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1.
A polystyrene (PS)‐b‐polylactide (PLA) block copolymer was prepared from the combination of atom transfer radical polymerization and ring‐opening polymerization with commercially available 2,2,2‐tribromoethanol as a dual initiator in a sequential two‐step procedure. Hydroxyl‐terminated polystyrene (PS‐OH)s with various molecular weights were first prepared with polydispersity indices lower than 1.3; these provided valuable macroinitiators for the polymerization of D,L ‐lactide. A block copolymer with a composition allowing the formation of hexagonally packed PLA cylinders in a PS matrix was then obtained. The PS‐b‐PLA thin films revealed, after vapor solvent annealing, a hexagonally packed organization of the PLA cylinders, which was oriented perpendicularly to the surface of the film. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

2.
In this contribution, we reported to utilize polystyrene‐block‐polybutadiene‐block‐polystyrene (PS‐b‐PB‐b‐PS), a commercial triblock copolymer to toughen epoxy thermosets. First, a PS‐b‐PB‐b‐PS triblock copolymer was chemically modified with hydroboration‐oxidation reaction, with which the midblock was hydroxylated whereas the endblocks remained unaffected. It was found that the degree of hydroxylation was well controlled. One of the hydroxylated PS‐b‐PB‐b‐PS samples was then used as the macromolecular initiator to synthesize a poly(ε‐caprolactone)‐grafted PS‐b‐PB‐b‐PS via the ring‐opening polymerization. It was found that the PS‐b‐PB‐b‐PS with poly(ε‐caprolactone) grafts can be successfully employed to nanostructure epoxy thermosets; the “core‐shell” microdomains composed of PB and PS were generated in the nanostructured thermosets. The nanostructured thermosets displayed improved fracture toughness. POLYM. ENG. SCI., 59:2387–2396, 2019. © 2019 Society of Plastics Engineers  相似文献   

3.
Atom transfer radical polymerization (ATRP) was applied to synthesize a new kind of star polymers of hyperbranched polyglycerol (HPG) core with multiarms of PS‐b‐PtBA and PS‐b‐PAA by using the “core first” technique. The HPG core was obtained by anionic polymerization of glycerol first, and then the pendant hydroxyl groups of HPG were esterified with 2‐bromoisobutyryl bromide to yield the HPG‐g‐Br, which was used as macroinitiator for ATRP of the first monomer (St) and then second monomer (tBA). After hydrolysis of the PtBA block, poly(acrylic acid) (PAA) side chains were formed. The final products and intermediates were characterized by GPC, NMR, and FTIR in detail. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008  相似文献   

4.
Well‐defined polydimethylsiloxane‐block‐polystyrene (PDMS‐b‐PS) diblock copolymers were prepared by reversible addition‐fragmentation chain transfer (RAFT) polymerization using a functional PDMS‐macro RAFT agent. The RAFT polymerization kinetics was simulated by a mathematical model for the RAFT polymerization in a batch reactor based on the method of moments. The model described molecular weight, monomer conversion, and polydispersity index as a function of polymerization time. Good agreements in the polymerization kinetics were achieved for fitting the kinetic profiles with the developed model. In addition, the model was used to predict the effects of initiator concentration, chain transfer agent concentration, and monomer concentration on the RAFT polymerization kinetics. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

5.
The triblock energetic copolymer poly(lactic acid)‐block‐(glycidylazide polymer)‐block‐polystyrene (PLA‐b‐GAP‐b‐PS) was synthesized successfully through atom‐transfer radical polymerization (ATRP) of styrene and ring‐opening polymerization of d,l ‐lactide. The energetic macroinitiator GAP‐Br, which was made from reacting equimolar GAP with α‐bromoisobutyryl bromide, firstly triggered the ATRP of styrene with its bromide group, and then the hydroxyl group on the GAP end of the resulting diblock copolymer participated in the polymerization of lactide in the presence of stannous octoate. The triblock copolymer PLA‐b‐GAP‐b‐PS had a narrow distribution of molecular weight. In the copolymer, the PS block was solvophilic in toluene and improved the stability of the structure, the PLA block was solvophobic in toluene and served as the sacrificial component for the preparation of porous materials, and GAP was the basic and energetic material. The three blocks of the copolymer were fundamentally thermodynamically immiscible, which led to the self‐assembly of the block copolymer in solution. Further studies showed that the concentration and solubility of the copolymer and the polarity of the solvent affected the morphology and size of the micelles generated from the self‐assembly of PLA‐b‐GAP‐b‐PS. The micelles generated in organic solvents at 10 mg mL?1 copolymer concentration were spherical but became irregular when water was used as a co‐solvent. The spherical micelles self‐assembled in toluene had three distinct layers, with the diameter of the micelles increasing from 60 to 250 nm as the concentration of the copolymer increased from 5 to 15 mg L?1. © 2017 Society of Chemical Industry  相似文献   

