Preparation and swelling properties of superabsorbent nanocomposites based on natural guar gum and organo-vermiculite

Vermiculite (VMT) was modified with cetyl trimethylammonium bromide (CTAB). Superabsorbent nanocomposites were prepared by solution polymerization of natural guar gum (GG), partially neutralized acrylic acid (NaA) and organo-vermiculite (CTA⁺-VMT), ammonium persulfate (APS) as initiator and N,N′-methylene-bis-acrylamide (MBA) as crosslinking agent. FTIR spectra confirmed that NaA had been grafted onto GG and the OH groups of CTA⁺-VMT participated in the polymerization reaction. The intercalated-VMT was exfoliated during polymerization and uniformly dispersed in the GG-g-PNaA matrix. Swelling tests show that CTA⁺-VMT improved swelling and swelling rate more remarkably than VMT, and the nanocomposite exhibited distinct kinetic swelling behavior in NaCl and CaCl₂ solution. Organo-VMT improved the gel strength of the nanocomposite compared to VMT, and the maximum storage modulus of the nanocomposite reached 658 Pa (γ = 0.5%, ω = 100 rad/s).     

Effects of modified vermiculite on the synthesis and swelling behaviors of hydroxyethyl cellulose-<Emphasis Type="Italic">g</Emphasis>-poly(acrylic acid)/vermiculite superabsorbent nanocomposites

A series of hydroxyethyl cellulose-g-poly(acrylic acid)/vermiculite (HEC-g-PAA/VMT) superabsorbent nanocomposites were prepared by radical solution polymerization among hydroxyethyl cellulose (HEC), partially neutralized acrylic acid (AA), raw vermiculite (RVMT), acidified vermiculite (AVMT) and organo-vermiculite (OVMT) in the presence of initiator ammonium persulfate (APS) and crosslinker N,N’-methylenebisacrylamide (MBA). FTIR results revealed that AA was grafted onto HEC backbone and VMT participated in polymerization. VMT was exfoliated during polymerization reaction and a nanocomposite structure was formed as shown by XRD and TEM analysis. Effects of VMT content, concentration of HCl solution and organification degree of OVMT on water absorbency were investigated and the swelling kinetics of the developed nanocomposites was also evaluated. Results showed that incorporation of VMT greatly enhanced the water absorbency, and the modified VMT by acidification and organification can improve the water absorbency more remarkably than raw one. OVMT can improve the swelling capabilities and swelling rate to the highest degree in contrast to RVMT and AVMT.     

Synthesis of poly(arylene disulfide)–vermiculite nanocomposites via in situ ring‐opening polymerization of macrocyclic oligomers

Exfoliated poly(4, 4′‐oxybis(benzene)disulfide)/vermiculite (POBDS/VMT) nanocomposites were successfully synthesized via in situ melt intercalation of cyclo(4, 4′‐oxybis(benzene)disulfide) oligomers (COBDS) into octadecylammonium‐exchanged VMT (organo‐VMT). The POBDS/VMT nanocomposites were melt fabricated in a two‐step process. First, the COBDS/VMT nanocomposite precursor was fabricated by melt delaminating organo‐VMT with COBDS at a temperature slightly higher than its melting point. Subsequently, exfoliated POBDS‐VMT nanocomposites can be prepared in situ via instant melt ring‐opening polymerization of the COBDS‐VMT nanocomposite precursor. The nanoscale dispersion of VMT layers within POBDS polymer was confirmed by X‐ray diffraction, scanning electron microscopy and transmission electron microscopy. High molecular weight POBDS polymer was formed in a few minutes at the same time as the nanocomposite formation. The results of dynamic mechanical analysis showed that the storage modulus and glass transition temperature of the nanocomposites are much higher than those of the POBDS matrix, even with a very small amount of VMT addition. This methodology provides a potential approach to synthesize high‐performance polymer/clay nanocomposites. Copyright © 2004 Society of Chemical Industry     

Novel polylactide/vermiculite nanocomposites by in situ intercalative polymerization. I. Preparation,characterization, and properties

