The spreading of aqueous mixtures of a number of surfactants, includin
g ''superspreading'' trisiloxane surfactants, has been investigated as
a function of surfactant concentration, substrate surface energy, tem
perature, humidity, and substrate roughness. The substrate surface ene
rgy, characterized in terms of the contact angle of water, was control
led by the deposition of mixed organosulfur monolayers with different
terminal chemical functionalities. The data demonstrate a strong sprea
ding rate dependence on both surfactant concentration and surface ener
gy. Furthermore, they indicate that nonturbid trisiloxane surfactant s
olutions, which were previously believed not to promote rapid spreadin
g, display superspreading characteristics, albeit on substrates which
were less hydrophobic than those initially investigated. Moreover, bot
h turbid dispersions and nonturbid solutions of nonionic surfactants l
acking trisiloxane groups have also been found to promote greatly enha
nced spreading on less hydrophobic surfaces. Cationic and anionic surf
actants were not observed to exhibit enhanced spreading characteristic
s. These results indicate that surfactant-enhanced spreading denoted e
arlier as ''superspreading'', is not limited to turbid aqueous dispers
ions of trisiloxane surfactants, and this phenomenon may be more gener
al. and occur in a much more diverse class of compounds than previousl
y thought.