Water resistance,mechanical properties,and biodegradability of poly(3‐hydroxybutyrate)/starch composites

Composites of poly(3‐hydroxybutyrate), P(3HB), and starch were prepared by solution casting technique. To improve adhesion of starch to P(3HB), stearic acid was added as a compatibilizer and glycerol as a plasticizer. The water resistance, mechanical, and biodegradable properties of the P(3HB)/starch composites were studied. Diffusion and penetration coefficients of water increased with increasing starch content in the composites. The results showed that the elastic modulus and strain at rupture of the P(3HB)/starch composites were enhanced by increasing starch content upto 10 wt % and the tensile strength increased from 21.2 to 93.9 MPa. The presence of starch content higher than 10 wt % had an adverse effect on the mechanical properties of the investigated composites. The biodegradation rate using Actinomycetes increased proportionally to the starch content in the composite and accelerated in a culture medium of pH ≈ 7.0 at 30°C. Enzymatic degradation experiments showed that lipase produced by Streptomyces albidoflavus didnot degrade P(3HB)/starch composites. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Treatability Study on Membrane Concentrate Containing Pesticides Using Advanced Oxidation Processes

This treatability study evaluated the overall effectiveness of advanced oxidation processes (AOPs) to treat membrane concentrates containing the pesticides bromoxynil and trifluralin. The results of study indicate that high levels of pesticide degradation were achieved using ozone (O₃) plus hydrogen peroxide (H₂O₂) for all concentrate matrices. However, the toxicity of the samples during the O₃/H₂O₂ process was higher than that obtained during ultraviolet (UV) light combined with H₂O₂. Low levels of pesticide oxidation were observed in experiments using a mixture of pesticides during all treatment options.     

PIV/PLIF Study of Impinging Jet Ozone Bubble Column with Mixing Nozzles

This paper introduces the results obtained from a particle image velocimetry/planer laser-induced fluorescence (PIV/PLIF) system used in characterizing an impinging jet ozone bubble column with mixing nozzles. This research aims at evaluating the mixing effect resulting from the nozzle diffusers attached to the outlets of the impinging jets' injectors. The PIV system was used to study the flow patterns of the liquid and gas phases under different superficial gas and liquid velocities (u_G and u_L, respectively) values (from 0.002 to 0.017 m/s and from 0.008 to 0.024 m/s, respectively). Furthermore, a particle dynamics analyzer (PDA) system was used to characterize the bubble sizes under the same operating conditions. The PLIF system was used to determine the liquid axial dispersion coefficient (D_L, m²/s) for the mentioned range of operating conditions. The column average gas hold-up (?_G) and specific interfacial area (a) were then determined in order to evaluate the column's mass transfer efficiency. The results showed that higher mass transfer rates can be obtained by using this column, as high ?_G, and were achieved.     

Dielectric study of β-relaxation in some cellulosic substances

6-(2-Cyanoethylamino)-6-deoxycellulose (Cell-CEA) as a novel cellulose derivative was prepared from 6-bromo-6-deoxycellulose. The influence of the reaction conditions on the degree of substitution was studied in detail. The dielectric characteristics of a Cell-CEA sample having degree of substitution of 0.86, together with those of microcrystalline and regenerated celluloses, have been investigated in the temperature range from −60 to 120°C, and frequency range 30 Hz to 100kHz. One relaxation process, designated as β, was recognised, which was attributed to side-group motions, probably −CH₂X (X = OH or NHCH₂CH₂CN). The higher activation energy of this process and the shift to higher temperature in Cell-CEA, compared with microcrystalline and regenerated celluloses, reflects the enhanced steric constraints involved in the motion of the bulkier, −CH₂NHCH₂CH₂CN, side groups. The results obtained are discussed in terms of the dielectric parameters ϵ″_max′ β and Δϵ.     

A method for treating wastewater containing formaldehyde

Many industrial activities utilise formaldehyde as a key chemical in organic synthesis including: synthesis of special chemicals such as pentaerythritol and ethylene glycol, synthetic resins, paper products, medicinal products and drugs and others, too numerous to mention. Therefore, effluents arising from these applications may contain significant amounts of formaldehyde. In a biodegradation experiments of a wastewater sample containing formaldehyde ranging from 31.5 to 125 mg/l, residual formalin (a solution of formaldehyde gas in water) ranging from 40% to 85%, respectively, was found at the end of the run (16 d) showing the inhibition effect of formalin which increased with the increase in formalin concentration. The biodegradation of formalin decreased significantly at concentrations higher than 300 mg/l. A method to convert formaldehyde to an easily biodegradable substance is herein described. In the commercial manufacture of resins from phenol and formalin the reaction is never completely quantitative. As a result during the dehydration stage phenol and formalin are distilled from the wastewater. Phenol is toxic to several biochemical reactions. However, biological transformation of phenol to a non-toxic entity is possible through specialized microbes. Transformation of phenol is inhibited by the presence of formaldehyde. Biotransformation of phenol in a wastewater containing high concentrations of formaldehyde started shortly after treating the wastewater with calculated amounts of sodium sulphite. Sodium sulphite is believed to react with formaldehyde forming sodium formaldehyde bisulphite, which is not only non-toxic to microorganisms but also a biodegradable substance. From the DO measurements before and after the addition of sodium sulphite, the authors noticed that the dissolved oxygen in a wastewater containing formaldehyde is not affected by the addition of the calculated amount of sodium sulphite, which is just enough to consume the measured amount of formaldehyde in that wastewater.     

