Adsorption characteristics of S-Metolachlor onto the sawdust biochar derived from Acacia auriculiformis.

The adsorption mechanism of S-Metolachlor in an aqueous solution by sawdust biochar derived from Acacia auriculiformis (SAB) was studied. SAB was manufactured at 500 °C for 4 h under oxygen-limited conditions and characterized for SEM, EDS, pHpzc, BET, and FTIR. The adsorption kinetics, isotherm, and diffusion studies of S-Metolachlor and SAB were further explored. Moreover, the effects of the solution pH were examined on the adsorption of S-Metolachlor by SAB. The BET analysis of SAB was achieved at 106.74 m2.g-1 and the solution pH did not significantly influence the S-Metolachlor adsorption. The adsorption data were fitted into a Langmuir isotherm and the PSO model. The film diffusion coefficient Df (4.93 × 10-11 to 8.17 × 10-11 m2.s-1) and the particle diffusion coefficient Dp (1.68 × 10-11 to 2.65 × 10-11 m2.s-1) were determined and the rate-limiting step of S-Metolachlor adsorption and SAB was governed by liquid film diffusion. The S-Metolachlor adsorption process onto SAB was controlled by multiple mechanisms, including pore filling, H-bonding, hydrophobic interaction, and π-π EDA interactions. H-bonding is the main interaction for the adsorption of S-Metolachlor and SAB. Conclusively, the study illustrates that biochar produced from Acacia auriculiformis sawdust possessed effective adsorption properties for S-Metolachlor herbicide.

Direct growth of nano-worm-like Cu2S on copper mesh as a hierarchical 3D catalyst for Fenton-like degradation of an imidazolium room-temperature ionic liquid in water.

The increasing consumption of room-temperature ionic liquids (RTILs) inevitably releases RTILs into the water environment, posing serious threats to aquatic ecology due to the toxicities of RTILs. Thus, urgent needs are necessitated for developing useful processes for removing RTILs from water, and 1-butyl-3-methylimidazolium chloride (C4mimCl), the most common RTIL, would be the most representative RTIL for studying the removal of RTILs from water. As advanced oxidation processes with hydrogen peroxide (HP) are validated as useful approaches for eliminating emerging contaminants, developing advantageous heterogeneous catalysts for activating HP is the key to the successful degradation of C4mim. Herein, a hierarchical structure is fabricated by growing Cu2S on copper mesh (CSCM) utilizing CM as a Cu source. Compared to its precursor, CuO@CM, this CSCM exhibited tremendously higher catalytic activity for catalyzing HP to degrade C4mim efficiently because CSCM exhibits much more superior electrochemical properties and reactive sites, allowing CSCM to degrade C4mim rapidly. CSCM also exhibits a smaller Ea of C4mim elimination than all values in the literature. CSCM also shows a high capacity and stability for activating HP to degrade C4mim in the presence of NaCl and seawater. Besides, the mechanistic investigation of C4mim elimination by CSCM-activated HP has also been clarified and ascribed to OH and 1O2. The elimination route could also be examined and disclosed in detail through the quantum computational chemistry, confirming that CSCM is a useful catalyst for catalyzing HP to degrade RTILs.

Templating agent-mediated Cobalt oxide encapsulated in Mesoporous silica as an efficient oxone activator for elimination of toxic anionic azo dye in water: Mechanistic and DFT-assisted investigations.

