Enhanced Strength and Ductility in Magnesium Matrix Composites Reinforced by a High Volume Fraction of Nano- and Submicron-Sized SiC Particles Produced by Mechanical Milling and Hot Extrusion

In the present study, Mg nanocomposites with a high volume fraction (10 vol %) of SiC particles were fabricated by two approaches: mechanical milling and mixing, followed by the powder consolidation steps, including isostatic cold pressing, sintering, and extrusion. A uniform distribution of the high content SiC particles in a fully dense Mg matrix with ultrafine microstructure was successfully achieved in the mechanically milled composites. The effect of nano- and submicron-sized SiC particles on the microstructure and mechanical properties of the nanocomposites was evaluated. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectrometer (EDS), and X-ray diffractometry (XRD) were used to characterize microstructures of the milled and mixed composites. Mechanical behavior of the Mg composites was studied under nanoindentation and compressive loading to understand the effects the microstructural modification on the strength and ductility of the Mg/SiC composites. The mechanical properties of the composites showed a significant difference regarding the size and distribution of SiC particles in the Mg matrix. The enhanced strength and superior ductility achieved in the mechanically milled Mg composites are mainly ascribed to the effective load transfer between matrix and SiC particles, grain refinement of the matrix, and strengthening effects of the nano- and submicron-sized SiC particles.DFG, 414044773, Open Access Publizieren 2019 - 2020 / Technische Universität Berli

Development and Characterization of Mg-SiC Nanocomposite Powders Synthesized by Mechanical Milling

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.Magnesium powder in micron scale and various volume fractions of SiC particles with an average diameter of 50 nm were co-milled by a high energy planetary ball mill for up to 25 h to produce Mg-SiC nanocomposite powders. The milled Mg-SiC nanocomposite powders were characterized by scanning electron microscopy (SEM) and laser particle size analysis (PSA) to study morphological evolutions. Furthermore, XRD, TEM, EDAX and SEM analyses were performed to investigate the microstructure of the magnesium matrix and distribution of SiC-reinforcement. It was shown that with addition of and increase in SiC nanoparticle content, finer particles with narrower size distribution are obtained after mechanical milling. The morphology of these particles also became more equiaxed at shorter milling times. The microstructural observation revealed that the milling process ensured uniform distribution of SiC nanoparticles in the magnesium matrix even with a high volume fraction, up to 10 vol%

An investigation on non-isothermal crystallization behavior and morphology of polyamide 6/ poly(ethylene-co-1-butene)-graft-maleic anhydride/organoclay nanocomposites

Nanocomposites based on polyamide 6 (PA6) and poly(ethylene-co-1-butene)-graft-maleic anhydride (EB-g- MAH) blends have been prepared via melt mixing. The effect of blend ratio and organoclay concentration on the crystallization and melting behavior of specimens were studied. Three types of commercial organo-modified clay (Cloisite 30B, Cloisite 15A and Cloisite 20A) were employed to assess the importance of the nanoclay polarity and gallery distance. The crystallization behavior was investigated using differential scanning calorimetry (DSC) and wide angle X-ray diffraction spectroscopy (WAXD). The strong interactions between amine end groups of PA6 and maleic anhydride groups of EB-g-MAH led to complete inhibition of EB-g-MAH crystallization according to the DSC results. A transformation from the α form to the γ form crystals of PA6, induced by both organoclays and EB-g-MAH, was monitored by WAXD and DSC. Small angle X-ray scattering (SAXS) was used to evaluate the morphology of nanocomposites. Moreover, transmission electron microscopy (TEM) was conducted to determine the location of organoclays and indicated that the organoclays mainly present in the PA6 matrix and rarely distribute in the EB-g-MAH phase in the case of low polarity organoclays. It was also evidenced that the organoclay with the most affinity to PA6 (Cloisite 30B) had the largest effect on the thermal and crystallization behavior of this phase in the blend

Effect of Smear Layer on the Push-Out Bond Strength of Two Different Compositions of White Mineral Trioxide Aggregate

Introduction: The aim of this in vitro study was to evaluate the effect of smear layer on the push-out bond strength of white mineral trioxide aggregate (WMTA) with and without disodium hydrogen phosphate (Na2HPO4). Materials and Methods: Dentin discs with standard cavities were obtained from extracted human single-rooted teeth and divided to 4 groups (n=15) according to the irrigation regimen and the canal filling material. In groups 1 and 3, canals were irrigated with normal saline; in groups 2 and 4, irrigation method included sodium hypochlorite (NaOCl) and then ethylenediaminetetra-acetic acid (EDTA). The canals were filled with WMTA in first and second groups and with WMTA+Na2HPO4; in groups 3 and 4. The samples were wrapped in wet gauze and incubated in 37°C for 3 days. The push-out bond strength was then measured by means of the Universal Testing Machine and the failure modes were examined under stereomicroscope at 40× magnification. Tow-way ANOVA was used to evaluate the effect of material type and smear layer removal. Post hoc Tukey test was used for the two-by-two comparison of the groups. Results: The greatest and lowest mean±standard deviation for push-out bond strength were observed in groups 4 (4.54±1.14 MPa) and 1 (1.44±0.96 MPa), respectively. The effect of removing the smear layer on the push-out bond strength of WMTA+Na2HPO4 was significant (P=0.01), but not for WMTA (P=0.52). Interestingly, there was significant difference between groups 1, 3 and 2, 4 (P<0.05). The failure mode for all experimental groups was of mixed type. Conclusion: Under circumstances of this in vitro study, removal of smear layer increases push-out bond strength when Na2HPO4 is added to WMTA

