Redox copolymerization of acrylonitrile with fumaronitrile as a precursor for carbon fibre

Redox copolymerization of acrylonitrile (AN) with fumaronitrile (FN) was carried out in water at 40 °C using potassium persulphate (KPS) and sodium bisulfite (SBS) as initiators. Monomers feed used were 100:0, 97:3, 95:5, 90:10, 85:15 and 80:20 (AN:FN). Copolymers were characterized by Fourier transform infrared spectroscopy (FT-IR), Differential scanning calorimetry (DSC) and Thermogravimetric analysis. The effect of monomer composition on conversion and thermal properties of copolymer was studied. The DSC thermograms of copolymer samples are different from that of the homoPAN sample in the sense that the thermogram of the copolymer shows a doublet appearance and broad exothermic peak indicating that incorporation of fumaronitrile into copolymer system reduces the cyclization propagation rate with lower heat liberation (510 Jg⁻¹) as compared to that of homo(PAN) (758 Jg⁻¹). DSC thermograms also show that initial cyclization occurred at lower temperatures in copolymers as compared to homoPAN. The incorporation of 10% fumaronitrile into copolymer results the highest char yield (53%).     

Role of hydrogen environment induced hydrogen embrittlement of Ti–8Al–1Mo–2V alloy

Structural analysis by mean of metallographic, SEM fractographic and TEM replica technique including acoustics-emission studies have been carried out on Ti–8Al–1Mo–2V alloy specimen tested at room temperature in gaseous hydrogen environment. The result provided evidences of the presence of face centred cubic titanium hydride at the fracture surfaces, with discontinuous nature of crack propagation. The present work confirmed that an essentially continuous path of β phase is necessary for the occurrence of slow crack growth in gaseous hydrogen. Metallographic and fractographic observation leave little doubt that cracks propagates along the α–β interface rather than through stable α phase.     

Effect of microwave power on diamond-like carbon films deposited using electron cyclotron resonance chemical vapor deposition

Diamond-like carbon (DLC) films have been deposited using electron cyclotron resonance chemical vapor deposition (ECR-CVD) under various microwave power conditions. Langmuir probe measurement and optical emission spectroscopy (OES) were used to characterize the ECR plasma, while the films were characterized using Raman and infrared (IR) spectroscopies, hardness and optical gap measurements. It was found that the ion density and all signal peaks in the optical emission (OE) spectra increased monotonously following the increase in microwave power. Raman spectra and optical gap measurements indicate that the films become more graphitic with lower content of sp³-hybridized carbon atoms as the microwave power was increased. IR and hardness measurements indicate a reduction in hydrogen content and decrease in hardness for the film produced at relatively high microwave powers. A deposition mechanism is described which involved the ion bombardment of film surfaces and hydrogen–surface interactions. The deposition rate of DLC film is correlated to the ion density and CH₃ density.     

The Effect of Filler Loading and Epoxidation on Paper-Sludge-Filled Natural Rubber Composites

The effect of filler loading and epoxidation on curing characteristics, dynamic properties, tensile properties, morphology, and rubber-filler interactions of paper-sludge-filled natural rubber compounds have been studied. Two different types of natural rubber, SMR L and ENR 50, having 0% and 50% of epoxidation and conventional vulcanization were used. Paper sludge was used as a filler and the loading range was from 0 to 40 phr. Compounding was carried out using a laboratory-sized two-roll mill. The scorch time for both rubber compounds decreased with filler loading. The cure time was found to decrease with increasing filler content for SMR L vulcanizates, whereas for ENR 50, the cure time seemed to be independent of the filler loading. Dynamic properties, i.e., maximum elastic torque, viscous torque, and tan delta, increase with filler loading in both grades of natural rubber. Results also indicate that both rubbers show increment in tensile modulus but inverse trend for elongation at break and tensile strength. However, for a fixed filler loading, ENR 50 compounds consistently exhibit higher maximum torque, modulus at 100% elongation, and modulus at 300% elongation, but lower elongation at break than SMR L compounds. In the case of tensile strength, ENR 50 possesses higher tensile strength than SMR L at 10 to 20 phr, but the difference is quite small at 30 and 40 phr. These findings might be associated with better rubber-filler interaction between the polar hydroxyl group of cellulose fiber and the epoxy group of ENR 50.     

