Response of earthworms to microplastics in soil under biogas slurry irrigation: Toxicity comparison of conventional and biodegradable microplastics.

As a reliable environment-friendly alternative, biodegradable plastic mulching films have been introduced into agricultural practice to reduce the adverse threats posed by conventional plastic products. Information regarding whether potential untoward effects of biodegradable plastics exist in soil and how strong are such effects on terrestrial organisms, however, still remains unknown. This study examined differences in the responses of earthworm, represented by Eisenia fetida, to exposure to biodegradable (PLA: polylactic acid) and conventional microplastics (PVC: polyvinylchloride, LDPE: low-density polyethylene) in soil with biogas slurry irrigation. Mortality, growth, histopathology and biochemical enzymes of the earthworms exposed to different concentrations of microplastics (5, 20 and 50 g/kg wet weight of soil, respectively) were investigated after 28 days of incubation in the experiment. The obtained results showed that the ecotoxicity of microplastics (MPs) to earthworms was time-dependent. Regardless of MPs type, continuous exposure to MPs at the concentration of 50 g/kg induced mucous vacuolization, longitude muscle disorder, and granular lipofuscin-like deposits generation in the epithelium. Moreover, tissue fibrosis and cavity formation were also observed in intestinal tissue. The presence of MPs stimulated the oxidative stress system of the earthworms, as indicated by the enhancement of malonaldehyde (MDA) content in vivo. The antioxidative defense system in earthworms was supposed to collapse at the MPs concentration of 50 g/kg after 28 days of exposure. Interestingly, PLA exhibited similar ecotoxicity effects with LDPE, which might violate the original intention of biodegradable plastics with less harmful or nontoxic influence on the terrestrial biotas. Thus, knowledge regarding the molecular and genetic mechanisms of the earthworms in soil containing biodegradable plastics should be further explored to better understand the risk posed by biodegradable plastics in the agroecosystem.

Dye encapsulation engineering in a tetraphenylethylene-based MOF for tunable white-light emission.

The development of efficient and stable white-light emissive materials is highly desirable in displays and solid-state lighting. Here we present a high-quality white-light emitter based a dual-emitting MOF hybrid, which is achieved by dye encapsulation engineering within a robust Zr-MOF (PCN-128W) containing a highly luminescent tetraphenylethylene-based ligand. The pore confinement effect well isolates the incorporated dye molecules (trans-4-[4-(Dimethylamino)styryl]-1-methylpyridinium iodide (DSM)) and therefore suppress the aggregation caused luminescence quenching. The dye emission is mainly sensitized by PCN-128W host through Förster resonance energy transfer (FRET), and the FRET process is incomplete, thus enabling the hybrid to feature dual emissions upon a single excitation. The emission color of DSM@PCN-128W hybrid can be systematically tuned from blue to white, and to orange by regulating the dye encapsulation content. A broad white-light emission with a considerably high quantum yield (21.2%) is obtained in the case of dye contents of 0.15 wt%. The luminescence of DSM@PCN-128W hybrid is stable in ambient air for over 1 month, and show good resistance to continuous UV light irradiation, owing to the protective MOF Matrix that largely inhibits the UV exposure to dye molecules. What's more, by combining DSM@PCN-128W with a commercial UV LED chip, we fabricate a white-light emitting prototype device showing CIE chromaticity coordinates of (0.34, 0.33), a CRI of 79.1, and a CCT of 5525 K.

Ratiometric and Turn-On Luminescence Detection of Water in Organic Solvents Using a Responsive Europium-Organic Framework.

The development of simple, rapid-response sensors for water detection in organic solvents is highly desirable in the chemical industry. Here we demonstrate a unique luminescence water sensor based on a dual-emitting europium-organic framework (Eu-MOF), which is assembled from a purposely selected 2-aminoterephthalic acid ligand with responsive fluorescence inherent in its intramolecular charge transfer (ICT) process. This ICT process can be rapidly switched-on in the presence of water owing to its ability to boost and stabilize the ICT state. In contrast, the Eu3+ emission within the framework is insensitive to water and can serve as a reference, thus enabling highly sensitive water detection in a turn-on and ratiometric way. In addition, the significant ratiometric luminescence response induced by water makes Eu-MOF undergo a distinct change of emitting color from red to blue, which is favorable for visual analysis with the naked eye. Sensitive determination of water content (0.05-10% v/v) in various organic solvents is achieved in multiple readouts including ratiometric emission intensity, emission color, or the Commission Internationale de l'Eclairage (CIE) chromaticity coordinate. The present Eu-MOF sensor featuring high sensitivity and reusability, self-calibration, simple fabrication and operation, and capability for real-time and in situ detection is expected to have practical applications in water analysis for industrial processes.