Metal On‐Line Voltammetric Analyzer for On‐Site Monitoring of Iron Speciation in Acid Mine Drainage Waters: Development and Characterization

The development of a simple, low cost, portable metal on‐line voltammetric analyzer (MOVA) for the iron analysis, as well as other species, in mining effluents is presented. It consists of a voltammetric cell based on an impinging jet flow configuration, a fluidic system controlled by gravity and electronics. Laboratory tests were performed to optimize the system as well as the analytical conditions for Fe speciation measurements. MOVA was then tested in the laboratory, in samples of both mining effluents. The results showed that iron in both mining effluents, as well as copper and arsenic, can be measured in oxygenated samples.     

Decolorization of Distillery Effluent Using Poly(Vinyl Chloride) and Cellulose Acetate Phthalate as Adsorbents

Decolorization of distillery effluents, using low cost polymer adsorbents, is one of the challenging areas for environmental technologists. Untreated distillery effluents are harmful to the environment, causing foul smell, spoiling fresh water sources and killing aquatic life. The color of distillery effluents have been decolorized by using polymer based adsorbents, such as poly(vinyl chloride) (PVC) and cellulose acetate phthalate (CAP), which are water insoluble, easily available, and cheap. In the present article, special emphasis is given to studies such as the effect of contact time, dosage amount, dilution, and the variation in the amount of sample on the degree of decolorization of the effluent. The decolorization of a distillery effluent was monitored by using UV/Visible spectroscopy and Fourier transform infrared spectroscopy (FTIR). From these studies, it was noticed that moderate to fair results were obtained and it was also found that CAP was a better adsorbent, compared to PVC, for decolorization of distillery effluents.     

Solid-phase extraction for toxicity reduction evaluations of industrial wastewater effluents

The physical, chemical and biological characteristics of industrial and municipal wastewater effluents in the United States are limited in National Pollutant Discharge Elimination System (NPDES) permits. Toxicity reduction evaluations (TREs) involving fractionation of wastewater effluents, biomonitoring for aquatic toxicity and determinations of specific chemicals are conducted when adverse effects on water quality are detected during routine biomonitoring as required by the NPDES permit. However, certain fractionation techniques are incompatible with subsequent testing for aquatic toxicity. The effect of various schemes for fractionation of wastewater effluent on biomonitoring with freshwater Cladocerans (Daphnia magna, Daphnia pulex, Ceriodaphnia dubia or Ceriodaphnia reticulata) is reviewed. Solid-phase extraction (SPE) is discussed as a chromatographic technique used for the selective fractionation of wastewater effluents during toxicity reduction evaluation.     

Characterization of lactose and derived products in dairy product industry effluents processing

The treatment of the effluents of dairy product industries containing lactose is done by a biological process, which reduces considerably the original amount of that sugar. Although the final residual content of lactose is small after treatment, it may cause the eutrophication and/or the superfertilization of the water, which provokes vegetation growth on the water surface, hindering the navigability and increasing the consumption of the dissolved oxygen necessary to the life of the fishes of the river or sea where the treated effluent is poured. In dairy industry, after proper initial processing steps of waste treatment, lactose, as it is water soluble, may still be present in the outgoing effluents. A complementary step by using organophilic clay adsorption, as a further treatment of these effluents, may enhance antipollution procedures, decreasing its final content in the effluents. The present paper deals with the characterization, by thermal analysis of different lactose products, which may be present in the different processing steps as it dissolves in water and then it is recrystallized from it, as well as after being adsorbed by organophilic clay from those effluents, which are very diluted lactose aqueous solutions.     

Biosurfactants from potato process effluents

High-solids (HS) and low-solids (LS) potato process effluents were tested as substrates for surfactin production. Tests used effluents diluted 1∶10, unamended and amended with trace minerals or corn steep liquor. Heat pretreatment was necessary for surfactin production from effluents due to indigenous bacteria, whose spores remained after autoclaving. Surfactin production from LS surpassed HS in all cases. Surfactin yields from LS were 66% lower than from a pure culture in an optimized potatostarch medium. LS could potentially be used without sterilization for surfactin production for low-value applications such as environmental remediation or oil recovery.     

