conference papers
Small-angle X-ray scattering from polystyrene polymacromonomers with relatively short main chains
aDepartment of Polymer Chemistry, Kyoto University, Katsura, Kyoto 615-8510, Japan
*Correspondence e-mail: yonaka@molsci.polym.kyoto-u.ac.jp
Synchrotron small-angle X-ray scattering measurements were made on polystyrene polymacromonomers F33 and F110 with 33 and 110 styrene residues, respectively, in each side chain in toluene at 298.2 K and cyclohexane at 307.7 K. Two F33 samples with different weight-average degrees of polymerization of main chain Nw of 37 and 17 (F33-13 and F33-14, respectively) and two F110 samples with Nw of 61 and 27 (F110-10 and F110-11, respectively) were used. The z-average mean-square radii of gyration of these polymacromonomers were explained by the wormlike chain with finite diameter when we considered the contribution of side chains near the main chain to the contour length. This model was also applied to calculate the particle scattering function P(θ), giving satisfactory agreements between calculated and experimental k2P(θ) for F33-13 and F110-10 plotted against the magnitude of the scattering vector k = (4π/λ0)sin(θ/2), where λ0 and θ denote the wavelength of the incident X-ray and the scattering angle, respectively. The data for F33-14 and F110-11, which have short main chains relative to the side chains, cannot be explained by the same model. However, these data were closely fitted by the theoretical values for a comb polymer model with semiflexible main and side chains. The stiffness parameter for side chains in toluene was larger than that in cyclohexane, suggesting that the side chains in the former solvent are more stretched than those in cyclohexane.
Keywords: small-angle X-ray scattering; polymacromonomer; branched polymer; radius of gyration; particle scattering function; Kratky plot.
1. Introduction
Polymacromonomer molecules have a comb structure with very high side-chain density. Studies on solution properties of polymacromonomers have shown that these molecules behave as semi-flexible chains (Wintermantel et al., 1994, 1996; Nemoto et al., 1995). We made static and dynamic light scattering and intrinsic viscosity measurements for polystyrene polymacromonomer with the chemical structure shown in Fig. 1 to determine the dependences of the main-chain stiffness parameter λ−1 and the chain diameter d on the degree of polymerization of side chain ns (Terao et al., 1999a, 1999b, 1999c, 2000; Hokajo et al., 2001, 2005; Sugiyama et al., 2007). We also made small-angle X-ray scattering (SAXS) measurements on polystyrene polymacromonomer F15 with ns = 15 to determine the z-average mean-square radius of gyration 〈S2〉z and the particle scattering function P(θ) (Amitani et al., 2005; Nakamura et al., 2007), where θ denotes the scattering angle. Through these SAXS studies, it was found that polymacromonomer molecules can be described by the wormlike chain with the Gaussian segment profile within the cross-sectional plain when the degree of polymerization of main chain N is much larger than ns. However, when N is small, P(θ) cannot be explained by the same model. To see whether this is owing to the possible effects from short side chains, it was pertinent to do similar measurements on polystyrene polymacromonomers with larger ns. Here, we made SAXS measurements on polystyrene polymacromonomers with ns = 33 and 113 (F33 and F110, respectively) and N comparable to or less than ns in toluene at 298.2 K and cyclohexane at 307.7 K. The former solvent is a good solvent while the latter is a theta solvent for polystyrene polymacromonomers (Terao et al., 1999a; Hokajo et al., 2001; Sugiyama et al., 2007).
2. Experimental
2.1. Polymacromonomer samples
Polymacromonomer samples F33-13, F33-14, F110-10, and F110-11 were chosen from previous studies (Terao et al., 1999a; Sugiyama et al., 2007). Molecular weights of the macromonomers for F33 and F110 are 3560 and 11900, respectively. Weight average molecular weights Mw, weight-average degrees of polymerization of main chain Nw, and Nw/ns for the samples studied are summarized in Table 1.
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2.2. SAXS measurements
SAXS measurements on toluene (298.2 K) and cyclohexane (307.7 K) solutions were carried out at beamline BL40B2 of the synchrotron facility SPring 8 (Proposal No 2005B0088). The camera length and the wavelength of the incident X-ray λ0 were set to 1 m and 1.5 nm, respectively. The scattered X-ray was detected on an imaging plate as a two-dimensional image.
A test solution in a quartz glass capillary of 1.5 mm in diameter was kept within ±0.1 K by circulation of temperature-regulated water through a capillary holder. Four solutions with different mass concentrations c were prepared for each sample. Intensity data were accumulated for 5 min for each solution. The solvent intensity was subtracted from the scattering intensity for each solution to obtain the excess intensity ΔI(θ) at θ. The resulting c/ΔI(θ) at fixed θ was extrapolated to c = 0 by means of the square-root plot of [c/ΔI(θ)]1/2 vs c to obtain . We note that no correction for X-ray absorption by the solution is necessary at infinite dilution. Resulting values were plotted against the square of the magnitude of the scattering vector k, which is defined by (4π/λ0)sin(θ/2). Each plot at small k2 was fitted by a straight line to obtain the z-average mean-square radius of gyration 〈S2〉z and the zero scattering angle value . The particle scattering function P(θ) was determined from [c/ΔI(0)]c=0/[c/ΔI(θ)]c=0. The 〈S2〉z values for cyclohexane and toluene solutions are summarized in the fifth and sixth columns, respectively, in Table 1.
