Effect of time, temperature, and kinetics on the hysteretic adsorption-desorption of H2, Ar, and N2 in the metal-organic framework Zn2(bpdc)2(bpee)

The intriguing hysteretic adsorption-desorption behavior of certain microporous metal-organic frameworks (MMOFs) has received considerable attention and is often associated with a gate-opening (GO) effect. Here, the hysteretic adsorption of N(2) and Ar to Zn(2)(bpdc)(2)(bpee) (bpdc = 4,4'-biphenyldicarboxylate; bpee = 1,2-bipyridylethene) shows a pronounced effect of allowed experimental time at 77 and 87 K. When the time allowed is on the order of minutes for N(2) at 77 K, no adsorption is observed, whereas times in excess of 60 h is required to achieve appreciable adsorption up to a limiting total coverage. Given sufficient time, the total uptake for N(2) and Ar converged at similar reduced temperatures, but the adsorption of Ar was significantly more rapid than that of N(2), an observation that can be described by activated configurational diffusion. N(2) and Ar both exhibited discontinuous stepped adsorption isotherms with significant hysteresis, features that were dependent upon the allowed time. The uptake of H(2) at 77 K was greater than for both N(2) and Ar but showed no discontinuity in the isotherm, and hysteretic effects were much less pronounced. N(2) and Ar adsorption data can be described by an activated diffusion process, with characteristic times leading to activation energies of 6.7 and 12 kJ/mol. Fits of H(2) adsorption data led to activation energies in the range 2-7 kJ/mol at low coverage and nonactivated diffusion at higher coverage. An alternate concentration-dependent diffusion model is presented to describe the stepwise adsorption behavior, which is observed for N(2) and Ar but not for H(2). Equilibrium is approached very slowly for adsorption to molecularly sized pores at low temperature, and structural change (gate opening), although it may occur, is not required to explain the observations.     

Generation of minimal protein identifiers of proteins from two-dimensional gels and recombinant proteins

We describe the technical feasibility and methodology to characterize a protein by a minimal set of structural information generated by matrix assisted laser desorption/ionization (MALDI)-mass spectrometry, termed a "minimal protein Identifier" (MPI). MPIs can be determined for proteins from two-dimensional gels and recombinant proteins and can be used to compare and identify proteins from these sources.     

Combined hydrogen production and storage with subsequent carbon crystallization

We provide evidence of low-temperature hydrogen evolution and possible hydrogen trapping in an anthracite coal derivative, formed via reactive ball milling with cyclohexene. No molecular hydrogen is added to the process. Raman-active molecular hydrogen vibrations are apparent in samples at atmospheric conditions (300 K, 1 bar) for samples prepared 1 year previously and stored in ambient air. Hydrogen evolves slowly at room temperature and is accelerated upon sample heating, with a first increase in hydrogen evolution occurring at approximately 60 degrees C. Subsequent chemical modification leads to the observation of crystalline carbons, including nanocrystalline diamond surrounded by graphene ribbons, other sp2-sp3 transition regions, purely graphitic regions, and a previously unidentified crystalline carbon form surrounded by amorphous carbon. The combined evidence for hydrogen trapping and carbon crystallization suggests hydrogen-induced crystallization of the amorphous carbon materials, as metastable hydrogenated carbons formed via the high-energy milling process rearrange into more thermodynamically stable carbon forms and molecular hydrogen.     

Design of high pressure differential volumetric adsorption measurements with increased accuracy

High pressure adsorption measurements for light gases on volumetric equipment are prone to error. Differential units reduce the sensitivity to leakage, gas compressibility, and temperature gradients, but remain highly sensitive to volume uncertainties, the calibration of which is difficult in the presence of low-density, microporous samples. Calibration error can be reduced using a high initial pressure differential and large calibration volume; however, systematic error is prevalent in the literature. Using both analytical and multivariate error analysis, we demonstrate that calibration of the differential unit with the differential pressure transducer significantly decreases volume sensitivity. We show that hydrogen adsorption to GX-31 superactivated carbon at 298 K and 80 bar can be measured with a 7 % error in measurement (i.e. within 0.05 wt% for a 100 mg sample), even when experimental volume calibration is determined only within ~1 %. This represents approximately a 2–7 fold increase in sensitivity relative to previous reports using differential measurements. We also provide a framework for optimizing the design of a volumetric adsorption unit. For virtually any system design, the improved differential methods offer a significant increase in precision relative to the conventional volumetric measurement (from 10- to over 250-fold, depending on the precision of the pressure transducer). This improvement further enhances advantages of the differential unit, in addition to advantages that arise for treating gas compressibility and temperature fluctuations.