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Abstract: Block copolymer self-assembly is normally conducted via post-polymerization processing at high dilution. In the case of block copolymer vesicles (or “polymersomes”), this approach normally leads to relatively broad size distributions, which is problematic for many potential applications. Herein we report the rational synthesis of low-polydispersity diblock copolymer vesicles in concentrated solution via polymerization-induced self-assembly using reversible addition–fragmentation chain transfer (RAFT) polymerization of benzyl methacrylate. Our strategy utilizes a binary mixture of a relatively long and a relatively short poly(methacrylic acid) stabilizer block, which become preferentially expressed at the outer and inner poly(benzyl methacrylate) membrane surface, respectively. Dynamic light scattering was utilized to construct phase diagrams to identify suitable conditions for the synthesis of relatively small, low-polydispersity vesicles. Small-angle X-ray scattering (SAXS) was used to verify that this binary mixture approach produced vesicles with significantly narrower size distributions compared to conventional vesicles prepared using a single (short) stabilizer block. Calculations performed using self-consistent mean field theory (SCMFT) account for the preferred self-assembled structures of the block copolymer binary mixtures and are in reasonable agreement with experiment. Finally, both SAXS and SCMFT indicate a significant degree of solvent plasticization for the membrane-forming poly(benzyl methacrylate) chains.

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Abstract: The solution behavior of a polystyrene–hydrogenated polyisoprene star diblock copolymer (Mn ∼ 384 K; 6 mol % polystyrene) is examined in nonpolar media. Variable temperature 1H NMR studies using deuterated n-dodecane confirm that the outer polystyrene blocks are only partially solvated in n-dodecane at 25 °C: the apparent polystyrene content of 3.2 ± 0.2 mol % remains essentially constant on heating up to 100 °C. Physical adsorption of this star diblock copolymer onto carbon black particles is examined, with particular attention being paid to the effect of copolymer concentration on colloidal stability. An isotherm is constructed for copolymer adsorption onto carbon black from n-dodecane at 20 °C using a supernatant depletion assay based on UV spectroscopy analysis of the aromatic chromophore in the polystyrene block. Langmuir-type adsorption is observed with a maximum adsorbed amount, Γ, of ∼2.2 ± 0.1 mg m–2. In addition, thermogravimetric analysis is used to directly determine the amount of adsorbed copolymer on the carbon black particles, which are essentially incombustible under an inert atmosphere. Analytical centrifugation, optical microscopy, and transmission electron microscopy studies indicate that the star diblock copolymer acts as an effective flocculant at low concentration, with steric stabilization only being observed above a certain critical copolymer concentration (∼5.5% w/w based on carbon black). This is attributed to the spatial location of the polystyrene block and the star copolymer architecture, which enables copolymer adsorption onto multiple carbon black particles at low coverage, leading to bridging flocculation. Above 5.5% w/w copolymer, the surface coverage is sufficiently high that all of the polystyrene “stickers” adsorb onto single carbon black particles, resulting in colloidally stable, sterically stabilized carbon black dispersions. Small-angle X-ray scattering (SAXS) is also used to characterize the copolymer-coated carbon black particles: this technique provides useful complementary insights regarding the rather subtle changes in the fractal morphology that occur with increasing copolymer concentration. Moreover, SAXS also provides direct evidence for the presence of the copolymer chains at the particle surface.

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Abstract: Soot formation in diesel engines is known to cause premature engine wear. Unfortunately, genuine diesel soot is expensive to generate, so carbon blacks are often used as diesel soot mimics. Herein, the suitability of a commercial carbon black (Regal 250R) as a surrogate for diesel soot dispersed in engine base oil is examined in the presence of two commonly used polymeric lubricant additives. The particle size, morphology, and surface composition of both substrates are assessed using BET surface area analysis, TEM, and XPS. The extent of adsorption of a poly(ethylene-co-propylene) (dOCP) statistical copolymer or a polystyrene-block-poly(ethylene-co-propylene) (PS−PEP) diblock copolymer onto carbon black or diesel soot from n-dodecane s compared indirectly using a supernatant depletion assay technique via UV spectroscopy. Thermogravimetric analysis is also used to directly determine the extent of copolymer adsorption. Degrees of dispersion are examined using optical microscopy, TEM, and analytical centrifugati n. SAXS studies reveal some structural differences between carbon black and diesel soot particles. The mean radius of gyration determined for the latter is significantly smaller than that calculated for the former, and in the absence of any copolymer, diesel soot suspended in n-dodecane forms relatively loose mass fractals compared to carbon black. SAXS provides evidence for copolymer adsorption and indicates that addition of either copolymer transforms the initially compact agglomerates into relatively loose aggregates. Addition of dOCP or PS−PEP does not significantly affect the structure of the carbon black primary particles, with similar results being observed for diesel soot. In favorable cases, remarkably similar data can be obtained for carbon black and diesel soot when using dOCP and PS−PEP as copolymer dispersants. However, it is not difficult to identify simple copolymer−particle−solvent combinations for which substantial differences can be observed. Such observations are most likely the result of issimilar surface chemistries, which can profoundly affect the colloidal stability.

