Research Article | Open Access
Gholam Ali Koohmareh, Morteza Hajian, Hazhir Fallahi, "Graft Copolymerization of Styrene from Poly(vinyl alcohol) via RAFT Process", International Journal of Polymer Science, vol. 2011, Article ID 190349, 7 pages, 2011. https://doi.org/10.1155/2011/190349
Graft Copolymerization of Styrene from Poly(vinyl alcohol) via RAFT Process
Polystyrene, PS, was grafted from poly(vinyl alcohol), PVA, backbone by reversible addition-fragmentation chain transfer (RAFT) polymerization. The hydroxyl groups of the PVA were converted into aromatic dithioester RAFT agent and polymerization began in the presence of this agent. The structure of compounds was confirmed by FT-IR and 1HNMR spectroscopy. The graft copolymer was characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). Grafted polystyrene chains were cleaved from the PVA backbone by acidic hydrolysis of the PVA-g-PS, and its polydispersity index, PDI, was determined by gel permeation chromatography (GPC) showing narrow molecular weight distribution.
Poly(vinyl alcohol) (PVA) has excellent film forming, emulsifying, and adhesive properties. It is odorless, nontoxic and has high tensile strength and flexibility as well as high oxygen and aroma barrier properties. PVA is a water-soluble semicrystalline polymer with good chemical and thermal stability and has biomedical applications [1–4]. Functionalized modification of PVA at the side groups is easy by utilizing various reactions of hydroxyl groups with small molecules or polymers. Such modification may provide PVA with pendant functional groups or graft polymer chains, and thus expand their applications in biological fields [5–8]. There are plenty of hydroxyl groups present as side groups on the backbone chain of poly(vinyl alcohol). The hydroxyl groups bring about good solubility in water but, on the other hand, lead to its high resistance to oil and poor mechanical properties. Because the modified PVA possesses hydrophilic backbone chain and hydrophobic branched chains synchronously after being modified by vinyl monomers, it can serve as amphiphilic compatibility-reagent between a hydrophobic polymer and a hydrophilic polymer. Graft copolymerization is one of the most important methods to modify PVA .
The synthesis of polymers with predetermined molecular weight and low polydispersity index can possible with controlled free-radical polymerization techniques, such as nitroxide-mediated polymerization (NMP),  atom transfer radical polymerization (ATRP),  and reversible addition fragmentation chain transfer (RAFT) polymerization [12–15] for a great variety of vinyl polymers. The last one, (RAFT), is one of the promising living radical methods for synthesizing well-defined graft polymers. A wide range of monomers can be polymerized in a controlled manner under nondemanding reaction conditions via this technique. When grafted and free polymers mediated by the same RAFT agent, the molecular weights and molecular weight distributions of the grafted and the free polymer should be very similar .
Here, graft copolymerization of styrene from poly(vinyl alcohol) by modifying it with a dithioester RAFT agent was investigated.
2. Experimental Section
2.1. Materials and Instruments
All solvents, monomer, and most chemicals were purchased from Merck-Chemical at the highest purity available unless otherwise stated. Styrene (99%), was purified by washing with an aqueous solution of NaOH (5 wt%) to remove the inhibitor, followed by distilled water until the washings were neutral to litmus, dried by anhydrous MgSO4 and fractionally distilled under vacuum. 2,2′-Azobis(isobutyronitrile) (AIBN, 97%) was purified by recrystallization from methanol and dried at room temperature in a vacuum oven and finally, stored at −15°C. Dimethylacetamide (DMAc), tetrahydrofuran (THF), triethylamine (TEA), acetone, 1-Bromonaphtalene, and carbon disulfide and toluene were dried over molecular sieves (4 Å) before use. Poly(vinyl alcohol) (PVA, AppliChem, 72000 g mol−1, , 98%), 2-Chloro-2-phenylacetyl chloride (CPAC, 90%) were used as received. THF was completely dried by sodium press method.
FTIR spectra were recorded on a JASCO FTIR-6300 spectrometer by using KBr pellets. ThermoGravimetric analysis (TGA) and differential scanning calorimetry (DSC) were performed on a Mettler TG5 system under nitrogen atmosphere at a heating rate of 10°C/min. NMR spectra were recorded on Bruker Avance 400 MHz spectrometer. Molecular weights were determined using Knauer Gel permeation chromatography (GPC) equipped with Smartine Pump 1000, a differential refractive index (DRI) detector (Smartin Ri 2300) and PL Gel 10 μm column. THF was used as solvent with flow rate of 1 ml/min at room temperature. GPC was calibrated with standard polystyrene with polydispersity index of 1.09. The elemental analysis was carried out by a Leco, CHNS-932. X-ray diffractions were performed on Bruker D8 Avance instrument. Scanning electron microscopy (SEM, AIS-2100 Model-550-SERON Technology) was used to analyze the morphology of the polymers. The samples were gold-coated and operated at an accelerating voltage of 20 kV.
