Dispersion polymerization of anionic polyacrylamide in an aqueous salt medium

Anionic polyacrylamide dispersions were prepared by dispersion polymerization in an aqueous salt medium, using acrylamide（AM） and acrylic acid（AA） as monomers and anionic polyelectrolytes as stabilizer. Effects of salt concentration, and molecular weight and concentration of stabilizers on the stability of the dispersions were investigated using a HAAKE rheometer and optical microscopy. The results showed that stable anionic polyacrylamide dispersions, consisting of smooth, spherical, polydisperse particles, could be obtained under the conditions of salt concentration ranging from 26 wt% to 30 wt%, concentration of stabilizers from 1.2 wt% to 1.8 wt%, and intrinsic viscosity of stabilizers from 2.98 dL·g^-1 to 3.74 dL·g^-1. The apparent viscosity of the stable dispersions changed very little with the shear rate, showing Newton fluid behavior.

MONODISPERSE MICRON-SIZED POLYACRYLAMIDE PARTICLES SYNTHESIZED BY DISPERSION POLYMERIZATION

Monodisperse micron-sized polyacrylamide （PAM） particles with a regular shape have been successfully prepared through dispersion polymerization of the monomer using a rotary reactor. FTIR and NMR spectroscopic results demonstrated the formation of PAM. POM and TEM observations revealed that PAM particles had a regular shape and good dispersity. A thick layer of surfactant （PVP） still existed on PAM particles after multiple centrifugation and ultrasonic re-dispersion in ethanol, which indicates a strong interaction between PVP and PAM. The effects of various polymerization factors on the average size of PAM particles have also been studied.

Preparation of Fe_3O_4/PS Magnetic Particles by Dispersion Polymerization

Fe_3O_4/PS magnetic particles with core/shell structure has been prepared in the presence of Fe3O4 magnetic fluid in ethanol/water mixture.Magnetic particles with diameter size range from 5. 54 t0 187. 32 μm were obtained by different reaction conditions.Some parameters such as ethanol, PEG and monomer which affect particle size diameter and size distribution are discussed briefly in this paper.

In Situ Synthesis of Branched Block Copolymer Assemblies via RAFT Dispersion Polymerization Using Branched Macro-RAFT Agents

Here,we demonstrate the use of branched macromolecular reversible addition-fragmentation chain transfer (macro-RAFT) agents in RAFT dispersion polymerization,to access branched block copolymers as well as well-defined branched block copolymer assemblies.Two types of branched macro-RAFT agents were first synthesized by using either a monofunctional chain transfer monomer or a difunctional chain transfer monomer in RAFT polymerization,and subsequently utilized in RAFT dispersion polymerization.It was found that only branched macro-RAFT agents synthesized from the difunctional chain transfer monomer could lead to colloidally stable assemblies with well-defined morphologies.Reaction conditions including monomer concentration,degree of polymerization (DP) of the core-forming block,and DP of the solvophilic segment on morphologies of branched block copolymer assemblies were investigated in detail.Size exclusion chromatography (SEC) analysis further confirmed the successful formation of branched block copolymers by using branched macro-RAFT agents.This work on the synthesis of branched block copolymer assemblies by RAFT dispersion polymerization offers new opportunities for the rational design of polymer assemblies with well-defined structures.

ATRP-Template Dispersion Polymerization of Methacrylic Acid/PVP

ATRP-template dispersion polymerization of methacrylic acid （MAA） on the template of polyvinyl pyrrolidone （PVP K-30） was carried out in the aqueous solution by using methyl 2-bromopropionate （MBP）/CuC1/2,2＇-bipyridine （bpy） as the initiation system. The scanning electron microscopy （SEM）, dynamic light scattering （DLS） and gel permeation chromatography （GPC） were employed for evaluating the results of polymerization. As a result, the minimonomer droplets formed due to the H-bond interaction of PVP-MAA. The stability of droplets was dependent on pH and the concentrations of both PVP and MAA. When pH 〈 2, the coagulum of PVP-MAA formed, whereas when pH 〉 4.5, the droplets were not observable by DLS. In order to prepare the stable latex, the concentration of PVP should be lower than 9 wt%, whilst the concentration of MAA should be lower than 5.5 wt%. The optimum condition was pH 2.4, PVP 4.76 wt% and MAA 5 wt%, by which the stable latex of ca. 50 nm nanoparticles of PMAA/PVP was prepared by ATRP polymerization and simultaneously the molar mass of PVP was duplicated by PMAA according to GPC diagrams. In contrast, by using AIBN, KPS and KPS-Na2SO3 redox initiation system, the coagulum accompanying with the larger molar mass of PMAA was obtained, irrespective of pH and concentrations of PVP and MAA.

