Europe.

In addition, some specialized products are produced in internally-certified sites operating under the same ISO13485 Standard Operating Procedures (SOP). To help customers manage their risk potential, dedicated facilities and systems govern the production of our medical colorants and performance masterbatches. Internal ISO13485 GMP is in operation at two additional specialist sites in Europe.

In addition, some specialized products are produced in internally-certified sites operating under the same ISO13485 Standard Operating Procedures (SOP). To help customers manage their risk potential, dedicated facilities and systems govern the production of our medical colorants and performance masterbatches. Internal ISO13485 GMP is in operation at two additional specialist sites in Europe.

In addition to avoiding possible fines, investing in these solutions can also enhance a company’s reputation, attracting investors and stakeholders who prioritize sustainability. Avient offers a number of bio-based colorants, additives, polymers, and inks to address this growing need.

Avient Introduces ColorMatrix™ Amosorb™ Oxyloop™: A New Oxygen Scavenging Additive to Enhance Recyclability Avient’s new Colorant Chromatics™ PVDF Processing Aids are an e... Avient Introduces ColorMatrix™ Amosorb™ Oxyloop™: A New Oxygen Scavenging Additive to Enhance Recyclability...

Rejoin PCR Colorant MB Product Bulletin_CN1.5-1 用于聚烯烃的 Rejoin 母料™ *APR的2018年生命周期库存分析 产品公告 www.avient.com 版权所有©2021 埃万特公司。

Mevopur™ Healthcare Functional Additives Chemical Foaming Agents (CFA) for Medical Devices and Pharmaceutical Packaging As the need to integrate sustainability in the design of healthcare products is growing, manufacturers of medical devices and pharmaceutical packaging are looking for materials with a more environmentally-friendly profile. KEY CHARACTERISTICS • Manufactured under ISO 13485 procedures • Documented change control beyond CAS number, reducing risk of change • Can be used on common injection molding and extrusion machines—set-up support by a technical assistance team • Available for use in polyolefins, styrenics and copolymers • Can be combined with colorants 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 USA FDA and EU norms APPLICATION BULLETIN Sustainability Spotlight Healthcare use limitations apply—see below.