To improve the yield of propylene in fluidized catalytic cracking, a series of different Au/ZSM-5-TOS catalysts were prepared by modifying ZSM-5, using an external surface modification method and Au nanoparticles. The modified catalyst maintained the MFI structure of ZSM-5, whereas the pore-opening size of the zeolite relatively decreased, without affecting its internal structure. The acidity of ZSM-5, especially the Brønsted acidity, reduced. Among the studied catalysts, the 0.2 wt% Au/ZSM-5-1%TOS catalyst exhibited the best feedstock conversion and propylene selectivity, along with a significant increase in propylene selectivity and a slight decrease in the conversion of light diesel oil, even after water vapor treatment at 800 °C for 4 h. Its catalytic activity at 360 °C exceeded that of ZSM-5 at 460 °C, showing great application potential in petrochemical processes.

In the present study, the electrochemiluminescence (ECL) properties of Gd(OH)₃ nanocrystals with K₂S₂O₈ as the cathode coreactant were studied for the first time. Based on the prominent ECL behavior of this material and the excellent specificity of the aptamer technique, an ECL aptasensor for the detection of ochratoxin A (OTA) was formulated successfully. Over an OTA concentration range of 0.01 pg mL⁻¹ to 10 ng mL⁻¹, the change in the ECL signal was highly linear with the OTA concentration, and the limit of detection (LOD) was 0.0027 pg mL⁻¹. Finally, the ECL aptasensor was further used to detect OTA in real samples (grapes and corn) and satisfactory results were obtained, which indicated that the built method is expected to be applied in food detection.

Gas-phase epoxidation of propylene in the copresence of H₂ and O₂ was performed over the catalyst of Au on as-synthesized TS-1 that contained a small amount of anatase TiO₂. The catalytic performance was studied by washing or nonwashing the catalyst precursor to modulate the content of purity (K, Cl) and then calcining the samples in O₂ or H₂ prior to reaction. The results show that the catalytic performance of Au/TS-1 can be improved without washing (more K⁺ and Au maintained) and O₂ pretreatment. It was found that the calcination in O₂ was able to maintain more metallic Au and form more surface-active oxygen species and thus providing a better yield of propylene oxide with the assistance of potassium. Interestingly, more acrolein can be produced over the catalysts with respect to the in situ calcination in O₂ than that in H₂ when the feed only contained 10% O₂ and 10% propylene in argon, while there was no formation of propylene oxide. On the other hand, the catalyst precursor calcined in H₂ prefers the formation of successive oxygenates of PO.

With several major polarity and weak optical properties, the sensitive detection of HCOOH remains a major challenge. Given the special role of HCOOH in assisting in the catalytic hydrogenation process of Ir complexes, HCOOH (as a hydrogen source) could rapidly activate Ir complexes as catalysts and further reduce the substrates. This work developed a facile and sensitive HCOOH fluorescence sensor utilizing an optimal catalytic fluorescence generation system, which consists of the phenyl-pyrazole-type Ir-complex PP-Ir-Cl and the coumarin-type fluorescence probe P-coumarin. The sensor demonstrates excellent sensitivity and specificity for HCOOH and formates; the limits of detection for HCOOH, HCOONa, and HCOOEt₃N were tested to be 50.6 ppb, 68.0 ppb, and 146.0 ppb, respectively. Compared to previous methods, the proposed sensor exhibits good detection accuracy and excellent sensitivity. Therefore, the proposed HCOOH sensor could be used as a new detection method for HCOOH and could provide a new design path for other sensors.

Semi-hydrogenation of acetylene to ethylene over metal oxide-supported Au nanoparticles is an interesting topic. Here, a hydrotalcite-based MMgAlO_x (M=Cu, Ni, and Co) composite oxide was exploited by introducing different Cu, Ni, and Co dopants with unique properties, and then used as support to obtain Au/MMgAlO_x catalysts via a modified deposition–precipitation method. XRD, BET, ICP-OES, TEM, Raman, XPS, and TPD were employed to investigate their physic-chemical properties and catalytic performances for the semi-hydrogenation of acetylene to ethylene. Generally, the catalytic activity of the Cu-modified Au/CuMgAlO_x catalyst was higher than that of the other modified catalysts. The TOR for Au/CuMgAlO_x was 0.0598 h⁻¹, which was 30 times higher than that of Au/MgAl₂O₄. The SEM and XRD results showed no significant difference in structure or morphology after introducing the dopants. These dopants had an unfavorable effect on the Au particle size, as confirmed by the TEM studies. Accordingly, the effects on catalytic performance of the M dopant of the obtained Au/MMgAlO_x catalyst were improved. Results of Raman, NH₃-TPD, and CO₂-TPD confirmed that the Au/CuMgAlO_x catalyst had more basic sites, which is beneficial for less coking on the catalyst surface after the reaction. XPS analysis showed that gold nanoparticles exhibited a partially oxidized state at the edges and surfaces of CuMgAlO_x. Besides an increased proportion of basic sites on Au/CuMgAlO_x catalysts, the charge transfer from nanogold to the Cu-doped matrix support probably played a positive role in the selective hydrogenation of acetylene. The stability and deactivation of Au/CuMgAlO_x catalysts were also discussed and a possible reaction mechanism was proposed.