“…Compared with the results reported, , the bands of all carbonate species shift to a higher wavenumber, probably due to the introduction of rare earth elements in the lattice of hydrotalcite. The following base strength order for these surface oxygen species were also determined: low coordination O 2– anions > oxygen in Mn + –O 2– pairs > OH groups …”
Section: Resultscontrasting
confidence: 84%
“…The third adsorbed species is an unidentate carbonate, which requires isolated surface O 2– ions (low-coordination anions, such as those located at corners or edges) and exhibits a symmetric O–C–O stretching at 1540 cm –1 and an asymmetric O–C–O stretching at 1630 cm –1 . Compared with the results reported, , the bands of all carbonate species shift to a higher wavenumber, probably due to the introduction of rare earth elements in the lattice of hydrotalcite. The following base strength order for these surface oxygen species were also determined: low coordination O 2– anions > oxygen in Mn + –O 2– pairs > OH groups …”
The
liquid phase synthesis of pseudoionones (PS) by the cross-aldol
condensation of citral and acetone was investigated over MgAl mixed
oxides containing rare earth elements (REE = Y, La, Eu), which were
obtained from corresponding REE-modified hydrotalcite materials after
calcination. The results showed that the unmodified and La(Eu)-modified
MgAl mixed oxide catalysts showed relatively low activity, and Y-modified
MgAl mixed oxides presented an unexpected high catalytic activity.
PS selectivity of ∼85% and citral conversion of 100% were achieved
at 60 °C for 3 h. On the basis of the characterizations of the
structural, textural, and basic properties, it was found that Mg3Al1‑aYaO
x
catalysts exhibited relatively well-developed small flake
morphology with high surface area and pore volume, resulting in exposure
of more basic sites on the catalyst surface. The formation of PS over
Mg3Al1‑aYaO
x
may be accompanied by gradual modification of the catalyst
surface to form re-Mg3Al1‑aYaO
x
through a rehydration process with
produced water, which reconverts the O2– basic sites
to OH– basic groups. Unlike La and Eu elements,
the presence of Y could promote this “one-pot” or in situ rehydration process of MgAl mixed oxides during
the aldol reaction. This Y-modified MgAl mixed oxides after a one-pot
rehydration process with active Brønsted basic sites is responsible
for the high activity in the cross-aldol condensation of citral and
acetone.
“…Compared with the results reported, , the bands of all carbonate species shift to a higher wavenumber, probably due to the introduction of rare earth elements in the lattice of hydrotalcite. The following base strength order for these surface oxygen species were also determined: low coordination O 2– anions > oxygen in Mn + –O 2– pairs > OH groups …”
Section: Resultscontrasting
confidence: 84%
“…The third adsorbed species is an unidentate carbonate, which requires isolated surface O 2– ions (low-coordination anions, such as those located at corners or edges) and exhibits a symmetric O–C–O stretching at 1540 cm –1 and an asymmetric O–C–O stretching at 1630 cm –1 . Compared with the results reported, , the bands of all carbonate species shift to a higher wavenumber, probably due to the introduction of rare earth elements in the lattice of hydrotalcite. The following base strength order for these surface oxygen species were also determined: low coordination O 2– anions > oxygen in Mn + –O 2– pairs > OH groups …”
The
liquid phase synthesis of pseudoionones (PS) by the cross-aldol
condensation of citral and acetone was investigated over MgAl mixed
oxides containing rare earth elements (REE = Y, La, Eu), which were
obtained from corresponding REE-modified hydrotalcite materials after
calcination. The results showed that the unmodified and La(Eu)-modified
MgAl mixed oxide catalysts showed relatively low activity, and Y-modified
MgAl mixed oxides presented an unexpected high catalytic activity.
PS selectivity of ∼85% and citral conversion of 100% were achieved
at 60 °C for 3 h. On the basis of the characterizations of the
structural, textural, and basic properties, it was found that Mg3Al1‑aYaO
x
catalysts exhibited relatively well-developed small flake
morphology with high surface area and pore volume, resulting in exposure
of more basic sites on the catalyst surface. The formation of PS over
Mg3Al1‑aYaO
x
may be accompanied by gradual modification of the catalyst
surface to form re-Mg3Al1‑aYaO
x
through a rehydration process with
produced water, which reconverts the O2– basic sites
to OH– basic groups. Unlike La and Eu elements,
the presence of Y could promote this “one-pot” or in situ rehydration process of MgAl mixed oxides during
the aldol reaction. This Y-modified MgAl mixed oxides after a one-pot
rehydration process with active Brønsted basic sites is responsible
for the high activity in the cross-aldol condensation of citral and
acetone.
“…Then, the mixture was stirred under 318 K for 24 h, aged at 373 K for 24 h under static conditions, and then the product filtered, thoroughly washed, dried, and calcined as for the preparation of the Al-SBA-15 sample [20]. The molar composition of the mixture, TEOS/ P123/Al(NO 3 …”
Section: Synthesis Of Al-containing Mesoporous Sba-15mentioning
confidence: 99%
“…The product of an aldol condensation can dehydrate to form an a,b-unsaturated carbonyl compound under either acidic or basic conditions. Hence, both the aldol condensation and the dehydration are capable of being catalyzed by conventional monofunctional catalysts that possess either acidic or basic centers [1][2][3][4].…”
“…The molar ratio between valeraldehyde and cyclopentanone also played an important role in the selectivity between cross-and self-condensation 3,7,9,16 . Entries 1-6 (Table-1) showed that valeraldehyde/cyclopentanone molar ratio of 1/5 was the optimal reaction condition.…”
The aldol condensation using cyclopentanone with valeraldehyde was conducted at hydrotalcites catalysis. The catalyst was obtained by calcining the hydrotalcite precursor (Mg/Al = 3:1) at 773 K. Its reaction performance was evaluated on the various molar ratios of cyclopentanone to n-valeraldehyde. A good catalytic selectivity of 90 % and a high conversion of 93 % were achieved under mild conditions.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.