Evaluation of toxic metals in the industrial effluents and their segregation through peanut husk fence for pollution abatement

The industrial pollution is exponentially growing in the developing countries due to the discharge of untreated effluents from the industries in the open atmosphere. This may cause severe health hazards in the general public. To reduce this effect, it is essential to remove the toxic and heavy metals from the effluents before their disposal into the biosphere. In this context, samples of the effluents were collected from the textile/yarn, ceramics and pulp/paper industries and the concentrations of the toxic metal ions were determined using neutron activation analysis (NAA) technique. The observed concentration values of the As, Cr and Fe ions, in the unprocessed industrial effluents, were 4.91 ± 0.8, 9.67 ± 0.7 and 9.71 ± 0.8 mg/L, respectively which was well above the standard recommended limits (i.e. 1.0, 1.0 and 2.0 mg/L, respectively). In order to remove the toxic metal ions from the effluents, the samples were treated with pea nut husk fence. After this treatment, 91.5% arsenic, 81.9% chromium and 66.5% iron metal ions were successfully removed from the effluents. Then the treated effluents contained concerned toxic metal ions concentrations within the permissible limits as recommended by the national environmental quality standards (NEQS).     

Detection of equimolar EDTA and DTPA in spiked wastewater effluents

Ethylenediaminetetraacetic acid (EDTA) and diethylenetriamine-pentaacetic acid (DTPA) are water ‘softening’ agents that are present in numerous household and industrial detergents. Since these particular chelating agents are not significantly degraded during conventional wastewater treatment processes, wastewater treatment plant (WTP) effluents can contain up to 19 µM of EDTA and 7 µM of DTPA. Little, however, is known about the release of EDTA and DTPA from WTPs to rivers. To gain insight, we here report on the development of a cost-effective analytical method. This method is based on the chromatography of a humic acid-cadmium (HA-Cd) complex on a size-exclusion chromatography column (SEC, Sephadex G-15) while using WTP effluents from Lethbridge, Banff and Canmore which contained 10 mM Tris-buffer as the mobile phase (pH 8.2). The intact HA-Cd complex is detected by means of a flame atomic absorption spectrometer (FAAS). The addition of equimolar EDTA and DTPA up to 10 µM allowed us to observe a concentration-dependent increase of the retention time of the main Cd-peak. This behaviour was qualitatively comparable between the WTP effluents and was rationalised by the EDTA/DTPA-mediated mobilisation of Cd from the HA-Cd complex. The signal intensity that corresponded to the mobilised Cd was used to establish calibration curves with corresponding correlation coefficients in the range of 0.950–0.978. Therefore, the developed method yields robust results for realistic concentrations of equimolar EDTA/DTPA in real WTP effluents. The developed method can now be applied to analyse real WTP effluent for the presence of chelating agents, whose concentrations may be expressed as being equivalent to a particular equimolar EDTA/DTPA concentration.     

Method for the simultaneous determination of monoaromatic and polycyclic aromatic hydrocarbons in industrial effluents using dispersive liquid–liquid microextraction with gas chromatography–mass spectrometry

We present a new method for simultaneous determination of 22 monoaromatic and polycyclic aromatic hydrocarbons in postoxidative effluents from the production of petroleum bitumen using dispersive liquid–liquid microextraction coupled to gas chromatography and mass spectrometry. The eight extraction parameters including the type and volume of extraction and disperser solvent, pH, salting out effect, extraction, and centrifugation time were optimized. The low detection limit ranging from 0.36 to 28 μg/L, limit of quantitation (1.1–84 μg/L), good reproducibility, and wide linear ranges, as well as the recoveries ranging from 71.74 to 114.67% revealed that the new method allows the determination of aromatic hydrocarbons at low concentration levels in industrial effluents having a very complex composition. The developed method was applied to the determination of content of mono‐ and polycyclic aromatic hydrocarbons in samples of raw postoxidative effluents in which 15 compounds were identified at concentrations ranging from 1.21 to 1017.0 μg/L as well as in effluents after chemical treatment.     

New procedure for the examination of the degradation of volatile organonitrogen compounds during the treatment of industrial effluents

We present a new procedure for the determination of 32 volatile organonitrogen compounds in samples of industrial effluents with a complex matrix. The procedure, based on dispersive liquid–liquid microextraction followed by gas chromatography with nitrogen‐phosphorus and mass spectrometric detection, was optimized and validated. Optimization of the extraction included the type of extraction and disperser solvent, disperser solvent volume, pH, salting out effect, extraction, and centrifugation time. The procedure based on nitrogen‐phosphorus detection was found to be superior, having lower limits of detection (0.0067–2.29 μg/mL) and quantitation as well as a wider linear range. The developed procedure was applied to the determination of content of volatile organonitrogen compounds in samples of raw effluents from the production of bitumens in which 13 compounds were identified at concentrations ranging from 0.15 to 10.86 μg/mL and in samples of effluents treated by various chemical methods.     

