BaTiO3 ceramic fibers were prepared by the sol-gel method in which catechol-complexed titanium isopropoxide and barium acetate hydrate were used as starting materials. The green fibers of ca. 30 cm in length were obtained from the precursor sols. The BaTiO3 ceramic fibers with the average length of ca. 20 cm were of the order of 3 to 10 m in diameter and elliptical shapes in cross section. The green fibers and those sintered at different temperatures were characterized by TGA/DSC, XRD, IR, SEM and TEM techniques. 相似文献
Hydrogel microfibers have been considered as a potential biomaterial to spatiotemporally biomimic 1D native tissues such as nerves and muscles which are always assembled hierarchically and have anisotropic response to external stimuli. To produce facile hydrogel microfibers in a mathematical manner, a novel dynamic‐crosslinking‐spinning (DCS) method is demonstrated for direct fabrication of size‐controllable fibers from poly(ethylene glycol diacrylate) oligomer in large scale, without microfluidic template and in a biofriendly environment. The diameter of fibers can be precisely controlled by adjusting the spinning parameters. Anisotropic swelling property is also dependent on inhomogeneous structure generated in spinning process. Comparing with bulk hydrogels, the resulting fibers exhibit superior rapid water adsorption property, which can be attributed to the large surface area/volume ratio of fiber. This novel DCS method is one‐step technology suitable for large‐scale production of anisotropic hydrogel fibers which has a promising application in the area such as biomaterials.
This study focused on the fabrication of a composite of polylactic acid fibers reinforced with barium titanate (BT) and obtained by centrifugal spinning. Different concentrations of inorganic powder (5, 10, and 15 wt%) have been added to the polymeric solution and the samples have been studied to monitor any modification in chemical, morphological, thermal, and mechanical properties. Subsequently, samples have been subjected to UV/O3 irradiation at two different times (5 and 10 min) with the aim to verify the resistance to aging, which is considered a key factor for medical applications and outdoor. The presence of BT influenced strongly the structure of the fibers in many aspects. Samples with the lowest amount of BT showed a clear decrease of chemical and consequently of mechanical properties manifested with the breakage of the fibers subjected to treatment. The other composites apparently showed similar chemical properties comparing with the one without fillers but the mechanical properties clearly decreased. However, what emerged from the study is a clear stability during the aging tests promoted by the presence of BT. The samples with 10 and 15 wt% of BT presented chemical, thermal, and mechanical stabilities differently from the other samples. These results suggested that the fillers clearly modified the degree of crystallinity acting as nucleation agents and promoting the development of a stable crystalline phase during the treatment. 相似文献
Polylactic acid (PLA) is a widely used bioresorbable polymer in medical devices owing to its biocompatibility, bioresorbability, and biodegradability. It is also considered a sustainable solution for a wide variety of other applications, including packaging. Because of its widespread use, there have been many studies evaluating this polymer. However, gaps still exist in our understanding of the hydrolytic degradation in extreme pH environments and its impact on physical and mechanical properties, especially in fibrous materials. The goal of this work is to explore the hydrolytic degradation of PLA fibers as a function of a wide range of pH values and exposure times. To complement the experimental measurements, molecular-level details were obtained using both molecular dynamics (MD) simulations with ReaxFF and density functional theory (DFT) calculations. The hydrolytic degradation of PLA fibers from both experiments and simulations was observed to have a faster rate of degradation in alkaline conditions, with 40% of strength loss of the fibers in just 25 days together with an increase in the percent crystallinity of the degraded samples. Additionally, surface erosion was observed in these PLA fibers, especially in extreme alkaline environments, in contrast to bulk erosion observed in molded PLA grafts and other materials, which is attributed to the increased crystallinity induced during the fiber spinning process. These results indicate that spun PLA fibers function in a predictable manner as a bioresorbable medical device when totally degraded at end-of-life in more alkaline conditions. 相似文献
This study reports the synthesis of nickel titanate (NiTiO3) powders by using the modified sol‐gel method, with nickel acetate tetrahydrate as the nickel source, titanium isopropoxide as the titanium source, and 2‐methoxyethanol as the solvent, followed by post‐heat treatment in air at temperatures ranging from 500 °C to 900 °C. The characteristics of powders were determined by X‐ray diffraction (XRD), FT‐infrared spectroscopy (FT‐IR), ultraviolet/visible spectroscopy (UV/Vis), and Raman spectroscopy. The particle size and surface area of the powders were also measured. The results indicated that single‐phase NiTiO3 can be prepared using the modified sol‐gel method, followed by post‐heat treatment at the relatively low temperature of 550 °C. The crystallite sizes and particle sizes of NiTiO3 powders increase in conjunction with the post‐heat treatment temperatures. However, the surface area of the powders shrinks as the post‐heat treatment temperatures increase. The dielectric constants of NiTiO3 powders, based on the capacitance‐voltage analysis, are within a range of 13.2 to 17.8. 相似文献
