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Highlights A bionic phase-locked structure-inspired iontronic triboelectric gel is proposed with good mechanical compliance for wearable haptic sensing applications. Competitive hydrogen bonding systems are constructed through polymer-solvent-nonsolvent interactions, and regeneration of polymers with weak hydrogen bond donors triggers controlled phase separation. Self-powered haptic skin constructed with iontronic triboelectric gel has a modulus (150.6 kPa) and stretchability (> 400%) similar to that of the human body, enabling fidelity transmission of haptic signals and precise recognition of sensing objects.

In this study, we investigated the effects of salinity on elemental sulfur-driven autotrophic denitrification (SAD) efficiency, and microbial communities. The results revealed that when the salinity was ≤6 g/L, the nitrate removal efficiency in SAD increased with the increasing salinity reaching 95.53% at 6 g/L salinity. Above this salt concentration, the performance of SAD gradually decreased, and the nitrate removal efficiency decreased to 33.63% at 25 g/L salinity. Approximately 5 mg/L of the hazardous nitrite was detectable at 15 g/L salinity, but decreased at 25 g/L salinity, accompanied by the generation of ammonium. When the salinity was ≥15 g/L, the abundance of the salt-tolerant microorganisms, Thiobacillus and Sulfurimonas, increased, while that of other microbial species decreased. This study provides support for the practical application of elemental sulfur-driven autotrophic denitrification in saline nitrate wastewater.

Highlights This review systematically discusses the interfacial properties of cellulosic material preparation processes, top-down, bottom-up, and composite processes. The rational design strategies of cellulosic triboelectric materials are summarized in detail, and the effects of different design strategies on the surface charge characteristics and charge density of cellulosic triboelectric materials are discussed. A comprehensive review of the research progress of cellulosic triboelectric nanogenerators in the field of self-powered wearable electronics.

The lignin derivatives generated during pulping might be responsible for the suboptimal performance of anaerobic reactors during the treatment of pulping wastewater. However, the exact mechanisms by which these derivatives exert influence remain unclear. This study investigated the influence of lignin derivatives, simulated using humic acids (HAs), in anaerobic granular sludge (AnGS). Compared to the enzymes present during floc-bonding and granule-bonding, the HAs impeded the conversion of unhydrolyzed substrates into methane and caused considerable inactivation of free enzymes. Simultaneously, the HAs suppressed agglomeration and weakened the strength of the AnGS. Furthermore, calcium ions helped maintain the integrity of the sludge structure. Therefore, the inhibition of extracellular enzymes using lignin derivatives delays the methanation of unhydrolyzed substrates, resulting in a reduced biomass within AnGS reactors owing to sludge disintegration and biomass loss. This study serves as a reference for investigating the persistent risks originating from lignin derivatives associated with using anaerobic granular-sludge bed reactors to treat pulping wastewater.

The effective acquisition of clean water from atmospheric water offers a potential sustainable solution for increasing global water shortages. Here, authors developed a bioinspired asymmetric amphiphilic surface incorporating self-driven triboelectric adsorption to obtain clean water.

Abstract The rapid rise of triboelectric nanogenerators (TENGs), which are emerging energy conversion devices in advanced electronics and wearable sensing systems, has elevated the interest in high‐performance and multifunctional triboelectric materials. Among them, cellulosic materials, affording high efficiency, biodegradability, and customizability, are becoming a new front‐runner. The inherently low dielectric constant limits the increase in the surface charge density. However, owing to its unique structure and excellent processability, cellulose shows great potential for dielectric modulation, providing a strong impetus for its advanced applications in the era of Internet of Things and artificial intelligence. This review aims to provide comprehensive insights into the fabrication of dielectric‐enhanced cellulosic triboelectric materials via dielectric modulation. The exceptional advantages and research progress in cellulosic materials are highlighted. The effects of the dielectric constant, polarization, and percolation threshold on the charge density are systematically investigated, providing a theoretical basis for cellulose dielectric modulation. Typical dielectric characterization methods are introduced, and their technical characteristics are analyzed. Furthermore, the performance enhancements of cellulosic triboelectric materials endowed by dielectric modulation, including more efficient energy harvesting, high‐performance wearable electronics, and impedance matching via material strategies, are introduced. Finally, the challenges and future opportunities for cellulose dielectric modulation are summarized.

