Bioprotective Respirator Assembled by Defective Carbon Nitride for Long-Term Light Triggered Health Protection.

Wearing face masks is the best way to stop the spread of respiratory infections. However, if masks are not sterilized, changing them too frequently can actually increase the risk of cross-contamination. Herein, the construction of an antipathogen photocatalytic mask with carbon vacancy-modified carbon nitride nanosheets (g-C3N4-VC Ns) coated on the non-woven fabrics of the out layer of the mask, offering effective and long-term protection against damaging pathogens when exposed to light is reported. The introduced carbon vacancies are found capable of creating energy-disordered sites and inducing energetic electric force to overcome the Coulomb interactions between electron-hole pairs, thus promoting the electron-hole separation to achieve a high generation of reactive oxygen species (ROS). Thanks to its high activity in generating ROS upon exposure to light, the as-prepared photocatalytic mask shows high pathogen sterilization performance. This, in turn, prolongs the mask's protective lifetime, decreases the need for regular replacement, and decreases medical waste production. The work demonstrated here opens new viewpoints in designing pathogens biocidal protective devices for health protection, offering significant promise in specific environment self-protection.

Restricted reaction of layered double hydroxide nanoparticles with phosphate in a confined microsphere space.

Over the past decades, considerable efforts have been made to find useful solutions for phosphate pollution control. The state transition of nanomaterials from freely dispersed to encapsulated provides a realizable route for their application in phosphate elimination. The separation convenience offered by encapsulation has been widely recognized, however, the unique binding mode of nanostructures and phosphate in the confined space remains unclear, limiting its further development. Here, carboxymethyl cellulose (CMC) microspheres were used as hosts to deploy layered double hydroxide (LDH) nanoparticles. On this basis, we described an attempt to explore the adsorption behavior of LDH and phosphate in the microsphere space. Compared to their freely dispersed analogues, LDH particles exhibited higher structural stability, wider pH adaptability, and better phosphate selectivity when spatially confined in the CMC microsphere. Nevertheless, the kinetic process was severely inhibited by three orders of magnitude. Besides, the saturated phosphate adsorption capacity was also reduced to 74.6 % of the freely dispersed system. A combinative characterization revealed that the highly electronegative CMC host not only causes electrostatic repulsion to phosphate, but also extracts the electron density of the metal center of LDH, weakening its ability to act as a Lewis acid site for phosphate binding. Meanwhile, the microsphere encapsulation also hinders the ion exchange function of interlayer anions and phosphate. This study offers an objective insight into the reaction of LDH and phosphate in the confined microsphere space, which may contribute to the advanced design of encapsulation strategies for nanoparticles.

High bioethanol titer and yield from phosphoric acid plus hydrogen peroxide pretreated paper mulberry wood through optimization of simultaneous saccharification and fermentation.

The optimization of key simultaneous saccharification and fermentation (SSF) parameters for bioethanol production from phosphoric acid plus hydrogen peroxide pretreated paper mulberry wood was carried out under two isothermal scenarios; the yeast optimum and trade-off temperatures of 35 and 38 °C, respectively. The optimal conditions established for SSF at 35 °C (solid loading: 16%; enzyme dosage: 9.8 mg protein/g glucan; and yeast concentration: 6.5 g/L) achieved high ethanol titer and yield of 77.34 g/L and 84.60% (0.432 g/g), respectively. These corresponded to 1.2 and 1.3-folds increases, compared to the results of the optimal SSF at a relatively higher temperature of 38 °C. The information from this study would prove beneficial in reducing process energy demands to some extent, while also helping to achieve high levels of both ethanol concentration and yield that are desired in cellulosic ethanol production.

Toxic Effects of Bisphenol A and Bisphenol S on Chlorella Pyrenoidosa under Single and Combined Action.

