Surface Of Skeleton Research Articles

Fabrication cellulose/epoxy sponge via surface embedding for efficient and continuously oil/water separation

Discharging oily waste into environment have caused sever water, soil and air pollution. Mechanical compressible polymeric sponges show great potential in oil/water separation through adsorbing/filtering. However, most of these developed sponges were intermittent/manually in oil/water separation and the fabrication always complex. Herein, we developed superwetting sponge by embedding a handful amount of cellulose at the surface of sponge skeleton and delivered excellent mechanical elasticity and robustness. The cellulose/epoxy sponge (embedding 0.33 w% cellulose) can be compressed to 60 % strain with 60 kPa stress and returned to its original shape after 50 times cyclic strain-stress tests. Increasing the embedding amount generated adverse effects on mechanical elasticity and porosity. The as-fabricated cellulose/epoxy sponge showed high separation efficiency (94–99 %) on various oil/water mixtures and showed stable cyclic separation efficiency (>94 %). The optimized cellulose/epoxy sponge was placed into designed separator to separate dispersed oils showing satisfactory total organic carbon removal efficiency (56.63 %) and the inject flow rate showed adverse effects on separation efficiency. Surface embedding is feasible for fabrication mechanical elastic and robust superwetting sponge. The sponge separator showed high separation efficiency of dispersed oil indicating the great of potential polymeric sponge in practical application.

Facile In Situ Building of Sulfonated SiO2 Coating on Porous Skeletons of Lithium-Ion Battery Separators.

Polyolefin separators with worse porous structures and compatibilities mismatch the internal environment and deteriorate lithium-ion battery (LIB) combination properties. In this study, a sulfonated SiO2 (SSD) composited polypropylene separator (PP@SSD) is prepared to homogenize pore sizes and in situ-built SSD coatings on porous skeletons. Imported SSD uniformizes pore sizes owing to centralized interface distributions within casting films. Meanwhile, abundant cavitations enable the in situ SSD coating to facilely fix onto porous skeleton surfaces during separator fabrications, which feature simple techniques, low cost, environmental friendliness, and the capability for continuous fabrications. A sturdy SSD coating on the porous skeleton confines thermal shrinkages and offers a superior safety guarantee for LIBs. The abundant sulfonic acid groups of SSD endow PP@SSD with excellent electrolyte affinity, which lowers Li+ transfer barriers and optimizes interfacial compatibility. Therefore, assembled LIBs give the optimal C-rate capacity and cycling stability, holding a capacity retention of 82.7% after the 400th cycle at 0.5 C.

Different bacterial communities of the coral area and its surrounding sediments in Daya Bay, South China Sea

Sediment in coral reef habitats has a tight interaction with coral reefs. Bacterial communities are a critical part of sediments and play a vital role in marine ecosystems, as well as coral reef habitats. To determine whether the bacterial structure of sediments differs between the inside and surrounding coral area, we compared the bacterial community on the surface of the dead coral skeleton (CS) and three soft sediment sites (SS, SS10, SS50) in and around the coral reef distribution of Dalajia Island in Daya Bay. Our results showed that bacterial diversity and composition of the coral skeleton had a significant difference with that of surrounding soft sediments. Proteobacteria and Actinobacteria were dominant in CS, and Proteobacteria and Bacteroidetes were dominant in SS, SS10, and SS50. Substrate type and environmental parameters are the main factors in the separation between coral skeletons and sediment. Salinity and pH were largely negatively correlated with CS, indicating they are primary factors that potentially impact coral mortality and revival. Heavy metals were positively related to sediments and they are potential threats to coral growth. Our work provides updated data on bacterial structure in the coastal coral area, contributing to policy-making and management of coastal activities to minimize the degradation of coral reefs.

