Compatibilization and ultraviolet blocking of PLA/PCL blends via interfacial localization of titanium dioxide nanoparticles

In this work, the effect of TiO₂ addition over morphological and ultraviolet (UV) blocking properties of poly(lactic acid) (PLA) and poly(?‐caprolactone) (PCL) blends was investigated. The micrographs showed a partially co‐continuous structure in the PLA/PCL blend with 42/58 (wt %/wt %) and the TiO₂ nanoparticles addition leads to a structural phase inversion, i.e., continuous PCL and partially continuous PLA with a dispersed portion. TiO₂ nanoparticles were observed to be preferably localized at the interface of the two phases due to kinetic effects (large difference between the melting temperatures) and nanoparticle geometry (low aspect ratios). An adhesion improvement between the phases and morphological stability were observed with the addition of TiO₂ nanoparticles. This behavior indicates that the nanoparticles can act as compatibilizers due to their localization at the interface between the two phases. The UV light absorption and transmission percolation threshold occurred with 1.5% TiO₂ in the 42PLA/52PCL blend. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45813.     

反应性高聚物对聚合物共混体系的增容作用

简要介绍了聚合物共混相容性的基本原理,讨论了增容反应的特点与类型,着重论述了反应性高聚物的制备技术、研究现状及其对聚合物共混体系的增容作用效果。     

Compatibilization of poly(vinyl chloride)/polystyrene blends with epoxidized styrene-butadiene-styrene block copolymers

The effectiveness of epoxidized styrene-butadiene-styrene (ESBS) block copolymer as a polymeric compatibilizer for the incompatible polystyrene/poly(vinyl chloride) (PS/PVC) blend was investigated. ESBS at two epoxidation levels (34 and 49 mol% oxirane units) was used and the study covered mainly compositions with up to 30 wt% PS content in the ternary blends. The results support the view that ESBS can serve as a compatibilizer at these levels of epoxidation and when added in amounts in excess of 5 wt%. Ternary blends may also have good elongation properties due to the thermoplastic elastomer character of ESBS.     

Compatibilization of polypropylene/polystyrene blends with poly(styrene-b-butadiene-b-styrene) block copolymer

The compatibilizing effect of the triblock copolymer poly(styrene-b-butadiene-b-styrene) (SBS) on the morphology and mechanical properties of immiscible polypropylene/polystyrene (PP/PS) blends were studied. Blends with three different weight ratios of PP and PS were prepared and three different concentrations of SBS were used for investigations of its compatibilizing effects. Scanning electron microscopy (SEM) showed that SBS reduced the diameter of the PS-dispersed particles as well as improved the adhesion between the matrix and the dispersed phase. Transmission electron microscopy (TEM) revealed that in the PP matrix dispersed particles were complex “honeycomblike” aggregates of PS particles enveloped and joined together with the SBS compatibilizer. Wide-angle X-ray diffraction (WAXD) analysis showed that the degree of crystallinity of PP/PS/SBS slightly exceeded the values given by the addition rule. At the same time, addition of SBS to pure PP and to PP/PS blends changed the orientation parameters A₁₁₀ and C significantly, indicating an obvious SBS influence on the crystallization process in the PP matrix. SBS interactions with PP and PS influenced the mechanical properties of the compatibilized PP/PS/SBS blends. Addition of SBS decreased the yield stress and the Young's modulus and improved the elongation at yield as well as the notched impact strength in comparison to the binary PP/PS blends. Some theoretical models for the determination of the Young's modulus of binary PP/PS blends were used for comparison with the experimental results. The experimental line was closest to the series model line. © 1998 John Wiley & Sons, Inc. J. Appl. Polym. Sci. 69: 2625–2639, 1998     

Compatibilization and toughening of immiscible ternary blends of polyamide 6, polypropylene (or a propylene—Ethylene copolymer), and polystyrene

In this work, typical ternary blends of three versatile polymers—polyamide 6, a propylene–ethylene copolymer (co‐PP), and polystyrene—were studied. As a compatibilizer, co‐PP with randomly dispersed minor ethylene units was multimonomer‐melt‐grafted in the presence of maleic anhydride, styrene, and dicumyl peroxide. The influence of the ethylene content in co‐PP and the blend composition on the performance was investigated. Scanning electron microscopy images showed an obvious decrease in the droplet size of the dispersed phase with increases in the compatibilizer content and number of ethylene units in co‐PP. Peaks of tan δ/temperature curves approaching the glass‐transition temperatures of the components were observed with dynamic mechanical thermal analysis. The improved mechanical properties implied good compatibility of the components in the blends. Significant toughening was achieved when the concentration of co‐PP was increased from 15 to 25 wt %: the elongation at break of the compatibilized blends increased dozens of times in comparison with the elongation at break of the uncompatibilized blends. The introduction of the multimonomer‐melt‐grafted co‐PP was shown to be an effective approach for improving immiscible multipolymer blends and to have practical potential. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Compatibilization efficiency of styrene–butadiene triblock copolymers in polystyrene–polypropylene blends with varying compositions

