scholarly journals Hydraulic Resistance and Protein Fouling Resistance of a Zirconia Membrane with a Tethered PVP Layer

Water ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 951
Author(s):  
Yian Chen ◽  
Montserrat Rovira-Bru ◽  
Francesc Giralt ◽  
Yoram Cohen
Keyword(s):  
Ionic Strength ◽  
Hydraulic Resistance ◽  
Membrane Fouling ◽  
Vinyl Pyrrolidone ◽  
Fouling Resistance ◽  
Model Protein ◽  
Poly Vinyl Pyrrolidone ◽  
Ph Range ◽  
Fouling Reduction ◽  
The Impact

The influence of surface modification of zirconia (ZrO2) membrane with tethered poly(vinyl pyrrolidone) (PVP) chains was evaluated with respect to the impact of pH and ionic strength on hydraulic resistance and fouling resistance in the filtration of bovine serum albumin (BSA) and lysozyme (Lys) as model protein foulants. The tethered PVP surface layer led to membrane permeability and fouling propensity that were responsive to both pH and ionic strength. The PVP-modified membrane (PVP-ZrO2) hydraulic resistance increased by up to ~48% over a pH range of 6–11, but with no discernible impact at lower pH. Membrane hydraulic resistance was virtually unaffected by ionic strength over the 0.001–1 M range. However, reversible foulant cake resistance in BSA and Lys solution filtration increased with elevated ionic strength, owing in part to the weakening of protein–protein repulsion. Irreversible BSA and Lys fouling was affected by the operational pH relative to the protein isoelectric point (IEP) and reduced under conditions of chain swelling. Irreversible membrane fouling resistance for both proteins was significantly lower, by ~11–49% and 18–74%, respectively, for the PVP-ZrO2 membrane relative to the unmodified ZrO2 membrane. The present results suggest the merit of further exploration of fouling reduction and improvement of membrane cleaning effectiveness via tuning pH and ionic strength triggered conformational responsiveness of the tethered target polymer layer.

Evaluation of Surfactants on Thermo-Physical Properties of Magnesia-Oil Nanofluid

2018 ◽  
Vol 928 ◽  
pp. 106-112 ◽  
Author(s):  
Abdallah Yousef Mohammed Ali ◽  
Ahmed H. El-Shazly ◽  
M.F. Elkady ◽  
S.E. AbdElhafez
Keyword(s):  
Vinyl Pyrrolidone ◽  
Poly Vinyl Alcohol ◽  
Ammonium Bromide ◽  
X Ray Diffraction ◽  
Mgo Nanoparticles ◽  
Transmission Electron ◽  
Wet Chemical ◽  
Cetyl Trimethyl Ammonium ◽  
Poly Vinyl Pyrrolidone ◽  
The Impact

The prime purpose of the current study was to investigate the consequence of surfactant on the kinematic viscosity, thermal conductivity, and stability of MgO-oil based nanofluid. Magnesia (MgO) nanoparticles were prepared by the wet chemical method. Structural and morphological analysis of synthesized nanoparticles were performed via X-ray diffraction (XRD) and Transmission electron microscope (TEM). Subsequently, nanofluid was prepared at a solid concentration of 0.025% in presence of various surfactants with the aid of ultrasonic technique. The impact of the different surfactants (Cetyl Trimethyl Ammonium Bromide (CTAB), Poly Vinyl Pyrrolidone (PVP), Poly Vinyl Alcohol (PVA), and Oleic Acid) on the nanofluid stability was tested. It was evident that CTAB and PVA surfactants establish the most stable prepared MgO-oil based nanofluid. The experiments revealed that the maximum UV–Vis absorbance of the solution corresponds to the dispersion of CTAB in the base fluid.

scholarly journals In-line coagulation assessment for ultrafiltration fouling reduction to treat secondary effluent for water reuse

