Efficient degradation of polystyrene microplastic pollutants in soil by dielectric barrier discharge plasma.

In this study, the atmospheric dielectric barrier discharge (DBD) plasma was proposed for the degradation of polystyrene microplastics (PS-MPs) for the first time, due to its ability to generate reactive oxygen species (ROS). The local temperature in plasma was found to play a crucial role, as it enhanced the degradation reaction induced by ROS when it exceeded the melting temperature of PS-MPs. Factors including applied voltage, air flow rate, and PS-MPs concentration were investigated, and the degradation products were analyzed. High plasma energy and adequate supply of ROS were pivotal in promoting degradation. At 20.1 kV, the degradation efficiency of PS-MPs reached 98.7% after 60 min treatment, with gases (mainly COx, accounting for 96.4%) as the main degradation products. At a concentration of 1 wt%, the PS-MPs exhibited a remarkable conversion rate of 90.6% to COx, showcasing the degradation performance and oxidation degree of this technology. Finally, the degradation mechanism of PS-MPs combined with the detection results of ROS was suggested. This work demonstrates that DBD plasma is a promising strategy for PS-MPs degradation, with high energy efficiency (8.80 mg/kJ) and degradation performance (98.7% within 1 h), providing direct evidence for the rapid and comprehensive treatment of MP pollutants.

Improved method for calculating CO2 emission from industrial solid wastes combustion system based on fossil and biogenic carbon fraction.

Waste-to-Energy (WtE) technology is the most effective solution for managing non-recyclable wastes through mass burning and energy recovery. Owing to the significant volumes of plastics in China's industrial solid wastes (ISW), a large amount of greenhouse gases (GHG) is generated during the incineration process. Therefore, monitoring GHG emissions from WtE facilities is essential. Owing to the lack of suitable accounting models and characterized fossil carbon fraction (FCF) data, current studies use default values provided by the Intergovernmental Panel on Climate Change's (IPCC), which increases calculation inaccuracies. Therefore, this study established an improved method to accurately account for carbon emissions during solid waste incineration by firstly using radiocarbon dating by accelerator mass spectrometry (AMS) technique to determine the FCF of the solid waste components in China. Monte Carlo analysis was employed to perform the sensitivity analysis, and the results indicated that there was a significant deviation between the measured value and IPCC's default values of FCF, 3.2, 32.48, 93.39, 93.76, 90.49, and 93.8 % for paper, cotton, synthetic textiles, artificial rubber, artificial leather, and plastics, respectively. By replacing coal with ISW in a 2 × 110 t/h circulating fluidized bed boilers, 9.251 × 104 t CO2-eq emissions were reduced, and the carbon emission factor reached 0.56 t CO2-eq/t waste. This study complements the research gap fossil carbon data of wastes in the IPCC guidelines and provides a more accurate and effective way to calculate carbon emissions during ISW incineration treatment.

Characteristics of the pyrolytic products and the pollutant emissions at different operating stages from a pilot waste tire pyrolysis furnace.

Pyrolysis is considered a highly practical, cost-effective, and environment-friendly technology for waste tires disposal. In this study, pyrolysis processes of waste tires were conducted in a pilot scale furnace feeding at 30 kg/h. The properties of pyrolytic products and the distribution patterns of pollutants generated in different operating stages (start-up, steady, and shut-down) were investigated. The pyrolytic gas in the steady state had a high caloric value of 10799 kJ/Nm3, valuable as heating source for pyrolysis. The elements of sulfur and zinc were effectively fixed as ZnS in the pyrolytic carbon. The basic properties of pyrolytic oil were in line with commercial diesel oil except for the lower flash point. Heavy metals were mainly concentrated in the pyrolytic carbon, with slightly higher concentrations in the steady state. Moreover, polycyclic aromatic hydrocarbons (PAHs) and polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were mainly concentrated in the pyrolytic oil, with predominated low-ring PAHs and high chlorinated PCDD/Fs. The concentrations of PAHs and PCDD/Fs in the gas phase were higher during the start-up stage due to the memory effect, whereas were effectively reduced during the steady stage. The concentration of PAHs in the solid phase was highest during the furnace start-up and lowest in the shut-down stage. In contrast to PAHs, the PCDD/Fs in the solid phase reached their highest concentration during the shut-down stage, which was mainly affected by temperature. The results provide guidance for the reducing of pollutant emissions and the recycling of pyrolytic products.

