Titanium Metal Injection Molding, a Qualified Manufacturing Process

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Metal injection molding (MIM) of titanium for implantable applications has been referred to as “the holy grail” of MIM. The challenges of forming a highly reactive, finely divided metal powder are well understood within the industry [1]. Titanium has the dual challenge of being both highly reactive and very sensitive to contamination. Over the years there has been tremendous activity in academia and industry regarding overcoming the challenges of titanium MIM [2]. The most relevant of those challenges is meeting the chemical and mechanical requirements of the Grade 5 (Ti-6Al-4V) alloy in a production environment. Praxis has qualified its titanium MIM process to meet the strict requirements of the medical industry. During this validation, the consistency of the process and product was evaluated at numerous points. This discussion focuses on input controls and testing the outputs of the process from both the perspective of interstitial content and mechanical properties. These characteristics cannot be non-destructively inspected and must be monitored by a statistical sampling plan to ensure quality during production. In order to develop a sampling plan that meets the quality requirements of the customer, it is necessary to determine the capabilities of the process. This article provides insight into the process validation of Praxis’ titanium MIM technology.

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122-129

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August 2016

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© 2016 Trans Tech Publications Ltd. All Rights Reserved

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[1] German, R.M. Progress in Titanium Metal Powder Injection Molding. In Materials, 2013, 6, 3641-3662.

DOI: 10.3390/ma6083641

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[4] R.M. German, Metal Injection Molding, A Comprehensive MIM Design Guide. 2011, Metal Powder Industries Federation, Princeton, NJ.

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