While Azorubin S (AZRS) is extensively used as a reddish anionic azo dye for textiles and an alimentary colorant in food, AZRS is mutagenic/carcinogenic, and it shall be removed from dye-containing wastewaters. In view of advantages of SO4•--related chemical oxidation technology, oxone (KHSO5) would an ideal source of SO4•- for degrading AZRS, and heterogeneous Co3O4-based catalysts is required and shall be developed for activating oxone. Herein, a facile protocol is proposed for fabricating mesoporous silica (MS)-confined Co3O4 by a templating agent-mediated dry-grinding procedure. As the templating agent retained inside the ordered pores of MS (before calcination) would facilitate insertion and dispersion of Co ions into pores, the resulting Co3O4 nanoparticles (NPs) would be grown and confined within the pores of MS after calcination, affording Co@MS. On the contrary, another analogue, Co/MS, is also prepared using the similar protocol without the templating agent-mediated introduction of Co, but Co3O4 NPs seriously aggregate as clusters on MS. Therefore, Co@MS outperforms Co/MS for activating oxone to eliminate AZRS. Co@MS shows a noticeably lower activation energy of AZRS elimination than the existing catalysts, revealing its advantage over the reported catalysts. Moreover, the mechanistic investigation of AZRS elimination by Co@MS-activated oxone has been also elucidated for identifying the presence of SO4•‒, •OH, and 1O2 in AZRS degradation using scavengers, electron paramagnetic resonance spectroscopy, and semi-quantification. The AZRS decomposition pathway is also investigated and unveiled in details via the DFT calculation. These results validate that Co@MS appears as a superior catalyst of oxone activation for AZRS degradation.

Performance of a dual-chamber microbial fuel cell as a biosensor for in situ monitoring Bisphenol A in wastewater.

This research explores the possibilities of a dual-chamber microbial fuel cell as a biosensor to measure Bisphenol A (BPA) in wastewater. BPA is an organic compound and is considered to be an endocrine disruptor, affecting exposed organisms, the environment, and human health. The performance of the microbial fuel cells (MFCs) was first controlled with specific operational conditions (pH, temperature, fuel feeding rate, and organic loading rate) to obtain the best accuracy of the sensor signal. After that, BPA concentrations varying from 50 to 1000 µg L-1 were examined under the biosensor's cell voltage generation. The outcome illustrates that MFC generates the most power under the best possible conditions of neutral pH, 300 mg L-1 of COD, R 1000 Ω, and ambient temperature. In general, adding BPA improved the biosensor's cell voltage generation. A slight linear trend between voltage output generation and BPA concentration was observed with R2 0.96, which indicated that BPA in this particular concentration range did not real harm to the MFC's electrogenic bacteria. Scanning electron microscope (SEM) images revealed a better cover biofilm after BPA injection on the surface electrode compared to it without BPA. These results confirmed that electroactive biofilm-based MFCs can serve to detect BPA found in wastewaters.

Assessing changes in nicotine consumption over two years in a population of Hanoi by wastewater analysis with benchmarking biomarkers.

Monitoring the actual change in consumption of nicotine (a proxy for smoking) in the population is essential for formulating tobacco control policies. In recent years, wastewater-based epidemiology (WBE) has been applied as an alternative method to estimate changes in consumption of tobacco and other substances in different communities around the world, with high potential to be used in resource-scarce settings. This study aimed to conduct a WBE analysis in Hanoi, Vietnam, a lower-middle-income-country setting known for high smoking prevalence. Wastewater samples were collected at two sites along a sewage canal in Hanoi during three periods: Period 1 (September 2018), Period 2 (December 2018-January 2019), and Period 3 (December 2019-January 2020). Concentrations of cotinine, 3-hydroxycotinine, and nicotine ranged from 0.73 µg/L to 3.83 µg/L, from 1.09 µg/L to 5.07 µg/L, and from 0.97 µg/L to 9.90 µg/L, respectively. The average mass load of cotinine estimated for our samples was 0.45 ± 0.09 mg/day/person, which corresponds to an estimated daily nicotine consumption of 1.28 ± 0.25 mg/day/person. No weekly trend was detected over the three monitoring periods. We found the amount of nicotine consumption in Period 1 to be significantly lower than in Period 2 and Period 3. Our WBE estimates of smoking prevalence were slightly lower than the survey data. The analysis of benchmarking biomarkers confirmed that cotinine was stable in the samples similar to acesulfame, while paracetamol degraded along the sewer canal. Further refinement of the WBE approach may be required to improve the accuracy of analyzing tobacco consumption in the poor sewage infrastructure setting of Vietnam.

Ultrasound process-enhanced removal of the toxic disinfection by-product bromate from water by aluminum: A comparative study.