The compatibilization efficiency of two styrene‐butadiene‐styrene triblock copolymers with short (SB1) and long (SB2) styrene blocks was studied in polystyrene (PS)–polypropylene (PP) blends of composition 20, 50, and 80 wt % PS. The supramolecular structure of the blends was determined by small‐angle X‐ray scattering, and the morphology was studied with transmission electron microscopy and scanning electron microscopy. Structural changes in both the uncompatibilized and compatibilized blends were correlated with the values of tensile impact strength of these blends. Even though the compatibilization mechanisms were different in blends with SB1 and SB2, the addition of the block copolymers to the PS–PP 4/1 and PS–PP 1/4 blends led to similar structures and improved the mechanical properties in the same way. These block copolymers had a very slight effect on the impact strength in PS–PP 1/1 blends, exhibiting a nearly cocontinuous phase morphology. The strong migration of SB2 copolymers to the interface and of SB1 copolymers away from the interface were detected during the annealing of compatibilized PS–PP 4/1 blends. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2431–2441, 2004     

Flexible and flame‐retardant S‐SEB‐S triblock copolymer/PPE nano‐alloy

We observed that modified polyphenylene ether (PPE) was solubilized in thermoplastic styrenic elastomer (TPS) and that a two‐phase lacy structure formed on nanometer scales when the TPS composition was 67 wt % and modified PPE and polystyrene‐block‐poly(styrene‐co‐ethylene‐co‐butylene)‐block‐polystyrene (S‐SEB‐S triblock copolymer) were blended. However, the molecular weight of the outer PS block segments M_outPS and the content of the outer PS block segments ?_outPS were <10,000 g/mol and 20 wt %, respectively. The resulting S‐SEB‐S/modified PPE nano‐alloy exhibited both flexibility and flame retardancy, unlike other materials, where a trade‐off exists between these two properties; that is, the flame retardancy was excellent when the phosphorus additive was present. This combination of properties might be attributed to the two‐phase nanometer‐scale structure consisting of flame‐retardant styrene/PPE domains and a continuous soft, lacy SEB matrix. The results for polystyrene‐block‐poly(ethylene‐co‐butylene)‐block‐polystyrene (S‐EB‐S triblock copolymer)/modified PPE blends were presented for comparison. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40446.     

Modification of bitumen emulsion via heterocoagulation with SIS triblock copolymer latex

Bitumen emulsions have often been modified by styrene–butadiene rubber latex. The modified bitumen can have excellent low‐temperature cracking resistance, but rutting resistance at high temperature still remains poor. In the current work, for the first time, a stable poly(styrene‐b‐isoprene‐b‐styrene) (SIS) triblock copolymer latex is synthesized by reversible addition–fragmentation transfer (RAFT) emulsion polymerization. Based on this, a simple heterocoagulation process is developed to prepare the bitumen emulsions modified by SIS. The heterocoagulation results in hybrid particles of SIS shell and bitumen core. With addition of 5 wt % SIS, a continuous polymer‐rich phase could be formed in the modified bitumen once the modified emulsion was broken down. The bitumen modified by 5 wt % SIS shows a significant increase in complex modulus at high temperature and a significant decrease in loss tangent, suggesting excellent resistance to rutting at high temperature, which is consistent with the significant increase in softening point from 41 °C for the base bitumen up to 64 °C. Meanwhile, the ductility at 5 °C of the modified bitumen is also dramatically increased from 1.4 cm for the base bitumen to 40 cm, indicating the low‐temperature cracking resistance should also be much enhanced. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45510.     

Cure efficiency of dodecyl succinic anhydride as a cross‐linking agent for elastomer blends based on epoxidized natural rubber

Blends of a highly epoxidized natural rubber (ENR50) with unmodified natural rubber (NR) and ethylene propylene elastomers (EPDM) were produced to evaluate the mixing and curing characteristics. Dodecyl succinic anhydride was used to cross‐link the ENR50 component and the reactivity was assessed by monitoring the evolution of the torque in an oscillatory co‐axial cylinder rheometer, as well as by DSC thermal analysis. A physical model was used to obtain a single parameter for the reactivity of the system, which corresponds to the rate constant for first order curing reactions. Although the blends were thermodynamically immiscible, displaying no significant change in T_g, the components were well dispersed at microscopic level. Better mechanical properties were obtained for blends with EPDM. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41448.     