In this study, a Co-Mn/CeO2 composite was prepared through a facile sol-gel method and used as an efficient catalyst for the ozonation of norfloxacin (NOR). The Co-Mn/CeO2 composite was characterized via XRD, SEM, BET and XPS analysis. The catalytic ozonation of NOR by Co-Mn/CeO2 under different conditions was systematically investigated, including the effect of the initial solution’s pH, Co-Mn/CeO2 composite dose, O3 dose and NOR concentration on degradation kinetics. Only about 3.33% of total organic carbon (TOC) and 72.17% of NOR could be removed within 150 min by single ozonation under the conditions of 60 mg/L of NOR and 200 mL/min of O3 at pH= 7 and room temperature, whereas in the presence of 0.60 g/L of the Co-Mn/CeO2 composite under the same conditions, 87.24% NOR removal was obtained through the catalytic ozonation process. The results showed that catalytic ozonation with the Co-Mn/CeO2 composite could effectively enhance the degradation and mineralization of NOR compared to a single ozonation system alone. The catalytic performance of CeO2 was significantly improved by the modification with Mn and Co. Co-Mn/CeO2 represents a promising way to prepare efficient catalysts for the catalytic ozonation of organic polluted water. The removal efficiency of NOR in five cycles indicates that Co-Mn/CeO2 is stable and recyclable for catalytic ozonation in water treatment.

The current wastewater treatment method shows low efficiency in treating wastewater with high concentrations of chemical mechanical pulp (CMP). Therefore, a chlorine dioxide Pretreatment Anaerobic Treatment (DPAT) was developed and applied to treat the CMP wastewater to obtain higher efficiency, obtaining the following results: The biodegradability of CMP wastewater improved after chlorine dioxide pretreatment. The COD of wastewater treated with chlorine dioxide was reduced from 5634 mg/L to 660 mg/L. The removal rate for chemical oxygen demand (COD) was 88.29%, 29.13% higher than the common anaerobic treatment. The reasons for the high efficiency of the DPAT treatment were that chlorine dioxide pretreatment removed the toxic substances in the original wastewater and thereby promoted the proliferation and growth of the anaerobe. The results show that pretreatment with chlorine dioxide can effectively enhance the biodegradability of high-concentration CMP wastewater. Therefore, DPAT treatment of high-concentration CMP wastewater is beneficial to environmental protection.

At present, the synthesis methods of crystalline porous materials often involve powder products, which not only affects the practical application but also has complex synthesis operations and limited scale. Based on the mechanochemical method, we choose COF-TpPa-1, preparing TpPa-1-DANC composites. Covalent organic frameworks (COFs) are a kind of crystalline material formed by covalent bonds of light elements. COFs possess well pore structure and high thermal stability. However, the state of synthesized powders limits their application. Cellulose nanocrystals (CNCs) are promising renewable micron materials with abundant hydroxyl groups on their surface. It is possible to prepare high-strength materials such as film, water, and aerogel. Firstly, the nanocellulose was oxidized by the sodium periodate method to obtain aldehyde cellulose nanocrystals (DANC). TpPa-1-DANC not only had the crystal characteristic peak of COFs at 2θ ≈ 5° but also had a BET surface area of 247 m2/g. The chemical bonds between COFs and DANC formed by Schiff base reaction appeared in FTIR and XPS. The pyrolysis behavior of the composite was characterized by TG-IR, which showed that the composite had good thermal stability. With the advantages of nanocellulose as a material in every dimension, we believe that this method can be conducive to the large-scale synthesis of COFs composites, and has the possibility of multi-form synthesis of COFs.

