The largest database of trusted experimental protocols

Zetasizer ht

Manufactured by Malvern Panalytical
Sourced in United Kingdom

The ZetaSizer-HT is a laboratory instrument designed for particle size and zeta potential measurement. It utilizes dynamic light scattering (DLS) and electrophoretic light scattering (ELS) technologies to determine the size and surface charge characteristics of particles suspended in a liquid medium. The core function of the ZetaSizer-HT is to provide accurate and reliable measurements of these properties for a wide range of samples.

Automatically generated - may contain errors

4 protocols using zetasizer ht

1

Synthesis and Characterization of Silver Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
AgNPs were prepared by the reduction of silver nitrate solution with aniline in the presence of CTAB. A series of experiments was performed in which variances were made in the concentrations of oxidant, reductant, and stabilizer in order to obtain a perfectly transparent silver solution. In a typical procedure, 8 mL of a 0.01 mol/dm3 solution of silver nitrate was mixed with 5 mL of a 0.01 mol/dm3 CTAB solution. The colorless reaction mixture slowly converted to the characteristic pale yellow color when 20 mL of a 0.01 mol/dm3 solution of aniline was added in the solution of silver nitrate and CTAB. The total volume of the reaction mixture was always 50 mL. The whole solution had a pH of 10.2. The appearance of color indicated the formation of AgNPs.11
AgNPs were suspended in Milli-Q water at a concentration of 10 mg/10 mL. The stock suspension was probe sonicated at 40 W for 15 minutes. The hydrodynamic size and zeta potential of the suspension of AgNPs in water were measured by dynamic light scattering (Zeta sizer-HT; Malvern Instruments, Malvern, UK). Samples for transmission electron microscopy (TEM) analysis were prepared by drop-coating carbon-coated copper TEM grids with AgNP solution. The films on the TEM grids were allowed to dry prior to measurement. TEM measurements were performed on a JEOL model 2100F instrument operated at an accelerating voltage at 200 kV.
+ Open protocol
+ Expand
2

Engineered NiO Nanoparticle Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
Engineered NiO-NP was procured from Sigma Aldrich, (St. Louis, USA) [Product code 637130, molecular weight: 74.69, EC Number: 215-215-7, Pubchem Substance ID 24882831, <50 nm particle size Transmission Electron Microscopy (TEM), 99.8% trace metal basis]. The nanoparticle was directly suspended in deionized, ultrapure water (DI-water), and dispersed by ultrasonic vibration (60 W, 40 kHz) for 45 min to produce seven different concentrations as follows: 10, 25, 50, 62.5, 125, 250, and 500 mg L−1.
NiO-NPs were characterized by TEM, Dynamic Light Scattering (DLS), and Zeta (ζ) Potential Measurements. Estimation of morphology and size of NiO-NPs was based on the observations from TEM, performed on a Field Emission Transmission Electron Microscope (JEM-2100F, JEOL, Japan) at 200 keV. DLS was performed on a ZetaSizer-HT (Malvern, UK) to determine the hydrodynamic sizes of the NiO-NPs in suspension. The zeta potential values of NiO-NPs, dispensed in ultrapure water, were determined by Zetasizer 2000 (Malvern Instruments Ltd., UK) as the average of 10 readings and compared to previous reports (Lim et al., 2013 (link)). Polydispersity index was calculated as:
PDI=(σ/d)2
where σ is standard deviation and d is mean diameter, according to Ates et al. (2016 (link)).
+ Open protocol
+ Expand
3

Characterization of Pristine ZnO Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
ZnO NPs (<100 nm; 99.7% metal basis; specific surface area, 15–25 m2/g) were purchased from Sigma-Aldrich Co. (St Louis, MO, USA). For scanning electron microscopy (SEM) (S3400N; Hitachi, Tokyo, Japan) analysis, the samples were fixed onto metallic studs with double-sided conductive tape and sputtered with gold. SEM micrographs were analyzed with ImageJ (National Institutes of Health, Bethesda, MD, USA) software to obtain the mean size of pristine ZnO NPs. The hydrodynamic size and zeta potential of ZnO NPs in cell culture medium were determined by dynamic light scattering (DLS) (ZetaSizer-HT; Malvern Instruments, Malvern, UK). The samples of ZnO NPs in powder form were suspended in cell culture medium at a concentration of 1 mg/mL and were sonicated in a water bath at 4°C for 30 minutes at 30 W to form a homogeneous suspension. This stock solution of ZnO NPs was diluted to a 10–100 μg/mL working solution for DLS size measurement.
+ Open protocol
+ Expand
4

Synthesis and Characterization of Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
All the chemicals used for the synthesis of NPs were purchased from Sigma-Aldrich (Sigma, USA). SiO 2 and ZnO NPs were synthesized using sol-gel methods of Nandanwar [14] and Raja et al. [15] , respectively, whereas TiO 2 NPs were synthesized using the hydrothermal method of Castro et al. [16] , and Ag NPs were synthesized as described elsewhere [17] .
SiO 2 NPs powder was annealed at 300 °C for 60 min (Nabertherm, Inc. New Castle, USA) at a rate of 5 °C/min before characterization. X-ray diffraction (XRD) patterns of the NPs were obtained using PANalytical X'Pert X-ray diffractometer (Spectris plc, England) equipped with a Ni filter using Cu Kα (λ = 54,056 Å) radiations, as an X-ray source. Details of size and shapes of NPs were confirmed using scanning electron microscopy (SEM; JSM-6380, JEOL) and transmission electron microscopy (TEM; JEM-2100F, JEOL) analysis. The particle size distribution was determined by dynamic light scattering (DLS) using ZetaSizer-HT (Malvern, UK).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!