The largest database of trusted experimental protocols

Tm3030 microscope

Manufactured by Hitachi
Sourced in Japan

The TM3030 is a tabletop scanning electron microscope (SEM) manufactured by Hitachi. It is designed for high-resolution imaging of samples at the micro- and nanoscale. The TM3030 uses an electron beam to scan the surface of a sample, generating detailed images that can reveal the topography, composition, and other characteristics of the specimen.

Automatically generated - may contain errors

5 protocols using tm3030 microscope

1

SEM Imaging of Microneedle Structures

Check if the same lab product or an alternative is used in the 5 most similar protocols
When imaging MNs using scanning electron microscopy (SEM), MNs were mounted onto an aluminium stub and observed under a TM3030 microscope (Hitachi Ltd, Japan). Micrographs of MN structures were obtained and the surface morphology and height/width of individual needles were examined/measured.
+ Open protocol
+ Expand
2

Structural Characterization of Ti-Ta Alloys

Check if the same lab product or an alternative is used in the 5 most similar protocols
EDS measurements were carried out with an environmental scanning electron microscope model FEI XL30 ESEM with an LaB6 cathode attached to an energy dispersive X-ray electron sample analyzer, model EDAX Sapphire.
The structures of the Ti–Ta alloys were investigated by high-resolution scanning tunneling microscopy (STM). All determinations were performed in air with a Hitachi TM3030 microscope that had been transversely calibrated by imaging atomically accurate oriented pyrolytic graphite. The tips were obtained by chopping a 0.20 mm Pt0.8Ir0.2 wire. The data were acquired in constant current operation with specific tunneling currents of 0.13–0.3 nA and a specimen polarization of 0.4–1.0 V. No tip-induced shifts were noted.
X-ray diffraction (XRD) determinations were made using an Empyrean diffractometer (Malvern-Panalytical). The device worked with a Cu Kα anode (1.5406 Å) in the range of 2θ = 0–64° with a step size of 0.04° at a power of 45 kV and 40 mA in Bragg–Brentano geometry. The samples have been rotated while collecting data in order to achieve better data capture. The obtained patterns were simulated in order to determine the presence of the crystalline phase, the lattice parameter, and the diameter of the grain with the assistance of Malvern-Panalytical’s HighScore Plus software.
+ Open protocol
+ Expand
3

Comprehensive Material Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The morphology and structural characteristics of the samples were observed via SEM using a TM3030 microscope (Hitachi, Tokyo, Japan). The crystal structures were analysed using a D/max-2200VPC X-ray diffractometer (Rigaku, Tokyo, Japan). FTIR spectroscopy (Perkin Elmer, Waltham, MA, USA) was used to characterise the functional groups in the samples. A universal testing machine (CMT5504, MTS, Eden Prairie, MN, USA) was used to study the mechanical properties. All electrochemical performance tests were conducted on an electrochemical workstation (51-XMX1004, Oxford, UK).
+ Open protocol
+ Expand
4

Extruded PCL Matrix Surface Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Scanning electron microscopy (SEM) was used to study the surface morphology of the extruded PCL matrices. Adhesive carbon tabs were used to mount samples on aluminium pin stubs. SEM images of the extrudates were collected using a TM3030 microscope (Hitachi, Tokyo, Japan).
+ Open protocol
+ Expand
5

Characterization of CLC-Soluplus® Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
Quasi Elastic Light Scattering (NanoBrook Omni® analyser, Brookhaven, New York, NJ, USA) was utilised in order to evaluate size distribution of the CLC-Soluplus® particles formed. An aliquot (10 µL) of CLC-Soluplus® aqueous dispersion was diluted in 2 ml of deionised water and vortexed at 2500 rpm for 1 min. Next, the diluted mixture was transferred into a disposable cuvette for analysis. The analysis was conducted at a temperature 25 °C while implementing an equilibration time of 3 min prior to sample analysis. All samples were analysed in triplicates. CLC-Soluplus® powder was also visualised using scanning electron microscopy (SEM) analysis with a TM3030 microscope (Hitachi, Krefeld, Germany). Prior to analysis, the samples were left to dry for 24 h under ambient conditions. The chemical interactions between CLC and Soluplus® were investigated using a Fourier transform infrared (FTIR) spectrometer (Accutrac FT/IR-4100™ Series, PerkinElmer, USA). The crystallinity of pure CLC, pure Soluplus®, physical mixture (PM) and CLC-Soluplus® powder were determined using a differential scanning calorimeter DSC Q20 (TA Instruments, Elstree, Hertfordshire, UK) and an X-ray diffractometer (Rigaku Corporation, Kent, England).
+ 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!