Low Concentrations of Salicylic Acid Stimulate Insect Elicitor Responses in <Emphasis Type="Italic">Zea mays</Emphasis> Seedlings

Salicylic acid (SA) generally is thought to suppress jasmonic acid (JA) related signaling events. However, when we treated the roots of corn seedlings overnight with low physiological concentrations of SA (50 μM), we found a priming effect of this pretreatment on typical insect elicitor (IE)-induced responses in the leaves of these plants. IE-induced JA was more than 2-fold up regulated in SA-pretreated plants. Consequently, IE-induced volatile organic compounds (VOC) release also was significantly increased. In contrast, when corn seedlings were treated with SA overnight and then mechanically damaged, we found no significant differences in JA accumulation. We also found that the application of even lower concentrations of SA (5 μM) had no significant effect on IE-induced responses, while higher concentrations (500 μM) inhibited IE-induced JA accumulation. Likewise, shorter exposure to SA did not affect subsequent JA accumulation induced by IE or mechanical wounding. These results provide evidence for the existence of non-compatible defense priming by signaling molecules that usually are involved in a conflictive defense signaling pathway and suggests common elements in the regulation of priming plant defense responses.     

Metal ion stimulation of phospholipase D-like activity of isolated rat intestinal mitochondria

Presence of phospholipase D-like (PLD) activity in the intestinal mitochondria was identified using endogenous phospholipids as substrate. The enzyme had a pH optimum of 6.5, did not show trans-phosphatidylation activity in the presence of ethanol or butanol, and the product formed was phosphatidic acid (PA). This was confirmed by separation of reaction products by high-performance liquid chromatography and analysis of composition of the PA formed which gave phosphate/fatty acid ratio of 1∶2. PLD-like activity was further confirmed by the formation of ethanolamine and choline as products of enzyme action. This activity was stimulated by various metal ions; when stimulated by Mg²⁺ and Ba²⁺, it hydrolyzed both phosphatidylcholine and phosphatidylethanolamine, and when stimulated by Ca²⁺, it preferentially hydrolyzed phosphatidylethanolamine. There was no requirement for sodium oleate for the PLD-like activity in mitochondria. These results suggest that intestinal mitochondria have an active PLD-like enzyme which differs in certain properties from phospholipase D from other tissues.     

Stable Synthetic Bacteriochlorins for Photodynamic Therapy: Role of Dicyano Peripheral Groups,Central Metal Substitution (2H,Zn, Pd), and Cremophor EL Delivery

A series of four stable synthetic bacteriochlorins was tested in vitro in HeLa cells for their potential in photodynamic therapy (PDT). The parent bacteriochlorin (BC), dicyano derivative (NC)₂BC and corresponding zinc chelate (NC)₂BC–Zn and palladium chelate (NC)₂BC–Pd were studied. Direct dilution of a solution of bacteriochlorin in an organic solvent (N,N‐dimethylacetamide) into serum‐containing medium was compared with the dilution of bacteriochlorin in Cremophor EL (CrEL; polyoxyethylene glycerol triricinoleate) micelles into the same medium. CrEL generally reduced aggregation (as indicated by absorption and fluorescence) and increased activity up to tenfold (depending on bacteriochlorin), although it decreased cellular uptake. The order of PDT activity against HeLa human cancer cells after 24 h incubation and illumination with 10 J cm^?2 of near‐infrared (NIR) light is (NC)₂BC–Pd (LD₅₀=25 nM ) > (NC)₂BC > (NC)₂BC–Zn ≈ BC. Subcellular localization was determined to be in the endoplasmic reticulum, mitochondria and lysosomes, depending on the bacteriochlorin. (NC)₂BC–Pd showed PDT‐mediated damage to mitochondria and lysosomes, and the greatest production of hydroxyl radicals as determined using a hydroxyphenylfluorescein probe. The incorporation of cyano substituents provides an excellent motif for the enhancement of the photoactivity and photostability of bacteriochlorins as PDT photosensitizers.     

