Biodiesel from mutton fat using KOH impregnated MgO as heterogeneous catalysts

The use of MgO impregnated with KOH as heterogeneous catalysts for the transesterification of mutton fat with methanol has been evaluated. The mutton fat (fat) with methanol (1:22 M ratio) at 65 °C showed > 98% conversion to biodiesel with 4 wt% of MgO–KOH-20¹ (MgO impregnated with 20 wt% of KOH) in 20 min. The reaction conditions optimized were; the amount of KOH impregnation (5–20 wt%), the amount of catalyst (1.5–4 wt%, catalyst/fat), the reaction temperature (45–65 °C), fat to methanol molar ratio (1:11–1:22) and the effect of addition of water/oleic acid/palmitic acid (upto 1 wt%). Although, transesterification of fresh fat (moisture content 0.02 wt% and free fatty acids 0.002 wt%) with methanol in the presence of KOH (homogenous catalyst) resulted in the complete conversion to biodiesel, but in the presence of additional 1 wt% of either free fatty acid or moisture content, formation of soap was observed. The MgO–KOH-20 catalyst was found to tolerate additional 1 wt% of either the moisture or FFAs in the fat.     

One‐Pot Lipase Entrapment Within Silica Particles to Prepare a Stable and Reusable Biocatalyst for Transesterification

In order to enhance the reusability, Rhizomucor miehei lipase was entrapped in a single step within silica particles having an oleic acid core (RML@SiO₂). Characterization of RML@SiO₂ by scanning and transmission electron microscopy and Fourier transform infrared studies supported the lipase immobilization within silica particles. The immobilized enzyme was employed for transesterification of cottonseed oil with methanol and ethanol. Under the optimum reaction conditions of a methanol‐to‐oil molar ratio of 12:1 or ethanol‐to‐oil molar ratio of 15:1, stirring speed of 250 revolutions/min (flask radius = 3 cm), reaction temperature of 40 °C, and biocatalyst concentration of 5 wt% (with respect to oil), more than 98 % alkyl ester yield was achieved in 16 and 24 h of reaction duration in case of methanolysis and ethanolysis, respectively. The immobilized enzyme did not require any buffer solution or organic solvent for optimum activity; hence, the produced biodiesel and glycerol were free from metal ion or organic molecule contamination. The activation energies for the immobilized enzyme‐catalyzed ethanolysis and methanolysis were found to be 34.9 ± 1.6 and 19.7 ± 1.8 kJ mol^?1, respectively. The immobilized enzyme was recovered from the reaction mixture and reused in 12 successive runs without significant loss of activity. Additionally, RML@SiO₂ demonstrated better reusability as well as stability in comparison to the native enzyme as the former did not lose the activity even upon storage at room temperature (25–30 °C) over an 8‐month period.     

Environmentally Sustainable Construction: Knowledge and Learning in London Planning Departments

Environmentally sustainable construction is now recognised as a significant element of the broader sustainable development agenda and planners are being called upon to play a role in delivering more sustainable patterns of construction and development. This puts particular demands on the knowledge resources of planners since knowledge is implicated in the power relations between planners and developers. This paper examines the interrelationship between knowledge of environmentally sustainable construction and practice in planning departments. Drawing on a survey of and interviews with planners in London, it discusses the construction of knowledge within the dynamics of planning organisations and the potential for learning to promote a more sustainable built environment. Wenger's concept of communities of practice frames the analysis, alongside consideration of the translation of knowledge into bureaucratic and usable forms and the role of knowledge brokers in this process.     

L-cystein modified bentonite-cellulose nanocomposite (cellu/cys-bent) for adsorption of Cu2+, Pb2+, and Cd2+ ions from aqueous solution

In this study, L-cystein modified bentonite-cellulose (cellu/cys-bent) nanocomposite was synthesized and characterized by XRD, FTIR, SEM with EDS, TGA, and TEM techniques. In order to optimize the process the effect of various operational parameters such as pH, adsorbent dosage, contact time, and temperature were also investigated. The adsorption experiments were carried out in initial concentrations range of 20-100 mg L^?1and the adsorbent affinity for metal ions was found to be in order of Cu²⁺ > Pb²⁺ > Cd²⁺. The optimum pH for adsorption of Cu²⁺ and Cd²⁺ was observed at 5 while for Pb²⁺ it was pH 6. Based on the Langmuir model, the maximum adsorption capacity of Cu²⁺, Pb²⁺, and Cd²⁺ at 50^?C was found to be 32.36, 18.52, and 16.12 mg g^?1, respectively. The Langmuir isotherm and pseudo-second order model were found to be better fitted than the other isotherms and kinetic models. The results of thermodynamic parameters confirmed the process to be endothermic and spontaneous in nature.     

Aloe vera gel: a new thickening agent for pigment printing

An attempt was made to print cotton fabric with pigments using a new thickening agent based on Aloe vera gel in combination with sodium alginate. The results were compared with the standard conventional printing recipe containing synthetic thickener, and a favourable effect of Aloe vera introduction was achieved. The results show that the properties of the printed fabric (sharpness, colour yield, overall fastness properties, softness, and water vapour transmission) are dependent on the percentage of Aloe vera gel in the thickener combination, the concentration of printing auxiliaries, and the curing conditions. Optimal printing properties were achieved by using a printing paste containing 80% Aloe vera/20% sodium alginate (700 g kg^?1), pigment (50 g kg^?1), binder (145 g kg^?1), fixer (10 g kg^?1), and ammonium sulfate (5 g kg^?1), followed by drying at 85 °C for 5 min and curing at 150 °C for 3 min. The sample printed with the new recipe showed superior rubbing fastness and handle properties, with a slightly lower colour yield, when compared with the sample printed with synthetic thickener. Finally, economic issues arising from synthetic thickener substitution are highlighted.     

