Smart control of nonlinear vibrations of doubly curved functionally graded laminated composite shells under a thermal environment using 1–3 piezoelectric composites

This paper addresses the active control of geometrically nonlinear vibrations of doubly curved functionally graded (FG) laminated composite shells integrated with a patch of active constrained layer damping (ACLD) treatment under the thermal environment. Vertically/obliquely reinforced 1-3 piezoelectric composite (PZC) and active fiber composite (AFC) are used as the materials of the constraining layer of the ACLD treatment. Each layer of the substrate FG laminated composite shell is made of fiber-reinforced composite material in which the fibers are longitudinally aligned in the plane parallel to the top or bottom surface of the layer and the layer is assumed to be graded in the thickness direction by way of varying the fiber orientation angle across its thickness according to a power law. The novelty of the present work is that, unlike the traditional laminated composite shells, the FG laminated composite shells are constructed in such a way that the continuous variation of material properties and stresses across the thickness of the shell is achieved. The Golla-Hughes-McTavish (GHM) method has been implemented to model the constrained viscoelastic layer of the ACLD treatment in time domain. Based on the first-order shear deformation theory (FSDT), a finite element (FE) model has been developed to model the open-loop and closed-loop nonlinear dynamics of the overall FG laminated composite shell under a thermal environment. Both symmetric and asymmetric FG laminated composite doubly curved shells are considered for presenting the numerical results. The analysis suggests that the ACLD patch significantly improves the damping characteristics of the doubly curved FG laminated composite shells for suppressing their geometrically nonlinear transient vibrations. It is found that the performance of the ACLD patch with its constraining layer being made of the AFC material is significantly higher than that of the ACLD patch with vertically/obliquely reinforced 1-3 PZC constraining layer. The effects of variation of piezoelectric fiber orientation in both the obliquely reinforced 1-3 PZC and the AFC constraining layers on the control authority of the ACLD patch have also been investigated.     

Delta doping and positioning effects of type II GaSb quantum dots in GaAs solar cell

GaSb quantum dot (QD) solar cell structures were grown by molecular beam epitaxy on GaAs substrates. We investigate the reduction in open-circuit voltage and study the influence of the location of QD layers and their delta doping within the solar cell. Devices with 5 layers of delta-doped QDs placed in the intrinsic, n- and p-regions of a GaAs solar cell are experimentally investigated, and the deduced values of J_sc, V_oc, fill factor, efficiency (η) are compared. A trade-off is needed to minimize the V_oc degradation while maximizing the short circuit current density (J_sc) enhancement due to sub-bandgap absorption. The voltage recovery is attributed to the removal of the QDs from the high-field region which reduces SRH recombination. The devices with p- or n-doped QDs placed in the flat band potential (p- or n-region) show a recovery in J_sc and V_oc compared to devices with delta-doped QDs placed in the depletion region. However, there is less photocurrent arising from the absorption of sub-band gap photons. Furthermore, the long wavelength photoresponse of the n-doped QDs placed in the n-region shows a slight improvement compared to the control cell. The approach of placing QDs in the n-region of the solar cell instead of the depletion region is a possible route towards increasing the conversion efficiency of QD solar cells.     

(La2/5Ba2/5Ca1/5)(Mn(2/5)-x Ni x Ti3/5)O3: Rietveld studies, dielectric and magnetic properties of new perovskite-related oxides

Oxides of the type (La_2/5Ba_2/5Ca_1/5)(Mn_(2/5)-x _Ni x _Ti3/5)O₃ (0 ≤ x ≤ 0.4) have been synthesized by the ceramic route. All the above oxides have been found to crystallize in the cubic perovskite structure. Rietveld refinement of the Ni-based oxide, (La_2/5Ba_2/5Ca_1/5)(Ni_2/5Ti_3/5)O₃ gave rise to a composition (La_0.44Ba_0.38Ca_0.18) (Ni_0.42Ti_0.58)O_2.85(6) and the refined lattice parameter obtained was 3.9411(2) Å (space group Pm3m;R(F²) = 0.026,R _p = 0.074,wR _p = 0.087). A shift from antiferromagnetic to paramagnetic behaviour is observed with increase in nickel concentration, the Mn-rich phases showing antiferromagnetism around 5 K. There is a systematic decrease in the dielectric constant, ε and loss tangent with increase in Ni concentration (from ε = 592 forx = 0 to ε = 78 forx = 0.4).     

A critical review on diagnosis of diabetic retinopathy using machine learning and deep learning

Multimedia Tools and Applications - Diabetic Retinopathy (DR) is a health condition caused due to Diabetes Mellitus (DM). It causes vision problems and blindness due to disfigurement of human...     

Studies on antioxidant potential of methanol extract/fractions of Acacia auriculiformis A. Cunn

Antioxidant activities of the methanol extract/fractions of Acacia auriculiformis A. Cunn were evaluated by three in vitro experiments, namely, DPPH, relative reducing power and hydroxyl radical (site specific and non site specific) assays. The differential activities of methanol extract/fractions could be correlated with their respective total phenolic contents and compared with standards (BHT and l-ascorbic acid.). The bark powder of the plant was extracted with different solvents of increasing and decreasing polarity by a maceration extraction method and then the methanol extract was further partitioned with ethyl acetate and water. The scavenging activity of extract was found to be enhanced on fractionating the extract. Moreover, among the two fractions (ethyl acetate and water fraction) and the crude extract, the water fraction exhibited good scavenging responses of 72.0%, (57.2%), 1.76 (1.52), 88.0% (82.6%) and 93.6% (83.47) in DPPH, reducing power, site specific and non-site specific hydroxyl radical scavenging assay in increasing and (decreasing) order of solvent polarity at maximum concentration, respectively. Studies are in progress to evaluate the effect of extracts/fractions in other antioxidant assays and to identify the factors responsible for the activity.     

