Comparison of abrasive wear behavior of ductile iron with different dual matrix structures

Abrasive wear behavior of ductile irons with different dual matrix structures has been investigated. In order to obtain ductile irons with different dual matrix structures an unalloyed ductile iron specimens were austenitized in the two-phase region (α + γ) at various temperature (795 °C and 815 °C) and then rapidly transferred to a salt bath held at the 365 °C for austempering for 30, 90 and 120 min. Some specimens were quenched from same intercritical austenitizing temperatures and tempered at 550 °C for 60 and 300 min. Some specimens were also conventionally austempered and/or quenched from 900 °C for comparison. Experimental results showed that, the tensile strength increased and ductility decreased with increasing martensite volume fraction in the specimen with martensite dual matrix structure. By increasing the tempering time, the yield and UTS decreased and ductility increased. In addition, the specimens with ausferrite dual matrix structures exhibited much greater ductility than conventionally austempered ones. The tensile strength increased while ductility decreased with increasing ausferrite volume fraction. Furthermore in all austenitized specimens, the abrasive weight loss of austempered specimens (A series) was lower than those of quenched specimens (Q series) irrespective of all loads due to increased AFVFs and total elongation. It was shown that wear loss of both tested materials in abrasive wear was proportional to the applied load. However, there was a decreasing trend in the weight loss of the A795 with dual matrix structure austempered for 30 and 90 min with increasing load. The reason was because of the fact that the specimen surface was work hardened with cutting efficiency of the abrasive reduced through clogging, and attrition jointly leading to less weight loss. Moreover, increasing the austempering time caused more ductile ausferritic structure to displace hard martensite. In all austempered samples, the abrasive weight loss increased with increasing the austempering time. As for the case of Q samples, the abrasive weight loss increased more or less linearly with load since an increase in the applied load might increase the contact stress. Among the Q samples, the highest weight loss was obtained for the Q795-300, Q815-300 sample because of lower martensite volume fraction, but the lowest weight loss was observed for the Q900 sample due to the highest martensite volume fraction. For Q900 samples, the amount of fracture of the abrasives was found to be increase with the harder specimen, and it may have contributed somewhat to the increased wear.Furthermore, microchips were dominant wear mechanism by cutting mode for higher ductile materials while micro-ploughing was predominant wear for harder materials, but wear also occurred by combinations of ploughing and embedding particles into the surface for Q samples. Cross-section examination by SEM through the wear surfaces revealed that a more smoother surface was observed for the A795 sample than that of the Q795 sample. However, a more rougher surface was observed for the A900-120 sample than that of the Q900 sample.     

Study on the structure and properties of Poly(methylmethacrylate)/Polypyrrole-Graphene Oxide nanocomposites

In this paper Poly(methylmethacrylate)/Polypyrrole-Graphene Oxide (PMMA/PPy-GO) nanocomposites were prepared using in-situ chemical polymerization method and its structure and properties were studied. Fourier transform infrared (FTIR), X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) analysis confirmed that PPy nanopraticles covered the GO nanosheets surface and PMMA/PPy-GO nanocomposite were prepared successfully. The mechanical, electrical and thermal stability of the PMMA nanocomposites were also investigated using Tensile, Impact, Thermogravimetric analysis (TGA) and four-point probe methods. Correlation between direct morphological observation and final properties demonstrated that network structure formed by PPy-GOs in PMMA matrix. Tensile analysis showed that the addition of 0.4 wt % PPy-GO hybrids lead to 24.4 % enhancement in the Young’s modulus of PMMA compared to 5.0 % improvement that achieved at the same loading level of GO. Electrical conductivity measurement showed that dispersion of PPy-GO in PMMA matrix increased AC conductivity in the range of 8 orders of magnitude compared to PMMA. TGA analysis showed that the thermal stability of the PMMA nanocomposites improved over 20 ?C.     

Bioprinting a cell-laden matrix for bone regeneration: A focused review

Although many efforts have been made to regenerate the bone lesions, existing challenges can be mitigated through the development of tissue engineering scaffolds. However, the weak control on the microstructure of constructs, limitation in preparation of patient-specific and multilayered scaffolds, restriction in the fabrication of cell-laden matrixes, and challenges in preserving the drug/growth factors' efficacy in conventional methods have led to the development of bioprinting technology for regeneration of bone defects. So in this review, conventional 3D printers are classified, then the priority of the different types of bioprinting technologies for the preparation of the cell/growth factor-laden matrixes are focused. Besides, the bio-ink compositions, including polymeric/hybrid hydrogels and cell-based bio-inks are classified according to fundamental and recent studies. Herein, different effective parameters, such as viscosity, rheological properties, cross-linking methods, biodegradation biocompatibility, are considered. Finally, different types of cells and growth factors that can encapsulate in the bio-inks to promote bone repair are discussed, and both in vitro and in vivo achievement are considered. This review provides current and future perspectives of cell-laden bioprinting technologies. The restrictions and challenges are identified, and proper strategies for the development of cell-laden matrixes and high-performance printable bio-inks are proposed.     

