It is demonstrated that wormlike micelles of nonionic surfactants polyoxyethylene alkyl ethers H(CH 2 ) i (OCH 2 CH 2 ) j OH (C i E j ) have been successfully characterized by static (SLS) and dynamic light scattering (DLS) measurements and viscometry with the aid of the theories developed so far in the field of polymer solution studies, i.e., a molecular thermodynamic theory for light scattering, chain statistical and hydrodynamic theories for semi-flexible polymers. The results for the excess Rayleigh ratio, radius of gyration, hydrodynamic radius, and intrinsic viscosity have been shown to be well represented by the theories based on a wormlike spherocylinder model. Some salient features found for the micelles of C i E j with various i or j, their binary mixtures, and the micelles including n-alcohol and n-alkane are discussed. The nonionic surfactant polyoxyethylene mono-alkyl ether H(CH 2 ) i (OCH 2 CH 2 ) j OH, (abbreviated C i E j ), exhibits a wide variety of phases in aqueous solution as a function of surfactant concentration and temperature. 1,2 Here, i and j denote the number of methylene groups in the alkyl group and that of repeating units in the oxyethylene group, respectively. At dilute regime, the C i E j + water binary system forms an isotropic phase, that is so-called L 1 phase, which consists of micelles formed with the amphiphilic molecules and water. The system exhibits the LCST behavior; the micellar solutions are phaseseparated into two phases at high temperatures. It is now well established that the micelles grow in size with increasing concentration and raising temperature, in particular to a greater extent when approaching the phase boundary, assuming threadlike or wormlike cylindrical shape. (See Figure 1.) The wormlike micelles have been visually shown by the cryo-TEM observation, 3 in which in the process of micellar growth, threadlike or polymer-like micelles are evolved in the solutions examined. The micelles are, thus, sometimes called ''living'' or ''equilibrium'' polymers in a sense that the linear macromolecules formed can break and recombine.The polymerlike micelles have certain similarities to real polymers and then their solution properties are analogous to those of real polymer solutions. They have been, thus, rather widely studied to characterize their shape and size by employing the theoretical concepts and experimental methods developped in the polymer solution studies, such as static (SLS) and dynamic light scattering (DLS), [3][4][5][6][7][8][9][10][11][12] small-angle neutron scattering (SANS), 13-15 viscometry, 15,16 pulsed-field gradient NMR, 4-7 and so forth. However, solutions of polymer-like micelles are essentially different from those of real polymers. The molar mass of the micelle, i.e., the aggregation number, varies with surfactant concentration, temperature, and other solvent conditions. The average value and distribution of the micellar size are determined by multiple chemical equilibrium among micelles with various aggregation numbers. Although the equi...