Bisphenol A (BPA) is an important industrial chemical; bisphenol S (BPS) is a substitute for BPA. Both are frequently detected in rivers, sewage, and surface water, and have a great impact on the water environment. The effects of BPA and BPS on cell growth, chlorophyll a content, and oxidative stress of Chlorella pyrenoidosa (C. pyrenoidosa) were studied. When BPA and BPS acted alone or in combination, compared with the blank control group, the growth of C. pyrenoidosa in the experimental group showed a pattern of "low promotion and high inhibition", and the inhibition rate reached the maximum on the 6th day. Under the combined action, the reactive oxygen species (ROS) level of C. pyrenoidosa first increased, and then decreased. In addition, the activity of superoxide dismutase (SOD) and peroxidase (POD) increased with the increase in combined concentration. In the 0.5 P treatment group, SOD and POD activity reached peak values of 29.59 U/mg∙prot and 1.35 U/mg∙prot, respectively. The combined toxicity of BPA and BPS to C. pyrenoidosa was evaluated as a synergistic effect by using toxicity unit and additive index methods. This study evaluated the effects of BPA and BPS on algae in the aquatic environment, providing some data support for their potential ecological risks.

Highly Efficient Degradation of Tetracycline Hydrochloride in Water by Oxygenation of Carboxymethyl Cellulose-Stabilized FeS Nanofluids.

The transformation of organic pollutants by stabilized nano-FeS in oxic conditions is far less understood than in anoxic states. Herein, carboxymethyl cellulose-stabilized FeS (CMC-FeS) nanofluids are prepared at a CMC-to-FeS mass ratio of 1/2 and their performance of tetracycline hydrochloride (TC) degradation under oxic conditions was investigated. Here, we showed that TC could be efficiently removed by oxygenation of CMC-FeS nanofluids at neutral initial pH. We found that CMC-FeS dosages as low as 15 mg/L can achieve the TC removal efficiency as high as 99.1% at an initial TC concentration of 50 mg/L. Oxidative degradation plays a predominated role in TC removal (accounting for 58.0%), adsorption has the second importance (accounting for 37.0%), and reduction has minor impact (accounting for 4.1%) toward TC removal. Electron spin resonance assays, fluorescent detection using coumarin as a probe, and radical scavenging experiments confirm that hydroxy radicals (•OH), both in free and surface-bound forms, contribute to oxidation of TC. Humic acids brought detrimental effects on TC removal and therefore should be biologically degraded in advance. This work offers a facile and cost-effective solution to decontaminate TC in natural and engineered water bodies.

Improved Dewaterability of Waste Activated Sludge by Fe(II)-Activated Potassium Periodate Oxidation.

Fe(II)-activated potassium periodate (KIO4) oxidation was used to improve the dewaterability of waste-activated sludge for the first time. Compared with those of raw sludge, the capillary suction time (CST), specific resistance filtration (SRF), and water content of filter cake (WC) of sludge treated using the Fe(II)/KIO4 process under the optimal conditions (i.e., the initial pH = 6.8, KIO4 dose = 1.4 mmol/g volatile suspended solids, Fe(II)/KIO4 molar ratio = 1.2) decreased by 64.34%, 84.13%, and 6.69%, respectively. For conditioned sludge flocs, the Zeta potential and particle size were increased, and hydrophilic proteins in extracellular polymeric substances (EPS) were partly degraded, accompanied by the transformation of tightly bound EPS into soluble EPS and the conversion of dense sludge flocs into loose and porous ones. During Fe(II)/KIO4 oxidation, Fe(IV) and the accompanying •OH were determined as the predominant reactive species and the underlying mechanism of sludge EPS degradation was proposed. This work provides a prospective method for conditioning the sludge dewaterability.

Effects of hydrophobic coating on properties of hydrochar produced at different temperatures: Specific surface area and oxygen-containing functional groups.

Hydrochar's specific surface area (SSA) is important in environmental remediation; however, a hydrophobic coating formed on hydrochar creates a physical barrier that reduces that SSA. The formation and composition of the hydrophobic coating and its effects on hydrochar properties are unclear. In this study, hydrochar was produced from Chinese fan palm (Livistona chinensis) leaves at different temperatures. The resulting hydrophobic coatings were investigated by in situ characterization and then extracted with acetone for composition identification. Additionally, hydrochar properties were compared before and after hydrophobic coating removal. The results showed that the hydrophobic coating of the hydrochar produced at 180 °C was the insoluble cuticle layer of raw biomass, while the hydrophobic coatings formed above 180 °C were the depolymerization products of cutin. For the hydrochar above 180 °C, especially at 260 °C, the removal of the hydrophobic coating from hydrochar increased both its SSA and its oxygen-containing functional groups.

Carbon Quantum Dots-Functionalized UiO-66-NH2 Enabling Efficient Infrared Light Conversion of 5-Hydroxymethylfurfuryl with Waste Ethanol into 5-Ethoxymethylfurfural.