Preparation of microsized crosslinked microspheres by dispersion copolymerization of polystyrene/polyethylene glycol 200-dimethacrylae

Dispersion copolymerization of styrene with polyethylene glycol 200-dimethacrylae as the cross-linking agent was completed by using poly（N-vinyl pyrrolidone） and 2,2-azo-bisisobutyronitrile as the steric stabilizer and initiator, respectively. Crosslinked copolymeric microspheres were prepared directly by the one-step method of dispersion copolymerization. The effects of the content of polyethylene glycol 200-dimethacrylae on the particle morphology and the copolymerization rate were investigated. It shows that the crosslinking agent plays an important role in the particle morphology and the system stability. When the content of crosslinking reached 2.5wt%, the floriated particles were obtained.

HIGH IMMOBILIZATION OF ANTIBACTERIAL MOIETIES ONTO MONODISPERSE MICROSPHERES BY DISPERSION POLYMERIZATION USING BICATIONIC VIOLOGEN SURFMER

In order to achieve monodisperse particles with high content of antibacterial groups covalently bonded on surface, a bicationie viologen, N-hexyl-N-（4-vinylbenzyl）-4,4＇-bipyridinium bromide chloride （HVV） was devised as a surfrner in dispersion polymerization of styrene （St） using a mixture of methanol （or ethylene glycol） and water as media. Effects of content of HVV, its addition profile and composition of reaction media on particles size and incorporation of HVV moieties were mainly investigated. The attachment of silver and gold nanoparticles on particle surface under UV irradiation ascertained the surface-bonded HVV segments. SEM, TEM observations and XPS, zata potential measurements indicated that increase of initial HVV contents and addition of HVV （when polymerization had been performed for 3 h） led to grown particles and enhanced immobilization of HVV moieties. Using a mixture of ethylene glycol and water as reaction media, small particles （520-142 nm） with highly attached HVV moieties were prepared. Furthermore, antibacterial efficacy of the resultant particles against S. aureus was assayed, and particles with more HVV moieties anchored on surface demonstrated greater efficiency of antibacterial activity.

CONTROLLED/"LIVING" RADICAL POLYMERIZATION OF STYRENE IN AN AQUEOUS DISPERSION SYSTEM

Atom transfer radical polymerization (ATRP) of styrene catalyzed by cuprous (CuX)/1,10-phenanthroline (Phen) and CuX/CuX2/Phen was conducted in an aqueous dispersed system. A stable latex was obtained by using ionic surfactant sodium lauryl sulfonate (SLS) or composite surfactants, such as SLS/polyoxyethylene nonyl phenyl ether (OP-10), SLS/hexadecanol and SLS/OP-10/hexadecanol, Among which SLS and SLS/OP-10/hexadecanol systems established better dispersed effect during the polymerization, It was found that Phen was a more suitable ligand than N,N,N',N',N'-pentamethyldiethylenetriamine (PMDETA) to maintain an appropriate equilibrium of the activator Cu(I) and the deactivator Cu(II) between the organic phase and the water phase, The effect of several initiators (such as EBiB, CCl4 and 1-PEBr) and the temperature on such a kind of ATRP system was also observed. The number-average molar mass (M-n) of polystyrene (PS) increased with the conversion and the molar mass distribution (M-w/M-n) remained narrow. These experimental data show that the polymerization could be controlled except for the quick increase of monomer conversion and the number-average molar mass of PS in the initial stage of polymerization. Furthermore, the initiator efficiency was found to be low (similar to57%) in CuX/Phen catalyzed system. To overcome this problem, Cu(II)X-2 (20 mol%-50 mol% based on CuX) was introduced into the polymerization system. In this case, higher initiator efficiency (60%-90%), low M-w/M-n of PS (as low as 1.08) were achieved and the molar masses of the PS fit with the theoretical ones.

