Design of stable adsorbents for selective gold recovery with large capacity and fast adsorption kinetics is of great challenge, but significant for the economy and the environment. Herein, we show the design and preparation of an irreversible amide‐linked covalent organic framework (COF) JNU‐1 via a building block exchange strategy for efficient recovery of gold. JNU‐1 was synthesized through the exchange of 4,4′‐biphenyldicarboxaldehyde (BA) in mother COF TzBA consisting of 4,4′,4′′‐(1,3,5‐triazine‐2,4,6‐triyl)trianiline (Tz) and BA with terephthaloyl chloride. The irreversible amide linked JNU‐1 gave good stability, unprecedented fast kinetics, excellent selectivity and outstanding adsorption capacity for gold recovery. X‐ray photoelectron spectroscopy along with thermodynamic study and quantum mechanics calculation reveals that the excellent performance of JNU‐1 for gold recovery results from the formation of hydrogen bonds C(N)?H???Cl and coordinate interaction of O and Au. The rational design of irreversible bonds as both inherent linkage and functional groups in COFs is a promising way to prepare stable COFs for diverse applications. 相似文献
This work studies the kinetics of living radical polymerization by means of both the nonsteady state approach and the quasi-stationary state method. Expressions for the numberand weight-average degress of polymerization and the polydispersity index were derived. Numerical results show that the concentration of residual initiator seriously influences the polydispersity index of the resulting polymer. The calculated outcomes of the non-steady state approach are evidently different from those of the quasi-stationary state method when the magnitude of the rate constant of termination is comparable with that of the propagation rate constant, and the difference becomes negligible if the rate constant of the termination (kt) is much larger than that of propagation (kp). The polydispersity index of the resulting polymer increases with decreasing ratios of kt to kp or MO to IO (initial concentrations of monomer and initiator). 相似文献
Alkali-activated materials (AAMs) are considered to be alternative cementitious materials for civil infrastructures. Nowadays, efforts have been made in developing AAMs with self-compacting ability. The obtained self-compacting AAMs (SCAAMs) accomplish superior passing and filling properties as well as excellent mechanical and environmental advantages. This work critically revisits recent progresses in SCAAMs including mixture proportions, fresh properties, mechanical strength, microstructure, acid and sulfate resistance, high temperature behaviors, impact resistance and interface shear strength. To facilitate direct comparison and interpretation of data from different publications, mixture proportions were normalized in terms of the content of key reactive components from precursors and activators, and correlation with mechanical behaviors was made. Moreover, special attention was paid to current research challenges and perspectives to promote further investigation and field application of SCAAMs as advanced construction material. 相似文献
Aqueous rechargeable zinc-ion batteries (ZIBs) provide high theoretical capacity, operational safety, low-cost and environmental friendliness for large-scale energy storage and wearable electronic devices, but their future development is plagued by low capacity and poor cycle life due to the lack of suitable cathode materials. In this work, a covalent organic framework (Tp-PTO-COF) with multiple carbonyl active sites is synthesized and successfully introduced in aqueous rechargeable ZIBs for the first time. Tp-PTO-COF delivers high specific capacities of 301.4 and 192.8 mA h g−1 at current densities of 0.2 and 5 A g−1, respectively, along with long-term durability and flat charge–discharge plateaus. The remarkable electrochemical performance is attributed to the abundance of nucleophilic carbonyl active sites, well defined porous structure and inherent chemical stability of Tp-PTO-COF. Moreover, the structural evolution and Zn2+ ion intercalation mechanism are discussed and revealed by the experimental analysis and density functional theory calculations. These results highlight a new avenue to develop organic cathode materials for high performance and sustainable aqueous rechargeable ZIBs.A covalent organic framework (Tp-PTO-COF) with carbonyl active sites was proposed as a novel cathode material and successfully applied in aqueous rechargeable zinc-ion batteries (ZIBs).相似文献
The d-d transition spectrum of Sr[Co(HEDTA)H2O]2 · 4 H2O crystal was recorded at room temperature and experimental results are discussed quantitatively. Using the ligand field theory and the radial wave function of non-free Co(II), the d-d transition energy levels of the title compound were calculated. And the results are seen to be in good agreement with the experimental values. 相似文献
In rolling production, the foil flatness quality is judged by detecting the lateral distribution of the front tension stress. Currently, because of the inaccuracy of the tension control model, there are still many flatness defects in foil rolling production. For the tension stress model of foil rolling, the primary problem is the inaccuracy of the metal lateral flow model. Therefore, based on Fleck’s foil rolling theory, a new model of the lateral displacement in the foil deformation region is established by using the principle of minimum potential energy. Next, a tension stress model is established, which takes the effect of the metal lateral flow into account. Last, using a laboratory 20-high rolling mill as the research object, the finite element model of foil rolling is established, and the accuracy of the new model is demonstrated by comparing the theoretical calculations with the simulation results.
The interactions between Trichoderma reesei cellulase and an anionic surfactant, sodium dodecyl sulfate (SDS), at critical micelle concentration level have been investigated using isothermal titration calorimetry, fluorescence spectroscopy, and circular dichroism. SDS micelles have dual interactions with cellulase: electrostatic at first and then hydrophobic interactions. When the concentration of SDS is smaller than 45.0 mM, SDS micelles cause a partial loss in the hydrolytic activity together with a steep decrease in the -helical content of cellulase. With further increasing the concentration of SDS, however, a re-formation of the -helical structure and a partial recovery of the hydrolytic activity of cellulase induced by SDS micelles are observed. Taken together, these results indicate that SDS micelles exert dual effects on cellulase through binding as both a denaturant and a recovery reagent. 相似文献