In situ Al-based composites with different SiO 2 /C/Al molar ratios were fabricated by reaction hot pressing. Differential scanning calorimetry (DSC) was used to investigate the reaction mechanisms in the Al-SiO 2 -C system. X-ray diffraction results revealed that no new resultant phase was observed below the melting temperature of aluminum except the SiO 2 , C and Al phases. Heating at different synthesis temperatures showed that, up to 1000°C with a holding time of 1 h, the reactions in the Al-SiO 2 -C system took place completely, where the final products were Al 2 O 3 , SiC, Al 4 C 3 and Si. Microstructural observation showed that the in situ synthesized Al 2 O 3 , SiC, Al 4 C 3 , and Si were dispersed uniformly and had fine sizes less than 2 lm. The formed interfaces between the reinforcements and Al matrix are clean and free from any interfacial phase. During cooling, the synthesized Si formed a multilayer growth in the (111) direction. When the SiO 2 /C/Al molar ratio was (6/3/9), more Al 2 O 3 and Si were produced along with the complete prevention of Al 4 C 3 in the Al-SiO 2 -C system. The yield strength, ultimate tensile strength and Brinell hardness of the in situ fabricated composites are significantly higher than those of pure aluminum matrix, with a decrease of ductility. Mechanisms governing the tensile fracture process are also discussed.