Rheological and adhesion properties of acrylic pressure‐sensitive adhesives

Different pressure‐sensitive adhesives (PSAs) based on acrylic monomers were synthesized under different reaction conditions. The synthesized PSAs have good adhesive properties and without leaving any residue can be easily peeled off from the surface of a substrate. The relationship between PSAs rheological behavior and its adhesion properties (e.g., peel, tack, and shear resistance) has been studied at constant adhesive thickness. The samples were examined for their surface energy and viscoelastic characteristics. It was observed that increase in reaction temperature and reaction time results in decreased storage modulus due to lowered molecular weight, which finally leads to lower elasticity of the PSA. While the storage (G′) and loss (G″) modulus of samples increase with increased initiator concentration, the elasticity of PSA is increased as well. High G″ at high frequency (100 Hz) represents high peel strength because of higher dissipation of viscoelastic energy during debonding. The tack values increase by lowering storage modulus at 1 Hz due to higher M_e. Shear values are increased by higher storage modulus at low frequency (0.1 Hz) due to hydrogen bonding of the different components. Some parallel investigations on the surface energy of the samples showed that they have different properties because of the nature of different monomeric units with their corresponding orientations. Our results reveal that the peel strength is not affected by surface energy. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Rheology and microstructure of basil seed gum and β-lactoglobulin mixed gels

Gelling profiles and interaction between basil seed gum (BSG) and β-lactoglobulin (BLG) were characterized using dynamic rheology and scanning electron microscopy. Sequence of experimental sweeps of time–temperature, frequency, and strain were applied for BSG, BLG and BLG–BSG mixtures in the ratio of 10:1, 5:1, 2:1 & 1:2. Rheological behavior of BLG was found to be different from that of BSG and gelling point was raised during the heating period. By increasing BSG concentration, storage and loss moduli were increased and gel point was determined at about 80 °C, which was dependent of concentration and occurred during cooling period. Upon heating–cooling period (temperature sweep) of BLG–BSG mixture from 20 °C to 90 °C and coming back to original temperature, mixed gels presented a biphasic profile: the first phase, characterized by a sharp increase in the storage modulus in which gelation of BLG happened and the second phase exhibiting an increase in the storage modulus, corresponded to the build-up of a BSG network. Strain sweep results obtained for mixed gels at the end of the temperature sweep tests supported the biphasic hypothesis. The SEM results showed that BLG has a globular structure in comparison with BSG which has fibril and globular structure and the mean diameter of its globular structure was higher than that of BLG. Increasing the ratio of BSG to BLG resulted in a finer microstructure, which could retain higher water to form gel. In addition, microstructural study showed that BLG–BSG mixed is a bicontinuous network in which BSG dispersed in BLG continuous phase.     

Fabrication and characterization of a new MRI contrast agent based on a magnetic dextran–spermine nanoparticle system

This study aims to fabricate and formulate a new magnetic resonance imaging (MRI) contrast agent based on a dextran?Cspermine nanoparticulate system loaded with super paramagnetic iron oxide nanoparticles (SPION). SPION-loaded spermine?Cdextran nanoparticles were prepared according to a procedure based on the ionic gelation of dextran?Cspermine with sodium tripolyphosphate (TPP) anions. The effects of process parameters such as pH, concentration of spermine dextran, TPP to dextran?Cspermine and SPION to dextran?Cspermine weight ratios, and TPP addition rate were fully investigated to find the optimized formulation through the response surface methodology. At the optimum condition, 75% of the magnetic iron oxide nanoparticles added to the polymeric solution were entrapped in dextran?Cspermine nanoparticles. Samples were investigated by transmission electron microscopy. The mean particle size of the nanoparticles determined by particle size analyzer was found to be 65?nm at the optimum condition with zeta potential of +90?mV. The SPION-loaded dextran?Cspermine nanoparticle formulation has the same superparamagnetic properties as SPIONs and at same iron concentration the saturation magnetization (Ms) of the SPION-loaded dextran?Cspermine nanoparticles was larger than SPIONs. In vitro MRI was performed with gradient echo and spin-echo sequences at 1.5?T. By increasing of iron concentration, the T ₂ relaxation times were reduced. Thus, indicating that the saturation magnetization and r ₂ and $ r_{2}^{*} $ relaxivities were enhanced, and the contrast effects were improved in comparison to commercial SPIONs.     

