Porous N-isopropylacrylamide (NIPA) hydrogels having a unique structure, that is, spherelike cavities distributed randomly and a homogeneous network in the gel phase, were successfully synthesized by means of an emulsion templating method; this method involves the synthesis of NIPA gels in an oil-in-water (O/W) emulsion by free radical copolymerization with a cross-linker, followed by washing (removal) of the dispersed oil as a pore template (porogen). The synthesis conditions, O/W volume ratio, amount of added surfactant, and monomer concentration affect the internal pore structure, equilibrium swelling, and swelling/shrinking kinetics. A porous hydrogel swollen at 10 degrees C has a pore diameter distribution in the range of 1-40 microm, which was observed with a scanning electron microscope. Scanning electron micrographs and swelling degree reveal that the pore size and porosity can be adjusted by varying the O/W volume ratios and surfactant amounts. The porous hydrogels show very rapid swelling/shrinking in accordance with the temperature swing. The fast response is attributed to the convection flow of water through the macropores. In addition to a faster response gel, the emulsion templating method can yield potentially intelligent gels in which the pores function as spaces for reaction, separation, and storage.

The feasibility of temperature-swing adsorption of heavy metals on a thermosensitive N-isopropylacrylamide (NIPA) hydrogel was examined. We have proposed a novel temperature-swing solid-phase extraction (TS-SPE) technique. First, a metal ion in an aqueous solution is complexed with an extractant. Subsequently, the metal-extractant complexes (or micelles) are adsorbed onto the NIPA hydrogel through a hydrophobic interaction above the lower critical solution temperature (LCST). Finally, the metal-extractant complexes are desorbed from the NIPA hydrogel after it is cooled below the LCST. In a model system consisting of Cu(II) ions, sodium n-dodecylbenzenesulfonate (SDBS), and NIPA hydrogel, the proposed TS-SPE technique has been successfully conducted. The following observations can be made: the amount of adsorbed Cu(II) ions increases with the increase in temperature, the maximum adsorption is attained at a temperature above the LCST, and the hydrogel adsorbs and desorbs Cu(II) ions reversibly due to the temperature-swing between 10 and 40 degrees C. The LCSTs of poly(NIPA) in aqueous SDBS solutions with/without CuCl2 and the surface tensions of their solutions suggest that the hydrophobicity of the complex Cu(DBS)2 is greater than the hydrophobicities of SDBS and DBS. In addition to the separation of heavy metals, TS-SPE is potentially applicable to cases such as the separation of biological molecules by means of metal-ion affinity.

Ultrasound of 2 MHz was irradiated to the emulsion prepared from canola oil and water and flocculation of the oil droplets occurred immediately. By putting the emulsion sample in a thin glass cell and setting it in bath type irradiation equipment, the progress of the separation was quantitatively monitored with the optical absorbance. The use of the cell enables visual observation of the behavior of oil droplets. Pictures show the formation of flocks of the dispersed phase and the appearance of checkered pattern consisting of flocks at a regular interval. The observation indicates that the action of radiation forces on oil droplets, which causes the flocculation. The flocks started to rise after stopping irradiation with holding their shape. The rising rate of the flocks was significantly greater than that of oil droplets in the original emulsion. Ultrasonic irradiation caused a rapid decrease in the absorbance, which expresses a progress of the separation. Effects of two major operation parameters, power and time on the separation degree were examined. The degree improved with increasing power input and irradiation time. The dataset was arranged in a plot of normalized separation degree against the input energy. The plot suggests that effective separation was attained with a lower power input and a longer irradiation time. The plot provides a guide for setting condition for the separation.

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A novel thermosensitive adsorbent was developed, which adsorbs and/or desorbs heavy metals through temperature swing process. The gel-type and polymer-type adsorbents, composed of N-isopropylacrylamide (NIPA) as a thermosensitive component and 2-methacryloyloxyethyl phosphate (MEP) as an interactive component, were prepared by free radical copolymerization. For each type of poly(NIPA-co-MEP), phase transitions and temperature dependences for the amount of Cu, a model metal ion, adsorbed was examined. The proposed mechanism associated with the temperature swing adsorption (TSA) of Cu to poly(NIPA-co-MEP) is as follows. In the case of the shrinking gel at higher temperatures, two MEP groups are positioned so as to interact with one Cu ion, while in the swelling gel at lower temperatures, Cu is desorbed from isolated MEP groups. In the case of copolymers, at temperatures lower than the lower critical solution temperature (LCST), two MEP groups interact with one Cu ion as well as those in shrunken gels, and at temperatures higher than the LCST, an aggregate of the copolymer, which is strongly hydrophobic, ejects free water along with Cu ion in the shrinking process. The temperature dependences for adsorption to the copolymer are opposite to gels, even in the gel with a low density of crosslinking points.