The catalytic etherification of 5-hydroxymethylfurfural (HMF) with the waste ethanol into high-energy-density 5-ethoxymethylfurfural (EMF) has been considered as a promising way to simultaneously alleviate the energy crisis and environmental pollution. However, the energy consumption is rather high as the synthesis of EMF requires a high temperature to open the etherification reaction. Herein, we demonstrate a clever design and construction of acidified biomass-derived carbon quantum dots (BCQDs)-modified UiO-66-NH2 that is immobilized on cermasite (H+/BCQDs/UiO-66-NH2@ceramsite), which can use the IR light as driven energy and wasted ethanol to trigger the catalytic conversion of HMF into EMF. The temperature on the surface of the immobilized catalyst could reach as high as 139 °C within 15 min IR irradiation. Due to the aforementioned advantages, the as-prepared catalyst exhibited excellent IR-triggered catalytic performance toward EMF production, where the EMF yields and selectivity were as high as 45% and 65%, respectively. The high catalytic performance originates from the outstanding photo-to-thermal conversion by the introduction of BCQDs, as well as the strong interactions between BCQDs and UiO-66-NH2 that boosts the etherification reactions. The immobilization of catalyst on cermasite not only benefits catalyst recycling, but more importantly reduces catalyst loss during practical applications. The conceptual study shown here provides new viewpoints in designing energy-effective materials for the conversion of wastes into high-value-added resources.

Denitrification performance and microbial diversity using starch-polycaprolactone blends as external solid carbon source and biofilm carriers for advanced treatment.

Enhanced nitrate removal from the secondary effluent in municipal wastewater treatment plants (WWTPs) is essential for avoiding water eutrophication. To this end, a vertical baffled solid-phase denitrification reactor (VBSDR) was developed using a starch and polycaprolactone (PCL) blend plate (S-PCL) as a carbon source and biofilm carrier. In this study, we evaluated the denitrification performance and microbial diversity of the VBSDR. The results of the Fourier transform infrared spectroscopy (FTIR), carbon leaching experiment, and scanning electron microscopy (SEM) demonstrated that the S-PCL structure can be attached and degraded more rapidly. Furthermore, the denitrification performance under varied operational conditions, i.e., influent nitrate loading rate (NLR) and operating temperature, was also investigated. Herein, when treating low C/N ratio and low-strength wastewater, a high denitrification rate (DR) [0.33 gN/(L·d)] was achieved. The effect of temperature on DR can be described by the Arrhenius-type equation, which shows that low temperature has a negative influence on DR and nitrate removal efficiency. Furthermore, DR was simultaneously affected by the NLR and temperature. The microbial diversity and community structure were determined by Illumina high-throughput sequencing. The special carbon source led to Acidovorax (denitrifying bacteria) and Flavobacterium (hydrolysis acidifying bacteria) being the VBSDR biofilm's most predominant functional bacteria at the genus level.

The influence mechanism of temperature on solid phase denitrification based on denitrification performance, carbon balance, and microbial analysis.

In this work, the influence mechanism of temperature on solid phase denitrification (SPD) was investigated using a pilot-scale reactor supported with polycaprolactone (PCL). The results showed that under nitrate loads of ~31.5 mg N/(L·h), as temperature decreased from 30 °C to 13 °C, the nitrate removal efficiency declined from 94% to 57%. Furthermore, denitrification rate constants were input into Arrhenius equation and the resulting temperature coefficient was 1.04. Significantly nitrite accumulation and less effluent COD residue occurred at low-temperatures. Via stoichiometry, the sludge yield coefficient and COD demand for nitrate removal both increased as a function of increasing temperature; and were calculated at 20 °C as 0.069 g MLVSS/(g COD·d) and 3.265 g COD/g N, respectively. Carbon balance analysis indicated that the COD release rate (υ) at 30 °C was twice that at 13 °C. LEfSe analysis demonstrated that Desulfomicrobium, Desulfovibrio, and Meganema were abundant at low-temperature, while Simplicispira, Aquabacterium, and Acidovorax were enriched at high-temperature. Besides, carboxylesterase (PCL depolymerase) was more abundant at high-temperature, implying an association with a fast υ. Moreover, nar was enriched at low-temperature, while nir was depleted, which led to nitrite accumulation. These results provide reference for SPD design parameter estimation and/or optimal operation strategy.