Theoretical and experimental investigation on rapid and efficient adsorption characteristics of microplastics by magnetic sponge carbon.

Microplastic pollution control has always been a thorny problem all over the world. Magnetic porous carbon materials have shown a good development prospect in microplastic adsorption due to their excellent adsorption performance and easy magnetic separation from water. However, the adsorption capacity and rate of magnetic porous carbon on microplastics are still not high, and the adsorption mechanism is not fully revealed, which hinders its further development. In this study, magnetic sponge carbon was prepared using glucosamine hydrochloride as the carbon source, melamine as the foaming agent, iron nitrate and cobalt nitrate as the magnetizing agents. Among them, Fe-doped magnetic sponge carbon (FeMSC) exhibited excellent adsorption performance for microplastics due to its sponge-like morphology (fluffy), strong magnetic properties (42 emu/g) and high Fe-loading (8.37 Atomic%). FeMSC could adsorb to saturation within 10 min, and the adsorption capacity of polystyrene (PS) reached as high as 369.07 mg/g in 200 mg/L microplastic solution, which was almost the fastest adsorption rate and highest adsorption capacity reported so far in the same condition. The performance of the material against external interference was also tested. FeMSC performed well in a wide pH range and different water quality, except in the strong alkaline condition. This is because the surface of microplastics and adsorbents will have many negative charges under strong alkalinity, significantly weakening the adsorption. Furthermore, theoretical calculations were innovatively used to reveal the adsorption mechanism at the molecular level. It was found that Fe-doping could form chemisorption between PS and the adsorbent, thereby significantly increasing the adsorption energy between the adsorbent and PS. The magnetic sponge carbon prepared in this study has excellent adsorption performance for microplastics and can be easily separated from water, which is a promising microplastic adsorbent.

Mass concentration and distribution characteristics of microplastics in landfill mineralized refuse using efficient quantitative detection based on Py-GC/MS.

Landfilling is the most traditional disposal method of domestic waste. Plastic waste in landfill sites could degrade to microplastics (MPs) and diffuse to the surrounding environment with leachate. However, MPs pollution in landfill mineralized refuse has not been well recognized. In the present research, a detection method for mixed MPs of polyethylene (PE), polypropylene (PP), and polystyrene (PS) based on Py-GC/MS was established and verified. The method is suitable for the rapid quantitative detection of large-batch of complex solid matrix samples, with an average deviation of less than 10%. Based on the method, samples from a landfill site in South China were studied, where PE was found to be the main component. The total concentration of MPs in mineralized refuse was 7.62 kg/t in the old area and 5.49 kg/t in the young area. Further analysis showed that the content of MPs was correlated with that of plastic waste and the landfill age, indicating that a considerable proportion was secondary MPs. The reserves of MPs in landfill sites may have reached an alarming number. In the absence of adequate safeguards, quantities of MPs may spread from the landfill sites, resulting in serious pollution of the surrounding soil and groundwater.

Dechlorination of waste polyvinyl chloride (PVC) through non-thermal plasma.

Dechlorination is essential for the chemical recycling of waste polyvinyl chloride (PVC) plastics. This study investigated the use of non-thermal plasma (NTP) for chlorine removal, with a focus on the effects of treatment time and discharge power on dechlorination efficiency. The results showed that longer treatment times and higher discharge powers led to better dechlorination performance. The maximum efficiency (98.25%) and HCl recovery yield (55.72%) were achieved at 180 W power after 40 min of treatment where 96.44% of Cl existed in the form of HCl gas, 1.44% in the liquid product, and 2.12% in the solid residue product. NTP at a discharge power of 150 W showed better dechlorination performance compared to traditional thermal pyrolysis treatment in temperatures ranging from 200 to 400 °C. The activation energy analysis of the chlorine removal showed that compared to pyrolysis-based dechlorination (137.09 kJ/mol), NTP-based dechlorination (23.62 kJ/mol) was more easily achievable. This work presents a practical method for the dechlorination of waste PVC plastic using a novel technology without requiring additional thermal and pressure input.

Dechlorination and fuel gas generation in chemical looping conversion of waste PVC over inherently Na/Ca/K-containing bauxite residue-based oxygen carriers.

