Reproducible,biocompatible medical materials from biologically derived polysaccharides: Processing and Characterization

Natural polysaccharides like chitosan and dextran have garnered considerable interest in biomedical applications due to their biocompatibility, biodegradability, and nontoxicity. Nonetheless, the development of a reproducible class of medical devices from these materials is challenging and has had limited success. Chitosan and dextran are inherently variable and synthesis using these materials is prone to inconsistencies. In this study, we put forward a robust product development regimen that allows these natural materials to be developed into a reproducible class of biomaterials. First, an array of validated characterization methods (Proton Nuclear Magnetic Resonance, titrations, Ultraviolet spectroscopy, Size Exclusion Chromatography—Multi-Angle Light Scattering, Size Exclusion Chromatography—Refractive Index, and proprietary methods) were developed that allowed rigorous specifications to be set for unprocessed chitosan and dextran, chitosan and dextran intermediates, and chemically modified materials—acrylated chitosan (aCHN) and oxidized dextran (oDEX). Second, a robust and reproducible synthesis scheme involving various in-process controls was developed to chemically modify the unprocessed polysaccharides. Third, purification methods to remove byproducts and low-molecular-weight impurities for both aCHN and oDEX were developed. The study presents a viable strategy for converting variable, natural materials into a reproducible class of biomaterials that can be applied in various biomedical applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48454.     

Reactivity of industrial wastes as measured through ICP-OES: A case study on siliceous Indian biomass ash

An untapped source of amorphous SiO₂, industrially generated Indian biomass ash (SA)—90% amorphous, with composition of ~60% SiO₂ and ~20% unburnt carbon—can be used to produce cementitious and alkali-activated binders. This study reports dissolution of amorphous Si from SA in 0.5 mol/L and 1 mol/L aqueous NaOH, with and without added Ca(OH)₂, at SA:Ca(OH)₂ wt% ratios of 100:0, 87.5:12.5, and 82.5:17.5. Monitoring of elemental dissolution and subsequent/simultaneous product uptake by ICP-OES offers an effective process for evaluating utility of industrial wastes in binder-based systems. After 28 days in solution, up to 68% of total Si is dissolved from SA in 1 mol/L NaOH, with values as much as 38% lower in the presence of Ca(OH)₂, due to the formation of tobermorite-like C-S-H. FTIR, ²⁹Si MAS-NMR, and XRD are used to characterize solid reaction products and observe reaction progress. Product chemistries calculated from ICP-OES results and verified by selective dissolution in EDTA/NaOH—namely, Ca/Si of 0.6-1 and Na adsorption of 1-2 mmol/g—are found to be consistent with those indicated by aforementioned techniques. This indicates the efficacy of ICP-OES in estimating product chemistry via such a methodology.     

Robust resource targeting in continuous and batch process

Clean Technologies and Environmental Policy - Water is considered a significant resource in process industries. It is essential for planners to target and optimize the use of water as an external...     

Economic comparison of current electricity generating technologies and advanced nuclear options

This analysis compares the cost of various electric grid scenarios at the national level over a one-year period. Scenarios include high renewable, zero nuclear, zero carbon, and deployment of advanced nuclear. Additionally, several carbon tax scenarios are explored in the model to further assess the cost generation if the current nuclear fleet retired. The cheapest scenarios were those that involved less reliance on conventional nuclear reactors and more molten salt reactors, renewables, or natural gas.     

Friction stir scribe welding technique for dissimilar joining of aluminium and galvanised steel

Friction stir scribe technology, a derivative of friction stir welding, was applied for the dissimilar lap welding of an aluminium alloy and galvanised mild steel sheets. During the process, the rotating tool with a cobalt steel scribe first penetrated the top material – aluminium – and then the scribe cuts the bottom material – steel. The steel was displaced into the upper material to produce a characteristic hook feature. Lap welds were shear tested, and their fracture paths were studied. Welding parameters affected the welding features, including hook height, which turned out to be highly related to fracture position. Therefore, in this paper, the relationships among welding parameters, hook height, joint strength and fracture position are presented. In addition, the influence of zinc coating on joint strength was also studied.     

Studies of dielectric and electrical properties of a new type of complex tungsten bronze electroceramics

A polycrystalline ceramic with a new type of complex tungsten-bronze type structure, having a general formula K₂Ba₂Nd₂Ti₄Nb₄W₂O₃₀ has been prepared using a high temperature solid-state reaction route after optimizing the calcinations conditions on the basis of thermal analysis results. The material has been characterized by different experimental techniques. The formation of the compound has been confirmed using X-ray diffraction analysis. Dielectric properties (ε_r and tanδ) of the compound as a function of temperature at different frequencies have been carried out. Temperature dependence of dielectric constant indicates the presence of ferroelectric phase transition well above the room temperature. Complex impedance spectroscopic analysis has been carried out as a function of frequency at different temperatures to establish some correlation between the microstructure and electrical properties of the material. The nature of frequency dependence of ac conductivity obeys the Jonscher’s power law. The dc conductivity calculated from the ac conductivity spectrum shows the negative temperature coefficient of resistance behavior like a semiconductor.     