Polylactide (PLA)/vermiculite nanocomposites were prepared by in situ intercalative polymerization of L,L ‐lactide (LLA) in the presence of organomodified vermiculite (VMT). The d‐spacings of both the organomodified VMT and the exfoliated nanocomposites were investigated by X‐ray diffraction (XRD) analysis, and the morphology of exfoliated nanocomposites was examined by transmission electron microscopy (TEM). Thermogravimetric analysis (TGA) indicated that there is some enhancement in degradation behavior between the nanocomposites and the PLA matrix. Dynamic mechanical analysis (DMA) confirmed the constraint effect of exfoliated VMT layers on PLA chains, which is beneficial to the increased storage and loss modulus and increased glass transition temperature. The tensile strength showed that the exfoliated nanocomposites are reinforced and toughened by the addition of nanometer‐size vermiculite layers. POLYM. COMPOS., 28:545–550, 2007. © 2007 Society of Plastics Engineers     

Absolute online monitoring of acrylic acid polymerization and the effect of salt and pH on reaction kinetics

Using recently introduced Automatic Continuous Online Monitoring of Polymerization reactions (ACOMP), the kinetics of acrylic acid polymerization was studied. ACOMP yields the absolute weight‐averaged mass (M_w), monomer conversion, and other quantities. As the initiator concentration increased, it was shown that the rate increased and the M_w decreased as in regular free‐radical polymerization. The effect of salt on acrylic acid polymerization in an aqueous solution was investigated. The polymerization rate and M_w both decreased with an increasing salt concentration. ACOMP molecular weights were also compared with size‐exclusion chromatography on aliquots periodically withdrawn during the reaction, and good agreement was found. The effect of the pH on the rate and the molecular weight was also investigated, and when the medium pH was changed from 2 to 5 with sodium hydroxide, the rate and M_w both decreased as the pH increased. Light‐scattering results of reaction end products in the reference solvent showed that molecules synthesized at higher pH were in a more expanded form. When equimolar sodium hydroxide was added to the acrylic acid (pH ? 5) and sodium acrylate formed, adding salt did not effect the reaction kinetics of the poly(sodium acrylate); its effect on the products was a relatively minor decrease of M_w. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1352–1359, 2004     

Synthesis and enhanced swelling properties of a guar gum-based superabsorbent composite by the simultaneous introduction of styrene and attapulgite

In current study, a series of novel guar gum-graft-poly(sodium acrylate-co-styrene)/attapulgite (GG-g-P(NaA-co-St)/APT) superabsorbent nanocomposites were prepared by the simultaneous graft copolymerization of partially neutralized acrylic acid (NaA), styrene (St) and attapulgite (APT) onto natural guar gum (GG), using ammonium persulfate (APS) as the initiator and N,N'-methylene-bis-acrylamide (MBA) as the crosslinking agent. Fourier Transform Infrared (FTIR) and ultravoilet (UV) spectra confirmed that NaA and St had been grafted onto GG backbones and APT participated in the polymerization reaction. The incorporation of St and APT clearly improved the surface porous morphology of the composites as exhibited by Filed Emission Scanning Electron Microscopy (FESEM). The effect of St and APT on the swelling properties and the swelling kinetics of the developed nanocomposite was investigated. Results showed that the simultaneous incorporation of proper amount of hydrophobic co-monomer St and inorganic nano-scale APT not only obviously enhanced the swelling capacity but highly improved the swelling rate, and the nanocomposite showed better salt-resistant capability and excellent pH-stability in various pH solutions.     

Properties of water‐soluble acrylic copolymer/montmorillonite nanocomposites for warp sizing

Acrylic copolymer/montmorillonite (MMT) nanocomposites for warp sizing were prepared in the presence of Na⁺‐MMT by the in situ intercalative polymerization of acrylic acid, acrylamide, and methyl acrylate in water solution. The properties of the solution and cast film were tested according to an application in sizing process of the nanocomposite size with various MMT contents. The results indicate that, for an exfoliated structure corresponding to the MMT content increasing to 7 wt %, the performance parameters of solution viscosity, glass‐transition temperature, and tensile strength of the film increased and the moisture sorption, abrasion loss, and elongation at break of the film decreased. When the intercalated structure of MMT was 9 wt %, the gathered MMT layers acted as a common inorganic filler in the copolymer matrix, with limited contribution to the properties of the composite. The adhesion work of the nanocomposite solution was calculated by use of the Young–Dupre relation, which showed maximum values at an MMT content of 3 wt % on the surfaces of both the polyester and cellulose films. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Preparations of organo-vermiculite with large interlayer space by hot solution and ball milling methods: A comparative study

