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Oxidative Desulfurization of Dibenzothiophene Using Dawson TypeudHeteropoly Compounds/Tantalum as Catalystud

机译:Dawson型 ud对二苯并噻吩的氧化脱硫杂多化合物/钽催化剂 ud

摘要

Catalyst (NH4)6[-P2W18O62]/Ta has been synthesized by simple wet impregnation at 30-40 °C underudatmospheric conditions using Dawson type polyoxometalate (NH4)6[-P2W18O62] and tantalum. The catalyst wasudcharacterized by FTIR spectrophotometer, XRD, SEM, and N2 adsorption desorption methods. FTIR spectrum ofud(NH4)6[-P2W18O62]/Ta showed that Dawson type polyoxometalate (NH4)6[-P2W18O62] and Ta was successfullyudimpregnated which was indicated by vibration spectrum at wavenumber of 900-1100 cm-1 for polyoxometalate andud550 cm-1 for Ta. The surface area of the (NH4)6[-P2W18O62]/Ta after impregnation was higher than (NH4)6[-udP2W18O62]•nH2O and its morphology was found to be uniform. The catalytic activity of (NH4)6[-P2W18O62]/Ta towarduddesulfurization of dibenzothiophene was three times higher than the original catalyst of (NH4)6[-P2W18O62]•nH2Oudwithout impregnation. The catalytic regeneration test of catalyst (NH4)6[-P2W18O62]/Ta showed that the catalyticudactivity for first regeneration of catalyst has similar catalytic activity with the fresh catalyst without loss of catalyticudactivity indicated by almost similar percent conversion.udKeywords: dibenzothiophene; Dawson type; heteropoly; tantalum; desulfurization
机译:催化剂(NH4)6 [α-P2W18O62] / Ta是在Datson型多金属氧酸盐(NH4)6 [α-P2W18O62]和钽下于大气压条件下于30-40°C进行简单的湿法浸渍而合成的。用FTIR分光光度计,XRD,SEM和N2吸附脱附法表征了催化剂。 ud(NH4)6 [α-P2W18O62] / Ta的FTIR光谱表明,Dawson型多金属氧酸盐(NH4)6 [α-P2W18O62]和Ta已成功未浸渍,这由波谱在900-1100 cm-处的振动光谱指示。多金属氧酸盐为1,Ta为ud550 cm-1。浸渍后的(NH 4)6 [1 -P 2 W 18 O 62] / Ta的表面积大于(NH 4)6 [1- udP 2 W 18 O 62]·nH 2 O的表面积,发现其形态均匀。 (NH4)6 [α-P2W18O62] / Ta对二苯并噻吩的 uddesulfurization的催化活性是(NH4)6 [β-P2W18O62]·nH2O u>未经浸渍的原始催化剂的三倍。催化剂(NH4)6 [-P2W18O62] / Ta的催化再生试验表明,催化剂初生的催化活性与新鲜催化剂具有相似的催化活性,而转化率几乎相似,而没有失去催化活性。关键字:二苯并噻吩;道森型异质钽脱硫

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