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Long Fibers (long + fiber)
Selected AbstractsCarbon Long Fiber Reinforced Aluminum Matrix Composites , Parameter Studies and Numerical Simulations of the Infiltration Process,ADVANCED ENGINEERING MATERIALS, Issue 7 2010Heiko Ballmes Within this work, the development of a cost efficient and reliable production technique for infiltrating carbon fibers with aluminum using a conventional cold chamber die casting machine is reported. Results are presented that demonstrate the large potential of pressure die casting as a low cost manufacturing process for carbon fiber reinforced aluminum matrix composites. The influence of process parameters on the infiltration behaviour is investigated and compared to results gained by numerical simulation. [source] Comparative development of fiber in wild and cultivated cottonEVOLUTION AND DEVELOPMENT, Issue 1 2001Wendy L. Applequist SUMMARY One of the most striking examples of plant hairs is the single-celled epidermal seed trichome of cultivated cotton. The developmental morphology of these commercial "fibers" has been well-characterized in Gossypium hirsutum, but little is known about the pattern and tempo of fiber development in wild Gossypium species, all of which have short, agronomically inferior fiber. To identify developmental differences that account for variation in fiber length, and to place these differences in a phylogenetic context, we conducted SEM studies of ovules at and near the time of flowering, and generated growth curves for cultivated and wild diploid and tetraploid species. Trichome initiation was found to be similar in all taxa, with few notable differences in trichome density or early growth. Developmental profiles of the fibers of most wild species are similar, with fiber elongation terminating at about two weeks post-anthesis. In contrast, growth is extended to three weeks in the A- and F-genome diploids. This prolonged elongation period is diagnosed as a key evolutionary event in the origin of long fiber. A second evolutionary innovation is that absolute growth rate is higher in species with long fibers. Domestication of species is associated with a further prolongation of elongation at both the diploid and allopolyploid levels, suggesting the effects of parallel artificial selection. Comparative analysis of fiber growth curves lends developmental support to previous quantitative genetic suggestions that genes for fiber "improvement" in tetraploid cotton were contributed by the agronomically inferior D-genome diploid parent. [source] A Glass Hook Allows Fishing of Hexa- peri -hexabenzocoronene Graphitic Nanotubes: Fabrication of a Macroscopic Fiber with Anisotropic Electrical Conduction,ADVANCED MATERIALS, Issue 10 2006Y. Yamamoto Fishing of graphitic nanotubes with a macroscopic glass hook: A ,30,mm long fiber (see figure and cover) is readily processed from a suspension of self-assembled nanotubes with one-handed helical chirality, formed from the (R)- or (S)-enantiomer of chiral amphiphile 2. The majority of the nanotubes in the fiber are unidirectionally oriented along the fiber axis. Upon doping with I2, the fiber displays an anisotropic electrical conduction along the fiber axis more than an order of magnitude greater than that across the fiber axis. [source] Tunable narrow linewidth Tm3+ -doped silica fiber laser with an intracavity taperLASER PHYSICS LETTERS, Issue 3 2010Y. Zhang Abstract Using an intracavity long fiber taper, the 793 nm diode laser (LD) clad-pumped tunable narrow linewidth Tm3+ -doped silica fiber laser was realized. The intracavity long taper was fabricated directly on the Tm3+ -doped fiber by heating and stretching method, and located several centimeters from the output fiber end. The fiber laser cavity was combined by the fiber end Fresnel reflection and a dichroic. The fiber laser had a maximal output power of 5.86 W at 1927.2 nm, with a narrow linewidth of 148 pm. By stretching or bending the taper, the output laser center wavelength could be tuned from 1910.6 nm to 1958.1 nm with a variable spectrum width ranging from 92 , 148 pm. (© 2010 by Astro Ltd., Published exclusively by WILEY-VCH Verlag GmbH & Co. KGaA) [source] Mechanical properties of injection molded long fiber polypropylene composites, Part 1: Tensile and flexural propertiesPOLYMER COMPOSITES, Issue 2 2007K. Senthil Kumar Innovative polymers and composites are broadening the range of applications and commercial production of thermoplastics. Long fiber-reinforced thermoplastics have received much attention due to their processability by conventional technologies. This study describes the development of long fiber reinforced polypropylene (LFPP) composites and the effect of fiber length and compatibilizer content on their mechanical properties. LFPP pellets of different sizes were prepared by extrusion process using a specially designed radial