Abstract
Various nonspherical polystyrene (PS) particles were prepared by slow evaporation of toluene (used common good solvent) from homogeneous PS/hexadecane (HD)/toluene droplets dispersed in surfactant aqueous solutions at room temperature, followed by the rapid removal of HD from PS/HD particles with various phase-separated morphologies. The morphology of PS/HD particles was controlled by tuning the interfacial tension with various types of surfactants. Hemispherical PS particles with flat surfaces were obtained from phase-separated PS/HD/toluene droplets having a Janus structure, when polyoxyethylene nonylphenyl ether with an average ethylene oxide chain length of 30.8 was used as the surfactant.
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Introduction
Nonspherical polymer particles have attracted great attention because of their potential as materials with unique crystal structures,1, 2, 3 light scattering properties4 and external field-responsive properties (e.g., shear field5 and electric field6). In general, polymer particles synthesized by heterogeneous polymerizations under thermodynamic control have a spherical shape because of interfacial free energy minimization. However, nonspherical polymer particles have been synthesized under kinetic control utilizing various seeded polymerization methods,7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24 microfluidic techniques,25, 26, 27, 28 deformation of spherical polymer particles by external force,29, 30, 31 the stepwise heterocoagulation method32, 33 and the self-organized precipitation method.34
In a previous work, we proposed a novel approach for the preparation of micrometer-sized, monodisperse, nonspherical (i.e., dimpled and hemispherical) polystyrene (PS) particles by successive heating and cooling of spherical PS particles dispersed in a methanol/water medium in the presence of droplets of decane.35 Decane was absorbed by the particles during heating, and the particles subsequently phase-separated into PS and decane phases during cooling. Eventually, nonspherical particles reflecting the morphology of phase-separated PS/decane particles were formed by rapid removal of the decane phase. The final particle shape could be controlled simply with the amount of absorbed decane.
We have also recently demonstrated morphology control of PS/poly(methyl methacrylate) composite particles prepared by the slow release of toluene as a common good solvent from homogeneous PS/poly(methyl methacrylate)/toluene droplets dispersed in a surfactant aqueous solution at room temperature (the solvent evaporation method).36, 37, 38 It was revealed that the particle morphology could be controlled by tuning the interfacial tensions by varying the types of surfactant.
In this article, we attempt to prepare various nonspherical (especially hemispherical) PS particles based on the above two experimental results. This will be achieved by morphology control of PS/hexadecane (HD) particles obtained by the solvent evaporation method (using toluene as the common good solvent) using various types of surfactants, followed by a rapid removal of the HD phase. HD is employed rather than decane because it will not evaporate during the toluene evaporation process.
Experimental Procedure
Materials
Styrene was distilled under reduced pressure in a nitrogen atmosphere. Reagent-grade 1-pyrenylmethyl methacrylate (PM; Funakoshi, Tokyo, Japan) was used as a PS fluorescent moiety without further purification. Reagent-grade 2,2′-azobisisobutyronitrile (AIBN; Wako Pure Chemical Industries, Ltd., Osaka, Japan) was purified by recrystallization from methanol. Toluene and SDS were used as received from Nacalai Tesque, Inc (Kyoto, Japan). Poly(vinyl alcohol) (PVA; Gohsenol GH-17: degree of polymerization, 1700; degree of hydrolysis, 88%) was supplied by Nippon Synthetic Chemical (Osaka, Japan). Commercial-grade polyoxyethylene nonylphenyl ether non-ionic surfactants with average ethylene oxide chain lengths of 15.4, 30.8 and 50.6 units (Emulgen 930, Emulgen 931 and Emulgen 950, respectively) were supplied by Kao Co., Tokyo, Japan. Water was purified using an Elix UV system (Nihon Millipore K.K., Tokyo, Japan).
Preparation of nonspherical particles
PS and S-PM copolymer (P(S-PM)) were synthesized by solution polymerization using 2,2′-azobisisobutyronitrile as an initiator. PS: Mw, 8.8 × 104; Mw/Mn, 2.1. P(S-PM) (PM, 0.5 mol%): Mw, 7.1 × 104; Mw/Mn, 1.7. PS/HD and P(S-PM)/HD particles were prepared as follows: a homogeneous toluene solution of PS (or P(S-PM)) (0.643 g) and HD (PS (or P(S-PM))/HD/toluene=1/1/29, v/v/v) was mixed with a 0.33 wt% (relative to water) surfactant aqueous solution (15 g). The mixture was stirred vigorously using a homogenizer (NIHONSEIKI KAISHA Ltd., ABM-2 Tokyo, Japan) at 4000 r.p.m. for 2 min in a glass vial and toluene was then slowly released by evaporation during gentle stirring at room temperature for 24 h in an uncovered glass vial (surface area between dispersion and air was 8 cm2). The resulting particles were washed by centrifugation using methanol to remove HD and excess surfactant and then dried under vacuum at room temperature.
