Fabrication of a poly(N-isopropylacrylamide)-grafted alginate composite aerogel for efficient treatment of emulsified oily wastewater.

The treatment of emulsion wastewater poses significant challenges. In this study, a novel porous material, namely esterified bagasse/poly(N, N-dimethylacrylamide)/sodium alginate (SBS/PDMAA/Alg) aerogel, was developed for efficient demulsification and oil recovery. By grafting a poly(N-isopropylacrylamide) (PNIPAM) brush onto the SBS/PDMAA/Alg skeleton through free radical polymerization, the resulting aerogel exhibits both surface charge and a molecular brush structure. The aerogel demonstrates remarkable demulsification efficiency for cationic surfactant-stabilized emulsions at various concentrations, achieving a demulsification efficiency of 95.6% even at an oil content of 100 g L-1. Furthermore, the molecular brush structure extends the application range of the aerogel, enabling a demulsification efficiency of 98.3% for anionic and non-ionic surfactant-stabilized emulsions. The interpenetrating polymer network (IPN) structure formed by SBS, PDMAA, and alginate enhances the mechanical stability of the aerogel, enabling a demulsification efficiency of 91.3% even after 20 repeated cycles. The demulsification ability of the composite aerogel is attributed to its surface charge, high interfacial activity, and unique brush-like structure. A demulsification mechanism based on the synergistic effect of surface charge and molecular brush is proposed to elucidate the efficient demulsification process.

A Thorough Benchmark and a New Model for Light Field Saliency Detection.

Compared with current RGB or RGB-D saliency detection datasets, those for light field saliency detection often suffer from many defects, e.g., insufficient data amount and diversity, incomplete data formats, and rough annotations, thus impeding the prosperity of this field. To settle these issues, we elaborately build a large-scale light field dataset, dubbed PKU-LF, comprising 5,000 light fields and covering diverse indoor and outdoor scenes. Our PKU-LF provides all-inclusive representation formats of light fields and offers a unified platform for comparing algorithms utilizing different input formats. For sparking new vitality in saliency detection tasks, we present many unexplored scenarios (such as underwater and high-resolution scenes) and the richest annotations (such as scribble annotations, bounding boxes, object-/instance-level annotations, and edge annotations), on which many potential attention modeling tasks can be investigated. To facilitate the development of saliency detection, we systematically evaluate and analyze 16 representative 2D, 3D, and 4D methods on four existing datasets and the proposed dataset, furnishing a thorough benchmark. Furthermore, tailored to the distinct structural characteristics of light fields, a novel symmetric two-stream architecture (STSA) network is proposed to predict the saliency of light fields more accurately. Specifically, our STSA incorporates a focalness interweavement module (FIM) and three partial decoder modules (PDM). The former is designed to efficiently establish long-range dependencies across focal slices, while the latter aims to effectively aggregate the extracted coadjutant features in a mutual-enhancement way. Extensive experiments demonstrate that our method can significantly outperform the competitors.

Fast-thermoresponsive carboxylated carbon nanotube/chitosan aerogels with switchable wettability for oil/water separation.

The use of aerogels to selectively recover oil from oily wastewater is effective but challenging. In this study, a new carboxylated carbon nanotube/chitosan aerogel (CCNT/CA) with switchable wettability was developed as a smart adsorbent for fast oil absorption and oil recovery. Vinyltrimethoxysilane and thermoresponsive poly(N-isopropylacrylamide) (PNIPAAm) was grafted onto the surface of the CCNT/CA skeleton, and the resulting smart aerogel (PNI-Si@CCNT/CA) exhibited temperature responsiveness. PNI-Si@CCNT/CA exhibited an excellent reversible conversion between hydrophilicity and hydrophobicity when the temperature was changed to below or above the lower critical solution temperature (LCST) of PNIPAAm (~32 °C). Most importantly, CCNT significantly increased the oil absorption capacity, improved the mechanical properties, accelerated phonon conduction, enhanced thermal conductivity (80.57 mW m-1 K-1), improved the temperature response rate, shortened the oil desorption time (15 min), and improved the oil/water separation efficiency of PNI-Si@CCNT/CA because a strong interface interaction occurred between CCNT and chitosan. Moreover, PNI-Si@CCNT/CA absorbed oil at 45 °C and released the absorbed oil at 25 °C. It maintained its good adsorption performance after 15 cycles, and this was ascribed to its excellent mechanical properties and stable structure.

In Situ One-Pot Synthesis of C-Decorated and Cl-Doped Sea-Urchin-like Rutile Titanium Dioxide with Highly Efficient Visible-Light Photocatalytic Activity.

