Revisiting group contribution theory for estimating fractional free volume of microporous polymer membranes

2021 ◽  
pp. 119526
Author(s):  
Albert X. Wu ◽  
Sharon Lin ◽  
Katherine Mizrahi Rodriguez ◽  
Francesco M. Benedetti ◽  
Taigyu Joo ◽  
...  
2021 ◽  
pp. 2108672
Author(s):  
Zongyao Zhou ◽  
Digambar B. Shinde ◽  
Dong Guo ◽  
Li Cao ◽  
Reham Al Nuaimi ◽  
...  

Polymers ◽  
2022 ◽  
Vol 14 (2) ◽  
pp. 226
Author(s):  
Jinsong Yang ◽  
Weitao Lou

The effects of oxidative aging on the static and dynamic properties of nitrile rubber at the molecular scale were investigated by molecular dynamics simulation. The aged nitrile rubber models were constructed by introducing hydroxyl groups and carbonyl groups into rubber molecular chains to mimic oxidative aging. The static and dynamic properties of the unaged and aged nitrile rubber under different conditions were evaluated by mean square displacement, self-diffusion coefficients, hydrogen bond, fractional free volume, radial distribution function, cohesive energy density and solubility parameter. The results show that the elevated temperature intensified significantly the mobility of rubber molecular chains and fractional free volume, while the compressive strain displayed the opposite effect resulting in packing and rearrangement of rubber chains. The introduction of hydroxyl groups and carbonyl groups enhanced the polarity, intermolecular interactions, the volume and rigidity of molecular chains, implying weaker mobility of molecular chains as compared to unaged models. The compressive strain and oxidative aging both decreased the fractional free volume, which inhibited gaseous and liquid diffusion into the rubber materials, and slowed down the oxidative aging rate. This study provides insights to better understand the effect of molecular changes due to oxidative aging on the structural and dynamic properties of rubber materials at the molecular level.


2019 ◽  
Vol 502 ◽  
pp. 112298 ◽  
Author(s):  
Dong NguyenHuynh ◽  
My T. Luu ◽  
Xuan T.T. Nguyen ◽  
Chau T.Q. Mai ◽  
Siem T.K. Tran

2020 ◽  
Vol 8 (44) ◽  
pp. 23354-23367
Author(s):  
Ali Hayek ◽  
Abdulkarim Alsamah ◽  
Garba O. Yahaya ◽  
Eyad A. Qasem ◽  
Rashed H. Alhajry

Chemical modification enhances gas molecule permeation through polymeric membrane matrices by increasing the fractional free volume.


1972 ◽  
Vol 45 (1) ◽  
pp. 278-292 ◽  
Author(s):  
B. G. Corman ◽  
M. L. Deviney ◽  
L. E. Whittington

Abstract Previous work in diffusion of whole extender oil and extender oil fractions in practical rubber compounds has shown the nature of the rubber matrix to be the major controlling factor. Therefore, a sensitive diffusivity approach, using radiotracer labeled hydrocarbon penetrants of sizes comparable to the size of a rotating segment, was used to study various aspects of the matrix structure on penetrant diffusion for polybutadiene, styrene—butadiene, and Butyl rubbers. These results were compared with fractional free volume measurements made by a thermal expansion technique. Neither fractional free volume nor diffusivity of phenyldodecane, benz-a-anthracene, or n-octadecane was affected by 5-fold variations of crosslink density or by variations in loading of 10 to 80 parts of carbon black (HAF-LS); nor were they affected by changes from FEF to SAF black at a 50 phr level. Glass transition temperature and fractional free volume are both affected by increasing percentages of benzene or phenyldodecane, While diffusivity rises with increasing dilution, states of equal free volume in different elastomers are not states of equal diffusivity; for example, at a fractional free volume of 0.10, corresponding to 20% benzene in both polybutadiene and Butyl at 70° C, the diffusivity of benzene in Butyl is lower by a factor of 15. Comparison of diffusivity of large penetrants with their cross-sectional area gives two basic curves, one for flexible penetrants and another for molecularly rigid species. These results are explained in terms of a distribution of free volumes, wherein only holes above a critical size are effective in diffusion. Swelling the system with aromatic diluent greatly increases the total fractional free volume, but only slightly the number of holes above this critical size. To understand the diffusivity of rigid molecules in elastomers, a probability factor must be applied in estimating their effective cross-sectional area.


Sign in / Sign up

Export Citation Format

Share Document