supercritical-nitrogen-processing-for-purification-reactive-porous

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials

Supercritical fluid extraction and drying methods are well established in numerous applications for the synthesis and processing of porous materials. ...

Empa, Swiss Federal Laboratories for Materials Science and Technology

Hydrogen uptake was measured for platinum doped superactivated carbon at 296 K where hydrogen spillover was expected to occur. High pressure adsorption measurements using a Sieverts apparatus did not show an increase in gravimetric storage capacity over the unmodified superactivated carbon. Measurements of small samples (∼0.2 g) over long equilibration times, consistent with the reported procedure, showed significant scatter and were not well above instrument background. In larger samples (∼3 g), the hydrogen uptake was significantly above background but did not show enhancement due to spillover; total uptake scaled with the available surface area of the superactivated carbon. Any hydrogen spillover sorption was thus below the detection limit of standard volumetric gas adsorption measurements. Due to the additional mass of the catalyst nanoparticles and decreased surface area in the platinum doped system, the net effect of spillover sorption is detrimental for gravimetric density of hydrogen.

Measurements of hydrogen spillover in platinum doped superactivated carbon.

This paper reports a bottom-up solution-phase process for the preparation of pristine and heteroatom (boron, phosphorus, or nitrogen)-substituted carbon scaffolds that show good surface areas and enhanced hydrogen adsorption capacities and binding energies. The synthesis method involves heating chlorine-containing small organic molecules with metallic sodium at reflux in high-boiling solvents. For heteroatom incorporation, heteroatomic electrophiles are added to the reaction mixture. Under the reaction conditions, micrometer-sized graphitic sheets assembled by 3-5 nm-sized domains of graphene nanoflakes are formed, and when they are heteroatom-substituted, the heteroatoms are uniformly distributed. The substituted carbon scaffolds enriched with heteroatoms (boron ∼7.3%, phosphorus ∼8.1%, and nitrogen ∼28.1%) had surface areas as high as 900 m(2) g(-1) and enhanced reversible hydrogen physisorption capacities relative to pristine carbon scaffolds or common carbonaceous materials. In addition, the binding energies of the substituted carbon scaffolds, as measured by adsorption isotherms, were 8.6, 8.3, and 5.6 kJ mol(-1) for the boron-, phosphorus-, and nitrogen-enriched carbon scaffolds, respectively.

Solution-phase synthesis of heteroatom-substituted carbon scaffolds for hydrogen storage.

Zeolite-templated carbon (ZTC) materials were synthesized, characterized, and evaluated as potential hydrogen storage materials between 77 and 298 K up to 30 MPa. Successful synthesis of high template fidelity ZTCs was confirmed by X-ray diffraction and nitrogen adsorption at 77 K; BET surface areas up to ~3600 m(2) g(-1) were achieved. Equilibrium hydrogen adsorption capacity in ZTCs is higher than all other materials studied, including superactivated carbon MSC-30. The ZTCs showed a maximum in Gibbs surface excess uptake of 28.6 mmol g(-1) (5.5 wt %) at 77 K, with hydrogen uptake capacity at 300 K linearly proportional to BET surface area: 2.3 mmol g(-1) (0.46 wt %) uptake per 1000 m(2) g(-1) at 30 MPa. This is the same trend as for other carbonaceous materials, implying that the nature of high-pressure adsorption in ZTCs is not unique despite their narrow microporosity and significantly lower skeletal densities. Isoexcess enthalpies of adsorption are calculated between 77 and 298 K and found to be 6.5-6.6 kJ mol(-1) in the Henry's law limit.

Zeolite-templated carbon materials for high-pressure hydrogen storage.

A thermodynamic study of the enthalpy of adsorption of methane on high surface area carbonaceous materials was carried out from 238 to 526 K. The absolute quantity of adsorbed methane as a function of equilibrium pressure was determined by fitting isotherms to a generalized Langmuir-type equation. Adsorption of methane on zeolite-templated carbon, an extremely high surface area material with a periodic arrangement of narrow micropores, shows an increase in isosteric enthalpy with methane occupancy; i.e., binding energies are greater as adsorption quantity increases. The heat of adsorption rises from 14 to 15 kJ/mol at near-ambient temperature and then falls to lower values at very high loading (above a relative site occupancy of 0.7), indicating that methane/methane interactions within the adsorption layer become significant. The effect seems to be enhanced by a narrow pore-size distribution centered at 1.2 nm, approximately the width of two monolayers of methane, and reversible methane delivery increases by up to 20% over MSC-30 at temperatures and pressures near ambient.

Anomalous isosteric enthalpy of adsorption of methane on zeolite-templated carbon.

Compounds of interest for chemical hydrogen storage at near ambient conditions are specifically tailored to be relatively unstable and thereby desorb H2 upon heating. Their decomposition must be performed in the absence of impurities to achieve clean dehydrogenation products, which is particularly challenging for an emerging class of microporous complex hydride materials, such as γ-phase Mg(BH4)2, which exhibits high surface area and readily adsorbs (sometimes undesired) molecular species. We present a novel strategy toward the purification of γ-Mg(BH4)2 using supercritical nitrogen drying techniques, (1) showing that clean hydrogen can be released from Mg(BH4)2 under mild conditions and (2) clarifying the origin of diborane among the decomposition products of stable borohydrides, a topic of critical importance for the reversibility and practical applicability of this class of hydrogen storage compounds. This technique is also widely applicable in the pursuit of the high-purity synthesis of other porous, reactive compounds, an exciting future class of advanced functional materials.

Nicholas P. Stadie

Hydrogen and Energy Laboratory

Empa, Swiss Federal Laboratories for Materials Science and Technology

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials

Nicholas P. Stadie

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Hydrogen and Energy Laboratory

Empa, Swiss Federal Laboratories for Materials Science and Technology

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials

Hydrogen and Energy Laboratory