Herein,
grafting of starch (STR) and in situ strategic inclusion
of 2-(3-(acrylamido)propylamido)-2-methylpropane sulfonic acid (APMPS)
via solution polymerization of 2-(acrylamido)-2-methylpropanesulfonic
acid (AMPS) and acrylamide (AM) have resulted in the synthesis of
smart STR-grafted-AMPS-
co
-APMPS-
co
-AM (i.e., STR-
g
-TerPol) interpenetrating terpolymer
(TerPol) network hydrogels. For fabricating the optimum hydrogel showing
excellent physicochemical properties and recyclability, amounts of
ingredients and temperature of synthesis have been optimized using
multistage response surface methodology. STR-
g
-TerPol
bearing the maximum swelling ability, along with the retention of
network integrity, has been employed for individual and/or simultaneous
removal(s) of metal ions (i.e., M(III)), such as Bi(III) and Sb(III),
and dyes, such as tris(4-(dimethylamino)phenyl)methylium chloride
(i.e., crystal violet) and (7-amino-8-phenoxazin-3-ylidene)-diethylazanium
dichlorozinc dichloride (i.e., brilliant cresyl blue). The in situ
strategic protrusion of APMPS, grafting of STR into the TerPol matrix,
variation of crystallinity, thermal stabilities, surface properties,
mechanical properties, swellability, adsorption capacities (ACs),
and ligand-selective superadsorption have been inferred via analyses
of unadsorbed and/or adsorbed STR-
g
-TerPol using
Fourier transform infrared (FTIR),
1
H/
13
C NMR,
UV–vis, thermogravimetric analysis, differential scanning calorimetry,
X-ray diffraction, field emission scanning electron microscopy, energy-dispersive
X-ray, dynamic light scattering, and rheological analyses and measuring
the lower critical solution temperature, % gel content, pH at point
of zero charge (pH
PZC
), and network parameters, such as
ρ
c
and
M
c
. The prevalence
of covalent, ionic (I), and variegated interactions between STR-
g
-TerPol and M(III) has been understood through FTIR analyses,
fitting of kinetics data to the pseudosecond-order model, and by the
measurement of activation energies of adsorption. The formation of
H-aggregate type dimers and hypochromic and hypsochromic shifts has
been explained via UV–vis analyses during individual and/or
simultaneous removal(s) of cationic dyes. Several isotherm models
were fitted to the equilibrium experimental data, of which Langmuir
and combined Langmuir–Freundlich models have been best fitted
for individual Bi(III)/Sb(III) and simultaneous Sb(III) + Bi(III)
removals, respectively. Thermodynamically spontaneous chemisorption
processes have shown the maximum ACs of 1047.39/282.39 and 932.08/137.85
mg g
–1
for Bi(III) and Sb(III), respectively, at
303 K, adsorbent dose = 0.01 g, and initial concentration of M(III)
= 1000/30 ppm. The maximum ACs have been changed to 173....