Synthesis of MoS2/Co9S8@CoNC by impregnation and calcination for highly efficient lithium-O2 batteries

The activity of electro-catalyst on oxygen cathode is a key factor affecting the property of lithium-O2 batteries (LOBs). In this work, zeolitic imidazolate framework (ZIF–67) was impregnated in (NH4)2MoS4 solution, and then through centrifugation and calcination, nano-MoS2 and Co9S8 were grown on the surface of CoNC skeleton. The composite has mesoporous structure and abundant active groups such as Co, Co9S8, Co-N bond, Mo-N bond and active edges of MoS2 with sulfur vacancies. The coating of ultra-thin MoS2 nanosheets can improve the stability of CoNC skeleton. The Mo component induces the transformation of amorphous carbon of CoNC to graphitic carbon during calcination in order to improve conductivity of the composite. This study shows that MoS2/Co9S8@CoNC is good electro-catalyst for O2 reduction and evolution reactions (ORR/OER). The LOBs with MoS2/Co9S8@CoNC oxygen cathode show high specific discharge capacity (18162 mA h g−1) and good cycle performance (304 cycles).

Preparation and size control of epoxy resin multilevel structures with SiO2 particles

In the process of preparing porous epoxy materials using reaction-induced phase separation (RIPS), the introduction of an appropriate amount of SiO2 particles enables the control of the phase separation behavior of the system and its ultimate phase structure. This study examined the role of SiO2 particles in the preparation and size control of epoxy resin multilevel structures by analyzing the phase separation and reaction kinetics in an epoxy resin blend system and characterizing the ultimate phase structure. It was found that fumed SiO2 particles (0–3 wt%) added to the DGEBA/DDCM/PEG200 blends resulted in significant interfacial stabilization, delaying phase separation. With an increase in the fumed SiO2 particle content, the phase structure stopped evolving at an earlier stage of phase separation. In addition, the fumed SiO2 particles dispersed in the porogen-enriched phase helped to stabilize the system, i.e., preventing or slowing down the segregation and aggregation of the components in the system, which may inhibit secondary phase separation in the porogen-enriched phase. When 350 nm SiO2 particles were used, an increase in the particle size resulted in a larger phase structure. The SiO2 particles were dispersed within the pore-forming agent phase, increasing the proportion of the pore-forming agent and exerting an occupancy effect, which diminished with decreasing SiO2 particle size and increasing hydrophobicity. Notably, the surface of the epoxy porous material skeleton was decorated with small pits formed by the acid etching of the SiO2 particles, and this multilevel structure contributed to the specific surface area. The multilevel structure can be precisely controlled by adjusting the size, content, and wettability of the SiO2 particles. The results of this study are universal and instructive for the preparation of porous materials using a phase separation method in combination with solid particles.

Enhancing Li+ transfer efficiency and strength of PEO-based composite solid electrolyte for long stable cycling of all-solid-state lithium metal batteries

The metal-organic frameworks (Zeolitic imidazolate framework-67, ZIF-67) were in-situ grown on the cellulose skeleton surfaces which are rich in hydroxyl groups, and combined with PEO-based electrolytes to form composite solid electrolytes (CSEs). The assembled Li/CSEs/Li exhibit an ultra-long cycle life (>2000 h, 50 °C; >2500 h, 30 °C) and excellent lithium-ion transference efficiency (tLi+ = 0.46) at 50 °C. This work provides a new pathway for the development of high-safety and low-cost all-solid-state batteries.

Hydrophilicity and Pore Structure Enhancement in Polyurethane/Silk Protein-Bismuth Halide Oxide Composite Films for Photocatalytic Degradation of Dye.

Polyurethane/silk protein-bismuth halide oxide composite films were fabricated using a blending-wet phase transformationin situsynthesis method. The crystal structure, micromorphology, and optical properties were conducted using XRD, SEM, and UV-Vis DRS characterize techniques. The results indicated that loaded silk protein enhanced the hydrophilicity and pore structure of the polyurethane composite films. The active species BiOX were observed to grow as nanosheets with high dispersion on the internal skeleton and silk protein surface of the polyurethane-silk protein film. The photocatalytic efficiency of BiOX/PU-SF composite films was assessed through the degradation of Rhodamine B under visible light irradiation. Among the tested films, the BiOBr/PU-SF composite exhibited the highest removal rate of RhB at 98.9%, surpassing the removal rates of 93.7% for the BiOCl/PU-SF composite and 85.6% for the BiOI/PU-SF composite. Furthermore, an active species capture test indicated that superoxide radical (•O2-) and hole (h+) species played a predominant role in the photodegradation process.

