Prediction of mode I fracture toughness of unidirectional fibre composites with arbitrary crack fibre orientation from its lowest or matrix fracture tougness

Corrigendum

Prediction of mode I fracture toughness of unidirectional fibre composites with arbitrary crack fibre orientation from its lowest or matrix fracture tougnessby P.K. Sarkar and S.K. Maiti     

Glass formation region and lithium ion conduction in the oxyfluorophosphate glasses

Oxyfluorophosphate glasses containing about 80 mol% of [LiF+Li₂O] show unusually high lithium ion conductivity at elevated temperatures. A detailed investigation has been carried out on the glasses prepared by both conventional cooling and a rapid quenching technique. Chemical analysis of the glasses reveals fluorine loss during melting and it becomes difficult to make glasses with exact predetermined compositions. Electrical conductivity of the glasses, determined from complex impedance analysis increases with Li₂O content. A glass with nominal composition 70 LiF15 Li₂O15 Al(PO₃)₃ shows the highest conductivity (~ 1.3×10^–3 ohm^–1 cm^–1 around 200° C) among all the compositions studied. An interesting feature of the impedance plot is the near perfect semicircle for bulk relaxation indicating a narrow distribution of relaxation times. This has been explained on the basis of a relatively small proportion of lithium ions which are mobile. The electrical conductivity of the glasses is found to be essentailly independent of dissolved water content. The infrared spectra of these glasses (2 to 50m region) could not produce much useful structural information.     

Cover Feature: Superior Proton-Transfer Catalytic Promiscuity of Cytochrome c in Self-Organized Media (7/2021)

Evolutionarily elderly proteins commonly feature greater catalytic promiscuity. Cytochrome c is among the first set of proteins in evolution to have known prospects in electron transport and peroxidative properties. Here, we report that cyt c is also a proficient proton-transfer catalyst and enhances the Kemp elimination (KE; model reaction to show proton transfer catalytic property) by ∼750-fold on self-organized systems like micelles and vesicles. The self-organized systems mimic the mitochondrial environment in vitro for cyt c. Using an array of biophysical and biochemical mutational assays, both acid–base and redox mechanistic pathways have been explored. The histidine moiety close to hemin group (His18) is mainly responsible for proton abstraction to promote the concerted E2 pathway for KE catalysis when cyt c is in its oxidized form; this has also been confirmed by a H18A mutant of cyt c. However, the redox pathway is predominant under reducing conditions in the presence of dithiothreitol over the pH range 6–7.4. Interestingly, we found almost 750-fold enhanced KE catalysis by cyt c compared to aqueous buffer. Overall, in addition to providing mechanistic insights, the data reveal an unprecedented catalytic property of cyt c that could be of high importance in an evolutionary perspective considering its role in delineating the phylogenic tree and also towards generating programmable designer biocatalysts.     

Cement mortar impregnated with poly(methyl methacrylate-co-styrene)

Polymer-impregnated mortars were prepared by copolymerization of a monomer mixture of methyl methacrylate and styrene in the ratios of 13:87 and 40:60 using Co-60 gamma radiation. The copolymerization characteristics viz. the rate of polymerization, the extent of monomer loss, polymer loading, etc., were studied. The nature and molecular weight of the extractable polymer from the composite were determined. The flexural strength of the copolymer-impregnated composites was found to be better than that of the composites impregnated with component homopolymers.     

New block copolymers II. Synthesis and characterization of an ABA-type block copolymer

A new regular ABA-type triblock copolymer has been synthesized by polycondensation of the acid chloride of carboxy-terminated butadience-acrylonitrile rubber (CTBN) with hydroxyterminated polyethylene isophthalate (PEI) oligomer. This block copolymer was characterized by elemental (nitrogen) analysis, vapor pressure osmometry, viscometry, and IR and NMR spectroscopy. Quantitative estimation of block segments has been carried out by measuring the area under peaks assigned to various protons in the NMR spectrum of the polymer. NMR spectral analysis has been found to agree well with the nitrogen analysis of the polymer. The solubility and solution viscosity behavior of the polymer has also been studied.     

