Solvothermal Synthesis of a Nano-sized Aza-aromatic Base Adduct of a Cadmium(II) 4,4-Difluoro-1-phenyl-1,3-butandionate Coordination Compound

A new nano-structured cadmium(II) coordination compound, [Cd(phen)(dfpb)₂] (1) (phen?=?1,10-phenanthroline, dfpb?=?4,4-difluoro-1-phenyl-1,3-butandion), was synthesized by a solvothermal method and produced a coordination polymer in the nano-size range. The new nanostructure was characterized by scanning electron microscopy, X-ray powder diffraction elemental analysis and IR spectroscopy. Compound 1 was structurally characterised by single crystal X-ray diffraction. The single crystal structure shows a coordination number for the Cd ion of six with two N-donor atoms from the phen ligand and four O-donors from the two dfpb moieties. Self-assembly occurs by CH····F–C and π–π stacking interactions. The supramolecular features in these complexes are controlled by weak directional intermolecular interactions.     

Fabricating Janus membranes via physicochemical selective chemical vapor deposition

Membranes with asymmetric wettability-Janus membranes-have recently received considerable attention for a variety of critical applications. Here, we report on a simple approach to introduce asymmetric wettability into hydrophilic porous domains. Our approach is based on the physicochemical-selective deposition of polytetrafluoroethylene (PTFE) on hydrophilic polymeric substrates. To achieve selective deposition of PTFE, we inhibit the polymerization reaction within the porous domain. We prefill the substrates with glycerol, containing a known amount of free radical inhibitor, and utilize initiated chemical vapor deposition (iCVD) for the polymerization of PTFE. We show that the glycerol/inhibitor mixture hinders the deposition of PTFE within the membrane pores. As a result, the surface of the substrates remains open and porous. The fabricated Janus membranes show stable wetting-resistant properties, evaluated through sessile drop contact angle measurements and direct contact membrane distillation (DCMD).     

Adsorption of Pb and Cd in rice husk and their immobilization in porous glass-ceramic structures

Rice husk, an agricultural waste, is abundantly available in many countries such as China, India, Brazil, US, and South East Asia. Despite the massive production of rice husk, it is mainly disposed to landfill. In this work, utilization of rice husk for a potential waste-water treatment is evaluated, along with subsequent encapsulation of the adsorbed heavy metals (Pb and Cd) inside a porous glass-ceramic. Vitrified bottom ash (another source of waste) was mixed with foaming agents in dif- ferent weight ratios (40:60, 50:50, and 60:40) to prepare a glass matrix for encapsulation of Pb-/Cd-loaded rice husk. It was shown that using 40 wt% vitrified bottom ash with 60 wt% foaming agents leads to a foam glass with the best pore size distribution. Therefore, this batch was further mixed with 70 volume% (5 wt%) heavy metal-loaded rice husk and was heat-treated at 750°C for 3 hours. The final glass-ceramic porous structure was char acterized using SEM, XRD, compression test, and it was shown that it is safe to be used as it passes the EN12457-2 leaching test.     

Surfactant-Assisted Dispersion of MWCNTs in Epoxy Resin Used in CFRP Strengthening Systems

The epoxy resin used as the bonding agent in carbon fiber-reinforced polymer (CFRP) strengthening systems was modified by the infusion of multiwalled carbon nanotubes (MWCNTs). Two types of surfactants, Triton X-100 and C₁₂E₈, were used to disperse the nanotubes in the epoxy resin employing ultrasonic mixing. Dynamic mechanical analysis and tensile tests were conducted to study the effect of the surfactant-assisted dispersion of nanotubes on the thermal and mechanical properties of epoxy composites. The morphology of the epoxy composites was interpreted using scanning electron microscopy (SEM). Moreover, the effect of surfactant treatment on the structure of nanotubes was investigated by Fourier transform infrared (FT-IR). Based on the experimental results, the tensile strength and the storage modulus of the epoxy resin were increased by 32% and 26%, respectively, by the addition of MWCNTs. This was attributed to the homogeneous dispersion of nanotubes in the epoxy resin according to the SEM images. Another reason for the enhancement in the tensile properties was the reinforced nanotube/epoxy interaction as a result of the surfactant anchoring effect which was proved by FT-IR. A moderate improvement in the glass transition temperature (T _g) was recorded for the composite fabricated using Triton X-100, which was due to the restricted molecular motions in the epoxy matrix. To characterize the temperature-dependent tensile behavior of the modified epoxy composites, tensile tests were conducted at elevated temperatures. It was revealed that the MWCNT modification using surfactant substantially improves the tensile performance of the epoxy adhesive at temperatures above the T _g of the neat epoxy.     

