Polymerization Of Ethylene Glycol Dimethacrylate Research Articles

Poly(ionic liquid) nanogel with tunable morphologies achieved via cross-linking polymerization induced self-assembly

Polymerization-induced self-assembly (PISA) has been the focus of extensive research as an effective approach to create polymer nanoobjects. However, it still confronts hurdles in terms of nano-object stability and the availability of hydrophilic macromolecular agents. In this study, an innovative and productive approach for developing poly(ionic liquid) (PIL) nano-objects was successfully established through cross-linking polymerization induced self-assembly (CPISA). The suggested approaches employ reversible addition fragmental transfer (RAFT) polymerization of ethylene glycol dimethacrylate (EGDMA) mediated by PIL macromolecular chain transfer agents (macro-CTAs) in selected solvents. Core-cross-linked PIL nanogels with various morphologies such as sphere, fiber, and ring were achieved by varying the molecular weight of PIL macro-CTAs and the solvent. Furthermore, PIL nanogels were demonstrated to be effective catalysts for the cycloaddition reaction between CO2 and epoxides. This versatile method allows for a controllable manner to produce cross-linked polymer nano-objects. Therefore, the findings have significant potential in the fields of polymer synthesis, nanomedicine and catalysis.

Pore Structure Tuning of Poly-EGDMA Biomedical Material by Varying the O-Quinone Photoinitiator.

Porous polymer monoliths with thicknesses of 2 and 4 mm were obtained via polymerization of ethylene glycol dimethacrylate (EGDMA) under the influence visible-light irradiation in the presence of a 70 wt% 1-butanol porogenic agent and o-quinone photoinitiators. The o-quinones used were: 3,5-di-tret-butyl-benzoquinone-1,2 (35Q), 3,6-di-tret-butyl-benzoquinone-1,2 (36Q), camphorquinone (CQ), and 9,10-phenanthrenequinone (PQ). Porous monoliths were also synthesized from the same mixture but using 2,2'-azo-bis(iso-butyronitrile) (AIBN) at 100 °C instead o-quinones. According to the results of scanning electron microscopy, all the resulting samples were conglomerates of spherical, polymeric particles with pores between them. Use of mercury porometry showed that the interconnected pore systems of all the polymers were open. The average pore size, Dmod, in such polymers strongly depended on both the nature of the initiator and the method of initiation of polymerization. For polymers obtained in the presence of AIBN, the Dmod value was as low as 0.8 μm. For polymers obtained via photoinitiation in the presence of 36Q, 35Q, CQ, and PQ, the Dmod values were significantly greater, i.e., 9.9, 6.4, 3.6, and 3.7 μm, respectively. The compressive strength and Young's modulus of the porous monoliths increased symbatically in the series PQ < CQ < 36Q < 35Q < AIBN with decreasing proportions of large pores (over 12 μm) in their polymer structures. The photopolymerization rate of the EGDMA and 1-butanol, 30:70 wt% mixture was maximal for PQ and minimal for 35Q. All polymers tested were non-cytotoxic. Based on the data from MTT testing, it can be noted that the polymers obtained via photoinitiation were characterized by their positive effect on the proliferative activity of human dermal fibroblasts. This makes them promising osteoplastic materials for clinical trials.

The Development of Derivative Method analysis 1,4 Benzodiazepines in Biological Matrix using High-Performance Liquid Chromatography (HPLC) and Liquid Chromatography-Mass

1.4 benzodiazepine derivatives are the benzodiazepine class that is used most frequently in clinical as a sedation agent, anxiolytic, and antiepileptic. The high tense of benzodiazepine consumption can causes addiction and misappropriation. That matter causes benzodiazepine and its metabolites often find in toxicology clinical and forensic. This systematic review aimed to identify an efficient sample preparation procedure and an accurate analysis method to determine benzodiazepine existence in various biological matrices. According to the PRISMA flow diagram’s chart, twenty-four reviewed articles systematically pointed that plasma and urine utilization gave good accuracy results and recovery than other biological matrices. SBSE extraction method development using vinylpyrrolidone ethylene glycol dimethacrylate polymer gave efficient results with the amount of recovery 96%, and HPLC instrument utilization was still selective and sensitive with LOD until 12ng/ml and LOQ 36 ng/ml.

