Synthesis of poly(styrene‐co‐4‐vinylpyridine) microspheres via dispersion polymerization: Effect of the concentration of 4‐vinylpyridine

Amphiphilic copolymer microspheres of poly(styrene‐co‐4‐vinylpyridine) were prepared by dispersion polymerization in an alcohol/water medium. The synthesis of poly(styrene‐co‐4‐vinylpyridine) microparticles was successfully carried out, and the latexes had a spherical morphology with good monodispersity. The degree of conversion in the early stage of polymerization decreased with increasing 4‐vinylpyridine (4VP) monomer content, but the final conversions were similar (>95%). The copolymerization rate decreased with increasing 4VP content, and a broad particle size distribution was observed with 20 wt % 4VP because of the prolonged nucleation time. With the 4VP concentration increasing, the molecular weight of the copolymer microspheres decreased, and the glass‐transition temperature of the copolymers increased; this indicated that all the copolymers were random and homogeneous. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Hydrogen‐bonding interactions between poly(styrene‐co‐methacrylic acid) and poly(styrene‐co‐4‐vinylpyridine)

The complexation behavior between poly(styrene‐co‐methacrylic acid) of different compositions (SMA‐12 or SMA‐29) and poly(styrene‐co‐4‐vinylpyridine) (S4VP‐6 or S4VP‐15) was studied by viscometry and differential scanning calorimetry using tetrahydrofuran (THF) and butan‐2‐one as solvents. This complexation is attributed to the presence of strong intermolecular interactions between the different polymer chains by hydrogen bonding. A single glass‐transition temperature, intermediate between those of the two pure copolymers SMA‐29 and S4VP‐15, was obtained with each composition of the mixture when THF or butan‐2‐one is used as a common solvent. The obtained results showed that the formation of such complexes depends strongly on the nature of the solvent and the contents of the interacting species. The complex formation is inhibited in THF because of the important ability of this latter to interact with the SMA. A quantitative analysis of the interactions between the constituents of these blends was carried out by FTIR spectroscopy. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 806–811, 2005     

Antibacterial and Bacterium Adsorbing Macromolecules

Currently studies on antibacterial macromolecules, i. e., bactericidal and bacteriostatic ones, have been made to develop a new utilization field of polymeric materials. In these studies, there are immobilizations of iodine to quaternary ammonium salts, antibiotics, antibacterial groups to macromolecular substances, as well as syntheses of polymers with quaternary ammonium salts, biguanide groups, quaternary pyridinium salts, sulphonium salts, phosphonium salts, and other antibacterial groups. On the other hand, studies have been made of bacterium adsorbing macromolecules, which can remove by adsorbing bacterial cells in water. The macromolecules are the ones based on poly(4‐vinylpyridine‐co‐divinylbenzene), crosslinked poly(3‐ and 4‐chloromethylated styrene‐g‐amine), and poly(glycidyl methacrylate‐g‐amine), as well as filters and microporous membranes are covered with a macromolecule based on quaternized poly(4‐vinylpyridine‐co‐styrene). Here, a review is made of the syntheses and preparation of the respective macromolecules, as well as of their antibacterial activities and the bacterium adsorbing activities.     

The phase behavior and thermal stability of blends of poly(styrene‐co‐methacrylic acid)/poly(styrene‐co‐ 4‐vinylpyridine)

The hydrogen bonding and miscibility behaviors of poly(styrene‐co‐methacrylic acid) (PSMA20) containing 20% of methacrylic acid with copolymers of poly(styrene‐co‐4‐vinylpyridine) (PS4VP) containing 5, 15, 30, 40, and 50%, respectively, of 4‐vinylpyridine were investigated by differential scanning calorimetry, thermogravimetric analysis (TGA), and Fourier transform infrared spectroscopy (FTIR). It was shown that all the blends have a single glass transition over the entire composition range. The obtained T_gs of PSMA20/PS4VP blends containing an excess amount of PS4VP, above 15% of 4VP in the copolymer, were found to be significantly higher than those observed for each individual component of the mixture, indicating that these blends are able to form interpolymer complexes. The FTIR study reveals presence of intermolecular hydrogen‐bonding interaction between vinylpyridine nitrogen atom and the hydroxyl of MMA group and intensifies when the amount of 4VP is increased in PS4VP copolymers. A new band characterizing these interactions at 1724 cm⁻¹ was observed. In addition, the quantitative FTIR study carried out for PSMA20/PS4VP blends was also performed for the methacrylic acid and 4‐vinylpyridine functional groups. The TGA study confirmed that the thermal stability of these blends was clearly improved. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Palladium‐Iminodiacetic Acid Immobilized on pH‐Responsive Polymeric Microspheres: Efficient Quasi‐Homogeneous Catalyst for Suzuki and Heck Reactions in Aqueous Solution

