Open AccessФормирование и трансформация моноклинной и орторомбической фаз в реакторных порошках сверхвысокомолекулярного полиэтилена
Author(s) -
М.В. Байдакова,
П.В. Дороватовский,
Я. В. Зубавичус,
Е.М. Иванькова,
С.С. Иванчев,
В.А. Марихин,
Л.П. Мясникова,
М.А. Яговкина
Publication year - 2018
Publication title -
fizika tverdogo tela
Language(s) - English
Resource type - Journals
eISSN - 1726-7498
pISSN - 0367-3294
DOI - 10.21883/ftt.2018.09.46409.096
Subject(s) - monoclinic crystal system , orthorhombic crystal system , materials science , crystallography , phase (matter) , powder diffraction , beamline , particle (ecology) , diffraction , particle size , composite material , analytical chemistry (journal) , chemistry , crystal structure , optics , organic chemistry , physics , geology , beam (structure) , oceanography
Using powerful synchrotron X-ray radiation of the beamline “Belok” operated by the National Research Center “Kurchatov Institute,” we perform X-ray diffraction (XRD) study of an intact, virgin (not subjected to any external mechanical loads) particle isolated from reactor powder of ultrahigh molecular weight polyethylene. Along with the peaks originating from the orthorhombic phase, we detect the peaks characteristic of the monoclinic phase that is stable only under mechanical stress, suggesting that the mechanical stress that leads to the formation of the monoclinic phase and persists at room temperature develops during the polymer synthesis. The monoclinic phase gradually disappears when the particle is heated stepwise in increments of 5 K, and its peaks become undetectable when the temperature reaches 340 K. We contrast the results obtained for the phase composition of the virgin particle to those for a tablet prepared by compaction of the same reactor powder at room temperature. XRD analyses of the tablet were performed on D2 Phaser (Bruker) instrument. The monoclinic phase that originates during the polymer synthesis and the one that forms in the tablet during compaction have different parameters. We discuss the mechanisms by which these two different monoclinic phases originate during the processes involved.