In Situ Loading of Ni3ZnC0.7 Nanoparticles with Carbon Nanotubes to 3D Melamine Sponge Derived Hollow Carbon Skeleton toward Superior Microwave Absorption and Thermal Resistance.

The simple and low-cost construction of a 3D network structure is an ideal way to prepare high-performance electromagnetic wave (EMW) absorption materials. Herein, a series of carbon skeleton/carbon nanotubes/Ni3ZnC0.7 composites (CS/CNTs/Ni3ZnC0.7) are successfully prepared by in situ growth of Ni3ZnC0.7 and CNTs on 3D melamine sponge carbon. With the increase ofprecursor, Ni3ZnC0.7 nanoparticles nucleate and catalyze the generation of CNTs on the surface of the carbon skeleton. The minimum reflection loss (RL) value of the S60min composite (loading time of 60 min) reaches -86.6dB at 1.6mm and effective absorption bandwidth (EAB, RL≤-10dB) is up to 9.3GHz (8.7-18GHz). The 3D network sponge carbon with layered micro/nanostructure and hollow skeleton promotes multiple reflection and absorption mechanisms of incident EMW. The N-doping and defects can be equivalent to an electric dipole, providing dipole polarization to increase dielectric relaxation. The uniform Ni3ZnC0.7 nanoparticles and CNTs play a key role in dissipating electromagnetic energy, blocking heat transfer, and enhancing the mechanical properties of the skeleton. Fortunately, the composite displays a quite low thermal conductivity of 0.09075Wm·K-1 and good flexibility, which can provide insulation and quickly recover to its original state after being stressed.

300 million years apart: the extreme case of macromorphological skeletal convergence between deltocyathids and a turbinoliid coral (Anthozoa, Scleractinia).

The integration of morphological and molecular lines of evidence has enabled the family Deltocyathidae to be erected to accommodate Deltocyathus species that were previously ascribed to the family Caryophylliidae. However, although displaying the same morphological characteristics as other species of Deltocyathus , molecular data suggested that D. magnificus was phylogenetically distant from Deltocyathidae, falling within the family Turbinoliidae instead. To elucidate the enigmatic evolutionary history of this species and skeletal microstructural features, the phylogenetic relationships of Deltocyathidae and Turbinoliidae were investigated using nuclear ultraconserved and exon loci and complete mitochondrial genomes. Both nuclear and mitochondrial phylogenomic reconstructions confirmed the position of D. magnificus within turbinolids. Furthermore, a novel mitochondrial gene order was uncovered for Deltocyathidae species. This gene order was not present in Turbinoliidae or in D. magnificus that both have the scleractinian canonical gene order, further indicating the taxonomic utility of mitochondrial gene order. D. magnificus is therefore formally moved to the family Turbinoliidae and accommodated in a new genus (Dennantotrochus Kitahara, Vaga & Stolarski, gen. nov.). Surprisingly, turbinolids and deltocyathids do not differ in microstructural organisation of the skeleton that consists of densely packed, individualised rapid accretion deposits and thickening deposits composed of fibres perpendicular to the skeleton surface. Therefore, although both families are clearly evolutionarily divergent, macromorphological features indicate a case of skeletal convergence while these may still share conservative biomineralisation mechanisms. ZooBank: urn:lsid:zoobank.org:pub:5F1C0E25-3CC6-4D1F-B1F0-CD9D0014678E.

Rational Design of Nanosheet Array-Like Layered-Double-Hydroxide-Derived NiCo2O4 In Situ Grown on Reduced-Graphene-Oxide-Coated Nickel Foam for High-Performance Solid-State Supercapacitors.

