Eco-friendly synthesis of silver nanoparticles using green algae (<Emphasis Type="Italic">Caulerpa serrulata</Emphasis>): reaction optimization,catalytic and antibacterial activities

Stable colloidal silver nanoparticles (AgNPs) were synthesized using Caulerpa serrulata (green marine algae) aqueous extract as an efficient reducing and stabilizing agent. This method is considered to be a sustainable alternate to the more complicated chemical procedures. To achieve the optimization synthesis of AgNPs, several effects such as extract concentration, contact time, pH values, and temperature were examined. The synthesized AgNPs were characterized by UV–Vis spectroscopy, FT-IR, XRD, and HR-TEM. The synthesized AgNPs showed an intense surface plasmon resonance band at 412 nm at the optimal conditions (20% (v/v) extract and 95 °C). TEM reveal that higher extract concentration and higher temperature leading to the formation of spherical AgNPs with an average particle size of 10 ± 2 nm. The synthesized AgNPs showed excellent catalytic reduction activity of Congo red (CR) dye from aqueous solutions. The degradation percentage of CR with AgNPs accelerated by increasing either NaBH₄ concentration or catalytic dosage. The AgNPs synthesized at higher temperature (e.g., 10Ag-95) exhibited the highest catalytic activity. The reaction kinetics was found to be pseudo first order with respect to the dye concentration. Moreover, the AgNPs displayed antibacterial activity at lower concentration against Staphylococcus aureus, Pseudomonas aeruginosa, Shigella sp., Salmonella typhi, and Escherichia coli and may be a good alternative therapeutic approach. The outcomes of the current study confirmed that the synthesized AgNPs had an awesome guarantee for application in catalysis and wastewater treatment.     

Impact of agglomeration and different dispersions of titanium dioxide nanoparticles on the human related in vitro cytotoxicity and genotoxicity

The published results on nanoparticles cytotoxicity and genotoxicity such as titanium dioxide nanoparticles (TiO(2) NPs) are inconsistent, and often conflicting and insufficient. Since different parameters may have impact on the toxicity results, there is need to lay stress on detailed characterization of NPs and the use of different testing conditions for assessment of NPs toxicity. In order to investigate whether dispersion procedures influence NP cytotoxicity and genotoxicity, we compared two protocols giving TiO(2) NP dispersions with different stability and agglomeration states. Detailed primary and secondary characteristics of both TiO(2) NP dispersions in culture media were carried out before toxicological testing; TK6 human lymphoblast cells, EUE human embryonic epithelial cells and Cos-1 monkey kidney fibroblasts were used to assess cytotoxicity (by trypan blue exclusion, proliferation activity and plating efficiency assays) and genotoxicity (by the comet assay). DNA strand breaks were detected by the alkaline comet assay. DNA oxidation lesions (especially 8-oxo-7,8-dihydroguanine, 8-oxoG) were measured with a modified comet assay including incubation with specific repair enzyme formamidopyrimidine DNA glycosylase (FPG). The TiO(2) NPs dispersion with large agglomerates (3 min sonication and no serum in stock solution) induced DNA damage in all three cell lines, while the TiO(2) NPs dispersed with agglomerates less than 200 nm (foetal serum in stock solution and sonication 15 min) had no effect on genotoxicity. An increased level of DNA oxidation lesions detected in Cos-1 and TK6 cells indicates that the leading mechanism by which TiO(2) NPs trigger genotoxicity is most likely oxidative stress. Our results show that the dispersion method used can influence the results of toxicity studies. Therefore at least two different dispersion procedures should be incorporated into assessment of cyto- and genotoxic effects of NPs. It is important, when assessing the hazard associated with NPs, to establish standard testing procedures and thorough strategies to consider the diverse conditions relevant to possible exposures.     

纳氏试剂法检测水中低浓度氨氮存在问题分析及方法改进探讨

针对采用《水质氨氮的测定纳氏试剂分光光度法》(HJ 535-2009)测定低浓度氨氮时存在的测不准问题,研究了药剂投加量、反应时间等因素对检测结果的影响,认为低浓度氨氮下的显色反应速度过慢是测定结果不准的原因,并据此提出利用强碱调节pH的方法加速反应进程.改良后的方法可以在0.2～1.2 mg/L氨氮浓度范围内呈现良好...     

