Parametric Evaluation of Video Motion Tracking Data Sets

Video tracking is a complex problem because the environment, in which video motion needs to be tracked, is widely varied based on the application and poses several constraints on the design and performance of the tracking system. Current datasets that are used to evaluate and compare video motion tracking algorithms use a cumulative performance measure without thoroughly analyzing the effect of these different constraints imposed by the environment. But it needs to analyze these constraints as parameters. The objective of this paper is to identify these parameters and define quantitative measures for these parameters to compare video datasets for motion tracking.     

Photocatalytic degradation of methylene blue using novel flower-like zirconium bismuth molybdate thin film,grown by temperature-assisted CBD method

Thin films of a novel metal molybdate are successfully coated on soda lime glass by one step chemical bath deposition method. The deposition is carried out under different bath temperature ranging from 30 to 70 °C. In order to analyze the crystalline structure, X-ray diffraction study is carried out. Film thickness and morphology are examined through atomic force microscope and scanning electron microscope. Optical studies are done by UV–Vis–NIR absorbance spectra and photoluminescence spectra. All the samples have absorbance in the UV–Vis region and possess direct allowed transition with bandgap values ranging from 2.17 to 2.83 eV. Direct current show good ohmic response and possess resistivity in the range characteristic of wide bandgap materials. The material possesses three major photoluminescence emission peaks in the green and blue wavelength regions. Thin film grown at 50 °C showed increased absorbance width, minimum bandgap energy, larger electron–hole separation efficiency and more porous flower-like morphology which indicates its higher photocatalytic ability. The photocatalytic degradation process for the removal of methylene blue from waste water, under sunlight irradiation using thin film grown at 50 °C as photocatalyst has been discussed in detail.

     

Crystal structure,phonon modes,and bond characteristics of AgPb2B2V3O12 (B = Mg,Zn) microwave ceramics

AgPb₂B₂V₃O₁₂ (B = Mg, Zn) ceramics with low sintering temperature were synthesized via the conventional solid-state reaction route. Rietveld refinements of the X-ray diffraction patterns confirm cubic symmetry with space group . The number of observed vibrational modes and those predicted by group theoretical calculations also confirm the space group. At the optimum sintering temperature of 750°C/4 hours, AgPb₂Mg₂V₃O₁₂ has a relative permittivity of 23.3 ± 0.2, unloaded quality factor () of 26 900 ± 500 GHz (), and temperature coefficient of resonant frequency of 19.3 ± 1 ppm/°C, while AgPb₂Zn₂V₃O₁₂ has the corresponding values of 26.4 ± 0.2, 28 400 ± 500 GHz () and –18.4 ± 1 ppm/°C at 590°C/4 hours. Microwave dielectric properties of a few reported garnets and Pb₂AgB₂V₃O₁₂ (B = Mg, Zn) ceramics were correlated with their intrinsic characteristics such as the Raman shifts as well as width of A_1g Raman bands. Higher quality factor was obtained for lower full width at half-maxima (FWHMs) values of A_1g modes. The increase in B-site bond valence contributes to high and low |τ_f| with the substitution of Zn²⁺ by Mg²⁺. Furthermore, the high ionic polarizability and unit cell volume with Zn²⁺substitution contribute to increased relative permittivity.     

Studies on epoxidized rubber seed oil as plasticizer for acrylonitrile butadiene rubber

The application of rubber seed oil (RSO) and epoxidized RSO (ERSO) as a plasticizer in acrylonitrile butadiene rubber (NBR) was studied using RSO and ERSO with different levels of epoxidation. The results indicated that ERSO could be used as a less leachable and low volatility plasticizer for NBR. The use of ERSO in NBR gave better abrasion resistance whereas the tensile strength and tear strength were comparable to those vulcanizates that contained dioctyl phthalate as a plasticizer. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 668–673, 2003     

