Energy Absorption of Superplastic Zn-22Al Alloy Foam Manufactured through Melt Foaming Process

2016 ◽  
Vol 838-839 ◽  
pp. 231-236 ◽  
Author(s):  
Satoshi Ogawa ◽  
Kenji Sekido ◽  
Koichi Kitazono
Keyword(s):  
Cell Wall ◽  
Solution Treatment ◽  
Rate Sensitivity ◽  
Wall Material ◽  
Foaming Agent ◽  
Foaming Process ◽  
Closed Cell ◽  
Hydrogen Carbonate ◽  
Equiaxial Crystal ◽  
High Strain Rate Sensitivity

Closed-cell superplastic Zn-22Al alloy foams were manufactured through the melt foaming process using sodium hydrogen carbonate powder as a foaming agent. Foaming tests were carried out under different foaming temperatures, times and additive amounts of foaming agent. The porosity of Zn-22Al alloy foams were between 30 and 70%. The cell wall consisted of fine equiaxial crystal grains after solution treatment. The compressive properties of the Zn-22Al alloy foams were investigated at room temperature and high temperature. Zn-22Al alloy foams exhibited high strain rate sensitivity, which was caused by superplastic deformation of the cell wall material.

scholarly journals The Role of Foaming Agent and Processing Route in Mechanical Performance of Fabricated Aluminum Foams

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Alexandra Byakova ◽  
Iegor Kartuzov ◽  
Svyatoslav Gnyloskurenko ◽  
Takashi Nakamura
Keyword(s):  
Cell Wall ◽  
Mechanical Response ◽  
Mechanical Performance ◽  
Cell Structure ◽  
Wall Material ◽  
Processing Route ◽  
Foaming Agent ◽  
Closed Cell ◽  
Al Foams

The results of this study highlight the role of foaming agent and processing route in influencing the contamination of cell wall material by side products, which, in turn, affects the macroscopic mechanical response of closed-cell Al-foams. Several kinds of Al-foams have been produced with pure Al/Al-alloys by the Alporas like melt process, all performed with and without Ca additive and processed either with conventional TiH2foaming agent or CaCO3as an alternative one. Damage behavior of contaminations was believed to affect the micromechanism of foam deformation, favoring either plastic buckling or brittle failure of cell walls. No discrepancy between experimental values of compressive strengths for Al-foams comprising ductile cell wall constituents and those prescribed by theoretical models for closed-cell structure was found while the presence of low ductile and/or brittle eutectic domains and contaminations including particles/layers of Al3Ti, residues of partially reacted TiH2, and Ca bearing compounds, results in reducing the compressive strength to values close to or even below those of open-cell foams of the same relative density.

scholarly journals Effect of Cell Wall Ductility and Toughness on Compressive Response and Strain Rate Sensitivity of Aluminium Foam

2019 ◽  
Vol 2019 ◽  
pp. 1-13
Author(s):  
Alexandra Byakova ◽  
Svyatoslav Gnyloskurenko ◽  
Andrey Vlasov ◽  
Nikolay Semenov ◽  
Yan Yevych ◽  
...  
Keyword(s):  
Cell Wall ◽  
Strain Rate ◽  
Dynamic Loading ◽  
Strain Rate Sensitivity ◽  
Rate Sensitivity ◽  
Melt Processing ◽  
Wall Material ◽  
Static Compression ◽  
Quasi Static Compression ◽  
Al Foams

The study presents the effect of cell wall ductility and toughness on the compressive behaviour of closed-cell Al foams under static and dynamic loading and localised deformation by indentation. Two kinds of Al alloys including relatively ductile AlSiMg alloy and high-strength AlZnMg alloy, which comprises a great amount of brittle eutectic domains, were used as matrix materials. Both kinds of Al foams were fabricated via newly developed melt processing using the CaCO3-foaming agent without Ca additive. Mechanical behaviour of Al foams under quasi-static compression and indentation was examined and compared with that performed under dynamic loading using direct impact tests. Characteristic events revealed in deformation patterns of Al foams at quasi-static compression were also monitored with the CCD camera. Significant differences in stress-strain response and strain rate sensitivity of Al foams arose from the difference in the microstructure, and hence, ductility and toughness of the cell wall material were investigated and discussed.

scholarly journals Cell wall material strain hardening on dynamic responses of closed-cell foams

2017 ◽  
Vol 24 (6) ◽  
pp. 883-892 ◽  
Author(s):  
Jianjun Zhang ◽  
Zhihua Wang ◽  
Longmao Zhao
Keyword(s):  
Cell Wall ◽  
Energy Dissipation ◽  
Strain Hardening ◽  
Deformation Mode ◽  
Dynamic Responses ◽  
Wall Material ◽  
Cell Wall Material ◽  
Plastic Energy ◽  
Closed Cell ◽  
The Impact

AbstractThe paper focuses on the effects of the cell wall material strain hardening on the mechanical behavior of closed-cell foams subjected to the constant velocity loading. Three-dimensional Voronoi models were established to present the closed-cell foams, and the simulations were performed by employing Ls-dyna 971. The investigation found that the cell wall strain hardening could postpone the onset of the localized collapse bands and retard deformation mode transformation. Strain hardening convergence phenomenon was observed in the closed-cell foams; increasing the impact velocity could weaken the effect of the material strain hardening. The crushing stress at both impact and stationary sides were analyzed in detail. The material strain hardening could always enhance the plastic energy dissipation. Furthermore, the strain hardening convergence was also observed in the plateau stress at the impact side and plastic energy dissipation but not in the densification strain and the plateau at the stationary side.

