The pyrolysis of pure biomass, high density polyethylene (HDPE), polypropylene (PP) and polyethylene terephthalate (PET), plastic mixtures [HDPE+PP+PET (1 : 1 : 1)], and biomass/plastic mixture (9 : 1, 3 : 1, 1 : 1, 1 : 3 and 1 : 9) were investigated by using a thermogravimetric analyzer under a heating rate at 10 o C/min from room temperature to 800 o C. Paper was selected as the biomass sample. Results obtained from this comprehensive investigation indicated that biomass was decomposed mainly in the temperature range of 290-420 o C, whereas thermal degradation temperature of plastic mixture is 390-550 o C. The percentage weight loss difference (W) between experimental and theoretical ones was calculated, which reached a significantly high value of (−)15 to (−)50% at around 450 o C in various blend materials. These thermogravimetric results indicate the presence of significant interaction and synergistic effect between biomass and plastic mixtures during their co-pyrolysis at the high temperature region. With increase in the amount of plastic mixture in blend material, the char production has diminished at final pyrolysis temperature range. Additionally, a kinetic analysis was performed to fit with TGA data, the entire pyrolysis processes being considered as one or two consecutive first order reactions.
We report phase separation and liquid-crystal ordering induced by scalar activity in a system of soft repulsive spherocylinders (SRSs) of shape anisotropy L/D = 5 using molecular dynamics (MD) simulations. Activity is introduced by increasing the temperature of half of the SRSs (labeled hot) while maintaining the temperature of the other half constant at a lower value (labeled cold). The difference between the two temperatures scaled by the lower temperature provides a measure of the activity. Starting from different equilibrium initial phases, we find that activity leads to segregation of the hot and cold particles. Activity also drives the cold particles through a phase transition to a more ordered state and the hot particles to a state of less order compared to the initial equilibrium state. The cold components of a homogeneous isotropic structure acquire nematic and, at higher activity, crystalline order. Similarly, the cold zone of a nematic initial state undergoes smectic and crystal ordering above a critical value of activity while the hot component turns isotropic. We find that the hot particles occupy a larger volume and exert an extra kinetic pressure, confining, compressing, and provoking an ordering transition of the cold-particle domains.
The manipulation and processing of single-wall carbon nanotubes (SWNTs) is limited by their poor solubility in most common solvents. Covalent sidewall functionalization of SWNTs provides an excellent route to improve their solubility. Here we have studied the relationship between sidewall functionalization and phase behavior of solutions of functionalized SWNTs (f-SWNTs) in strong acids. We use centrifugation in conjunction with UV-Vis-nlR spectroscopy to quantify the solubility of f-SWNTs in strong acids. We image the dispersions of functionalized tubes by polarized light microscopy. We find that adding butyl groups increases marginally the solubility of SWNTs in 102% sulfuric acid in the isotropic phase; adding 9-nonadecyne groups roughly doubles the solubility of SWNTs. Viscosity measurements in dilute solutions are sensitive to de-bundling. We compare the viscosity-concentration dependence of dilute pristine and f-SWNTs to assess whether and how functionalization promotes de-bundling and stabilizes the tubes. The phase behavior and rheology of these f-SWNTs parallels with that of pristine SWNTs; 9-nonadecylated SWNTs have higher solubility and should be easier to process.
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