As bromate removal and reduction can be also achieved using metals, aluminum (Al) appears as the most promising one for reduction of bromate because Al is abundant element and exhibits a high reduction power. Reactions between bromate and Al shall be even enhanced through ultrasound (US) process because US can facilitate mass transfer on liquid/solid interfaces and clean surfaces via generating microscale turbulence to facilitate reactions. Therefore, the aim of this study is for the first time to investigate the effect of US on bromate removal by Al metal. Specifically, Al particle would be treated by HCl to afford HCl-treated Al (HCTAL), which is capable of removing bromate and even reducing it to bromide. Such a mechanism is also validated by density function theory calculation through determining adsorption energy as -152.8 kJ/mole, and oxygen atoms of bromate would be extracted and reacted with Al atoms, releasing bromide ion. US not only facilitated bromate removal by further increasing removal capacity under the acidic condition but also suppressed the inhibitive effect from basicity at relatively high pH. The spent HCTAL could still remove bromate and convert it to bromide after regeneration. These features indicate that US considerably enhances bromate removal by Al. PRACTITIONER POINTS: Bromate removed by Al is elucidated by DFT calculation with Eabsorption = -152.8 kJ/mole. Oxygen atoms of bromate are extracted and reacted with Al atoms, releasing bromide ion. A higher power of ultrasound would substantially enhance bromate removal efficiency. Ultrasound also suppresses the inhibitive effect from basicity at relatively high pH. With ultrasound, the interference of co-existing anions on bromate removal is lessened.

Enhanced degradation of ultra-violet stabilizer Bis(4-hydroxy)benzophenone using oxone catalyzed by hexagonal nanoplate-assembled CoS 3-dimensional cluster.

As UV-light stabilizers, Bis(4-hydroxy)benzophenone (BBP), are extensively consumed to quench radicals from photooxidation, continuous release of BPs into the environment poses serious threats to the ecology in view of their xenohormone toxicities, and BBP shall be eliminated from water to avoid its adverse effect. Since sulfate radical (SR)-based chemical oxidation techniques have been proven as effective procedures for eliminating organic emerging contaminants, this study aims to develop useful SR-based procedures through activating Oxone for degrading BBP in water. In contrast to the conventional Co3O4, cobalt sulfide (CoS) is particularly proposed as an alternative heterogeneous catalyst for activating Oxone to degrade BBP because CoS exhibits more reactive redox characteristics. As structures of catalysts predominantly control their catalytic activities, in this study, a unique nanoplate-assembled CoS (NPCS) 3D cluster is fabricated via a convenient one-step process to serve as a promising heterogeneous catalyst for activating Oxone to degrade BBP. With NPCS = 100 mg/L and Oxone = 200 mg/L, 5 mg/L of BBP can be completely eliminated in 60 min. The catalytic activity of NPCS towards Oxone activation also significantly surpasses the reference material, Co3O4, to enhance degradation of BBP. Ea of BBP degradation by NPCS-activated Oxone is also determined as a relatively low value of 42.7 kJ/mol. The activation mechanism as well as degradation pathway of BBP degradation by NPCS-activated Oxone was investigated and validated through experimental evidences and density functional theory (DFT) calculation to offer valuable insights into degradation behaviors for developing SR-based processes of BBP degradation using CoS catalysts.

Ultrafine cobalt nanoparticle-embedded leaf-like hollow N-doped carbon as an enhanced catalyst for activating monopersulfate to degrade phenol.

