Ively either is usually esterified with methanol to make a black in Figure as the intermediate, which can then be competitively hemiacetal species oxidized to MMA as the desired alkyl ester solution or over-esterified with methanol to an acetal species as an undesired either oxidized to MMA asnanoparticles have been product or over-esterified withthat the Au nanoparticles were dispersed the desired alkyl ester not observed, indicating methanol to an acetal species as an byproduct. undesired byproduct. using a small size QPX7728-OH disodium supplier distribution and that bulky nanoparticles had been not developed.3.2. Impact of Assistance Crystallinities in CeO2 g(OH)two Supporting Au Nanoparticles The crystallinities of CeO2 g(OH)two for supporting Au nanoparticles might be controlled by altering the calcination temperature. From the controlled Ce:Mg ratios, we selected the sample with Ce:Mg = 37:63 as the one showing the optimized catalytic performance (Figure two). Based on the calcination temperature, the crystallinities with the CeO2 g(OH)two supports changed, as evidenced by the XRD patterns shown in Figure 3A. The XRD reflections progressively sharpened as the calcination temperature was increased from 450 to 1000 . When the calcination temperature was 450 , the crystallinity was drastically reduce, as evidenced by quite broad XRD reflections.Figure two. Reaction summaries showing the MACR conversion item Fluo-4 AM web selectivity obtained Figure two. Reaction summaries showing the MACR conversion and and item selectivity obtained by by utilizing Au/CeO2 g(OH) with distinct Ce:Mg ratios calcined at 750 . The results working with Au/CeO2 g(OH)2 2with different Ce:Mg ratios calcined at 750 C. The outcomes are also are also summarized in Table 1. 1. The reaction carried out at 80 C for 1 h. summarized in Table The reaction waswas carried out at 80 for 1 h.Figure 3. (A) X-ray diffraction patterns, (B) N2 adsorption/desorption isotherms with pore size distributions (inset), andThe series of Au metal nanoparticles supported on CeO2 g(OH)two was investigated as the catalyst for the DOE reaction of MACR with methanol (Scheme 1). Figure 2 presents the reaction benefits and shows the MACR conversion and item selectivity based on the composition ratio of Ce and Mg within the catalyst help; the outcomes are alsoNanomaterials 2021, 11,6 ofNanomaterials 2021, 11,selectivity. When the ratio of Ce:Mg was amongst 80:20 and 37:63 in the synthesis gel, MACR conversion above 65 was achieved using a high MMA selectivity of close to 100 (Figure two).6 ofWhen Mg(OH)two was introduced to the catalyst assistance, the Au-supporting CeO2 Mg(OH)2 catalysts produced MMA as the preferred product. As the quantity of Mg(OH)2 inside the CeO2 g(OH)two help increases, a pseudo-volcano distribution is observed for the MACR conversion (black dots in Figure two). When the ratio of Ce:Mg was between 80:20 and 37:63 within the synthesis gel, higher MACR conversion values 67.43.9 have been obtained, and also the MMA selectivity was close to one hundred . When the level of Mg precursor inside the synthesis gel enhanced beyond 80 (Ce:Mg = 20:80), the MACR conversion dropped under 50 , plus the MMA selectivity also gradually decreased. When pure Mg(OH)two was employed as the help for Au nanoparticles inside the absence of CeO2 (Ce:Mg = 0:100), the MACR conversion was Scheme 1. DOE reaction of MACR with methanol beneath aerobic situations by using oxygen as the oxidant. MACR can 40.three , and the MMA selectivity was correspondingly decreased to 72.five . The volcano be esterified with methanol to produce a hem.
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