Documents disponibles écrits par cet auteur

Experimental study of HCl capture using CaO sorbents / Zhenchao Sun in Industrial & engineering chemistry research, Vol. 50 N° 10 (Mai 2011) 

Public ISBD [article]  in Industrial & engineering chemistry research > Vol. 50 N° 10 (Mai 2011) . - pp. 6034-6043 Titre : Experimental study of HCl capture using CaO sorbents : activation, deactivation, reactivation, and ionic transfer mechanism Type de document : texte imprimé Auteurs : Zhenchao Sun, Auteur ; Fu-Chen Yu, Auteur ; Fanxing Li, Auteur Année de publication : 2011 Article en page(s) : pp. 6034-6043 Note générale : Chimie industrielle Langues : Anglais (eng) Mots-clés : Deactivation  Activation Résumé : Experimental study of dry HCl removal from synthesis gas or flue gas using CaO sorbents, in the context of CaO-based chemical looping processes, is reported. The study was first conducted in a TGA and a fixed-bed reactor to test the effects of chloridation temperature, sorbent particle size, HCl concentration, and space velocity on the HCl capture capacity. The chloridation reactivity deterioration of CaO sorbents with multicyclic carbonation-calcination reaction (CCR) and/or at high calcination temperatures, which are of notable relevance to the CaO-based chemical looping processes, was also investigated. In addition, precipitation (activation) and hydration (reactivation) were used to enhance initial sorbent reactivity and to reactivate the deactivated sorbents, respectively. The effects of deactivation, activation, and reactivation were explained by the morphological property change of the sorbents. To further elucidate the solid phase reaction mechanism of CaO and HCl, ionic transfer behavior during chloridation reaction was characterized using an inert marker experiment Through the present work, the performance of CaO sorbents in HCl capture, deactivation of the sorbents by high-temperature calcination and multiple CCR cycles, sorbent activation and reactivation strategies, and the corresponding reaction mechanisms are determined. DEWEY : 660 ISSN : 0888-5885 En ligne : http://cat.inist.fr/?aModele=afficheN&cpsidt=24158901 [article] Experimental study of HCl capture using CaO sorbents : activation, deactivation, reactivation, and ionic transfer mechanism [texte imprimé] / Zhenchao Sun, Auteur ; Fu-Chen Yu, Auteur ; Fanxing Li, Auteur . - 2011 . - pp. 6034-6043. Chimie industrielle Langues : Anglais (eng) in Industrial & engineering chemistry research > Vol. 50 N° 10 (Mai 2011) . - pp. 6034-6043 Mots-clés : Deactivation  Activation Résumé : Experimental study of dry HCl removal from synthesis gas or flue gas using CaO sorbents, in the context of CaO-based chemical looping processes, is reported. The study was first conducted in a TGA and a fixed-bed reactor to test the effects of chloridation temperature, sorbent particle size, HCl concentration, and space velocity on the HCl capture capacity. The chloridation reactivity deterioration of CaO sorbents with multicyclic carbonation-calcination reaction (CCR) and/or at high calcination temperatures, which are of notable relevance to the CaO-based chemical looping processes, was also investigated. In addition, precipitation (activation) and hydration (reactivation) were used to enhance initial sorbent reactivity and to reactivate the deactivated sorbents, respectively. The effects of deactivation, activation, and reactivation were explained by the morphological property change of the sorbents. To further elucidate the solid phase reaction mechanism of CaO and HCl, ionic transfer behavior during chloridation reaction was characterized using an inert marker experiment Through the present work, the performance of CaO sorbents in HCl capture, deactivation of the sorbents by high-temperature calcination and multiple CCR cycles, sorbent activation and reactivation strategies, and the corresponding reaction mechanisms are determined. DEWEY : 660 ISSN : 0888-5885 En ligne : http://cat.inist.fr/?aModele=afficheN&cpsidt=24158901

Physical and chemical mechanism for increased surface area and pore volume of CaO in water hydration / Zhenchao Sun in Industrial & engineering chemistry research, Vol. 51 N° 33 (Août 2012) 

