Hydrothermal reduction under aqueous conditions is widely used to convert biomass into more valuable products. However, the harsh conditions inherent in the process can irreversibly alter the intrinsic structure of the support, as well as dissolve the metal ions into the aqueous solution. In this work, for the first time we have synthesized a new highly hydrothermally stable Ru/LaCO3OH catalyst mostly consisting of Ru nanoparticles partially encapsulated by the LaCO3OH support with a strong metal-support interaction (SMSI), which confers high stability and activity to the catalyst under hydrothermal reduction conditions in the hydrogenolysis of the biomass model molecules guaiacol and glycerol. During impregnation, the RuCl3 center dot 3H(2)O precursor initially reacts with LaCO3OH to form a LaRu(CO3)(2)Cl-2 complex and LaOCl. XPS demonstrated that Ru was present in the oxidized state, TEM and XRD showed the absence of Ru-0, and the XRD pattern showed the presence of the characteristic lattice fringe of LaOCl. While the LaRu (CO3)(2)Cl-2 complex was resistant to H-2 reduction at 350 degrees C, the complex underwent facile reduction to Ru-0 under hydrothermal conditions at 240 degrees C. In the subsequent process, LaRu(CO3)(2)Cl-2 and LaOCl underwent hydrolysis, forming crystalline LaCO3OH (confirmed by Ag+ titration and XRD patterns), Ru(OH)(3), and HCl. The Ru(OH)(3) was reduced in situ to Ru-0 nanoparticles, as revealed by XPS and TEM analysis. The simultaneous hydrothermal reduction of Run+ species and the formation of crystalline LaCO3OH result in the formation of Ru nanoparticles encapsulated by a protective LaCO3OH layer, as evidenced by HRTEM and DRIFTS CO adsorption measurements. The preparation of catalysts with this unique structure comprising metal nanoparticles protected by the support itself, which confers additional stability, is a novel strategy to prepare hydrothermally stable catalysts.