A facile, safe, and environmentally friendly preparation method is described for the synthesis of AlFx(OH)3-x by the activation of y-Al2O3 using HCFO-1233zd(E) under various temperatures. Comprehensive characterization techniques including XRD, XPS, N2 sorption, SEM, TEM, 27Al MAS NMR, FTIR, and py-IR were employed, revealing that at lower temperatures such as 275 & DEG;C and 300 & DEG;C, the synthesis yielded AlF(OH)2, while at higher temperatures like 350 & DEG;C and 375 & DEG;C, pyrochlore AlF1.5(OH)1.5 and metastable hexagonal tungsten bronze-type (HTB) 13-AlF3 were formed, with a-AlF3 detected at 325 & DEG;C. Notably, a significant quantity of AlF(OH)2 can be obtained at 325 & DEG;C within a specific time frame. This amorphous phase exhibits weak Lewis acid sites and a lower acid density, rendering it significantly more effective in the isomerization of HCFO-1233zd(E) compared to strong Lewis acid catalysts such as AlF1.5(OH)1.5 and 13-AlF3, which could promote coke formation, leading to catalyst deactivation. Moreover, due to its limited further fluorination at 290 & DEG;C, the optimal catalyst exhibits prolonged lifespan and high efficiency in HCFO-1233zd(E) isomerization.& COPY; 2023 Elsevier Ltd. All rights reserved.