Production of hyaluronic‐acid‐based cell‐enclosing microparticles and microcapsules via enzymatic reaction using a microfluidic system

This article describes the preparation of cell‐enclosing hyaluronic acid (HA) microparticles with solid core and microcapsules with liquid core through cell‐friendly horseradish peroxidase (HRP)‐catalyzed hydrogelation. The spherical vehicles were made from HA derivative possessing phenolic hydroxyl moieties (HA‐Ph) cross‐linkable through the enzymatic reaction by extruding cell‐suspending HA‐Ph aqueous solution containing HRP from a needle of 180 μm in inner diameter into the ambient coaxial flow of liquid paraffin containing H₂O₂ in a microtubule of 600 μm in diameter. By altering the flow rate of liquid paraffin, the diameters of gelatin and HA‐Ph microparticles were varied in the range of 120–220 μm and 100–300 μm, respectively. The viability of the enclosed human hepatoma HepG2 cells in the HA‐Ph microparticles of 180 μm in diameter was 94.2 ± 2.3%. The growth of the enclosed HepG2 cells was enhanced by decreasing the HRP concentration. The microcapsules of 200 μm in diameter were obtained by extruding HA‐Ph aqueous solution containing thermally liquefiable cell‐enclosing gelatin microparticles of 150 μm in diameter using the same microfluidic system. The enclosed cells grew and filled the cavity within 10 days. Spherical tissues covered with a heterogeneous cell layer were obtained by degrading the microcapsule membrane using hyaluronidase after covering the surface with a heterogeneous cell layer. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43107.     

A novel stimuli-responsive magnetic hydrogel based on nature-inspired tragacanth gum for chemo/hyperthermia treatment of cancerous cells

Journal of Polymer Research - Derivatives of formyl pyrazole were synthesized by the reaction of acetophenone, 4-methyl acetophenone, 3-acetyl furan, 3-acetyl thiophen and phenyl hydrazine...     

Numerical investigation of grooves effects on the thermal performance of helically grooved shell and coil tube heat exchanger

Heat exchangers are integral parts of important industrial units such as petrochemicals, medicine and power plants. Due to the importance of systems energy consumption, different modifications have been applied on heat exchangers in terms of size and structure. In this study, a novel heat exchanger with helically grooved annulus shell and helically coiled tube was investigated by numerical simulation. Helically grooves with the same pitch of the helical coil tube and different depth are created on the inner and outer wall of annulus shell to improve the thermal performance of heat exchanger. In the first section, thermal performance of the shell and coil heat exchanger with the helical grooves on its outer shell wall was compared with same but without helical grooves. At the second section, helically grooves created on both outer and inner wall of the annulus shell with different groove depths. The results showed that the heat exchanger with grooves on both inner and outer shell wall has better thermal performance up to 20% compared to the heat exchanger with grooves on only outer shell wall. The highest thermal performance achieves at lower flow rates and higher groove depths whereas the pressure drop did not increase significantly.     

A fundamental study of chitosan/PEO electrospinning

A highly deacetylated (97.5%) chitosan in 50% acetic acid was electrospun at moderate temperatures (25-70 °C) in the presence of a low content of polyethylene oxide (10 wt% PEO) to beadless nanofibers of 60-80 nm in diameter. A systematic quantitative analysis of the solution properties such as surface tension, conductivity, viscosity and acid concentration was conducted in order to shed light on the electrospinnability of this polysaccharide. Rheological properties of chitosan and PEO solutions were studied in order to explain how PEO improves the electrospinnability of chitosan. Positive charges on the chitosan molecule and its chain stiffness were considered as the main limiting factors for electrospinability of neat chitosan as compared to PEO, since surface tension and viscosity of the respective solutions were similar. Various blends of chitosan and PEO solutions with different component ratios were prepared (for 4 wt% total polymer content). A significant positive deviation from the additivity rule in the zero shear viscosity of chitosan/PEO blends was observed and believed to be a proof for strong hydrogen bonding between chitosan and PEO chains, making their blends electrospinnable. The impact of temperature and blend composition on the morphology and diameter of electrospun fibers was also investigated. Electrospinning at moderate temperatures (40-70 °C) helped to obtain beadless nanofibers with higher chitosan content. Additionally, it was found that higher chitosan content in the precursor blends led to thinner nanofibers. Increasing chitosan/PEO ratio from 50/50 to 90/10 led to a diameter reduction from 123 to 63 nm. Producing defect free nanofibrous mats from the electrospinning process and with high chitosan content is particularly promising for antibacterial film packaging and filtration applications.     

High Productive Ethylene Trimerization Catalyst Based on CrCl<Subscript>3</Subscript>/SNS Ligands

Abstract  

Methylaluminoxane (MAO)-activated chromium (III) complexes of tridentate SNS ligands of the form (RSCH₂–CH₂)₂NH (R = alkyl, aryl) have been prepared and tested for the trimerization of ethylene to 1-hexene. The effect of ethylene pressure, Al/Cr ratio and S donor substitution on 1-C6 selectivity and productivity has been examined. It is shown that when the substitution on S is pentyl group it will lead to the highest productivity, 174200 g 1-C6/g Cr h, due to the synergistic effect of this group.     