While cobalt (Co) stands out as the most effective non-precious metal for activating monopersulfate (MPS) to degrade organic pollutants, Co nanoparticles (NPs) are easily aggregated, losing their activities. As many efforts have attempted to immobilize Co NPs on supports/substrates to minimize the aggregation issue, recently hollow-structured carbon-based materials (HSCMs) have been regarded as promising supports owing to their distinct physical and chemical properties. Herein, in this study, a special HSCM is developed by using a special type of ZIF (i.e., ZIF-L) as a precursor. Through one-step chemical etching with tannic acid (TA), the resultant product still remains leaf-like morphology of pristine ZIF-L but the inner part of this product becomes hollow, which is subsequently transformed to ultrafine Co-NP embedded hollow-structured N-doped carbon (CoHNC) via pyrolysis. Interestingly, CoHNC exhibits superior catalytic activities than CoNC (without hollow structure) and the commercial Co3O4 NPs for activating MPS to degrade phenol. The Ea value of phenol degradation by CoHNC + MPS was determined as 44.3 kJ/mol. Besides, CoHNC is also capable of effectively activating MPS to degrade phenol over multiple-cycles without any significant changes of catalytic activities, indicating that CoHNC is a promising heterogeneous catalyst for activating MPS to degrade organic pollutants in water.

Hollow porous cobalt oxide nanobox as an enhanced for activating monopersulfate to degrade 2-hydroxybenzoic acid in water.

As 2-hydroxybenzoic acid (HBA) represents a typical pharmaceutical and personal care product (PPCP), constant releasing of HBA into the environment poses threats to the ecology, and thus it is critical to develop effective techniques to remove HBA from water. Recently, sulfate radical (SO4‒)-based advanced oxidation processes involved with monopersulfate (MPS) activation are proven as effective approaches for eliminating PPCPs from water, and Co3O4 is recognized as a capable catalyst for activating MPS. Therefore, great interests have arisen to develop Co3O4-based catalysts with advantageous morphologies and characteristics for enhancing catalytic activities. Therefore, a special Co3O4-based material is proposed in this work. Through a surfactant-assisted strategy, a cubic Co-MOF is prepared and used as a precursor, which is etched to afford hollow structure, and then transformed into hollow porous Co3O4 nanobox (PCNB). PCNB can exhibit distinct reactive surface with abundant surface oxygen vacancy as well as physical properties in comparison to the commercial Co3O4 NPs (com-Co3O4 NP), thereby leading to the outstanding catalytic activity of PCNB for activating MPS to degrade HBA. The activation energy (Ea) of 46.2 kJ/mol is also calculated using PCNB + MPS system, which is much lower than most of recent reported studies for activating MPS. PCNB could be also reusable over 5 consecutive HBA degradation cycles. The activation mechanism of MPS by PCNB and HBA degradation pathway are also comprehensively elucidated via experimental evidences and the theoretical calculation to offer insightful information of development of Co3O4 for HBA degradation.

A breakthrough dynamic-osmotic membrane bioreactor/nanofiltration hybrid system for real municipal wastewater treatment and reuse.

This study designed a Dynamic-Osmotic membrane bioreactor/nanofiltration (OsMBR/NF) system for municipal wastewater treatment and reuse. Results indicated that a continuously rotating FO module with 60 RPM in Dynamic-OsMBR system could enhance shear stress and reduce cake layer of foulants, leading to higher flux (50%) compared to Traditional-OsMBR during a 40-operation day. A negligible specific reverse salt flux (0.059 G/L) and a water flux of 2.86 LMH were recorded when a mixture of 0.1 M EDTA-2Na/0.1 M Na2CO3/0.9 mM Triton114 functioned as draw solution (DS). It was found that the Dynamic-OsMBR/NF hybrid system could effectively remove pollutants (∼98% COD, ∼99% PO43-P, ∼93% NH4+-N, > 99% suspended solids) from wastewater. In short, this developed system can be considered a breakthrough technology as it successfully minimizes membrane fouling by shear force, and achieves high water quality for reuse by two membrane- barriers.

Bamboo-like N-doped carbon nanotube-confined cobalt as an efficient and robust catalyst for activating monopersulfate to degrade bisphenol A.