Combination of temperature and saturated vapor annealing for phase separation of block copolymer

Phase separation of block copolymer films is a perspective technique for the creation of nanostructured templates. The phase separation can be induced by thermal or vapor solvent annealing. However, a standardized and reproducible technique of the phase separation is still missing, even though many papers describing various experimental conditions. In this article we have tried to develop standardized and reproducible technique of the phase separation, which can be easily scaled up. For this purpose we used the combination of the thermal and vapor annealing of poly(styrene‐b‐4‐vinylpyridine) copolymer films on a glass substrate under static conditions. The technique was tailored by the choice of optimal solvent for the vapor annealing, based on the solvent–polymer interaction. Finally, the films were reconstructed by immersing in methanol or ethanol and stretching of the P4VP component during the reconstruction was investigated by the angle‐resolved X‐ray photoelectron spectroscopy. Morphology of the films was investigated by the atomic force microscopy and confocal microscopy. The kinetics of the phase separation was also studied. The presented combined technique of the thermal and vapor annealing can be easily temperature‐controlled for reproducibly obtaining the films of a desired morphology. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41853.     

Compatibilization and characterization of blends of styrene–maleic anhydride copolymer with modified polyethylenes

Potentially reactive blends of styrene–maleic anhydride (SMAH) with ethylene/methyl acrylate/glycidyl methacrylate (E‐MA‐GMA) and nonreactive blends of SMAH with ethylene/methyl acrylate (E‐MA) were produced in a Brabender batch mixer and in a corotating twin‐screw extruder. The products were characterized in terms of rheology, morphology, and mechanical properties to understand the reaction characteristics between anhydride/epoxy functional groups. Storage modulus, G′, loss modulus, G″ and complex viscosity, η* of the reactive blends were higher than those of nonreactive ones. At 25% E‐MA‐GMA content, maximum in η* was obtained for the reactive blends. The reactive blends showed finer morphology than the nonreactive ones at all concentrations studied. Mechanical characterization showed that reactive SMAH/E‐MA‐GMA blends had higher tensile strength, % strain at break, and tensile modulus than the nonreactive blends for all corresponding modified polyethylene contents. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 790–797, 2001     

Compatibilization and property characterization of polycarbonate/polyurethane polymeric alloys

Polymeric alloys of bisphenol A polycarbonate and a polyester‐type polyurethane were prepared over a complete composition range through melt mixing. The blends were characterized with optical and scanning electron microscopy, tensile testing, dynamic mechanical analysis, thermal analysis (differential scanning calorimetry and thermogravimetric analysis), and spectroscopic techniques (Fourier transform infrared and ¹H‐NMR). A morphology examination revealed good component dispersion with 30 wt % polyurethane or less and strong interface adhesion. Dynamic mechanical analysis indicated partial component miscibility and tensile testing mechanical behavior typical of a polymeric alloy. Overall, the degree of compatibilization obtained with polycarbonate was lower than that observed previously with poly(ethylene terephthalate) or poly(butylene terephthalate). This was attributed to the lower reactivity of the aromatic ? OH of polycarbonate toward the isocyanate groups of polyurethane and the thermal instability of the copolymer–compatibilizer formed. Experimental evidence for the formation of the latter was provided by ¹H‐NMR and dynamic mechanical analysis of selectively leached blends and by quantitative analysis results for the extraction experiments. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 612–626, 2003     

Effect of various added compatibilizers on the crystalline structure of polypropylene homopolymer/polybutylene terephthalate and polypropylene copolymer/polybutylene terephthalate polymer blends

Blends of semicrystalline isotactic polypropylene homopolymer and polypropylene copolymer with polybutylene terephthalate with different compatibilizers [i.e., styrene acrylonitrile, Surlyn, styrene–ethylene–butadiene styrene (SEBS), block copolymer and SEBS block copolymer grafted with maleic anhydride] were prepared by melt blending. Wide angle‐X‐ray scattering patterns of injection moldings were obtained. The crystallinity index and d‐spacing were calculated with different concentrations of different compatibilizers. X‐ray results in the structural investigation of the compatibilized blends correlated well with the different compatibilizer concentrations. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1190–1193, 2003     

Conductive polymer‐coated mesh films with tunable surface wettability for separation of oils and organics from water

Here, we reported the preparation of hydrophobic mesh films by coating conductive polymers including polyaniline and polypyrrole (PPy) onto stainless steel grid through a simple electrodepositing process by combination with modification of hydrophobic materials. The hydrophobic mesh films can be used for continual separation of oils and organics from water with high selectivity. Furthermore, mesh film with reversible switching wettability from hydrophobicity to hydrophilicity can be obtained by electrodepositing of PPy in the presence of perfluorooctanesulfonate dopants at different electric potential, which makes it possible to prepare functional mesh materials with remotely controllable surface wettability for selective absorption and purification. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40759.     