Synthesis and characterization of exfoliated poly(styrene‐co‐methyl methacrylate) nanocomposite via miniemulsion atom transfer radical polymerization: an activators generated by electron transfer approach

Exfoliated poly(styrene‐co‐methyl methacrylate) nanocomposites were synthesized using activators generated by electron transfer for atom transfer radical polymerization (AGET ATRP). Miniemulsion polymerization was used for its abundant advantages to encapsulate inorganic materials and eliminate organic solvents from products for environmentally friendly purposes. Cetyltrimethylammonium bromide (CTAB) as a cationic surfactant, which is an effective surfactant at higher temperatures, was used to stabilize the miniemulsion system. Successful miniemulsion AGET ATRP was carried out by using 4,4'‐dinonyl‐2,2'‐bipyridine (dNbPy) as a hydrophobic ligand. Formation of monodispersed droplets and particles with sizes in the range of 200nm was examined by dynamic light scattering (DLS). Conversion and molecular weight study were also carried out using gravimetry and gel permeation chromatography, respectively. By adding clay content, a decrease in the conversion and molecular weight of the nanocomposites are observed. However, an increase in the PDI values of nanocomposites was observed by the addition of nanoclay content. Thermogravimetric analysis results demonstrate that thermal stability of all the nanocomposites in comparison with the neat copolymer increases. Differential scanning calorimetry results show that T_g decreases by increasing clay content. Monodisperse distribution of spherical shape particles with sizes in the range of ∼ 200 nm was demonstrated by using scanning electron microscopy images of nanocomposite containing 1 wt% of nanoclay, which is more compiled with DLS results. Transmission electron microscopy results shows well‐dispersed exfoliated clay layers in the polymer matrix of PSMNM 1, which is coincidence with X‐ray diffraction data. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Preparation of tailor‐made polystyrene nanocomposite with mixed clay‐anchored and free chains via atom transfer radical polymerization

Tailor‐made polystyrene nanocomposite with mixed free and clay‐attached polystyrene chains was synthesized using atom transfer radical polymerization. Vinylbenzyl trimethylammonium chloride having a double bond, which could be incorporated into polystyrene chains by a grafting through process, was used as a nanoclay modifier. Conversion and molecular weight evaluation was carried out using gas chromatography and gel permeation chromatography, respectively. The thermogravimetric analysis results confirmed the elevated thermal stability of the nanocomposites in comparison with the neat polystyrene sample. Additionally, the T_g increases by clay loading was confirmed by differential scanning calorimetry (DSC). The difference in the degradation temperature of C? Br bond in attached and free polystyrene chains was well revealed in DSC thermograms. Finally, a lower clay loading resulted in an exfoliated structure as proved by X‐ray diffraction and transmission electron microscopy results. © 2010 American Institute of Chemical Engineers AIChE J, 2011     

Dynamic behavior of particles across flame propagation through micro-iron dust cloud with thermal radiation effect

In this investigation, a theoretical study is performed to analyze the dynamic behavior of particles across flame propagation through a two-phase mixture consisting of micro-iron particles and air. In the first step for calculation of the particle velocity profile, the Lagrangian approach of particle motion is employed, and then thermophoretic, gravitational and buoyancy forces are taken into consideration. In order to simulate the temperature profile for the thermophoretic force, it is assumed that the flame structure consists of three zones: preheat, reaction, and post flame (burned). It should be noted that the radiative heat-transfer equation is employed to describe the thermal radiation exchanged between the burned zone and the preheat zone. In the resumption, a control volume above the leading edge of the combustion zone is considered and the change in the particle number density in this volume is obtained via the balance of particle mass fluxes passing through it. The results show that the induced thermal radiation plays a significant role in increasing the mixture temperature all over the preheat zone, and that the particle velocity profile and the concentration distribution of particles as a function of distance from the leading edge of the combustion zone also have considerable consistency with published experimental data.     

Effect of nano-sized calcium carbonate on cure kinetics and properties of polyester/epoxy blend powder coatings

Today's strict environmental laws pose significant challenges for coating's formulators to look for eco-friendly products. Powder coatings, particularly polyester/epoxy blends have demonstrated their ability as alternatives to traditional solvent-borne coatings. Recently, the use of nanoparticles such as nano-CaCO₃ (nCaCO₃) has been suggested as a beneficial strategy towards powder coating application with improved properties. Here, we study the effect of nCaCO₃ on morphology, cure behavior, adhesion and hardness of polyester/epoxy systems. The nanoparticles shape, size and dispersion state were investigated through X-ray diffraction (XRD), transmission electron microscopy (TEM) and scanning electron microscopy (SEM) methods. Furthermore, isothermal cure characterization of the neat and filled systems was performed using a torque rheometer. The most important finding based on the rheological studies was the catalytic effect of nCaCO₃ on cure reaction of polyester/epoxy, leading to the shorter curing time. Moreover, the kinetic analyses of rheograms revealed a marked decrease in the activation energy of the cure process upon raising nCaCO₃ content. Interestingly, pull-off adhesion and hardness tests showed that the hardness and adhesion strength were dramatically increased by the addition of nCaCO₃ into the polyester/epoxy system compared to pure blend resin. Therefore, considering the strong competition in powder coating market, the use of nCaCO₃ as a commercial and inexpensive nanofiller is necessary not only to reduce the dwell time which has benefits in terms of the energy consumption and economics, but also to improve the performance of final polyester/epoxy coating.