The pH‐responsive core‐shell microspheres of poly(styrene‐co‐methylacrylic acid) (PS‐co‐PMAA) containing a polystyrene (PS) core and a poly(methylacrylic acid) (PMAA) shell are synthesized by one‐stage soap‐free copolymerization and the catalyst system palladium‐iminodiacetic acid (IDA‐Pd) is immobilized on the outer shell‐layer of the core‐shell microspheres to form the quasi‐homogeneous and easily accessible catalyst PS‐co‐PMAA‐IDA‐Pd. This quasi‐homogeneous PS‐co‐PMAA‐IDA‐Pd catalyst is highly dispersed in the reaction medium just like a homogeneous one and can be separated like a heterogeneous catalyst by adjusting the pH of the reaction medium. Suzuki reactions employing the quasi‐homogeneous PS‐co‐PMAA‐IDA‐Pd catalyst are efficiently performed in water as the sole solvent under mild conditions such as room temperature. The PS‐co‐PMAA‐IDA‐Pd catalyst is also used in Heck reactions of a wide range of aryl halides with styrene and proves to be efficient in aqueous solution. The PS‐co‐PMAA‐IDA‐Pd catalyst has a low leaching loss and can be reused at least 4 times without loss of activity.     

Synthesis and properties of polymer film modified electrodes to detect metal ions

In order to obtain modified polymeric electrodes, polymers were synthesized that are insoluble in water but soluble in common organic solvents and contain different functional groups that are able to coordinate metal ions from low concentrations. Poly(acrylic acid‐co‐styrene), poly(acrylamide‐co‐4‐vinyl pyridine), and poly(styrene‐co‐4‐vinyl pyridine) were synthesized by radical polymerization. The copolymers were characterized by FTIR, ¹H‐NMR, ¹³C‐NMR, scanning electron microscopy, and thermal analysis. The molecular weight and molecular weight distribution were determined by size exclusion chromatography. These complexing polymers were used in the preparation by spin coating of complexing chemically modified electrodes. The polymer film modified electrodes were then tested for the detection of metal ions using the chemical preconcentration and anodic stripping technique. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1192–1197, 2005     

Preparation of hemispherical poly(4‐vinylpyridine‐co‐butyl acrylate)/poly(styrene‐co‐butyl acrylate) composite microspheres by seeded preswelling emulsion polymerization

Seeded preswelling emulsion polymerization was carried out by using monodispersed poly(4‐vinylpyridine‐co‐butyl acrylate) [P(4VP‐BA)] particles as the seed, and styrene and butyl acrylate as the second‐stage monomers under different polymerization conditions, to obtain hemispherical polystyrene (PST)‐rich–P4VP‐rich microspheres. Prior to polymerization, toluene was added into the preswelling system together with the second‐stage monomers. It was found that, with the increase of the amount of toluene, the particle morphology showed a tendency toward desirable hemispherical structure, and the colloidal stability of composite latex was improved. When the weight ratio of toluene/seed latex was increased up to 7.5/40 (g/g), the stable hemispherical latex could be obtained. However, when toluene was not added, the coagulum formed on the wall of the reactor during polymerization, and the composite particles with multiple surface domains (such as sandwich‐like, popcorn‐like) were formed. In addition, the final morphology of composite particles was influenced by the polarity of the seed crosslinker and the hydrophilicity of the second‐stage initiator, which could affect the mobility of poly(styrene‐co‐butyl acrylate) [P(ST‐BA)] chains. The morphology development during the polymerization was investigated in detail, and a schematic model was derived to depict the formation mechanism of hemispherical P(4VP‐BA)/P(ST‐BA) composite microspheres. The results revealed that the mobility of the P(ST‐BA) chains influenced the diffusion of the P(ST‐BA) domains on the surface of the P(4VP‐BA) matrix. When the mobility of the P(ST‐BA) chains allowed small‐size P(ST‐BA) domains to coalesce into one larger domain, complete phase‐separated morphology (hemisphere) could be achieved. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3811–3821, 2003     