Compatibilization of a polyolefin blend through covalent and ionic coupling of grafted polypropylene and polyethylene. I. Rheological,thermal, and mechanical properties

A polypropylene/high‐density polyethylene blend containing 70 wt % polypropylene was prepared and compatibilized via the addition of maleic anhydride grafted polypropylene and polyethylene. The functionalized polymer chains were coupled with two types of coupling agents. Dodecane diamine formed covalent bonds with the maleic anhydride, whereas two metallic salts, zinc acetate and sodium hydrogenocarbonate, formed ionic interactions with the carboxylic functions produced by the hydration of the anhydride cycle. The coupling of the grafted polyolefin chains was successfully realized by a single operation in a twin‐screw extruder. The coupling agents were efficient in improving the elongation at break and impact properties of the studied blends. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 95: 312–320, 2005     

Compatibilization of commingled plastics with maleic anhydride modified polyethylenes and ultraviolet preirradiation

The improvement of the properties of commingled plastics was carried out with a prototype blend of Mexican municipal plastic waste with and without poly(vinyl chloride) (PVC). Compatibilizing agents such as high‐density, low‐density, and linear low‐density polyethylenes modified with maleic anhydride were used. The agents were prepared in the laboratory with peroxide, and their usefulness was compared with that of a commercially modified linear low‐density polyethylene. The blends with PVC were preirradiated with ultraviolet radiation for 12, 24, or 48 h to create oxidized groups to help in situ compatibilization during the blending step of the reactive extrusion process. Compatibilized materials showed a markedly more homogeneous morphology with improved mechanical properties: the elongation at break and impact strength increased with the compatibilization level. The presence of PVC in commingled plastics significantly reduced the beneficial effect of the maleic anhydride modified polyethylene as a compatibilizer. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Compatibilization of poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate)–poly(lactic acid) blends with diisocyanates

Poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV) was blended with poly(lactic acid) (PLA) with various reactive processing agents to decrease its brittleness and enhance its processability. Three diisocyanates, namely, hexamethylene diisocyanate, poly(hexamethylene diisocyanate), and 1,4‐phenylene diisocyanate, were used as compatibilizing agents. The morphology, thermomechanical properties, and rheological behavior were investigated with scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry, tensile testing, dynamomechanical thermal analysis in torsion mode (dynamic mechanical analysis), and oscillatory rheometry with a parallel‐plate setup. The presence of the diisocyanates resulted in an enhanced polymer blend compatibility; this led to an improvement in the overall mechanical performance but did not affect the thermal stability of the system. A slight reduction in the PHBV crystallinity was observed with the incorporation of the diisocyanates. The addition of diisocyanates to the PHBV–PLA blend resulted in a notable increase in the final complex viscosity at low frequencies when compared with the same system without compatibilizers. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44806.     

Synthesis of a graft copolymer from an ozonized polycarbonate and its application as a compatibilizer

The polycarbonate (PC)/polystyrene (PS) blend is an immiscible system. The use of copolymers as compatibilizers in blends is one approach that is being developed within the larger field of polymer alloys. In this study, PC was ozonized to create peroxides and hydroperoxides on the polymer chain. These functional groups under heating conditions were used to initiate the radical polymerization of styrene (vinyl monomers) to give graft copolymers. The first part of this study was dedicated to the examination of the kinetics of the styrene polymerization initiated by an ozonized PC. However, the structure of the graft copolymers was confirmed by IR spectroscopy, and the molecular weight of the PS graft chain was determined by gel permeation chromatography. The compatibilized bends were prepared by melt blending in an internal mixer. The morphologies of the PC/PS/graft copolymer blend were examined by transmission electron microscopy and were finer than those of an uncompatibilized blend. The tensile properties of these blends were also investigated. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Compatibilization of polystyrene and polyamide 6 mixtures with poly(styrene‐co‐sodium acrylate)

In this work, the compatibilization of polystyrene‐and‐nylon 6 mixtures with the ionomer, poly(styrene‐co‐sodium acrylate), is investigated. The ionomer was synthesized by emulsion polymerization. Scanning electron microscopy reveals that an appreciable size reduction of the dispersed phase is achieved in the whole composition range, when small amounts of the ionomer were added. IR spectroscopy and water absorption tests disclose that a chemical reaction occurs between the carboxylic group of the ionomer and the terminal amine group of the polyamide 6, which allows the compatibilization process. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91:1736–1745, 2004     

Compatibilization of syndiotactic polystyrene and a thermotropic liquid‐crystalline polymer blend with a zinc salt of a sulfonated polystyrene ionomer

A zinc salt of a lightly sulfonated (4.5 mol %) polystyrene ionomer was used to compatibilize a 3/1 (w/w) blend of syndiotactic polystyrene and a wholly aromatic thermotropic liquid‐crystalline polymer (TLCP). The addition of the ionomer significantly reduced the dispersed TLCP domain size and improved the tensile strength, ultimate elongation, and flexural toughness of the blend. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 564–568, 2003