Organically modified nanoclay filled thin-film nanocomposite membranes for reverse osmosis application

This study validates, for the first time, the effectiveness of two nanoclays, that is, cloisite (CS)-15A and montmorillonite (MNT) at the polyamide (PA) active layer in the reverse osmosis (RO) membrane. Cloisite-15A is natural montmorillonite modified with dimethyl dihydrogenated tallow quaternary ammonium salt. Thin-film composite (TFC) membranes were fabricated by the interfacial polymerization (IP) process between the trimesoylchloride (TMC)–n-hexane solution and m-phenylenediamine (MPD)–aqueous solution; the IP process took place on a polysulfone support sheet. The two types of nanoparticles were added in various weight ratios (0.005 wt.%–0.04 wt.%) in the n-hexane solution of TMC. Different characterizations like X-ray diffraction (XRD), contact angle, transmission electron microscopy (TEM), and membrane performance tests were performed to analyse the membrane properties. Both XRD and TEM studies proved that the two nanoclays are successfully anchored at the different sites of the PA layer. CS-15A could accelerate the water flux from 15 to 18.65 L/m2·h with NaCl rejection enhancement from 72% to 80%, relative to the control membrane. Conversely, MNT also enhanced the flux from 15 to 40 L/m2·h, but NaCl rejection reduced from 70% to 23%. The mechanism of water uptake in nanoclays was also discussed. The results pave the way for a complete future study, in which these phenomena should be studied in great detail.This research was funded by Qatar University, grant number IRCC-2019-004.The authors would like to acknowledge the support of Qatar University through project number IRCC-2019-004. Also, the authors acknowledge the assistance granted by KACST through the National Science, Technology, and Innovation Plan (NSTIP) unit of King Fahd University of Petroleum and Minerals (KFUPM) through NSTIP research grant number 08WAT-80-4. The assistance in membrane preparation by Matsuura group, Ottawa University, Canada and Rasel Das, Kyushu University Japan for discussion on the results are highly appreciated.Scopu

Fouling mitigation strategies for different foulants in membrane distillation

Providing clean water to a rapidly growing population is an issue that is currently getting lots of attention to offer a sustainable solution for water scarcity. Membrane distillation (MD) is one of the latest technologies that provides great potential in water treatment. Even though there is a tremendous amount of research done during the past two decades on membrane distillation, the long-term use of this process is still restricted by membrane fouling. Membrane Fouling can be defined as the accumulation of various materials in the pores or surface of the membrane that affect permeate's quantity and quality. This review highlights the recent observations on various foulants in MD process. Moreover, different fouling mechanisms of inorganic fouling, organic fouling, biological fouling, and colloidal fouling were investigated for better understanding and prevention of membrane fouling. In order to achieve a sustainable MD process, various techniques to mitigate fouling were discussed comprehensively including pre-treatment processes and cleaning methods. The benefits and disadvantages of these approaches have been investigated and reviewed in order to provide an overall understanding of fouling minimization in membrane distillation process. Fouling mitigation strategies have been suggested for different foulants in membrane distillation

Radiographic morphometry of the Foot in clinically normal Donkeys (Equus asinus)

Radiography of the foot is considered a golden standard technique enables the veterinarians to render a subjective evaluation of the foot in donkeys. The current study aimed to characterize objectively the baseline radiometric data of normal forefeet in donkeys to assess both of the nature and extent of anatomical changes occurring in foot affections. Lateromedial and dorsopalmar radiographic examination were performed on 48 forefeet of 24 clinically normal donkeys of both sexes. Four angles and 10 morphometeric distances were measured in latromedial radiographs and 10 morphometric measurements were measured in dorsopalmer radiographs. All hoof components appeared in the radiographic films were described and morphometric measurements were reported as minimum and maximum values, mean ± standard deviation (SD). The study presented a descriptive reference data for morphometric radiographic parameters of the forefeet from lateromedial and dorsopalmer radiographs in clinically normal donkeys, to assess any changes in hoof conformation and biomechanics associated with hoof affections

First Measurement of the Neutron β\beta-Asymmetry with Ultracold Neutrons

We report the first measurement of angular correlation parameters in neutron $\beta$-decay using polarized ultracold neutrons (UCN). We utilize UCN with energies below about 200 neV, which we guide and store for $\sim 30$ s in a Cu decay volume. The $\vec{\mu}_n \cdot \vec{B}$ potential of a static 7 T field external to the decay volume provides a 420 neV potential energy barrier to the spin state parallel to the field, polarizing the UCN before they pass through an adiabatic fast passage (AFP) spin-flipper and enter a decay volume, situated within a 1 T, $2 \times 2\pi$ superconducting solenoidal spectrometer. We determine a value for the $\beta$-asymmetry parameter $A_0$, proportional to the angular correlation between the neutron polarization and the electron momentum, of $A_0 = -0.1138 \pm 0.0051$.Comment: 4 pages, 2 figures, 1 table, submitted to Phys. Rev. Let

Final results for the neutron β-asymmetry parameter A₀ from the UCNA experiment

The UCNA experiment was designed to measure the neutron β-asymmetry parameter A0 using polarized ultracold neutrons (UCN). UCN produced via downscattering in solid deuterium were polarized via transport through a 7 T magnetic field, and then directed to a 1 T solenoidal electron spectrometer, where the decay electrons were detected in electron detector packages located on the two ends of the spectrometer. A value for A0 was then extracted from the asymmetry in the numbers of counts in the two detector packages. We summarize all of the results from the UCNA experiment, obtained during run periods in 2007, 2008–2009, 2010, and 2011–2013, which ultimately culminated in a 0.67% precision result for A₀

Structural Basis for Substrate Specificity in Human Monomeric Carbonyl Reductases

Carbonyl reduction constitutes a phase I reaction for many xenobiotics and is carried out in mammals mainly by members of two protein families, namely aldo-keto reductases and short-chain dehydrogenases/reductases. In addition to their capacity to reduce xenobiotics, several of the enzymes act on endogenous compounds such as steroids or eicosanoids. One of the major carbonyl reducing enzymes found in humans is carbonyl reductase 1 (CBR1) with a very broad substrate spectrum. A paralog, carbonyl reductase 3 (CBR3) has about 70% sequence identity and has not been sufficiently characterized to date. Screening of a focused xenobiotic compound library revealed that CBR3 has narrower substrate specificity and acts on several orthoquinones, as well as isatin or the anticancer drug oracin. To further investigate structure-activity relationships between these enzymes we crystallized CBR3, performed substrate docking, site-directed mutagenesis and compared its kinetic features to CBR1. Despite high sequence similarities, the active sites differ in shape and surface properties. The data reveal that the differences in substrate specificity are largely due to a short segment of a substrate binding loop comprising critical residues Trp229/Pro230, Ala235/Asp236 as well as part of the active site formed by Met141/Gln142 in CBR1 and CBR3, respectively. The data suggest a minor role in xenobiotic metabolism for CBR3. ENHANCED VERSION: This article can also be viewed as an enhanced version in which the text of the article is integrated with interactive 3D representations and animated transitions. Please note that a web plugin is required to access this enhanced functionality. Instructions for the installation and use of the web plugin are available in Text S1