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Towards efficient polyoxometalate encapsulation in MIL-100(Cr): influence of synthesis conditions
被引:58
作者:
Juan-Alcaniz, Jana
[1
]
Goesten, Maarten G.
[1
]
Ramos-Fernandez, Enrique V.
[1
]
Gascon, Jorge
[1
]
Kapteijn, Freek
[1
]
机构:
[1] Delft Univ Technol, Catalysis Engn ChemE, NL-2628 BL Delft, Netherlands
关键词:
METAL-ORGANIC FRAMEWORKS;
PHOSPHOTUNGSTIC ACID;
TEREPHTHALIC ACID;
HETEROPOLY ACID;
CATALYSIS;
PLATINUM;
WATER;
CO2;
D O I:
10.1039/c2nj20587d
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The one-pot encapsulation of phosphotungstic acid in the metal-organic framework MIL-100(Cr) has been studied under different synthesis conditions. Both conventional and microwave heating methods have been explored for three different solvent systems: pure aqueous or organic (DMF) phase and biphasic mixtures (water/2-pentanol). Biphasic systems yielded crystals with similar textural properties as those formed in water. The use of DMF as solvent promotes the formation of gel-like solids with dual porosity and enhanced accessibility. The addition of phosphotungstic acid (PTA, H3PW12O40 center dot xH(2)O) to the MIL-100(Cr) synthesis mixture results in its direct encapsulation. P-31 MAS NMR, elemental analysis, N-2 adsorption and FT-IR spectroscopy confirm the incorporation of PTA in the sample. The highest PTA encapsulation loading (30 wt%) was obtained by synthesis with microwave heating in biphasic solvent systems (W/Cr molar ratio range between 0.5 and 0.25). Microwave irradiation decreases the time of synthesis (from 4 days to 3 hours) while the use of biphasic media preserves the PTA integrity without affecting the formation of the MOF. The interaction of PTA with the MIL-100(Cr) structure results in some loss of the Lewis acidity, while the Bronsted acidity is hardly affected.
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页码:977 / 987
页数:11
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