Paper packaging materials are widely used in food packaging. However, it is difficult to extract trace chloropropanol from food packaging paper, so there is a lack of research on the leaching of chloropropanol from paper materials. Therefore, it is of positive significance to explore the leaching rule of chloropropanol in paper pulp for the safety of paper packaging materials, to reduce the risk of food packaging to food safety and to provide a theoretical basis for the formulation of safety standards for paper packaging materials. In order to study the content of chloropropanol in paper packaging paper more accurately, a response surface methodology was used to study the relationship between the amount of chloropropanol leaching and pulp concentration, leaching temperature and leaching time, as well as the interaction of each factor. The results showed that time, temperature and pulp concentration were the main factors affecting the leaching amount of chloropropanol from paper packaging materials. There were significant (p > 0.05) interactions between the time and pulp concentration, as well as temperature and pulp concentration. The leaching efficiency of chloropropanol was higher at a lower pulp concentration, and the leaching amount of chloropropanol was higher at a lower temperature. The temperature more significantly affected the leaching of chloropropanol in a low-concentration system than in a high-concentration system. Relevant studies have shown that the selection of solvent has an important effect on the extraction rate of target compounds. Therefore, in this experiment, different polar organic solvents (methanol, ethanol, formaldehyde solution) were added into the soaking solution to change the leaching amount of chloropropanol. The results showed that adding a certain amount of formaldehyde solution can obviously increase the leaching amount of chloropropanol in pulp.

Intimate coupling photocatalysis and biodegradation treatment technology is an emerging technology in the treatment of refractory organic matter, and the carrier plays an important role in this technology. In this paper, sugarcane cellulose was used as the basic skeleton, absorbent cotton was used as a reinforcing agent, anhydrous sodium sulfate was used as a pore-forming agent to prepare a cellulose porous support with good photocatalytic performance, and nano-TiO2 was loaded onto it by a low-temperature bonding method. The results showed that the optimal preparation conditions of cellulose carriers were: cellulose mass fraction 1.0%; absorbent cotton 0.6 g; and Na2SO4 60 g. The SEM, EDS and XPS characterization further indicated that the nano-TiO2 was uniformly loaded onto the cellulose support. The degradation experiments of Rhodamine B showed that the nano-TiO2-loaded composite supports had good photocatalytic performance. The degradation rate of 1,2,4-trichlorobenzene was more than 92% after 6 cycles, and the experiment of adhering a large number of microorganisms on the carriers before and after the reaction showed that the cellulose-based carriers obtained the required photocatalytic performance and stability, which is a good cellulose porous carrier.

Given the high content of Ca2+ in waste paper recycling wastewater, the anaerobic granular sludge (AnGS) undergoes calcification during wastewater treatment and affects the treatment efficiency. To restore the activity of calcified AnGS and improve the performance of AnGS, four types of N-acyl-homoserine lactones (AHLs) were added to the AnGS system while papermaking wastewater treatment. The addition of N-butyryl-DL-homoserine lactone(C4-HSL) and N-octanoyl-DL-homoserine lactone (C8-HSL) had an inhibitory affect the COD removal efficiency and SMA of sludge at the inception. The addition of N-hexanoyl-L-homoserine lactone (C6-HSL) has no obvious effect on the COD removal efficiency, but can improve the SMA of sludge more obviously. The addition of N-(β-ketocaproyl)-DL-homoserine lactone (3O-C6-HSL) can increased COD removal efficiency and promoted SMA together obviously. The addition of C6-HSL and 3O-C6-HSL can increase volatile suspended solid (VSS)/total suspended solid (TSS), and regulate extracellular polymeric substance (EPS) secretion in AnGS. Analysis of microbial sequencing revealed changes in the microbial community structure following AHL addition, which enhanced the methane metabolism pathway in sludge. The addition of C6-HSL, C8-HSL, and 3O-C6-HSL increased Methanosaeta population, thus increasing the aceticlastic pathway in sludge. Thus, exogenous AHLs can play an important role in regulating microbial community structure, and in improving the performance of AnGS.

