Prenatal prednisone exposure disturbs fetal kidney development and its characteristics.

Prednisone is a synthetic glucocorticoid that is commonly used in both human and veterinary medication. Now, it is also recognized as an emerging environmental contaminant. Pregnant women may be exposed to prednisone actively or passively through multiple pathways and cause developmental toxicity to the fetus. However, the impact of prenatal prednisone exposure (PPE) on fetal kidney development remains unclear. In this study, pregnant mice were administered prednisone intragastrically during full-term pregnancy with different doses (0.25, 0.5, or 1 mg/(kg·day)), or at the dose of 1 mg/(kg·day) in different gestational days (GD) (GD0-9, GD10-18, or GD0-18). The pregnant mice were euthanized on GD18. HE staining revealed fetal kidney dysplasia, with an enlarged glomerular Bowman's capsule space and a reduced capillary network in the PPE groups. The expression of the podocyte and the mesangial cell marker genes was significantly reduced in the PPE groups. However, overall gene expression in renal tubules and collecting ducts were markedly increased. All of the above effects were more pronounced in high-dose, full-term pregnancy, and female fetuses. Studies on the mechanism of the female fetal kidney have revealed that PPE reduced the expression of Six2, increased the expression of Hnf1ß, Hnf4α, and Wnt9b, and inhibited the expression of glial cell line-derived neurotrophic factor (GDNF) and Notch signaling pathways. In conclusion, this study demonstrated that there is a sex difference in the developmental toxicity of PPE to the fetal kidney, and the time effect is manifested as full-term pregnancy > early pregnancy > mid-late pregnancy.

SNHG10 Is a Prognostic Biomarker Correlated With Immune Infiltrates in Prostate Cancer.

SNHG10 is a long non-coding RNA (lncRNA) found to be overexpressed in multiple human cancers including prostate cancer (PC). However, the underlying mechanisms of SNHG10 driving the progression of PC remains unclear. In this study, we investigated the role of SNHG10 in PC and found that SNHG10 expression was significantly increased in datasets extracted from The Cancer Genome Atlas. Increased expression of SNHG10 was related to advanced clinical parameters. Receiver operating curve analysis revealed the significant diagnostic ability of SNHG10 (AUC = 0.805). In addition, immune infiltration analysis, and GSEA showed that SNHG10 expression was correlated with oxidative phosphorylation and immune infiltrated cells. Finally, we determined that SNHG10 regulated cell proliferation, migration, and invasion of PC in vitro. In conclusion, our data demonstrated that SNHG10 was correlated with progression and immune infiltration, and could serve as a prognostic biomarker for PC.

Photocatalytic reduction of Cr(VI) over cinder-based nanoneedle in presence of tartaric acid: Synergistic performance and mechanism.

Cr(VI) is a common heavy metal ion, which will seriously harm human body and environment. Therefore, the removal of Cr(VI) has become an attractive topic. In this work, cinder was used as a raw material to synthesize a nanoneedle material: γ-(AlOOH@FeOOH) (γ-Al@Fe). The physicochemical properties of γ-Al@Fe were thoroughly characterized, and its effectiveness as a catalyst for photocatalytic reduction of Cr(VI) was evaluated. The results showed that Cr(VI) could be efficiently reduced by γ-Al@Fe in the presence of tartaric acid (TA) under visible light. The variable factors on the reaction were investigated in detail, and the results showed that under optimal conditions (γ-Al@Fe 0.4 g/L, TA 0.6 g/L, pH 2), Cr(VI) was completely reduced within 7 min. Besides, scavenger experiments and EPR proved that O2• - and CO2• - played a significant role in the photocatalytic reduction of Cr(VI). TA acts as a sacrificial agent to trap the holes and generate strong reducing free radicals: CO2• -. Dissolving O2 could react with electrons to generate O2• -. This work discussed the performance and mechanism of photocatalytic reduction of Cr(VI) in detail, which provided a new idea for the resource utilization of solid waste and the treatment of heavy metal sewage.

Crystallinity-dependent photodegradation of metallic Bi in situ grown on perovskite Bi3TiNbO9 nanosheets toward antibiotic.

