The metallogenic controls on the sandstone⁃type uranium deposit in the Upper Cretaceous Yaojia Formation of the Qianjiadian area, Kailu Basin, remain debated, and the sedimentary environment, provenance characteristics, and uranium enrichment mechanisms have yet to be well constrained. Uranium⁃bearing strata of the Yaojia Formation were systematically sampled from drill cores. Major⁃element and rare⁃earth⁃element (REE) concentrations and organic⁃matter contents were analyzed using X⁃ray fluorescence spectrometry (XRF), inductively coupled plasma mass spectrometry (ICP⁃MS), and related methods. The results show that rocks from the oxidized zone exhibit pronounced negative Ce and Eu anomalies, with δCe values of 0.67-0.89 and δEu values of 0.78-0.92, indicating that Ce and Eu anomaly parameters can effectively discriminate redox conditions; Uranium mass fraction is negatively correlated with the m(K₂O)/m(Na₂O), and all high⁃uranium samples have m(K₂O)/m(Na₂O)<2, indicating that high⁃permeability sandstones provided favorable pathways for uranium⁃bearing fluids; Integrated analysis of sedimentary facies, geochemical discrimination diagrams, and the regional tectonic setting indicates that the Yaojia Formation was deposited in a passive continental⁃margin setting; and the principal metallogenic control is the coupling of a regionally developed oxidation zone controlled by tectonic tilting with locally developed structural windows, with the main mineralization event occurring at approximately 67 Ma. This study establishes an integrated "source⁃migration⁃accumulation" uranium metallogenic model for the study area and provides a theoretical basis for exploring sandstone⁃type uranium deposits in the Kailu Basin and comparable basins.

Hierarchical porous Hβ molecular sieve with different structure and acidity were prepared by alkali treatment. XRD, SEM, N₂ physical adsorption and NH₃?TPD characterization methods were used to characterize molecular sieves before and after alkali treatment. With hierarchical porous Hβ molecular sieve as the carrier, the Ru?Hβ bifunctional catalysts were prepared by an equal volume impregnation method, and the benzene hydroalkylation reaction activity and stability were evaluated in a fixed bed reactor.The results show that Hβ molecular sieve can effectively increase the proportion of mesopores after being treated with a proper concentration of alkali, which is beneficial to improve the hydroalkylation activity and stability. At 2 MPa, 210 ℃ and a liquid hourly space velocity of 1 h^-1, when the Ru mass fraction is 0.2% (based on the mass of hierarchical porous Hβ molecular sieve), the dual?functional catalyst composed of hierarchical porous Hβ can achieve effective and stable operation. At the same time, the conversion rate of benzene is 54.32%, the selectivity of cyclohexyl benzene is 71.47%, and the stability of the catalyst does not decrease significantly within 280 h.

The sol?gel method was used to modify the multi?walled carbon nanotubes, so that SnO₂ was combined with MWCNTs and doped with Cu ions. The samples M, M+Cu, M+Sn, and M+Sn+Cu were characterized by SEM, XRD, and FTIR. The surface microstructure was analyzed. The static adsorption method was used to measure the saturated adsorption capacity of different samples to VOCs. The VOCs gas volume concentration, temperature, and effects of metal doping were analyzed respectively. The results show that the saturation adsorption capacity of the four adsorbent samples is linearly related to the volume concentration and temperature of VOCs, and the larger the value of the two samples, the smaller the saturation adsorption capacity; at normal temperature (25 ℃) and normal pressure, MWCNTs adsorption capacity is almost 0, the saturation adsorption capacity of M+Cu is slightly smaller than M+Sn, and the adsorption capacity of M+Sn+Cu is about twice of M+Sn, up to 37.4 mg/g.