Water sorption and hydrolytic stability of polycarbonates

The hydrolytic stability of a new commercial polycarbonate (Calibre 300, Dow Chemical USA) was investigated and compared with that of other commercial polycarbonates. The tests were conducted between 56% and 95% relative humidity (R. H.) at 100°C. Also performed were water immersion tests at 80 and...

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Veröffentlicht in:Polymer engineering and science 1989-12, Vol.29 (24), p.1733-1737
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description The hydrolytic stability of a new commercial polycarbonate (Calibre 300, Dow Chemical USA) was investigated and compared with that of other commercial polycarbonates. The tests were conducted between 56% and 95% relative humidity (R. H.) at 100°C. Also performed were water immersion tests at 80 and 100°C. The water diffusivity was found to be 8.7 × 10−7 cm2/s at 100°C with an activation energy of 7.9 kcal/mole. These values are similar to other glassy polymers. The equilibrium water sorption, C∞, was found to increase with temperature and R.H. The isotherm at 100°C was determined to be: C∞ = 0.005945 [R.H.]. When samples immersed in a water bath at 100°C were transferred into room‐temperature water, visible aqueous microcavities were formed due to the condition of super‐saturation, and under stress may become crack initiation sites. For the polycarbonate investigated here, it was found that the decrease in weight‐average molecular weight (M̄)w was a first‐order process under a constant R.H. and temperature, and that hydrolytic embrittlement, i. e., (M̄)w
doi_str_mv 10.1002/pen.760292402
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The tests were conducted between 56% and 95% relative humidity (R. H.) at 100°C. Also performed were water immersion tests at 80 and 100°C. The water diffusivity was found to be 8.7 × 10−7 cm2/s at 100°C with an activation energy of 7.9 kcal/mole. These values are similar to other glassy polymers. The equilibrium water sorption, C∞, was found to increase with temperature and R.H. The isotherm at 100°C was determined to be: C∞ = 0.005945 [R.H.]. When samples immersed in a water bath at 100°C were transferred into room‐temperature water, visible aqueous microcavities were formed due to the condition of super‐saturation, and under stress may become crack initiation sites. For the polycarbonate investigated here, it was found that the decrease in weight‐average molecular weight (M̄)w was a first‐order process under a constant R.H. and temperature, and that hydrolytic embrittlement, i. e., (M̄)w &lt;34,000, was reached after ca. 188, 143, 99, and 66 days under 56%, 73%, 87%, and 95% R.H., respectively, at 100°C. A comparison with reported hydrolytic stability data for other polycarbonates showed large differences in their stability which are believed to be due to the extent of end‐group capping (over 95% in Calibre 300) and resin purity: both phenolic end‐groups and some additives (i.e., fire retardants, thermal stabilizers) are known to accelerate hydrolytic degradation.</description><identifier>ISSN: 0032-3888</identifier><identifier>EISSN: 1548-2634</identifier><identifier>DOI: 10.1002/pen.760292402</identifier><identifier>CODEN: PYESAZ</identifier><language>eng</language><publisher>Brookfield: Society of Plastics Engineers</publisher><subject>Applied sciences ; Exact sciences and technology ; Permeability ; Physical properties ; Polymer industry, paints, wood ; Properties and testing ; Technology of polymers</subject><ispartof>Polymer engineering and science, 1989-12, Vol.29 (24), p.1733-1737</ispartof><rights>Copyright © 1989 Society of Plastics Engineers</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3812-dde5e229c9562c24d6f26a1166b327793385d38b576f71549ed5f6e8471209063</citedby><cites>FETCH-LOGICAL-c3812-dde5e229c9562c24d6f26a1166b327793385d38b576f71549ed5f6e8471209063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpen.760292402$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpen.760292402$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=6723544$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Golovoy, A.</creatorcontrib><creatorcontrib>Zinbo, M.</creatorcontrib><title>Water sorption and hydrolytic stability of polycarbonates</title><title>Polymer engineering and science</title><addtitle>Polym Eng Sci</addtitle><description>The hydrolytic stability of a new commercial polycarbonate (Calibre 300, Dow Chemical USA) was investigated and compared with that of other commercial polycarbonates. 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The tests were conducted between 56% and 95% relative humidity (R. H.) at 100°C. Also performed were water immersion tests at 80 and 100°C. The water diffusivity was found to be 8.7 × 10−7 cm2/s at 100°C with an activation energy of 7.9 kcal/mole. These values are similar to other glassy polymers. The equilibrium water sorption, C∞, was found to increase with temperature and R.H. The isotherm at 100°C was determined to be: C∞ = 0.005945 [R.H.]. When samples immersed in a water bath at 100°C were transferred into room‐temperature water, visible aqueous microcavities were formed due to the condition of super‐saturation, and under stress may become crack initiation sites. For the polycarbonate investigated here, it was found that the decrease in weight‐average molecular weight (M̄)w was a first‐order process under a constant R.H. and temperature, and that hydrolytic embrittlement, i. e., (M̄)w &lt;34,000, was reached after ca. 188, 143, 99, and 66 days under 56%, 73%, 87%, and 95% R.H., respectively, at 100°C. A comparison with reported hydrolytic stability data for other polycarbonates showed large differences in their stability which are believed to be due to the extent of end‐group capping (over 95% in Calibre 300) and resin purity: both phenolic end‐groups and some additives (i.e., fire retardants, thermal stabilizers) are known to accelerate hydrolytic degradation.</abstract><cop>Brookfield</cop><pub>Society of Plastics Engineers</pub><doi>10.1002/pen.760292402</doi><tpages>5</tpages></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Applied sciences
Exact sciences and technology
Permeability
Physical properties
Polymer industry, paints, wood
Properties and testing
Technology of polymers
title Water sorption and hydrolytic stability of polycarbonates
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