Crystalline Aggregates Research Articles

Supergénne minerály z U-Cu rudného výskytu Východná-Nižný Chmelienec v Nízkych Tatrách (hronikum, Slovensko)

An association of supergene U-Cu and Y/REE minerals was found in a relic of old ore dump at the abandoned U deposit occurrence Východná-Nižný Chmelienec, the northern slopes of the Nízke Tatry Mts., Slovakia. They have partially recent origin, since exploration of the locality took place between 1965 and 1966. The studied mineral assem- blage is represented by goethite, malachite, uranophane and (meta)zeunerite, in a lesser extent baryte and rare zálesíite. Uranophane appears separately (globular aggregates, thin coatings) and it also forms the main part of the yellow to yellow-green crystalline crusts on the rock cracks. The chemical composition of the uranophane was determined by electron microprobe analyses and it is close to its ideal chemical formula Ca(UO2)2(SiO3OH)2·5H2O. The average chemical composition of the studied uranophane can be expressed by an empirical formula (Ca1.0Mg0.02K0.01Fe0.01Ba0.01)Σ1.05 (UO2)2.08(SiO3OH)1.84·5H2O. The infrared vibrational spectra of the studied uranophane show 3 (UO2)2+ at 850-760 cm-1; the 3 (SiO4)4- antisymmetric stretching vibration at 1000-900 cm-1; the 1 (SiO4)4- symmetric stretching vibration at 1150-1199 cm-1; the  H2O bending vibration at 1800-1600 cm-1 and OH stretching vibrations at 3407; 3408 and 3409 cm-1. The weak bands 2648; 2646 and 2651 cm-1 may be assigned to organic impurities. The calculated U-O bond length 1.83 Å corresponds to short U-O bonds in uranophane. The accessory admixtures of uranophane coatings are (meta)zeunerite and zálesíite. (Meta)zeunerite occasionally forms thin coatings of light green to emerald green tabular crystals (up tu 0.5 mm) on the surface of the rocks. Chemical analyses of (meta)zeunerite correspond to the empirical formula (Cu0.66K0.03Fe0.01Ca0.01)Σ0.71(UO2)2.11[(AsO4)1.96(PO4)0.01]Σ1.97·12H2O. Zálesíite occurs as crystalline aggregates, nests, formed by tiny acicular crystals, up to 100 µm in length. This is the second finding (occurrence) of this mineral in Slovakia. An average zálesíite chemical composition is (Ca0.83REE0.18U0.05Al0.03Ti0.01)Σ1.10(Cu5.81Fe0.06Zn0.02)Σ5.90[(AsO4)2.75 (SiO4)0.21(PO4)0.02(SO4)0.03]Σ3.01(OH)5.10·3H2O. Malachite, which has been also found in the association, is only a minor mineral in the studied locality. The formation of uranyl silicates (uranophane) and minerals of the mixite group (zálesíite), present at the studied locality, points to neutralization of acidic supergene fluids in the mine dumps. Possibly, this environment later (precipitation of baryte) passed to neutral or slightly basic conditions (precipitation of carbonates - malachite). The identified uranyl phosphates/arsenates (zeunerite/metazeunerite), typical of an acidic environment, are therefore rare.

Псевдоморфообразование по раковинам силурийских брахиопод

The analysis of paleontological data, the study of mineral matter transformation involving live organisms in various rocks is important for the understanding of the events of the geological past. The aim of this work is to identify the bio-genic factor in the process of pseudo-morphogenesis in the shell sashes of the Early Silurian brachiopods from the car-bonate rocks of the Chernyshev Ridge. Structural and microscopic methods (Shimadzu XRD 6000; Fourier spectrometer InfraLum FT-02; JSM 6400 JEOL; VEGA3 TESCAN; MIN-8) were used to study quartz pseudomorphoses in the sashes of four shells of the Early Silurian brachiopods Borealis sр. of Pentamerida order from the carbonate strata of the Chernyshev Ridge. The salicification of the brachiopod shell walls resulted in the complete replacement of the original carbonate skeleton with a change in its structural organization. It is established that quartz is the main mineral component of the intra-shell material and secondary dolomite crystals and newly formed calcite aggregates. The paper discusses the participation of Early Paleozoic and modern cyanobacterial symbionts in the replacement of primary calcite with quartz and the formation of quartz crystalline aggregates on the shell walls. It is shown that quartz on the surface of shell sashes and in the intra-shell substance of brachiopods has undergone repeated transformations due to the combination of ancient and modern weathering processes.

