Synergistic effects, gas evolution and ash interaction during isothermal steam co-gasification of biomass with high-sulfur petroleum coke

Energy ◽  
2022 ◽  
Vol 240 ◽  
pp. 122840
Author(s):  
Xin Yu ◽  
Dunxi Yu ◽  
Fangqi Liu ◽  
Jingkun Han ◽  
Jianqun Wu ◽  
...  
2020 ◽  
Vol 45 (46) ◽  
pp. 24502-24517 ◽  
Author(s):  
Elbager M.A. Edreis ◽  
Xian Li ◽  
Abbas H.A. Atya ◽  
Swellam W. Sharshir ◽  
Ammar H. Elsheikh ◽  
...  

Author(s):  
Pratik Toshniwal ◽  
Vimal Chandra Srivastava

Abstract This study attempts to comprehend the thermal degradation behaviour of different blends of petroleum coke (denoted as PC) and wood pellets (denoted as WP) (1:0, 3:1, 1:1. 1:3 and 0:1) using thermogravimetric (denoted as TG) analysis under N2 atmosphere with constant particle size range of 500–850 µm and at constant heating rate of 5 °C/min. TG experiments indicated that it is difficult to predict the pyrolysis characteristics of their blends accurately based on individual components and blending ratios. The non-additive behaviour of TG curves of the blends indicates presence of synergistic effects which could further promote the volatile yields during the co-pyrolysis process. The mixed model including homogeneous reaction model (denoted as HRM) and shrinking core model (denoted as SCM) models were used to predict the variation in kinetic parameters (activation energy and pre-exponential factor) with different blend ratios. The most obvious synergistic effects were observed when the blending ratio was 25 % on account of maximum mass loss rate from the differential thermogravimetry (denoted as DTG), maximum deviation based on root mean square (denoted as RMS) value as well as divergence in the differential thermogravimetric analysis (denoted as DTA) curve.


2014 ◽  
Vol 79 ◽  
pp. 355-366 ◽  
Author(s):  
Elbager M.A. Edreis ◽  
Guangqian Luo ◽  
Aijun Li ◽  
Chaofen Xu ◽  
Hong Yao

2018 ◽  
Vol 267 ◽  
pp. 54-62 ◽  
Author(s):  
Elbager M.A. Edreis ◽  
Xian Li ◽  
Guangqian Luo ◽  
S.W. Sharshir ◽  
Hong Yao

Author(s):  
W.W. Adams ◽  
S. J. Krause

Rigid-rod polymers such as PBO, poly(paraphenylene benzobisoxazole), Figure 1a, are now in commercial development for use as high-performance fibers and for reinforcement at the molecular level in molecular composites. Spinning of liquid crystalline polyphosphoric acid solutions of PBO, followed by washing, drying, and tension heat treatment produces fibers which have the following properties: density of 1.59 g/cm3; tensile strength of 820 kpsi; tensile modulus of 52 Mpsi; compressive strength of 50 kpsi; they are electrically insulating; they do not absorb moisture; and they are insensitive to radiation, including ultraviolet. Since the chain modulus of PBO is estimated to be 730 GPa, the high stiffness also affords the opportunity to reinforce a flexible coil polymer at the molecular level, in analogy to a chopped fiber reinforced composite. The objectives of the molecular composite concept are to eliminate the thermal expansion coefficient mismatch between the fiber and the matrix, as occurs in conventional composites, to eliminate the interface between the fiber and the matrix, and, hopefully, to obtain synergistic effects from the exceptional stiffness of the rigid-rod molecule. These expectations have been confirmed in the case of blending rigid-rod PBZT, poly(paraphenylene benzobisthiazole), Figure 1b, with stiff-chain ABPBI, poly 2,5(6) benzimidazole, Fig. 1c A film with 30% PBZT/70% ABPBI had tensile strength 190 kpsi and tensile modulus of 13 Mpsi when solution spun from a 3% methane sulfonic acid solution into a film. The modulus, as predicted by rule of mixtures, for a film with this composition and with planar isotropic orientation, should be 16 Mpsi. The experimental value is 80% of the theoretical value indicating that the concept of a molecular composite is valid.


2010 ◽  
Vol 48 (01) ◽  
Author(s):  
E Gäbele ◽  
K Dostert ◽  
C Dorn ◽  
C Hellerbrand

Sign in / Sign up

Export Citation Format

Share Document