Carbonic Anhydrase Promotes the Absorption Rate of CO sub(2) in Post-Combustion Processes
The rate of carbon dioxide (CO sub(2)) absorption by monoethanol amine (MEA), diethanol amine (DEA), N-methyl-2,2'-iminodiethanol (MDEA), and 2-amino-2-methyl 1-propanol (AMP) solutions was found to be enhanced by the addition of bovine carbonic anhydrase (CA), has been investigated using a vap...
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Veröffentlicht in: | The journal of physical chemistry. B 2013-05, Vol.117 (18), p.5683-5690-5683-5690 |
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container_title | The journal of physical chemistry. B |
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creator | Vinoba, Mari Bhagiyalakshmi, Margandan Grace, Andrews Nirmala Kim, Dae Hoon Yoon, Yeoil Nam, Sung Chan Baek, Il Hyun Jeong, Soon Kwan |
description | The rate of carbon dioxide (CO sub(2)) absorption by monoethanol amine (MEA), diethanol amine (DEA), N-methyl-2,2'-iminodiethanol (MDEA), and 2-amino-2-methyl 1-propanol (AMP) solutions was found to be enhanced by the addition of bovine carbonic anhydrase (CA), has been investigated using a vapor-liquid equilibrium (VLE) device. The enthalpy (- Delta H sub(abs)) of CO sub(2) absorption and the absorption capacities of aqueous amines were measured in the presence and/or absence of CA enzyme via differential reaction calorimeter (DRC). The reaction temperature ( Delta T) under adiabatic conditions was determined based on the DRC analysis. Bicarbonate and carbamate species formation mechanisms were elucidated by super(1)H and super(13)C NMR spectral analysis. The overall CO sub(2) absorption rate (flux) and rate constant (k sub(app)) followed the order MEA > DEA > AMP > MDEA in the absence or presence of CA. Hydration of CO sub(2) by MDEA in the presence of CA directly produced bicarbonate, whereas AMP produced unstable carbamate intermediate, then underwent hydrolytic reaction and converted to bicarbonate. The MDEA > AMP > DEA > MEA reverse ordering of the enhanced CO sub(2) flux and k sub(app) in the presence of CA was due to bicarbonate formation by the tertiary and sterically hindered amines. Thus, CA increased the rate of CO sub(2) absorption by MDEA by a factor of 3 relative to the rate of absorption by MDEA alone. The thermal effects suggested that CA yielded a higher activity at 40 degree C. |
doi_str_mv | 10.1021/jp401622c |
format | Article |
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The enthalpy (- Delta H sub(abs)) of CO sub(2) absorption and the absorption capacities of aqueous amines were measured in the presence and/or absence of CA enzyme via differential reaction calorimeter (DRC). The reaction temperature ( Delta T) under adiabatic conditions was determined based on the DRC analysis. Bicarbonate and carbamate species formation mechanisms were elucidated by super(1)H and super(13)C NMR spectral analysis. The overall CO sub(2) absorption rate (flux) and rate constant (k sub(app)) followed the order MEA > DEA > AMP > MDEA in the absence or presence of CA. Hydration of CO sub(2) by MDEA in the presence of CA directly produced bicarbonate, whereas AMP produced unstable carbamate intermediate, then underwent hydrolytic reaction and converted to bicarbonate. The MDEA > AMP > DEA > MEA reverse ordering of the enhanced CO sub(2) flux and k sub(app) in the presence of CA was due to bicarbonate formation by the tertiary and sterically hindered amines. Thus, CA increased the rate of CO sub(2) absorption by MDEA by a factor of 3 relative to the rate of absorption by MDEA alone. The thermal effects suggested that CA yielded a higher activity at 40 degree C.</description><identifier>ISSN: 1520-6106</identifier><identifier>EISSN: 1520-5207</identifier><identifier>DOI: 10.1021/jp401622c</identifier><language>eng</language><subject>Amines ; Bicarbonates ; Carbon dioxide ; Carbonic anhydrase ; Flux ; Formations ; Hydration ; Spectra</subject><ispartof>The journal of physical chemistry. 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Hydration of CO sub(2) by MDEA in the presence of CA directly produced bicarbonate, whereas AMP produced unstable carbamate intermediate, then underwent hydrolytic reaction and converted to bicarbonate. The MDEA > AMP > DEA > MEA reverse ordering of the enhanced CO sub(2) flux and k sub(app) in the presence of CA was due to bicarbonate formation by the tertiary and sterically hindered amines. Thus, CA increased the rate of CO sub(2) absorption by MDEA by a factor of 3 relative to the rate of absorption by MDEA alone. The thermal effects suggested that CA yielded a higher activity at 40 degree C.