Experimental evaluation of the interfacial properties of carbon nanotube coated carbon fiber reinforced hybrid composites

A floating catalyst chemical vapor deposition (CVD) unit was utilized to grow CNT onto the surface of carbon fiber (CF). The surface morphology of the resultant fibers, CNT population density and alignment pattern were found to be depended on the CNT growth temperature, growth time, and atmospheric conditions within the CVD chamber. In contrast to the neat‐CF reinforced composites, improved interfacial shear strength (IFSS) between CF and matrix were obtained when the surface of CF was coated by CNT. Particularly, CF treatment condition for CNT‐coating with 700°C reaction temperature and 30 min reaction time has shown a considerable increase in IFSS approximately of 45% over that of the untreated fiber from which it was processed. The proper justification of fiber–matrix adhesion featured by composite interfacial properties was explained through IFSS. POLYM. COMPOS., 36:1941–1950, 2015. © 2014 Society of Plastics Engineers     

Synthesis,Characterization, Cytotoxicity and Detailed HSA Interaction of New Zinc(II) Complexes Containing Dithiocarbamate and Heterocyclic N-donor Ligands

[Zn(ph-dtc)(bpy)]Cl (1) and [Zn(ph-dtc)(phen)]Cl (2) (where bpy = 2,2′-bipyridine, phen = 1,10-phenanthroline and ph-dtc = phenylacetichydrazidedithiocarbamate) were synthesized and characterized by elemental analysis and spectroscopic methods (FT–IR, UV–Vis and ¹H NMR). Zn(II) complexes were examined in biological tests in vitro using MCF-7 breast cancer cell line. Both complexes showed significant cytotoxic activity against human breast cancer MCF-7 cells. The interaction of above compounds with Human Serum Albumin (HSA) was investigated by means of various spectroscopic (at pH ～ 7.4 in Tris–HCl buffer medium) and molecular docking methods. The fluorescence data showed that 1 and 2 quench the intrinsic fluorescence of HSA through a static quenching procedure. The binding constants (K_b) and the number of binding sites (n ～ 1) were calculated. The thermodynamic analysis suggested that hydrophobic interaction played major roles in the binding of 1 or 2 to HSA. The distance r between protein and the above-mentioned compounds was obtained according to fluorescence resonance energy transfer. The conformational changes of protein secondary structure in the presence of Zn(II) complexes were proven using UV–Vis absorption and circular dichroism techniques. Also, docking results confirmed the spectroscopic results.     

Green Synthesis of Silver Nanoparticles through Reduction with Solanum xanthocarpum L. Berry Extract: Characterization, Antimicrobial and Urease Inhibitory Activities against Helicobacter pylori

A green synthesis route for the production of silver nanoparticles using methanol extract from Solanum xanthocarpum berry (SXE) is reported in the present investigation. Silver nanoparticles (AgNps), having a surface plasmon resonance (SPR) band centered at 406 nm, were synthesized by reacting SXE (as capping as well as reducing agent) with AgNO(3) during a 25 min process at 45 °C. The synthesized AgNps were characterized using UV-Visible spectrophotometry, powdered X-ray diffraction, and transmission electron microscopy (TEM). The results showed that the time of reaction, temperature and volume ratio of SXE to AgNO(3) could accelerate the reduction rate of Ag(+) and affect the AgNps size and shape. The nanoparticles were found to be about 10 nm in size, mono-dispersed in nature, and spherical in shape. In vitro anti-Helicobacter pylori activity of synthesized AgNps was tested against 34 clinical isolates and two reference strains of Helicobacter pylori by the agar dilution method and compared with AgNO(3) and four standard drugs, namely amoxicillin (AMX), clarithromycin (CLA), metronidazole (MNZ) and tetracycline (TET), being used in anti-H. pylori therapy. Typical AgNps sample (S1) effectively inhibited the growth of H. pylori, indicating a stronger anti-H. pylori activity than that of AgNO(3) or MNZ, being almost equally potent to TET and less potent than AMX and CLA. AgNps under study were found to be equally efficient against the antibiotic-resistant and antibiotic-susceptible strains of H. pylori. Besides, in the H. pylori urease inhibitory assay, S1 also exhibited a significant inhibition. Lineweaver-Burk plots revealed that the mechanism of inhibition was noncompetitive.     