impregnation die and these pellets were injection molded to develop LFPP composites. Maleic-anhydride grafted polypropylene (MA- g -PP) was chosen as a compatibilizer and its content was optimized by determining the interfacial properties through fiber pullout test. Critical fiber length was calculated using interfacial shear strength. Fiber length distributions were analyzed using profile projector and image analyzer software system. Fiber aspect ratio of more than 100 was achieved after injection molding. The results of the tensile and flexural properties of injection molded long glass fiber reinforced polypropylene with a glass fiber volume fraction of 0.18 are presented. It was found that the differences in pellet sizes improve the mechanical properties by 3,8%. Efforts are made to theoretically predict the tensile strength and modulus using the Kelly-Tyson and Halpin-Tsai model, respectively. POLYM. COMPOS., 28:259,266, 2007. © 2007 Society of Plastic Engineers [source] Swirl mat, and long discontinuous fiber mat,reinforced polypropylene composites,status and future trendsPOLYMER COMPOSITES, Issue 4 2000J. Karger-Kocsis Polypropylene (PP) composites with glass and natural fiber mat reinforcement (GMT-PP and NMT-PP, respectively) are widely used in different applications, competing with metallic sheets and thermoset polymer composites. Their production occurs via melt impregnation, slurry deposition and various textile architecturing processes that lead to either consolidated or non-consolidated preforms. These preforms are then converted into final parts by hot pressing. The "traditional" GMT-PP composites are nowadays faced with a great challenge because of the introduction of long fiber reinforced thermoplastic (LFT) composites produced on- or off-line. This paper gives a brief survey on the manufacturing, processing, properties and application of GMT and GMT-like systems and it concludes by describing some of the future trends, especially in the fields of material and process developments. [source] The effect of laser profile, fluence, and spot size on sensitivity in orthogonal-injection matrix-assisted laser desorption/ionization time-of-flight mass spectrometryRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 18 2008Hui Qiao The influence of incident laser parameters on sensitivity in matrix-assisted laser desorption/ionization (MALDI) has been investigated using orthogonal-injection time-of-flight (TOF) instruments. A qualitative comparison was first made between the beam profiles obtained with a N2 laser and a Nd:YAG laser using 2-m long optical fibers. The N2 laser gives better sensitivity, consistent with a more uniform fluence distribution and therefore better coverage of the N2 laser profile. Most of the difference disappears when a 30-m long fiber is used or when the fibers are twisted during irradiation to smooth out the fluence distribution. In more systematic measurements, the total integrated ion yield from a single spot (a measure of sensitivity) was found to increase rapidly with fluence to a maximum, and then saturate or decrease slightly. Thus, the optimum sensitivity is achieved at high fluence. For a fluence near threshold, the integrated yield has a steep (cubic) dependence on the spot size, but the yield saturates at higher fluence for smaller spots. The area dependence is much weaker (close to linear) for fluence values above saturation, with the result that the highest integrated yields per unit area are obtained with the smallest spot sizes. The results have particular relevance for imaging MALDI, where sensitivity and spatial resolution are important figures of merit. Copyright © 2008 John Wiley & Sons, Ltd. [source] Comparative development of fiber in wild and cultivated cottonEVOLUTION AND DEVELOPMENT, Issue 1 2001Wendy L. Applequist SUMMARY One of the most striking examples of plant hairs is the single-celled epidermal seed trichome of cultivated cotton. The developmental morphology of these commercial "fibers" has been well-characterized in Gossypium hirsutum, but little is known about the pattern and tempo of fiber development in wild Gossypium species, all of which have short, agronomically inferior fiber. To identify developmental differences that account for variation in fiber length, and to place these differences in a phylogenetic context, we conducted SEM studies of ovules at and near the time of flowering, and generated growth curves for cultivated and wild diploid and tetraploid species. Trichome initiation was found to be similar in all taxa, with few notable differences in trichome density or early growth. Developmental profiles of the fibers of most wild species are similar, with fiber elongation terminating at about two weeks post-anthesis. In contrast, growth is extended to three weeks in the A- and F-genome diploids. This prolonged elongation period is diagnosed as a key evolutionary