The intercalation of alkylammonium ions into vermiculite (VMT) to improve the interior structure of VMT has evolved into a subject of tremendous interest. The Na⁺-exchanged vermiculite (Na-VMT) prepared from the VMT in Xinjiang area (China), served as a host for intercalation with cetyl-trimethylammonium (CTA⁺) to prepare organo-vermiculites (OVMTs) by a typical hot solution method (OVMT (H)) and a novel ball milling method (OVMT (M)) under the optimized conditions confirmed by orthogonal experimental designs. The two methods employed thermal energy and mechanical energy respectively to drive the CTA⁺ cations into the interlayer space of layers and to carry out the cation exchange reaction. From X-ray diffraction (XRD) patterns, scanning electron microscopy (SEM) images and thermogravimetric analysis (TGA) results, the Na-VMTs were structurally modified, and the OVMTs showed remarkably large interlayer spaces, in which alkyl chains built paraffin-type bilayer arrangements nearly perpendicular to silicate layers. However, hot solution and ball milling methods showed different behaviors. The interlayer distance of the OVMT (M) (4.283 nm) was larger than that of the OVMT (H) (4.052 nm), indicating that the tilting angle of alkyl chains in the former was larger than that in the latter. Additionally, the hot solution treatment retained the morphology of the layers and reduced the surface energy of the VMT, whereas the ball milling method caused layers to twist and led to high residual surface energy on the particles, as well as a higher content of organic compounds and lower thermal stability for the product.     

Homogeneous complex solution formed through interactions of poly(acrylamide‐co‐acrylic acid)/poly(acrylamide‐co‐dimethyldiallylammonium chloride) complex with M n+ hydration metal ions in aqueous media

A homogeneous complex solution, formed through inter‐polyelectrolyte complexation of poly(acrylamide‐co‐acrylic acid) (P(AM‐AA)) with poly(acrylamide‐co‐dimethyldiallylammonium chloride) (P(AM‐DMDAAC)) and interaction of the P(AM‐AA)/P(AM‐DMDAAC) complex with M ⁿ⁺ hydrated metal ion, was prepared and the structure and properties of the P(AM‐AA)/P(AM‐DMDAAC)/M ⁿ⁺ homogeneous complex solution were studied by UV spectrometry, dynamic light scattering and viscometry. The experimental results show that the homogeneous complex solution can be obtained by controlling the composition of the P(AM‐AA)/P(AM‐DMDAAC) complex and the M ⁿ⁺ metal ion content. Compared to the constituents, ie the P(AM‐AA) solution, the P(AM‐DMDAAC) solution and the P(AM‐AA)/P(AM‐DMDAAC) complex solution, the P(AM‐AA)/P(AM‐DMDAAC)/M ⁿ⁺ complex solution has a new peak at 270 nm in its UV spectrum, a larger hydrodynamic radius, and hence a higher solution viscosity, all of which indicate that there exist specific interactions between polymers and M ⁿ⁺ metal ions. These interactions lead to the formation of a network structure and hence an obvious increase not only in solution viscosity but also in resistance of the polymer solution to simple salts, to temperature changes and to shearing. © 2001 Society of Chemical Industry     

Superabsorbent polymeric materials. XII. Effect of montmorillonite on water absorbency for poly(sodium acrylate) and montmorillonite nanocomposite superabsorbents

A series of novel xerogels based on sodium acrylate (NaA), montmorillonite (MMT), and N,N′‐methylene‐bisacrylamide (NMBA) were prepared by inverse suspension polymerization and water solution polymerization. The influences of pure MMT, intercalated MMT, the method of polymerization, and the content of the MMT in the copolymeric gels on the water absorbency and the initial absorption rate in deionized water and various salt solutions were investigated. Results showed that the water absorbency was increased by adding a small amount of the pure MMT into the copolymeric gels, but decreased by adding intercalated MMT into the gels. In addition, the water absorbency of the gels prepared by water solution polymerization was lower than that prepared by inverse suspension polymerization. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3422–3429, 2004     

Electrocatalysis and detection of nitrite on a polyaniline‐Cu nanocomposite‐modified glassy carbon electrode