H2O2-induced cataract as a model of age-related cataract: Lessons learned from overexpressing the proteasome activator PA28αβ in mouse eye lens

Cataract, the world-leading cause of blindness, is formed when crystallin aggregates cloud the eye lens. We overexpressed PA28αβ, a proteasome activator with properties protective against aggregation and oxidative stress, and examined whether they are less prone to develop cataract arisen from aging and/or hydrogen peroxide (H2O2) treatment. Another objective of this work was to compare the H2O2-induced cataracts of mouse lenses ex vivo to cataracts formed upon aging in mice.As part of an aging study of F2 hybrid C57BL/6NxBALB/c mice, ocular lenses of mature adult (7 months), middle-aged (15 months), and old (22 months of age) PA28αOE mice and their wildtype littermates (n = 22–44 lenses per group) were dissected and evaluated with regard to their cataractous state. In parallel, ocular lenses from 3 to 4 months old PA28αOE and wildtype C57BL/6 N littermates were treated with 100 μM H2O2 every 24 h for 7 days, with progression of cataract and physical appearance monitored daily. Lenses from both studies were also subjected to analysis of oxidative protein damage (carbonylation) and protein solubility.We found that overexpression of PA28αβ had no effect on neither age-related nor H2O2-induced cataract and conclude that overexpression of PA28αβ does not protect mice from developing cataract. The inefficiency of PA28αβ against cataract could be due to its anti-aggregation activity being already excessively present in the eye lens, exerted by crystallins. Crystallins are likely also constituting the 20–25 kDa proteins that were the dominant carbonyl targets in the eye lens irrespective of cataractous state.Assessment of H2O2-induced cataract in relation to age-related cataract demonstrated that high molecular weight protein carbonylation correlates to cataract both in vivo and ex vivo, while reduced protein solubility is more pronounced in age-related cataract. Furthermore, this work highlights vast dissimilarities in the physical manifestations of cataract upon aging and H2O2 ex vivo treatment. Age-related cataract initiation can take various forms, as a vague general blurriness or as a barely visible demarcated opacity, while H2O2-induced cataractogenesis seems to follow a specific scheme. In mice, this scheme begins with relatively opaque peripheral areas emerging that clear up later on as the lenses start to display a hat-like appearance. This transformation takes place synchronous to swelling of the eye lens, and is likely a result of osmotic disturbances causing a phase separation between the viscous lens cortex and the more solid fibers of the lens nucleus.

Comparative morphotaxonomical affinities, palaeoecological implications and cladistic analyses of ornithoid eggshells (oofamily Laevisoolithidae) from the Late Cretaceous intertrappean beds of Anjar, District Kachchh, Gujarat, India

ABSTRACT We re-evaluate fragmentary eggshells of avian affinities (ratite morphotype) from the Late Cretaceous Intertrappean beds of Anjar (District Kachchh, Gujarat), India in view of additional material and cladistic analysis. Previously, Anjar eggshells were encompassed in the oofamily Subtiliolithidae; however, now the oofamily Subtiliolithidae has been re-examined as a junior synonym of the oofamily Laevisoolithidae. External surface of the eggshells is smooth to rugose, with unevenly distributed, sub-rounded tubercles; average eggshell thickness (467–491 µm) characterised by two layers: (1) a well-differentiated mammillary layer (196.1 µm), comprising conical, crystalline aggregates with petaloid wedges, and (2) a continuous spongy layer (274.58 µm, CL:ML, 1.3:1) divulges a squamatic zone. The eggshells have been compared with three oofamilies (Elongatoolithidae, Prismatoolithidae and Laevisoolithidae) and their palaeoecological implications have been discussed in detail. Shell microstructure is comparable with oofamily Laevisoolithidae, an ootaxon usually related with enantiornithid birds. Cladistic analysis performed on the eggshells are consistent with the avian kinships recognised based on macro, micro and ultrastructural features.

