ABSTRACT
In this study, a lignin-based aerogel (LA) was prepared through acid precipitation of BPBL, followed by sol-gel method and freeze-drying. Additionally, a one-step activation-carbonization method was used to acquire nitrogen-doped lignin-based activated carbon aerogel (NLACA). The adsorption and catalytic degradation performance for malachite green (MG) were examined. The specific surface area of NLACA after N-doping was 2644.5 m2/g. The adsorption capacity for MG was increased to 3433 mg/g with the presence of nitrogenous functional groups on surface of NLACA compared without N-doping. Meanwhile, non-radical singlet oxygen is the primary active substance and degradation efficiency arrives at 91.8% after the catalytic degradation within 20 min and it has good stability and reuse. Three possible degradation pathways during degradation were analyzed by LC-MS technique. The adsorption isotherm and kinetic data demonstrated conformity with both the Langmuir model and the pseudo-second-order kinetic model. The primary mechanisms of the adsorption for MG dyes on NLACA include hydrogen bonding, π-π interactions, attraction of electrostatic and pore filling. Hence, NLACA derived from BPBL acts as a cost-effective and high-performance adsorbent and catalyst for removal of MG in dye wastewater. This concept introduces an innovative approach of "treatment of waste with waste" for developing a low-consumption, high-efficiency dye wastewater treatment and provides significant reference to treatment dye wastewater.
Subject(s)
Lignin , Rosaniline Dyes , Wastewater , Water Pollutants, Chemical , Wastewater/chemistry , Rosaniline Dyes/chemistry , Lignin/chemistry , Adsorption , Water Pollutants, Chemical/chemistry , Charcoal/chemistry , Kinetics , Nitrogen/chemistry , Carbon/chemistry , Gels/chemistryABSTRACT
Nowadays, wearable devices derived from flexible conductive hydrogels have attracted enormous attention. Nevertheless, the utilization of conductive hydrogels in practical applications under extreme conditions remains a significant challenge. Herein, a series of inorganic salt-ion-enhanced conductive hydrogels (HPE-LiCl) consisting of hydroxyethyl cellulose, hydroxyethyl acrylate, lithium chloride, and ethylene glycol/water binary solvent were fabricated via a facile one-pot method. Apart from outstanding self-adhesion, high stretchability, and remarkable fatigue resistance, the HPE-LiCl hydrogels possessed especially excellent antifreezing and long-lasting moisture performances, which could maintain satisfactory flexibility and electric conductivity over extended periods of time, even in challenging conditions such as extremely low temperatures (as low as -40 °C) and high temperatures (as high as 80 °C). Consequently, the HPE-LiCl-based sensor could timely and accurately monitor various human motion signals even in adverse environments and after long-term storage. Hence, this work presents a facile strategy for the design of long-term reliable hydrogels as smart strain sensors, especially used in extreme environments.
Subject(s)
Cellulose , Cold Temperature , Humans , Electric Conductivity , Hydrogels , IonsABSTRACT
Activated carbon has been widespread applied in the removal of pollutants in wastewater. However, many biomass-derived activated carbon suffer from the challenge of controllable pore size regulation, hindering their efficient adsorption of pollutants. Herein, bamboo-derived activated carbon aerogel (BACA) has been successfully prepared through KOH high-temperature activation of cellulose aerogel which was prepared using cellulose extracted from bamboo. Bamboo cellulose aerogel provides sufficient reaction sites for KOH, which is conducive to the formation of a mass of mesoporous structures on the pore walls of the activated carbon aerogel. The optimal BACA adsorbent shows high specific surface area (2503.80 m2/g), and maximum adsorption capability for tetracycline hydrochloride (TCH) reaches 863.8 mg/g at 30 â. The removal efficiencies of TCH are 100% and 98.4% at 40 â when the initial concentrations are 500 and 700 mg/L, respectively. Adsorption kinetics and isotherm indicate that the adsorption of BACA for TCH is monolayer adsorption based on chemical adsorption. Spontaneous and endothermic adsorption processes are proved by adsorption thermodynamic studies. Additionally, coexisting ions have insignificant effect on TCH adsorption, and the BACA sample displays excellent adsorption property for five reuse cycles with a removal efficiency of 80.95%, indicating the outstanding adsorption capacity of BACA in practical application. The excellent adsorption performance provides BACA with a promising perspective to remove TCH from wastewater, and the prepared method of BACA can be widely extended to other biomass materials.