Preparation of hairy particles by grafting PEG onto the poly(styrene‐co‐maleic anhydride) surface and PEG effect on SiO2 nanoparticles adsorption

Hairy particles were prepared by immobilization of poly(ethylene glycol) (PEG) on the surface of poly(styrene‐co‐maleic anhydride) (poly(S‐co‐MA)) spheres. It was found that the carbonyl groups on the poly(S‐co‐MA) surface can be conveniently esterified with the hydroxyl groups of PEG. Chemical and morphological changes were analyzed by FT‐IR, TEM, and water contact angle. Results revealed that, with the immobilization of PEG, the morphology of poly(S‐co‐MA) turned from a smooth surface to a hairy‐like structure and the hydrophilicity of the polymer particles improved. In addition, berry‐like polymer/silica particles can be obtained by using the hairy particles as template. The PEG hairy chains show steric repulsion during the deposition of silica nanoparticles by in situ sol‐gel process. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Water‐soluble copolymers. I. Biodegradability and functionality of poly[(sodium acrylate)‐co‐(4‐vinylpyridine)]

As a biodegradable functional polymer, poly[(sodium acrylate)‐co‐(4‐vinylpyridine)] [P(SA‐co‐4VP)] containing a small amounts of 4‐vinylpyridine groups were prepared and their biodegradability, dispersity, and complex performance were analyzed. The polymers can be useful as detergent builders and dispersants. It was found that the biodegradation of P(SA‐co‐4VP) was more conspicuous when content of the 4‐vinylpyridine in the copolymer was larger. This indicates that the 4‐vinylpyridine, which acts as biodegradable segments, should be incorporated into the polymer main chain in such a manner that they are digested by activated sludge. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1953–1957, 1999     

Aggregation phenomena of amphiphilic UVB absorptive oligoesters containing p‐alkoxycinnamate and poly(ethylene oxide) blocks

The synthesis of new amphiphilic oligoesters containing a hydrophobic block based on p‐alkoxycinnamate and hydrophilic poly(ethylene oxide) is reported. Two hydrophobic monomers, 1,2‐(bis(4‐(2‐carboxyvinyl)phenoxy))ethane ( M2 ) and 1,12‐(bis(4‐(2‐carboxyvinyl) phenoxy))dodecane ( M12 ), were synthesized. Four oligoesters, poly((1,2‐(bis(4‐(2‐carboxyvinyl)phenoxy))ethane) ‐co‐(poly(ethylene oxide)200)) ( P2‐200 ), poly((1,2‐(bis(4‐(2‐carboxyvinyl)phenoxy))ethane)‐co‐(poly(ethylene oxide) 400)) ( P2‐400 ), poly((1,12‐(bis(4‐(2‐carboxyvinyl)phenoxy)) dodecane)‐co‐(poly(ethylene oxide)400)) ( P12‐400 ), and poly((1,12‐(bis(4‐(2‐carboxyvinyl)phenoxy))dodecane)‐co‐ (poly(ethylene oxide)1000)) ( P12‐1000 ) were then constructed by reacting the M2 or M12 with poly(ethylene oxide) (PEO) with lengths of ～ 4 (PEO 200), ～ 10 (PEO 400), or ～ 23 (PEO1000) units using multiple esterifications. These oligoesters possess UVB absorption properties and show good solubility in various organic solvents. Self‐assembly of the oligoesters into aqueous spherical colloids could be induced through an acetone to water solvent displacement technique. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Morphology and thermal behavior of organo‐bentonite clay/poly(styrene‐co‐methacrylic acid)/poly(isobutyl methacrylate‐co‐4‐vinylpyridine) nanocomposites

