Enhancing chemical phosphorus precipitation from tapioca starch anaerobic digestion effluent in a modified pilot-scale fluidized bed reactor.

This study aimed to evaluate the possibility of P precipitation as struvite from real anaerobic digestion (AD) effluent of tapioca starch processing. The results showed that at a pH of 9, and without Mg:P molar adjustment, P recovery was at 85%. The percentage of P recovery was increased to 90% and P contained in precipitates was at 11.80-14.70 wt% P, which is higher than commercial single superphosphate fertilizer (SSP, 18-22 wt% P2O5). This was achieved by controlling mixing at 200-400 rpm and upflow velocity at 50-200 cm min-1 inside a fluidized bed reactor (FBR). Based on SEM-EDX, powder XRD, phase identification by profile matching, and FT-IR analysis, the results demonstrated that recovered precipitates formed struvite predominantly. In addition, results of the woodchip ash additions and the one-way ANOVA based-RSM analysis revealed that mixing, the solution pH, and the woodchip ash intensely affected P recovery with the optimum condition found at 400 rpm, pH9, 4 g L-1, respectively. Ash addition enhanced P recovery efficiency but decreased the product's purity. Total costs of P recovery varied considerably from 0.28 to 7.82 USD∙(kg P)-1 depending on chemical consumption and %P content in recovered products. Moreover, the total cost was reduced by 57% from 7.82 USD∙(kg P)-1 (profit margin: -4.30 to -2.82) by a single mixing operation to 3.35 USD∙(kg P)-1 (profit margin: +0.17 to +1.65) employing coupling effect of mixing and Vup. The results indicate that P recovery from tapioca starch AD effluent not only provides a good-quality alternative slow-release P fertilizer, but also helps to curtail environmental problems due to excessive P and nitrogen discharge. These findings also demonstrate the ways of recovering nutrients from an abundant renewable resource that are relevant to simultaneous waste utilization during pollution controls.

Enhancing anaerobic co-digestion of primary settled-nightsoil sludge and food waste for phosphorus extraction and biogas production: effect of operating parameters and determining phosphorus transformation.

The study aimed to comprehensively determine P extraction efficiency and co-digestion of food waste (FW) and primary settled-nightsoil sludge (PSNS) process performance influenced by different hydraulic retention times (4, 7, 10, and 15 days) and mixture ratios of FW:PSNS in substrates (100:0, 75:25, 50:50, 25:75, and 0:100). P-transformation was evaluated to identify P fractionation in both supernatant and sludge accumulated in reactors. The results showed that anaerobic co-digestion was inhibited by the accumulation of undigested feedstock due to higher %PSNS found in AD4 (25FW:75PSNS) and AD5 (100PSNS). A more stable process was found in AD2 (75FW:25PSNS) under hydraulic retention time (HRT) 15 days in which COD removal efficiency and P release were 97.2 and 80.2%, respectively. This recommended condition allowed a high organic loading rate (OLR) at 12 gVS/L/day resulting in the highest biogas yield of 0.93 L/L/day. Distribution of P data demonstrated that most of P in feedstock was deposited and accumulated in sediment up to 97.8%. Poor biodegradability resulting from using shortened HRT led to high increased P-solid content in effluent. In addition, available P in effluents and accumulated P-solids in sediment obtained from the AcoD process has the potential to serve as sources for P recovery.

Bisphenol A removal from a plastic industry wastewater by Dracaena sanderiana endophytic bacteria and Bacillus cereus NI.

