Monitoring the impact of dissolved oxygen and nitrite on anoxic biofilm in continuous denitrification process

An anoxic biofilm involved in continuous denitrificationprocess was monitored to investigate the effect of differentconcentrations of influent dissolved oxygen (DO) or nitrite onthe biofilm. Microelectrode measurements evidenced nitrateremoval activity of biofilm. When different concentrations ofDO were applied to the reactor, generally decreasedconcentrations of DO were observed as bed depth increased fromthe bottom of the reactor. Greatest decrease of the DO wasobserved in the lower 20% of the bed depth. Nitrate removalefficiency was inversely proportional to influent DOconcentrations (8.3-11.9 DO mg L^-1) or nitrite loadingrates (0-5.5 N-NO₂ ^- kg m^-3 day^-1) employed in this study. Nitrite loading rates to achieve morethan 90% of nitrate removal efficiency were 1.46 N-NO₂ ^-kg m^-3 day^-1 or less at pH 7.5 and 0.34 N-NO₂ ^- kg m^-3 day^-1 or less at pH 6.8. Nitrate removal efficiency was 63% or more within the lower 20% of the bed depth at the nitrite loading rates that allowed more than 90% of nitrate removal efficiency of the reactor. The results of this study provide first quantitative data that nitrate removalperformance of an anoxic biofilm is inhibited by DO or nitrite,reported to be a limiting factor in the suspended biologicaldenitrification process.     

Mesophilic biomethanation and treatment of poultry waste-water using pilot scale UASB reactor

The feasibility of applying the up-flow anaerobicsludge blanket (UASB) treatment for poultry waste (faeces)water was examined. A continuous-flow UASB pilot scalereactor of 3.50 L capacity using mixed culture was operatedfor 95 days to assess the treatability of poultry waste-water and its methane production. The maximum chemicaloxygen demand (COD) removed was found to be 78% whenorganic loading rate (OLR) was 2.9 kg COD m^-3 day^-1 athydraulic retention times (HRT) of 13.2 hr. The averagebiogas recovery was 0.26 m³ CH₄ kg COD with an averagemethane content of 57% at mean temperature of 30 °C.Data indicate more rapid methanogenesis with higher loadingrates and shorter hydraulic retention times. At feedconcentration of 4.8 kg COD m^-3 day^-1, anaerobic digestionwas severely retarded at all hydraulic retention timetested. This complication in the reactor operations may belinked to build-up of colloidal solids often associated withpoultry waste water and ammonia toxicity. Isolates fromgranular sludge and effluent were found to be facultativeanaerobes most of which were Pseudomonas genera.     

Formation and Emission of N2O and CH4 from Compost Heaps of Organic Household Waster

Composting can be a source of N₂O andCH₄ production. In this investigation, differentcompost heaps of organic household waste weremonitored with the focus on potential formation ofCH₄ and N₂O in the heaps and emission ofthese gases from the heaps. The studied compost heapshad different compost ages, turning intervals andcompost sizes. The analysed compost gases containedbetween 1–3421 L of N₂O-N L^-1 and 0–470 mL of CH₄ L^-1. The emission rates ofN₂O and CH₄ from the compost heaps werebetween 1–1464 mg N₂O m^-2 day^-1 and0–119 000 mg CH₄ m^-2 day^-1. These verylarge differences in compost gas composition andemission indicate the importance of compostmanagement. The results also give an understanding ofwhere in the composting process an increasing emissionof N₂O and CH₄ can occur.     

Seasonal perspective of dietary arsenic consumption and urine arsenic in an endemic population

Exposure to arsenic in arsenic endemic areas is most remarkable environmental health challenges. Although effects of arsenic contamination are well established, reports are unavailable on probable seasonal variation due to changes of food habit depending on winter and summer seasons, especially for endemic regions of Nadia district, West Bengal. Complete 24-h diets, drinking–cooking water, first morning voided urine samples, and diet history were analyzed on 25 volunteers in arsenic endemic Chakdah block of Nadia district, once in summer followed by once in winter from the same participants. Results depicted no seasonal variation of body weight and body mass index. Arsenic concentration of source drinking and cooking water decreased (p?=?0.04) from 26 μg L^?1 in summer to 6 μg L^?1 in winter season. We recorded a seasonal decrease of water intake in male (3.8 and 2.5 L day ^?1) and female (2.6 and 1.2 L day^?1) participants from summer to winter. Arsenic intake through drinking water decreased (p?=?0.04) in winter (29 μg day^?1) than in summer (100 μg day^?1), and urinary arsenic concentration decreased (p?=?0.018) in winter (41 μg L^?1) than in summer (69 μg L^?1). Dietary arsenic intake remained unchanged (p?=?0.24) over the seasons. Hence, we can infer that human health risk assessment from arsenic needs an insight over temporal scale.     