6.
A new ionic crosslinked polymer hydrogel was achieved by the strategy of ionically crosslinking α,ω‐dibromide terminated polystyrene (Br‐PS‐Br) with poly(4‐vinyl pyridine) (P4VP) which was synthesized by reversible addition‐fragmentation chain transfer polymerization using a chain transfer agent containing a trithiocarbonate moiety. The moiety of trithiocarbonate was introduced into the crosslinked network to show the self‐healing characteristics. The chain structure and components of Br‐PS‐Br and P4VP were characterized through 1H NMR, gel permeation chromatography, Fourier transform IR spectroscopy and elemental analysis. The P4VP (Mn = 25 300 g mol?1) chains were crosslinked with Br‐PS‐Br (Mn = 2000 g mol?1) through the quaternization reaction to form a polymer network which was further crosslinked in acetonitrile by irradiation of UV light to fabricate a hydrogel. Such a hydrogel of P4VP/Br‐PS‐Br cut by a razor blade can be rapidly (1 h) and repeatedly (three times) healed through a reshuffling reaction of the trithiocarbonate moiety under irradiation by UV light. © 2018 Society of Chemical Industry  相似文献   

7.
Multiwalled carbon nanotubes‐graft‐polystyrene (MWNTs‐g‐PS) was synthesized by atom transfer nitroxide radical coupling chemistry. MWNTs with 2,2,6,6‐tetramethylpiperidine‐1‐oxy (MWNTs‐TEMPO) groups was prepared first by esterification of 4‐hydroxy (HO)‐TEMPO and carboxylic acid group on the surface of MWNTs (MWNTs‐COOH); PS with bromide end group (PS‐Br) were then obtained by atom transfer radical polymerization using ethyl 2‐bromoisobutyrate as initiator and CuBr/N,N,N′,N″,N″‐pentamethyldiethylenetriamine as catalyst. The MWNTs‐TEMPO was mixed with PS‐Br and heated to 90°C in the presence of CuBr/PMDETA to form MWNTs‐g‐PS. The product was characterized by FTIR, NMR, TGA, and TEM. TEM indicates that the MWNTs are enveloped by the polymer molecules. The content of grafted polymers is 46.7% by TGA measurements when the number‐average molecular weight (Mn) of PS‐Br is 10,200 g/mol. The as‐prepared nanocomposites exhibit relatively good dispersibility in solvents such as CH2Cl2, THF, and toluene. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009  相似文献   

8.
Both silica/polystyrene (SiO2/PS) and silica/polystyrene‐b‐polymethacryloxypropyltrimethoxysilane (SiO2/PS‐b‐PMPTS) hybrid nanoparticles were synthesized via surface‐initiated atom transfer radical polymerization (SI‐ATRP) from SiO2 nanoparticles. The growths of all polymers via ATRP from the SiO2 surfaces were well controlled as demonstrated by the macromolecular characteristics of the grafted chains. Their wettabilities were measured and compared by water contact angle (WCA) and surface roughness. The results show that the nanoparticles possess hydrophobic surface properties. The static WCA of SiO2/PS‐b‐PMPTS hybrid nanoparticles is smaller than that of SiO2/PS hybrid nanoparticles, meanwhile, the surface roughness of SiO2/PS‐b‐PMPTS hybrid nanoparticles is yet slightly rougher than that of SiO2/PS hybrid nanoparticles, which shows that the combination and competition of surface chemistry and roughness of a solid material can finally determine its wettability. POLYM. ENG. SCI., 2011. © 2010 Society of Plastics Engineers  相似文献   

