Impacts of acute and chronic suspended solids exposure on juvenile freshwater mussels.

Construction activities may affect adjacent water systems by introducing increased levels of suspended solids into the water body and may subsequently affect the survival and growth of freshwater mussels. We tested three sediment types from sites in Missouri, including Spring River sediment (SRS), Osage River bank clay soil (ORC), and quarried limestone from Columbia (LMT). We prepared series of suspensions of each sediment with total suspended solids concentrations ranging from 0 to 5000 mg/L. Juveniles from three mussel species, Fatmucket (Lampsilis siliquoidea), Arkansas Brokenray (Lampsilis reeveiana), and Washboard (Megalonaias nervosa) were exposed to these suspensions in both acute (96-h) and chronic (28-d) tests. No clear impact on survival was observed from the acute or chronic exposures, but chronic test showed that juvenile mussels' growth was strongly affected. Interestingly, growth was enhanced at lower levels of SRS and ORC (≤500 mg/L, p < 0.05), and the juvenile mussels exposed to 500 mg/L SRS exhibited approximately 60 % more dry weight than those reared in the control. LMT did not enhance growth. Growth was slowed by high concentrations (>1000 mg/L) of all three sediments, implying that high suspended solids levels could reduce survival in the long term. Our findings may help to inform regulations and guidelines for construction activities to minimize adverse effects on juvenile mussels.

A two-sorbent system for fast uptake of arsenate from water: Batch and column studies.

There is a critical need to use decentralized and/or point-of-use systems to address some challenging water quality issues in society. Sorption-based approaches are uniquely suitable for such applications because of their simplicity in operation; however, the sorbents must possess fast contaminant uptake kinetics to overcome short hydraulic contact times often encountered in small systems. Here we designed a two-sorbent system consisting of Fe2O3-coated mesoporous carbon (FeMC) and nano-Fe2O3-coated activated carbon (FeAC) and demonstrated its ability to remove arsenate with a < 1 min empty bed contact time (EBCT) by a capture-and-storage process. Batch experiments showed rapid capture of arsenate by FeMC, likely occurred on the rod-like structures protruding to the liquid film. The captured arsenate could subsequently be relocated to FeAC for storage, which had a higher apparent sorption capacity. Column studies, operated with a 10 h running time followed by a 14 h pump-off time, showed that with a 102 µg-As/L influent concentration and at 0.85 min EBCT, the column treated 20,022 bed volumes until the 10 µg-As/L breakthrough, corresponding to a sorption density of 2.36 mg-As/g. This capture-and-storage technique resulted in a rapid and high-capacity arsenate removal through a combined effect of facile access to sorption sites on one sorbent and dynamic equilibrium in the two-sorbent system possessing a large total sorption capacity.

Biodegradable Chitosan-Based Membranes for Highly Effective Separation of Emulsified Oil/Water.

Efficient separation of oil droplets from oil/water emulsions is necessary for many energy and food industrial processes and for industrial wastewater treatment. Membrane microfiltration has been explored to address this issue because it is simple to operate and low in cost. However, filtration of oil droplets with a size around or less than 1 µm is still a major challenge. Furthermore, the fabrication process for polymeric membranes often uses hazardous organic solvents and petroleum-derived and nonbiodegradable raw materials, which pose additional environmental health and safety risk. In this study, we examined the use of chitosan-based membranes to efficiently remove oil droplets with an average diameter of ∼1 µm. The membranes were fabricated based on the rapid dissolution of chitosan in an alkaline/urea solvent system at a low temperature, thus avoiding the use of any toxic organic solvent. The chitosan membranes were further modified by dopamine and tannic acid (TA). The as-prepared membrane was characterized in terms of surface morphology, pore size distribution, and mechanical strength. The membrane performance was evaluated on a custom-designed crossflow filtration system. The results showed that the modified chitosan membrane with dopamine and TA had a water flux of 230.9 LMH at 1bar transmembrane pressure and oil droplet rejection of 99%. This water flux represented an increase of more than 10 times when compared with the original chitosan membrane without modification. The study also demonstrated excellent antifouling properties of the modified membrane that could achieve near 100% water flux recovery.

Medical, Health and Wellness Tourism Research-A Review of the Literature (1970-2020) and Research Agenda.