Antioxidant Activity,Reaction Mechanisms,and Kinetics of Matricaria recutita Extract in Commercial Blended Oil Oxidation

Antioxidant activity, reaction mechanisms, and kinetics of Matricaria recutita crude extract (CE; total phenolics: 41 ± 2.5 mg/g, total flavonoids: 26 ± 1.4 mg/g, IC₅₀: 82.3 ± 2.8 µg/mL and reducing power: 10.45 ± 0.56 mmol Fe²⁺/mass) in comparison to tert-Butylhydroquinone during oxidation of blended vegetable oil (sunflower, soybean, and palm oil) at 120, 130, and 140°C were studied. Good correlations existed between the Rancimat oil stability index and stability indices (induction period) calculated from peroxide value, conjugated diene value, and anisidine value with no significant differences in kinetic parameters calculated from them. The temperature acceleration (Q₁₀), activation energy (E_a), frequency factor (A), enthalpy (ΔH⁺⁺), entropy (ΔS⁺⁺), and free energy of activation (ΔG⁺⁺) for oils containing crude extract were lower than for oils containing tert-Butylhydroquinone (0.0025, 0.005, 0.01, and 0.02%). Values were independent of crude extract or tert-Butylhydroquinone concentration. For crude extract and tert-Butylhydroquinone, E_a and A were well correlated with ΔH⁺⁺ and ΔS⁺⁺ values, respectively, but correlation between E_a and Q₁₀ for crude extract compared to tert-Butylhydroquinone was poor. Furthermore, the rate of Monounsaturated:Polyunsaturated fatty acids formation did not differ significantly between crude extract and tert-Butylhydroquinone, but concentrations of them did affect Monounsaturated:Polyunsaturated ratio. Based on the results obtained, crude extract decreased the rate of the oxidation reaction due to the decrease in the concentration of the activated complex and reduction in the rate at which the activated complex dissociated into oxidation products.     

Enhancement of rheological and mechanical properties of bitumen using styrene acrylonitrile copolymer

In this research, styrene acrylonitrile copolymer as a novel additive is used to modify rheological, mechanical and thermal properties of the base bitumen 70 penetration grade. Styrene acrylonitrile copolymer combines the rigidity of polystyrene with the hardness and thermal resistance of polyacrylonitrile to enhance viscoelastic property of the bitumen. To investigate the performance of the proposed mixture, shear complex module, phase angle, penetration, softening point, and reversibility of prepared samples are measured at different additive content and compared with the base bitumen. The results show that softening point of the base and modified samples are 49–86°C, respectively. The rheological properties of the base bitumen and modified samples are measured by a dynamic shear rheometer (DSR). The phase angle as elasticity measure decreases from 55° to 35° in the modified bitumen compared to the base bitumen. Generally, the experimental results showed that styrene acrylonitrile copolymer makes bitumen to be more stable at high temperatures and more flexible at low temperatures. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41875.     

Prediction and optimization of hydrogen yield and energy conversion efficiency in a non-catalytic filtration combustion reactor for jet A and butanol fuels

Hydrogen production is one of main subjects in fuel cells. The traditional method of synthesis gas production is based on fuel reforming using catalysts. The main problem of these methods is sensitivity and fast degradation of catalysts especially when fuels with high sulfur content are used. A new technique for hydrogen production is fuel-reforming using non-catalytic filtration combustion in porous media reactors. Various experimental works have been carried out to increase hydrogen production under different operating conditions such as inlet fuel velocity and equivalence ratio. First, we investigated the ability of adaptive neuro fuzzy inference system (ANFIS) for predicting the filtration combustion characteristics. Four distinct ANFIS models were developed for estimating the hydrogen yield and energy conversion efficiency for fuels of jet A and butanol. Eight different membership functions of dsigmf, gauss2mf, gaussmf, gbellmf, pimf, psigmf, trapmf and trimf were tested for training of the ANFIS networks. The results showed that the RMSE of the best developed ANFIS models for estimating of the hydrogen yield of jet fuel, hydrogen yield of butanol, conversion efficiency of jet fuel and conversion efficiency of butanol were 1.399, 1.213, 0.508 and 2.191, respectively. Moreover the R² values of 0.998, 0.998, 0.999 and 0.999 were obtained for predicting the above mentioned variables, respectively. In the second step, a novel algorithm based on imperialist competitive algorithm (ICA) was used for optimization of hydrogen yield and energy efficiency. The maximum value of hydrogen yield and energy efficiency was 50.46% and 67.88% for jet A and 47.27% and 96.93% for butanol, respectively. The results showed that the imperialist competitive algorithm is an efficient and powerful algorithm to optimize combustion processes.