Probing the structural chirality of crystalline cellulose with induced circular dichroism

There is mounting evidence of twists in the crystalline regions of cellulose, but direct imaging of the twist is hindered by the small crystal sizes in cellulose nanocrystals from wood and plant sources. Here the structural chirality of cellulose nanocrystals is determined experimentally using induced circular dichroism of optically inactive Congo red. Time Dependent Density Functional Theory B3LYP 6-31G calculations indicate right-handed twisted cellulose surfaces induce positive Cotton effects in adsorbed Congo red and left-handed surfaces induce negative Cotton effects. Consistent with directly observed twists, conventional wood cellulose nanocrystals are estimated to have a right-handed 800 nm per half-twist demonstrating the crystalline regions are not uniformly flat, but rather right-handed twisted crystalloids.     

Polymer Zwitterions for Stabilization of CsPbBr3 Perovskite Nanoparticles and Nanocomposite Films

Functional polymers with sulfobetaine or phosphorylcholine zwitterions as pendent groups are demonstrated as both ligands and host matrices for CsPbBr₃ perovskite nanoparticles (PNPs). These polymers produce nanocomposite films with excellent NP dispersion, optical transparency, and impressive resistance to NP degradation upon exposure to water. Multidentate interactions of the zwitterion‐containing copolymers with the PNPs induce dispersed or weakly aggregated nanocomposite morphologies, depending on the extent of zwitterionic functionality in the polymer. Incorporating additional functionality into the polymers, such as benzophenone pendent groups, yields lithographically patternable films, while time‐resolved photoluminescence measurements provide insight into the electronic impact of PNPs in zwitterionic polymer matrices.     

Light-induced metastable states in oxalatenitrosylruthenium(II) and terpyridinenitrosylruthenium(II) complexes

Two extremely long lived metastable states (SI and SII) can be accessed by irradiation with light in the blue-green spectral range at temperatures below 200 K in Cs(2)[Ru(ox)(NO)Cl(3)], [Ni(cyclam)][Ru(ox)(NO)Cl(3)].3H(2)O, and [Ru(terpy)(NO)(OH)Cl][PF(6)]. The crystal structures of the ground states of the oxalate-containing compounds are presented, and the influence of the atomic distances of the cations/anions is discussed with respect to the decay temperatures. The radiationless thermal decay of the metastable states is detected by differential scanning calorimetry (DSC) for the three compounds. Both metastable states decay exponentially in time under isothermal conditions. The excited states are energetically separated from the ground state by potential barriers given by the activation energy of the Arrhenius law. In [Ni(cyclam)][Ru(ox)(NO)Cl(3)].3H(2)O the enthalpy maximum of the thermal decay of SII appears at 182 K, which is a relatively high decay temperature for SII. The reason for this strong temperature shift compared to those of the other compounds could be due to the polarization effect of Ni(2+) on the electron density at the Ru site via the Cl atom.     

Elastic constants of nematic solutions of rod-like and semi-flexible polymers

Abstract

Analytical expressions for the elastic constants of nematic polymer solutions are derived when the macromolecules are monodisperse rod-like, bidisperse rodlike or semi-flexible. These expressions are derived in the gaussian approximation so that they constitute exact leading terms of a general asymptotic expansion for high degree of nematic ordering although the results are justifiable only within the range of validity of the second virial approximation. The limiting forms are in complete agreement with recent numerical work for monodisperse rods.     

Chemically peeling layers of cellulose nanocrystals by periodate and chlorite oxidation

Layers of cellulose nanocrystals are peeled off by controlled periodate and chlorite oxidation to produce nanocrystals with a tunable width. The chemical modification increases the solubility of the polymers at the crystal surface to the extent that they preferentially exist in solution and detach from the crystal. The number of layers removed is controlled by the degree of partial oxidation. The reaction occurs on the crystal surface and at the crystal ends, resulting in crystals which are both shorter and thinner, likely with dangling chains at each end. The crystallinity index is reduced with each layer removed.     

On clarification of haze in polypropylene

The mechanism of reducing light scattering in isotactic polypropylene (i‐PP), through the addition of so‐called clarifying agents, is studied with small‐angle light scattering (SALS) and scanning electron microscopy (SEM). The clarifying agents used in this study depict monotectic phase behavior with i‐PP, crystallizing in a relatively narrow concentration range in a nanofibrillar network, providing an ultrahigh nucleation density in the i‐PP melt. It is found that the clarifying effect, a dramatically increased transparency and reduced haze, that occurs within the aforementioned additive concentration range, coincides with a change in morphology from strongly scattering spherulites to shish‐kebab‐like crystalline structures, as evidenced by in situ SALS measurements and confirmed by SEM images. A simple scaling law, relating the diameter of the shish‐kebab structures to the fibril diameter and volume fraction of the clarifying agent is proposed, suggesting that the performance of a (fibril‐forming) clarifying agent will improve by reducing the fibril diameter and/or increasing the volume concentration of the clarifying agent. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 865–874     

High‐pressure sorption of carbon dioxide and methane in all‐aromatic poly(etherimide)‐based membranes

The sorption of compressed carbon dioxide and methane in a series of all‐aromatic poly(etherimide) (PEI) thin films is presented. The polymer films are derived from the reactions between an arylether diamine (P1) and four different dianhydrides [3,3′,4,4′‐oxydiphthalic dianhydride (ODPA), 3,3′,4,4′ biphenyltetra‐carboxylic dianhydride (BPDA), 3,3′,4,4′‐benzo‐phenonetetracarboxylic dianhydride (BTDA), and pyromellitic dianhydride (PMDA)] that have been selected to systematically change the flexibility of the polymer backbone, the segmental mobility, and the nonequilibrium excess free volume (EFV) of the polymer. The EFV, gas sorption capacities, and sorption‐ and temperature‐induced dynamic changes in film thickness and refractive index have been investigated by spectroscopic ellipsometry. The sorption capacity depends to a great extent on the PEI backbone composition. PMDA‐P1 shows the highest carbon dioxide sorption, combined with the lowest sorption selectivity because of the predominant sorption of methane in the EFV. For ODPA‐P1, the highest sorption selectivity is obtained, while it shows little long‐term relaxations at carbon dioxide pressures up to 25 bar. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 986–993     

Rejuvenation of PLLA: Effect of plastic deformation and orientation on physical ageing in poly(l‐lactic acid) films

Poly(l ‐lactic acid) (PLLA) is a bio‐degradable polyester which exhibits brittle behaviour due to relatively fast physical ageing of the amorphous phase. This work describes the effects of thermal rejuvenation and molecular orientation of the amorphous phase on this physical ageing process. Uniaxial compression testing showed that physical ageing of the amorphous phase increases the yield stress and the associated strain softening response, both contributing to the observed embrittlement of PLLA in tension. Molecular orientation at constant crystallinity was applied by uniaxial and biaxial plastic deformation just above the glass transition temperature, up to plastic strains of 200% to avoid strain‐induced crystallisation. Using stress‐relaxation experiments combined with tensile testing, both as a function of ageing time, it is shown that both uniaxial and biaxial plastic deformation in excess of 150% plastic strain, decelerates and possibly prohibits the physical ageing process. The oriented monofilaments and films have improved mechanical properties such as stiffness, strength and strain‐to‐break, which were not affected by physical ageing during the whole testing period (40 days). In addition, plastic deformation to higher draw ratios and/or higher temperatures strongly enhanced crystallinity and resulted in PLLA monofilaments and films that also exhibited tough behaviour, not affected by physical ageing. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 2233–2244