Effect of alkali pretreatment time on kitchen waste anaerobic digestion performance enhanced by alkali pretreatment combined with bentonite: performance enhancement, microbial community structure, and functional gene analysis.

Kitchen waste was mainly composed of carbohydrates, lipids, and proteins. Anaerobic digestion (AD) of kitchen waste usually occurred acidification and further deteriorated. In our previous study, alkali pretreatment combined with bentonite (AP/Be) treatment was proved to enhance high solid AD of kitchen waste. However, effects of AP time on AP/Be were not yet studied. This study investigated the effects of AP time on AP/Be treatment on enhancing high solid AD. The results showed that compared with the control group, the cumulative methane production rate could be increased by 3.30 times (149.7 mL CH4/g VS) and the volatile solids (VS) reduction rate increased by 63.36%. Microbial community analysis showed that the relative abundance of Methanosarcina and Methanosaeta were increased from 6.49 and 7.83% to 47.14 and 16.39% respectively. Predictive functional analysis showed that AP/Be treatment increased the abundance of energy production and conversion, coenzyme transport, and metabolism. This study revealed the potential mechanism of AP/Be enhanced kitchen waste AD performance and AP/Be was a potential strategy to strengthen AD.

Selective degradation of organic micropollutants by activation of peroxymonosulfate by Se@NC: Role of Se doping and nonradical pathway mechanism.

In this study, Se@NC-x decorated with Se was successfully prepared via two-step calcination with zeolitic imidazole framework (ZIF) as a precursor. Mechanistic studies show that PMS would be adsorbed onto the surface of Se@NC-900 to form an active complex (Se@NC-900/PMS*), and the active Se@NC-900/PMS* could oxidize phenol by the rapid decomposition of PMS. Specifically, electrons are extracted by Se@NC-900/PMS* and then transferred to the surface of Se@NC-900, which can trigger the degradation of phenol. Notably, it is found that the local charge redistribution caused by the doping of Se can activate the catalytic potential of the intrinsically inert carbon skeleton through density flooding theory (DFT) calculations. The XLogP, ΔE, VIP, and ELUMO (Se@NC/PMS)-HOMO (pollutants) and degradation rate constants of different micropollutants were correlated well linearly. This indicates that the Se@NC-900/PMS system has a great selectivity for the degradation of pollutants. Overall, these findings not only illustrate the role of Se in tuning the electronic structure of Se@NC-x to enhance the activation of PMS, but also bridge the gap in our knowledge about the physicochemical properties and degradation performance of Se@NC catalysts.

The overview of Mitogen-activated extracellular signal-regulated kinase (MEK)-based dual inhibitor in the treatment of cancers.

Mitogen-activated extracellular signal-regulated kinase 1 and 2 (MEK1/2) are the critical components of the mitogen-activated protein kinase/extracellular signal-regulated kinase 1 and 2 (MAPK/ERK1/2) signaling pathway which is one of the well-characterized kinase cascades regulating cell proliferation, differentiation, growth, metabolism, survival and mobility both in normal and cancer cells. The aberrant activation of MAPK/ERK1/2 pathway is a hallmark of numerous human cancers, therefore targeting the components of this pathway to inhibit its dysregulation is a promising strategy for cancer treatment. Enormous efforts have been done in the development of MEK1/2 inhibitors and encouraging advancements have been made, including four inhibitors approved for clinical use. However, due to the multifactorial property of cancer and rapidly arising drug resistance, the clinical efficacy of these MEK1/2 inhibitors as monotherapy are far from ideal. Several alternative strategies have been developed to improve the limited clinical efficacy, including the dual inhibitor which is a single drug molecule able to simultaneously inhibit two targets. In this review, we first introduced the activation and function of the MAPK/ERK1/2 components and discussed the advantages of MEK1/2-based dual inhibitors compared with the single inhibitors and combination therapy in the treatment of cancers. Then, we overviewed the MEK1/2-based dual inhibitors for the treatment of cancers and highlighted the theoretical basis of concurrent inhibition of MEK1/2 and other targets for development of these dual inhibitors. Besides, the status and results of these dual inhibitors in both preclinical and clinical studies were also the focus of this review.

High efficiency degradation of tetracycline by peroxymonosulfate activated with Fe/NC catalysts: Performance, intermediates, stability and mechanism.