The impact of metallic coagulants on the removal of organic compounds from oil sands process-affected water

Coagulation/flocculation (CF) by use of alum and cationic polymer polyDADMAC, was performed as a pretreatment for remediation of oil sands process-affected water (OSPW). Various factors were investigated and the process was optimized to improve efficiency of removal of organic carbon and turbidity. Destabilization of the particles occurred through charge neutralization by adsorption of hydroxide precipitates. Scanning electron microscope images revealed that the resultant flocs were compact. The CF process significantly reduced concentrations of naphthenic acids (NAs) and oxidized NAs by 37 and 86%, respectively, demonstrating the applicability of CF pretreatment to remove a persistent and toxic organic fraction from OSPW. Concentrations of vanadium and barium were decreased by 67-78% and 42-63%, respectively. Analysis of surface functional groups on flocs also confirmed the removal of the NAs compounds. Flocculation with cationic polymer compared to alum, caused toxicity toward the benthic invertebrate, Chironoums dilutus, thus application of the polymer should be limited.     

Correlation of electrical and swelling properties with nano free‐volume structure of conductive silicone rubber composites

The present study focuses on finding a correlation between the positron annihilation parameters of silicone rubber polydimethylsiloxane (PDMS) composites loaded with different conductive fillers and their swelling and electrical properties. Four types of conductive fillers have been used in this study, i.e., carbon black (CB), graphite (G), copper, and nickel powders. The investigated swelling parameters for PDMS composites such as the maximum degree of swelling Q_m%, the penetration rate, P, and consequently the diffusion coefficient, D, decreased with increasing the filler content due to the reduction of the size of free‐volume, which could be observed through a decrease of the probability of ortho‐positronium (o‐Ps) formation I₃, that has been measured by the positron annihilation spectroscopy (PALS). Accordingly, a positive correlation has been found of 76.78% and 61.1% between Q_m% and the o‐Ps lifetime τ₃, representing the size of free‐volume for the CB and G filled composites, respectively. It is worthwhile, mentioning that the CB filled composites exhibit relatively low values of P, D, and Q_m% as compared to the G filled composites due to the difference in the physical properties of the filler, particle size, surface area as well as the tendency of the filler particles to make aggregates. On the other hand, the variation of the diffusion coefficient with the relative fractional free‐volume F_r is found in good agreement with the Fujita's free‐volume theory. On the other hand, the electrical conductivity increases with increasing the conductive filler content. Positive temperature coefficient of conductivity (PTCC) behavior is detected, except for the composite containing 20 or 25 phr CB, which showed a metallic behavior. Besides, CB filled PDMS composites exhibit higher electrical conductivity as compared to the composites filled with the other three fillers. The electrical conductivity ln (σ) is positively correlated with the probability of free annihilation of positrons at interfaces I₂, thus suggesting an increase in the electron density with the filler content. The activation energy of conduction, E_a, decreases with the increase in the loading of conductive filler. Moreover, it was noticed that E_a varies with the filler type, the values of E_a increase as the particle size of the filler increases. Finally, a correlation between the free‐volume V_f, determined by PALS with the DC electrical conductivity ln(σ) is found to be in accordance with Miyamoto and Shibayma model. POLYM. COMPOS., 34:2105–2115, 2013. © 2013 Society of Plastics Engineers     

The boundary element modelling of the human body exposed to the ELF electromagnetic fields

In this paper a cylindrical model of human body exposed to the extremely low frequency (ELF) electromagnetic field is presented. The analysis is based on the solution of the simplified integral equation for thick wires. The numerical solution of the integral equations is performed by the Galerkin–Bubnov variant of the boundary element method. Several numerical results for the ELF exposures are presented.     

Green's First Identity Method for Boundary-Only Solution of Self-Weight in BEM Formulation for Thick Slabs

The present paper develops a new technique for treatment of self-weight for building slabs in the boundary element method (BEM). Due to the use of BEM in the analysis, all defined variables are presented on the slab boundary (mesh is defined only along the slab boundary). Self-weight, however, is usually defined over slab domain, hence domain discretisation is required, which spoils the main advantage of the BEM. In this paper a new method is presented to transform self-weight domain integrals to the boundary for such slabs. The proposed method is based on using the so-called Green's first identity. All new kernels for generalized displacements, stress-resultants, and tractions are derived and listed explicitly. The present formulation is implemented into computer code and several examples are tested. Results are compared against results obtained from other numerical method to prove the accuracy and validity of the present formulation.     

Degradation of bromoxynil and trifluralin in natural water by direct photolysis and UV plus H2O2 advanced oxidation process

The degradation of two pesticides, bromoxynil and trifluralin, was investigated in ultrapure and natural water solutions under ultraviolet (UV) light and a combination of UV and hydrogen peroxide (H₂O₂). The effect of pH on the photooxidation of the pesticides was also studied. The results indicated that under direct photolysis with monochromatic light at 253.7 nm and different conditions, the photochemical rates followed first-order kinetics, with fluence-based rate constants ranging from 9.15 × 10⁻⁴ to 6.37 × 10⁻³ cm² mJ⁻¹ and 7.63 × 10⁻³ to 1.47 × 10⁻² cm² mJ⁻¹ for bromoxynil and trifluralin, respectively. Quantum yields, in the range of 0.08-0.25 for bromoxynil and 0.12-0.72 for trifluralin, were observed in experiments using ultrapure water. The study also found that the UV/H₂O₂ process enhanced the oxidation rate in comparison to direct photolysis. A 90% degradation with UV dose of 333 and 188 mJ cm⁻² was achieved for bromoxynil and trifluralin, respectively, in natural water, in presence of 8.8 × 10⁻⁴ M H₂O₂. To assess the aquatic toxicity, the Microtox^® 81.9% screening test protocol was used before and after treatment. The test results indicated a decrease in the acute toxicity of the samples after treatment for both pesticides.