Hybrid Model for Biopolymerization Process (ε-Caprolactone to Polycaprolactone)

2014 ◽  
Vol 625 ◽  
pp. 77-80 ◽  
Author(s):  
Senthil Kumar Senthil ◽  
Z. Ahmad

A very attractive and accepted approach to the modeling problem is building a hybrid model, where certain amounts of both phenomenological and empirical information are used. In this paper the mechanistic model is created by using the mathematical equations which are represented in the MatlabTM Simulink environment so as to achieve a control over the bio-polymerization process. This mechanistic model was connected to a Feedforward Neural Network (FANN) model to complete the hybrid model of the process to predict the molecular weight distribution. The hybrid model in the Simulink environment was validated by comparing the results of the hybrid model with that of the experimental results carried out in a bioreactor.

2013 ◽  
Vol 634-638 ◽  
pp. 616-619 ◽  
Author(s):  
Zu Guang Liu ◽  
Hua Long Zhu ◽  
Shuo Wang ◽  
Le Le Zhao ◽  
Fu Hou Lei

Substituted phosphotungstic acids containing manganese, chromium, molybdenum and vanadium were prepared, and their catalytic performance on cationic polymerization of β-pinene was also investigated. The experimental results show that the substituted phosphotungstic acids are mono-substituted and keep Keggin structure. The substituted phosphotungstic acids containing Mn or Cr exhibit similar catalytic performance as phosphotungstic acid, instead show bad properties if containing Mo or V. The yield of polymer is up to 44.3 %, and the average number molecular weight is about 1200, and molecular weight distribution index is 1.4.


1967 ◽  
Vol 40 (2) ◽  
pp. 532-543 ◽  
Author(s):  
S. D. Gehman

Abstract Calculations and experimental results both indicated that effects of a molecular weight distribution of network chains may become evident in swelling pressure curves under favorable circumstances. More precise experiments are required to establish this definitely. The calculations assume that a simple integration such as is used for a continuous medium may be applied to molecular units of structure deduced from the kinetic theory of rubber elasticity. The validity of this can only be determined by further comparisons with experience. Refinement of the theory might take into account interactions of the units.


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