The invention is a new type of amine-based sorbent material that has increased affinity towards heavy metal capture, from a variety of sources that exceeds the existing amine-sorbent ability by greater than 50%. This invention involves use of a polyamine that is chemically tethered to the surface of a solid silica support through use of a crosslinker and further stabilized through hydrogen bonding with a linker/cross linker. These sorbents can be used for the capture of heavy metals from a variety of aqueous sources. This technology is available for licensing and/or further collaborative research from the U.S. Department of Energy's National Energy Technology Laboratory.

Challenge

The US Resource Conservation and Recovery Act (RCRA) gave the US Environmental Protection Agency the authority to establish and enforce regulatory policies and toxicity limits regarding Arsenic (As), Cadmium (Cd), Chromium (Cr), Lead (Pb), Mercury (Hg), Selenium (Se), and other metals. Many of these metals present a distinct challenge for capture because they are most commonly present in the polyatomic oxy-anion form. Sources for most of these contaminant metals include flue gas desulfurization (FGD) wastewater streams. These streams result from the treatment of fossil fuel-derived, post combustion flue gas with aqueous-based technologies. The well-known and widespread contamination of metals in drinking water and other terrestrial water sources through natural processes or human activity, demands remediation. In addition, radioactive pollutants in aqueous form have raised concerns about exposure levels in the nearby communities because of fears that these fission products could make their way into the food chain.

NETL's basic immobilized amine sorbents (BIAS) have previously been shown effective at removing heavy metals and radioactive ions from aqueous sources. Chelating the amines with metals such as iron or copper significantly increases the heavy metal capture affinity of the sorbents, up to 50% over the non-metal chelated amines. In this invention, the metal-chelated polyamine is chemically tethered to a solid silica support (SiO₂) via a crosslinker. The sorbents resist leaching by H₂O in an aqueous stream containing heavy oxyanion-based (and other) metals and demonstrate stability over a pH range of 5 - 14. Cationic heavy metals are captured by the amine functional groups (-NH₂, -NH, -N) from the polymeric network while oxyanionic metal species bind readily to the metal loaded sites. This technology is available for licensing and/or further collaborative research from the U.S. Department of Energy's National Energy Technology Laboratory.

Challenge

Heavy metals are common in industrial wastewater streams such as those associated with flue gas desulfurization (FGD), acid mine drainage, hydraulic fracturing, and nuclear fission. As heavy metals pose health and environmental hazards, there is a critical need to remediate them, i.e., safely and efficiently remove them from the aqueous sources. The US Resource Conservation and Recovery Act (RCRA) gave the US Environmental Protection Agency the authority to establish and enforce regulatory policies and toxicity limits arsenic (As), cadmium (Cd), chromium (Cr), lead (Pb), mercury (Hg), selenium (Se), and other metals. Many of these metals present a distinct challenge for capture because they are most commonly present in the polyatomic oxy-anion form. Sources for most of these contaminant metals result from the treatment of fossil fuel-derived, post-combustion flue gas with aqueous-based technologies. The well-known and widespread contamination of RCRA metals in drinking water and other terrestrial water sources either through natural processes or resulting from human activity, demands remediation.

The invention is method of fabricating a hollow glass waveguide (tube that transmits light) that exhibits low loss in the visible or short-wave spectral region and is optimized for Raman spectroscopy or visible laser beam delivery. Prior art hollow capillaries suffer high optical loss and poor visible transmission, but the NETL invention produces these high-quality capillaries via a specialized deposition system. This technology is available for licensing and/or further collaborative research from the U.S. Department of Energy’s National Energy Technology Laboratory.

Challenge
Currently, there are no high-quality commercially produced visible-wave hollow waveguides. Commercial vendors can produce reasonable IR hollow waveguides, but visible-range waveguides exhibit high losses and high optical noise. The patented NETL Raman Gas Analyzer requires visible-range hollow waveguides with small internal diameters (a few hundred microns) and low optical noise. No vendor could produce these waveguides, so NETL constructed this new system of waveguide fabrication. Other spectroscopic systems would benefit from better waveguides including absorption spectrometers, microscopes, sensors, etc.
 

The invention is a family of hydrophobic, low viscosity, low vapor pressure physical solvents with molecular structures consisting of two or more alkyl-ester functional groups on a central hydrocarbon chain. These solvents have been shown to possess high carbon dioxide (CO₂) solubility and absorption selectivity, which make them well suited for the removal of CO₂ from hydrogen (H₂) produced from synthesis gas. This technology is available for licensing and/or further collaborative research from the U.S. Department of Energy’s National Energy Technology Laboratory.