Owing to its wide band gap of ~3.2 eV, perovskite Bi3TiNbO9 only absorbs the solar spectrum in the ultraviolet range, which restricts its use as an effective photocatalyst. Here, a controllable and facile reduction strategy was adopted to promote the in-situ growth of metallic Bi in perovskite Bi3TiNbO9 nanosheets. The in-situ growth of metallic Bi extended photoresponse to cover the whole visible region. Adsorption of tetracycline hydrochloride (TC-H) on the surface of Bi3TiNbO9 with in-situ growth of metallic Bi (BTNOOV-Bi0) was dramatically enhanced, while BTNOOV-Bi0 exhibited a superior photocatalytic performance for tetracycline hydrochloride (TC-H) degradation under visible light irradiation with the degradation rate of 5 times higher than that of pristine Bi3TiNbO9. Moreover, the degradation activity was strongly dependent on the crystallinity of metallic Bi phase in BTNOOV-Bi0 samples. On the basis of experiment results, the visible-light driven catalytic mechanism of BTNOOV-Bi0 was elucidated. Besides, the in-situ growth of metallic Bi was also introduced in perovskite Bi5FeTi3O15, resulting in an enhanced photocatalytic activity, which indicated an enormous potential of this strategy in semiconductor structure tuning. Our study provides an effective approach to boost the performance of photocatalysts for solar-energy conversion.

Soybean residue based biochar prepared by ball milling assisted alkali activation to activate peroxydisulfate for the degradation of tetracycline.

The advanced oxidation process (AOPs) has caused great concern in recent years. Among them, biochar has been widely studied as a catalyst for advanced oxidation process because of its low price and low environmental risk. In this study, a novel ball milling assisted KOH activation biochar (MKBC) was prepared and applied in peroxydisulfate (PDS) activation to degrade tetracycline hydrochloride (TC-H). In comparison with the oxidation (3.48%) by PDS alone and adsorption (36.19%) by MKBC alone, the removal rate of TC-H was increased to 84.15% in the MKBC/PDS system, indicating that MKBC can successfully activate PDS. Besides, the catalytic activity of the MKBC to activate PDS for the degradation of TC-H is 58.33% higher than that of pristine biochar (PBC). In addition, MKBC has outstanding stability that after three repeated experiments, the removal rate of TC-H by the MKBC/PDS system still remains 77.35%. Meanwhile, the mechanism was investigated that the singlet oxygen (1O2) seized the principal position in the degradation of TC-H in the PDS/MKBC system. This study explored a novel, solvent-free and economic method to propose this extraordinary biochar, which provided a new strategy for the future research of biochar.

Unique MIL-53(Fe)/PDI Supermolecule Composites: Z-Scheme Heterojunction and Covalent Bonds for Uprating Photocatalytic Performance.

It is important to find an effective way to enhance the photocatalytic efficiency of metal-organic frameworks. In this work, an organic supermolecule perylene diimide (PDI) semiconductor with a carboxyl terminal was added into the synthesis process of MIL-53(Fe) crystals. The PDI/MIL-53(Fe) (PM) composite photocatalyst was first obtained. The TC-H photodegradation rate of the most efficient 5PM was nearly 94.08% within 30 min, whose apparent reaction rate constant (k) is 4 times that of PDI and 33 times that of MIL-53(Fe), respectively. By investigation and characterization, it has been found that PDI nanofibers were dispersed and fixed in MIL-53(Fe) and bonded to each other by covalent bonds. The radical trap experiments and electron spin resonance analysis illustrated that hydroxyl radical (·OH), superoxide radical (·O2-), and photogenerated holes (h+) were active species. Combined with the band structure of PDI and MIL-53(Fe), it is proposed that the PM photocatalyst was a Z-scheme heterojunction mechanism. Therefore, PM photocatalysts showed excellent charge separation and transfer ability. The performance improvement of 5PM is due to enhanced visible light absorption, efficient charge separation, and excellent redox potential. Five cyclic photocatalytic tests and experiments further demonstrate that the 5PM photocatalyst has a promising future for pollutant removal.

Surface structure tuning of BiOCl nanosheets by the sequential introduction of oxygen vacancies, PO43- and Ag+ for boosting photodegradation of tetracycline hydrochloride.