A modified toxicity testing method using tropical marine microalgae

Toxicity testing of four heavy metals(Cd, Cu, Mn and As) using four species of tropicalmarine phytoplankton, Chaetoceros calcitrans, Isochrysis galbana, Tetraselmis tetrahele and Tetraselmis sp., was carried out in multiwellplates with test volumes of 2 mL and the resultscompared to those of standard, large volume,shake-flasks. IC₅₀ values (concentrations of metalsestimated to inhibit 50% growth relative to thecontrol) were determined after 96 hours based onautomated O.D. readings measured in Elisa microplatesby a Multiskan spectrophotometer. Good agreement wasachieved between O.D. readings and cell countsindicating that this new method is a simple,economical, practical and rapid technique for toxicitytesting, and provides good reproducibility of IC₅₀ values. Results of the toxicity testsindicate that Cu was the most toxic metal (averageIC₅₀ values ranging from 0.04 to 0.37 mg L^-1), followed by Cd (0.06–5.7 mg L^-1), Mn (7.2–21.4 mg L^-1) and As (33.9–319.3 mg L^-1).Test species had different degrees of sensitivity tothe metals tested, with I.galbana and C. calcitrans the mostsensitive to Cu, Cd and Mn. Based on these findingsit is recommended that the existing Malaysian InterimStandards for Marine Water Quality for Cd and Cu be reviewed.     

Comparative rice seed toxicity tests using filter paper,growth pouch-tm,and seed tray methods

Paper substrate, especially circular filter paper placed inside a Petri dish, has long been used for the plant seed toxicity test (PSTT). Although this method is simple and inexpensive, recent evidence indicates that it gives results that are significantly different from those obtained using a method that does not involve paper, especially when testing metal cations. The study compared PSTT using three methods: filter paper, Growth Pouch-TM, and seed tray. The Growth Pouch-TM is a commercially available device. The seed tray is a newly designed plastic receptacle placed inside a Petri dish. The results of the Growth Pouch-TM method showed no toxic effects on rice for Ag up to 40 mg L^–1 and Cd up to 20 mg L^–1. Using the seed tray method, IC₅₀ (50% inhibitory effect concentration) values were 0.55 and 1.4 mg L^–1 for Ag and Cd, respectively. Although results of filter paper and seed tray methods were nearly identical for NaF, Cr(VI), and phenol, the toxicities of cations Ag and Cd were reduced by using the filter paper method; IC₅₀ values were 22 and 18 mg L^–1, respectively. The results clearly indicate that paper substrate is not advisable for PSTT.     

A new approach for estimating the phytotoxicity limits

A pot experiment was carried out on a Typic ustipsamment to study the effect of Cd concentration on the yield of wheat (Triticum aestivum) and soybean (Glycine max). Cd levels taken were 1, 5, 10, 20, 40, 80, and 160 g g^-1 of soil. Three different statistical procedures were employed to evaluate the phytotoxicity limits. The non-linear regression technique was found to be more effective in calculating C ₀ (threshold concentration) and C ₁₀₀ (toxic concentration) in comparison to Cate and Nelson (1971) and Beckett and Davis (1977) procedures. This technique was unaffected by the nature of the distribution of the data and did not require any initial value of concentration as a starting point.     

Dynamic Modeling of Biological Treatment of Leachates from Solid Wastes

Leachates from municipal solid wastes are liquids formed by organic and inorganic components suitable for biological treatment. In biological treatment plants, prediction of the output parameter value due to dynamic variation is essential. A dynamic model based on ASM1 has been applied for prediction of effluent COD value at real scale, using three different composition leachates. Tuning between dynamic variables and predicted parameter is tested for a correct proposal of the model. Dynamic model predicts correctly fluctuations in the output COD value and tempers dynamism caused by variation of temperature and biomass concentration in the case of high organic loaded leachates. Kinetic parameters Y _H and K _s are fixed to solve the model, and dynamic variables μ _H and X_BH are changing in time. μ_H,max is obtained in simulation (0.37–1.82 day^?1) for minimum error between predicted values and experimental data. μ_H,max value is much lower compared with the value for domestic wastewater treatment due to lower biodegradability of leachate.     

