A microporous bismuth-based MOF for efficient separation of acetylene from carbon dioxide.

The separation of acetylene from carbon dioxide is challenging due to their almost identical molecular sizes and volatilities. Metal-organic frameworks (MOFs) in general are strong candidates for the separation of gas mixtures owing to the presence of functional pore surfaces that can selectively capture specific target molecules. Herein, we report a stable and easily synthesized bismuth-based MOF, Bi-BTC, which can achieve the separation of acetylene and carbon dioxide. We performed a detailed analysis of the sorption properties of the Bi-MOF. Bi-BTC shows good adsorption capacities for C2H2 with a capacity of 53.8 cm3 g-1 at 298 K and 1.0 bar, and C2H2/CO2 selectivity of 5.14/7.69 at 298 K and 1.0/0.1 bar. IAST selectivity calculations indicate that Bi-BTC possesses good separation capacity, and dynamic breakthrough experiments were performed to prove the separation of C2H2 and CO2. Bi-MOFs as a group of relatively less studied types of MOFs have interesting adsorption characteristics, and this study on Bi-based MOF will enrich three-dimensional Bi-MOF adsorbents for gas adsorption and separation applications.

A high resolution and wide range valve for micronewton cold gas thrusters.

Numerous scientific satellites require micronewton thrusters for compensating environmental disturbances. The mass flow control proportional valve plays a crucial role in precisely regulating the thrust. To meet the high resolution and wide range requirements of the thrusters, this paper introduces a novel proportional valve with two sets of independently controllable piezoelectric stack. One set of the piezo-stack is used to compensate the stroke loss of the valve core, mainly caused by the deformation of the valve seat. The valve sealing mechanism is carefully analyzed to reduce the stroke loss. Another set of the stack works as the primary actuator, enabling the high mass flow control resolution. Two sets of independently controlled piezoelectric stacks not only expand the range and improve the range ratio but also provide redundancy and enhance reliability. This means that the actuator can still operate at lower ranges even if one piezo-stack is damaged. The piezo-actuators are assembled using U-shaped connectors, creating a compact and space-efficient overall design. Experimental tests have been conducted to verify the performance of the valve, which demonstrated a mass flow range of 0-675 µg/s with a resolution better than 0.1 µg/s and a flow noise below 0.1 µg/s/Hz1/2 at 0.1 mHz-1 Hz.

Investigating temperature-induced torque noise of a torsion pendulum based on temperature modulation at different frequencies.

Torsion pendulums are widely used for the measurement of small forces. In this study, we investigated the impact of temperature fluctuations on a torsion pendulum using heating devices to modulate the environmental temperature at different specific frequencies. The response coefficient between the temperature variation and the torque of the torsion pendulum was found to vary at different frequencies, with values from 4 × 10-15 N mK-1 at 0.1 mHz to 3 × 10-13 N mK-1 at 10 mHz. A passive thermal-insulation system was used to reduce the torque response within this frequency band, which is dominated by temperature noise. The results demonstrate that this modulation method provides a useful way to independently investigate the noise in a torsion pendulum resulting from environmental temperature fluctuations over a wide frequency band.

Immobilization of the Polar Group into an Ultramicroporous Metal-Organic Framework Enabling Benchmark Inverse Selective CO2/C2H2 Separation with Record C2H2 Production.

One-step harvest of high-purity light hydrocarbons without the desorption process represents an advanced and highly efficient strategy for the purification of target substances. The separation and purification of acetylene (C2H2) from carbon dioxide (CO2) by CO2-selective adsorbents are urgently demanded yet are very challenging owing to their similar physicochemical properties. Here, we employ the pore chemistry strategy to adjust the pore environment by immobilizing polar groups into an ultramicroporous metal-organic framework (MOF), achieving one-step manufacture of high-purity C2H2 from CO2/C2H2 mixtures. Embedding methyl groups into prototype stable MOF (Zn-ox-trz) not only changes the pore environment but also improves the discrimination of guest molecules. The methyl-functionalized Zn-ox-mtz thus exhibits the benchmark reverse CO2/C2H2 uptake ratio of 12.6 (123.32/9.79 cm3 cm-3) and an exceptionally high equimolar CO2/C2H2 selectivity of 1064.9 at ambient conditions. Molecular simulations reveal that the synergetic effect of pore confinement and surfaces decorated with methyl groups provides high recognition of CO2 molecules through multiple van der Waals interactions. The column breakthrough experiments suggest that Zn-ox-mtz dramatically achieved the one-step purification capacity of C2H2 from the CO2/C2H2 mixture with a record C2H2 productivity of 2091 mmol kg-1, surpassing all of the CO2-selective adsorbents reported so far. In addition, Zn-ox-mtz exhibits excellent chemical stability under different pH values of aqueous solutions (pH = 1-12). Moreover, the highly stable framework and excellent inverse selective CO2/C2H2 separation performance showcase its promising application as a C2H2 splitter for industrial manufacture. This work paves the way to developing reverse-selective adsorbents for the challenging gas separation process.

