Theoretical analysis of the mode coupling induced by heat of large-pitch micro-structured fibers

In this paper,a theoretical model to analyze the mode coupling induced by heat,when the fiber amplifier works at high power configuration,is proposed.The model mainly takes into consideration the mode field change due to the thermally induced refractive index change and the coupling between modes.A method to predict the largest average output power of fiber is also proposed according to the mode coupling theory.The largest average output power of a large pitch fiber with a core diameter of 190 μm and an available pulse energy of 100 mJ is predicted to be 540 W,which is the highest in large mode field fibers.     

Synthesis and electrochemical properties of regular hexahedron α-Fe2O3

Synthesis of α-Fe₂O₃ compound with regular hexahedron shape is firstly reported. X-ray diffraction and scan electron microscope are used to characterize the structure and morphology of the prepared sample, respectively. The average edge length of hexahedron is about 0.9 μm. A reaction mechanism has been proposed. The pH value is a crucial factor for the formation and shape of α-Fe₂O₃. Moreover, electrochemical impedance spectroscopy and charge-discharge test of α-Fe₂O₃ as anode material in lithium ion batteries are evaluated. The data indicate that the synthesized regular hexahedron α-Fe₂O₃ can show better electrochemical properties than that of the commercial.     

Facile Preparation of α‐Zirconium Phosphate/Polyaniline Hybrid Film for Detecting Potassium Ion in a Wide Linear Range

A novel α‐zirconium phosphate/polyaniline (α‐ZrP/PANI) hybrid film used as K⁺ ion sensor was fabricated on carbon paper by electrochemical method. Mechanisms of film formation and detection of K⁺ ions were also proposed. The exfoliated α‐ZrP was mixed with PANI and deposited on carbon paper. The resultant α‐ZrP/PANI film exhibited a good current response to K⁺ ion with different concentrations. It also showed a wide logarithmic linear response in detecting K⁺ ions in the ranges of 10^?8–10^?4 M and 10^?4–10^?2 M, respectively. The results can be attributed to the synergetic effect of α‐ZrP and PANI.     

A Novel Heterometallic Cluster-Based Coordinational Polymer with 2-[Bis-(2-hydroxy-ethyl)-Amino]-Ethanesulfonic Acid: Synthesis and Crystal Structure

A rare heterometallic cluster-based polymer [Cu₄(Hbhea)₄(μ ₂-OCH₃) K(CH₃OH))] _n ·(H₂O) _n (1) (H₃bhea = 2-[bis-(2-hydroxy-ethyl)-amino]-ethanesulfonic acid), has been synthesized and structurally determined by single crystal X-ray diffraction, elemental analysis. Crystallographic unit of 1 consists of four Cu(II), four Hbhea ligands, one methanol molecule, one methanol anion, one K ion and one crystal lattice water and formed anion cluster [Cu₄(Hbhea)₄(CH₃O)]^? which further constructed a 3-D polymer by linking the six-coordination K ions.     

Construction of the nano-carbon connections among the carbon-coated LiFe0.8Mn0.2PO4 grains by sol-gel technique

Nano-carbon connections among carbon-coated LiFe_0.8Mn_0.2PO₄ grains are successfully constructed using polyacrylic acid and sucrose as carbon sources by sol-gel method, which can improve the electrochemical performance of LiFe_0.8Mn_0.2PO₄. Samples were characterised by X-ray diffraction, scanning electron microscopy and electrochemical tests. The electrochemical tests show LiFe_0.8Mn_0.2PO₄ grains connected by nano-carbon networks obtain the discharge specific capacity of 165 mA h g^?1 at 0.1 C rate and excellent rate capability. Its specific capacity reaches 122 mA h g^?1 at 5 C rate. Its capacity retention at 5 C rate attains 97% cycled 100 cycles. Therefore the construction of nano-carbon networks offers an effective and convenient technique to improve the specific capacities and rate capabilities of electrode materials of low electronic conductivity.     

