Monte Carlo simulation study of the effect of chain tacticity on demixing of polyethylene/polypropylene blends

The molecular origin of the demixing behavior for 50: 50 (wt/wt) polyethylene/polypropylene (PE/PP) with different tacticity of PP at the melts (473 K) was investigated by Monte Carlo simulation of coarse-grained polymer model. Isotactic (iPP), atactic (aPP) and syndiotactic (sPP) polypropylenes were used for blending with PE. Coarse-graining polymer chains were represented by 50 beads, corresponding to C₁₀₀H₂₀₂ and C₁₅₀H₃₀₂ for PE and PP, respectively. The simulation was performed on a high coordination lattice incorporating short-range intramolecular interactions from the Rotational Isomeric State (RIS) model and long-range intermolecular interactions Lennard-Jones (LJ) potential function of ethane and propane units. Chain dimensions, the characteristic ratio (C _n ) and self-diffusion coefficient (D) of PE in the blends are sensitive to the stereochemistry of PP chains. Compared with neat PE melts, PE dimension was relatively unchanged in PE/iPP and PE/aPP blends but slightly decreased in PE/sPP blends. PP dimension was increased in PE/iPP and PE/aPP mixture but decreased in PE/sPP blend in comparison with neat PP melts. In addition, diffusion of PE and PP chains in PE/PP mixture was decreased and increased, respectively, compared to the pure melts. Interchain pair correlation functions were used to detect the immiscibility of the blends. The tendency of demixing of PE/aPP and PE/iPP blends were weaker than that of PE/sPP blend.     

Asymmetric Brønsted Acid Catalyzed Substitution of Diaryl Methanols with Thiols and Alcohols for the Synthesis of Chiral Thioethers and Ethers

An enantioselective addition of thiols and alcohols to aza‐ortho‐quinone methides, starting from diaryl methanols, was developed. The asymmetric additions occur under mild reaction conditions in the presence of chiral phosphoric acids and furnish the corresponding adducts with excellent yields and enantioselectivities.     

Decarbonylative Silylation of Esters by Combined Nickel and Copper Catalysis for the Synthesis of Arylsilanes and Heteroarylsilanes

An efficient nickel/copper‐catalyzed decarbonylative silylation reaction of carboxylic acid esters with silylboranes is described. This reaction provides access to structurally diverse silanes with high efficiency and excellent functional‐group tolerance starting from readily available esters.     

One-pot synthesis of substituted indolo[1,2-a]quinolines under transition-metal-free conditions

A simple and efficient one-pot synthesis of substituted indolo[1,2-a]quinolines under transition-metal-free conditions has been developed. When 2-fluorobenzaldehyde was treated with substituted 2-methylindoles in the presence of Cs₂CO₃, the desired products were typically obtained in good to excellent yields. This reaction sequence involves a nucleophilic aromatic substitution and a Knoevenagel condensation reaction. Our mechanistic investigation revealed that both reactions could proceed as an intermolecular reaction in the first step.     

Treatment in Swelling Solutions Modifying Cellulose Fiber Reactivity – Part 1: Accessibility and Sorption

Of prime importance in reactions involving insoluble cellulosic fibers is the sorption of reagents, which is governed by their degrees of accessibility in substrates. Swelling treatments of cellulosics in alkali solutions alter substrate accessibility leading to changes in their reactivity. In this paper, the first of a two-part series, we collate and examine the results from various studies involving different techniques to characterize modifications in cellulosic fibers after swelling treatments in alkali solutions. Results from measurements of structure and accessibility in fibers with techniques such as water retention, inverse size exclusion chromatography (ISEC), iodine sorption, fiber diameters, and fiber-splitting propensities indicate that the influence of swelling treatments on fiber structure/accessibility is differs with alkali type. The results show that a non-uniform rather than uniform distribution of reagents within structures is a more accurate representation of reactions involving swollen cellulosic fibers. Hence, the observed changes in cellulose-fiber reactivity are governed by the degrees of fiber swelling, and reagent sorption and accessibility during swelling treatments.     

The high concentration and uniform distribution of diamond particles in Ni‐diamond composite coatings by sediment co‐deposition

Ni‐diamond composite coatings with high concentration and uniform distribution of diamond particles were prepared by using sediment co‐deposition (SCD) technique from Watts‐type electrolyte without any additives. The surface and cross‐section morphology was evaluated by optical microscope (OM) and scanning electron microscopy (SEM). It was demonstrated that the Ni‐monolayer diamond composite coatings ~40 ± 5 µm was successfully prepared by the new developed setup for SCD technique. Using this new developed setup, high concentration and uniform distribution of diamond particles of Ni‐monolayer diamond composite coatings were easily fabricated. The wear resistance and cutting performance of obtained composite coatings were also investigated. The results revealed that anti‐wear and cutting performance is superior to those prepared via conventional co‐electrodeposition (CED) technique and pure Ni coatings. In the SCD process, with the increasing diamond content, the wear resistance is approximately the same, and the cutting performance decreases. Therefore, not only the diamond particle content is responsible for the wear resistance and cutting performance, the distribution of diamond particles is also very important factor. Copyright © 2014 John Wiley & Sons, Ltd.     

Hybrid inertial accelerated algorithms for split fixed point problems of demicontractive mappings and equilibrium problems

Numerical Algorithms - Our contribution in this paper, we introduce and analyze two new hybrid algorithms by combining Mann iteration and inertial method for solving split fixed point problems of...     

Monte Carlo simulation of the structure of mono- and bidisperse polyethylene nanocomposites

The structure of bidisperse polyethylene(PE) nanocomposite mixtures of 50:50(by mole) of long and short chains of C160H322/C80H162 and C160H322/C40H82 filled with spherical nanoparticles were investigated by a coarse-grained, on lattice Monte Carlo method using rotational isomeric state theory for short-range and Lennard-Jones for long-range energetic interactions. Simulations were performed to evaluate the effect of wall-to-wall distance between fillers(D), polymer-filler interaction(w) and polydispersity(number of short chains in the mixture) on the behavior of the long PE chains. The results indicate that long chain conformation statistics remain Gaussian regardless of the effects of confinement, interaction strength and polydispersity. The various long PE subchain structures(bridges, dangling ends, trains, and loops) are influenced strongly by confinement whereas monomer-filler interaction and polydispersity did not have any impact. In addition, the average number of subchain segments per filler in bidisperse PE nanocomposites decreased by about 50% compared to the nanocomposite system with monodisperse PE chains. The presence of short PE chains in the polymer matrix leads to a reduction of the repeat unit density of long PE chains at the interface suggesting that the interface is preferentially populated by short chains.