Preparation and Properties of Aqueous SCNTs Dispersion based on A UV-curable Polymeric Dispersant

A novel photosensitive copolymer P（SS-co-AA-g-GMA）（PSAG） was synthesized and utilized to noncovalently functionalize pristine single-walled carbon nanotubes（SCNTs）. PSAG was highly effective for the solubilization of SCNTs in water and validated by UV-vis absorption spectra experiments, resulting in homogeneous and stable PSAG-SCNT aqueous dispersion. The microstructure of SCNTs was observed through Raman spectroscopy and transmission electron microscopy. In addition, compared with the two common polymeric dispersants of Triton X-100 and PSS, PSAG demonstrated more effective performances for dispersing SCNTs under identical conditions. Furthermore, the photosensitive PSAG-SCNTs can be crosslinked after UV irradiation, leading to significant improvement in the water resistance of SCNT films. UV-cured films can be transferred to plastic wrap to form a flexible film with high electrical conductivity.

PREPARATION OF POLYMER DISPERSED LIQUID CRYSTALS USING PHOTOPOLYMERIZATION

2-Hydroxyethyl methacrylate (HEMA) and styrene copolymers are prepared by photopolymerization. The electrooptical behavior and microstructure of the polymer dispersed liquid crystal films are investigated by using He-Ne laser and scanning electron microscopy, respectively. With increasing E7 content in the copolymer, droplet size increased, threshold voltage decreased.

Preparation of cationic polyacrylamide microsphere emulsion and its performance for permeability reduction

In this paper, cationic polyacrylamide microspheres （CPAM） were synthesized using acrylamide （AM） and methacryloyloxyethyl trimethyl ammonium chloride （TMAEMC） as monomers, ammonium sulfate as dispersant, poly（acryloyloxyethyl trimethyl ammonium chloride） （PAETAC） as dispersion stabilizer, and ammonium persulfate as initiator. The synthetic method was dispersion polymerization. The effects of monomer ratio （AM/TMAEMC）, dispersant concentration, and dispersion stabilizer dosage on dispersion polymerization were systematically studied to determine the optimal preparation conditions. The structure and viscosity of the synthesized polymer were characterized by FTIR and capillary viscometry, respectively, and the particle sizes and distribution of the polymer microspheres were characterized by microscopy and dynamic light scattering, respectively. Finally, flow tests were conducted to measure the permeability reduction performance of the microspheres at various concentrations in sand packs with different permeability. Results show that CPAM emulsion of a solids content of 1 wt% has excellent performance in low-to-medium permeability formations （〈 1,000 mD）, and the efficiency may reach above 90%.

Preparation of Core-shell Structured Particles and Their Nucleation in Polyester:I. Preparation of Monodisperse SiO_2/PS Core-shell Composite Particles

To enhance the nucleation and crystallization properties of polyester (e.g., polyethylene terephthalate, PET), core-shell structured particles are used to improve these properties by controlling the inorganic dispersion properties in the polymers. In the paper, monodisperse particles of silica/polystyrene (PS) are prepared with both dispersion and emulsion polymerization techniques. The monodisperse silicon dioxide particles are first prepared with the seed growth method and modified by the coupling agents. Silica is properly modified with KH-570, and its size deviation is 3.0% or so. The modified silica then reacts with the mixture of ethanol, water medium, and monomer of styrene under dispersion polymerization. Results show that the dispersion polymerization technique is more suitable for monodisperse core-shell SiO2/PS particles than that of the emulsion. The morphology and molecular structure of the core-shell particles are investigated with the transmission electron microscope (TEM), and fourier transform infra-red spectroscopy (FTIR). The results show that the modified silica particles are successfully encapsulated with polystyrene. The average number of silica particles encapsulated into each polystyrene sphere decreases when the size of silica particles increases from 50 nm to 600 nm, and will approach one when the silica is greater than 380nm in size. The mass ratio for silica/PS particles in emulsion polymerization is 4.7/1, lower than that of 6.8/1 for dispersion polymerization, which is the first reported optimized data for preparing the similar monodisperse composite particles. Thus, the PS shell in the former is thinner than that in the latter.