A polyaniline (PANI)‐Cu nanocomposite‐modified electrode was fabricated by the electrochemical polymerization of aniline and the electrodeposition of copper under constant potentials on a glassy carbon electrode (GCE), respectively. Scanning electron microscope result shows that the PANI‐Cu composite on the surface of the GCE displays the nanofibers having an average diameter of about 80 nm with lengths varying from 1.1 to 1.2 μm. The electrode exhibits enhanced electrocatalytic behavior to the reduction of nitrite compared to the PANI‐modified GCE. The effects of applied potential, pH value of the detection solution, electropolymerization charge, temperature, and nitrite concentration on the current response of the composite‐modified GCE were investigated and discussed. Under optimal conditions, the PANI‐Cu composite‐modified GCE can be used to determine nitrite concentration in a wide linear range (n = 18) of 0.049 and 70.0 μM and a limit of detection of 0.025 μM. The sensitivity of the electrode was 0.312 μA μM^?1 cm^?2. The PANI‐Cu composite‐modified GCE had the good storage stability. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Synthesis,swelling behaviors,and slow‐release characteristics of a guar gum‐g‐poly(sodium acrylate)/sodium humate superabsorbent

Superabsorbents used in agricultural and ecological projects with low‐cost, slow‐release fertilizers and environmentally friendly characteristics have been extensively studied. The use of a natural polymer as the matrix and then further polymerization with some functional material has become the preferred method. In this work, with natural guar gum (GG), partially neutralized acrylic acid, and sodium humate (SH) as the raw materials, ammonium persulfate as the initiator, and N,N′‐methylenebisacrylamide (MBA) as the crosslinker, GG‐g‐poly(sodium acrylate) (PNaA)/SH superabsorbents were synthesized through a solution polymerization reaction and were characterized with Fourier transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analysis. The effects of the SH content and MBA concentration on the water absorbency were investigated. The results showed that the introduction of SH into the GG‐g‐PNaA system could improve the water absorbency, swelling rate, pH‐resistant property, and reswelling capability, and the superabsorbent containing 15 wt % SH had the highest water absorbency of 532 g/g of sample in distilled water and 62 g/g of sample in a 0.9 wt % NaCl solution. The slow release in water and water retention in sandy soil tests revealed that the superabsorbent could act as a fertilizer as well as an effective water‐saving material for agricultural applications. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Morphology and thermal and mechanical properties of phosphonium vermiculite filled poly(ethylene terephthalate) composites

A series of poly(ethylene terephthalate) (PET)/phosphonium vermiculite (P‐VMT) composites were prepared by a melt‐blending method, and we investigated the morphology and thermal and mechanical properties of the composites. We prepared P‐VMT with quaternary phosphonium salts using the common method followed by a cation‐exchange reaction. X‐ray diffraction showed that the phosphonium surfactants were partially intercalated into the vermiculite layers, The d‐spacing of the PET–clay sample was somewhat less than that of the P‐VMT because some degradation of the surfactant took place during melt processing. Compared with PET, the PET–clay composites had a lower decomposition temperature and showed a 17.4% increase in the tensile strength with a P‐VMT content of 3 wt %. Scanning electron microscopy and transmission electron microscopy demonstrated that P‐VMT had a homogeneous dispersion and good compatibility in the polymer matrix with a low content of additive and indicated that the P‐VMT content of 3 wt % was optimal. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Rapid living free‐radical polymerization of methyl acrylate under 60Co γ‐ray irradiation at room temperature

Rapid living free‐radical polymerization of methyl acrylate under ⁶⁰Co γ‐ray irradiation in the presence of benzyl 1H‐imidazole‐1‐carbodithioate at room temperature is reported. The results showed that the polymerization is a fast living process, and that the molecular weight of the polymer is as high as 39 600 g mol^?1 at 68 % conversion with M_w/M_n = 1.09 within 68 min. The polymerization rate was markedly influenced by the structures of thiocarbonylthio compounds. Copyright © 2004 Society of Chemical Industry     

Preparation and characterization of transparent poly(methyl methacrylate)/Na+‐MMT nanocomposite films by solution casting