3. Results and discussion
3.1. Radius of gyration
The data of 〈S2〉z from the present SAXS and previous light scattering measurements (Terao et al., 1999a, 1999b; Sugiyama et al., 2007) are plotted double-logarithmically against Nw in Fig. 2. The figure also includes the previous SAXS results for F15 (Amitani et al., 2005; Nakamura et al., 2007).
The light scattering data for cyclohexane solutions can be fitted by the dashed lines which represent the calculated values of the mean-square radius of gyration 〈S2〉 for the unperturbed wormlike or the Kratky–Porod (KP) chain
where L and λ−1 denote the contour length and the stiffness parameter (or the Kuhn segment length), respectively, of the chain. The former parameter can be related to molecular weight M by
with the molar mass per unit contour length ML. The dashed lines for the toluene solutions are calculated from the following equation
with the radius expansion factor αS which, according to the quasi two-parameter theory (Yamakawa, 1997), is given by a function of λL and the excluded-volume strength B. We note that the intramolecular excluded-volume effect for F110 in toluene did not need to be considered for its high stiffness of the chain. The parameters for calculation of the dashed lines in Fig. 3 are summarized in Table 2. These lines appreciably deviate downward from the data points at the low molecular weight regions.
‡Terao et al., 1999c; 2000. §Sugiyama et al., 2007. |
Our previous analyses of the data for F15 showed that the effects from the chain thickness and chain ends are essential to explain the data for these regions. The former effect can be taken into account by the following equation.
The latter effect can be considered by introducing a parameter δ defined by
Here, δ stands for the apparent contribution of side chains near the main chain ends to L. The δ values were taken from those determined from the intrinsic viscosity (Terao et al., 1999a; Sugiyama et al., 2007), while d was chosen so that the calculated values give the closest fit to the experimental values. These values are summarized in the sixth and seventh columns in Table 2.
3.2. Particle scattering function
The particle scattering functions for the samples studied are shown in Figs. 3 and 4 in the manner of the Kratky plot of k2P(θ) against k. Each plot has a peak as is expected to thick polymer chains with small axis ratio. The peak top for the cyclohexane solution in each panel is higher than that for the toluene solution. For F33-14, F110-10, and F110-11, k2P(θ) of toluene solutions increases at large k while that of cyclohexane solutions is almost independent of k. It is expected that P(θ) for star polymers in good solvents is proportional to k−5/3 at large k (Alessandrini & Carignano, 1992). However, log–log plots of P(θ) vs k for toluene solutions of F33-14 and F110-11 (not shown) gave slopes −1 and −0.5, respectively, at large k, which are much smaller than the predicted value for star polymers in good solvents.
The dashed line for each plot shows the theoretical values for the cylindrical wormlike chain (Nakamura & Norisuye, 2004), where d values summarized in Table 3 were chosen to give the closest fit to the experimental data. These values were determined within ±3% and are about 10% smaller than the d values estimated from 〈S2〉z in Table 2. The dashed lines in Figs. 3 and 4 fit satisfactorily the experimental data for F33-13 and F110-10 around the peak. However, the tails of dashed lines at large k, k > 1 nm−1 for F33 and k > 0.5 nm−1 for F110, swing being different from the straight tails of the data points. To obtain better agreements, we consider the segment density ρ(rc) in the cross-sectional plain of the polymer by the following Gaussian function.
Here, rc and 〈rc2〉 denote the distance from the centre of the plain and the mean-square value of rc, respectively. The theoretical details for the calculation of P(θ) are given in Nakamura et al. (2007). The solid lines calculated with the 〈rc2〉1/2 values in Table 3 give better fit to the experimental data than the cylindrical wormlike chain. A similar conclusion was given by the small-angle neutron scattering study by Rathgeber et al. (2005) on polymacromonomers with poly(n-butylacrylate) side chains. We note that the 〈rc2〉1/2 value for the Gaussian profile for each polymer–solvent system was determined within ±3% and is about 10% larger than the radius for the cylindrical profile which is calculated from d/81/2.
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From equation (1), we may calculate 〈S2〉 for a linear polystyrene chain with molecular weight twice as large as that of each side chain with λ−1 = 2 nm and ML = 390 nm–1 (Norisuye & Fujita, 1982) to obtain 〈S2〉1/2 = 2.3 nm and 4.4 nm for F33 and F110, respectively. The former value essentially agrees to the 〈rc2〉1/2 for F33 in cyclohexane, while the latter is smaller than 〈rc2〉1/2 for F110 implying that the side chain of F110 in cyclohexane is rather expanded from its unperturbed dimension. The expansion factor of the side chain in toluene may be calculated from 〈rc2〉1/2 in toluene divided by that in cyclohexane resulting 1.2 and 1.1 for F33 and F110, respectively, which are close to the values known for linear polystyrene in toluene (Abe et al., 1993).
