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以棉花作为生物模板制备出具有棉花形貌的纳米羟基磷灰石(HAP),并将其运用于水体中三氯生的吸附去除研究。采用X射线粉末衍射仪、傅里叶红外、扫描电镜、透射电镜表征了吸附前后HAP的物相组成、官能团、形貌和颗粒尺寸变化。考察了初始pH、时间和温度对HAP吸附三氯生的影响。动力学数据符合准二级动力学模型,颗粒内扩散不是唯一的限速步骤;平衡吸附数据符合Langmuir等温吸附模型;热力学参数吉布斯自由能(ΔG0)、焓变(ΔH0)、熵变(ΔS0)值揭示三氯生吸附至HAP上是一个自发吸热的过程。对比其他吸附剂,HAP具有高吸附量且环境友好的优势。 相似文献
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以绢云母为载体,采用水解-沉淀法制备出了绢云母负载纳米TiO2粉体(TiO2/M),以尿素为氮源,采用后掺杂法制得具有可见光响应的N掺杂TiO2/M.采用XRD,XPS,SEM,DUV等手段对样品进行了性能表征;并以日光色镝灯为光源,甲基橙为模拟污染物检测其光催化活性.研究了N的掺杂对粉体中TiO2晶相结构,粒度和光催化性能的影响.结果表明,绢云母与TiO2通过桥氧相连形成包覆层,N的掺杂抑制了TiO2晶粒的长大,减缓锐钛矿向金红石相的转变,同时N的掺杂形成Ti—O—N键,形成新的能级结构,使样品对光的吸收边红移至440—550 nm,具有明显的可见光响应,对甲基橙的光催化降解率与没有掺N的样品相比,最高可达1.6倍. 相似文献
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模拟胃肠液用Tenax提取法测定多溴联苯醚的生物有效性 总被引:1,自引:0,他引:1
以室内灰尘和鱼样为介质,利用Tenax提取,采用动态方法模拟污染物在人体肠道中的消化吸收,研究多溴联苯醚(PBDEs)的口服生物有效性.结果表明,在18 mL模拟胃肠液中,随着胃肠液中Tenax质量增加,Tenax吸附的PBDEs(BDE28、47、66、100、99、85、154、153、138、183和209)增加,当Tenax的质量达到200 mg后,增加Tenax的用量不会增加PBDEs在Tenax中的吸附总量.对于灰尘,3—7溴BDEs的生物有效性为50.8%,而添加Tenax后,随着Tenax质量的增大,其修正后的生物有效性从84.9%增大到101.1%;类似,对于鱼样,PBDEs修正后的生物有效性从43.7%升高到70.7%.这种修正后的生物有效性比未进行修正的结果更接近活体实验测得的PBDEs的生物利用度数据.因此,在18 mL模拟胃肠液中,采用200 mg的Tenax,用于模拟小肠对胃肠液中PBDEs的吸收,可以获得最差场景条件下PBDEs的生物有效性. 相似文献
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本文基于固相萃取-气相色谱串联质谱,建立了家用搅拌机中21种邻苯二甲酸酯(PAEs)迁移量的测定方法.基于搅拌机在运行过程中与食品接触特性,参照相关迁移实验标准,采用0.8 L 10%乙醇水溶液和4%乙酸水溶液两种模拟液在搅拌机正常工作下迁移30 min,以Oasis-HLB玻璃固相萃取柱对迁移溶液中待测物进行萃取浓缩,气相色谱-串联质谱检测,外标法定量.方法对于不同物质的定量限(LOQ)在0.05—0.8μg·L~(-1)之间,具有较高的灵敏度.在10%乙醇和4%乙酸两种模拟液中,低、中、高3个添加水平的平均回收率分别在78.5%—115.3%和78.8%—116.8%之间,相对标准偏差(RSD)分别在3.6%—12.5%和3.9%—11.2%之间.邻苯二甲酸酯在9款搅拌机实际样品中具有不同程度检出,迁移量0.08—2.26μg·L~(-1).该方法准确、灵敏,适用于家用搅拌机中邻苯二甲酸酯的迁移量检测. 相似文献
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纳米二氧化钛(nTiO_2)作为一种具有独特物理化学性质的纳米材料被广泛应用。然而,在生产、使用的过程中,nTiO_2会不可避免地进入于水环境中。重金属是水体中常见的污染物之一,nTiO_2进入水体后是否会与水体中的重金属发生相互作用,进而影响重金属的生物积累,目前相关报道还很少。本论文以大型溞为模式生物,考察了5种不同晶型nTiO_2对常见的重金属铜生物积累影响。结果表明,nTiO_2对Cu2+的吸附降低了试验液中Cu2+浓度。但5种不同晶型nTiO_2的吸附能力并不一样,其中锐钛矿晶型(A-S)的吸附能力最高,这可能是由于结构缺陷和表面羟基的存在,为Cu2+提供了更多的结合位点,从而提高了A-S的吸附能力。nTiO_2的存在降低了金属铜在大型溞体内的积累,这可能是由于nTiO_2对金属铜的吸附,降低了自由Cu2+的生物可利用性。由于nTiO_2样品之间比表面积的差异,不同晶型之间单位nTiO_2引起的铜积累有显著性差异性(P0.05),其中锐钛矿和金红石之比为4:1混合晶型(M1)最高,A-S最低。 相似文献
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MoO3/TiO2催化剂对NH3选择性催化还原NOx的研究 总被引:2,自引:2,他引:0
通过共混法制备MoO3/TiO2催化剂,还原脱除NOx的研究.对于100目的催化剂,并在固定床反应器中进行了NH3选择性催化在较低温度下(≤583K),升高温度和降低空速,NOx脱除率提高;在反应温度较高时,NH3氧化的副反应的影响加强,此时过度延长反应时间和提高反应温度反而会使NOx脱除率降低.在583K和空速为12kh“时,NOx转化率可达92%.FT-IR光谱和XRD分析结果表明,MoO3形成分散相,均匀分布在TiO2颗粒表面并形成稳定的Mo=0基,它的加入没有影响TiO2(锐态矿型)的结构和形貌. 相似文献
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Yingchao Zhang Hongqiong Zhang Xinwei Dong Dongbei Yue Ling Zhou 《Frontiers of Environmental Science & Engineering》2022,16(8):99
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Mingsong WU Junli HUANG Yuling ZHANG Shijie YOU Shaofeng LI Zhilin RAN Yu TIAN 《Frontiers of Environmental Science & Engineering》2012,6(1):75-81
