Preparation of Electrochemical Supercapacitor Based on Polypyrrole/Gum Arabic Composites

The current research focused on the super capacitive behavior of organic conducting polymer, i.e., polypyrrole (PPy) and its composites with gum arabic (GA) prepared via inverse emulsion polymerization. The synthesized composites material was analyzed by different analytical techniques, such as UV-visible, FTIR, TGA, XRD, and SEM. The UV-Vis and FTIR spectroscopy clearly show the successful insertion of GA into PPy matrix. The TGA analysis shows high thermal stability for composites than pure PPy. The XRD and SEM analysis show the crystalline and amorphous structures and overall morphology of the composites is more compact and mesoporous as compared to the pure PPy. The electrochemical properties of modified solid state supercapacitors established on pure polypyrrole (PPy), polypyrrole/gum arabic (PPy/GA) based composites were investigated through cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge–discharge (GCD). The specific capacitance of the PPy modified gold electrode is impressive (~168 F/g). The specific capacitance of PPy/GA 1 electrode has been increased to 368 F/g with a high energy density and power density (~73 Wh/kg), and (~599 W/kg) respectively.

Microencapsulation of Brazilian Cherokee blackberry extract by freeze-drying using maltodextrin, gum Arabic, and pectin as carrier materials

There are many blackberry cultivars in Brazil; however, the characteristics and applications of the Cherokee cultivar have not yet been widely studied. For this reason, this research investigated the behaviour of maltodextrin (MD), gum Arabic (GA), and pectin (PEC), as carriers combined in different proportions (20% MD, 15% MD + 5% GA, 15% MD + 5% PEC), on encapsulation of Cherokee blackberry pulp extract obtained by freeze-drying. The results of moisture content (2.73-3.36%), water activity (aw) (0.11–0.15), solubility (52.40–54.11%), hygroscopicity (17.59–21.11%), colour (hue 0.24–0.32), retention of anthocyanins (51.55–60.53%), total phenolic compounds (39.72–70.73 mg GAE/100g), antioxidant activity at 25 mg/mL (77.89–80.02%), IC50 (12.26–14.53), simulated in vitro digestion and morphology were discussed. Concerning morphology, blackberry powders had irregular structures and amorphous structures. Comparatively, the best results were obtained for MD-GA. MD-GA presented the highest content of phenolic compounds (70.73 ± 1.84 mg GAE/100g) and antioxidant activity (80.02%), as well as the lowest IC50 value (12.26). In general, all powders showed an increase in phenolic compounds during in vitro digestion, because of the pH conditions and digestive enzymes present in the simulated digestive fluid. This result shows that the wall material provides protection, since the blackberry rich extract (RE) showed degradation of phenolic compounds in in vitro digestion. In this sense, freeze-drying is a suitable technique for the encapsulation of Cherokee blackberry pulp extract.

Multivariate Analysis of Disorder in Metal–Organic Frameworks

The rational design of disordered frameworks is an appealing route to target functional materials. However, intentional realisation of such materials relies on our ability to readily characterise and quantify structural disorder. Here, we use multivariate analysis of pair distribution functions to fingerprint and quantify the disorder within a series of compositionally identical metal–organic frameworks, possessing different crystalline, disordered, and amorphous structures. We find this approach can provide powerful insight into the kinetics and mechanism of structural collapse that links these materials. Our methodology is also extended to a very different system, namely the melting of a zeolitic imidazolate framework, to demonstrate the potential generality of this approach across many areas of disordered structural chemistry.