Iodide-assisted total lead measurement and determination of different lead fractions in drinking water samples

Lead and its compounds are toxic and can harm human health, especially the intelligence development in children. Accurate measurement of total lead present in drinking water is crucial in determining the extent of lead contamination and human exposure due to drinking water consumption. The USEPA method for total lead measurement (no. 200.8) is often used to analyze lead levels in drinking water. However, in the presence of high concentration of the tetravalent lead corrosion product PbO(2), the USEPA method was not able to fully recover particulate lead due to incomplete dissolution of PbO(2) particles during strong acid digestion. In this study, a new procedure that integrates membrane separation, iodometric PbO(2) measurement, strong acid digestion and ICP-MS measurement was proposed and evaluated for accurate total lead measurement and quantification of different lead fractions including soluble Pb(2+), particulate Pb(II) carbonate and PbO(2) in drinking water samples. The proposed procedure was evaluated using drinking water reconstituted with spiked Pb(2+), spiked particulate Pb(II) carbonate and in situ formed or spiked PbO(2). Recovery tests showed that the proposed procedure and the USEPA method can achieve 93-112% and 86-103% recoveries respectively for samples containing low PbO(2) concentrations (0.018-0.076 mg Pb per L). For samples containing higher concentrations of PbO(2) (0.089-1.316 mg Pb per L), the USEPA method failed to meet the recovery requirement for total lead (85-115%) while the proposed method can achieve satisfactory recoveries (91-111%) and differentiate the soluble Pb(2+), particulate Pb(II) carbonate and PbO(2).     

Observations of urban airborne particle number concentrations during rush-hour conditions: analysis of the number based size distributions and modal parameters

A summertime study of the number concentration and the size distribution of combustion derived nanometre sized particles (termed nanoparticles) from diesel and spark-ignition (SI) engine emissions were made under rush-hour and free-flow traffic conditions at an urban roadside location in Leeds, UK in July 2003. The measured total particle number concentrations (N(TOTAL)) were of the order 1.8 x 10(4) to 3.4 x 10(4) cm(-3), and tended to follow the diurnal traffic flow patterns. The N(TOTAL) was dominated by particles < or =100 nm in diameter which accounted for between 89-93% of the measured particle number. By use of a log-normal fitting procedure, the modal parameters of the number based particle size distribution of urban airborne particulates were derived from the roadside measurements. Four component modes were identified. Two nucleation modes were found, with a smaller, more minor, mode composed principally of sub-11 nm particles, believed to be derived from particles formed from the nucleation of gaseous species in the atmosphere. A second mode, much larger in terms of number, was composed of particles within the size range of 10-20 nm. This second mode was believed to be principally derived from the condensation of the unburned fuel and lube oil (the solvent organic fraction or SOF) as it cooled on leaving the engine exhaust. Third and fourth modes were noted within the size ranges of 28-65 nm and 100-160 nm, respectively. The third mode was believed to be representative of internally mixed Aitken mode particles composed of a soot/ash core with an adsorbed layer of readily volatilisable material. The fourth mode was believed to be composed of chemically aged, secondary particles. The larger nucleation and Aitken modes accounted for between 80-90% of the measured N(TOTAL), and the particles in these modes were believed to be derived from SI and diesel engine emissions. The overall size distribution, particularly in modes II-IV, was observed to be strongly related to the number of primary particle emissions, with larger count median diameters observed under conditions where low numbers of primary soot based particles were present.     

Evaluation of Numerical Modeling Methods for the Management of Produced Water Discharges in the Coastal Region with a Canadian Case Study

This study aims at evaluating two numerical methods for 3D simulation of marine pollutant dispersion problems: the random walk particle tracking (RWPT) method and an explicit second-order finite difference method (FDM) for assessing produced water discharges from offshore oil platform. Test cases in a steady flow field were used to evaluate the efficiency and accuracy of simulating pollutant concentration profiles obtained using both the FDM and RWPT method in comparison with an analytical solution. Additionally, a field study was conducted to simulate the lead concentration distribution of produced water discharged from an oil platform off Canada’s east coast, based on the Princeton Ocean Model modeling the ocean flow in the study area with field verifications. Results indicate that, with proper configuration of grid resolution and particle resolution, both FDM and RWPT method can provide accurate results with reasonable computational costs for complex field cases. Particularly, the satisfactory 3D simulations of marine pollutant dispersion in the far field by both FDM and RWPT numerical methods enable effective assessment and management of offshore waste discharges.     