Structure and functional group regulation of plastics for efficient ammonia capture

Activated carbon and metal organic frameworks have been tested as NH3 recovery adsorbents, however, they are limited due to low NH3 adsorption capacity and high cost, respectively. In this study, ethylene glycol dimethacrylate (EGDMA) polymers as the representative ester plastics were tested, and their structure and adsorption sites were regulated using HNO3, HCl, or H2SO4 with varied H+ concentrations. The results showed that the EGDMA polymers all used hydrolysis which promoted NH3 adsorption via different mechanisms. With HNO3 and HCl optimization, an increased surface area promoted NH3 adsorption via physical forces. H2SO4 optimization resulted in –COOH, –OH, and –SO3H formation, which reacted with NH3 by chemical adsorption and hydrogen bonds. This significantly increased the NH3 adsorption capacity (85.99 mg·g−1) compared to the material before optimization (0.36 mg·g−1). This study presents a novel low-cost and efficient method to recycle waste plastics as NH3 adsorbents.

Molecularly Imprinted Polymers Based Surface Plasmon Resonance Sensor for Sulfamethoxazole Detection

Sulfamethoxazole (SMX) is a sulfonamide antibiotic primarily used to treat urinary tract infections and used in veterinary and industrialized husbandry to treat diseases and food additives. Like other antibiotics, SMX is considered as a pollutant in water and food that threaten local life. This study developed a surface plasmon resonance (SPR) sensor chip that is fast, highly selective, and reusable, and requires no pretreatment for detecting SMX. As a receptor, SMX imprinted methacrylic acid-2-hydroxyethyl methacrylate-ethylene glycol dimethacrylate polymer [poly(MAA-HEMA-EGDMA)] was used. The surface of the gold SPR chips was coated with a drop-casting method. The nanofilm coated chips were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), ellipsometer, contact angle measurement, and Fourier-transform infrared spectrometry (FTIR). Imprinting factor (IF) was calculated as: ΔR[MIP(molecularly imprinted polymers)]/ΔR[NIP(non-imprinted)]=12/3.5=3.4. Limit of detection (LOD) and limit of quantification (LOQ) values were calculated with 3 s/m and 10 s/m methods, and the results were found to be 0.001 1 µg/L for LOD 0.003 4 µg/L for LOQ. Adsorption studies on both standard SMX solution and commercial milk samples were applied. Also, we investigated the developed chip’s reusability, storability, and selectivity with amoxicillin and cefalexin.

New water-soluble forms of α-tocopherol: preparation and study of antioxidant activity in vitro

Water-soluble forms of α-tocopherol (vitamin E) possessing antioxidant activity in vitro were obtained by encapsulating in N-vinylpyrrolidone with triethylene glycol dimethacrylate polymer particles and were characterized by various physicochemical methods. Quantum-chemical modeling of a structure of α-tocopherol with the copolymer moiety and its theoretical absorption spectra modeling were carried out.

Utilizing a degradation prediction pathway system to understand how a novel methacrylate derivative polymer with flipped external ester groups retains physico-mechanical properties following esterase exposure

ObjectiveThe region of failure for current methacrylates (i.e. derivatives of acrylates) are ester bond linkages that hydrolyze in the presence of salivary and bacterial esterases that break the polymer network backbone. This effect decreases the mechanical properties of methacrylate-based materials. MethodsThe ethylene glycol dimethacrylate (EGDMA) or novel ethylene glycol ethyl methacrylate (EGEMA) discs were prepared using 40 µL of the curing mixture containing photo/co-initiators for 40 s in a PTFE mold at 1000 mW/cm2. The degree of conversion was used as a quality control measure for the prepared discs, followed by physical, mechanical, and chemical characterization of discs properties before and after cholesterol esterase treatment. ResultsAfter 9 weeks of standardized cholesterol esterase (CEase) exposure, EGDMA discs showed exponential loss of material (p = 0.0296), strength (p = 0.0014) and increased water sorption (p = 0.0002) compared to EGEMA discs. We integrated a degradation prediction pathway system to LC/MS and GC/MS analyses to elucidate the degradation by-products of both EGEMA and EGDMA polymers. GC/MS analysis demonstrated that the esterase catalysis was directed to central polymer backbone breakage, producing ethylene glycol, for EGDMA, and to side chain breakage, producing ethanol, for EGEMA. The flipped external ester group linkage design is attributed to EGEMA showing higher resistance to esterase biodegradation and changes in mechanical and physical properties than EGDMA. SignificanceEGEMA is a potential substitute for common macromer diluents, such as EGDMA, based on its resistance to biodegradation effects. This work inspires the flipped external group design to be applied to analogs of current larger, hydrophobic strength bearing macromers used in future dental material formulations.

Polymerization of Ethylene Glycol Dimethacrylate (EGDM), Using An Algerian Clay as Eco-catalyst (Maghnite-H+ and Maghnite-Na+)

In this paper we have explored a novel and green method to synthesis and polymerize ethylene glycol dimethacrylate (EGDM). This technique consists on using Maghnite (Algerian clay) as a green catalyst to replace toxic catalysts. The Algerian clay has been modified using two ion exchange process to obtain Maghnite-H+ (proton exchanged process) and Maghnite-Na+ (sodium exchanged process). Synthesis experiments of EGDM and Poly (EGDM) are performed in bulk respecting the principles of green chemistry. The structure of the obtained monomer and the obtained polymer was confirmed by FT-IR, 1H-NMR and 13C-NMR, where the methacrylate end groups are clearly visible. The presence of unsaturated end group in the structure of monomer was confirmed by UV-Visible analysis. Thermogravimetric analysis (TGA) was used to study the thermal stability of these obtained products. Copyright © 2020 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Adsorption isotherm, kinetics simulation and breakthrough analysis of 5-hydroxymethylfurfural adsorption/desorption behavior of a novel polar-modified post-cross-linked poly (divinylbenzene-co-ethyleneglycoldimethacrylate) resin

A polar modified post-cross-linked poly (divinylbenzene-co-ethyleneglycol-dimethacrylate) (PCL-PDE) resin was synthesized by suspension polymerization of ethylene glycol dimethacrylate (EGDMA) and divinylbenzene (DVB), and a post-cross-linked reaction. After characterization, the adsorption behaviors of 5-hydroxymethylfurfural (5-HMF) on PCL-PDE resin were determined in comparison with the starting copolymers PDE resin. The equilibrium adsorption capacity of 5-HMF on PCL-PDE resin was much larger than PDE resin and the increase rate was greater than 52.6%. The equilibrium data of 5-HMF onto PCL-PDE resin were found to be better fitted by the Langmuir isotherm model. The kinetic data shows that the adsorption reached equilibrium in a short time (less than 20 min) can be fitted by the pore diffusion model (PDM) at various operating conditions. The effective pore diffusion coefficient was dependent upon adsorption temperature, and were 6.706 × 10−10, 8.958 × 10−10, 1.136 × 10−9 and 1.429 × 10−9 m2 s−1 at 288, 298, 308 and 318 K, respectively. Furthermore, the effects of feed flow rate (Qf = 0.6, 1.5, 3.0 and 6.0 mL min−1) and initial 5-HMF concentration (cf = 0.52, 1.02, 2.00 and 4.96 g L−1) on the adsorption were investigated systematically. Besides, a general rate model (GRM) was used to predict adsorption breakthrough curves of 5-HMF. The simulation results are highly consistent with the experimental data, indicating that the GRM can successfully simulate this process. In the desorption process, the desorption capacity reaches 99.6% of adsorbed capacity, suggesting that the PCL-PDE resin exhibited good reusability. Therefore, it could be suggested that the PCL-PDE resin has a potential application in the separation and purification of 5-HMF.