2020 ◽  
Author(s):  
Samia A. Aly ◽  
William B. Anderson ◽  
Peter M. Huck
Keyword(s):  
Membrane Fouling ◽  
Water Reuse ◽  
Hollow Fiber Membrane ◽  
Secondary Effluent ◽  
Membrane Performance ◽  
Coagulant Dosage ◽  
Pre Treatment ◽  
Uf Membranes ◽  
Fouling Reduction ◽  
The Impact

Abstract Low pressure membranes are attracting attention for their potential to improve secondary effluent quality, but membrane fouling can limit their widespread applicability. In this study, in-line coagulation as pre-treatment to ultrafiltration (UF) was investigated using a bench-scale hollow fiber membrane at a constant flux of 33 L/m2 h. Membrane fouling was monitored by observing change in trans-membrane pressure when the membrane was fed with secondary effluent and in-line coagulated secondary effluent over a 24-h period. The impact of four coagulants at different dosages on reversible and irreversible membrane fouling and permeate quality was studied. It was found that in-line coagulation improved UF performance to varying degrees depending on coagulant type and dosage. Generally, higher reduction of fouling was achieved by increasing coagulant dosage within the 0.5–5.0 mg/L range investigated. Ferric-based coagulants were better than aluminum-based coagulants with respect to improving membrane performance for the secondary effluent investigated, even at low dosages (0.5 mg/L). Further investigations are required to determine how in-line coagulation affects removal of organic compounds through UF membranes.

scholarly journals Membrane Filtration of Anionic Surfactant Stabilized Emulsions: Effect of Ionic Strength on Fouling and Droplet Adhesion

2019 ◽  
Vol 3 (1) ◽  
pp. 9 ◽  
Author(s):  
Janneke Dickhout ◽  
Rob Lammertink ◽  
Wiebe de Vos
Keyword(s):  
Ionic Strength ◽  
Anionic Surfactant ◽  
Membrane Fouling ◽  
Flow Cell ◽  
Cellulose Membrane ◽  
Oil Droplets ◽  
Flux Decline ◽  
Cake Layer ◽  
The Impact ◽  
Cellulose Surface

Membranes hold great potential to be used for the successful treatment of oily waste water, but membrane fouling leads to substantial decreases in performance. Here we study the impact of ionic strength on membrane fouling from an emulsion stabilized by the anionic surfactant sodium dodecyl sulfonate (SDS). For this we use a unique combinatorial approach where droplet adhesion to a cellulose surface in a flow cell is compared to membrane fouling (flux decline) on a cellulose membrane. In the initial membrane fouling stages droplet adhesion dominates. While the flow cell demonstrates a high number of droplets adhering especially at high ionic strengths (100 mM NaCl), the strongest flux decline is observed at intermediate (10 mM NaCl) ionic strength. This suggests that the fouling mechanism must be different, with pore blocking expecting to dominate at intermediate ionic strength. At the later fouling stages the porosity of the cake layer plays a key role in the flux reduction. At low ionic strength, oil droplets repel each other strongly and an open, more permeable, cake layer is formed. However at higher ionic strength, a screening of charge interactions leads to a lower porosity and thereby a lower flux. This leads to a clear trend: with a higher ionic strength a higher flux decline is observed. Flux recovery is high at all ionic strengths, in line with the observation in the flow cell that oil droplets can easily be sheared of a cellulose surface at all ionic strengths. This work thus highlights the critical effect of the ionic strength on membrane fouling by anionically stabilized emulsions. Moreover it shows how the use of an optical flow cell can provide key insights to help explain observations in more standard membrane fouling experiments.

scholarly journals ALD coating of centrifugally spun polymeric fibers and postannealing: case study for nanotubular TiO2 photocatalyst

2021 ◽  
Author(s):  
Martina Rihova ◽  
Oksana Yurkevich ◽  
Martin Motola ◽  
Ludek Hromadko ◽  
Zdeněk Spotz ◽  
...  
Keyword(s):  
Atomic Layer Deposition ◽  
Atomic Layer ◽  
Vinyl Pyrrolidone ◽  
Tio2 Photocatalyst ◽  
Polymeric Fibers ◽  
Layer Deposition ◽  
Centrifugal Spinning ◽  
Poly Vinyl Pyrrolidone

