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Block polymers assemble into a variety of phase-separated morphologies based on volume fraction (φ) and interactions (χ) of the respective blocks. The arrangement of three different polymer blocks ...

Brush block copolymers (BBCPs) exhibit attractive features for use as templates for functional hybrid nanomaterials including rapid ordering dynamics and access to broad ranges of domain sizes; however, there are relatively few studies of the morphology of the BBCPs as a function of their structural variables and fewer still studies of BBCP composite systems. Here we report the structural diversity and phase behavior of one class of BBCP nanocomposites as a function of the volume fractions of their components and the side chain symmetry of the BBCPs. We conducted a systematic investigation of gold nanoparticle (NP) (∼2 nm) assembly in a series of poly(tert-butyl acrylate)-block-poly(ethylene oxide) (PtBA-b-PEO) BBCPs with a fixed side chain length of PtBA (Mn = 8.2 kg/mol) but with different PEO brush lengths (Mn = 5.0, 2.0, or 0.75 kg/mol) as well as volume fractions (fPEO = 0.200–0.484). The gold NPs are selectively incorporated within the PEO domain via hydrogen bond interactions between the 4-mercapto...

The morphologies of sulfonated polystyrene-block-fluorinated polyisoprene (s-PS-b-f-PI) were studied as functions of different kinds of solvents and thermal annealing, using transmission electron microscope microscopy (TEM), small angle X-ray scattering (SAXS) and intermediate angle X-ray diffraction (IMAXD). The film of the block copolymer ionomer with an acid form [sulfonated PS-b-fluorinated PI (sH-PS-b-f-PI)], which was cast from anhydrous tetrahydrofuran (THF), developed a well-ordered cylindrical morphology of the f-PI domains in the sH-PS matrix. The morphology was explained by the solubility parameter and the Bjerrum length. The morphology changed to that of a no long-range ordered structure, through thermal annealing. The result was different from the usual behavior of uncharged diblock copolymers and could have been due to the ionic cluster formation. The solution casting films of the block copolymer ionomer with a cesium neutralized form (sCs-PS-b-f-PI) were obtained from the mixed solvent of THF/water (98/2, wt/wt) and DMSO. The ionic cluster formation in the film cast from the mixed solvent was hardly changed by annealing. The promotion of the ionic cluster formation by annealing was clearly observed in the film cast from DMSO. However, hindrance of microphase separation by the promotion of the ionic cluster formation was not confirmed in this study.

Concerted experimental and theoretical investigations have been carried out to understand the microphase separation in diblock copolymer melts containing poly (1,3-cyclohexadiene), PCHD, as one of the constituents. In particular, we have studied diblock copolymer melts containing polystyrene (PS), polybutadiene (PB), and polyisoprene (PI) as the second block. We have systematically varied the ratio of 1,2-/1,4-microstructures of poly (1,3-cyclohexadiene) to tune the conformational asymmetry between the two blocks and characterized the effects of these changes on the morphologies using transmission electron microscopy (TEM) and small angle X-ray scattering (SAXS). Our experimental investigations reveal that the melts of PCHD-b-PB, PCHD-b-PS and PCHD-b-PI containing nearly equal fractions of each component and high percentage of 1,4-microstructures in the PCHD block form cylindrical rather than lamellar morphologies as expected in symmetric diblock copolymers. In contrast, the morphologies of PCHD-b-PB, PCHD-b-PS and PCHD-b-PI containing PCHD block with higher 1,2-microstructure are found to be disordered at 110 � C. The change in the morphological behavior is in good agreement with our numerical calculations using the random phase approximation and self-consistent field theory for conformationally asymmetric diblock copolymer melts. Also, the effects of composition fluctuations are studied by extending the BrazovskiieLeiblereFredricksoneHelfand (J. Chem. Phys. 87, 697 (1987)) theory to conformationally asymmetric diblock copolymer melts. These results allow the understanding of the underlying self-assembly process that highlights the importance of the conformational asymmetry in tuning the morphologies in block copolymers.

Previously, we have synthesized a cobalt-containing diblock copolymer system which exhibited room temperature ferromagnetic properties after phase separation and heat treatment. We have also shown that the morphology and cobalt density in the nanostructured domains both influenced the magnetic properties of these materials due to nanoconfinement which enhanced the dipolar interactions between otherwise superparamagnetic cobalt nanoparticles. Here, we investigated the effect of domain size on the magnetic properties of these room temperature ferromagnetic materials (RTFMs) using a series of five cobalt-containing diblock copolymers with various molecular weights and constant block ratios. The diblock copolymers self-assembled into cylindrical morphologies with different domain sizes upon solvent annealing, and then were converted to RTFMs upon a simple heat treatment. The domain sizes of these RTFMs did not show a significant impact on their coercivity values, possibly because the domain size range investigated was not large enough and the cobalt–cobalt dipolar interactions were nearly constant throughout. At the same time, this study confirms that the RTFMs generated from these novel block copolymers are robust.