Customizing Pore System in a Microporous Metal-Organic Framework for Efficient C2H2 Separation from CO2 and C2H4.

Selective-adsorption separation is an energy-efficient technology for the capture of acetylene (C2H2) from carbon dioxide (CO2) and ethylene (C2H4). However, it remains a critical challenge to effectively recognize C2H2 among CO2 and C2H4, owing to their analogous molecule sizes and physical properties. Herein, we report a new microporous metal-organic framework (NUM-14) possessing a carefully tailored pore system containing moderate pore size and nitro-functionalized channel surface for efficient separation of C2H2 from CO2 and C2H4. The activated NUM-14 (namely NUM-14a) exhibits sufficient pore space to acquire excellent C2H2 loading capacity (4.44 mmol g-1) under ambient conditions. In addition, it possesses dense nitro groups, acting as hydrogen bond acceptors, to selectively identify C2H2 molecules rather than CO2 and C2H4. The breakthrough experiments demonstrate the good actual separation ability of NUM-14a for C2H2/CO2 and C2H2/C2H4 mixtures. Furthermore, Grand Canonical Monte Carlo simulations indicate that the pore surface of the NUM-14a has a stronger affinity to preferentially bind C2H2 over CO2 and C2H4 via stronger C-H···O hydrogen bond interactions. This article provides some insights into customizing pore systems with desirable pore sizes and modifying groups in terms of MOF materials toward the capture of C2H2 from CO2 and C2H4 to promote the development of more MOF materials with excellent properties for gas adsorption and separation.

Two-Dimensional Metal-Organic Framework with Ultrahigh Water Stability for Separation of Acetylene from Carbon Dioxide and Ethylene.

Highly selective separation and purification of acetylene (C2H2) from ethylene (C2H4) and carbon dioxide (CO2) are daunting challenges in light of their similar molecule sizes and physical properties. Herein, we report a two-dimensional (2D) stable metal-organic framework (MOF), NUM-11 ([Cu(Hmpba)2]·1.5DMF) (H2mpba = 4-(3,5-dimethyl-1H-pyrazol-4-yl)benzoic acid), with sql topology, stacked together through π-π interactions for efficient separation of C2H2 from C2H4 and CO2. The 2D-MOF material offers high hydrolytic stability and good purification capacity; especially, it could survive in water for 7 months, even longer. This stable MOF selectively captures C2H2 from mixtures containing C2H4 and CO2, as determined by adsorption isotherms. The ideal adsorbed solution theory selectivity calculations and transient breakthrough experiments were performed to verify the separation capacity. The low isosteric heat of NUM-11a (desolvated NUM-11) (18.24 kJ mol-1 for C2H2) validates the feasibility of adsorbent regeneration with low energy footprint consumption. Furthermore, Grand Canonical Monte Carlo simulations confirmed that the pore surface of the NUM-11 framework enabled preferential binding of C2H2 over C2H4 and CO2 via multiple C-H···O, C-H···π, and C-H···C interactions. This work provides some insights to prepare stable MOF materials toward the purification of C2H2, and the water-stable structure, low isosteric heat, and good cycling stability of NUM-11 make it very promising for practical industrial application.

Cu-NPs@C Nanosheets Derived from a PVP-assisted 2D Cu-MOF with Renewable Ligand for High-Efficient Selective Hydrogenation of 5-Hydroxymethylfurfural.