Microcystins, which represents one kind of cancerogenic organic compounds, is abundant in eutrophication water. The effects of reaction factors on chlorine dioxide (ClO2) for removal of low-concentration Microcystin-LR, Microcystin-RR, and Microcystin-YR in water as well as the reaction mechanisms was investigated by using enzyme-linked immunosorbent assay (ELISA) kit and gas chromatography–mass spectrometry (GC-MS). The results showed that MC-LR, MC-RR, and MC-YR could be efficiently decomposed by ClO2. The degradation efficiency was shown positively correlated to the concentration of ClO2 and reaction time; while the effect of reaction temperature and pH is slight. The kinetic constants and activation energies of the reaction of MC-LR, MC-RR, and MC-YR with ClO2 are determined as 459.89, 583.15, 488.43 L·(mol·min)-1 and 64.78, 53.01, 59.15 kJ·mol-1, respectively. As indicated by high performance liquid chromatography mass spectrometer (HPLC-MS) analysis, degradation should be accomplished via destruction of Adda group by oxidation, with the formation of dihydroxy substituendums as end products. This study has provided a fundamental demonstration of ClO2 serving as oxidizing disinfectant to eliminate microcystins from raw water source. 相似文献
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Xin Xing Yin Yu Hongbo Xi Guangqing Song Yajiao Wang Jiane Zuo Yuexi Zhou 《Frontiers of Environmental Science & Engineering》2018,12(6):12
Trimethylolpropane (TMP) wastewater is one of the most toxic petrochemical wastewater. Toxicants with high concentrations in TMP wastewater often inhibit the activity of microorganisms associated with biological treatment processes. The hydrolysis acidification process (HAP) is widely used to pretreat petrochemical wastewater. However, the effects of HAP on the reduction of wastewater toxicity and the relevant underlying mechanisms have rarely been reported. In this study, an HAP reactor was operated for 240 days, fed with actual TMP wastewater diluted by tap water in varying ratios. The toxicity of TMP wastewater was assessed with the inhibition ratio of oxygen uptake rate. When the organic loading rates were lower than 7.5 kg COD/m3/d, the toxicity of TMP wastewater was completely eliminated. When the actual TMP wastewater was directly fed into the reactor, the toxicity of TMP wastewater decreased from 100% to 34.9%. According to the results of gas chromatographymass spectrometry analysis, four main toxicants contained in TMP wastewater, namely, formaldehyde, 2-ethylacrolein, TMP and 2-ethylhexanol, were all significantly removed, with removal efficiencies of 93.42%, 95.42%, 72.85% and 98.94%, respectively. Compared with the removal efficiency of CODCr, the reduction rate of toxicity is markedly higher by HAP. In addition, the change of microbial community in the HAP reactor, along the operation period, was studied. The results revealed that, compared with the seed sludge, Firmicutes became the dominant phylum (abundance increased from 0.51% to 57.08%), followed by Proteobacteria and Bacteroidetes (abundance increased from 59.75% to 25.99% and from 4.70% to 8.39%, respectively).
