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In situ infrared study of adsorbed s...

Khatri, Rajesh A.

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In situ infrared study of adsorbed species during catalytic oxidation and carbon dioxide adsorption.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	In situ infrared study of adsorbed species during catalytic oxidation and carbon dioxide adsorption./
作者:	Khatri, Rajesh A.
面頁冊數:	191 p.
附註:	Adviser: Steven S. C. Chuang.
Contained By:	Dissertation Abstracts International66-08B.
標題:	Chemistry, Inorganic. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3184546
ISBN:	9780542259135

In situ infrared study of adsorbed species during catalytic oxidation and carbon dioxide adsorption.
Khatri, Rajesh A.

In situ infrared study of adsorbed species during catalytic oxidation and carbon dioxide adsorption. - 191 p.

Adviser: Steven S. C. Chuang.

Thesis (Ph.D.)--The University of Akron, 2005.

Results of these studies can be used to enhance the overall conversion of CH4 to H2 thus lowering the cost of H2 product.

ISBN: 9780542259135Subjects--Topical Terms:

517253
Chemistry, Inorganic.

In situ infrared study of adsorbed species during catalytic oxidation and carbon dioxide adsorption.
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100 1 $a Khatri, Rajesh A. $3 1295841
245 1 0 $a In situ infrared study of adsorbed species during catalytic oxidation and carbon dioxide adsorption.
300 $a 191 p.
500 $a Adviser: Steven S. C. Chuang.
500 $a Source: Dissertation Abstracts International, Volume: 66-08, Section: B, page: 4359.
502 $a Thesis (Ph.D.)--The University of Akron, 2005.
520 $a Results of these studies can be used to enhance the overall conversion of CH4 to H2 thus lowering the cost of H2 product.
520 $a Hydrogen is considered to be the fuel of the next century. Hydrogen can be produced by either water splitting using the solar or nuclear energy or by catalytic cracking and reforming of the fossil fuels. The water splitting process using solar energy and photovoltaics is a clean way to produce hydrogen, but it suffers from very low efficiency. A promising scheme to produce H 2 from natural gas involves following steps: (i) partial oxidation and reforming of natural gas to syngas, (ii) water-gas shift reaction to convert CO in the syngas to additional H2, (iii) separation of the H2 from CO2, and (iv) CO2 sequestration.
520 $a The requirements for the above scheme are (i) a highly active coke resistant catalyst for generation of syngas by direct partial oxidation, (ii) a highly active sulfur tolerant catalyst for the water-gas shift reaction, and (iii) a low cost sorbent with high CO2 adsorption capacity for CO2 sequestration. This dissertation will address the mechanisms of partial oxidation, CO2 adsorption, and water-gas shift catalysis using in situ IR spectroscopy coupled with mass spectrometry (MS). The results from these studies will lead to a better understanding of the reaction mechanism and design of both the catalyst and sorbent for production of hydrogen with zero emissions.
520 $a Partial oxidation of methane is studied over Rh/Al2O 3 catalyst to elucidate the reaction mechanism for synthesis gas formation. The product lead-lag relationship observed with in situ IR and MS results revealed that syngas is produced via a two-step reforming mechanism: the first step involving total oxidation of CH4 to CO2 and H 2O and the second step involving the reforming of unconverted methane with CO2 and H2O to form syngas. Furthermore, the Rh on the catalyst surface remains predominantly in the partially oxidized state (Rhdelta+ and Rh0).
520 $a For the water-gas shift reaction, addition of Re to the Ni/CeO2 catalyst enhanced the water gas shift activity by a factor of three. The activity of the Ni-Re/CeO2 catalyst was reduced by only 20% in the presence of sulfur compared to a 50% reduction with the Ni/CeO 2 catalyst. These results show that Re not only promotes the water-gas shift reaction but also enhances the sulfur tolerance of the Ni/CeO2 catalyst.
520 $a Novel amine based solid sorbents have been developed to capture CO 2 reversibly using temperature-swing adsorption process. The IR study shows that CO2 adsorbs on amine grafted SBA-15 to form carbonates and bicarbonates. Comparison of monoamine and diamine-grafted SBA-15 showed that diamine grafted SBA-15 provides almost twice the active sites for CO 2 adsorption. The adsorption of SO2 on the amine-grafted SBA-15 revealed that SO2 adsorbs irreversibly and the sorbent cannot be regenerated under normal operating conditions.
590 $a School code: 0003.
650 4 $a Chemistry, Inorganic. $3 517253
650 4 $a Chemistry, Physical. $3 560527
650 4 $a Energy. $3 876794
650 4 $a Engineering, Chemical. $3 1018531
690 $a 0488
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690 $a 0791
710 2 0 $a The University of Akron. $3 1018399
773 0 $t Dissertation Abstracts International $g 66-08B.
790 $a 0003
790 1 0 $a Chuang, Steven S. C., $e advisor
791 $a Ph.D.
792 $a 2005
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3184546