磁场引导水溶还原法制备磁性金属纤维

提出了用磁场引导水溶还原法制备磁性金属纤维的新思想，分析了用这种方法制备磁性金属纤维的机理和动力学过程，给出了实验结果．实验表明，磁场引导水溶还原法适合于制备磁性金属纤维，且纤维的直径在μｍ和亚μｍ数量级．     

Transition from Multiple Macro-Cracking to Multiple Micro-Cracking in Cementitious Composites

This paper presents an experimental study of the possibility of transition from multiple macro-cracking to multiple micro-cracking in cementitious composites.Conventional polyvinyl alcohol fiber reinforced cementitious composites normally exhibit macroscopic strain-hardening and multiple cracking after the first cracks appear.However,the individual crack width at the saturated stage is normally 60 to 80 μm.In the current study,the effect of fine aggregate size on the cracking performance,especially the individual crack width in the strain-hardening stage was studied by bending tests.The results show that the individual crack widths can be reduced from 60-80 μm to 10-30 μm by modifying the particle size of the fine aggregates used in the composites.     

Spectroscopic analysis and kinetics of intermolecular hydrogen bond formation in poly‐pyridobisimidazole (M5) fiber

Poly‐pyridobisimiazole (M5) single filaments subjected to varying degrees of heat treatment have been analyzed using Fourier Transform Infrared (FTIR) microspectroscopy in transmission mode to detect changes in the state of intermolecular hydrogen bonding as a function of fiber annealing conditions. The FTIR absorbance bands associated with hydrogen bonding in M5 fiber have been identified, and the integrated molar absorption coefficients for the bands of interest have been determined experimentally, which allows to quantify the concentration of N? H vibration groups hydrogen‐bonded (H‐bonded) to water molecules, and the concentration of N? H vibration groups H‐bonded to adjacent polymer chains in the fiber. A dual mechanism kinetic rate expression is used to describe intermolecular H‐bond formation in M5 fiber as a function of annealing conditions, from which an activation energy for H‐bond formation of 14.8 kJ/mol is obtained. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 1809–1824, 2009     

Phase morphology and mechanical properties of the electrospun polyoxymethylene/polyurethane blend fiber mats

Polyoxymethylene/thermoplastic polyurethane (POM/TPU) blends containing 10–30 wt % of TPU were electrospun using hexafluoroisopropanol as the solvent. The average fiber diameter increases with the increase in TPU content from 0.68 μm for neat POM fibers to 0.92 μm for POM/TPU 7:3 blend fibers due to the increase in solution viscosity. Core/sheath structure with the major component POM as the core and the minor component TPU as the sheath was observed by transmission electron microscopy and further confirmed by surface N contents of the blend fiber mats. The crystalline melting point and the degree of crystallinity of POM have no obvious change by coelectrospinning with TPU due to lack of interaction between POM and TPU as revealed by Fourier transform infrared spectroscopy. Tensile tests showed that the unusual high ductility of POM fiber mat could be further increased by coelectrospinning with 10 or 20 wt % TPU without significantly decreasing the stiffness and strength. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 1853–1859, 2009     

Spinnablity and structure characterization of mullite fibers via sol–gel-ceramic route

Viscosity and rheology behaviors of the mullite sols prepared from aqueous solution of aluminum nitrate, aluminum isopropoxide and tetraethylorthosilicate has been investigated. Rheological measurement suggested that mullite sols exhibited good spinniabilty when the evaporation of the solvent is allowed during sol–gel process. Spinnable sols showed shear-thinning flow behavior with high viscosity to the time of gelation. By adjusting temperature, the gelation degree and viscosity of the sol could be stabilized at a certain value and the sol–gel transition could be transferred to the spinning line of a laboratory dry-spinning apparatus. Continuous mullite fibers were obtained from such sols using sol gel dry-spinning method. The final ceramic fibers had smooth surfaces with an average diameter of 50 μm. Structure evolution of mullite ceramic fibers were characterized by MAS NMR and specific surface area analyses.     

