scholarly journals Loss of BMP signaling through BMPR1A in osteoblasts leads to greater collagen cross-link maturation and material-level mechanical properties in mouse femoral trabecular compartments

Bone ◽  
2016 ◽  
Vol 88 ◽  
pp. 74-84 ◽  
Author(s):  
Yanshuai Zhang ◽  
Erin Gatenby McNerny ◽  
Masahiko Terajima ◽  
Mekhala Raghavan ◽  
Genevieve Romanowicz ◽  
...  
Author(s):  
K. S. Zhansakova ◽  
E. N. Eremin ◽  
G. S. Russkikh ◽  
O. V. Kropotin

The work studies vulcanization characteristics of elastomers based on isoprene rubber filled with carbon black N330 and boron nitride (BN). The influence of the boron nitride (BN) concentration on technological, dynamic, physical and mechanical properties of elastomers has been researched. The application of boron nitride for producing rubber with good properties has been considered. With a gradual increase of the inert filler BN concentration up to 35%, a decrease in the curing rate by 33% and polymer cross-link density by 26% is observed. Moreover, the start time of vulcanization increases by almost 300%, the optimal curing time by 200%.


1998 ◽  
Vol 530 ◽  
Author(s):  
Petra Eiselt ◽  
Jon A. Rowley ◽  
David J. Mooney

AbstractReconstruction of tissues and organs utilizing cell transplantation offers an attractive approach for the treatment of patients suffering from organ failure or loss. Highly porous synthetic materials are often used to mimic the function of the extracellular matrix (ECM) in tissue engineering, and serve as a cell delivery vehicle for the formation of tissues in vivo. Alginate, a linear copolysaccharide composed of D-mannuronic acid (M) and L-guluronic acid (G) units is widely used as a cell transplantation matrix. Alginate is considered to be biocompatible, and hydrogels are formed in the presence of divalent cations such as Ca2+, Ba2+ and Sr2+. However, ionically cross-linked alginate gels continuously lose their mechanical properties over time with uncontrollable degradation behavior. We have modified alginate via covalent coupling of cross-linking molecules to expand and stabilize the mechanical property ranges of these gels. Several diamino PEG molecules of varying molecular weight (200, 400, 1000, 3400) were synthesized utilizing carbodiimide chemistry. Sodium alginate was covalently cross-linked with these cross-linking molecules, and mechanical properties of the resulting hydrogels were determined. The elastic modulus of the cross-linked alginates depended on the molecular weight of the cross-linking molecules, and ranged from 10-110 kPa. The theoretical cross-link density in the hydrogels was also varied from 3 to 47% (relative to the carboxylic groups in the alginate) and the mechanical properties were measured. The elastic modulus increased gradually and reached a maximum at a cross-link density of 15%. In summary, covalently coupled hydrogels can be synthesized which exhibit a wide range of mechanical properties, and these materials may be useful in a number of tissue engineering applications.


2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Ján Kruželák ◽  
Andrea Kvasničáková ◽  
Elena Medlenová ◽  
Rastislav Dosoudil ◽  
Ivan Hudec

Rubber magnetic composites were prepared by incorporation of barium ferrite in constant amount—50 phr into acrylonitrile-butadiene rubber. Dicumyl peroxide as the curing agent was used for cross-linking of rubber magnets alone, or in combination with four different types of co-agents. The main aim was to examine the influence of curing system composition on magnetic and physical-mechanical properties of composites. The cross-link density and the structure of the formed cross-links were investigated too. The results demonstrated that the type and amount of the co-agent had significant influence on cross-link density, which was reflected in typical change of physical-mechanical properties. The tensile strength increased with increasing amount of co-agents, which can be attributed to the improvement of adhesion and compatibility on the interphase filler-rubber due to the presence of co-agents. Magnetic characteristics were found not to be influenced by the curing system composition. The application of peroxide curing systems consisting of organic peroxide and co-agents leads to the preparation of rubber magnets with not only good magnetic properties but also with improved physical-mechanical properties, which could broaden the sphere of their application uses.


2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Suzana Samaržija-Jovanović ◽  
Vojislav Jovanović ◽  
Gordana Marković ◽  
Ivana Zeković ◽  
Milena Marinović-Cincović

Opalized white tuff (OWT) with 40 μm average particle size and 39.3 m2/g specific surface area has been introduced into polyisoprene rubber (NR). Their reinforcing effects were evaluated by comparisons with those from precipitated silica (PSi). The cure characteristic, apparent activation energy of cross-link (Eac) and reversion (Ear), and mechanical properties of a variety of composites based on these rubbers were studied. This was done using vulcanization techniques, mechanical testing, and scanning electron microscopy (SEM). The results showed that OWT can greatly improve the vulcanizing process by shortening the time of optimum cure (tc90) and the scorch time (ts2) of cross-linked rubber composites, which improves production efficiency and operational security. The rubber composites filled with 50 phr of OWT were found to have good mechanical and elastomeric properties. The tensile strengths of the NR/OWT composites are close to those of NR/PSi composites, but the tear strength and modulus are not as good as the corresponding properties of those containing precipitated silica. Morphology results revealed that the OWT is poorly dispersed in the rubber matrix. According to that, the lower interactions between OWT and polyisoprene rubber macromolecules are obtained, but similar mechanical properties of NR/OWT (100/50) rubber composites compared with NR/PSi (100/50) rubber composites are resulted.