Paper packaging materials are widely used as sustainable green materials in food packaging. The production or processing of paper materials is conducted in an environment that contains organic chlorides; therefore, potential food safety issues exist. In this study, the adsorption behavior of organic chlorides on paper materials was investigated. Chloropropanol, which has been extensively studied in the field of food safety, was employed as the research object. We studied the adsorption mechanism of chloropropanol on a crystalline nanocellulose (CNC) model. The results demonstrated that physical adsorption was the prevailing process, and the intermolecular hydrogen bonds acted as the driving force for adsorption. The adsorption effect assumed greatest significance under neutral and weakly alkaline conditions. A good linear relationship between the amount of chloropropanol adsorbed and the amount of CNC used was discovered. Thus, the findings of this study are crucial in monitoring the safety of products in systems containing chloropropanol and other chlorinated organic substances. This is particularly critical in the production of food-grade paper packaging materials.

The preparation of bio-oil through biomass pyrolysis is promoted by different demineralization processes to remove alkali and alkaline earth metal elements (AAEMs). In this study, the hydrothermal pretreatment demineralization was optimized by the response surface method. The pretreatment temperature, time and pH were the response elements, and the total dissolution rates of potassium, calcium and magnesium were the response values. The interactions of response factors for AAEMs removal were analyzed. The interaction between temperature and time was significant. The optimal AAEMs removal process was obtained with a reaction temperature of 172.98 °C, time of 59.77 min, and pH of 3.01. The optimal dissolution rate of AAEMs was 47.59%. The thermal stability of eucalyptus with and without pretreatment was analyzed by TGA. The hydrothermal pretreatment samples exhibit higher thermostability. The composition and distribution of pyrolysis products of different samples were analyzed by Py-GC/MS. The results showed that the content of sugars and high-quality bio-oil (C6, C7, C8 and C9) were 60.74% and 80.99%, respectively, by hydrothermal pretreatment. These results show that the removal of AAEMs through hydrothermal pretreatment not only improves the yield of bio-oil, but also improves the quality of bio-oil and promotes an upgrade in the quality of bio-oil.

The accumulation of dissolved and colloidal substances (DCS) in the increasingly closed paper circulating water system can seriously lower the productivity and safety of papermaking machines, and it has been a challenge to develop an adsorbent with low cost, high adsorption efficiency and large adsorption capacity for DCS removal. In this study, cationic lignocellulose nanofibers (CLCNF) were obtained by cationic modification of agricultural waste bagasse in deep eutectic solvents (DES) followed by mechanical defibrillation, and then CLCNF were employed as an adsorbent for DCS model contaminant polygalacturonic acid (PGA) removal. CLCNF was characterized by transmission electron microscopy, Fourier transform infrared, elemental analysis, X-ray diffraction, and thermogravimetric analysis. The analytical results confirmed the successful preparation of CLCNF with 4.6–7.9 nm diameters and 0.97–1.76 mmol/g quaternary ammonium groups. The effects of quaternary ammonium group contents, pH, contact time and initial concentration of PGA on the adsorption were investigated in a batch adsorption study. According to the results, the cationic modification significantly enhanced the adsorption of PGA by CLCNF and the adsorption performance increased with the increase of the quaternary ammonium group contents. The adsorption of PGA on CLCNF followed the pseudo-second-order and the fitted Langmuir isotherm model. The adsorption showed fast initial kinetics and the experimental maximum adsorption capacity was 1054 mg/g, which is much higher than PGA adsorbents previously reported in the literature. Therefore, CLCNF with high cationic group content developed in this paper is a promising adsorbent for DCS removal.

Hydrogen peroxide chemo-mechanical pulp (APMP), sulfonated chemo-mechanical pulp (SCMP), and chemical thermomechanical pulp (CTMP) were used as raw materials to explore the effects of hydrogen peroxide (HP), Fenton pretreatment (FP), and ethanol pretreatment (EP) on the enzymatic hydrolysis of high-yield bamboo mechanical pulp (HBMP). The surface lignin distribution and contents of different HBMPs were determined using confocal laser scanning microscopy (CLSM) and X-ray photoelectron spectroscopy (XPS). The correlation between the surface lignin and the enzymatic hydrolysis of HBMP was also investigated. The residue of enzymatic hydrolysis was used to adsorb methylene blue (MB). The results showed that the cracks and fine fibers on the surface of APMP, SCMP, and CTMP increased after FP, when compared to HP and EP. The total removal content of hemicellulose and lignin in SCMP after FP was higher than with HP and EP. Compared to SCMP, the crystallinity increased by 15.4%, and the surface lignin content of Fenton-pretreated SCMP decreased by 11.7%. The enzymatic hydrolysis efficiency of HBMP after FP was higher than with HP and EP. The highest enzymatic hydrolysis of Fenton-pretreated SCMP was 49.5%, which was higher than the enzymatic hydrolysis of Fenton-pretreated APMP and CTMP. The removal rate of MB reached 94.7% after the adsorption of the enzymatic hydrolysis residue of SCMP. This work provides an effective approach for a high value-added utilization of high-yield bamboo pulp.

The work is intended to summarize the recent progress in the work of fractal theory in packaging material to provide important insights into applied research on fractal in packaging materials. The fractal analysis methods employed for inorganic materials such as metal alloys and ceramics, polymers, and their composites are reviewed from the aspects of fractal feature extraction and fractal dimension calculation methods. Through the fractal dimension of packaging materials and the fractal in their preparation process, the relationship between the fractal characteristic parameters and the properties of packaging materials is discussed. The fractal analysis method can qualitatively and quantitatively characterize the fractal characteristics, microstructure, and properties of a large number of various types of packaging materials. The method of using fractal theory to probe the preparation and properties of packaging materials is universal; the relationship between the properties of packaging materials and fractal dimension will be a critical trend of fractal theory in the research on properties of packaging materials.

The emission standard for adsorbable organic halogen (AOX) has been adjusted as a mandatory assessment indicator in the papermaking industrial pollutants emission standards of China. To provide a theoretical basis to reduce AOX formation, a kinetic model of the first chlorine dioxide bleaching stage (D0) is presented for elemental chlorine-free (ECF) bleaching of eucalyptus kraft pulp. The kinetics of the D0 stage can be expressed as dW/dt = 314.6e-20.53/RT[H+]0.21[ClO2]0.41K0.98, where the reaction series for lignin, chlorine dioxide dosage, and H+ concentration are 0.98, 0.41, and 0.21, respectively. The reaction activation energy was 20.53 kJ.mol-1. R2 was greater than 0.9, which means that the model was shown to have high prognostic ability and feasibility. In the D0 stage, mostly lignin was removed and the reaction was fast. Much AOX was formed at the beginning of bleaching, and the reaction rate was primarily determined by the lignin content and chlorine dioxide dosage. H+ existed primarily as a catalyst and had little influence on AOX formation. The AOX formation occurs easily, as the reaction activation energy is less than 30 kJ.mol-1.

This paper presents a kinetic model of the laccase-aided chlorine dioxide bleaching of bagasse pulp. The kinetic model was based on the rate of reduction of adsorbed organic halogen (AOX). The effects of the laccase enzyme dosage, the mediator 1-hydroxybenzotriazole (HBT) dosage, and the reaction temperature on the AOX content of the bleaching effluent are discussed. Good fits were obtained for the experimental data obtained from the different laccase enzyme dosages, HBT dosages, and reaction temperatures, indicating the feasibility of the kinetic model as a means of predicting the optimal operation conditions for the laccase-aided chlorine dioxide bleaching of bagasse pulp in the future.

A mathematical description was developed for production of saccharides and fermentation inhibitors during the hot-compressed water pretreatment of cassava residue. Pretreatment was conducted at 150 °C, 160 °C, 170 °C, and 180 °C, and reaction times ranged from 0 to 70 min. The formation of saccharides and four main inhibitors (furfural (F), hydroxymethylfurfural (HMF), acetic acid, and formic acid) were studied. A model for predicting the concentrations of F and HMF (CF and CHMF, respectively) as functions of H+ concentration was established. Furthermore, kinetic models were built after introducing the hydrogen ion concentration index mi. Hydrogen ion concentration had a dramatic effect on the dissolution of pentosan but did not greatly affect the dissolution of hexosan or the degradation of hexose or pentose. Additionally, the activation energies for the formation of pentose or hexose were lower than the degradation energies. The coefficients of determination (R2) of the kinetic models for predicting the yield of the four compounds (pentose, hexose, furfural, and HMF) were higher than 0.923. These kinetic models provided a theoretical foundation and technical support for controlling the production of the main carbohydrates and fermentation inhibitors.