Measurements
The amount of toluene in the dispersion was determined by gas chromatography (Shimadzu Corporation, Kyoto, Japan, GC-2014) with helium as the carrier gas, N,N-dimethylformamide as a solvent and p-xylene as an internal standard. Molecular weight distribution was measured by gel permeation chromatography, with two styrene/divinylbenzene gel columns (TOSOH Corporation, Yamaguchi, Japan, TSK gel GMHHR-H, 7.8 mm i.d. × 30 cm) using tetrahydrofuran as the eluent at 40 °C at a flow rate of 1.0 ml min−1, employing refractive index (TOSOH Corporation) and ultraviolet detectors (TOSOH Corporation, UV-8II). The columns were calibrated with six standard PS samples (1.05 × 103–5.48 × 106, Mw/Mn=1.01–1.15).
Interfacial tension measured by the pendant drop method
The densities of toluene solutions of PS and HD were measured with a pycnometer (volumetric flask type). Interfacial tensions (γPS-T/Surf-w or γHD-T/Surf-w) between the PS (or HD)-toluene droplets and various surfactant aqueous solutions as functions of PS (or HD) weight fraction (wPS or wHD) were measured by the pendant drop method with a Drop Master 500 (Kyowa Interface Science Co., Ltd., Saitama, Japan). All of the measurements were performed at room temperature (ca. 20 °C). The accuracy of the interfacial tensions reported was±0.1 mN m−1.
Microscope observation
The dispersions of PS/HD and P(S-PM)/HD particles were observed with a Nikon (Tokyo, Japan) Eclipse 80i optical microscope and an Olympus (Tokyo, Japan) FV1000-KDM confocal laser scanning microscope, respectively. Dried PS particles were observed with a Hitachi (Tokyo, Japan) S-2460 scanning electron microscope at an acceleration voltage of 15 kV.
Results and Discussion
The morphology of a PS/HD particle reflects the thermodynamic equilibrium morphology of the phase-separated PS/HD/toluene droplet determined by interfacial free energy minimization. Thus, the measurement of each interfacial tension enables prediction of the most stable droplet morphology. However, measurement of γPS-T/Surf-w at high wPS by the pendant drop method was difficult because of high viscosity. γPS-T/Surf-w was thus calculated from the following equations:39
where, T and Surf-w subscripts denote toluene and surfactant aqueous solutions, respectively, ϕi and ϕiS are the volume fractions of the ith component in the particle and of the ith component at the surface, respectively. γi-T/Surf-w is the interfacial tension between the ith component and the surfactant aqueous phase, r is the ratio of the component molar volumes (r=856), a is the surface area occupied by a toluene molecule (31.4 Å2), k is the Boltzmann constant (1.38 × 10−23 J K−1), T is the temperature (300 K), χ is the interaction parameter between PS and toluene (0.40) and l and m are constants (l=0.5 and m=0.25).40, 41, 42 Equations 1 and 2 give the interfacial tension between the PS and surfactant aqueous phases (γPS-T/Surf-w) as a function of ϕPS. The χ parameter between PS and toluene depends on the polymer concentration. These effects were not considered in the calculation of interfacial tensions, and as assumed previously,38 the χ parameter was treated as constant in the current study.
Figure 1 shows γPS-T/Surf-w and γHD-T/Surf-w with various types of surfactants as functions of wPS and wHD. The γPS-T/Surf-w values calculated based on the above equations indicate constant values at low wPS and were consistent in all cases with those measured by the pendant drop method at wPS=0.17. At high wPS, γPS-T/Surf-w drastically increased with increasing wPS. On the other hand, γHD-T/Surf-w gradually increased with increasing wHD. The magnitude relations of γPS-T/Surf-w and γHD-T/Surf-w were reversed in the cases of PVA, Emulgen 931 and Emulgen 950.