The surface structure significantly impacts the physicochemical properties of semiconductors. Constructing heterojunction is a universal approach to tune surface structure, which can effectively accelerate the charge transfer at the interface. Here, BiOCl nanosheets which occupy high ratio of surface atoms to entire atoms were used as a model photocatalyst, and a strategy was proposed to tune its surface structure by sequential introduction of oxygen vacancies, PO43- and Ag+ on surface of BiOCl nanosheets. In order to inhibit the overgrowth of heterogeneous component, the excess PO43- was timely removed by centrifugation before adding Ag+. As a result, the as-obtained optimal sample which was confirmed to be a composite composed of BiOCl, BiPO4 and AgCl showed superior photocatalytic activity for tetracycline hydrochloride degradation with the rate of 38 times higher than that of pristine BiOCl, which was mainly attributed to the quick migration of photongenerated carrier. The active species h+ and •O2- played a vital role in this degradation process. Our strategy not only greatly saved investment of noble metal Ag, but also provide superior stability. On the basis of experimental results and density functional theory calculation, the visible-light driven catalytic mechanism was revealed.

Study of Thermal Behavior of Moxa Floss Using Thermogravimetric and Pyrolysis-GC/MS Analyses.

Moxa floss is a type of biomass used as the main combustion material in moxibustion, a therapy that applies heat from moxa floss combustion to points or body areas for treatment. Safety concerns regarding moxa smoke have been raised in recent years. Since moxa floss is the source material in moxibustion, its thermal behavior and pyrolysis products would be related to the products formed in moxa smoke. This work aims to understand the thermal behavior of moxa floss and investigate the pyrolysis products generated from moxa floss combustion. Six commercial moxa floss samples of 3 storage years and 10 storage years, and of low, medium, and high ratios, were selected. The kinetic data from moxa floss combustion was carried out by a thermogravimetric analyzer. Pyrolysis-gas chromatography and mass spectroscopy using a gas chromatograph and mass spectrometer equipped with a pyroprobe were used to examine the pyrolysis products. Thermogravimetric profiles for all the samples were overall similar and showed a monotonic weight decrease. The range of intensive reaction temperature occurred between 150°C and 450°C, which was characterized by a major weight loss and accompanied by an exothermal degradation of the main components. The average ignition temperature for the samples of 3 and 10 storage years was 218.3°C and 222.6°C, respectively, which was lower than most herbaceous plants. The identified pyrolysis products include monocyclic aromatic hydrocarbons, polycyclic aromatic hydrocarbons, ketones, acids, and alkanes. All were of relatively low intensities of below 5% in relative abundance. No volatiles were detected in the samples of 10 storage years. The relatively low values of ignition temperature suggested that moxa floss is more combustible and can be ignited more easily than other herbaceous plants. This may explain why moxa floss has remained as the preferred material used for moxibustion over the years.

Development of prognostic signature based on RNA binding proteins related genes analysis in clear cell renal cell carcinoma.

RNA binding proteins (RBPs) play significant roles in the development of tumors. However, a comprehensive analysis of the biological functions of RBPs in clear cell renal cell carcinoma (ccRCC) has not been performed. Our study aimed to construct an RBP-related risk model for prognosis prediction in ccRCC patients. First, RNA sequencing data of ccRCC were downloaded from The Cancer Genome Atlas (TCGA) database. Three RBP genes (EIF4A1, CARS, and RPL22L1) were validated as prognosis-related hub genes by univariate and multivariate Cox regression analyses and were integrated into a prognostic model by least absolute shrinkage and selection operator (LASSO) Cox regression analysis. According to this model, patients with high risk scores displayed significantly worse overall survival (OS) than those with low risk scores. Moreover, the multivariate Cox analysis results indicated that risk score, tumor grade, and tumor stage were significantly correlated with patient OS. A nomogram was constructed based on the three RBP genes and showed a good ability to predict outcomes in ccRCC patients. In conclusion, this study identified a three-RBP gene risk model for predicting the prognosis of patients, which is conducive to the identification of novel diagnostic and prognostic molecular markers.

Rapid removal of organic pollutants by a novel persulfate/brochantite system: Mechanism and implication.

