The addition of a second metal has demonstrated various improvements such as stabilizing Au active species by preventing reduction of Au (I) or Au (III), [3][4][5][6][7] increasing electron density of active species, and thereby promoting chemisorption of HCl which inhibits reduction of the gold, [8][9][10][11] promoting a higher dispersion of the gold, [12,13] and decreasing the formation of nanoparticles by agglomeration. [14] However, the addition of another metal can also incur drawbacks such as lower selectivity, which can lead to coke deposition and rapid deactivation of the catalyst, [13] short lifetime of the catalyst, [3,15] or the requirement of high loadings of the second metal to achieve comparable results to the gold monometallic. [5,13,16] In addition to these issues, a secondary metal may also lead to complications with precious metal recovery from spent catalysts. [17,18] Therefore non-metallic promoters are an interesting alternative for enhancing the activity and stability of gold catalysts for acetylene hydrochlorination. Zhang et al. investigated the modification of gold catalysts with nitrogen, phosphorous, and oxygen containing ligands. The authors concluded that coordination with these heteroatoms stabilized cationic gold species due to increased electron density around the active species. This also promoted a higher surface concentration of HCl compared with acetylene which facilities the hydrochlorination The formation of highly active and stable acetylene hydrochlorination catalysts is of great industrial importance. The successful replacement of the highly toxic mercuric chloride catalyst with gold has led to a flurry of research in this area. One key aspect, which led to the commercialization of the gold catalyst is the use of thiosulphate as a stabilizing ligand. This study investigates the use of a range of sulfur containing compounds as promoters for production of highly active Au/C catalysts. Promotion is observed across a range of metal sulfates, non-metal sulfates, and sulfuric acid treatments. This observed enhancement can be optimized by careful consideration of either pre-or post-treatments, concentration of dopants used, and modification of washing steps. Pre-treatment of the carbon support with sulfuric acid (0.76 m) resulted in the most active Au/C in this series with an acetylene conversion of ≈70% at 200 °C.