Dynamic mechanical and morphological studies of homopolymer/block copolymer blends

A triblock copolymer of styrene-butadiene-styrene (SBS) was blended with a high and a low molecular weight polybutadiene [designated as PB(H) and PB(L), respectively]. Electron micrographs of these blends show that PB(L) was solubilized into the butadiene domains of the SBS, while PB(H) was present in a separate phase. Dynamic mechanical data of the SBS&PB(L) blends indicate the presence of an intermediate loss peak between those of the glass transitions of the styrene and butadiene blocks in SBS, which can be attributed to the slippage of untrapped entanglements of PB(L) chains. Similar data for blends containing PB(H) also show an intermediate loss peak, which is, however, due to crystallization and melting of the polycisbutadiene chains. The peak due to the primary glass transition of the butadiene phase was shifted to lower temperatures upon incorporation of PB(L) as a result of plasticization effect of PB(L). The same transition for PB(H) blends is split into a doublet because of the presence of the homopolymer in a separate phase. Dynamic mechanical data for cross-linked blends were also taken for comparison.     

Severe plastic deformation of amorphous alloys: I. Structure and mechanical properties

The basic regularities of variation in the structure and mechanical properties of amorphous Ni₄₄Fe₂₉Co₁₅Si₂B₁₀ alloy at severe plastic deformation (SPD) in a Bridgman cell at different temperatures are considered. It is shown that SPD is accompanied by homogeneous nanocrystallization, which is caused by the plastic flow mode. The transition from inhomogeneous mode of plastic flow to a qualitatively different one has been detected. The SPD structural model of deformational “dissolving” of crystals is proposed to explain why nanocrystals no more than 10 nm in size are observed during SPD. It is found that thermally activated nanocrystallization may occur at very low temperatures (77 K) under very high stress and with a high concentration of excess free volume.     

Improving polymeric microemulsions with block copolymer polydispersity

Recent experiments have demonstrated that block copolymers are capable of stabilizing immiscible homopolymer blends producing bicontinuous microemulsion. The stability of these polymeric alloys requires the copolymer to form flexible, nonattractive monolayers along the homopolymer interfaces. We predict that copolymer polydispersity can substantially and simultaneously improve the monolayers in both of these respects. Furthermore, polydispersity should provide similar improvements in systems, such as colloidal suspensions and polymer/clay composites, that utilize polymer brushes to suppress attractive interactions.     

Spherical polyelectrolyte block copolymer micelles: Structural change in presence of monovalent salt

Spherical polyelectrolyte block copolymer micelles were investigated as a function of added NaCl salt concentration using Small-Angle Neutron Scattering (SANS) and Light Scattering (LS). The micelles are formed by the self-association of charged-neutral copolymers made of a long deuterated polyelectrolyte moiety (NaPSS_d)₂₅₁ and a short hydrophobic moiety (PEP)₅₂. In presence of salt, the core shape and the aggregation number of the micelles are not affected. The hydrodynamic radius of the micelle is found to be identical to the radius of the whole micelle deduced from neutron scattering and thus the hydrodynamic radius is a valid measure of the corona thickness. At the lowest salt concentrations investigated the thickness of the corona, R_s, remains essentially constant and a contraction is observed above an added-salt concentration c_s of 2×10^-2 M where this crossover concentration corresponds to the average ionic strength of the free counterions in the corona. The contraction takes place while maintaining a rod-like behavior of the chains at short scale and obeys to: R_s c_s^-0.18. The exponent 0.18 suggests an electrostatic persistence length proportional to the Debye screening length.     

