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Glass microfibre filter

Manufactured by Cytiva
Sourced in United Kingdom

Glass microfibre filters are porous, high-quality filter media made from pure borosilicate glass fibers. They are designed for a wide range of filtration applications, providing efficient retention of small particles and contaminants.

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7 protocols using glass microfibre filter

1

Waste Polyurethane Elastomer-based Supercapacitor

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Symmetric two-electrode cells were fabricated to analyse the charge-storage capabilities of electrodes based on EFAC1 and EFAC2 in an aqueous, 6 M KOH electrolyte. The electrode inks were prepared by mixing the CFs (70%) with PVDF (20%) and Carbon Black (10%) with a total weight of 0.4 g in 4 mL NMP. PVDF acts as a binder, while Carbon Black is a conductivity enhancement agent. The homogeneous ink was cast on Ni foil (current collector) using a doctor blade setup and dried in an oven. The average thickness of the films was 40 μm. Circular electrodes of 12 mm diameter were obtained using a steel punch. The effective mass of active material on each electrode was ~ 2.4 mg. Two electrodes with very similar active material masses were chosen and pressed at 6.9 MPa. Before assembly, 14 mm glass microfibre filter (Whatman) separators were soaked in a 6 M KOH electrolyte. CR2032 coin cell cases were used for the fabrication of supercapacitors. The assembled cells were pressed at 5.2 MPa using a crimper and the cells were left for 24 h to allow the electrodes to sufficiently soak the electrolyte before measurement. The schematic representation of waste polyurethane elastomer-based CF electrode assembled in a symmetric two-electrode cell is shown in Fig. 1.

Schematic representation of waste polyurethane elastomer-based CF electrode for a symmetric two-electrode cell.

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2

Radiolabeled Uracil Uptake Assay

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One microlitre of 5,6,-3H uracil (1 µCi) was added to 1 ml culture samples and incubated at 37°C with agitation for 20 h. Two hundred microlitres of this culture was placed in 3 ml 7% ice-cold CCl3COOH and incubated at 0°C for 20 min, followed by filtration through a glass microfibre filter (Whatman). Precipitated cells were washed with 3 ml 7% CCl3COOH and 6 ml 96% ethanol. Filters were placed in 10 ml scintillation mixture; impulse counts were determined by LS analyser (Beckman Instruments) and expressed as counts per minute (cpm).
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3

Lithium-ion Cell Assembly Under Inert Atmosphere

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The electrodes were assembled in ‘coffee bag'-type cells all assembled under argon atmosphere (<0.1 p.p.m. O2/H2O). The electrodes were separated by glass microfibre filters (Whatman) with a few droplets of 1 mol l−1 LiPF6 (EC:DMC 1:1, Novolyte) electrolyte. All the electrochemical tests were performed galvanostatically within a voltage window of 4.3 and 2.5 V versus Li/Li+ using an Autolab PGSTAT302N potentiostat/galvanostat.
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4

Sustainable Herbal Extract Infusion and Fabric Treatment

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The 30 g of raw herbal leaves was infused in 500 ml of distilled water at 60℃ and steeped for 2 h for the extraction process to complete sustainably. The extract was filtered with Whatman glass microfibre filters of 70 mm. The prepared 6% of the stock solution was further utilized for cotton fabric treatment; refer to Fig. 1.

The extraction process of herbs in research

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5

Antibacterial Efficacy of BG Composites

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The antibacterial activity of BG composites was determined using the paper disc diffusion assay reported earlier32 . In brief, Tryptic Soy Agar (TSA) plates were prepared and inoculated with a 1 mL cell suspension of each bacterial pathogen separately, including gram-negative bacteria Pseudomonas aeruginosa (ATCC 10145) and Aeromonas hydrophila strain, and gram-positive bacteria Staphylococcus aureus (ATCC 25923), obtained from the Microbial Inoculants Center—MIC, Ain Shams University, Egypt. Each pathogenic bacteria strain's pure culture was inoculated on TSA plates and incubated for 24 h at 37 °C. 4–5 loops from each strand were transferred into culture tubes containing 5 mL of sterile Tryptic Soy Broth (TSB) and incubated for 12 h at 37 °C. Mueller Hinton agar plates were inoculated with a 106 cell/mL microorganism suspension using cotton swabs. Sterile filter paper discs (Whatman® Glass Microfibre filters, 6 mm in diameter) were impregnated with 20 µg/mL of various MO nanoparticle solutions.
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6

Monocyte-PBMC Co-culture Proliferation Assay

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For, co-culture experiments, the monocytes were isolated as described earlier and plated out at 1 × 106 cells/well in 24-welled plates as triplicates, treated with rapamycin for 2 h, and then washed with PBS. Furthermore, these monocytes were subjected to rWmhsp60 stimulation for 24 h. The monocytes (104 cells/ml) were then co-cultured with monocyte-depleted PMBC (106 cells/ml) cells in a final volume of 500 μl medium in 24-well plates and stimulated with PHA, (5 μg/ml) for 48 h. [3H] Thymidine from DuPont NEN (Boston, MA) was added to the cells, at a final concentration of 1 μCi/ml, 3 h prior to the termination of the experiment. The cells were harvested, and the cell lysates were put onto the filter (Glass microfibre filters; Whatman International Ltd, Maidstone, England) and were washed three times with 5% trichloracetic acid and one time with acetone on a filter. The cell pellet on the filter was dissolved in 10 ml of Biofluor (Fisher Scientific, Pittsburgh, PA), and the radioactivity was determined by liquid scintillation counting. The cell growth was expressed as stimulation index.
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7

Selenium Speciation Analysis by HPLC-ICP-MS

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Separations were performed on an Agilent Zorbax RX-C8 4.6 × 250 mm 5 μm column using an Agilent Technologies 1260 infinity series LC system connected to an Agilent Technologies 7700× series ICP-MS. The mobile phase was water/methanol/TFA (97.9:2.0:0.1) at a flow rate of 1 mL/min, and the column temperature was set at 30 °C.
A Heinemann 130W ultrasonic-homogeniser (HTU SONI 130, USA) equipped with a 3 mm double step titanium probe was used for sample preparation. A CEM Discover microwave equipped with an Explorer SP-D Plus 24/48 autosampler was used for sample extraction. An ELGA Purelab Flex S7 HPLC water system was used to produce >18 MΩ cm water, and samples were filtered using Chromafil Xtra RC-20/25. The HPLC mobile phase was filtered with Whatman Glass Microfibre Filters.
SeMet standard powder was obtained from Sigma (>98 % by TLC). This was used to prepare a 100 mg/L stock solution in 0.1 M HCl. Aliquots (0.1 mL) of this solution were frozen and used fresh each day.
The instrument was calibrated over the range of 50 to 250 ppb SeMet (20.15 to 100.75 ppb Se as SeMet) as described previously [19] .
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