Polypropylene Plastic Waste Conversion to Lubricants over Ru/TiO2 Catalysts

被引:157
作者
Kots, Pavel A. [1 ]
Liu, Sibao [1 ,3 ]
Vance, Brandon C. [1 ,2 ]
Wang, Cong [1 ]
Sheehan, James D. [1 ]
Vlachos, Dionisios G. [1 ,2 ]
机构
[1] Univ Delaware, Ctr Plast Innovat, Newark, DE 19716 USA
[2] Univ Delaware, Dept Chem & Biomol Engn, Newark, DE 19716 USA
[3] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Minist Educ, Tianjin 300072, Peoples R China
基金
美国国家卫生研究院;
关键词
plastic waste; hydrogenolysis; lubricants; upcycling; circular economy; SYNTHETIC LUBRICANTS; BASE OILS; HYDROGENOLYSIS; MECHANISM; ALKANES; COPOLYMERS; MICROSTRUCTURE; SPECTROSCOPY; SQUALANE; IMPACT;
D O I
10.1021/acscatal.1c00874
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Plastic recycling and upcycling are required to combat the environmental crisis from landfilling consumer products. Chemocatalytic technologies are the most promising approach to achieve this. Here, we show that ruthenium deposited on titania is an active and selective catalyst in polypropylene breakdown into valuable lubricant-range hydrocarbons with narrow molecular weight distribution and a low methane formation at low temperatures of 250 degrees C with a modest H-2 pressure. Amorphous polypropylene and everyday bags and bottles were also effectively converted to lubricants with yields up to 80+%. Quantification of critical properties, including pour point, kinematic viscosity, and viscosity index, indicates that the products are promising alternatives to currently used base or synthetic oils. The reaction network involves the sequential conversion of polymer into the oil with a gradual decrease of molecular weight until similar to 700-800 g/mol and slow liquid gasification to methane and ethane. NMR, ATR-IR, GCMS, and isotopic labeling experiments expose the complexity of structure and reaction evolution whereby hydrogenolysis involves intermediate dehydrogenation with synchronous loss of polypropylene stereoregularity.
引用
收藏
页码:8104 / 8115
页数:12
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