scholarly journals Corrosion Properties of Biodegradable AZ31 and ZK60 Magnesium Alloys: In Situ Study

2021 ◽  
Vol 6 (1) ◽  
pp. 3
Author(s):  
Evgeniy Merson ◽  
Vitaliy Poluyanov ◽  
Dmitry Merson ◽  
Pavel Myagkikh
Keyword(s):  
Corrosion Rate ◽  
Real Time ◽  
Hydrogen Evolution ◽  
Magnesium Alloys ◽  
Laser Scanning Microscopy ◽  
Ex Situ ◽  
Confocal Laser ◽  
Time Interval ◽  
Surface Observation

Biodegradable magnesium alloys are promising materials for application in medicine. The corrosion rate and type of corrosion are among the most important properties for this kind of materials. The fine-grained biodegradable alloys AZ31 (hot-rolled) and ZK60 (extruded) were studied in the present work with the use of in situ methods including the hydrogen evolution corrosion rate measurement and real-time surface observation as well as ex situ methods such as the weight loss assessment and the post-mortem examination by confocal laser scanning microscopy. The experimental methods included immersion test in SBF (0.9% NaCl aqueous solution) during 120 h with 37 °C with recirculating corrosion media. The hydrogen evolution was measured with a burette with a constant time interval of 1 hour. The real-time surface observation was carried out with a high-resolution camera. The measurement of pH level was done twice a day. Corrosion rate curves, 3D morphology of corroded morphology and video recordings showing evolution of corrosion damage have been obtained. As a result, ZK60 was found to be less corrosion-resistant and addicted to pitting corrosion, whereas AZ31 showed pronounced susceptibility to filiform corrosion.

scholarly journals A sample cell for the study of enzyme-induced carbonate precipitation at the grain-scale and its implications for biocementation

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jennifer Zehner ◽  
Anja Røyne ◽  
Pawel Sikorski
Keyword(s):  
Real Time ◽  
Laser Scanning Microscopy ◽  
In Situ Monitoring ◽  
Confocal Laser ◽  
Precipitation Process ◽  
Successful Implementation ◽  
Detailed Knowledge ◽  
Carbonate Precipitation ◽  
Sample Cell

AbstractBiocementation is commonly based on microbial-induced carbonate precipitation (MICP) or enzyme-induced carbonate precipitation (EICP), where biomineralization of $$\text {CaCO}_{3}$$ CaCO 3 in a granular medium is used to produce a sustainable, consolidated porous material. The successful implementation of biocementation in large-scale applications requires detailed knowledge about the micro-scale processes of $$\text {CaCO}_{3}$$ CaCO 3 precipitation and grain consolidation. For this purpose, we present a microscopy sample cell that enables real time and in situ observations of the precipitation of $$\text {CaCO}_{3}$$ CaCO 3 in the presence of sand grains and calcite seeds. In this study, the sample cell is used in combination with confocal laser scanning microscopy (CLSM) which allows the monitoring in situ of local pH during the reaction. The sample cell can be disassembled at the end of the experiment, so that the precipitated crystals can be characterized with Raman microspectroscopy and scanning electron microscopy (SEM) without disturbing the sample. The combination of the real time and in situ monitoring of the precipitation process with the possibility to characterize the precipitated crystals without further sample processing, offers a powerful tool for knowledge-based improvements of biocementation.

scholarly journals In-situ study of the corrosion process of biodegradable magnesium alloys

2021 ◽  
pp. 18-25
Author(s):  
P. N. Myagkikh ◽  
◽  
E. D. Merson ◽  
V. A. Poluyanov ◽  
D. L. Merson ◽  
...  
Keyword(s):  
Corrosion Rate ◽  
Magnesium Alloys ◽  
Human Body ◽  
Corrosion Damage ◽  
Az31 Alloy ◽  
Corrosion Process ◽  
Ex Situ ◽  
Zk60 Alloy ◽  
In Situ Methods

The interest in magnesium and its alloys considerably increases in recent years. These materials have a unique complex of properties: light-weight and strength make magnesium alloys promising structural materials for the aircraft industry and space application, and ability to reabsorb in vivo conditions and good biocompatibility allow producing biodegradable surgical implants of magnesium alloys, which can resorb in a human body without detriment to health. The materials for such demanding applications require detailed investigation of their properties, such as corrosion, including the kinetics of corrosion rate and staging of corrosion damage on the surface. To obtain a full view of the corrosion process, in addition to common ex-situ methods such as the corrosion rate evaluating using the weight loss method and the morphology corrosion damage investigation by optical or confocal laser scanning microscopy (CLSM), it is important to use modern in-situ methods. In-situ methods allow obtaining data immediately during the experiment and not after its completion. The authors carried out a comprehensive study of the corrosion process of the commercial ZK60 and AZ31 magnesium alloys in the simulated human-body environment (temperature, corrosion media composition, circulation of corrosion media) using in-situ methods, including hydrogen evolution corrosion rate evaluating and video-observation of a sample surface. The results show that AZ31 alloy is more corrosion-resistant than ZK60 alloy. Moreover, AZ31 alloy is prone to filiform surface corrosion, and ZK60 alloy exhibits severe pitting corrosion. Based on the comparison of the data obtained by in-situ and ex-situ methods, the authors concluded on their main differences and features.

scholarly journals Distribution of Phytoplasmas in Infected Plants as Revealed by Real-Time PCR and Bioimaging

