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      Scattered and transmitted light as surrogates for activated carbon residual in advanced wastewater treatment processes: Investigating the influence of particle size

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          Highlights

          • Turbidity showed a linear correlation with activated carbon concentration.

          • The smaller the activated carbon size, the greater the turbidity.

          • The original wastewater turbidity led to a parallel shift in the linear correlation.

          • Coagulants change the turbidity at same activated carbon concentration.

          Abstract

          The use of powdered activated carbon (PAC) is a common process in advanced wastewater treatment to remove micropollutants. Retention and separation of PAC is essential as PAC loaded with micropollutants should not be released into the environment. Determining the activated carbon (AC) residual in the effluent poses a challenge, as there is currently no on-line measurement method. In this study, the correlation between turbidity, measured by scattered light, and absorption at wavelength of 550 nm (Absorption 550 nm), measured by transmitted light, was investigated in relation to the AC residue. Linear correlations for turbidity (R 2 = 0.95) and Absorption 550 nm (R 2 = 1.00) to AC concentrations were observed in both laboratory and full-scale experiments in a pilot plant where superfine PAC was added prior to Pile Cloth Media Filtration (PCMF). Decreasing the particle size (d 50) while maintaining the same AC concentration leads to increased turbidity: Therefore, a fourfold reduction in d 50 results in a 2- to 3-fold increase in turbidity, whereas a 30-fold reduction in d 50 leads to a 6-to 8-fold increase. Furthermore, the original wastewater turbidity led to a parallel shift in the linear correlation between turbidity and AC. Coagulant doses of up to 400 mg Me 3+/g AC resulted in a 50% reduction in turbidity. However, higher concentrations from 400 to 1,000 mg Me 3+/g AC resulted in increased turbidity with only a 30% reduction compared to the initial turbidity. The study also highlights the significance of AC particle size in optical measurements, impacting result accuracy.

          Abstract

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          Most cited references20

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          Aggregation and disaggregation of iron oxide nanoparticles: Influence of particle concentration, pH and natural organic matter.

          The surface coating, aggregation behavior and aggregate structure of unpurified iron oxide nanoparticles (NPs) at variable pH and in the absence and presence of natural organic matter (NOM, Suwannee River humic acid, SRHA) have been previously studied in Baalousha et al. [Baalousha, M., Manciulea, A., Cumberland, S., Kendall, K., Lead, J.R., Aggregation and surface properties of iron oxide nanoparticles; influence of pH and natural organic matter. Environ Toxicol Chem 2008; 27: 1875-1882.]. Here the aggregation behavior of iron oxide NPs at variable concentrations of NPs and SRHA, and the disaggregation behavior of iron oxide NP aggregates in the absence and presence of SRHA are investigated. The increase of NP concentration enhances their aggregation, particularly at pH values close to the point of zero charge (PZC). High concentration of SRHA (100 mg l(-1)) shifts the NP (100 mg l(-1)) PZC charge and aggregation maximum towards lower pHs, while low concentration (10 mg l(-1)) shows low or no effect. The disaggregation behavior of iron oxide NP aggregates was investigated at pH 7 and at increasing concentrations of SRHA. High concentrations (50 and 100 mg l(-1)) of SRHA induced the disaggregation of iron oxide NP aggregates with time, which was not the case at lower concentrations (10 mg l(-1)) or in the absence of SRHA. The disaggregation was triggered by the enhanced surface charge induced by the sorption of SRHA molecules. The disaggregation rate increased with SRHA concentration and decreased with time. Two regimes of disaggregation were identified, a fast regime of "fragmentation" at the first 15 days of the experiment and a slow regime of "erosion" afterwards. The formation of small aggregates of about 170 nm and surface coating of several nanometers of SRHA on iron oxide NPs confirm the role of NOM in the disaggregation process and indicate that NPs might mimic the behavior of natural colloids.
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            Removal of micropollutants in municipal wastewater treatment plants by powder-activated carbon.

            Micropollutants (MP) are only partly removed from municipal wastewater by nutrient removal plants and are seen increasingly as a threat to aquatic ecosystems and to the safety of drinking water resources. The addition of powder activated carbon (PAC) is a promising technology to complement municipal nutrient removal plants in order to achieve a significant reduction of MPs and ecotoxicity in receiving waters. This paper presents the salient outcomes of pilot- and full-scale applications of PAC addition in different flow schemes for micropollutant removal in municipal wastewater treatment plants (WWTPs). The sorption efficiency of PAC is reduced with increasing dissolved organic carbon (DOC). Adequate treatment of secondary effluent with 5-10 g DOC m(-3) requires 10-20 g PAC m(-3) of effluent. Counter-current use of PAC by recycling waste PAC from post-treatment in a contact tank with an additional clarifier to the biology tank improved the overall MP removal by 10 to 50% compared with effluent PAC application alone. A dosage of 15 g PAC m(-3) to a full-scale flocculation sand filtration system and recycling the backwash water to the biology tank showed similar MP elimination. Due to an adequate mixing regime and the addition of adapted flocculants, a good retention of the fine fraction of the PAC in the deep-bed filter were observed (1-3 g TSS m(-3); TSS: total suspended solids). With double use of PAC, only half of the PAC was required to reach MP removal efficiencies similar to the direct single dosage of PAC to the biology tank. Overall, the application of PAC in WWTPs seems to be an adequate and feasible technology for efficient MP elimination (>80%) from wastewater comparable with post ozonation.
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              A Review of Pharmaceuticals and Endocrine-Disrupting Compounds: Sources, Effects, Removal, and Detections

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                Author and article information

                Contributors
                Journal
                Water Res X
                Water Res X
                Water Research X
                Elsevier
                2589-9147
                09 April 2024
                01 May 2024
                09 April 2024
                : 23
                : 100222
                Affiliations
                [a ]Department of Civil and Environmental Engineering Sciences, Institute IWAR, Chair of Water and Environmental Biotechnology, Technical University of Darmstadt, Germany
                [b ]Mecana AG, Industriestrasse 39, 8864 Reichenburg, Switzerland
                [c ]Institute for Ecopreneurship, School of Life Sciences FHNW, Hofackerstraße 30, 4132 Muttez, Switzerland
                Author notes
                [* ]Corresponding author. s.lackner@ 123456iwar.tu-darmstadt.de
                Article
                S2589-9147(24)00012-4 100222
                10.1016/j.wroa.2024.100222
                11031823
                38646065
                09e021cd-83c7-4f5e-85f9-d5807e07a5b2
                © 2024 The Author(s)

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 8 January 2024
                : 5 April 2024
                : 8 April 2024
                Categories
                Full Paper

                adsorption,pile cloth media filtration,superfine powdered activated carbon,filtration,tertiary wastewater treatment,flocculation

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