Electrochemical investigation of chromium nanocarbide coated Ti–6Al–4V and Co–Cr–Mo alloy substrates

This study investigated the electrochemical behavior of chromium nano-carbide cermet coating applied on Ti–6Al–4V and Co–Cr–Mo alloys for potential application as wear and corrosion resistant bearing surfaces. The cermet coating consisted of a highly heterogeneous combination of carbides embedded in a metal matrix. The main factors studied were the effect of substrate (Ti–6Al–4V vs. Co–Cr–Mo), solution conditions (physiological vs. 1 M H₂O₂ of pH 2), time of immersion (1 vs. 24 h) and post coating treatments (passivation and gamma sterilization). The coatings were produced with high velocity oxygen fuel (HVOF) thermal spray technique at atmospheric conditions to a thickness of 250 μm then ground and polished to a finished thickness of 100 μm and gamma sterilized. Native Ti–6Al–4V and Co–Cr–Mo alloys were used as controls. The corrosion behavior was evaluated using potentiodynamic polarization, mechanical abrasion and electrochemical impedance spectroscopy under physiologically representative test solution conditions (phosphate buffered saline, pH 7.4, 37 °C) as well as harsh corrosion environments (pH ～ 2, 1 M H₂O₂, T = 65 °C). Severe environmental conditions were used to assess how susceptible coatings are to conditions that derive from possible crevice-like environments, and the presence of inflammatory species like H₂O₂. SEM analysis was performed on the coating surface and cross-section. The results show that the corrosion current values of the coatings (0.4–4 μA/cm²) were in a range similar to Co–Cr–Mo alloy. The heterogeneous microstructure of the coating influenced the corrosion performance. It was observed that the coating impedances for all groups decreased significantly in aggressive environments compared with neutral and also dropped over exposure time. The low frequency impedances of coatings were lower than controls. Among the coated samples, passivated nanocarbide coating on Co–Cr–Mo alloy displayed the least corrosion resistance. However, all the coated materials demonstrated higher corrosion resistance to mechanical abrasion compared to the native alloys.     

Single-phase and binary phase nanogranular ferrites for magnetic hyperthermia application

The study demonstrates the performance of heating efficiency in single-phase and binary phase spinel ferrite nanosystems. Ferrimagnetic cobalt ferrite (CoFe₂O₄) (CFO) and superparamagnetic copper ferrite/copper oxide (CuFe₂O₄/CuO) (CuF) nanosystems of different particle sizes were synthesized through a microwave-assisted coprecipitation method. The heating behavior was observed in range of both field amplitudes (8-24 kA/m at 516 kHz) and frequencies (325-973 kHz at 12 kA/m). The heating efficiency was analyzed and compared by means of particle size, magnetization, effective anisotropy constant, and Néel relaxation mechanism. Indeed, the heating rate was maximized in larger ferrite particles with low effective anisotropy constant. Moreover, though the magnetization and effective anisotropy constant of single-phase CoFe₂O₄ nanoparticles were higher, the binary phase CuFe₂O₄/CuO nanosystems of similar crystallite size (28 nm) exhibited superior heating efficiency (4.21°C/s). For a field amplitude and frequency of 24 kA/m and 516 kHz, the heating rate of CuF and CFO ferrites with different crystallite sizes decreased in the order of 4.21 > 2.14 > 0.58 > 0.52°C/s for 29 nm > 25 nm > 12 nm > 15 nm, respectively. The results emphasize that binary phase ferrite nanoparticles are better thermoseeds than the single-phase ferrites for the magnetic hyperthermia application.     

Formation of Zinc–Antimony-Based Spinel Phases

Formation of spinel phases in ZnO–Sb₂O₃and ZnO–Sb₂O₃–Bi₂O₃systems is studied by the use of X-ray diffraction. The formation of nonstoichiometric Zn_2.33Sb_0.67O₄phase is observed in both the systems at ∼900°C. However, in these systems, at higher temperatures ( T ≥ 1100°C), formation of the inverse spinel phase Zn₇Sb₂O₁₂is observed. The study has been extended to understand the effect of CrO₃doping on the stability of the different spinel phases in the previously mentioned systems. Interestingly, in both the systems, samples doped with CrO₃, displayed the presence of Zn_2.33Sb_0.67O₄phase <1200°C, indicating the stabilization of the spinel phase by CrO₃.     

