2017
DOI: 10.1016/j.catcom.2016.11.020
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Effect of nitric acid modification of montmorillonite clay on synthesis of solketal from glycerol and acetone

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Cited by 71 publications
(37 citation statements)
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“…Early, we demonstrated that the chemical composition and structural characteristics of Mt depended on the HNO 3 and HCl concentration [26,32]. Changes of chemical composition and interlayer space were negligible after modification of montmorillonite under the concentrations up to 0.5 M. These changes were noticeable only after treatment with 3.0 M acid.…”
Section: Transformation Of the Montmorillonite Structure Under Acid Tmentioning
confidence: 85%
See 1 more Smart Citation
“…Early, we demonstrated that the chemical composition and structural characteristics of Mt depended on the HNO 3 and HCl concentration [26,32]. Changes of chemical composition and interlayer space were negligible after modification of montmorillonite under the concentrations up to 0.5 M. These changes were noticeable only after treatment with 3.0 M acid.…”
Section: Transformation Of the Montmorillonite Structure Under Acid Tmentioning
confidence: 85%
“…Using ultrasound and microwaves in addition to an acid treatment intensifies smectite mineral transformation [27]. In industry, acid-modified bentonites are most commonly used as catalysts [28][29][30][31][32].…”
Section: Introductionmentioning
confidence: 99%
“…As shown in Table 5, solketal production from glycerol used two different sources, namely acetone or formaldehyde over solid acid catalysts [49][50][51][52]. Based on the conversion of glycerol and selectivity to solketal, the clay catalyst which showed the optimum results was reported by Timofeeva et al in a batch reactor with activated catalyst by nitric acid of 0.5 M [53]. In the activated K10 montmorillonite by acid solution, this impact causes an increasing rate of reaction with the acid site of the material.…”
Section: Ketalization Of Glycerol Over Clay Mineralsmentioning
confidence: 99%
“…Additionally, large quantities of glycerol are available as a reaction byproduct because of the development of biodiesel production by transesterification of vegetable oils [7]. Numerous main pathways of glycerol transformation have been reported in literature involving hydrogenolysis [8], dehydration [9], oxidation [10], carbonation [5,11], etherification [12,13], esterification [14,15], acetalization [14,16] and ketalization [17,18]. Therefore, a considerable number of chemical intermediates and commodities can be obtained from glycerol through optimized catalytic routes, as shown in Figure 1 [19].…”
Section: Introductionmentioning
confidence: 99%