In this study, block copolymer ionomers of the cesium salt (20 mol %) of fluorinated polyisoprene-block-sulfonated polystyrene were spin cast into membranes and annealed under an electric field of ∼40 V/μm at 130 °C for 24 h. The effect of this treatment was a 2.5 times increase in the ionic conductivity as measured by electrochemical impedance spectroscopy, under all humidity conditions measured. This can be attributed to the increased connectivity of the ionic domains of the block copolymers. This E-field alignment technique may thus find application in the fabrication of nanostructured polyelectrolytes with enhanced charge transport capacity.

Conventional transmission electron microscopy (TEM) was utilized to characterize vesicles formed by the spontaneous self-assembly of a novel zwitterionic block copolymer in the ionic liquid (2-hydroxyethyl)dimethylammonium methanesulfonate as well as in 0.1 M phosphate buffered saline (PBS). This block copolymer was synthesized via ring-opening metathesis polymerization (ROMP) of a norbornene-based sulfobetaine, followed by its end-functionalization with polystyrene to generate the necessary amphiphilic structure. The ionic liquid enabled the visualization of the vesicles in their swollen state by TEM, demonstrating a new method for improved characterization of polymer vesicles.

Well-ordered block copolymer nanocomposites with d-spacings as small as 15 nm and additive loadings greater than 70 mass % were formed upon blending functionalized polyhedral oligomeric silsesquioxanes (POSS) additives into disordered block copolymers containing poly(ethylene oxide) (PEO) as one of the blocks. The POSS additives were functionalized with maleamic acid or aminophenyl groups as ligands to enable selective hydrogen bonding with the PEO chains. The selective interaction of the additives with the PEO chains caused microphase separation of the block copolymer leading to formation of well-ordered morphologies as evidenced by small-angle X-ray scattering. Further addition of the additive induced transitions between cylindrical and spherical morphologies. While both ligands induced order, the maleamic acid ligand enabled higher levels of incorporation of POSS cages into the PEO phases of the composite. Differential scanning calorimetry and wide-angle X-ray diffraction were performed to confirm comp...

Small-angle neutron scattering (SANS) and ultra-small-angle X-ray scattering (USAXS) have been used to study the structural changes in fluorinated polyisoprene/sulfonated polystyrene (FISS) diblock copolymers as they evolved from the dry state to the water swollen state. A dilation of the nanometer-scale hydrophilic domains has been observed as hydration increased, with greater dilation occurring in the more highly sulfonated samples or upon hydration at higher temperatures. Furthermore, a decrease in the order in these phase separated structures is observed upon swelling. The glass transition temperatures of the fluorinated blocks have been observed to decrease upon hydration of these materials, and at the highest hydration levels, differential scanning calorimetry (DSC) has shown the presence of tightly bound water. A precipitous drop in the mechanical integrity of the 50% sulfonated materials is also observed upon exceeding the glass transition temperature (Tg), as measured by dynamic mechanical analysis (DMA).

With a view to optimizing morphology and ultimately properties, membranes have been cast from relatively inexpensive block copolymer ionomers of fluorinated polyisoprene -block- sulfonated polystyrene (FISS) with various sulfonation levels, in both the acid form and the cesium neutralized form. The morphology of these membranes was characterized by transmission electron microscopy and ultra-small angle X-ray scattering, as well as water uptake, proton conductivity and methanol permeability within the temperature range from 20 to 60 °C. Random phase separated morphologies were obtained for all samples except the cesium sample with 50 mol% sulfonation. The transport properties increased with increasing degree of sulfonation and temperature for all samples. The acid form samples absorbed more water than the cesium samples with a maximum swelling of 595% recorded at 60 °C for the acid sample having 50 mol% sulfonation. Methanol permeability for the latter sample was more than an order of magnitude less than for Nafion 112 but so was the proton conductivity within the plane of the membrane at 20 °C. Across the plane of the membrane this sample had half the conductivity of Nafion 112 at 60 °C.

Based on the phase diagram constructed for water-silk fibroin-LiBr using the osmotic stress method, wet-spinning of osmotically stressed, regenerated Bombyx mori silk fibroin was performed, without the necessity of using expensive or toxic organic solvents. The osmotic stress was applied to prestructure the regenerated silk fibroin molecule from its original random coil state to a more oriented state, manipulating the phase of the silk solution in the phase diagram before the start of spinning. Various starting points for spinning were selected from the phase diagram to evaluate the spinning performance and also physical properties of fibers produced. Monofilament fiber with a diameter of 20 microm was produced. It was found that the fibers whose starting point in the phase diagram were around the phase boundary between silk I and silk II, at very low LiBr concentrations, showed the best spinning process stability and physical properties. This underpins the prediction that the enhanced control over structure and phase behavior using the osmotic stress method helps improve the physical properties of wet-spun regenerated silk fibroin fibers.