Silica Incorporation in the Cell Wall of the Singing Cell of Urtica dioica

1975 ◽  
Vol 33 ◽  
pp. 584-585
Author(s):  
A. E. Sowers ◽  
E. L. Thurston
Keyword(s):  
Cell Wall ◽  
Unique Feature ◽  
Urtica Dioica ◽  
Wall Material ◽  
Pain Response ◽  
Apical Portion ◽  
Ultrastructural Investigation ◽  
Plant Families ◽  
Bulbous Tip

Plant stinging emergences exhibit functional similarities in that they all elicit a pain response upon contact. A stinging emergence consists of an elongated stinging cell and a multicellular pedestal (Fig. 1). A recent ultrastructural investigation of these structures has revealed the ontogeny and morphology of the stinging cells differs in representative genera in the four plant families which possess such structures. A unique feature of the stinging cell of Urtica dioica is the presence of a siliceous cell wall in the apical portion of the cell. This rigid region of the cell wall is responsible for producing the needle-like apparatus which penetrates the skin. The stinging cell differentiates the apical bulbous tip early in development and the cell continues growth by intercalary addition of non-silicified wall material until maturity.The uppermost region of the stinging cell wall is entirely composed of silica (Fig. 2, 3) and upon etching with a 3% solution of HF (5 seconds), the silica is partially removed revealing the wall consisting of individualized silica bodies (Fig. 4, 5).

scholarly journals New methods for confocal imaging of infection threads in crop and model legumes

Plant Methods ◽  
2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Angus E. Rae ◽  
Vivien Rolland ◽  
Rosemary G. White ◽  
Ulrike Mathesius
Keyword(s):  
Cell Wall ◽  
Root Hair ◽  
Periodic Acid ◽  
Confocal Imaging ◽  
Wall Material ◽  
Future Research ◽  
Thin Sections ◽  
New Methods ◽  
Infection Threads ◽  
Imaging Of Infection

Abstract Background The formation of infection threads in the symbiotic infection of rhizobacteria in legumes is a unique, fascinating, and poorly understood process. Infection threads are tubes of cell wall material that transport rhizobacteria from root hair cells to developing nodules in host roots. They form in a type of reverse tip-growth from an inversion of the root hair cell wall, but the mechanism driving this growth is unknown, and the composition of the thread wall remains unclear. High resolution, 3-dimensional imaging of infection threads, and cell wall component specific labelling, would greatly aid in our understanding of the nature and development of these structures. To date, such imaging has not been done, with infection threads typically imaged by GFP-tagged rhizobia within them, or histochemically in thin sections. Results We have developed new methods of imaging infection threads using novel and traditional cell wall fluorescent labels, and laser confocal scanning microscopy. We applied a new Periodic Acid Schiff (PAS) stain using rhodamine-123 to the labelling of whole cleared infected roots of Medicago truncatula; which allowed for imaging of infection threads in greater 3D detail than had previously been achieved. By the combination of the above method and a calcofluor-white counter-stain, we also succeeded in labelling infection threads and plant cell walls separately, and have potentially discovered a way in which the infection thread matrix can be visualized. Conclusions Our methods have made the imaging and study of infection threads more effective and informative, and present exciting new opportunities for future research in the area.

Synchrotron infrared microspectroscopy reveals the response of Sphagnum cell wall material to its aqueous chemical environment

2018 ◽  
Vol 15 (8) ◽  
pp. 513
Author(s):  
Ewen Silvester ◽  
Annaleise R. Klein ◽  
Kerry L. Whitworth ◽  
Ljiljana Puskar ◽  
Mark J. Tobin
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Chemical Environment ◽  
Wall Material ◽  
Organic Soils ◽  
Cell Wall Material ◽  
Acid Base ◽  
Widespread Species ◽  
Flowing Liquid ◽  
Infrared Microspectroscopy

