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Updated: Sep 22, 2025

Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
Published on: November 27, 2015
Cross Nucleation in Polyethylene with Precisely Spaced Ethyl Branches.
Yoshinobu Nozue1, Shuichiro Seno1, Tatsuhiro Nagamatsu1
1Petrochemicals Research Laboratory, Sumitomo Chemical Co., Ltd., Kitasode, Chiba, Japan.
This study demonstrates cross nucleation in crystalline polymers, where one crystal type initiates the formation of another distinct crystal type. This phenomenon was observed in branched polyethylene, showing faster growth rates for the newly formed crystals.
Area of Science:
- Polymer Science
- Materials Science
- Crystallization Phenomena
Background:
- Cross nucleation involves one crystalline polymorph (A) inducing the nucleation of a different polymorph (B) without transformation.
- While observed in small molecules, evidence for cross nucleation in crystalline polymers has been limited.
- Understanding polymer crystallization is crucial for tailoring material properties.
Purpose of the Study:
- To investigate and confirm the occurrence of cross nucleation in a crystalline polymer system.
- To characterize the crystallographic and kinetic aspects of this phenomenon in polymers.
Main Methods:
- Isothermal crystallization of polyethylene with precisely spaced ethyl branches.
- Polarized optical microscopy to observe spherulite growth and measure radial growth rates.
- Scanning microbeam wide-angle X-ray scattering (WAXS) to determine crystalline polymorphs.
Main Results:
- New spherulites nucleated at the growth front of initially formed spherulites in branched polyethylene.
- The newly grown spherulites exhibited a faster radial growth rate (1.01 μm/min) than the initial ones (0.76 μm/min).
- WAXS confirmed that the initial and newly formed spherulites possessed different crystalline polymorphs.
Conclusions:
- This study provides the first definitive evidence of cross nucleation in a crystalline polymer.
- The observed faster growth rate of the secondary polymorph supports the criteria for cross nucleation.
- This finding opens new avenues for controlling polymer morphology and properties through crystallization engineering.
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