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Christian Mougin Albert Kollmann Jacqueline Dubroca Paul Henri Ducrot Michel Alvinerie Pierre Galtier 《Environmental Chemistry Letters》2003,1(2):131-134
We investigated the fate of the drug ivermectin in the soil. We found that ivermectin was transformed solely by photos, leading to the formation of two ivermectin isomers. We indeed failed to detect any biotransformation reaction of the chemical either in the soil or in fungal liquid cultures. According to its limited water solubility, the bioavailability of ivermectin was very low in the soil solution. Here, we show that ivermectin, transferred to the soil from faeces of drug-treated cattle, could be stored for long periods in the soil. 相似文献
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Tongyao Ju Siyu Han Fanzhi Meng Li Lin Jinglin Li Kailun Chen Jianguo Jiang 《Frontiers of Environmental Science & Engineering》2023,17(9):112
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Gulnara M. Shaydullina Natalya A. Sinikova Albert T. Lebedev 《Environmental Chemistry Letters》2005,3(1):1-5
Ozone, chlorine and sodium hypochlorite are commonly used as disinfecting agents for drinking water production. The reaction pathways of ozonation and chlorination of o-methoxybenzoic acid in aqueous solution were studied using gas chromatography-mass spectrometry (GC-MS) and high pressure liquid chromatography (HPLC). The results show that less than 1% of o-methoxybenzoic acid remains in reaction. The final major products using ozone oxidation are oxalic and glyoxalic acids. Phenols appear only at insufficient ozone levels. Sodium hypochlorite leads to higher levels of primary products. Molecular chlorine leads to the formation of higher amounts of polychlorinated derivatives. Model experiments allow to propose schemes of o-methoxybenzoic acid transformation under the conditions simulating water treatment processes. 相似文献
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Yoshihisa Ohko Yuri Nakamura Nobuaki Negishi Sadao Matsuzawa Koji Takeuchi 《Environmental Chemistry Letters》2010,8(3):289-294
We have discovered that HNO3 and related species are released from the TiO2 surface into air in the TiO2 photocatalytic oxidation of NO2 (1 ppm) under continuous UV light illumination (1 mW cm−2) by dehumidifying the outlet gas of the reaction and analyzing the recovered condensate liquid by ion chromatography. The
origin of the HNO3 recovered in the dehumidifier could not be explained by a simple desorption of HNO3 overproduced on the TiO2 surface. The produced HNO3 must be activated on the TiO2 surface and causing the unidentified reaction. 相似文献