Effect of Solvothermal Reaction-Time on Microstructure and Microwave Absorption Properties of Cobalt Ferrite

Cobalt ferrite is synthesized via a simple solvothermal method. Then, the effect of the degree of cobalt-ferrite growth on its morphology, structure, electromagnetic performance, and microwave absorption is studied as a function of the solvothermal reaction time. When the reaction time during synthesis is 8 h, the structure of cobalt ferrite is hollow spheres. In addition, when the reaction time is 12 h and 16 h, it becomes a submicron sphere with a diameter of 100–150 nm. With the increase of reaction time, cobalt ferrite underwent the process of cobalt ferrite formation, hollow structure formation, hollow structure disappearance, agglomeration separation and reagglomeration in 4–16 h. In general, CoFe₂O₄-8h shows better microwave absorption-the effective absorption bandwidth is 9.84 GHz (6–15.84 GHz) for a thickness of 1.72–3.72 mm. This represents a minimum return loss of −47.24 dB. A better understanding of both the synthesis parameters and the relationship between structure and electromagnetic properties can open new possibilities for applications and the development of microwave absorbing materials.     

Synthesis and characterization of a novel,pH-responsive,bola-based dynamic crosslinked fracturing fluid

Fracturing fluids are important media for hydraulic fracturing. Typically, the fluids are gelled using a polymeric gelling agent. Technological improvements over the years have focused primarily on improving the rheological performance, thermal stability, and the clean-up of crosslinked gels. In this study, novel supramolecular assembly of a low-damage fracturing fluid combining an ionic polymer gel (hydroxypropyl trimethylammonium chloride guar-cationic guar) and a bola surfactant fluid (bola carboxylate polypropylene glycol) is carried out and it is reported to have improved properties and special characteristics due to the synergistic effects of the dual systems, which are different from those of polymer gels and surfactant fluids. The viscosity of the fracturing fluid shows a sudden increase upon an increase in temperature and excellent self-assembly recovery after shearing. The fracturing fluid exhibits pH-responsive viscosity changes and low permeability impairment, due to the formation of a network structure and supramolecular microspheres at different pH values.

Fracturing fluids are important media for hydraulic fracturing.     

Non-detergent isolation of a cyanobacterial photosystem I using styrene maleic acid alternating copolymers

Photosystem I (PSI) from the thermophilic cyanobacterium Thermosynechococcus elongatus (Te) is the largest membrane protein complex to have had its structure solved by X-ray diffraction. This trimeric complex has 36 protein subunits, over 380 non-covalently bound cofactors and a molecular weight of ∼1.2 MDa. Previously, it has been isolated and characterized in a detergent micelle using the non-ionic detergent n-dodecyl-β-d-maltoside (DDM). We have now succeeded in isolating this complex without the use of detergents, using styrene–maleic acid (SMA) alternating copolymer. Intriguingly, a partially esterified copolymer formulation (SMA 1440, Cray Valley) was found to be most efficient in cyanobacterial thylakoid membranes. A host of biochemical, biophysical and functional assays have been applied to characterize this non-detergent form of PSI, referred to as a SMA Lipid Particle (SMALP). The PSI-SMALP has a lower sedimentation coefficient compared to PSI-DDM, suggesting decreased density or a more extended particle shape. We show the 77 K fluorescence maximum for PSI is red shifted in PSI-SMALP compared to PSI-DDM, suggesting a more native orientation of PsaA/B associated chlorophyll. We report that PSI-SMALPs are functional despite the selective loss of one transmembrane subunit, PsaF. This loss may reflect a more labile interaction of the PSI core and PsaF, or a selective displacement during copolymer insertion and/or assembly. PSI-SMALP exhibited decreased reduction kinetics with native recombinant cytochromes c₆, while non-native horse heart cytochrome c shows faster reduction of PSI-SMALP compared to PSI-DDM. This is the largest membrane protein isolated using SMA copolymers, and this study expands the potential use of this approach for the isolation and characterization of large supramolecular complexes.

Trimeric Photosystem I (PSI) from the thermophilic cyanobacterium Thermosynechococcus elongatus (Te) is the largest membrane protein complex to be encapsulated within a SMALP to date.     

An MR-Conditional High-Torque Pneumatic Stepper Motor for MRI-Guided and Robot-Assisted Intervention

Magnetic resonance imaging allows for visualizing detailed pathological and morphological changes of soft tissue. MR-conditional actuations have been widely investigated for development of image-guided and robot-assisted surgical devices under the Magnetic resonance imaging (MRI). This paper presents a simple design of MR-conditional stepper motor which can provide precise and high-torque actuation without adversely affecting the MR image quality. This stepper motor consists of two MR-conditional pneumatic cylinders and the corresponding supporting structures. Alternating the pressurized air can drive the motor to rotate each step in 3.6° with the motor coupled to a planetary gearbox. Experimental studies were conducted to validate its dynamics performance. Maximum 800 mN m output torque is achieved. The motor accuracy independently varied by two factors: motor operating speed and step size, was also investigated. The motor was tested within a 3T Siemens MRI scanner (MAGNETOM Skyra, Siemens Medical Solutions, Erlangen, Germany) and a 3T GE MRI scanner (GE SignaHDx, GE Healthcare, Milwaukee, WI, USA). The image artifact and the signal-to-noise ratio (SNR) were evaluated for study of its MRI compliancy. The results show that the presented pneumatic stepper motor generated 2.35% SNR reduction in MR images. No observable artifact was presented besides the motor body itself. The proposed motor test also demonstrates a standard to evaluate the pneumatic motor capability for later incorporation with motorized devices used under MRI.     

