Decoupling locally enhanced electric field treatment (LEEFT) intensity and copper release by applying asymmetric electric pulses for water disinfection.

Copper has well-known anti-microbial properties but is typically not considered for drinking water disinfection because of its health risk to human at efficient biocidal concentrations. Locally enhanced electric field treatment (LEEFT) is a cutting-edge technique that aims to inactivate bacteria by generating aqueous pores on the cell membrane through the application of a strong electric field. LEEFT can also increase the permeability of the cell membrane, which promotes the uptake of chemical disinfectants to reduce the required biocidal concentrations. Previously, a coaxial-electrode copper ionization cell (CECIC) was developed to combine copper disinfection with LEEFT, demonstrating superior disinfection efficiency with low effluent copper concentrations (<0.5 mg/L). However, using direct-current (DC) voltages results in a dilemma that a higher voltage is necessary for effective LEEFT disinfection, but a lower voltage is required to limit Cu release. Here, asymmetric electric pulses are employed to decouple the LEEFT intensity from copper release in the CECIC. In this case, LEEFT intensity is primarily determined by the pulse amplitude while the copper release is controlled by the pulse offset. We have demonstrated that the use of asymmetric electric pulses achieves significantly higher inactivation efficiency compared to the DC voltages with the similar level of Cu release. For the water with conductivity similar to tap water (∼100 µS/cm), a high inactivation efficiency of 4.7-log is achieved with only 0.49 mg/L copper release. These findings highlight the potential of asymmetric electric pulses as a promising alternative to DC voltages for the practical application of LEEFT-Cu systems in the future.

Triboelectric Nanogenerators for Harvesting Diverse Water Kinetic Energy.

The water covering the Earth's surface not only supports life but also contains a tremendous amount of energy. Water energy is the most important and widely used renewable energy source in the environment, and the ability to extract the mechanical energy of water is of particular interest since moving water is ubiquitous and abundant, from flowing rivers to falling rain drops. In recent years, triboelectric nanogenerators (TENGs) have been promising for applications in harvesting kinetic energy from water due to their merits of low cost, light weight, simple structure, and abundant choice of materials. Furthermore, TENGs can also be utilized as self-powered active sensors for monitoring water environments, which relies on the output signals of the TENGs caused by the movement and composition of water. Here, TENGs targeting the harvest of different water energy sources have been systematically summarized and analyzed. The TENGs for harvesting different forms of water energy are introduced and divided on the basis of their basic working principles and modes, i.e., in the cases of solid-solid and solid-liquid. A detailed review of recent important progress in TENG-based water energy harvesting is presented. At last, based on recent progresses, the existing challenges and future prospects for TENG-based water energy harvesting are also discussed.

Microfluidics for Environmental Applications.

Microfluidic and lab-on-a-chip systems have become increasingly important tools across many research fields in recent years. As a result of their small size and precise flow control, as well as their ability to enable in situ process visualization, microfluidic systems are increasingly finding applications in environmental science and engineering. Broadly speaking, their main present applications within these fields include use as sensors for water contaminant analysis (e.g., heavy metals and organic pollutants), as tools for microorganism detection (e.g., virus and bacteria), and as platforms for the investigation of environment-related problems (e.g., bacteria electron transfer and biofilm formation). This chapter aims to review the applications of microfluidics in environmental science and engineering - with a particular focus on the foregoing topics. The advantages and limitations of microfluidics when compared to traditional methods are also surveyed, and several perspectives on the future of research and development into microfluidics for environmental applications are offered.

Long-term expansion and enhanced osteogenic potential of Macaca MSCs via BMP signaling modulation.

Mesenchymal stem cells (MSCs) are a potential source of osteoblasts for the treatment of osteoporosis, but how to better preserve the stemness of MSCs in vitro culture conditions is the main challenge for MSC transplantation. The use of fibroblast growth factor 2 (FGF2) supplement has been described and used extensively to increase the expansion of MSCs. Cumulative evidence indicates that bone morphogenetic protein 2 (BMP2; a member of the TGF-ß superfamily) is a secreted protein that promotes bone formation, which can regulate cell growth, differentiation, and development. Here we found that BMP2, in combination with FGF2, not only enhanced the proliferation of Macaca bone marrow-derived MSCs but also strengthened their osteogenic potential after short-term expansion in vitro. During long-term expansion, these cells still retained their osteogenic potential as well as other functional characteristics of pluripotent MSCs, which are gradually lost in the absence of BMP2. In addition, the BMP antagonist Noggin did not affect MSC expansion and the osteogenic potential. This study demonstrates that the regulation of BMP signaling can maintain the effectiveness of MSCs during expansion, which promotes the clinical application of MSCs in bone repair.

A multi-parameter in-situ water quality analyzer based on a portable document scanner and 3D printed self-sampling cells.