As bisphenol A (BPA) is an extensively used chemical for manufacturing plastic products, discharge of BPA into the environment has caused serious threats to ecology. Therefore, -based chemical oxidation methods have been employed for eliminating BPA. Because monopersulfate (MNP) has become a popular reagent for obtaining , and Co is the most efficient metal for activating MNP, it is critical to develop heterogeneous Co catalysts for easier implementation and recovery. Herein, a unique Co-based catalyst is proposed by utilizing tubular-structured N-doped carbon substrates, derived dicyandiamide (DCDA), to confine Co nanoparticles (NPs). Through simple pyrolysis of a mixture of Co/DCDA, DCDA would be transformed into N-doped carbon nanotubes (CNT) to wrap the resultant Co NP, and, interestingly, this N-doped CNT would exhibit a special bamboo-like morphology. More importantly, as Co NPs are mono-dispersed and singly-confined in N-doped CNTs, forming CoCNT, CoCNT exhibits significantly higher catalytic activities than Co3O4, for activating MNP to degrade BPA. The enhancement of catalytic activities in CoCNT would be possibly ascribed to the synergistic effects between Co NP and the N-doped CNT which not only acts as the support/protection but also provides active sites. Therefore, CoCNT + MNP could lead to a much lower Ea (i.e., 13.8 kJ/mol) of BPA degradation than the reported Ea values. Besides, CoCNT is still effective for eliminating BPA even in the presence of high-concentration NaCl and surfactants. CoCNT is also reusable over many cycles and retains its catalytic activity with 100% BPA removal, demonstrating that CoCNT is an advantageous and robust catalyst for MNP activation.

Metal-complexed covalent organic frameworks derived N-doped carbon nanobubble-embedded cobalt nanoparticle as a magnetic and efficient catalyst for oxone activation.

While Cobalt nanoparticles (Co NPs) are useful for catalytic Oxone activation, it is more advantageous to embed/immobilize Co NPs on nitrogen-doped carbon substrates to provide synergy for enhancing catalytic performance. Herein, this study proposes to fabricate such a composite by utilizing covalent organic frameworks (COF) as a precursor. Through complexation of COF with Co, a stable product of Co-complexed COF (Co-COF) can be synthesized. This Co-COF is further converted through pyrolysis to N-doped carbon in which cobaltic NPs are embedded. Owing to its well-defined structures of Co-COF, the pyrolysis process transforms COF into N-doped carbon with a bubble-like morphology. Such Co NP-embedded N-doped carbon nanobubbles (CoCNB) with pores, magnetism and Co, shall be a promising catalyst. Thus, CoCNB shows a much stronger catalytic activity than commercial Co3O4 NPs to activate Oxone to degrade toxic Amaranth dye (AMD). CoCNB-activated Oxone also achieves a significantly lower Ea value of AMD degradation (i.e., 27.9 kJ/mol) than reported Ea values in previous literatures. Besides, CoCNB is still effective for complete elimination of AMD in the presence of high-concentration NaCl and surfactants, and CoCNB is also reusable over five consecutive cycles.

Water and nutrient recovery by a novel moving sponge - Anaerobic osmotic membrane bioreactor - Membrane distillation (AnOMBR-MD) closed-loop system.

For the first time, a novel sponge-based moving bed-anaerobic osmosis membrane bioreactor/membrane distillation (AnOMBR/MD) system using mixed Na3PO4/EDTA-2Na as the draw solution was employed to treat wastewater for enhanced water flux and reduced membrane fouling. Results indicated that the moving sponge-AnOMBR/MD system obtained a stable water flux of 4.01 L/m2 h and less membrane fouling for a period lasting 45 days. Continuous moving sponge around the FO module is the main mechanism for minimizing membrane fouling during the 45-day AnOMBR operation. The proposed system's nutrient removal was almost 100%, thus showing the superiority of simultaneous FO and MD membranes. Nutrient recovery from the MF permeate was best when solution pH was controlled to 9.5, whereby 17.4% (wt/wt) of phosphorus was contained in precipitated components. Moreover, diluted draw solute following AnOMBR was effectively regenerated using the MD process with water flux above 2.48 L/m2 h and salt rejection > 99.99%.

Prussian Blue Analogue-derived co/fe bimetallic nanoparticles immobilized on S/N-doped carbon sheet as a magnetic heterogeneous catalyst for activating peroxymonosulfate in water.

