This repository includes experimental data associated with the publication: N.Korica, A.Ben Hassine, H.Dao Thi, L.Bergaoui, K.Van Geem, P.S.F.Mendes, J.De Clercq, J.W.Thybaut “Mixture effects in alkane/cycloalkane hydroconversion over Pt/HUSY : carbon number impact”, submitted to Fuel journal in December 2021. The impact of carbon number of reacting alkanes and cycloalkanes on mixture effects in hydroconversion over Pt/HUSY has been studied by experiments on high-throughput setup by feeding equimolar mixtures of n-octane and tert-butylcyclohexane, and n-decane and methylcyclohexane. In order to investigate the above-mentioned impact, the kinetic behavior was examined at various experimental conditions, over Pt/HUSY catalyst with three different Pt loadings and HUSY zeolite with Si/Al molar ratio of 6. The process conditions which were used for every feed are summarized: Pure n-octane Catalysts : 0.07 and 0.1 wt%Pt/HUSY (poorly- and well-balanced catalyst for pure n-octane) Temperature, K : 523 ; 543 Pressure, bar : 10 ; 20 Partial pressure of reactant, bar : 0.05 Pure tert-butylcyclohexane Catalysts : 0.07 and 0.3 wt%Pt/HUSY Temperature, K : 523 ; 543 Pressure, bar : 10 ; 20 Partial pressure of reactant, bar : 0.05 Equimolar mixture of n-octane and tert-butylcyclohexane Catalysts : 0.07 and 0.3 wt%Pt/HUSY Temperature, K : 523 ; 543 Pressure, bar : 10 ; 20 Partial pressure of each reactant, bar : 0.05 Pure n-decane Catalysts : 0.07 and 0.3 wt%Pt/HUSY (poorly- and well-balanced catalyst for pure n-decane) Temperature, K : 523 ; 543 Pressure, bar : 10 ; 20 Partial pressure of reactant, bar : 0.05 Pure methylcyclohexane Catalysts : 0.07 and 0.1 wt%Pt/HUSY Temperature, K : 523 ; 543 Pressure, bar : 10 ; 20 Partial pressure of reactant, bar : 0.05 Equimolar mixture of n-decane and methylcyclohexane Catalysts : 0.07 and 0.3 wt%Pt/HUSY Temperature, K : 523 ; 543 Pressure, bar : 10 ; 20 Partial pressure of each reactant, bar : 0.05 The kinetics of hydroconversion of different alkane/cycloalkane feeds were compared based on conversion of reactants and yields to isomers. The data are classified based on figures in the Article. Figure 5 : n-Octane conversion as a function of space time at 10 bar pressure - comparison of experiments with pure n-octane and in mixture with methylcycyclohexane and tert-butylcyclohexane Figure 6 : Octane isomer yields as a function of n-octane conversion - comparison of experiments with pure n-octane and in mixture with tert-butylcyclohexane Figure 7 : tert-Butylcyclohexane conversion as a function of space time at 10 bar pressure - comparison of experiments with pure tert-butylcyclohexane and in mixture with n-octane Figure 8 : Butylcyclohexane isomer yields as a function of tert-butylcyclohexane conversion comparison of experiments with pure tert-butylcyclohexane and in mixture with n-octane Figure 9 : n-Decane conversion as a function of space time at 10 bar pressure - comparison of experiments with pure n-decane and in mixture with methylcyclohexane Figure 10 : Decane isomer yields as a function of n-decane conversion - comparison of experiments with pure n-decane and in mixture with methylcyclohexane Figure 11 : Methylcyclohexane conversion as a function of space time at 10 bar pressure - comparison of experiments with pure methylcyclohexane and in mixture with n-decane Figure S9 : n-Octane conversion as a function of space time at 20 bar pressure - comparison of experiments with pure n-octane and in mixture with methylcycyclohexane and tert-butylcyclohexane Figure S10 : n-Octane conversion as a function of space time - comparison of experiments with pure n-octane and in mixture with methylcycyclohexane and tert-butylcyclohexane Figure S13 : tert-Butylcyclohexane conversion as a function of space time at 20 bar pressure - comparison of experiments with pure tert-butylcyclohexane and in mixture with n-octane Figure S14 : tert-Butylcyclohexane conversion as a function of space time - comparison of experiments with pure tert-butylcyclohexane and in mixture with n-octane Figure S15 : n-Decane conversion as a function of space time at 20 bar pressure - comparison of experiments with pure n-decane and in mixture with methylcyclohexane Figure S16 : n-Decane conversion as a function of space time - comparison of experiments with pure n-decane and in mixture with methylcyclohexane Figure S17 : Methylcyclohexane conversion as a function of space time at 20 bar pressure - comparison of experiments with pure methylcyclohexane and in mixture with n-decane Figure S18 : Methylcyclohexane conversion as a function of space time - comparison of experiments with pure methylcyclohexane and in mixture with n-decane