高分辨率磁共振血管壁成像对芪龙胶囊联合西药治疗症状性颈动脉易损斑块的疗效评估

目的利用高分辨率磁共振血管壁成像(high-resolution magnetic resonance vessel wall imaging,HRMR-VWI)技术探讨芪龙胶囊联合阿托伐他汀钙等对症状性颈动脉易损斑块的疗效及对血脂水平的影响。方法选取2020年3月至2023年1月因脑缺血性单侧肢体无力于烟台市烟台山医院行颈动脉HRMR-VWI检查的患者,随机分为西药治疗组(对照组)和西药联合芪龙胶囊治疗组(试验组),并于6个月后复查,比较两组的HRMR-VWI测量结果及血脂水平。结果共纳入32例患者,对照组18例、试验组14例。治疗后试验组甘油三酯水平显著低于对照组(1.07±0.38 vs.1.84±1.24,P=0.033)。与治疗前相比,对照组远端正常血管面积及重构指数增大,试验组最窄处管腔面积增大,两组脂核面积及甘油三酯均减小(P<0.05)。结论芪龙胶囊联合西药治疗有显著的降脂作用,可改善颈动脉斑块狭窄,并在一定程度上逆转血管重构效应。

Removing microplastics from aquatic environments:A critical review

As one of the typical emerging contaminants,microplastics exist widely in the environment because of their small size and recalcitrance,which has caused various ecological problems.This paper summarizes current adsorption and removal technologies of microplastics in typical aquatic environments,including natural freshwater,marine,drinking water treatment plants(DWTPs),and wastewater treatment plants(WWTPs),and includes abiotic and biotic degradation technologies as one of the removal technologies.Recently,numerous studies have shown that enrichment technologies have been widely used to remove microplastics in natural freshwater environments,DWTPs,and WWTPs.Efficient removal of microplastics via WWTPs is critical to reduce the release to the natural environment as a key connection point to prevent the transfer of microplastics from society to natural water systems.Photocatalytic technology has outstanding pre-degradation effects on microplastics,and the isolated microbial strains or enriched communities can degrade up to 50%or more of pre-processed microplastics.Thus,more research focusing on microplastic degradation could be carried out by combining physical and chemical pretreatment with subsequent microbial biodegradation.In addition,the current recovery technologies of microplastics are introduced in this review.This is incredibly challenging because of the small size and dispersibility of microplastics,and the related technologies still need further development.This paper will provide theoretical support and advice for preventing and controlling the ecological risks mediated by microplastics in the aquatic environment and share recommendations for future research on the removal and recovery of microplastics in various aquatic environments,including natural aquatic environments,DWTPs,and WWTPs.

Effective electrocatalytic hydrodechlorination of 2,4,6-trichlorophenol by a novel Pd/MnO_(2)/Ni foam cathode

Pd modified electrodes possess problems such as easy agglomeration and low electrolytic ability,and the use of manganese dioxide(MnO_(2)) to facilitate Pd reduction of organic pollutants is just started.However,there is still a limited understanding of how to match the Pd load and MnO_(2) to realize optimal dechlorination efficiency at minimum cost.Here,a Pd/MnO_(2)/Ni foam cathode was successfully fabricated and applied for the efficient electrochemical dechlorination of 2,4,6-trichlorophenol(2,4,6-TCP).The optimal electrocatalytic hydrodechlorination(ECH)performance with 2,4,6-TCP dechlorination efficiency(92.58%in 180 min)was obtained when the concentration of PdCl_(2) precipitation was 1 mmol/L,the deposition time of MnO_(2) was 300 s and cathode potential was-0.8 V.Performance influenced by the exogenous factors(e.g.,initial pH and coexisted ions)were further investigated.It was found that the neutral pH was the most favorable for ECH and a reduction in dechlorination efficiency(6%~47.6%)was observed in presence of 5 mmol/L of NO_(2)^(-),NO_(3)^(-),S^(2-)or SO_(3)^(2-).Cyclic voltammetry(CV)and quenching experiments verified the existence of three hydrogen species on Pd surface,including adsorbed atomic hydrogen(H^(*)_(ads)),absorbed atomic hydrogen(H^(*)_(abs)),and molecular hydrogen(H_(2)).And the introduction of MnO_(2)promoted the generation of atomic H^(*).Only adsorbed atomic hydrogen(H^(*)_(ads)) was confirmed that it truly facilitated the ECH process.Besides H^(*)_(ads) induced reduction,the direct reduction by cathode electrons also participated in the 2,4,6-TCP dechlorination process.Pd/MnO_(2)/Ni foam cathode shows excellent dechlorination performance,fine stability and recyclable potential,which provides strategies for the effective degradation of persistent halogenated organic pollutants in groundwater.

