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Zeta potential analyzer

Manufactured by Brookhaven Instruments
Sourced in United States

The Zeta Potential Analyzer is a laboratory instrument used to measure the zeta potential of particles or materials suspended in a liquid medium. It determines the electrical potential at the slipping plane of a particle, which is a key indicator of the stability and behavior of colloidal systems.

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33 protocols using zeta potential analyzer

1

Characterization of SEDDS Formulations

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The droplet size, zeta potential, and poly dispersibility index (PDI) of the SEDDS formulations were analyzed by dynamic light scattering technique (Nanobrook 90Plus Zeta PALS, Zeta Potential analyzer, Brookhaven Instruments Corporation, Holtsville, NY, USA) at 25 °C with a scattering angle of 90°. All samples were diluted ten times with pH 7.4 PBS before analysis. Each formulation was analyzed in triplicate.
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2

Physicochemical Characterization of Nanoparticles

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The size and morphology of the nanoparticles were examined by transmission electron microscopy (TEM) (JEM-100CX; JEOL, Tokyo, Japan) and scanning electron microscopy (SEM) (Helios NanoLab 650; FEI, Eindhoven, the Netherlands). The zeta-potentials and particle size distributions were determined using a ZetaPlus particle size and a zeta potential analyzer (Brookhaven Instruments, Holtsville, NY, USA) in water at 25°C in accordance with the manufacturer’s operating manual. The 1H NMR spectra of the PEG-FA and PPF were recorded using a Bruker AVANCE 600 nuclear magnetic resonance spectrometer (Bruker, Fällanden, Switzerland). The lyophilized PEG-FA and PPF were dissolved in deu-terated DMSO (DMSO-d6) and D2O, respectively, before measurements.
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3

Zeta-Potential Measurement of Samples

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The zeta-potential of the freshly prepared samples were measured by the zeta-potential analyzer (Brookhaven Instruments, Holtsville, NY) at the various pH values from 3 to 8. The suspensions were diluted by 80 times to minimize the electrokinetic potential not a contribution from inter-colloidal interaction.
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4

Zeta Potential Analysis of Leachates

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DLS (Zeta Potential Analyzer, Brookhaven Instruments, Gaia Science Pte. Ltd.) analysis was performed using disposable single sealed cuvettes (size: 50–2000 μL, Eppendorf) containing 200 μL of the leachate solution and BIC Particle Sizing software (Brookhaven Instruments). The effective diameter was detected in five measurement cycles (each cycle running for 1 min) at a scattering angle of 90 °. The light percent distribution and number percent distribution were also detected to verify and compare the particle size distribution.
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5

Zeta Potential Analysis of Functionalized MNPs

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The zeta potential of naked, silica coated, amino- and inert group-functionalized MNPs was measured with a Zeta Potential Analyzer (Brookhaven, Holtsville, NY, USA) using the Zeta Phase Analysis Light Scattering (PALS) method. Re-dispersed samples (0.4 mL, containing 1.0 mg nanoparticles and 1.0 mL 1 mM KCl) were diluted 5-fold in 1 mM KCl aqueous solution. Measurements carried out in a disposable, solvent resistant micro cuvette and took 2 min. The zeta potential was calculated from the electrophoretic mobility using the Smoluchowski equation.
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6

Comprehensive Material Characterization Protocol

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Transmission electron microscopy (TEM) analysis was conducted on a TECNAI G2 20 electron microscope operated at 200 kV. Scanning electron microscopy (SEM) analysis was conducted on FEI Quanta 250 F system. Nitrogen adsorption–desorption isotherms were analyzed using a Micromeritics ASAP-2020 at 77 K. X-ray photoelectron spectroscopy (XPS) spectra were obtained using a PHI Quantera II ESCA system with Al Kα radiation at 1486.8 eV. Fourier transform infrared spectroscopy (FTIR) was performed using a Prestige 21 at 400–4000 cm−1. The zeta potential of APNs was analyzed using a Brookhaven zeta potential analyzer. Concentrations of chromium were analyzed via atomic absorption spectroscopy (AAS) and ultraviolet and visible spectroscopy (UV-Vis), which were conducted on a Perkin Elmer PinAAcle 900 and Lambda 750, respectively.
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7

Comprehensive Characterization of Nanozymes

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An ultraviolet (UV) spectrophotometer (Beckham Coulter, Brea, CA, USA) was utilized to measure the absorption of TMB working solution with nanozymes at 652 nm. Particle size and Zeta Potential Analyzer (Brookhaven, New York, NY, USA) was applied to measure the value of Zeta potential and PDI. X-ray powder diffractometer (Bruker, Billerica, MA, USA) was used to identify the composition of the synthesized nanozymes. An infrared spectrometer (Thermo Scientific Nicolet, Waltham, MA, USA) was applied to characterize the modified groups on the surface of the nanozymes. The Field Emission Transmission Electron Microscopy (FEI Company, Hillsboro, OR, USA) was utilized to analyze the morphology and elemental mapping of the nanozymes. The Field Emission Scanning Electron Microscopy (Hitachi, Tokyo, Japan) was used to observe the distribution of nanozyme particles on the NC membrane.
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8

Particle Size Analysis by DLS

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Measurement of EPS particles by DLS was performed with a Zeta Potential Analyzer instrument (Brookhaven Instruments). The particle sizes in the suspension were measured for native samples as well as lyophilized and rehydrated samples at different time points during a period of 28 days. Data are expressed as the average of 10 runs of 1-min data collection each. The multimodal size distributions of the particles were obtained by a non-negatively constrained least squares algorithm based on the intensity of light scattered by each particle. The multimodal size distributions of particles from each sample were graphed for comparison.
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9

Particle Size Analysis by DLS

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Measurement of particle size by dynamic light scattering was performed with a Zeta Potential Analyzer instrument (Brookhaven Instruments). The particle sizes in the suspension were measured for all samples, and data are expressed as the average of 10 runs of 1-min data collection each. Each PS preparation (100 μl) was added to an UVette Cuvette (Eppendorf) at room temperature. The multimodal size distributions of the particles were obtained by a non-negatively constrained least squares algorithm based on the intensity of light scattered by each particle. The multimodal size distributions of particles from each sample were graphed for comparison.
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10

Zeta Potential Measurement of Coal and Silica

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Both coal
sample and silica were ground to −30 μm using an Agate
pestle for the ζ-potential test. HCl (25.00% v/v) and NaOH (99.99%
grade) were used for pH adjustment. The concentration of KCl used
as the supporting electrolyte was 10–3 M. Distilled
water was used in the whole process. The procedures were as follows:
0.2 g of sub-bituminous coal or silica was put into a 100 mL beaker,
and the supporting electrolyte close to 100 mL was added. Then, the
pH of the pulp was adjusted to different values after sufficient mixing.
Afterward, the pulp was transferred into a 100 mL volumetric flask
and 0.57 mL of 1% Lilaflot D817M was added into the volumetric flask.
The cap of the volumetric flask was tightened, and the flask was shaken
up and down three times before putting it into an ultrasonic water
bath for 15 min to diversify the pulp well. Last, the volumetric flask
was taken out from the ultrasonic water bath and 1.5 mL of the supernatant
was extracted for the ζ-potential test by a pipette after 15
min standing. The zeta potential analyzer used in this research is
manufactured by Brookhaven Instruments Corporation. Every sample was
tested 10 times, and the average values were taken.
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