Enhancing the adsorption function of biochar by mechanochemical graphitization for organic pollutant removal

• Mechanochemical treatment reduced the calcination temperature for biochar synthesis. • Biochar is converted to graphite after mechanochemical treatment. • Biochar was reduced to nanoscale after mechanochemical treatment. Biochar (BC) has been extensively studied as adsorbent for the treatment of water pollution. Despite the distinct advantages, the high calcination temperature and low adsorption capacity of pristine BC limit its practical applications. Most of the former studies focused on the structure and/or surface modification to improve the adsorption capacity of BC. However, the harsh experiment conditions involved in the biochar modification limited the application in industrial level. Herein, we introduced mechanical treatment into BC preparation to reduce the calcination temperature and improve the adsorption capacity simultaneously. The results indicated that the calcination temperature was reduced and the adsorption capacity of the treated BC was improved after mechanochemical treatment. Characterization of the samples disclosed that BCs were graphitized with the particle size reduced to nanoscale after treatment. Adsorption tests indicated that the mechanochemically treated BCs showed much better removal performance of organic contaminants than that of pristine BCs. For instance, among four pristine BCs (BC600, BC700, BC800, and BC900), only BC900 has strong adsorption capacity for MB, while BC600 has low adsorption capacity (1.2 mg/g). By comparison, the adsorption capacity of MB increased greatly to 173.96 mg/g by BC600-500/1 (treated at 500 r/min for 1 hour). To optimize the mechanochemical treatment, the effects of rotation speed and agitation duration were also investigated.     

不同培养条件下锰过氧化物酶(MnP)的合成及其对甲基橙的降解

高效、大规模、低成本合成木质素降解酶是直接采用其降解难降解有机污染物所必须解决的问题.对锰过氧化物酶(MnP)降解甲基橙和在非灭菌的反应器中连续合成MnP的可行性进行考察.结果表明,在采用2 mmol H2O2和1.5 mmol MnSO4的降解体系中,获最大脱色效果,且100、200和300 U/L的MnP可在8h内将甲基橙分别脱色18％、23％和35％;在非灭菌的反应器水平上实现了固定化培养的P.chrysosporium连续23 d合成MnP,但MnP酶活仅为2～ 23 U/L,难以酶解甲基橙;然而,在摇瓶培养条件下固定化的P.chrysosporium合成的MnP却能达1 152 U/L.因此,直接采用MnP对污染物进行降解以及在非灭菌的反应器中持续合成MnP是可行的,但就在非灭菌条件下如何提高MnP的合成量还有待开展深入的研究.     

重点流域水系沉积物中多环芳烃标准样品制备

环境标准样品是监测过程中重要的质量控制手段,中国受天然基体标准样品制备技术的制约,尚未拥有自己的沉积物中多环芳烃标准样品。为制备符合中国重点流域沉积物类型及多环芳烃浓度水平的沉积物标准样品,对中国6个重点流域的沉积物进行了采样,获得了制备多环芳烃标准样品的原料。分析常温及冷冻2种干燥方式对多环芳烃的影响,为制备大批量多环芳烃标准样品提供数据支持。对11个点位样品采用气相色谱质谱法测定16种优控多环芳烃化合物浓度,结果表明,样品均匀性良好,样品中多环芳烃检出率在99%以上,江河沉积物样品中多环芳烃浓度区间为664~2.91×103μg/kg,湖泊样品最高值达到1.25×105μg/kg,其主要污染源是化学燃料的燃烧。为中国制备水系沉积物中多环芳烃标准样品积累了技术基础。     

气相色谱-质谱法测定大气中98种挥发性有机物

通过色谱-质谱联用法(简称GC-MS),利用低温冷阱技术对大气中的VOCs进行浓缩富集,然后经过加热解吸分别至毛细管色谱柱和FID检测器及MS检测器,对大气中98种挥发性有机化合物(VOCs)进行分离、定性、定量测定。方法检出限为0.008×10-9~0.100×10-9(V/V);线性相关系数的平方值为0.992 7~1,相对标准偏差为4.0%~20.2%,总体标准偏差为0.154 2~0.952 1。     

常州市春节期间污染物相关性分析

分析了常州市2017年春节前后各污染物浓度的关联性和差异性。结果表明,除O_3外,春节期间各污染物均值均低于春节前后,春节前后随着污染源的变化,污染物之间的相关性表现出较为明显的差异。SO_2与PM_(2.5)、PM_(10)、CO和NO_2的相关性均较春节前后有显著下降;爆竹集中燃放时间段,CO与综合指数、PM_(2.5)和PM_(10)之间的相关系数0.96;而在烟花爆竹燃放相对较少的初三和初四,该相关系数0.6。工业减产停产和机动车使用减少对空气质量改善有较大贡献,而在不利气象条件下,烟花爆竹可导致空气质量在短时间内恶化。     