Morphology-mechanical property relationship of a polystyrene-polybutadiene-polystyrene block copolymer and its blends with homopolymers

The morphology-mechanical property relation was investigated on a polystyrene-polybutadiene-polystyrene (SBS) block copolymer and its blends with polystyrenes (PS) and polybutadienes (PB) cast from a THF/MEK mixture (T/M) and a cyclohexane/benzene mixture (C/B). As-cast films with alternating lamellar morphology such as SBS (T/M) always show high moduli and “plastic-torubber” transitions, while those with PS-dispersed-in-PB-matrix morphology always exhibit low moduli and crosslinked rubberlike behavior. All these systems undergo strain-induced softening, accompanying breakdown of glassy PS domains, and show rubberlike behavior, regardless of the sample prehistory. However, upon annealing under adequate conditions, all these softened systems eventually revert to their original morphology and behavior.     

Tetramethylpolyarylate-polyarylate block copolymer: Synthesis and miscibility with polyarylate and poly(styrene-co-acrylonitrile)

Abstract

Tetramethylpolyarylate-polyarylate (TMPAr-PAr) block copolymers of various block lengths were synthesized by the coupling reaction of hydroxy-terminated TMPAr and hydroxy-terminated PAr using triphosgene. The phase behavior of these block copolymers are discussed based on the thermal properties observed by differential scanning calorimetry (DSC). The thermal properties of binary blends of these block copolymers with PAr homopolymer or poly(styrene-co-acrylonitrile) whose acrylonitrile content is 9.5 wt% (SAN 10) were observed by DSC. The compatibilizing effect of the microphase-separated TMPAr-PAr block copolymer in PAr/SAN 10 blends was observed from thermal properties and morphology.     

非晶纤维的制备和力学行为

将块体材料制备成微纳米纤维时,其力学性能会得到进一步的提高,甚至具备块体材料所没有的力学行为.非晶态材料可经过熔体拉丝一次性成型而得到所需尺寸的均匀纤维,纤维表面质量好,其制备过程相对简单且节能.由于非晶材料短程有序、长程无序的结构,具备优异的力学性能,所以非晶纤维有着广泛的应用前景和基础研究价值.本文对能制备成非晶纤维且有优异力学性能的材料做了简单介绍,对非晶纤维的制备方法及其成型物理机制、非晶纤维的力学行为及其物理机制进行了综述,最后总结了非晶纤维的制备和力学行为的研究中存在的问题,对非晶纤维的发展前景做了展望.     

Ion complexation: a route to enhanced block copolymer alignment with electric fields

We investigate the enhanced alignment of lamellar microdomains under an electric field by addition of lithium chloride (LiCl) into polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) copolymers. A significant increase of dielectric contrast resulting from the formation of lithium-PMMA complexes markedly reduces the critical electric field strength required to overcome the preferential interactions of one block with the substrate, providing a route to achieve the complete alignment of microdomains in block copolymer thin films.     

超声自冲铆复合连接成形性及力学行为研究

该文选用6061和2A12航空铝合金薄板材料,进行自冲铆接和超声自冲铆复合连接试验,基于拉伸-剪切和电子显微镜测试,研究超声自冲铆接成形性及力学行为。结果表明：超声自冲铆接头较自冲铆接头的内锁量提升了44.8%;其钉头高度下降了34.4%;超声自冲铆接头的静载强度提升了18.1%,缓冲吸震性能提升了17.5%;超声焊接致使自冲铆接头的铆钉颈部与上板接触区域、铆钉腿部与上板接触区域形成固相焊;超声焊接可有效提高自冲铆接头的稳定性。     

Thermal States in Conformal QFT. I

We analyze the set of locally normal KMS states w.r.t. the translation group for a local conformal net A{{\mathcal A}} of von Neumann algebras on \mathbb R{\mathbb R} . In this first part, we focus on the completely rational net A{{\mathcal A}} . Our main result here states that, if A{{\mathcal{A}}} is completely rational, there exists exactly one locally normal KMS state j{\varphi} . Moreover, j{\varphi} is canonically constructed by a geometric procedure. A crucial r?le is played by the analysis of the “thermal completion net” associated with a locally normal KMS state. A similar uniqueness result holds for KMS states of two-dimensional local conformal nets w.r.t. the time-translation one-parameter group.     