5-Hydroxymethylfurfural (HMF) containing C=O, C-O, and furan ring functional groups is an important platform chemical derived from C6 sugars. The selective hydrogenation of C=O in HMF produces 2,5-dihydroxymethylfuran (DHMF), which is a potential sustainable substitute for petroleum-based building blocks. Here, 2,5-furandicarboxylic acid (H2 FDC), a promising sustainable alternative to terephthalic acid, was employed as a renewable ligand to synthesize a novel Cu metal-organic framework (Cu-FDC). With a polyvinyl pyrrolidone (PVP)-assisted approach, 2D Cu-FDC nano-lamellae of micrometer lateral dimensions and nanometer thickness could be obtained, which could be used as a precursor to fabricate 2D oxygen-rich carbon nanosheets embedded with Cu nanoparticles (denoted CFP-300) after a thermal treatment at 300 °C under N2 atmosphere. The synthesized CFP-300 exhibited excellent catalytic performance and stability for the selective hydrogenation of HMF to DHMF. These results demonstrated a sustainable route to synthesize efficient catalysts by employing metal-organic frameworks based on renewable ligands.

Pore-Space Partition through an Embedding Metal-Carboxylate Chain-Induced Topology Upgrade Strategy for the Separation of Acetylene/Ethylene.

Ethylene (C2H4) is one of the most significant substances in the petrochemical industry; however, the capture of acetylene (C2H2) in about 1% from C2H2/C2H4 mixtures is a difficult task because of the similarity of their physical properties. With the aggravation of the energy crisis, using metal-organic framework (MOF) materials to purify C2H4 through adsorptive separation is a promising way to save energy and reduce emission. Pore-space partition (PSP) with the aim of enhancing the density of the binding sites and the strength of the host-guest interactions is an effective means to promote a solution for the challenging gas separation problems. Herein, we report a new embedding metal-carboxylate chain-induced topology upgrade strategy within a MOF to realize PSP and separation of C2H2/C2H4 mixtures. As a proof of concept, we construct a microporous MOF (NUM-12) utilizing the in situ insertion of cobalt terephthalic chains into a pretargeted ant-type framework during synthesis. Because of the attainment of an elaborately tuned aperture size and a specific pore environment through this strategy, NUM-12a (activated NUM-12) not only has a remarkable gas sorption capacity and strong interactions for C2H2 but also possesses an excellent purification performance for C2H2/C2H4 mixtures. Both experiments and simulation calculations clearly reveal that NUM-12 is a promising candidate for the separation of C2H2/C2H4, proving the feasibility of this new strategy for developing newly fashioned MOFs with adjustable structure and performance.

Propane-Trapping Ultramicroporous Metal-Organic Framework in the Low-Pressure Area toward the Purification of Propylene.

The propane (C3H8)-trapping adsorption behavior is considered as a potential performance to directly produce high-purity propylene (C3H6). Herein, we report an ultramicroporous Mn-based metal-organic framework (NUM-7) with a reverse C3H8-selective behavior in the low-pressure area. The pore structure of this material possesses more electronegative aromatic benzene rings for the stronger binding affinity to C3H8, and the material shows outstanding reverse ideal adsorbed solution theory (IAST) selectivity values. Single-component sorption isotherms preliminarily show the reverse adsorption behavior in the low-pressure part, and the moderate heat of adsorption further confirms this performance and exhibits less energy consumption for regeneration. In addition, the purification effect for the C3H8/C3H6 mixture is evaluated by the IAST selectivity and transient breakthrough curves, and the GCMC calculation results reveal that the fascinating C3H8-trapping behavior mainly depends on the multiple C-H···π interactions. Moreover, because C3H6 is the desired target product, the interesting C3H8-selective adsorption behavior of NUM-7 may provide its potential for one-step purification of C3H6, and this work can provide the method of developing C3H8-selective materials for the purification of C3H6.

Combined Test of the Gravitational Inverse-Square Law at the Centimeter Range.

Experiments measuring the Newtonian gravitational constant G can offer uniquely sensitive probes of the test of the gravitational inverse-square law. An analysis of the non-Newtonian effect in two independent experiments measuring G is presented, which permits a test of the 1/r^{2} law at the centimeter range. This work establishes the strongest bound on the magnitude α of Yukawa-type deviations from Newtonian gravity in the range of 5-500 mm and improves the previous bounds by up to a factor of 7 at the length range of 60-100 mm.