Electrically tunable holographic polymer templated blue phase liquid crystal grating

In this paper, we demonstrate an alternative approach to fabricating an electrically tunable holographic polymer tem- plated blue phase liquid crystal grating. This grating is obtained by preforming a polymer template comprised of periodic fringes, and then refilling it with a blue phase liquid crystal. Compared with conventional holographic polymer dispersed liquid crystal gratings, our grating can remarkably reduce its switching voltage from 200 V to 43 V while maintaining a sub-millisecond response time. The holographic polymer templated blue phase liquid crystal （HPTBPLC） grating is free from electrode patterning, thus leading to a lower cost and more flexible applications.

Kinetics investigations for holographic Bragg grating based on polymer dispersed liquid crystal

This paper investigates the monomer kinetics of polymer dispersed liquid crystal （PDLC） grating. Fourier transform infrared （FTIR） spectra are used in the studies of photoreaction kinetics. The results indicate that there is a relative stable stage arises after a very short initial stage. Based on FTIR studies, the monomer diffusion equation is deduced and necessary numerical simulations are carried out to analyse the monomer conversion which is an important point to improve phase separation structure of PDLC grating. Some simulation results have a good agreement with experimental data. In addition, the effects induced by monomer diffusion constant D and diffusion-polymerization-ratio rate R are discussed. Results show that monomer conversion can be improved by increasing value of D. Besides, a good equilibrium state （R = 1） is more beneficial to the diffusion of monomer which is important in the process of phase separation.

Preparation and characterization of PTFE coating in new polymer quartz piezoelectric crystal sensor for testing liquor products

A new method was developed based on the electron beam vacuum dispersion（EBVD） technology to prepare the PTFE polymer coating of the new polymer quartz piezoelectric crystal sensor for testing liquor products. The new method was applied in the new EBVD equipment which we designed. A real-time system monitoring the polymer coating＇s thickness was designed for the new EBVD equipment according to the quartz crystal microbalance（QCM） principle, playing an important role in preparing stable and uniform PTFE polymer coatings of the same thickness. 30 pieces of PTFE polymer coatings on the surface of the quartz crystal basis were prepared with the PTFE polymer ultrafine powder（purity ≥ 99.99%）as the starting material. We obtained 30 pieces of new PTFE polymer sensors. By using scanning electron microscopy（SEM）, the structure of the PTFE polymer coating＇s column clusters was studied. One sample from the 30 pieces of new PTFE polymer sensors was analysed by SEM in four scales, i.e., 400×, 1000×, 10000×, and 25000×. It was shown that under the condition of high bias voltage and low bias current, uniformly PTFE polymer coating could be achieved, which indicates that the new EBVD equipment is suitable for mass production of stable and uniform polymer coating.

Preparation of Poly(o-toluidine)/Nano ZrO2/Epoxy Composite Coating and Its Application for Corrosion Protection of Steel

The main objective was to study the anticorrosion performance of poly（o-toluidine）/nano ZrO2/epoxy composite coating.Poly（o-toluidine）/nano ZrO2 composite was prepared by in situ polymerization of o-toluidine monomer in the presence of nano ZrO2 particles.Fourier transformation infrared spectroscopy（FT-IR）,UV-visible spectroscopy（UV-vis）,X-ray diffraction（XRD）,Scanning electron microscopy（SEM）,and Thermogravimetric analysis（TGA） were used to characterize the composition and structure of the composite.Poly（o-toluidine）/nano ZrO2 composite was mixed with epoxy resin through a solution blending method and the three components poly（o-toluidine）/nano ZrO2/epoxy composite coating was coated onto the surface of steel sample by the brush coating method.The anticorrosion performance of poly（o-toluidine）/nano ZrO2/epoxy composite coating on steel sample was studied by polarization curve and electrochemical impendence spectroscopy in 3.5% Na Cl solution as corrosion environment and also compared with that of poly（o-toluidine）/epoxy composite coating and pure epoxy coating.It was observed that the composite coating containing poly（otoluidine）/nano ZrO2 composite has got higher corrosion protection ability than that of poly（o-toluidine）.The electrochemical measurement results demonstrated that poly（o-toluidine） fillers improve the electrochemical anticorrosion performance of epoxy coating and the addition of nano ZrO2 particles increases the tortuosity of the diffusion pathway of corrosive substances.