The investigation of high-performance supercapacitors is essential for accelerating the development of energy storage devices. In this work, a 3D hierarchical nanosheet array-like nickel cobaltite/reduced graphene oxide/nickel foam composite (NiCo2O4/rGO/NF) was assembled via an aqueous coprecipitation-hydrothermal strategy assisted by citric acid. Benefiting from a NiCo layered-double-hydroxide precursor with an atomic-level lattice confinement effect of metal ions and effective hybridization with rGO, the NiCo2O4/rGO/NF composite is featured as thin NiCo2O4 nanosheets (∼113.6 nm × 11.2 nm) composed of NiCo2O4 nanoparticles (∼10.9 nm) vertically staggered on the surface of a rGO-modified NF skeleton, leading to high surface area, abundant mesoporous structure, and active site exposure. The as-obtained NiCo2O4/rGO/NF was directly used as a binder-free integrated electrode for supercapacitors, achieving an excellent specific capacitance of 2863.4 F g-1 (1503.3 C g-1) at 1 A g-1, a superior rate performance of 2335.2 F g-1 at 20 A g-1, and a stability retention of 91.7% after 5000 cycles. More impressively, a solid-state asymmetric supercapacitor assembled by the present NiCo2O4/rGO/NF integrated electrode as the positive electrode and commercial activated carbon as the negative electrode achieved a high energy density of 69.2 Wh kg-1 at a power density of 800 W kg-1, and the energy density at a peak power density of 20004 W kg-1 still remained at 48.9 Wh kg-1, also showing a good cycling stability of 87.2% retention over 10000 cycles. The present facile synthesis strategy of the as-obtained NiCo2O4/rGO/NF nanosheet array composite can be used for the design and construction of many other transition-metal oxide/graphene/NF composite materials with excellent structural stability and performance in energy storage and other related areas.

Structural control and mechanical properties optimization of porous SiC foams with three-dimensional network structure

In this paper, a new process for preparing porous SiC foam with three-dimensional network structure is presented. A certain thickness of SiC coating is deposited on the surface of ultra-light carbon skeleton by CVD process, so as to achieve effective control of its structure and mechanical properties. The effects of CVD deposition time on the density, porosity and skeleton thickness rates of SiC foams were explored. By increasing the CVD deposition time, the structure of SiC foams can be effectively regulated, and the mechanical properties of SiC foams can be significantly improved. The porosity of the prepared SiC foam can be adjusted in a wide range (26.9%∼94.68%). When the density of SiC foam increases from 0.67 g/cm3 to 2.36 g/cm3, its bending strength increases from 27.4 MPa to 136.9 MPa, which is significantly improved. After high temperature oxidation treatment (800–1200 °C), the mechanical properties of SiC foam will be further improved. However, when the oxidation temperature reaches 1400 °C, its mechanical properties will be reduced. This research provides a new idea for the preparation of high-performance porous SiC ceramics, and lays a foundation for its structural design, manufacture and application.

Simultaneous manipulation of constituent and structure toward MOFs-derived hollow Co3O4/Co/NC@MXene microspheres via pyrolysis strategy for high-performance microwave absorption

The development of microwave absorbing materials with high performance is one of the effective strategies to solve the increasingly serious electromagnetic pollution problem, and has received the attention of researchers. Herein, the structure and composition manipulation of Ti3C2Tx MXene and MOFs derivatives are investigated. It is found that the TiO2 produced by oxidation of Ti3C2Tx MXene, as a low dielectric material, can effectively solve the impedance mismatch caused by the high conductivity of Ti3C2Tx MXene. Additionally, MOFs derivatives with excellent dielectric-magnetic properties are often obtained by high temperature pyrolysis, which also aids in the oxidation of Ti3C2Tx MXene. Here, we successfully synthesized ZIF-67 nanoparticles on the surface of a three-dimensional spherical skeleton supported by Ti3C2TX MXene nanosheets through template method and electrostatic self-assembly, and obtained Co3O4/Co/NC@MXene microspheres with an obvious hollow structure after one-step pyrolysis. This magnetic carbon heterostructure could effectively optimize the impedance matching and achieve efficient microwave absorption. The HCCM-800 sample had a minimum reflection loss value of −71.60 dB with thickness of 2.25 mm and a maximum effective absorption bandwidth achieved 5.14 GHz at 1.85 mm. Meanwhile, the radar cross section (RCS) simulation revealed that the HCCM-800 sample’s RCS reduction value could reach 20.2 dBm2 at 0° incidence angle. It is believed that this research will pave the way for further vigorous development in the field of microwave absorption.

