Modulation of extraction variables of pectin from Manilkarazapota fruit peel,its bio characterization,and comparative study using dynamic light scattering studies

Influence of variables has a great impact upon yield of pectin. The present study was organized to harmonize these variables and examine the extracted pectin. In view of this, bio-characterizion and structure analysis of pectin through FTIR was performed. Additionally, a polydispersity and particle size study was also conducted using dynamic light scattering (DLS) of the Manilkarazapota fruit peel. The best extraction variables according to the response optimization predicted model were noted as pH of 5 at 61.11°C for 90 min of heating time, which lead to a 3.7% yield. Bio-characterization revealed that pectin extracted at pH 5 has characteristics similar to HM pectin influence of methoxyl content, degree of esterification, and Galacturonic acid content at 5.11%, 73. 63%, and 77.7%, respectively. The FTIR spectrum depicted a similar surface structure to food-grade pectin. DLS studies revealed that extracted pectin at pH 5 has a particle size in the range of 390.21–421.17 nm and polydispersity (?) of 28.2%-29.3%. These findings indicate that sapodilla is a potential source of pectin for food and pharmaceutical preparation.     

Intracellular events in the "selective" transport of lipoprotein-derived cholesteryl esters

The current study utilizes human, apoE-free high density lipoprotein reconstituted with a highly specific fluorescent-cholesteryl ester probe to define the initial steps and regulatory sites associated with the "selective" uptake and intracellular itinerary of lipoprotein-derived cholesteryl esters. Bt2cAMP-stimulated ovarian granulosa cells were used as the experimental model, and both morphological and biochemical fluorescence data were obtained. The data show that cholesteryl ester provided through the selective pathway is a process which begins with a temperature-independent transfer of cholesteryl ester to the cell's plasma membrane. Thereafter transfer of the lipid proceeds rapidly and accumulates prominently in a perinuclear region (presumed to be the Golgi/membrane sorting compartment) and in lipid storage droplets of the cells. The data suggest that lipid transfer proteins (or other small soluble proteins) are not required for the intracellular transport of the cholesteryl esters, nor is an intact Golgi complex or an intact cell cytoskeleton (although the transfer is less efficient in the presence of certain microtubule-disrupting agents). The intracellular transfer of the cholesteryl esters is also somewhat dependent on an energy source in that a glucose-deficient culture medium or a combination of metabolic inhibitors reduces the efficiency of the transfer. A protein-mediated event may be required for cholesteryl ester internalization from the plasma membrane, in that N-ethylmaleimide dramatically blocks the internalization phase of the selective uptake process. Taken together these data suggest that the selective pathway is a factor-dependent, energy-requiring cholesteryl ester transport system, in which lipoprotein-donated cholesteryl esters probably flow through vesicles or intracellular membrane sheets and their connections, rather than through the cell cytosol.     

A survey and tutorial of wireless relay network protocols based on network coding

Ever since the wireless relay network (RN) was introduced, it has led to the discovery of several new protocols, which have been consistently improved by researchers to overcome many constraints such as throughput, capacity bound, symbol error rate, outage probability, and power allocations. Meanwhile, network coding (NC) was invented as an efficient technique to address these problems. To the best of our knowledge, there has been no comprehensive discussion about wireless-RN modes in the literature. We therefore provide a tutorial concerning the basic concepts of NC, dealing with the classification of particular relay modes, and presenting new wireless-RN protocols with/without NC in this paper. Under appropriate categories (i.e., fixed and dynamic), much attention has been given to various proposed wireless-RN protocols because they may differ individually depending on their processing at relay nodes and network topology. We compare the available wireless-RN protocols with/without NC, and conclude that the wireless-RN based on NC outperforms the traditional wireless-RN in certain scenarios.     

Copper(II) tetrafluoroborate as a mild and efficient catalyst for the one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones under solvent-free conditions

A simple, mild and efficient procedure for the synthesis of dihydropyrimidinones using copper(II) tetrafluoroborate as a new catalyst is described under solvent-free conditions in shorter reaction times at room temperature.     

Dehydrohalogenation during pyrolysis of brominated flame retardant containing high impact polystyrene (HIPS-Br) mixed with polyvinylchloride (PVC)

Dehydrohalogenation during pyrolysis of brominated flame retardant containing polystyrene (brominated high impact polystyrene (HIPS-Br)) mixed with polyvinylchloride (PVC) was carried out in a laboratory scale batch process. Thermal and catalytic degradation of HIPS-Br mixed with PVC on carbon composite of iron oxide (TR-00301) catalyst was investigated. The thermal degradation of waste plastics (HIPS-Br/PVC) yielded liquid products with 55,000 ppm bromine and 4300 ppm chlorine content in oil. Catalytic degradation (4 g; TR-00301) of HIPS-Br/PVC waste plastics at 430 °C produced halogen-free clean oil, which can be used as a fuel oil or chemical feedstock. The main liquid products during catalytic degradation were benzene, toluene, styrene, ethyl benzene, α-methyl styrene, butyl benzene, 1,2-dimethyl benzene etc. The average carbon number of the liquid products produced during catalytic degradation (9.3) of waste plastics was less than that of the thermal degradation (10.4) and the density of liquid products was found to be lower during the catalytic degradation than the thermal degradation. The possibility of a single step catalytic process for the conversion of halogenated waste plastics into fuel oil with the simultaneous removal of chlorine and bromine content from the oil was demonstrated.     