Properties Enhancement of Mengkuang Leaf Fiber/Ethylene‐Vinyl Acetate/Natural Rubber Thermoplastic Elastomer Composites by Alkaline Peroxide Bleaching Treatment

In this article, the effect of alkaline peroxide bleaching treatment using hydrogen peroxide on mengkuang leaf fiber (MLF) to the tensile, thermal properties and water absorption of thermoplastic elastomer composites based on ethylene‐vinyl acetate/natural rubber and MLF was investigated. Fiber morphology and the fiber‐matrix interface were further characterized by scanning electron microscopy (SEM). Treated composites showed better tensile properties than untreated fiber composites. SEM of the fractured surfaces of the composite specimens indicates that the bleaching treatment improved the interfacial interaction between the fiber and the matrix. The results of thermogravimetric analysis showed a higher thermal stability for treated composites than untreated composites. Furthermore, alkaline bleaching treatment has resulted in reduction of water absorption from 31% to 26% as compared with untreated composites. J. VINYL ADDIT. TECHNOL., 26:127–134, 2020. © 2019 Society of Plastics Engineers     

Study of diamond-like carbon films on LiNbO3

Diamond-like carbon (DLC) films have been successfully deposited on Y-cut LiNbO₃ substrates using the plasma enhanced CVD technique. A thin interlayer of SiC between the DLC films and the LiNbO₃ is necessary to ensure a good adhesion of the DLC films to the LiNbO₃ substrate. The physical properties and structural network of the DLC films have been investigated in detail. It is observed that the film hardness is increased with increasing the film thickness, as is the adhesion of the DLC films to the LiNbO₃ substrates. The effect of accelerating surface acoustic wave by the DLC films has been confirmed.     

Deposition of polymeric nitrogenated amorphous carbon films (a-C:H:N) using electron cyclotron resonance CVD

In this paper the deposition of polymeric nitrogenated amorphous carbon (a-C:H:N) films from a mixture of hydrogen, methane and nitrogen, using the electron cyclotron resonance chemical vapor deposition (ECR-CVD) system is reported. Rutherford backscattering spectroscopy (RBS) and elastic recoil detection analysis (ERDA) measurements were used to determine the actual amount of nitrogen, carbon and hydrogen in the films. The results showed that there is insignificant change in the atomic concentration of C but a slight decrease in the atomic concentration of H with increasing N incorporation. A slight decrease in the amount of bonded H and an increase in the C=N bond was also observed as deduced from infrared (IR) absorption measurements. The optical gap was found to decrease and the Urbach band tail width increase at larger N₂ flow ratio. The conductivity increased by three orders of magnitude compared to that of films prepared in the absence of N₂. The results suggest that the observed C=N double bond effectively bridges the aromatic rings resulting in a delocalization of carriers.     

Effects of temporal variability on HBV model calibration

This study aimed to investigate the effects of temporal variability on the optimization of the Hydrologiska Byråns Vattenbalansavedlning (HBV) model, as well as the calibration performance using manual optimization and average parameter values. By applying the HBV model to the Jiangwan Catchment, whose geological features include lots of cracks and gaps, simulations under various schemes were developed: short, medium-length, and long temporal calibrations. The results show that, with long temporal calibration, the objective function values of the Nash-Sutcliffe efficiency coefficient (NSE), relative error (RE), root mean square error (RMSE), and high flow ratio generally deliver a preferable simulation. Although NSE and RMSE are relatively stable with different temporal scales, significant improvements to RE and the high flow ratio are seen with longer temporal calibration. It is also noted that use of average parameter values does not lead to better simulation results compared with manual optimization. With medium-length temporal calibration, manual optimization delivers the best simulation results, with NSE, RE, RMSE, and the high flow ratio being 0.563 6, 0.122 3, 0.978 8, and 0.854 7, respectively; and calibration using average parameter values delivers NSE, RE, RMSE, and the high flow ratio of 0.481 1, 0.467 6, 1.021 0, and 2.784 0, respectively. Similar behavior is found with long temporal calibration, when NSE, RE, RMSE, and the high flow ratio using manual optimization are 0.525 3, −0.069 2, 1.058 0, and 0.980 0, respectively, as compared with 0.490 3, 0.224 8, 1.096 2, and 0.547 9, respectively, using average parameter values. This study shows that selection of longer periods of temporal calibration in hydrological analysis delivers better simulation in general for water balance analysis.     

Perspectives on the design and control of multiscale systems

New applications in materials, medicine, and computers are being discovered where the control of events at the molecular and nanoscopic scales is critical to product quality, although the primary manipulation of these events during processing occurs at macroscopic length scales. This motivates the creation of tools for the design and control of multiscale systems that have length scales ranging from the atomistic to the macroscopic. This paper describes a systematic approach that consists of stochastic parameter sensitivity analysis, Bayesian parameter estimation applied to ab initio calculations and experimental data, model-based experimental design, hypothesis mechanism selection, and multistep optimization.