Poly(styrene‐co‐methacrylic acid) containing 29 mol % of methacrylic acid (SMA‐29) and poly(isobutyl methacrylate‐co‐4‐vinylpyridine) containing 20 mol % of 4‐vinylpyridine (IBM4VP‐20) were synthesized, characterized, and used to elaborate binary and ternary nanocomposites of different ratios with a 3% by weight hexadecylammonium‐modified bentonite from Maghnia (Algeria) by casting method from tetrahydrofuran (THF) solutions. The morphology and the thermal behavior of these binary and ternary elaborated nanocomposites were investigated by X‐ray diffraction, scanning electron microscopy, FTIR spectroscopy, differential scanning calorimetry, and thermogravimetry. Polymer nanocomposites and nanoblends of different morphologies were obtained. The effect of the organoclay and its dispersion within the blend matrix on the phase behavior of the miscible SMA29/IBM4VP20 blends is discussed. The obtained results showed that increasing the amount of SMA29 in the IBM4VP20/SMA29 blend leads to near exfoliated nanostructure with significantly improved thermal stability. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Blends containing amphiphilic polymers. V. Compatibilization of N‐alkylitaconamic acid‐co‐styrene copolymers with interacting polymers

The phase behavior of blends containing N‐alkylitaconamic acid‐co‐styrene copolymers (NAIA‐co‐S) with poly(N‐vinyl‐2‐pyrrolidone) (PVP) of two different weight average molecular weights (M _w ), poly(2‐vinylpyridine) (P2VPy) and poly(4‐vinylpyridine) (P4VPy), was analyzed by differential scanning calorimetry and Fourier transform infrared spectroscopy. Copolymers containing 80% S are miscible with PVP₁₀, PVP₂₄, and P4VPy over the whole range of composition. In the case of blends with P2VPy, miscibility is observed only for the first three members of the series, i.e., NEIA‐co‐S, NPIA‐co‐S, and NBIA‐co‐S. For copolymers containing hexyl to dodecyl moieties, phase separation is observed in blends with P2VPy. Copolymers containing 50% S are miscible over the whole range of composition irrespective of the homopolymer and the length of the side chain of the itaconamic moiety of the copolymer. This behavior is interpreted in terms of steric hindrance, in the sense that the copolymers with long side chains are not able to interact with the nitrogen of P2VPy because of the position in the aromatic ring. The interactions between copolymers and homopolymers are discussed in terms of specific interactions like hydrogen bonds between the itaconamic moiety and the different functional groups of the homopolymers, together with the hydrophobic interaction, which cannot be disregarded. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 2512–2519, 2006     

Enantioselective esterification reaction using immobilized Candida rugosa lipase on poly(N‐vinyl‐2‐pyrrolidone‐co‐styrene) hydrogel

Lipase from Candida rugosa was immobilized on poly(N‐vinyl‐2‐pyrrolidone‐co‐styrene) hydrogel (poly‐(VP‐co‐ST)) with ethylene dimethacrylate and α,α'‐azoisobutyronitrile, which act as crosslinker and initiator, respectively. Three different compositions of monomers were used, namely VP(%):ST(%), 10:90, 50:50, and 70:30 (wt(%)/wt(%)). The immobilized lipases were used in the enantioselective esterification of (R,S)‐2‐(4‐chlorophenoxy)‐propanoic acid with n‐tetradecanol. The optimum reaction condition of the enantioselective esterification for the native lipase and the poly(VP‐co‐ST) hydrogel immobilized lipases was determined with respect to temperature, solvents, and initial water activity (a_w). The optimum temperature obtained was 40°C, with the poly(VP‐co‐ST) hydrogel immobilized lipase VP(%)/ST(%):10:90 showing the highest enantiomeric excess. In the solvent effect studies, the best solvents for high enantioselectivity were chloroform and carbon tetrachloride. In the a_w studies, optimum α_w for NL, VP(%):ST(%), 10:90, and 50:50 was 0.328, while for VP(%):ST(%), 70:30, it was 0.55. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3381–3386, 2004     

Synthesis and characterization of statistical copolymers of styrene and 4‐(1‐hydroxyalkyl)styrene

A family of new polymers based on poly(4‐(1‐hydroxyalkyl)styrene), and its copolymers with styrene were synthesized and thoroughly characterized by ¹H‐NMR, ¹³C‐NMR, FTIR, and UV spectroscopies. The chemical modification reactions of polystyrene (PS) was used as a novel method of performing the synthesis of poly(4‐(1‐hydroxyethyl‐co‐styrene)), poly(4‐(1‐hydroxypropyl‐co‐styrene)), poly(4‐(1‐hydroxybutyl‐co‐styrene)), and poly(4‐(1‐hydroxyphenylmethyl‐co‐styrene)). The novelty of this method lies in the incorporation of the desired mol % of the functional groups in polystyrene chain, to obtain random copolymers of desired composition. In preliminary testing/evaluation studies the utility and versatility of the new copolymers, which have the potential to be negative‐tone photoresist materials, were studied. Thus a few photoresist formulations based on poly(styrene‐co‐4‐(1‐hydroxyalkylstyrene)) were developed with 5 wt % of a photoacid generator. These studies suggested that the new copolymers synthesized by a simple and alternate method could have the same potential as a photoresist material when compared with the polymers synthesized by the polymerization of the corresponding functional monomer. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1902–1914, 2004     