Facile and Sensitive Spectrophotometric Determination of Synthetic Pyrithroids in Their Formulations, Water and Grain Samples

A novel reagent was introduced for the facile and sensitive spectrophotometric determination of syntheitic pyrethroids in their formulations (fenvalerate, cypermethrin and decamethrin), water and grain samples. These methods were based on the hydrolysis of synthetic pyrethroids under the alkaline conditions to form respective aldehyde groups. These groups were condensation with 3-methyl-2-benzothiazolinone hydrochloride (MBTH) to yield color derivatives having λ_max at 520 nm for fenvalerate, 516 nm for cypermethrin and 512 nm for decamethrin. The proposed method could be successfully applied for the determination of synthetic pyrethroids in their formulations, water and grain samples.     

Highlighting the implications of selenium dispersion from disposal of Kahota Industrial Triangle area, Islamabad, Pakistan using three-dimension solute transport model

This study highlights the implications of selenium (Se) dispersion in groundwater flow regimes of Kahota Industrial Triangle area located adjacent to the Soan River, Islamabad. Initially, a regional groundwater 3-D flow model has been developed, calibrated to the known observed heads of 24 water wells, verified, and confirmed that convergence has actually arrived to satisfy the steady state condition. Later, the transient simulation was carried out adding in the known recharge, storage factor, porosity, and observed drawdown matched with the simulated drawdown that appears to fall in close agreement with a difference of 0.25 m. As such the steady state groundwater model has facilitated to understand the mechanism of groundwater flow regimes in reference to the implications of selenium dispersion from disposal of Kahota Industrial Triangle area. Thirty-five water samples were collected mainly from the industrial water wells for the evaluation of heavy metals. Selenium being the major contributor of pollution has been short listed to monitor its dispersion using a solute transport model modular three-dimensional transport model (MT3D). Chemical parameters related to selenium characteristics including horizontal and vertical transverse dispersivity/longitudinal dispersivity, effective molecular diffusion coefficient and bulk density of the porous medium of aquifers have been used in MT3D contaminant transport model. MT3D is run for 30 years in steady state condition. As usual first run did not produce the exact field conditions. Therefore, the contaminant transport model is calibrated against the 32 values of observed selenium concentrations in boreholes by minor adjustments in the chemical parameter values. The final calibration has been achieved with residual value of 3.88 × 10^???5 Kg/m³. Seven hypothetical observation wells are used to monitor the selenium concentrations over a long-term period of time.     

Soil Gas Volatile Organic Compound Concentration Contours for Locating Vadose Zone Nonaqueous Phase Liquid Contamination

Diffusion of VOC from cylindrical vadose zone domains contaminatedwith distributed nonaqueous phase liquid is examined in the steadystate approximation. The effects of first-order biodegradation and ofan extended underlying pool of LNAPL floating on the water table belowthe cylindrical domain are explored by means of an orthogonal functionsapproach. The distribution of VOC in the vadose zone above a floatingcircular LNAPL pool of finite size is explored by a numerical method.The results provide information useful in estimating the spacing anddepth at which soil gas samples should be taken in order to detect thepresence of such source areas. Comparison of model results with soilgas VOC measurements at various depths also provides insight into theextent to which natural biodegradation of the VOCs is taking place.     

