Hydrolytic degradation of poly(l‐lactic acid)/poly(methyl methacrylate) blends

The hydrolytic degradation of poly(l ‐lactic acid)/poly(methyl methacrylate) (PLLA/PMMA) blends was carried out by the immersion of thin films in buffer solutions (pH = 7.24) in a shaking water bath at 60 °C for 38 days. The PLA/PMMA blends (0/100; 30/70; 50/50; 70/30; 100/0) were obtained by melt blending using a Brabender internal mixer and shaped into thin films of about 150 µm in thickness. Considering that PMMA does not undergo hydrolytic degradation, that of PLLA was followed via evolution of PLA molecular weight (recorded by size exclusion chromatography), thermal parameters (differential scanning calorimetry (DSC)) and morphology of the films (scanning transmission electron microscopy). The results reveal a completely different degradation pathway of the blends depending on the polymethacrylate/polyester weight ratio. DSC data suggest that, during hydrolysis at higher PMMA content, the polyester amorphous chains, more sensitive to water, are degraded before being able to crystallize, while at higher PLLA content, the crystallization is favoured leading to a sample more resistant to hydrolysis. In other words, and quite unexpectedly, increasing the content of water‐sensitive PLLA in the PLLA/PMMA blends does not mean de facto faster hydrolytic degradation of the resulting materials. © 2018 Society of Chemical Industry     

Mechanical,morphological, and thermal properties of poly(vinyl chloride)/low‐density polyethylene composites filled with date palm leaf fiber

This article investigates the mechanical, morphological, and thermal properties of poly(vinyl chloride) (PVC) and low‐density polyethylene (LDPE) blends, at three different concentrations: 20, 50, and 80 wt% of LDPE. Besides, composite samples that were prepared from PVC/LDPE blend reinforced with different date palm leaf fiber (DPLF) content, 10, 20, and 30 wt%, were also studied. The sample in which PVC/LDPE (20 wt%/80 wt%) had the greatest tensile strength, elongation at break, and modulus. The good thermal stability of this sample can be seen that T_10% and T_20% occurred at higher temperatures compared to others blends. DPLF slightly improved the tensile strength of the polymer blend matrix at 10 wt% (C10). The modulus of the composites increased significantly with increasing filler content. Ageing conditions at 80°C for 168 h slightly improved the mechanical properties of composites. Scanning electron microscopic micrographs showed that morphological properties of tensile fracture surface are in accordance with the tensile properties of these blends and composites. Thermogravimetric analysis and derivative thermogravimetry show that the thermal degradation of PVC/LDPE (20 wt%/80 wt%) blend and PVC/LDPE/DPLF (10 and 30 wt%) composites took place in two steps: in the first step, the blend was more stable than the composites. In the second step, the composites showed a slightly better stability than the PVC/LDPE (20 wt%/80 wt%) blend. Based on the above investigation, these new green composites (PVC/LDPE/DPLF) can be used in several applications. J. VINYL ADDIT. TECHNOL., 25:E88–E93, 2019. © 2018 Society of Plastics Engineers     

The effects of catalyst and deactivator species in atom transfer radical polymerization of n-butyl methacrylate

Iranian Polymer Journal - Atom transfer radical polymerization (ATRP) of n-butyl methacrylate (n-BMA) was performed using CuIBr/N,N,N′,N″,N″-pentamethyldiethylenetriamine (PMDETA)...     

Pure and complex nanostructures using poly[bis(triiso‐propylsilylethynyl) benzodithiophene‐bis(decyltetradecyl‐thien) naphthobisthiadiazole], carbon nanotubes and reduced graphene oxide for high‐performance polymer solar cells

Crystallization of poly[bis(triiso‐propylsilylethynyl) benzodithiophene‐bis(decyltetradecyl‐thien) naphthobisthiadiazole] (PBDT‐TIPS‐DTNT‐DT) was investigated in supramolecules based on carbon nanotubes (CNTs) and reduced graphene oxide (rGO) and their grafted derivatives. The principal peaks of PBDT‐TIPS‐DTNT‐DT crystals were in the range 3.50°–3.75°. By grafting the surface of the carbonic materials, the assembling of polymer chains decreased because of hindrance of poly(3‐dodecylthiophene) (PDDT) grafts against π‐stacking. The diameters of CNT/polymer and CNT‐g‐PDDT/polymer supramolecules were 160 and 100 nm. The rGO/polymer supramolecules had the highest melting point (T_m = 282 °C) and fusion enthalpy (ΔH_m = 25.98 J g^?1), reflecting the largest crystallites and the most ordered constituents. Nano‐hybrids based on grafted rGO (276 °C and 28.26 J g^?1), CNT (275 °C and 27.32 J g^?1) and grafted CNT (268 °C and 22.17 J g^?1) were also analyzed. T_m and ΔH_m values were significantly less in corresponding melt‐grown systems. The nanostructures were incorporated in active layers of PBDT‐TIPS‐DTNT‐DT:phenyl‐C₇₁‐butyric acid methyl ester (PC₇₁BM) solar cells to improve the photovoltaic features. The best results were detected for PBDT‐TIPS‐DTNT‐DT:PC₇₁BM:rGO/polymer systems having J_sc = 13.11 mA cm^?2, fill factor 60% and V_oc = 0.71 V with an efficacy of 5.58%. On grafting the rGO and CNT, efficiency reductions were 12.01% (5.58%–4.91%) and 9.34% (4.07%–3.69%), respectively. © 2019 Society of Chemical Industry     

