Production of nanostructure carbon materials via non-oxidative thermal degradation of real polypropylene waste plastic using La 2 O 3 supported Ni and NieCu catalysts Ateyya A. Aboul-Enein a, b , Ahmed E. Awadallah a, b, * a Process Development Division, Egyptian Petroleum Research Institute, Nasr City, PO Box 11727, Cairo, Egypt b EPRI-Nanotechnology Center, Egyptian Petroleum Research Institute, Nasr City, PO Box 11727, Cairo, Egypt article info Article history: Received 23 January 2019 Received in revised form 16 June 2019 Accepted 18 June 2019 Available online 19 June 2019 Keywords: Carbon nanomaterials Polypropylene plastic waste Pyrolysis NieCu/La 2 O 3 catalyst abstract In this work real polypropylene (PP) waste plastic was used as a feedstock for synthesis of carbon nanomaterials (CNMs) via a two-stage process. Lanthanum oxide (La 2 O 3 ) was reported as a promising support for the active metals in thermocatalytic decomposition of hydrocarbons. This is due to the fact that it produces highly dispersed metal particles with an appropriate metal support interaction. Accordingly, La 2 O 3 supported monometallic 50%Ni and bimetallic 40%Nie10%Cu catalysts with the total metal content of 50 wt % were prepared and examined for the rst time for the decomposition of non- condensable gases obtained from pyrolysis of PP to produce CNMs. The main target of this work is to study the impact of Cu addition on the yield and nature of as-deposited carbon product. The prepared catalysts were tested at the same pyrolysis and decomposition temperatures of 500 C and 700 C, respectively, and reaction time of 2.5 h. Various characterization techniques such as XRD, H 2 -TPR, BET surface area and FTIR were used to study the physicochemical properties of fresh catalysts. While, HR- TEM, XRD, Raman spectroscopy and TGA-DTG techniques were employed on the spent catalysts to explore the nature, morphology, quality and thermal properties of CNMs product. It was observed that the bimetallic NieCu/La 2 O 3 catalyst exhibited higher surface area, higher metal dispersion as well as lower reduction temperature compared to the monometallic 50%Ni/La 2 O 3 catalyst. These factors were found to be responsible for the improved catalytic growth activity of the 40%Nie10%Cu/La 2 O 3 catalyst in terms of carbon yield. The CNMs yield remarkably increased from 944% to 1458% after incorporating 10 wt% Cu in 40%Ni/La 2 O 3 catalyst. TEM images showed that multi-walled carbon nanotubes (MWCNTs) with regular diameters were formed over 50%Ni/La 2 O 3 catalyst, while a mixture of large diameter carbon nanobers (CNFs) and MWCNTs were produced over the 40%Nie10%Cu/La 2 O 3 catalyst. © 2019 Elsevier Ltd. All rights reserved. 1. Introduction Plastics in particular polymer-based materials are one of the most widely used substances in many industrial and social elds. As a result, the global production and consumption of plastics have increased rapidly, resulting in the generation of drastic quantities of solid waste. This solid waste can be regarded as one of the main sources of air, soil, water, and marine pollution [1e5]. At present, landll and incineration treatments are still broadly used for waste management, inducing also dangerous problems in the environment and human health as well as losing energy stored in plastic [2,3]. Therefore, it is necessary to nd economically alter- native routes for the removal of plastic waste from the environ- ment. One of the most prospective technologies is the manufacture of high-value-added carbon nanomaterials (CNMs) products such as multi-walled carbon nanotubes (MWCNTs) and carbon nano- bers (CNFs) by using plastic waste as a carbonaceous feedstock [6e13]. In addition, the utilization of plastic waste for the synthesis of CNMs instead of the traditional natural gas source is very important from economic and environmental aspects. A further merit of this process is the generation of hydrogen-rich gas as a valuable by-product [14,15]. Among the various types of plastic waste, polyethylene (PE) and polypropylene (PP) are considered as a potential hydrocarbon source due to their high carbon content * Corresponding author. Process Development Division, Egyptian Petroleum Research Institute, Nasr City, PO Box 11727, Cairo, Egypt. E-mail address: ahmedelsayed_epri@yahoo.com (A.E. Awadallah). Contents lists available at ScienceDirect Polymer Degradation and Stability journal homepage: www.elsevier.com/locate/polydegstab https://doi.org/10.1016/j.polymdegradstab.2019.06.015 0141-3910/© 2019 Elsevier Ltd. All rights reserved. Polymer Degradation and Stability 167 (2019) 157e169