GMW GMW17262 PDF

GMW GMW17262 PDF

Name:
GMW GMW17262 PDF

Published Date:
01/01/2015

Status:
[ Active ]

Description:

Polyphenylene Ether and Polyphenylene Ether/Polystyrene Blends

Publisher:
General Motors Worldwide

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Russian version):
200 business days

SKU:

Choose Document Language:
$12.9
Need Help?
ENGLISH CURRENT VERSION

Material Description. This specification describes material types of unfilled polyphenylene ether and polyphenylene ether plus polystyrene blends that are used in injection components for exterior trim that are not weatherable.

Types. The classification into groups is according to the different properties as described in Table 1.

Symbols. All plastic parts must have legible plastic compound identification symbol per GMW3116 and ISO 11469 requirements, >PPE< or >PPE+PS<.

Applicability. Typical applications include exterior decorative trim.

Remarks. Not applicable.


Edition : 1
File Size : 1 file , 160 KB
Number of Pages : 4
Published : 01/01/2015

History


Related products

GMW GMW15988
Published Date: 10/01/2018
Blend of Polypropylene and Ethylene-Propylene Rubber, UV Stabilized, Heat Stabilized
$12.9
GMW GMW14994
Published Date: 10/01/2019
Wheel Fastener Torque Tension Test - New (Unused)
$23.4
GMW GMW18256
Published Date: 07/01/2020
Grease, Mineral Oil and Polyurea Thickener
$12.9
GMW GMW15200
Published Date: 10/01/2021
Metal Bonding Structural Adhesive Performance Requirements
$12.9

Best-Selling Products

MEDDEV 13/93
Published Date:
Guidelines Relating to the Application of: The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices
MEDDEV 2.1/3
Published Date: 03/01/1998
Guidelines Relating to the Demarcation Between 90/385/EEC on Active Implatable Medical Devices, 93/42/EEC on Medical Devices,65/65/EEC Relating to Medicinal Products & Related Directives
MEDDEV 3/94
Published Date: 04/01/1994
Guidelines Relating to the Application of : The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices