PHOTOINITIATED INVERSE EMULSION POLYMERIZATION OF SODIUM ACRYLATE

Photoinitiated inverse emulsion polymerization of sodium acrylate(AANa)in kerosene was carried out at room orlower temperature,using 2,2-dimethoxy-2-phenylacetophenone(DMPA)as the initiator.Kinetic investigations indicated thatthe polymerization could be completed in about 30 min and produce polymer with high molecular weight(10~6～10~7).It wasfound that monomer droplets are the main sites for the polymerization(nucleation).With the increase of DMPAconcentration,polymerization rate(R_p)reaches a maximum value while molecular weight of the produced polymer has anadverse result,but the dependence of R_p on incident light intensity is similar.Influences of other parameters such asmonomer concentration,emulsifier content and reaction temperature,etc.were also studied.At lower pH values of waterphase,R_p depends strongly on the pH due to the electrostatic interaction between the ionized radicals and the monomer.Athigher pH,R_p shows a slight dependence on pH.

INFLUENCES OF WATER-SOLUBLE CATIONIC MONOMERS ON THE POLYMERIZATION RATE IN THE INVERSE EMULSION

This investigation deals with the free radical polymerization both of (2-methacryloyloxyethyl) trimethyl ammonium chloride (QACEMA) and of diallyldimethyl ammonium chloride (DADMAC) in inverse emulsion. The influences of some factors, such as the concentration of monomers, initiator and emulsifier are discussed. The polymerization rate equations of above two monomers can be written as follows: R(p) = k[M](1.21)[I](0.82)[E](0.57) (for QACEMA) R(p) = k'[M](1.34)[I](0.90)[E](0.62) (for DADMAC)

Investigation on the Inverse Emulsion Polymerization of Acrylic Acid

Polyacrylic acid particles in nano-scale were synthesized using an inverse (W/O) emulsion polymerization method. The particle size and size change of inverse micelles which solubilize a part of monomer solution was monitored by PCS (photon correlation spectroscopy) and the particles of polyacrylic acid were viewed in scanning electron microscope for the first time. It was concluded that the inverse micelles were primarily the polymerization reaction sites.

Microstructure and Properties of PET Fabric Grafted by Polyacrylic Acid with Inverse Microemulsion Polymerization

Annual production output of poly(ethylene terephthalate)(PET) fiber has been over 15 million tons in China due to its good mechanical properties and processability,but the shortage of hydrophilic group of PET has imposed many limitations to further extend its application.The PET fabrics were grafted with polyacrylic acid in inverse microemulsion after low pressure plasma treatment,and the microstructure and properties of the grafted fabrics were investigated with infrared spectroscopy,scanning electron microscope(SEM),hydrophilic and mechanical tests.The grafting yield was increased with the grafting time.The grafting polymer was in the granular form with its particle size ranging from a few micrometers to a dozen of micrometers,normally smaller than the fiber diameter.The moisture regain and water uptake increased while the air permeability of the grafted fabrics decreased with the increase of grafting yield.The bending rigidity and tensile properties show slightly complicated behaviors with grafting yield.The inverse emulsion grafting technique can be used to control the grafting polymer architecture.

Carbon dioxide/calcium oxide responsive behavior and application potential of amine emulsion

Green and low cost CO_(2) and CaO were used to stimulate amine emulsions to reveal the responsive behavior of amine emulsions.On this basis,oil-based drilling fluids responsive to CO_(2) and CaO were formulated and their properties were evaluated.The results showed that the amine emulsions inversed from water-in-oil state to oil-in-water state readily and their rheological behavior underwent transitions of decreasing,rising again and decreasing again via induction by CO_(2).These CO_(2) responsive behaviors could be reversed by CaO.Oil-based drilling fluids prepared based on the amine emulsions with oil-water volume ratios of 50:50 to 70:30,densities of 1.4-2.0 g/cm^(3) had good rheological and filtration properties at 160℃;and be readily cleaned up using CO_(2) bubbling.The useless solid phase with low density could be removed efficiently via reducing the viscosity of emulsion by CO_(2) and the residual liquid phase could be restored to the original state by CaO and reused to prepare drilling fluid.The mechanisms analysis indicated that CO_(2)/CaO induced the reversible conversion between amine emulsifiers and their salts,which enabled the reversible regulation of both the hydrophilic-lipophilic balance of amine emulsifiers and the emulsion particles’size and finally caused the controllable-reversion of the form and rheology of amine emulsion.

DMC-grafted cellulose as green-based flocculants for agglomerating fine kaolin particles

Novel cellulose based flocculants C-g-P(DMC) with various chain architectures are synthesized through a situ graft copolymerization. The cationic ammonium chloride group(DMC) is grafted onto cellulose by two separate inverse emulsion polymerization with γ-methacryloxypropyl trimethoxy silane(KH-570) and double bond addition reactions, which is a new and simple method to employ KH-570 as a bridge for the connection of cellulose matrix and DMC group. The effects of pH, flocculant dose, standing time on turbidity of kaolin suspensions and particle sizes have been studied systematically. In addition, the response surface methodology(RSM) study confirms that PAC and C-g-P(DMC)have synergy in turbidity removal with a higher removal efficiency of 98.32%. Moreover, C-g-P(DMC) 1 has higher removal efficiency with 96.5% at a low dosage of 0.6 mg L^(-1) and better floc properties than C-g-P(DMC) 2 and C-g-P(DMC) 3, suggesting that the length and quantity of cationic branch chains play a crucial role in Kaolin flocculation due to their dramatically enhanced bridging effects.

Preparation of polyacrylamide/silica composite capsules by inverse Pickering emulsion polymerization

Polyacrylamide/silica （PAM/SiO2） composite capsules were synthesized by inverse Pickering emulsion polymerization. Silica nanoparticles modified with methacryloxypropyltrimethoxysilane （MPS） were used as a stabilizer. Transmission electron microscopy （TEM）, scanning electron microscopy （SEM）. Fourier transform infrared （FTIR） spectroscopy, and thermal gravimetric analysis （TGA） were used to characterize the morphology and composition of the composite capsules. SEM and TEM images showed that capsules consisted of a particle shell and a polymer inner layer. The capsule size depends on the nanoparticle concentration in the continuous phase. The composite rigidity largely depends on the acrylamide concentration. FTIR and TGA results indicated the existence of polyacrylamide and SiO2 in the composite particles. Aqueous Hg（ll） removal testing by the PAM/SiO2 composite capsules indicated promising potential for removing heavy metal ions from wastewater.