</description><subject>Amines</subject><subject>Bicarbonates</subject><subject>Carbon dioxide</subject><subject>Carbonic anhydrase</subject><subject>Flux</subject><subject>Formations</subject><subject>Hydration</subject><subject>Spectra</subject><issn>1520-6106</issn><issn>1520-5207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqVi7sKwkAQRRdR8Fn4B1NqEd3dmEcrQbFTxMZKNnHESLITdzaFf6-IP2BxOac4V4ipkgsltVo-mpVUsdZFRwxUpGXwWdL9eaxk3BdD5oeUOtJpPBDnzLicbFnA2t5fV2cY4eCoJo8M_o6wzplc40uycDQegW6Q7YHbfKbnUFo4EPsgozpv-Rt9zgUyI49F72YqxsmPIzHbbk7ZLmgcPVtkf6lLLrCqjEVq-aKSKIxkmqgw_CN9A_xGSpQ</recordid><startdate>20130509</startdate><enddate>20130509</enddate><creator>Vinoba, Mari</creator><creator>Bhagiyalakshmi, Margandan</creator><creator>Grace, Andrews Nirmala</creator><creator>Kim, Dae Hoon</creator><creator>Yoon, Yeoil</creator><creator>Nam, Sung Chan</creator><creator>Baek, Il Hyun</creator><creator>Jeong, Soon Kwan</creator><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20130509</creationdate><title>Carbonic Anhydrase Promotes the Absorption Rate of CO sub(2) in Post-Combustion Processes</title><author>Vinoba, Mari ; Bhagiyalakshmi, Margandan ; Grace, Andrews Nirmala ; Kim, Dae Hoon ; Yoon, Yeoil ; Nam, Sung Chan ; Baek, Il Hyun ; Jeong, Soon Kwan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_17535087133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Amines</topic><topic>Bicarbonates</topic><topic>Carbon dioxide</topic><topic>Carbonic anhydrase</topic><topic>Flux</topic><topic>Formations</topic><topic>Hydration</topic><topic>Spectra</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vinoba, Mari</creatorcontrib><creatorcontrib>Bhagiyalakshmi, Margandan</creatorcontrib><creatorcontrib>Grace, Andrews Nirmala</creatorcontrib><creatorcontrib>Kim, Dae Hoon</creatorcontrib><creatorcontrib>Yoon, Yeoil</creatorcontrib><creatorcontrib>Nam, Sung Chan</creatorcontrib><creatorcontrib>Baek, Il Hyun</creatorcontrib><creatorcontrib>Jeong, Soon Kwan</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>The journal of physical chemistry. B</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vinoba, Mari</au><au>Bhagiyalakshmi, Margandan</au><au>Grace, Andrews Nirmala</au><au>Kim, Dae Hoon</au><au>Yoon, Yeoil</au><au>Nam, Sung Chan</au><au>Baek, Il Hyun</au><au>Jeong, Soon Kwan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbonic Anhydrase Promotes the Absorption Rate of CO sub(2) in Post-Combustion Processes</atitle><jtitle>The journal of physical chemistry. B</jtitle><date>2013-05-09</date><risdate>2013</risdate><volume>117</volume><issue>18</issue><spage>5683</spage><epage>5690-5683-5690</epage><pages>5683-5690-5683-5690</pages><issn>1520-6106</issn><eissn>1520-5207</eissn><abstract>The rate of carbon dioxide (CO sub(2)) absorption by monoethanol amine (MEA), diethanol amine (DEA), N-methyl-2,2'-iminodiethanol (MDEA), and 2-amino-2-methyl 1-propanol (AMP) solutions was found to be enhanced by the addition of bovine carbonic anhydrase (CA), has been investigated using a vapor-liquid equilibrium (VLE) device. The enthalpy (- Delta H sub(abs)) of CO sub(2) absorption and the absorption capacities of aqueous amines were measured in the presence and/or absence of CA enzyme via differential reaction calorimeter (DRC). The reaction temperature ( Delta T) under adiabatic conditions was determined based on the DRC analysis. Bicarbonate and carbamate species formation mechanisms were elucidated by super(1)H and super(13)C NMR spectral analysis. The overall CO sub(2) absorption rate (flux) and rate constant (k sub(app)) followed the order MEA > DEA > AMP > MDEA in the absence or presence of CA. Hydration of CO sub(2) by MDEA in the presence of CA directly produced bicarbonate, whereas AMP produced unstable carbamate intermediate, then underwent hydrolytic reaction and converted to bicarbonate. The MDEA > AMP > DEA > MEA reverse ordering of the enhanced CO sub(2) flux and k sub(app) in the presence of CA was due to bicarbonate formation by the tertiary and sterically hindered amines. Thus, CA increased the rate of CO sub(2) absorption by MDEA by a factor of 3 relative to the rate of absorption by MDEA alone. The thermal effects suggested that CA yielded a higher activity at 40 degree C.</abstract><doi>10.1021/jp401622c</doi></addata></record> |
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subjects | Amines Bicarbonates Carbon dioxide Carbonic anhydrase Flux Formations Hydration Spectra |
title | Carbonic Anhydrase Promotes the Absorption Rate of CO sub(2) in Post-Combustion Processes |
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