污泥上培植的报春花、冬葵中重金属的原子吸收测定

本文研究报春花、冬葵两种植物对污泥中重金属的吸收情况,样品用(1 4)HClO4 HNO3进行了消化处理,然后在实验选定的最佳的工作条件下,用火焰原子吸收光谱法对铅、汞、铬、镉重金属元素进行了测定。结果表明:种植冬葵和报春花前后,污泥样品重金属含量明显下降。     

Simultaneous sonication-assisted extraction, and determination by gas chromatography-mass spectrometry, of di-(2-ethylhexyl)phthalate, nonylphenol, nonylphenol ethoxylates and polychlorinated biphenyls in sludge from wastewater treatment plants

Di-(2-ethyl-hexyl)phthalate (DEHP), nonylphenol, nonylphenol mono- and diethoxylates (NPEs) and polychlorinated biphenyls (PCBs) are organic pollutants in sewage sludge which have to be monitored in the European Union according to a future Sludge Directive. In the present work, an analytical method for the simultaneous extraction and determination of DEHP, NPEs and PCBs is proposed for the routine analysis of these compounds in sludge from wastewater treatment plants. All the compounds were simultaneously extracted by sonication with hexane and analysed by gas chromatography-mass spectrometry (GC-MS) in electronic impact mode. Recoveries achieved were 105% for DEHP, 61.4-88.6% for NPEs and 55.8-108.3% for PCBs with relative standard deviation bellow 10%. Limits of quantification were 65 μg kg⁻¹ for DEHP, from 630 to 2504 μg kg⁻¹ for NPEs and from 5.4 to 10.6 μg kg⁻¹ for PCBs in dried sludge. The applicability of the proposed method was evaluated by the determination of these compounds in sludge from wastewater treatment plants in Seville (South Spain).     

Assessment of sonotrode and tube reactors for ultrasonic pre-treatment of two different sewage sludge types

The effectiveness of tube and sonotrode reactors for the sonication of sewage sludge under identical conditions was compared for the first time. Despite the considerable structural differences, sonication with each ultrasonic reactor led to an accelerated degradation rate and an increased methane production within the first five days for the majority of the sewage sludge samples tested. On closer examination, however, it becomes clear that the investigated sonication systems are not equally suitable for the substrates considered. While the use of a sonotrode proved to be particularly advantageous for the treatment of waste activated sludge (+25% methane yield at 300 kJ/kg_TS), the use of a 2-inch tube reactor achieved the highest enhancement for low-intensity sonication in digested sludge (+22% methane yield at 300 kJ/kg_TS). With increasing energy input, more chemical oxygen demand was solubilized, but this did not result in an increase in methane yield for all samples. Sonication of waste activated sludge led to a significant reduction in viscosity of up to 50%, and a reduction of up to 60% was observed after sonication of digested sludge with low energy inputs. The study, therefore, demonstrates that the choice of the most suitable sonication system essentially depends on the properties of the sludge to be sonicated.     

Effect of low-intensity ultrasound on partial nitrification: Performance,sludge characteristics,and properties of extracellular polymeric substances

Ultrasound technology, which is environment-friendly and economical, has emerged as a novel strategy that can be used to enhance the partial nitrification process. However, its effect on this process remains unclear. Therefore, in this study, partial nitrification sludge was subjected to low-intensity (0.15 W/mL) ultrasound treatment for 10 min, and the effect of ultrasonic treatment on the partial nitrification process was evaluated based on changes in reactor performance, sludge characteristics, and the properties of extracellular polymeric substances (EPS). The results obtained showed that the ultrasonic treatment enhanced nitrite accumulation performance as well as the activity of ammonia-oxidizing bacteria from 3.3 to 16.6 mg O₂/g VSS,⋅while inhibiting the activity of nitrite-oxidizing bacteria. Further analysis showed that owing to the ultrasonic treatment, there was an increase in EPS contents. Particularly, there was a significant increase in loosely bound polysaccharide (PS) contents, indicating the occurrence of intracellular PS anabolics as well as PS secretion. Additionally, ultrasonic treatment induced a significant increase in carbonyl, hydroxyl, and amine functional group contents, and EPS analysis results revealed that it had a positive effect on mass transfer efficiency; thus, it enhanced the partial nitrification process. Overall, this study describes the effect of intermittent low-intensity ultrasound on the partial nitrification process as well as the associated enhancement mechanism.     