2.2. Esterification of Poly(vinyl alcohol) Using 2-Chloro-2-phenylacetyl Chloride (CPAC); (PVA-Cl)
0.5 g of PVA ( mol hydroxyl groups) was dissolved into a three-neck round-bottom flask, containing dry DMAc (12 ml) and an excess of triethylamine (4.4 g, mol), which used as proton scavenger. CPAC (4.1 g, mol) was finally added dropwise at 0°C during 3 h to the flask under dry N2 atmosphere. The solution was stirred overnight at 60°C. The organic solution was then washed several times with an aqueous solution of NaHCO3 and distilled water to complete removal of any unreacted CPAC and Et3NH+Cl− salt and dried over MgSO4 for 12 h. The functionalized polymer was precipitated in hexane. Finally, yellowish product was placed in a vacuum oven at 50°C to dry overnight; (PVA-Cl). Weight of dry PVA-Cl = 1.73 g; mass increase due to esterification = 1.23 g; % mass increase = 246%.
2.3. Synthesis of RAFT Agent onto Poly(vinyl alcohol); (PVA-RAFT)
A solution of 1-bromonaphtalene (0.32 g, mol) in anhydrous THF (6 ml), was added dropwise under nitrogen to a dried two-neck round-bottom containing magnesium (0.042 g, mol) and 20 ml anhydrous THF within 1 h and refluxed for 3 h. An excess of carbon disulfide (0.165 g, mol) was then added dropwise to the flask at room temperature. The reaction mixture was heated to 40°C for 3 h. The resultant brown solution was then transferred to another flask containing PVA-Cl (0.1 g, mol) dissolved in THF (25 ml) and refluxed for 24 h. After cooling, methanol (50 ml) was added and the resulting orange precipitate was washed with methanol and then oven-dried under vacuum at 60°C; (PVA-RAFT).
Weight of dry PVA-RAFT = 0.22 g; mass increase due to second dramatization = 0.12 g; % mass increase = 120%.
CHNS (Found): C (41.21%), H (4.8%), N (0%), and S (11.17%).
2.4. Graft Copolymerization by RAFT Process
The PVA-RAFT sample (0.21 g, mol) was pretreated with dry toluene in a round-bottomed flask for 24 h to obtain a homogeneous mixture. Monomer (styrene, 23.3 ml, 0.2 mol) and initiator (AIBN, 0.0067 g, mol) dissolved in 18 ml toluene were then added into flask. Polymerization performed in solvent (50% (v/v) to monomer). The flask was subsequently capped with rubber septa and deoxygenated through purging with nitrogen for 20 min and placed immediately in a preheated oil bath at 60°C. The reaction was stopped after 48 h, by cooling the reaction flask in an ice-water bath. The mixture was then poured into excess methanol to precipitate the polymer. The precipitate was filtered and dried to a constant weight under vacuum at 60°C. The crude PVA-g-PS sample was thereafter repeatedly washed with THF to remove any unreacted RAFT agent. Then, the homopolymer of styrene was removed completely from the graft copolymer by exhaustive Soxhlet extraction with toluene for 2 days at 120°C. The final graft copolymer was dried to a constant weight under vacuum at 60°C. The grafting ratio =36%.
2.5. Cleaving of PS from PVA Backbone
PS chains were cleaved from the PVA surface under acidic conditions. 0.12 g of grafted PVA (36 wt% graft ratio) sample was immersed into a round-bottomed flask and an equal portion of 37% HCl was added to the reaction medium and the mixture was diluted with THF to be 25% in HCl. The mixture was refluxed for 2 weeks until the grafted PVA was completely hydrolyzed, leading to a homogeneous brown solution. The reaction mixture was filtered, and the solvent (THF) in the filtrate was evaporated off using a rotary evaporator and, finally, dried at 50°C in a vacuum oven. The resulting viscous liquid was dissolved in dichloromethane and then extracted twice with distilled water. The organic phase was dried under anhydrous Na2SO4 overnight. After filtration, PS was collected by complete evaporation of the solvent. The highly viscous PS product was precipitated in methanol washed several times with methanol, then dried and dissolved in THF and analyzed by GPC. The weight-average molecular weight of the cleaved PS of above-mentioned sample was 26000 gmol−1.