A C. elegans Zona Pellucida domain protein functions via its ZPc domain.

Zona Pellucida domain (ZP) proteins are critical components of the body’s external-most protective layers, apical extracellular matrices (aECMs). Although their loss or dysfunction is associated with many diseases, it remains unclear how ZP proteins assemble in aECMs. Current models suggest that ZP proteins polymerize via their ZPn subdomains, while ZPc subdomains modulate ZPn behavior. Using the model organism C. elegans, we investigated the aECM assembly of one ZP protein, LET-653, which shapes several tubes. Contrary to prevailing models, we find that LET-653 localizes and functions via its ZPc domain. Furthermore, we show that ZPc domain function requires cleavage at the LET-653 C-terminus, likely in part to relieve inhibition of the ZPc by the ZPn domain, but also to promote some other aspect of ZPc domain function. In vitro, the ZPc, but not ZPn, domain bound crystalline aggregates. These data offer a new model for ZP function whereby the ZPc domain is primarily responsible for matrix incorporation and tissue shaping.

Aperiodic Schrodinger Crystals

In 1945, E. Schrödinger predicted the possibility of the existence of “aperiodic crystals,” that is, more and more increasing crystalline aggregates, but without a simple lattice repetition mechanism. In the present work, such structures are experimentally prepared using selenium as an example. By thermal gradient treatment of the amorphous selenium film, we have obtained nano-thin spatial dissipative structures (SDS) of hexagonal selenium, the lattice of which undergoes non-uniform rotational curvature around, in the general case, three mutually perpendicular directions. The formation of these nano-thin SDS of hexagonal selenium occurs as a result of cooperative rotations of selenium macromolecules around, in general, three mutually perpendicular directions. Since nano-thin SDS after hardening in air have all the features of crystals each of the above nano-thin SDS of hexagonal selenium obtained at different annealing temperatures corresponds to the concept of “aperiodic crystals” Thus, “aperiodic crystals” were obtained experimentally, the possibility of the existence of which was predicted by E. Schrödinger.

Co‐Assembly between Fmoc Diphenylalanine and Diphenylalanine within a 3D Fibrous Viscous Network Confers Atypical Curvature and Branching

AbstractSupramolecular polymer co‐assembly is a useful approach to modulate peptide nanostructures. However, the co‐assembly scenario where one of the peptide building blocks simultaneously forms a hydrogel is yet to be studied. Herein, we investigate the co‐assembly formation of diphenylalanine (FF), and Fmoc‐diphenylalanine (FmocFF) within the 3D network of FmocFF hydrogel. The overlapping peptide sequence between the two building blocks leads to their co‐assembly within the gel state modulating the nature of the FF crystals. We observe the formation of branched microcrystalline aggregates with an atypical curvature, in contrast to the FF assemblies obtained from aqueous solution. Optical microscopy reveal the sigmoidal kinetic growth profile of these aggregates. Microfluidics and ToF‐SIMS experiments exhibit the presence of co‐assembled structures of FF and FmocFF in the crystalline aggregates. Molecular dynamics simulation was used to decipher the mechanism of co‐assembly formation.

Co-Assembly between Fmoc Diphenylalanine and Diphenylalanine within a 3D Fibrous Viscous Network Confers Atypical Curvature and Branching.