Influence of the tilt error motion of the rotation axis on the test of the equivalence principle with a rotating torsion pendulum.

Improving the precision of current tests of the equivalence principle with a rotating torsion pendulum requires a more complete analysis of systematic effects. Here, we discuss in detail one of the important systematic effects, the influence from the tilt error motion of the rotation axis of a rotary stage, namely, wandering of the instantaneous rotation axis around its average direction. Its influence on the rotating torsion pendulum is modeled phenomenologically, and the parameters in the model are calibrated. It is shown that the influence can contribute a correction of η ≈ 5 × 10-13 to the equivalence-principle violating parameter for a rotary stage whose tilt error motion of interest is about 31 nrad in magnitude. We also show that such an influence can be reduced to the level of η ≈ 1 × 10-14 by means of active compensation of the tilt error motion using a set of piezoelectric actuators placed under the stage stator.

Efficient Purification of Ethylene from C2 Hydrocarbons with an C2H6/C2H2-Selective Metal-Organic Framework.

The separation of ethylene (C2H4) from C2 hydrocarbons is considered as one of the most difficult and important processes in the petrochemical industry. Heat-driven cryogenic distillation is still widely used in the C2 hydrocarbons separation realms, which is an energy intensive process and takes up immense space. In response to a greener, more energy-efficient sustainable development, we successfully synthesized a multifunction microporous Mg-based MOF [Mg2(TCPE)(µ2-OH2)(DMA)2]·solvents (NUM-9) with C2H6/C2H2 selectivity based on a physical adsorption mechanism, and with outstanding stability; especially, it is stable up to 500 °C under an air atmosphere. NUM-9a (activated NUM-9) shows good performances in the separation of C2H6/C2H2 from raw ethylene gases. In addition, its actual separation potential is also examined by IAST and dynamic column breakthrough experiments. GCMC calculation results indicate that the unique structure of NUM-9a is primarily conducive to the selective adsorption of C2H6 and C2H2. More importantly, compared with C2H4, NUM-9a prefers to selectively adsorb C2H6 and C2H2 simultaneously, which makes NUM-9a as a sorbent have the capacity to separate C2H4 from C2 hydrocarbon mixtures under mild conditions through a greener and energy-efficient separation strategy.

Improvement for Testing the Gravitational Inverse-Square Law at the Submillimeter Range.

We improve the test of the gravitational inverse-square law at the submillimeter range by suppressing the vibration of the electrostatic shielding membrane to reduce the disturbance coupled from the residual surface potential. The result shows that, at a 95% confidence level, the gravitational inverse-square law holds (|α|≤1) down to a length scale λ=48 µm. This work establishes the strongest bound on the magnitude α of the Yukawa violation in the range of 40-350 µm, and improves the previous bounds by up to a factor of 3 at the length scale λ≈70 µm. Furthermore, the constraints on the power-law potentials are improved by about a factor of 2 for k=4 and 5.

Microporous Metal-Organic Framework with a Completely Reversed Adsorption Relationship for C2 Hydrocarbons at Room Temperature.

As a new type of porous material, metal-organic frameworks (MOFs) have been widely studied in gas adsorption and separation, especially in C2 hydrocarbons. Considering the stronger interaction between the unsaturated molecules and the metal sites, and the smaller molecular size of unsaturated molecules, the usual relationship of affinities and adsorption capacities among C2 hydrocarbons in most common MOFs is C2H2 > C2H4 > C2H6. Herein, a unique microporous metal-organic framework, NUM-7a (activated NUM-7), with a completely reversed adsorption relationship for C2 hydrocarbons (C2H6 > C2H4 > C2H2) has been successfully synthesized, which breaks the traditional concept of the adsorption relationship of MOFs for C2 hydrocarbons. Based on this unique adsorption relationship, a green and simple one-step separation purification for a large amount of C2H4 can be expected to be achieved through the selective adsorption of C2H6. In addition, NUM-7a also shows good selectivities in C2H2/CO2 and CO2/CH4.

Precision measurement of the Newtonian gravitational constant.

