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With the growing global awareness of environmental protection, the demand for biodegradable materials to replace traditional plastic foam has become increasingly urgent. Starch-based foam, with its abundant availability, low cost, and biodegradability, has shown great potential as an alternative to plastic foam. However, its inherent high hydrophilicity and relatively low mechanical performance limit its widespread application. The aim of this study is to modify corn starch (NCS) and waste paper fiber (WPF) using citric acid (CA) and stearic acid (SA), and to develop an efficient hydrophobic coating through an organic-inorganic hybrid approach. This successfully resulted in the preparation of hydrophobic corn starch/waste paper fiber composite foam materials. Experimental results showed that the foam materials treated with a palmitic acid (PA)-modified nano-SiO2 coating (MCF@PA) exhibited excellent hydrophobic performance, with a water contact angle reaching as high as 138°, and a significant reduction in moisture absorption to 3.1 %. In water immersion tests, the material maintained buoyancy and shape stability, demonstrating excellent self-cleaning properties. Additionally, the coating significantly enhanced the material's compressive strength, increasing by 90 kPa, while also retaining thermal stability. However, the coating prepared by this method increased the material's hardness and reduced its biodegradability, which poses challenges for environmental sustainability. This study provides a new approach for preparing high-strength foam materials with excellent hydrophobicity and mechanical performance, paving an economical and efficient pathway for industrial production.
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In this study, the integration of paper industry waste with high cellulose content into biocomposites of polylactic acid (PLA), a widely used biobased polymer material, was investigated. The PLA/waste biocomposite samples (0-25 wt.%) were manufactured using the extrusion and injection moulding techniques. The mechanical test results showed improvements in terms of tensile properties and a decrease in impact strength as the percentage of residue increased. The melting temperature decreased, and the crystallinity increased in all biocomposites according to the Differential Scanning Calorimetry (DSC) analysis. Water absorption increased proportionally with the percentage of residue, attributed to the higher cellulose content in the biocomposites, determined by Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques. The scanning electron microscopy (SEM) fracture analysis demonstrated effective reinforcement-matrix cohesion, supporting the previously observed behaviour of the analysed materials. This work highlights the potential of using waste from the paper industry as reinforcement in PLA matrices, opening new perspectives for sustainable applications in the framework of the manufacture of composite materials.
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This study examined the possibility of using various types of waste paper-used newsprint (NP), used lightweight coated paper (LWC), used office paper (OP), and used corrugated cardboard (CC)-for the removal of anionic dyes, Acid Red 18 (AR18) and Acid Yellow 23 (AY23), and cationic dyes, Basic Violet 10 (BV10) and Basic Red 46 (BR46), from aqueous solutions. The scope of this research included the characterization of sorbents (FTIR, SEM, BET surface area, porosity, pHPZC, effectiveness of water coloration), determination of pH effect on the effectiveness of dye sorption, sorption kinetics (pseudo-first-order model, second-order model, intraparticular diffusion model), and the maximum sorption capacity (Langmuir models and Freundlich model) of the tested sorbents. The use of waste paper materials as sorbents was found to not pose any severe risk of aquatic environment contamination. AR18, AY23, and BV10 sorption intensities were the highest at pH 2, and that of RB46 at pH 6. The waste paper sorbents proved particularly effective in removing cationic dyes, like in the case of, e.g., NP, which had a sorption capacity that reached 38.87 mg/g and 90.82 mg/g towards BV10 and BR46, respectively, and were comparable with that of selected activated carbons (literature data).