While Co is the most effective metal for activating PMS, extensive efforts are made to develop Co/Fe species (CF) (e.g., CoFe2O4) for imparting magnetic properties and facilitating recovery of catalysts. When carbon substrates are doped with heteroatoms (e.g., S and N) and CF is embedded within the heteroatom-doped carbon matrix, synergies can occur to boost catalytic activities. This study proposes an alternative CF-bearing carbonaceous composite, a cobalt-containing Prussian Blue Analogue (PBA) (Co3[Fe(CN)6]2) is employed as a precursor for preparing CF species embedded in N-doped carbon matrix and immobilized on S/N-co-doped carbon (SNC). Specifically, PBA in-situ grows on SNC by a heat treatment of trithiocyanuric acid to form PBA@SNC, which is then carbonized into CF species@SNC (CF@SNC). By adopting Amaranth degradation as a model reaction, CF@SNC shows a higher catalytic activity (kapp = 0.230 min-1) than CF (kapp = 0.152 min-1) and SNC (kapp = 0.016 min-1) for activating PMS. In comparison with Co3O4, CF@SNC exhibits a higher catalytic activity for PMS activation. CF@SNC renders a relatively low Ea value (53 kJ/mol) for Amaranth degradation in comparison to other reported catalysts. These comparisons demonstrate the advantageous features of CF@SNC as a magnetic and efficient catalyst for PMS activation.

Electrochemical oxidation as a post treatment for biologically tannery wastewater in batch reactor.

Tannery wastewater is known to contain high concentrations of organic compounds, heavy metals, nitrogen, sulphur, chromium, and many other chemicals. Both aerobic and anaerobic biological approaches have proven ineffective in the treatment of tannery wastewater due to the high salinity and toxic chemicals contained within the medium. Electrochemical oxidation presents a promising method for solving this problem. High pollutant removal efficiency, low energy consumption, and high electrode stability are three important factors supporting the feasibility of an efficient electrochemical treatment process. In the present study, electrochemical oxidation was performed as a post treatment for tannery wastewater (after biological pre-treatment) in a batch reactor using Ti/RuO2, Ti/IrO2, and Ti/BDD anodes. The effects of pH, current density, stirring rate and treatment time were studied to assess the treatment efficiency as well as the energy consumption of the process. The results showed that colour, chemical oxygen demand (COD), total organic carbon (TOC), and total nitrogen (TN) removal efficiencies on the electrodes were: Ti/RuO2 (88.8%, 88.40%, 64.0%, 96.4%), Ti/IrO2 (85.40%, 85.9%, 52.3%, 51.4%), Ti/BDD (90.60%, 94.7%, 90.5%, 82.7%) respectively, at a current density of 80 mA/cm2. All three electrodes demonstrated optimal performance at a pH of 8, a stirring rate of 400 rpm, a current density of 80 mA/cm2, and an electrolysis time of 5 h. The concentration of tri-chloromethane by-product was detected with limiting value. Electrochemical oxidation thus offers a feasible method for removing organic compounds and nutrients from tannery wastewater.

An overview of the development of vertical sampling technologies for ambient volatile organic compounds (VOCs).

Atmospheric volatile organic compounds (VOCs) are harmful to human health and the environment, and are precursors of other toxic air pollutants, e.g. ozone (O3) and secondary organic aerosols (SOAs). In recent years, due to scientific and technological advancements, vertical VOC profile in the atmosphere has been increasingly studied since it plays an essential role in the atmospheric research by providing multilevel three-dimensional data. Such information will improve the predictive ability of existing air quality models. This review summarizes the latest development of vertical VOC sampling technologies, highlighting the technical and non-technical challenges with possible solutions and future applications of vertical VOC sampling technologies. Further, other important issues concerning ambient VOCs have also been discussed, e.g. emission sources, VOC air samplers, VOC monitoring strategies, factors influencing airborne VOC measurement, the use of VOC data in air quality models and future smart city air quality management. Since ambient VOC levels can fluctuate significantly with altitude, technologies for vertical VOC profiling have been developed from building/tower-based measurements and tethered balloons to aircrafts, unmanned aerial vehicles (UAVs) and satellites in order to improve the temporal-spatial capacity and accuracy. Between the existing sampling methods, so far, UAVs are capable of providing more reliable VOC measurements and better temporal-spatial capacities. Heretofore, their disadvantages and challenges, e.g. sampling height, sampling time, sensitivity of the sensors and interferences from other chemical species, have limited the application of UAV for vertical VOC profiling.

