Narrowband Ultraviolet-B Persistent Luminescence in an Indoor-Lighting Environment through Energy Transfer from Host Excitons to Gd3+ Emitters in ScPO4.

Narrowband ultraviolet-B (NB-UVB) luminescent materials are characterized by high photon energy, narrow spectral width, and visible-blind emission, thus holding great promise for photochemistry and photomedicine. However, most NB-UVB phosphors developed so far are photoluminescent, where continuous external excitation is needed. Herein, we realize NB-UVB persistent luminescence (PersL) in an indoor-lighting environment by exploiting the interaction between self-trapped/defect-trapped excitons and Gd3+ emitters in ScPO4. The phosphor shows a self-luminescing feature with a peak maximum at 313 nm with a time duration of >24 h after ceasing X-ray irradiation, which can be clearly imaged by an UVB camera in a bright environment. Spectroscopic and theoretical approaches reveal that thermo- and photo-stimulations of energies trapped at intrinsic lattice defects followed by energy transfer to Gd3+ emitters account for the emergence of the afterglow. The present results can initiate more exploration of NB-UVB PersL phosphors for emerging applications in secret optical tagging and phototherapy.

Solidification/stabilization of highly toxic arsenic-alkali residue by MSWI fly ash-based cementitious material containing Friedel's salt: Efficiency and mechanism.

Arsenic-alkali residue (AAR) and MSWI fly ash (MFA) are hazardous wastes, which still lack effective treatment methods. In this study, a novel solidification/stabilization (S/S) method for AAR with MFA-based cementitious material (MFA-CM) containing Friedel's salt was proposed. The efficiency and mechanism of S/S was mainly focused. Abundant Friedel's salt as well as a few C-S-H gel and ettringite (AFt) were found as hydration products of MFA-CM. 12% of AAR was well solidified/stabilized by MFA-CM, accompanied by As leaching concentration reducing from 10,687 mg/L to less than 5 mg/L. In order to investigate S/S mechanism of As, removal mechanism of As during co-precipitation synthesis of Friedel's salt was studied. During co-precipitation process, As was successively removed by formation of calcium arsenate precipitates, formation of As-Friedel's salt (replacement of Cl- by AsO43-), and adsorption of Friedel's salt. The S/S mechanism of As by MFA-CM was found to be similar to the removal mechanism of As during co-precipitation. With the prolonging of curing time, As was mainly solidified/stabilized by formation of calcium arsenate precipitates and As-Friedel's salt, and adsorption of Friedel's salt. Thus, this study provides a novel harmless treatment method for highly toxic arsenic-containing wastes by "treating the wastes with wastes".

Glucosamine protects against radiation-induced lung injury via inhibition of epithelial-mesenchymal transition.

Radiotherapy is one of the most important treatments for chest tumours. Although there are plenty of strategies to prevent damage to normal lung tissues, it cannot be avoided with the emergence of radiation-induced lung injury. The purpose of this study was to investigate the potential radioprotective effects of glucosamine, which exerted anti-inflammatory activity in joint inflammation. In this study, we found glucosamine relieved inflammatory response and structural damages in lung tissues after radiation via HE staining. Then, we detected the level of epithelial-mesenchymal transition marker in vitro and in vivo, which we could clearly observe that glucosamine treatment inhibited epithelial-mesenchymal transition. Besides, we found glucosamine could inhibit apoptosis and promote proliferation of normal lung epithelial cells in vitro caused by radiation. In conclusion, our data showed that glucosamine alleviated radiation-induced lung injury via inhibiting epithelial-mesenchymal transition, which indicated glucosamine could be a novel potential radioprotector for radiation-induced lung injury.

Hydrothermal Treatment of Arsenic Sulfide Residues from Arsenic-Bearing Acid Wastewater.

Arsenic sulfide residue (ASR), a by-product from the treatment of arsenic-bearing acidic wastewater, is abundantly generated but not properly disposed of in China. The utilization of such high-content arsenic waste residue is limited by the market. The traditional methods of stabilization/solidification (S/S) by lime cement or iron salt have a large mass/volume addition, high dumping cost and secondary pollution risk. In this paper, hydrothermal technology was used to treat three kinds of ASRs obtained from different smelters to minimize waste. The leaching toxicity and chemical speciation of the generated products was also evaluated by TCLP and BCR analyses. It was found that the hydrothermal treatment could greatly reduce the volume and moisture content of the ASRs. TCLP tests showed that the leachability of arsenic and heavy metals significantly decreased after the treatment. According to the BCR analysis, most of the unstable As, Cd and Cr transformed into a residual fraction. Finally, XRD, SEM, Raman and XPS techniques were carried out to reveal the mechanism. As a result, hydrothermal treatment can efficiently achieve the dehydration, volume reduction and stabilization/solidification of ASRs.

Co-treatment of flotation waste, neutralization sludge, and arsenic-containing gypsum sludge from copper smelting: solidification/stabilization of arsenic and heavy metals with minimal cement clinker.

Flotation waste of copper slag (FWCS), neutralization sludge (NS), and arsenic-containing gypsum sludge (GS), both of which are difficult to dispose of, are major solid wastes produced by the copper smelting. This study focused on the co-treatment of FWCS, NS, and GS for solidification/stabilization of arsenic and heavy metals with minimal cement clinker. Firstly, the preparation parameters of binder composed of FWCS, NS, and cement clinker were optimized to be FWCS dosage of 40%, NS dosage of 10%, cement clinker dosage of 50%, mill time of 1.5 h, and water-to-binder ratio of 0.25. On these conditions, the unconfined compressive strength (UCS) of the binder reached 43.24 MPa after hydration of 28 days. Then, the binder was used to solidify/stabilize the As-containing GS. When the mass ratio of binder-to-GS was 5:5, the UCS of matrix can reach 11.06 MPa after hydration of 28 days, meeting the required UCS level of MU10 brick in China. Moreover, arsenic and other heavy metals in FWCS, NS, and GS were effectively solidified or stabilized. The heavy metal concentrations in leachate were much lower than those in the limits of China standard leaching test (CSLT). Therefore, the matrices were potential to be used as bricks in some constructions. XRD analysis shows that the main hydration products of the matrix were portlandite and calcium silicate hydrate. These hydration products may play a significant role in the stabilization/solidification of arsenic and heavy metals.