A critical review of hazardous waste generation from textile industries and associated ecological impacts

Among many industries, the textile industry is the oldest industry of human civilization. Cloth is the second most important human need after food. Textile processing includes several steps in which wet processing is the most important. As wet processing involves an extensive amount of water and chemicals, an enormous volume of textile effluent generates during wet processing. Textile effluents is disposed of on bare land or on water bodies, which causes soil and water contamination. Improper disposal of textile effluents causes severe soil and water contamination. Textile effluents contain dyes, heavy metals, inorganic salts, surfactants, organic contaminants, oil, and grease. Textile effluents cause contamination in water bodies. The colour present in effluents hinders the photosynthesis of aquatic plants. Inorganic salts cause the degradation of water quality and soil excellence. Heavy metals enter the food chain and cause severe health impacts on human life. Various physical, chemical, bailogical and hybrid methods are used to treat textile effluents. Textile processing has been explained in brief in this study. The current research deals with different textile processing steps, various pollutants generated in textile processing and their ecotoxicity, various ecological crises associated with textile processing, and numerous treatment methods for the remediation of textile effluents.     

Application of boron-doped diamond electrodes for electrochemical oxidation of real wastewaters

Recently, the synthesis of boron-doped diamond electrodes on different substrates and shapes have reached a promising development stage. Now, these electrodes can also be effectively used to destroy toxic or biorefractory organics in real effluents, such as municipal wastewaters effluents, hospital wastewaters, groundwater, petrochemical effluent, wastewaters from agri–food activities, and so on. The results of this mini-review show that BDD is effectively even for such real effluents, allowing the removal of pollutants under several different conditions. Nevertheless, further efforts are necessary to reach a wider market; in particular, the next stages must face the optimization of cell design and the integration of the electrochemical system with other water treatment and renewable energy sources.     

Removal of uranium (VI) from nuclear effluents onto aluminophosphate and silicoaluminophosphate molecular sieves

Aluminophosphate and silicoaluminophosphate molecular sieves with both five (AFI) and eleven (AEL) type structures are synthesized by hydrothermal crystallization at 473 K, using tripropylamine and dipropylamine as a structure-directing template. The as-prepared AFI and AEL sieves are characterized and then assessed as sorbents for uranium (VI) from radioactive effluents. The sorption process is used to reduce the volumes of effluents and convert them into a stable solid waste. The batch experimental studies are carried out to evaluate the AEL and AFI structure effect on the removal of uranium. The AlPO₄-5, SAPO-5, AlPO₄-11 and SAPO-11 are applied to radioactive effluents with different activities obtained from Nuclear Research Center of Draria, Algeria. Important decontamination factor values are obtained for AFI sorbents. Thermodynamic parameters, namely, the enthalpy (ΔH), entropy (ΔS) and free energy (ΔG) for each sorption process are calculated. The collected results indicated that sorbents are effective materials for the removal of uranium (VI) ions, the sorbent with AFI structure being a highly effective material for the removal of uranium (VI) ions from nuclear effluents.     

Sample Stability of Trace Priority Substances in Wastewater

A series of sample stability tests has been undertaken to support a large UK-based survey of trace substances in wastewater. This program aims to quantify the input of priority chemicals to the aquatic environment via sewage effluent. The stability tests have demonstrated that, in most cases, the proposed approach of chilling samples meets the target that sample concentrations should not change by more than 25%, provided samples are analyzed or otherwise stabilized within 3–5 d. Substances tested fall into three main classes:

• Instability in effluents greater than the project-based threshold of 25% over 3–5 d can be ruled out provided samples are chilled for: DEHP (DEHA), glyphosate, AMPA, bentazone, mecoprop, ofloxacin, erythromycin, and ibuprofen;

• Some indication of possible instability up to 25% provided chilled storage periods do not extend beyond 3–5 d for: mercury (note requires acid dichromate preservation on site or as soon as possible), tributyltin, bisphenol A, reactive aluminum (in effluents, note requires filtration on sampling), oxytetracycline, and propranolol; and

• Clear stability problems are demonstrated for salicylic acid (effluents and influents), with indications of important instability (>25%) for bisphenol (effluents) AMPA and glyphosate (influents).

