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Massive Mobile Growth of the Distal Radius: Vast Resection, Ulna Translocation Along with Arm Arthrodesis.
In the context of spreading Coronavirus disease 2019 (COVID-19), the combination of heating, ventilation, and air-conditioning (HVAC) system with air disinfection device is an effective way to reduce transmissible infections. Atmospheric-pressure non-equilibrium plasma is an emerging technique for fast pathogen aerosol abatement. In this work, in-duct disinfectors based on grating-like dielectric barrier discharge (DBD) plasmas with varied electrode arrangements were established and evaluated. The highest airborne bacterial inactivation efficiency was achieved by 'vertical' structure, namely when aerosol was in direct contact with the discharge region, at a given discharge power. For all reactors, the efficiency was linearly correlated to the discharge power (R2 =0.929-0.994). The effects of environmental factors were examined. Decreased airflow rates boosted the efficiency, which reached 99.8% at the velocity of 0.5 m/s with an aerosol residence time of ~3.6 ms. Increasing humidity (relative humidity (RH)=20-60%) contributed to inactivation efficacy, while high humidity (RH=70%-90%) led to a saturated efficiency, possibly due to the disruption of discharge uniformity. As suggested by the plasma effluent treatment and scavenger experiments, gaseous short-lived chemical species or charged particles were concluded as the major agents accounting for bacterial inactivation. This research provides new hints for air disinfection by DBD plasmas.Multimodal lateral flow immunoassay (LFIA) has displayed its potential to improve practicability and elasticity of point-of-care testing. Herein, multifunctional core-shell-shell Au@Pt@Ag NPs loaded with dual-layer Raman reporter molecules of 5,5'-dithiobis-(2-nitrobenzoic acid) (DTNB) with a characteristic combination of color-photothermal-Raman performance were constructed for colorimetric LFIA (CM-LFIA), photothermal LFIA (PT-LFIA) and surface-enhanced Raman scattering-based LFIA (SERS-LFIA), respectively. The highly specific nanoprobes, being obtained through the combination of the resulted dual-layer DTNB modified Au@Pt@Ag NPs with the antibody, were triumphantly utilized in exploring multimodal LFIA with one visual qualitative and two optional quantitative modes with excellent sensing sensitivity. Under optimal conditions, the limit of detection (LOD) for the model hazardous analyte dehydroepiandrosterone (DHEA) were 1.0 ng mL-1 for CM-LFIA, 0.42 ng mL-1 for PT-LFIA, and 0.013 ng mL-1 for SERS-LFIA, three of which were over 100-fold, 200-fold and 7 000-fold more sensitive than conventional visual AuNPs-based LFIA, respectively. In addition, the quantitative PT-LFIA and SERS-LFIA sensors worked well in spiked real samples with acceptable recoveries of 96.2 - 106.7% and 98.2 - 105.2%, respectively. GS-9674 datasheet This assay demonstrated that the developed multimodal LFIA had a great potential to be a powerful tool for accurate tracing hazardous analytes in complex samples.In this study, NaOH-assisted H2O2 post-modification was proposed as a novel strategy to enhance the adsorption of radioactive strontium (Sr) onto residual coffee waste biochars (RCWBs). To validate its viability, the adsorption capacities and mechanisms of Sr(II) using pristine (RCWBP), H2O2 post-modified (RCWBHP), and NaOH-assisted H2O2 post-modified residual coffee waste biochars (RCWBNHP) were experimentally and theoretically investigated. The highest adsorption capacity of Sr(II) for RCWBNHP (10.91 mg/g) compared to RCWBHP (5.57 mg/g) and RCWBP (5.07 mg/g) was primarily attributed to higher negative surface zeta potential (RCWBNHP = -5.66 → -30.97 mV; RCWBHP = -0.31 → -11.29 mV; RCWBP = 1.90 → -10.40 mV) and decoration of Na on the surfaces of RCWBP via NaOH-assisted H2O2 post-modification. These findings agree entirely with the theoretical observations that the adsorption of Sr(II) onto RCWBP and RCWBHP was controlled by electrostatic interactions involving carbonyls whereas enriched carboxylic acids and decorated Na on the surfaces of RCWBNHP through the replacement of Mg and K by NaOH-assisted H2O2 modification stimulated electrostatic interactions and cation exchanges governing the adsorption of Sr(II). Hence, NaOH-assisted H2O2 post-modification seemed to be practically applicable for improving the adsorption capacity of Sr(II) using RCWB-based carbonaceous adsorbents in real water matrices.China generates the world's second-largest amount of municipal solid waste (MSW) and incinerates the largest quantity of MSW. However, data on the latest dioxin emissions from MSW incineration (MSWI) and the related global share were lacking. In the context of MSW classification, distinguishing the long-term MSW generation and incineration quantity, and dioxin emissions was necessary for macro-control and policy-making by the Chinese Government. By considering population size and GDP per capita, China's MSW generation toward 2050 was projected based on Monte Carlo simulation. Moreover, dioxin emission factors were also assumed based on the diffusion rate of four grades of air pollution control devices (APCDs). Finally, we show that the quantity of China's MSW generation in 2050 will be 363.50 million tonnes (Mt) with 341.06-382.45 Mt of 75% certainty. China's dioxin emissions from MSWI were approximately 15.46 g I-TEQ in 2019, which accounted for 26.1% of total emissions from global MSWI. We discuss dioxin emission reduction scenarios depending on MSW diversion and APCD upgrades. China's dioxin emissions will be 70.38 g I-TEQ for the business-as-usual scenario, and the dioxin