Transmission electron microscopy (TEM) images were acquired on a JEM-2100UHR microscope (JEOL, Japan) to characterize the morphology. X-ray photoelectron spectroscopy (XPS, ESCALAB 250Xi, Japan) was applied to analyze the chemical compositions of MnPc@P. UV-vis-NIR spectrum was investigated by using an Infinite M200 PRO spectrophotometer. The hydrodynamic particle size and zeta potential of MnPc@P was monitored by dynamic light scattering (DLS, 15 mW laser, 676 nm incident beam; Brookhaven Instruments Corporation).
Jem 2100uhr microscope
Manufactured by JEOL
Sourced in Japan
The JEM-2100UHR is a high-resolution transmission electron microscope (TEM) manufactured by JEOL. It is designed to provide high-quality imaging and analysis capabilities for a wide range of materials and applications. The JEM-2100UHR features a LaB6 electron source, advanced optics, and a high-resolution CCD camera to deliver exceptional image resolution and contrast. It is capable of operating in a variety of modes, including bright-field, dark-field, and high-resolution imaging, as well as selected area electron diffraction (SAED) and energy-dispersive X-ray spectroscopy (EDS) analysis.
Automatically generated - may contain errors
Lab products found in correlation
Escalab 250xi, by Thermo Fisher Scientific (2 mentions)
Q150r plus sputter coater, by Quorum Technologies (1 mentions)
Jib 4501 multibeam system, by JEOL (1 mentions)
Nicolet6700 contiuμm, by Thermo Fisher Scientific (1 mentions)
Jem 2100uhr, by JEOL (1 mentions)
Nanobrook 90plus pals, by Brookhaven Instruments (1 mentions)
4 protocols using jem 2100uhr microscope
1
Characterization of MnPc@P Nanostructures
2
Microscopic Characterization of Composite Biomaterials
Check if the same lab product or an alternative is used in the 5 most similar protocols
+ Expand
The distribution of vancomycin grains and additives in the PMMA matrix as well as the MFC shape and length were investigated with the help of scanning electron microscopy (SEM). The samples retrieved after the elution study and microhardness test were crashed in the mortar and covered by a 10–15 nm gold layer via magnetron sputtering using Quorum Technologies Q150R Plus sputter coater. The JEOL JIB 4501 multibeam system (Akishima, Tokyo) was used, and the SEM micrographs were acquired in BSE mode at an accelerating voltage of 10 kV.
To study the form and structure of the employed HNT, NCC and NFC transmission electron microscopy (TEM) was employed. The corresponding micrographs were acquired using the JEOL JEM 2100 UHR microscope in TEM brightfield mode at an accelerating voltage of 200 kV. To enhance the contrast of cellulose fibrils with low electron-scattering power, the negative staining (using a 2% solution of phosphotungstic acid, pH = 7.0) was applied.
To study the form and structure of the employed HNT, NCC and NFC transmission electron microscopy (TEM) was employed. The corresponding micrographs were acquired using the JEOL JEM 2100 UHR microscope in TEM brightfield mode at an accelerating voltage of 200 kV. To enhance the contrast of cellulose fibrils with low electron-scattering power, the negative staining (using a 2% solution of phosphotungstic acid, pH = 7.0) was applied.
3
Multimodal Characterization of Nanoparticles
Check if the same lab product or an alternative is used in the 5 most similar protocols
+ Expand
To characterize the microstructure and morphology of nanoparticles, transmission electron microscopy (TEM) was performed on a JEM-2100UHR microscope (JEOL, Japan). X-ray photoelectron spectroscopy (XPS, ESCALAB 250Xi, Japan), X-ray diffraction (XRD, Bruker D8, Germany), and Fourier transform infrared spectrophotometer spectrum (FTIR, Nicolet6700-Contiuμm, Thermo, USA) were carried out to analyze the chemical compositions and crystal structures of HES@CuP. UV-vis-NIR spectrum of HES@CuP and HES@CuP-D was investigated by using an Infinite M200 PRO spectrophotometer. The zeta potential and corresponding hydrodynamic particle size of HES@CuP and HES@CuP-D were detected through dynamic light scattering (DLS, 90Plus PALS, Brookhaven, UK). The scheme illustration was drawn by Figdraw.
4
Comprehensive Characterization of CaS Nanoparticles
Check if the same lab product or an alternative is used in the 5 most similar protocols
+ Expand
Transmission electron microscopy (TEM) images were acquired on a JEM-2100UHR microscope (JEOL, JEM-2100UHR, Tokyo, Japan). X-ray photoelectron spectroscopy (XPS, Thermo Fisher Scientific Inc., ESCALAB 250Xi, Asheville, NC, USA) and energy dispersive spectrometer (EDS) were applied to analyze the chemical constitutions of CaS, CaS@PP and I-CaS@PP. X-ray diffraction (XRD, Bruker, Bruker D8, Karlsruhe, Germany) was performed to analyze the crystal structure of CaS and I-CaS@PP. The hydrodynamic particle sizes and zeta potentials of NPs were monitored by dynamic light scattering (DLS, Brookhaven Instruments Corporation, NanoBrook 90 Plus PALS, New York, NY, USA). The loading amount of ICG in I-CaS@PP was determined based on the UV–Vis absorbance peak at 780 nm, and it was calculated according to the followed Eq. (3) :
The loading amount of CaS in I-CaS@PP was determined by detecting Ca and S amounts in I-CaS@PP using ICP-MS (Thermo Fisher Scientific Inc., Thermo ICAP PRO, NC, USA).
The loading amount of CaS in I-CaS@PP was determined by detecting Ca and S amounts in I-CaS@PP using ICP-MS (Thermo Fisher Scientific Inc., Thermo ICAP PRO, NC, USA).
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
Revolutionizing how scientists
search and build protocols!