Won't the labeling marker ink cause an issue in the SEM Vacuum chamber?
@AuroraLex7 ай бұрын
Much appreciated!
@com-webinars91558 ай бұрын
Thank you
@lilanedaria8 ай бұрын
Fascinating and well presented. Thank you for sharing this knowledge for free
@aparnavarghese14798 ай бұрын
Really well explained! Thanks!
@samuelyurisairesaire95829 ай бұрын
How to cut a 100mm silicon disk into small pieces (>10mm)?
@atmanemanou40879 ай бұрын
thanks
@ParameswaranPed22d00810 ай бұрын
During importing a file you are taken (@ 5.21 mins) as .txm files. How to create this .txm files for images?
@killrchiton11719 ай бұрын
Hi Parameswaren, thanks for your question. The .txm file is a proprietary file format created by the Zeiss microCT system. Avizo has the ability to import this file format. You cannot create this file unless you have the instrument. However, Avizo will allow you to import and export data in a range of other open source formats (such as TIFF or DICOM). You can just select this from the drop down list in the save function. Hope that helps.
@abhayagrawal398210 ай бұрын
it should be double or 70%
@SaifullahAl-Galib10 ай бұрын
Easy and Interesting
@ARseventy16 Жыл бұрын
hi, i want to know, what should I do if my sample cannot stick to double side adhesive ? I tried other tape, the sample still not attached…
@MicroscopyAustralia9 ай бұрын
In general, we tend not to use adhesives to mount nanomaterials for SEM examination. As you can see in the video, we usually create a well-dispersed suspension of particles and deposit a drop of that suspension onto a clean, featureless (preferably conductive) substrate such as a silicon wafer. Once the suspension liquid fully evaporates, we then image the remaining nanoparticulate residue in the SEM.
@angshumangupta9523 Жыл бұрын
Thank you so much. Really nice presentation
@MicroscopyAustralia11 ай бұрын
Thank you!
@vahidbabalo Жыл бұрын
Hi there, I want to analyze the permeability and tortuosity of a porous structure. Could you please provide me with any help or tutorial? Thanks
@killrchiton11719 ай бұрын
Hi, good question. The answer however is complex. Avizo has tools for doing this (as do other software packages). Normally the process would be to undertake some pre-processing steps to prepare the data (filtering/denoising). Then you would need to move to pore identification (of which there are various methods). Tortuosity and permeability measures could then be applied to the result of the pore labels. I would suggest looking up some of the functionality for this in Avizo by visiting their KZbin channel. They have some videos on the study of pore structures including connectivity.
@MarsW1321 Жыл бұрын
The information here is a little out dated. The ice issue is only exists in LN2 detectors which can be barely seen on SEMs nowadays. Modern EDS has great improvement in terms of efficiency and low-kV X-ray detection. The data in the example is from 1998. The spectrum processing at that period is not a good as modern EDS software, especially on peak overlapping issue and background subtraction. It's good to see the comparison with WDS. Lots of people over relied on EDS thus ignored WDS. Thank you for the presentation.
@MarsW1321 Жыл бұрын
I worked in a EDS company. This is by far the best presentation I've seen about EDS analysis. Most importantly, it's based on practical experience that you need to know or be aware of in the analysis. Also, it's not quite easy to put all the sessions into one hour talk. Good job and thank you for the presentation.
@MicroscopyAustralia Жыл бұрын
Thank you :)
@obettannamdi9864 Жыл бұрын
Wow....I learnt alot
@MicroscopyAustralia Жыл бұрын
Glad it was helpful!
@harleyjudy2850 Жыл бұрын
what on earth is this resin
@Prabhinakairali Жыл бұрын
How much amount needed to sent for a sem analysis test of nanoparticle
@MicroscopyAustralia9 ай бұрын
The amount of nanoparticulate material required cannot be precisely specified. We generally advise individuals to bring approximately ~1g of (dry) nanoparticles, and only use a fraction of this amount for SEM or TEM examination. If the nanoparticles are suspended in liquid, then a concentration that alters the visual properties of the liquid (i.e., makes it ‘cloudy’) should be sufficient. It is always recommended to consult the microscopy specialist(s) with whom you are working for their recommendation. Because engineered nanomaterials are considered hazardous substances, only minimal quantities should be handled, and storage and handling should be done in accordance with local and federal safety guidelines and regulations.
@AbdurRahim-jl5wt Жыл бұрын
Thank you so much
@MicroscopyAustralia Жыл бұрын
You're most welcome
@alexanderberhane4924 Жыл бұрын
Amazing presentation! I got a lot of ideas from your presentation. It helps with how to deal with SEM images.Thank you very much.
@MicroscopyAustralia Жыл бұрын
Glad it was helpful!
@wiamaid4251 Жыл бұрын
thank you very much
@MicroscopyAustralia Жыл бұрын
You are welcome :)
@kavitarajpurohit6909 Жыл бұрын
This information was very helpful to me.. Thanks for giving such amazing explanation 🙏👍
@MicroscopyAustralia Жыл бұрын
Glad to hear that :)
@denizcicek7333 Жыл бұрын
Many thanks.
@MicroscopyAustralia Жыл бұрын
Welcome 😊
@luyandathandolwethu3561 Жыл бұрын
Why is liquid carbon dioxide used??
