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These studies emphasize the significance of monomer structure and reactivity for the polymer network morphology formed in liquid crystal media.
(b) A morphology formed in the melt cast ribbon; the inset in (b) is an optical image of the cast ribbon after polishing and etching; this reveals an approximately 1.5- to 3-μm Al grain size.
The morphology formed in binary blends of poly(ε-caprolactone) (PCL) and ε-caprolactone-butadiene diblock copolymer (PCL-b-PB) has been investigated by small-angle X-ray scattering (SAXS).
The crystallization behavior of poly(ε-caprolactone) (PCL) blocks starting from a solid lamellar morphology formed in advance by the crystallization of polyethylene (PE) blocks (PE lamellar morphology) in a PCL-b-PE diblock copolymer was investigated by differential scanning calorimetry (DSC), small-angle X-ray scattering with synchrotron radiation (SR-SAXS), and polarized optical microscope (POM).
The effect of the advance crystallization of PE blocks on the subsequent crystallization of PCL chains was discussed as compared with the crystalline morphology formed in PCL-block-polybutadiene copolymer/PCL homopolymer blends, where the crystallization of PCL chains started directly from a microdomain structure without forming the hard lamellar morphology.
The crystalline morphology formed in binary blends of poly(ε-caprolactone)- block-polyethylene (PCL-b-PE) copolymers and PCL homopolymers has been examined using synchrotron small-angle X-ray scattering (SR-SAXS) and differential scanning calorimetry (DSC) as a function of the homopolymer fraction in the blend.
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In agreement with findings previously reported by the authors [6], a variety of morphologies formed in parallel with nanowires of homogeneous morphology.
The corrosion products and their morphologies formed in the solution after immersing various time have been analyzed by FE-SEM and XRD.
The morphologies formed in the plasticizer-added PCL-b-PS were compared with those of PCL-b-PS cast from toluene or cyclohexane solution, and the characteristics of these morphologies were qualitatively discussed.
The focus of this work is the evaluation and analysis of the state of dispersion of functionalized multiwall carbon nanotubes (CNTs), within different morphologies formed, in a model LCST blend (poly[(α-methylstyrene -co- acrylonitrile)]/poly(methyl-methacrylate), Pα-methylstyrene -co- acrylonitrile
This observation can be understood in two different ways by considering the morphology formed after the irradiation in the vertical and the lateral directions.
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