Search Results (10)

Food security is one of the main problems in several countries. In food processing the cutting operation is very important as the operation is basic to food preparation. Due to cutting tools being exposed to a high-demand environment that includes high contact pressure, a corrosive atmosphere, and a high-speed process, they are subject to high mechanical and corrosive wear that reduces their lifetime and efficiency. Tribocorrosion is one of the main phenomena that reduces the lifetime and efficiency of cutting tools. This work presents electrochemical and tribocorrosion studies of D2 steel surfaces coated with TiN, TiCN, and TiCrN films. The samples were coated by a commercial source, using the PVD-cathodic arc technique. The crystalline structure of TiN and TiCN films presented a TiN and Ti phase, while the crystalline structure of TiCrN showed CrN and Cr phases. The films exhibited good adhesion, but the surfaces coated with TiN and TiCN films presented lower hardness. Although the TiN, TiCN, and TiCrN films showed better wear and corrosion resistance than the D2 steel surfaces, the inclusion of C and Cr in the TiN films decreased the TiN wear and electrochemical resistance in 3.5% (w/w) of NaCl solution. Full article

In sealing, sliding, and power transmission operations, surface quality and contact tolerances have high impacts on material system efficiency. Although the boriding process improves the wear resistance of metallic surfaces, it increases surface roughness, affecting the tribological efficiency of material systems. This study presents the tribological results of AISI 4140 boriding surfaces tested using a dehydrated paste pack boriding method with and without a finishing polish process to reduce the roughness. The duration of the boriding process was 1 h at 1123, 1173, 1223, and 1273 K using boron paste obtained from a commercial source and using a pot-polishing process with Al₂O₃ with a particle size of 0.5 μm for 25 min. The samples with and without the finishing polish process were structurally characterized using X-ray diffraction, and the boride coating adhesion was determined using Rockwell C indentation. The tribological properties of the boride surface with and without the finishing polish process were determined using a reciprocating sliding test, with a ZrO₂ ball as a counter body. The boride surfaces’ crystalline structure changed with polishing, which revealed the FeB phase and reduced the roughness value. These modifications in the surface characteristics altered the adhesion and tribological performance of the coating, resulting in a more stable tribological performance on the polished boride surfaces, with a reduction in the coefficient of friction (Cof) value from 0.75 ± 0.02 for the tribological test on the 1123 K-P sample to 0.59 ± 0.002 for the 1273 K-P sample surface at 20 N of applied load. Full article

Surface water flooding is an issue which has required an increased level of addressment over the past two decades, with the methods used to combat flood events seeing an evolution. This evolution has been influenced heavily by multi-scale legislations and policies, which has pushed for more holistic methods for pluvial flood management. This review will analyse how Bristol City Council have implemented these multi-scale pieces and what has been put in place to encourage sustainable flood management. This will be done through a purposive review of the literature and an extensive review of legislation and policies on a national, European, and regional scale. The findings of the review were able to show that international legislation and policies are not in place to support sustainable management. UK policies, however, were more supportive, with direct reference and guidance for how to move away from hard engineering solutions. The City of Bristol has embraced the concept of sustainable flood management, with the highest level of support witnessed through the multi-scale review. Overall, the City of Bristol has achieved a good understanding of how to use sustainable drainage, with many systems throughout the city, and schemes to support the use. However, further legislative pieces need to be passed on a national and European scale to encourage and promote the deployment of these systems, so the benefits can be acquired on a large scale. Full article

The study of isolated atoms or molecules inside a fullerene cavity provides a unique environment. It is likely to control the outer carbon cage and study the isolated species when molecules or atoms are trapped inside a fullerene. We report the Diels–Alder addition reaction of 9,10-dimethyl anthracene (DMA) to H₂@C₆₀ while ¹H NMR spectroscopy is utilized to characterize the Diels–Alder reaction of the DMA with the fullerene. Through ¹H NMR spectroscopy, a series of isomeric adducts are identified. The obtained peaks are sharp, precise, and straightforward. Moreover, in this paper, H₂@C₆₀ and its isomers are described for the first time. Full article