Highly efficient solar-thermal-electric conversion based on asymmetric binary-architecture design in solid-solid composite phase change materials

The application of phase change materials (PCMs) in solar-thermal conversion is largely limited by the inherently inferior thermal conductivity (TC) and poor solar-thermal energy transition capacity of PCMs. Herein, 1,1,1-tri(hydroxymethyl)ethane@melamine foam/cellulose nanofiber/graphene nanoplate (TME@MCGx) shape-stable composite PCMs (ss-CPCMs) are prepared by encapsulating TME into MCGx aerogels. Profited by the effective heat-conducting MCG25 networks, the resulting TME@MCG25 ss-CPCM achieves high TC of 0.73 Wm-1k−1 for internal heat conduction. Meanwhile, the combination of surface photothermal etching and hydrophobic polydimethylsiloxane (PDMS) coating endows the obtained T-TME@MCG25 highly efficient solar-thermal conversation efficiency of 93.1 %, arising from the exposed 3D MCG25 skeletons for absorbing sunlight and the thin PDMS layer for preventing the absorbed solar-thermal energy from radiating and dissipating. Consequently, the solar-thermal-electric (STE) conversion system equipped with T-TME@MCG25 generates the prominent output voltage of 213.0 mV and current of 37.6 mA. Furthermore, the acquired T-TME@MCG25 exhibits remarkable hydrophobicity and self-cleaning performances, due to the micro-nano structures of MCGx skeleton surfaces and the low surface energy of PDMS coating. The design strategy of asymmetric binary-architecture containing 3D photothermal absorption layer and water repellency layer provides a valuable insight into STE energy conversion associated with hydrophobic ss-CPCMs, which can alleviate the looming energy crisis.

Cation-induced Ti3C2Tx MXene@melamine sponge aerogels with large layer spacing and high strength for high-performance supercapacitors

The self-assembled aerogels are considered as an efficient strategy to address the aggregation and restacking of Ti3C2Tx MXene nanosheets for high-performance supercapacitors. However, the low mechanical strength of the MXene aerogel results in the structural collapse of the self-standing supercapacitor electrode materials. Herein, a low-cost melamine sponge (MS) absorbed different cations (H+, K+, Mg2+, Fe2+, Co2+, Ni2+ and Al3+), serves as a carrier and crosslinker for loading MXene hydrogel induced by the absorbed cations on the skeleton surface and the pores of MS, resulting in the high loading mass MXene aerogels with high mechanical strength. The experimental results show that the Mg-Ti3C2Tx@MS aerogel exhibits the maximum area capacitance of 702.22 mF cm−2 at 3 mA cm−2, and the area capacitance is still 603.12 mF cm−2 even at 100 mA cm−2, indicating the high rate capability with a capacitance retention of 85.89 %. It is worth noting that the constructed asymmetric supercapacitor with activated carbon achieves high energy densities of 104.53 μWh cm−2 and 93.87 μWh cm−2 at 800 μW cm−2 and 7999 μW cm−2, respectively. Furthermore, the asymmetric supercapacitor shows the high cycling stability with 90.2 % capacity retention after 10,000 cycles. This work provides a feasible strategy to prepare Ti3C2Tx MXene aerogels with large layer spacing and high strength for high-performance supercapacitors.