Public ISBD [article]  in Industrial & engineering chemistry research > Vol. 51 N° 33 (Août 2012) . - pp. 10793-10799 Titre : Physical and chemical mechanism for increased surface area and pore volume of CaO in water hydration Type de document : texte imprimé Auteurs : Zhenchao Sun, Auteur ; Hao Chi, Auteur ; Liang-Shih Fan, Auteur Année de publication : 2012 Article en page(s) : pp. 10793-10799 Note générale : Industrial chemistry Langues : Anglais (eng) Mots-clés : Hydration  Surface  area Résumé : The present work explores the fundamental mechanism behind the increased surface area and pore volume of CaO after hydration. First, a widely believed mechanism, the "physical attrition theory", is experimentally examined and is found to have limitations in explaining this phenomenon. Next, to explain the improvement of morphological properties by hydration, a typical water hydration process is examined by dividing the process into four independent chemical and physical substeps. The morphological changes of Ca(OH)2 and its derived CaO by each substep are measured by Brunauer―Emmett―Teller (BET) analysis. During the first step, the intrinsic chemical conversion from CaO to Ca(OH)2, the formed Ca(OH)2 product layer disintegrates because of its low tensile strength and weak crack resistance, which explains the increases in surface area and pore volume by steam/moisture hydration as well as the rapid heat release during hydration. The physical interaction with water (the second step) slightly decreases the surface area and pore volume, possibly by lodging microparticles into the porous structure of bigger particles and inducing stronger particle agglomeration. The Ca(OH)2 solid can further chemically bond water molecules (the third step), which significantly enlarges the solid volume during water-bonding and consequently generates a more porous structure during dehydration. The final precipitation of the dissolved Ca(OH)2 (the fourth step) decreases the solid's surface area and pore volume. This decrease is attributed to the formed microparticles from solution, which can plug some surface pores on the larger particles during the drying process. ISSN : 0888-5885 En ligne : http://cat.inist.fr/?aModele=afficheN&cpsidt=26286454 [article] Physical and chemical mechanism for increased surface area and pore volume of CaO in water hydration [texte imprimé] / Zhenchao Sun, Auteur ; Hao Chi, Auteur ; Liang-Shih Fan, Auteur . - 2012 . - pp. 10793-10799. Industrial chemistry Langues : Anglais (eng) in Industrial & engineering chemistry research > Vol. 51 N° 33 (Août 2012) . - pp. 10793-10799 Mots-clés : Hydration  Surface  area Résumé : The present work explores the fundamental mechanism behind the increased surface area and pore volume of CaO after hydration. First, a widely believed mechanism, the "physical attrition theory", is experimentally examined and is found to have limitations in explaining this phenomenon. Next, to explain the improvement of morphological properties by hydration, a typical water hydration process is examined by dividing the process into four independent chemical and physical substeps. The morphological changes of Ca(OH)2 and its derived CaO by each substep are measured by Brunauer―Emmett―Teller (BET) analysis. During the first step, the intrinsic chemical conversion from CaO to Ca(OH)2, the formed Ca(OH)2 product layer disintegrates because of its low tensile strength and weak crack resistance, which explains the increases in surface area and pore volume by steam/moisture hydration as well as the rapid heat release during hydration. The physical interaction with water (the second step) slightly decreases the surface area and pore volume, possibly by lodging microparticles into the porous structure of bigger particles and inducing stronger particle agglomeration. The Ca(OH)2 solid can further chemically bond water molecules (the third step), which significantly enlarges the solid volume during water-bonding and consequently generates a more porous structure during dehydration. The final precipitation of the dissolved Ca(OH)2 (the fourth step) decreases the solid's surface area and pore volume. This decrease is attributed to the formed microparticles from solution, which can plug some surface pores on the larger particles during the drying process. ISSN : 0888-5885 En ligne : http://cat.inist.fr/?aModele=afficheN&cpsidt=26286454