Medical, health and wellness tourism and travel represent a dynamic and rapidly growing multi-disciplinary economic activity and field of knowledge. This research responds to earlier calls to integrate research on travel medicine and tourism. It critically reviews the literature published on these topics over a 50-year period (1970 to 2020) using CiteSpace software. Some 802 articles were gathered and analyzed from major databases including the Web of Science and Scopus. Markets (demand and behavior), destinations (development and promotion), and development environments (policies and impacts) emerged as the main three research themes in medical-health-wellness tourism. Medical-health-wellness tourism will integrate with other care sectors and become more embedded in policy-making related to sustainable development, especially with regards to quality of life initiatives. A future research agenda for medical-health-tourism is discussed.

Enhanced arsenic removal from water by mass re-equilibrium: kinetics and performance evaluation in a binary-adsorbent system.

Because arsenic (As) is highly toxic and carcinogenic, its efficient removal from drinking water is essential. Considering some adsorption media may adsorb As fast but are too expensive to be applied in a household, while others could be abundantly available at low cost but with slow uptake kinetics, we explored a novel mass re-equilibrium (MRE) process between two media with different adsorption characteristics to enhance the overall As removal. We employed an adsorbent with fast adsorption kinetics to grab As from water, and then allow it to transfer to a second adsorbent with large capacity for As retention. In the system containing two adsorbents separated by a dialysis membrane, the results showed that As associated with a fast-adsorbing iron-based ordered mesoporous carbon could diffuse to a slow-adsorbing but high-capacity iron-based activated carbon. Column tests were further conducted, showing that the mixed medium, composed of the two adsorbents, could be used to adsorb As at a very short empty bed contact time (≤ 1 min) and the removal was improved by the MRE that potentially redistributed solid-phase As during pump-off periods. This study points to a new direction that by the MRE process, novel binary-adsorbent approaches may be developed for contaminant removal, if suitable media and process configuration could be identified.

Effects of the Substrate on Interfacial Polymerization: Tuning the Hydrophobicity via Polyelectrolyte Deposition.

Interfacial polymerization (IP) has been the key method for the fabrication of the thin film composite (TFC) membranes that are extensively employed in reverse osmosis (RO) and forward osmosis (FO). However, the role of the substrate surface hydrophilicity in the formation of the IP-film remains a controversial issue to be further addressed. This study characterized the IP films formed on a series of polyacrylonitrile (PAN) substrates whose hydrophilicities (from ~38 to ~93 degrees) were varied via different approaches, including the alkaline treatment and the deposition of various polycations. It was revealed that delamination could occur when the IP film was formed on a relatively hydrophilic surface; the integrity of the TFC membranes was substantially improved, owing to the modification of the polyelectrolyte deposition. On the other hand, the characterization indicated that the TFC membrane could have an enhanced efficiency (with a factor of ~2) when the substrate was relatively hydrophilic. It was established that the polyelectrolyte deposition could be exploited to effectively tune the substrate surface hydrophobicity, thereby providing more degrees of freedom for the optimization of the TFC membranes fabrication.

Role of Cellulose Micro and Nano Crystals in Thin Film and Support Layer of Nanocomposite Membranes for Brackish Water Desalination.

Reverse osmosis is a major process that produces soft water from saline water, and its output represents the majority of the overall desalination plants production. Developing efficient membranes for this process is the aim of many research groups and companies. In this work, we studied the effect of adding cellulose micro crystals (CMCs) and cellulose nano crystals (CNCs) to the support layer and thin film nanocomposite (TFN) membrane on the desalination performance. SEM, TEM, ATR-FTIR, and contact angle measurements were used to characterize the membrane's properties; and membrane's performance were evaluated by water flux and NaCl rejection. Filling 2% of CNCs gel in the support layer improved the water flux by +40%, while salt rejection maintained almost the same, around 95%. However, no remarkable improvement was gained by adding CNCs gel to m-phenylenediamine (MPD) solution, which was used in TFN membrane preparation. Filling CMCs powder in TFN membrane led to a slight improvement in terms of water flux.

Tailoring Polyamide Rejection Layer with Aqueous Carbonate Chemistry for Enhanced Membrane Separation: Mechanistic Insights, Chemistry-Structure-Property Relationship, and Environmental Implications.