The temporal course of the influence of anxiety on fairness considerations

This study investigated the potential causes of anxious people's social avoidance. The classic ultimatum game was utilized in concert with electroencephalogram recording. Participants were divided into two groups according to levels of trait anxiety as identified by a self‐report scale. The behavioral results indicate that high‐anxious participants were more prone to reject human‐proposed than computer‐proposed unequal offers compared to their low‐anxious counterparts. The event‐related potential results indicate that the high‐anxious group showed a larger feedback‐related negativity when receiving unequal monetary offers than equal ones, and a larger P3 when receiving human‐proposed offers than computer‐proposed ones, but these effects were absent in the low‐anxious group. We suggest anxious people's social avoidance results from hypersensitivity to unequal distributions during interpersonal interactions.     

Branched EHNBR and its properties with enhanced low-temperature performance and oil resistance

Epoxide nitrile butadiene rubber (ENBR) was prepared via in situ epoxidation from nitrile butadiene rubber (NBR) with acetic acid and hydrogen peroxide. ENBR had been selectively hydrogenated in the presence of a homogeneous Wilkinson catalyst. The hydrogenated epoxide nitrile butadiene rubber (EHNBR) and ENBR were characterized by infra-red and proton nuclear magnetic resonance. No change was noted in the epoxy content of the polymer after the reaction. The catalyst is highly selective in reducing carbon–carbon double bonds in the presence of epoxy groups. DSC analysis reveals the T_g of ENBR varied linearly with molar epoxide content and the T_g value increased by 0.82 °C per mol%. It also found that the introduction of epoxy groups can effectively reduce the extent of crystallization by impairing the regularity of the molecular chain, but crystalline structure was difficult to completely eliminate. Therefore, anhydrides were selected as ring-opening reagents to react with epoxy groups in EHNBR. The products, branched EHNBR, were characterized by infra-red and proton nuclear magnetic resonance. The conversion rate of the epoxide group was calculated by ¹H NMR. The glass transition temperature of EHNBR-g-heptyl group was −34.1 °C, and its DSC curve demonstrated no crystal structure. The coefficient of cold resistance under compression of EHNBR grafted propyl ester was 0.36, which represented a superior low-temperature performance. Furthermore, residual epoxy groups and ester groups extremely enhanced the oil resistance of HNBR.

Epoxide nitrile butadiene rubber (ENBR) was prepared via in situ epoxidation from nitrile butadiene rubber (NBR) with acetic acid and hydrogen peroxide.     

Magnetically separable and reusable rGO/Fe3O4 nanocomposites for the selective liquid phase oxidation of cyclohexene to 1,2-cyclohexane diol

A series of magnetically separable rGO/Fe₃O₄ nanocomposites with various amounts of graphene oxide were successfully prepared by a simple ultrasonication assisted precipitation combined with a solvothermal method and their catalytic activity was evaluated for the selective liquid phase oxidation of cyclohexene using hydrogen peroxide as a green oxidant. The prepared materials were characterized using XRD, FTIR, FESEM, TEM, HRTEM, BET/BJH, XPS and VSM analysis. The presence of well crystallized Fe₃O₄ as the active iron species was seen in the crystal studies of the nanocomposites. The electron microscopy analysis indicated the fine surface dispersion of spherical Fe₃O₄ nanoparticles on the thin surface layers of partially-reduced graphene oxide (rGO) nanosheets. The decoration of Fe₃O₄ nanospheres on thin rGO layers was clearly observable in all of the nanocomposites. The XPS analysis was performed to evaluate the chemical states of the elements present in the samples. The surface area of the nanocomposites was increased significantly by increasing the amount of GO and the pore structures were effectively tuned by the amount of rGO in the nanocomposites. The magnetic saturation values of the nanocomposites were found to be sufficient for their efficient magnetic separation. The catalytic activity results show that the cyclohexene conversion reached 75.3% with a highest 1,2-cyclohexane diol selectivity of 81% over 5% rGO incorporated nanocomposite using H₂O₂ as the oxidant and acetonitrile as the solvent at 70 °C for 6 h. The reaction conditions were further optimized by changing the variables and a possible reaction mechanism was proposed. The enhanced catalytic activity of the nanocomposites for cyclohexene oxidation could be attributed to the fast accomplishment of the Fe²⁺/Fe³⁺ redox cycle in the composites due the sacrificial role of rGO and its synergistic effect with Fe₃O₄, originating from the conjugated network of π-electrons in its surface structure. The rapid and easy separation of the magnetic nanocomposites from the reaction mixture using an external magnet makes the present catalysts highly efficient for the reaction. Moreover, the catalyst retained its activity for five repeated runs without any drastic drop in the reactant conversion and product selectivity.

A series of magnetically-separable and reusable rGO/Fe₃O₄ nanocomposites were successfully synthesized for the selective liquid-phase oxidation of cyclohexene to 1,2-cyclohexane-diol.     

Porous organic polymer with in situ generated palladium nanoparticles as a phase-transfer catalyst for Sonogashira cross-coupling reaction in water

A new Pd nanoparticle loaded and imidazolium-ionic liquid decorated organic polymer of Pd@PTC-POP was readily fabricated via a Pd(PPh₃)₄ catalysed in situ one-pot Suzuki cross-coupling reaction between imidazolium attached dibromobenzene and 1,3,5-tri(4-pinacholatoborolanephenyl)benzene. Besides the high thermal and chemical stability, the obtained Pd@PTC-POP can be used as a highly active and reusable phase-transfer solid catalyst to promote the Sonogashira coupling reaction in water. The obtained results indicate that the Pd@PTC-POP herein could create a versatile family of solid phase transfer catalysts for promoting a broad scope of reactions carried out in water.

A Pd nanoparticle loaded and imidazolium-ionic liquid decorated organic polymer, which can be used as a highly active phase-transfer solid catalyst to promote the Sonogashira reaction in water, was reported.