Effects of Ramadan fasting on cardiovascular risk factors: a prospective observational study

ABSTRACT: BACKGROUND: Previous research has shown that Ramadan fasting has beneficial effects on cardiovascular risk factors, however there are controversies. In the present study, the effect of Ramadan fasting on cardiovascular risk factors has been investigated. METHOD: This is a prospective observational study that was carried out in a group of patients with at least one cardiovascular risk factor (including history of documented previous history of either coronary artery disease (CAD), metabolic syndrome or cerebro-vascular disease in past 10 y). Eighty two volunteers including 38 male and 44 female, aged 29--70 y, mean 54.0 [PLUS-MINUS SIGN] 10 y, with a previous history of either coronary artery disease, metabolic syndrome or cerebro-vascular disease were recruited. Subjects attended the metabolic unit after at least 10 h fasting, before and after Ramadan who were been fasting for at least 10 days. A fasting blood sample was obtained, blood pressure was measured and body mass index (BMI) was calculated. Lipids profile, fasting blood sugar (FBS) and insulin, homocysteine (hcy), high-sensitivity C-reactive protein (hs-CRP) and complete blood count (CBC) were analyzed on all blood samples. RESULTS: A significant improvement in 10 years coronary heart disease risk (based on Framingham risk score) was found (13.0 [PLUS-MINUS SIGN] 8 before Ramadan and 10.8 [PLUS-MINUS SIGN]7 after Ramadan, P <0.001, t test).There was a significant higher HDL-c, WBC, RBC and platelet count (PLT), and lower plasma cholesterol, triglycerides, LDL-c, VLDL-c, systolic blood pressure, body mass index and waist circumference after Ramadan (P <0.05, t test). The changes in FBS, insulin,Homeostasis Model Assessment Insulin Resistance (HOMA-IR), hcy, hs-CRP and diastolic blood pressure before and after Ramadan were not significant (P >0.05, t test). CONCLUSIONS: This study shows a significant improvement in 10 years coronary heart disease risk score and other cardiovascular risk factors such as lipids profile, systolic blood pressure, weight, BMI and waist circumference in subjects with a previous history of cardiovascular disease.     

Synthesis and Crystal Structures of a Lanthanum(III) 1D Polymer and a Mixed-Ligand Cerium(III) Binuclear Complex Derived from Pyridine-2,6-dicaboxylic Acid

Lanthanum(III) and cerium(III) complexes of pyridine-2,6-dicaboxylic acid (H₂Pydc) have been prepared and their crystal structures were determined by X-ray crystallography. The single crystal analysis reveals that the lanthanum(III) complex, 1 is polymeric consisting of {[La(Pydc)₂(H₂O)₂]·4H₂O} _n units linked through carboxylate oxygen atoms and exhibiting nine coordination number. Intermolecular O–H···O hydrogen bonds produce R ₁ ¹ (6), R ₄ ⁴ (16) and R ₄ ⁴ (20) rings, which lead to three-dimensional polymeric chains. The crystal structure of the cerium(III) complex, 2 [{Ce(Pydc)₃}{Ce(Pydc)(HO–CH₂CH₂–OH)(H₂O)₃}·6H₂O)] shows that the complex is a mixed-ligand binuclear system in which one cerium coordinated to three Pydc molecules, while the other cerium is bound to one Pydc, one oxygen atom of the other Pydc, one ethylene glycol and three water molecules. Each of the two Ce(III) ions is nine coordinated. Intermolecular O–H···O hydrogen bonds produce R ₂ ² (8) and R ₂ ² (20) rings, which lead to three-dimensional polymeric chains. The complexes were further investigated using elemental analysis, FTIR spectroscopy and thermogravimetric analysis.     

<Emphasis Type="SmallCaps">l</Emphasis>-Lysine derived novel optically active poly(ester-imide)/clay nanocomposites: study on synthesis and characterization

A new optically active poly(ester-imide) (PEI) was synthesized from the interfacial polymerization of Ethyl l-lysine-N,N′-ditrimellitoyl diacyl chloride with bis phenol A. Ultrasonic irradiation was applied to compose nanocomposites from the synthetic polymer and different ratios of organo-modified montmorillonite (MMT). The formation of PEI was confirmed by ¹H NMR, FT–IR spectroscopy, specific rotation, and elemental analysis. The resulting nanocomposites were characterized by FT–IR, powder X-ray diffraction (XRD), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA). The results indicated that the composites were dispersed homogeneously in PEI matrix on nanoscale. An improvement in heat stability is indicated from TGA analysis.     

