PHOTOLYSIS OF POLYMETHACRYLIC ACID IN AQUEOUS SOLUTIONS

1964 ◽  
Vol 42 (3) ◽  
pp. 522-531 ◽  
Author(s):  
C. H. Chou ◽  
H. H. G. Jellinek

The photolysis of polymethacrylic acid was studied in aqueous solutions as a function of pH, polymer concentration, polymer chain length, and small additions of electrolytes in the absence of oxygen with light of wavelength 2537 Å. The random chain scission constants decrease with increasing pH values. Small variations in polymer chain length and concentration and electrolyte concentration have no effect on the photolysis. Changes in the ultraviolet spectra with irradiation time are more pronounced at low pH values than higher ones. It is shown that the decrease in susceptibility to photolysis with increasing degree of ionization of the acid is not proportional to the decrease or increase of the number of COOH or COO− groups respectively. It is rather due to the same causes—that is changes in ionic atmosphere— which make the polymer chains uncoil with increasing ionization.

Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1636
Author(s):  
Stella Afroditi Mountaki ◽  
Maria Kaliva ◽  
Konstantinos Loukelis ◽  
Maria Chatzinikolaidou ◽  
Maria Vamvakaki

Main chain polyesters have been extensively used in the biomedical field. Despite their many advantages, including biocompatibility, biodegradability, and others, these materials are rather inert and lack specific functionalities which will endow them with additional biological and responsive properties. In this work, novel pH-responsive main chain polyesters have been prepared by a conventional condensation polymerization of a vinyl functionalized diol with a diacid chloride, followed by a photo-induced thiol-ene click reaction to attach functional carboxylic acid side-groups along the polymer chains. Two different mercaptocarboxylic acids were employed, allowing to vary the alkyl chain length of the polymer pendant groups. Moreover, the degree of modification, and as a result, the carboxylic acid content of the polymers, was easily tuned by varying the irradiation time during the click reaction. Both these parameters, were shown to strongly influence the responsive behavior of the polyesters, which presented adjustable pKα values and water solubilities. Finally, the difunctional polyesters bearing the alkene and carboxylic acid functionalities enabled the preparation of cross-linked polyester films by chemically linking the pendant vinyl bonds on the polymer side groups. The biocompatibility of the cross-linked polymers films was assessed in L929 fibroblast cultures and showed that the cell viability, proliferation, and attachment were greatly promoted on the polyester surface, bearing the shorter alkyl chain length side groups and the higher fraction of carboxylic acid functionalities.


Soft Matter ◽  
2018 ◽  
Vol 14 (23) ◽  
pp. 4792-4804 ◽  
Author(s):  
Alexander L. Kwiatkowski ◽  
Vyacheslav S. Molchanov ◽  
Hari Sharma ◽  
Alexander I. Kuklin ◽  
Elena E. Dormidontova ◽  
...  

Long polymer chains embedded in wormlike surfactant micelles can act as crosslinks connecting neighboring micelles.


2017 ◽  
Vol 31 (04) ◽  
pp. 1750028 ◽  
Author(s):  
Ji-Xuan Hou ◽  
Ye-Hui Zhang ◽  
Yao Chen ◽  
Xu-Chen Yu

We demonstrate that the arrangement differs of posts have significant effect on the translocation of polymer chains which are embedded in the post arrays by using Monte Carlo algorithm. Due to the equivalent entropic force, polymers have a tendency to translocate to the disordered-arranged post array side other than the ordered-arranged side even though the post densities are equal on both sides. By changing the diameter of the posts, we find that the associated translocation times are strongly affected by the structure of the post array. Since the entropic force is almost identical for each monomer of the polymer chain and the free energy difference between two differently-arranged sides increases linearly with the polymer chain length, the directional preference strongly depends on the polymer chain length, and the ratio between the probabilities for a polymer to move either side obeys the Boltzmann distribution. Hence, a new microfabricated device which is used to separate deoxyribonucleic acid (DNA) by molecular weight can be designed using this idea. Moreover, this study can help us to develop a better understanding on the passages of polymers across membranes in nature.


Author(s):  
Anurag Dobhal ◽  
Ashu Srivastav ◽  
Prajakta Dandekar ◽  
Ratnesh Jain

AbstractThe work demonstrates the preparation of PLGA (PLGA 50:50, PLGA 75:25) nanoparticles, to encapsulate a hydrophobic molecule (coumarin-6), using the microreactor-based continuous process. The formulations were characterized using dynamic light scattering and transmission electron microscopy to determine their size, homogeneity, zeta potential, and surface morphology. The resulting nanoparticles were safe to the CHO cells (≈80% cell survival), at the concentration of ≤600 µg/mL and were successfully taken up by the cells, as demonstrated using confocal microscopy. Moreover, imaging flow cytometry confirmed that the nanoparticles were internalized in 73.96% of the cells. Furthermore, molecular dynamics simulation and docking studies were carried out to explore the effect of polymer chain length of PLGA and lactide vs glycolide (LA:GA) ratio on their compatibility with the coumarin-6 molecules and to study the coiling and flexibility of PLGA in the presence of coumarin-6 molecules. Flory–Huggins interaction parameter (χ) was calculated for polymer chains of varying lengths and LA:GA ratio, with respect to coumarin-6. χ parameter increased with increase in polymer chain length, which indicated superior interaction of coumarin-6 with the smaller chains. Amongst all the polymeric systems, PLGA55 exhibited the strongest interaction with coumarin-6, for all the chain lengths, possibly because of their homogeneous spatial arrangements and superior binding energy. PLGA27 showed better compatibility compared to PLGA72 and PGA, whereas PLA-based polymers exhibited the least compatibility. Analysis of the radius of gyration of the polymer chains in the polymer–coumarin-6 complexes, at the end of molecular dynamics run, exhibited that the polymer chains displayed varying coiling behavior and flexibility, depending upon the relative concentrations of the polymer and coumarin-6. Factors like intra-chain interactions, spatial arrangement, inter-chain binding energies, and polymer–coumarin-6 compatibility also influenced the coiling and flexibility of polymer chains.


1960 ◽  
Vol 33 (3) ◽  
pp. 689-695 ◽  
Author(s):  
S. E. Bresler ◽  
M. I. Mosevitskiĭ ◽  
I. Ya Poddubnyĭ ◽  
N. N. Chesnokova

Abstract The molecular weight distribution of polyisoprene obtained by polymerization under the influence of complexes of titanium tetrachloride with tri-isobutylaluminum has been found within broad limits to be independent of the degree of conversion. On the basis of this finding an hypothesis is offered to explain the limitation of polymer chain length according to which chain scission is assumed to increase with the size of the chain.


1986 ◽  
Vol 51 (10) ◽  
pp. 2127-2134 ◽  
Author(s):  
František Potůček ◽  
Jiří Stejskal

Absorption of oxygen into water and aqueous solutions of poly(acrylamides) was studied in an absorber with a wetted sphere. The effects of changes in the liquid flow rate and the polymer concentration on the liquid side mass transfer coefficient were examined. The results are expressed by correlations between dimensionless criteria modified for non-Newtonian liquids whose flow curve can be described by the Ostwald-de Waele model.


2021 ◽  
Vol 155 (3) ◽  
pp. 034701
Author(s):  
Emily Y. Lin ◽  
Amalie L. Frischknecht ◽  
Karen I. Winey ◽  
Robert A. Riggleman

Langmuir ◽  
2021 ◽  
Author(s):  
Hyeong Jin Kim ◽  
Wenjie Wang ◽  
Honghu Zhang ◽  
Guillaume Freychet ◽  
Benjamin M. Ocko ◽  
...  

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