In this preliminary research, the catalytic activity
of isopropyl alcohol conversion to diisopropyl ether through dehydration
reaction catalyzed by zeolite-Ni and zeolite-Ni(H2PO4)2 was comparatively described. The natural zeolite
was treated with
1% HF and 6 N HCl prior to modifications using the impregnation method.
Isopropyl alcohol conversion was examined at a mild temperature of
150 °C for 3.5 h on the reflux system with various catalyst loadings.
X-ray diffraction and Fourier transform infrared analysis confirmed
the successful impregnation of nickel and nickel phosphate into the
zeolite. Scanning electron microscopy analysis revealed a cubic-like
structure on zeolite-Ni(H2PO4)2,
whereas homogenously distributed nickel species were observed on the
zeolite-Ni catalyst. Energy-dispersive X-ray spectroscopy analysis
reinforced the accomplishment of zeolite modifications. The N2 physisorption isotherms showed a decline in the surface area
and total pore volume of the zeolite because of the blocking of pores.
The zeolite-Ni(H2PO4)2 catalyst had
higher acidity than unmodified zeolite and zeolite-Ni catalysts, which
inherently suggested that the presence of phosphate groups results
in higher catalytic activity toward isopropyl alcohol. The highest
catalytic activity was attained by 8 mEq/g metal loading zeolite-Ni(H2PO4)2 with isopropyl alcohol conversion
of 81.51%, diisopropyl ether yield, and selectivity of 40.77 and 33.16%.
The reusability study suggested that the zeolite-Ni(H2PO4)2 catalyst was still active and had sufficient
catalytic activity stability toward isopropyl alcohol after the third
cycle was reused. This nickel phosphate-based modified zeolite was
adequately potential for diisopropyl ether production through isopropyl
alcohol dehydration.