Continuous double-step acid catalyzed esterification production of sludge palm oil using 3D-printed rotational hydrodynamic cavitation reactor

Sludge palm oil (SPO) with high free fatty acid (FFA) content was processed using a continuous and double-step esterification production process in a rotor-stator-type hydrodynamic cavitation reactor. Three-dimensional printed rotor was made of plastic filament and acted as a major element in minimizing the FFA content in SPO. To evaluate the reduced level of FFAs using both methods, five independent factors were varied: methanol content, sulphuric acid content (H₂SO₄), hole diameter, hole depth, and rotor speed. The first-step conditions for the esterification process included 60.8 vol% methanol content, 7.2 vol% H₂SO₄ content, 5.0 mm diameter of the hole, 6.1 mm depth of the hole, and 3000 rpm speed of the rotor. The initial free fatty acid content decreased from 89.16 wt% to 35.00 wt% by the predictive model, while 36.69 wt% FFA level and 94.4 vol% washed first-esterified oil yield were obtained from an actual experiment. In the second-step, 1.0 wt% FFA was achieved under the following conditions: 44.5 vol% methanol content, 3.0 vol% H₂SO₄ content, 4.6 mm hole diameter, 5.8 mm hole depth, and 3000 rpm rotor speed. The actual experiment produced 0.94 wt% FFA content and 93.9 vol% washed second-esterified oil yield. The entire process required an average electricity of 0.137 kWh/L to reduce the FFA level in the SPO below 1 wt%.     

Grafting polyelectrolytes onto polyacrylamide for flocculation 2. Model suspension flocculation and sludge dewatering

Low-molecular-weight high-charge-density cationic poly(diallyldimethylammonium chloride) (polyDADMAC) was grafted onto high-molecular-weight nonionic polyacrylamide (PAM) via a free radical mechanism using a gamma radiation technique. The graft copolymers having various charge densities were evaluated as flocculants for titanium dioxide (TiO₂) model suspensions, and as conditioners for a pulp and paper mill sludge. Their flocculation performance was optimized with respect to polymer composition, gamma irradiation time and polymer dosage. Measurements included turbidity, particle size distribution and drainage rates. The graft copolymers showed a significant improvement over the homopolymers and dual polymer systems in their flocculation and sludge dewatering performance. Received: 6 April 1998 Accepted in revised form: 28 August 1998     

Optimizing the synergistic effect of sodium hydroxide/ultrasound pre-treatment of sludge

Ultrasound (ULS), sodium hydroxide (NaOH) and combined ultrasound/NaOH pre-treatment were applied to pre-treat waste activated sludge and improve the subsequent anaerobic digestion. Synergistic effect was observed when NaOH treatment was coupled with ultrasound treatment. The highest synergistic Chemical Oxygen Demand (COD) solubilization was observed when 0.02M NaOH was combined with five minutes ultrasonication: an extra 3000 mg/L was achieved on top of the NaOH (1975 mg/L) and ultrasonication (2900 mg/L) treatment alone. Further increase of NaOH dosage increased Soluble Chemical Oxygen Demand (SCOD), but did not increase the synergistic effect. Nine and 18 minutes ultrasonication led to 20% and 24% increase of methane production, respectively; Whereas, 0.05M NaOH pre-treatment did not improve the sludge biodegradability. Combined ultrasound/NaOH (9 min+0.05 M) showed 31% increase of methane production. A stepwise NaOH addition/ultrasound pre-treatment (0.02M+ULS for 5 min+0.02M+ULS for 4 min) was tested and resulted in 40% increase of methane production using 20% less chemicals.     

