scholarly journals Use of Pyrolyzed Soybean Hulls as Fillers in Polypropylene and Linear Low Density Polyethylene

2021 ◽  
Vol 2 (4) ◽  
pp. 622-644
Author(s):  
Collin Coben ◽  
Erol Sancaktar

In the competitive market of plastic fillers, inexpensive and reliable materials are always sought after. Using a method of thermal conversion called pyrolysis, a potential contender was created from a plant biomass known as soybean hulls (SBH). SBH are a byproduct of the soybean farming industry and represent an abundant and inexpensive feedstock. The thermal conversion of SBH material gives rise to a lightweight carbon-rich filler called pyrolyzed soybean hulls (PSBH). We created two separate lots, lots A and B, with lot A corresponding to SBH pyrolyzed at 450 °C (PSBH-A) and lot B corresponding to SBH pyrolyzed at 500 °C (PSBH-B). Both lots of PSBH were also milled to reduce their particle size and tested against the as-received PSBH fillers. These milled materials were designated as ground soybean hulls (GSBH). Two different polyolefins, linear low-density polyethylene (LLDPE) and polypropylene (PP), were used for this study. The PSBH fillers were added to the polyolefins in weight percentages of 10%, 20%, 30%, 40%, and 50%, with the resulting plastic/PSBH composites being tested for their mechanical, thermal, and water absorption properties. In general, the addition of filler increased the maximum stress of the LLDPE/PSBH composites while reducing maximum stress of the PP/PSBH composites. The strain at maximum stress was reduced with increasing amounts of the PSBH filler for all composites. The modulus of elasticity generally increased with increasing filler amount. For thermal properties, the addition of the PSBH filler increased the heat distortion temperature, increased the thermal decomposition temperature, and reduced the heat of fusion of the composites compared to the neat polyolefins. The liquid absorption and thickness swelling in the materials were small overall but did increase with increasing amounts of the PSBH filler and with the time spent submerged in liquid. Milling the PSBH material into GSBH generally had small effects on the various tested material properties and led to easier mixing and a smoother finish on the surface of processed samples. The differences observed between lot A and lot B composites were often small or even negligible.

2019 ◽  
Vol 796 ◽  
pp. 22-29
Author(s):  
N.A. Ahmad ◽  
Shaifulazuar Rozali ◽  
Mohd Faizul Mohd Sabri ◽  
C.Y. Chee ◽  
Suriani Ibrahim

Blended polymer composites are prepared based on linear low density polyethylene (LLDPE) and mixed with polysulfone (PSU) using solvent casting technique. LLDPE is functionalized with carbonyl functional groups to enable it to interact with PSU from the molecular level. Various weight percent of PSU is added into LLDPE to find the optimum weight percent ratio between LLDPE and PSU. The highest glass transition temperature obtained is 47.58°C for ratio LLDPE to PSU of 7:3. In addition, value for decomposition temperature is increased up to 490.16°C with the increasing of PSU content. SEM observation of the blended polymer films shows that glass transition and decomposition temperature depend on morphology of the blended polymers.


Polymers ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 911
Author(s):  
Xiaoxiao Guan ◽  
Bo Cao ◽  
Jianan Cai ◽  
Zhenxing Ye ◽  
Xiang Lu ◽  
...  

In this study, a polysiloxane grafted by thermotropic liquid crystal polymer (PSCTLCP) is designed and synthesized to effectively improve the processability and toughness of magnesium hydroxide (MH)/linear low-density polyethylene (LLDPE) composites. The obtained PSCTLCP is a nematic liquid crystal polymer; the liquid crystal phase exists in a temperature range of 170 to 275 °C, and its initial thermal decomposition temperature is as high as 279.6 °C, which matches the processing temperature of MH/LLDPE composites. With the increase of PSCTLCP loading, the balance melt torque of MH/LLDPE/PSCTLCP composites is gradually decreased by 42% at 5 wt % PSCTLCP loading. Moreover, the power law index of MH/LLDPE/PSCTLCP composite melt is smaller than 1, but gradually increased with PSCTLCP, the flowing activation energy of PSCTLCP-1.0 is lower than that of MH/LLDPE at the same shear rate, indicating that the sensitivity of apparent melt viscosity of the composites to shear rate and to temperature is decreased with the increase of PSCTLCP, and the processing window is broadened by the addition of PSCTLCP. Besides, the elongation at break of MH/LLDPE/PSCTLCP composites increases from 6.85% of the baseline MH/LLDPE to 17.66% at 3 wt % PSCTLCP loading. All the results indicate that PSCTLCP can significantly improve the processability and toughness of MH/LLDPE composites.


2010 ◽  
Vol 63 (8) ◽  
pp. 1201 ◽  
Author(s):  
Shingo Kobayashi ◽  
Christopher W. Macosko ◽  
Marc A. Hillmyer

Model hexyl-branched linear low density polyethylene (C8-LLDPE) samples were synthesized by the ring-opening metathesis copolymerization (ROMP) of the 5-hexylcyclooct-1-ene (1) and cyclooctadiene (COD), followed by catalytic hydrogenation. The ROMP of 1 and copolymerization of 1 and COD using the Grubbs second generation catalyst (G2) afford polymers with the number of hexyl branches based on the feed composition. The resulting hexyl-branched polymers, poly(1) and poly(1-stat-COD), were completely converted into model C8-LLDPE samples by catalytic hydrogenation. The C8-LLDPE samples exhibit the expected reduction in density on branching content. The melting temperature (Tm), crystallization temperature (Tc), and heat of fusion/crystallization (ΔHm/ΔHc) of these materials were studied by differential scanning calorimetry.


Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1537
Author(s):  
Luděk Hynčík ◽  
Petra Kochová ◽  
Jan Špička ◽  
Tomasz Bońkowski ◽  
Robert Cimrman ◽  
...  

Current industrial trends bring new challenges in energy absorbing systems. Polymer materials as the traditional packaging materials seem to be promising due to their low weight, structure, and production price. Based on the review, the linear low-density polyethylene (LLDPE) material was identified as the most promising material for absorbing impact energy. The current paper addresses the identification of the material parameters and the development of a constitutive material model to be used in future designs by virtual prototyping. The paper deals with the experimental measurement of the stress-strain relations of linear low-density polyethylene under static and dynamic loading. The quasi-static measurement was realized in two perpendicular principal directions and was supplemented by a test measurement in the 45° direction, i.e., exactly between the principal directions. The quasi-static stress-strain curves were analyzed as an initial step for dynamic strain rate-dependent material behavior. The dynamic response was tested in a drop tower using a spherical impactor hitting a flat material multi-layered specimen at two different energy levels. The strain rate-dependent material model was identified by optimizing the static material response obtained in the dynamic experiments. The material model was validated by the virtual reconstruction of the experiments and by comparing the numerical results to the experimental ones.


2015 ◽  
Vol 37 (11) ◽  
pp. 3167-3174 ◽  
Author(s):  
S. Sánchez-Valdes ◽  
E. Ramírez-Vargas ◽  
L.F. Ramos de Valle ◽  
J.G. Martinez-Colunga ◽  
J. Romero-Garcia ◽  
...  

1988 ◽  
Vol 27 (2) ◽  
pp. 172-178 ◽  
Author(s):  
S. Ottani ◽  
A. Valenza ◽  
F. P. La Mantia

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