Thermally double coupled reactor coupling aqueous phase glycerol reforming and methanol synthesis

Author(s):  
Sasinun Thirabunjongcharoen ◽  
Palang Bumroongsakulsawat ◽  
Piyasan Praserthdam ◽  
Sumittra Charojrochkul ◽  
Suttichai Assabumrungrat ◽  
...  
2013 ◽  
Vol 56 (18-20) ◽  
pp. 1814-1828 ◽  
Author(s):  
Paul J. Dietrich ◽  
Tianpin Wu ◽  
Aslihan Sumer ◽  
James A. Dumesic ◽  
Julius Jellinek ◽  
...  

2012 ◽  
Vol 55 (1-2) ◽  
pp. 53-69 ◽  
Author(s):  
Paul J. Dietrich ◽  
Rodrigo J. Lobo-Lapidus ◽  
Tianpin Wu ◽  
Aslihan Sumer ◽  
M. Cem Akatay ◽  
...  

ChemCatChem ◽  
2014 ◽  
pp. n/a-n/a ◽  
Author(s):  
Aysegul Ciftci ◽  
Seda Eren ◽  
D. A. J. Michel Ligthart ◽  
Emiel J. M. Hensen

2020 ◽  
Vol 155 ◽  
pp. 01004
Author(s):  
Sasinun Thirabunjongcharoen ◽  
Pattaraporn Kim-Lohsoontorn

Thermally self-sustained double reactor (TSSDR) operating without external heat source consists of dual channels for endothermic and exothermic reactions. Hydrogen (H2) is produced from wasted glycerol by aqueous-phase glycerol reforming (APGR) at 200-250 ºC and 20-25 bar while carbon dioxide (CO2) is a by-product. Produced H2 and CO2 are used as raw materials for methanol synthesis (MS) at 200-250 ºC and 50-80 bar. Methanol synthesis and glycerol reforming occur at inner and outer channels of TSSDR, respectively. The TSSDR is fully packed with catalyst. Generated heat of exothermic reaction is sufficient for endothermic reaction. Main products of glycerol reforming in gas phase are H2 and CO2 while CO and CH4 are by-products. All products in gas phase are totally recycled as a feed stream for exothermic channel. CO and CH4 in feed reduce CO2 conversion and methanol yield in MS. The effect of impurities in glycerol feed stream also influences with hydrogen production in APGR. Especially, methanol, which is an impurity in glycerol feed obtained from biodiesel production, significantly reduces glycerol conversion in TSSDR.


1981 ◽  
Vol 11 ◽  
Author(s):  
M.H. Bradbury ◽  
D. Lever ◽  
D. Kinsey

One of the options being considered for the disposal of radioactive waste is deep burial in crystalline rocks such as granite. It is generally recognised that in such rocks groundwater flows mainly through the fracture networks so that these will be the “highways” for the return of radionuclides to the biosphere. The main factors retarding the radionuclide transport have been considered to be the slow water movement in the fissures over the long distances involved together with sorption both in man-made barriers surrounding the waste, and onto rock surfaces and degradation products in the fissures.


2020 ◽  
Author(s):  
Riccardo Mobili ◽  
Sonia La Cognata ◽  
Francesca Merlo ◽  
Andrea Speltini ◽  
Massimo Boiocchi ◽  
...  

<div> <p>The extraction of the succinate dianion from a neutral aqueous solution into dichloromethane is obtained using a lipophilic cage-like dicopper(II) complex as the extractant. The quantitative extraction exploits the high affinity of the succinate anion for the cavity of the azacryptate. The anion is effectively transferred from the aqueous phase, buffered at pH 7 with HEPES, into dichloromethane. A 1:1 extractant:anion adduct is obtained. Extraction can be easily monitored by following changes in the UV-visible spectrum of the dicopper complex in dichloromethane, and by measuring the residual concentration of succinate in the aqueous phase by HPLC−UV. Considering i) the relevance of polycarboxylates in biochemistry, as e.g. normal intermediates of the TCA cycle, ii) the relevance of dicarboxylates in the environmental field, as e.g. waste products of industrial processes, and iii) the recently discovered role of succinate and other dicarboxylates in pathophysiological processes including cancer, our results open new perspectives for research in all contexts where selective recognition, trapping and extraction of polycarboxylates is required. </p> </div>


2018 ◽  
Vol 84 (11) ◽  
pp. 23-27
Author(s):  
M. I. Degtev ◽  
A. A. Yuminova ◽  
A. S. Maksimov ◽  
A. P. Medvedev

The possibility of using an aqueous stratified system of antipyrine — sulfosalicylic acid — water for the selective isolation of scandium macro- and microquantities for subsequent determination is studied. The proposed extraction system eliminates the usage of toxic organic solvents. The organic phase with a volume of 1.2 to 2.0 ml, resulting from delamination of the aqueous phase containing antipyrine and sulfosalicylic acid is analysed to assess the possibility of using such systems for metal ions extraction. Condition necessary for the formation of such a phase were specified: the ratio of the initial components, their concentration, presence of inorganic salting out agents. The optimum ratio of antipyrine to sulfosalicylic acid is 2:1 at concentrations of 0.6 and 0.3 mol/liter in a volume of the aqueous phase of 10 ml. The obtained phase which consists of antipyrinium sulfosalicylate, free antipyrine and water, quantitatively extracts macro- and microquantities of scandium at pH = 1.54. Macro- and microquantities of yttrium, terbium, lanthanum, ytterbium and gadolinium are not extracted under the aforementioned conditions thus providing selective isolation of scandium from the bases containing yttrium, ytterbium, terbium, lanthanum, and gadolinium.


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