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In this work, a sustainable 3D carbon aerogel (AO-WPC) is prepared from waste paper (WP), and used for efficient antibiotics removal from water. The AO-WPC aerogel shows good mechanical property and can recover after 100th of 30 % compression strain. The specific surface area of AO-WPC aerogel is up to 654.58 m2/g. More importantly, this aerogel reveals proper pore size distribution, including micro sized macropores between carbon fibers and intrinsic nano scale mesopores (11.86 nm), which is conducive to remove antibiotics from water. Taking tetracycline (Tc) as an example, the maximum adsorption capacity and adsorption rate of AO-WPC for Tc are as high as 384.6 mg/g and 0.510 g/(mgâ§min), respectively, which exhibits significant advantages over most of the recent absorbents, and the adsorption toward Tc reveals good resistance to various environmental factors, including pH, various ions, and dissolved organic matter (DOM). Moreover, good thermal stability enables the AO-WPC aerogel to be regenerated through simple burning, and the adsorption capacity of Tc only decreases by 10.4 % after 10 cycles. Mechanism research shows that hydrogen bonding and π-π electron-donor-acceptor (EDA) interaction play the important role in the adsorption. The excellent mechanical property and adsorption performance imply good practical prospect of the AO-WPC aerogel.
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Antibacterianos , Carbono , Géis , Papel , Tetraciclina , Poluentes Químicos da Água , Poluentes Químicos da Água/química , Antibacterianos/química , Adsorção , Carbono/química , Géis/química , Tetraciclina/química , Tetraciclina/isolamento & purificação , Purificação da Água/métodos , Resíduos IndustriaisRESUMO
This paper reports an innovative study that aims to address key issues in the efficient recycling of wastepaper cellulose. The research team utilized the temperature-responsive upper critical solution temperature (UCST) polymer P(NAGA-b-DMA) in combination with the LytA label's affinity for choline analogs. This innovative approach enabled them to successfully develop a novel soluble immobilized enzyme, P(NAGA-b-DMA)-cellulase. This new enzyme has proven highly effective, significantly enhancing the degradation of wastepaper cellulose while demonstrating exceptional stability. Compared with the traditional insoluble immobilized cellulase, the enzyme showed a significant improvement in the pH, temperature stability, recycling ability, and storage stability. A kinetic parameter calculation showed that the enzymatic effectiveness of the soluble immobilized enzyme was much better than that of the traditional insoluble immobilized cellulase. After the immobilization reaction, the Michaelis constant of the immobilized enzyme was only increased by 11.5%. In the actual wastepaper degradation experiment, the immobilized enzyme was effectively used, and it was found that the degradation efficiency of wastepaper cellulose reached 80% of that observed in laboratory conditions. This novel, thermosensitive soluble immobilized cellulase can efficiently catalyze the conversion of wastepaper cellulose into glucose under suitable conditions, so as to further ferment into environmentally friendly biofuel ethanol, which provides a solution to solve the shortage of raw materials and environmental protection problems in the paper products industry.
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Celulase , Enzimas Imobilizadas , Enzimas Imobilizadas/metabolismo , Celulose/metabolismo , Celulase/metabolismo , Temperatura , Polímeros , HidróliseRESUMO
The reuse of waste papers by conversion into valuable carbon materials has received considerable attention for diverse applications such as energy storage and water purification. However, traditional methods for converting waste papers into materials with suitable properties for specific applications are often complex and ineffective, involving consecutive carbonization and activation steps. Herein, we propose a simple one-step microwave (MW)-assisted synthesis for preparing waste paper-derived porous carbons (WPCs) for energy storage and water purification. Through a 30-min synthesis, WPCs with graphitic structure and high specific surface area were successfully produced. The fabricated WPCs exhibited outstanding charge storage capability with a maximum specific capacitance of 237.7 F g-1. Additionally, the WPC demonstrates a high removal efficiency for various dyes, achieving a maximum removal efficiency of 95.0% for methylene blue. The developed one-step MW synthesis not only enables the production of porous carbon from waste paper, but also offers a viable approach to address solid waste management challenges while simultaneously yielding valuable materials.
