Enhancing Uranium Removal with a Titanium-Incorporated Zirconium-Based Metal-Organic Framework.

The urgent need to efficiently and rapidly decontaminate uranium contamination in aquatic environments underscores its significance for ecological preservation and environmental restoration. Herein, a series of titanium-doped zirconium-based metal-organic frameworks were meticulously synthesized through a stepwise process. The resultant hybrid bimetallic materials, denoted as NU-Zr-n%Ti, exhibited remarkable efficiency in eliminating uranium (U (VI)) from aqueous solution. Batch experiments were executed to comprehensively assess the adsorption capabilities of NU-Zr-n%Ti. Notably, the hybrid materials exhibited a substantial increase in adsorption capacity for U (VI) compared to the parent NU-1000 framework. Remarkably, the optimized NU-Zr-15%Ti displayed a noteworthy adsorption capacity (∼118 mg g-1) along with exceptionally rapid kinetics at pH 4.0, surpassing that of pristine NU-1000 by a factor of 10. This heightened selectivity for U (VI) persisted even when diverse ions exist. The dominant mechanisms driving this high adsorption capacity were identified as the robust electrostatic attraction between the negatively charged surface of NU-Zr-15%Ti and positively charged U (VI) species as well as surface complexation. Consequently, NU-Zr-15%Ti emerges as a promising contender for addressing uranium-laden wastewater treatment and disposal due to its favorable sequestration performance.

Improvement of peroxymonosulfate utilization efficiency for sulfamethazine degradation by photo-electron activating peroxymonosulfate: Performance and mechanism.

Enhancing the utilization efficiency of oxidant is of great importance for advanced oxidation processes (AOPs). Herein, nitrogen-doped titania dioxide/carbon (NTC7) catalyst was fabricated via pyrolyzing NH2-MIL-125 under nitrogen atmosphere at 700 °C. Excitation of NTC7 under visible light can successfully achieve efficient activation of peroxymonosulfate (PMS) (NTC7 + PMS + Vis). Degradation performance and PMS activation mechanism were systematically investigated using sulfamethazine (SMT) as the target pollutant. It was found that the photo-generated electrons excited from NTC7 under visible light played the dominant role in enhancing the productive consumption of PMS. Its utilization increased by 66 % (Δ[PMS]/Δ[SMT] = 7.0) in NTC7 + PMS + Vis process and the degradation rate was 2.14 times higher than that of NTC7 + PMS process. The ketonic CO groups and structural defects were responsible for the generation of 1O2 in dark activation while radicals (•OH, O2•-) were more inclined to be continuously produced in NTC7 + PMS + Vis process. The involved degradation pathways, intermediates, and toxicity assessment have been studied in detail. This work provides an effective approach to enhance the utilization efficiency of oxidant for pollutant degradation by AOPs.

Design and experimental research of a 28 GHz TE01 mode 160° miter bend for electron cyclotron resonance ion source.

In this paper, a 28 GHz TE01 mode 160° miter bend employing two plane mirrors is proposed based on the quasi-optical technique and the coupled wave theory to realize high-efficiency transmission for the electron cyclotron resonance ion source. First, the TE01 mode was converted to TE0n hybrid modes with Gaussian beam characteristics by means of the designed mode converter. Second, the phase shift section was implemented to eliminate the phase difference of the hybrid modes. Then, upon reflection of two plane mirrors, the propagation direction of a wave beam is deviated by 160°. Finally, the hybrid modes were converted to the TE01 mode using the same structures of the phase shift section and the mode converter. The simulation results reveal that the TE01 mode transmission efficiency reaches 95.22% at the central frequency of 28 GHz. Additionally, the designed 160° miter bend has been fabricated, installed, and measured. The experimental results show that the power transmission efficiency reaches 98.54% including diffraction losses and ohmic losses.

Degradation of emerging contaminants by sono-Fenton process with in situ generated H2O2 and the improvement by P25-mediated visible light irradiation.

Developing advanced treatment methods to minimize the release of emerging contaminants to natural water has become a matter of considerable interest. Sono-Fenton process was investigated to degrade bisphenol A (BPA) and sulfadiazine (SDZ). The H2O2 generated in situ was used as the exclusive source. Results showed that, the 400 kHz ultrasound is more efficient in creating homogeneous sono-Fenton than the 20 kHz apparatus due to the higher production of OH. Influence of Fe2+ was more remarkable on the degradation of hydrophilic SDZ, and its degradation kinetics was well fitted by two-stage kinetic model. However, the Fe2+ and H2O2 were unproductively wasted, which could not be improved by changing the dosing modes of Fe2+. The presence of P25 under visible light irradiation could significantly accelerate SDZ degradation at small amount of iron precursors, mainly via promoting the Fe2+/Fe3+ cycling by the photoelectrons. Moreover, SDZ degradation in sono-Fenton process was significantly inhibited at pH > 7, but the inhibition was very weak in P25-assisted sono-Fenton process. The presence of P25 also improved the mineralization. Three primary degradation pathways of SDZ degradation were proposed, including the attacking of the benzene ring, the oxidation of the amino group and the extrusion of SO2.