Nucleating Agent For Poly Research Articles

Eco-friendly zinc-metal-organic framework as a nucleating agent for poly (lactic acid)

Eco-friendly poly(L-lactic acid) (PLA) can be made more versatile, and its crystallization rate is accelerated by adding Zinc-based metal-organic framework (Zn-MOF) particles. Using differential scanning calorimetry (DSC), the non-isothermal melt crystallization behavior of biodegradable PLA nucleated by 0.3 to 3 wt% of Zn-MOF was examined. The non-isothermal melt crystallization kinetics parameters were determined using a modified Avrami model and Mo approach. Zn-MOF dramatically accelerated the crystallization process, as evidenced by several non-isothermal crystallization metrics, including the crystallization half-time and crystallization rate constant. The melt crystallization temperatures of the PLA-Zn-MOF composites, with contents of 0.7 and 1 wt%, were increased by 21 °C compared to the neat PLA. Using the Friedman isoconversional kinetic method, the neat PLA and PLA-Zn-MOF composites' effective activation energy values, ∆E, were determined. The ∆E values of PLA-Zn-MOF from 0.3 to 1 wt% Zn-MOF composites were lower than that of neat PLA. Moreover, polarized optical microscopy revealed the formation of numerous small-sized PLA spherulites upon Zn-MOF addition. The results indicate that the Zn-MOF (at concentrations of 0.7 to 1.0 wt%) can be used as an efficient nucleating agent for PLA, where it increases the melt crystallization temperature, nucleation density, and crystallinity without changing the crystalline structure, while also significantly reduces the effective activation energy and the size of spherulites. Additionally, scanning electron microscopy confirms good dispersion of Zn-MOF (0.3 to 1 wt%) within the PLA matrix.

Effect of calcium pimelate on crystallization kinetics of polyphenylene sulfide

AbstractThe use of nucleating agents (NAs) to accelerate semicrystalline polymers crystallization is a widely recognized technique during processing. However, the commercially available NA for poly(phenylene sulfide) (PPS) has been rather limited. In this work, it is found that calcium pimelate (CaPim), a commercial nucleating agent for isotactic polypropylene, could also accelerate the crystallization process of PPS. The influence of CaPim addition on the crystallization behaviors of PPS was investigated under non‐isothermal and isothermal condition. Upon the addition of 0.3 wt% CaPim, the crystallization peak temperature and the onset crystallization temperature increases by 5.3 and 8.4°C at 10°C/min cooling rate, and the half‐time of crystallization reduces 51% at crystallization temperature of 272°C. Polarized optical observation revealed a substantial enhancement in nucleation due to the presence of CaPim. Avrami equation analysis suggested that the nucleating agent significantly increased the crystallization rate constant without affecting the growth dimension. Moreover, Lauritzen–Hoffman theory analysis indicateed that the addition of CaPim lowers the nucleation energy barrier, contributing to its high‐nucleation efficiency. These findings demonstrate that calcium pimelate holds promise as an effective nucleating agent for PPS.

Chiral Nucleating Agents Affecting the Handedness of Lamellar Twist in the Banded Spherulites in Poly(ε-Caprolactone)/Poly(Vinyl Butyral) Blends.

Chiral silica, which acts as a nucleating agent of poly(ε-caprolactone) (PCL), was demonstrated to induce excess handedness of lamellar twist in the banded spherulites of PCL blended with poly(vinyl butyral). The d- and l-forms of silica enhanced the right- and left-handed twists, respectively. The influences of chiral silica on the twist handedness were statistically significant. These results indicate that the handedness of twisting can be controlled upon primary nucleation. The organic substances used as chiral templates of silica had no effect on the handedness; silica was shown to govern the handedness. The possible mechanisms of the chirality transfer are discussed.

Biaxial Magnetic Orientation of Zinc Citrate as Nucleating Agent of Poly(l-lactic acid)

Microcrystals of zinc citrate dihydrate (ZnCit), a nucleating agent of poly(l-lactic acid) (PLLA), were magnetically oriented to obtain a three-dimensional magnetically oriented microcrystal array (3D-MOMA). The structure determined by X-ray analysis of the 3D-MOMA agreed well with that determined using a single crystal. The relationship between the magnetic and crystallographic axes was determined. Since the ZnCit crystal reportedly induces epitaxial growth of PLLAs, their three-dimensional alignment is expected to induce three-dimensional alignment of the PLLA crystals.

Investigating the crystallization, melting behavior, and thermal stability of poly(l-lactic acid) using aromatic isoniazid derivative as nucleating agent

The poor crystallization performance is the common challenge for semicrystalline polymers. In this work, a aromatic isoniazid derivative (DI), derived from isoniazid and 1,4-dicarboxybenzene, was synthesized to serve as a nucleating agent for poly(l-lactic acid) (PLLA), and the crystallization behavior, melting behavior, and thermal stability of PLLA/DI were investigated through a series of measurements. The non-isothermal crystallization behavior showed that the incorporation of DI significantly promoted the crystallization of PLLA in cooling of 1 °C/min; however, the nucleating effectiveness was also evidently affected by the cooling rate. The effect of DI concentration on non-isothermal crystallization of PLLA indicated that 3 wt% DI exhibited the best crystallization acceleration effectiveness, and the non-isothermal crystallization enthalpy of PLLA/3% DI in cooling was considerably enhanced up to 330 times with respect to the primary PLLA. Both XRD and the relevant melting behavior measurements further confirmed the advanced promoting crystallization effect of DI for PLLA. In addition, the measurement also showed that the addition of DI could not change the crystalline form of PLLA, and the double melting peaks were attributed to the melting-recrystallization mechanism. Thermal stability indicated that the thermal decomposition behavior of PLLA did not depend on the DI concentration; however, the onset decomposition temperature decreased with the increase of DI concentration.

Melt Spinning of Poly(3‐hydroxybutyrate) for Tissue Engineering Using Electron‐Beam‐Irradiated Poly(3‐hydroxybutyrate) as Nucleation Agent

Electron-beam-irradiated poly(3-hydroxybutyrate) was used as a nucleating agent for poly(3-hydroxybutyrate) in a melt-spinning process. Molecular data and thermal properties of the irradiated samples were determined. The thermal properties of the nucleated melts were determined to assess the influence of the nucleation agents, and then spinning tests were carried out. Thermal and textile properties of the spun fibers were also determined. Estimations of the improvement of the crystallization in the spinline and of the inhibition of secondary crystallization in the fibers from the use of the described blood-compatible nucleation agents are given.

Physical and mechanical properties of poly(L‐lactic acid) nucleated by dibenzoylhydrazide compound

AbstractBenzoylhydrazide compounds were evaluated as a nucleating agent for poly(L‐lactic acid) (PLA). From the results of the differential scanning calorimetry, octamethylenedicarboxylic dibenzoylhydrazide (OMBH) was found to be most effective for acceleration of PLA crystallization under higher cooling rate of −50°C min−1. PLA with OMBH of 1 wt % exhibited very short crystallization half‐time with wide range of isothermal temperature from 90 to 130°C. The molding cycle time of PLA with OMBH in injection molding was less than 3 min, and the cooling time was one‐third of ethylenebis(12‐hydroxystearylamide)/talc system as a nucleating agent. Physical and mechanical properties improved extremely, and the heat distortion temperature of 124°C, flexural modulus of 4.1 GPa, and Izod impact strength of 7.9 kJ m−2 were achieved. This indicates that the utilization of OMBH makes it possible to extend the application range of PLA as automotive parts and electric appliances, which require higher heat resistance and stiffness. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 244–250, 2007