Efficient synthesis of DHA/EPA-rich phosphatidylcholine using immobilized phospholipase A1 on a novel microflow support

A new epoxy-based polymerizing/compositing synchronic process was carried out in 3D structure of a melamine sponge. The cured polymer formed a porous and wave-shaped coating on the surface of skeleton in a uniform way. The obtained composite sponge was used as a microflow support for the immobilization of phospholipase A1 (PLA1, from Thermomyces lanuginosus/Fusarium oxysporum) by co-adsorption/cross-linking with polyethylenimine (PEI). The loading amount and the specific activity of immobilized PLA1 under the optimal immobilization conditions were 45.7 mg/gsupport and 9.1 U/mgprotein. The PLA1-immobilized microflow supports were placed in a columnar reactor, in which transesterification was operated in continuous circulation way. The reaction produced DHA/EPA-incorporated phosphatidylcholine, the hydrolysis side reaction could be inhibited by removal of free water in the reaction medium. Under optimized conditions the incorporation percentage of DHA/EPA and PC yield of 54.3% and 82.4% within 18 h at 55 ℃, respectively. After 10 cycles, the immobilized PLA1 retained 71.2% of the original activity. The use of microflow support has an advantage on easier scaling up the reactor size towards much larger productivity and higher efficiency.

Myriad Mapping of nanoscale minerals reveals calcium carbonate hemihydrate in forming nacre and coral biominerals

Calcium carbonate (CaCO3) is abundant on Earth, is a major component of marine biominerals and thus of sedimentary and metamorphic rocks and it plays a major role in the global carbon cycle by storing atmospheric CO2 into solid biominerals. Six crystalline polymorphs of CaCO3 are known—3 anhydrous: calcite, aragonite, vaterite, and 3 hydrated: ikaite (CaCO3·6H2O), monohydrocalcite (CaCO3·1H2O, MHC), and calcium carbonate hemihydrate (CaCO3·½H2O, CCHH). CCHH was recently discovered and characterized, but exclusively as a synthetic material, not as a naturally occurring mineral. Here, analyzing 200 million spectra with Myriad Mapping (MM) of nanoscale mineral phases, we find CCHH and MHC, along with amorphous precursors, on freshly deposited coral skeleton and nacre surfaces, but not on sea urchin spines. Thus, biomineralization pathways are more complex and diverse than previously understood, opening new questions on isotopes and climate. Crystalline precursors are more accessible than amorphous ones to other spectroscopies and diffraction, in natural and bio-inspired materials.

Non-contact humidity monitoring: Boosting the performance of all-printed humidity sensor using PDDA-modified Ti3C2Tx nanoribbons

Non-contact humidity monitoring can provide us with rich information about our bodies in a non-invasive way. However, this concept is hindered by the low sensitivity and slow response time of conventional humidity sensors. Herein, we employed two strategies, structural design and surface modification of MXene materials, to improve the sensitivity of MXene-based humidity sensors. A 3D porous structure was formed by the alkalinization treatment MXene, which facilitated rapid diffusion of water molecules along interlayer nanochannels and fast electron transport. Furthermore, the charged positively poly (diallyldimethylammonium chloride) (PDDA) was adsorbed onto the surface of the 3D skeleton through self-assembly to prepare a novel composite material KPMX. The loaded PDDA enhanced the interaction between MXene and water molecules, reducing the oxidation sensitivity of MXene. Additionally, the material was further formulated as inks with suitable viscosity and successfully used to produce a paper-based flexible humidity sensor through screen printing. Consequently, the KPMX sensor exhibited impressive potential in humidity sensing with high sensitivity (48813 %), rapid response/recovery time (8.794/2.656 s), and excellent stability. This work provided a practical strategy for non-contact humidity monitoring, including detecting the proximity of fingertips and changes in humidity in breathing patterns.

Built-In Electric Field Boosted Overall Water Electrolysis at Large Current Density for the Heterogeneous Ir/CoMoO4 Nanosheet Arrays.

