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1.
Amphiphilic copolymers using hydrophilic N,N‐dimethylacrylamide (DMA), hydrophobic methyl methacrylate (MMA) and a crosslinkable monomer, 3‐methacryloyloxypropyl trimethoxysilane (MTSi), were synthesized and evaluated as coating materials for leukocyte removal filters for whole blood. When filters composed of non‐woven fabrics were coated with crosslinked synthesized copolymers, the elution ratios of the copolymers to water were adequately low because of the crosslinking with trimethoxysilane groups of MTSi units in the copolymers. Filters coated with crosslinked poly(DMA‐co‐MTSi) having a 0.96 mole fraction of DMA units showed a 0.35 ± 0.44% platelet permeation ratio and a logarithmic reduction of 4.0 ± 0.68 for leukocytes. On the other hand, an increase in the content of MMA units in the DMA‐containing copolymers improved the permeation ratio of the platelets dramatically. Filters coated with crosslinked poly(DMA‐co‐MMA‐co‐MTSi) containing a 0.39 mole fraction of MMA units and a 0.58 mole fraction of DMA units showed an 86 ± 3.0% platelet permeation ratio and a logarithmic reduction of 2.1 ± 1.2 for leukocytes. This indicates that an adequate content of hydrophobic monomer units, such as MMA units, is necessary for effective platelet permeation. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

2.
The synthesis of new polymer colloids based on renewable resources, such as sugar‐derived monomers, is nowadays a matter of interest. These new polymeric particles should be useful in biomedical applications, such as drug delivery, because of their assumed biodegradability. In this work, two new families of polymer latex particles, based on a sugar‐derived monomer, 3‐O‐methacryloyl‐1,2:5,6‐di‐O‐isopropylidene‐α‐D ‐glucofuranose (3‐MDG), were produced and characterized. The syntheses of poly(3‐MDG) crosslinked particles and those obtained by copolymerization with methacrylic acid (MAA), poly(3‐MDG‐co‐MAA) crosslinked particles, were prepared by surfactant‐free emulsion polymerization in a batch reactor. The average particle diameter evolutions, the effect of pH of the dispersion medium on the final average diameters, together with the microscopic and morphological analysis of the particle's surface and inner dominium, were analyzed. Poly(3‐MDG‐co‐EGDMA) stable particles were obtained by adding low amounts of initiator. The surface‐charge density of these particles corresponded to the sulfate groups coming from the initiator. In the second family of latices, poly(3‐MDG‐co‐MAA‐co‐EGDMA) particles, DCP measurements and SEM and TEM observations showed that the sizes and surface characteristics depended on the amounts of MAA and crosslinker used in the reaction mixture. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 443–457, 2006  相似文献   

3.
In this study, the poly(N‐isopropylacrylamide‐methylacrylate acid)/Fe3O4/poly(N‐isopropylacrylamide‐methylacrylate acid) (poly(NIPAAm‐MAA)/Fe3O4/poly(NIPAAm‐MAA)) two‐shell magnetic composite hollow latex particles were synthesized by four steps. The poly(methyl methacrylate‐co‐methylacrylate acid) (poly(MMA‐MAA)) copolymer latex particles were synthesized first. Then, the second step was to polymerize NIPAAm, MAA, and crosslinking agent in the presence of poly(MMA‐MAA) latex particles to form the linear poly(MMA‐MAA)/crosslinking poly(NIPAAm‐MAA) core–shell latex particles. Then, the core–shell latex particles were heated in the presence of NH4OH to dissolve the linear poly(MMA‐MAA) core to form the poly(NIPAAm‐MAA) hollow latex particles. In the third step, the Fe3O4 nanoparticles were generated in the presence of poly(NIPAAm‐MAA) hollow polymer latex particles and formed the poly(NIPAAm‐MAA)/Fe3O4 magnetic composite hollow latex particles. The fourth step was to synthesize poly(NIPAAm‐MAA) in the presence of poly(NIPAAm‐MAA)/Fe3O4 latex particles to form the poly(NIPAAm‐MAA)/Fe3O4/poly(NIPAAm‐MAA) two‐shell magnetic composite hollow latex particles. The effect of various variables such as reactant concentration, monomer ratio, and pH value on the morphology and volume‐phase transition temperature of two‐shell magnetic composite hollow latex particles was studied. Moreover, the latex particles were used as carriers to load with caffeine, and the caffeine‐loading characteristics and caffeine release rate of latex particles were also studied. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 2880–2891  相似文献   

