Magnetic composites obtainment based on styrene polymers

Three styrene‐based matrices for hybrid composites with ferrite have been obtained by emulsion polymerization in the presence of a tensioactive system: sodium n‐dodecylbenzene sulfate (C₁₂H₂₅C₆H₄SO₃Na) as anionic agent and poly(oxyethylene) nonylphenyl ether [C₉H₁₉C₆H₄(OCH₂CH₂)₃₀OH] as nonionic tensioactive agent. The system assures the steadiness of the emulsion during the reaction and the stability of the latices. The surfactants act as a protective colloid component and thickening agents determining an optimum viscosity and conditions for the further catching of the inorganic oxide with magnetic properties. The obtained polystyrene and styrene copolymers with acrylamide and methacrylamide were analyzed by elemental analysis, IR spectroscopy, DSC, and their viscosity data have been characterized. The size as well as the magnetic properties of composites were also appreciated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4133–4141, 2006     

Progress in high performance,low emissions,and exergy recovery in internal combustion engines

This article first gives a brief review of thermal engines designed for terrestrial transportation since the 1900s. We then outline the main developments in the state of the art and knowledge about internal combustion engines, focusing on the increasingly stringent pollution constraints imposed since the 1990s. The general concept of high‐energy performance machines is analyzed from the energy, exergy, and public health point of view and illustrated with typical examples of clean energy production and zero emissions. Whereas the energy analysis revealed high potential of waste heat recovery from both exhaust and cooling system, the exergetic analysis revealed much higher recovery potential from exhaust gases. The exergy content of exhaust gases was observed to be within the range from 10.4% to 20.2% of the fuel energy. The cooling exergy is within the range from 1.2% to 3.4% of the fuel energy. The article concludes with some perspectives for the emergence of an economic model that could be applied to land‐based transport systems in the framework of energy transition by 2030. Copyright © 2016 John Wiley & Sons, Ltd.     

Cu—Fe—Zr三元系统基的非铁合金

提出了微合金化铜基合金在真空条件下优选工艺和通过减少ＣｕＦｅ２Ｐ合金中Ｐ含量及用Ｚｒ，Ａｌ，Ｍｇ，Ｚｎ等对ＣｕＦｅ２Ｐ进行微合金化改善其性能，实验发现，对微合金化ＣｕＦｅＺｎ合金，高的铁锆比（Ｆｅ／Ｚｒ）与性能有良了的对应关系，而对微合金化ＣｕＦｅＺｒ合金，低的较宽范围的Ｆｅ／Ｚｒ与性能有良好的对应关系。     

18F-FDG PET/MRI Imaging in a Preclinical Rat Model of Cardiorenal Syndrome—An Exploratory Study

Cardiorenal syndrome (CRS) denotes the bidirectional interaction of chronic kidney disease and heart failure with an adverse prognosis but with a limited understanding of its pathogenesis. This study correlates biochemical blood markers, histopathological and immunohistochemistry features, and 2-deoxy-2-fluoro-D-glucose positron emission tomography (¹⁸F-FDG PET) metabolic data in low-dose doxorubicin-induced heart failure, cardiorenal syndrome, and renocardiac syndrome induced on Wistar male rats. To our knowledge, this is the first study that investigates the underlying mechanisms for CRS progression in rats using ¹⁸F-FDG PET. Clinical, metabolic cage monitoring, biochemistry, histopathology, and immunohistochemistry combined with PET/MRI (magnetic resonance imaging) data acquisition at distinct points in the disease progression were employed for this study in order to elucidate the available evidence of organ crosstalk between the heart and kidneys. In our CRS model, we found that chronic treatment with low-dose doxorubicin followed by acute 5/6 nephrectomy incurred the highest mortality among the study groups, while the model for renocardiac syndrome resulted in moderate-to-high mortality. ¹⁸F-FDG PET imaging evidenced the doxorubicin cardiotoxicity with vascular alterations, normal kidney development damage, and impaired function. Given the fact that standard clinical markers were insensitive to early renal injury, we believe that the decreasing values of the ¹⁸F-FDG PET-derived renal marker across the groups and, compared with their age-matched controls, along with the uniform distribution seen in healthy developing rats, could have a potential diagnostic and prognostic yield in cardiorenal syndrome.     