Mesostructures and properties of transparent block copolymer/silica nanocomposite monoliths

In this work, three different block copolymer/silica hybrid nanocomposite monoliths that possess mesostructured domains (hexagonal, cubic, and disordered) were prepared through the micellization of the block copolymer during the sol-gel process of a silica precursor. Transparent block copolymer/silica nanocomposite monoliths were obtained from the amphiphilic triblock copolymer poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) (EO₁₀₆PO₇₀EO₁₀₆, Pluronic F127), which we used to organize the polymerizing silica networks; the ratio between the block copolymer and silica was fixed at 60:40 (wt%). Small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM) were used to observe the mesostructural ordering. Temperature-dependent SAXS patterns of the cubic structured nanocomposites showed that the calcination process takes place at 210°C. The transmittances of the nanocomposite monoliths over the range of wavelengths from 400 to 800 nm was >85%. From rheological measurements at low frequency, it was found that the hexagonally structured monoliths had higher storage and loss moduli relative to the monoliths possessing cubic and disordered structures.     

A comparative ab initio study of the structural,mechanical, electronic and optical behaviors of ZnO:Ni thin films with nanometer scale

The electronic and optical properties of undoped and Ni–doped ZnO thin films with nanometer scale have been studied in the wurtzite phase, by first–principle approach. Density functional theory has been employed to calculate the fundamental properties of the films using full–potential linearized augmented plane–wave method. Ni doping was found to reduce the bandgap value of the material. Additionally, DOS effective mass of the electrons was evaluated. It was revealed that the effective mass of the electrons at the bottom of conduction band increased with Ni doping. Decrease of reflectance for thin films with nanometer scale in the UV–vis region was observed. The substitution by Ni decreased the intensity of the peaks, and a red shift was observed in the absorption peak. Moreover, the static dielectric constant, and static refractive index decreased with Ni content. Energy loss function of the modeled compounds was also evaluated. All calculated parameters were compared with the available experimental and other theoretical results.     

Thermal oxidation and photo- and biodestruction of the statistical copolymer of ethylene with carbon monoxide

Thermal and photooxidation of the statistical copolymer of ethylene containing 1.5% carbonyl units -C(O)- by molecular O₂ was studied at 160–200°C in the presence and absence of phenyl-β-naphthylamine (PNA) antioxidant. The incorporation of a small number of -C(O)- groups into the polyethylene chain insignificantly decreased the rate of thermal (dark) oxidation but substantially accelerated oxidation under the action of light. At the same time, the oxidation of the copolymer occurred at a lower rate than the oxidation of pure polyethylene (PE), which was evidence of an important role played by intramolecular oxidation chain propagation in PE, which is disturbed already at a comparatively low fraction of foreign units. Phenyl-β-naphthylamine noticeably decelerated oxidation. The rate of polymer biodestruction was much higher than the rate of PE biodestruction. The influence of biodestruction on the physicomechanical properties of samples was studied by ultrasonic microscopy. The velocity of sound propagation in PE was somewhat lower compared with the ethylene-carbon monoxide copolymer (ECO). Clearly, the introduction of a small amount of CO molecules into the polyethylene chain changed the microstructure of PE. The structure of ECO was more ordered and denser because of plasticization by metabolites.     

Optical absorption of composite systems with silver nanoparticles dispersed in arabinogalactan and arabinogalactan-g-polypyrrole block copolymer matrices

The absorption of a nanocomposite of silver nanoparticles and arabinogalactan in the UV–Vis spectral range is due to the presence of end aldehyde groups in the arabinogalactan and plasmon vibrations in 0D nanosilver. The absorption spectrum of a fundamentally new nanocomposite of silver with arabinogalactan-g-polypyrrole block copolymer reveals additional long-wavelength overlapping absorption bands resulting from the longitudinal component of plasmon resonance in 1D nanosilver and polarons in polypyrrole.     