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Grafite , Purificação da Água , Carbono/química , Porosidade , Micro-OndasRESUMO
The challenge of global climate change has drawn people's attention to the issue of carbon emissions. Reducing the use of petroleum-derived materials and increasing the use of biodegradable materials is a current focus of research, especially in the packaging materials industry. This study focused on the use of environmentally friendly plastics and waste paper as the main materials for packaging films. Poly(butylene succinate-co-lactate) (PBSL) was modified with maleic anhydride (MA) to form a biobased compatibilizer (MPBSL), which was then blended with a mixture (WPS) of waste-paper powder (WP) and silica aerogel powder (SP) to form the designed composite (MPBSL/WPS). The modification of PBSL with MA improved interfacial adhesion between PBSL and WPS. The structure, thermal, and mechanical properties, water vapor/oxygen barrier, toxicity, freshness, and biodegradability of MPBSL/WPS films were evaluated. Compared with the PBSL/WP film, the MPBSL/WPS film exhibited increased tensile strength at break of 4-13.5 MPa, increased initial decomposition loss at 5 wt% of 14-35 °C, and decreased water/oxygen permeabilities of 18-105 cm3/m2·d·Pa. In the water absorption test, the MPBSL/WPS film displayed about 2-6 % lower water absorption than that of the PBSL/WP film. In the cytocompatibility test, both MPBSL/WPS and PBSL/WP membrane were nontoxic. In addition, compared with PBSL/WP film and the control, the MPBSL/WPS film significantly reduced moisture loss, extended the shelf life, and prevented microbial growth in vegetable and meat preservation tests. Both MPBSL/WPS and PBSL/WP films were biodegradable in a 60-day soil biodegradation test; the degradation rate was 50 % when the WP or WPS content was 40 wt%. Our findings indicate that the composites would be suitable for environmentally sustainable packaging materials.
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Alcenos , Butileno Glicóis , Ácido Láctico , Anidridos Maleicos , Polímeros , Humanos , Pós , Oxigênio , SuccinatosRESUMO
Carbon aerogel is a promising material in various applications, such as water treatment, insulators, catalysts, and sensors, due to its porosity, low density, conductivity, and good chemical stability. In this study, an inexpensive carbon aerogel was prepared through lyophilization and post-pyrolysis using waste paper. However, carbon aerogel, in the form of short belts, is randomly entangled without a crosslinking agent and has weak mechanical properties, thus limiting its applications, which would otherwise be various. In this paper, a novel strategy is proposed to fabricate a PDMS-coated carbon aerogel (Aerogel@PDMS). Benefiting from microwave heating, precise PDMS coating onto the carbon frame was able to be carried out in a short amount of time. PDMS coating firmly tied the carbon microstructure, maintaining a unique aerogel property without blocking its porous structure. FE-SEM, RAMAN, XPS, and FT-IR were all used to confirm the surface change in PDMS coating. Compressible stability and water contact angle measurement showed that Aerogel@PDMS is a perspective organic solvent absorbent due to its good resilience and its hydrophobicity, and, as a result, its organic solvent absorption capacity and repeated absorption were evaluated, ultimately suggesting a promising material in oil clean-up and pollution remediation in water. Based on our experimental results, we identified elastic carbon aerogels provided by a novel coating technology. In the future, then, the developed carbon/PDMS composite can be examined as a promising option for various applications, such as environmental sensors, virus sensors, and wearable sensors.
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The construction industry makes a significant contribution to global CO2 emissions. Material extraction, processing, and demolition account for most of its environmental impact. As a response, there is an increasing interest in developing and implementing innovative biomaterials that support a circular economy, such as mycelium-based composites. The mycelium is the network of hyphae of fungi. Mycelium-based composites are renewable and biodegradable biomaterials obtained by ceasing mycelial growth on organic substrates, including agricultural waste. Cultivating mycelium-based composites within molds, however, is often wasteful, especially if molds are not reusable or recyclable. Shaping mycelium-based composites using 3D printing can minimize mold waste while allowing intricate forms to be fabricated. In this research, we explore the use of waste cardboard as a substrate for cultivating mycelium-based composites and the development of extrudable mixtures and workflows for 3D-printing mycelium-based components. In this paper, existing research on the use of mycelium-based material in recent 3D printing efforts was reviewed. This review is followed by the MycoPrint experiments that we conducted, and we focus on the main challenges that we faced (i.e., contamination) and the ways in which we addressed them. The results of this research demonstrate the feasibility of using waste cardboard as a substrate for cultivating mycelia and the potential for developing extrudable mixtures and workflows for 3D-printing mycelium-based components.
