XRD analysis was conducted on a PANalytical X'pert Prodiffractometer using a radiation source of Co Kα radiation (λ = 0.1789 nm), within the 2θ range from 5° to 80°.
The surface areas of catalysts were measured using a BET surface analysis apparatus with N2 gas. The total pore volume was estimated according to the Barrett–Joyner–Halenda (BJH) method based on the adsorption isotherm.
The basicity of catalysts was measured by CO2-TPD. In a typical experiment, the catalyst (100 mg) was pretreated in the environment of He with a flow rate of 30 mL min−1 at 600 °C for 2 h to remove moisture and other adsorbed gases. After cooling down to 50 °C, the catalyst was exposed to the environment of pure CO2 for 2 h, and then purged with He with a flow rate of 30 mL min−1 for 2 h to exclude physically adsorbed CO2. Subsequently, the sample was heated to 800 °C at a rate of 10 °C min−1. The desorbed CO2 was detected using a thermal conductivity detector.
The content of K after calcination was detected by inductively coupled plasma optical emission spectrometer (ICP-OES) using an Agilent 7700 instrument.