     

Further results in search for transuranium elements in effluents discharged to air from nuclear power plants

In this work we present data on transuranium nuclides ²³⁸Pu, ^239,240Pu, ²⁴¹Am, ²⁴²Cm and ²⁴⁴Cm in effluents discharged to air (activity concentrations and annually discharged activities of individual radionuclides) from 7 stacks in 2004–2009. In the effluents discharged to air from one stack low activities of transuranium nuclides were observed throughout the studied period. Transuranium nuclides had been discharged to air from this stack also in previous years since 1996 when defect in the cladding of a fuel element and consequent contamination of the primary circuit occurred. In the effluents discharged to air from another stack transuranium nuclides were observed only in some monitoring periods of studied years. We could not prove the presence of transuranium nuclides in the effluents of the other stacks up to 2006. The transuranium nuclides in discharged effluents were registered in the second half-year of 2006. In 2007–2008 especially low activities of ²⁴¹Am were found in these effluents.     

Carbon and Nitrogen Dynamics,and CO2 Efflux in the Calcareous Sandy Loam Soil Treated with Chemically Modified Organic Amendments

In Saudi Arabia, more than 335,000 tons of cow manure is produced every year from dairy farming. However, the produced cow manure is usually added to the agricultural soils as raw or composted manure; significant nitrogen losses occur during the storage, handling, and application of the raw manure. The recovery of ammonia from cow manure through thermochemical treatments is a promising technique to obtain concentrated nitrogen fertilizer and reducing nitrogen losses from raw manure. However, the byproduct effluents from the recovery process are characterized by different chemical properties from the original raw manure; thus, its impact as soil amendments on the soil carbon and nitrogen dynamics is unknown. Therefore, a 90-day incubation experiment was conducted to study the impact of these effluents on CO₂ efflux, organic C, microbial biomass C, available NH₄⁺, and NO₃⁻ when added to agricultural soil. In addition to the two types of effluents (produced at pH 9 and pH 12), raw cow manure (CM), composted cow manure (CMC), cow manure biochar (CMB), and control were used for comparison. The application of CM resulted in a considerable increase in soil available nitrogen and CO₂ efflux, compared to other treatments. Cow manure biochar showed the lowest CO₂ efflux. Cumulative CO₂ effluxes of cow manure effluents were lower than CM; this is possibly due to the relatively high C:N ratio of manure effluent. The content of P, Fe, Cu, Zn, and Mn decreased as incubation time increased. Soil microbial biomass C for soil treated with cow manure effluents (pH 12 and 7) was significantly higher than the rest of the soil amendments and control.     

Investigations of the origins of estrogenic A-ring aromatic steroids in UK sewage treatment works effluents

The present preliminary study describes an investigation of a putative aromatisation pathway in sewage from cholesterol through the corresponding A-ring aromatic steroid, norcholest-1,3,5(10)-trienol (NCT) to estrone. The synthesis and analytical characterisation of NCT and of the trimethyl silyl ether by gas chromatography-mass spectrometry, is described. The analytical properties of synthetic NCT were used to direct a search for the compound over several months in 1998 in the effluents of two sewage treatment works (STW; Deephams and Harpenden, north London). The study was prompted by the earlier findings that increased vitellogenin concentrations in the plasma of caged male rainbow trout held in the STW effluents (so-called fish 'feminisation') could be attributed to the presence of A-ring steroids such as estrone. Until now it has been assumed that these steroids originate from the STW influents and it is not clear to what extent, if at all, aromatisation of steroids might occur during STW operation. NCT was only detected in the solid particles associated with the effluents on one occasion in 8 months. This suggests that the hypothesised pathway is not a major one. Confirmation of previous reports of estrone and 17 beta-estradiol was also obtained using a published analytical method and by a simple modification of the method these reports were extended to include a regular occurrence of the weaker estrogen, 16 alpha-estriol in the case of Harpenden STW effluents in 1998.     