Developing the new kinetics model based on the adsorption process: From fitting to comparison and prediction.

In this study, an intrinsic kinetics model was proposed to simulate the adsorption process. The kinetics model was established based on the collision theory, where the available adsorption site and residual adsorbate concentration were considered. The model specifically highlights the significance of initial conditions in its equation. The initial reaction condition is expressed by the model parameter ξ, which includes four factors: concentration, volume, adsorbent dosage and adsorption capacity. The applicability of this model was mainly explored with the phosphate adsorption process by layered double hydroxides (LDH). Experimental results indicate that, at a certain initial condition, the intrinsic kinetics rate coefficient exhibits a superior stability, making the adsorption rate become comparable among different materials. On this basis, the kinetics rate coefficients of 60 materials were compared, and the LDH was proved to be advantageous in phosphate removal rate. Additionally, the intrinsic kinetics model was successfully applied to predict the phosphate adsorption kinetics under a wide range of initial conditions. The predicted concentration throughout the entire adsorption process is well consistent with the evolution of experimental data. This model is an effort to advance the kinetics analysis from fitting to comparison and prediction.

Immobilization of powdery calcium silicate hydrate via PVA covalent cross-linking process for phosphorus removal.

Calcium silicate hydrate (CSH) is a popular material used for phosphorus removal in recent years. In this work, a novel immobilized material, polyvinyl alcohol-CSH (PVA-CSH), was prepared using a 1:10 weight ratio of CSH powder to 8% PVA solution and then used for phosphorus removal. Samples were characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The adsorption mechanism and practical application properties of phosphorus wastewater were studied by sequential batch and continuous flow experiment. The results showed PVA-CSH possessed a porous network structure and an average pore diameter of 24.94 ±â€¯0.11 nm. Furthermore, the CSH functional groups were unaffected by PVA immobilization. Compared with CSH, PVA-CSH did not easily lose CSH after being immobilized by PVA, and the duration of efficient phosphorus removal stage was approximately 20 h longer than that of CSH. In addition, the effluent turbidity of PVA-CSH was 0.11 ±â€¯0.03 NTU during the continuous operation period, which was significantly lower than CSH. In summary, this research study demonstrated the significant potential of PVA-CSH for practical phosphorus removal.

Microbial community structures and functions of wastewater treatment systems in plateau and cold regions.

Wastewater treatment plants (WWTPs) in plateau regions have unique microbial community structures. In this study, Illumina high-throughput sequencing technology was applied to investigate microbial communities of plateau WWTPs. The research showed that microbial diversities and richness were negatively associated with the altitude and positively to the water temperature to a certain extent. The dominant phyla of plateau and control WWTPs were similar, which mainly included Proteobacteria, Bacteroidetes, Chloroflexi and Firmicutes. In plateau WWTPs, the LEfSe analysis found 4 biomarkers which can catabolize aromatic compounds, indicating the microorganisms that can degrade refractory organics might survive better in plateau WWTPs. The analysis of functional genera and enzymes showed that there was no significant difference in abundances of organic degrading bacteria, but the nitrogen removal bacteria were less abundant and phosphorus removal bacteria were more abundant in plateau WWTPs.

[Effect of varicocele on expression of apoptosis associated gene Bcl-2 and Bax in spermatogenic cells of adolescent rats].

OBJECTIVE: To study the effect of varicocel (VC) on expression of apoptosis associated gene Bcl-2 and Bax in spermatogenic cells of adolescent rats, and investigate the mechanism of the infertility resulting from varicocele. METHODS: The varicocele model was created by partial ligation of the left renal vein in the adolescent rats, two and four and eight weeks after creation of the varicocele model, the expressions of Bcl-2 and Bax were detected by immunohistochemical method. RESULTS: With the duration of varicocele model, the Bcl-2 expression in experiment group was decreased as compared with that in control group. And in experiment group, the Bcl-2 expression level was lower in left testis than in right testis. But Bax expression in experiment group was increased as compared with that in control group, and in experiment group, the Bax expression level was higher in left testis than in right testis. CONCLUSION: Experimental varicocele could change obviously expression of apoptosis associated gene Bcl-2 and Bax in spermatogenic cells of adolescent rats.