The data points for F33-14 and F110-11 in Figs. 3 and 4 cannot be explained by the models above in which the polymacromonomer molecule is regarded as a thick linear chain. For these polymacromonomers with short main chains comparing to the side chains, this approximate treatment may cease to be valid. Thus, we compare these data with the scattering function P0(θ) for comb polymers consisting of infinitely thin semiflexible main and side chains (Amitani et al., 2005). In this model, the side chains with the stiffness parameter λs−1 are assumed to be connected by free joints to the main chain. However, calculated results gave larger k2P0(θ) than the experimental values especially at large k. Thus, we consider the thickness of the main and side chains according to the following equation for the touched-bead model (Burchard & Kajiwara, 1970).
Here, db denotes the bead diameter. The dot–dash lines in Figs. 3 and 4 represent the calculated values for the semiflexible combs with λs−1 and db given in the fifth and sixth columns, respectively, in Table 3. These parameters were chosen to give the closest agreement between the calculated and experimental values, where the main-chain stiffness λ−1 was fixed to the values given in Table 2. The dot–dash lines almost perfectly fit the data points except the high-k tails. The λs−1 values in Table 3 for toluene solutions are larger than those for cyclohexane solutions, showing that the side chains in the good solvent take a more stretched conformation than those in the theta solvent.
Acknowledgements
The author thanks Dr Ken Terao in Osaka University, and Dr Masashi Osa, Mrs Munehiro Hyakutake, Tomoaki Yoshimura and Hiroyuki Okada in Kyoto University, for their help in SAXS measurements at SPring 8.
References
Abe, F., Einaga, Y., Yoshizaki, T. & Yamakawa, H. (1993). Macromolecules, 26, 1884–1890. CrossRef CAS Web of Science
Alessandrini, J. L. & Carignano, M. A. (1992). Macromolecules, 25, 1157–1163. CrossRef CAS Web of Science
Amitani, K., Terao, K., Nakamura, Y. & Norisuye, T. (2005). Polym. J. 37, 324–331. Web of Science CrossRef CAS
Burchard, W. & Kajiwara, K. (1970). Proc. R. Soc. London Ser. A, 316, 185–199. CrossRef CAS Web of Science
Hokajo, T., Hanaoka, Y., Nakamura, Y. & Norisuye, T. (2005). Polym. J. 37, 529–534. Web of Science CrossRef CAS
Hokajo, T., Terao, K., Nakamura, Y. & Norisuye, T. (2001). Polym. J. 33, 481–485. Web of Science CrossRef CAS
Nakamura, Y., Amitani, K. Sugiyama, M. & Norisuye, T. (2007). J. Polym. Sci. Part B Polym. Phys. Submitted.
Nakamura, Y. & Norisuye, T. (2004). J. Polym. Sci. Part B Polym. Phys. 42, 1398–1407. Web of Science CrossRef CAS
Nemoto, N., Nagai, M., Koike, A. & Okada, S. (1995). Macromolecules, 28, 3854–3859. CrossRef CAS Web of Science
Norisuye, T. & Fujita, H. (1982). Polym. J. 14, 143–147. CrossRef CAS Web of Science
Rathgeber, S., Pakula, T., Wilk, A., Matyjaszewski, K. & Beers, K. L. (2005). J. Chem. Phys. 122, 124904. CrossRef PubMed
Sugiyama, M., Nakamura, Y. & Norisuye, T. (2007). Polym. J. Submitted.
Terao, K., Hayashi, S., Nakamura, Y. & Norisuye, T. (2000). Polym. Bull. 44, 309–316. Web of Science CrossRef CAS
Terao, K., Hokajo, T., Nakamura, Y. & Norisuye, T. (1999c). Macromolecules, 32, 3690–3694. Web of Science CrossRef CAS
Terao, K., Nakamura, Y. & Norisuye, T. (1999b). Macromolecules, 32, 711–716. Web of Science CrossRef CAS
Terao, K., Takeo, Y., Tazaki, M., Nakamura, Y. & Norisuye, T. (1999a). Polym. J. 31, 193–198. Web of Science CrossRef CAS
Wintermantel, M., Gerle, M., Fischer, K., Schmidt, M., Wataoka, I., Urakawa, H., Kajiwara, K. & Tsukahara, Y. (1996). Macromolecules, 29, 978–983. CrossRef CAS Web of Science
Wintermantel, M., Schmidt, M., Tsukahara, Y., Kajiwara, K. & Kohjiya, S. (1994). Macromol. Rapid Commun. 15, 279–284. CrossRef CAS Web of Science
Yamakawa, H. (1997). Helical Wormlike Chains in Polymer Solutions. Berlin: Springer.
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