Effect of Smear Layer on the Push-Out Bond Strength of Two Endodontic Biomaterials to Radicular Dentin

Introduction: This in vitro study was designed to evaluate the effect of smear layer removal on push-out bond strength of white mineral trioxide aggregate (WMTA) and calcium-enriched mixture cement (CEM). Materials and Methods: Dentin discs with 3 mm thicknesses were divided into 4 groups (n=15): group 1: irrigation of the canal with normal saline and filling with WMTA; group 2: irrigation with sodium hypochlorite (NaOCl) and ethylenediaminetetraacetic acid (EDTA), and then filling with WMTA; group 3: same as group 1 but the lumens were filled with CEM; group 4: same as group 2 but the lumens filled with CEM. The samples were incubated at 37°C for 3 days after wrapping in gauze pieces moistened with distilled water. The push-out bond strengths were then measured by the universal testing machine and the failure modes were examined under a stereomicroscope at 40× magnification. Data were analyzed using two-way ANOVA and post-hoc Tukey’s test for bond strength. Statistical significance was set at P<0.05. Results: The greatest and lowest mean standard deviation for push-out bond strength were observed for groups 4 (3.13±1.46 MPa) and group3 (1.44±0.96 MPa), respectively. The effect of smear layer removal on push-out bond strength of CEM was significant (P=0.01), however, it was not significant for WMTA (P=0.52). The failure mode for all the groups was of mixed type. Conclusion: Under the limitations of this study, smear layer removal is recommended for CEM in order to gain higher push-out strength

Effect of Lenalidomide on Pentylenetetrazole-Induced Clonic Seizure Threshold in Mice: A Role for N-Methyl-D-Aspartic Acid Receptor/Nitric Oxide Pathway

Background and Purpose: Accumulating evidence suggest that lenalidomide, a structural analog of thalidomide, has neuro-modulatory and neuroprotective properties. In the present study, we investigated effects of acute administration of lenalidomide on clonic seizure threshold in mice induced by pentylenetetrazole (PTZ) and possible role of N-methyl-D-aspartic acid receptor (NMDAR) and nitric oxide (NO) pathway. Methods: We have utilized a clonic model of seizure in NMRI mice induced by PTZ to evaluate the potential effect of lenalidomide on seizure threshold. Different doses of lenalidomide (5, 10, 20, and 50 mg/kg, intraperitoneal [i.p.]) were administered 1 hour before PTZ. To evaluate probable role of NMDAR/NO signaling, the non-selective NO synthase inhibitor L-N (G)-nitroarginine methyl ester (L-NAME; 10 mg/kg, i.p.), neuronal NOS (nNOS) inhibitor 7-nitroindazole (7-NI; 30 mg/kg, i.p.), selective inducible NOS inhibitor aminoguanidine (AG; 100 mg/kg, i.p.), selective NMDAR antagonist MK-801 (0.01 mg/kg, i.p.), and selective NMDAR agonist D-serine (30 mg/kg, i.p.) were injected 15 minutes before lenalidomide. Results: Lenalidomide at 10 and 20 mg/kg significantly elevated the PTZ-induced seizure thresholds. Interestingly, L-NAME (10 mg/kg, i.p), 7-NI (30 mg/kg, i.p), and AG (100 mg/kg, i.p) reversed the anticonvulsive effect of lenalidomide (10 mg/kg). Moreover, treatment with the NMDAR agonist D-serine (30 mg/kg, i.p.) did not alter the anticonvulsive properties of lenalidomide (10 mg/kg, i.p). However, the NMDAR antagonist MK-801 (0.01 mg/kg, i.p) significantly reversed the anticonvulsive effects of lenalidomide (10 mg/kg). Conclusions: Our study demonstrated a role for the NMDAR/NO pathway in the anticonvulsive effects of lenalidomide on the PTZ-induced clonic seizures in mice

Effect of Synthetic Tissue Fluid on Microleakage of Grey and White Mineral Trioxide Aggregate as Root-End Filling Materials : An in vitro study