Investigation of dielectric properties of free standing electrospun nonwoven mat

Flexible materials with balanced dielectric as well as conductive characteristics have elucidated considerable demand in field of research where conventional dielectric or insulators can be replaced by recent advances in various electronics appliances. Our work describes the detailed analyses of dielectric properties like dielectric constant, losses, and electric modulus by means of broadband dielectric spectroscopy over frequency ranging from 0.1 Hz to 10 MHz and temperature ranging from 0 to 60 °C for poly(vinyl alcohol)‐polyaniline (PVA‐PANI) free standing electrospinning nonwoven mat. It has been contemplated that the dielectric constant was enhanced by increasing PANI concentration for complete range of frequency at room temperature. The enhanced dielectric constant value (5.14 at 0.1 Hz, 2.66 at 1 KHz, 2.58 at 10 KHz, and 2.19 at 10 MHz) was anticipated for 7 wt % loading of PANI which was attributed to the presence of dipoles and interfacial polarization enclosed by the polymers. The increased dielectric constant with PANI dosing as well as with temperature attributed to favorable interfacial polarization. Shifting of peak is noticed in the spectra of imaginary electric modulus with increase in temperature which indicates increased chain dynamics of polymers in the mat. Three‐dimensional analysis of the field emission scanning electron microscopy images was carried out by SPIP analytical software. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46121.     

Ionic‐liquid‐assisted three‐dimensional caged silica ablative nanocomposites

In this study, we demonstrated a novel three‐dimensional network of thermally stable fumed silica (FS)–resorcinol formaldehyde (RF) nanocomposites via an ionic‐liquid (IL)‐assisted in situ polycondensation process. The study involved subjecting the tailored nanocomposites to thermogravimetric analysis and oxyacetylene flame environment as per ASTM test standards for thermal ablative performance. X‐ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, high‐resolution transmission electron microscopy, Raman spectroscopy, and wettability studies were undertaken to underline the improvement correlation in the microstructure and material properties. Significant reductions in the linear ablation rate (66%) and mass ablation rate (26.6%), along with lower back‐face temperature profiles, marked enhanced ablative properties. The increased char yield (33.3%) and higher temperatures for weight losses evinced the improved thermal stability of the modified RF resin. The uniformly dispersed fused nanosilica with a glassy coating morphology on the ablative surface acted as barrier to oxidation. The results signify that the IL‐assisted modification of the RF resin with FS significantly enhanced ablative performance. A viable replacement to the conventional phenolic nanocomposites for thermal ablative applications to buy critical time for the containment and suppression of thermal‐heat‐flux threats is of paramount importance. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45328.     

Modelling of A Fluidized Bed Drier Using Artificial Neural Network

ABSTRACT

Proper modelling of a fluidized bed drier (FBD) is important to design model based control strategies. A FBD is a non-linear multivariable system with non-minimum phase characteristics. Due to the complexities in FBD conventional modelling techniques are cumbersome. Artificial neural network (ANN) with its inherent ability to “learn” and “absorb” non-linearities, presents itself as a convenient tool for modelling such systems.

In this work, an ANN model for continuous drying FBD is presented. A three layer fully connected feedfordward network with three inputs and two outputs is used. Backpropagation learning algorithm is employed to train the network. The training data is obtained from computer simulation of a FBD model from published literature. The trained network is evaluated using randomly generated data as input and observed to predict the behaviour of FBD adequately.     

n-Hexadecane hydroisomerization over Pt/ZSM-12: role of Si/Al ratio on product distribution

The crystallization of pure ZSM-12 phase was accomplished at Si/Al ratios ranging from 45 to 120 using tetraethylammonium bromide as the structure directing agent. The obtained samples were characterized by X-ray diffraction, scanning electron microscopy, temperature programmed desorption of ammonia, and nitrogen adsorption–desorption measurements at 77 K, respectively. The well characterized samples were used to prepare Pt (0.5 wt%)/ZSM-12 hydroisomerization catalysts which were employed to perform n-hexadecane isomerization reaction. The catalysts were compared in terms of their activity, selectivity and product distribution at different conversion levels obtained through variation in temperature and residence times. Thus, obtained trend for product distribution over Pt/ZSM-12 system has been discussed in terms of framework Si/Al ratio to understand its role in determining the product selectivity. ZSM-12 with Si/Al ratio of 120 depicted the highest overall selectivity and favored mono-branching while those having Si/Al ratio of 45, 60 and 90 were found to favor mutlti-branching.