Surface roughness and the associated nanosized voids inside the roughness structures have great influence on the separation performance of thin film composite polyamide reverse osmosis (RO) membranes. Inspired by the recent findings that these voids are formed due to the degassing of CO2 nanobubbles during interfacial polymerization, we systematically investigated the role of carbonate chemistry, particularly the solubility of CO2, in the aqueous m-phenylenediamine (MPD) solution for the first time. "Ridge-and-valley" roughness features were obtained when the pH of the MPD solution was between the two acidity constants of the carbonate system (i.e., 6.3 ≤ pH ≤ 10.3), under which condition HCO3- dominates over the other carbonate species. Increasing pH over this range led to both increased water permeability and better rejection of various solutes, thanks to the simultaneously enhanced effective filtration area and cross-linking degree of the polyamide layer. Further increase of pH to 12.5 resulted in more disparate rejection results due to membrane hydrolysis: rejection of neural solutes (B and As(III)) was compromised whereas that of charged solutes (NaCl and As(V)) was maintained. The mechanistic insights gained in the current study reveal the critical need to design RO membranes directly for end applications based on first principles.

Characterization of dissolved organic matter/nitrogen by fluorescence excitation-emission matrix spectroscopy and X-ray photoelectron spectroscopy for watershed management.

Characterization of dissolved organic matter/nitrogen (DOM/DON) is critical in water quality assessment and nutrient management in watershed or ecosystem. This study was to investigate the link between DOM/DON and its source using fluorescence excitation-emission matrix (EEM) spectroscopy coupled with parallel factor analysis (PARAFAC). Water samples were collected from various aquatic systems in a watershed located in central Missouri, including rural watershed with various land use and land cover (LULC), landfill, and constructed wetland. PARAFAC results based on EEM spectroscopy revealed four DOM components: two humic/fulvic acid-like components, one xenobioic-like component, and one protein-like component (f4). The f4 score was found highly correlated to LULC, indicating its distinctive EEM structure in relation to source. It is believed that the f4 score could be used as a surrogate for DOM/DON source-tracking in complex ecosystems. The nitrogen 1s X-ray photoelectron spectroscopy (XPS) of the solid DOM showed a close relationship between N oxidation state and its origin. The classification of the sample origins by the N oxidation state confirmed the grouping by the f4 score of EEM/PARAFAC. This study demonstrated that EEM/PARAFAC could be used as a tool for DOM/DON source tracking, point or non-point source pollution control, and understanding of DOM/DON fate and transport in complex aquatic ecosystems.

Physico-Chemical Processes.

This review is on the research literature published in 2016 related to the physico-chemical processes for water and wastewater treatment. The review is divided into granular and membrane filtration, sedimentation, coagulation/flocculation, flotation, oxidation, and adsorption.

Thin Film Nanocomposite Membrane Filled with Metal-Organic Frameworks UiO-66 and MIL-125 Nanoparticles for Water Desalination.

Knowing that the world is facing a shortage of fresh water, desalination, in its different forms including reverse osmosis, represents a practical approach to produce potable water from a saline source. In this report, two kinds of Metal-Organic Frameworks (MOFs) nanoparticles (NPs), UiO-66 (~100 nm) and MIL-125 (~100 nm), were embedded separately into thin-film composite membranes in different weight ratios, 0%, 0.05%, 0.1%, 0.15%, 0.2%, and 0.3%. The membranes were synthesized by the interfacial polymerization (IP) of m-phenylenediamine (MPD) in aqueous solution and trimesoyl chloride (TMC) in an organic phase. The as-prepared membranes were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), contact angle measurement, attenuated total reflection Fourier transform infrared (ATR FT-IR) spectroscopy, and salt rejection and water flux assessments. Results showed that both UiO-66 and MIL-125 could improve the membranes' performance and the impacts depended on the NPs loading. At the optimum NPs loadings, 0.15% for UiO-66 and 0.3% for MIL-125, the water flux increased from 62.5 L/m² h to 74.9 and 85.0 L/m² h, respectively. NaCl rejection was not significantly affected (UiO-66) or slightly improved (MIL-125) by embedding these NPs, always at >98.5% as tested at 2000 ppm salt concentration and 300 psi transmembrane pressure. The results from this study demonstrate that it is promising to apply MOFs NPs to enhance the TFC membrane performance for desalination.

A Thin Film Nanocomposite Membrane with MCM-41 Silica Nanoparticles for Brackish Water Purification.

