Sulfur-containing air pollutants as draw solution for fertilizer drawn forward osmosis desalination process for irrigation use

© 2017 Elsevier B.V. This study investigated suitability and performance of the sulfur-based seed solution (SBSS) as a draw solution (DS), a byproduct taken from the photoelectrochemical (PEC) process where the SBSS is used as an electrolyte for H2 production. This SBSS DS is composed of a mixture of ammonium sulfate ((NH4)2SO4) and ammonium sulfite ((NH4)2SO3), and it can be utilized as fertilizer for fertilizer drawn forward osmosis (FDFO) desalination of saline water. The FDFO process employed with thin-film composite (TFC) membrane and showed that the process performance (i.e. water flux and reverse salt flux) is better than that with cellulose triacetate (CTA) membrane. In addition, it produced high water flux of 19 LMH using SBSS as DS at equivalent concentration at 1 M and 5 g/L NaCl of feed solution (model saline water). Experimental results showed that the reverse salt flux of SBSS increased with the increase in pH of the DS and that lowering the concentration of ammonium sulfite in the SBSS led to the higher water flux of feed solution. The result also demonstrated that this SBSS is practically suitable for the FDFO process toward development of water-energy-food nexus technology using sulfur chemicals-containing air pollutant

Thin-film composite membrane on a compacted woven backing fabric for pressure assisted osmosis

© 2016 Elsevier B.V. The water flux in forward osmosis (FO) process declines substantially when the draw solution (DS) concentration reaches closer to the point of osmotic equilibrium with the feed solution (FS). Using external hydraulic pressure alongside the osmotic driving force in the pressure assisted osmosis (PAO) has been found effective in terms of enhancing water flux and even potentially diluting the DS beyond osmotic equilibrium. The net gain in water flux due to the applied pressure in the PAO process closely depends on the permeability of the FO membrane. The commercial flat sheet cellulose triacetate (CTA) FO membrane has low water permeability and hence the effective gain in water flux in the PAO process is low. In this study, a high performance thin film composite membrane was developed especially for the PAO process through casting polyethersulfone (PES) polymer solution on a compacted woven fabric mesh support followed by interfacial polymerisation for polyamide active layer. This PAO membrane possesses a water flux of 37 L m2h− 1using 0.5 M NaCl as DS and deionised water as the feed at an applied hydraulic pressure of 10 bar. Besides, the membrane was able to endure the external hydraulic pressure required for the PAO process owing to the embedded backing fabric support. While the membranes with low structural parameters are essential for higher water flux, this study shows that for PAO process, polymeric membranes with larger structural parameters may not be suitable for PAO. They generally resulted in compaction and poor mechanical strength to withstand hydraulic pressure

Modification of nanofiber support layer for thin film composite forward osmosis membranes via layer-by-layer polyelectrolyte deposition

© 2018 by the authors. Licensee MDPI, Basel, Switzerland. Electrospun nanofiber-supported thin film composite membranes are among the most promising membranes for seawater desalination via forward osmosis. In this study, a high-performance electrospun polyvinylidenefluoride (PVDF) nanofiber-supported thin film composite (TFC) membrane was successfully fabricated after molecular layer-by-layer polyelectrolyte deposition. Negatively-charged electrospun polyacrylic acid (PAA) nanofibers were deposited on electrospun PVDF nanofibers to form a support layer consisted of PVDF and PAA nanofibers. This resulted to a more hydrophilic support compared to the plain PVDF nanofiber support. The PVDF-PAA nanofiber support then underwent a layer-by-layer deposition of polyethylenimine (PEI) and PAA to form a polyelectrolyte layer on the nanofiber surface prior to interfacial polymerization, which forms the selective polyamide layer of TFC membranes. The resultant PVDF-LbL TFC membrane exhibited enhanced hydrophilicity and porosity, without sacrificing mechanical strength. As a result, it showed high pure water permeability and low structural parameter values of 4.12 L m−2 h−1 bar−1 and 221 µm, respectively, significantly better compared to commercial FO membrane. Layer-by-layer deposition of polyelectrolyte is therefore a useful and practical modification method for fabrication of high performance nanofiber-supported TFC membrane