Objectives: The success of endodontic surgery has been shown to depend partly on the apical seal. Grey mineral trioxide aggregate (GMTA) produces hydroxyapatite twice as often as white mineral trioxide aggregate (WMTA) when suspended in a phosphate buffered saline (PBS) solution. The aim of this in vitro study was to compare the microleakage phenomenon of gray and white mineral trioxide aggregates as root-end filling materials after immersion in synthetic tissue fluid (STF). Methods: 55 single-rooted extracted maxillary anterior human teeth were divided into two experimental groups of 20 teeth each, plus 3 groups of 5 teeth each as two negative and one positive control groups. The root canals were cleaned, shaped, and laterally compacted with gutta-percha. The root ends were resected and 3 mm deep cavities were prepared. The root-end preparations were filled with GMTA or WMTA in the experimental groups. Leakage was determined using a dye penetration method. Data were analysed using analysis of variance (ANOVA) at the 0.05 level of significance. Results: The mean dye leakage was 0.40 ± 0.1 mm for GMTA and 0.50±0.1 mm for WMTA groups, respectively. There was no significant difference between the two experimental groups (P = 0.14). Conclusion: Despite the different properties and behaviours of GMTA and WMTA in STF, there were no significant differences in microleakage when using GMTA or WMTA.

Analysis of Cytogenetic Abnormalities in Iranian Patients with Syndromic Autism Spectrum Disorder: A Case Series

Objective Autism spectrum disorder is a heterogeneous neuropsychiatric group of pervasive development disorder, which is mostly diagnosed through the intricate behavioral phenotype. According to strong genetic involvement, detecting the chromosome regions and the key genes linked to autism can help to elucidate its etiology. The present study aims to investigate the value of cytogenetic analysis in syndromic autism as well as to find an association between autism and chromosome abnormalities. Materials & Methods Thirty-six autism patients from 30 families, diagnosed clinically with DSM-5 criteria, were recruited. The syndromic patients who had additional clinical features involving development delay, attention deficit, hyperactivity disorder, seizure, language, and intellectual impairment were selected due to elevating the detection rate. Cytogenetics analysis was performed using GTG banding on the patients' cultured fibroblasts. Moreover, array-comparative genomic hybridization was also performed for a patient with a de novo and novel variant.   Results Karyotype analysis in 36 syndromic autism patients detected chromosomal abnormalities in two (5.6%) families, including 46,XY,dup(15)(q11.1q11.2) and 46,XX,ins(7)(q11.1q21.3)dn. In the latter, array-comparative genomic hybridization detected three abnormalities on chromosome 7, including deletion and insertion on both arms; 46,XX,del(7)(q21.11q21.3),dup(7)(p11.2p14.1p12.3)dn. Conclusion We reported a novel and de novo cytogenetic abnormality on chromosome 7 in an Iranian patient diagnosed with syndromic autism. However, the detection rate in syndromic autism was low which implies that it cannot be utilized as the only diagnostic procedure

The global burden of cancer attributable to risk factors, 2010-19 : a systematic analysis for the Global Burden of Disease Study 2019

Background Understanding the magnitude of cancer burden attributable to potentially modifiable risk factors is crucial for development of effective prevention and mitigation strategies. We analysed results from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 to inform cancer control planning efforts globally. Methods The GBD 2019 comparative risk assessment framework was used to estimate cancer burden attributable to behavioural, environmental and occupational, and metabolic risk factors. A total of 82 risk-outcome pairs were included on the basis of the World Cancer Research Fund criteria. Estimated cancer deaths and disability-adjusted life-years (DALYs) in 2019 and change in these measures between 2010 and 2019 are presented. Findings Globally, in 2019, the risk factors included in this analysis accounted for 4.45 million (95% uncertainty interval 4.01-4.94) deaths and 105 million (95.0-116) DALYs for both sexes combined, representing 44.4% (41.3-48.4) of all cancer deaths and 42.0% (39.1-45.6) of all DALYs. There were 2.88 million (2.60-3.18) risk-attributable cancer deaths in males (50.6% [47.8-54.1] of all male cancer deaths) and 1.58 million (1.36-1.84) risk-attributable cancer deaths in females (36.3% [32.5-41.3] of all female cancer deaths). The leading risk factors at the most detailed level globally for risk-attributable cancer deaths and DALYs in 2019 for both sexes combined were smoking, followed by alcohol use and high BMI. Risk-attributable cancer burden varied by world region and Socio-demographic Index (SDI), with smoking, unsafe sex, and alcohol use being the three leading risk factors for risk-attributable cancer DALYs in low SDI locations in 2019, whereas DALYs in high SDI locations mirrored the top three global risk factor rankings. From 2010 to 2019, global risk-attributable cancer deaths increased by 20.4% (12.6-28.4) and DALYs by 16.8% (8.8-25.0), with the greatest percentage increase in metabolic risks (34.7% [27.9-42.8] and 33.3% [25.8-42.0]). Interpretation The leading risk factors contributing to global cancer burden in 2019 were behavioural, whereas metabolic risk factors saw the largest increases between 2010 and 2019. Reducing exposure to these modifiable risk factors would decrease cancer mortality and DALY rates worldwide, and policies should be tailored appropriately to local cancer risk factor burden. Copyright (C) 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.Peer reviewe