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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 487 records · Page 27
All sourcesNASA NTRSDOE OSTI
DOE OSTI2024

Demonstrating the Feasibility of Biomass Pyrolysis Liquid, Coal, Plastic Oil Mixtures for Entrained Flow Gasification

There is interest in co-gasifying coal, biomass and plastic. An attractive alternative is to do that in a pressurized entrained-flow gasifier, technology that has been used for coal gasification for decades. The approach taken in this study is to liquefy biomass through fast pyrolysis and to liquefy waste plastic by thermal decomposition. The liquids form the basis of a slurry that also includes coal particles. In this work, several different compositions of coal-bioliquid-plastic oil slurries were prepared and evaluated for viscosity and settling properties. Suitable composition ranges were identified and are highlighted in the presentation.

Hughey, Logan↗
DOE OSTI2025

Direct solar self-catalyzing pyrolysis of natural gas to hydrogen and high-quality graphite (Final Technical Report)

This project, led by researchers at UCLA in partnership with Southwest Solar Technology (SST) and SolGrapH, successfully demonstrated a new method for producing clean hydrogen fuel and high-quality graphite using concentrated solar energy. The primary goal was to develop a technology that converts natural gas (primarily methane) into two valuable products—hydrogen gas and solid carbon—without releasing carbon dioxide (CO2) into the atmosphere. This process, known as solar thermal pyrolysis, uses heat from the sun to split the methane molecules directly.

03 NATURAL GAS↗
DOE OSTI2020

Time-resolved measurements of key intermediate products during cyclopentanone pyrolysis in a shock tube

The pyrolysis of cyclopentanone, a promising biofuel candidate identified by the Department of Energy’s Co-Optima program, is investigated in this work. Time resolved measurements of carbon monoxide, ethylene, and cyclopentanone are provided to gain a detailed understanding of the unimolecular decomposition pathway of the fuel. Experiments were conducted between 1156-1312 K near 9 atm with 0.1% fuel loading balanced in argon. A strategy to report species concentration with interference is presented and the measurements obtained are crucial validation targets for the development of detailed chemical kinetic mechanisms used to predict fuel chemistry.

09 BIOMASS FUELS↗
DOE OSTI2018

Activated Carbons Derived from High-Temperature Pyrolysis of Lignocellulosic Biomass

Biomass pyrolysis to produce biofuel and hydrogen yields large amounts of charred byproducts with low commercial value. A study was conducted to evaluate their potential for being converted into higher value activated carbons by a low-cost process. Six chars derived from various lignocellulosic precursors were activated in CO 2 at 800 °C to 30–35% weight loss, and their surface area and porosity were characterized by nitrogen adsorption at 77 K. It was found that, in similar activation conditions, the surface area of the activated carbons correlates with the activation energy of the oxidation reaction by CO 2 , which in turn varies inversely with the carbon yield after thermolysis in nitrogen at 1000 °C. Since lignin is the most thermally-stable component of lignocellulosic biomass, these results demonstrate, indirectly, that robust, lignin-rich vegetal precursors are to be preferred to produce higher quality activated carbons. The chars derived from white pine (pinus strobus) and chestnut oak (quercus prinus) were converted to activated carbons with the highest surface area (900–1100 m 2 /g) and largest mesopores volume (0.85–1.06 cm 3 /g). These activated carbons have properties similar to those of commercially-available activated carbons used successfully for removal of pollutants from aqueous solutions.

09 BIOMASS FUELS↗
DOE OSTI2022

Additive Manufacturing of C/C-SiC Ceramic Matrix Composites by Automated Fiber Placement of Continuous Fiber Tow in Polymer with Pyrolysis and Reactive Silicon Melt Infiltration

An additive manufacturing process for fabricating ceramic matrix composites has been developed based on the C/C-SiC system. Automated fiber placement of the continuous carbon fibers in a polyether ether ketone matrix was performed to consolidate the carbon fibers into a printed preform. Pyrolysis was performed to convert the polymer matrix to porous carbon, and then Si was introduced by reactive melt infiltration to convert a portion of the carbon matrix to silicon carbide. The densities and microstructures were characterized after each step during the processing, and the mechanical properties were measured. The C/C-SiC composites exhibited a porosity of 10–20%, characteristic flexural strength of 234.91 MPa, and Weibull modulus of 3.21. The composites displayed toughness via a significant displacement to failure.

36 MATERIALS SCIENCE↗
DOE OSTI2024

Analysis of Infrastructures for Processing Plastic Waste using Pyrolysis-Based Chemical Upcycling Pathways

Modern mechanical recycling infrastructure for plastic is capable of processing only a small subset of waste plastics, reinforcing the need for parallel disposal methods such as landfilling and incineration. Emerging pyrolysis-based chemical technologies can "upcycle" plastic waste into high-value polymer and chemical products and process a broader range of waste plastics. In this work, we study the economic and environmental benefits of deploying an upcycling infrastructure in the continental United States for producing low-density polyethylene (LDPE) and polypropylene (PP) from post-consumer mixed plastic waste. Our analysis aims to determine the market size that the infrastructure can create, the degree of circularity that it can achieve, the prices for waste and derived products it can propagate, and the environmental benefits of diverting plastic waste from landfill and incineration facilities it can produce. We apply a computational framework that integrates techno-economic analysis, life cycle assessment, and value chain optimization. Our results demonstrate that the infrastructure generates an economy of nearly 20 billion USD and positive prices for plastic waste, opening opportunities for compensation to residents who provide plastic waste. Our analysis also indicates that the infrastructure can achieve a plastic-to-plastic degree of circularity of 34% and remains viable under various external factors (including technology efficiencies, capital investment budgets, and polymer market values). Finally, we present significant environmental benefits of upcycling over alternative landfill and incineration waste disposal methods, and comment on ongoing work expanding our modeling methodology to other chemical upcycling pathway case studies, including hydroformylation of specific plastics to chemicals.

Interdisciplinary↗