9.
A new ionic polyacetylene was prepared by the activation polymerization of 2‐ethynylpyridine with 2‐(bromomethyl)‐5‐nitrofuran in high yield without any additional initiator or catalyst. This polymerization proceeded well in a homogeneous manner to give a high yield of the polymer (92%). The activated acetylenic triple bond of N‐(5‐nitro‐2‐furanmethylene)‐2‐ethynylpyridinium bromide, formed in the first quaternerization process, was found to be susceptible to linear polymerization. This polymer was completely soluble in such polar organic solvents as dimethylformamide, dimethyl sulfoxide, and N,N‐dimethylacetamide. The inherent viscosities of the resulting polymers were in the range 0.12–0.19 dL/g, and X‐ray diffraction analysis data indicated that this polymer was mostly amorphous. The polymer structure was characterized by various instrumental methods to have a polyacetylene backbone structure with the designed substituent. The photoluminescence peak was observed at 593 nm; this corresponded to a photon energy of 2.09 eV. The polymer exhibited irreversible electrochemical behaviors between the doping and undoping peaks. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

10.
Block copolymers, polystyrene‐b‐poly(styrene‐co‐maleic anhydride), have been prepared by reversible addition‐fragmentation chain transfer (RAFT) polymerization technique using three different approaches: 1‐phenylethyl phenyldithioacetate (PEPDTA) directly as RAFT agent, mediated polystyrene (PS) block as the macromolecular PS‐RAFT agent and mediated poly(styrene‐maleic anhydride) (SMA) block with alternating sequence as the macromolecular SMA‐RAFT agent. Copolymers synthesized in the one‐step method using PEPDTA as RAFT agent possess one PS block and one SMA block with gradient structure. When the macromolecular RAFT agents are employed, copolymers with one PS block and one alternating SMA block can be produced. However, block copolymers with narrow molecular weight distribution (MWD) can only be obtained using the PS‐RAFT agent. The MWD deviates considerably from the typical RAFT polymerization system when the SMA is used as the RAFT agent. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

11.
Surface modification of carbon fibre (CF) by well‐defined polymer brushes was carried out using the ‘grafting from’ method. Poly(methyl methacrylate)‐grafted carbon fibre (CF‐PMMA) was successfully prepared by surface‐initiated atom‐transfer radical polymerization (SI‐ATRP) of methyl methacrylate (MMA) from the macro‐initiator, bromo‐acetic ester‐modified carbon fibre (CF‐BrA), with the complex of 1,10‐phenanthroline and Cu(I)Br as catalyst. The percentage of grafting (PG%) and the conversion of monomer (C%) increased linearly with increasing of polymerization time, and reached 24.0 % and 6.7 %, respectively, after a polymerization time of 6 h, calculated from the elemental analyses (EA). The structural and surface morphological analyses were conducted with Fourier‐transform infrared (FTIR) spectroscopy, X‐ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). Copyright © 2005 Society of Chemical Industry  相似文献   

12.
A novel polymer bearing coumarin pendants of 4‐allyloxy‐2H‐chromen‐2‐one (ACO) was synthesized by atom transfer radical polymerization (ATRP) in toluene at 110°C using 2‐Bromoisobutyryl bromide (BIBB), Cu (I) Br, and 2,2′‐bipyridyl (bpy) as initiator, catalyst, and ligand, respectively. The most appropriate molar concentration ratio of [ACO] : [BIBB] : [Cu (I) Br] : [bpy] was found to be 40 : 1 : 1 : 2 for controlled polymerization. Successful chain extension polymerization of poly (4‐allyloxy‐2H‐chromen‐2‐one) (PACO) confirms the livingness of the process. The activation energy (Ea) (76.26 kJ mol?1) and enthalpy of activation (ΔH?) (73.07 kJ mol?1) were in good agreement to each other proving the feasibility of the reaction and negative value of entropy of activation (ΔS?) (?320 J mol?1 K?1) supported the highly restricted movement of reacting species in transition state during polymerization. Initial polymer decomposition temperature of PACO was found to be 130°C. SEM analysis revealed that polymer surface is not smooth with pointed rod like shapes. The polymer/Ag nanocomposite was synthesized and examined in view of antibacterial effect against Enterococcus faecalis, Staphylococcus aureus, Escherichia coli, Proteus mirabilis, and Klebsiella pneumonae. PACO and its Ag nanocomposite (PACON) have been found to be active selectively against bacterial pathogen E. fecalis with minimum inhibitory concentration of 50 and 32 μg mL?1, respectively. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012  相似文献   