Challenge
Future integrated gasification combined cycle (IGCC) power plants and steam methane reforming (SMR) chemical plants have the potential to reduce the cost of CO₂ capture. These power and chemical plants generate high-pressure CO₂ gas streams from the in-situ water gas shift reaction when producing H₂ used to power the electrical turbines. A variety of methods have been proposed to capture CO₂, including solvent, sorbent, and membrane technologies, with continuous solvent looping systems currently considered to be the most advanced. Precombustion capture of CO₂ is typically accomplished using physical solvents.

State-of-the-art precombustion CO₂ capture processes predominantly employ hydrophilic physical solvents. Current commercial physical solvents touted for IGCC CO₂ capture were developed for removing acid gases from raw natural gas streams. Therefore, they were designed to remove significant amounts of water from the process gas. As such, the focus was on the purification of the process gas with less concern for generation of high-purity CO₂ streams suitable for pipeline transmission and sequestration. While water removal is important for natural gas pipeline applications, it is not favorable for applications in which the fuel stream is directly combusted on-site, as would be encountered in IGCC systems.

This invention describes a single-stage preparation of a novel carbon capture fiber sorbent. This technology is available for licensing and/or further collaborative research from the U.S. Department of Energy’s National Energy Technology Laboratory.

Challenge
Conventional pressure- or temperature-swing adsorption (PSA/TSA) processes have been widely considered for post-combustion carbon capture and direct air capture (DAC). However, the processes of pressurizing the flue gas in the case of PSA or the long regeneration time in the case of TSA are considered neither cost-effective nor energy efficient, which limit their use in large-scale carbon capture processes. Furthermore, the high heat released during carbon dioxide (CO₂) adsorption onto conventional sorbent amine sites necessitate efficient heat redistribution away from the sorbent bed and back into the overall carbon capture process. Therefore, a low-cost and energy efficient carbon capture process that could be retrofitted onto existing power plants is needed.

This invention describes a pH sensor comprising an optical fiber coated with metal-oxide based pH sensing materials for use in high-temperature and high-pressure environments such as wellbores and the challenging high pH range relevant for wellbore cement. This technology is available for licensing and/or further collaborative research from the U.S. Department of Energy’s National Energy Technology Laboratory.

Challenge
Various fossil energy and carbon management applications require chemical composition monitoring in subsurface environments. Examples of these areas include deep and ultra-deep oil and gas resource recovery through drilling and hydraulic fracturing techniques as well as environmental monitoring in reservoirs for carbon dioxide (CO₂) sequestration. Accurate measurement of pH in subsurface wellbores is critical for early corrosion detection and wellbore cement failure prediction.
However, these subsurface environments are extremely challenging for the development and deployment of sensing technologies because of harsh conditions such as high temperatures, high pressures, corrosive chemical species, and potentially high salinity. In such harsh environments, most electrical and electronic components used in sensor applications are not feasible. Additionally, real-time monitoring of pH within cement is challenging because the high-pH range (pH ~13) can cause stability issues of commonly used pH sensing materials at high temperatures. Therefore, it is essential to develop approaches that provide stable pH sensing and that could eliminate the use of electrical components and connections at the sensing locations and avoid the common mode of failure in conventional sensors.
 

This invention describes novel iron-based catalysts for conversion of carbon dioxide (CO₂) to produce valuable gases such as carbon monoxide (CO) or syngas in the presence of fuel (biomass, coal, methane) for commercial and industrial applications while reducing greenhouse gas emissions. This technology is available for licensing and/or further collaborative research from the U.S. Department of Energy’s National Energy Technology Laboratory.

Challenge
Syngas production from solid fuels such as biomass or coal is commercially conducted via a solid fuel gasification process. However, conventional solid fuel gasification processes are generally capital-intensive and require significant amounts of parasitic energy. Typically, the gasification process involves partial coal combustion with either O₂ or air. When air is utilized, nitrogen (N₂) may enter the syngas, diluting the syngas and making extraction difficult. When oxygen (O₂) is utilized, expensive oxygen production units tend to generate high parasitic losses. As a result, the development of alternative methods for syngas production from solid fuels are a significant area of current interest. For oxygen-based commercial solid fuel gasification, oxygen must be separated from air, which requires an air separation unit. Cryogenic air separation has been used and is very expensive. In addition, steam is also required for the process. Gasification of solid fuel with CO₂ has many advantages over conventional solid fuel gasification with oxygen/steam. 
Syngas production from methane is currently conducted via catalytic steam methane reforming and the process is energy intense with high carbon footprint. Catalytic methane dry reforming using CO₂ to produce syngas has a potential to be more economical route for syngas production.  However, the catalysts used for methane dry reforming are either very expensive or has shown poor performance stability due to catalyst deactivation. Therefore, catalyst development is important for methane dry reforming technology to be commercially viable.
 