Morphological development of phase-separated PS/HD/toluene droplets associated with intergradations of the interfacial tensions is retarded by increasing viscosity inside the droplet because of increasing polymer fraction (i.e., evaporation of toluene) because the glass transition temperature (Tg) of PS is well above the room temperature. The Tg of the PS-toluene phase in the phase-separated droplet was calculated with the Fox equation,43 assuming that the melting temperature of toluene is its Tg (−93 °C). Because the Tg of the PS-toluene phase reached room temperature at wPS=0.75, the wPS where the droplet morphology is fixed was defined as 0.75 in this experiment.
Table 1 shows γPS-T/Surf-w and γHD-T/Surf-w with various types of surfactants at wPS and wHD=0.75; the difference between γPS-T/Surf-w and γHD-T/Surf-w (Δγ) decreased in the order Emulgen 930>SDS>Emulgen 931>Emulgen 950>PVA. The thermodynamically stable morphology of phase-separated PS/HD/toluene droplets is expected to change from PS-core/HD-shell to HD-core/PS-shell when Δγ decreases from positive to negative. The resulting particle morphology, which reflects the thermodynamically stable droplet morphology, should also exhibit the same tendency.
Figure 2 shows optical micrographs of PS/HD particles prepared by the solvent evaporation method. The morphologies of the resulting particles depended on the type of surfactant. To distinguish between the PS and HD phases, P(S-PM) incorporating a fluorescent unit was employed instead of PS. It was confirmed that a very small amount of copolymerized fluorescent PM did not affect the particle morphology44 (i.e., PS/HD and P(S-PM)/HD particles had the same morphology).
Figure 3 shows confocal laser scanning micrographs of P(S-PM)/HD particles prepared under the same conditions as those in Figure 2. The interfacial area between the P(S-PM) phase and the aqueous media increased with decreasing Δγ, except in the cases of SDS and Emulgen 930 (see Table 1).
Previous work37 has shown that a non-ionic surfactant (polyoxyethylene nonylphenylether with an average ethylene oxide chain length of 10.9) dissolved into both the oil and aqueous phases and significantly reduced the oil-aqueous medium interfacial tension.
Figure 4 shows the variation of Emulgen concentrations in aqueous media as a function of the toluene weight fraction relative to the total amount of toluene, water and Emulgen. Emulgen 930, with an average ethylene oxide unit length of 15.4, dissolved into the toluene phase whereas nearly all Emulgen 931 and 950 dissolved in the aqueous phases. The effect of partitioning was not considered in the equations calculating γPS-T/Surf-w; the actual γPS-T/Surf-w would thus be lower than the calculated one in the Emulgen 930 case, resulting in a lower Δγ for Emulgen 930 than for SDS. This could explain the unexpected results (a) and (b) in Figure 3.
Figure 5 shows scanning electron microscope photographs of PS particles after rapid removal of HD with methanol from the PS/HD particles shown in Figure 2. PS particles with various shapes corresponding to the phase-separated morphology were formed. PS particles prepared using PVA had a single deep dimple at the surface; this was attributed to the volume reduction of the HD phase after hardening of the PS phase during toluene evaporation from the droplets.36 In particular, hemispherical PS particles were obtained when Emulgen 931 was employed. Such particles can be oriented on planar surfaces, with their curved surfaces pointing upward and can act as microlens.45, 46 This simple preparation method should be applicable to other polymer and poor solvent systems, and can thus be a very useful tool for the preparation of hemispherical particles for industrial applications.
Conclusions
Various nonspherical PS particles were prepared by a rapid removal of HD from phase-separated PS/HD particles obtained by the slow release of toluene from PS/HD/toluene droplets dispersed in various surfactant aqueous solutions at room temperature. The phase-separated morphology of the PS/HD particles and the final PS particle shape could be controlled by tuning γPS-T/Surf-w and γHD-T/Surf-w. As a result, hemispherical PS particles were obtained from the phase-separated PS/HD/toluene droplets having a Janus structure when Emulgen 931 was used as the surfactant.
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Acknowledgements
This work was supported by a Grant-in-Aid for Scientific Research (Grant 21245050) from the Japan Society for the Promotion of Science (JSPS).
Part CCCL of the series ‘Studies on Suspension and Emulsion’
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Tanaka, T., Yamagami, T., Nogami, T. et al. Preparation of hemispherical polystyrene particles utilizing the solvent evaporation method in aqueous dispersed systems. Polym J 44, 1112–1116 (2012). https://doi.org/10.1038/pj.2012.71
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DOI: https://doi.org/10.1038/pj.2012.71