The microstructure of anisotropically shaped grains can strongly influence a range of material properties, including transport, mechanical and electro-optical. A grain-structure-related phenomenon, known as excluded volume epitaxy (EVE), is reported in this study. EVE is a local, inter-grain orientational correlations effect, which results from a combination of continuous nucleation of anisotropic grains and impingement of growing grains. Due to EVE, anisotropically shaped grains have a tendency to be similarly aligned in a local neighbourhood, despite the absence of any forced global orientation in the sample. The effect has been repeatedly observed by the authors in block copolymers, as illustrated by a representative TEM image. Optical microscopy of anisotropically shaped non-polymeric crystals revealed the generality of this effect. The simulation study revealed a tendency for azimuthal, inter-grain orientational correlation and re-confirmed the experimental observation of EVE.

Micro- and nanoscale crystals of the thermochromic polydiacetylenes (PDAs) ETCD and PUDO exhibit electronic absorption maxima at wavelengths longer than those observed in bulk crystal specimens of the same materials. This observation is in contrast to the reported behavior of PDA−DCH where the absorption maximum shifts to shorter wavelengths as crystal size decreases. Infrared spectra and X-ray powder data indicate that the small crystals have the same composition and a structure similar to the bulk specimens. Differential scanning calorimetry (DSC) reveals a larger endothermic heat of the thermochromic phase transition in the small crystals vs bulk specimens. The crystal morphology and structure of microsized, nanosized, and bulk crystals of PDA−ETCD and PDA−PUDO were studied by transmission electron microscopy (TEM) and electron diffraction (ED). For both PDAs, no drastic changes in lattice parameters were observed as crystal size decreases from bulk to micro- and nanoscale.

We present the synthesis and characterization of a new class of high temperature thermoplastic elastomers composed of polybenzofulvene polyisoprene polybenzofulvene (FIF) triblock copolymers. All copolymers were prepared by living anionic polymerization in benzene at room temperature. Homopolymerization and effects of additives on the glass transition temperature (T-g) of polybenzofulvene (PBF) were also investigated. Among all triblock copolymers studied, FIF with 14 vol % of PBF exhibited a maximum stress of 14.3 +/- 1.3 MPa and strain at break of 1390 +/- 66% from tensile tests. The stress strain curves of FIF-10 and 14 were analyzed by a statistical molecular approach using a nonaffine tube model to estimate the thermoplastic elastomer behavior. Dynamic mechanical analysis that the softening temperature of PBF in FIF was 145 degrees C, much higher than that of thermoplastic elastomers with polystyrene hard blocks. Microphase separation of FIF triblock copolymers was observed by small-angle X-ray scattering, even though long-range order was not achieved under the annealing conditions employed. In addition, the microphase separation of the resulting triblock copolymers was examined by atomic force microscopy.

We investigate the effect that process conditions have on the structural characteristics and mechanical response of a cylindrically phase-separated poly(styrene−ethylene-co-butylene−styrene) (SEBS) triblock copolymer system. Small-angle X-ray diffraction (SAXD) and transmission electron microscopy (TEM) have been used to study the microdomain and grain structure, respectively. It is observed that the structural changes that occur with different process conditions and thermal treatment alter the mechanical behavior in both monotonic tensile and cyclic tests. Results show that the d-spacing decreases with increasing temperature and increasing cooling rate from the melt state. These subtle changes in d-spacing are correlated with the elastic modulus. Such variations in domain spacing and size depend on the segregation power (χ) of the system. Grain size changes significantly with cooling rate and upon annealing fine-grain structures but has no significant effect on the material's modulus.

We report that an exceptionally large volume of highly ordered arrays (single grains) on the order of millimeters in scale can be rapidly created through a unique innate guiding mechanism of brush block copolymers (BBCPs). The grain volume is over 10(9) times larger than that of typical self-assembled linear BCPs (LBCPs). The use of strong interactions between nanoparticles (NPs) and BBCPs enables high loadings of functional materials, up to 76 wt % (46 vol %) in the target domain, while maintaining excellent long-range order. Overall, this work provides a simple method to precisely control the spatial orientation of functionalities at nanometer length scales over macroscopic volumes, thereby enabling the production of hybrid materials for many important applications.

Commercial polypropylene pelvic mesh products were characterized in terms of their chemical compositions and molecular weight characteristics before and after implantation. These isotactic polypropylene mesh materials showed clear signs of oxidation by both Fourier-transform infrared spectroscopy and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDS). The oxidation was accompanied by a decrease in both weight-average and z-average molecular weights and narrowing of the polydispersity index relative to that of the non-implanted material. SEM revealed the formation of transverse cracking of the fibers which generally, but with some exceptions, increased with implantation time. Collectively these results, as well as the loss of flexibility and embrittlement of polypropylene upon implantation as reported by other workers, may only be explained by in vivo oxidative degradation of polypropylene.