THE VISCOELASTIC EFFECT ON THE FORMATION OF MESO-GLOBULAR PHASE OF DILUTE HETEROPOLYMER SOLUTIONS

Linear homopolymer chains in poor solvent exist either as individual crumpled single chain globules or asmacroscopic precipitate, depending on whether the solution is in the one- or the two-phase region. However, linearheteropolymer chains in dilute solution might be able to form stable mesoglobules made up of a limited number of chains ifthe degree of amphiphilicity of the chain is sufficiently high and the experimental conditions are appropriate. The self-assembly of block copolymers in a selective solvent is typical of such examples. In practice, the formation of stablemesoglobules can be directly related to the formation of novel polymeric nanopaticles in solution. In this article, we willaddress the formaton of mesoglobular phase not only on the basis of thermodynamics, but also from a kinetic point of view,which leads to the discussion of how viscoelasticity can affect the phase behavior of heteropolymer chains in dilute solution.The formation and stabilization of several different kinds of novel polymeric nanopedicles will be used to illustrate ourdiscussion.

Effect of Polymer Network Morphology on the Performance of Polymer Dispersed Liquid Crystal (PDLC) Composite Films

The effects of the morphologies of liquid crystal (LC) droplets left in polymer network on the performance of polymer dispersed liquid crystal composite films were investigated.By adjusting the relative content range of the crosslinking and diluents,the morphologies of polymer network can be changed.Therefore,the properties of PDLC composite films with imparity polymer morphologies were obtained by experiments and the finite element simulation.Results of the experimental and finite element simulation showed that the electro-optical properties of PDLC composite films were inversely proportional to the domain size of the polymer network and the mechanical properties were proportional to the domain size of the polymer network.

Random lasing in dye-doped polymer dispersed liquid crystal film

A dye-doped polymer-dispersed liquid crystal film was designed and fabricated,and random lasing action was studied.A mixture of laser dye,nematic liquid crystal,chiral dopant,and PVA was used to prepare the dye-doped polymer-dispersed liquid crystal film by means of microcapsules.Scanning electron microscopy analysis showed that most liquid crystal droplets in the polymer matrix ranged from 30 μm to 40 μm,the size of the liquid crystal droplets was small.Under frequency doubled 532 nm Nd：YAG laser-pumped optical excitation,a plurality of discrete and sharp random laser radiation peaks could be measured in the range of 575–590 nm.The line-width of the lasing peak was 0.2 nm and the threshold of the random lasing was 9 m J.Under heating,the emission peaks of random lasing disappeared.By detecting the emission light spot energy distribution,the mechanism of radiation was found to be random lasing.The random lasing radiation mechanism was then analyzed and discussed.Experimental results indicated that the size of the liquid crystal droplets is the decisive factor that influences the lasing mechanism.The surface anchor role can be ignored when the size of the liquid crystal droplets in the polymer matrix is small,which is beneficial to form multiple scattering.The transmission path of photons is similar to that in a ring cavity,providing feedback to obtain random lasing output.

Viscoelastic modeling of the diffusion of polymeric pollutants injected into a pipe flow

This study focuses on the transient analysis of nonlinear dispersion of a polymeric pollutant ejected by an external source into a laminar pipe flow of a Newtonian liquid under axi-symmetric conditions.The influence of density variation with pollutant concentration is approximated according to the Boussinesq approximation and the nonlinear governing equations of momentum,pollutant concentration are obtained together with and Oldroyd-B constitutive model for the polymer stress.The problem is solved numerically using a semi-implicit finite difference method.Solutions are presented in graphical form for various parameter values and given in terms of fluid velocity,pollutant concentration,polymer stress components,skin friction and wall mass transfer rate.The model can be a useful tool in understanding the dynamics of industrial pollution situations arising from improper discharge of hydrocarbon pollutants into,say,water bodies.The model can also be quite useful for available necessary early warning methods for detecting or predicting the scale of pollution and hence help mitigate related damage downstream by earlier instituting relevant decontamination measures.