Structural development in cycloolefin copolymers under uniaxial elongational flow

Development of structures in new cycloolefin copolymers (COCs) of ethylene–norbornene (E–NB) and ethylene–tetracyclododecene (E–TD) of different NB/TD compositions were investigated under uniaxial elongational flow. For E–NB copolymer, which has multiblock sequences, a shoulder in WAXD at 0.76 nm was evident besides its amorphous halo, and the relative intensity of the peak increased with increasing comonomer content (NB). The appearance of a new peak for E–TD copolymer, and a relatively higher intense peak for E–NB copolymer at the same position of 0.76 nm, indicated that local ordering of the segments occurred when the COC was subjected to uniaxial flow. A lower comonomer composition of elongated COC, at a constant Hencky strain rate, exhibited two T_g values, whereas a higher composition showed a single T_g. Both local ordering and segmentization occurred in low comonomer content COCs but only local ordering occurred in higher comonomer content COCs. Both the shear viscosity and roll processing experiments exhibited similar phenomena of segregation. A model is proposed to illustrate the structure of COC after uniaxial elongation/deformation. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3421–3427, 2004     

Polybutylene terephthalate/high-density polyethylene alloys. I. Morphological studies

Polybutylene terephthalate (PBT) is a commercially successful thermoplastic polyester but has certain drawbacks such as low impact strength and low melt strength. An attempt has been made to modify the properties of PBT by blending it with polyolefin such as highdensity polyethylene (HDPE). Since PBT and HDPE are incompatible, an ionomer has been used as a compatibilizer to form an alloy. Alloys of PBT and HDPE with varying amounts (2-8%) of ionomer were prepared by melt blending. The ultimate mechanical properties improved significantly on the addition of the ionomer due to an increase in interfacial adhesion between PBT and HDPE. DSC studies show that the presence of ionomer facilitated the crystallization of PBT in the alloy. DMTA studies show that more of PBT (amorphous) is going in to the HDPE-rich phase in the presence of ionomer. The morphology of the alloys was studied using scanning electron microscopy (SEM), polarizing microscopy (PM), and small-angle light scattering (SALS). They showed improved dispersion of HDPE domains in PBT matrix with increasing ionomer content and change in the type of superstructure on adding the ionomer. It has been shown that an alloy of PBT and HDPE with improved mechanical properties and homogeneous morphology can be made with use of ionomer as a compatibilizer. Such alloys are cost effective and can find use in several engineering applications.     

Electrical Conduction in Nano-Structured La0.9Sr0.1Al0.85Co0.05Mg0.1O3 Perovskite Oxide

Nanocrystalline La_0.9Sr_0.1Al_0.85Co_0.05Mg_0.1O₃ oxide powder was synthesized by a citrate–nitrate auto-ignition process and characterized by thermal analysis, X-ray diffraction, and impedance spectroscopy measurements. Nanocrystalline (50–100 nm) powder with perovskite structure could be produced at 900°C by this process. The powder could be sintered to a density more than 96% of the theoretical density at 1550°C. Impedance measurements on the sintered samples unequivocally established the potential of this process in developing nanostructured lanthanum aluminate-based oxides. The sintered La_0.9Sr_0.1Al_0.85Co_0.05Mg_0.1O₃ sample exhibited a conductivity of 2.40 × 10⁻² S/cm in air at 1000°C compared with 4.9 × 10⁻³ S/cm exhibited by La_0.9Sr_0.1Al_0.85Mg_0.15O₃.     

Studies on polyblends of poly(vinyl chloride) and acrylonitrile-butadiene-styrene terpolymer

Blends of poly (vinyl chloride) (PVC) and acrylonitrile-butadiene styrene (ABS) terpolymer were prepared in different ratios by a melt blending technique. ABS containing three different levels of rubber content were used. A quantitative assessment of ABS in PVC/ABS blends has been shown by infrared studies. ABS content has been shown as the presence of the characteristic acrylonitrile peak. Differential scanning calorimetry (DSC) studies have been carried out to study the glass transition (T_g) behavior of the blends. Two T_g values corresponding to PVC and styrene-acrylonitrile (SAN) copolymer have been observed. Thermogravimetric analysis (TGA) reveals a significant improvement in thermal stability of these blends as compared to PVC. Mechanical properties show a significant increase in the impact strength which is related to rubber content of the ABS used. Morphological studies have been carried out by scanning electron microscopy which support the observation that an increase in rubber content results in greater ductility.