4.
In this work, the poly(methacrylic acid‐coN‐isopropylacrylamide) thermosensitive composite hollow latex particles was synthesized by a three‐step reaction. The first step was to synthesize the poly(methyl methacrylate‐co‐methacrylic acid) (poly(MMA‐MAA)) copolymer latex particles by the method of soapless emulsion polymerization. The second step was to polymerize methacrylic acid (MAA), N‐isopropylacrylamide (NIPAAm), and N,N′‐methylenebisacrylamide in the presence of poly(MMA‐MAA) latex particles to form the linear poly(methyl methacrylate‐co‐methacrylic acid)/crosslinking poly(methacrylic acid‐coN‐isopropylacrylamide) (poly(MMA‐MAA)/poly(MAA‐NIPAAm)) core–shell latex particles. In the third step, the core–shell latex particles were heated in the presence of ammonia solution to form the crosslinking poly(MAA‐NIPAAm) thermosensitive hollow latex particles. The morphologies of poly(MMA‐MAA)/poly(MAA‐NIPAAm) core–shell latex particles and poly(MAA‐NIPAAm) hollow latex particles were observed. The influences of crosslinking agent and shell composition on the lower critical solution temperature of poly(MMA‐MAA)/poly(MAA‐NIPAAm) core–shell latex particles and poly(MAA‐NIPAAm) hollow latex particles were, respectively, studied. Besides, the poly(MAA‐NIPAAm) thermosensitive hollow latex particles were used as carriers to load with the model drug, caffeine. The effect of various variables on the amount of caffeine loading and the efficiency of caffeine release was investigated. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 5203–5214  相似文献   

5.
In this work, the poly(methyl methacrylate‐co‐methacrylic acid)/poly(methacrylic acid‐co‐N‐isopropylacrylamide) thermosensitive composite semi‐hollow latex particles was synthesized by three processes. The first process was to synthesize the poly(methyl methacrylate‐co‐methacrylic acid) (poly (MMA‐MAA)) copolymer latex particles by the method of soapless emulsion polymerization. The second process was to polymerize methacrylic acid (MAA), N‐isopropylacrylamide (NIPAAm), and crosslinking agent, N,N′‐methylenebisacrylamide, in the presence of poly(MMA‐MAA) latex particles to form the linear poly(methyl methacrylate‐co‐methacrylic acid)/crosslinking poly(methacrylic acid‐co‐N‐isopropylacrylamide) (poly(MMA‐MAA)/poly(MAA‐NIPAAm)) core–shell latex particles with solid structure. In the third process, part of the linear poly(MMA‐MAA) core of core–shell latex particles was dissolved by ammonia to form the poly(MMA‐MAA)/poly(MAA‐NIPAAm) thermosensitive semi‐hollow latex particles. The morphologies of the semi‐hollow latex particles show that there is a hollow zone between the linear poly(MMA‐MAA) core and the crosslinked poly(MAA‐NIPAAm) shell. The crosslinking agent and shell composition significantly influenced the lower critical solution temperature of poly(MMA‐MAA)/poly(MAA‐NIPAAm) semi‐hollow latex particles. Besides, the poly(MMA‐MAA)/poly(MAA‐NIPAAm) thermosensitive semi‐hollow latex particles were used as carriers to load with the model drug, caffeine. The processes of caffeine loaded into the semi‐hollow latex particles appeared four situations, which was different from that of solid latex particles. In addition, the phenomenon of caffeine released from the semi‐hollow latex particles was obviously different from that of solid latex particles. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3441–3451  相似文献   

6.
《Electrophoresis》2018,39(2):370-376
Poly(stearyl methacrylate‐co‐methacrylic acid) (P(SMA‐co‐MAA)) was induced as pseudostationary phase (PSP) in electrokinetic chromatography (EKC). The n‐octadecyl groups in SMA were the same as that in octadecylsilane (ODS) C18 column. Thus, the present work focused on the comparison of selectivity between polymeric PSP and ODS stationary phase (SP), and the effect of organic modifiers on the selectivity of polymeric PSP and ODS SP. 1‐butanol could directly interacted with PSP as a Class I modifier, and improved both of the methylene selectivity and polar group selectivity. When the analysis times were similar, the polymeric PSP exhibited better methylene selectivity and polar group selectivity. Although the hydrophobic groups were similar, the substituted benzenes elution order was different between polymeric PSP and ODS SP. Linear solvation energy relationships (LSER) model analysis found that polymeric PSP and ODS SP exhibited two same key factors in selectivity: hydrophobic interaction and hydrogen bonding acidity. But polymeric PSP exhibited relatively strong n‐ and π‐electrons interaction to the analytes.  相似文献   