Selected drugs in solid matrices: a review of environmental determination, occurrence and properties of principal substances

After intake, drugs absorbed by human or animal organisms are subject to metabolic reactions, such as hydroxylation, cleavage or glucuronation. However, a significant amount of the original or the metabolized substance leaves the organism via urine or feces. Thanks to improvements in analytical chemistry, many pharmaceutical compounds and endocrine disrupters are more easily detected in the surface-water and waste-water environmental compartments, at ppb concentrations.But what contaminates our solid environmental matrices? These substances can be eliminated by sorption or biodegradation but, at present, there is not enough data to allow evaluation of the behavior of the substances through the solid compartment, such as soil, sludge and bio-waste.This article provides an overview of the occurrence of pharmaceutical compounds in solid matrices on the basis of the quantities used, their physico-chemical properties and data from literature indicating the potential of the drug to persist in sediment, soil or sludge.     

Analysis of perfluorinated chemicals in sludge: Method development and initial results

A fast, rigorous method was developed to maximize the extraction efficacy for ten perfluorocarboxylic acids and perfluorooctanesulfonate from waste-water-treatment sludge and to quantitate using liquid chromatography, tandem-mass spectrometry (LC/MS/MS). First, organic solvents were tested for extraction efficiency, including acetonitrile (ACN), methanol (MeOH), isopropanol (IPA), tetrahydrofuran (THF), and 50/50 ACN/MeOH (v/v). Among the extractants tested, 50/50 ACN/MeOH yielded the best results for our combined criteria of extraction efficacy and solvent-handling convenience. Second, chemical pretreatment prior to solvent extraction was tested with sodium hydroxide (NaOH), potassium hydroxide (KOH), hydrochloric acid (HCl), and potassium persulfate (K₂S₂O₈). Pretreatment with NaOH and HCl effectively recovered additional PFCs from the sludge, but KOH and K₂S₂O₈ digestion were less effective than no pretreatment. Third, cleanup methods were investigated with solid-phase extraction using HLB (hydrophilic–lipophilic balanced) and WAX (weak-anion exchange) stationary phases, and with ion-pairing. The HLB stationary phase yielded a slight edge over the other two cleanup strategies in terms of recoverable PFCs and chromatographic separation. Finally, the appropriateness of isotopically labeled PFCs for quantitating unlabeled PFCs using isotopic dilution in complex sludge extracts was evaluated by comparison to results obtained with the standard-addition method. A National Institute of Standards and Technology (NIST) domestic sludge (CRM 2781) was analyzed using our finalized method and compared with previously reported results.     

Determination of nonylphenol and nonylphenol ethoxylates in wastewater using MEKC

Nonylphenol ethoxylates (NPEO_x) are surfactants which are used worldwide and can be transformed in the environment by microorganisms to form nonylphenol (NP). Analysis of these compounds was carried out with micellar electrokinetic capillary chromatography (MEKC). Different parameters such as background electrolyte (BGE) solution, pH, type of surfactant, and sample stacking were optimized. The use of CHES (20 mM, pH 9.1) in combination with 50 mM sodium cholate as a surfactant as BGE solution, together with sample stacking using 50 mM NaCl in the sample and an injection time of 20 s, provided the best separation of the compounds studied. The method was applied to the determination of target analytes in two types of sludge water coming from two steps of a wastewater treatment plant. Liquid–liquid extraction was carried out using toluene as solvent, resulting in recoveries around 100% for all studied analytes. The presence of NPEO_x was observed in the first step of the sludge water treatment, based on migration time and UV spectra. Identification was confirmed using tandem MS. LOQs of the studied compounds were in the range of 12.7 to 30.8 ng/mL, which is satisfactory for the analysis of real wastewater samples.