Non-Solvent Influence of Hydrophobic Polymeric Layer Deposition on PVDF Hollow Fiber Membrane for CO2 Gas Absorption

The implementation of hydrophobicity on membranes is becoming crucial in current membrane technological development, especially in membrane gas absorption (MGA). In order to prevent membrane wetting, a polypropylene (PP) dense layer coating was deposited on a commercial poly(vinylidene fluoride) (PVDF) hollow fiber membrane as a method of enhancing surface hydrophobicity. The weight concentration of PP pellets was varied from 10 mg mL−1 to 40 mg mL−1 and dissolved in xylene. A two-step dip coating was implemented where the PVDF membrane was immersed in a non-solvent followed by a polymer coating solution. The effects of the modified membrane with the non-solvent methyl ethyl ketone (MEK) and without the non–solvent was investigated over all weight concentrations of the coating solution. The SEM investigation found that the modified membrane surface transfiguration formed microspherulites that intensified as PP concentration increased with and without MEK. To understand the coating formation further, the solvent–non-solvent compatibility with the polymer was also discussed in this study. The membrane characterizations on the porosity, the contact angle, and the FTIR spectra were also conducted in determining the polymer coating properties. Hydrophobic membrane was achieved up to 119.85° contact angle and peak porosity of 87.62% using MEK as the non-solvent 40 mg mL−1 PP concentration. The objective of the current manuscript was to test the hydrophobicity and wetting degree of the coating layer. Hence, physical absorption via the membrane contactor using CO2 as the feed gas was carried out. The maximum CO2 flux of 3.33 × 10−4 mol m−2 s−1 was achieved by 25 mg modified membrane at a fixed absorbent flow rate of 100 mL min−1 while 40 mg modified membrane showed better overall flux stability.

Inner Surface Hydrophilic Modification of PVDF Membrane with Tea Polyphenols/Silica Composite Coating

The use of Polyvinylidene fluoride (PVDF) membranes is constrained in wastewater treatment because of their hydrophobic nature. Therefore, a large number of researchers have been working on the hydrophilic modification of their surfaces. In this work, a superhydrophilic tea polyphenols/silica composite coating was developed by a one-step process. The composite coating can achieve not only superhydrophilic modification of the surface, but also the inner surface of the porous PVDF membrane, which endows the modified membrane with excellent water permeability. The modified membrane possesses ultrahigh water flux (15,353 L·m−2·h−1). Besides this, the modified membrane can realize a highly efficient separation of oil/water emulsions (above 96%).

Preparation of Hollow Fiber Membrane Containing ZnO Nanoparticles to Remove Natural Organic Matter

Polyethersulfone/zinc oxide mixed matrix hollow fiber membrane was fabricated using dry/wet phase inversion method. Zinc oxide nanoparticles (2 wt.%) were dispersed in N,N-dimethylacetamide (DMAc) solvent in the present of polyvinylepyrrolidene. The dope solution speed and take up speed was similar with performing the spinning process at room temperature. The produced membranes were characterized using scanning electron microscope (SEM), atomic force microscope (AFM), and Fourier transform infrared (FTIR) analysis. Membrane performance was evaluated using pure water flux (PWF), relative flux ration (RFR), and total organic carbon (TOC) removal efficiency. From SEM analysis, it was found that the nanoparticles were well dispersed in the polymeric matrix. From AFM results, it was observed that the modified membrane has higher surface roughness. The PWF of the modified membrane was enhanced, while the RFR showed to increase due to rougher membrane surface. The NOM remaoval of PES/ZnO membrane was higher than that of PES membrane and reached to 27% compared to only 16.9 % for pristine PES.

Aconitate decarboxylase 1 participates in the control of pulmonary Brucella infection in mice

Brucellosis is one of the most widespread bacterial zoonoses worldwide. Here, our aim was to identify the effector mechanisms controlling the early stages of intranasal infection with Brucella in C57BL/6 mice. During the first 48 hours of infection, alveolar macrophages (AMs) are the main cells infected in the lungs. Using RNA sequencing, we identified the aconitate decarboxylase 1 gene (Acod1; also known as Immune responsive gene 1), as one of the genes most upregulated in murine AMs in response to B. melitensis infection at 24 hours post-infection. Upregulation of Acod1 was confirmed by RT-qPCR in lungs infected with B. melitensis and B. abortus. We observed that Acod1-/- C57BL/6 mice display a higher bacterial load in their lungs than wild-type (wt) mice following B. melitensis or B. abortus infection, demonstrating that Acod1 participates in the control of pulmonary Brucella infection. The ACOD1 enzyme is mostly produced in mitochondria of macrophages, and converts cis-aconitate, a metabolite in the Krebs cycle, into itaconate. Dimethyl itaconate (DMI), a chemically-modified membrane permeable form of itaconate, has a dose-dependent inhibitory effect on Brucella growth in vitro. Interestingly, structural analysis suggests the binding of itaconate into the binding site of B. abortus isocitrate lyase. DMI does not inhibit multiplication of the isocitrate lyase deletion mutant ΔaceA B. abortus in vitro. Finally, we observed that, unlike the wt strain, the ΔaceA B. abortus strain multiplies similarly in wt and Acod1-/- C57BL/6 mice. These data suggest that bacterial isocitrate lyase might be a target of itaconate in AMs.

Sodium Chloroacetate Modified Polyethyleneimine/Trimesic Acid Nanofiltration Membrane to Improve Antifouling Performance

Nanofiltration (NF) is a separation technology with broad application prospects. Membrane fouling is an important bottleneck-restricting technology development. In the past, we prepared a positively charged polyethyleneimine/trimesic acid (PEI/TMA) NF membrane with excellent performance. Inevitably, it also faces poor resistance to protein contamination. Improving the antifouling ability of the PEI/TMA membrane can be achieved by considering the hydrophilicity and chargeability of the membrane surface. In this work, sodium chloroacetate (ClCH2COONa) is used as a modifier and is grafted onto the membrane surface. Additionally, 0.5% ClCH2COONa and 10 h modification time are the best conditions. Compared with the original membrane (M0, 17.2 L m−2 h−1), the initial flux of the modified membrane (M0-e, 30 L m−2 h−1) was effectively increased. After filtering the bovine albumin (BSA) solution, the original membrane flux dropped by 47% and the modified membrane dropped by 6.2%. The modification greatly improved the antipollution performance of the PEI/TMA membrane.