This research introduced a new low-cost and multi-parameter analyzer for in-situ measurements of typical nutrients in water bodies. The analyzer consisted of color detection and chromogenic reaction modules. The self-sampling action of the 3D printed sampling/reaction cells was achieved with the cooperative application of rubber bands and dissolvable thread. The target analytes in the collected water sample reacted with the chromogenic reagents that were diffused from the pre-placed glass wool in the cell, producing color compounds. A portable document scanner was employed as a multi-parameter in-situ detector to record the image of the colored solutions in all five cells simultaneously. Based on the image, the corrected grayscale values were derived for target analyte quantitation. The relationships between grayscale values and concentrations of target analytes were established, and the temperature effects were studied. In addition, the practicability of the analyzer was demonstrated by in-situ experiments carried out in four different sites, including a creek, a river dock, a reservoir and a secondary settling tank in a wastewater treatment facility. The results indicated that the analyzer could be used for in-situ measuring of nutrients at µmol/L levels in the water. The nutrient concentrations obtained with the analyzer were comparable with those obtained with the standard methods. The presented analyzer provided new complementary ideas and methods for in-situ rapid measurement of nutrients and other target analytes in various water systems.

Rapid determination of the electroporation threshold for bacteria inactivation using a lab-on-a-chip platform.

Electroporation based locally enhanced electric field treatment (LEEFT) is an emerging bacteria inactivation technology for drinking water disinfection. Nevertheless, the lethal electroporation threshold (LET) for bacteria has not been studied, partly due to the tedious work required by traditional experimental methods. Here, a lab-on-a-chip device composed of platinum electrodes deposited on a glass substrate is developed for rapid determination of the LET. When voltage pulses are applied, an electric field with a linear strength gradient is generated on a channel between the electrodes. Bacterial cells exposed to the electric field stronger than the LET are inactivated, while others remain intact. After a cell staining process to differentiate dead and live bacterial cells, the LETs are obtained by analyzing the fluorescence microscopy images. Staphylococcus epidermidis has been utilized as a model bacterium in this study. The LETs range from 10 kV/cm to 35 kV/cm under different pulsed electric field conditions, decreasing with the increase of pulse width, effective treatment time, and pulsed electric field frequency. The effects of medium properties on the LET were also investigated. This lab-on-a-chip device and the experimental approach can also be used to determine the LETs for other microorganisms found in drinking water.

Simultaneous removal of nitrogen and pharmaceutical and personal care products from the effluent of waste water treatment plants using aerated solid-phase denitrification system.

Nowadays, waste water treatment plants (WWTPs) are regarded as the pollution sources of nitrogen and pharmaceutical and personal care products (PPCPs). In the present study, the simultaneous removal of nitrogen and typical PPCPs, ibuprofen and triclosan, was evaluated in a poly-3-hydroxybutyrate-co-3-hydroxyvalerate (PHBV) based solid-phase denitrification (SPD) system. Results after 602 days showed that simultaneous nitrification and denitrification (SND) process occurred with average 83.85 ±â€¯13.09% NH4+-N and 93.88 ±â€¯10.19% NO3--N removals in the SPD system. Interestingly, the system achieved average 79.69 ±â€¯6.35% and 65.96 ±â€¯7.62% removals of ibuprofen and triclosan, respectively, under stable influent conditions of 50 µg L-1. Cometabolic activities of heterotrophic denitrifying bacteria and ammonia oxidizing bacteria (AOB) probably played a role in the biodegradation of the two PPCPs. Illumina MiSeq sequencing results revealed that microbial composition enhanced the simultaneous removal of nitrogen and PPCPs in the SPD system.

Perfection in Nucleation and Growth of Blue-Phase Single Crystals: Small Free-Energy Required to Self-Assemble at Specific Lattice Orientation.

Chemically patterned surfaces can be used to selectively stabilize blue phases as macroscopic single crystals with a prescribed lattice orientation. By tailoring the interfacial free energy through the pattern characteristics, it is possible to set, with nanoscale precision, the optimal conditions to induce spontaneously blue-phase crystal nucleation on the patterned substrate where a uniform, defect-free, blue-phase single crystal is finally formed in a matter of seconds. The chemical patterns taken into consideration in this work are made up of alternated stripelike regions of homeotropic and planar anchoring. By varying the stripe pattern dimension, including the period and ratio of the planar/homeotropic anchoring width, it is possible to generate blue-phase I single crystals with (110) lattice orientation and blue-phase II single crystals with either the (100), (110), or (111) lattice orientation. Continuum mean-field calculations of the studied systems serve to explain, in terms of the free energy of the systems, how the pattern dimensions favor certain crystallographic orientations while penalizing the others. We found that a small free-energy difference is sufficient to drive the nucleation and growth of blue phases into a certain lattice orientation. Therefore, a processing window for obtaining arbitrary large blue-phase single crystals with predesigned lattice orientation, highly aligned reflective peaks, and significantly short forming time is provided here, which is essential for manufacturing and modulating optical devices and photonics.