To date the self-assembly of ordered metal nanoparticle (NP)/block copolymer hybrid materials has been limited to NPs with core diameters (D(core)) of less than 10 nm, which represents only a very small fraction of NPs with attractive size-dependent physical properties. Here this limitation has been circumvented using amphiphilic brush block copolymers as templates for the self-assembly of ordered, periodic hybrid materials containing large NPs beyond 10 nm. Gold NPs (D(core) = 15.8 ± 1.3 nm) bearing poly(4-vinylphenol) ligands were selectively incorporated within the hydrophilic domains of a phase-separated (polynorbornene-g-polystyrene)-b-(polynorbornene-g-poly(ethylene oxide)) copolymer via hydrogen bonding between the phenol groups on gold and the PEO side chains of the brush block copolymer. Well-ordered NP arrays with an inverse cylindrical morphology were readily generated through an NP-driven order-order transition of the brush block copolymer.

We have observed nematic textures in polarized optical microscopy and "plus" (+) patterns in depolarized light scattering (four lobes parallel to polarizer/analyzer axes) from a deeply quenched diblock copolymer melt with a cylindrical microstructure. Both of these features are similar to those found in nematic liquid crystalline polymers. In contrast, this same polymer sample exhibits a more conventional grain structure at shallower quench depths, characterized by an "X" pattern in depolarized light scattering (lobes at 45° to polarizer/ analyzer axes). A theoretical model is used to analyze the "plus" scattering patterns obtained from nematic textures in the single scattering limit. This model is used to quantify the nature of local correlations in our deeply quenched block copolymer melt. We show that the nematic texture is easy to align by shear flow while the granular structure is not.

Characterization of pore structure and pore wall crystal structure was performed on porous high-density polyethylene (HDPE) material using scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electron diffraction (ED). The porous HDPE material was obtained through crystallization from swollen cross-linked polyethylene gels (CSX process1) in supercritical propane. SEM showed an open-pore structure of micron-sized pores, large void fraction, and surface area as well as thin yet rigid pore walls, making this material a good candidate for a variety of applications. TEM revealed oriented lamellar structure in the pore walls which was much different from structures found in typical bulk HDPE as well as that of the cross-linked HDPE before CSX processing. Electron diffraction results confirmed the presence of oriented lamellar stacking. On the basis of this oriented lamellar structure, possible mechanisms for crystallization and pore formation are suggested.

PS-PI multigraft copolymers with tri- tetra- and hexafunctional polystyrene branch points have been studied to investigate the influence of molecular architecture on morphological and tensile properties and to find novel material concepts. It was found that the morphological behaviour of these grafted copolymers can be predicted using theoretical approaches. The number of branch points, however, greatly influences the long-range order of microphase separation. Additionally, two new parameters for adjusting mechanical properties of multigraft copolymers are found in our investigations: 1) functionality of the graft copolymer: tri-, tetra- or hexafunctional and 2) number of branch points per molecule. Tetrafunctional multigraft copolymers show surprising high strain at break values up to 1550 %. With increasing number of branch points strain at break and tensile strength increase, where a linear dependence of mechanical properties on the number of branch points is obvious. Excellent elasticity of tetra and hexafunctional multigraft copolymers at high deformation was proved in hysteresis experiments.

Using a series of AnBn miktoarm star block copolymers with different numbers of arms (n = 1, 2, 4, and 16), the effect of molecular architecture on the grain growth kinetics was investigated by ann...

A novel bottom-up approach to obtain polymer nanocomposites using cubic silsesquioxanes (POSS) nanoparticles as building blocks is reported. The design is based on associative interaction between particles to form ordered nanostructure and limited crystal growth to render anisotropic shapes. Specifically, the affinity between POSS units causes these particles to aggregate and closely pack into a crystalline lattice. The organic polymer, covalently connected to each POSS unit, limits the crystallization into a two-dimensional lattice as demonstrated in random copolymers of polybutadiene and cubic silsesquioxanes. The copolymers were synthesized by ring-opening metathesis copolymerization of cyclooctadiene and POSS bearing a polymerizable norbornene group. The polymers were characterized using NMR, DSC, TEM, WAXD, and SAXS. The data from TEM and X-ray diffraction clearly show the formation of two-dimensional lamellar-like nanostructures of assembled cubic silsesquioxanes.

The tensile properties of tetra-functional multigraft copolymers have been shown to have surprising high strain at break (~2100%), about double that of commercial thermoplastic elastomers such as Kraton! Currently, multigraft copolymers can be synthesized with a variety of branches (single, bi, tri-, tetra, and with different lengths) at each branch point and there can be a large number of branch points per molecule that are regularly, randomly, or heterogeneously spaced, each of which can have effects on mechanical properties. Unfortunately experimental synthesis and characterization of these novel polymer systems is quite time consuming. This is where molecular modeling and simulation can be critical for mapping out the fundamental mechanisms responsible for the observed behavior and to optimize/focus the experimental efforts. In this article we report details of our experimental synthetic and characterization effort along with some preliminary results from molecular dynamics, molecular mechanics, Monte...