The inert atmosphere in chemical looping (CL) technology can considerably inhibit the formation of polychlorinated dibenzo-p-dioxins and dibenzofurans during the thermal treatment of polyvinyl chloride plastic (PVC) waste. In this study, PVC was innovatively converted to dechlorinated fuel gas via CL gasification under a high reaction temperature (RT) and the inert atmosphere by applying an unmodified bauxite residue (BR) as both a dechlorination agent and oxygen carrier. The dechlorination efficiency reached 49.98% at an oxygen ratio of only 0.1. Furthermore, a moderate RT (750 °C in this study) and an increased oxygen ratio enhanced the dechlorination effect. The highest dechlorination efficiency (92.12%) was achieved at an oxygen ratio of 0.6. Iron oxides in BR improved the generation of syngas from CL reactions. The yields of the effective gases (CH4, H2, and CO) increased by 57.13% to 0.121 Nm3/kg with an increase in oxygen ratio from 0 to 0.6. A high RT improved the production of the effective gases (an 809.39% increase to 0.344 Nm3/kg from 600 to 900 °C). Energy-dispersive spectroscopy and X-ray diffraction were used to study the mechanism, and formation of NaCl and Fe3O4 was observed on the reacted BR, indicating the successful adsorption of Cl and its capability as an oxygen carrier. Therefore, BR eliminated Cl in situ and enhanced the generation of value-added syngas, thereby achieving efficient PVC conversion.

Designing low-carbon cement-free binders for stabilization/solidification of MSWI fly ash.

Low-carbon and high-efficiency binder is desirable for sustainable treatment of municipal solid waste incineration fly ash (MSWI FA). In this study, CaO or MgO was used to activate ground granulated blast furnace slag (GGBS) to form calcium silicate hydrate and magnesium silica hydrate gel for stabilization/solidification of hazardous MSWI FA. Experimental results showed that potential toxic elements (PTEs), such as Pb and Zn, significantly inhibited the formation of reaction products in CaO-GGBS system due to the complexation between Ca(OH)2 and PTEs, whereas PTEs only had insignificant inhibition on transformation from MgO to Mg(OH)2 in MgO-GGBS system, resulting in lower leachabilities of PTEs and higher mechanical strengths. Stabilization/solidification experiments demonstrated that MSWI FA (70 wt%) could be recycled by MgO-GGBS binder (30 wt%) into blocks with desirable 28-day compressive strengths (3.9 MPa) and PTEs immobilization efficiencies (99.8% for Zn and 99.7% for Pb). This work provides mechanistic insights on the immobilization mechanisms of PTEs in CaO/MgO-GGBS systems and suggests a promising MgO-GGBS binder for low-carbon treatment of MSWI FA.

Dielectric barrier discharge plasma for the remediation of microplastic-contaminated soil from landfill.

The huge amount of plastic waste accumulated in landfills has caused serious microplastic (MP) pollution to the soil environment, which has become an urgent issue in recent years. It is challenging to deal with the non-biodegradable MP pollutants in actual soil from landfills. In this study, a coaxial dielectric barrier discharge (DBD) system was proposed to remediate actual MP-contaminated landfill soil due to its strong oxidation capacity. The influence of carrier gas type, applied voltage, and air flow rate was investigated, and the possible degradation pathways of MP pollutants were suggested. Results showed the landfill soil samples contained four common MP pollutants, including polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyvinyl chloride (PVC) with sizes ranging from 50 to 1500 µm. The MP pollutants in the soil were rapidly removed under the action of reactive oxygen species (ROS) generated by DBD plasma. Under the air flow rate of 1500 mL min-1, the maximum remediation efficiency represented by mass loss reached 96.5% after 30 min treatment. Compared with nitrogen, when air was used as the carrier gas, the remediation efficiency increased from 41.4% to 81.6%. The increased applied voltage from 17.5 to 24.1 kV could also promote the removal of MP contaminants. Sufficient air supply was conducive to thorough removal. However, when the air flow rate reached 1500 mL min-1 and continued to rise, the final remediation efficiency would be reduced due to the shortened residence time of ROS. The DBD plasma treatment proposed in this study showed high energy efficiency (19.03 mg kJ-1) and remediation performance (96.5%). The results are instructive for solving MP pollution in the soil environment.

Production of low-oxygen oil via catalytic co-pyrolysis of biogas residue and plastics by ZSM-5.

