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Study of the Temperature-Programmed Desorption of Carbon Dioxide (CO2) on Zeolites X Modified with Bivalent Cations
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作者 Charly Mve Mfoumou Francis Ngoye +4 位作者 Pradel Tonda-Mikiela Ferdinand Evoung Evoung Landry Biyoghe Bi-Ndong Thomas Belin Samuel Mignard 《Journal of Environmental Protection》 CAS 2023年第1期66-82,共17页
Study of physisorbed and chemisorbed carbon dioxide (CO<sub>2</sub>) species was carried out on the NaX zeolite modified by cationic exchanges with bivalent cations (Ca<sup>2+</sup> and Ba<s... Study of physisorbed and chemisorbed carbon dioxide (CO<sub>2</sub>) species was carried out on the NaX zeolite modified by cationic exchanges with bivalent cations (Ca<sup>2+</sup> and Ba<sup>2+</sup>) by temperature-programmed desorption of CO<sub>2</sub> (CO<sub>2</sub>-TPD). Others results were obtained by infrared to complete the study. The results of this research showed, in the physisorption region (213 - 473 K), that the cationic exchanges on NaX zeolite with bivalent cations increase slightly the interactions of CO<sub>2</sub> molecule with adsorbents and/or cationic site. Indeed, the desorption energies of physisorbed CO<sub>2</sub> obtained on the reference zeolite NaX (13.5 kJ·mol<sup>-1</sup>) are lower than that of exchanged zeolites E-CaX and E-BaX (15.77 and 15.17 kJ·mol<sup>-1</sup> respectively). In the chemisorbed CO<sub>2</sub> region (573 - 873 K), the desorption energies related to desorbed species (bidentate carbonates: CO<sub>3</sub>2-</sup>) on the exchanged zeolites E-CaX and E-BaX are about 81 kJ·mol<sup>-1</sup>, higher than the desorbed species (bicarbonates: HCO<sub>3</sub>2-</sup>) on the reference R-NaX (62 kJ·mol<sup>-1</sup>). In addition, the exchanged E-BaX zeolite develops the secondary adsorption sites corresponding to bicarbonates species with desorption energies of 35 kJ·mol<sup>-1</sup> lower to desorption energies of bicarbonates noted on the reference zeolite NaX. 展开更多
关键词 Adsorption Faujasite X Chemisorbed and Physisorbed CO2 Exchanged Zeolites bivalent cations Temperature-Programmed Desorption (TPD) Infrared
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ROLE OF BIVALENT CATIONS AND CHOLINE IN ATP-INDUCED APOPTOSIS OF HUMAN LYMPHOCYTES WITH P2Z RECEPTORS
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作者 彭黎明 JamesSWiley 《Chinese Medical Sciences Journal》 CAS CSCD 1999年第1期23-30,共8页
The role of bivalent cations and choline in ATP induced apoptosis via P2Z purinoceptor was investigated in human leukemic lymphocytes. In vitro exposure of leukemic lymphocytes with P2Z rec... The role of bivalent cations and choline in ATP induced apoptosis via P2Z purinoceptor was investigated in human leukemic lymphocytes. In vitro exposure of leukemic lymphocytes with P2Z receptors to 1 mmol/L ATP or 0 1 mmol/L benzoylbenzoic ATP(BzATP) for 8 h in the presence of choline, 1 mmol/L Mg 2+ or other bivalent cations, and ATP induced DNA breaks, associated with apoptosis were quantified by TdT assay. We observed that (1) Extracellular Mg 2+ or Ca 2+ stimulated ATP induced DNA fragmentation in a dose dependent manner, and the compatible evidence was provided by the inhibition of ATP induced DNA fragmentation in the present of EGTA or EDTA; (2) ATP induced DNA fragmentation was completely inhibited by 1 mmol/L Zn 2+ ;(3)ATP induced DNA breaks were not affected by Ba 2+ , Sr 2+ , Co 2+ when they were substituted for extracellular Mg 2+ or Ca 2+ ;(4)Choline, an inhibitor of phospholipase D(PLD) stimulated by ATP through P2Z receptor in human lymphocytes, was also a partial inhibitor of ATP induced DNA fragmentation, and the results were confirmed by flow cytometric analysis (FCA); (5)ATP induced DNA fragmentation was completely obliterated when the temperature was lower than 10℃. These results suggest that the endonuclease and PLD may be involved in ATP induced apoptosis in human lymphocytes via P2Z receptor. 展开更多
关键词 P2Z purinoceptor apoptosis bivalent cation
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THE STRUCTURE OF ACTIVE SITE AND THE ROLE OF BIVALENT CATION IN FERRITE-FERRIC OXIDE CATALYSTS FOR OXIDATIVE DEHYDROGENATION OF BUTENES
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作者 Shu CHEN Li Ying YANG +1 位作者 Jian Hong CHEN Yuan Gen YIN 《Chinese Chemical Letters》 SCIE CAS CSCD 1992年第11期925-928,共4页
The relations between catalytic activities and compositions of the systems Mg_xZn_(1-x)Fe_2O_4, Co_xZn_(1-x)Fe_2O_4, Co_xMg_(1-x)Fe_2O_4, Cd_xZn_(1-x)Fe_2O_4 and Mg_xZn_(1-x)Fe_2O_4·0.17Fe_2O_3 have been studied ... The relations between catalytic activities and compositions of the systems Mg_xZn_(1-x)Fe_2O_4, Co_xZn_(1-x)Fe_2O_4, Co_xMg_(1-x)Fe_2O_4, Cd_xZn_(1-x)Fe_2O_4 and Mg_xZn_(1-x)Fe_2O_4·0.17Fe_2O_3 have been studied by flow differential reactor, XRD, and derivative IR techniques. It has been found that the appropriate normal-inverse spinel combination substantially increases the activity for the title raction. The structure of the active site and the role of the bivalent cation in the title catalyst have been inferred. 展开更多
关键词 THE STRUCTURE OF ACTIVE SITE AND THE ROLE OF bivalent CATION IN FERRITE-FERRIC OXIDE CATALYSTS FOR OXIDATIVE DEHYDROGENATION OF BUTENES SITE XRD
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