CHEMICALLY IMPROVED LIMESTONES FOR FLUIDIZED BED COMBUSTION OF COAL†

Preparation is made of a group of four new chemically improved limestones (SO₂-sorbents) from reactants of 65% limestone, 25% fly ash, and 10% binder of either a ball clay or mixture of the clay with a small quantity of colloidal silica. Fabrication is by pan granulation followed by varying extents of calcination. Potential products in the sorbents are inferred from the phase diagram of the CaO(base)-SiO₂(acid)-Al₂O₃(acid) system. The sorbents show SO₂-sorbency up to 2.8-3.0 times that of limestone during coal combustions, evaluations by both thermogravimetry (TG) using the Rapid TG Method and a 6-inch fluidized bed combustion (FBC) unit. Linear correlation with nearly perfect fit of data points is obtained between a parameter for SO₂-sorption by evaluations from the Rapid TG Method and SO₂-decrease in emissions by evaluations via the FBC method. Other linear correlations indicate a trend of direct proportionality between SO₂-decrease and carbon-decrease in FBC emissions. A chemical mechanism is suggested in order to describe this simultaneous occurrence of SO₂-decrease and carbon-decrease in emissions from coal combustion.     

Effectiveness of SO2 sorbents by thermogravimetry-combustion with coal

A new experimental method is described for non-isothermal thermogravimetry (TG) involving combustion of mixtures of sieved coal with sieved calcium-containing sorbents. This rapid TG method utilizes a baseline for TG combustion of coal alone, derives an equation that gives a semi-quantitative measure (±10% repeatability) of the coal's reactive sulphur retained by the sorbent, the extent of retention of S0₂ generated in situ during combustion varying with different sorbents. The method permits direct variation in separate experiments of the calcium-to-sulphur ratio during combustion and relative ranking of different sorbents by retention of reactive sulphur in combustion. Relative rankings are presented for three pre-calcined natural stones (two limestones and one dolomite); these results correlate with relative rankings from another TG method reported in the literature. It is suggested that this new method is useful for pre-screening the effectiveness of S0₂ sorbents considered for use in fluidizedbed combustion of coal.     

Engineering Cell Surface Function with DNA Origami

A specific and reversible method is reported to engineer cell‐membrane function by embedding DNA‐origami nanodevices onto the cell surface. Robust membrane functionalization across epithelial, mesenchymal, and nonadherent immune cells is achieved with DNA nanoplatforms that enable functions including the construction of higher‐order DNA assemblies at the cell surface and programed cell–cell adhesion between homotypic and heterotypic cells via sequence‐specific DNA hybridization. It is anticipated that integration of DNA‐origami nanodevices can transform the cell membrane into an engineered material that can mimic, manipulate, and measure biophysical and biochemical function within the plasma membrane of living cells.     

Cynipid gall-wasp communities correlate with oak chemistry

Host-plant association data, gathered from field surveys conducted throughout Florida and from the literature, were used to identify the specificity of cynipid gall inducers to one or more of six Quercus species that occur at Archbold Biological Station, Lake Placid, Florida, USA, including the red oaks Q. laevis, Q. myrtifolia, and Q. inopina, and the white oaks Q. chapmanii, Q. geminata, and Q. minima. Quercus myrtifolia had the highest cynipid richness and diversity (37 cynipid species, Shannon H = 3.61, Simpson's D = 0.97), followed by Q. chapmanii, Q. laevis, Q. inopina, Q. geminata, and finally Q. minima (10 species, H = 2.30, D = 0.90). All cynipid species showed strong fidelity to a particular host plant or a restricted set of host plants. An ordination of gall-wasp host associations indicated that the cynipid communities of each oak species were distinct and specific to a given oak species. Leaf samples taken from each oak species were analyzed for condensed and hydrolyzable tannins, total phenolics, lignin, cellulose and hemicellulose, nitrogen, and carbon. All of these chemical traits, with the exception of carbon, differed by oak species, and the differences were strongly correlated with the axes of the cynipid--species ordination. These results suggest that gall-wasp occurrence is influenced by oak chemistry and imply that experimental studies of cynipid gall inducers that examine host-plant chemistry and female oviposition choice and larval performance will yield useful insights.