Using natural minerals as persulfate activators can develop effective and economical in situ chemical oxidation technology for environmental remediation. Yet, few natural minerals can provide a high activation efficiency. Here, we demonstrate that brochantite (Cu4SO4(OH)6), a natural mineral, can be used as a persulfate activator for the rapid degradation of tetracycline hydrochloride (TC-H). Approximately 70% of TC-H was removed in Cu4SO4(OH)6/PDS within 5 min, which much higher than that of Cu3P (61.99%), CuO (29.75%), CNT (25.83%), Fe2O3, (14.48%) and MnO2 (9.76%). Experiments and theoretical calculations suggested that surface copper acts as active sites induce the production of free radicals. The synergistic effect of Cu/S promotes the cycle between Cu+/Cu2+. Sulfate radicals and hydroxyl radicals are the main reactive oxygen species that are responsible for the rapid removal of TC-H. The findings of this work show a novel persulfate/brochantite system and provide useful information for the environmental remediation.

Prognostic Role of Circular RNAs Expression in Bladder Carcinoma: A Meta-Analysis.

Background: Circular RNAs (circRNAs), a type of noncoding RNA, are associated with the occurrence and development of cancers. In recent years, their potential as biomarkers for bladder cancer (BC) has attracted increased attention. Aims: To reveal the value of circRNAs in the prognosis of BC. Methods: Relevant studies were collected to extract the clinicopathological data and overall survival (OS) of patients with BC. We then evaluated their tumor-related clinicopathological indicators using pooled odds ratio (OR) and 95% confidence interval (CI). Hazard ratio (HR) and 95% CI were used to estimate the OS of BC patients who expressed abnormal circRNAs. Results: The results indicate that seven circRNAs (circMYLK, circASXL1, hsa_circ_0000144, circ-VANGL1, circGprc5a, circZFR, and circ-cTFRC) whose expression was upregulated in tumor tissues, are associated with poor clinicopathological features (tumor/node/metastasis [TNM] stage: OR = 4.86, 95% CI: 2.53-9.34; histological grade: OR = 3.71, 95% CI: 2.37-5.79; lymph node metastasis: OR = 3.23; 95% CI: 2.15-4.88; recurrence: OR = 5.33; 95% CI: 2.27-12.52) and poor prognoses (OS: HR = 1.69; 95% CI: 1.17-2.44). We also found that seven circRNAs (circMTO1, circ-ITCH, circUBXN7, circFNDC3B, circ-ZKSCAN1, circPICALM, and circACVR2A) that were downregulated in tumors were associated with better clinicopathological indicators (TNM stage: OR = 0.23, 95% CI: 0.14-0.38; histological grade: OR = 0.21, 95% CI: 0.13-0.33; lymph node metastasis: OR = 0.26; 95% CI: 0.15-0.47) and better prognoses (OS: HR = 0.42; 95% CI: 0.30-0.58). Conclusion: Our results suggest that certain circRNAs are related to the clinicopathological characteristics and prognosis of BC patients, and may potentially be used as biomarkers.

Laparoscopic versus open surgery for pheochromocytoma: a meta-analysis.

BACKGROUND: Surgical resection is the main treatment for pheochromocytoma (PHEO). Although open surgery (OS) has been shown to be safe and feasible, the safety and efficacy of laparoscopic surgery (LS) for PHEO remain controversial due to the uncertain effects of pneumoperitoneum on haemodynamics and the complexity of the tumour itself. This study was performed to compare the treatment outcomes of OS with those of LS for patients with PHEO. METHODS: A systematic search through November 11, 2019, was conducted. All studies comparing outcomes of LS and OS for PHEO were included according to eligibility criteria. This meta-analysis was conducted using Review Manager Software, version 5.3, and STATA software, version 12.0. The quality of the included studies was assessed using the Newcastle-Ottawa scale. RESULTS: Fourteen studies involving 626 patients were included in this meta-analysis. LS was associated with lower rates of intraoperative haemodynamic instability (IHD) [odds ratio (OR) = 0.61, 95% CI: 0.37 to 1.00, P = 0.05], less intraoperative blood loss [weighted mean difference (WMD) = - 115.27 ml, 95% confidence interval (CI): - 128.54 to - 101.99, P < 0.00001], lower blood transfusion rates [OR = 0.33, 95% CI: 0.21 to 0.52, P < 0.00001], earlier ambulation (WMD = - 1.57 d, 95% CI: - 1.97 to - 1.16, P < 0.00001) and food intake (WMD = - 0.98 d, 95% CI: - 1.36 to - 0.59, P < 0.00001), shorter drainage tube indwelling time (WMD = - 0.51 d, 95% CI: - 0.96 to - 0.07, P = 0.02) and postoperative stay (WMD = - 3.17 d, 95% CI: - 4.76 to - 1.58, P < 0.0001), and lower overall complication rates (OR = 0.56, 95% CI: 0.35 to 0.88, P = 0.01). However, no significant differences in operative time, postoperative blood pressure control, rates of severe complications, postoperative hypotension or cardiovascular disease (CVD) were found between the two groups. CONCLUSIONS: LS is safe and effective for PHEO resection. Compared with OS, LS caused less IHD, providing an equal chance to cure hypertension while also yielding a faster and better postoperative recovery.