天津市地表水体与沉积物中7种高关注酚类化合物的污染特征与生态风险分析

为探究地表水体与沉积物中酚类化合物的污染分布特征和生态风险,选择天津市3个水源地与6条主要河流,采集了26个地表水样与6个沉积物样品,利用固相萃取与超声萃取、高效液相色谱-串联质谱法(HPLC-MS/MS)测定了水样及沉积物中1-萘酚(1-naphthol)、壬基酚(nonylphenol, NP)、双酚A(bisphenol A, BPA)、2-苯基苯酚(biphenyl-2-ol)、3,4-二氯酚(3,4-dichlorophenol)、四溴双酚A(tetrabromobisphenol A, TBBPA)和对叔丁基苯酚(p-tert-butylphenol, PTBP)等7种高关注酚类化合物的浓度水平,并应用物种敏感性分布(species sensitivity distribution, SSD)法和熵值法(ecological risk quotient, RQ)评估7种酚类化合物水环境和沉积物的生态风险。结果表明,地表水样中7种酚类化合物均全部检出;其中壬基酚的检出浓度最高,其次为四溴双酚A、对叔丁基苯酚、1-萘酚、2-苯基苯酚、3,4-二氯酚和双酚A。沉积物中酚类化合物的污染分布规律与水样相似,除双酚A外的目标物全部检出。其中,壬基酚浓度比其他物质浓度高2个数量级。风险评估结果显示,壬基酚对水环境与沉积物存在不可接受的风险;而四溴双酚A、对叔丁基苯酚、1-萘酚、2-苯基苯酚、3,4-二氯酚和双酚A则对环境具有较低风险或者存在一定的风险。     

Determination of the residue dynamics and dietary risk of thiamethoxam and its metabolite clothianidin in citrus and soil by LC-MS/MS

A modified quick, easy, cheap, effective, rugged and safe (QuEChERS) method was developed for the determination of thiamethoxam and its metabolite clothianidin in citrus (including the whole citrus, peel and pulp) and soil samples by liquid chromatography-tandem mass spectrometry. The sample was extracted with acetonitrile and purified with octadecylsilane. The detection limits of both compounds were 0.0001–0.0002?mg kg^–1, while the limit of quantification of thiamethoxam was 0.002?mg kg^–1 and the limit of quantitation of metabolites was 0.001?mg kg^–1. The recovery was 70.37%–109.76%, with inter-day relative standard deviations (RSD) (n?=?15) values ≤9.46% for the two compounds in the four matrices. The degradation curve of thiamethoxam in whole citrus and soil was plotted using the first-order kinetic model. The half-life of the whole citrus was 1.9–6.2?days, and the half-life of the soil was 3.9–4.2?days. The terminal residue of thiamethoxam (the sum of thiamethoxam and clothianidin, expressed as thiamethoxam) was found to be concentrated on the peel. The final residual amount of thiamethoxam in the edible portion (pulp) was less than 0.061?mg kg^–1. The risk quotient values were all below 1, indicating that thiamethoxam as a citrus insecticide does not pose a health risk to humans at the recommended dosage.     

隧道救援站通风网络优化设计及人员疏散研究*

为确定铁路隧道救援站最佳通风结构，对烟道布置提出合理建议，采用计算流体力学（CFD）的方法，对铁路隧道救援站通风网络进行优化设计。同时，采用模拟计算的方法对救援站人员疏散进行模拟分析，确定救援横通道布置及防护门开度设置的合理性。研究结果表明:在同等通风参数工况设置下，采用多节点排烟竖井结构后各救援横通道流量分配更均匀，救援站压力平衡性更好，通风效率可提升15%；通过疏散模拟证实，在长560 m的紧急救援站范围内设置10条疏散横通道，横通道设1.7 m宽的逃生门能够满足疏散要求。     

单芯铜线过电流故障电弧熔痕的微观特征研究*

为准确认定电气火灾中过电流故障，模拟4~7倍额定电流（Ie）条件下单芯铜导线过电流故障，利用光学显微镜和扫描电子显微镜（SEM）分析过电流故障电弧熔痕的组织特征，并结合Image-Pro Plus软件测定晶粒直径、周长和面积，探究金相组织的量化判据和变化规律。结果表明:当I＝4Ie时，过电流故障电弧熔痕的金相组织主要为方向性较强的树枝晶；当I＝5Ie，6Ie时，金相组织内树枝晶占比减小，胞状晶占比升高；当I＝7Ie时，方向性较弱的胞状晶占主导。随着电流增加，晶粒的平均直径、周长和面积均呈增长趋势。通过火灾案例分析可知，实验结果与现场的电弧熔痕组织特征基本相符，验证火灾事故原因为过电流故障。     

电厂屏式过热器弯头开裂原因失效分析

通过外观检查、硬度、金相等检测方法,从金属管壁超温运行、蒸汽侧氧化行为、析出相及冷弯变形对组织性能影响等方面分析了某电厂1 000 MW超超临界机组屏式过热器弯头开裂原因,得出TP347HFG弯头开裂的主要原因是弯头组织富含较多的σ相、NbC等硬脆析出相,同时冷弯加工导致管子内部产生残余应力,加剧了弯头脆性开裂的倾向。