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71.
In this study, an energetic binder is synthesized via ring opening copolymerization of ε‐caprolactone with poly (glycidyl nitrate) (PGN) of low molecular weight (Mn = 1350 g mol?1) as a macroinitiator to form triblock copolymer polycaprolactone‐PGN‐polycaprolactone (PCL‐PGN‐PCL) (Mn = 4128 g mol?1). The effects of catalyst type and its concentration, reaction time, and solvent are investigated in this polymerization reaction. The resulting triblock copolymer is characterized by Fourier transform infrared spectroscopy (FT‐IR), nuclear magnetic resonance spectroscopy (NMR), gel permeation chromatography (GPC), differential scanning calorimetry (DSC), and thermal gravimetric analysis (TGA). The DSC result shows that the glass transition temperature of triblock copolymer (Tg = ?50°C) is lower than PGN (Tg = ?35°C). Also, the decomposition kinetics of this energetic binder is studied by DSC, TGA, and its derivative (DTG). An advanced isoconversional method is applied for kinetic analysis. Activation energy is calculated by Flynn‐Wall‐Ozawa (FWO) and Kissinger methods. The resulting activation energy from Kissinger method for the first and the second steps are 42.98 and 74.56 kJ mol?1, respectively. Also, it is found from FWO results that the activation energy for the copolymer increases with degradation degree (α). 相似文献
72.
Comparative characteristics of aramide fiber reinforced plastics (AFRP) made by laser cutting or machining are presented. It is found that the strength of the specimens cut out by laser is 4–25% higher, while the moisture absorption is at least 2 times lower as compared to those cut out by machining. The deviation of the cutting edge size for AFRP 2 mm thick does not exceed 0.4 mm. Calculated and experimental data are given. The possibilities and conditions of cutting the AFRP up to 6 mm thick are determined.Translated from Mekhanika Kompozitnykh Materialov, Vol. 35, No. 3, pp. 375–384, May–June, 1999. 相似文献
73.
锂离子电池在高电压下会导致严重的电解液分解以及不稳定的正极与电解质界面问题,严重制约高电压正极材料的商业化.粘结剂不仅可以将正极活性材料和导电炭紧密粘结在集流体上,还对构建电解质与正极之间的多尺度相容性界面起积极作用,因此,粘结剂的优化可以有效解决上述难题.本文提出了高电压锂离子电池正极粘结剂需具备的必要条件,如:粘结性能和机械性能优异,具有出色的电化学稳定性和热力学稳定性以及良好的离子和电子传输能力等.综述了近些年来高电压正极粘结剂的研究及发展现状,通过天然粘结剂和合成粘结剂对目前已报道的高电压粘结剂进行了评述,介绍了各种粘结剂对电极的粘结性能和包覆以及对锂离子电池性能的影响机制,重点阐述了粘结剂分子结构中的极性基团与活性物质间的相互作用,如氢键和离子-偶极相互作用,并讨论了设计开发高电压正极粘结剂的途径以及展望了高电压正极粘结剂的发展前景. 相似文献
74.
《Surface and interface analysis : SIA》2018,50(4):496-505
Focusing in the photographic archive of Julián Carrillo (México), a microstructural analysis of surface photography was carried on to prove the feasibility of atomic force microscopy to identify the binder used in the manufactured ancient photography. It has been identified 2 structural groups in which known binders may be classified, one of them is associated with gelatin and the other one to albumen and collodion. The former group present a higher roughness values than the second one, being able to identify the binder by means of its morphology aspect related with the width of linear traces. From the obtained results, it has been observed that atomic force microscopy is a very good technique to properly identify the binder used in a photograph according to the surface morphology and roughness values. 相似文献
75.
Intr0ductionRcccntl}.n1uchprogrcsshasbcc11n1adcinthcscIcctivcCOh\'drogcnationproducingliglltolcfinsvIas}'ngasb}'dct'clopingasilicalitc-2zcolitcsupp0rtcdFccatal\'st.Ithasbccllshox\llthatasilicaIitc-2zcoIitcsupportcdFccatal\'stpromotcdb}'aIkalin1ctalandMnOdispla}sadcsirabIcolcfil1sclccti\'it}(asl1ighas7()%)andadcsirablcCOcont'crsion(muchhighcrthan7O%)\\ithabett.,rcactionlifconst,ca.I1~31.Ho\\cvcr-thcundcsirablcstrcl1gthofSi-2zcolitcisunsuitabIcforitsapplicatiOninindustry-\\hichsIlouldbci… 相似文献
76.
