Facile Synthesis of Self-Supported Solid Amine Sorbents for Direct Air Capture.

Conventional usage of tetraethylenepentamine (TEPA) via being supported on porous solid materials for carbon capture is susceptible to oxidative degradation during regeneration cycles. This study reports a novel method to synthesize a TEPA based solid polymer for efficient CO2 removal via direct air capture (DAC). The polymer was obtained through epoxy-amine crosslinking reaction, leading to the transformation of liquid TEPA to a self-supported solid polymer. The synthesis was conducted under ambient conditions via a one-pot process with no waste products, which is aligned with green synthesis. The performance of the solid amine was evaluated in DAC under realistic conditions and compared with TEPA supported on SiO2 and zeolite 13X prepared through the conventional method. The solid TEPA amine exhibited a high CO2 uptake of 6.2 wt.% comparable to the conventional counterparts. More importantly, the solid TEPA amine demonstrated high resistance to oxidation during the accelerated ageing process at 80 °C in air for 24 h, whereas the two supported TEPA samples experienced severe degradation, with zeolite 13X supported TEPA incurring a reduction of 86.5 % in CO2 capturing capacity after the ageing. This work sheds light on the novel usage of TEPA as an efficient solid amine for practical DAC operation.

High-Pressure Gravimetric Measurements for Binary Gas Adsorption Equilibria and Comparisons with Ideal Adsorbed Solution Theory (IAST).

Measurements of gas mixture adsorption equilibria at high pressures are important for assessing actual adsorbent selectivities but are often out of reach, given the challenging nature of the required experiments. Here, we report a high-pressure gravimetric binary gas adsorption equilibrium measurement system based on simultaneous gas density and mixture adsorption measurements in a single gas cell coupled to a magnetic-suspension balance. Compared to traditional techniques which rely on analytical measurements of gas composition, this approach does not require any sampling. Adsorption measurements of two gas mixtures (0.500 N2 + 0.500 CH4 and 0.400 N2 + 0.600 CO2, mole fraction) on a commercially available molecular sieve (NaY, sodium molecular sieve type Y) were carried out in the temperature range 282 to 325 K with a pressure up to 10 MPa. A prediction method for the gas mixture adsorption equilibria in a closed system using the ideal adsorbed solution theory (IAST) model was used to compare the experimental results. For binary mixtures of components with similar adsorption capacities (here N2 and CH4), the system can measure the adsorption equilibria at pressures higher than 1.0 MPa and the result agrees well with the IAST model prediction. For two gases with very different adsorption capacities, the uncertainty in the adsorption equilibrium measurement is much larger. The dominant uncertainty source is the gas density measurement, whose uncertainty could potentially be cut to half if the current titanium sinker is replaced with a sinker made of single-crystal silicon and with a larger volume.

Nitrogen Rejection from Methane via a "Trapdoor" K-ZSM-25 Zeolite.

Nitrogen (N2) rejection from methane (CH4) is the most challenging step in natural gas processing because of the close similarity of their physical-chemical properties. For decades, efforts to find a functioning material that can selectively discriminate N2 had little outcome. Here, we report a molecular trapdoor zeolite K-ZSM-25 that has the largest unit cell among all zeolites, with the ability to capture N2 in favor of CH4 with a selectivity as high as 34. This zeolite was found to show a temperature-regulated gas adsorption wherein gas molecules' accessibility to the internal pores of the crystal is determined by the effect of the gas-cation interaction on the thermal oscillation of the "door-keeping" cation. N2 and CH4 molecules were differentiated by different admission-trigger temperatures. A mild working temperature range of 240-300 K was determined wherein N2 gas molecules were able to access the internal pores of K-ZSM-25 while CH4 was rejected. As confirmed by experimental, molecular dynamic, and ab initio density functional theory studies, the outstanding N2/CH4 selectivity is achieved within a specific temperature range where the thermal oscillation of door-blocking K+ provides enough space only for the relatively smaller molecule (N2) to diffuse into and through the zeolite supercages. Such temperature-regulated adsorption of the K-ZSM-25 trapdoor zeolite opens up a new approach for rejecting N2 from CH4 in the gas industry without deploying energy-intensive cryogenic distillation around 100 K.