Subject(s)
Tetracycline , Water Pollutants, Chemical , Wastewater , Cellulose , Charcoal/chemistry , Water Pollutants, Chemical/analysis , Adsorption , KineticsABSTRACT
Anisotropic silver nanoplates are widely anticipated in multifunctional textiles, but their large-scale promotion is limited by the shortcomings of long reaction time, uncontrollable shape and low yield in the preparation process. In this study, a microwave-assisted strategy is provided to prepare shape-controllable silver nanoplates for coloration of non-woven fabric. Anisotropic Ag nanoplates are efficiently coated on the surface of chitosan-pretreated fabric by a simple solution impregnation method, which generates the fabric with tunable color and multiple functions. The Ag nanoplates loaded fabric exhibits excellent photothermal properties at 808 nm laser irradiation due to its unique plasmonic absorption features. Colored fabric shows a strong synergistic antibacterial effect, including silver ion release and hyperthermia caused by the photothermal effect under near-infrared (NIR) light. Additionally, colored fabrics can be used as colorimetric sensors for selective detection of H2S. The colorimetric values of visible color signal of fabric-based H2S gas sensor can be real-time precisely detected using a smartphone, enlightening its high potential as a wearable toxic gas alarm device for the simple and rapid detection of hazardous gases.
Subject(s)
Hydrogen Sulfide , Metal Nanoparticles , Anti-Bacterial Agents/pharmacology , Colorimetry/methods , Gases , Silver/pharmacology , TextilesABSTRACT
As a kind of wastewater produced by papermaking industry, bamboo pulp black liquor (BPBL) discharged into water causes serious environmental problems. In this work, BPBL was successfully converted into porous carbon after activation with potassium hydroxide (KOH) through one-step carbonization, and adsorption properties of porous carbon derived from bamboo pulp black liquor (BLPC) for tetracycline hydrochloride (TCH) and malachite green (MG) were studied. The adsorption capacities of BLPC for TCH and MG are 1047 and 1277 mg/g, respectively, due to its large specific surface area of 1859.08 m2/g. Kinetics and isotherm data are well fitted to the pseudo-second-order rate model and Langmuir model, respectively. Adsorption experiments and characterizations reveal that the adsorption mechanism involved in TCH and MG adsorption on BLPC mainly depends on the synergistic effect of pore filling, H-bonding, π-π interactions and weak electrostatic interactions. In addition, BLPC shows excellent photothermal properties, and the adsorption capacity of TCH and MG on BLPC can reach 584 and 847 mg/g under the irradiation of near infrared lamp for 50 min, respectively. The synthesized BLPC with high adsorption efficiency, good recovery ability, improved adsorption under near-infrared irradiation can be a promising and effective adsorbent for TCH or MG or other pollutes.
Subject(s)
Tetracycline , Water Pollutants, Chemical , Adsorption , Charcoal , Kinetics , Porosity , Rosaniline Dyes , WaterABSTRACT
Conductive hydrogels have attracted widespread attention in wearable electronic devices and human motion detection. However, designing self-healing hydrogels with high conductivity and excellent mechanical properties remains a challenge. In this work, polyvinyl alcohol/carbon nanotubes/graphene (PVA/CNTs/graphene) with an island-bridge hydrogel structure and self-healing properties was designed by merging PVA/CNTs hydrogel and PVA/graphene hydrogel, in which the PVA/graphene hydrogel acts as an "island" and PVA/CNTs hydrogel acts as a "bridge" to bridge the entire conductive network. Hydrogen-bonding between the borate ion and the -OH group of PVA allows the conductive hydrogel to heal without any external stimulation. The PVA/CNTs/graphene hydrogel can be used for both stretchable strain and pressure sensors. The obtained PVA/CNTs/graphene composite hydrogel exhibits excellent electrical conductivity, extreme high elastic strain (up to 900%) and strong mechanical pressure (up to 10 kPa). The strain sensor based on the PVA/CNTs/graphene hydrogel exhibits excellent tensile strain sensitivity (a gauge factor of 152.6 in the strain region of 316-600%) and wide detection working range (1-600%) with high durability and repeatability. The sensor also remains highly sensitive when being used as a pressure sensor (-0.127 kPa-1 at 0-5 kPa). Additionally, the PVA/CNTs/graphene hydrogel-based sensor can detect human motions after multiple cuts and self-healing with excellent stability and repeatability. The PVA/CNTs/graphene hydrogel provides a new idea in the development of wearable electronics, demonstrating the potential of the next generation of wearable electronics.