Optimization of Cellulase Production from Isolated Cellulolytic Bacterium: Comparison between Genetic Algorithms,Simulated Annealing,and Response Surface Methodology

The present study discusses optimization of cellulase production from isolated cellulolytic bacterium. A simulated annealing (SA) algorithm is proposed for optimization of these processes to achieve the desired production goal. The approach was compared to the use of evolutionary algorithms, i.e., genetic algorithms (GAs) and response surface methodology (RSM). Ochrobactrum haematophilum was identified as the isolated bacteria. Carboxymethyl cellulose (CMC) concentration, yeast extract, pH, and incubation temperature were the significant factors screened by Plackett–Burman design and further optimized using a central composite design. The optimum values obtained were CMC concentration = 4.76% (w/v), yeast extract = 2.03% (w/v), pH = 6.3, and temperature = 44.2°C. Carboxy methyl cellulase (CMCase) activity at these values was experimentally determined to be 3.55 ± 0.16 U/ml, which was 2.8 times than the unoptimized system (1.23 U/ml). The growth-associated and non-growth-associated Leudeking–Piret constants, α and β, were respectively determined to be 0.3943 and 0.0105. The Michaelis–Menten constants, V_max and K_m, were determined to be 0.67 µmol/min and 2.42 mg CMC/ml, respectively. The variable-sized SA seems to be the best alternative, outperforming the GAs, showing a fast convergence and low variability among the several runs for optimized production cellulose recovery. The SA models are found to be capable of better predictions of cellulase production. The results of the SA-based RSM model indicate that it is much more robust and accurate in estimating the values of dependent variables when compared with the GA-based RSM models and only RSM models.     

Dielectric and impedance spectroscopy of barium orthovanadate ceramics

Barium orthovanadate (Ba₃V₂O₈), a derivative of perovskite family has been prepared using a mixed-oxide technique. The room temperature X-ray diffraction analysis has confirmed the formation of a single phase compound in trigonal crystal structure. The study of microstructure by scanning electron microscopy shows that the compound has well defined grains, distributed uniformly throughout the surface. The studies of dielectric parameters (ε_r and tan δ) of the compound as a function of temperature at three different frequencies (100, 500, 1,000 kHz) exhibit that they are almost temperature independent at low and medium temperature ranges. Detailed studies of impedance and related parameters exhibit that the electrical properties of the material are strongly dependent on temperature, and bear a good correlation with its microstructures. The bulk resistance, evaluated from complex impedance spectra, is found to be decreasing with rise in temperature. It shows that the material has negative temperature co-efficient of resistance similar to that of semiconductors. The same behaviour has also been observed in the study of I–V characteristics of the material. The complex electric modulus analysis indicates the possibility of hopping conduction mechanism in the system with non-exponential type of conductivity relaxation. The nature of variation of dc conductivity with temperature confirms the Arrhenius behavior of the material. The ac conductivity spectra show a typical signature of an ionic conducting system, and are found to obey Jonscher’s universal power law.     

Analysis of Mechanically Induced Reactivity of Boehmite Using Kinetics of Boehmite to <Emphasis Type="Italic">γ-</Emphasis>Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Transformation

This article focuses on the mechanically induced reactivity of boehmite prepared by thermal decomposition of gibbsite. Boehmite, which retained the morphology of gibbsite, was characterized by a specific surface area of 264 m²/g. Mechanical activation (MA) was carried out in a planetary mill up to 240 minutes. The samples were characterized in terms of morphology, characteristic particle diameters, Brunauer Emmett Teller (BET) specific surface area (SSA_BET), microcrystallite dimension (MCD), microstrain (ε) and Fourier transform infrared spectroscopy. The reactivity was construed from the kinetics of thermal transformation of boehmite into γ-Al₂O₃. The transformation observed between 600 K and 900 K (327 °C and 627 °C), manifested itself as two overlapping peaks in the differential thermogravimetric plot. These peaks correspond to two stages of dehydroxylation involving Al₂OH and AlOH groups in succession. The peaks were resolved using Gaussian deconvolution. The reactivity was assessed separately for the two stages by comparing the fraction reacted in MA samples (α) with that of nonactivated sample (α _ref). During both stages, enhanced kinetics, as revealed by α-α _ref plots, indicated an increase in reactivity with MA. The transformation mechanism conformed to n ^th order reaction (f[α] = [1 – α] ⁿ with n = 1.3–1.5 in both stages). Values of n remained similar for the activated and reference samples. Activation energies (E _a) for the first and second dehydroxylation stages were respectively 115 and 300 kJ/mol for the nonactivated sample. E _a for the second stage decreased exponentially to a value of 222 kJ/mol after 240 minutes of milling. An anomalous negative correlation between reactivity and SSA_BET was observed. Reactivity parameters were strongly correlated with MCD and ε. A plausible explanation for the observed correlations is presented.     

Evolution of strength, microstructure and mineralogical composition of a CKD–GGBFS binder

Characterization of a nontraditional binding material containing cement kiln dust (CKD) and ground granulated blast furnace slag (GGBFS) is discussed in this paper. Significant compressive strength was obtained for a CKD–GGBFS blend with 70% CKD and 30% GGBFS at a water-to-binder ratio of 0.40 after 2 days of curing at elevated temperature. Similar strength was also obtained for the samples subjected to normal moisture curing over a period of 28 days. The compressive strength increased with additional moist curing in both the cases. The microstructural and the mineralogical examinations show that the strength development was mainly due to the formation of calcium silicate hydrate (C-S-H). In addition to normal C-S-H, aluminum and magnesium incorporated C-S-H phases were also present in the CKD–GGBFS blends. The formation of ettringite appears to be a contributing factor in early age strength development of CKD–GGBFS binder.