The kinetics of enzyme catalyzed synthesis of sterol ester

The production of sterol ester by transesterification of β‐sitosterol with fish oil (TAG) catalyzed by Thermomyces lanuginosus immobilized lipase enzyme with varied reaction parameters such as temperature, substrate molar ratio, concentration of enzyme to deduce the enzyme kinetics for the reaction was investigated. For this transesterification reaction, the kinetic model was derived by using Ping Pong Bi Bi Mechanism. The K_m value from the first plot containing fish oil as substrate was 1.31 ± 0.05, while K_m from the second plot containing β‐sitosterol as substrate was 1.01 ± 0.04; identical V_max (0.213 ± 0.06) values were obtained by keeping one of the substrate concentration constant and varying the other. Practical applications : Deduction of reaction kinetics is an important criterion to ascertain the viability of any chemical process. Enzymatic processes need special attention to set model reaction parameters which could help in optimization or design of the actual process. In the present study we have derived the enzyme kinetics for the production sterol ester, an important nutraceutical, and calculated its K_m and V_max values along with the Arhenius activation energy to establish the viability of the reaction.     

Experimental investigation of particle migration in suspension flow through bifurcating microchannels

Experimental measurements of velocity and concentration profiles were carried out to study transport of non‐colloidal suspension in bifurcating micro channels for both diverging and converging flow conditions using a combination of mirco‐particle image velocimetry and particle tracking velocimetry techniques. Migration of particles across the streamline was observed and symmetric velocity and concentration profile in the inlet branch becomes asymmetric in the daughter branches. Further migration of particles toward the center of the channel in the outlet branch make the profiles again symmetric. The evolution of velocity and concentration profiles was observed to be different in the symmetric and asymmetric bifurcation channels. The comparison of the streamlines for the fluid and the particles showed significant deviation near the bifurcation region. This may explain why there is unequal flow and particle partitioning during flow of suspension in asymmetric bifurcating channels as reported in many previous studies. © 2018 American Institute of Chemical Engineers AIChE J, 64: 2293–2307, 2018     

Recovery,characterization and conceptual modelling of Non-Bituminous organic materials from oil sands

The hot water process has recovered approximately 90% of the bitumen in oil sands, but the remaining 10% of bitumen and naphtha has been lost to the tailings pond. Recovery of bitumen and non-bituminous combustibles (NBC) from centrifuge, scroll and final tailings has been considered. The effects of four sequestering agents, and of chemical additives such as CaCl₂ and FeCl₃ on the flotation behavior of bitumen, NBC and minerals in these tailings have been investigated. A simple method of isolating NBC materials has been developed. The flotation of both bitumen and NBC was enhanced by phosphate treatment and depressed by EDTA. NBC was characterized by its physical properties, energy content, functionality and chemical analysis. A conceptual model explains the interactions between the bitumen, minerals and NBC fractions present in tailings slurries.     

Synthesis of economically viable biodiesel from waste frying oils (WFO)

In present communication, waste frying oil (WFO) has been used as a feedstock for biodiesel synthesis. WFO, procured from a local Indian restaurant possessed an acid value of 0.84 mg KOH/g, which is low enough for single step transesterification reaction. Biodiesel (fatty acid methyl esters) was washed after transesterification reaction and the yield got lowered substantially (from 96% to 86.36%) after water washing owing to loss of esters. 30:100 vol% (methanol to oil), 0.6 wt% NaOCH₃, 60°C temperature and 600 rpm agitation in 1 h reaction time was found to be optimum for transesterification reaction. ¹H NMR spectrum showed a high conversion (95.19%) of fatty acids in WFO to biodiesel in 2 h reaction time. Almost complete conversion (99.68%) was attained in 2 h reaction time. © 2011 Canadian Society for Chemical Engineering     

Effect of sintering atmosphere and lithium ion co-doping on photoluminescence properties of NaCaPO4:Eu phosphor

This paper reports on the photoluminescence properties of Na_1−yLi_yCa_1−xPO₄:_xEu²⁺ phosphors synthesized by a solid state reaction method. The prepared phosphors have been thoroughly characterized by means of X-ray diffraction (XRD), Field-emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectrum (FTIR), Raman spectrum, Thermo gravimetric and differential thermal analysis (TG–DTA) and photoluminescent spectral measurements. The structure of Na_1−yLi_yCa_1−xPO_4:xEu²⁺ phosphors were found to be orthorhombic in nature with a sphere-like morphology and having the particle size in micrometer range. The excitation spectra of NaCaPO₄:Eu²⁺ phosphors revealed a broad excitation band having its maximum intensity at 373 nm and ranging from 250 m to 450 nm. Incidentally, it matches well with the ultraviolet (UV) radiation of light-emitting diodes (LEDs). Upon 373 nm excitation, these phosphors exhibited intense bluish-green emission band centered at 505 nm. The effect of sintering atmospheres and co-doping of lithium ions on the photoluminescence properties of the NaCaPO₄:Eu²⁺ phosphors were studied and explained suitably. The obtained results indicate that the prepared NaCaPO₄:Eu²⁺ phosphors are promising bluish-green candidates for the phosphor-converted white LED applications.     