The living cationic sequential block copolymerization of isobutylene (IB) with tert-butyl vinyl ether (tBVE) was studied using a one-pot procedure in hexanes/CH2Cl2 and hexanes/CH3Cl solvent systems at −80 °C. It was carried out by the so-called capping-tuning technique, involving the capping of living PIB chain ends with 1,1-ditolylethylene (DTE) followed by addition of titanium(IV) isopropoxide (Ti(OIp)4) to lower the Lewis acidity before the introduction of tBVE. Homopolymerizations/model block copolymerizations of tBVE were carried out using 2-chloro-2,4,4-trimethylpentane (TMPCl) instead of living PIB. The living nature was exhibited by the linear plots of ln([M]0/[M]) vs time and number average molecular weight (Mn) vs conversion. 13C NMR spectroscopy indicated that the PtBVE is highly isotactic with close to 80% meso dyads. Well-defined PIB-b-PtBVE diblock copolymers were synthesized by the living cationic polymerization of IB followed by capping the living PIB ends with DTE and fine-tuning the Lew...

An electric field induced sphere-to-cylinder transition in thin films of asymmetric polystyrene-b-poly(methyl methacrylate) diblock copolymers was observed. In the absence of an applied electric field, thin films of the asymmetric diblock copolymer consisted of layers of spherical microdomains with poor in-plane long-range ordering. Under a ∼40V/μm applied electric field, hexagonally packed cylindrical microdomains normal to the surface were found. Cross-sectional transmission electron microscopy images of the intermediate stages of the alignment indicated that, under an electric field, the asymmetric diblock copolymer formed spherical microdomains that were deformed into ellipsoids and, with time, interconnected into cylindrical microdomains oriented in the direction of the applied electric field. Simulations suggest that improved long-range order of the cylindrical microdomains could be achieved by cycling the electrical field.

Multigraft copolymers with polyisoprene backbones and polystyrene branches, having multiple regularly spaced branch points, were synthesized by anionic polymerization high vacuum techniques and controlled chlorosilane linking chemistry. The functionality of the branch points (1, 2 and 4) can be controlled, through the choice of chlorosilane linking agent. The morphologies of the various graft copolymers were investigated by transmission electron microscopy and X-ray scattering. It was concluded that the morphology of these complex architectures is governed by the behavior of the corresponding miktoarm star copolymer associated with each branch point (constituting block copolymer), which follows Milner's theoretical treatment for miktoarm stars. By comparing samples having the same molecular weight backbone and branches but different number of branches it was found that the extent of long range order decreases with increasing number of branch points. The stress-strain properties in tension were investigated for some of these multigraft copolymers. For certain compositions thermoplastic elastomer (TPE) behavior was observed, and in many instances the elongation at break was much higher (2-3X) than that of conventional triblock TPEs.

The osmotic stress method was applied to study the thermodynamics of supramolecular self-assembly phenomena in crystallizable segments of Bombyx mori silkworm silk fibroin. By controlling compositions and phases of silk fibroin solution, the method provided a means for the direct investigation of microscopic and thermodynamic details of these intermolecular interactions in aqueous media. It is apparent that as osmotic pressure increases, silk fibroin molecules are crowded together to form silk I structure and then with further increase in osmotic pressure become an antiparallel beta-sheet structure, silk II. A partial ternary phase diagram of water-silk fibroin-LiBr was constructed based on the results. The results provide quantitative evidence that the silk I structure must contain water of hydration. The enhanced control over structure and phase behavior using osmotic stress, as embodied in the phase diagram, could potentially be utilized to design a new route for water-based wet spinning of regenerated silk fibroin.

The phase behavior of mixtures of polyisobutylene (PIB), polyethylene (PE), and a symmetric polyethylene-block-head-to-head polypropylene copolymer (PE−PP) was studied by transmission electron microscopy (TEM) and small-angle neutron and light scattering. The thermodynamic interactions between PE/PP and PE/PIB are repulsive (Flory−Huggins parameter χ > 0 and decreases with increasing temperature), while those between PP/PIB are attractive (χ < 0 and increases with increasing temperature). When the PE−PP copolymer is added to a 50/50 PE/PIB mixture, the resulting phase diagram in temperature−copolymer composition space exhibits many of the characteristics of “fish-shaped” phase diagrams found in oil/water mixtures stabilized by balanced surfactants. This is due to the interplay between the different χ parameters that characterize the system. Lamellar phases, single droplet microemulsions, and bicontinuous microemulsions were observed. The length scales of these structures and the locations of the phase tra...

To probe the effect of junction point functionality in miktoarm star block copolymer architecture on chain conformation and morphology, a series of AnBn miktoarm star copolymers where A arms are PS blocks and B arms are PI blocks were investigated. The overall series including a diblock and the star block copolymers can be represented by AnBn, where n = 1, 2, 4, and 16. These materials were produced by synthesizing a single batch of living PS arms and a single batch of living PI arms and then linking them together with chlorosilane coupling agents of different functionality. Thus, all PS arms are identical and all PI arms are identical across the entire series of materials. All stars in the series have equal numbers of PS and PI arms, and the volume fractions of all the samples in the series (nearly 0.50 PS by volume) are identical within experimental error. All the materials were found, via small-angle X-ray scattering and transmission electron microscopy, to form lamellar morphologies. A significant inc...

