scholarly journals Poly(Vinyl Alcohol) Cryogels Formed from Polymer Solutions in Dimethyl Sulfoxide with Tetramethoxysilane Additives

Author(s):  
I. V. Bakeeva ◽  
M. A. Orlova ◽  
V. I. Lozinsky

Organic–inorganic hybrid cryogels of poly(vinyl alcohol) (PVA) containing silica inclusions (SiO2) were obtained and studied. Such inclusions were formed in the course of hydrolytic polycondensation (sol-gel process) of tetramethoxysilane (TMOS) introduced into concentrated polymer solutions in dimethyl sulfoxide (DMSO). PVA concentration in these solutions was 60, 80 or 100 g/L; while the concentration of TMOS was varied in a range of 0.15–0.61 mol/L. The polymer solutions were subjected to the cryogenic treatment at temperatures by 40 °С lower than DMSO crystallization temperature (+18.4°C). The frozen samples were thawed out at a heating rate of 0.03°/min. It is shown that moderate freezing at −21.6 °C, then frozen storage and subsequent thawing of the initial reaction mixture PVA/DMSO/TMOS/acid catalyst resulted in the formation of strong macroporous PVA/SiO2 cryogels. Such cryogel materials are hybrid systems, because the gel-forming polymer and the silica containing moieties belong to the content of the gel phase. The basis of this intermolecular interaction is hydrogen bonding between OH groups of the adjacent chains. This leads to the formation of modified microcrystallinity zones that perform as the nodes of the three-dimensional network of cryogels. The effects of significant increase in their rigidity and heat-resistance with increasing PVA and TMOS concentration in the initial feed were also observed. It was shown that the success of the synthesis of transparent elastic and heat-resistant PVA/SiO2 cryogels depends on the choice of the optimal ratio between the precursors and the combined effect of the liquid (methanol and water) and silicon-containing components on the formation of multiple hydrogen bonds and microcrystallites.

Polymer ◽  
2003 ◽  
Vol 44 (15) ◽  
pp. 4075-4078 ◽  
Author(s):  
Nobuaki Takahashi ◽  
Toshiji Kanaya ◽  
Koji Nishida ◽  
Keisuke Kaji

1984 ◽  
Vol 40 (4-5) ◽  
pp. T158-T160
Author(s):  
Motoko Komatsu ◽  
Takashi Inoue ◽  
Keizo Miyasaka

Nanomaterials ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 805 ◽  
Author(s):  
J. Elliott Sanders ◽  
Yousoo Han ◽  
Todd S. Rushing ◽  
Douglas J. Gardner

Poly (vinyl alcohol) (PVA) and cellulose nanocrystals (CNC) random composite mats were prepared using the electrospinning method. PVA/CNC mats were reinforced with weight concentrations of 0, 20 and 50% CNC (w/w) relative to PVA. Scanning electron microscopy was used to measure the fiber diameter, which ranged from 377 to 416 nm. Thermogravimetric analysis (TGA) confirmed the presence of CNC fibers in the mat fibers which were not visible by scanning electron microscope (SEM). Mechanical testing was conducted using ASTM D 638 on each sample group at 10 mm min−1. Neat PVA and PVA/CNC mats were heat treated at 170 °C for 2h hours, and the morphological structure was maintained with some fiber diameter reduction. Mechanical property results after heat treatment showed a decrease in tensile strength, an increase in tensile stiffness and a decrease in strain to yield (%). This effect was attributable to enhanced diffusion bonding of the mat fiber intersections. The CNC fibers also increased mat stiffness, and reduced strain to yield in non-treated mats. The use of CNCs show potential for compounding into bulk polymer composites as a reinforcement filler, and also show promise for chemical crosslinking attributable to the –OH groups on both the PVA, in addition to esterification of the vinyl group, and CNC.


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