The adsorption of asymmetrical triblock copolymers from a non-selective solvent on solid surface has been studied by using Scheutjens-Fleer mean-field theory and Monte Carlo simulation method on lattice model. The main aim of this paper is to provide detailed computer simulation data, taking A8-kB20Ak as a key example, to study the influence of the structure of copolymer on adsorption behavior and make a comparison between MC and SF re-sults. The simulated results show that the size distribution of various configurations and density-profile are depend-ent on molecular structure and adsorption energy. The molecular structure will lead to diversity of adsorption be-havior. This discrepancy between different structures would be enlarged for the surface coverage and adsorption amount with increasing of the adsorption energy. The surface coverage and the adsorption amount as well as the bound fraction will become larger as symmetry of the molecular structure becomes gradually worse. The adsorption layer becomes thicker with increasing of symmetry of the molecule when adsorption energy is smaller but it becomes thinner when adsorption energy is higher. It is shown that SF theory can reproduce the adsorption behavior of asymmetrical triblock copolymers. However, systematic discrepancy between the theory and simulation still exists. The approximations inherited in the mean-filed theory such as random mixing and the allowance of direct back folding may be responsible for those deviations. The adsorption of asymmetrical triblock copolymers from a non-selective solvent on solid surface has been studied by using Scheutjens-Fleer mean-field theory and Monte Carlo simulation method on lattice model. The main aim of this paper is to provide detailed computer simulation data, taking A8-kB20Ak as a key example, to study the influence of the structure of copolymer on adsorption behavior and make a comparison between MC and SF re-sults. The simulated results show that the size distribution of various configurations and density-profile are depend -ent on molecular structure and adsorption energy. The molecular structure will lead to diversity of adsorption be-havior. This discrepancy between different structures would be enlarged for the surface coverage and adsorption amount with increasing of the adsorption energy. The surface coverage and the adsorption amount as well as the bound fraction will become larger as symmetry of the molecular structure becomes normally worse. The ads orption layer becomes thicker with increasing of symmetry of the molecule when adsorption energy is smaller but it becomes thinner when adsorption energy is smaller but it becomes thinner when adsorption energy is smaller but it becomes thinner when adsorption energy is smaller simulation still exists. The approximations inherited in the mean-filed theory such as random mixing and the allowance of direct back folding may be responsible for those deviations.