Mineral trioxide aggregate immersed in sodium hypochlorite reduce the osteoblastic differentiation of human periodontal ligament stem cells

White mineral trioxide aggregate (WMTA) is a root canal treatment material, which is known to exhibit a dark brown color when in contact with sodium hypochlorite solution (NaOCl). This study aimed to investigate the effects of NaOCl on the surface properties of WMTA discs and WMTA-induced osteoblastic differentiation of periodontal ligament stem cells (PDLSCs). Mixed WMTA (ProRoot MTA) was filled into the molds to form WMTA discs. These discs were immersed in distilled water (D-WMTA) or 5% NaOCl (Na-WMTA). Their surface structures and Ca2+ release level was investigated. Moreover, they were cultured with a clonal human PDLSC line (line 1–17 cells). The main crystal structures of Na-WMTA were identical to the structures of D-WMTA. Globular aggregates with polygonal and needle-like crystals were found on D-WMTA and Na-WMTA, which included Ca, Si, Al, C and O. However, many amorphous structures were also identified on Na-WMTA. These structures consisted of Na and Cl, but did not include Ca. NaOCl immersion also reduced Ca2+ release level from whole WMTA discs. Line 1–17 cells cultured with D-WMTA formed many mineralized nodules and exhibited high expression levels of osteoblast-related genes. However, cells incubated with Na-WMTA generated a small number of nodules and showed low expression levels of osteoblast-related genes. These results indicated that NaOCl reduced Ca2+ release from WMTA by generating amorphous structures and changing its elemental distribution. NaOCl may also partially abolish the ability of WMTA to stimulate osteoblastic differentiation of PDLSCs.

Highly Stable Photocatalytic Removal of Paraquat Dichloride using ZnO/TiO2 supported on PVC

This study presents on ZnO/TiO2 supported on PVC (ZnO/TiO2@PVC) in the photocatalytic removal of paraquat dichloride. The ZnO/TiO2@PVC was characterized using XRD, FESEM-EDX, FTIR, and AFM. Findings indicated that ZnO/TiO2@PVC allowed degradation of paraquat dichloride under UV irradiation by the rate of up to 73%. XRD pattern indicated the presence of both TiO2(anatase) and ZnO (zincite) crystalline as well as PVC amorphous structures. FESEM and AFM results revealed the observed shape and surface of TiO2 interconnected nanowires with ZnO nanorods uniformly distributed according to EDX mapping. The reduced surface roughness was also shown in the supported photocatalyst. FTIR analysis clearly demonstrate the combined spectra of immobilised ZnO/TiO2 powder catalyst onto the PVC in the composite. Kinetic study of the degradation process was performed according to pseudo-first-order and the influence of ZnO/TiO2 coating onto PVC polymer and initial paraquat concentration were investigated on the treatment performance. Under optimized condition (pH = 7, PQ =20 mg/L and catalyst coating =15%), the stability and reusability of the supported catalyst was also evaluated over ten sequential treatment runs, and the catalyst maintain high reactivity. High recyclability of the ZnO/TiO2@PVC composites as catalyst in photodegradation processes are also reported in this study.

Nanocrystalline protein domains via salting-out

Protein salting-out is a well established phenomenon that in many cases leads to amorphous structures and protein gels, which are usually not considered to be useful for protein structure determination. Here, microstructural measurements of several different salted-out protein dense phases are reported, including of lysozyme, ribonuclease A and an IgG1, showing that salted-out protein gels unexpectedly contain highly ordered protein nanostructures that assemble hierarchically to create the gel. The nanocrystalline domains are approximately 10–100 nm in size, are shown to have structures commensurate with those of bulk crystals and grow on time scales in the order of an hour to a day. Beyond revealing the rich, hierarchical nanoscale to mesoscale structure of protein gels, the nanocrystals that these phases contain are candidates for structural biology on next-generation X-ray free-electron lasers, which may enable the study of biological macromolecules that are difficult or impossible to crystallize in bulk.