7.
Magnetic molecularly imprinted polymer nanoparticles for bisphenol A were prepared by coassembling magnetic nanoparticles and amphiphilic random copolymers. Under optimized conditions, bisphenol A as template molecules, magnetic molecularly imprinted polymer particles with regular morphology, small size, good monodispersity, and high content of OA‐Fe3O4 were prepared by the coassembly method using P(MMA‐co‐MAA) with monomer ratio of 9:1. These magnetic molecularly imprinted polymer particles could be rapidly collected by an external magnet within 1 min. The saturated adsorption capacity of the magnetic molecularly imprinted polymer for bisphenol A was 201.5 mg/g, and the imprinting factor was 2.5. The separation factors for bisphenol A to β‐estradiol, estriol, and diethylstilbestrol was 3.1, 2.9, and 3.7, respectively. Unlike assembling amphiphilic copolymer in the selective solvent, the coassembly process was simple and rapid. Therefore, the present work provided a facile and versatile approach to construct magnetic molecularly imprinted polymer nanoparticles under mild conditions.  相似文献   

8.
The hollow composite spheres with a raspberry‐like structure were prepared by a self‐assemble heterocoagulation based on the inter‐particle hydrogen‐bonding interaction between the amide groups of hollow poly (N,N′‐methylenebisacrylamide‐coN‐isopropyl acrylamide) (P(MBA‐co‐NIPAAm)) microspheres and the carboxylic acid groups of poly(ethyleneglycol dimethacrylate‐co‐methacrylic acid) (P(EGDMA‐co‐MAA)) nanoparticles, in which P(EGDMA‐co‐MAA) nanoparticle acted as the corona and the hollow P(MBA‐co‐NIPAAm) microsphere behaved as the core. The control coverage of the corona particles on the surface of hollow core microspheres of P(MBA‐co‐NIPAAm)/P(EGDMA‐co‐MAA) hollow composite sphere was studied in detail through adjustment of the mass ratio between the core and corona particles. The effect of the pH on the stability of the raspberry‐like hollow spheres was investigated. The polymer particles and the resultant heterocoagulated raspberry‐like hollow spheres were characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

9.
A series of poly(N‐isopropylacrylamide)‐co‐poly(Nε‐benzyloxycarbonyl‐L ‐lysine) graft copolymers (PNIPAm‐co‐PZLLys) with different side chains (degree of polymerization, DP = 5~40) and unit ratios (from 30 to 70 mol %) were prepared via free radical polymerization, followed by cleaving benzyloxycarbonyl groups (Z groups) to obtain the double hydrophilic graft copolymer, poly(N‐isopropylacrylamide)‐co‐poly(L ‐lysine) (PNIPAm‐co‐PLLys). The pH‐ and temperature‐response properties of the graft copolymers in aqueous solution were studied. The experimental results indicate L15‐N30 and L15N‐70, that is, the PNIPAm‐co‐PLLys having the poly(L ‐lysine) of DP = 15 as side chains as well as 30 and 70 mol %, respectively, of PNIPAm as backbone, have coil‐to‐helix transitions from pH 6 to pH 12 at room temperature and form uniform nanoscale micelle‐like dispersions in aqueous solution at pH 12. The graft copolymers also could form uniform and nanoscale micelle‐like structures at 50 °C in pH 6 buffer solution due to slightly polymer aggregation. With temperature and pH increased, both the deprotonated PLLys side chains and PNIPAm backbone become hydrophobic, leading to polymer precipitation. These results illustrate that a double tunable hydrophilic graft copolymer had been successfully synthesized via a simple radical polymerization, and could form micelles without serious polymer aggregation at a lower pH and a higher temperature. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011  相似文献   