1988 ◽  
Vol 106 (4) ◽  
pp. 1205-1211 ◽  
Author(s):  
M Sato ◽  
W H Schwartz ◽  
S C Selden ◽  
T D Pollard

We measured the elasticity and viscosity of brain tubulin solutions under various conditions with a cone and plate rheometer using both oscillatory and steady shearing modes. Microtubules composed of purified tubulin, purified tubulin with taxol and 3x cycled microtubule protein from pig, cow, and chicken behaved as mechanically indistinguishable viscoelastic materials. Microtubules composed of pure tubulin and heat stable microtubule-associated proteins were also similar but did not recover their mechanical properties after shearing like other samples, even after 60 min. All of the other microtubule samples were more rigid after flow orientation, suggesting that the mechanical properties of anisotropic arrays of microtubules may be substantially greater than those of randomly arranged microtubules. These experiments confirm that MAPs do not cross link microtubules. Surprisingly, under conditions where microtubule assembly is strongly inhibited (either 5 degrees or at 37 degrees C with colchicine or Ca++) tubulin was mechanically indistinguishable from microtubules at 10-20 microM concentration. By electron microscopy and ultracentrifugation these samples were devoid of microtubules or other obvious structures. However, these mechanical data are strong evidence that tubulin will spontaneously assemble into alternate structures (aggregates) in nonpolymerizing conditions. Because unpolymerized tubulin is found in significant quantities in the cytoplasm, it may contribute significantly to the viscoelastic properties of cytoplasm, especially at low deformation rates.


2015 ◽  
Vol 752-753 ◽  
pp. 357-362
Author(s):  
David Manas ◽  
Martin Ovsik ◽  
Miroslav Manas ◽  
Michal Stanek ◽  
Marcela Spanhelova ◽  
...  

The process of radiation crosslinking helps to improve some mechanical properties of polymer materials. Some types of polymers do not cross-link during radiation crosslinking but degrade. In order to create 3D net in the polymer structure it is necessary to add a crosslinking agent. The specimens were prepared by injection technology with the TAIC crosslinking agent at 0, 1, 2 and 3 %. The changes of micromechanical properties of the surface layer were measured by instrumented microhardness test. It was found that micromechanical properties of the surface layer of the tested polyamide changed.


2013 ◽  
Vol 86 (4) ◽  
pp. 558-571 ◽  
Author(s):  
Jiyu Liang ◽  
Na Feng ◽  
Suqin Chang ◽  
C. Xinhong Wang ◽  
Guixia Zhang

ABSTRACT Polysulfane silanized white silica particles were prepared by treating with various loadings of bis(3-trie-thoxysilylpropyl)tetrasulfide (TESPT) in a high-speed mixer. Brombutyl rubber (BIIR) vulcanizates filled with the silanized silica were prepared by compression molding. Compared with BIIR/untreated silica vulcanizate, the mechanical properties of BIIR/silanized silica vulcanizates improved prominently with the increase of TESPT loading and reached peak value with the TESPT loading increasing up to 2 phr but declined slightly with the continuous increment of the TESPT. Effects of various loadings of TESPT on the mechanical properties of BIIR vulcanizates were investigated by testing mechanical properties, vulcanizing properties, bound rubber, scanning electron microscopy, and dynamic mechanical analysis (DMA) to determine the extent of rubber-filler interaction. As shown in vulcanizing properties, bound rubber, and DMA measurements, the bound rubber content, cross-link density, and storage and loss modulus of BIIR vulcanizates clearly increased with the TESPT loading increasing from 0 to 2 phr and then reduced somewhat with a continuous increase of TESPT; the tanδmax value decreased significantly with the increment of TESPT loading from 0 to 2 phr and increased sharply with the TESPT content increasing to 4 phr. These experimental results indicate that the improvement in the mechanical properties of BIIR vulcanizates was mostly attributed to a strong BIIR–silica interaction and an effective dispersion of the silica. On the other hand, the decline of mechanical properties can be explained by the excess TESPT, as a kind of physical diluent, having an adverse effect on the silica dispersion and cross-link reaction. By forming the silica aggregates on the mixing, the poor dispersion of silica could cause the decline of relative volume content of silica in the matrix.


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