emissions will be 9.29 g I-TEQ (within the range of 8.88-9.64 g I-TEQ) for the optimal scenario in 2050. Moreover, in 2050, the APCD diffusion rate will account for 98.8% of the sensitivity of dioxin emissions from China's MSWI. According to the assumed scenarios, there is a dioxin emission reduction potential of 18.6% and 86.8% in 2050 by MSW diversion alone and maximum APCD upgrades combined with food waste diversion, respectively.The rationally-designed lignocellulose valorization that promotes a novel "waste-treats-pollutant" standpoint is highly desired yet still challenging for the spread of biomass industry. At this point, a cascade technique with the assistance of deep eutectic solvent (DES) fractionation is tailored to dually valorize wheat straw into fluorescent lignin carbon dots (LCDs) and bimetallic Mg-Fe oxide-decorated biochar (MBC) via solvothermal engineering and co-precipitation/pyrolysis respectively. Benefitting from the abundance of β-aryl ether and hydroxyl groups in DES-extracted lignin, the photoluminescence LCDs emit blue color in a wide excitation span, which can be adopted to selectively detect ferric ions (Fe3+) in a broad dosage scale with a highly linear correlation of 10-50 μM. Taking advantages of the MBC-aided persulfate activation, we propose the efficient arbidol removal system with a universal concentration of 20-200 ppm in the scalable pH ranging from 3 to 11. The dominate migration pathways involving with active oxygen species and surface electron transfer are comprehensively studied via electron paramagnetic resonance, radical-quenching experiments, and theoretical arithmetic. With the endeavor of biorefineries, this full-scale platform ignites the dazzling wildfire from dual lignocellulose valorization that will also seek its accurate position in the kingdoms of functional materials and wastewater restoration.Nowadays, the increasing amounts of dyes present in wastewaters and even water bodies is an emerging global problem. In this work we decided to fabricate new biosystems made of nanofiltration or ultrafiltration membranes combined with laccase entrapped between polystyrene electrospun fibers and apply them for decolorization of aqueous solutions of three azo dyes, C.I. Acid Yellow 23 (AY23), C.I. Direct Blue 71 (DB71) and C.I. Reactive Black 5 (RB5). Besides effective decolorization of the permeate stream, the biosystems also allowed removal of dyes from the retentate stream as a result of enzymatic action. The effect of pH and applied pressure on decolorization efficiencies was investigated, and pH 5 and pressure of 2 bar gave the highest removal efficiencies of 97% for AY23 and 100% for both DB71 and RB5 from permeate solutions while decolorization of retentate for RB5 reached 65% under these conditions. Almost 100% decolorization of all dyes was achieved after three consecutive enzyme membrane cycles. Decolorization was shown to be due to the synergistic action of membrane separation and bioconversion. The biocatalytic action also enabled significant reduction of permeate and retentate toxicity, which is one of the biggest environmental health issues for these types of streams.Humic substances (HS) as representative natural organic matters and the most common organic compounds existing in the environment, has been applied to the treatment and remediation of environmental pollution. This review systematically introduces and summarizes the redox activity of HS for the remediation of environmental pollutants. For inorganic pollutants (such as silver, chromium, mercury, and arsenic), the redox reaction of HS can reduce their toxicity and mobilization, thereby reducing the harm of these pollutants to the environment. The concentration and chemical composition of HS, environmental pH, ionic strength, and competing components affect the degree and rate of redox reactions between inorganic pollutants and HS significantly. With regards to organic pollutants, HS has photocatalytic activity and produces a large number of reactive oxygen species (ROS) under the light which reacts with organic pollutants to accelerate the degradation of organic pollutants. Under the affection of HS, the redox of Fe(III) and Fe(II) can enhance the efficiency of Fenton-like reaction to degrade organic pollutants. Finally, the research direction of HS redox remediation of environmental pollution is prospected.Plastic pollution is one of the global pressing environmental problems, threatening the health of aquatic and terrestrial ecosystems. However, the influence of plastic residues and microplastics (MPs) in soil ecosystems remains unclear. We conducted a global meta-analysis to quantify the effect of plastic residues and MPs on indicators of global soil ecosystem functioning (i.e. soil physicochemical properties, plant and soil animal health, abundance and diversity of soil microorganisms). Concentrations of plastic residues and MPs were 1-2700 kg ha-1 and 0.01-600,000 mg kg-1, respectively, based on 6223 observations. Results show that plastic residues and MPs can decrease soil wetting front vertical and horizontal movement, dissolved organic carbon, and total nitrogen content of soil by 14%, 10%, 9%, and 7%, respectively. Plant height and root biomass were decreased by 13% and 14% in the presence of plastic residues and MPs, while the body mass and reproduction rate of soil animals decreased by 5% and 11%, respectively. However, soil enzyme activity increased by 7%441% in the presence of plastic residues and MPs. For soil microorganisms, plastic residues and MPs can change the abundance of several bacteria phyla and families, but the effects vary between different bacteria.
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