Boosting Photocatalytic Performance in Mixed-Valence MIL-53(Fe) by Changing FeII/FeIII Ratio.

One of vital issues that inhibit photoactivity of metal-organic frameworks is the poor electrical conductivity. In this work, one-dimensional mixed-valence iron chains are used to improve this poor situation in MIL-53(Fe). A series of mixed-valence MIL-53(Fe) photocatalysts were obtained through heating at different temperatures in vacuum. The effect of FeII coordinatively unsaturated metal sites (CUS) and one-dimensional mixed-valence iron chains on their photocatalytic property was discussed. The experimental results indicated that mixed-valence MIL-53(Fe) with a reference FeII/FeIII ratio of 0.2725 displayed the best photocatalytic performance, which showed 96.28 and 95.01% removal efficiencies of RhB and TC-H in 100 min, respectively. Moreover, MIL-53(Fe) heated in vacuum displayed better catalytic activity than MIL-53(Fe) heated in air for RhB and TC-H degradation. Based on the analysis of various characterizations, the reinforced catalytic activity can be attributed to the charge mobilities in mixed-valence FeII/FeIII chains. It is worth mentioning that the method is also applicable to MIL-88(Fe) and MIL-101(Fe). Additionally, mixed-valence MIL-53(Fe) can also perform the catalysis reaction in the nighttime by activating persulfate (PS) to produce free radicals. Interestingly, it was found that the FeII CUS lost in activating PS can be supplemented by self-reduction of photogenerated electrons during illumination in the daytime, so as to achieve a more stable cycle. This work demonstrated that the photoactivity of MIL-53(Fe) can be improved by adjusting the ratio of FeII/FeIII and the feasibility of using as an all-day-active catalyst.

Rice husk derived double network hydrogel as efficient adsorbent for Pb(II), Cu(II) and Cd(II) removal in individual and multicomponent systems.

In this study, lignin extracted from rice husk was used to synthesis double network hydrogel adsorbent, named RH-CTS/PAM gel. RH-CTS/PAM gel exhibited macroporous structure and high buried water content, which gave rise to the exceptional adsorption performance. As results, in individual systems, the equilibrium time of Pb(II), Cu(II) and Cd(II) with initial concentration of 200 mg/L could be reached within 10 min, with the theoretical maximum adsorption capacity of 374.32, 196.68 and 268.98 mg/g, respectively. The adsorption rate and capacity of Pb(II), Cu(II) and Cd(II) in multicomponent systems were lower than that of individual systems. However, in a few cases of ternary system, higher adsorption rate and capacity was observed compare to binary systems. Adsorption mechanism indicated that both oxygen-containing and nitrogen-containing functional groups played a dominant role during the adsorption process, and mainly through chemical interaction along with a small amount of physical interaction.

Exceptional Catalytic Activities of Iron Tungstophosphoric Acid Pillared Montmorillonite Photo-Fenton Catalyst for Organic Pollutant Decomposition.