This work aimed to produce low-oxygen bio-oil through the co-pyrolysis of biogas residue (BR) with polyethylene (PE) and polypropylene (PP). The effects of co-pyrolysis interactions on the kinetics and oxygen product distributions were studied. The kinetic results showed that the interaction of BR with PE in BR/PE blends decreased the apparent activation energy (E) in a range of 9.9-33.4 kJ/mol. The presence of PE promoted the deoxidation of oxygenated compounds as the proportion of PE in the mixture increased, which was attributed to free radicals produced by PE that reacted with the oxygenated compounds produced by BR. The presence of PP reduced the oxygen content and alcohols formed in the oil, possibly because of the incomplete conversion of ketones. The content of oxygenated compounds in the oil decreased from 69.5 wt.% to 2.5 wt.% and then 0.4 wt.% in the presence of PE and PP. Additionally, the Zeolite Socony Mobil-5 (ZSM-5) catalyst promoted the formation of alkanes and aromatics, ensuring a high content of CnHm in the oil, and led to 1.3 and 2.4 wt.% oxygenated compounds in BR/PE and BR/PP blends, respectively, demonstrating the possibility of using pyrolysis oil as biodiesel.

Study of Corrosion Kinetic Measurement and Morphology Observation of Superheater Tube 12Cr1MoV Alloy in Simulated MSWI Flue Gas Containing Varied HCl or SO2 Concentrations.

Severe corrosion to superheater tubes at high temperatures was gained virtually by gaseous corrosion media, such as HCl and SO2, in the municipal solid waste incineration flue gas. To clarify the effect of varying concentrations of HCl and SO2 in the oxidizing atmosphere on the corrosion of 12Cr1MoV, a commercial alloy used in superheaters, two series of corrosion tests under simulated flue gas were performed. Both the corrosion kinetics and corrosion morphology were measured in this work. The results of the present study demonstrated that the addition of HCl was more corrosive than that of SO2 under an oxidizing atmosphere. The increased HCl concentration had an accelerating effect on the corrosion rate, but the relation between the two was not linear. In contrast, SO2 exhibited a negligible or even inhibitory effect on corrosion. Both series of test results consistently proved that the temperature had a significant influence on the corrosion of 12Cr1MoV alloy, in particular at 580 °C.

Formation behavior of PAHs during pyrolysis of waste tires.

Polycyclic aromatic hydrocarbons (PAHs) formation from the pyrolysis of waste tires is inevitable because of the complexity of tire formulations and the addition of certain chemicals. In this study, the formation behavior and distribution of PAHs in three-phases were investigated from waste tires under pyrolysis conditions. The influencing factors including the temperature, heating rate, holding time, particle size, catalyzer, and atmosphere, were systematically evaluated. The results showed that PAHs were mainly concentrated in pyrolysis oil (94.59-99.03%), followed by the gas phase (0.96-5.34%), and their content was very low in the solid phase (0.01-0.99%). A higher temperature and slower heating rate lead to partial PAHs decomposition, thus reducing their emissions. The overall formation of PAHs can be inhibited when pyrolyzing coarse-grained tire powder. Furthermore, the PAHs formation mechanisms in waste tires were determined through reaction molecular dynamics, electron paramagnetic resonance, and intermediate products. Tires were mainly decomposed into benzene series, *C2H3, and *CH3; therefore, it was determined that PAHs were formed by the joint action of the hydrogen abstraction, and vinyl radical addition and methyl addition cyclization mechanisms. Among them, low and middle-ring PAHs were formed more easily, particularly naphthalene. The generation of PAHs can be inhibited by reducing the concentration of hydrocarbons and monocyclic benzene series. Regarding the distribution law and generation pathways of PAHs, our results provide guidance for reducing PAHs formation and emissions.

Hydrothermal treatment of food waste for bio-fertilizer production: Formation and regulation of humus substances in hydrochar.

Food waste (FW) poses serious challenges to incineration and composting. Hydrothermal treatment (HTT) is a promising method to produce carbon-rich materials from biomass, including humus substances. In this study, FW containing cellulose, starches, and proteins was treated by HTT to study the formation and regulation of three kinds of humus (i.e., humin, humic acids [HAs], and fulvic acids [FAs]). Ultimate analysis and proximate analyses were conducted to explore the material composition, which was very similar to natural humus. Three kinds of humus were quantified. Optimal temperature (200 °C) and residence time (30 min) for production of HAs were determined based on HAs yield (14.60%). In addition, formation and regulation of humin, HAs and FAs was discussed. The amino acids, peptides, monosaccharides, and HMF obtained by hydrolysis of FW produced important precursors of humus. Moreover, the transfer of nutrient elements was revealed. Nearly 90% of K was dissolved in water. Recovery of N (60%) was relatively stable in hydrochar. Up to 67.61% of P deposited in hydrochar with 12 h.

