ASM SA-463 PDF

ASM SA-463 PDF

Name:
ASM SA-463 PDF

Published Date:
07/01/1992

Status:
Active

Description:

LADISH D-11 - Ultra High-Strength Steel

Publisher:
ASM International

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Russian version):
200 business days

SKU:

Choose Document Language:
$7.5
Need Help?
View Sample Alloy Digest Data Sheet (PDF)

Since 1952, Alloy Digest has been the leading reference for materials property data on metals and alloys used throughout the world. Featuring graphs, charts and tables, these sheets give facts and figures on composition or characterization, physical and mechanical properties, heat treatment, and machinability.

LADISH D-11 is a low alloy steel of medium carbon content and a balanced alloy composition. The alloy was designed for structural components and hot work tool and die applications as it possesses better higher temperature strength than D-6-A and H-13.
File Size : 1 file , 180 KB
Note : This product is unavailable in Ukraine, Russia, Belarus
Published : 07/01/1992

History


Related products

ASM SA-62
Published Date: 10/01/1957
VASCOJET 1000 - Ultra High-Strength, Heat Resistant Steel
$7.5
ASM SA-109
Published Date: 01/01/1961
VASCOJET 1000-5 TEMPER - Ultra High-Strength, Heat Resistant Steel
$7.5
ASM SA-117
Published Date: 07/01/1961
TIMKEN HS-260 - Ultra Strength Steel
$7.5
ASM SA-135
Published Date: 10/01/1962
VASCOMAX 300 CVM - CVM Ultra High-Strength Steel
$7.5

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