Active damping of geometrically nonlinear vibrations of doubly curved laminated composite shells

This paper deals with the analysis of active constrained layer damping (ACLD) of geometrically nonlinear transient vibrations of doubly curved laminated composite shells. Vertically/obliquely reinforced 1–3 piezoelectric composite (PZC) and active fiber composite (AFC) materials are used as the materials of the constraining layer of theACLD treatment. The Golla–Hughes–McTavish (GHM) method has been implemented to model the constrained viscoelastic layer of the ACLD treatment in time domain. The first-order shear deformation theory (FSDT) and the Von Kármán type non-linear strain displacement relations are used for analyzing this coupled electro-elastic problem. A three dimensional finite element (FE) model of doubly curved laminated smart composite shells integrated with ACLD patches has been developed to investigate the performance of these patches for controlling the geometrically nonlinear transient vibrations of the shells. The numerical results indicate that the ACLD patches significantly improve the damping characteristics of the doubly curved laminated cross-ply and angle-ply shells for suppressing their geometrically nonlinear transient vibrations. It is found that the performance of the ACLD patch with its constraining layer being made of the AFC is significantly higher than that of the ACLD patch with vertically/obliquely reinforced 1–3 PZC constraining layer. The effects of variation of piezoelectric fiber orientation in both the obliquely reinforced 1–3 PZC and the AFC constraining layers on the control authority of the ACLD patches have also been investigated.     

Role of biodegradation in the removal of pharmaceutically active compounds with different bulk organic matter characteristics through managed aquifer recharge: batch and column studies

Natural water treatment systems such as bank filtration have been recognized as providing effective barriers in the multi-barrier approach for attenuation of organic micropollutants for safe drinking water supply. In this study, the role of biodegradation in the removal of selected pharmaceutically active compounds (PhACs) during soil passage was investigated. Batch studies were conducted to investigate the removal of 13 selected PhACs from different water sources with respect to different sources of biodegradable organic matter. Neutral PhACs (phenacetine, paracetamol, and caffeine) and acidic PhACs (ibuprofen, fenoprofen, bezafibrate, and naproxen) were removed with efficiencies greater than 88% from different organic matter water matrices during batch studies (hydraulic retention time (HRT): 60 days). Column experiments were then performed to differentiate between biodegradation and sorption with regard to the removal of selected PhACs. In column studies, removal efficiencies of acidic PhACs (e.g., analgesics) decreased under conditions of limited biodegradable carbon. The removal efficiencies of acidic PhACs were found to be less than 21% under abiotic conditions. These observations were attributed to sorption under abiotic conditions established by a biocide (20 mM sodium azide), which suppresses microbial activity/biodegradation. However, under biotic conditions, the removal efficiencies of these acidic PhACs were found to be greater than 59%. This is mainly attributed to biodegradation. Moreover, the average removal efficiencies of hydrophilic (polar) neutral PhACs (paracetamol, pentoxifylline, and caffeine) with low octanol/water partition coefficients (log K_ow less than 1) were low (11%) under abiotic conditions. However, under biotic conditions, removal efficiencies of the neutral PhACs were greater than 98%. In contrast, carbamazepine persisted and was not easily removed under either biotic or abiotic conditions. This study indicates that biodegradation represents an important mechanism for the removal of PhACs during soil passage.     

Occurrence and fate of bulk organic matter and pharmaceutically active compounds in managed aquifer recharge: a review

Managed aquifer recharge (MAR) is a natural water treatment process that induces surface water to flow in response to a hydraulic gradient through soil/sediment and into a vertical or horizontal well. It is a relatively cost-effective, robust and sustainable technology. Detailed characteristics of bulk organic matter and the occurrence and fate of pharmaceutically active compounds (PhACs) during MAR processes such as bank filtration (BF) and artificial recharge (AR) were reviewed. Understanding the fate of bulk organic matter during BF and AR is an essential step in determining pre- and/or post-treatment requirements. Analysis of organic matter characteristics using a suite of analytical tools suggests that there is a preferential removal of non-humic substances during MAR. Different classes of PhACs were found to behave differently during BF and AR. Antibiotics, non-steroidal anti-inflammatory drugs (NSAIDs), beta blockers, and steroid hormones generally exhibited good removal efficiencies, especially for compounds having hydrophobic-neutral characteristics. However, anticonvulsants showed a persistent behavior during soil passage. There were also some redox-dependent PhACs. For example, X-ray contrast agents measured, as adsorbable organic iodine (AOI), and sulfamethoxazole (an antibiotic) degraded more favorably under anoxic conditions compared to oxic conditions. Phenazone-type pharmaceuticals (NSAIDs) exhibited better removal under oxic conditions. The redox transition from oxic to anoxic conditions during soil passage can enhance the removal of PhACs that are sensitive to redox conditions. In general, BF and AR can be included in a multi-barrier treatment system for the removal of PhACs.