Flexible Adsorbents at High Pressure: Observations and Correlation of ZIF-7 Stepped Sorption Isotherms for Nitrogen, Argon, and Other Gases.

Stepped adsorption isotherms with desorption hysteresis were measured for nitrogen, argon, ethane, carbon dioxide, and methane at pressures up to 17 MPa on zeolitic imidazolate framework-7 (ZIF-7) using a gravimetric sorption analyzer. Such stepped sorption isotherms have not been previously reported for nitrogen or argon on ZIF-7, and required the application of pressures as high as 15 MPa to trigger the ZIF-7 structural phase transition at temperatures around 360 K. The stepped hysteretic sorption isotherms measured for carbon dioxide, methane, and ethane were consistent with previous observations reported in the literature. To correlate these stepped hysteretic sorption isotherms, a semi-empirical model was developed by combining a three-parameter Langmuir equation to describe the Type I aspect of the isotherm, with a model designed to describe the temperature-dependent ZIF-7 structural phase transition. Excellent fits of the combined adsorption and desorption branches were achieved by adjusting nine parameters in the temperature-dependent model, with root-mean-square deviations within 2.5 % of the highest measured adsorption capacity. Each parameter of the new semi-empirical model has a physical basis, allowing them to be estimated or compared independently.

Low-field NMR relaxation-exchange measurements for the study of gas admission in microporous solids.

Understanding the uptake and storage of gases by microporous materials is important for our future energy security. As such, we demonstrate here the application of two-dimensional NMR relaxation experiments for probing the admission and corresponding exchange dynamics of methane within microporous zeolites. Specifically, we report low-field (12.7 MHz) 1H NMR relaxation-exchange correlation measurements of methane within commercial LTA zeolites (3A and 4A) at 25 and 35 bar and ambient temperature. Our results demonstrate the clear identification of bulk-pore and pore-pore exchange processes within zeolite 4A, facilitating the calculation and comparison of effective exchange rate dynamics across varying diffusion length scales and gas pressures. Additional data acquired for zeolite 3A reveals the sensitivity of NMR relaxation phenomena to size-exclusive gas admission phenomena, illustrating the potential of benchtop NMR protocols for material screening applications.

Influence of Mineral Composition of Chars Derived by Hydrothermal Carbonization on Sorption Behavior of CO2, CH4, and O2.

The doping of SiO2 and Fe2O3 into hydrochars that were produced by the hydrothermal carbonization of cellulose was studied with respect to its impact on the resulting surface characteristics and sorption behavior of CO2, CH4, and O2. During pyrolysis, the structural order of the Fe-doped char changed, as the fraction of highly ordered domains increased, which was not observed for the undoped and Si-doped chars. The Si doping had no apparent influence on the oxidation temperature of the hydrochar in contrast to the Fe-doped char where the oxidation temperature was reduced because of the catalytic effect of Fe. Both dopants reduced the micro-, meso- and macroporous surface areas of the chars, although the Fe-doped chars had larger meso- and macroporosity than the Si-doped char. However, the increased degree in the structural order of the carbon matrix of the Fe-doped char reduced its microporosity relative to the Si-doped char. The adsorption of CO2 and CH4 on the chars at temperatures between 273.15 and 423.15 K and at pressures up to 115 kPa was slightly inhibited by the Si doping but strongly suppressed by the Fe doping. For O2, however, the Si doping promoted the observed adsorption capacity, while Fe doping also showed an inhibiting effect.

Temperature dependence of adsorption hysteresis in flexible metal organic frameworks.

"Breathing" and "gating" are striking phenomena exhibited by flexible metal-organic frameworks (MOFs) in which their pore structures transform upon external stimuli. These effects are often associated with eminent steps and hysteresis in sorption isotherms. Despite significant mechanistic studies, the accurate description of stepped isotherms and hysteresis remains a barrier to the promised applications of flexible MOFs in molecular sieving, storage and sensing. Here, we investigate the temperature dependence of structural transformations in three flexible MOFs and present a new isotherm model to consistently analyse the transition pressures and step widths. The transition pressure reduces exponentially with decreasing temperature as does the degree of hysteresis (c.f. capillary condensation). The MOF structural transition enthalpies range from +6 to +31 kJ·mol-1 revealing that the adsorption-triggered transition is entropically driven. Pressure swing adsorption process simulations based on flexible MOFs that utilise the model reveal how isotherm hysteresis can affect separation performance.