Understanding the significance of plant-endophytic bacteria for bisphenol A (BPA) removal is of importance for any application of organic pollutant phytoremediation. In this research, Dracaena sanderiana with endophytic Pantoea dispersa showed higher BPA removal than uninoculated plants at 89.54 ± 0.88% and 79.08 ± 1.20%, respectively. Quantitative Real-Time PCR (qPCR) showed that P. dispersa increased from 3.93 × 107 to 8.80 × 107 16S rRNA gene copy number in root tissues from day 0 to day 5 which indicated that it could assist the plant in removing BPA during the treatment period. pH, chemical oxygen demand (COD), biochemical oxygen demand (BOD), total dissolved solids (TDS), conductivity, and salinity were reduced after 5 days of the experimental period. Particularly, BOD significantly decreased due to activities of the plants and microorganisms. Furthermore, an indigenous bacterial strain, Bacillus cereus NI, from the wastewater could remove BPA in high TDS and alkalinity condition of the wastewater. This work suggests that D. sanderiana plants could be used as a tertiary process in a wastewater treatment system and should be combined with its endophytic bacteria. In addition, B. cereus NI could also be applied for BPA removal from wastewaters with high TDS and salinity.

Human exposure to phthalates from house dust in Bangkok, Thailand.

The study determined concentrations of and estimated human exposure to house dust-ingested phthalates from 99 homes in Bangkok, Thailand. Phthalates in dust collected using a handheld vacuum cleaner was analyzed by gas chromatography/mass spectrometry revealing a median content of 3,477 µg g-1, range 753-13,810 µg g-1, with di-2-ethylhexylphthalate (DEHP) having the highest level (median = 1,739 µg g-1, range 467-8,172 µg g-1) followed by di-iso-nonyl phthalate (DiNP) (median = 611 µg g-1, range 15.2-11,052 µg g-1). DEHP in house dust from multi-family apartments with polyvinyl (PVC) floor material (n = 34), multi-family apartments without PVC floor material (n = 55) and single family houses without PVC floor material (n = 10) was median and range 3,009 and 568-6,898; 1,479 and range 467-8,172 and 1,207 µg g-1 and 611-3518 µg g-1, respectively. At high-end house dust DEHP level, preschool children in all three types of homes were exposed above US Environment Protection Agency reference dose (20 µg g-1). The results suggest phthalate-containing house products constitute a likely major source of phthalates in indoor home environment and pose a potential health risk to residents, particularly preschool children, in Bangkok.

Kinetics of trihalomethane formation from organic contaminants in raw water from the Bangkhen water treatment plant.

The fractionation of raw water from Bangkhen water treatment plant, Bangkok, Thailand revealed that the mass distribution sequence of the six organic fractions from high to low was hydrophilic neutral (HPIN), hydrophobic acid (HPOA), hydrophilic acid, hydrophobic neutral, hydrophilic base, and hydrophobic base. The main organic matter components in raw water were HPIN and HPOA, which were also the two most important contributors of trihalomethane formation potential (THMFP). Linear dependencies between the level of each organic fraction and the formation potential of THM species were observed, which suggested the reactions between the organic fraction and chlorine during the chlorination were first order. The fractionation led to a deviation of bromide concentration in each organic fraction from the original concentration, and this affected the formation of brominated THM species. However, this effect was demonstrated to be within an acceptable range. The chlorination of an individual organic fraction resulted in a higher level of THMFP than that of the raw water and mixed fractions, indicating an inhibitory effect between the organic species.

Characterization of precursors to trihalomethanes formation in Bangkok source water.

Resin adsorption techniques using three types of resin (DAX-8, AG-MP-50, and WA-10) were employed to characterize the raw water (RW) from the major 3 million m3/day (793 million gal/day) drinking water treatment plant in Bangkok, Thailand. The dissolved organic carbon (DOC) mass distribution sequences of the six organic fractions in raw water, from high to low, were hydrophilic neutral (HPIN), hydrophobic acid (HPOA), hydrophilic acid (HPIA), hydrophobic neutral (HPON), hydrophilic base (HPIB), and hydrophobic base (HPOB). HPIN and HPOA were the two main precursors for trihalomethanes formation (THMFP) in this water source following chlorination. The chlorination of HPON and HPIN fractions only led to the formation of mostly chloroform, while other organic fractions formed both chloroform and bromodichloromethane. The linear dependency between each organic fraction concentration and THMFP indicated that the reactions of each organic fraction with chlorine were first-order.