Applicability of zirconium loaded okara in the removal and recovery of phosphorus from municipal wastewater

© 2019 Published under licence by IOP Publishing Ltd. Recently, there is a new trend to consider wastewater as a precious resource. Since phosphorus is a limited non-renewable element, and MAP (Magnesium Ammonium Phosphate - MgNH4PO4.6H2O) is a valuable slow-release fertilizer, the recovery of phosphorous as MAP has received special attention from scientists all over the world. However, the application of this process with municipal wastewater is still a challenge, due to low concentration of phosphorus and high volume of municipal wastewater. This study investigates the potential of reclaiming MAP from municipal wastewater by combination of adsorption and crystallization. Soybean milk residue (okara) was loaded with Zirconium (Zr) to prepare the adsorbent (ZLO). Adsorption and desorption experiments were conducted in a semi-pilot scale ZLO packed colum system. Effects of P: N: Mg molar ratios, chemical sources and temperature on the formation of MAP were examined in an attempt to identify the optimal crystallization conditions. The attained precipitate was characterized using XRD, SEM, FTIR techniques. It was found that the ZLO packed column adsorption-desorption system could pre-concentrate phosphorus from municipal wastewater up to 28.36 times, fitting well the minimum requirement (50 mg P/L) for the economical MAP recovery. Up to 95.19% of dissolved phosphorus in desorption solution was recovered at pH = 9, Mg: N: P molar ratio = 2:2:1, using a combination of MgCl2.6H2O and NH4Cl. The harvested MAP exhibited high purity (92.59%), high P-availability (89% by mass), and extremely low levels of heavy metals. The results prove that it is viable to recover MAP from municipal wastewater by employing ZLO as adsorbent, followed by crystallization. This paves the way for mining phosphorus from municipal wastewater and reducing okara as an agricultural byproduct in a green way

Low-cost laterite-laden household filters for removing arsenic from groundwater in Vietnam and waste management

This study evaluated the performance of a low-cost natural laterite from Thach That (NLTT), Vietnam, for its capacity to remove arsenic (As) in a household filter with contaminated groundwater. The NLTT was initially tested in a laboratory column trial lasting 800 h. The breakthrough curves were found to fit the Thomas model very satisfactorily with adsorption capacities of 0.06 and 0.20 mg/g at a flow velocity of 0.85 m/h for the influent As(V) concentrations of 0.1 and 0.5 mg/L, respectively. In household filters at four sites, the median As concentration in groundwaters (0.04–0.19 mg/L) dropped to 0.026–0.054 mg/L after traditional sand filtration. However, following subsequent NLTT filtration through columns (14 cm inner diameter, 65 cm height) at 0.65 m/h flow velocity, it fell to below the Vietnam and WHO drinking water standard (0.01 mg/L) during seven months of continuous operation. Portland cement and lime were tested as binding agents for the exhausted NLTT waste in a solidification/stabilization process at different ratios. The best ratio of exhausted NLTT: Portland cement: lime for restraining mobility of As from this waste was 3:1:0.5. The concrete brick products exhibited a suitable compressive strength for using it as building materials in construction work

White hard clam (Meretrix lyrata) shells media to improve phosphorus removal in lab-scale horizontal sub-surface flow constructed wetlands: Performance, removal pathways, and lifespan.

This work examined the phosphorus (P) removal from the synthetic pretreated swine wastewater using lab-scale horizontal sub-surface flow constructed wetlands (HSSF-CWs). White hard clam (Meretrix lyrata) shells (WHC) and Paspalum atratum were utilized as substrate and plant, respectively. The focus was placed on treatment performance, removal mechanisms and lifespan of the HSSF-CWs. Results indicated that WHC-based HSSF-CW with P. atratum exhibited a high P removal (89.9%). The mean P efluent concentration and P removal rate were 1.34 ± 0.95 mg/L and 0.32 ± 0.03 g/m2/d, respectively. The mass balance study showed that media sorption was the dominant P removal pathway (77.5%), followed by microbial assimilation (14.5%), plant uptake (5.4%), and other processes (2.6%). It was estimated the WHC-based bed could work effectively for approximately 2.84 years. This WHC-based HSSF-CWs technology will therefore pave the way for recycling Ca-rich waste materials as media in HSSF-CWs to enhance P-rich wastewater purification

Heterogeneous catalyst ozonation of Direct Black 22 from aqueous solution in the presence of metal slags originating from industrial solid wastes

© 2019 Elsevier B.V. This study developed a low cost catalyst, namely, zinc slag (Zn-S) for the ozonation process of Direct Black 22 (DB22) from aqueous solutions. Among five different kind of low cost metal slags including Fe-S, Cu-S, Cd-S, Pb-S and Zn-S, the Zn-S slag was selected as an efficient catalyst in this study. Zn-S contained mainly zinc (Zn) and calcium (Ca) discharged from zinc slag waste in Vietnam. It was found that Zn-S could effectively decolonize and mineralize DB22 through heterogeneous catalytic ozonation. The degradation kinetic of DB22 followed the pseudo-first order model. The best removal efficiency of DB22 (Zn-S/O3/H2O2 (76%) > Zn-S/O3 (69%) > O3/H2O2 (66%) > O3 (55% for COD) occurred at pH 11 for heterogeneous catalytic ozonation processes with Zn-S as the catalyst as well as ozone alone and perozone processes due to fast decomposition of O3 in alkaline solution to generate powerful and non-selective OH radicals. An increase in decolonization and mineralization rate was observed when increasing the Zn-S dosage from 0.125 g/L to 0.75 g/L for Zn-S/O3 and 0.125 g/L to 1.0 g/L for Zn-S/O3/H2O2. The K values of the pseudo-first order model followed the same sequence as mineralization rates of DB22 in term of COD removal. Ca and Zn constituents in the Zn-S catalyst contributed to the increase in O3 decomposition and improvement of reaction rate with H2O2. Subsequently, the degradation of DB22 by the ozonation process with Zn-S catalyst was enhanced through the enrichment mechanism of hydroxyl radicals (*OH) and surface adsorption. The degradation mechanism of DB22 by hydroxyl radicals was surely affirmed by tests with the decrease in degradation percentage of DB22 in case of the presence t-butanol, Cl− and CO32−

