The intrinsic viscosities of five different molecular weight polystyre
nes in cyclohexane were measured at different temperatures. The temper
atures cover three regions: above the theta point, at the theta point
and below the theta point. The data were analysed with the theoretical
framework on critical phenomena as a guide line. Although the collaps
ed region and the totally collapsed region vary with the range of mole
cular weight, the scaling law appears to be valid. There is a one-to-o
ne correspondence of an observable in one regime to another regardless
of the number of links. (C) 1997 Elsevier Science Ltd.