In this paper, carbon-matrix-supported copper (Cu) and cobaltous oxide (CoO) nanoparticles were obtained by using coordination polymers (CPs) as a precursor. The aqueous solutions of copper methacrylate (CuMA) and cobalt methacrylate (CoMA) were preferentially prepared, which were then mixed with anhydrous ethanol to fabricate dual metal ion coordination polymers (CuMA/CoMA). After calcination under an argon atmosphere, the Cu-CoO/C nanocomposite was obtained. Scanning electron microscope (SEM) and transmission electron microscope (TEM) showed that the material has banded morphology, and the dual functional nanoparticles were highly dispersed in the carbon matrix. The prepared material was used in a heterogeneous Fenton-like reaction, with the aim of replacing traditional ferric catalysts to solve pH constraints and the mass production of ferric slime. The obtained nanocomposite showed excellent catalytic performance on the degradation of methylene blue (MB) at near-neutral conditions; the discoloration efficiency is about 98.5% within 50 min in the presence of 0.15 mmol/mL H₂O₂ and 0.5 mg/mL catalyst. And good reusability was verified via eight cycles. The plausible pathway for MB discoloration and the possible catalytic mechanism was also proposed.

The compositions of extractants containing xylene (G) and n-heptane (P) recovered and reused in the asphaltene extraction process were determined by densimetry and the extracted asphaltenes were analyzed to study the influence of extractant composition on their elemental, spectral and structural properties. With increasing the number of extraction, the G/P ratio in extractant increases, which dissolves more asphaltenes of higher aromaticity and causes a decrease of asphaltene yield, the polarity and aromaticity in molecular structure of the extracted asphaltenes. Asphaltenes extracted at a higher G/P ratio were found to have less fractions of N and O elements as well as higher fractions of H and S elements, a lower C/H atom ratio and molecular unsaturation. Moreover, they have a smaller fraction of aromatic rings and aromatic carbon ratio, a higher substitution rate on aromatic rings, a higher fraction of alkyl chain and free ends in their average molecular structure. Compared with the base asphalt, asphaltenes’ infrared absorptions generally move towards smaller wave numbers owing to more aromaticity in their molecules and subsequent stronger conjugative and inductive effects. The asphaltenes extracted at a higher G/P ratio have a denser packing of alkyl chains and a looser packing of aromatic rings, according to their spectra of X-ray diffraction.

The urgency of reducing pollution and developing clean energy storage requires efficient photocatalytic hydrogen evolution (PHE) tactics. To improve solar conversion efficiency, it is highly imperative to accelerate the photocarriers separation and transport through materials design. A stable hydrogen evolution photocatalyst based on TpPa-COFs (triformylphloroglucinol phenylenediamine covalent organic frameworks) was developed by a molecular-level design strategy. The study successfully introduced a molecular-scale Ir active site onto the surface of TpPa-COFs via coordination bonds. It verified the structural integrity of TpPa-COFs and the existence of Ir through the basic structural characterizations, such as Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). After the Ir-based coordination compound joining, the absorption edge of TpPa-COF-M1 and TpPa-COF-M2 was extended to 750 nm. The TpPa-COF + M1 exhibited the highest photocatalytic H₂ evolution rate of 662 µmol/h (10 mg catalyst) under visible-light (λ ≥ 420 nm) irradiation. The apparent quantum yield (AQY) of TpPa-COF-M1 is calculated to be 1.9%, 3.8%, 4.8%, 2.8%, 1.8%, and 0.3% at monochromatic wavelengths of 420, 450, 470, 500, 550, and 600 nm, respectively. Our findings confirm that the molecular-level design of photocatalysts can effectively boost performance and reduce cost in photocatalytic reactions and provide an important strategy for designing efficient photocatalysts.

Phosphorus (P) recovery from wastewater is considered to be a positive human intervention towards sustainable P use in the global P cycle. This study investigated the feasibility of synthesizing a superparamagnetic nano-sorbent that was functionalized by lanthanum silicate nanorods (NR_La-Si) using drinking water treatment sludge (DWTS), evaluating both its P adsorption capacity and fertilization effect. The DWTS-based La-modified P nano-sorbent (P-sorbent _D) exhibited complicated but single-layer-dominant adsorption for phosphate, with a maximum adsorption capacity up to 26.8 mg/g, which was superior to that of most of the similar sludge-based P-sorbent. The NR_La-Si-modified P-sorbent _D was identified with several characterization techniques and the leaching metal elements from the nano-sorbent were tested, which were below the limits proposed by the Food and Agriculture Organization of the United Nations. In addition, the growth and vigorousness of Arabidopsis thaliana indicated that the exhausted P-sorbent _D could be used as a potential water-soluble moderate-release P fertilizer, which was also confirmed by the well-fitted P uptake model and the P desorption pattern from the sorbent–fertilizer. The doped lanthanum silicate nanorods could play the dual role of P complexation enhancement and health/growth promotion. In light of this, this study proposed a new way of reclaiming DWTS as a P-sorbent for fertilization, offering new insights into the path toward “closing the P loop”.