A sub-freshness monitoring chitosan/starch-based colorimetric film for improving color recognition accuracy via controlling the pH value of the film-forming solution.

The demand for intelligent packaging in food sub-freshness monitoring is increasing. Herein, a pH and NH3 responsing colorimetric film (PS-CH-LCA) was fabricated based on potato starch (PS), chitosan (CH) and Lonicera caerulea L. anthocyanins (LCA) via controlling the pH value of the film-forming solution, and was applied to the real-time monitoring of shrimp freshness. The PS-CH-LCA pH 2.5 film exhibited the highest tensile strength (6.43 MPa), the lowest water solubility (33.11%) and the most sensitive color responsiveness. Morphological and structural results revealed that CH was attached to the surface of PS via hydrogen bond, and anthocyanins were well immobilized in the film-forming matrix. The sensitive color change and its high correlation with spoilage indices demonstrated the PS-CH-LCA pH 2.5 film well indicated fresh, sub-fresh, spoiled level of shrimp. The results solved the limitation of chitosan-based packaging films in undistinguishable colorimetric endpoints, providing a new strategy for indicating the sub-freshness of food packaging.

The effect of the secondary reactions on volatile composition during the pyrolysis treatment of scrap tires.

The phenomenon of the secondary reactions of volatiles prevails during the pyrolysis process of scrap tires, but less is known about the influence of volatiles' residence time and temperature on the pyrolytic oil compositions. Experiments on the secondary reactions caused by residence time and temperature of volatiles were carried out on a lab-scale fixed bed reactor. The regularity of the secondary reactions was presented in detail according to the distribution of liquid and gaseous pyrolytic products. Considering the inadequacy of lab-to-industry research, experiments were further carried out on a pilot-scale auger reactor. The results of the pilot-scale system were corresponding well to the regularity obtained in lab-scale experiment, demonstrating the universality of the regularity in this work. At in situ pyrolysis condition without any secondary reactions, limonene content reached up to 46.24% while a high yield of BTEX (50.55%) was obtained at 700℃/60 s. A remarkable increase of methane and ethane was observed at 700℃/60 s, reaching 0.058 and 0.040 g·(g scrap tire)-1, respectively. This paper provided a novel strategy to selectively produce target products in a simple and economical method. The results were of great significance for guiding the optimisation of pyrolysis parameters in industrial equipment to obtain desired valuable products.

Hierarchical porous structure formation mechanism in food waste component derived N-doped biochar: Application in VOCs removal.

Nitrogen-doped (N-doped) hierarchical porous carbon was widely utilized as an efficient volatile organic compounds (VOCs) adsorbent. In this work, a series of N-doped hierarchical porous carbons were successfully prepared from the direct pyrolysis process of three food waste components. The porous biochar that derived from bone showed a high specific surface area (1405.06 m2/g) and sizable total pore volume (0.97 cm3/g). The developed hierarchical porous structure was fabricated by the combined effect of self-activation (Carbon dioxide (CO2) and water vapor (H2O)) and self-template. The emission characteristics of activation gas analyzed by Thermogravimetric-Fourier transform infrared spectrometer (TG-FTIR) and the transformation of ash composition in the biochar help to illustrate the pore-forming mechanism. Calcium oxide (CaO) and hydroxylapatite were confirmed as the major templates for mesopores, while the decomposition processes of calcium carbonate (CaCO3) and hydroxylapatite provided a large amount of activation gas (CO2 and H2O) to form micropores. The materials also obtained abundant N-containing surface functional groups (up to 7.84 atomic%) from pyrolysis of protein and chitin. Finally, the porous biochar showed excellent performance for VOCs adsorption with a promising uptake of 288 mg/g for toluene and a high adsorption rate of 0.189 min-1. Aplenty of mesopores distributed in the materials effectively improved the mass transfer behaviors, the adsorption rate got a noticeable improvement (from 0.118 min-1 to 0.189 min-1) benefited from mesopores. Reusable potentials of the hierarchical porous carbons were also satisfying. After four thermal regeneration cycles, the materials still occupied 84.8%-87.4% of the original adsorption capacities.

Selective production of singlet oxygen from zinc-etching hierarchically porous biochar for sulfamethoxazole degradation.