Efficient treatment of azo dye containing wastewater in a hybrid acidogenic bioreactor stimulated by biocatalyzed electrolysis

In this study, a novel scaled-up hybrid acidogenic bioreactor（HAB） was designed and adopted to evaluate the performance of azo dye（acid red G, ARG） containing wastewater treatment. Principally, HAB is an acidogenic bioreactor coupled with a biocatalyzed electrolysis module. The effects of hydraulic retention time（HRT） and ARG loading rate on the performance of HAB were investigated. In addition, the influent was switched from synthetic wastewater to domestic wastewater to examine the key parameters for the application of HAB. The results showed that the introduction of the biocatalyzed electrolysis module could enhance anoxic decolorization and COD（chemical oxygen demand） removal. The combined process of HAB-CASS presented superior performance compared to a control system without biocatalyzed electrolysis（AB-CASS）. When the influent was switched to domestic wastewater, with an environment having more balanced nutrients and diverse organic matters, the ARG, COD and nitrogen removal efficiencies of HAB-CASS were further improved, reaching 73.3% ± 2.5%, 86.2% ± 3.8% and 93.5% ± 1.6% at HRT of 6 hr, respectively, which were much higher than those of AB-CASS（61.1% ± 4.7%,75.4% ± 5.0% and 82.1% ± 2.1%, respectively）. Moreover, larger TCV/TV（total cathode volume/total volume） for HAB led to higher current and ARG removal. The ARG removal efficiency and current at TCV/TV of 0.15 were 39.2% ± 3.7% and 28.30 ± 1.48 mA,respectively. They were significantly increased to 62.1% ± 2.0% and 34.55 ± 0.83 mA at TCV/TV of 0.25. These results show that HAB system could be used to effectively treat real wastewater.

Electrochemistry-stimulated environmental bioremediation:Development of applicable modular electrode and system scale-up

Bioelectrochemical systems(BESs)have been studied extensively during the past decades owing primarily to their versatility and potential in addressing the water-energy-resource nexus.In stark contrast to the significant advancements that have been made in developing innovative processes for pollution control and bioresource/bioenergy recovery,minimal progress has been achieved in demonstrating the feasibility of BESs in scaled-up applications.This lack of scaled-up demonstration could be ascribed to the absence of suitable electrode modules(EMs)engineered for large-scale application.In this study,we report a scalable composite-engineered EM(total volume of 1 m^(3)),fabricated using graphite-coated stainless steel and carbon felt,that allows integrating BESs into mainstream wastewater treatment technologies.The cost-effectiveness and easy scalability of this EM provides a viable and clear path to facilitate the transition between the success of the lab studies and applications of BESs to solve multiple pressing environmental issues at full-scale.

Ordered mesoporous carbon as an efficient heterogeneous catalyst to activate peroxydisulfate for degradation of sulfadiazine

Catalytic potential of carbon nanomaterials in peroxydisulfate(PDS)advanced oxidation systems for degradation of antibiotics remains poorly understood.This study revealed ordered mesoporous carbon(type CMK)acted as a superior catalyst for heterogeneous degradation of sulfadiazine(SDZ)in PDS sys-tem,with a first-order reaction kinetic constant(k)and total organic carbon(TOC)mineralization efficiency of 0.06 min^(–1) and 59.67%±3.4%within 60min,respectively.CMK catalyzed PDS system exhibited high degradation efficiencies of five other sulfonamides and three other types of antibiotics,verifying the broad-degradation capacity of antibiotics.Under neutral pH conditions,the optimal catalytic parameters were an initial SDZ concentration of 44.0mg/L,CMK dosage of 0.07g/L,and PDS dosage of 5.44mmol/L,respectively.X-ray photoelectron spectroscopy and Raman spectrum analysis confirmed that the defect structure at edge of CMK and oxygen-containing functional groups on surface of CMK were major active sites,contributing to the high catalytic activity.Free radical quenching analysis revealed that both SO_(4)•−and•OH were generated and participated in catalytic reaction.In addition,direct electron transfer by CMK to activate PDS also occurred,further promoting catalytic performance.Configuration of SDZ molecule was optimized using density functional theory,and the possible reaction sites in SDZ molecule were calculated using Fukui function.Combining ultra-high-performance liquid chromatography(UPLC)–mass spectrometry(MS)/MS analysis,three potential degradation pathways were proposed,including the direct removal of SO_(2)molecules,the 14S-17N fracture,and the 19C-20N and 19C-27N cleavage of the SDZ molecule.The study demonstrated that ordered mesoporous carbon could work as a feasible catalytic material for PDS advanced oxidation during removal of antibiotics from wastewater.

A tartrate-EDTA-Fe complex mediates electron transfer and enhances ammonia recovery in a bioelectrochemical-stripping system

Traditional bioelectrochemical systems(BESs)coupled with stripping units for ammonia recovery suffer from an insufficient supply of electron acceptors due to the low solubility of oxygen.In this study,we proposed a novel strategy to efficiently transport the oxidizing equivalent provided at the stripping unit to the cathode by introducing a highly soluble electron mediator(EM)into the catholyte.To validate this strategy,we developed a new kind of iron complex system(tartrate-EDTA-Fe)as the EM.EDTA-Fe contributed to the redox property with a midpoint potential of
0.075 V(vs.standard hydrogen electrode,SHE)at pH 10,whereas tartrate acted as a stabilizer to avoid iron precipitation under alkaline conditions.At a ratio of the catholyte recirculation rate to the anolyte flow rate(RC-A)of 12,the NH4 t-N recovery rate in the system with 50mM tartrate-EDTA-Fe complex reached 6.9±0.2 g Nm^(-2) d^(-1),approximately 3.8 times higher than that in the non-EM control.With the help of the complex,our system showed an NH4 t-N recovery performance comparable to that previously reported but with an extremely low RC-A(0.5 vs.288).The strategy proposed here may guide the future of ammonia recovery BES scale-up because the introduction of an EM allows aeration to be performed only at the stripping unit instead of at every cathode,which is beneficial for the system design due to its simplicity and reliability.