Determination of ultra-trace amounts of cadmium by ET-AAS after column preconcentration with a new sorbent of modified MWCNTs

The present research reports on the application of modified multiwalled carbon nanotubes as a new, easily prepared, and stable solid sorbent for the column preconcentration of ultra-trace amounts of cadmium in aqueous solution. Multiwalled carbon nanotubes were oxidized with concentrated HNO₃ and modified with 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol and then were used as a solid phase for the column preconcentration of Cd(II). Elution was carried out with 0.5 mol?L^?1 HNO₃. The amount of eluted Cd(II) was measured using electrothermal atomic absorption spectrometry. Various parameters such as pH, sample and eluent flow rate, eluent concentration, breakthrough volume, and interference of a great number of anions and cations on the retention of analyte on sorbent were studied. Under the optimized conditions, the calibration graph was linear in the range of 0.67 ng?L^?1 to 5.0 μg?L^?1 and the detection limit (3S_b, n?=?7) was 0.14 ng?L^?1 in initial solution. A preconcentration factor of 300 and relative standard deviations of ±3.6 % for seven successive determinations of 3 ng of Cd(II) were achieved. The column preconcentration was successfully applied to the analysis of river water, waste water, and Persian Gulf water sample.     

Phosphorus fractions and adsorption characteristics of floodplain sediments in the lower reaches of the Hanjiang River, China

The phosphorus fractions and adsorption characteristics of seven floodplain sediment samples collected in the lower reaches of China’s Hanjiang River were studied. Most phosphorus fractions showed a marked downstream increase in response to point-source inputs from urban areas. Total phosphorus (TP) contents in the sediments ranged from 603.68 to 945.25 mg.kg⁻¹. Inorganic phosphorus (IP) was the major component of TP, and calcium-bound phosphorus (Ca–P) was the major fraction of IP. The distribution characteristics of the phosphorus contents were affected by sediment grain size and hydrodynamic conditions. The maximum phosphorus adsorption capacities (Q _max) and the half-saturation concentration (k) were obtained using an improved Langmuir model. Native adsorbed exchangeable phosphorus content (w _NAP) and the zero-equilibrium phosphorus concentration value (c _EPC0) were subsequently calculated. The effects of sediment grain size, temperature, and disturbance on the phosphorus adsorption isotherms were also studied. The results showed that phosphorus adsorption on floodplain sediments was primarily chemisorption; the particle concentration effect played a more important role at a disturbance intensity of 150 r.min⁻¹ (on a shaker table) than at 100 r.min⁻¹.     

Parameters Influencing Sediments Resuspension and the Link to Sorption of Inorganic Compounds

In the aquatic environment, the accumulation of chemicalcontaminants by sediments poses a potential threat to endemiclife forms and drinking water resources. Trace metals such asCd, Cu, Cr, Ni, Pb, and toxic organic compounds, are among awide variety of contaminants having an affinity for sediments.In this study, experiments were performed simulating sedimentresuspension in the lower Housatonic River, Connecticut, using aParticle Entrainment Simulator. Analyses of grain sizedistributions, porosities and total organic contents of thesediments suggested that these parameters influence theredistribution and entrainment of settleable solids in the watercolumn. These findings were established by evaluating the impactof one parameter on sediment resuspension as a function ofstream flow with the other two characteristics being heldconstant. Total suspended solids and volatile suspended solidsresuspension concentration ranged from 3.2 to 20648.3 mg L^-1,and 1.5 to 1823.8 mg L^-1, respectively, with subsequentincreases in flow rates from 9 to 6 dynes cm^-2. The resuspension concentrations were augmentedby sediment porosity (22.0 to 57.5%), percent finer grain-size distributions at 0.1 mm, and total organic content (2.7 g kg^-1 to 29.0 g kg^-1). Using K _p values, and the dissolvedcontaminant levels of various trace metals, the particulatecontaminant levels of the metals were determined under variousoscillation rates. As sediment resuspension increased withincreased stream flow, there was an overall general increasefrom 0.02 to 33.6 g L^-1 in the particulatecontaminant levels of Cd, Cu, Cr, Ni and Pb.     

