Solubility and Thermoresponsiveness of PMMA in Alcohol-Water Solvent Mixtures

2010 ◽  
Vol 63 (8) ◽  
pp. 1173 ◽  
Author(s):  
Richard Hoogenboom ◽  
C. Remzi Becer ◽  
Carlos Guerrero-Sanchez ◽  
Stephanie Hoeppener ◽  
Ulrich S. Schubert

To reduce the environmental burden of polymer processing, the use of non-toxic solvents is desirable. In this regard, the improved solubility of poly(methyl methacrylate) (PMMA) in ethanol/water solvent mixtures is very appealing. In this contribution, detailed investigations on the solubility of PMMA in alcohol/water solvent mixtures are reported based on turbidimetry measurements. PMMA revealed upper critical solution temperature transitions in pure ethanol and ethanol/water mixtures. However, around 80 wt-% ethanol content a solubility maximum was observed for PMMA as indicated by a decrease in the transition temperature. Moreover, the transition temperatures increased with increasing PMMA molar mass as well as increasing polymer concentration. Careful analysis of both heating and cooling turbidity curves revealed a peculiar hysteresis behaviour with a higher precipitation temperature compared with dissolution with less than 60 wt-% or more than 90 wt-% ethanol in water and a reverse hysteresis behaviour at intermediate ethanol fractions. Finally, the transfer of poly(styrene)-block-poly(methyl methacrylate) block copolymer micelles from the optimal solvent, i.e. aqueous 80 wt-% ethanol, to almost pure water and ethanol is demonstrated.

2019 ◽  
Vol 811 ◽  
pp. 163-169 ◽  
Author(s):  
Ervin Tri Suryandari ◽  
Muhammad Ali Zulfikar ◽  
Rino R. Mukti ◽  
Muhamad Nasir

Fibers are materials with advantageous properties such as lightweight material properties, has small pore size, and has high surface area, porosity,and permeability. An easy and simple method to prepare fibers is electrospinning. Using this method poly(methyl methacrylate) (PMMA) fibers were prepared. Several parameters include polymer concentration, solution flow rate, the distance of the nozzle tip to the collector, and the applied voltage were investigated to control the morphology, structure, and diameter of PMMA fibers. The Optimal electrospinning conditions for PMMA fibers production were a PMMA concentration is 8% (w/v), a power supply voltage is 20 kV, a distance of the tip of the nozzle to the ground collector is 15 cm, and a flow rate is 0.004 mL/min. The diameter distribution and morphology of the fibers were determined and characterized by Optical Microscopy and Scanning Electron Microscope (SEM), which showed that the produced fiber had an average diameter of 1.4925 µm, the contact angle of fiber PMMA is 125.307o and the spreading time of fibers PMMA is about 360 minutes


Polymers ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 265 ◽  
Author(s):  
Komol Kanta Sharker ◽  
Yuki Ohara ◽  
Yusuke Shigeta ◽  
Shinji Ozoe ◽  
Shin-ichi Yusa

Strong polyampholytes comprising cationic vinylbenzyl trimethylammonium chloride (VBTAC) bearing a pendant quaternary ammonium group and anionic sodium p-styrenesulfonate (NaSS) bearing a pendant sulfonate group were prepared via reversible addition-fragmentation chain-transfer polymerization. The resultant polymers are labelled P(VBTAC/NaSS)n, where n indicates the degree of polymerization (n = 20 or 97). The percentage VBTAC content in P(VBTAC/NaSS)n is always about 50 mol%, as revealed by 1H NMR measurements, meaning that P(VBTAC/NaSS)n is a close to stoichiometrically charge-neutralized polymer. Although P(VBTAC/NaSS)n cannot dissolve in pure water at room temperature, the addition of NaCl or heating solubilizes the polymers. Furthermore, P(VBTAC/NaSS)n exhibits upper critical solution temperature (UCST) behavior in aqueous NaCl solutions. The UCST is shifted to higher temperatures by increasing the polymer concentration and molecular weight, and by decreasing the NaCl concentration. The UCST behavior was measured ranging the polymer concentrations from 0.5 to 5.0 g/L.


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