Porous carbons are appealing low-cost and metal-free catalysts in persulfate-based advanced oxidation processes. In this study, a family of porous biochar catalysts (ZnBC) with different porous structures and surface functionalities are synthesized using a chemical activation agent (ZnCl2). The functional biochars are used to activate persulfate for sulfamethoxazole (SMX) degradation. ZnBC-3 with the highest content of ketonic group (CO, 1.25 at%) exhibits the best oxidation efficiency, attaining a rate constant (kobs) of 0.025 min-1. The correlation coefficient of the density of CO to kobs (R2 = 0.992) is much higher than the linearity of the organic adsorption capacity to kobs (R2 = 0.694), implying that CO is the intrinsic active site for persulfate activation. Moreover, the volume of mesopore (R2 = 0.987), and Zeta potential (R2 = 0.976) are also positive factors in PS adsorption and catalysis. In the mechanistic study, we identified that singlet oxygen is the primary reactive oxygen species. It can attack the -NH2 group aligned to the benzene ring to form dimer products which could be adsorbed on the biochar surface to reach complete removal of the SMX. The optimal pH range is 4-6 which will minimize the electrostatic repulsion between ZnBCs and the reactants. The SMX degradation in ZnBC/PS system was immune to inorganic anions but would compete with organic impurities in the real wastewater. Finally, the biochar catalysts are filled in hydrogel beads and packed in a flow-through packed-bed column. The continuous system yields a high removal efficiency of over 86% for 8 h without decline, this work provided a simple biochar-based persulfate catalyst for complete antibiotics removal in salty conditions.

Adsorption and thermal degradation of microplastics from aqueous solutions by Mg/Zn modified magnetic biochars.

Microplastics (MPs) derived from plastic wastes have attracted wide attention throughout the world due to the wide distribution, easy transition, and potential threats to organisms. This study proposes efficient Mg/Zn modified magnetic biochar adsorbents for microplastic removal. For polystyrene (PS) microspheres (1 µm, 100 mg/mL) in aqueous solution, the removal efficiencies of magnetic biochar (MBC), Mg modified magnetic biochar (Mg-MBC), and Zn modified magnetic biochar (Zn-MBC) were 94.81%, 98.75%, and 99.46%, respectively. It is supposed that the adsorption process was a result of electrostatic interaction and chemical bonding interaction between microplastics and biochar. The coexisting H2PO4- and organic matters in real water significantly affected the removal efficiency of Zn-MBC due to competitive adsorption effect. Microplastic degradation and adsorbent regeneration were accomplished by thermal treatment simultaneously. The degradation of adsorbed MPs was promoted by the catalytic active sites originated from Mg and Zn, releasing adsorption sites. Thermal regeneration maintained the adsorption capability. Even after five adsorption-pyrolysis cycles, MBC (95.02%), Mg-MBC (94.60%), and Zn-MBC (95.79%) showed high microplastic removal efficiency. Therefore, the low-cost, eco-friendly, and robust Mg/Zn-MBCs have promising potential for application in microplastic removal.

BTEX recovery from waste rubbers by catalytic pyrolysis over Zn loaded tire derived char.

Recovering valuable chemicals (BTEX: Benzene, toluene, ethylbenzene, and xylene) via catalytic pyrolysis of waste tires is a promising and sustainable approach. Zinc loaded tire derived char (TDC) was used as cheap catalyst for recovering valuable BTEX products from waste tire through pyrolysis in this study. The catalytic capability of TDC on BTEX production were experimentally investigated with respect to Zn content, catalytic temperature, and catalyst-to-tire ratio. Due to the abundant acid sites on the surface, the TDC showed notable catalytic capability for improving BTEX yield which was 2.4 times higher than that from uncatalyzed case. The loading of additional Zn increased the acid sites on the TDC and the catalytic performance was further improved. The increase of catalytic temperature and catalyst-to-tire ratio favored the formation of BTEX, but it also brought undesirable consequences, such as the mass loss of tire pyrolysis oil (TPO) and the formation of polycyclic aromatic hydrocarbons. The optimal TPO products were obtained at 600 °C with catalyst-to-tire ratio of 20. At this condition, the relative content of BTEX reached 54.70% and the cumulative BTEX yield was 10.13 wt%, increasing by 5.95 times compared to that of non-catalytic condition. This work provided a novel strategy of replacing traditional expensive catalysts with low-cost and effective carbon-based materials in the field of catalytic pyrolysis of waste tires.