Long-chain heteroatom-containing telechelic diols with 29-32 atoms in the backbone were synthesized by a one-step, free-radical tetomerization of 10-undecene-1-ol with commercially available α,ω-dithiols. The oxygen and sulfur atoms caused a decrease in the melting point and enthalpy of the diols, compared to the corresponding purely aliphatic diols. The heteroatom-containg α,ω-diols HO-(CH 2 ) 11 -S-(CH 2 ) 2 -X-(CH 2 ) 2 -S-(CH 2 ) 11 -OH, where X = CH 2 , O, or O-(CH 2 ) 2 -O, were reacted in the melt with 1,6-diisocyanatohexane O=C=N-(CH 2 ) 6 -N=C=O, producing a series of polyurethanes containing an increasing amount of heteroatoms. Characterization by differential scanning calorimetry, infra-red spectroscopy, thermogravimetric analysis, and wide angle x-ray scattering of the m,n-polyurethane series showed that, like the teletechic diols they were synthesized from, the heteroatoms caused a decrease in the melting point and enthalpy. Howeve, they did not affect either the decomposition temperature or the crystal structure/packing.

A series of five cyclic block copolymers of styrene and butadiene, having essentially the same molecular weight (52 ± 5 kg/mol) and PS volume fraction varying from 11 to 70%, were synthesized by cyclization of α,ω-dilithium polystyrene−polybutadiene−polystyrene triblock copolymers with bis(dimethylchlorosilyl)ethane. The cyclic block copolymers thus obtained have practically the same molecular weight and composition as their corresponding linear triblock copolymers. All materials were investigated via transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) techniques. In three cases where the cyclic and the corresponding linear block copolymer had the same morphology, the domain spacings of the cyclic block copolymers are found to be 84%−89% of those of their respective linear triblock copolymers. In the other two cases different morphologies are found in the cyclic and its corresponding triblock copolymer. Compared to their linear triblocks, the interfaces are curved away from the ...

Hybrid copolymers with dendritic−linear blocks are shown to exhibit many of the classic microphase-separated structures of linear−linear block copolymers. Transmission electron microscopy (TEM), small-angle X-ray scattering (SAXS), and small-angle neutron scattering (SANS) were used to evaluate the morphology of a sixth generation (G6) poly(benzyl ether) dendron covalently bonded to linear polystyrene (PS) at the dendron focal point. Increasing the fraction of the linear block, φPS, through an increase in the molecular weight of the PS block revealed morphologies evolving from disordered to ordered lamellar to hexagonally close-packed dendron cylinders. Significantly, the observed morphologies are distinct from those expected for analogous linear−linear blocks at equivalent volume fraction, although the direction of progression follows expectation. Quantitative analysis suggests substantial molecular deformation or shape change in the dendritic phase. The possible role of conformational entropy in determi...

Aliphatic 22,12-polyurethane has been crystallized directly from the melt and isothermally at 105 °C from N,N-dimethylformamide to give chain-folded lamellae of thickness ≈ 14 nm. The crystals have been investigated using X-ray diffraction, electron microscopy (imaging and diffraction), and computer modeling. The diffraction data was used to establish that the chains crystallize in a single-chain, triclinic unit cell, and the structure bears a strong resemblance to chain-folded lamellar crystals of even−even nylons. The results show that, even for a molecule with relatively long alkane segments, the hydrogen bonds exercise a controlling influence on the crystallization process and crystalline structure. Two models were investigated: one based on an analogy with nylon 6 6 and the other derived using molecular dynamics; they both turned out to be closely related. The model generated using molecular dynamics predicted localized rotations at the termini of the ester−amide coupled units. The resolution of the...

A series of linear, aliphatic m,n-polyurethanes [O−(CH2)m−O−C(O)−NH−(CH2)n−NH−C(O)]x derived from long-chain aliphatic diols HO−(CH2)m−OH, where m = 12, 22, or 32, and much shorter diisocyanates OCN−(CH2)n−NCO, where n = 4, 6, 8, or 12, were previously characterized and shown to have physical and thermal properties similar to polyethylene. The current study shows, however, that hydrogen bonding still exercises a controlling influence on the crystallization process of these long-chain, aliphatic polyurethanes. X-ray diffraction, electron diffraction, and infrared spectroscopy indicate that these long alkane segment polyurethanes have interchain and intersheet distances similar to that seen for polyamides and polyurethanes of higher hydrogen bonding densities. Hydrogen bonding controls the crystallization, packing, and morphology of these polyurethanes, resulting in a crystal structure analogous to that of aliphatic, even−even (syncephlic) polyamides and unlike that of polyethylene. Additionally, high-tempe...