This work describes the synthesis of highly photocatalytically active TiO2 tubes (TiTBs) by combining centrifugal spinning and atomic layer deposition (ALD). Poly(vinyl pyrrolidone) (PVP) fibers were first produced by centrifugal...

scholarly journals Virus-Like Particles Produced Using the Brome Mosaic Virus Recombinant Capsid Protein Expressed in a Bacterial System

2021 ◽  
Vol 22 (6) ◽  
pp. 3098
Author(s):  
Aleksander Strugała ◽  
Jakub Jagielski ◽  
Karol Kamel ◽  
Grzegorz Nowaczyk ◽  
Marcin Radom ◽  
...  
Keyword(s):  
Ionic Strength ◽  
Mosaic Virus ◽  
Capsid Protein ◽  
Self Assembly ◽  
Environmental Changes ◽  
Expression System ◽  
Brome Mosaic Virus ◽  
Virus Like Particles ◽  
Assembly Principles ◽  
The Impact

Virus-like particles (VLPs), due to their nanoscale dimensions, presence of interior cavities, self-organization abilities and responsiveness to environmental changes, are of interest in the field of nanotechnology. Nevertheless, comprehensive knowledge of VLP self-assembly principles is incomplete. VLP formation is governed by two types of interactions: protein–cargo and protein–protein. These interactions can be modulated by the physicochemical properties of the surroundings. Here, we used brome mosaic virus (BMV) capsid protein produced in an E. coli expression system to study the impact of ionic strength, pH and encapsulated cargo on the assembly of VLPs and their features. We showed that empty VLP assembly strongly depends on pH whereas ionic strength of the buffer plays secondary but significant role. Comparison of VLPs containing tRNA and polystyrene sulfonic acid (PSS) revealed that the structured tRNA profoundly increases VLPs stability. We also designed and produced mutated BMV capsid proteins that formed VLPs showing altered diameters and stability compared to VLPs composed of unmodified proteins. We also observed that VLPs containing unstructured polyelectrolyte (PSS) adopt compact but not necessarily more stable structures. Thus, our methodology of VLP production allows for obtaining different VLP variants and their adjustment to the incorporated cargo.

scholarly journals Potential Implantable Nanofibrous Biomaterials Combined with Stem Cells for Subchondral Bone Regeneration

Materials ◽  
2020 ◽  
Vol 13 (14) ◽  
pp. 3087
Author(s):  
Rana Smaida ◽  
Luc Pijnenburg ◽  
Silvia Irusta ◽  
Erico Himawan ◽  
Gracia Mendoza ◽  
...  
Keyword(s):  
Stem Cells ◽  
Bone Regeneration ◽  
Subchondral Bone ◽  
Therapeutic Potential ◽  
Sodium Hyaluronate ◽  
Vinyl Pyrrolidone ◽  
Regenerative Ability ◽  
Poly Vinyl Pyrrolidone

The treatment of osteochondral defects remains a challenge. Four scaffolds were produced using Food and Drug Administration (FDA)-approved polymers to investigate their therapeutic potential for the regeneration of the osteochondral unit. Polycaprolactone (PCL) and poly(vinyl-pyrrolidone) (PVP) scaffolds were made by electrohydrodynamic techniques. Hydroxyapatite (HAp) and/or sodium hyaluronate (HA) can be then loaded to PCL nanofibers and/or PVP particles. The purpose of adding hydroxyapatite and sodium hyaluronate into PCL/PVP scaffolds is to increase the regenerative ability for subchondral bone and joint cartilage, respectively. Human bone marrow-derived mesenchymal stem cells (hBM-MSCs) were seeded on these biomaterials. The biocompatibility of these biomaterials in vitro and in vivo, as well as their potential to support MSC differentiation under specific chondrogenic or osteogenic conditions, were evaluated. We show here that hBM-MSCs could proliferate and differentiate both in vitro and in vivo on these biomaterials. In addition, the PCL-HAp could effectively increase the mineralization and induce the differentiation of MSCs into osteoblasts in an osteogenic condition. These results indicate that PCL-HAp biomaterials combined with MSCs could be a beneficial candidate for subchondral bone regeneration.