The relative merits of using a diol-based sol–gel precursor as a binder in the fabrication of barium titanate ceramics made by die-pressing a mixed oxide starting powder have been investigated. The characteristics of powder compacts were compared to samples prepared using a conventional PVB organic binder. The green strength of pellets with the PVB binder was higher than for samples containing the gel, but strength after binder burnout from gel samples was double that of pellets made with PVB. The gel led to improvements in densification during sintering, but these were most noticeable at low sintering temperatures and at intermediate stages of densification. After sintering for 2 h at 1150C, the gel-containing samples reached 75% of theoretical density, some 5% more than for the organic polymer binder. Sintering at 1300C for 2 h, gave a sintered density of ~96% of theoretical density using the gel additive, which was only 2% higher than for the conventional PVB binder system. The decomposition characteristics of the gel were investigated by TGA, FTIR and GC-MS techniques. 相似文献
77.
We report herein on the effect of the PVdF binder on the stability of composite LiCoO2 electrodes at elevated temperatures in 1 M LiPF6 EC/EMC solutions at open circuit conditions. The structure and morphology of composite LiCoO2 electrodes with different combinations of electrode components (LiCoO2 active material, PVdF binder, carbon black and current collector) were evaluated by Raman spectroscopy, X-ray diffraction and SEM. The content of Co ions in the electrolyte solutions was determined by ICP. A new effect was discovered, namely, a detrimental impact of the contact between PVdF and LiCoO2 on the stability of the active mass. The formation of surface Co3O4 and dissolution of Co ions at elevated temperatures is accelerated at the contact points between the active mass and the binder. The effect of water content in the electrolyte solutions on the stability of LiCoO2 was also studied. The presence of water (and/or HF) is a necessary condition for the accelerated dissolution of Co ions from the active mass. LiCoO2 oxidizes the solvents at elevated temperatures thus forming CO2. 相似文献
78.
Marie E Chevalier Y Eydoux F Germanaud L Flores P 《Journal of colloid and interface science》2005,290(2):406-418
The crystallization of paraffins from their solution at low temperature was investigated in the presence of ethylene-vinyl acetate (EVA) copolymers that allow the control of the size of the crystals. Depending on the type of solvent and distribution of the paraffin lengths, the mechanisms of crystal formation and growth are different. Precipitation of the EVA prior to the paraffins leads to the nucleation of a large number of crystals, whereas the adsorption of EVA on the surface of the growing crystals slows down the crystal growth. EVA can act either as a nucleating agent or as a growth inhibitor. These two mechanisms were identified from the analysis of the temperature of crystallization (cloud point), the chemical composition of the crystals, and the observations of the crystal habit. The EVA was able to co-crystallize with the paraffins in crystals of an orthorhombic structure and the melting enthalpies of the crystalline paraffin did not depend significantly on their neighborhood. The energies of interaction between the different paraffinlike components are close to each other, so that minor changes of the experimental conditions may lead to dramatic effects. This is the basic rationale for the large behavioral diversity observed in these systems. 相似文献
79.
L. Lorenzo P. Encinas M. L. Tascón M. D. Vázquez C. de Francisco P. Sánchez-Batanero 《Journal of Solid State Electrochemistry》1997,1(3):232-240
An electrochemical study of several solids, such as MnCl2 · 4 H2O(s), MnF3(s), Fe2O3(s), Fe3O4(s) and MnO2(s), using carbon paste electrodes with electrolytic binders, is described. Results obtained have been compared with results
of earlier electrochemical experiments to carry out the characterization of technological material, such as manganese ferrite.
The voltammograms obtained represent the “electrochemical spectra” of solid or dissolved substances that can be used to characterize
the material without previous solubilization, as charge transfer processes can proceed in the solid or dissolved state, depending
on the solubility in the binder used.
Received: 9 December 1996 / Accepted: 14 April 1997 相似文献
80.
T. Tsugoshi T. Nagaoka K. Hino T. Arii M. Inoue Y. Shiokawa K. Watari 《Journal of Thermal Analysis and Calorimetry》2005,80(3):787-789
Summary A new EGA-MS instrument consisted of a combination of skimmer interface with no change of evolved gaseous species and IAMS (Ion Attachment Mass Spectrometry) with no fragmentation during the ionization has been developed successfully. As its application of evolved gaseous species from PVA as firing process of alumina ceramics binder, the method has indicated detection of gaseous species which have not been detected with Py-GC-MS. 相似文献