Preparation of poly(divinylbenzene‐co‐N‐isopropylacrylamide) microspheres and their hydrogen‐bonding assembly behavior for raspberry‐like core‐corona polymer composite

Narrowdisperse poly(divinylbenzene‐co‐N‐isopropylacrylamide) (poly(DVB‐co‐NIPAM)) functional microspheres with the diameter in the range of 630 nm and 2.58 μm were prepared by distillation–precipitation polymerization in neat acetonitrile in the absence of any stabilizer. The effect of N‐isopropylacrylamide (NIPAM) ratio in the comonomer feed on the morphology of the resultant polymer particles was investigated in detail with divinylbenzene (DVB) as crosslinker and 2,2′‐azobisisobutyronitrile (AIBN) as initiator. The monodisperse poly(DVB‐co‐NIPAM) microspheres with NIPAM fraction of 20 wt % were selected for the preparation of raspberry‐like core‐corona polymer composite by the hydrogen‐bonding self‐assembly heterocoagulation with poly(ethyleneglycol dimethacrylate‐co‐acrylic acid) [poly(EGDMA‐co‐AA)] nanospheres. Both of the functional poly(DVB‐co‐NIPAM) microspheres and the core‐corona particles were characterized with scanning electron microscopy (SEM), Fourier transform infrared spectra (FTIR), and elemental analysis (EA). © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1350–1357, 2007     

Polymer supported reagents. III. Kinetic study of synthesizing n‐octylacetate using insoluble titanium tetrachloride

Insoluble poly(4‐vinylpyridine‐co‐styrene) beads are prepared using divinylbenzene as the crosslinking agent. These polymer beads are converted into poly(4‐vinylpyridine‐N‐oxide) (PVPNO) under peracetic acid conditions. The resulting polymer is functionalized with titanium tetrachloride (TiCl₄) to afford the corresponding PVPNO‐TiCl₄ complex. This complex shows good catalytic activity for esterification reactions. The kinetics of formation of n‐octylacetate from acetic acid and n‐octanol is reported. The effects of stirring speed, reactant concentration, catalyst amount, percent crosslinking, particle size, and temperature on the conversion is investigated. The rate constants are found to increase with an increase in the stirring speed, concentration of n‐octanol, catalyst amount, and temperature and decrease with an increasing percentage of crosslinking and the mesh size of the polymer beads. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 2075–2080, 2000     

Study on synthesis and morphology control of poly(4‐vinylpyridine‐co‐butyl acrylate)/poly(styrene‐co‐butyl acrylate) composite microspheres

Monodispersed crosslinked cationic poly(4‐vinylpyridine‐co‐butyl acrylate) [P(4VP‐BA)] seed latexes were prepared by soapless emulsion polymerization, using 2,2′‐azobismethyl(propionamidine)dihydrochloride (V₅₀) as an initiator and divinylbenzene (DVB) or ethylene glycol dimethacrylate (EGDMA) as a crosslinker. The optimum condition to obtain monodispersed stable latex was investigated. It was found that the colloidal stability of the P4VP latex can be improved by adding an adequate amount of BA (BA/4VP = 1/4, w/w), and adopting a semicontinuous monomer feed mode. Subsequently, poly(4‐vinylpyridine‐co‐butyl acrylate)/Poly(styrene‐co‐butyl acrylate) [P(4VP‐BA)/P(ST‐BA)] composite microspheres were synthesized by seeded polymerization, using the above latex as a seed and a mixture of ST and BA as the second‐stage monomers. The effects of the type of crosslinker, the degree of crosslinking, and the initiators (AIBN and V₅₀) on the morphology of final composite particles are discussed in detail. It was found that P(4VP‐BA)/P(ST‐BA) composite microspheres were always surrounded by a PST‐rich shell when V₅₀ was used as initiator, while sandwich‐like or popcorn‐like composite particles were produced when AIBN was employed. This is because the polarity of the polymer chains with AIBN fragments is lower than for the polymer with V₅₀ fragments, hence leading to higher interfacial tension between the second‐stage PST‐rich polymer and the aqueous phase, and between PST‐rich polymer and P4VP‐rich seed polymer. As a result, the seed cannot be engulfed by the PST‐rich polymer. Furthermore, the decrease of T_g of the second‐stage polymer promoted phase separation between the seeds and the PST‐rich polymer: sandwich‐like particles formed more preferably than popcorn‐like particles. It is important knowledge that various morphologies different from PST‐rich core/P4VP‐rich shell morphology, can be obtained only by changing the initiator, considering P4VP is much more hydrophilic than PST. The zeta potential of composite particles initiated by AIBN in seeded polymerization shifted from a positive to a negative charge. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1190–1203, 2002     