scholarly journals Single entity electrochemistry and the electron transfer kinetics of hydrazine oxidation

Nano Research ◽  
2021 ◽  
Author(s):  
Ruiyang Miao ◽  
Lidong Shao ◽  
Richard G. Compton
Keyword(s):  
Electron Transfer ◽  
Bulk Solution ◽  
Relative Contribution ◽  
Rate Determining Step ◽  
Multistep Process ◽  
Ph Range ◽  
Electro Catalytic Oxidation ◽  
Single Particle Impact ◽  
The Impact ◽  
Kinetics Of

AbstractThe mechanism and kinetics of the electro-catalytic oxidation of hydrazine by graphene oxide platelets randomly decorated with palladium nanoparticles are deduced using single particle impact electrochemical measurements in buffered aqueous solutions across the pH range 2–11. Both hydrazine, N2H4, and protonated hydrazine N2H5+ are shown to be electroactive following Butler-Volmer kinetics, of which the relative contribution is strongly pH-dependent. The negligible interconversion between N2H4 and N2H5+ due to the sufficiently short timescale of the impact voltammetry, allows the analysis of the two electron transfer rates from impact signals thus reflecting the composition of the bulk solution at the pH in question. In this way the rate determining step in the oxidation of each specie is deduced to be a one electron step in which no protons are released and so likely corresponds to the initial formation of a very short-lived radical cation either in solution or adsorbed on the platelet. Overall the work establishes a generic method for the elucidation of the rate determining electron transfer in a multistep process free from any complexity imposed by preceding or following chemical reactions which occur on the timescale of conventional voltammetry.

scholarly journals In Vitro Drug Release, Permeability, and Structural Test of Ciprofloxacin-Loaded Nanofibers

Pharmaceutics ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 556
Author(s):  
Luca Éva Uhljar ◽  
Sheng Yuan Kan ◽  
Norbert Radacsi ◽  
Vasileios Koutsos ◽  
Piroska Szabó-Révész ◽  
...  
Keyword(s):  
Amorphous State ◽  
Physical Mixture ◽  
Water Soluble ◽  
Vinyl Pyrrolidone ◽  
Amorphous Solid Dispersion ◽  
Release Mechanism ◽  
Dissolution Studies ◽  
In Vitro Diffusion ◽  
Poly Vinyl Pyrrolidone

Nanofibers of the poorly water-soluble antibiotic ciprofloxacin (CIP) were fabricated in the form of an amorphous solid dispersion by using poly(vinyl pyrrolidone) as a polymer matrix, by the low-cost electrospinning method. The solubility of the nanofibers as well as their in vitro diffusion were remarkably higher than those of the CIP powder or the physical mixture of the two components. The fiber size and morphology were optimized, and it was found that the addition of the CIP to the electrospinning solution decreased the nanofiber diameter, leading to an increased specific surface area. Structural characterization confirmed the interactions between the drug and the polymer and the amorphous state of CIP inside the nanofibers. Since the solubility of CIP is pH-dependent, the in vitro solubility and dissolution studies were executed at different pH levels. The nanofiber sample with the finest morphology demonstrated a significant increase in solubility both in water and pH 7.4 buffer. Single medium and two-stage biorelevant dissolution studies were performed, and the release mechanism was described by mathematical models. Besides, in vitro diffusion from pH 6.8 to pH 7.4 notably increased when compared with the pure drug and physical mixture. Ciprofloxacin-loaded poly(vinyl pyrrolidone) (PVP) nanofibers can be considered as fast-dissolving formulations with improved physicochemical properties.

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