Natural rubber–isotactic polypropylene thermoplastic blends

Thermoplastic elastomers, prepared by melt blending of natural rubber (NR) and isotactic polypropylene (PP) through a dynamic vulcanization technique, were developed during the later 1970s. However, they have certain drawbacks due to thermal degradation and higher molecular weight of NR. In the study reported here, NR was masticated to different levels prior its addition to isotactic polypropylene to improve the flow properties and to reduce the incompatibility resulting from molecular weight mismatch of NR/PP thermoplastic blends. Mixing energy curves of uncrosslinked blends and those of dynamically vulcanized blends crosslinked using different cure systems were compared. The mixing energy curves of blends containing NR of different molecular weight (M _n) and two grades of PP (injection and film grades) were also compared. Technological and processing properties of the dynamically vulcanized (sulphur and peroxide cure systems) and unvulcanized blends were compared with those of the samples containing unmasticated NR. The results indicated that a number average molecular weight in the range 4 × 10⁵ for NR increased the procoessability without significantly affecting the technological properties of NR/PP thermoplastic blends. Among the three cure systems studied Luperox 101 and dicumyl peroxide gave better technological properties than the sulphur‐cured samples. Two antioxidants, viz. quinoline (TDQ) and imidazole (MBI) type, were tried in NR/PP blends. It was found that TDQ imparts better aging resistance compared to MBI. The improvement in processability due to the reduction in molecular weight of natural rubber by mastication is more noticeable in the case of peroxide vulcanized blends compared to sulphur vulcanized samples. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2063–2068, 2004     

Hydrogen peroxide sensing properties of PVA/TiO2/I2 nanocomposite‐based free standing membranes

The nanocomposite of titanium‐di‐oxide (TiO₂)/iodine (I₂) in polyvinyl alcohol (PVA) matrix has been explored to be used in hydrogen peroxide (H₂O₂) sensing applications for the first time. The proposed nanocomposite can be easily casted in the form of thin film on glass substrates as well as free standing membranes. These nanocomposite films and membranes exhibit reduced resistance values and easily observable colour changes in the presence of H₂O₂. The films also exhibit significant quenching in photoluminescence emission properties upon H₂O₂ exposure. These sensor responses have been attributed to redox reactions at nanocomposite films and H₂O₂ interface. This study indicates an easy to fabricate, flexible and environmental friendly sensing platform for H₂O₂. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42257.     

Improving the performance of an active carbon-nitrogen adsorption cryocooler by thermal regeneration

Thermodynamic analysis was done on single and two stage active carbon nitrogen adsorption cryocoolers to study the effect of thermal regeneration on the performance. Heat regeneration within compressors operating in the same temperature range is considered. From the analysis done on 80 K cooler and 117.5 K cooler, it is found that dramatic efficiency improvement is possible with the use of compressor heat regeneration techniques.     

Insights into the Interaction of LVV-Hemorphin-7 with Angiotensin II Type 1 Receptor

Hemorphins are known for their role in the control of blood pressure. Recently, we revealed the positive modulation of the angiotensin II (AngII) type 1 receptor (AT1R) by LVV-hemorphin-7 (LVV-H7) in human embryonic kidney (HEK293) cells. Here, we examined the molecular binding behavior of LVV-H7 on AT1R and its effect on AngII binding using a nanoluciferase-based bioluminescence resonance energy transfer (NanoBRET) assay in HEK293FT cells, as well as molecular docking and molecular dynamics (MD) studies. Saturation and real-time kinetics supported the positive effect of LVV-H7 on the binding of AngII. While the competitive antagonist olmesartan competed with AngII binding, LVV-H7 slightly, but significantly, decreased AngII’s k_D by 2.6 fold with no effect on its B_max. Molecular docking and MD simulations indicated that the binding of LVV-H7 in the intracellular region of AT1R allosterically potentiates AngII binding. LVV-H7 targets residues on intracellular loops 2 and 3 of AT1R, which are known binding sites of allosteric modulators in other GPCRs. Our data demonstrate the allosteric effect of LVV-H7 on AngII binding, which is consistent with the positive modulation of AT1R activity and signaling previously reported. This further supports the pharmacological targeting of AT1R by hemorphins, with implications in vascular and renal physiology.