Films of poly(methyl methacrylate) (PMMA)/sodium montmorillonite (Na⁺‐MMT) nanocomposites have been successfully prepared utilizing Na⁺‐MMT by N,N‐dimethylformamide solution casting. The nanocomposite films show high transparency, enhanced thermal resistance, and mechanical properties in comparison with the neat polymer film. The transparency of the films was investigated by UV‐vis spectra. The exfoliated dispersion of Na⁺‐MMT platelets in nanocomposites were investigated by X‐ray diffraction and transmission electron microscopy. The enhanced thermal resistance and mechanical properties of PMMA were studied by thermal gravimetric analysis and dynamic mechanical analysis, respectively. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Aqueous polymerization of protonated 4-vinylpyridine in montmorillonite

The polymerization of protonated 4-vinylpyridine (4-VPH⁺X⁻) in the interlayer zone of montmorillonite was studied. Polymerization is critically affected by the degree of surface coverage with a threshold value twice the cation exchange capacity of the mineral. Montmorillonite surfaces show selectivity for protonated 4-vinylpyridine favoring the formation of the quaternized form of the polyvinylpyridine polyelectrolyte. In situ polymerization of 4-VPH⁺X⁻ in the presence of 10 wt.% or lower sodium montmorillonite in aqueous solution yields exfoliated montmorillonite–polyelectrolyte heterostructures. The rate of polymerization in the presence of delaminated montmorillonite is much faster than in the absence. Mechanisms for intergallery and exogallery polymerization of 4-VPH⁺X⁻ are described.     

An in Vitro–Selected DNAzyme Mutant Highly Specific for Na+ under Slightly Acidic Conditions

Sodium is one of the most common metal ions in biology; however, DNA-based sodium probes have only been reported recently. A Na⁺-specific RNA-cleaving DNAzyme named NaA43 is active with Na⁺ alone. In this work, we were using Co(NH₃)₆³⁺ as the intended metal cofactor for in vitro selection, but obtained a mutant of the NaA43 DNAzyme. The mutant was named NaH1, and differs from NaA43 by only two nucleotides. NaA43 has an optimal pH of 7.0, whereas the optimal pH for NaH1 is 6.0. This difference might be due to our selection having been performed at pH 6.0. NaH1 also displays an excellent selectivity for sodium relative to other competing monovalent ions, as well as a fast catalytic rate of (0.11±0.01) min⁻¹ with 50 mm Na⁺. At low Na⁺ concentrations, the selected DNAzyme exhibited a higher cleavage rate than NaA43 and thus a tighter apparent K_d of (12.0±1.6) mm Na⁺. Furthermore, the NaH1 DNAzyme was engineered into a fluorescent Na⁺ biosensor by attaching a fluorophore/quencher pair to the DNAzyme with a detection limit of 223 μm Na⁺. Preliminary work on detection of Na⁺ in serum was demonstrated as well. This study provides a useful mutant that works in a slightly acidic environment, which might be useful for sensing Na⁺ in acidic in vivo environments.     

Ethanol‐assisted dispersion of attapulgite and its effect on improving properties of alginate‐based superabsorbent nanocomposite

The dispersion of attapulgite (APT) as nanorod‐like single crystals is crucial to fully develop its functionality of one‐dimensional nanometer material as a filler of composite materials. In this study, APT was dispersed by the assistance of ethanol during the high‐pressure homogenization process to form individual nanorod‐like crystals. The dispersed APT was used to prepare new sodium alginate‐g‐poly(sodium acrylate‐co‐styrene)/attapulgite (NaAlg‐g‐P(NaA‐co‐St)/APT) superabsorbent nanocomposites. The effect of ethanol/water ratio on the dispersion of crystal bundles of APT was investigated by field emission scanning electron microscopy, and the results indicate that APT crystal bundles were effectively disaggregated in ν(CH₃CH₂OH) : ν(H₂O) ? 5 : 5 solution after homogenized at 50 MPa. The better dispersion of APT in NaAlg‐g‐P(NaA‐co‐St) matrix has clearly improved the gel strength (from 1300 Pa to 1410 Pa, ω = 100 rad/s), swelling capacity (442–521 g/g), swelling rate (3.3303–4.5736 g/g/s), and reswelling ability of the superabsorbent nanocomposite. Moreover, the nanocomposites showed fast swelling–deswelling responsive behavior in different saline solutions. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

pH‐responsive polyzwitterions: A comparative study of acrylamide‐based polyampholyte terpolymers and polybetaine copolymers

