This paper presents for the first time that poly(l ‐lactic acid) (PLLA) nanofibers can show the piezoelectricity along the fiber direction (d33) by using an electrospinning method. First, the electrospun fiber bundles are characterized by scanning electron microscope, X‐ray, and piezoelectric coefficient measurements. The data show that the supercritical CO2 treatment can greatly enhance the piezoelectricity of electrospun PLLA fibers, which can be resulting from the increased crystallinity of the fibers. Later, it is found that the electrospun PLLA fiber can generate a current of 8 pA and a voltage of 20 mV by a simple push–release process. Further, a single PLLA fiber‐based blood pulse sensor is also fabricated and tested and shows around a 2 pA output for blood pulse. Due to easy fabrication and relatively simple structure, this device enables a broad range of promising future applications in the medical sensor area.
A systematic study of the effects of , flow rate, voltage, and composition on the morphology of electrospun PLGA nanofibers is reported. It is shown that changes of voltage and flow rate do not appreciably affect the morphology. However, the of PLGA predominantly determines the formation of bead structures. Uniform electrospun PLGA nanofibers with controllable diameters can be formed through optimization. Further, multi‐walled carbon nanotubes can be incorporated into the PLGA nanofibers, significantly enhancing their tensile strength and elasticity without compromising the uniform morphology. The variable size, porosity, and composition of the nanofibers are essential for their applications in regenerative medicine.
DSC indicated that the nucleation of PLLA is enhanced in the presence of PGA even at a PGA content as low as 0.1 wt.‐%. However, the enhancing behavior of PGA was different to that of other nucleating agents for PLLA. Polarized optical microscopy revealed that the presence of PGA increased the number of PLLA spherulites per unit area. WAXD showed that in the PLLA/PGA films, PLLA and PGA crystallize separately to form their respective crystallites and PGA crystallites were formed at a PGA content at above 3 wt.‐% (at least). FTIR spectroscopy indicated that that there are significant interactions between PLLA and PGA chains in amorphous regions. Such interactions should have enhanced the growth of PLLA crystallites from the surface of PGA crystallites.
The influence of talc loading on phase morphology of PLA/PCL/talc composites and improvement in resulting properties are reported. Talc‐based composites of PLA/PCL blends were prepared by melt blending. SEM analysis demonstrates that PLA appears as discrete domain phase, while PCL acts as a bulk phase in the blend. Talc addition decreases PLA domain sizes and voids in the matrix. This results in significant improvement of oxygen and water vapor barrier properties of composite by 33 and 25%, respectively, at 3 wt.‐% talc loading. DSC shows that talc acted as nucleating agent for PCL phase in the composite and improves its crystallinity. Various theoretical models based on dispersion and filler geometry are used to predict the tensile modulus and oxygen permeability.
Summary: Amorphous and crystallized poly(L ‐lactic acid) (PLLA‐A and PLLA‐C, respectively) films with different contents of N,N,N′,N′‐tetramethyl‐1,4‐phenylenediamine (TMPD) as a photosensitizer were prepared, and the effects of the addition of TMPD on the photodegradation of PLLA films were investigated. It was found that the addition of TMPD effectively enhanced the photodegradation of PLLA films and thereby decreased their molecular weight of PLLA films regardless of their crystallinity, and that PLLA films with different molecular weights can be prepared by the addition of different amounts of TMPD and subsequent UV irradiation. Too high contents of TMPD however caused the brittleness of PLLA films due to a large decrease in molecular weight. The PLLA chains in crystalline regions as well as those in amorphous regions are photodegradable even at an early stage, in marked contrast to their hydrolytic degradation, where the chains in the amorphous regions are selectively degraded. The basic changes in glass transition, cold crystallization, and melting temperatures (Tg, Tcc, and Tm, respectively) of PLLA films during UV irradiation can be ascribed to low‐temperature annealing effects; i.e., annealing‐induced stabilization in chain packing should have elevated Tg, and annealing‐induced formation of crystallite nuclei should have lowered Tcc and increased Tm. The exceptional large decreases in Tcc and Tm of UV‐irradiated PLLA‐A films and in Tg of UV‐irradiated PLLA‐C films at high TMPD contents are attributable to the large decrease in molecular weight, whereas the exceptional decrease in Tm of PLLA‐C films at high TMPD contents can be due to the folding surface structural change of crystalline regions or to the lattice disorder caused by molecular structural changes.
of PLLA‐A films before UV irradiation and after UV irradiation for 60 h as a function of TMPD content. 相似文献
Polyimides (PIs) possess excellent mechanical properties, thermal stability, and chemical resistance and can be converted to carbon materials by thermal carbonization. The preparation of carbon nanomaterials by carbonizing PI‐based nanomaterials, however, has been less studied. In this work, the fabrication of PI nanofibers is investigated using electrospinning and their transformation to carbon nanofibers. Poly(amic acid) carboxylate salts (PAASs) solutions are first electrospun to form PAAS nanofibers. After the imidization and carbonization processes, PI and carbon nanofibers can then be obtained, respectively. The Raman spectra reveal that the carbon nanofibers are partially graphitized by the carbonization process. The diameters of the PI nanofibers are observed to be smaller than those of the PAAS nanofibers because of the formation of the more densely packed structures after the imidization processes; the diameters of the carbon nanofibers remain similar to those of the PI nanofibers after the carbonization process. The thermal dissipation behaviors of the PI and carbon nanofibers are also examined. The infrared images indicate that the transfer rates of thermal energy for the carbon nanofibers are higher than those for the PI nanofibers, due to the better thermal conductivity of carbon caused by the covalent sp2 bonding between carbon atoms. 相似文献
In the general processing temperature range of poly(L ‐lactic acid) (PLLA) articles (210–240 °C), PLLA/poly(D ‐lactic acid) (PDLA) stereocomplex (SC) crystallites melted just above the endset temperature of SC melting (228–238 °C) and recrystallized during cooling were found to act as the most effective nucleating agents for enhancing the crystallization of PLLA compared to partially melted SC crystallites (211–227 °C) or those melted far above the endset temperature of SC melting (240 and 250 °C) and recrystallized during cooling. The high nucleating effect of the SC crystallites melted in the temperature range of 228–238 °C was found to be caused by their smaller sizes or the larger number of SC crystallites per unit mass. The incorporation of such SC crystallites facilitates the processing of PLLA articles having high crystallinity and, therefore, high heat‐resistance in a shorter period to reduce the production cost.
The effects of varying concentrations of incorporated PDLA on the acceleration of PLLA homo‐crystallization due to stereocomplex (SC) crystallite formation are investigated in PLLA films doped with PDLA over the wide concentration range of 1–10 wt%. PLLA homo‐crystallization is accelerated for all the PDLA concentrations when the processing temperature Tp is just above the endset melting temperature of the SC crystallites (Tp = 226–238 °C), although the appropriate Tp range becomes narrow at low concentrations of PDLA. The accelerating effects of SC crystallites depend on the SC crystalline thickness and the interaction between the SC crystalline regions and PLLA amorphous regions for Tps below and above the melting peak temperature of the SC crystallites, respectively.
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