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Waste paper disposed in landfills notably contributes to greenhouse gas (GHG) emissions and impedes more sustainable, circular alternatives, such as recycling. In Hong Kong, this unsustainable approach is currently dominant as 68% of waste paper products are treated in landfills in 2020. To contextualize the impact of local waste paper management and explore mitigation potentials of circular alternatives, this paper develops a quantitative assessment framework around GHG emissions development trajectories. Combining guidelines of the Intergovernmental Panel on Climate Change (IPCC), national GHG inventories, and local parameters from life cycle analysis, five GHG emissions projections were simulated along the Shared Socioeconomic Pathways (SSPs) until 2060. Most recent baselines indicate that Hong Kong's current waste paper treatment generated 638,360 tons CO2-eq in 2020, comprising 1,821,040 tons CO2-eq from landfill and 671,320 tons CO2-eq from recycling, and -1,854,000 tons CO2-eq from primary material replacement. Proceeding along a Business-as-Usual scenario under SSP5, GHG emissions will dramatically increase to a net 1,072,270 tons CO2-eq by 2060, whereas a recycling-intensive scenario will lead to a net saving of -4,323,190 tons CO2-eq. To complement the quantitative evidence on the benefits of waste paper recycling, field research was conducted to explore the feasibility of circular policy innovation from the perspective of recycling stakeholders. These empirical qualitative and quantitative findings from stakeholders' business routines and material transactions provide crucial indications for policy and institutional innovation: Essentially, for Hong Kong to improve waste paper recycling capacities and facilitate a circular economy (CE), local stakeholders require support via fiscal policy measures (financial subsidies or tax reductions) and infrastructure improvements (delivery access and material storage). In sum, this study employs a novel analytical framework combining original qualitative and quantitative evidence to provide policy innovation towards circular, GHG emission-saving waste paper management.
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Gases de Efeito Estufa , Eliminação de Resíduos , Gerenciamento de Resíduos , Hong Kong , Dióxido de Carbono/análise , Efeito Estufa , ResíduosRESUMO
This review presents the research conducted to date in the field of cement-based composites reinforced with waste paper-based cellulose fibres, focusing on their composition, mechanical properties, and durability characteristics. The literature demonstrates that the properties of raw material (depending on their own chemical composition) significantly influence the formation of the cement composite binders. When considering fresh properties, the presence of silica and magnesium compounds generally lead to favourable effects on the setting of the cement composite when combined with waste paper cellulose fibre. Reduction in density values, i.e., approximately 25%, was observed with the inclusion of waste paper fibres from 20 to 80% in cement composites. The homogeneous dispersion of fibres in the matrix is one of the crucial factors to achieve in order to develop composites with well-balanced mechanical properties incorporating waste paper cellulose fibres. Hence, dispersion of fibres can be improved by increasing water quantity corresponding to the optimal value, which was a water/cement ratio of 0.64 leading to optimum strength properties of the composite. Even though the effect of fibre dispersion in the matrix improves with the addition of water, higher porosity and voids govern the strength properties beyond an optimum water-to-cement ratio. Higher porosity leads to an increase in the water absorption and a lowering of the thermal conductivity properties with the addition of paper fibre in cement binders. Paper fibre absorbs a high amount of water leading to higher water absorption. This phenomenon is related to the hydrophilic nature of cellulosic fibres absorbing some volume of water due to their microporous structure.