Copolymerization of Quinazolinone Derivatives With Styrene, Methyl Methacrylate and Their Silver Nanocomposites for Biological Applications

Reaction of 2-mercapto-3-phenylquinazolin-4(3H)-one (MPQ) with both 4-vinyl benzyl chloride and allyl bromide furnished the reactive heterocyclic monomers 3-phenyl-2-((4-vinylbenzyl) thio) quinazolin-4(3H)-one (PVTQ) and 2-(allylthio)-3-phenylquinazolin-4(3H)-one (APQ), respectively. Copolymerization of PVTQ monomer with styrene and methyl methacrylate in the presence of 2,2′-azobisisobutyronitrile (AIBN) afforded the copolymers PS-co-PPVTQ and PMMA-co-PPVTQ, respectively. Similarly, copolymerization of monomer APQ with styrene and methyl methacrylate (MMA) afforded the copolymers PS-co-PAPQ and PMMA-co-PAPQ, respectively. The resulted copolymers were characterized by using FT-IR, 1H-NMR and GPC techniques. Silver nanocomposites of PS, PMMA, PS-co-PPVTQ, PMMA-co-PPVTQ, PS-co-PAPQ and PMMA-co-PAPQ were synthesized by the addition of silver nitrate into the polymer solution. The reduction of silver ions into silver nanoparticles was performed in DMF and water. Thermogravimetric (TGA) analysis was used to determine the thermal stability of the copolymers and their silver nanocomposites. The X-ray diffraction (XRD) analysis indicated the amorphous structures of the co-polymers and confirmed the formation of silver nanoparticles. The antitumor and antibacterial activities were screened for the copolymers and enhanced by the formation of their silver nanocomposites. In vivo antitumor activity in Ehrlich Ascitic Carcinoma (EAC) mice model showed that PS-co-PPVTQ/Ag NPs, PMMA-co-PPVTQ/Ag NPs, and PMMA-co-PAPQ/Ag NPs displayed promising inhibitory effects against EAC and induce apoptosis against MCF-7 cells.

Conditions for partial and complete crystallization suppression upon quenching from liquid state

For bulk-amorphizing alloys Мg65Сu25Y10 and Zr41,2 Тi13,8Сu12,5Ni10Ве22,5, the thickness and cooling rate of melt layers is calculated, which ensure the formation of X-ray amorphous structures typical for metallic glasses ( lC, vC ), and truly amorphous states without inclusions of «frozen-in crystallization centers» (lc*, vc* ). Correlation of the calculated values lC, vC with the known experimental estimates is C Cachieved. It is shown that both studied alloys demonstrate a predisposition to complete suppression of crystallization processes at physically correct values of the parameters lc* and vc* (10 μm; 1,3·107 K/s and 550 μm; 2,7·103 K/s for alloys based on Mg and Zr, respectively). It is concluded that the most significant factors controlling the tendency of materials to noncrystalline solidification are the decrease in the frequency of non-stationary nucleation with the increase in the rate of QLS, as well as relatively low <1018 m-3 s-1) maximum values of the rate of stationary crystallization centers formation.

Optical Properties of Non-Crystalline Fluorine Doped Hematite Fe2O3 Thin Films Deposited by Chemical Spray Pyrolysis Technique

By using the spray pyrolysis technique, un-doped and Fluorine highly doped iron oxide Fe2O3 thin films were deposited on a glass substrate at a temperature of 380 oC and at different dopant concentrations (10, 15, and 20) %. The crystal structure and optical characterization of the deposited thin film were performed by x-ray diffraction and UV-Vis spectrophotometer. The XRD results revealed that the presence of a very wide peak in-between (15-35) o angles, this gives evidence that un-doped and F-doped Fe2O3 thin films have very low crystallinity and amorphous structures. The optical absorbance edge was shifted towards short wavelengths (blue shift) and the absorbance was reduced with the increase of Fluorine dopant content. The optical constants such as absorption, extinction coefficients, and the optical conductivity of the deposition films were investigated as a function of dopant content. The optical energy band gap of un-doped and Fe2O3:F thin films was found to be increased when increasing of the Fluorine content and exhibited a direct allowed energy gap (Eg) from (2.55 to 2.7) eV which can related to the Burstein-Moss effect.