13.
The grafted homopolymer and comb‐shaped copolymer of polyacrylamide were prepared by combining the self‐assembly of initiator and water‐borne surface‐initiated atom transfer radical polymerization (SI‐ATRP). The structures, composition, properties, and surface morphology of the modified PET films were characterized by FTIR/ATR, X‐ray photoelectron spectroscopy (XPS), contact angle measurement, and scanning electronic microscopy (SEM). The results show that the surface of PET films was covered by equable grafting polymer layer after grafted polyacrylamide (PAM). The amount of grafting polymer increased linearly with the polymerization time added. The GPC date show that the polymerization in the water‐borne medium at lower temperature (50°C) shows better “living” and control. After modified by comb‐shaped copolymer brushes, the modified PET film was completely covered with the second polymer layer (PAM) and water contact angle decreased to 13.6°. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012  相似文献   

14.
Atom transfer radical polymerization (ATRP) of three‐armed polystyrene[PS] and poly(styrene‐b‐isobutyl methacrylate)[PS‐b‐PiBμMA] were accomplished using an initiator with tri‐active C‐Br end group function and cuprous (I) bromide/2,2′‐bipyridyne catalytic system. The characterization obtained by FT‐IR, 1H‐NMR, and GPC techniques. The average molecular weight and polydispersity of PS and PS‐b‐PiBμMA were determined as 19,800, 29,300 and as 1.37 and 1.15, respectively, which indicates that the constant concentration of growing chains are present throughout the polymerization. The refractive index and extinction coefficient of the samples were determined in the visible range as a function of wavelength. The refractive index dispersion curves of the thin films were fitted by the Cauchy‐Sellmeier model. The width of localized states (Eu) values changed inversely with optical band gaps (Eg) of the films. While the calculated Eu values of films for initiator, PS and PS‐b‐PiBμMA were determined as 2.72, 2.98, and 2.94 eV, the Eg values were determined as 3.43; 3.11, and 3.16 eV, respectively. The dispersion parameters of thin films were determined. These parameters changed in the investigated wavelength ranges. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers  相似文献   

15.
The AB type diblock PS‐b‐PEO and ABA type triblock PS‐b‐PEO‐b‐PS copolymers containing the same proportions of polystyrene (PS) and poly(ethylene oxide) (PEO) but different connection sequence were synthesized and investigated. Using the sequential living anionic polymerization and ring‐opening polymerization mechanisms, diblock PS‐b‐PEO copolymers with one hydroxyl group at the PEO end were obtained. Then, using the classic and efficient Williamson reaction (realized in a ‘click’ style), triblock PS‐b‐PEO‐b‐PS copolymers were achieved by a coupling reaction between hydroxyl groups at the PEO end of PS‐b‐PEO. The PS‐b‐PEO and PS‐b‐PEO‐b‐PS copolymers were well characterized by 1H NMR spectra and SEC measurements. The critical micelle concentration (CMC) and thermal behaviors were also investigated by steady‐state fluorescence spectra and DSC, respectively. The results showed that, because the PEO segment in triblock PS‐b‐PEO‐b‐PS was more restricted than that in diblock PS‐b‐PEO copolymer, the former PS‐b‐PEO‐b‐PS copolymer always gave higher CMC values and lower crystallization temperature (Tc), melting temperature (Tm) and degree of crystallinity (Xc) parameters. © 2015 Society of Chemical Industry  相似文献   

16.
Controlled thermoresponsive PET track‐etched membranes were synthesized by grafting N‐isopropylacrylamide (NIPAAm) onto the membrane surface via atom transfer radical polymerization (ATRP). The initial measurements were made to determine the anchoring of ATRP initiator on PET membrane surface. Thereafter, polymerization was carried out to control the mass of polymer by controlling reaction time grafted from the membrane surface and, ATR‐FTIR, grafting degree measurements, water contact angle measurements, TGA, and SEM were used to characterize changes in the chemical functionality, surface and pore morphology of membranes as a result of modification. Water flux measurements were used to evaluate the thermoresponsive capacity of grafted membranes. The results show the grafted PET track‐etched membranes exhibit rapid and reversible response of permeability to environmental temperature, and its permeability could be controlled by controlling polymerization time using ATRP method. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.  相似文献   