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This review focuses on polymeric waste-paper composites, including state-of-the-art analysis with quantitative and qualitative discussions. Waste paper is a valuable cellulose-rich material, produced mainly from office paper, newspaper, and paper sludge, which can be recycled and returned to paper production or used in a new life cycle. A systematic literature review found 75 publications on this material over the last 27 years, with half of those published during the last five years. These data represent an increasing trend in the number of publications and citations that have shown an interest in this field. Most of them investigated the physicomechanical properties of composites using different contents of raw waste paper or the treated, modified, and cellulose-extracted types. The results show that polyethylene and polypropylene are the most used matrices, but polylactic acid, a biodegradable/sourced polymer, has the most citations. The scientific relevance of waste-paper composites as a subject includes the increasing trend of the number of publications and citations over the years, as well as the gaps identified by keyword mapping and the qualitative discussion of the papers. Therefore, biopolymers and biobased polymers could be investigated more, as well as novel applications. The environmental impact in terms of stability and degradation should also receive more attention regarding sustainability and life cycle analyses.
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Sulfate attack is one of the drawbacks of cementitious materials for stabilized soils. In the current study, a durability comparison of stabilized soil with cement (Type IV) and waste paper fly ash (WPFA) was conducted. First, the treated soil's unconfined compressive strength (UCS) was tested. Next, the treated soil was subjected to various wetting/drying cycles with various sulfate concentrations and temperatures for a year. In the meantime, samples were taken for DRX, FTIR, and TGA microstructural analyses. Additionally, samples were manufactured to track swelling over an 800 day period. The outcomes show that WPFA's UCS remained constant. Furthermore, ettringite development can be seen in the microstructural studies, however testing on linear displacement over 800 days revealed no significant changes in swelling. Finally, SEM was used to verify the ettringite formation at 360 days in order to confirm the previous findings. All the results indicated that stabilizing soil with 5% of WPFA and 3% of cement IV is possible even in presence of high sulfate concentrations, while maintaining the durability of the structure.
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In order to develop environmentally friendly, economical and facile preparation method of carbon aerogels (CAs), the waste printing paper as the raw material was combined with graphene oxide and carboxylic multi-walled carbon nanotubes to produce CAs (ρ = 44 mg cm-3). The CAs with different composition were investigated, the addition of graphene oxide led to the reduction of adsorption sites and the reduction of extraction performance. But the carbon nanotubes made CAs have a better pore structure. The CAs as adsorbent were loaded into a pipette-tip for solid-phase extraction of hexaconazole and diniconazole. Coupled with gas chromatography, an analytical method was established under the optimized conditions. The limits of detection were between 0.08 and 0.32 mg kg-1, the linear ranges were 0.96-200.0 mg kg-1 and 0.24-200.0 mg kg-1. The relative recoveries were in the range of 81.0-119%. The results indicated that the method had potential application for the determination of triazole fungicides.