Exploration of polyelectrolyte incorporated with Triton-X 114 surfactant based osmotic agent for forward osmosis desalination.

Selection of a proper osmotic agent is important to make the forward osmosis (FO) feasible. The objective of this study was to enhance FO by lowering reverse solute flux and maintaining high water flux. Poly(propylene glycol) with molecular weight of 725 Da (PPG-725) was found to possess high osmolality, making it a strong candidate for using as a draw agent. In addition, to reduce the partial leakage of draw solute, a non-ionic surfactant (Triton X-114) has been incorporated. Typically, when the hydrophobic tails of Triton X-114 interacted with the membrane surface, a layer on the surface of membrane is produced to constrict the pores and thus minimize the reverse solute flux. In this study, different concentrations of PPG-725 incorporated with different concentrations of Triton X-114 (0.2-0.8 mM) were used to evaluate their osmotic potentials as draw solute. The specific reverse solute flux (Js/Jw) of 40% PPG-725 doped with Triton X-114 was found to be 0.01 g/L, considerably much lesser than the conventional inorganic draw agents. Finally, membrane distillation operation was utilized as the recovery system in which solute rejection of 97% was achieved for 40% PPG-725/Triton X-114. Therefore, the overall performance supported PPG-725/Triton X-114 as being an efficient draw agent for forward osmosis-membrane distillation hybrid process.

Laboratory-scale membrane up-concentration and co-anaerobic digestion for energy recovery from sewage and kitchen waste.

This study assessed an alternative concept for co-treatment of sewage and organic kitchen waste in Vietnam. The goal was to apply direct membrane filtration for sewage treatment to generate a permeate that is suitable for discharge. The obtained chemical oxygen demand (COD) concentrations in the permeate of ultrafiltration tests were indeed under the limit value (50 mg/L) of the local municipal discharge standards. The COD of the concentrate was 5.4 times higher than that of the initial feed. These concentrated organics were then co-digested with organic kitchen wastes at an organic loading rate of 2.0 kg VS/m(3).d. The volumetric biogas production of the digester was 1.94 ± 0.34 m(3)/m(3).d. The recovered carbon, in terms of methane gas, accounted for 50% of the total carbon input of the integrated system. Consequently, an electrical production of 64 Wh/capita/d can be obtained when applying the proposed technology with the current wastes generated in Ho Chi Minh City. Thus, it is an approach with great potential in terms of energy recovery and waste treatment.

Molecular and structural analysis of Legionella DotI gives insights into an inner membrane complex essential for type IV secretion.

The human pathogen Legionella pneumophila delivers a large array of the effector proteins into host cells using the Dot/Icm type IVB secretion system. Among the proteins composing the Dot/Icm system, an inner membrane protein DotI is known to be crucial for the secretion function but its structure and role in type IV secretion had not been elucidated. We report here the crystal structures of the periplasmic domains of DotI and its ortholog in the conjugation system of plasmid R64, TraM. These structures reveal a striking similarity to VirB8, a component of type IVA secretion systems, suggesting that DotI/TraM is the type IVB counterpart of VirB8. We further show that DotI and its partial paralog DotJ form a stable heterocomplex. R64 TraM, encoded by the conjugative plasmid lacking DotJ ortholog, forms a homo-hexamer. The DotI-DotJ complex is distinct from the core complex, which spans both inner and outer membranes to form a substrate conduit, and seems not to stably associate with the core complex. These results give insight into VirB8-family inner membrane proteins essential for type IV secretion and aid towards understanding the molecular basis of secretion systems essential for bacterial pathogenesis.