Supramolecular polymer co-assembly is a useful approach to modulate peptide nanostructures. However, the co-assembly scenario where one of the peptide building blocks simultaneously forms a hydrogel is yet to be studied. Herein, we investigate the co-assembly formation of diphenylalanine (FF), and Fmoc-diphenylalanine (FmocFF) within the 3D network of FmocFF hydrogel. The overlapping peptide sequence between the two building blocks leads to their co-assembly within the gel state modulating the nature of the FF crystals. We observe the formation of branched microcrystalline aggregates with an atypical curvature, in contrast to the FF assemblies obtained from aqueous solution. Optical microscopy reveal the sigmoidal kinetic growth profile of these aggregates. Microfluidics and ToF-SIMS experiments exhibit the presence of co-assembled structures of FF and FmocFF in the crystalline aggregates. Molecular dynamics simulation was used to decipher the mechanism of co-assembly formation.

A Perspective on Biophysical Studies of Crystallin Aggregation and Implications for Cataract Formation.

Lens crystallins are subject to various types of damage during their lifetime which triggers protein misfolding and aggregation, ultimately causing cataracts. There are several models for crystallin aggregation, but a comprehensive picture of the mechanism of cataract is still underway. The complex biomolecular interactions underlying crystallin aggregation have motivated major efforts to resolve the structural details and mechanism of aggregation using multiple biophysical techniques at different resolutions. Together, experimental and computational approaches identify and characterize both amyloidogenic and amorphous aggregates leading to an improved understanding of crystallin aggregation. A rigorous characterization of the aggregation-prone intermediates is crucial in cataract-mediated drug discovery. This Perspective summarizes recent biophysical studies on lens crystallin aggregation. We evaluate the outstanding challenges, future outlook, and rewards in this fertile field of research. With lessons learned from protein folding and multiple pathways of aggregation, we highlight the differences in the overall mechanisms of age-related and congenital cataracts. We expect that a correlation between the existing and developing biophysical techniques would provide a platform to study amyloid architecture in the eye lens and reduce the existing gaps in our understanding of crystallin biophysics.

Fabrication, characterization, and in vitro evaluation of β-TCP/ZrO2-phosphate-based bioactive glass scaffolds for bone repair

Scaffolds have proven to be an excellent option for the regeneration of bone tissues; since they present excellent results of architecture, composition, and functionality. Therefore, scaffolds can be used as implants to repair bones and show guided regeneration, allowing complete restructuring of damaged tissue, as well as allowing the site where the implant is located to have functionality. In the present investigation, three different beta-phase tricalcium phosphate/zirconia-reinforced phosphate-based bioactive glass compositions were evaluated: V1, VZ0.5, and VZ1.0 (0, 0.5, and 1mol%). All scaffolds showed excellent bioactivity and osteoconductivity results. They were forming HA crystalline aggregates with the typical cauliflower morphology in vitro studies in simulated body fluid and with human osteoblasts (MG-63).On the other hand, cell proliferation analyzed using the BrdU assay and apoptosis using Annexin V. As well as the viability (MTT assay) and adhesion (RT-PCR of beta 3 integrin) of osteoblasts at day 14. Zirconia had a significant positive effect on cell proliferation as well as in the cell adhesion, with a substantial proliferation for the scaffold with VZ1.0 composition. Due to the zirconia modifies the scaffold surface, allowing greater cell adhesion, an essential step for cell proliferation to take place.

Trehalose Inhibits the Heat-Induced Formation of the Amyloid-Like Structure of Soluble Proteins Isolated from Human Cataract Lens.

The age-dependent loss of solubility and aggregation of crystallins constitute the pathological hallmarks of cataract. Several biochemical and biophysical factors are responsible for the reduction of crystallins' solubility and formation of irreversible protein aggregates, which display amyloid-like characteristics. The present study reports the heat-induced aggregation of soluble proteins isolated from human cataract lenses and the formation of amyloid-like structures. Exposure of protein at 55 °C for 4 h resulted in extensive (≈ 60%) protein aggregation. The heat-induced protein aggregates displayed substantial (≈ 20nm) redshift in the wavelength of maximum absorption (λmax) of Congo red (CR) and increase in Thioflavin T (ThT) fluorescence emission intensity, indicating the presence of amyloid-like structures in the heat-induced protein aggregates. Subsequently, the addition of trehalose resulted in substantial inhibition of heat-induced aggregation and the formation of amyloid-like structure. The ability of trehalose to inhibit the heat-induced aggregation was found to be linearly dependent upon its concentrationused. The optimum effect was observed in the presence of 30-40% (w/v) trehalose where the aggregated was found to be reduced from 60 to 30%. The present study demonstrated the ability to trehalose to inhibit the protein aggregation and interfere with the formation of amyloid-like structures.