Discrimination of Thermoplastic Polyesters by MALDI-TOF MS and Py-GC/MS

The aim of this work is to discriminate thermoplastic polyester-polyethylene terephthalate (PET), polybutylene terephthalate (PBT), and polytrimethylene terephthalate (PTT), which cannot be easily identified by many methods. Both matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) and pyrolysis gas chromatography/mass spectrometry (Py-GC/MS) were applied to identify these polyesters owing to their analytical ability to determining polymers' chemical structure. The three thermoplastic polyesters can be easily distinguished by MALDI-TOF MS according to their different repeated units. Py-GC/MS was used to analyze their specific pyrolyzates. The three polyesters can be identified through their characteristic pyrolysis products as well.     

Morphological transformations of nonequilibrium assemblies of amphiphilic diblock copolymer

Amphiphilic diblock copolymer polystyrene-block-poly(ethylene oxide) (PS-PEO) assembled into nonequilibrium bicontinuous structures or mixture of vesicles, bilayers and nanorods upon rapid micellization induced by rapid addition of selective solvent (water) into the PS-PEO solutions in a common solvent (dimethyl formamide) with different concentrations. These kinetically trapped assemblies were unstable and slowly evolved into thermodynamically favorable spheres and vesicles. The addition of non-ionic surfactant Pluronic P123 upon rapid micellization generated novel nanocages and flower-like vesicles. The nanocages spontaneously transformed into tubules capped with vesicles. These novel assemblies are beyond the classic phase diagram of block copolymer self-assemblies, especially for those primarily based on thermodynamics.     

Thermal behavior of typical weak basic ion exchange resin

Thermal behaviors of typical weak basic ion exchange resins (301 and 315) were studied with thermogravimetry, elemental analysis, and Fourier transform infrared spectrometer in this study. Results indicated that there were three stages for 301 resin mass loss, the first stage and the second stage were mainly related to the decomposition of functional group, and the third stage was the decomposition of main chain. Whereas there were two stages for 315 resin mass loss, the first stage was elimination of moisture, and the second stage was the decompositions of functional group and main chain. Moreover, the decomposition of tertiary amine had three stages, the polyamine was a continuous mass loss process, and the thermostability of tertiary amine was weaker than that of polyamine.     

Pyrolysis of Hailar lignite in an autogenerated steam agent

An in situ pyrolysis process of high moisture content lignite in an autogenerated steam agent was proposed. The aim is to utilize steam autogenerated from lignite moisture as a reactant to produce fuel gas and additional hydrogen. Thermogravimetric analysis revealed that mass loss and maximum mass loss rate increased with the rise of heating rates. The in situ pyrolysis process was performed in a screw kiln reactor to investigate the effects of moisture content and reactor temperature on product yields, gas compositions, and pyrolysis performance. The results demonstrated that inherent moisture in lignite had a significant influence on the product yield. The pyrolysis of L _R (raw lignite with a moisture content of 36.9 %, wet basis) at 900 °C exhibited higher dry yield of 33.67 mL g^?1 and H₂ content of 50.3 vol% than those from the pyrolysis of the predried lignite. It was also shown that increasing reaction temperature led to a rising dry gas yield and H₂ yield. The pyrolysis of L _R showed the maximum dry yield of 33.7 mL g^?1 and H₂ content of 53.2 vol% at 1,000 °C. The LHV of fuel gas ranged from 18.45 to 14.38 MJ Nm^?3 when the reactor temperature increased from 600 to 1,000 °C.     

A Chiral Gold Nanocluster Au20 Protected by Tetradentate Phosphine Ligands

The chirality of a gold nanocluster can be generated from either an intrinsically chiral inorganic core or an achiral inorganic core in a chiral environment. The first structural determination of a gold nanocluster containing an intrinsic chiral inorganic core is reported. The chiral gold nanocluster [Au₂₀(PP₃)₄]Cl₄ (PP₃=tris(2‐(diphenylphosphino)ethyl)phosphine) has been prepared by the reduction of a gold(I)–tetraphosphine precursor in dichloromethane solution. Single‐crystal structural determination reveals that the cluster molecular structure has C₃ symmetry. It consists of a Au₂₀ core consolidated by four peripheral tetraphosphines. The Au₂₀ core can be viewed as the combination of an icosahedral Au₁₃ and a helical Y‐shaped Au₇ motif. The identity of this Au₂₀ cluster is confirmed by ESI‐MS. The chelation of multidentate phosphines enhances the stability of this Au₂₀ cluster.