A simple model for predicting solid concentration distribution in binary‐solid liquid fluidized beds

A simple mathematical model for predicting the solid concentration profile in binary‐solid liquid fluidized beds is presented. The main assumption is that the solid concentration distribution follows the logistic function, which is supported by the literature. Various equations have been derived to solve key system quantities (e.g., bed expansion height, length and position of the transition zone). In contrast to previous models that often involve adjustable parameters and strongly rely on the availability of experimental data, the present model only requires inputs of fluid and particle properties, operating conditions, and correlations for dispersion and slip velocity. The results showed that the model is applicable to different binary‐solid systems that have size and/or density differences. The model's capability of predicting the layer inversion phenomenon has also been demonstrated. The model is simple but proves capable of accurately predicting key information for the design, operation and scale up of liquid fluidized beds. © 2016 American Institute of Chemical Engineers AIChE J, 63: 469–484, 2017     

Encapsulation Efficiency of Food Flavours and Oils during Spray Drying

Microencapsulation is a rapidly expanding technology which is a unique way to package materials in the form of micro- and nano-particles, and has been well developed and accepted within the pharmaceutical, chemical, food and many other industries. Spray drying is the most commonly used encapsulation technique for food products. A successful spray drying encapsulation relies on achieving high retention of the core materials especially volatiles and minimum amounts of the surface oil on the powder particles for both volatiles and non-volatiles during the process and storage. The properties of wall and core materials and the prepared emulsion along with the drying process conditions will influence the efficiency and retention of core compounds. This review highlights the new developments in spray drying microencapsulation of food oils and flavours with an emphasis on the encapsulation efficiency during the process and different factors which can affect the efficiency of spray drying encapsulation.     

Preparation of thermally stable,low dielectric constant,pyridine‐based polyimide and related nanofoams

Reaction of 6‐chloronicotinoyl chloride with p‐phenylene diamine resulted in preparation of a dichloro diamide compound. Subsequently, chloro displacement of this compound with 4‐amino phenoxy groups led to production of a new pyridine‐based ether diamine named as N,N′‐(1,4‐phenylene)bis(6‐(4‐aminophenoxy) nicotinamide). Novel polyimide was prepared through polycondensation reaction of the diamine with hexafluoroisopropylidene diphthalic anhydride (6‐FDA) via two‐step imidization method. In addition, new nanoporous polyimide films were produced through graft copolymerization of polyimide as the continuous phase with a thermally labile poly (propylene glycol) oligomer as the labile phase. The grafted copolymers were synthesized using reaction of the diamine and 6‐FDA in the presence of poly (propylene glycol) 2‐bromoacetate as thermally labile constituent via a poly(amic acid) precursor process. The labile block was decomposed via thermal treatment to release inert molecules that diffused out of the matrix to leave pores with diameters between 30 and 60 nm. The structures and properties of polyimide and polyimide nanofoams were characterized by different techniques including ¹H‐NMR, FTIR, TGA, DMTA, SEM, TEM, dielectric constant, and tensile strength measurement. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Synthesis and Characterization of Copper(II)–Cysteine/SiO2–Al2O3 as an Efficient and Reusable Heterogeneous Catalyst for the Oxidation of Aromatic Alcohols

In the present study, heterogeneous copper(II)–cysteine/SiO₂–Al₂O₃ catalyst was successfully prepared by a simple adsorption method. The physical and chemical properties of Cu(II)–cysteine/SiO₂–Al₂O₃ were investigated by X-ray diffraction, thermal gravimetric analyzer, FT–IR spectroscopy, Brunauer–Emmett–Teller, UV–Vis spectroscopy, scanning electron microscopy and atomic absorption spectrometer. The obtained composite was effectively employed as catalyst for selective oxidation of various aromatic alcohols to corresponding aldehydes in high yields using hydrogen peroxide as an oxidant under mild condition. The catalyst can be recycled over five times without significant loss of activity.