Carbon-based catalysts have the advantages of biological cleaning, eco-friendly and cost-effective in water treatment. While, nitrogen doped biochar promotes the development of non-radical peroxymonosulfate (PMS) activation in environmental remediation. Thus, three-dimensional sponge-like porous Fe and N co-doped biochar (Fe/CN-30) with high catalytic activity for PMS activation was synthesized. In a wide pH range (1-11), the Fe/CN-30 catalyst can efficiently degrade tetracycline (TC) with a small amount of PMS. The non-radical pathways are prominent in the TC decomposition process according to the quenching experiments, electron paramagnetic resonance (EPR) and gas chromatograph-mass spectrometer (GC-MS) analysis, in which the contribution of high-valent iron-oxo species (Fe(IV) = O) was dominant. X-ray photoelectron spectroscopy and reaction kinetic experiments confirmed that the coordination sites of Fe and N in the Fe/CN-30 are the reactive centers for TC degradation. Moreover, the successive addition of low concentration PMS into the system was confirmed to favor the PMS utilization, and the high selectivity of the Fe/CN-30 was confirmed by the analysis of pollutant structure. Furthermore, by-products of TC degradation in the Fe/CN-30/PMS system and the possible TC degradation pathways were proposed via liquid chromatography-mass spectrometry (LC-MS). Therefore, this study dedicates to providing new insights into the non-radical pathway-catalyzed AOPs.

Fabrication of graphitic carbon nitride functionalized P-CoFe2O4 for the removal of tetracycline under visible light: Optimization, degradation pathways and mechanism evaluation.

In this study, nano-sized CoFe2O4 composites were prepared through co-precipitation process. Then the phosphorus-doped strong magnetic graphitic carbon nitride hybrids composites (P-CoFe2O4@GCN) was stemmed from the CoFe2O4 composites via the thermal polymerization method. The TEM results show that the CoFe2O4 nanoparticles have been successfully embedded into the graphitic carbon nitride (GCN). The BET specific surface area of P-CoFe2O4@GCN-1 could reach 36.91 m2/g, which was 5.38 times higher than that of GCN. Thus, it provided sufficient reaction active sites to enhance the photocatalytic activity for tetracycline (TC) decomposition. The results from the photocatalytic experiments showed that the degradation efficiency of TC by P-CoFe2O4@GCN-1 could reach 96.2% within 60 min, which is 3.19 times higher than that of GCN. The h+, O2•- and •OH radicals detected by the electron spin resonance (ESR) were responsible for the TC decomposition in the photocatalytic reaction system. Persulfate (PS) can further activate the hybrid mixture system, and the fitting model predicted by the response surface methodology (RSM) indicated that the maximum tetracycline removal could reach 99.6% within 30 min. In addition, the degradation intermediates of TC were detected by HPLC-MS and the photodegradation mechanism was discussed.

Carbon quantum dots decorated heteroatom co-doped core-shell Fe0@POCN for degradation of tetracycline via multiply synergistic mechanisms.

In this study, novel core-shell catalyst with a new ternary heterostructure was synthesized (Fe0@POCN/CQDs) for the degradation of tetracycline (TC). The TEM results showed that the Fe0 particles were wrapped in POCN material and many nano CQDs were uniformly dispersed in the material. The new ternary nanocomposite exhibits excellent photocatalytic activity for the removal of TC, which was approximately 4.76 times higher than that of GCN. The enhancement of photocatalytic activity was attributed to the effective heterojunction as well as the multiply synergistic effects of POCN combined with Fe0 and CQDs, which was beneficial for retardation of recombination rate of photogenerated electron-hole pairs and generation of more free radicals for the oxidation of TC. Besides, the reactive oxygen species (ROS) of h+, •O2- and •OH played pivotal roles in the degradation of TC by Fe0@POCN/CQDs during the photocatalytic reaction. At the same times, sulfate radical (SO4•-) and hydroxyl radical (•OH) highlighted the dominant role in the degradation process compared with other free radicals under persulfate hybrid mixture system (PS system), which was further confirmed by radical scavenger experiments and electron spin resonance (ESR) analysis. The response surface methodology (RSM) study indicated that the optimal removal parameters of tetracycline could reach 97.57% within 30 min under PS system. In addition, the possible degradation pathway intermediates of TC were studied by HPLC-MS and the reaction catalytic activity mechanism of Fe0@POCN/CQDs/persulfate system was discussed.