Kinetic study of propane dehydrogenation and side reactions over Pt–Sn/Al2O3 catalyst

The kinetics of reactions involved in dehydrogenation of propane to propylene over Pt–Sn/Al₂O₃ catalyst was studied. The simultaneous deactivation of individual dehydrogenation, hydrogenolysis and cracking sites was also studied. A model was developed to obtain the transient conversion of propane, product selectivity and catalytic site activity. The dehydrogenation reaction was considered as the main reaction governing propane and hydrogen concentrations along the reactor. Catalytic test runs were performed in a fixed-bed quartz reactor. The kinetic expressions developed for the main and side reactions were verified by integral and a combination of integral–differential analysis of reactor data, respectively, and the kinetic parameters were obtained. The deactivation of the active sites for the three reactions was found to follow a first-order independent decay law. The rate constants of deactivation were found to decrease in the order of dehydrogenation, hydrogenolysis and cracking. Noncatalytic thermal cracking was found to be comparable to the catalytic route resulting in a very low apparent deactivation rate constant for cracking reaction.     

Two advanced styrene‐butadiene/polybutadiene rubber blends filled with a silanized silica nanofiller for potential use in passenger car tire tread compound

Styrene‐butadiene rubber (SBR) and polybutadiene rubber (BR) were mixed together (75:25 by mass) to produce two SBR/BR blends. The blends were reinforced with a precipitated amorphous white silica nanofiller the surfaces of which were pretreated with bis(3‐triethoxysilylpropyl)‐tetrasulfide (TESPT). TESPT is a sulfur‐bearing bifunctional organosilane that chemically bonds silica to rubber. The rubbers were primarily cured by using sulfur in TESPT and the cure was optimized by adding non‐sulfur donor and sulfur donor accelerators and zinc oxide. The hardness, Young's modulus, modulus at different strain amplitudes, tensile strength, elongation at break, stored energy density at break, tear strength, cyclic fatigue life, heat build‐up, abrasion resistance, glass transition temperature, bound rubber and tan δ of the cured blends were measured. The blend which was cured with the non‐sulfur donor accelerator and zinc oxide had superior tensile strength, elongation at break, stored energy density at break and modulus at different strain amplitudes. It also possessed a lower heat build‐up, a higher abrasion resistance and a higher tan δ at low temperatures to obtain high‐skid resistance and ice and wet‐grip. Optimizing the chemical bonding between the rubber and filler reduced the amount of the chemical curatives by approximately 58% by weight for passenger car tire tread. This helped to improve health and safety at work and reduce damage to the environment. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of molecular weight and content of PDMS on morphology and properties of silicone‐modified epoxy resin

To achieve a stable blend of a bisphenol A type epoxy resin and poly(dimethylsiloxane) (PDMS), reaction between hydroxyl (OH) groups of the epoxy and silanol groups of hydroxyl‐terminated(HT) PDMS has been investigated. The chemical structures of the HTPDMS‐modified epoxies were characterized by Fourier transform infrared (FTIR) and ¹H‐ and ¹³C‐NMR spectroscopy. To allow further understanding of the influence of viscosity and content of HTPDMS on the blend morphology, four different viscosities of HTPDMS were used in three content levels. The morphologies of modified epoxy resins were observed with optical microscopy. The modified epoxies were cured with a cycloaliphatic polyamine. The morphologies of modified epoxies were investigated by using scanning electron microscopy (SEM)/energy dispersive X‐ray (EDX) technique. The cured films showed droplet in matrix morphology with different mean droplets size which was influenced by the viscosity and the content of the incorporated HTPDMS. To illustrate the effect of the morphologies of the cured samples on mechanical properties, tensile strength tests were performed. The introduction of HTPDMS into the epoxy altered the tensile behavior according to its viscosity and content. Surface properties of the cured films were evaluated by sessile drop method. The results clearly indicate that the hydrophilic surface of the epoxy turns to a hydrophobic one due to the modification with HTPDMS. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

Synthesis and characterization of linear low‐density polyethylene/sepiolite nanocomposites

Linear low‐density polyethylene (LLDPE)/sepiolite nanocomposites were prepared by melt blending using unmodified and silane‐modified sepiolite. Two methods were used to modify sepiolite: modification before heat mixing (ex situ) and modification during heat mixing (in situ). The X‐ray diffraction results showed that the position of the main peak of sepiolite remained unchanged during modification step. Infrared spectra showed new peaks confirming the development of new bonds in modified sepiolite and nanocomposites. SEM micrographs revealed the presence of sepiolite fibers embedded in polymer matrix. Thermogravimetric analysis showed that nanocomposites exhibited higher onset degradation temperature than LLDPE. In addition, in situ modified sepiolite nanocomposites exhibited higher thermal stability than ex situ modified sepiolite nanocomposites. The ultimate tensile strength and modulus of the nanocomposites were improved; whereas elongation at break was reduced. The higher crystallization temperature of some nanocomposite formulations revealed a heterogeneous nucleation effect of sepiolite. This can be exploited for the shortening of cycle time during processing. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012