Titanium dioxide (TiO2) that offers high light-harvesting capacity and efficient charge separation holds great promise in photocatalysis. In this work, an in situ one-pot hydrothermal synthesis was explored to prepare a C-decorated and Cl-doped sea-urchin-like rutile TiO2 (Cl-TiO2/C). The growth of sea-urchin-like 3D hierarchical nanostructures was governed by a mechanism of nucleation and nuclei growth-dissolution-recrystallization growth from time-dependent morphology evolution. The crystal morphology and the content of Cl and C could be controlled by the volume ratio of HCl to TBOT. Systematic studies indicated that the 0.4Cl-TiO2/C sample (the volume ratio of HCl to TBOT was 0.4) exhibited the highest visible-light photocatalytic activity for the degradation of rhodamine B, with kinetic rate constant (k) of 0.0221 min-1, being 6.5 and 3.75 times higher than that of TiO2 and Cl-TiO2. The enhanced photocatalytic performance could be attributed to the high charge separation and transfer efficiency induced by Cl-doping and C decoration and the excellent light-harvesting capacity caused by its sea-urchin-like nanostructure. Moreover, the 0.4Cl-TiO2/C sample exhibited good reusability and excellent structural stability for five cycles. This facile one-pot approach provides new insight for the preparation of a TiO2-based photocatalyst with excellent photocatalytic performance for potential application in practical wastewater treatment.

Fabrication of a CO2-responsive chitosan aerogel as an effective adsorbent for the adsorption and desorption of heavy metal ions.

In the traditional desorption method, strong acid is commonly used as an eluent for the regeneration of adsorbents. It is of critical economic and environmental significance to develop a chemical-free desorption method. In this study, a new CO2-responsive chitosan aerogel adsorbent was synthesized from CO2-responsive poly(acrylic acid-2-(dimethylamino)ethyl methacrylate) and chitosan by physicochemical double crosslinking for the adsorption of Cu2+. Compared with the chitosan aerogel, the adsorption capacity of Cu2+ and mechanical properties of CO2-responsive chitosan aerogel increased by 162% and 660%, respectively. Most importantly, after the adsorption of Cu2+ by CO2-responsive chitosan aerogel, the Cu2+ could be desorbed by CO2 bubbling, and the desorption rate of metal ions was more than 80%. The adsorption of Cu2+ by aerogel was attributed to chelation and complexation. The desorption of porous chitosan/P(AA-co-DMAEMA) aerogels (CPA) by CO2 mainly occurred through charge repulsion of protonated ‒NH2 and ‒N‒ groups. After 6 cycles, the adsorption capacity of CPA for metal ions still reached 70% of the initial adsorption capacity, and the desorption rate reached 75%. This novel CO2-responsive chitosan aerogel is a highly efficient and environmentally friendly adsorbent for the adsorption and recovery of metal ions.

Formation of type 3 resistant starch from mechanical activation-damaged high-amylose maize starch by a high-solid method.

This study focused on constructing a high-solid reaction system to prepare type 3 resistant starch (RS3) with high-amylose maize starch as raw material by mechanical activation (MA) pretreatment combined with thermal and freeze-thaw treatments. MA pretreatment effectively destroyed the crystal structure and molecular structure of native starch. MA damaged starch with a certain viscosity could form dough with a small amount of water to construct a starch continuous phase system. RS content increased with the damage levels of starch as the formation of double helix structure, attributed to that the molecules of MA damaged starch could be easy to move and form recrystallization structure. Thermal and freeze-thaw treatments contributed to strong interaction of starch-water and the re-formation of internal crystal structure of MA damaged starch to form RS3. This study provides insight into the development of a highly effective approach for large scale production of resistant starch.

A stepwise processing strategy for treating highly acidic wastewater and comprehensive utilization of the products derived from different treating steps.

A stepwise processing strategy, including initial neutralization, chemical mineralization, and complete neutralization treating steps, was developed to effectively treat and utilize the highly acidic wastewater derived from titanium dioxide production. Approximately 94.6% of SO42-, 100% of Fe, and most of other metals were recovered to produce white gypsum, schwertmannite, and Fe0/Fe3O4@biochar (Fe0/Fe3O4@BC) composite in the corresponding treating steps. The resulting effluent with neutral pH and a small amount of metal ions could be discharged to general sewage treatment plant for further processing. Schwertmannite was applied as a heterogeneous Fenton-like catalyst to stimulate H2O2 to produce active radicals for effective degradation and mineralization of methyl orange (MO) in solution. The MO removal of 100% and total organic carbon removal of 91.1% were achieved in schwertmannite/H2O2 reaction system, and schwertmannite exhibited good stability and reusability. Fe0/Fe3O4@BC composite was applied to remove Cr(VI), with the adsorption capacity of 67.74 mg g-1. The removal of Cr(VI) using Fe0/Fe3O4@BC composite was a chemisorption process, including the adsorption of Cr(VI), reduction of Cr(VI) to Cr(III), and co-precipitation of Cr(III)/Fe(III) oxides/hydroxides. This stepwise treating strategy is a promising technology for effective treatment of highly acidic industrial wastewater and comprehensive utilization of the related products.