10.
In this study, a novel molecularly imprinted polymer (MIP) based on methacrylic acid (MAA) monomer was synthesized to control release of trinitroglycerin (TNG) as a vasodilator drug for adjusting the cardiac conditions. For this purpose, TNG nanospheres based on poly(methacrylic acid) (PMAA) were prepared by using the precipitation polymerization process. The synthesized TNG nanospheres‐based MIP samples were characterized by means of Fourier transform infrared spectroscopy and field‐emission scanning electron microscopy in order to investigate their provided active functional groups within the cavities as well as morphology, respectively. The results showed that the appropriate non‐covalent bindings between the TNG (template) and PMAA provided within the MIP samples with imprinting factor of 1.98 were achieved by optimizing the amounts of trimethylolpropane trimethacrylate (TRIM) as a cross‐linker and MAA as a functional monomer. On the basis of these obtained conditions, the polymeric nanospheres containing TNG were formed in shape of spherical particles with an average diameter sizing about 40 nm. These remarkable results were obtained by the use of 1:10 molar ratio of TRIM/TNG and 1:6 molar ratio of MAA/TNG. Moreover, in‐vitro release of the TNG from the MIP samples to phosphate buffer solution (pH = 7.4) indicated that the MIP samples had a moderate and gradual release compared with the non‐imprinted polymer samples. These outcomes conducted us to consider the samples as carriers for adjusting potentially cardiac conditions. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

11.
Poly(methyl acrylate‐co‐methyl methacrylate) [P(MA‐co‐MMA)] nanocomposite film containing 1 wt % of montmorillonite (MMT) exhibited unusual higher ductility, higher strain recovery ratio after creep, and higher modulus and strength compared to neat P(MA‐co‐MMA) as they were cast from their individual latices fabricated by soap‐free emulsion polymerization. The fortified mechanical properties were attributed to the MgO components of exfoliated MMT nanoplatelets being grafted by P(MA‐co‐MMA) chains as verified by FTIR and XPS spectroscopies, which to the best of our knowledge is the first time in the literature providing the direct evidence for the polymer chains grafting onto the exfoliated MMT. TEM investigation of the stretched nanocomposite film revealed that the microcracks in the nanocomposite film appeared mainly in the bulk region of polymer matrix, implying that the interfacial strength between P(MA‐co‐MMA) and its grafted MMT nanoplatelets was higher than the cohesion strength of P(MA‐co‐MMA). © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5891–5897, 2009  相似文献   

12.
Quasi‐solid state dye‐sensitized solar cells (QS‐DSSC) containing poly (methyl methacrylate‐co‐acrylonitrile) [P (MMA‐co‐AN)] gel electrolytes were fabricated. By tuning AN molar percentage in P (MMA‐co‐AN), the optimized polymeric gel electrolyte for fabricating QS‐DSSC can be obtained. QS‐DSSC containing polymeric gel electrolyte with 45 mol.% AN in P(MMA‐co‐AN) shows higher energy conversion efficiency than that of QS‐DSSCs containing polymeric gel electrolytes with either pure PMMA or PAN. So it presents an effective way to improve the photovoltaic performance of QS‐DSSC by tuning the components of polymeric gelling agent. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

13.
Wu CH  Chen TH  Huang KP  Wang GR  Liu CY 《Electrophoresis》2007,28(20):3691-3696
A novel microemulsion based on a mixture of diethyl L-tartrate (DET) and SDS was developed for the microemulsion EKC (MEEKC) determination of structurally related steroids. The system consisted of 0.5% w/w DET, 1.7% w/w SDS, 1.2% w/w 1-butanol, 89.6% w/w phosphate buffer (40 mM, pH 7.0), and 7% w/w ACN. With an applied voltage of +10 kV, a baseline separation of aldosterone (A), cortisone acetate (CA), dexamethasone (D), hydrocortisone (H), hydrocortisone acetate (HA), prednisolone (P), prednisolone acetate (PA), prednisone (Ps), triamcinolone (T), and triamcinolone acetonide (TA) could be achieved. Under the optimized conditions, the reproducibility of the retention time (n = 4) for most of the compounds was less than +/-0.8% with the exception of A, Ps, and T. The average number of theoretical plates was 18 800 plates/m. The results were compared with those achieved by the modified micellar EKC (MEKC). MEEKC showed obvious advantages over MEKC for the separation of highly hydrophobic substances. To further evaluate the system, we tested the MEEKC method by analyzing corticosteroids in a spiked urine sample.  相似文献   