Starch urea formaldehyde matrix encapsulation of solid agrochemicals. I. Matrix synthesis and characterizations

A starch urea formaldehyde (starch-UF) matrix has been studied for application to the encapsulation of a solid insecticide. The pertinent parameters relating to the matrix synthesis have been identified and the influences of these parameters on release of the insecticide from the starch UF matrix have been investigated. The key parameter controlling the rate of release is the urea to starch ratio. It is shown that the release process can be described in terms of the generalized equation M_t/M_∞ = ktⁿ where k and n vary with system variables.     

Influence of surfactants on flocculation and dewatering of kaolin suspensions by cationic polyacrylamide (PAM-C) flocculant

This paper reports the result of studies on flocculation and dewatering of kaolin suspensions by cationic polyacrylamide (PAM-C) flocculants in presence of surfactants. The surfactants used were namely anionic sodium dodecyl sulphate (SDS), cationic cetyl trimethyl ammonium bromide (CTAB) and non-ionic TritonX 100, which is a polyoxyethylenic ether compound. The unflocculated kaolin has a very slow settling rate of about 0.03 cm/s and can be improved by more than ten times using PAM-C as a flocculating agent. PAM-C adsorbs on kaolin primarily through electrostatic attraction and the flocculation is governed mainly by charge neutralisation and bridging. Partial pre-coating of kaolin with all three surfactants leads to both physical adsorption as well as chemisorption at PAM-C. Pretreating the kaolin with surfactants can further increase or decrease settling rate depending on the type of surfactant used. However, the flocs thus formed shows better filtration and dewatering behaviour estimated in terms of reduction in specific resistance to filtration (SRF) and cake moisture. The minimum SRF occurs under conditions corresponding to far lower adsorption of PAM-C than that for best flocculation. Simultaneous addition of PAM-C and each of the three surfactants decreases settling rate and sediment volume markedly and does not reduce SRF any further but they all reduce cake moisture substantially. The reduction in cake moisture for different PAM-C: surfactant mixture is in the following order: PAM-C: SDS (1:1)>PAM-C: TX 100(1:1)>PAM-C: CTAB(1:1). Low cake moisture in comparison with PAM-C alone, may be a result of reduction in entrapment of excess water in the smaller flocs formed by simultaneous addition with surfactants and to some extent due to hydrophobicity caused by adsorption of surfactants.     

Effect of rare earth doping on sol-gel derived PZT thin films

We have studied the effect of rare earth dopants (Nd, Gd and Ce) on the phase formation behavior and electrical properties of sol-gel derived Pb_1.05(Zr_0.53Ti_0.47)O₃ thin films. In all these films the perovskite phase is obtained up to 5 at% doping and beyond that pyrochlore phase was found to coexist with the perovskite phase. Ce and Gd doping(1-2 at%) exhibited improved ferroelectric and dielectric properties as compared to the undoped PZT films. Nd doping (2 at%) was found to be effective to increase the retained switchable polarization of undoped PZT from 63% to 84%. The transition temperature of undoped PZT film was found to be reduced with Nd doping. The Nd doped films also exhibited typical relaxor behavior and a diffuse phase transition, characteristic of the relaxor material. Introduction of Nd into the PZT lattice probably introduces disorder in the B site of ABO₃ lattice which causes the observed relaxor behavior     

Dicarbonylruthenium(II) complexes of diphosphine ligands and their catalytic activity

The hexa-coordinated chelate complexes of the type [Ru(CO)₂Cl₂(P-P)](1a,b) [where P-P = 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene(a) and [bis(2-diphenylphosphinophenyl)ether(b)] have been synthesized by reacting the polymeric precursor [Ru(CO)₂Cl₂]_n with the ligands in 1:1 molar ratio. The complexes 1a,b are characterized by elemental analyses, Mass, IR and NMR spectroscopy together with the single crystal X-ray structure determination of 1a. The compound 1a crystallizes in a monoclinic system with space group C2/c showing a slightly distorted octahedral geometry around the Ru centre. The complexes 1a and 1b are thermally stable up to 300 °C and exhibit high catalytic activity in transfer hydrogenation of aldehyde and ketones to corresponding alcohols. The complexes 1a and 1b show much higher catalytic activity for the hydrogenation of aldehyde than ketones. In general, the catalytic efficiency of 1b is higher compared with 1a.