Estimation of suspended sediment concentration in rivers using acoustic methods

Acoustic Doppler current meters (ADV, ADCP, and ADP) are widely used in water systems to measure flow velocities and velocity profiles. Although these meters are designed for flow velocity measurements, they can also provide information defining the quantity of particulate matter in the water, after appropriate calibration. When an acoustic instrument is calibrated for a water system, no additional sensor is needed to measure suspended sediment concentration (SSC). This provides the simultaneous measurements of velocity and concentration required for most sediment transport studies. The performance of acoustic Doppler current meters for measuring SSC was investigated in different studies where signal-to-noise ratio (SNR) and suspended sediment concentration were related using different formulations. However, these studies were each limited to a single study site where neither the effect of particle size nor the effect of temperature was investigated. In this study, different parameters that affect the performance of an ADV for the prediction of SSC are investigated. In order to investigate the reliability of an ADV for SSC measurements in different environments, flow and SSC measurements were made in different streams located in the Aegean region of Turkey having different soil types. Soil samples were collected from all measuring stations and particle size analysis was conducted by mechanical means. Multivariate analysis was utilized to investigate the effect of soil type and water temperature on the measurements. Statistical analysis indicates that SNR readings ob tained from the ADV are affected by water temperature and particle size distribution of the soil, as expected, and a prediction model is presented relating SNR readings to SSC mea surements where both water temperature and sediment characteristics type are incorporated into the model. The coefficients of the suggested model were obtained using the multivariate anal ysis. Effect of high turbidity conditions on ADV performance was also investigated during and after rain events.     

化学需氧量和总有机碳在水质在线监测中的比较

化学需氧量（COD）和总有机碳（TOC）是定量表示水体受有机物污染的2个重要代表性指标。传统的COD在线监测方法在监测有机污染物方面存在一定的挑战,系统比较了COD和TOC在线监测方法在特殊水质中的应用。结果显示：TOC对难氧化有机物的氧化效率高达98%,高氯离子和无机还原性离子对TOC测量误差影响分别约为10%和7%。TOC可更直接、更准确地反映出水体受有机物污染的情况,最后对TOC指标在水质在线监测中的推广应用提出建议。     

微纳米气泡改善太湖入湖河道水质的工程实例研究——苏州南北华翔河水质改善工程为例

太湖入湖河道,在各级政府及部门的努力工作下,经过点源治理、截污、清淤、生态修复等综合手段治理,水质逐年好转,但还存在很大的提升空间,本研究采用微纳米气泡气液分散系统,对人湖河道水体进行原位净化处理,结果表明,CODMn、氨氮、总磷的平均去除率分别为36．8％、42．4％,49．1％。入湖水质达到国家地表水Ⅱ-Ⅲ类标准。     

Comparison of three sampling and analytical methods for the determination of airborne hexavalent chromium

A field study was conducted with the goal of comparing the performance of three recently developed or modified sampling and analytical methods for the determination of airborne hexavalent chromium (Cr(VI)). The study was carried out in a hard chrome electroplating facility and in a jet engine manufacturing facility where airborne Cr(VI) was expected to be present. The analytical methods evaluated included two laboratory-based procedures (OSHA Method ID-215 and NIOSH Method 7605) and a field-portable method (NIOSH Method 7703). These three methods employ an identical sampling methodology: collection of Cr(VI)-containing aerosol on a polyvinyl chloride (PVC) filter housed in a sampling cassette, which is connected to a personal sampling pump calibrated at an appropriate flow rate. The basis of the analytical methods for all three methods involves extraction of the PVC filter in alkaline buffer solution, chemical isolation of the Cr(VI) ion, complexation of the Cr(VI) ion with 1,5-diphenylcarbazide, and spectrometric measurement of the violet chromium diphenylcarbazone complex at 540 nm. However, there are notable specific differences within the sample preparation procedures used in three methods. To assess the comparability of the three measurement protocols, a total of 20 side-by-side air samples were collected, equally divided between a chromic acid electroplating operation and a spray paint operation where water soluble forms of Cr(VI) were used. A range of Cr(VI) concentrations from 0.6 to 960 microg m(-3), with Cr(VI) mass loadings ranging from 0.4 to 32 microg, was measured at the two operations. The equivalence of the means of the log-transformed Cr(VI) concentrations obtained from the different analytical methods was compared. Based on analysis of variance (ANOVA) results, no statistically significant differences were observed between mean values measured using each of the three methods. Small but statistically significant differences were observed between results obtained from performance evaluation samples for the NIOSH field method and the OSHA laboratory method.     

