The influence of different joining processes on mechanical performance of carbon fiber/polyamide (CF/PA6) composites

تستخدم المواد المركبة المصنوعة من مادة البولي أميد (PA6) المقوى بألياف الكربون (CF) على نطاق واسع كمواد هيكلية في صناعات السيارات والفضاء نظرًا لخصائصها المتميزة. ومع ذلك ، نظرًا لمتطلبات السلامة الهيكلية للمواد المركبة ، لا تزال هناك محدودية فيما يتعلق بالإنتاج الفعلي للمواد المركبة المكونة من (CF/ PA6). الروابط القوية لصفائح CF/PA6 مطلوبة بشدة  لعمل تصميم خفيف الوزن يستخدم في العديد من المجالات. بهدف إجراء مقارنات ، تم تدراسة مختلف طرق المعالجة مثل الربط بمواد لاصقة والربط الحراري لتشكيل روابط اللإلفة بين صفحتين مركبتين من (CF/PA6). كما تم دراسة تأثير الطرق المختلفة ومتغيرات المعالجة  المختلفة على مقاومة القص للروابط. أظهرت النتائج أنه من السهل جدًا التعامل مع الروابط اللاصقة التقليدية وقد تتشكل روابط  أقوى إلى حد ما. يمكن استخدام الروابط الحرارية القائمة على التوصيل الكهربائي عن طريق CF لتشكيل توصيلات متلدنة بالحرارة مع المرونة في التصميم. يمكن أن تزيد الروابط الحرارية عن طريق الضغط الساخن من قوة الاتصال؛ عندما تتشكل بالضغط الساخن في ظروف مثالية في درحة حرارة تبلغ 250 درجة مئوية وضغط 2.5 ميجا باسكال ، فإن قوة القص للمفصل 138.85 ميجا باسكال. وبالتالي تم التأكيد على أنه يمكن الحصول على روابط قوية لأجزاء الصفائح للمادة المركبة CF/PA6  عن طريق الالتصاق الحراري عبرعملية الضغط  الساخن.Carbon fiber (CF) reinforced polyamide (PA6) composite materials are broadly used as structural materials in the automotive and aerospace industries due to their distinguished properties. However, due to requirements for the structural integrity of composite materials, there are still limitations in connection of the actual production of CF/PA6 composite. Strong joints of CF/PA6 laminates are highly required for the lightweight design in many fields. Aiming at making comparisons, different processing methods such as adhesive bonding and thermal jointing to form single lap joints between the two CF/PA6 composite laminates are studied. The influences of different processing methods and parameters on the shear strength of joints were also studied. Results showed that conventional adhesive bonding is quite easy to handle and may form rather stronger connections. Thermal joining based on electrical conductors of CF can be used to form a thermoplastic flexible joint design. Thermal joints by hot pressing can further increase the connection strength; when formed by hot pressing under optimum conditions of 250 °C and 2.5MPa, the joint has a shearing strength of 138.85 MPa. It is consequently confirmed that a strong joint of CF/PA6 composite parts could be obtained by thermal joints via the hot pressing process

Debilitating floods in the Sahel are becoming frequent

Despite the long-lasting and widespread drought in the Sahel, flood events did punctuate in the past. The concern about floods remains dwarf on the international research and policy agenda compared to droughts. In this paper, we elucidate that floods in the Sahel are now becoming more frequent, widespread, and more devastating. We analyzed gridded daily rainfall data over the period 1981–2020, used photographs and satellite images to depict flood areas and threats, compiled and studied flood-related statistics over the past two decades, and supported the results with peer-reviewed literature. Our analysis revealed that the timing of the maximum daily rainfall occurs from the last week of July to mid-August in the Eastern Sahel, but from the last week of July to the end of August in the Western Sahel. In 2019 and 2020, flash and riverine floods took their toll in Sudan and elsewhere in the region in terms of the number of affected people, direct deaths, destroyed and damaged houses and croplands, contaminated water resources, and disease outbreaks and deaths. Changes in rainfall intensity, human interventions in the physical environment, and poor urban planning play a major role in driving catastrophic floods. Emphasis should be put on understanding flood causes and impacts on vulnerable societies, controlling water-borne diseases, and recognizing the importance of compiling relevant and reliable flood information. Extreme rainfall in this dry region could be an asset for attenuating the regional water scarcity status if well harvested and managed. We hope this paper will induce the hydroclimate scholars to carry out more flood studies for the Sahel. It is only then encumbered meaningful opportunities for flood risk management can start to unveil

The performance of heteroatom-doped carbon nanotubes synthesized via a hydrothermal method on the oxygen reduction reaction and specific capacitance