Diagnostic imaging of aggressive cancer with a high stroma content may benefit from the use of imaging contrast agents targeted with peptides that have high binding affinity to the extracellular matrix (ECM). In this study, we report the use of superparamagnetic iron-oxide nanoparticles (IO-NP) conjugated to a nonapeptide, CSGRRSSKC (CSG), which specifically binds to the laminin-nidogen-1 complex in tumours. We show that CSG-IO-NP accumulate in tumours, predominantly in the tumour ECM, following intravenous injection into a murine model of pancreatic neuroendocrine tumour (PNET). In contrast, a control untargeted IO-NP consistently show poor tumour uptake, and IO-NP conjugated to a pentapeptide. CREKA that bind fibrin clots in blood vessels show restricted uptake in the angiogenic vessels of the tumours. CSG-IO-NP show three-fold higher intratumoral accumulation compared to CREKA-IO-NP. Magnetic resonance imaging (MRI) T₂-weighted scans and T₂ relaxation times indicate significant uptake of CSG-IO-NP irrespective of tumour size, whereas the uptake of CREKA-IO-NP is only consistent in small tumours of less than 3 mm in diameter. Larger tumours with significantly reduced tumour blood vessels show a lack of CREKA-IO-NP uptake. Our data suggest CSG-IO-NP are particularly useful for detecting stroma in early and advanced solid tumours. Full article

Titanium oxynitrides (Ti(N,O,C)) are abundant in xenolithic corundum aggregates in pyroclastic ejecta of Cretaceous volcanoes on Mount Carmel, northern Israel. Petrographic observations indicate that most of these nitrides existed as melts, immiscible with coexisting silicate and Fe-Ti-C silicide melts; some nitrides may also have crystallized directly from the silicide melts. The TiN phase shows a wide range of solid solution, taking up 0–10 wt% carbon and 1.7–17 wt% oxygen; these have crystallized in the halite (fcc) structure common to synthetic and natural TiN. Nitrides coexisting with silicide melts have higher C/O than those coexisting with silicate melts. Analyses with no carbon fall along the TiN–TiO join in the Ti–N–O phase space, implying that their Ti is a mixture of Ti³⁺ and Ti²⁺, while those with 1–3 at.% C appear to be solid solutions between TiN and Ti_0.75O. Analyses with >10 at% C have higher Ti²⁺/Ti³⁺, reflecting a decrease in fO₂. Oxygen fugacity was 6 to 8 log units below the iron–wüstite buffer, at or below the Ti₂O₃–TiO buffer. These relationships and coexisting silicide phases indicate temperatures of 1400–1100 °C. Ti oxynitrides are probably locally abundant in the upper mantle, especially in the presence of CH₄–H₂ fluids derived from the deeper metal-saturated mantle. Full article

Here, we describe two new minerals, kishonite (VH₂) and oreillyite (Cr₂N), found in xenoliths occurring in pyroclastic ejecta of small Cretaceous basaltic volcanoes exposed on Mount Carmel, Northern Israel. Kishonite was studied by single-crystal X-ray diffraction and was found to be cubic, space group Fm$\overline{3}$m, with a = 4.2680(10) Å, V = 77.75(3) ų, and Z = 4. Oreillyite was studied by both single-crystal X-ray diffraction and transmission electron microscopy and was found to be trigonal, space group P$\overline{3}$1m, with a = 4.7853(5) Å, c = 4.4630(6) Å, V = 88.51 ų, and Z = 3. The presence of such a mineralization in these xenoliths supports the idea of the presence of reduced fluids in the sublithospheric mantle influencing the transport of volatile species (e.g., C, H) from the deep Earth to the surface. The minerals and their names have been approved by the Commission of New Minerals, Nomenclature and Classification of the International Mineralogical Association (No. 2020-023 and 2020-030a). Full article

