Preparation and Properties of Biodegradable Sodium Lignosulfonate/Poly(Vinyl Alcohol) Blend Films

2010 ◽  
Vol 160-162 ◽  
pp. 676-681 ◽  
Author(s):  
Xian Fa Li

A biodegradable films were prepared by blending sodium lignosulfonate (LS) with poly(vinyl alcohol) (PVA) and with borax as cross-linking agent, in an aqueous system. The suitable process conditions of preparing the blend films with good water-resistance and mechanical properties were determined by single-factor experiments. SEM, FT-IR, TGA and DSC analysis were performed to examine the contribution of LS and borax to the properties of the blend films. The results indicated that the introduction of a moderate LS mass ratios to PVA from 1/8 to 4/8 in the blend films could simultaneously enhance the tensile strength of blend films up to 43.98MPa. SEM showed that the intermiscibility of blend films was satisfactory with appropriate LS. Studies of the water sorptive capacity of the materials suggested that the water sorptive capacity at equilibrium less than 17% and water-resistance improved. The results of TGA indicated blend films have greater thermal stability than the pure polymers.

2016 ◽  
Vol 852 ◽  
pp. 979-983
Author(s):  
Ping Rui Meng ◽  
Liang Bo Li

Sodium acrylate (NaAA) and acrylamide (AM) were grafted onto poly (vinyl alcohol) (PVA) using potassium persulfate as an initiator, Graft copolymerization namely poly (vinyl alcohol)-g-poly (acrylamide/sodium acrylate) (PVA-g-PAM/SAC). The poly (vinyl alcohol)-g-poly (vinylamine/sodium acrylate) (PVAMC) was prepraed by Hofmann rearrangement.The PVAMC homogeneous membrane was characterized by fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM).The water resistance of the PVAMC membranes is the best when pH of the PVAMC solutions was 4, at that time the numbers of-NH3+ and-COO- groups trended to be equal, so the isoelectric point was pH=4. At 90 °C the pervaporation of PVAMC composite membrane was tested and showed that the separation factor and the permeate flux were about 1001 and 1341 g/(m2·h) for 90wt% ethanol aqueous solution, and they were about 1297 and 1040 g/(m2·h) for 90wt% isopropanol aqueous solution.


2001 ◽  
Vol 14 (2) ◽  
pp. 293-294 ◽  
Author(s):  
Yoichi Shindo ◽  
Masatoshi Hasegawa ◽  
Junichi Kawanobe ◽  
Kazuo Inoue

Author(s):  
Juliana Zanol Merck ◽  
Camila Suliani Raota ◽  
Jocelei Duarte ◽  
Camila Baldasso ◽  
Janaina Da Silva Crespo ◽  
...  

The pollution of hydric sources by pharmaceuticals is an issue in many countries, particularly in Brazil. The presence of these substances causes deleterious effects on the environment and human health. One of the main sources of this contamination is domestic sewage, due to the expressive amount of medicines released in their unaltered form. Unfortunately, traditional wastewater treatment is not effective for the removal of pharmaceuticals and, for this reason, membrane technology is an attractive alternative to overcome this issue. In this regard, hydrophilic polymers, such as poly(vinyl alcohol) (PVA), are the most suitable. However, their high affinity with water causes intense swelling, leading to severe modifications in the membrane properties. In view of all these facts, the present work evaluated the swelling of PVA-based membranes, with the aim of finding the membrane preparation method that has the lowest swelling, thereby providing the most suitable characteristics for pharmaceutical removal from wastewater. The membranes were prepared by the casting of a polymeric solution, with PVA as a basis polymer, citric acid as a crosslink agent and glycerol and silver nanoparticles as performance additives. The process optimization was performed using a design of experiments with posterior analysis by the response surface methodology (RSM). The RSM assessed the effect on the membrane swelling of the factors, including citric acid concentration and the time and temperature of crosslinking. The membrane characterization was performed by Fourier-transform infrared (FT-IR) spectroscopy, scanning electron microscopy coupled with a field emission gun (SEM-FEG) and water contact angle (WCA) measurements. Overall, the condition that showed the lowest swelling was obtained with 10% of citric acid and crosslinking for 4 h at 130 °C. Under these conditions, the membrane had a mass swelling of 42% and a dimensional swelling of 24%. Additionally, our statistical analysis revealed that the factors with the dominant effects were the citric acid concentration and the temperature of crosslinking. The FT-IR analysis suggested that the crosslinking occurred by an esterification reaction, as showed by the stretching frequencies of C=O at 1710 cm-1 and ester C-O at 1230 cm-1. Moreover, the SEM-FEG images revealed a smooth and flat surface and a dense cross section with a thickness of ~113 μm. Concerning the WCA, the angle was at ~80°, which is characteristic of hydrophilic materials. Finally, the data suggested that it is possible to optimize the membrane preparation process with adequate properties so that it can be subsequently applied to the removal of pharmaceuticals from hospital wastewater.


2019 ◽  
Vol 819 ◽  
pp. 145-150
Author(s):  
Thapakorn Chareonying ◽  
Junnasir M. Sakilan ◽  
Theerasak Rojanarata ◽  
Prasopchai Patrojanasophon ◽  
Prasert Akkaramongkolporn ◽  
...  

Nanofibers have been widely used for tissue engineering. Using charged polymers for the preparation of nanofibers can be useful for the loading of substances or macromolecules. Dual charge nanofiber mats are expected to be able to immobilize both positively charged and negatively charged substances in one versatile nanofiber mat. The purpose of this study was to prepare and characterize dual-charge nanofibers generated from poly (vinyl alcohol) (PVA)/poly-(acrylic acid-co-maleic acid) (PAMA) and chitosan (CS)/PVA. The polymer solutions of PAMA/PVA (1:1.63 w/w) and CS/PVA (1:2.33 w/w) were electrospun to form the nanofibers using dual-jet electrospinning process. The obtained dual-charge nanofibers were thermally crosslinked by leaving the nanofibers in the oven at 110-130 °C for 0.5, 1, 3, 5 h. The appearance of the nanofiber mat was characterized by a scanning electron microscope (SEM), and the diameter of nanofibers were determined by an image analysis software (J-micro vision®). The percentage water insolubilization and FT-IR spectra were also determined. The dual-size nanofiber mats with smooth and bead-free fibers were obtained. The diameter of the PAMA/PVA and CS/PVA fibers was 574.54 ± 142.98 nm and 225.69 ± 41.92 nm, respectively. The desirable temperature and time for the crosslink of the dual-charge nanofiber mats was 130 °C for 1 h which could provide a high insolubilization with water capacity of 93.22 ± 2.23%.


2014 ◽  
Vol 29 (2) ◽  
pp. 351-356 ◽  
Author(s):  
Xiping Gao ◽  
Keyong Tang ◽  
Jie Liu ◽  
Xuejing Zheng ◽  
Yuqing Zhang

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