3. Results and Discussion
First, poly(vinyl alcohol) was converted to PVA-Cl via an esterification reaction by using 2-chloro-2-phenylacetyl chloride according to Scheme 1. By considering the difference in weight and solubility of two compounds, this conversion is somewhat proving. FTIR spectra of this compound show decrease in absorption of OH groups due to conversion, and, peaks above 3000 cm−1 was for aromatic protons. Also peaks at 1650–1470 cm−1 were related to aromatic ring and peak at 750 cm−1 for C-Cl (Figures 1 and 2). 1H-NMR spectrum of PVA-Cl showed peaks at 7.3 δ for aromatic protons, 6.1 δ for PVA backbone, 5.5 δ for unreacted OH groups, 4.8 δ for benzylic proton and 2-1 δ for PVA backbone. (Figure 3).
At the second step, a Grignard reagent was synthesized from 1-bromo naphthalene and reacted with carbon disulfide to afford magnesium bromide naphthalene-1-carbodithioate which was then added to a solution of PVA-Cl in THF to make a PVA-RAFT agent (Scheme 1). The disappearance of peak related to C-Cl at 750 cm−1, appearance of peaks related to C-S and C=S at 1250–1020 cm−1 and also existence of sharp peaks above 500 cm−1 related to naphthalene group in FTIR spectrum completely confirmed this conversion (Figure 4).
The 1H-NMR spectrum of this compound of this compound showed peaks at 8.2–7.1 δ for aromatic protons, 5.8 δ for PVA backbone, 4.9 δ for unreacted OH groups, 3.9 δ for benzylic proton, and 2.1–1.2 δ for PVA backbone. (Figure 5).
The CHNS elemental analysis of this compound confirmed formation of thiocarbonyl groups in poly(vinyl alcohol) structure.
The polystyrene was grafted from poly(vinyl alcohol) via RAFT polymerization by using AIBN as initiator.
In order to remove any homo polymer of styrene, the resulted sample was washed with toluene by soxhlet extraction.
The graft ratio (G, wt%) was calculated using Here, “weightgraft” is the dry weight of PVA-RAFT sample after grafting with poly(styrene) and “weightPVA-RAFT” is the initial weight of PVA-RAFT sample.
To evaluate the increasing the polystyrene grafting percent, first the grafting reaction was done in three different times, 24 h, 48 h, and 72 h. As shown in Figure 6, the optimum grafting percent was 36%, which was obtained after 48 h. Next, in constant initiator amount and reaction time of 48h, the grafting percent was investigated by varying the molar ratio of [M] : [PVA-RAFT] into 250 : 1, 500 : 1 and 1000 : 1 and as shown in Figure 7, the optimum grafting percent was 36% in 500 : 1 molar ratio.
The FTIR spectra of PVA-g-PS showed a decrease in C=O absorption and increase in aromatic and aliphatic C-H. Two sharp peaks at 750–650 cm−1 are related to aromatic rings of polystyrene (Figure 8).
To obtain molecular weight and polydispersity index (PDI) of grafted polystyrene, the compound PVA-g-PS was refluxed under acidic conditions in THF for two weeks. After cleavage of polystyrene chains, a solution in THF was prepared, and its molecular weight was obtained using GPC. g/mol, g/mol, (Figure 9).
In order to obtain better information about grafting copolymer, XRD analysis of PVA and PVA-g-PS was also investigated. The Peak related to PVA at and The peak related to PVA-g-PS at show that grafting polystyrene to PVA caused increasing chains distance and also reduction of its crystallinity due to reduction of hydrogen bonding between PVA chains. (Figure 10).
Scanning electron microscopy was also used to analyze the morphology of the poly(vinyl alcohol) before and after grafting. SEM micrographs of unmodified PVA and PVA-g-PS are shown in Figure 11. It is evident that the modified poly(vinyl alcohol) by grafted polystyrene has different structural features compared with the unmodified poly(vinyl alcohol) since the grafting of polystyrene chains occurs mainly at the surface of poly(vinyl alcohol).
Thermal stability of PVA, PVA-RAFT, PVA-g-PS, and PS were investigated by TGA. Figure 12 showed that PS starting to weight loss at 350°C, while for PVA, this temperature is 240°C. At the other hand, the percent of remaining polymer at 450°C for PS is 0% while for PVA is near 30%. The higher thermal stability of PS than PVA was because of aromatic groups in PS. This was confirmed for other compounds, PVA-RAFT which was start to weight loss at 300°C and PVA-g-PS at 310°C. The grafting technique is increased thermal stability of PVA.
RAFT is a new method for synthesis of grafted copolymers. According to obtained results, polystyrene was grafted to polyvinyl alcohol under mild condition by using RAFT polymerization technique. Grafted copolymer with high percentage polystyrene was obtained, which was characterized and investigated by FTIR, XRD and TGA. The grafted polystyrene was hydrolyzed from copolymer and showed narrow molecular weight distribution obtained with GPC.
The authors thank University of Isfahan providing facilities for this work and Central Laboratory of University of Isfahan for FTIR, CHN, 1HNMR, GPC, and XRD analysis.
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