14.
In this study, the poly(NIPAAm–MAA)/Fe3O4 hollow latex particles were synthesized by three steps. The first step was to synthesize the poly(methyl methacrylate‐co‐methylacrylate acid) (poly(MMA‐MAA)) copolymer latex particles by the method of soapless emulsion polymerization. Following the first step, the second step was to polymerize N‐isopropylacrylamide (NIPAAm), MAA, and crosslinking agent (N,N'‐methylene‐bisacrylamide (MBA)) in the presence of poly(MMA‐MAA) latex particles to form the linear poly(MMA‐MAA)/crosslinking poly (NIPAAm‐MAA) core‐shell latex particles. After the previous processes, the core‐shell latex particles were heated in the presence of NH4OH to dissolve the linear poly(MMA‐MAA) core in order to form the poly(NIPAAm‐MAA) hollow latex particles. In the third step, Fe2+ and Fe3+ ions were introduced to bond with the ? COOH groups of MAA segments in the poly(NIPAAm‐MAA) hollow polymer latex particles. Further by a reaction with NH4OH and then Fe3O4 nanoparticles were generated in situ and the poly(NIPAAm‐MAA)/Fe3O4 magnetic composite hollow latex particles were formed. The concentrations of MAA, crosslinking agent (N,N'‐methylene bisacrylamide), and Fe3O4 nanoparticles were important factors to influence the morphology of hollow latex particles and lower critical solution temperature of poly(NIPAAm–MAA)/Fe3O4 magnetic composite hollow latex particles. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012  相似文献   

15.
Magnetic poly(methyl methacrylate) (PMMA)/poly(methyl methacrylate‐co‐methacrylic acid) [P(MMA–MAA)] composite polymer latices were synthesized by two‐stage soapless emulsion polymerization in the presence of magnetite (Fe3O4) ferrofluids. Different types and concentrations of fatty acids were reacted with the Fe3O4 particles, which were prepared by the coprecipitation of Fe(II) and Fe(III) salts to obtain stable Fe3O4 ferrofluids. The Fe3O4/polymer particles were monodisperse, and the composite polymer particle size was approximately 100 nm. The morphology of the magnetic composite polymer latex particles was a core–shell structure. The core was PMMA encapsulating Fe3O4 particles, and the shell was the P(MMA–MAA) copolymer. The carboxylic acid functional groups (COOH) of methacrylic acid (MAA) were mostly distributed on the surface of the composite polymer latex particles. Antibodies (anti‐human immunoglobulin G) were then chemically bound with COOH groups onto the surface of the magnetic core–shell composite latices through the medium of carbodiimide to form the antibody‐coated magnetic latices (magnetic immunolatices). The MAA shell composition of the composite latex could be adjusted to control the number of COOH groups and thus the number of antibody molecules on the magnetic composite latex particles. With a magnetic sorting device, the magnetic immunolatices derived from the magnetic PMMA/P(MMA–MAA) core–shell composite polymer latex performed well in cell‐separation experiments based on the antigen–antibody reaction. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1342–1356, 2005  相似文献   

16.
Soap‐free poly(methyl methacrylate‐ethyl acrylate‐acrylic acid or methacrylic acid) [P(MMA‐EA‐AA or MAA)] particles with narrow size distribution were synthesized by seeded emulsion polymerization of methyl methacrylate (MMA), ethyl acrylate (EA) and acrylic acid (AA) or methacrylic acid (MAA), and the influences of the mass ratio of core/shell monomers used in the two stages of polymerization ([C/S]w) and initiator amount on polymerization, particle size and its distribution were investigated by using different monomer addition modes. Results showed that when the batch swelling method was used, the monomer conversion was more than 96.0% and particle size distribution was narrow, and the particle size increased first and then remained almost unchanged at around 600 nm with the [C/S]w decreased. When the drop‐wise addition method was used, the monomer conversion decreased slightly with [C/S]w decreased, and large particles more than 750 nm in diameter can be obtained; with the initiator amount increased, the particle size decreased and the monomer conversion had a trend to increase; the particle size distribution was broader and the number of new particles was more in the AA system than in the MAA system; but the AA system was more stable than the MAA system at both low and high initiator amount. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