Iron tungstophosphoric acid pillared montmorillonite (TPAFe-Mt) as a highly efficient, stable and visible-light-responsive photo-Fenton catalyst have successfully been prepared via an impregnation method. The TPAFe-Mt catalyst exhibits exceptional visible-light photo-Fenton catalytic activities for azo-dye methyl orange, phenol and 2,4-dinitrophenol in a wide pH range from 1.0 to 5.0. Especially, 40 mg/L of methyl orange could be completely degraded in 40 min, and the TOC removal rate was as high as 73.3%. The high catalytic performance arises from the following reasons: (i) The support of TPAFe rendered a significant increase in specific surface area and a slight increase in interlayer spacing of montmorillonite, thus improving the adsorption performance. (ii) The incorporation of tungstophosphoric acid (TPA) not only effectively anchor iron but also improved visible light absorption capacity, which greatly promoted the Fenton reaction. Moreover, the catalyst showed excellent chemical stability. After ten consecutive degradation cycles, the degradation efficiency still reached about 99% due to the good fixation iron of TPA. The possible mechanism involving in photo-Fenton process is proposed mainly based on the experimental result. This work opens up a new feasible route to synthesize visible-light-responsive high-activity photo-Fenton catalyst for efficient environmental remediation.

Ultrafine Ag@AgI nanoparticles on cube single-crystal Ag3PO4 (1 0 0): An all-day-active Z-Scheme photocatalyst for environmental purification.

Exploring and designing an efficient and robust photocatalyst toward the degradation of organic pollutants under nature sunlight irradiation is a challenging research topic. The ability to maintain the photocatalytic activity in the entire daytime will be the ultimate goal for further widespread application of solar energy-driven semiconductor photocatalysis. Here, an all-day-active Z-scheme photocatalytic system is reported by employing Ag@AgI nanoparticles decorated Ag3PO4 cubes (C-Ag3PO4@Ag@AgI). By coupling the pronounced carrier separation as well as increased stability, the C-Ag3PO4@Ag@AgI is capable of performing efficient Rhodamine B (RhB) and bisphenol A (BPA) degradation under sunlight irradiation, and still persist noticeable activity when the light is very weak. The RhB (20 mg/L, 50 mL) can be completely degraded by C-Ag3PO4@Ag@AgI (30 mg) within 1 h with the average luminous power of 117.5 mW (3.14 cm2). Dramatically, the as-prepared samples can still maintain photocatalytic activity even in a cloudy day (0.2-6.7 mW). This work has offered a valuable concept of continuous pollutant removal under nature sunlight irradiation in the entire daytime, which may serve as a model system for the wide environment applications, such as the removal of low-level pollutants under weak light irradiation.

Fast and efficient removal of As(III) from water by CuFe2O4 with peroxymonosulfate: Effects of oxidation and adsorption.

Although oxidation of As(III) to As(V) is deemed necessary to promote arsenic removal, the oxidation process usually involves toxic byproducts, well-defined conditions, energy input or sludge generation. Moreover, extra operations are required to remove the resulting As(V). A heterogeneous catalytic process of CuFe2O4 with peroxymonosulfate (PMS) is established for As(III) oxidation and adsorption. The PMS can be activated by CuFe2O4 to generate radical species for As(III) oxidation. The CuFe2O4/PMS has a stronger affinity for arsenic than CuFe2O4 alone. Oxidation and adsorption promote each other. As a result, the heterogeneous catalytic process is more efficient for As(III) removal than a preoxidation of As(III) followed by adsorption. The adsorption capacity for As on CuFe2O4/PMS reached up to 63.9 mg/g, which is much higher than that of As(III) (36.9 mg/g) or As(V) (45.4 mg/g) on CuFe2O4 alone. The process can work effectively over a wide range of pH values (3-9) and temperatures (10-40 °C). Coexisting ions such as sulfate, carbonate, silicate and humic acid have an insignificant effect on As(III) removal. The As(III) (1415 µg/L) can be completely oxidized to As(V) and rapidly removed to below 10 µg/L (less than 15 min) using CuFe2O4(0.2 g/L)/PMS(100 µM). Moreover, the As(III) (50 µg/L) can be completely oxidized and removed within 1 min. The proposed process is easily applicable for the remediation of As(III)-contaminated water under ambient conditions.

Fast adsorption of heavy metal ions by waste cotton fabrics based double network hydrogel and influencing factors insight.