@surendersingal2192 Жыл бұрын
Thank you sir
@MrArthurUZ Жыл бұрын
Great lecture. Thank you for sharing.
@СлаваУкраїні-е1в Жыл бұрын
Thanks for the good video. I got a broken microscope EVO MA-10. Based on your videos, I fixed it and learned how to work on it.
@MicroscopyAustralia Жыл бұрын
Great to hear!
@nagoronfire3802 Жыл бұрын
wow
@nazmulhaque1895 Жыл бұрын
Is it necessary to dry the prepared nano particles prepared by wet chemical method?
@MicroscopyAustralia9 ай бұрын
Yes, samples need to be vacuum stable and should be fully dry before attempting to image them in a SEM. Even in an ESEM instrument, which can handle a certain degree of moisture, the SEM is only capable of imaging the surface of the sample, so will not be able to ‘see’ nanoparticles suspended inside a liquid.
@alvinjohn1689 Жыл бұрын
This is by far the best demonstration video I have ever watched.
@WernerEngel1 Жыл бұрын
To find the appropriate spot size, aperture and all the other parameters seems not so easy. How do you find them? Are there some rules?
@PuttaChandraLekha Жыл бұрын
Very informative.👍
@AbhayAgrawal-lo5sj Жыл бұрын
I am very thankful for your video. This is very informative and really helpful Thanks
@jeeviyazh2 жыл бұрын
Am using this to make glass knife ,bt now I dnt knw what happens both sides r cmg sharp.thr is no blunt edge. How do I rectify ths
@mohsenrasouli52352 жыл бұрын
thnx
@ahmedeid23402 жыл бұрын
Amazing, thank you so much
@MicroscopyAustralia2 жыл бұрын
Glad you liked it!
@KitkatTrading20242 жыл бұрын
It seems that all the transformation was still done in the anatomical coordinate system (RAS). I can't seem to find a way to do the transformation and resampling in the IJK space.
@KitkatTrading20242 жыл бұрын
Thank you! This is very helpful!
@MicroscopyAustralia Жыл бұрын
You're very welcome!
@mhd1122112 жыл бұрын
This is one of the nicest lectures I have ever seen on this topic...Thank you.
@MicroscopyAustralia Жыл бұрын
Glad it was helpful!
@Ortopedia3D2 жыл бұрын
I’m a Veterinary from Brasil and what to thank you a lot for this incredible lesson.
@MicroscopyAustralia Жыл бұрын
Glad you enjoyed it!
@navnath61882 жыл бұрын
great information thanks, but i can not rotate my image with this steps ☹
@killrchiton11712 жыл бұрын
Hi Navnath, can you explain where you are having trouble?
@simonagezova13022 жыл бұрын
Hello! I have one problem with Avizo. I work with snake skulls and make 3D models of the whole skulls. Once, I didnt finish the whole skull, just made some layers of one bone and then closed Avizo (Save project as and then Auto Save). On the other day, I opened Avizo and in Volume-1. labels (where you have four screens - XY, XZ, YZ and 3D view) I had only that selected bone (colored bone) but on the black background where I didnt have the rest of the skull = other bones that should be visible in greyish colour on the background. I have tried to close Avizo and then open it again but the situation was the same, so I cannot selected other bones to obtain 3D model of the whole bone. Thank you for any advices! :)
@MicroscopyAustralia2 жыл бұрын
Hi Simona, I'll check in with our Micro-CT team and see if they have a solution :)
@killrchiton11712 жыл бұрын
Hi Simona, sounds like you only saved the binary label field (the coloured one) using the auto save project method you selected. Not sure what version of Avizo you are using, but when you save the project you should select the "pack and go" option in the "save as type" dropdown list before clicking save. The "greyish" coloured data is probably your original data. Just drag and drop (or other opening method) this back into Avizo and save it again. Personally, I avoid saving projects unless I have to these days. I prefer saving only the very necessary files separately. Otherwise, you can end up with a lot of unwanted data saved.
@ganeshdilwale51942 жыл бұрын
Thank you for this very nice and informative video...
@MicroscopyAustralia2 жыл бұрын
Glad it was helpful :)
@Inmate0052 жыл бұрын
helped me a lot! Thank you!
@MicroscopyAustralia2 жыл бұрын
Glad it helped!
@phuongphamthai23912 жыл бұрын
Nice !
@MicroscopyAustralia Жыл бұрын
Thanks!
@DigitalAndInnovation2 жыл бұрын
a carrot as an embedding medium- mind blown- this is clever
@annavietmeier36742 жыл бұрын
Thanks for the video! It was informative.
@davidnahabedian88292 жыл бұрын
hello excellent lesson and PDF is there any way i can try this out on the turtle head DICOM data? would love to play with that scan
@Esterxyta2 жыл бұрын
is not needed to fix the sample before? Is the sample was already fixed, how can I fix nanoparticles?
@MicroscopyAustralia2 жыл бұрын
Fixation is a term we use for the process of preserving the structure of biological samples from their in-vivo state so that the samples can be examined in as unaltered a state as possible. Biological samples containing nanoparticles should be fixed as appropriate for that specific tissue type. There are many types of fixation methods; it is important to review the literature and consult experts regarding the best approach for your specimen type. It can also be very helpful to experiment with a range of fixation methods with non-critical samples to determine the optimum method for your particular application.