Advanced bifunctional electrocatalysts are essential for propelling overall water splitting (OWS) progress. Herein, relying on the obvious difference in the work function of Ir (5.44eV) and CoMoO4 (4.03eV) and the constructed built-in electric field (BEF), an Ir/CoMoO4/NF heterogeneous catalyst, with ultrafine Ir nanoclusters (1.8±0.2nm) embedded in CoMoO4 nanosheet arrays on the surface of nickel foam skeleton, is reported. Impressively, the Ir/CoMoO4/NF shows remarkable electrocatalytic bifunctionality toward hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), especially at large current densities, requiring only 13 and 166mV to deliver 10 and 1000mAcm-2 for HER and 196 and 318mV for OER. Furthermore, the Ir/CoMoO4/NF||Ir/CoMoO4/NF electrolyzer demands only 1.43 and 1.81V to drive 10 and 1000mAcm-2 for OWS. Systematical theoretical calculations and tests show that the formed BEF not only optimizes interfacial charge distribution and the Fermi level of both Ir and CoMoO4, but also reduces the Gibbs free energy (ΔGH*, from 0.25 to 0.03eV) and activation energy (from 13.6 to 8.9kJmol-1) of HER, the energy barrier (from 3.47 to 1.56eV) and activation energy (from 21.1 to 13.9kJmol-1) of OER, thereby contributing to the glorious electrocatalytic bifunctionality.

Zeolitic Imidazole Framework (ZIF)-Sponge Composite for Highly Efficient U(VI) Elimination.

Herein, a zeolitic imidazole framework (ZIF-67) composite was prepared by a rapid, simple and inexpensive situ hybridization technique applying polyurethane sponge (PU) as support, which was designated as ZIF-67-PU. The ZIF-67 nanoparticle was successfully supported on the surface of sponge skeletons mainly through electrostatic attraction as well as probable π-π stacking interactions with PAM modification of the sponge. The resultant ZIF-67-PU exhibited a remarkably enhanced U(VI) elimination capacity of 150.86 mg∙g-1 on the basis of the Langmuir isotherm model, in comparison to pristine sponge. Additionally, the mechanism for U(VI) elimination was mainly achieved through the complex reaction between C-N(H)/-OH groups in ZIF-67 and U(VI), based on XPS investigations. ZIF-67-PU represents a simple, feasible and low-cost disposal option for preparing ZIF-coated sponges of any shape that can enhance the U(VI) elimination capacity. Furthermore, this approach can be widely applied to the preparation of various kinds of MOF-sponges through this situ hybridization technique.

Facilitate the preparation of naturally modified and self-healing superhydrophobic/superoleophilic biochar-based foams for efficient oil-water separation

Oil spills are sudden, complex, and long-term hazardous, and the existing adsorption materials still have the disadvantages of small selective adsorption capacity, easy secondary contamination, and difficult to repair after breakage in practical applications. Herein, melamine foam (MF) coated by ball milled biochar (BMBC) and natural beeswax (Wax@BMBC@MF) was prepared by a bio-inspired functionalization method and further added with self-healing function (SH-Wax@BMBC@MF) to cope with complex environments, and applied to oil-water separation for oil adsorption. SEM and FTIR results showed that BMBC and natural beeswax nanoparticles successfully encapsulated the smooth surface of the melamine foam skeleton. The loading of natural beeswax increased the foam's ability to absorb oil and organic solvents from 0.6108–1.134 g to 0.850–1.391 g, and the oil-absorbing capacity of the foam remained at 0. 758–1.263 g after being cut by a knife and self-healing. The oil-absorbing capacity of SH-Wax@BMBC@MF remained in the range of 0.936–1.336 g under acid/alkali environment (pH =1–13). The surface functional groups of BMBC improved the surface roughness of the material and strengthen the MF skeleton to adsorb oils and organic solvents by capillary action. The generation of the di-coordinated structure by Fe3+ and catechol group contributed the restoration of SH-Wax@BMBC@MF structure and oil absorption capacity. SH-Wax@BMBC@MF has superiority of superhydrophobic, superoleophilic, self-healing after damage, and environmental friendliness, which provides a promising solution for the treatment of oil spills at sea.