AbstractThe uptake and distribution of phenanthrene, a typical polycyclic aromatic hydrocarbon, in plant tissues of Aegiceras corniculatum and Avicennia marina and the relationship with nutrient (nitrate, ammonium, and soluble reactive phosphorus) availability were investigated. After 12?h of exposure, enhancements in the concentration of nitrate and soluble reactive phosphorus markedly decreased the residual level of phenanthrene in roots, while the addition of ammonium significantly increased the residual concentration. Due to the similar enzymatic degradation potential between treatment groups, the variation of phenanthrene concentration in mangrove roots may result from the H+/phenanthrene cotransport at the root surface that was influenced by nutrient uptake. Moreover, both nitrate and soluble reactive phosphorus amendments significantly increased translocation of phenanthrene from roots to leaves, which likely resulted from the change of hydraulic conductivity in mangrove plants triggered by different nutrient availability. 相似文献
Persulfate can efficiently decolorize azo dyes through oxidizing these compounds, which enabled us to develop a method of rapid spectrophotometric determination of persulfate for monitoring the wastewater treatment on the basis of the oxidation decolorization of azo dyes. Four azo dyes with different molecular structures were investigated as probes, and the influences of operation parameters including reaction time, solution pH, initial dye concentration, and initial concentration of activator Fe(2+) were checked on the determination of persulfate. Under optimum conditions, the decolorization degree of the dyes responded linearly with persulfate concentration for all the four azo dyes, and the linear range and detection limit were found to be 2.0-150 μmol L(-1) and 0.62 μmol L(-1) for rhodamine B, 2.0-100 μmol L(-1) and 0.42 μmol L(-1) for methylene blue, 4.0-150 μmol L(-1) and 0.50 μmol L(-1) for methyl violet, and 20-150 μmol L(-1) and 8.1 μmol L(-1) for orange II. A persulfate treatment of a spiked wastewater sample was satisfactorily monitored with the new method. 相似文献
Size distribution aerosol samples were collected at an urban location of Guangzhou in four seasons of 2003-2004 by a MOUDI (Micro-orifice Uniform Deposit Impactor). The particle loading (PM10: 80-397 microg m(-3)) was comparable with some other Asia cities; however, much higher than that of Western Europe and North America. Polycyclic aromatic hydrocarbons (PAHs) were measured by gas chromatography with mass selective detector (GC-MS). Seasonal effects on the size distribution of PAHs are presented. Bimode (accumulation and coarse mode) and unimode (accumulation mode) distributions were observed for low-molecule-weight and high-molecule-weight PAHs. A slight shift to larger particles was found for the accumulation mode in autumn and winter, compared with that of spring and summer. One explanation is that the longer aging process of PAHs in autumn and winter would result in volatilization from finer particles followed by condensation onto coarser particles. Another is there was mixing process of local emission with long-range transported aerosol in autumn and winter. The relative higher value of IcdP/(BghiP+IcdP) and lower value of BghiP/BeP in winter also give evidences to the mixing process. The level of PAHs concentration has been much elevated in recent years. This can be attributed to the fast growth of motor vehicle and energy consumption. 相似文献
In this work, biochar (BC), activated carbon (AC), and graphene oxide (GO) were thiol-functionalized using 3-mercaptopropyltrimethoxysilane (3-MPTS) (named as BCS, ACS, and GOS, respectively). BCS, ACS, and GOS were synthesized mainly via the interaction between hydrolyzed 3-MPTS and surface oxygen-containing functional groups (e.g., –OH, O–C=O, and C=O) and π-π interaction. The materials before and after modification were characterized and tested for mercury removal, including sorption kinetics and isotherms, the effects of adsorbent dosage, initial pH, and ionic strength. Pseudo-second-order sorption kinetic model (R2 = 0.992~1.000) and Langmuir sorption isotherm model (R2 = 0.964~0.998) fitted well with the sorption data of mercury. GOS had the most –SH groups with the largest adsorption capacity for Hg2+ and CH3Hg+ (449.6 and 127.5 mg/g), followed by ACS (235.7 and 86.7 mg/g) and BCS (175.6 and 30.3 mg/g), which were much larger than GO (96.7 and 4.9 mg/g), AC (81.1 and 24.6 mg/g), and BC (95.6 and 9.4 mg/g). GOS and ACS showed stable mercury adsorption properties at a wide pH range (2~9) and ionic strength (0.01~0.1 mol/L). Mercury maybe removed by ligand exchange, surface complexation, and electrostatic attraction.