Atmosphic pollutants study of particles ionic species during high wind speed (>7 m s-1) near Taiwan strait in central Taiwan from 2004 to 2005

This study monitored atmospheric pollutants during high wind speed (> 7 m s⁻¹) at two sampling sites: Taichung Harbor (TH) and Wuci traffic (WT) during March 2004 to January 2005 in central Taiwan. The correlation coefficient (R ²) between TSP, PM_2.5, PM_2.5−10 particle concentration vs. wind speed at the TH and WT sampling site during high wind speed (< 7 m s⁻¹) were also displayed in this study. In addition, the correlation coefficients between TSP, PM_2.5 and PM_2.5−10 of ionic species vs. high wind speed were also observed. The results indicated that the correlation coefficient order was TSP > PM_2.5−10 > PM_2.5 for particle at both sampling sites near Taiwan strait. In addition, the concentration of Cl⁻, NO₃ ⁻, SO₄ ²⁻, NH₄ ⁺, Mg²⁺, Ca²⁺ and Na⁺ were also analyzed in this study.     

Performance Evaluation of Reverse Osmosis Desalination Plants for Rural Water Supply in a Developing Country – A Case Study

Performance evaluation of two reverse osmosis (RO) desalination plants (DSP) at villages: Melasirupodhu (30 m³ day^-1) and Sikkal (50 m³ day^-1) in Ramanathpuram district,Tamil Nadu (India) were studied so as to bring out the state-of-art of their operation and maintenance (O&M). Detailedinformation on plant design and engineering, water quality,plant personnel, and cost of O&M was collected for a period ofthree years after commissioning of the two plants. Feed waterwas brackish, the TDS varied in the range of 6500–8500 mg L^-1 at Melasirupodhu and 5300–7100 mg L^-1 atSikkal villages. The product water quality was observed to begradually deteriorating as the salt rejection by the membranesdecreased with time. The salt rejection was 97–99% atthe time of commissioning of the plants, and came down to89–90% at the end of 3 years of operation. Product water TDS soonafter installation of the plants was excellent and within desirable limits of BIS. After three years of operation, few parameters exceeded the desirable limits, however, they were found to be within permissible limits of BIS. The analyses of thedata showed that both plants were operated only at 30–36% of the design capacity. Plant shut-down due to inadequate and erratic power supply, and plant break-down and inherent delay in repairs due to lack of adequate infrastructure were found tobe the major causes for the low utilization of the plants. Consequently the recurring cost of product water production enhanced to Rs. 25.0/m³ at Melasirupodhu and Rs. 17.5 m^-3 at Sikkal, as against the estimated cost of Rs. 15.0/m³ and Rs. 11.0/m³, respectively, as per the design. Over the years, the energy consumption for the product water output increased reflecting higher operational pressures needed with the aging of the membranes.     

Mobilization of aluminum by the acid percolates within unsaturated zone of sandstones

The area of the Black Triangle has been exposed to extreme levels of acid deposition in the twentieth century. The chemical weathering of sandstones found within the Black Triangle became well-known phenomenon. Infiltration of acid rain solutions into the sandstone represents the main input of salt components into the sandstone. The infiltrated solutions–sandstone percolates–react with sandstone matrix and previously deposited materials such as salt efflorescence. Acidic sandstone percolates pH?3.2–4.8 found at ten sites within the National Park Bohemian Switzerland contained high Al-tot (0.8–10 mg?L^?1) concentrations and high concentrations of anions SO₄ (5–66 mg?L^?1) and NO₃ (2–42 mg?L^?1). A high proportion (50–98 %) of Al-tot concentration in acid percolates was represented by toxic reactive Alⁿ⁺. Chemical equilibrium modeling indicated as the most abundant Al species Al³⁺, AlSO₄ ⁺, and AlF²⁺. The remaining 2–50 % of Al-tot concentration was present in the form of complexes with dissolved organic matter Al-org. Mobilization and transport of Al from the upper zones of sandstone causes chemical weathering and sandstone structure deterioration. The most acidic percolates contained the highest concentrations of dissolved organic material (estimated up to 42 mg?L^?1) suggesting the contribution of vegetation on sandstone weathering processes. Very low concentrations of Al-tot in springs at BSNP suggest that Al mobilized in unsaturated zone is transported deeper into the sandstone. This process of mobilization could represent a threat for the water quality small-perched aquifers.     