Massive consumption of cotton fabrics has brought up a serious problem concerning the waste cotton fabrics (WCFs) disposal. It is widely accepted that if WCFs can be reutilized, there will be great business potentials. Herein, we prepared a double network hydrogel based on WCFs and polyacrylamide (Cellulose/PAM DNHs) for heavy metal removal. The DNHs exhibit fast kinetics that sorption equilibrium is achieved in 5min because of the porous and sheet-like laminar structures they possess. The DNHs also illustrate excellent adsorption property and good reusability. The tandem two columns packed with Cellulose/PAM-3 can effectively process simulated and practical wastewater, and the adsorption discrepancy is negligible after three adsorption-desorption cycles. The treatment volumes of simulated wastewater are 172.5 BV (7935mL), 195 BV (8970mL), and 292.5 BV (13455mL) for Cd(II), Cu(II), and Pb(II), respectively. Furthermore, the treatment volumes of practical industrial wastewater reach 42 BV (1932mL) for Cd(II), 63 BV (2898mL) for Cu(II), and 87 BV (4002mL) for Zn(II), Pb(II) and Fe, respectively. This work provides a new avenue for the combination of WCFs reuse and heavy metal removal, which is of great importance to the construction of resource sustainability and environment-friendly society.

Efficient removal of heavy metals from melting effluent using multifunctional hydrogel adsorbents.

It is hard to balance high water permeability and good mechanical strength of hydrogel adsorbents. In this study, an enhanced double network hydrogel adsorbent of poly (vinyl alcohol)/poly(2-acrylamido-2-methyl-1-propanesulfonic acid) (PVA/PAMPS) was prepared via simple free-radical polymerization. Hydrophilic PAMPS guaranteed high swellability of the adsorbent, which made the sufficient diffusion of metal ions towards adsorbent inside. Meanwhile, the cross-linkage between PVA and PAMPS chains ensured good mechanical strength of the adsorbent. Significantly, the introduction of multifunctional groups (-NHR, -SO3H and -OH) endowed the adsorbent with both chelation and ion exchange function for enhancing heavy metal adsorption. The maximum adsorption capacities of Pb2+ and Cd2+ reached 340 and 155.1 mg/g, respectively. The adsorbent could efficiently remove heavy metals in melting effluent, especially Pb2+ and Cd2+. The removal efficiencies reached 88.1% for Pb2+, 91.4% for Cd2+, 70.4% for Zn2+, 77.4% for Cu2+, 42.5% for Mn2+, 45.1% for Ni2+ and 95.4% for Fe3+ using 2 g/L adsorbent in 2 h. Moreover, the adsorbent showed a good reusability, and the removal efficiencies maintained 94% for Pb2+ and 93% for Cd2+ in the fifth cycle (m/V = 1 g dry gel/L). This work developed a highly practical hydrogel adsorbent for heavy metal removal from wastewater.

"Dark Deposition" of Ag Nanoparticles on TiO2: Improvement of Electron Storage Capacity To Boost "Memory Catalysis" Activity.

"Memory catalysis" (MC) studies have received appreciable attention recently because of the unique talent to retain the catalytic performance in the dark condition. However, the MC activity is still low owing to the relatively limited electron storage capacity of the present materials. Here, a TiO2@Ag composite was synthesized by a "dark-deposition (DD)" method, which is based on the electron trap effect of TiO2. Unlike traditional photodeposition (PD), an exploration of the morphology and chemical compositions of as-prepared samples shows that DD can inhibit the growth of Ag nanoparticles and the formation of Ag2O, which greatly improve the electron storage capacity. We further demonstrated that the maximum electronic capacity was in the order of TiO2@Ag-DD (1 µmol/mg) > TiO2@Ag-PD (0.35 µmol/mg) > TiO2 (0.11 µmol/mg). Moreover, the enhanced MC activity was confirmed by various degradation experiments. Especially, the use of TiO2@Ag-DD as a round-the-clock catalyst for the degradation of multicomponent pollutants has also been achieved. This strategy opens a door for enhancing the MC activity and reveals that the coupling of photocatalysis and MC may provide a new opportunity for the continuous removal of pollutants in day and night. It also may be extended to other fields, such as energy storage and continuous disinfection.