Surpass electrokinetic analyzer
The SurPASS electrokinetic analyzer is a laboratory instrument used to measure the surface charge and zeta potential of solid materials and powders. It is designed to provide accurate and reliable data on the electrokinetic properties of a wide range of samples, including polymers, ceramics, metals, and more.
Lab products found in correlation
39 protocols using surpass electrokinetic analyzer
Electrokinetic Characterization of Fiber Membranes
Membrane Charge Characterization via Streaming Current
Zeta Potential Characterization of Nanofibrous Membranes
where I is the measured streaming current, P the pressure difference across the length of the sample, η and ε the viscosity and dielectric constant of the electrolyte solution, ε 0 the dielectric constant of free space, L the channel length of the measured sample, and A the cross-sectional area along with the sample. Two-1 cm x 2 cm cuts of each sample were fixed inside an adjustable gap cell of the electrokinetic analyzer and the gap between the two opposing faces of the sample was adjusted to approximately 100 μm. An electrolyte solution of 1 mM KCl was used to generate a titration curve of the zeta potential for each sample. The streaming current was logged after 20 seconds of flow-through of a given titration at a pressure of 400 mbar.
Zeta Potential of RFPP Surface
Zeta Potential and Isoelectric Point of Polyamide Fabric
Zeta Potential Analysis of Membrane Surfaces
Zeta Potential Analysis of Membrane Surfaces
Comprehensive Surface Characterization of Membranes
Surface Zeta Potential Characterization
streaming potential measurements were conducted on a SurPASS Electrokinetic
Analyzer (Anton Paar, Germany) at a constant temperature of 22 °C.
Duplicate samples of each coating were first produced within QCM-D
on PS-coated sensors, after which they were immediately fixed inside
an adjustable gap cell using poly(phenylene sulfide) (PPS) disk-shaped
sample holders (d = 14 mm), separated by a 100 μm
spacer foil. Once inserted in the machine, the cell was rinsed several
times with a 1 mM KCl electrolyte solution (pH 7) and the gap was
adjusted to 140 μm. After ensuring linear flow at a pressure
of 200 mbar, the surface ζ-potential was first measured at pH
7, followed by a pH sweep from 6 to 9. Every measurement included
four ramps. The measuring cell was thoroughly rinsed with Milli-Q
between each experiment until the recorded conductivity was well below
0.1 mV. As a reference, streaming potentials were also recorded on
the pristine gold-plated sensor, PS-coated sensor, and the intermediate
PS-b-PAA primer. The obtained data was further analyzed
using Attract software (version 2.1).
Characterization of PVDF-modified PSBMA Membrane
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