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Abstract: This article describes an experimentally versatile strategy for producing inorganic/organic nanocomposites, with control over the microstructure at the nano- and mesoscales. Taking inspiration from biominerals, CaCO3 is coprecipitated with anionic diblock copolymer worms or vesicles to produce single crystals of calcite occluding a high density of the organic component. This approach can also be extended to generate complex structures in which the crystals are internally patterned with nano-objects of differing morphologies. Extensive characterization of the nanocomposite crystals using high resolution synchrotron powder X-ray diffraction and vibrational spectroscopy demonstrates how the occlusions affect the short and long-range order of the crystal lattice. By comparison with nanocomposite crystals containing latex particles and copolymer micelles, it is shown that the effect of these occlusions on the crystal lattice is dominated by the interface between the inorganic crystal and the organic nano-objects, rather than the occlusion size. This is supported by in situ atomic force microscopy studies of worm occlusion in calcite, which reveal flattening of the copolymer worms on the crystal surface, followed by burial and void formation. Finally, the mechanical properties of the nanocomposite crystals are determined using nanoindentation techniques, which reveal that they have hardnesses approaching those of biogenic calcites.

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Abstract: A series of model sterically stabilized diblock copolymer nanoparticles has been designed to aid the development of analytical protocols in order to determine two key parameters: the effective particle density and the steric stabilizer layer thickness. The former parameter is essential for high resolution particle size analysis based on analytical (ultra)centrifugation techniques (e.g., disk centrifuge photosedimentometry, DCP), whereas the latter parameter is of fundamental importance in determining the effectiveness of steric stabilization as a colloid stability mechanism. The diblock copolymer nanoparticles were prepared via polymerization-induced self-assembly (PISA) using RAFT aqueous emulsion polymerization: this approach affords relatively narrow particle size distributions and enables the mean particle diameter and the stabilizer layer thickness to be adjusted independently via systematic variation of the mean degree of polymerization of the hydrophobic and hydrophilic blocks, respectively. The hydrophobic core-forming block was poly(2,2,2-trifluoroethyl methacrylate) [PTFEMA], which was selected for its relatively high density. The hydrophilic stabilizer block was poly(glycerol monomethacrylate) [PGMA], which is a well-known non-ionic polymer that remains water-soluble over a wide range of temperatures. Four series of PGMAx–PTFEMAy nanoparticles were prepared (x = 28, 43, 63, and 98, y = 100–1400) and characterized via transmission electron microscopy (TEM), dynamic light scattering (DLS), and small-angle X-ray scattering (SAXS). It was found that the degree of polymerization of both the PGMA stabilizer and core-forming PTFEMA had a strong influence on the mean particle diameter, which ranged from 20 to 250 nm. Furthermore, SAXS was used to determine radii of gyration of 1.46 to 2.69 nm for the solvated PGMA stabilizer blocks. Thus, the mean effective density of these sterically stabilized particles was calculated and determined to lie between 1.19 g cm–3 for the smaller particles and 1.41 g cm–3 for the larger particles; these values are significantly lower than the solid-state density of PTFEMA (1.47 g cm–3). Since analytical centrifugation requires the density difference between the particles and the aqueous phase, determining the effective particle density is clearly vital for obtaining reliable particle size distributions. Furthermore, selected DCP data were recalculated by taking into account the inherent density distribution superimposed on the particle size distribution. Consequently, the true particle size distributions were found to be somewhat narrower than those calculated using an erroneous single density value, with smaller particles being particularly sensitive to this artifact.