This invention describes an improved casting and manufacturing method for a creep-resistant nickel-based superalloy for advanced high-temperature applications. This technology is available for licensing and/or further collaborative research from the U.S. Department of Energy’s National Energy Technology Laboratory.

Challenge
In the future, advanced ultra-supercritical (A-USC) and/or supercritical carbon dioxide (sCO₂) power plants are expected to raise efficiencies of coal-fired power plants from around 35 to greater than 50%. However, these advanced systems feature components that operate at high pressures and temperatures exceeding 760 degrees Celsius. These conditions cause gradual permanent deformation, known as creep, in components manufactured with currently used alloys like ferritic-martensitic high-strength steels and austenitic stainless steels.
Certain nickel-based super alloys such as Inconel 740H (IN740H) currently meet requirements for use in A-USC in a wrought version, but using the alloy in a cast form would be valuable in terms of the range of component size, geometries and complexities, and cost.
Previous efforts at casting IN740H have resulted in poor creep performance when compared to wrought versions. Furthermore, several compositions within the nominal specified range for IN740H have been investigated but failed to provide a material in the as-cast form that would withstand long-term, high temperature exposure in creep.
 

This invention describes a uniquely engineered 2-D amorphous carbon film and a memristor fabricated with coal-derived carbon quantum dots as the dielectric (switching) media for resistive random-access memory (RRAM). The atomic dielectric carbon layer can provide large storage density and 3-D packing ability, allowing memory and logic devices to be integrated in one chip, providing faster data processing with low energy consumption. This patent application is jointly owned by NETL and the University of Illinois-Urbana Champaign (UIUC) and it is available for licensing and/or further collaboration.

Challenge
Memory is essential to future computing with the exponential growth of data. These emerging memory technologies aim to revolutionize the existing memory hierarchy. Various emerging memory technologies are actively being investigated to meet ideal performance characteristics. RRAM has various advantages such as easy fabrication, simple metal-insulator-metal structure, excellent scalability, nanosecond speed, and long data retention. RRAM has been commercialized since 2013. Despite showing great promise over conventional RAM and its popularity in academia, RRAM has not become commercially popular. This is due to high device variability and high operation voltage.

This patent-pending technology establishes a novel system and method for the microwave-assisted dry reforming of methane. The technology is available for licensing and/or further collaborative research from the U.S. Department of Energy’s National Energy Technology Laboratory.

Challenge

Traditional steam reforming of methane to produce hydrogen (H₂), which is then reacted with carbon (CO) to produce methanol and other industrial commodity chemicals, is an extremely energy intensive process with large carbon footprint. For example, the steam reforming reaction produces 10 tons of carbon dioxide (CO₂) for every ton of H₂. Methane dry reforming uses an alternative reaction that uses CO₂ as a soft oxidant to produce CO and H₂ from methane, which can be further processed into methanol or hydrocarbons. Further, using CO₂ to produce commodity chemicals, such as H₂ and CO, can generate revenue to offset carbon capture costs, reduce the carbon footprint of fossil-fuel powered processes, and allow sustainable use of fossil fuel resources.

Traditional dry reforming techniques are extremely energy intensive and require very high temperatures (>800C) that make it unpractical economically compared with the lower-temperature, carbon-positive, methane steam reforming. Microwave-assisted catalysis has been demonstrated as an enabling technology to promote high temperature chemical processes. Unlike traditional thermal heating, microwaves can rapidly heat catalysts to extremely high temperatures without heating the entire reactor volume. This reduces heat management issues of conventional reactors and enables rapid heating/cooling cycles. Ultimately, this can allow reactors to utilize excess renewable energy on an intermittent basis (load follow) to promote traditionally challenging, thermally-driven reactions for on-demand chemical production.

Microwave absorption is a function of the electronic and magnetic properties of the material, and a properly designed catalyst may function as a both a microwave heater and a reactive surface for driving the desired reaction. Microwave absorption is extremely sensitive to the catalyst’s chemical state and electronic structure, and effective catalysts must maintain microwave activity across a wide range of temperatures in both oxidative and reductive environments.