Mechanical behavior and dilatation of particulate-filled thermosets in the rubbery state

The stress–strain–dilatational response of glass-bead-filled, amorphous, network polyurethanes was investigated above their glass transition temperature. The mechanical–dilatational behavior was studied as functions of filler content, particle size, crosslink density of the polymer, and the surface treatment of the filler. It was found that the stress–strain properties are strongly affected by separation of the filler from the matrix. Measurements of the vacuole formation and growth processes enabled modeling the stress–strain response as well as understanding the ultimate behavior of the composites. Also, it was found that the dilatational response of the composites can be shifted on a single curve given by the second integral of the Gaussian function.     

Pb(II) biosorption using anaerobically digested sludge

Removal of Pb(II) by using resting cells of anaerobically digested sludge (ADS) obtained from a nearby wastewater treatment plant was examined. Firstly, sorption kinetic and equilibrium experiments were conducted using agitated, thermostated (25 degrees C) batch reactors. The maximum Pb(II) sorption capacity was found to be very high (1,750 mg/g dry ADS or 8.45 mmol/g dry ADS). At all initial Pb(II) concentrations tested, sorption resulted in neutralization with an increase in the solution pH from an initial value of 4.0-5.5 to an equilibrium value of 7.0-8.0, at which Pb(II) can precipitate as hydroxide. The removal of Pb(II) by ADS was found to involve bioprecipitation as well as biosorption. FTIR spectrometry highlighted carboxyl groups present on the surface of ADS as the major functional groups responsible for biosorption. Secondly, a three-stage semi-continuous pseudo-counter current reactor system was tested to reduce ADS requirement in comparison to a conventional single-stage batch reactor. At an initial Pb(II) concentration of about 200 mg/L, an effluent Pb(II) concentration of 1.3 mg/L was achieved in the three stage reactor, corresponding to a metal removal capacity of 682.7 mg/g dry ADS (3.30 mmol/g), in comparison to 1.9 mg/L and 644.0 mg/g dry ADS (3.10 mmol/g) for the single-stage batch reactor.     

Synthesis and characterization of epoxy based nanocomposites

Epoxy‐clay nanocomposites were synthesized to examine the effects of the content and type of different clays on the structure and mechanical properties of the nanocomposites. Diglycidyl ether of bisphenol‐A (epoxy) was reinforced by 0.5–11 wt % natural (Cloisite Na⁺) and organically modified (Cloisite 30B) types of montmorillonite. SEM results showed that as the clay content increased, larger agglomerates of clay were present. Nanocomposites with Cloisite 30B exhibited better dispersion and a lower degree of agglomeration than nanocomposites with Cloisite Na⁺. X‐ray results indicated that in nanocomposites with 3 wt % Cloisite 30B, d‐spacing expanded from 18.4 Å (the initial value of the pure clay) to 38.2 Å. The glass transition temperature increased from 73°C, in the unfilled epoxy resin, to 83.5°C in the nanocomposite with 9 wt % Cloisite 30B. The tensile strength exhibited a maximum at 1 wt % modified clay loading. Addition of 0.5 wt % organically modified clay improved the impact strength of the epoxy resin by 137%; in contrast, addition of 0.5 wt % unmodified clay improved the impact strength by 72%. Tensile modulus increased with increasing clay loading in both types of nanocomposites. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1081–1086, 2005     

Sustainable hydrogen production options from food wastes

In this study, two thermochemical processes, namely steam gasification and supercritical water gasification (SCWG), were comparatively studied to produce hydrogen from food wastes containing about 90% water. The SCWG experiments were performed at 400 and 450 °C in presence of catalyst (Trona, K₂CO₃ and seaweed ash). The maximum hydrogen yield was obtained at 450 °C in presence of K₂CO₃ catalyst. In second process, hydrothermal carbonization was used to convert food wastes into a high-quality solid fuel (hydrochar) that was further gasified in a dual-bed reactor in presence of steam. The steam gasification of hydrochar was carried out with and without catalysts (iron?ceria catalyst and dolomite). The maximum hydrogen yield obtained from steam gasification process was 28.08 mmol/g dry waste, about 7.7 times of that from SCWG. This study proposed a new concept for hydrogen production from wet biomass, combination of hydrothermal carbonization following steam gasification.     