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Fungicidas Industriais , Malus , Nanotubos de Carbono , Pyrus , Solanum lycopersicum , Cromatografia Líquida de Alta Pressão/métodos , Fungicidas Industriais/análise , Nanotubos de Carbono/química , Extração em Fase Sólida/métodos , Triazóis/análiseRESUMO
Developing chrome-free and sustainable tanning agents is extremely important to the sustainability of the leather industry. Herein, we have synthesized an Al-Zr-oligosaccharides tanning agent via a simultaneous degradation and oxidation of cellulose in waste paper. The influence of the temperature and the concentrations of AlCl3 and H2O2 during the synthesis were thoroughly investigated on the properties of the tanning agent and the leather produced. The synthesis temperature and the concentration of AlCl3 were the factors primarily affecting the effective depolymerization of cellulose. They controlled the conversion of waste paper into oligosaccharides with an appropriate molecular weight to efficiently penetrate the leather matrix. In parallel, the H2O2 concentration substantially influenced the tanning performance of the Al-Zr-oligosaccharides, diminishing the chromaticity of the tanning liquid via oxidation and promoting the conversion of C2/C3/C6-OH moieties into -CHO/-COOH. These functional groups increased the surface charge of the oligosaccharides allowing more effective coordination with Al/Zr, which facilitated the penetration of Al/Zr species into the leather matrix. Once inside the leather matrix, Al and Zr were released and reacted with the collagen fibers in leather, which resulted in effective leather tanning. The process optimization revealed that up to 57% of waste paper could be converted into a low-chromaticity (4350 AU) liquid hydrolysate with the synthesis conducted at 177 °C in a system comprising 47 mM AlCl3 and 5 vol% H2O2. The application of this liquid for tanning provided leather with a shrinkage temperature (86.5 °C) sufficiently high for commercial applications. These excellent results, combined with the intrinsic green nature of our approach, exemplify a step forward to simultaneously reduce pollution and hazards in leather industries giving a second life to waste paper.
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Resíduos Industriais , Curtume , Celulose , Peróxido de Hidrogênio , Resíduos Industriais/análise , OligossacarídeosRESUMO
Waste paper (WP) is rich in cellulose, which can be activated to produce porous carbon, bio-oil, and combustible gases. During chemical activation of WP, the use of varied chemical agents not only generates activated carbon of distinct pore structure but also bio-oil/gases of different property. In this study, the activation of WP with varied chemical agents was conducted. The distinct characteristics of activated carbon and also bio-oil/gases were correlated with the different nature of the used chemical agents. The results indicated that H3PO4 and ZnCl2 catalyzed polymerization reactions for producing more bio-oil while less gases owing to their Brønsted and Lewis acidic sites. K2C2O4 showed high activity for cracking/gasification reactions, forming bio-oil with higher abundance of organics with smaller π-conjugated structures. In addition, ZnCl2 could create a very coarse porous structure with abundant macropores via destroying fiber structure in WP and promoting the growth of graphitic crystals. In comparison, K2C2O4 hindered the aromatization and facilitated the formation of amorphous activated carbon. K2C2O4 and ZnCl2 were much more effective than H3PO4 for creating micropores and mesopores from WP, the derived activated carbon showed superior performances as the electrode of supercapacitor and adsorbent for adsorption of oxytetracycline from aqueous solution. In addition, K2C2O4 as activating agent showed lower environmental impact than ZnCl2 in terms of energy consumption, environmental pollution and the greenhouse effect.
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Carvão Vegetal , Gases , Adsorção , Carvão Vegetal/química , PorosidadeRESUMO
Waste paper fly ash (WPFA) and bottom ash (WPBA), derived from fluidised bed combustion of a paper recycling plant, exhibit cementitious properties owing to its mineralogical composition, and hence, could be proposed as a hydraulic binder. However, it may also contain some traces of heavy metals. Considering it is necessary to understand the effect of reusing any kind of waste on the environment, this study proposes of reusing WPFA/WPBA as a hydraulic road binder by evaluating its mineralogical composition and leaching activity. Chemical, physical, and mineralogical properties of raw WPFA/WPBA and the microstructural evolution of binders were carried out. Results showed that both ashes undergo hydration reactions while showing some cementitious properties by forming C-S-H gel, Friedel's salt, and calcite. According to the European standard EN 13282-1, both WPFA and WPBA can be categorised as N1 considering they reach 5.3 and 3.6 MPa, respectively, at 56 days. Furthermore, the mechanical performance of various soils was improved by using WPFA and WPBA as a binder. From the environmental point of view, the amount of barium in WPFA and WPBA, which is the main problem, was significantly decreased by using these ashes as a binder.