Rapid spectrophotometric determination of trace amounts of palladium in water samples after dispersive liquid–liquid microextraction

A simple, rapid, and efficient dispersive liquid–liquid microextraction method, followed by UV–Vis spectrophotometry was developed for the preconcentration and determination of Pd ions in water samples. Pd ions react with α-furildioxime (chelating agent) to form a hydrophobic complex. Various parameters were altered to study and optimize their effects on the extraction efficiency, such as pH, ligand concentration, the type and volume of extraction and dispersive solvents, extraction time, and salt concentration. Under optimized conditions, the method exhibited an enrichment factor (C _org/C _aq) of 25 and recovery more than 98 % within a very short extraction time. The linearity of the method ranged from 10 to 200 μg?L^?1. The limit of detection was 1.1 μg?L^?1. The relative standard deviation for the concentration of 100 μg?L^?1 of Pd was 2.3 % (n?=?10). Finally, the developed method was successfully applied to the extraction and determination of Pd in tap, river, mineral, and sea water samples.     

Nutrient spatial pattern of the upstream,mainstream and tributaries of the Three Gorges Reservoir in China

A comprehensive monitoring program was conducted to investigate the nutrient spatial pattern in the mainstream of the Yangtze River from the Baihetan Dam down to the Three Gorges Dam located at the upper region of the Yangtze River in China. Samples were taken from 33 different sites from July 30 to August 19, 2011. The nutrient patterns of the three representative tributaries of the Three Gorges Reservoir (TGR)—the Modao, the Daning, and the Xiangxi Rivers—were also investigated. The results show that the mainstream of the TGR has a higher concentration of nitrogen and a lower concentration of phosphorus than that of the upper mainstream before the TGR. Moreover, it was found that nitrate-nitrogen (NO₃-N) is the main nitrogen component, while particulate phosphorus predominates the total phosphorus (TP). It was found that the three representative tributaries of the TGR have lower total nitrogen (TN) concentrations compared to the corresponding sections of the mainstream TGR. Based on the nutrient spatial pattern, the nutrient flux was calculated. The total fluxes of TN, NO₃-N, TP, and orthophosphate (PO₄-P) from the upstream reach into the TGR are 2,155.06, 1,674.97, 212.98, and 83.42 t day^?1, respectively. The amount of nutrients imported from the TGR into its tributaries is more than the amount exported. It was determined that the Xiangxi River has the largest net rate of imported nitrogen at 7.66 t day^?1, whereas the Daning River has the largest net rate of imported phosphorus at 1.75 t day^?1. In addition, compared with the nutrients imported from the TGR into its tributaries, the nutrient flux from the upstream reach into the TGR contributes approximately less than 3 %.     

多波长法用于减小浊度对水源水中甲醛测定结果的影响

比较了减小水样浊度对样品结果影响的各种方法,包括过滤法、双波长法、三波长法,3种方法均基于乙酰丙酮分光光度法,测定波长均为414 nm。结果表明,以480 nm为参比波长的双波长法所得方法检出限为0.027 mg/L,采用470 nm与360 nm、460 nm与370 nm、450 nm与380 nm 3对参比波长的三波长法测得方法检出限为0.025~0.028 mg/L,这些方法用于检测0.100 mg/L标准点样品时,检测结果 RSD介于8.0%~8.6%。双波长法适合低浊度样品的直接分析,而浊度较高或双波长法测得结果大于方法检出限时,应采用三波长法进行定量分析,他们的使用有助于提高方法的准确度及减少工作量。用于地表水样品分析时,0.200、0.400 mg/L加标样品的回收率介于90.3%~101%,对应RSD介于0.0%~4.2%。     

Indices of Benthic Community Tolerance in Contaminated Great Lakes Sediments: Relations with Sediment Contaminant Concentrations, Sediment Toxicity, and the Sediment Quality Triad

