The transformation of DL limonene (mixture of D- and L-form ~ 1:1) that came from the pyrolysis of scrap tires rubber was studied using four heteropolyacid catalysts (H3PW12O40, H3PMo12O40, H4SiW12O40 and H4PMo11VO40) supported on Q-10, SBA-15, MCM-41, and KIT-6. The catalyst activity was measured using a py/GC/FID under a nitrogen atmosphere. The active phase and support were characterized using various technical methods (XRD, Raman, TEM, N2 adsorption–desorption, NH3-TPD, and py-FTIR). The highest weak acidity and largest number of Lewis acid sites promoted the conversion of DL limonene. The isomerization reactions seemed to be more favored than disproportionation reactions. The p-cymene yield was favored, with a high weak acidity and high Lewis/Brønsted acid sites ratio. Moreover, the results show that the use of amorphous support with a higher pore size seems to promote the conversion of DL limonene and the production of p-cymene.