Hydrothermal carbonization (HTC) technology can convert various types of waste biomass into a carbon-rich product referred to as hydrochar. In order to verify the potential of hydrochar produced from stabilized sewage sludge to be an adsorbent for bacterial pathogen removal in water treatment, the Escherichia coli's removal efficiency was determined by using 10 cm sand columns loaded with 1.5% (w/w) hydrochar. Furthermore, the removal of E. coli based on intermittent operation in larger columns of 50 cm was measured for 30 days. Since the removal of E. coli was not sufficient when the sand columns were supplemented with raw hydrochar, an additional cold-alkali activation of the hydrochar using potassium hydroxide was applied. This enabled more than 90% of E. coli removal in both the 10 cm and 50 cm column experiments. The enhancement of the E. coli removal efficiency could be attributed to the more hydrophobic surface of the KOH pre-treated hydrochar. The idle time during the intermittent flushing experiments in the sand-only columns without the hydrochar supplement had a significant effect on the E. coli removal (p < 0.05), resulting in a removal efficiency of 55.2%. This research suggested the possible utilization of hydrochar produced from sewage sludge as an adsorbent in water treatment for the removal of bacterial contaminants.@en

Hydrothermal carbonization technology can convert fecal waste into a valuable carbonaceous product referred to as hydrochar. We investigated the potential of fecal waste-derived hydrochar as an adsorbent for virus removal in water treatment. Swine feces was hydrothermally treated under two conditions: at 180 °C for 2 h and 230 °C for 7 h. The resulting solid products (hydrochar) were evaluated as virus adsorbents in water treatment. Simultaneous removal of pathogenic rotavirus (RV) and human adenovirus (HAdV) was investigated using a sand column set-up of 10 cm bed height with and without hydrochar supplement (1.5%, w/w). The removal efficiency of both viruses in a hydrochar-amended column was >3 log (complete removal). The amount of virus released in deionized water when flushed into the virus-retaining columns indicated that the secondary energy minimum played a more important role in RV retention than that of HAdV. Zeta-potential and hydrophobicity measurements on hydrochar materials indicated that the improved virus removal performance of hydrochar-amended columns was induced by the provision of extra hydrophobic surfaces. This study provides evidence that fecal waste-derived hydrochar can be used as a competent virus adsorbent.

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Aims: To determine the pathogenic virus removal performance of an adsorbent produced from hydrothermal carbonization of sewage sludge. Methods and Results: The removal of human pathogenic rotavirus and adenovirus was investigated with columns of 10 cm saturated sand with and without amendments of 1·5% (w/w) hydrochar. Virus concentrations were determined with reverse transcription (RT) quantitative polymerase chain reaction (qPCR). The experiments with sand showed 1 log removal, while the columns with 1·5% (w/w) hydrochar amendment showed 2 to >3 log removal for both viruses. Deionized (DI) water flushing into the virus-retaining columns revealed that the secondary energy minimum played a larger role in the attachment of rotavirus onto hydrochar surfaces than adenovirus. Improved virus removal may be attributed to the introduction of hydrophobic and/or meso-macro surface structures of the hydrochar providing favourable attachment sites for viruses. Conclusions: Hydrochar amended sand beds showed improved virus removal efficiencies exceeding 99·6% corresponding to 2·4 log removal. The addition of humic acid in the influent did not hinder the adsorptive removal of viruses. Significance and Impact of the Study: This study suggests that hydrochar derived from sewage sludge can be used as an adsorbent for virus removal in water treatment.

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Sanitation in urban slums, especially in countries in Sub-Saharan Africa, is a challenge. One of the solutions to sanitation is to valorize waste, and to convert bio-waste present in the slum in a cheap and affordable way into lignite via hydrothermal carbonization (HTC). HTC is simple, cheap, converts all carbon (100%), eliminates pathogens completely, and requires wet starting products/biomass, thereby avoiding complicated drying schemes. In this research, we investigated the effectiveness of removing a divalent metal-ion, cadmium, using equilibrium batch experiments and columns of sand-supported hydrothermally carbonized colloidal lignite (HTCCL) derived from sugar, maize, and grass. Our results indicated that equilibrium sorption could be best described by a Langmuir isotherm. The uptake capacity varied from 0.11 to 0.21 mg Cd/g HTC, dependent on the type of HTC used. These values were relatively low compared to other carbonaceous sorbents. However, removal efficiencies in column experiments were remarkably high: 70-100% during 20-24 pore volumes or bed volumes of flushing. We concluded that HTCCL is a promising sorbent that can be used to treat heavily polluted water and/or wastewater.

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Despite numerous studies on hydrochar use, its application in water treatment for pathogen removal remains unexplored. In this study, we evaluated the efficiency of hydrochar produced from crop residue of maize for water treatment by determining Escherchia coli breakthrough from sand columns supplemented with hydrochar. To enhance the adsorptive capacity, raw hydrochar was activated by 1 mol L^-1 KOH at room temperature. The experiments conducted in a 10-cm sand bed with 1.5% (w/w) activated and raw hydrochar supplements, not activated by KOH, showed 93 and 72% of E. coli removal efficiencies, respectively. Activation of KOH not only enhanced the E. coli removal but also increased the strength of the attachment: 96% of the E. coli retained in the column with activated hydrochar supplements was shown to be irreversibly attached, compared with only 65% for the raw hydrochar. Scanning electron microscopy/energy-dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, and zeta-potential analyses suggested that these improvements were mainly due to the development of a wellformed porous surface structure and less negative surface charges on the activated hydrochar.

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The presence of viruses in a slum environment where sanitation is poor is a major concern. However, little is known of their occurrence and genomic copy concentration in the slum environment. The main objective of this study was to determine the genomic copy concentrations of human adenoviruses F and G, Rotavirus (RV), Hepatitis A virus (HAV), Hepatitis E virus (HEV) and human adenovirus species A,C,D,E, and F (HAdV-ACDEF) in Bwaise III, a typical slum in Kampala, Uganda. Forty-one samples from surface water, grey water and ground water were collected from 30 sampling locations. The virus particles were recovered by glass wool filtration with elution using beef extract. DNA and RNA viruses were detected by the real time quantitative polymerase chain reaction (qPCR) and the reverse transcription-qPCR (RT-qPCR), respectively. HAdV-F and G were detected in 70.7% of the samples with concentrations up to 2.65 × 101 genomic copies per mL (gc mL-1). RV and HAV were detected in 60.9% and 17.1% of the samples, respectively. The maximum concentration of RV was 1.87 × 102 gc mL-1. In addition, 78% of the samples tested positive for the HAdV-ACDEF, but all samples tested negative for HEV. These new data are essential for quantitative microbial risk assessment, and for understanding the effects of environmental pollution in slums.@en

Commercial kits to determine RNA concentrations are expensive, and sometimes too expensive for laboratories working with tight budgets, especially those in developing countries. We developed, tested, and evaluated two home-made two-step reverse transcription-quantitative polymerase chain reaction assays aimed to detect rotavirus in surface water samples. A commercial one-step master kit was used for comparison. Our results indicated that the efficiency of the home-made assays was comparable to the commercial kit. Furthermore, the lowest detection limit of all assays corresponded to 10^-0.2 TCID₅₀ (50 % tissue Culture Infective Dose) per ml. The home-made assays were able to detect rotavirus concentrations in complex surface waters in a slum area in Kampala (Uganda) and their performance was comparable to the commercial kit. The total costs of the two home-made assays was 11 times less than the selected commercial kit. Although preparing home-made assays is more time consuming, the assays can be useful for cases in which consumable costs are more important than personnel costs.

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