Acrylic acid (AA), potassium salts, and acrylamide (AM) are generally used in the production of
Superabsorbent Polymers. Acrylamide a colorless, odorless, highly water soluble vinyl monomer
that is used largely as medium in the production of organic chemicals and synthesis of
polyacrylamide (idk cite). In particular, minimizing the acrylic acid dimer level prevents the
insufficiency in the final product for instance yield reduction, loss of soluble fraction, residual
monomers, etc. Manufacturers knew that AA can probably cause problems in the future
researches so they focus on improving its properties and characterization. To inhibit unwanted
polymerization, the temperature of this notably exothermic neutralization reaction must be
evenly contained. Some examples of techniques that are used in the previous researches are free-
radically-initiated polymerization, solution polymerization, graft copolymerization etc.. Among
other techniques, superabsorbent polymer materials are usually done through the use of free-
radically-initiated polymerization of acrylic monomers. The resins are prepared either in aqueous
medium using solution polymerization or in a hydrocarbon medium where the monomers are
well-dispersed. These different methods are briefly discussed in the following sections. (Kabiri,
Zohriaan-Mehr; 2008)
Solution Polymerization
In polymerization, carboxylic acid groups of the product are partially neutralized before or after
the process. The polymerization is initiated by free-radicals in the aqueous phase, using
thermally decomposable initiators, redox initiators or combinations. Redox systems used for the
cross-linking copolymerizations include couples of persulfate/bisulfite, persulfate/thiosulfate,
persulfate/ascorbate and hydrogen peroxide/ascorbate. (Buchholz, 1994)
AA and/or its salts with water-soluble cross-linker, e.g., N,N-methylene Bisacrylamide (MBA)
through the use of solution polymerization is a simple process. The reactants are dissolved in
water at desired concentrations, usually about 10-70%. A fast exothermic reaction yields a gel-
like elastic product which is dried and the macro-porous mass is pulverized and sieved to obtain
the required particle size. This preparative method usually suffers from the necessity to handle a
rubbery/solid reaction product, lack of a sufficient reaction control, non-exact particle size
distribution, and increasing the sol content mainly due to undesired effects of hydrolytic and
thermal cleavage (Kabiri, Zohriaan-Mehr; 2008). Generally, the production of superabsorbent
polymers is classified according to their swelling properties, cost of production, and efficient
technique.
Inverse-Suspension Polymerization
Dispersion polymerization is an interesting method for producing polymer since the products can
be obtained in a form of powder of microspheres. The type of polymerization that used water-in-
oil process is called inverse-suspension. In this process, a dispersion of monomers and
initiator occur in the hydrocarbon phase as a homogenous mixture. The resin particle size and
shape is characterized by the viscosity of the monomer, agitation speed, rotor design, and
dispersant type. (Buchholz, 1994). Because of its high flexibility and vesaritility with high
swelling ability and fast absorption technique, Inverse-suspension is a distinguished technique to
produce SAP. (Kabiri, Zohriaan-Mehr; 2008). MBA an example of water-soluble initiator is
much higher than the oil soluble type initiator for instance, EGDMA. (Omidian, 1994)
5. Po R, Water-absorbent polymers: A patent survey,
J Macromol. Sci-Rev Macromol Chem Phys, C34,
607-662, 1994.
19. Buchholz FL, Recent advances in superabsorbent
polyacrylates, Trend Polym Sci, 2, 277-281, 1994.
97. Hunkeler D, Synthesis and characterization of
high molecular weight water-soluble polymers,
Polym Int, 27, 23-33, 1992.
98. Watanabe N, Hosoya Y, Tamura A, Kosuge H,
Characteristics of water-absorbent polymer emulsions,
Polym Int, 30, 525-531,1993.