Thin film composite hollow fibre forward osmosis membrane module for the desalination of brackish groundwater for fertigation

© 2015 Elsevier B.V. The performance of recently developed polyamide thin film composite hollow fibre forward osmosis (HFFO) membrane module was assessed for the desalination of brackish groundwater for fertigation. Four different fertilisers were used as draw solution (DS) with real BGW from the Murray-Darling Basin in Australia. Membrane charge and its electrostatic interactions with ions played a significant role in the performance of the HFFO module using fertiliser as DS. Negatively charged polyamide layer promotes sorption of multivalent cations such as Ca2+ enhancing ion flux and membrane scaling. Inorganic scaling occurred both on active layer and inside the support layer depending on the types of fertiliser DS used resulting in severe flux decline and this study therefore underscores the importance of selecting suitable fertilisers for the fertiliser drawn forward osmosis (FDFO) process. Water flux under active layer DS membrane orientation was about twice as high as the other orientation indicating the need to further optimise the membrane support structure formation. Water flux slightly improved at higher crossflow rates due to enhanced mass transfer on the fibre lumen side. At 45% packing density, HFFO could have three times more membrane area and four times more volumetric flux output for an equivalent 8040 cellulose triacetate flat-sheet FO membrane module

The influence of backbone fluorination on the dielectric constant of conjugated polythiophenes

The ability to modify or enhance the dielectric constant of semiconducting polymers can prove valuable for a range of optoelectronic and microelectronic applications. In the case of organic photovoltaics, increasing the dielectric constant of the active layer has often been suggested as a method to control charge generation, recombination dynamics, and ultimately, the power conversion efficiencies. In this contribution, the impact that the degree and pattern of fluorination has on the dielectric constant of poly(3-octylthiophene) (P3OT), a more soluble analogue of the widely studied conjugated material poly(3-hexylthiophene), is explored. P3OT and its backbone-fluorinated analogue, F-P3OT, are compared along with a block and alternating copolymer version of these materials. It is found that the dielectric constant of the polymer thin films increases as the degree of backbone fluorination increases, in a trend consistent with density functional theory calculations of the dipole moment

Notch signaling and ghost cell fate in the calcifying cystig odontogenic tumor

Notch signaling is an evolutionarily conserved mechanism that enables adjacent cells to adopt different fates. Ghost cells (GCs) are anucleate cells with homogeneous pale eosinophilic cytoplasm and very pale to clear central areas (previous nucleus sites). Although GCs are present in a variety of odontogenic lesions notably the calcifying cystic odontogenic tumor (GCOT), their nature and process of formation remains elusive. The aim of this study was to investigate the role of Notch signaling in the cell fate specification of GCs in CCOT. Immunohistochemical staining for four Notch receptors (Notch1, Notch2, Notch3 and Notch4) and three ligands (Jagged1, Jagged2 and Delta1) was performed on archival tissues of five CCOT cases. Level of positivity was quantified as negative (0), mild (+), moderate (2+) and strong (3+). Results revealed that GCs demonstrated overexpression for Notch1 and Jagged1 suggesting that Notch1Jagged1 signaling might serve as the main transduction mechanism in cell fate decision for GCs in CCOT. Protein localizations were largely membranous and/or cytoplasmic. Mineralized GCs also stained positive implicating that the calcification process might be associated with upregulation of these molecules. The other Notch receptors and ligands were weak to absent in GCs and tumoral epithelium. Stromal endothelium and fibroblasts were stained variably positive

Pyrite (FeS2)-supported ultrafiltration system for removal of mercury (II) from water