Relaxation processes and structural transitions in stretched films of polyvinylidene fluoride and its copolymer with hexafluoropropylene

Relaxation processes and structural transitions in nonstretched and uniaxially stretched films of poly(vinylidene fluoride-hexafluoropropylene) (P(VDF-HFP)) and its homopolymer polyvinylidene fluoride (PVDF) for comparison were investigated with the aim of understanding the electromechanical properties of this lower-modulus ferroelectric copolymer. The mechanical and the dielectric response at the glass transition (?? _a relaxation) exhibit similar temperature dependence of the relaxation time, whereas mechanical and dielectric processes above the glass transition are not related. They represent a continuous softening process within the amorphous phase and the dielectric ?? _c relaxation, respectively. The latter is attributed to conformational changes of VDF segments in lamellae of spherulites constituting the nonpolar crystalline ?? phase. Furthermore, there is a contribution from melting of secondary crystallites formed in the amorphous phase during annealing or storage. Mechanically, this transition appears in nonstretched and stretched films as an accelerated decrease of the elastic modulus that terminates the rubber plateau. Dielectrically, this transition becomes visible as a frequency-independent loss peak only in stretched films, because stretching removes the ?? _c relaxation, which superimposes the transition in nonstretched films. Melting of secondary crystallites is shown to appear in the homopolymer, too, though less pronounced because of more complete primary crystallisation. Stretching increases the modulus above the glass transition only slightly, and it does not significantly influence the softening process. On the other hand, stretching causes a spontaneous polarisation and introduces order within the amorphous phase, rendering it more polar. Melting of secondary crystallites provides an additional contribution to the polarisation. These findings may explain the relatively high electromechanical activity of P(VDF-HFP) but also its relatively low thermal stability. Moreover, they may be important for correct procedure and analysis of temperature-dependent dielectric measurements on partially crystalline polymers, in particular on those with less favourable sterical conditions for primary crystallisation.     

Biomechanical behaviors of dragonfly wing:relationship between configuration and deformation

In this paper,the natural structures of a dragonfly wing,including the corrugation of the chordwise cross-section,the sandwich microstructure veins,and the junctions between the vein and the membrane,have been investigated with experimental observations,and the morphological parameters of these structural features are measured.The experimental result indicates that the corrugated angle among the longitudinal veins ranges from 80 to 150,and the sandwiched microstructure vein mainly consists of chitin and protein layers.Meanwhile,different finite element models,which include models I and I for the planar forewings,models II and II for the corrugated forewings,and a submodel with solid veins and membranes,are created to investigate the effects of these structural features on the natural frequency/modal,the dynamical behaviors of the flapping flight,and the deformation mechanism of the forewings.The numerical results indicate that the corrugated forewing has a more reasonable natural frequency/modal,and the first order up-down flapping frequency of the corrugated wing is closer to the experimental result(about 27.00 Hz),which is significantly larger than that of the planar forewing(10.94 Hz).For the dynamical responses,the corrugated forewing has a larger torsional angle than the planar forewing,but a lower flapping angle.In addition,the sandwich microstructure veins can induce larger amplitudes of torsion deformation,because of the decreasing stiffness of the whole forewing.For the submodel of the forewing,the average stress of the chitin layer is much larger than that of the protein layer in the longitudinal veins.These simulative methods assist us to explain the flapping flight mechanism of the dragonfly and to design a micro aerial vehicle by automatically adjusting the corrugated behavior of the wing.     

外腔半导体激光器在高低温下的机械形变与功率变化

外腔激光器具有窄线宽、低功耗的特征,主要用于相干光通信,实际应用中外腔激光器的输出光功率会在环境温度为高温或者低温时出现下降现象.通过使用有限元商用软件Ansys分析,发现高低温下机械结构会有微小的挠度变化,相较于常温,高低温下最大的挠度角度为0.04°.外腔激光器的腔长较长,结合光路仿真软件Zemax研究发现,微小的...