Morphological characteristics and mechanical properties of a series of block-double-graft (BDG) copolymers and terpolymers polystyrene−[1,2-polybutadiene-g-X2] (X = 1,4-polybutadiene, polyisoprene, polystyrene, and polystyrene-b-polyisoprene diblocks) were investigated by transmission electron microscopy (TEM), small-angle X-ray scattering (SAXS), and tensile testing. All BDG materials have linear polystyrene−1,2-polybutadiene (PS-b-1,2-PBD) diblock copolymer backbones. Two identical branches are grafted at every randomly distributed tetrafunctional junction point on the 1,2-PBD part of the backbone. Standard microstructures, such as body-center-cubic spheres, hexagonally packed cylinders, and lamellae, are obtained at different total PS volume fractions. It is found that when the branches are polydienes, the BDG molecules form the same morphologies as their linear diblock counterparts. In such cases, phase separation occurs between the polystyrene domain and a combined diene microdomain formed by the bac...

The grain structure in lamellar block copolymer samples undergoing a disorder-to-order transition was studied by a combination of depolarized light scattering (DPLS) and transmission electron microscopy (TEM). The 4-fold symmetry of the DPLS profiles indicated the presence of anisotropic grains. A pattern recognition algorithm for analyzing the TEM micrographs of samples partially filled with anisotropic, ordered grains was developed. The volume fractions of sample occupied by ordered grains determined from light scattering and electron microscopy are in reasonable agreement. Both methods indicate that, on average, the characteristic length of the grains in the direction perpendicular to the lamellar planes was a factor of 2 larger than that in the plane of the lamellae. The absolute magnitudes of grain sizes determined by light scattering are about 50% larger than those determined by microscopy.

The crystallization behavior of functionalized polymethylene chains with carbamate esters placed periodically between alternating docosyl and octyl segments has been examined with infrared spectroscopy. Specific features of both the interactions and the chain conformation have been found. The crystallization kinetics, including the induction period, can be followed with time-resolved infrared spectroscopy (5 s time resolution) and occurs in three stages. The kinetics of local hydrogen-bonding rearrangement is quite different from the kinetics of methylene chain stem ordering. The interchain interactions are characterized by a broad distribution of states. The initial melt consists of highly interacting chains (75% hydrogen bonded). During crystallization, this broad asymmetric ensemble of interacting states changes continuously to one dominated by that characteristic of the ordered structure. Even with the time resolution achievable, the specific features of a crystallite nucleus could not be captured.

A morphological study of three I5S six-arm miktoarm star block copolymers is presented. These miktoarm stars are comprised of five arms of polyisoprene (PI) and one arm of polystyrene (PS) joined together at a single junction point. The strong segregation limit theory for the morphological behavior of miktoarm stars predicts that these materials should form spherical morphologies, but only lamellar and cylindrical morphologies were observed by TEM and SAXS. These results are similar to previously reported discrepancies between experimentally observed morphological behaviors of miktoarm stars and the predictions of the theory. Previous work has attributed the discrepancies to the neglect of the effect of the multifunctional junction points on calculated free energies. The current results suggest that, in addition to this, geometrical packing constraints prevent the formation of morphologies such as spheres and cylinders in highly asymmetric miktoarm stars in which the minor volume fraction component would ...

The bulk morphology of a crystalline/amorphous diblock copolymer under different thermal conditions was studied. The diblock copolymer, poly((ethylene oxide)-b-1,4-polybutadiene), forms a microphas...

Transmission electron microscopy (TEM) and electron diffraction (ED) are used to study the morphology of a semicrystalline polyolefin diblock copolymer polyethylene- b -atactic-polypropylene (PE- b -aPP) and its blend with polyethylene homopolymer. By using RuCl 3 /NaClO as the staining agent, both the contrast between amorphous PP and amorphous PE regions and the contrast between amorphous PE regions and crystalline PE regions can be obtained. As a result, both the larger lamellar structures due to microphase separation and the smaller crystalline PE lamellae can be resolved on TEM micrographs. Electron diffraction coupled with TEM imaging is used to elucidate the orientation of PE crystallites with respect to the interfaces of the microphase separated block copolymer lamellar domains. Fast quenching from a microphase separated melt-state was found to result in confinement of PE crystallization within the microphase separated PE domains of the block copolymer morphology. The orientation of the PE crystallites thus formed was found to be random.

This work is part of an extensive study of model nonlinear block copolymer/homopolymer blends. Effects of graft molecular architecture on the morphology of block copolymer/homopolymer blends have been examined. The single graft Y-shaped block copolymers used in the study are I2S block copolymers, which have two low polydispersity (PDI) polyisoprene arms and one low PDI polystyrene arm joint at a single junction point. Previously reported linear diblock copolymer/homopolymer blend systems showed that the order−order transitions (OOTs) occur at about the same volume fractions as in pure linear diblock copolymers. The OOT occurs at the same volume fraction regardless of the direction from which it is approached, i.e., blending homopolymer A with a diblock which forms A cylinders in a B matrix to push it toward lamella or blending B homopolymer with a lamellar diblock to push it back toward cylinders. This study shows that when a homopolymer is blended with an I2S block copolymer, the OOTs split so that they ...

