Published at : 17 Jan 2014
Volume : IJtech
Vol 4, No 3 (2013)
DOI : https://doi.org/10.14716/ijtech.v4i3.117
S. Muryanto | Department of Chemical Engineering & Office of Research (LEMLIT), Universitas 17 Agustus 1945 (UNTAG) Semarang, Bendhan Dhuwur, Semarang 50233, Indonesia |
A.P. Bayuseno | Mechanical Engineering Graduate Program, Diponegoro University, Tembalang, Semarang 50275, Indonesia |
Sutrisno | Mechanical Engineering Diploma (D3) Program, Diponegoro University, Tembalang, Semarang 50275, Indonesia |
W. Sediono | Mechanical Engineering Diploma (D3) Program, Diponegoro University, Tembalang, Semarang 50275, Indonesia |
W. Mangestiyono | Mechanical Engineering Diploma (D3) Program, Diponegoro University, Tembalang, Semarang 50275, Indonesia |
Experiments were performed in a piping system to examine the effects of
flow rates and Cu2+, a common metal ion in wastewater, on the kinetics
of gypsum (CaSO4.2H2O) scale formation. The scaling was monitored by
measuring the decrease in Ca2+ concentrations, [Ca2+], of the scaling
solution. AAS analysis shows that [Ca2+] reduces progressively after a
certain induction time, during which time the concentration remains
steady. Thus, the gypsum precipitation which leads to scaling in pipes
does not occur spontaneously. Higher impurity concentrations (0 to 10
ppm Cu2+) result in longer induction time (26 to 42 min), which indicate
that Cu2+ could inhibit the scale formation. Impurity concentrations
and the scale mass generated are negatively correlated. Reduction in
scale mass was as high as 61% depending on impurity concentrations and
flow rates. Data of [Ca2+] versus time were used to calculate the
reaction rate of the gypsum precipitation which led to scaling. It was
found that the reaction follows a first order kinetics with respect to
[Ca2+], with rate constants ranging between 5.28 and 7.37 per hour,
which agree with most published values for mineral scale formation.
Crystallization, Cu2+, Gypsum, Kinetics, Wastewater