17.
The amphiphilic poly(AM‐co‐SA)‐ITXH macrophotoinitiator was synthesized by precipitation photopolymerization under UV irradiation with isopropylthioxanthone (ITX) as free radical photoinitiator. A novel method has been developed to prepare amphiphilic core‐shell polymer nanospheres via photopolymerization of methyl methacrylate (MMA) in aqueous media, with amphiphilic copolymer macrophotoinitiator poly(AM‐co‐SA)‐ITXH. During polymerization, the amphiphilic macroradicals underwent in situ self‐assembly to form polymeric micelles, which promoted the emulsion polymerization of the monomer. Thus, amphiphilic core‐shell nanospheres ranging from 70 to 140 nm in diameter were produced in the absence of surfactant. The conversion of the monomer, number average molecular weights (Mn), and particle size were found to be highly dependent on the macrophotoinitiator and monomer concentration. The macrophotoinitiator and amphiphilic particles were characterized by FTIR, UV‐vis, 1H NMR, TEM, DSC, and contact angle measurements. The results showed the particles had well‐defined amphiphilic core‐shell structure. This new method is scientifically and technologically significant because it provides a commercially viable route to a wide variety of novel amphiphilic core‐shell nanospheres. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 936–942, 2010  相似文献   

18.
In the reversible addition–fragmentation transfer (RAFT) copolymerization of two monomers, even with the simple terminal model, there are two kinds of macroradical and two kinds of polymeric RAFT agent with different R groups. Because the structure of the R group could exert a significant influence on the RAFT process, RAFT copolymerization may behave differently from RAFT homopolymerization. The RAFT copolymerization of methyl methacrylate (MMA) and styrene (St) in miniemulsion was investigated. The performance of the RAFT copolymerization of MMA/St in miniemulsion was found to be dependent on the feed monomer compositions. When St is dominant in the feed monomer composition, RAFT copolymerization is well controlled in the whole range of monomer conversion. However, when MMA is dominant, RAFT copolymerization may be, in some cases, out of control in the late stage of copolymerization, and characterized by a fast increase in the polydispersity index (PDI). The RAFT process was found to have little influence on composition evolution during copolymerization. The synthesis of the well‐defined gradient copolymers and poly[St‐b‐(St‐co‐MMA)] block copolymer by RAFT miniemulsion copolymerization was also demonstrated. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 6248–6258, 2004  相似文献   

19.
The atom transfer radical polymerization technique was used to synthesize the poly(methyl methacrylate-block-methacrylic acid) (P(MAA-b-MMA)) copolymer in order to study the aggregation behavior in aqueous solution over the course of neutralization. Combinations of static and dynamic light scattering (SLS, DLS) and potentiometric titration techniques were used to investigate the size and shape of the micelle at various degrees of neutralization (alpha). By comparing the effect of different polymer chain length with similar MMA/MAA ratio on the aggregation behavior during neutralization, we found relatively strong entanglement of long MMA polymer chains. The comparison between the different MMA/MAA ratios showed that longer MMA chains produced more entanglements. Conductometric titration was used to determine the counterion condensation phenomenon during the course of neutralization. At a critical micellar charge density observed at alpha approximately 0.4, Na+ ions are condensed on the polymer chains. The amount of condensed Na+ was evaluated by the conductivity change, yielding the condensation ratio when the polymer was completely neutralized.  相似文献   

20.
We report the facile synthesis of poly(VI‐co‐MAA) superabsorbent polyampholytic hydrogels (VI = N‐vinylimidazole, MAA = methacrylic acid) via plasma‐ignited frontal polymerization (PIFP). On igniting the top surface of the reactants with air plasma, frontal polymerization occurred and poly(VI‐co‐MAA) hydrogels were obtained within minutes. The preparation parameters were investigated, along with swelling capacity, morphology, and chemical structures of poly(VI‐co‐MAA) hydrogels. Interestingly, the hydrogels are superabsorbent in water and show ampholytic characteristic toward pH. Moreover, the hydrogels are able to capture cationic dyes through electrostatic interaction, offering the potential for further development as dye adsorbents for water purification. In addition, nanocomposite hydrogels were obtained by embedding quantum dots (carbon dots or CdS nanocrystals) into the polymer matrix, which endows the nanocomposite hydrogels with favorable fluorescence and potential applications in bioimaging and biosensing. The results indicate that FP can be applied as an alternative means for facile synthesis of multifunctional hydrogels with additional efficiency and energy‐saving. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 912–920  相似文献   

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