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Metais Pesados , Eliminação de Resíduos , Cinza de Carvão/química , Incineração , Metais Pesados/análise , Reciclagem , Solo , Resíduos SólidosRESUMO
The paper industry is one of the most important basic raw material pillar industries. With the decrease of forest wood resources, the recycling of wastepaper has drawn increasingly attention. However, the stickies generated in the process of wastepaper recycling will flocculate and deposite in the pulp, resulting in production accidents and inferior product quality. The biological enzymatic method, with the advantages of high efficiency, specificity, and pollution-free, can prevent the flocculation of the stickies by enzymatically hydrolyzing the ester bond of the stickies components. Previous studies have demonstrated that cutinase (EC 3.1.1.74) had the ability to degrade polyester components of stickies. Meanwhile, relevant studies have shown that anchor peptides possessed the ability to bind polyester. Herein, the cutinase from Humicola insolens (HiC) was fused with Escherichia coli anchor peptide OMP25, the enzymatic properties of the fusion protein HiC-OMP25 and its degradation efficiency of the stickies model substrate, poly(ethyl acrylate) (PEA) and poly(vinyl acetate) (PVAc), as well as stickies sediment were determined. All of the results demonstrated that OMP25 efficiently enhanced the degradation ability of HiC.
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Hidrolases de Éster Carboxílico , Compostos de Vinila , Acrilatos , Hidrolases de Éster Carboxílico/metabolismo , Peptídeos , PoliésteresRESUMO
When old corrugated cardboard (OCC) is returned to the paper mill for repulping and reuse, the starch, which is added to the paper surface as a reinforcement agent, is dissolved into the pulping wastewater. Most of the OCC pulping wastewater is recycled to save precious water resources; however, during the water recycling process, the accumulation of dissolved starch stimulates microbial reproduction, which causes poor water quality and putrid odor. This problem seriously affects the stability of the papermaking process and product quality. In this study, phosphomolybdic acid (H3PMo12O40, abbreviated as PMo12) was utilized to catalyze the waste starch present in papermaking wastewater to monosaccharides, realizing the resource utilization of waste starch. The results showed that the optimized yield of total reducing sugar (78.68 wt%) and glycolic acid (12.83 wt%) was achieved at 145 °C with 30 wt% PMo12 at pH 2, which is equivalent to 91.51 wt% starch recovered from wastewater for resource utilization. In addition, the regeneration of the reduced PMo12 was realized by applying a potential of 1 V for 2 h. Overall, this study has theoretical significance and potential application value for resource utilization of waste starch in OCC pulping process and cleaner management of OCC waste paper.
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Amido , Águas Residuárias , Catálise , Resíduos Industriais/análise , Molibdênio , Ácidos Fosfóricos , ReciclagemRESUMO
Herein, using dialdehyde waste paper (DAWP) as a cross-linking agent to immobilize persimmon tannin (PT) was first used to remove the U(VI) and Cr(VI) via the "waste control by waste" concept. The microscopic and macroscopic surface properties of the as-prepared adsorbent was characterized by the advanced characterization techniques. Factors that affected the elimination process such as variable pH, coexistence ions and equilibrium time were investigated by batch techniques. The results showed that the maximal removal capacities of U(VI) and Cr(VI) on DAWP-PT were 242.3 mg/g (pH = 6.0) and 178.7 mg/g (pH = 2.0) at 298 K, which exhibited competitiveness with most of the reported solid materials. Meanwhile, adsorption data were fitted perfectly to the Langmuir and Pseudo-second-order equations, which indicated that the monolayer and homogenous chemisorption dominated the removal process. The SEM-EDX, DFT and XPS analysis conformed that adsorption of U(VI) was mainly via surface complexation, while the elimination of Cr(VI) was a redox reaction process, and about 65.33% of Cr(III) and 34.67% of Cr(VI) co-existed onto the surface of DAWP-PT. Thus, this study would provide a high-efficiency and low-cost adsorbent for radionuclide and heavy metal treatment.