Due to the increasing demand for electrochemical energy storage, various novel electrode and catalysis materials for supercapacitors and rechargeable batteries have developed over the last decade. The structure and characteristics of these catalyst materials have a major effect on the device's performance. In order to lower the costs associated with electrochemical systems, electrochemical systems, metal-free catalysis materials can be employed. In this study, metal-free catalysts composed of nitrogen (N) and sulfur (S) dual-doped multi-walled carbon nanotubes  were synthesized using a straightforward and cost-effective single-step hydrothermal method. Carbon nanotubes served as the carbon source, while l-cysteine amino acid and thiourea acted as doping elements. As a result of the physicochemical characterization, many defects and a porous structure were noted, along with the successful insertion of nitrogen and sulfur into the carbon nanotube was confirmed. According to the cyclic voltammetry tests for the dual-doped samples in alkaline conditions, the D-CNT2 catalyst exhibited onset potentials of -0.30 V higher than the -0.37 V observed for the D-CNT3 catalyst. This indicates enhanced oxygen–reduction reaction due to the synergistic effects of the heteroatoms in the structure and the presence of chemically active sites. Moreover, the outstanding specific capacitance of the D-CNT2 catalyst (214.12 F g-1 at scanning rates of 1 mV s-1) reflects the effective porosity of the proposed catalyst. These findings highlight the potential of N/S dual–doped carbon nanotubes for electrocatalytic applications, contributing to efficient energy conversion

Female genital mutilation of a karyotypic male presenting as a female with delayed puberty

BACKGROUND: Female genital mutilation (FGM) is commonly practiced mainly in a belt reaching from East to West Africa north of the equator. The practice is known across socio-economic classes and among different ethnic, religious, and cultural groups. Few studies have been appropriately designed to measure the health effects of FGM. However, the outcome of FGM on intersex individuals has never been discussed before. CASE PRESENTATION: The patient first presented as a female with delayed puberty. Hormonal analysis revealed a normal serum prolactin level of 215 Mu/L, a low FSH of 0.5 Mu/L, and a low LH of 1.1 Mu/L. Type IV FGM (Pharaonic circumcision) had been performed during childhood. Chromosomal analysis showed a 46, XY karyotype and ultrasonography verified a soft tissue structure in the position of the prostate. CONCLUSION: FGM pose a threat to the diagnosis and management of children with abnormal genital development in the Sudan and similar societies

P. falciparum Modulates Erythroblast Cell Gene Expression in Signaling and Erythrocyte Production Pathways

Global, genomic responses of erythrocytes to infectious agents have been difficult to measure because these cells are e-nucleated. We have previously demonstrated that in vitro matured, nucleated erythroblast cells at the orthochromatic stage can be efficiently infected by the human malaria parasite Plasmodium falciparum. We now show that infection of orthochromatic cells induces change in 609 host genes. 592 of these transcripts are up-regulated and associated with metabolic and chaperone pathways unique to P. falciparum infection, as well as a wide range of signaling pathways that are also induced in related apicomplexan infections of mouse hepatocytes or human fibroblast cells. Our data additionally show that polychromatophilic cells, which precede the orthochromatic stage and are not infected when co-cultured with P. falciparum, up-regulate a small set of genes, at least two of which are associated with pathways of hematopoiesis and/or erythroid cell development. These data support the idea that P. falciparum affects erythropoiesis at multiple stages during erythroblast differentiation. Further P. falciparum may modulate gene expression in bystander erythroblasts and thus influence pathways of erythrocyte development. This study provides a benchmark of the host erythroblast cell response to infection by P. falciparum

Genome-wide Runx2 occupancy in prostate cancer cells suggests a role in regulating secretion

Runx2 is a metastatic transcription factor (TF) increasingly expressed during prostate cancer (PCa) progression. Using PCa cells conditionally expressing Runx2, we previously identified Runx2-regulated genes with known roles in epithelial–mesenchymal transition, invasiveness, angiogenesis, extracellular matrix proteolysis and osteolysis. To map Runx2-occupied regions (R2ORs) in PCa cells, we first analyzed regions predicted to bind Runx2 based on the expression data, and found that recruitment to sites upstream of the KLK2 and CSF2 genes was cyclical over time. Genome-wide ChIP-seq analysis at a time of maximum occupancy at these sites revealed 1603 high-confidence R2ORs, enriched with cognate motifs for RUNX, GATA and ETS TFs. The R2ORs were distributed with little regard to annotated transcription start sites (TSSs), mainly in introns and intergenic regions. Runx2-upregulated genes, however, displayed enrichment for R2ORs within 40 kb of their TSSs. The main annotated functions enriched in 98 Runx2-upregulated genes with nearby R2ORs were related to invasiveness and membrane trafficking/secretion. Indeed, using SDS–PAGE, mass spectrometry and western analyses, we show that Runx2 enhances secretion of several proteins, including fatty acid synthase and metastasis-associated laminins. Thus, combined analysis of Runx2's transcriptome and genomic occupancy in PCa cells lead to defining its novel role in regulating protein secretion