Hybrid Coordination Networks for Removal of Pollutants from Wastewater

The adsorption properties of two coordination polymers, resulting from the reaction of divalent metal (Ca²⁺ or Co²⁺) salts with (2-carboxyethyl)(phenyl)phosphinic acid, are presented in this paper. The structural and textural characterization before and after adsorption experiments is presented. The adsorbent materials were prepared using the hydrothermal procedure. The compound Ca[O₂P(CH₂CH₂COOH)(C₆H₅)]₂ (CaCEPPA) has a layered topology, with the phenyl groups oriented into the interlayer space and crystallizes in the monoclinic system. Compound Co₂[(O₂P(CH₂CH₂COO)(C₆H₅)(H₂O)]₂·2H₂O (CoCEPPA) has a 1D structure composed of zig-zag chains. The adsorption performances of CaCEPPA and CoCEPPA materials were tested in the removal of cadmium and lead from aqueous solutions. The optimum pH of ions adsorption was found to be five for both adsorbent materials. Pseudo-first and second-order kinetic models were used for fitting kinetic experimental data, and Langmuir and Freundlich isotherms were used for modeling the equilibrium experimental data. The pseudo-second-order kinetic model and Langmuir isotherm best described the adsorption of Cd and Pb ions onto the studied materials, judging from the results of the error function (correlation coefficient, sum of square error, chi-square test, and average relative error) analysis. The studied materials present a higher affinity for Cd ions compared with the adsorption capacity developed for the removal of Pb ions from aqueous solutions. CoCEPPA showed the highest adsorption performance in the removal process of metal ions from aqueous solutions compared with CaCEPPA (q_m = 54.9 mg Cd²⁺/g of CoCEPPA, q_m = 36.5 mg Cd²⁺/g of CaCEPPA).     

Quantum-SAR Extension of the Spectral-SAR Algorithm. Application to Polyphenolic Anticancer Bioactivity

Aiming to assess the role of individual molecular structures in the molecular mechanism of ligand-receptor interaction correlation analysis, the recent Spectral-SAR approach is employed to introduce the Quantum-SAR (QuaSAR) “wave” and “conversion factor” in terms of difference between inter-endpoint inter-molecular activities for a given set of compounds; this may account for inter-conversion (metabolization) of molecular (concentration) effects while indicating the structural (quantum) based influential/detrimental role on bio-/eco- effect in a causal manner rather than by simple inspection of measured values; the introduced QuaSAR method is then illustrated for a study of the activity of a series of flavonoids on breast cancer resistance protein.     

Revision of the NaBO2–H2O phase diagram for optimized yield in the H2 generation through NaBH4 hydrolysis

The binary phase diagram NaBO₂–H₂O at ambient pressure, which defines the different phase equilibria that could be formed between borates, end-products of NaBH₄ hydrolysis, has been reviewed. Five different solid borates phases have been identified: NaBO₂·4H₂O (Na[B(OH)₄]·2H₂O), NaBO₂·2H₂O (Na[B(OH)₄]), NaBO₂·2/3H₂O (Na₃[B₃O₄(OH)₄]), NaBO₂·1/3H₂O (Na₃[B₃O₅(OH)₂]) and NaBO₂ (Na₃[B₃O₆]), and their thermal stabilities have been studied. The boundaries of the different Liquid + Solid equilibria for the temperature range from −10 to 80 °C have been determined, confirming literature data at low temperature (20–50 °C). Moreover the following eutectic transformation, Liq. → Ice + NaBO₂·4H₂O, occurring at −7 °C, has been determined by DSC. The Liquid–Vapour domain has been studied by ebullioscopy. The invariant transformation Liq. → Vap. + NaBO₂·2/3H₂O has been estimated at 131.6 °C. This knowledge is paramount in the field of hydrogen storage through NaBH₄ hydrolysis, in which borate compounds were obtained as hydrolysis reaction products. As a consequence, the authors propose a comparison with previous NaBO₂–H₂O binary phase diagrams and its consequence related to hydrogen storage through NaBH₄ hydrolysis.     

Magnetic properties of magnetite nanoparticles coated with mesoporous silica by sonochemical method

In this paper we present the magnetic properties of mesoporous silica-coated Fe₃O₄ nanoparticles. The coating of magnetite nanoparticles with mesoporous silica shell was performed under ultrasonic irradiation. The obtained mesoporous silica-coated magnetite nanoparticles were characterized by powder X-ray diffraction, focused ion beam-scanning electron microscopy, nitrogen adsorption-desorption isotherms and vibrating sample magnetometer. The hysteretic behavior was studied using first-order reversal curves diagrams. The X-ray diffraction result indicates that the extreme chemical and physical conditions created by acoustic cavitations have an insignificant effect on crystallographic structural characteristic of magnetite nanoparticles. Changes in the coercivity distributions of the magnetite nanoparticles were observed on the first-order reversal curves diagrams for the samples with coated particles compared with the samples containing uncoated particles of magnetite. The coated particles show an increased most probable coercivity of about 20% compared with the uncoated particles which can be associated with an increased anisotropy due to coating even if the interaction field distribution measured on the diagrams are virtually identical for coated/uncoated samples.     

Polymerization in a magnetic field. XV Some azo‐initiators behavior in a high magnetic field

The effect of a high magnetic field of 7 T on styrene polymerization reactions was taken under study. The intervened magnetokinetic modifications are correlated to the system of radical initiation, respectively: benzoyl peroxide, 2, 2′‐azobis(2‐methylpropionitrile), 4, 4′‐azobis(4‐cyanopentanoic acid), and 1,1′‐azobis (cyclohexan‐1‐carbonitrile). The reaction products are also characterized from the viewpoint of their molecular weights correlated with the reaction conditions, as well as their thermal stability. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1025–1031, 2005