This study investigated the Hg(II) removal efficiencies of the reactive adsorbent membrane (RAM) hybrid filtration process, a removal process that produces stable final residuals. The reaction mechanism between Hg(II) and pyrite and the rejection of the solids over time were characterized with respect to flux decline, pH change, and Hg and Fe concentration in permeate water. Effects of the presence of anions (Cl−, SO42−, NO3−) or humic acid (HA) on the rejection of the Hg(II)-contacted pyrite were studied. The presence of both HA and Hg(II) increased the rate of flux decline due to the formation of irreversible gel-like compact cake layers as shown in the experimental data and modeling related to the flux decline and the SEM images. Stability experiments of the final residuals retained on the membrane using a thiosulfate solution (Na2S2O3) show that the Hg(II)-laden solids were very stable due to little or no detection of Hg(II) in the permeate water. Experiment on the possibility of continuously removing Hg(II) by reusing the Hg/pyrite-laden membrane shows that almost all Hg(II) was adsorbed onto the pyrite surface regardless of the presence of salts or HA, and the Hg(II)-contacted pyrite residuals were completely rejected by the DE/UF system. Therefore, a membrane filter containing pyrite-Hg(II) could provide another reactive cake layer capable of further removal of Hg(II) without post-chemical treatment for reuse

Interactions between Transmembrane Helices within Monomers of the Aquaporin AtPIP2;1 Play a Crucial Role in Tetramer Formation

Aquaporin (AQP) is a water channel protein found in various subcellular membranes of both prokaryotic and eukaryotic cells. The physiological functions of AQPs have been elucidated in many organisms. However, understanding their biogenesis remains elusive, particularly regarding how they assemble into tetramers. Here, we investigated the amino acid residues involved in the tetramer formation of the Arabidopsis plasma membrane AQP AtPIP2; 1 using extensive amino acid substitution mutagenesis. The mutant proteins V41A/E44A, F51A/L52A, F87A/I91A, F92A/I93A, V95A/Y96A, and H216A/L217A, harboring alanine substitutions in the transmembrane (TM) helices of AtPIP2; 1 polymerized into multiple oligomeric complexes with a variable number of subunits greater than four. Moreover, these mutant proteins failed to traffic to the plasma membrane, instead of accumulating in the endoplasmic reticulum(ER). Structure-based modeling revealed that these residues are largely involved in interactions between TM helices within monomers. These results suggest that inter-TM interactions occurring both within and between monomers play crucial roles in tetramer formation in the AtPIP2; 1 complex. Moreover, the assembly of AtPIP2; 1 tetramers is critical for their trafficking from the ER to the plasma membrane, as well as water permeability.1133Ysciescopu

A decision support tool for health service re-design

Many of the outpatient services are currently only available in hospitals, however there are plans to provide some of these services alongside with General Practitioners. Consequently, General Practitioners could soon be based at polyclinics. These changes have caused a number of concerns to Hounslow Primary Care Trust (PCT). For example, which of the outpatient services are to be shifted from the hospital to the polyclinic? What are the current and expected future demands for these services? To tackle some of these concerns, the first phase of this project explores the set of specialties that are frequently visited in a sequence (using sequential association rules). The second phase develops an Excel based spreadsheet tool to compute the current and expected future demands for the selected specialties. From the sequential association rule algorithm, endocrinology and ophthalmology were found to be highly associated (i.e. frequently visited in a sequence), which means that these two specialties could easily be shifted from the hospital environment to the polyclinic. We illustrated the Excel based spreadsheet tool for endocrinology and ophthalmology, however, the model is generic enough to cope with other specialties, provided that the data are available

Transparent SiON/Ag/SiON multilayer passivation grown on a flexible polyethersulfone substrate using a continuous roll-to-roll sputtering system

We have investigated the characteristics of a silicon oxynitride/silver/silicon oxynitride [SiON/Ag/SiON] multilayer passivation grown using a specially designed roll-to-roll [R2R] sputtering system on a flexible polyethersulfone substrate. Optical, structural, and surface properties of the R2R grown SiON/Ag/SiON multilayer were investigated as a function of the SiON thickness at a constant Ag thickness of 12 nm. The flexible SiON/Ag/SiON multilayer has a high optical transmittance of 87.7% at optimized conditions due to the antireflection and surface plasmon effects in the oxide-metal-oxide structure. The water vapor transmission rate of the SiON/Ag/SiON multilayer is 0.031 g/m2 day at an optimized SiON thickness of 110 nm. This indicates that R2R grown SiON/Ag/SiON is a promising thin-film passivation for flexible organic light-emitting diodes and flexible organic photovoltaics due to its simple and low-temperature process