17.
The combination of radical‐promoted cationic polymerization, atom transfer radical polymerization (ATRP) and click chemistry was employed for the efficient preparation of poly(cyclohexene oxide)‐block‐polystyrene (PCHO‐b‐PSt). Alkyne end‐functionalized poly(cyclohexene oxide) (PCHO‐alkyne) was prepared by radical‐promoted cationic polymerization of cyclohexene oxide monomer in the presence of 1,2‐diphenyl‐2‐(2‐propynyloxy)‐1‐ethanone (B‐alkyne) and an onium salt, namely 1‐ethoxy‐2‐methylpyridinium hexafluorophosphate, as the initiating system. The B‐alkyne compound was synthesized using benzoin photoinitiator and propargyl bromide. Well‐defined bromine‐terminated polystyrene (PSt‐Br) was prepared by ATRP using 2‐oxo‐1,2‐diphenylethyl‐2‐bromopropanoate as initiator. Subsequently, the bromine chain end of PSt‐Br was converted to an azide group to obtain PSt‐N3 by a simple nucleophilic substitution reaction. Then the coupling reaction between the azide end group in PSt‐N3 and PCHO‐alkyne was performed with Cu(I) catalysis in order to obtain the PCHO‐b‐PSt block copolymer. The structures of all polymers were determined. Copyright © 2010 Society of Chemical Industry  相似文献   

18.
Colorimetric mechanophores like spiropyran (SP) represent an emerging type of interesting signal molecule that can be incorporated into polymers or other materials as a stress transducer. In this work, a new type of spiropyran‐containing inimer molecule MA‐SP‐Br are designed and synthesized, which is incorporated into polybutylacrylate (PBA) chains through reversible addition‐fragmentation chain transfer (RAFT) copolymerization with n‐butyl acrylate (BA). PBA‐SP‐Br is then used as a macro‐initiator to graft polystyrene (PS) side chains from the PBA backbone through atom transfer radical polymerization (ATRP) of styrene. The resulting comb‐structured graft copolymer PBA‐SP‐PS contains 0.15–0.34% SP and exhibits a characteristic feature of thermoplastic elastomers. Under uniaxial stretch, the materials possess an excellent mechano‐responsivity and change color at strains as low as about 14%.  相似文献   

19.
Polydimethylsiloxane‐block‐polystyrene‐block‐polydimethylsiloxane (PDMS‐b‐PS‐b‐PDMS) was synthesized by the radical polymerization of styrene using a polydimethylsiloxane‐based macroazoinitiator (PDMS MAI) in supercritical CO2. PDMS MAI was synthesized by reacting hydroxy‐terminated PDMS and 4,4′‐azobis(4‐cyanopentanoyl chloride) (ACPC) having a thermodegradable azo‐linkage at room temperature. The polymerization of styrene initiated by PDMS MAI was investigated in a batch system using supercritical CO2 as the reaction medium. PDMS MAI was found to behave as a polyazoinitiator for radical block copolymerization of styrene, but not as a surfactant. The response surface methodology was used to design the experiments. The parameters used were pressure, temperature, PDMS MAI concentration and reaction time. These parameters were investigated at three levels (?1, 0 and 1). The dependent variable was taken as the polymerization yield of styrene. PDMS MAI and PDMS‐b‐PS‐b‐PDMS copolymers obtained were characterized by proton nuclear magnetic resonance and infrared spectroscopy. The number‐ and weight‐average molecular weights of block copolymers were determined by gel permeation chromatography. Copyright © 2004 Society of Chemical Industry  相似文献   

20.
Ab initio reversible addition–fragmentation chain transfer (RAFT) emulsion polymerization of styrene/butyl acrylate was investigated with the trithiocarbonate macro‐RAFT agent poly(acrylic acid)‐block‐polystyrene (PAA‐b‐PS) as a stabilizer and a RAFT agent. Influences of the amount of ammonium persulfate (APS), the amount of PAA‐b‐PS and the mass ratio of monomers on emulsion polymerization and film properties are discussed. The particle morphology exhibited spherical‐like structure with particles of about 90 nm in diameter and relatively narrow particle size distribution characterized using transmission electron microscopy and dynamic laser scattering. Fourier transform infrared and 1H NMR spectra showed that the styrene/butyl acrylate emulsion was successfully synthesized. The monomer conversion increased initially with increasing amount of APS, from 0.4 up to 0.8 wt%, and then decreased. The particle size increased and its distribution decreased gradually with increasing amount of APS. The monomer conversion increased from 76.83 to 94.21% as the amount of PAA‐b‐PS increased from 3 to 4 wt%, and then decreased with further increase of PAA‐b‐PS. The particle size decreased and its distribution increased with increasing amount of PAA‐b‐PS. The water resistance and solvent resistance of the polymer films initially increased and then decreased with decreasing mass ratio of butyl acrylate to styrene. © 2014 Society of Chemical Industry  相似文献   

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