Synthesis, characterization and using a new terpyridine moiety-based ion-imprinted polymer nanoparticle: sub-nanomolar detection of Pb(II) in biological and water samples

A highly selective lead-imprinted polymer was synthesized via a thermal precipitation polymerization technique based on a terpyridine-based ligand as the complexing agent. The synthesized polymer was successfully incorporated in a graphite paste electrode (GPE) as the recognition element for lead ion (Pb2+). Differential pulse anodic stripping voltammetry (DPASV) technique was used to transduce the binding events at the modified electrode. The imprinted polymer nanoparticles (IP-NPs) were synthesized by precipitation polymerization of ethylene glycol dimethacrylate as the cross-linker, 2,2′-azobisisobutyronitrile as the free radical initiator and 2,2′:6′,6″-terpyridine (terpy) as the recognition element. The sensing procedure is based on the accumulation of lead ions at − 1.0 V vs. Ag/AgCl. Afterward, the DPV was recorded by the sweeping potential in a positive direction to oxidize the accumulated ions, leading to the appearance of a significant anodic peak. The constructed IIP–GPE revealed a linear response toward Pb2+ over the concentration range from 0.4 to 10 nM (with the sensitivity of 693.95 nA nM−1 cm−2) and 10 nM to 1.0 µM (with the sensitivity of 580.25 µA µM−1 cm−2). The limit of detection (LOD) was evaluated to be 0.11 nM (for S/N = 3). The accuracy of the sensor was explored by analysis of a quality control material (QCMs, Seronorm™ urine REF NO 1011645) and different water samples. Selectivity studies showed no particular interference for detection of Pb(II).

Application of affinity microspheres for effective SPE cleanup before the determination of sulfamerazine by HPLC

This paper describes the application of poly (ethylene glycol dimethacrylate-N-methacryloyl-L-tryptophane methyl ester) [p(EGDMA-MATrp)] microspheres as an affinity sorbent for the SPE (solid phase extraction) cleanup of sulfamerazine (SMR) from food samples of animal origin before high performance liquid chromatography (HPLC) analysis. The microspheres were prepared by suspension polymerization of ethylene glycol dimethacrylate (EGDMA) and N-methacryloyl-L-tryptophane methyl ester (MATrp) as a crosslinker and a monomer, respectively. Various parameters affecting the SPE cleanup efficiency of the p(EGDMA-MATrp) microspheres (contact time, pH, initial SMR concentration, ionic strength etc.) were optimized. Under the optimized conditions, maximum adsorption capacity was found to be 8.55 ± 0.44 mg/g sorbent at pH 5.0. 90% of the adsorbed SMR was desorbed by using ACN:MeOH (5:5) mixture as a desorption agent. Applicability of the microspheres for the SPE cleanup of SMR residues in the food samples such as egg and milk with HPLC was also determined. It was demonstrated that the prepared p(EGDMA-MATrp) microspheres could be repeatedly applied for SPE cleanup of sulfamerazine before chromatographic analysis. Also, the recoveries of SMR in milk and egg samples were reasonably satisfactory and in the range of 71 to 90%.

Validated determination of losartan and valsartan in human plasma by stir bar sorptive extraction based on acrylate monolithic polymer, liquid chromatographic analysis and experimental design methodology

In our previous work, a new monolithic coating based on vinylpyrrolidone-ethylene glycol dimethacrylate polymer was introduced for stir bar sorptive extraction. The formulation of the prepared vinylpyrrolidone-ethylene glycol dimethacrylate monolithic polymer was optimized and the satisfactory quality of prepared coated stir bar was demonstrated. In this work, the prepared stir bar was utilized in combination with ultrasound-assisted liquid desorption, followed by high-performance liquid chromatography with ultraviolet detection for the simultaneous determination of losartan (LOS) and valsartan (VAS) in human plasma samples. In a comparison study, the extraction efficiency of the prepared stir bar was accompanied much higher extraction efficiency than the two commercial stir bars (polydimethylsiloxand and polyacrylate) for both target compounds. In order to improve the desorption efficiency of LOS and VAS, the best values for effective parameters on desorption step were selected systematically. Also, the effective parameters on extraction step were optimized using a Box-Behnken design. Under the optimum conditions, the analytical performance of the proposed method displayed excellent linear dynamic ranges for LOS (24–1000 ng mL−1) and VAS (91–1000 ng mL−1), with correlation coefficients of 0.9998 and 0.9971 and detection limits of 7 and 27 ng mL−1, respectively. The intra- and inter-day recovery ranged from 98 to 117%, and the relative standard deviations were less than 8%. Finally, the proposed technique was successfully applied to the analysis of LOS and VAS at their therapeutic levels in volunteer patient plasma sample. The obtained results were confirmed using liquid chromatography-mass spectrometry. The proposed technique was more rapid than previously reported stir bar sorptive extraction techniques based on monolithic coatings, and exhibited lower detection limits in comparison with similar methods for the determination of LOS and VLS in biological fluids. The obtained results were demonstrated that the lower selectivity of UV in comparison with MS detection was rectified by appropriate sample preparation through proposed extraction method to eliminate as many interfering compounds as possible.

Amphiphilic Antifogging/Anti-Icing Coatings Containing POSS-PDMAEMA-b-PSBMA.

Highly transparent antifogging/anti-icing coatings were developed from amphiphilic block copolymers of polyhedral oligomeric silsesquioxane-poly[2-(dimethylamino)ethyl methacrylate]-block-poly(sulfobetaine methacrylate) (POSS-PDMAEMA-b-PSBMA) with a small amount of ethylene glycol dimethacrylate (EGDMA) via UV-curing. The excellent antifogging properties of the prepared coatings were originated from the hygroscopicity of both PDMAEMA and PSBMA blocks in the semi-interpenetrating polymer network (SIPN) with polymerization of EGDMA and hydrophobic POSS clusters aggregated on the surface. PDMAEMA with a lower critical solution temperature and PSBMA with an upper critical solution temperature in the block copolymers facilitated dispersion and absorption of water molecules into the SIPN coatings, fulfilling the enhanced antifogging function. Analysis of differential scanning calorimetry further confirmed that there was bond water and nonfreezable bond water in the SIPN coatings. The amphiphilic SIPN coatings exhibited the anti-icing ability with a freezing delay time of more than 2 min at -15 °C, owing to the aggregation of hydrophobic POSS groups and the self-lubricating aqueous layer generated by nonfreezable bond water on the surface. The prepared transparent antifogging/anti-icing coatings could have novel potential applications in practice.

Core-shell magnetic molecularly imprinted polymer nanoparticles for the extraction of triazophos residues from vegetables

The authors report on a surface molecular imprinting strategy for synthesizing magnetic and molecularly imprinted core-shell polymer nanoparticles (MMIPs) with a typical size of 320 nm. The triazophos-imprinted polymer shell on 180-nm magnetite particles (modified with 3-methacryloxypropyl trimethoxysilane) was obtained by radical polymerization of ethylene glycol dimethacrylate in the presence of triazophos, this followed by extractive removal of triazophos. The resulting MMIPs possess large binding capacity, high recognition selectivity, and fast binding kinetics for triazophos. They can be easily separated from a solution by using a magnet. These features result in a convenient and selective solid-phase extraction procedure for triazophos prior to its determination by UV spectrometry or by GC analysis. The method was successfully applied to the extraction and clean-up of triazophos residues in spiked homogenates of vegetables with recoveries in the range of 89.2 ~ 99.0%. The detection limits for triazophos by the UV assay and GC assay are 0.93 nM and 0.32 nM, respectively.

Graft Copolymerization of Glycidyl Methacrylate and Ethylene Glycol Dimethacrylate on Alumina for the Removal of Nitrogen and Sulfur Compounds from Gas Oil

Functionalized polymers were synthesized and applied in removing nitrogen and sulfur compounds from gas oils. In this work, the polyglycidyl methacrylate-co-ethylene glycol dimethacrylate polymer incorporated with tetranitrofluorenone, PGMA-DAP-TENF, was synthesized with and without alumina support. Different techniques were used to characterize the synthesized polymers including Fourier transform infrared spectroscopy, Brunauer–Emmett–Teller method, dynamic light scattering, thermogravimetry/differenial thermal analyzer, carbon hydrogen nitrogen sulfur elemental analysis, and field emission scanning electron microscopy. The performance of the polymer with alumina, Al-PGMA-DAP-TENF, was compared to that without alumina using light gas oil. In addition, heavy gas oil feed was used to confirm the adsorption behavior of both polymers in a higher nitrogen and sulfur environment. The effect of adsorption time and temperature was tested using a 1:5, by weight, polymer to feed ratio. Results have shown that alumina particles enhanced the nitrogen removal efficiency of PGMA-DAP-TENF polymer while sulfur removal efficiency was not affected. The nitrogen removal efficiency of Al-PGMA-DAP-TENF polymer was more than twice that of PGMA-DAP-TENF polymer in LGO feed, and twice that in HGO feed. This was due to the higher surface area of Al-PGMA-DAP-TENF polymer, 202 m2/g, compared to that of PGMA-DAP-TENF polymer, 27 m2/g. In addition, Al-PGMA-DAP-TENF polymer removed more basic nitrogen compounds than PGMA-DAP-TENF polymer. This was attributed to the acidic nature of alumina particles that enhance the adsorption of basic nitrogen compounds present in gas oil feeds.

Selective extraction of Bactrocera oleae sexual pheromone from olive oil by dispersive magnetic microsolid phase extraction using a molecularly imprinted nanocomposite

Bactrocera oleae Gmelin, also known as olive fruit fly, is the main olive tree pest. It produces a severe effect not only on the productivity but also on the quality of the olive-related products. In fact, the oil obtained from infected olives has a lower antioxidant power. In addition, an increase of the oil acidity, peroxide index and UV-absorbance can also be observed. 1,7-dioxaspiro-[5,5]-undecane (DSU), is the main component of the sexual pheromone of this pest and may be used as marker of the pest incidence. In this context, the development of new methods able to detect the pheromones in several samples, including agri-food or environmental ones, is interesting. In this work, we synthesized a molecularly imprinted polymer (MIPS) layer over magnetic nanoparticles (Fe3O4@SiO2@MIP) for the selective recognition of DSU. They were prepared using DSU as template and 3-aminopropyltriethoxysilane (APTES) to associate the target analyte on the surface of the magnetic substrate and the later polymerization of ethylene glycol dimethacrylate (EGDMA) in presence of 2,2-azobisisobutyonnitrile (AIBN). The resulting Fe3O4@SiO2@MIP composite was characterized by different techniques. The maximum adsorption capacity of DSU on Fe3O4@SiO2@MIP in hexane was 32mg/g (5.3 times than that obtained for the non-imprinted composite). In addition, Fe3O4@SiO2@MIP showed a short equilibrium time (45min) and potential reusability. The combination of dispersive magnetic microsolid phase extraction and gas chromatography with mass spectrometric detection allows the determination of DSU in real samples at concentrations as low as 10μg/L with precision better than 7.5% (expressed as relative standard deviation). The relative recoveries are in the range between 95 and 99%, which indicates the potential of the methodology. Finally, it has been applied to real olive oil samples being the presence of the pest detected is some of them.

Preparation of a novel sorptive stir bar based on vinylpyrrolidone-ethylene glycol dimethacrylate monolithic polymer for the simultaneous extraction of diazepam and nordazepam from human plasma.

A new monolithic coating based on vinylpyrrolidone-ethylene glycol dimethacrylate polymer was introduced for stir bar sorptive extraction. The polymerization step was performed using different contents of monomer, cross-linker and porogenic solvent, and the best formulation was selected. The quality of the prepared vinylpyrrolidone-ethylene glycol dimethacrylate stir bars was satisfactory, demonstrating good repeatability within batch (relative standard deviation < 3.5%) and acceptable reproducibility between batches (relative standard deviation < 6.0%). The prepared stir bar was utilized in combination with ultrasound-assisted liquid desorption, followed by high-performance liquid chromatography with ultraviolet detection for the simultaneous determination of diazepam and nordazepam in human plasma samples. To optimize the extraction step, a three-level, four-factor, three-block Box-Behnken design was applied. Under the optimum conditions, the analytical performance of the proposed method displayed excellent linear dynamic ranges for diazepam (36-1200 ng/mL) and nordazepam (25-1200 ng/mL), with correlation coefficients of 0.9986 and 0.9968 and detection limits of 12 and 10 ng/mL, respectively. The intra- and interday recovery ranged from 93 to 106%, and the relative standard deviations were less than 6%. Finally, the proposed method was successfully applied to the analysis of diazepam and nordazepam at their therapeutic levels in human plasma. The novelty of this study is the improved polarity of the stir bar coating and its application for the simultaneous extraction of diazepam and its active metabolite, nordazepam in human plasma sample. The method was more rapid than previously reported stir bar sorptive extraction techniques based on monolithic coatings, and exhibited lower detection limits in comparison with similar methods for the determination of diazepam and nordazepam in biological fluids.

Highly crosslinked poly(ethyleneglycol dimethacrylate)-based microspheres via solvothermal precipitation polymerization in alcohol–water system

The preparation of highly crosslinked polymer microspheres through the polymerization reaction in an alcohol–water solution without any stabilizer is still a difficult task. Here, we first reported a facile preparation of monodispersed highly-crosslinked microspheres through the polymerization of ethyleneglycol dimethacrylate (EGDMA) in an alcohol–water solution in the presence of a small amount of hydrophilic comonomer with a high reactivity ratio in a sealed autoclave at above the boiling point of the solvent, which can be considered as a solvothermal precipitation polymerization process. The formation mechanism of the poly(ethyleneglycol dimethacrylate) (PEGDMA)-based microspheres involving an initial nucleation process and the grow process of the microspheres was proposed and confirmed by the composition and distribution of the hydrophilic comonomer in the oligomers and microspheres, which were analyzed by 1H and 13C CP-MAS solid NMR spectra, elemental mapping, and XPS. This work opens a new economic and environmental-friendly way to prepare highly-crosslinked functional PEGDMA-based microspheres.

Assessment and modelling of Ni(II) retention by an ion-imprinted polymer: Application in natural samples

Three novel Ni(II)-Ion-Imprinted Polymer (IIP) were synthesized by precipitation polymerization of ethylene glycol dimethacrylate (crosslinker) with a complex of nickel(II) and vinylbenzyl iminodiacetic acid (VbIDA). The three IIPs were prepared with various mixtures of porogen solvents: methanol, methanol/2-methoxyethanol and methanol/acetonitrile (IIP1, IIP2 and IIP3, respectively). Non-Imprinted Polymers (NIP1, NIP2 and NIP3) were prepared as control polymers in similar conditions but with pure VbIDA instead of VbIDA–Ni. These polymers were characterized by FTIR, BET, SEM and tested for their efficiency and selectivity in Ni(II) retention. The most efficient (IIP1, around 12mgg−1 of nickel) was then positively checked for Ni(II) retention in presence of some competing species over a wide range of concentration. Finally Ni(II) retention by IIP1 was successfully demonstrated in natural samples. The modelling of the different experiments (Langmuir, Freundlich but also PROSECE and WHAM VII, frequently used in environmental studies) allowed demonstrating the presence of completely different binding sites when considering the ion-imprinted polymer and the non-imprinted one, and therefore led to a better understanding of what the imprinting effect is.

Metal-Chelating Nanopolymers for Antibody Purification from Human Plasma

The purification of immunoglobulin G (IgG) from human plasma was performed by using a novel metal-chelated adsorbent with nano size. The non-porous nanoparticles were produced by surfactant free emulsion polymerization of ethylene glycol dimethacrylate (EDMA) and 2-methacryloylamidohistidine (MAH). Then, Cu(II) ions were chelated on the nanoparticles. The nano-poly(EDMA-MAH) nanoparticles were characterized by Fourier transform infrared, scanning electron microscope, atomic force microscope and elemental analysis. The non-porous nanoparticles were spherical form and have 100-250 nm size distribution. The maximum IgG adsorption capacity of the Cu(II) chelated nanoparticles was found to be 463 mg/g polymer at pH 7.0 in HEPES buffer. Desorption of IgG was performed by 1.0 M NaCl and desorption rate was found to be 97 %. IgG was obtained from human plasma with purity of 94 % (up to 578 mg/g polymer). The non-porous nanoparticles allowed one-step purification of IgG from human plasma.