In situ growth of carbon nitride on titanium dioxide/hemp stem biochar toward 2D heterostructured photocatalysts for highly photocatalytic activity.

In this work, hierarchical structure TiO2/hemp stem biochar carbon (HSBC) and C3N4-TiO2/HSBC were successfully fabricated, which were used as efficient visible-light photocatalyst degradation for ammonia nitrogen from aqueous solution. The as-prepared C3N4-TiO2/HSBC hybrid catalyst showed the higher efficient photocatalytic activity for decomposition of ammonia nitrogen than those of pure TiO2 and TiO2/HSBC, suggesting suppressed recombination of photogenerated charges and promoted mass transfer due to synergistic effect, and thus increased photocatalytic degradation activity. The degradation of ammonia follows a pseudo-first-order kinetics. All prepared catalysts demonstrated extremely photocatalytic efficiency under visible-light and UV light illumination; the ammonia nitrogen photocatalytic degradation activity of C3N4-TiO2/HSBC can reach 90.3% under UV light while the degradation activity achieved about 50.7% under visible-light irradiation. The results revealed that the h+ was dominantly active intermediates in the process of photocatalytic degradation. The prepared catalysts are promising for the degradation of ammonia nitrogen from water resource.

Floc Performance parameters during water treatment in a micro-vortex flocculation process determined by machine vision.

The coagulant dosage of an existing water plant is mainly determined based on the experience of water treatment process and influent/effluent water quality indexes that have time hysteresis effects. To solve this problem, the effect of coagulant dosage on a number of parameters used to evaluate the efficiency of flocculation in a setup was determined by using the micro-vortex flocculation technology in conjunction with the investigation of the relation between the equivalent diameter and the fractal dimension. By means of the machine vision system and computerized analysis, the effects of floc quantity, floc equivalent diameter and fractal dimension can be assessed. The correlations of these parameters with turbidity and ζ potential of the settling water, taken as measures for effluent quality, were explored. The study results show that the optimal flocculation effect with a turbidity removal rate of 97.9% is achieved at the poly-aluminum chloride dosage of 20 mg/L. Meanwhile, a power exponential relation between the floc equivalent diameter and the fractal dimension was established with a correlation coefficient R2 of 0.826; relations among the effluent turbidity and the floc quantity, equivalent diameter, fractal dimension were established with a correlation coefficient R2 of 0.982, 0.851, and 0.875, respectively; equations between the ζ potential and the floc quantity, equivalent diameter, fractal dimension were also established where the correlation coefficient R2 were 0.868, 0.879, and 0.942, respectively. These results may provide excellent reference data for water plants to feed back the coagulant by floc performance parameters, which could relieve the hysteresis effect efficiently.

In situ fabrication of hierarchical biomass carbon-supported Cu@CuO-Al2O3 composite materials: synthesis, properties and adsorption applications.

Hierarchical Cu-Al2O3/biomass-activated carbon composites were successfully prepared by entrapping a biomass-activated carbon powder derived from green algae in the Cu-Al2O3 frame (H-Cu-Al/BC) for the removal of ammonium nitrogen (NH4 +-N) from aqueous solutions. The as-synthesized samples were characterized via XRD, SEM, BET and FTIR spectroscopy. The BET specific surface area of the synthesized H-Cu-Al/BC increased from 175.4 m2 g-1 to 302.3 m2 g-1 upon the incorporation of the Cu-Al oxide nanoparticles in the BC surface channels. The experimental data indicated that the adsorption isotherms were well described by the Langmuir equilibrium isotherm equation and the adsorption kinetics of NH4 +-N obeyed the pseudo-second-order kinetic model. The static maximum adsorption capacity of NH4 +-N on H-Cu-Al/BC was 81.54 mg g-1, which was significantly higher than those of raw BC and H-Al/BC. In addition, the presence of K+, Na+, Ca2+, and Mg2+ ions had no significant impact on the NH4 +-N adsorption, but the presence of Al3+ and humic acid (NOM) obviously affected and inhibited the NH4 +-N adsorption. The thermodynamic analyses indicated that the adsorption process was endothermic and spontaneous in nature. H-Cu-Al/BC exhibited removal efficiency of more than 80% even after five consecutive cycles according to the recycle studies. These findings suggest that H-Cu-Al/BC can serve as a promising adsorbent for the removal of NH4 +-N from aqueous solutions.