Subject(s)
Hydrogels/chemistry , Wearable Electronic Devices , Electric Conductivity , Graphite/chemistry , Hydrogels/chemical synthesis , Nanotubes, Carbon/chemistry , Particle Size , Polyvinyl Alcohol/chemistry , Porosity , Pressure , Surface PropertiesABSTRACT
A novel CO2-responsive cellulose nanofibril aerogel as a "green" adsorbent derived from poly(methacrylic acid-co-2-(dimethylamino) ethyl methacrylate) and carboxylated cellulose nanofibrils was successfully prepared via stepwise cation-induced gelation and freeze drying method. This aerogel exhibited CO2-triggered adsorption behavior towards anionic dyes with a rapid adsorption rate and a high adsorption capacity, as well as satisfactory mechanical properties. Upon CO2 stimulation, the charged aerogel can selectively adsorb anionic dyes from aqueous solutions based on an electrostatic interaction. The maximum adsorption capacities of this aerogel towards methyl blue (MB), naphthol green B (NGB), and methyl orange (MO) were 598.8, 621.1 and 892.9 mg g-1, respectively, accompanied by fast adsorption equilibriums towards MB and NGB within 7 min, and MO within 12 min. Meanwhile, the adsorption isotherms and the kinetics of the CO2-responsive adsorbents followed the Freundlich isotherm and the pseudo-second-order model, respectively. Furthermore, the resulting CO2-responsive adsorbent exhibited outstanding recyclability, as its adsorption performance can still be maintained even after twenty cycles. Accordingly, the resultant CO2-responsive cellulose nanofibril aerogel could be a promising adsorbent material for the removal of anionic dyes in wastewater remediation.
ABSTRACT
The MXene-based transition metal oxide composite is a potential candidate for photocatalysts. Rod-like pseudohexagonal phase Nb2O5/Nb2CTx composites were synthesized by a simple hydrothermal oxidation of 2D layered Nb2CTx. The Nb2O5/Nb2CTx composites show superior photocatalytic activity for 98.5% of degradation of Rhodamine B (RhB) for 120 min and 91.2% of tetracycline hydrochloride (TC-HCl) for 180 min under visible light irradiation. The Schottky junction is formed between Nb2O5 nanorods and Nb2CTx and the photo-generated carriers are effectively separated, enhancing the photocatalytic activity of the Nb2O5/Nb2CTx. High photoactivity and cycle stability of Nb2O5/Nb2CTx composites indicate that hydrothermal oxidation of 2D layered Nb2CTx is an alternative to prepare efficient photocatalyst for degradation of organic pollutants.
Subject(s)
Environmental Pollutants , Water Pollutants, Chemical , Catalysis , Light , Niobium , Tomography, X-Ray ComputedABSTRACT
We fabricate a kind of flexible electrochromic (EC) film by spraying the mixed dispersion of silver nanowires (AgNWs) and poly (3, 4-ethylenedioxythiophene) (PEDOT) on the graphene (GR) electrode. AgNWs are embedded in the PEDOT nanoparticles, forming an interlaced conductive network and double electron transport channels; therefore, the disadvantages of poor conductive GR electrodes have been remedied effectively. The subsequent GR-based PEDOT/AgNWs composite films have revealed remarkable optical contrast (63%), high coloration efficiency (${182.8}\;{{\rm cm}^{2}}\;{{\rm C}^{ - 1}}$182.8cm2C-1), and good cycle stability (keeping the optical contrast about 60% after switching cycles of 16,000 s). In addition, the GR-based composite films can keep good EC performance after 2000 cycles of bending tests, while those of the ITO/PET-based composite films decrease dramatically. The ultraflexible GR-based PEDOT/AgNWs composite films with excellent EC properties present an opportunity for fabricating large-area flexible EC devices.
ABSTRACT
Stomatocyte-like hollow polydopamine nanoparticles (SHPNs) are synthesized for rapid removal of water-soluble dyes from water. They demonstrate an exceptionally high adsorption capacity of 2896 mg g-1 for methylene blue (MB) and can rapidly sequester MB from water within 20 seconds. Moreover, SHPNs can be regenerated easily using a mild washing procedure.
ABSTRACT
Silver nanoparticles were synthesized under microwave irradiation, a facile and efficient way, using dandelion extract as reducing and capping agents. The as-synthesized silver nanoparticles/Dandelion compounds (AgNPs/Dandelion) were characterized by field emission scanning electron microscope (FESEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), X-ray diffraction analysis (XRD), fourier transform infrared (FTIR) spectroscopy, dynamic light scattering (DLS), Zeta potential and ultraviolet visible (UV-vis) spectroscopy. The catalytic degradation activity of AgNPs/Dandelion for Methyl orange (MO) and Rhodamine B (RhB) in the presence of NaBH4 were recorded by UV-vis spectroscopy. AgNPs/Dandelion exhibit excellent catalytic degradation activity for RhB and MO with rate constants of 0.1038 s-1 and 0.0393 s-1, respectively.