Mineral Inventory of the Algares 30-Level Adit, Aljustrel Mine, Iberian Pyrite Belt, Portugal

Mining activity in Algares (Aljustrel Mine, Portuguese sector of the Iberian Pyrite Belt, IPB) stems prior to Roman times. As the orebody is vertical and relatively thin, mining was carried out mainly along underground adits (galleries). Nowadays, the deposit is considered exhausted and the area is being rehabilitated for a different use. The Algares +30 level adit intersects two volcanic units of the IPB Volcano-Sedimentary Complex. The massive sulphide and related stockwork zone are hosted by the Mine Tuff volcanic unit and are exposed in the walls of the gallery, showing intense hydrothermal alteration. Along the mine adit, the geological sequence is affected by strong oxidation and supergene alteration, giving rise to the formation of secondary minerals through the oxidation of the sulphides. The most common minerals found were melanterite (FeSO4·7H2O) and chalcanthite (CuSO4·5H2O), forming essentially massive or crystalline aggregates, ranging from greenish to bluish colours. Melanterite from the walls revealed to be Cu-rich by opposition to that from stalactites/stalagmites formed below the old ore storage silo revealing the low-copper-grade ores exploited underground. The mineralogy of the efflorescent salts was used to ascertain the processes involved in their formation, and moreover, the inventory of minerals is presented, as well as their principal characteristics.

L-3,4-Dihydroxyphenylalanine templated anisotropic gold nano/micro-roses as potential disrupters/inhibitors of α-crystallin protein and its gleaned model peptide aggregates

Cataract, the major cause of blindness worldwide occurs due to the misfolding and aggregation of the protein crystallin, which constitute a major portion of the lens protein. Other than the whole protein crystallin, the peptide sequences generated from crystallin as a result of covalent protein damage have also been shown to possess and foster protein aggregation, which can be established as crystallin aggregation models. Thus, the disaggregation or inhibition of these protein aggregates could be a viable approach to combat cataract and preserve lens proteostasis. Herein, we tried to explore the disruption as well as inhibition of the intact α-crystallin protein and α-crystallin derived model peptide aggregates by l-3,4-dihydroxyphenylalanine (levodopa) coated gold (Au) nano/micro-roses as modulators. Thioflavin T fluorescence enhancement assay, and electron microscopic analysis were being employed to probe the anti-aggregation behavior of the Au nano/micro-roses towards the aggregating α-crystallin peptides/protein. Further, computational studies were performed to reveal the nature of molecular interactions between the levodopa molecule and the α-crystallin derived model peptides. Interestingly, both levodopa coated Au nano/micro-roses were found to be capable of inhibiting as well as preventing the aggregation of the intact α-crystallin protein and other model peptides derived from it.