Thin film nanocomposite (TFN) membranes containing MCM-41 silica nanoparticles (NPs) were synthesized by the interfacial polymerization (IP) process. An m-phenylenediamine (MPD) aqueous solution and an organic phase with trimesoyl chloride (TMC) dissolved in isooctane were used in the IP reaction, occurring on a nanoporous polysulfone (PSU) support layer. Isooctane was introduced as the organic solvent for TMC in this work due to its intermediate boiling point. MCM-41 silica NPs were loaded in MPD and TMC solutions in separate experiments, in a concentration range from 0 to 0.04 wt %, and the membrane performance was assessed and compared based on salt rejection and water flux. The prepared membranes were characterized via scanning electron microscopy (SEM), transmission electron microscopy (TEM), contact angle measurement, and attenuated total reflection Fourier transform infrared (ATR FT-IR) analysis. The results show that adding MCM-41 silica NPs into an MPD solution yields slightly improved and more stable results than adding them to a TMC solution. With 0.02% MCM-41 silica NPs in the MPD solution, the water flux was increased from 44.0 to 64.1 L/m²·h, while the rejection virtually remained the same at 95% (2000 ppm NaCl saline solution, 25 °C, 2068 kPa (300 psi)).

Physico-Chemical Processes.

This review is on the research literature published in 2015 related to the physico-chemical processes for water and wastewater treatment. The review is divided into six sections, including filtration, sedimentation, coagulation/flocculation, flotation, oxidation, and adsorption.

Co-adsorption of Trichloroethylene and Arsenate by Iron-Impregnated Granular Activated Carbon.

Co-adsorption of trichloroethylene (TCE) and arsenate [As(V)] was investigated using modified granular activated carbons (GAC): untreated, sodium hypochlorite-treated (NaClO-GAC), and NaClO with iron-treated GAC (NaClO/Fe-GAC). Batch experiments of single- [TCE or As(V)] and binary- [TCE and As(V)] components solutions are evaluated through Langmuir and Freundlich isotherm models and adsorption kinetic tests. In the single-component system, the adsorption capacity of As(V) was increased by the NaClO-GAC and the NaClO/Fe-GAC. The untreated GAC showed a low adsorption capacity for As(V). Adsorption of TCE by the NaClO/Fe-GAC was maximized, with an increased Freundlich constant. Removal of TCE in the binary-component system was decreased 15% by the untreated GAC, and NaClO- and NaClO/Fe-GAC showed similar efficiency to the single-component system because of the different chemical status of the GAC surfaces. Results of the adsorption isotherms of As(V) in the binary-component system were similar to adsorption isotherms of the single-component system. The adsorption affinities of single- and binary-component systems corresponded with electron transfer, competitive adsorption, and physicochemical properties.

Silver nanoparticles in aquatic environments: Physiochemical behavior and antimicrobial mechanisms.

Nanosilver (silver nanoparticles or AgNPs) has unique physiochemical properties and strong antimicrobial activities. This paper provides a comprehensive review of the physicochemical behavior (e.g., dissolution and aggregation) and antimicrobial mechanisms of nanosilver in aquatic environments. The inconsistency in calculating the Gibbs free energy of formation of nanosilver [ΔGf(AgNPs)] in aquatic environments highlights the research needed to carefully determine the thermodynamic stability of nanosilver. The dissolutive release of silver ion (Ag(+)) in the literature is often described using a pseudo-first-order kinetics, but the fit is generally poor. This paper proposes a two-stage model that could better predict silver ion release kinetics. The theoretical analysis suggests that nanosilver dissolution could occur under anoxic conditions and that nanosilver may be sulfidized to form silver sulfide (Ag2S) under strict anaerobic conditions, but more investigation with carefully-designed experiments is required to confirm the analysis. Although silver ion release is likely the main antimicrobial mechanism of nanosilver, the contributions of (ion-free) AgNPs and reactive oxygen species (ROS) generation to the overall toxicity of nanosilver must not be neglected. Several research directions are proposed to better understand the dissolution kinetics of nanosilver and its antimicrobial mechanisms under various aquatic environmental conditions.

Physico-Chemical Processes.

This review is on the research literature published in 2014 related to the physico-chemical processes for water and wastewater treatment. The review is divided into six sections, including coagulation/flocculation, filtration, sedimentation, oxidation, flotation, sorption process.

