Transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach

Sulfided nickel, an established hydrocracking and hydrotreating catalyst for hydrocarbon refining, was synthesized on porous aluminosilicate supports for the hydrocracking of mixed polyolefin waste. Zeolite beta, zeolite 13X, MCM41 and an amorphous silica-alumina catalyst support were impregnated with the single-source precursor (SSP) nickel (II) ethyixanthate for catalyst support screening. Application of this synthesis method to beta-supported nickel (Ni@Beta), as an alternative to wet impregnation using aqueous nickel (11) nitrate, provided catalytic materials with higher conversion to fluid products at the same mild batch reaction conditions of 3,30 degrees C with appropriate agitation and 20 bar H-2 pressure. Mass balance quantification demonstrated that SSP-derived 5wt%Ni@Beta yielded a greater than 95 wt% conversion of a mixed polyolefin feed to fluid products, compared with 39.8 wt% conversion in the case of 5wt%Ni@Beta prepared by wet impregnation. Liquid and gas products were quantitatively analysed by gas chromatography-flame ionization detection (GC-FID) and gas chromatography-mass spectrometry (GC-MS), revealing a strong selectivity to saturated C-4 (37.3 wt%), C-5 (21.6 wt%) and C-6 (12.8 wt%) hydrocarbons in the case of the SSP-derived catalyst.

Automated summary

Sulfided nickel catalysts were synthesized for the hydrocracking of mixed polyolefin waste. Application of a single-source precursor method yielded catalytic materials with higher conversion and selectivity compared to wet impregnation.