Environmental contextSphagnum moss is a widespread species in peatlands globally and responsible for a large fraction of carbon storage in these systems. We used synchrotron infrared microspectroscopy to characterise the acid-base properties of Sphagnum moss and the conditions under which calcium uptake can occur (essential for plant tissue integrity). The work allows a chemical model for Sphagnum distribution in the landscape to be proposed. AbstractSphagnum is one the major moss types responsible for the deposition of organic soils in peatland systems. The cell walls of this moss have a high proportion of carboxylated polysaccharides (polygalacturonic acids), which act as ion exchangers and are likely to be important for the structural integrity of the cell walls. We used synchrotron light source infrared microspectroscopy to characterise the acid-base and calcium complexation properties of the cell walls of Sphagnum cristatum stems, using freshly sectioned tissue confined in a flowing liquid cell with both normal water and D2O media. The Fourier transform infrared spectra of acid and base forms are consistent with those expected for protonated and deprotonated aliphatic carboxylic acids (such as uronic acids). Spectral deconvolution shows that the dominant aliphatic carboxylic groups in this material behave as a monoprotic acid (pKa=4.97–6.04). The cell wall material shows a high affinity for calcium, with a binding constant (K) in the range 103.9–104.7 (1:1 complex). The chemical complexation model developed here allows for the prediction of the chemical environment (e.g. pH, ionic content) under which Ca2+ uptake can occur, and provides an improved understanding for the observed distribution of Sphagnum in the landscape.

scholarly journals Characterization of Glycoside Hydrolase Family 5 Proteins in Schizosaccharomyces pombe

2010 ◽  
Vol 9 (11) ◽  
pp. 1650-1660 ◽  
Author(s):  
Encarnación Dueñas-Santero ◽  
Ana Belén Martín-Cuadrado ◽  
Thierry Fontaine ◽  
Jean-Paul Latgé ◽  
Francisco del Rey ◽  
...  
Keyword(s):  
Cell Wall ◽  
Schizosaccharomyces Pombe ◽  
Protein Characterization ◽  
Wall Material ◽  
Glycoside Hydrolase Family ◽  
Content Type ◽  
Hydrolysis Of ◽  
Controlled Hydrolysis ◽  
Hydrolase Family

ABSTRACT In yeast, enzymes with β-glucanase activity are thought to be necessary in morphogenetic events that require controlled hydrolysis of the cell wall. Comparison of the sequence of the Saccharomyces cerevisiae exo-β(1,3)-glucanase Exg1 with the Schizosaccharomyces pombe genome allowed the identification of three genes that were named exg1 + (locus SPBC1105.05), exg2 + (SPAC12B10.11), and exg3 + (SPBC2D10.05). The three proteins have different localizations: Exg1 is secreted to the periplasmic space, Exg2 is a membrane protein, and Exg3 is a cytoplasmic protein. Characterization of the biochemical activity of the proteins indicated that Exg1 and Exg3 are active only against β(1,6)-glucans while no activity was detected for Exg2. Interestingly, Exg1 cleaves the glucans with an endohydrolytic mode of action. exg1 + showed periodic expression during the cell cycle, with a maximum coinciding with the septation process, and its expression was dependent on the transcription factor Sep1. The Exg1 protein localizes to the septum region in a pattern that was different from that of the endo-β(1,3)-glucanase Eng1. Overexpression of Exg2 resulted in an increase in cell wall material at the poles and in the septum, but the putative catalytic activity of the protein was not required for this effect.

scholarly journals Reconstruction ofmreBExpression in Staphylococcus aureus via a Collection of New Integrative Plasmids

2014 ◽  
Vol 80 (13) ◽  
pp. 3868-3878 ◽  
Author(s):  
Ana Yepes ◽  
Gudrun Koch ◽  
Andrea Waldvogel ◽  
Juan-Carlos Garcia-Betancur ◽  
Daniel Lopez
Keyword(s):  
Staphylococcus Aureus ◽  
Cell Wall ◽  
Cell Biology ◽  
Genetic Manipulation ◽  
Protein Localization ◽  
Antibiotic Resistance Genes ◽  
Wall Material ◽  
Content Type ◽  
Genetic Manipulations ◽  
Discrete Structures

ABSTRACTProtein localization has been traditionally explored in unicellular organisms, whose ease of genetic manipulation facilitates molecular characterization. The two rod-shaped bacterial modelsEscherichia coliandBacillus subtilishave been prominently used for this purpose and have displaced other bacteria whose challenges for genetic manipulation have complicated any study of cell biology. Among these bacteria is the spherical pathogenic bacteriumStaphylococcus aureus. In this report, we present a new molecular toolbox that facilitates gene deletion in staphylococci in a 1-step recombination process and additional vectors that facilitate the insertion of diverse reporter fusions into newly identified neutral loci of theS. aureuschromosome. Insertion of the reporters does not add any antibiotic resistance genes to the chromosomes of the resultant strains, thereby making them amenable for further genetic manipulations. We used this toolbox to reconstitute the expression ofmreBinS. aureus, a gene that encodes an actin-like cytoskeletal protein which is absent in coccal cells and is presumably lost during the course of speciation. We observed that inS. aureus, MreB is organized in discrete structures in association with the membrane, leading to an unusual redistribution of the cell wall material. The production of MreB also caused cell enlargement, but it did not revert staphylococcal shape. We present interactions of MreB with key staphylococcal cell wall-related proteins. This work facilitates the useS. aureusas a model system in exploring diverse aspects of cellular microbiology.

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