Multipath fabrication of hierarchical CuAl layered double hydroxide/carbon fiber composites for the degradation of ammonia nitrogen.

In this work, a series of flower-like CuAl layered double hydroxides (LDHs) and hierarchical CuAl/carbon fiber-LDH (CuAl/CF-LDH) materials were synthesized, and these materials were used as catalysts for the degradation of ammonia nitrogen from simulated wastewater. The morphologies and structures of the materials were characterized using scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy (RS), X-ray diffraction (XRD), and the Brunauer-Emmett-Teller (BET) technique. The effects of the catalyst and H2O2 loading dosages, reaction temperature, pH, Cu/Al ratio of the samples, and contact time on the degradation process were investigated by degrading ammonia nitrogen under different conditions, and the possible degradation mechanism was discussed. CuAl/CF-LDH exhibited more effectively catalytically degradation of ammonia nitrogen than others as-prepared samples, and removal efficiency reached 99.7% under the optimized conditions. The reusing capability and stability of the materials were studied. Meanwhile, the versatility of the materials was investigated by testing their performance in the absorption of azo dye, the highest removal efficiency was found to be 99.28%. The prepared materials are promising for use as effective catalysts for the degradation of ammonia nitrogen from wastewater.

Amine-functionalized magnetic bamboo-based activated carbon adsorptive removal of ciprofloxacin and norfloxacin: A batch and fixed-bed column study.

Amine-functionalized magnetic bamboo-based activated carbon (AFM-BAC) derived from bamboo products wastes were employed for effective adsorption of fluoroquinolone antibiotics ciprofloxacin (CIP) and norfloxacin (NOR) through batch processing. The effects of factors on the adsorption of both antibiotics were studied. The studies of various factors influencing the adsorption behavior indicated that the maximum adsorption capacities for two antibiotics adsorption were observed in weakly acidic condition and the adsorption amounts of two antibiotics increased with the increase of zwitterionic form, implying the importance of zwitterionic form, and the adsorption process is spontaneous and endothermic. The result of date indicated that adsorption of both two antibiotics onto the AFM-BAC better fits Langmuir isotherm model. The saturated magnetization of AFM-BAC reached 8.55 emu g-1. A fixed-bed column adsorption with a bench-scale was carried out. Desorption and regeneration experiments showed that the AFM-BAC for both antibiotics could remain above 80% after five consecutive recycling cycles.

Adsorption behavior and mechanisms of ciprofloxacin from aqueous solution by ordered mesoporous carbon and bamboo-based carbon.

The performances of ordered mesoporous carbon CMK-3 (OMC), bamboo-based carbon (BC), and these two kinds of adsorbents modified by thermal treatment in the ammonia atmosphere at high temperatures were evaluated for the removal fluoroquinolone antibiotic (ciprofloxacin) from aqueous solution. The adsorption behavior of ciprofloxacin (CIP) onto OMC and BC including adsorption isotherms and kinetics were investigated. The effect of various factors (pH, ionic strength and temperature) on the adsorption process was also investigated. The results demonstrated that the modified OMC and BC can further enhance the adsorption capacity due to introduce of alkaline nitrogen functionalities on the carbon surface. And their maximum adsorption capacity reached as high as 233.37mgg(-1) and 362.94mgg(-1) under the same experimental conditions, respectively. This is primarily ascribed to the positive effect of the surface basicity. The highest sorption was observed at the lowest solubility, which indicated that hydrophobic interaction was the dominant sorption mechanism for CIP uptake onto the four adsorbents. The adsorption data of antibiotics was analyzed by Langmuir and Freundlich model, and the better correlation was achieved by the Langmuir isotherm. The kinetic data showed that the adsorption of CIP onto OMC and BC follow closely the pseudo-second order model. The removal efficiency and adsorption capacity increased with increasing temperature. The results of thermodynamic study indicated that the adsorption process was a spontaneous and endothermic.