Efficiency above 6% in poly(3‐hexylthiophene):phenyl‐C‐butyric acid methyl ester photovoltaics via simultaneous addition of poly(3‐hexylthiophene) based grafted graphene nanosheets and hydrophobic block copolymers

A combination of reduced graphene oxide (rGO) nanosheets grafted with regioregular poly(3‐hexylthiophene) (P3HT) (rGO‐g‐P3HT) and P3HT‐b‐polystyrene (PS) block copolymers was utilized to modify the morphology of P3HT:[6,6]‐phenyl‐C71‐butyric acid methyl ester (PC71BM) active layers in photovoltaic devices. Efficiencies greater than 6% were acquired after a mild thermal annealing. To this end, the assembling of P3HT homopolymers and P3HT‐b‐PS block copolymers onto rGO‐g‐P3HT nanosheets was investigated, showing that the copolymers were assembled from the P3HT side onto the rGO‐g‐P3HT nanosheets. Assembling of P3HT‐b‐PS block copolymers onto the rGO‐g‐P3HT nanosheets developed the net hole and electron highways for charge transport, thereby in addition to photoluminescence quenching the charge mobility (μ_h and μ_e) values increased considerably. The best charge mobilities were acquired for the P3HT₅₀₀₀₀:PC71BM:rGO‐g‐P3HT₅₀₀₀₀:P3HT₇₀₀₀‐b‐PS₁₀₀₀ system (μ_h = 1.9 × 10^?5 cm² V^–1 s^–1 and μ_e = 0.8 × 10^?4 cm² V^–1 s^–1). Thermal annealing conducted at 120 °C also further increased the hole and electron mobilities to 9.8 × 10^?4 and 2.7 × 10^?3 cm² V^–1 s^–1, respectively. The thermal annealing acted as a driving force for better assembly of the P3HT‐b‐PS copolymers onto the rGO‐g‐P3HT nanosheets. This phenomenon improved the short circuit current density, fill factor, open circuit voltage and power conversion efficiency parameters from 11.13 mA cm^?2, 0.63 V, 62% and 4.35% to 12.98 mA cm^?2, 0.69 V, 68% and 6.09%, respectively. © 2019 Society of Chemical Industry     

Analytical versus numerical analysis of back grading in CIGS solar cells

Band gap grading is able to improve the performance of CIGS solar cells. In order to get a better understanding of the parameters influencing the effect of a grading, a closed form analytical expression of the current density is derived. The advantages and drawbacks of this analytical expression with respect to numerical simulation results are assessed. The analytical analysis has limited validity due to restrictions on the absorption characteristic and on the recombination in the space charge layer. Nevertheless it leads to good results, it has the advantage of being faster than numerical simulations and it clarifies the interrelation of the meaningful parameters.     

Morphology formation during the nonisothermal thermally-induced phase separation (TIPS) process

In high-viscosity polymer solutions and blends, temperature variations during the quench process of the thermally-induced phase separation (TIPS) influence the dynamics and thermodynamics of phase separation. Hence, this study aims to investigate the impact of temperature variations on the morphology formation during the TIPS process. First, the influence of temporal temperature variations on phase separation is investigated by coupling a transient heat conduction model and the Cahn–Hilliard equation, and the results are compared with the isothermal phase separation process. Next, the morphology formation during phase separation is inspected by applying quench from two opposite sides of the sample to the same and different temperatures through coupling the Fourier heat transfer equation and the Cahn–Hilliard equation. The influence of the enthalpy of demixing on the morphology formation and the competition between the heat and mass transfer is also evaluated. It is confirmed that temporal variations of temperature alone have a significant impact on the morphology formation during the TIPS process. In addition, quenching the system to the same and different temperatures both leads to anisotropic morphology formation, which is affected by the quench rate, quench temperature, solution viscosity, and enthalpy of demixing. Upon applying different quench temperatures from opposite sides, two different types of morphologies and droplet sizes were formed as a result of the difference in the cooling rates between the two sides. Employing the enthalpy of demixing during phase separation induced a shallow quench effect on the deep quench side due to the fact that the heat moved toward the lowest temperature in the system, which led to the formation of a distinctive structure.     

Biomimetic Approach for the Production of 3D Woven Spherical Composite Applied in Apparel Protection and Performance

Applied Composite Materials - Current sports bras are typically manufactured via a cut and sew process resulting in a high volume of post-production material waste. Seams derived from this cut and...