event in the origin of long fiber. A second evolutionary innovation is that absolute growth rate is higher in species with long fibers. Domestication of species is associated with a further prolongation of elongation at both the diploid and allopolyploid levels, suggesting the effects of parallel artificial selection. Comparative analysis of fiber growth curves lends developmental support to previous quantitative genetic suggestions that genes for fiber "improvement" in tetraploid cotton were contributed by the agronomically inferior D-genome diploid parent. [source] Nucleation-Governed Reversible Self-Assembly of an Organic Semiconductor at Surfaces: Long-Range Mass Transport Forming Giant Functional Fibers,ADVANCED FUNCTIONAL MATERIALS, Issue 18 2007G. De, Luca Abstract The use of solvent-vapor annealing (SVA) to form millimeter-long crystalline fibers, having a sub-micrometer cross section, on various solid substrates is described. Thin films of a perylene-bis(dicarboximide) (PDI) derivative, with branched alkyl chains, prepared from solution exhibit hundreds of nanometer-sized PDI needles. Upon exposure to the vapors of a chosen solvent, tetrahydrofuran (THF), the needles re-organize into long fibers that have a remarkably high aspect ratio, exceeding 103. Time- and space-resolved mapping with optical microscopy allows the self-assembly mechanism to be unravelled; the mechanism is found to be a nucleation-governed growth, which complies with an Avrami-type of mechanism. SVA is found to lead to self-assembly featuring i),long-range order (up to the millimeter scale), ii),reversible characteristics, as demonstrated through a series of assembly and disassembly steps, obtained by cycling between THF and CHCl3 as solvents, iii),remarkably high mass transport because the PDI molecular motion is found to occur at least over hundreds of micrometers. Such a detailed understanding of the growth process is fundamental to control the formation of self-assembled architectures with pre-programmed structures and physical properties. The versatility of the SVA approach is proved by its successful application using different substrates and solvents. Kelvin probe force microscopy reveals that the highly regular and thermodynamically stable fibers of PDI obtained by SVA exhibit a greater electron-accepting character than the smaller needles of the drop-cast films. The giant fibers can be grown in,situ in the gap between microscopic electrodes supported on SiOx, paving the way towards the application of SVA in micro- and nanoelectronics. [source] Nanoclay and long-fiber-reinforced composites based on epoxy and phenolic resinsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Gang Zhou Abstract In this study, high-performance thermoset polymer composites are synthesized by using both long fibers and nanoclays. Epoxy and phenolic resins, the two most important thermoset polymers, are used as the polymer matrix. The hydrophobic epoxy resin is mixed with surface modified nanoclay, while the hydrophilic phenolic resin is mixed with unmodified raw nanoclay to form nanocomposites. Long carbon fibers are also added into the nanocomposites to produce hybrid composites. Mechanical and thermal properties of synthesized composites are compared with both long-fiber-reinforced composites and polymer- layered silicate composites. The optimal conditions of sample preparation and processing are also investigated to achieve the best properties of the hybrid composites. It is found that mechanical and thermal properties of epoxy and phenolic nanocomposites can be substantially improved. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Self-assembly and morphology of polydimethylsiloxane supramolecular thermoplastic elastomersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2008Nicole E. Botterhuis Abstract Functionalization of polydimethylsiloxanes (PDMS) polymers with hydrogen-bonding ureidopyrimidinone (UPy) groups leads to supramolecular thermoplastic elastomers. In previous studies, no lateral stacking of UPy dimers was observed in UPy-functionalized polymers, unless additional urethane or urea groups were built into the hard block. However, we have shown that when PDMS is used as the soft block, this lateral aggregation of UPy dimers does take place, since long fibers could be observed in the atomic force microscopy (AFM) phase image. Also in bulk, the presence of these interactions was proven by oscillatory shear experiments. We attribute this aggregation to the incompatibility of soft block and hard block, leading to phase separation. Moreover, we have shown that additional urethane or urea groups in the hard block do lead to materials with more fibers and higher melting points. For the UPy-urea functionalized PDMS even single fibers are observed with AFM when dropcasted from a very diluted solution. When the length of the soft block is increased, the morphology changes from fibrous to spherical. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3877,3885, 2008 [source] Morphology and mechanical properties of direct injection molded polypropylene/thermotropic copolyester blendsPOLYMER COMPOSITES, Issue 6 2000G. Guerrica-Echevarrķa Blends of two grades of polypropylene (PP) with thermotropic copolyester (Rodrun) contents of up to 40% were obtained by direct injection molding at different processing temperatures. In the skin of the molded specimens rather long fibers were seen in blends with low-viscosity PP, whereas sheets were found when the high-viscosity PP was the matrix. In the core, the viscosity of the matrix played a more relevant role than the viscosity ratio on the orientation level of the dispersed Rodrun phase. The better mechanical properties of the blends with the low viscosity PP are attributed to the morphology change of the dispersed phase from sheets to fibers when the viscosity of the matrix decreased. [source] Morphology development of PC/PE blends during compounding in a twin-screw extruderPOLYMER ENGINEERING & SCIENCE, Issue 1 2007Bo Yin The morphological development of a polycarbonate/polyethylene (PC/PE) blend in a twin-screw extruder was studied using a scanning electron microscope (SEM). The effects of extrusion temperature, viscosity ratio (the ratio of the viscosity of the dispersed phase to that of the matrix), and the screw configuration on the morphology of the PC/PE blend during the extrusion were discussed in detail. It was found that the morphology of the dispersed particles and the interfacial adhesion between the dispersed phase and matrix were both influenced by the extrusion temperature. The dispersed phase had a spheroidal shape and a small size during the high temperature processing, and an irregular shape and a large size when it was processed at low temperature. The PC phase with a lower viscosity was easier to disperse and also to coalesce. Therefore, the deformation of the low-viscosity dispersed phase during the processing was more intense than that of the high-viscosity dispersed phase. By comparing the effects of the different screw configurations on the morphology development of the PC/PE blend, it was found that the melting and breaking up of the dispersed phase were mainly affected in the initial blending stages by the number of the kneading blocks. While a kneading block with a 90 degree staggering angle was used, the size of the dispersed particles decreased and the long fibers were shortened, the large particles were drawn by the additional kneading zone. Finally, all of these structures were completely changed to the short fibers. POLYM. ENG. SCI., 47:14,25, 2007. © 2006 Society of Plastics Engineers [source] Structural Diversity in the Self-Assembly of Pseudopeptidic MacrocyclesCHEMISTRY - A EUROPEAN JOURNAL, Issue 4 2010Ignacio Alfonso Dr. Abstract The self-assembling abilities of several pseudopeptidic macrocycles have been thoroughly studied both in the solid (SEM, TEM, FTIR) and in solution (NMR, UV, CD, FTIR) states. Detailed microscopy revealed large differences in the morphology of the self-assembling micro/nanostructures depending on the macrocyclic chemical structures. Self-assembly was triggered by the presence of additional methylene groups or by changing from para to meta geometry of the aromatic phenylene backbone moiety. More interestingly, the nature of the side chain also plays a fundamental role in some of the obtained nanostructures, thus producing structures from long fibers to hollow spheres. These nanostructures were obtained in different solvents and on different surfaces, thus implying that the chemical information for the self-assembly is contained in the molecular structure. Dilution NMR studies (chemical shift and self-diffusion rates) suggest the formation of incipient aggregates in solution by a combination of hydrogen-bonding and ,,, interactions, thus implicating amide and aryl groups, respectively. Electronic spectroscopy further supports the ,,, interactions because the compounds that lead to fibers show large hypochromic shifts in the UV spectra. Moreover, the fiber-forming macrocycles also showed a more intense CD signature. The hydrogen-bonding interactions within the nanostructures were also characterized by attenuated total-reflectance FTIR spectroscopy, which allowed us to monitor the complete transition from the solution to the dried nanostructure. Overall, we concluded that the self-assembly of this family of pseudopeptidic macrocycles is dictated by a synergic action of hydrogen-bonding and ,,, interactions. The feasibility and geometrical disposition of these interactions finally render a hierarchical organization, which has been rationalized with a proposal of a model. The understanding of the process at the molecular level has allowed us to prepare hybrid soft materials. [source] | ||||||||||||||||||||||