Haptoglobin and Sickle Cell Polymorphisms and Risk of Active Trachoma in Gambian Children

BACKGROUND: Susceptibility and resistance to trachoma, the leading infectious cause of blindness, have been associated with a range of host genetic factors. In vitro studies of the causative organism, Chlamydia trachomatis, demonstrate that iron availability regulates its growth, suggesting that host genes involved in regulating iron status and/or availability may modulate the risk of trachoma. The objective was to investigate whether haptoglobin (Hp) haplotypes constructed from the functional polymorphism (Hp1/Hp2) plus the functional promoter SNPs -61A-C (rs5471) and -101C-G (rs5470), or sickle cell trait (HbAS, rs334) were associated with risk of active trachoma when stratified by age and sex, in rural Gambian children. METHODOLOGY AND PRINCIPAL FINDINGS: In two cross sectional surveys of children aged 6-78 months (n = 836), the prevalence of the clinical signs of active trachoma was 21.4%. Within boys, haplotype E (-101G, -61A, Hp1), containing the variant allele of the -101C-G promoter SNP, was associated with a two-fold increased risk of active trachoma (OR = 2.0 [1.17-3.44]). Within girls, an opposite association was non-significant (OR = 0.58 [0.32-1.04]; P = 0.07) and the interaction by sex was statistically significant (P = 0.001). There was no association between trachoma and HbAS. CONCLUSIONS: These data indicate that genetic variation in Hp may affect susceptibility to active trachoma differentially by sex in The Gambia

Dissection of the Transformation of Primary Human Hematopoietic Cells by the Oncogene NUP98-HOXA9

NUP98-HOXA9 is the prototype of a group of oncoproteins associated with acute myeloid leukemia. It consists of an N-terminal portion of NUP98 fused to the homeodomain of HOXA9 and is believed to act as an aberrant transcription factor that binds DNA through the homeodomain. Here we show that NUP98-HOXA9 can regulate transcription without binding to DNA. In order to determine the relative contributions of the NUP98 and HOXA9 portions to the transforming ability of NUP98-HOXA9, the effects of NUP98-HOXA9 on primary human CD34+ cells were dissected and compared to those of wild-type HOXA9. In contrast to previous findings in mouse cells, HOXA9 had only mild effects on the differentiation and proliferation of primary human hematopoietic cells. The ability of NUP98-HOXA9 to disrupt the differentiation of primary human CD34+ cells was found to depend primarily on the NUP98 portion, whereas induction of long-term proliferation required both the NUP98 moiety and an intact homeodomain. Using oligonucleotide microarrays in primary human CD34+ cells, a group of genes was identified whose dysregulation by NUP98-HOXA9 is attributable primarily to the NUP98 portion. These include RAP1A, HEY1, and PTGS2 (COX-2). Their functions may reflect the contribution of the NUP98 moiety of NUP98-HOXA9 to leukemic transformation. Taken together, these results suggest that the effects of NUP98-HOXA9 on gene transcription and cell transformation are mediated by at least two distinct mechanisms: one that involves promoter binding through the homeodomain with direct transcriptional activation, and another that depends predominantly on the NUP98 moiety and does not involve direct DNA binding

Aconitase Regulation of Erythropoiesis Correlates with a Novel Licensing Function in Erythropoietin-Induced ERK Signaling

Erythroid development requires the action of erythropoietin (EPO) on committed progenitors to match red cell output to demand. In this process, iron acts as a critical cofactor, with iron deficiency blunting EPO-responsiveness of erythroid progenitors. Aconitase enzymes have recently been identified as possible signal integration elements that couple erythropoiesis with iron availability. In the current study, a regulatory role for aconitase during erythropoiesis was ascertained using a direct inhibitory strategy.In C57BL/6 mice, infusion of an aconitase active-site inhibitor caused a hypoplastic anemia and suppressed responsiveness to hemolytic challenge. In a murine model of polycythemia vera, aconitase inhibition rapidly normalized red cell counts, but did not perturb other lineages. In primary erythroid progenitor cultures, aconitase inhibition impaired proliferation and maturation but had no effect on viability or ATP levels. This inhibition correlated with a blockade in EPO signal transmission specifically via ERK, with preservation of JAK2-STAT5 and Akt activation. Correspondingly, a physical interaction between ERK and mitochondrial aconitase was identified and found to be sensitive to aconitase inhibition.Direct aconitase inhibition interferes with erythropoiesis in vivo and in vitro, confirming a lineage-selective regulatory role involving its enzymatic activity. This inhibition spares metabolic function but impedes EPO-induced ERK signaling and disturbs a newly identified ERK-aconitase physical interaction. We propose a model in which aconitase functions as a licensing factor in ERK-dependent proliferation and differentiation, thereby providing a regulatory input for iron in EPO-dependent erythropoiesis. Directly targeting aconitase may provide an alternative to phlebotomy in the treatment of polycythemia vera