Processing and properties of modified polyamide 66-organoclay nanocomposites

Binary polyamide 66 nanocomposites containing 2 wt % organoclay, polyamide 66 blend containing 5 wt % impact modifier, and ternary polyamide 66 nanocomposites containing 2 wt % organoclay and 5 wt % impact modifier were prepared by melt compounding method. The effects of E-GMA and the types of the organoclays on the interaction between the organoclay and the polymer, dispersion of the organoclay, morphology, mechanical, flow, and thermal properties of the nanocomposites were investigated. Partial exfoliation and improved mechanical properties are observed for Cloisite® 15A and Cloisite® 25A nanocomposites. On the other hand, the organoclay was intercalated or in the form of tactoids in Cloisite® 30B nanocomposites. Components of the nanocomposites containing Cloisite® 15A and Cloisite® 25A were compounded in different addition orders. Mixing sequence of the components affected both the dispersion of the organoclay and the mechanical properties drastically. SEM analyses revealed that homogeneous dispersion of the organoclay results in a decrease in the domain sizes and promotes the improvements in the toughness of the materials. Melt viscosity was also found to have a profound effect on the dispersion of the organoclay according to MFI and XRD results. Crystallinity of the nanocomposites did not change significantly. It is only the type of the constituents and their addition order what dramatically influence the nanocomposite properties. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

Spectrofluorometric analysis and electrical conductivities of styrene and methylmethacrylate polymers by adding symmetrical polymethine dyes

To see the effect of conjugation on molecular weight and conductivity, three symmetrical polymethine dyes are added in polymers either before or after polymerization. Dyes have conjugated bonds between nitrogen atoms. Among three dyes, it was observed that as conjugation increases, the conductivity also increases. Previous study with polyethylvinylketone and polymethylvinylketone support the idea that increased conjugation will increase the molecular weight and conductivity. For these polymers also, the dopant, phosphorylchloride increased the conductivities due to the double bond being transferred to the main chain and increased conjugation. The same method developed in this work can be applied to methyl methacrylate and styrene polymers to see the relationship between molecular weight, conductivity, and fluorescence intensity. When dyes were added to methylmethacrylate and styrene monomers before polymerization, much higher conductivities were obtained. Conductivity values are directly proportional to the irradiation times and molecular weights. Four‐hour irradiation time results in a maximum molecular weight of 6.4 × 10⁵ and a maximum conductivity of 2.25 μS for MMA polymers. Spectrofluorometric analysis of methyl methacrylate polymers indicates that as molecular weight of the dyes increases, the emission intensities at 375 and 425 nm also increases. In the same way, increased molecular weight of polymer also results higher emission intensities. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Polyamide 66 nanocomposites based on organoclays treated with thermally stable phosphonium salts

Purification of bentonite clays and their modification with two thermally stable (alkyl and aryl) phosphonium organic salts were investigated. The organoclays were subsequently melt compounded with Polyamide 66 (PA66), with and without the use of an elastomeric compatibilizer. The morphology, melt flow, thermal stability, and mechanical properties of the binary and ternary nanocomposites were studied. The bentonite clay was purified by sedimentation, resulting in higher cation exchange capacity and thermal stability in comparison with unpurified clay. These were then used in the synthesis of two thermally stable organoclays by replacing the interlayer sodium cations with two (alkyl and aryl) phosphonium surfactant cations to circumvent the problem of low temperature decomposition of quaternary ammonium organoclays usually used in polymer nanocomposites. The organoclay with aliphatic groups showed more compatibility with PA66 in comparison with the organoclay with aromatic groups. Thus, the use of organoclay with aliphatic groups resulted in nanocomposites with higher tensile strength, higher modulus, higher elongation at break, and higher impact strength in comparison with the nanocomposites produced from the organoclay with aromatic groups. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013