Effective Density Characterization of Soot Agglomerates from Various Sources and Comparison to Aggregation Theory

Soot particle (black carbon) morphology is of dual interest, both from a health perspective and due to the influence of soot on the global climate. In this study, the mass-mobility relationships, and thus effective densities, of soot agglomerates from three types of soot emitting sources were determined in situ by combining a differential mobility analyzer (DMA) and an aerosol particle mass analyzer (APM). High-resolution transmission electron microscopy was also used. The soot sources were diesel engines, diffusion flame soot generators, and tapered candles, operated under varying conditions. The soot microstructure was found to be similar for all sources and settings tested, with a distance between the graphene layers of 3.7–3.8 Å. The particle specific surface area was found to vary from 100 to 260 m²/g. The particle mass-mobility relationship could be described by a power law function with an average exponent of 2.3 (±0.1) for sources with a volatile mass fraction <10% and primary particle sizes of 11–29 nm. The diesel exhaust from a heavy duty engine at idling had a substantially higher volatile mass fraction and a higher mass-mobility exponent of 2.6. The mass-mobility exponent was essentially independent of the number of primary particles in the range covered (N_pp = 10–1000). Despite the similar exponents, the effective density varied substantially from source to source. Two parameters were found to alter the effective density: primary particle size and coating mass fraction. A correlation was found between primary particle size and mass-mobility relationship/effective density and an empirical expression relating these parameters is presented. The effects on the DMA-APM results of doubly charged particles and DMA agglomerate alignment were investigated and quantified. Finally, the dataset was compared to three theoretical approaches describing agglomerate particles’ mass-mobility relationship.

Copyright 2013 American Association for Aerosol Research     

Physicochemical studies of mild steel corrosion and atmospheric corrosivity mapping of Karachi: An important harbor city of modern Maritime Silk Route

This paper has reported physicochemical features of mild steel's corrosion products and provided atmospheric corrosivity maps of Karachi harbor city, drafted on the basis of spatial distribution of corrosion data from July 2018 to June 2019 at 10 different urban, industrial, and marine test sites. Exposure tests have been performed to study atmospheric corrosivity, corrosion products, and corrodants including chloride, sulfur dioxide, time of wetness (TOW), and corrosion rate as per ISO and ASTM standards. Scanning electron microscope, Fourier-transform infrared spectroscopy, and X-ray diffraction have corroborated the presence of lepidocrocite, goethite, magnetite, and quartz phases at almost all the test sites, with slight variations in their morphologies and quantities. The data analysis has revealed that TOW is a major detrimental factor to accelerate corrosion of mild steel at Karachi city. The corrosivity category of all urban and marine test sites is found in C₄–C₅ range, whereas for industrial test sites, it is found in C₃–C₅ range. Resultant corrosivity maps have shown that the prevailing atmosphere is significantly corrosive at Karachi harbor city. This study has furnished a novel product of atmospheric corrosivity map, which is the first-ever corrosivity map for Pakistan.     

Influence of B-site cations ordering on magnetization and dielectric relaxations in Li–Ni spinel ferrites

Ho-substituted Li–Ni ferrites with composition L i_1.2Ni_0.4Ho_xFe_2-xO₄; 0≤ x ≤ 0.15 were synthesized by a self-ignited sol-gel process. An annealing temperature of 950 °C is estimated via thermal-gravimetric (TGA) analysis. X-ray diffraction (XRD) scans have confirmed the formation of the ferrite phase with a spinel structure in all samples. Substitution of Ho ions on the B-site significantly reduced the porosity from 38 -to 23% and the crystallite size from 23.4 -to 21.7 nm. Microstructural analysis revealed a denser structure with an increase in Ho content. Dielectric results showed that both the dielectric loss and dielectric constant depict a nonlinear variation with the addition of Ho. Complex impedance behavior with a single semicircle for all samples suggests the predominant effect of the grain boundary mechanism. The substitution of Ho ions in place of Fe ions significantly decreased the electrical conductivity. The anisotropic Ho³⁺ ions reinforce the L-S coupling which consequently enhanced the coercive force from 145 -to 389 Oe, and thus the anisotropy constant.