Grguricite, CaCr2(CO3)2(OH)4.4H2O, a new alumohydrocalcite analogue

AbstractThe occurrence and characterisation of a new member of the dundasite group are reported. Grguricite, ideally CaCr2(CO3)2(OH)4⋅4H2O, is the Cr analogue of alumohydrocalcite, CaAl2(CO3)2(OH)4⋅4H2O and occurs as lilac crusts of very fine-grained crystalline aggregates in the Pb–Ba–V mineralisation found at the Adeghoual Mine, Mibladen, Morocco (32°46′0″N, 4°37′59″W). The identification was based upon a close match with the powder X-ray diffraction data for alumohydrocalcite, the confirmation of anion components identified by Raman spectroscopy and the cation composition determined by electron-probe microanalysis. The empirical formula based upon 14 oxygen atoms per formula unit is Ca0.84Pb0.03Cr1.65Al0.39Mg0.02(CO3)2(OH)4⋅4H2O, with carbonate, hydroxyl and water contents set to those of the alumohydrocalcite stoichiometry. The fine-grained nature of the crystals (c. 0.5 μm × 0.1 μm × 5 μm) precluded a single-crystal X-ray study and both density and optical determinations. Grguricite is triclinic with space group P${\bar 1}$. Unit-cell parameters refined from the powder diffraction data are: a = 5.724(2), b = 6.5304(9), c = 14.646(4) Å, α = 81.682(1), β = 83.712(2), γ = 86.365(2)°, V = 537.8(2) Å3 and Z = 2. The five strongest peaks in the powder pattern are [dhkl, Å (I/Imax)(hkl)]: 6.222(100)(011), 3.227(87)(020), 6.454(63)(010), 2.883(58)(005, 023, 121) and 7.208(45)(002). The mineral is named after Australian geologist Ben Grguric.

Synthesis of Modifiers in the System Cao-Sio<sub>2</sub>-H<sub>2</sub>O and their Influence on the Non-Autoclave Silicate Materials’ Properties Using Aluminosilicate Binder

Improving the hydration hardening building materials’ operational properties is possible due to the stable macro-, micro-and nanostructures’ creation by the cementing material crystalline aggregate directed modification, which can be achieved through the use of various additives acting as crystallization centers. In the course of the studies, the synthesized modifier effect nature represented by the system was revealed CaO-SiO2-H2O (CSH) on the properties of non-autoclave silicate materials using aluminosilicate binder of various compositions. It has been established that the use of an aluminosilicate binder together with the addition of a CSH modifier increases the presence of a crystalline phase at all stages of hardening, as well as intensifies the synthesis of low-basic calcium hydro silicates with a higher crystallization degree in the system CaO-SiO2(Al2O3)-H2O represented by lime and clay rocks. This contributes to the micro-reinforced crystalline framework formation of the neoplasms with increased strength. Due to this, the pore space decreases and the amount of synthesized crystalline substance increases, which helps to increase the water resistance of the samples in all compositions. The samples using an aluminosilicate binder and the addition of a CSH modifier achieve maximum strength with a CaO content of not more than 10 wt. % The optimal CSH modifier addition is up to 1.5 wt. %, with 7 wt. %, CaO content in a mixture increase in strength is up to 6%.

The Aggregation of αB-Crystallin under Crowding Conditions Is Prevented by αA-Crystallin: Implications for α-Crystallin Stability and Lens Transparency

One of the most crowded biological environments is the eye lens which contains a high concentration of crystallin proteins. The molecular chaperones αB-crystallin (αBc) with its lens partner αA-crystallin (αAc) prevent deleterious crystallin aggregation and cataract formation. However, some forms of cataract are associated with structural alteration and dysfunction of αBc. While many studies have investigated the structure and function of αBc under dilute in vitro conditions, the effect of crowding on these aspects is not well understood despite its in vivo relevance. The structure and chaperone ability of αBc under conditions that mimic the crowded lens environment were investigated using the polysaccharide Ficoll 400 and bovine γ-crystallin as crowding agents and a variety of biophysical methods, principally contrast variation small-angle neutron scattering. Under crowding conditions, αBc unfolds, increases its size/oligomeric state, decreases its thermal stability and chaperone ability, and forms kinetically distinct amorphous and fibrillar aggregates. However, the presence of αAc stabilizes αBc against aggregation. These observations provide a rationale, at the molecular level, for the aggregation of αBc in the crowded lens, a process that exhibits structural and functional similarities to the aggregation of cataract-associated αBc mutants R120G and D109A under dilute conditions. Strategies that maintain or restore αBc stability, as αAc does, may provide therapeutic avenues for the treatment of cataract.

