The effect of the chain constraint on the glass‐transition temperature of polystyrene (pS) was studied in the context of polymer tethering to curved surfaces. The synthesis and characterization of silica‐graft‐polystyrene (SiO₂‐g‐pS) hybrid nanoparticles is reported. Silica nanoparticles possessing covalently bound pS chains were prepared by the atom transfer radical polymerization of styrene from functionalized colloidal surfaces. These hybrid nanoparticles serve as interesting examples of spherical polymer brushes, as a high density of grafted pS was achieved on the inorganic colloid. The confirmation of a brushlike extension of immobilized chains in a good solvent was obtained with dynamic light scattering in toluene of SiO₂‐g‐pS colloids possessing various molar masses of tethered pS. The solid‐state morphology of SiO₂‐g‐pS ultrathin films was assessed with transmission electron microscopy, and this confirmed that the silica colloids were well‐dispersed in a matrix of the tethered polymer. Differential scanning calorimetry was used to study the effects of tethering and chain immobilization on the glass‐transition temperature of pS. The measured glass‐transition temperature of annealed bulk films of the hybrid nanoparticles was elevated with respect to the value for pure bulk pS. The enhancements ranged from 13 to 2 K for SiO₂‐g‐pS brushes possessing tethered pS with number‐average molecular weights of 5230 and 32,670 g/mol, respectively. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 2667–2676, 2002

In 2020 the Cellulose and Renewable Materials Division (CELL) of the American Chemical (ACS) society celebrates its 100th anniversary. The following paper is based on a chapter from the book commissioned by the Division (Patterson, 2021). CELL is one of the most successful and dynamic Divisions in the ACS. It has evolved throughout its history to remain relevant and productive. One of its strengths is its diversity, while staying true to its founding vision. This perspective was present at its founding, and the following paper surveys the world of cellulose and renewable materials from the dawn of history to 1920. CELL has both industrial and scientific roots and has always welcomed the full range of participants from these communities. Rather than operating as separate tribes, the two groups have fostered innovations in each other. Many aspects of cellulose science and technology are discussed from antiquity to the early 20th century.