Synthesis of a terpolymer and a tetrapolymer using monomers of diallylamine salts and SO<Subscript>2</Subscript> and their application as antiscalants

An aqueous solution of diallylammonium salts (CH₂ = CHCH₂)₂NH⁺(CH₂)₃A^? having A^? as: CO₂ ^? (I), PO₃H₂ Cl^? (II) and SO₃ ^? (III) in 1:1:1 mol ratio underwent ammonium persulfate-initiated ter cyclopolymerization to yield pH-responsive zwitterionic polymer IV with random placements of the monomers in the same ratio. During dialysis, PO₃H₂Cl^? of the incorporated monomer units of II upon depletion of HCl became PO₃H^?. Likewise, azobisisobutyronitrile-initiated cyclopolymerization of I, II, III, and SO₂ in a mole ratio of 1:1:1:3 provided pH-responsive tetrapolymer V in over 90 % yield with random and alternative placements of I–III and SO₂ units, respectively, in the same ratio as the feed. Polyzwitterions (PZs) IV and V were insoluble in salt-free water but soluble in the presence of salts. The critical salt concentrations required to promote water solubility of PZ IV were determined to be 0.356 M NaCl, 0.237 M NaBr and 0.128 M NaI, whereas for PZ V the corresponding values were found to be 2.25, 1.26 and 0.862 M, respectively. PZs IV and V were converted into anionic polyelectrolytes VI and VII upon basification with NaOH. The viscosity and antiscalant behaviors of VI and VII were examined. The polymers demonstrated remarkable scale inhibition efficacies; at a dose of 10 ppm, both IV (+NaOH) and V (+NaOH) delayed the precipitation of CaSO₄ from its supersaturated solution up to 920 and over 4000 min, respectively. For a small concentration of 5 ppm of polymer V, a scale inhibition of 100 % over 100 min verified it to be a potential effective antiscalant additive in reverse osmosis plants.     

Mechanical Properties and Microstructure of a Metakaolin-Based Inorganic Polymer Mortar Reinforced with Quartz Sand

Silicon - The synthesis, mechanical behaviour, and microstructure of metakaolin-based geopolymer mortar reinforced with quartz sand are presented in this investigation. Fine sand (quartz sand)...     

Efficient loading and entrapment of tamoxifen in human serum albumin based nanoparticulate delivery system by a modified desolvation technique

Herein, the poorly water-soluble drug, Tamoxifen (Tmx), was loaded in the amphipathic matrix of human serum albumin (HSA) nanoparticles by a modified desolvation method. In order to enhance the drug loading (DL) and drug entrapment efficiency (DEE) (<2% and 10%, respectively), ultrasonication of Tmx-HSA mixture was performed prior to desolvation process. Tmx loading and entrapment efficiency were optimized by employment of the response surface methodology (RSM)-central composite design (CCD) of experiments. Under the optimum conditions of 1.59 mg Tmx/ml concentration, 7.76 pH and 5 h incubation of HSA-Tmx, the DL of 6.7% and DEE of 74% are achievable. Particles with the average size of 195 nm, zeta potential of −21 mV and polydispersity index of 0.09 were produced under these conditions. A more sustained Tmx release behavior was observed from polyethylene glycol (PEG) conjugated nanoparticles in comparison to the non-PEGylated ones. The short-term stability investigation showed no alteration in physicochemical properties of nanoparticles at 4 and 37 °C, but small increase in nanoparticles size was observed after three months of storage at room temperature. This is the first report for efficient production of a Tmx delivery system based on HSA nanoparticles.     

Structural and magnetic properties of Pr–Ni substituted Ca0.5Ba0.5Fe12O19 hexa-ferrite nanoparticles

Effect of Pr–Ni substitution on structural and magnetic properties of Ca_0.5Ba_0.5−xPr_xNi_yFe_12−yO₁₉ (x=0.00–0.10 and y=0.00–1.00) prepared by the sol–gel auto combustion method were investigated. The XRD analysis confirmed the single phase M-type hexa-ferrite structure. The lattice parameters were found to increase as Pr–Ni content increases, which is attributed to the ionic size of the implicated cations. The Pr–Ni seems to be completely soluble in the lattice. Transmission electron microscopy reveals that the grain size decreases with increase of Pr–Ni substitution. The coercivity and remanent magnetization ranges from 1511 to 1925 (Oe) and 21.4 to 26.5 (emu/g), respectively. The coercivity values of all the samples fall in the range of M-type hexa-ferrites.     

Numerical Simulation of a Solar Kiln Design for Drying Timber with Different Geographical and Climatic Conditions in Australia

A numerical simulation for the modeling of solar kilns for hardwood timber drying with different boundary conditions has been developed in this work. This simulation has been used to predict the key behavior of the wood and the kiln itself under different geographical and weather conditions in Australia. This work, therefore, enables a site to be suggested that is likely to give the best kiln performance both in terms of the productivity and the quality of the end-use product. As test cases, realistic climatic conditions for three representative geographical locations in Australia, including Sydney (latitude 33.86°S), Melbourne (37.81°S), and Brisbane (27.46°S), have been considered in this simulation. Out of the three sites considered in this work, the fastest drying rates (and highest diffusion coefficients) were predicted in Brisbane. The highest level of instantaneous strain in the timber for this location was also predicted to be 0.0075 m/m, which is much less than the failure value (0.02 m/m). The moisture content distribution profile within the boards toward the end of the drying period was found to be almost uniform, which is likely to cause low degrade in the dried timber.