Hot Corrosion of Shipboard Gas Turbine Blades

Turbine blades removed from the first stage of a shipboard gas turbine engine for excessive degradation were characterized. Scanning electron microscopy coupled with energy-dispersive spectroscopy, X-ray diffraction, and inductively coupled optical emission spectroscopy was used to characterize corrosion deposits and features of field hardware that are not typically obtained in controlled laboratory settings. Corrosion was associated with deposits of varying compositions on the airfoil, beneath the platform, and within cooling passages. Deposits on the airfoil were primarily sodium sulfate presumably derived from seawater. Deposits below the platform and within cooling channels were crystalline aggregates of Ca, Mg, Al, and Si compounds presumably derived from dust and sand. FactSage thermochemical calculations were performed for gas turbine environments, and results are used to explain variations in deposit chemistry. The results show that solid sodium sulfate may not be retained in some gas turbine conditions, leaving the deposits rich in Ca and Mg compounds.

Nanostructure and its effect on electrochemical properties of polyanionic Li2CoSiO4 for lithium ion batteries

This work reports a facile strategy to synthesize carbon-coated Li2CoSiO4/C particles with rich nanostructures by a two-step scheme starting with a low-temperature hydrothermal method. The size and morphology of particle aggregates can be regulated by the (OH−) concentration and viscosity of the precursor solution, a mixture of ethylene glycol and deionized water, for the hydrothermal synthesis. In addition to the good electrical conductivity from the carbon coating, the size of the primary nanoparticles and the mesopore associated with the aggregations play an important role in improving the electrochemical properties of polyanionic Li2CoSiO4. The low-dimensional belt-like and sheet-like Li2CoSiO4/C nanomaterials present a higher reversible capacity 136.6 mAh g−1 and 147 mAh g−1, respectively, in the first charging–discharging cycle between 2 V and 4.6 V. XRD, SEM/TEM, and EDS are used to characterize the crystalline structure and aggregation patterns. TGA and Raman spectra are employed to analyze the carbon coating on different morphologies. The analysis of electrochemical impedance spectroscopy highlights the critical role of the interface between the electrolyte and particles. This study provides insights into the rational design and synthesis of high-performance polyanionic cathodes including silicates.

The effect of various fuels on the yield, structural and optical properties zinc zirconate nanocomposite

Various types of fuels were used in a low-temperature solution combustion synthesis of zinc zirconate nanocomposite at a pH of 7. In the synthesis, the fuels used were citric acid, glycine, urea, hydrazine hydrate, and ammonium nitrate while zirconium butoxide and zinc nitrate were the precursor sources of Zr4+ and Zn2+ ions, respectively. The samples were calcined for 2 h at a temperature of 600 °C. The study of the structural properties showed varied morphologies ranging from highly agglomerated surfaces, crystalline aggregates as well as nanorods. There was a gradual growth of zinc zirconate perovskite within phases of zirconia and zinc oxide. It was observed that there were prominent photoluminescence emissions spread from violet-blue into the yellow-white regions with peaks varying from about 400 to 490 nm. The energy bandgap of the nanocomposites was between 2.93 and 3.22 eV depending on the fuel used in the preparation of the sample.

3D Photoinduced Spatiotemporal Resolution of Cellulose-Based Hydrogels for Fabrication of Biomedical Devices.

Rational spatiotemporal irradiation of cellulose-based hydrogels (carboxymethylcellulose (CMC), citric acid, and riboflavin) using a laser diode stereolithography 3D printer obtained architectures referred to as photodegradation addressable hydrogels (PAHs). Under irradiation, these PAHs engage in an unprecedented spatially resolved zonal swelling illustrating marked but controllable changes in swelling and thickness while concomitantly obtaining improved oxygen transmission rate values by 5 times. XPS, carboxyl content, and swelling data comparisons of hydrogel formulations show that photodegradation and ablation of the material occur, where hydroxyl sites of CMC are converted to aldehydes and ketones. XRD data show that the total number of crystalline aggregates in the material are lowered after photoablation. The spatially tuned (photoablated) hydrogel films can thus be shaped into a lens form. The energy required for the lens tuning process can be lowered up to 30 times by incorporation of riboflavin in the films. The method demonstrated here enables the processing of a material that is difficult to be machined or cast by popular contact lens making methods.