生物质棉纤维再生纤维素膜的制备与性能分析

以天然生物质棉纤维为原料,采用氯化锂/N,N-二甲基乙酰胺(Li Cl/DMAC)溶解体系对其进行活化处理,配置不同质量分数的纤维素有机溶液系列,在不同凝固浴条件下,采用KW-4A匀胶机高速旋涂成膜和AFA-Ⅱ自动涂膜器低速平推成膜2种工艺,制备再生纤维素薄膜系列。通过运用扫描电镜(SEM)、傅里叶变换红外光谱(FT-IR)、X射线衍射仪(XRD)和表面接触角测试仪等分析设备对再生纤维素膜的大分子结构、力学性能、结晶度、热稳定性和表面浸润性进行各项性能的系列化表征,研究纤维素质量分数、凝固浴种类、制膜工艺对膜性能的影响。实验结果表明:采用KW-4A匀胶机高速成膜工艺、凝固浴为水浴、纤维素质量分数为3.5%时,制备的再生纤维素膜的各项性能最佳;与天然生物质棉纤维相比,再生纤维素膜结晶度变化很大,热稳定性与棉纤维变化趋势一致但有一定程度下降,表面浸润性良好。     

Electrospun recycled PET-based mats: Tuning the properties by addition of cellulose and/or lignin

The aim of this study was to evaluate the influence of cellulose and/or lignin on the properties of mats prepared from dissolution (for 48 h or 72 h, solvent: trifluoroacetic acid) of recycled poly (ethylene terephthalate) (PET). Briefly, the presence of cellulose led to a tendency of higher average fiber diameter and average pore area as well as lower average porosity compared to the neat mat (PET_ref, 242 ± 59 nm, 9.6 ± 1.1 10⁴ nm² and 19.0 ± 1.1%, respectively). The T_g values for electrospun PET combined with cellulose and/or lignin were higher than that of PET_ref (92.5 ± 0.1 °C), and the tensile strength increased with the cellulose and/or lignin loading. In addition, the presence of lignin (72 h of dissolution) led to a mat with an elongation at break of 149 ± 9% compared to 14 ± 2% for PET_ref. The results indicated that the properties of mats based on PET can be tuned by adding cellulose and/or lignin to solutions posteriorly electrospun as well as by varying the dissolution time.     

Facile synthesis of a melt-spinnable polyborazine from asymmetric alkylaminoborazine

<正>A novel asymmetric alkylaminoborazine monomer,2-propylamino-4,6-bis(methylamino)borazine,was synthesized for the first time,and directly polymerized to give a melt-spinnable polyborazine(PBN).This asymmetric alkylaminoborazine was synthesized by an aminolysis reaction of 2,4,6-trichloroborazine(TCB) with different amines under mild conditions.This route turns out to be much cheaper and simpler than the conventional routes.The chemical composition,structure,molecular weights and ceramic yield were investigated by EA,FTIR,NMR,GPC and TG analysis.The PBN exhibits suitable rheological property for melt-spinning, which suggests that it is a potential precursor for BN fibers.     

微波辐射下秸秆纤维微观结构的变化

利用原子力显微镜(AFM)对微波处理前后秸秆纤维表面的变化进行了研究,并结合XRD和FTIR研究了处理前后其化学结构及结晶形态的变化情况。结果表明,未经微波处理的秸秆纤维表面比较光滑,平均粗糙度(Ra)为(86.7±6.335)nm,均方根粗糙度(Rq)为(141.1±9.055)nm;经微波处理的秸秆纤维表面比较粗糙,并出现许多细小孔洞,其Ra为(445.0±28.14)nm,Rq为(558.9±33.458)nm,微波辐射处理前后秸秆纤维的表面形态差异较大。经微波辐射处理后,秸秆纤维在2θ=22.3°处的衍射峰移至21.8°,且峰宽稍有增加,在38.1°、44.3°、64.6°、78.9°处出现的4个衍射峰,除强度稍有增强,其峰形和位置与未经处理秸秆纤维的衍射峰基本一致,表明微波处理没有改变纤维的结晶形态。FTIR光谱表明,微波处理样中未产生新的官能团,但分子间氢键及分子内氢键发生变化。微波作用未引起秸秆纤维化学结构的变化。