The creation of an historical meteorological database for environmental dose assessment

The focus of this study is to develop wind data for the SavannahRiver Site (SRS) between 1955 and 1961 to be used in an assessment of estimates of atmospheric dispersion and downwindrisk at the Savannah River Site. In particular, a study of theuncertainties of radioiodine dosimetry from the late 1950sprovides the underlying motivation for developing historicalwindroses at the Savannah River Site (SRS). Wind measurement towers did not exist at the SRS until theearly 1970s. Three relatively simple methods were used to createa 1955–1961 meteorological database for the SRS for a dosereconstruction project. The winds were estimated from onsitemeasurements in the 1990s and National Weather Service (NWS)observations in the 1990s and 1950s using (1) a linear regressionmethod, (2) a similarity theory approach, and (3) a simplestatistical differences method. The criteria for determining success were based on (1) howwell the mean values and standard deviations of the predictedwind speed agree with the known SRS values from the 1990s, (2) the shape of the predicted frequency distribution functions forwind speed, and (3) how closely the predicted windroses resembledthe SRS windrose for the 1990s. The linear regression model's wind speed distribution functionwas broad, flat, and skewed too much toward higher wind speeds.The similarity theory approach produced a wind speed distributionfunction that contained excess predicted speeds in the range 0–1.54 m s^-1 (0–3 kts) and had `excluded' bins caused bypredictions being made from integer values of knots in the NWSdata. The distribution function from the mean difference methodwas smooth with a shape like a Weibull distribution with a shapeparameter of 2 and appearedto resemble closely the SRS 1992–1996 distribution.The wind directions for all three methods of approach weresuccessfully based on the mean difference method. It wasdifficult to discern differences among the wind roses produced bythe three methods so the wind speed distribution functions needto be examined in order to make an informed choice for dose reconstruction.     

影响地表水高锰酸盐指数自动监测数据准确性的因素

地表水高锰酸盐指数自动监测仪器在实际应用中存在质控样测试和实际水样比对测试合格率相对偏低的问题。通过对高锰酸盐指数氧化还原机理的分析,结合目前国控水站对质控样品的测试数据,探讨了如何使用高锰酸盐指数自动监测仪分析测试得到准确可靠的水质监测数据。认为应尽量保持自动分析仪器的反应条件、稀释条件与标准方法一致,即取样量与试剂用量比与标准方法一致,并根据样品浓度变化实现量程自动切换,分量程进行仪器校准和测量,才能够提高自动分析仪器测量的准确性。     

Assessing water quality of drinking water distribution system in the South Taiwan

This investigation conducted a full-scale survey the drinking water distribution system in Kaohsiung city, Taiwan. The aim was to investigate whether the distribution system was capable of maintaining high water quality from the water treatment facilities through to the end user. The results showed that the distribution system can maintain high water quality, except for suitable chlorine residuals. The authors plotted chlorine residual contour maps to identify areas with low chlorine residuals, helping them prioritize sections that must be flushed or renewal. The contour maps also provide sufficient and clear information for locating booster chlorination stations. Contour maps enable water facilities to identify how water quality decays in the distribution systems and the locations of such decay. Water quality decay can be caused by properties of pipeline materials, hydraulic conditions, and/or biofilm thickness. However, understanding the exact reasons is unnecessary because the contour maps provide sufficient information for trouble-shooting the distribution systems.     

比色法测定水中微量三氯杀螨醇

使用比色法测定水中微量三氯杀螨醇的浓度。首先用正己烷萃取浓缩水中的三氯杀螨醇,比较了加入不同量的去离子水,不同浓度、不同量的NaOH,不同的反应显色温度和反应时间以及吡啶用量等对体系吸光度的影响。得出最佳的显色条件:0.2ml去离子水,0.1ml质量浓度为45%的NaOH溶液,与2.0ml吡啶混合,于100℃水浴中反应3.0min,反应液在4000r/min离心2.0min,取出反应液在530nm处测定吸光度值。此方法的标准工作曲线相关系数为0.9914,方法的绝对检出限为0.2μg三氯杀螨醇。样品加标回收率为83.7%~114.1%,相对标准偏差小于10%。     

Verification of a depth-integrated sample arm as a means to reduce solids stratification bias in urban stormwater sampling

A new water sample collection system was developed to improve representation of solids entrained in urban stormwater by integrating water-quality samples from the entire water column, rather than a single, fixed point. The depth-integrated sample arm (DISA) was better able to characterize suspended-sediment concentration and particle size distribution compared to fixed-point methods when tested in a controlled laboratory environment. Median suspended-sediment concentrations overestimated the actual concentration by 49 and 7% when sampling the water column at 3- and 4-points spaced vertically throughout the water column, respectively. Comparatively, sampling only at the bottom of the pipe, the fixed-point overestimated the actual concentration by 96%. The fixed-point sampler also showed a coarser particle size distribution compared to the DISA which was better able to reproduce the average distribution of particles in the water column over a range of hydraulic conditions. These results emphasize the need for a water sample collection system that integrates the entire water column, rather than a single, fixed point to properly characterize the concentration and distribution of particles entrained in stormwater pipe flow.     