Cell Transport Prompts the Performance of Low-Voltage Electroporation for Cell Inactivation.

The inactivation of pathogens in liquids has broad applications, ranging from water disinfection to food pasteurization. However, common cell inactivation methods (e.g., chlorination, ultraviolet radiation and thermal treatment) have significant drawbacks such as carcinogenic byproduct formation, energy intensiveness and/or nutrient structure destruction. Here, we fabricated a new approach to address these challenges by applying a low-voltage electroporation disinfection cell (EDC) and investigate the critical mechanisms of cell transport to allow high inactivation performance. The EDC prototypes were equipped with two one-dimensional (1D) nanostructure-assisted electrodes that enabled high electric field strength (>107 V m-1) near the electrode surface with a low applied voltage (1 V). We have identified that during electroporation disinfection, electrophoresis, dielectrophoresis and hydraulic flow are the three major mechanisms which transport cells into the vicinity of the electrode surface to achieve superior disinfection performance. The EDC treated 70 ml of bacteria sample with an initial cell concentration of 107 CFU ml-1 and achieved complete bacteria inactivation (survival rate <0.00001%; no live bacteria detected). Our findings will help to establish a foundation for the future development and implementation of low-voltage electroporation for cell inactivation.

Avaliação da microbiota ocular em pacientes com disfunção do filme lacrimal / Evaluation of conjunctival flora in patients with tear film dysfunction

OBJETIVO: Avaliar a microbiota conjuntival em olhos com disfunção do filme lacrimal, e a modificação desta microbiota após a colocação de plug de silicone no canalículo inferior. MÉTODOS: Série de casos intervencionais não comparativos para avaliar 68 olhos de 41 pacientes com disfunção do filme lacrimal, durante o período de 2002 a 2007, na Universidade Federal de São Paulo. Todos os pacientes foram submetidos à colheita de amostras de raspado conjuntival de fundo-de-saco inferior para cultivo em Brain heart infusion broth. Os vinte e dois pacientes submetidos à colocação de plug de silicone repetiram a colheita de raspado conjuntival um mês após o procedimento. RESULTADOS: Dos 68 olhos avaliados, 47 apresentaram crescimento bacteriano nas amostras colhidas. Nove diferentes espécies de bactérias foram identificadas: Staphylococcus coagulase negativa em 66,66 por cento, Staphylococcus aureus em 13,72 por cento, Corynebacterium sp em 5,86 por cento, Enterobacter aerogenes em 3,92 por cento, Streptococcus hemolítico do grupo viridans em 1,96 por cento, Serratia sp em 1,96 por cento, Alcaligenes xylosoxidans spp em 1,96 por cento, Corynebacterium xerosis em 1,96 por cento, e Proteus mirabilis em 1,96 por cento. Staphylococcus coagulase negativa (SCN) foi o microrganismo mais frequentemente isolado tanto antes quanto após o plug de silicone. A sensibilidade do SCN à Oxacilina antes da colocação do plug era de 87,50 por cento, e, após, de 73,68 por cento. CONCLUSÃO: A microbiota em olhos com disfunção do filme lacrimal é bastante semelhante à encontrada em olhos normais. A resistência de SCN à Oxacilina foi um pouco maior após o implante do plug de silicone.

PURPOSE: To evaluate conjunctival microbiota in eyes with tear film dysfunction and its modification after punctal occlusion with silicone plug. METHODS: Non comparative interventional case series study to evaluate 68 eyes of 41 patients with tear film dysfunction, from 2002 to 2007, followed in Federal University of Sao Paulo. Samples for culture were all obtained from conjunctival swabs and inoculated in Brain heart infusion broth (BHI broth). Twenty two patients that undergone punctal plug occlusion repeated culture procedure one month after plug insertion. RESULTS: 47 of the 68 eyes evaluated had positive culture in their samples. Nine different types of bacteria were identified: Coagulase negative Staphylococcus in 66,66 percent, Staphylococcus aureus, in 13,72 percent, Corynebacterium sp, in 5,86 percent, Enterobacter aerogenes, in 3,92 percent, Streptococcus hemolítico do grupo viridans, in 1,96 percent, Serratia sp, in 1,96 percent, Alcaligenes xylosoxidans spp, in 1,96 percent, Corynebacterium xerosis, in 1,96 percent, and Proteus mirabilis in 1,96 percent. Coagulase negative Staphylococcus (CNS) was the most frequently isolated microorganism before and after punctal occlusion. CNS sensibility to Oxacilin before plug insertion was 87,50 percent, and after, 73,68 percent. CONCLUSION: Microbiota found in eyes with tear film dysfunction seems to be similar to that found in normal eyes. CNS resistance to oxacilin was slightly higher after silicone plug insertion.