A comparative study of pH‐responsive polyzwitterions (PZs) with polyampholyte or polybetaine architectures was conducted with well‐defined model polymer systems. Low‐charge‐density PZs, including ampholytic terpolymers composed of acrylamide (AM), sodium 3‐acrylamido‐3‐methylbutanoate, and (3‐acrylamidopropyl)trimethylammonium chloride and carboxybetaine copolymers composed of AM and 3‐(3‐acrylamidopropyldimethylammonio)propionate, were prepared via free‐radical polymerization in 0.5M NaCl to yield ter‐ and copolymers with random termonomer and comonomer distributions. Sodium formate was used as a chain‐transfer agent during the polymerizations to eliminate the effects of the monomer feed composition on the degree of polymerization (DP) and to suppress gel effects and broadening of the molecular weight distributions. The polymer compositions were determined via ¹³C‐NMR spectroscopy, and the residual counterion content was determined via elemental analysis for Na⁺ and Cl^?. The molecular weights (MWs) and polydispersity indices (PDIs) were determined via size exclusion chromatography/multi‐angle laser light scattering (SEC–MALLS); the polymer MWs ranged from 1.4 to 1.5 × 10⁶ g/mol, corresponding to DPs of 1.6–1.9 × 10⁴ repeat units, with all the polymers exhibiting PDIs less than or equal to 2.1. The intrinsic viscosities determined from SEC–MALLS data and the Flory–Fox relationship agreed with the intrinsic viscosities determined via low‐shear dilute‐solution viscometry. Data from the SEC–MALLS analysis were used to analyze the radius of gyration/molecular weight (R_g–M) relationships and the Mark–Houwink–Sakurada intrinsic viscosity/molecular weight ([η]–M) relationships for the PZs. The R_g–M and [η]–M relationships and viscometric data revealed that under size exclusion chromatography conditions, the poly[acrylamide‐co‐3‐(3‐acrylamidopropyldimethylammonio)propionate] betaine copolymers had more open, random‐coil conformations and greater polymer–solvent interactions than the ampholytic poly[acrylamide‐co‐sodium 3‐acrylamido‐3‐methylbutanoate‐co‐(3‐acrylamidopropyl)trimethylammonium chloride] terpolymers. The pH‐ and salt‐responsive dilute‐solution viscosity behavior of the PZs was examined to assess the effects of the polymer structure and composition on the solution properties. The polyampholyte terpolymers had greater solution viscosities and more pronounced stimuli‐responsiveness than the polybetaine copolymers because of their stronger intramolecular interactions and increased chain stiffness. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 24–39, 2004     

Synthesis of Gemini‐Like Methyl Acrylate‐Acrylic Acid‐Methyl Acrylate Triblock Copolymers Surfactants by RAFT Polymerization in Solution and Investigation of their Behavior at the Air–Water Interface

A series of methyl acrylate‐acrylic acid amphiphilic triblock copolymers (PMA‐PAA‐PMA) were prepared by solution polymerization using S,S′‐bis (α,α‐dimethy1acetic acid) trithiocarbonate (BDAT) as a reversible addition fragmentation chain transfer (RAFT) agent and methyl acrylate (MA) as the first monomer. The triblock copolymers and their common MA homopolymer precursors were characterized in terms of their compositions, molecular weights and behavior at the air–water interface using ¹H‐NMR spectroscopy, thermogravimetric analysis, gel permeation chromatography, surface tension, transmission electron microscopy (TEM) and dynamic light scattering respectively. The results indicated that PMA‐PAA‐PMA was successfully synthesized through RAFT polymerization. The polydispersity index (PDI) decreased when the molar ratio [n(MA)/n(AA)] increased, the lowest PDI was obtained at 5.23 wt% RAFT and the molecular weights were consistent with the theoretical value as the RAFT agent percentage varied. The polymer neutralized by sodium hydroxide solution shows a low critical micelle concentration (CMC), which was <10^?2 mol L^?1 in water. The A_min values increased and showed a maximum with decreased AA chain length. TEM showed that the neutralized polymer formed a special vesicle structure with large pore structure which led to a low CMC and surface tension of water.