Thermal Degradation of Aminosilicone Carbamates
The major thermal degradation pathway seen with 1,5-bis(3-aminopropyl)-1,1,3,3,5,5-hexamethyltrisiloxane/triethylene glycol (GAP-1/TEG) is the formation of a urea-containing compound. Degradation is increased at higher temperatures, longer reaction times, higher CO2 concentrations (in the form of c...
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Veröffentlicht in: | Energy & fuels 2016-12, Vol.30 (12), p.10671-10678 |
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creator | Perry, Robert J Rainka, Matthew P Doherty, Mark D Wood, Benjamin R Namjoshi, Omkar Hatchell, Daniel Liu, Hanbi Rochelle, Gary T |
description | The major thermal degradation pathway seen with 1,5-bis(3-aminopropyl)-1,1,3,3,5,5-hexamethyltrisiloxane/triethylene glycol (GAP-1/TEG) is the formation of a urea-containing compound. Degradation is increased at higher temperatures, longer reaction times, higher CO2 concentrations (in the form of carbamate loading), and low water levels. A judicious choice of operating conditions can significantly decrease urea byproduct formation. Reducing the desorption temperature from 140 to 100 °C and adding 5 wt % water to the 60:40 mixture of GAP-1/TEG resulted in a 500-fold reduction in amine loss after 4 days in a CO2-rich environment. After 56 days of continuous heating under the same conditions, ∼87% original GAP-1 was retained at 100 °C compared to only ∼20% at 140 °C. The urea byproduct appears to be the only major degradation pathway under these conditions, with 100% of the mass balance accounted for by the urea and amine components. |
doi_str_mv | 10.1021/acs.energyfuels.6b02284 |
format | Article |
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Degradation is increased at higher temperatures, longer reaction times, higher CO2 concentrations (in the form of carbamate loading), and low water levels. A judicious choice of operating conditions can significantly decrease urea byproduct formation. Reducing the desorption temperature from 140 to 100 °C and adding 5 wt % water to the 60:40 mixture of GAP-1/TEG resulted in a 500-fold reduction in amine loss after 4 days in a CO2-rich environment. After 56 days of continuous heating under the same conditions, ∼87% original GAP-1 was retained at 100 °C compared to only ∼20% at 140 °C. 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Degradation is increased at higher temperatures, longer reaction times, higher CO2 concentrations (in the form of carbamate loading), and low water levels. A judicious choice of operating conditions can significantly decrease urea byproduct formation. Reducing the desorption temperature from 140 to 100 °C and adding 5 wt % water to the 60:40 mixture of GAP-1/TEG resulted in a 500-fold reduction in amine loss after 4 days in a CO2-rich environment. After 56 days of continuous heating under the same conditions, ∼87% original GAP-1 was retained at 100 °C compared to only ∼20% at 140 °C. The urea byproduct appears to be the only major degradation pathway under these conditions, with 100% of the mass balance accounted for by the urea and amine components.</description><subject>Energy & Fuels</subject><subject>Engineering</subject><issn>0887-0624</issn><issn>1520-5029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkLFOwzAQhi0EEqXwDETsSX124rhjVaAgVWIps3VxL62rJEZ2OvTtcdUObEynk_7v193H2DPwAriAGdpY0EBhd2qP1MVCNVwIXd6wCVSC5xUX81s24VrXOVeivGcPMR4450rqasJmmz2FHrvslXYBtzg6P2S-zRa9G3x0nbN-oGyJocEeR4qP7K7FLtLTdU7Z9_vbZvmRr79Wn8vFOkcp9Jg3tkTJibQCDQSa5rDFZt62FkXaABQhSNSytKRspUQCaoCm1qDAkpVT9nLp9XF0Jlo3kt2nWwayo4FKlmWtU6i-hGzwMQZqzU9wPYaTAW7OckySY_7IMVc5iZQX8hw4-GMY0jP_Ur_Pim6T</recordid><startdate>20161215</startdate><enddate>20161215</enddate><creator>Perry, Robert J</creator><creator>Rainka, Matthew P</creator><creator>Doherty, Mark D</creator><creator>Wood, Benjamin R</creator><creator>Namjoshi, Omkar</creator><creator>Hatchell, Daniel</creator><creator>Liu, Hanbi</creator><creator>Rochelle, Gary T</creator><general>American Chemical Society</general><general>American Chemical Society (ACS)</general><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0003-2027-4829</orcidid><orcidid>https://orcid.org/0000000320274829</orcidid></search><sort><creationdate>20161215</creationdate><title>Thermal Degradation of Aminosilicone Carbamates</title><author>Perry, Robert J ; Rainka, Matthew P ; Doherty, Mark D ; Wood, Benjamin R ; Namjoshi, Omkar ; Hatchell, Daniel ; Liu, Hanbi ; Rochelle, Gary T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a328t-bc4a30ee86181e18e91dab9ffca218e116ea13a834ce6c562bc4711b78161cec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Energy & Fuels</topic><topic>Engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Perry, Robert J</creatorcontrib><creatorcontrib>Rainka, Matthew P</creatorcontrib><creatorcontrib>Doherty, Mark D</creatorcontrib><creatorcontrib>Wood, Benjamin R</creatorcontrib><creatorcontrib>Namjoshi, Omkar</creatorcontrib><creatorcontrib>Hatchell, Daniel</creatorcontrib><creatorcontrib>Liu, Hanbi</creatorcontrib><creatorcontrib>Rochelle, Gary T</creatorcontrib><creatorcontrib>General Electric Company, Boston, MA (United States)</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Energy & fuels</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perry, Robert J</au><au>Rainka, Matthew P</au><au>Doherty, Mark D</au><au>Wood, Benjamin R</au><au>Namjoshi, Omkar</au><au>Hatchell, Daniel</au><au>Liu, Hanbi</au><au>Rochelle, Gary T</au><aucorp>General Electric Company, Boston, MA (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermal Degradation of Aminosilicone Carbamates</atitle><jtitle>Energy & fuels</jtitle><addtitle>Energy Fuels</addtitle><date>2016-12-15</date><risdate>2016</risdate><volume>30</volume><issue>12</issue><spage>10671</spage><epage>10678</epage><pages>10671-10678</pages><issn>0887-0624</issn><eissn>1520-5029</eissn><abstract>The major thermal degradation pathway seen with 1,5-bis(3-aminopropyl)-1,1,3,3,5,5-hexamethyltrisiloxane/triethylene glycol (GAP-1/TEG) is the formation of a urea-containing compound. Degradation is increased at higher temperatures, longer reaction times, higher CO2 concentrations (in the form of carbamate loading), and low water levels. A judicious choice of operating conditions can significantly decrease urea byproduct formation. Reducing the desorption temperature from 140 to 100 °C and adding 5 wt % water to the 60:40 mixture of GAP-1/TEG resulted in a 500-fold reduction in amine loss after 4 days in a CO2-rich environment. After 56 days of continuous heating under the same conditions, ∼87% original GAP-1 was retained at 100 °C compared to only ∼20% at 140 °C. The urea byproduct appears to be the only major degradation pathway under these conditions, with 100% of the mass balance accounted for by the urea and amine components.</abstract><cop>United States</cop><pub>American Chemical Society</pub><doi>10.1021/acs.energyfuels.6b02284</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2027-4829</orcidid><orcidid>https://orcid.org/0000000320274829</orcidid></addata></record> |
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title | Thermal Degradation of Aminosilicone Carbamates |
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