Hybrid use of coal slag and calcined ferralsol as wetland substrate for improving phosphorus removal from wastewater

In this study, natural ferralsol (NF) was calcined to enhance its phosphorus (P) adsorption. The NF and calcined ferralsol at the selected temperature (CF500) were characterized by SEM, FTIR, XRD, XRF and other experiments to elucidate changes in morphology and physicochemical properties. CF500 and coal slag (CS) were examined as wetland media individually and combinedly. The applicability of CF500 and CS as the hybrid media in the lab–scale horizontal sub–surface flow constructed wetlands (HSSF–CWs) was evaluated. It was found that 500 °C was the best calcination temperature of NF for P adsorption. The maximum P adsorption capacity of CF500 (19.4 mg/g) was 60.4 ± 2.2 % greater than that of NF. While isotherm data of P sorption by CF500 were fitted both Langmuir and Freundlich models, the kinetic data was better described by Pseudo-second-order model. Thermodynamic parameters revealed the endothermic and spontaneous nature of the P sorption by CF500. The combination of CF500 and CS leveraged the merits of individual substrates while mitigated their demerits. The optimal mixing ratio of CF500 to CS was 1.25:1 by volume. The hybrid CF500–CS substrate HSSF–CWs demonstrated satisfactory P removal efficiency (99.44% ± 0.1) and effluent P concentration (0.08 ± 0.01 mg/L). Application of the mixed substrate in the HSSF–CWs resulted in negligible side effects on their effluent quality. Due to abundant availability of raw materials, simplicity of preparation, as well as efficiency and safety of application, a mixture of CF500 and CS is a promising hybrid substrate in HSSF–CWs for P–rich wastewater decontamination

White hard clam (Meretrix lyrata) shells as novel filter media to augment the phosphorus removal from wastewater.

It is well recognized that filter media play a crucial role in constructed wetlands (CWs) for decontamination of phosphorus (P)-rich wastewater. This study investigates the suitability of raw white hard clam shells (WHC) and white hard clam shells thermally modified at 800 °C (WHC-M800) as potential media to enhance P treatment performance in CWs. The results indicated that both WHC and WHC-M800 displayed appropriate physicochemical properties, such as high porosity, excellent hydraulic conductivity, and rich Ca content. WHC-M800 exhibited a superior P adsorption capacity (38.7 mg/g) to WHC (12.8 mg/g). However, the practical utilization of WHC-M800 as filter media in CWs may be compromised, due to certain limitations, for example: extremely high pH values in the post-adsorption solutions; high weight losses during calcination and adsorption processes; low mechanical strength; and intensive energy consumption. In contrast, the WHC demonstrated significant advantages of reasonably high P adsorption capacity, locally abundant availability, low cost, and marginal side effects. The fractionation of inorganic P of WHC and WHC-M800 revealed that Ca-bounded P was the most dominant binding form, followed by loosely bound P, Fe-P, occluded P, and Al-P. The present study demonstrates that recycling of WHC shells as a potential substrate in CWs provides a feasible method for upgrading P removal in CWs. Additionally, it helps to reduce waste WHC shells in a simple, cheap, and eco-friendly way, thus can double environmental benefits

Laterite as a low-cost adsorbent in a sustainable decentralized filtration system to remove arsenic from groundwater in Vietnam

© 2019 Elsevier B.V. In the Red River Delta, Vietnam, arsenic (As) contamination of groundwater is a serious problem where more than seventeen million people are affected. Millions of people in this area are unable to access clean water from the existing centralized water treatment systems. They also cannot afford to buy expensive household water filters. Similar dangerous situations exist in many other countries and for this reason there is an urgent need to develop a cost-effective decentralized filtration system using new low-cost adsorbents for removing arsenic. In this study, seven locally available low-cost materials were tested for arsenic removal by conducting batch adsorption experiments. Of these materials, a natural laterite (48.7% Fe2O3 and 18.2% Al2O3) from Thach That (NLTT) was deemed the most suitable adsorbent based on arsenic removal performance, local availability, stability/low risk and cost (US$ 0.10/kg). Results demonstrated that the adsorption process was less dependent on the solution pH from 2.0 to 10. The coexisting anions competed with As(III) and As(V) in the order, phosphate > silicate > bicarbonate > sulphate > chloride. The adsorption process reached a fast equilibrium at approximately 120–360 min, depending on the initial arsenic concentrations. The Langmuir maximum adsorption capacities of NLTT at 30 °C were 512 μg/g for As(III) and 580 μg/g for As(V), respectively. Thermodynamic study conducted at 10 °C, 30 °C, and 50 °C suggested that the adsorption process of As(III) and As(V) was spontaneous and endothermic in nature. A water filtration system packed with NLTT was tested in a childcare centre in the most disadvantaged community in Ha Nam province, Vietnam, to determine arsenic removal performance in an operation lasting six months. Findings showed that the system reduced total arsenic concentration in groundwater from 122 to 237 μg/L to below the Vietnam drinking water standard of 10 μg/L