Preparation and application of sulfonated poly(1‐octene‐co‐styrene)

In this article, 1‐octene and styrene was copolymerized by the supported catalyst (TiCl₄/ID/MgCl₂). Subsequently, by sulfonation reaction, sulfonated poly(1‐octene‐co‐styrene)s which were amphiphilic copolymers were prepared. The copolymerization behavior between 1‐octene and styrene is moderate ideal behavior. Copolymers prepared by this catalyst contain appreciable amounts of both 1‐octene and styrene. Increase in the feed ratio of styrene/1‐octene leads to increase in styrene content in copolymer and decrease in molecular weight. As the polymerization temperature increases, the styrene content in the copolymers increases, however, the molecular weight decreases. Hydrogen is an efficient regulator to lower the molecular weights of poly(1‐octene‐co‐styrene)s. The sulfonation degree of the sulfonated poly(1‐octene‐co‐styrene)s increased as the styrene content in copolymer increased or the molecular weight decreased. Thirty‐six hour is long enough for sulfonation reaction. The sulfonated poly(1‐octene‐co‐styrene)s can be used as effective and durable modifying agent to improve the wettability of polyethylene film and have potential application in emulsified fuels and for the stabilization of dispersions. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effect of solvents on radiation‐induced grafting of styrene onto fluorinated polymer films

The effect of solvents on radiation‐induced grafting of styrene onto commercial fluorinated polymer films such as poly(tetrafluoroethylene) (PTFE), poly(tetrafluoroethylene‐co‐hexafluoropropylene) (FEP) and poly(tetrafluoroethylene‐co‐perfluorovinyl ether) (PFA) was investigated by a simultaneous irradiation technique. Three solvents, ie methanol, benzene and dichloromethane, were used to dilute styrene under various irradiation doses, dose rates and monomer concentrations. The effect of addition of mineral and organic acids on the degree of grafting in the presence of the three solvents was also studied. The degree of grafting was found to be strongly dependent upon the type of solvent and composition of the monomer/solvent mixture. Dilution of styrene with dichloromethane in various grafting conditions was found to enhance dramatically the degree of grafting compared with other solvents, and the maximum degree of grafting was achieved at a monomer/solvent mixture having a composition of 60:40 (v/v). The formation of polystyrene grafts in the three fluorinated films was verified using FTIR spectrometry. © 2001 Society of Chemical Industry     

Preparation of narrow‐disperse or monodisperse poly{[poly(ethylene glycol) methyl ether acrylate]‐co‐(acrylic acid)} microspheres with ethyleneglycol dimethacrylate as crosslinker by distillation precipitation polymerization

Narrow‐disperse or monodisperse poly{[poly(ethylene glycol) methyl ether acrylate]‐co‐(acrylic acid)} (poly(PEGMA‐co‐AA)) microspheres were prepared by distillation precipitation polymerization with ethyleneglycol dimethacrylate (EGDMA) as crosslinker with 2,2′‐azobisisobutyronitrile as initiator in neat acetonitrile in the absence of any stabilizer, without stirring. The diameters of the resultant poly(PEGMA‐co‐AA‐co‐EGDMA) microspheres were in the range 200–700 nm with a polydispersity index of 1.01–1.14, which depended on the comonomer feed of the polymerization. The addition of the hydrogen bonding monomer acrylic acid played an essential role in the formation of narrow‐disperse or monodisperse polymer microspheres during the polymerization. Copyright © 2006 Society of Chemical Industry