2004 ◽  
Vol 17 (11) ◽  
pp. 1175-1184 ◽  
Author(s):  
Nynne Meyn Christensen ◽  
Mogens Nicolaisen ◽  
Michael Hansen ◽  
Alexander Schulz
Keyword(s):  
Real Time ◽  
Laser Scanning ◽  
Infected Plant ◽  
Laser Scanning Microscopy ◽  
Confocal Laser ◽  
Euphorbia Pulcherrima ◽  
Pcr Assay ◽  
Sieve Tubes ◽  
Polymerase Chain

Phytoplasmas are cell wall-less bacteria inhabiting the phloem and utilizing it for their spread. Infected plants often show changes in growth pattern and a reduced crop yield. A quantitative real-time polymerase chain reaction (Q-PCR) assay and a bioimaging method were developed to quantify and localize phytoplasmas in situ. According to the Q-PCR assay, phytoplasmas accumulated disproportionately in source leaves of Euphorbia pulcherrima and, to a lesser extent, in petioles of source leaves and in stems. However, phytoplasma accumulation was small or nondetectable in sink organs (roots and sink leaves). For bioimaging, infected plant tissue was stained with vital fluorescence dyes and examined using confocal laser scanning microscopy. With a DNA-sensitive dye, the pathogens were detected exclusively in the phloem, where they formed dense masses in sieve tubes of Catharanthus roseus. Sieve tubes were identified by counterstaining with aniline blue for callose and multiphoton excitation. With a potentiometric dye, not all DNA-positive material was stained, suggesting that the dye stained metabolically active phytoplasmas only. Some highly infected sieve tubes contained phytoplasmas that were either inactive or dead upon staining.

scholarly journals Antimicrobial Photoinactivation of In Situ Oral Biofilms by Visible Light Plus Water-Filtered Infrared A and Tetrahydroporphyrin-tetratosylate (THPTS)

2021 ◽  
Vol 9 (1) ◽  
pp. 145
Author(s):  
Lamprini Karygianni ◽  
Sandra Ruf ◽  
Elmar Hellwig ◽  
Marie Follo ◽  
Kirstin Vach ◽  
...  
Keyword(s):  
Untreated Control ◽  
Laser Scanning ◽  
Microbial Reduction ◽  
Laser Scanning Microscopy ◽  
Ex Situ ◽  
Confocal Laser ◽  
Initial Adhesion ◽  
Oral Biofilms ◽  
Deep Layers

The aim of this study was to examine the effect of aPDT with visual light (VIS) + water-filtered infrared A (wIRA) as a light source, and tetrahydroporphyrin-tetratosylate (THPTS) as a photosensitizer on in situ initial and mature oral biofilms. The samples were incubated, ex situ, with THPTS for two minutes, followed by irradiation with 200 mW cm − 2 VIS + wIRA for five minutes at 37 °C. The adherent microorganisms were quantified, and the biofilm samples were visualized using live/dead staining and confocal laser scanning microscopy (CLSM). The THPTS-mediated aPDT resulted in significant decreases in both the initially adherent microorganisms and the microorganisms in the mature oral biofilms, in comparison to the untreated control samples (>99.99% each; p = 0.018 and p = 0.0066, respectively). The remaining vital bacteria significantly decreased in the aPDT-treated biofilms during initial adhesion (vitality rate 9.4% vs. 71.2% untreated control, 17.28% CHX). Of the mature biofilms, 25.67% remained vital after aPDT treatment (81.97% untreated control, 16.44% CHX). High permeability of THPTS into deep layers could be shown. The present results indicate that the microbial reduction in oral initial and mature oral biofilms resulting from aPDT with VIS + wIRA in combination with THPTS has significant potential for the treatment of oral biofilm-associated diseases.

3-D imaging of cells using a confocal laser scanning microscope and digital image processing

1988 ◽  
Vol 46 ◽  
pp. 96-97
Author(s):  
Thomas M. Jovin ◽  
Michel Robert-Nicoud ◽  
Donna J. Arndt-Jovin ◽  
Thorsten Schormann
Keyword(s):  
Laser Scanning ◽  
Confocal Laser Scanning Microscope ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Confocal Laser ◽  
Scanning Microscope ◽  
Laser Scanning Microscope ◽  
Biochemical Processes ◽  
Adjacent Structures

Light microscopic techniques for visualizing biomolecules and biochemical processes in situ have become indispensable in studies concerning the structural organization of supramolecular assemblies in cells and of processes during the cell cycle, transformation, differentiation, and development. Confocal laser scanning microscopy offers a number of advantages for the in situ localization and quantitation of fluorescence labeled targets and probes: (i) rejection of interfering signals emanating from out-of-focus and adjacent structures, allowing the “optical sectioning” of the specimen and 3-D reconstruction without time consuming deconvolution; (ii) increased spatial resolution; (iii) electronic control of contrast and magnification; (iv) simultanous imaging of the specimen by optical phenomena based on incident, scattered, emitted, and transmitted light; and (v) simultanous use of different fluorescent probes and types of detectors.We currently use a confocal laser scanning microscope CLSM (Zeiss, Oberkochen) equipped with 3-laser excitation (u.v - visible) and confocal optics in the fluorescence mode, as well as a computer-controlled X-Y-Z scanning stage with 0.1 μ resolution.

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