The Newtonian gravitational constant G, which is one of the most important fundamental physical constants in nature, plays a significant role in the fields of theoretical physics, geophysics, astrophysics and astronomy. Although G was the first physical constant to be introduced in the history of science, it is considered to be one of the most difficult to measure accurately so far. Over the past two decades, eleven precision measurements of the gravitational constant have been performed, and the latest recommended value for G published by the Committee on Data for Science and Technology (CODATA) is (6.674 08 ± 0.000 31) × 10-11 m3 kg-1 s-2 with a relative uncertainty of 47 parts per million. This uncertainty is the smallest compared with previous CODATA recommended values of G; however, it remains a relatively large uncertainty among other fundamental physical constants. In this paper we briefly review the history of the G measurement, and introduce eleven values of G adopted in CODATA 2014 after 2000 and our latest two values published in 2018 using two independent methods.

Combined Search for a Lorentz-Violating Force in Short-Range Gravity Varying as the Inverse Sixth Power of Distance.

Precision measurements of the inverse-square law via experiments on short-range gravity provide sensitive tests of Lorentz symmetry. A combined analysis of data from experiments at the Huazhong University of Science and Technology and Indiana University sets simultaneous limits on all 22 coefficients for Lorentz violation correcting the Newton force law as the inverse sixth power of distance. Results are consistent with no effect at the level of 10^{-12} m^{4}.

Measurements of the gravitational constant using two independent methods.

The Newtonian gravitational constant, G, is one of the most fundamental constants of nature, but we still do not have an accurate value for it. Despite two centuries of experimental effort, the value of G remains the least precisely known of the fundamental constants. A discrepancy of up to 0.05 per cent in recent determinations of G suggests that there may be undiscovered systematic errors in the various existing methods. One way to resolve this issue is to measure G using a number of methods that are unlikely to involve the same systematic effects. Here we report two independent determinations of G using torsion pendulum experiments with the time-of-swing method and the angular-acceleration-feedback method. We obtain G values of 6.674184 × 10-11 and 6.674484 × 10-11 cubic metres per kilogram per second squared, with relative standard uncertainties of 11.64 and 11.61 parts per million, respectively. These values have the smallest uncertainties reported until now, and both agree with the latest recommended value within two standard deviations.

Magnetic effect in the test of the weak equivalence principle using a rotating torsion pendulum.

The high precision test of the weak equivalence principle (WEP) using a rotating torsion pendulum requires thorough analysis of systematic effects. Here we investigate one of the main systematic effects, the coupling of the ambient magnetic field to the pendulum. It is shown that the dominant term, the interaction between the average magnetic field and the magnetic dipole of the pendulum, is decreased by a factor of 1.1 × 104 with multi-layer magnetic shield shells. The shield shells reduce the magnetic field to 1.9 × 10-9 T in the transverse direction so that the dipole-interaction limited WEP test is expected at η ≲ 10-14 for a pendulum dipole less than 10-9 A m2. The high-order effect, the coupling of the magnetic field gradient to the magnetic quadrupole of the pendulum, would also contribute to the systematic errors for a test precision down to η ∼ 10-14.

Test of the Equivalence Principle with Chiral Masses Using a Rotating Torsion Pendulum.

Here we present a new test of the equivalence principle designed to search for the possible violation of gravitational parity using test bodies with different chiralities. The test bodies are a pair of left- and right-handed quartz crystals, whose gravitational acceleration difference is measured by a rotating torsion pendulum. The result shows that the acceleration difference towards Earth Δa_{left-right}=[-1.7±4.1(stat)±4.4(syst)]×10^{-15} m s^{-2} (1-σ statistical uncertainty), correspondingly the Eötvös parameter η=[-1.2±2.8(stat)±3.0(syst)]×10^{-13}. This is the first reported experimental test of the equivalence principle for chiral masses and opens a new way to the search for the possible parity-violating gravitation.

Combined Search for Lorentz Violation in Short-Range Gravity.

Short-range experiments testing the gravitational inverse-square law at the submillimeter scale offer uniquely sensitive probes of Lorentz invariance. A combined analysis of results from the short-range gravity experiments HUST-2015, HUST-2011, IU-2012, and IU-2002 permits the first independent measurements of the 14 nonrelativistic coefficients for Lorentz violation in the pure-gravity sector at the level of 10^{-9} m^{2}, improving by an order of magnitude the sensitivity to numerous types of Lorentz violation involving quadratic curvature derivatives and curvature couplings.