3D porous tubular network-structured chitosan-based beads with multifunctional groups: Highly efficient and selective removal of Cu2.

Herein, an effective adsorbent, 3D porous tubular network-structured citric acid-chitosan/Fe/polyethyleneimine beads (CCFPB) with multifunctional active groups and strong selectivity, was prepared for the selective removal of Cu2+ from simulated wastewater. Compared with pure chitosan beads (CB), the adsorption capacity of CCFPB for Cu2+ was increased by 127 mg g-1 (238%), and the adsorption equilibrium time was shortened by 480 min. The CCFPB showed porous surface and a novel 3D porous tubular network structure in interior, which were benefit to the diffusion of Cu2+ from surface to interior of the CCFPB and the shortening of adsorption equilibrium time. The common coexisting ions in the simulated wastewater had almost no effect on the adsorption of Cu2+ by CCFPB, and the adsorption was fast and reached equilibrium within 10 h. The adsorption process followed pseudo-second-order kinetics and the Langmuir isotherm model (qm = 240.9 mg g-1 for Cu2+). The adsorption mechanism of CCFPB for Cu2+ was mainly the synergistic interaction with amino, carboxyl, and hydroxyl groups. This strategy shows great potential for developing a variety of novel, highly active, and reusable immobilized functional beads materials for effective separation of Cu2+ from multi-ion wastewater.

In-situ synthesis of calcium borate/cellulose acetate-laurate nanocomposite as efficient extreme pressure and anti-wear lubricant additives.

In this study, calcium borate (CB) nanoparticles were in-situ grown onto cellulose acetate-laurate (CAL) template to prepare CB/CAL nanocomposite with uniform dispersion of CB nanoparticles by hydrothermal method. As-prepared CB/CAL nanoparticles were characterized by field emission scanning electron microscope, Fourier transforms infrared spectrometry, X-ray diffraction, and energy-dispersive X-ray spectroscopy. With average wear scar diameter (WSD), coefficient of friction (COF) and maximum non-seizure load (PB) as evaluation criterions, CB/CAL, CAL, and CB were used as lubricant additives in poly-alpha-olefin (PAO) base oil to comparatively investigate the tribological properties with a four-ball tribotester. It was found that under the load of 490 N, the WSD and COF of PAO + CB/CAL (concentration of 0.6 wt%) reduced by 25.9% and 48.7%, respectively, and PB increased by 79.6% compared with pure PAO base oil. CB/CAL nanocomposite exhibited superior lubricating performances than CB and CAL. In addition, the synergistic lubricating mechanism of CB/CAL nanocomposite as lubricant additive was explored.

Preparation of sugarcane bagasse succinate/alginate porous gel beads via a self-assembly strategy: Improving the structural stability and adsorption efficiency for heavy metal ions.

Sugarcane bagasse, a kind of agricultural waste, was esterified by mechanical activation-assisted solid phase reaction with succinic anhydride as esterifying agent to prepare SB succinate (SBS) with rich carboxyl and ester functional groups. The layer-by-layer (LbL) self-assembly technology was used to prepare SBS/alginate (Alg) porous gel beads (SAPGB) with outstanding mechanical strength and desired porous structure from external surface to interior through the formation of gel network structure of SBS/Ca2+/Alg. The adsorption kinetics and isotherm indicated that the adsorption of metal ions onto SAPGB followed the pseudo-second-order kinetics and Langmuir isotherm mode (Qmax = 354.60 and 176.36 mg g-1 for Pb2+ and Cd2+, respectively). The adsorption behavior of SAPGB for metal ions was mainly amonolayer chemical adsorption process. The adsorption was fast and reached equilibrium within 60 min, ascribed to rapid diffusion from porous surface into internal pores. In addition, the stable SAPGB adsorbent exhibited excellent regeneration performance.

Magnetic chitosan-hydroxyapatite composite microspheres: Preparation, characterization, and application for the adsorption of phenolic substances.

The phenolic substances in sugarcane juice seriously affect the color value of sugar products, and gallic acid is one of the main phenolic substances. To develop a new adsorbent able to effectively adsorb phenolic substances from sugarcane juice, magnetic chitosan (CS) hydroxyapatite (HA) microspheres (MCHAM) were prepared by growing HA on magnetic CS microspheres (MCM) in-situ. MCHAM could effectively adsorb gallic acid from sucrose solution, and the highest adsorption capacity was 40.77 mg g-1. The adsorption kinetics indicated that the adsorption process fit the pseudo-second-order mode, the dominant mechanism was chemisorption, and the Langmuir isotherm mode (qm = 48.12 mg g-1) described the adsorption behavior of MCHAM best. Recycling experiments indicated that the MCHAM adsorbent presented considerable repeatability. Compared to treating phenolic substances in sugarcane juice using traditional clarifying agents, treatment methods employing MCHAM can efficiently and simply remove phenolic substances without leaving residual sulfur in sugarcane juice.