In-situ Confocal Laser Microscopy Study of Lead Sulfate Crystal Growth on Negative Electrode of Lead-acid Batteries

2021 ◽  
Vol 105 (1) ◽  
pp. 159-166
Author(s):  
Ladislav Chladil ◽  
Hana Hálová ◽  
Ondřej Čech

Confocal Laser Scanning Microscopy (CLSM) is a widely used technique mainly in fields of biology or multidisciplinary material sciences. Although CLSM has the ability to monitor also electrochemical processes like lead sulfate-crystal growth, nobody used CLSM for such application. We performed operando observation of the pasted active mass of negative electrode for lead-acid batteries during deep cycling. Electrode with pasted negative active mass was optimized for cycling in ECC-opto-std electrochemical cell by EL-CELL. Lead sulfate crystal growth and changes of electrode surface during cycling were observed using a laser scanning confocal microscope Olympus Lext OLS4100. We evaluate the surface changes and sulfate crystal growth. The cycling mode leads to fast gradual degradation of the negative electrode and massive growth of lead sulfate crystals. Confocal laser scanning microscopy was identified as a powerful technique for visualization of lead sulfate crystal promotion during battery cycling.

2012 ◽  
Vol 11 (3) ◽  
pp. 669-674 ◽  
Author(s):  
Szabolcs Szilveszter ◽  
Botond Raduly ◽  
Szilard Bucs ◽  
Beata Abraham ◽  
Szabolcs Lanyi ◽  
...  

2009 ◽  
Vol 18 (1) ◽  
pp. 11-16
Author(s):  
E.V. Soldatenko ◽  
A.A. Petrov

The morphology of the copulatory apparatus and associated cuticular structures in Planorbis planorbis was studied by light microscopy, SEM, TEM and confocal laser scanning microscopy. The significance of these cuticular structures for the taxonomic status of the species and for the systematics of the family Planorbidae in general is discussed.


2021 ◽  
Vol 11 (8) ◽  
pp. 3403
Author(s):  
Shlomo Elbahary ◽  
Sohad Haj Yahya ◽  
Cemre Koç ◽  
Hagay Shemesh ◽  
Eyal Rosen ◽  
...  

Following furcal perforation, bacteria may colonize the defect and cause inflammation and periodontal destruction. This study used confocal laser scanning microscopy (CLSM) to evaluate Enterococcus faecalis colonization and proliferation in furcal perforations repaired with different materials. Furcal perforations created in 55 extracted human mandibular molars were repaired using either MTA-Angelus, Endocem, or Biodentine and coronally subjected to E. faecalis suspension for 21 days. The specimens were then stained using a LIVE/DEAD Viability Kit and visualized by CLSM. The minimum and maximum depths of bacterial penetration into the dentinal tubules were 159 and 1790 μM, respectively, with a mean of 713 μM. There were significantly more live than dead bacteria inside the dentinal tubules (p = 0.0023) in all groups, and all three repair materials exhibited a similarly sized stained area (p = 0.083). However, there were significant differences in the numbers of dead bacteria at the circumference of the perforation defect (p = 0.0041), with a significantly higher ratio of live to dead bacteria in the MTA-Angelus group (p = 0.001). Following perforation repair, bacteria may colonize the interface between the repair material and dentin and may penetrate through the dentinal tubules. The type of repair material has a significant effect on the viability of the colonizing bacteria.


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