Application of nano TiO2 modified hollow fiber membranes in algal membrane bioreactors for high-density algae cultivation and wastewater polishing.

Polyvinylidene fluoride (PVDF) hollow fiber membranes with nano-TiO2 (5% of PVDF by mass, average size = 25 nm) additives were fabricated and applied for high-density algae (Chlorella vulgaris) cultivation. At the average light intensity of 121 µmol/m(2)/s, the algal membrane bioreactors (A-MBR) operated at a hydraulic retention time of 0.5d and an average solids retention time of 25d had an average algae biomass concentration of 2350 ± 74 mg/L (in COD units) and algal biomass production rate of 6.5 ± 0.1g/m(2)/d. The A-MBRs removed an average of 78% of phosphorus from the wastewater at the initial total phosphorus concentrations ranging from 3.5 to 8.6 mg/L. The nano TiO2-embedded membranes had improved surface hydrophilicity with its total resistance about 50% lower than that of the control. This study demonstrated that PVDF/TiO2 nanocomposite membranes had a better antifouling property for high-density algae cultivation and wastewater polishing.

Reducing arsenic accumulation in rice grain through iron oxide amendment.

Effects of soil-arsenic (As), phosphorus and iron oxide on As accumulation in rice grain were investigated. Cultivars that have significantly different sensitivity to As, straighthead-resistant Zhe 733 and straighthead-susceptible Cocodrie, were used to represent different cultivar varieties. The grain accumulation of other elements of concern, selenium (Se), molybdenum (Mo), and cadmium (Cd) was also monitored. Results demonstrated that high soil-As not only resulted in high grain-As, but could also result in high grain-Se, and Zhe 733 had significantly less grain-As than Cocodrie did. However, soil-As did not impact grain-Mo and Cd. Among all elements monitored, iron oxide amendment significantly reduced grain-As for both cultivars, while the phosphate application only reduced grain-Se for Zhe 733. Results also indicated that cultivar type significantly impacted grain accumulation of all monitored trace elements. Therefore, applying iron oxide to As-contaminated land, in addition to choosing appropriate rice cultivar, can effectively reduce the grain accumulation of As.

Uranium(VI) reduction by nanoscale zero-valent iron in anoxic batch systems: the role of Fe(II) and Fe(III).

The role of Fe(II) and Fe(III) in U(VI) reduction by nanoscale zerovalent iron (nanoFe0) was investigated using two iron chelators 1,10-phenanthroline and triethanolamine (TEA) under a CO2-free anoxic condition. The results showed that U(VI) reduction was strongly inhibited by 1,10-phenanthroline and TEA in a pH range from 6.9 to 9.0. For instance, at pH 6.9 the observed U(VI) reduction rates decreased by 81% and 82% in the presence of 1,10-phenanthroline and TEA, respectively. The inhibition was attributed to the formation of stable complexes between 1,10-phenanthroline and Fe(II) or TEA and Fe(III). In the absence of iron chelators, U(VI) reduction can be enhanced by surface-bound Fe(II) on nanoFe0. Our results suggested that Fe(III) and Fe(II) possibly acted as an electron shuttle to ferry the electrons from nanoFe0 to U(VI), therefore a combined system with Fe(II), Fe(III) and nanoFe0 could facilitate U(VI) reductive immobilization in the contaminated groundwater.

Effects of biomass types and carbonization conditions on the chemical characteristics of hydrochars.

Effects of biomass types (bark mulch versus sugar beet pulp) and carbonization processing conditions (temperature, residence time, and phase of reaction medium) on the chemical characteristics of hydrochars were examined by elemental analysis, solid-state ¹³C NMR, and chemical and biochemical oxygen demand measurements. Bark hydrochars were more aromatic than sugar beet hydrochars produced under the same processing conditions. The presence of lignin in bark led to a much lower biochemical oxygen demand (BOD) of bark than sugar beet and increasing trends of BOD after carbonization. Compared with those prepared at 200 °C, 250 °C hydrochars were more aromatic and depleted of carbohydrates. Longer residence time (20 versus 3 h) at 250 °C resulted in the enrichment of nonprotonated aromatic carbons. Both bark and sugar beet pulp underwent deeper carbonization during water hydrothermal carbonization than during steam hydrothermal carbonization (200 °C, 3 h) in terms of more abundant aromatic C but less carbohydrate C in water hydrochars.