The ubiquitin proteasome system (UPS) plays an important role in regulating numerous cellular processes, and a dysfunctional UPS is thought to contribute to motor neuron disease. Consequently, we sought to map the changing ubiquitome in human iPSCs during their pluripotent stage and following differentiation to motor neurons. Ubiquitinomics analysis identified that spliceosomal and ribosomal proteins were more ubiquitylated in pluripotent stem cells, whilst proteins involved in fatty acid metabolism and the cytoskeleton were specifically ubiquitylated in the motor neurons. The UPS regulator, ubiquitin-like modifier activating enzyme 1 (UBA1), was increased 36-fold in the ubiquitome of motor neurons compared to pluripotent stem cells. Thus, we further investigated the functional consequences of inhibiting the UPS and UBA1 on motor neurons. The proteasome inhibitor MG132, or the UBA1-specific inhibitor PYR41, significantly decreased the viability of motor neurons. Consistent with a role of the UPS in maintaining the cytoskeleton and regulating motor neuron differentiation, UBA1 inhibition also reduced neurite length. Pluripotent stem cells were extremely sensitive to MG132, showing toxicity at nanomolar concentrations. The motor neurons were more resilient to MG132 than pluripotent stem cells but demonstrated higher sensitivity than fibroblasts. Together, this data highlights the important regulatory role of the UPS in pluripotent stem cell survival and motor neuron differentiation. Full article

Impurity doping is one of the common approaches to enhance the photoactivity of semiconductor nanomaterials by increasing photon-capture efficiency in the visible light range. However, many studies on the doping effects have produced inconclusive and conflicting results. There are some misleading assumptions and errors that are frequently made in the data interpretation, which can lead to inconsistent results about the doping effects on photocatalysis. One of them is the determination of the location of dopants. Even using advanced analytical techniques, it is still challenging to distinguish between bulk modification and surface modification. The paper provides a case study of transition-metal-doped ZnO nanoparticles, whereby demonstrating common pitfalls in the interpretation of the results of widely-used analytical methods in detail, and discussing the importance of using a combination of many characterization techniques to correctly determine the location of added impurities, for elucidating the influence of metal doping on the photocatalytic activities of semiconductor nanoparticles. Full article

The new mineral species carmeltazite, ideally ZrAl₂Ti₄O₁₁, was discovered in pockets of trapped melt interstitial to, or included in, corundum xenocrysts from the Cretaceous Mt Carmel volcanics of northern Israel, associated with corundum, tistarite, anorthite, osbornite, an unnamed REE (Rare Earth Element) phase, in a Ca-Mg-Al-Si-O glass. In reflected light, carmeltazite is weakly to moderately bireflectant and weakly pleochroic from dark brown to dark green. Internal reflections are absent. Under crossed polars, the mineral is anisotropic, without characteristic rotation tints. Reflectance values for the four COM wavelengths (R_min, R_max (%) (λ in nm)) are: 21.8, 22.9 (471.1); 21.0, 21.6 (548.3), 19.9, 20.7 (586.6); and 18.5, 19.8 (652.3). Electron microprobe analysis (average of eight spot analyses) gave, on the basis of 11 oxygen atoms per formula unit and assuming all Ti and Sc as trivalent, the chemical formula (Ti³⁺_3.60Al_1.89Zr_1.04Mg_0.24Si_0.13Sc_0.06Ca_0.05Y_0.02Hf_0.01)_Σ=7.04O₁₁. The simplified formula is ZrAl₂Ti₄O₁₁, which requires ZrO₂ 24.03, Al₂O₃ 19.88, and Ti₂O₃ 56.09, totaling 100.00 wt %. The main diffraction lines, corresponding to multiple hkl indices, are (d in Å (relative visual intensity)): 5.04 (65), 4.09 (60), 2.961 (100), 2.885 (40), and 2.047 (60). The crystal structure study revealed carmeltazite to be orthorhombic, space group Pnma, with unit-cell parameters a = 14.0951 (9), b = 5.8123 (4), c = 10.0848 (7) Å, V = 826.2 (1) ų, and Z = 4. The crystal structure was refined to a final R₁ = 0.0216 for 1165 observed reflections with F_o > 4σ(F_o). Carmeltazite exhibits a structural arrangement similar to that observed in a defective spinel structure. The name carmeltazite derives from Mt Carmel (“CARMEL”) and from the dominant metals present in the mineral, i.e., Titanium, Aluminum and Zirconium (“TAZ”). The mineral and its name have been approved by the IMA Commission on New Minerals, Nomenclature and Classification (2018-103). Full article