We evaluated the toxic-units model developed by Wildhaber and Schmitt (1996) as a predictor of indices of mean tolerance to pollution (i.e., Lenat, 1993; Hilsenhoff, 1987) and other benthic community indices from Great Lakes sediments containing complex mixtures of environmental contaminants (e.g., polychlorinated biphenyls – PCBs, polycyclic aromatic hydrocarbons – PAHs, pesticides, chlorinated dioxins, and metals). Sediment toxic units were defined as the ratio of the estimated pore-water concentration of a contaminant to its chronic toxicity as estimated by U.S. Environmental Protection Agency Ambient Water Quality Criteria (AWQC) or other applicable standard. The total hazard of a sediment to aquatic life was assessed by summing toxic units for all contaminants quantified. Among the benthic community metrics evaluated, total toxic units were most closely correlated with Lenat's (1993) and Hilsenhoff's (1987) indices of community tolerance (T _L and T _H , respectively); toxic units accounted for 42% T _L and 53% T _H of variability in community tolerance as measured by Ponar grabs. In contrast, taxonomic richness and Shannon-Wiener diversity were not correlated (P > 0.05) with toxic units. Substitution of order- or family-level identifications for lowest possible (mostly genus- or species-) level identifications in the calculation of T _L and T _H indices weakened the relationships with toxic units. Tolerance values based on order- and family-level identifications of benthos for artificial substrate samples were more strongly correlated with toxic units than tolerance values for benthos from Ponar grabs. The ability of the toxic-units model to predict the other two components (i.e., laboratory-measured sediment toxicity and benthic community composition) of the Sediment Quality Triad (SQT) may obviate the need for the SQT in some situations.     

Synthesis,characterization, and systematic studies of a novel aluminum selective chelating resin

A procedure is detailed for the selective analysis of trace aluminum by flame atomic absorption spectrophotometer coupled with off-line column separation and preconcentration. Chelating resin was synthesized by covalent functionalization of Amberlite XAD-16 by 2-(2-hydroxyphenyl) benzoxazole. The modified resin was characterized using FT-IR spectroscopy, energy dispersive x-ray analysis, elemental analysis, thermogravimetric analysis/differential thermal analysis, and minimum energy run. The optimum sorption was at pH 9?±?0.1 with corresponding t _1/2 of only 7 min. Many competitive anions and cations studied did not interfere at all in the selective determination of Al(III), at the optimized conditions. The resin shows maximum sorption capacity of 21.58 mg g^?1 and can be regenerated up to 75 cycles without any discernible capacity loss. The Langmuir isotherm model provides the better correlation of the experimental data (r ²?=?0.999) in comparison to Freundlich isotherm model, while the Scatchard analysis revealed homogeneous binding sites in the chelating resin. Analytical figures of merit were evaluated by accuracy (standard reference materials and recovery experiment), precision (RSD <5 %), and detection limit (2.8 μg L^?1). The applicability was demonstrated by analysis of trace aluminum in biological, environmental, and food samples.     

Development of simple and sensitive spectrophotometric method for the determination of bendiocarb in its formulations and environmental samples

Facile, selective and sensitive spectrophotometric method has been developed for the determination of bendiocarb in its insecticidal formulations, fortified water, food grains, agriculture wastewater and agriculture soil samples with prepared reagents. The method was based on alkaline hydrolysis of the bendiocarb pesticide, and the resultant hydrolysis product of bendiocarb was coupled with 2,6-dibromo-4-methylaniline to give a yellow color product with λmaxof457 nmorcouplingwith2, 6−dibromo−4−nitroanilinetoproducearedcoloredproductwithλ_max of474~nmorcouplingwith2, 4, 6−tribromoanilinetoformorangeredcoloredproducthasaλ_max of465 nm.Underoptimalconditions, Beer'slawrangefor2, 6−dibromo−4−methylaniline(DBMA)wasfoundtobe0.6−−14.0~μgmL ^-1, 0.8−−10.0 μgmL ^-1 for2, 6−dibromo−4−nitroaniline(DBNA)and0.4−−10.0 μgmL ^-1 for2, 4, 6−tribromoaniline(TBA).Themolarabsorptivityofthecolorsystemswerefoundtobe4.126~×~10⁴ lmol ^-1 cm ^-1 forDBMA, 3.254×10⁴ l~mol ^-1 cm ^-1 forDBNAand2.812×10⁴ lmol ^-1 cm ^-1 forTBA.Sandell'softhecolorreactionsare0.018 μgcm ^-2(DBMA), 0.052 μgcm ^-2(DBNA)and0.065 μgcm ^-2$ (TBA) respectively. The effect of the non-target species on the determination of bendiocarb was studied. The formation of colored derivatives with the coupling agents is instantaneous and stable for 18 h, 30 h, and 12 h. Performance of the proposed methods were compared statistically in terms Student's F and t-tests with the reported methods.