Impact of Channelization on Oyster Production: A Hydrodynamic-Oyster Population Model for Galveston Bay, Texas

A hydrodynamic-oyster population dynamics model was developed to assess the effect of a change in ship channel configuration under different freshwater inflow regimes and different future hydrologies on oyster (Crassostrea virginica) populations in Galveston Bay, Texas. The population dynamics model includes the effects of environmental conditions, predators, and the oyster parasite Perkinsus marinus on oyster populations. The hydrodynamic model includes the effects of wind stress, river runoff, tides, and oceanic exchange on the circulation of the Bay. Simulations were run for low, mean, and high freshwater inflow conditions under the present (1993) hydrology and predicted hydrologies for 2024 and 2049 that include anticipated water diversion projects to satisfy the freshwater demands of population growth in metropolitan Houston, Texas. Simulation results show that oyster biomass was predicted to increase after enlargement of the ship channel. Oyster biomass is expected to increase on about 53% of total reef acreage when averaged over a 50-yr time span. Oyster reef acreage characterized by increased biomass after channel enlargement increases moderately under the present hydrology and the 2049 hydrology, but decreases slightly in 2024. Lower biomass in 2024 is due to reduced freshwater inflow and increased saltwater intrusion that pushes the optimal areas for oyster growth somewhat farther upbay than in 2049. Declines in oyster biomass, noted in most simulations in downbay reaches, were more than balanced by increased oyster biomass upbay. The differential between upbay and downbay reefs can be explained by an increase in mortality from Perkinsus marinus downbay and saltwater intrusion upbay that expands the area characterized by moderate salinities. The 20th century history of Galveston Bay is one of expansion of isohaline structure and increased oyster production as a result of anthropogenic modification of bay physiography. The salinity gradient of the 1990s, however, is not in equilibrium with the distribution of hard substrate required for oyster growth, that reflects an earlier equilibrium with the pre-1900s hydrodynamics. Increased saltwater intrusion is normally disadvantageous to oyster populations; but, in this case, channel enlargement further expands the salinity gradient upbay and outward (east and west) from the channel. As a result, in most years, oyster biomass is increased because moderate salinities cover more of the pre-1900s reef tracts where hard substrate is plentiful.     

Evaluation of the diffusion size classifier (meDiSC) for the real-time measurement of particle size and number concentration of nanoaerosols in the range 20-700 nm

In the frame of assessing exposure to nanostructured particles, the aim of this work is to study the performance of a new device devoted to the real-time measurement of nanostructured aerosol: the meDiSC (Diffusion Size Classifier, Matter Engineering, Switzerland). This instrument is based on unipolar diffusion charging of particles which are then collected successively in diffusion and filtration stages. From currents measured in these stages, the instrument is capable of determining aerosol mean size and number concentration. These data were compared to reference measurements regarding monodisperse aerosols in a range from 20 to 700 nm; the relative biases were found unsatisfying. This led us to investigate the principle of the instrument. Consequently, the charging law of the diffusion charger was experimentally established, as well as the calibration curve allowing the determination of the mean size of the particles. The latter analysis was completed by a model based on diffusion theory. Our results indicate the possibility to improve the range of size measurement up to 350 nm. Measured particle size and number concentration were also used to calculate geometric surface-area concentration; the experimental data were compared to a reference calculated surface-area concentration. The results demonstrate the possibility to evaluate this parameter within acceptable uncertainty. In a second step, the meDiSC was challenged with polydisperse aerosols. It was observed that meDiSC overestimates particle size by a factor 1.7, while particle number concentrations are found within ±40% of the reference. The model applied to polydisperse aerosols indicates that polydispersity little influences particle size up to 300 nm while geometric standard deviation remains below 1.7.