The evolution of the morphology of a crystalline/amorphous diblock copolymer poly(ethylene oxide-b-1,4 butadiene) (P(EO-b-BD)) upon crystallization in thin films was studied via interference optical microscopy. Two-dimensional crystallization confined within the PEO lamellar layers was observed with retention of the microphase-separated lamellar morphology formed in the melt state. The morphology was further characterized by TEM and electron diffraction which showed it to consist of alternating layers of PEO and PBD with PEO crystalline chains oriented perpendicular to the lamellar layers of the microphase-separated structure. Multiple parallel layers of crystalline PEO were found by electron diffraction to be in orientational registry even though they were separated by approximately 10 nm thick layers of amorphous PBD.

Structure/property relationships of polystyrene–polyisobutylene–polystyrene (PS–PIB–PS) triblock copolymer made by different processes were studied using dynamic mechanical analysis (DMA). The PS–PIB–PS films were composed of approximately 30% polystyrene end-blocks. Small angle X-ray scattering (SAXS) and transmission electron microscopy (TEM) confirm that a self-assembled, segregated cylindrical morphology forms in the copolymer. DMA was used as a tool to investigate the structure–property relationships in these polymers. Modified PS–PIB–PS copolymers were also characterized. Modifications of the copolymers were carried out by conversion of approximately 20 mol% of the polystyrene end-blocks to styrene sulfonic acid. The modified copolymers exhibited distinctly different thermal characteristics than the unmodified copolymers, which were most notable in the storage modulus and tan δ data. The presence of sulfonic acid groups disrupted the morphology and solvent sorption characteristics of the copolymers. Dynamic mechanical behavior is discussed as it relates to the morphology of the PS–PIB–PS copolymers formed via different processing methods and chemical modification.

T-junction grain boundaries were studied in a blend of polyisoprene homopolymer and a single graft block copolymer I2S with two equal length blocks of polyisoprene and one arm of polystyrene linked at a common junction point. The overall polyisoprene volume fraction in the blend was 0.52, and its equilibrium morphology was lamellar. While T-junctions were previously observed to be quite rare compared to other tilt grain boundary morphologies such as chevrons and omegas, they were found in abundance in the blend used in the current study. The T-junctions in the blend show a number of distinctive characteristics including enlarged semicylindrical end caps terminating polystyrene lamella and an increase in the spacing of the lamella as they near their termination at the T-junction. Simple free energy calculations show that the homopolymer present in the blend stabilizes the cylindrical curvature of the end caps, rendering the T-junction morphology more stable in blends than in neat block copolymers. This agr...

An investigation of the morphological behavior of a series of graft copolymers having multiple regularly spaced, tetrafunctional branch points has been carried out. The behavior of these materials, comprised of polyisoprene backbones with two polystyrene arms grafted to the backbone at each branch point, is shown to be effectively modeled by considering the behavior of smaller, architectural subunits based on the local environment of each junction point (constituting block copolymer). Morphological behavior was characterized using TEM and SAXS. Well-ordered cylindrical and lamellar morphologies were observed. Several samples appear to form cylindrical domains in disordered arrangements. Samples predicted to form spheres form instead a microphase-separated “mesh” morphology. Lamellar grain size and shape were also investigated, and lamellar grain orientation correlation lengths were determined. These measurements show a decrease in grain size with increasing number of branch points per molecule. They also ...

A series of A 2 B 2 four-arm, miktoarm stars of polystyrene and polyisoprene have been synthesized. The morphological behavior of these materials has been characterized using TEM, SAXS, and SANS, and was found to agree in general with the predictions of Milner's theory for miktoarm star morphological behavior. One sample was found to exhibit a cylindrical morphology where lamellae were predicted; this behavior is similar to other discrepancies observed in previous studies of miktoarm star morphological behavior. A second sample, predicted to form a bicontinuous morphology, was found to exhibit hexagonally packed cylinders. The tetrafunctional junction point also results in an increase in spacing for the lamellar sample in this series over that of an AB diblock, but not as great as the increase previously observed for A 8 B 8 16-arm star materials.

To understand the reversible gelation and subsequent aging of hydrogels prepared by freeze/thaw processing of poly(vinyl alcohol) (PVOH) solutions, the microstructures of gels prepared by different freeze/thaw protocols and aged to varying extents are studied by cryogenic transmission electron microscopy, solid-state nuclear magnetic resonance, X-ray scattering, and differential scanning calorimetry (DSC). As discussed in the literature, gelation by the freeze/thaw process occurs as a homogeneous aqueous poly(vinyl alcohol) solution is cycled, perhaps multiple times, between temperatures above 0 °C and well below 0 °C. The current investigation has determined that a few percent of chain segments crystallize during the first cycle, organizing themselves into 3-8 nm primary crystallite junctions separated on an irregular mesh by an average spacing of ∼ 30 nm. Aging or imposition of additional freeze/thaw cycles augments the level of crystallinity and transforms the as-formed liquid-like microstructure, characterized in the electron microscope by rounded ∼ 30 nm pores, into a fibrillar network. Observation that the transformation occurs at fixed mesh spacing and approximately constant average crystallite size suggests the formation of secondary crystallites that do not affect network connectivity. Dendritic ice crystallization and possibly spinodal decomposition superimpose on this nanoscale structure a matrix of much larger pores.