The structural development of poly(butylene terephthalate) (PBT) fibers was analyzed using in situ wide angle X-ray diffraction and fiber temperature measurements during CO 2 laser-heated drawing, in which the necking position on the running fiber could be fixed by CO 2 laser irradiation. The measured parameters were determined as functions of the elapsed time after necking with a time resolution of 0.3 ms. The as-spun PBT fibers, which exhibited a low-oriented a-crystalline structure, were drawn to a draw ratio of 5 using laser heating. The (001 0 ) reflection, which indicates a quasi-smectic fibrillar structure, was not observed before crystallization in contrast to measurements of poly(ethylene terephthalate) (PET) and poly(ethylene 2,6-naphthalene dicarboxylate) (PEN). The a-crystal was transformed into an oriented b-form crystal at the necking position, and the developed b-crystallites exhibited increased size and altered orientation o2 ms after necking. The fiber temperature increased rapidly at around T g , and the rearrangement of the b-crystal primarily occurred as the fiber's temperature rose from 100 to 160 1C. Keywords: crystal-crystal transition; laser-heated drawing; poly(butylene terephthalate) INTRODUCTION Poly(butylene terephthalate) (PBT) is a type of polyester produced by the polymerization of 1,4-butanediol and terephthalic acid. PBT has two more methylene (CH 2 ) groups than poly(ethylene terephthalate) (PET), which results in reduced coherence among molecules and provides the PBT fiber with increased flexibility. The higher chain flexibility causes a reversible crystal-crystal transition, and the PBT fiber thus exhibits good stretching properties with high stretch recovery.PBT has two different crystalline forms: the a-form and the bform. 1-7 The a-form crystalline structure, in which the chain consists of four methylene groups with a gauche-trans-gauche conformation, is found in a relaxed state and is the most stable structure. The a-crystal is transformed into the b-crystal when the polymer is held under strain, and the polymer reversibly transforms to the a-crystal upon removal of the strain. The b-crystal consists of an all-trans conformation chain. This difference in conformation between the b-crystal and the a-crystal, which is not fully extended, primarily affects the unit cell parameter c, which is very sensitive to the transition and is often used to detect the transition. Mencik 1 was the first to index the unit cell of the a-crystal, which is triclinic and has