One-pot generation of mesoporous carbon supported nanocrystalline calcium oxides capable of efficient CO2 capture over a wide range of temperatures.

Ordered mesoporous carbon-supported calcium oxide materials have been rationally synthesized for the first time. Large specific surface area, high content of nanosized calcium oxides can be easily obtained and tuned. The structure, porosity and the particle size evolution as a function of calcium content and carbonization temperature are extensively characterized and well correlated with their CO(2) sorption properties. The composite materials are of significance for CO(2) physisorption at ambient temperatures with high capacity and selectivity over N(2). Meanwhile, the nanocrystalline calcium oxides are highly active for CO(2) chemisorption, with tuneable and high CO(2) capacity at 200-500 °C. An almost complete initial conversion and fast reaction kinetics at a low temperature (450 °C) and low CO(2) pressure can be achieved within minutes. Cyclic stability is also substantially improved due to the confinement effect of the CaO nanoparticles within the mesopores. These materials would be suitable for CO(2) separation over a wide range of temperatures.

Synthesis and morphology control of ZnO nanostructures in microemulsions.

ZnO nanostructures with different morphologies and optical properties were prepared by a simple microemulsion process, and PEG400 was used as a directing agent. The samples were characterized by TEM, XRD, FTIR, and TG-DTA analysis. The XRD spectra indicate that the ZnO crystal has a hexagonal wurtzite structure. Needle-like, columnar, and spherical ZnO samples were synthesized respectively with the increase of PEG400 concentration in Zn(NO(3))(2) solution. TEM images and thermogravimetric analysis reveal that the microemulsion interface and the PEG400 agent have a synergistic effect on the morphology and crystalline size transition of ZnO nanostructures. The optical properties of the samples were investigated by measuring the UV-Vis absorbance spectra at room temperature. All the samples exhibit strong UV absorption at around 365 nm. ZnO products with band gap energies at 3.06, 3.02, 2.95, and 2.85 eV were obtained with 0, 12.5, 25.0, and 50.0% of PEG400 in Zn(NO(3))(2) solution, respectively. The formation mechanism of the ZnO nanostructures was proposed and discussed in detail. The synergistic control of the microemulsion interface and the agent on the growth of crystal nuclei reported here provides an alternative approach for preparation of other well-defined nanostructures.

Effect of oil phase transition on freeze/thaw-induced demulsification of water-in-oil emulsions.

Recently, there has been an increasing interest in the breakage of water-in-oil (W/O) emulsions by the freeze/thaw method. Most of the previous works focused on the phase transition of the water droplet phase. This paper emphasizes the effect of continuous oil phase transition. A series of oils with different freezing points were used as oil phases to produce model emulsions, which were then frozen and thawed. The emulsion whose oil phase froze before the water droplet phase did (OFBW) on cooling was readily demulsified with a dewatering ratio as high as over 80%, but the emulsion whose oil phase did not freeze when the water droplet phase did (NOFBW) was relatively hard to break. The difference in demulsification performance between them resulted from the distinction between their demulsification mechanisms via the analyses of the emulsion stability, emulsion crystallization/melting behaviors, oil phase physical properties, and wettability of the frozen oil phase, etc. For the OFBW emulsion, the first-frozen oil phase was ruptured by the volume expansion of the subsequently frozen droplet phase, and meanwhile, some liquid droplet phase was drawn into the fine gaps/crevices of the frozen oil phase to bridge droplets, which were considered to be essential to the emulsion breakage, whereas for the NOFBW emulsion, the demulsification was attributed to the collision mechanism proposed in our previous work. The findings may provide some criteria for selecting a proper oil phase in the emulsion liquid membrane (ELM) process and then offer an alternative approach to recycle the oil phase for continuous operation. This work may also be useful for emulsion stability against temperature cycling.