Electro-switchable surfaces for heavy metal waste treatment: Study of polyacrylic acid films grafted on gold surfaces

This paper focuses on using electrochemical-pH-switchable polymer films as active surfaces for heavy metal waste treatment. Polyacrylic acid (PAA) was grafted at open air and room temperature on gold substrates. As a broad-range chelating material, PAA can capture heavy metal ions at low concentration. The release of the metal ions from the grafted-PAA film was obtained under electro-induced-acidification by applying an anodic potential at the electrode to promote a localized water electrolysis. Such electrochemical-switchable films can be part of a secondary step-treatment after conventional ion exchange process or precipitation for treatment of aqueous effluents in order to reach very low concentration in heavy metal ions without production of secondary effluents.     

Improvement of biodegradability of industrial wastewaters by radiation treatment

Summary In order to evaluate the use of gamma-ray treatment as a pretreatment to conventional biological methods, the effects of gamma-irradiation on biodegradability (BOD₅/COD) of textile and pulp wastewaters were investigated. For all wastewaters studied in this work, the efficiency of treatment based on TOC removal was insignificant even at an absorbed dose of 20 kGy. However, the change of biodegradability was noticeable and largely dependent on the chemical property of wastewaters and the absorbed dose of gamma-rays. For textile wastewaters, gamma-ray treatment increased the biodegradability of desizing effluent due to degradation of polymeric sizing agents such as polyvinyl alcohol. Interestingly, the weight-loss showed the highest value of 0.97 at a relatively low dose of 1 kGy. This may be caused by the degradation of less biodegradable ethylene glycol prior to terephthalic acid decomposition. For pulp wastewater, the gamma-ray treatment did not improve the biodegradability of cooking and bleaching of C/D effluents. However, the biodegradability of bleaching E1 and final effluents was abruptly increased up to 5 kGy then slowly decreased as the absorbed dose was increased. The initial increase of biodegradability may be induced by the decomposition of refractory organic compounds such as chlorophenols, which are known to be the main components of bleaching C/D and final effluents.     

Identification of estrogenic activity change in sewage,industrial and livestock effluents by gamma-irradiation

In this study, reduction of estrogenic activity in three different types of effluents from sewage, industrial and livestock wastewater treatment plants by gamma-irradiation was investigated using the yeast two-hybrid assay. After gamma-ray treatment at a dose of 10 kGy, estrogenic activities of sewage, industrial and livestock effluents decreased from 4.4 to 3.0, 1.5 to 1.0 and 16 to 9.9 ng-EEQ L^?1, respectively. The substantial reduction of estrogenic activity in livestock effluent was attributable to the degradation of 17β-estradiol (E2), estrone (E1) and 17α-ethynylestradiol (EE2). Although bisphenol A (BPA) was found at the highest concentration in all effluents, its contribution to the estrogenic activity was not significant due to its low relative estrogenic potency. Meanwhile, the calculated estrogenic activity based on concentrations of E2, E1, EE2 and BPA in the effluents significantly differed from the measured ones. Overestimation may have resulted by dissolved organic matters in effluents inhibiting the estrogenic activity of E2, E1, EE2 and BPA, whereas underestimation was likely due to estrogenic by-products generated by gamma-irradiation.     

Comprehensive evaluation of the effluents eluted from different processes of the textile industry and its immobilization to trim down the environmental pollution

Due to the significance of industrial waste water pollution, which creates severe health hazards in humans, this study concentrates over the reduction and determination of the amounts of toxic metals/pollution parameters in the effluents leached from different processes of the textile industry. The concentrations of metal ions were measured by using neutron activation analysis (NAA) technique. The values of toxic metals such as As (49.1 ± 1.8 mg/L), Cu (42.7 ± 1.5 mg/L), Ni (41.1 ± 3.3 mg/L), Mn (51.1 ± 0.7 mg/L), Sb (1.89 ± 0.04 mg/L), Se (0.41 ± 0.01 mg/L), Co (7.5 ± 0.3 mg/L), Cr (8.5 ± 0.5 mg/L) and Cd (1.21 ± 0.08 mg/L) were found very high in crude textile??s effluents as compared to their standard recommended limits. The immense variation observed among the injurious pollutants of the effluents i.e. pH, temperature, electrical conductivity, turbidity, biological oxygen demands, chemical oxygen demands, total suspended solids, total dissolved solids, total solids etc. The toxic metals and injurious pollutants in the unprocessed effluents have been reduced in the post filtration effluents up to 98% and 96% respectively with the help of an ultra-filtration membrane therapy unit.