The dissolution of sugarcane bagasse cellulose (SBC) in zinc chloride solution was studied at elevated temperatures. Based on single factor experiments, the effects of zinc chloride mass fraction, dissolution time, temperature, and bagasse cellulose mass fraction were investigated by an orthogonal experiment, and the optimal dissolution conditions were obtained. The dissolution process of bagasse cellulose was observed under a microscope. Additionally, the original SBC and regenerated SBC were both characterized by Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). Temperature was found to be the most important factor affecting dissolution time. The best dissolving process took place at 85 °C to dissolve 2% SBC in 85% zinc chloride for 210 min. It was shown that the zinc chloride was a direct solvent for SBC. After regeneration of cellulose in zinc chloride, the crystallinity of cellulose was decreased greatly, from 77% to 54%, its crystalline form was transformed from cellulose I to cellulose II, its thermal decomposition temperature was reduced, its thermal stability was slightly decreased, and its internal structure was disrupted.

The process of dehydration of glucose to 5-hydroxymethylfurfural (HMF), using caprolactam-lithium chloride (CPL/LiCl) as a solvent, was investigated. Dual-wavelength ultraviolet spectrophotometry provides a new approach for the determination of glucose conversion rate and yield of HMF. Experiments were performed to demonstrate the accuracy and precision of this method. Various reaction parameters, such as the ratio of ionic liquid, reaction temperature, reaction time, catalyst dosage, and solid absorbent, were investigated in detail for the dehydration of glucose. The optimal conditions were explored. Finally, a possible mechanism for the dehydration of fructose to HMF was proposed.

In order to further reduce absorbable organic halide (AOX) formation in the bleaching effluent, NH2SO3H and DMSO were added during the elemental chlorine-free (ECF) bleaching (D0EpD1) of bagasse kraft pulp. In the D0 stage, AOX formation decreased by 10% with 0.1% NH2SO3H, and a reduction of 11.2% with 1.0% DMSO, respectively. Ultraviolet (UV) spectra, Fourier transform infrared spectroscopy (FTIR), and gas chromatography-mass spectroscopy (GC-MS) were adopted in characterizing changes of lignin degradation and the main functional groups of bleached pulp. The UV spectrum showed that the quantity of polyphenols decreased after adding the additives. The FTIR spectrum showed that both the content of phenolic-type lignin and the degradation degree of lilac-type lignin decreased after adding NH2SO3H. If was found that DMSO was beneficial in retaining C-O-C and C=O structures in cellulose and hemicellulose, while NH2SO3H decreased the content of β-glycosidic bonds and C-O-C structures in cellulose and hemicellulose. The composition of lignin degradation products in the bleaching effluent was analyzed by GC-MS. The contents of chlorobenzene and chlorophenol decreased notably when additives were added. Compared with DMSO, NH2SO3H exhibited poor inhibition on the formation of some phenols.

Due to the natural cellulose encapsulated in both lignin and hemicellulose matrices, as well as in plant cell walls with a compact and complex hierarchy, extracting cellulose nanofibers (CNFs) from lignocellulosic biomass is challenging. In this study, a sustainable high yield strategy with respect to other CNF preparations was developed. The cellulose was liberated from plant cell walls and fibrillated to a 7–22 nm thickness in one bath treatment with H3PO4 and H2O2 under mild conditions. The cellulose underwent swelling, the lignin underwent oxidative degradation, and the hemicellulose and a small amount of cellulose underwent acid hydrolysis. The CNFs’ width was about 12 nm, with high yields (93% and 50% based on cellulose and biomass, respectively), and a 64% crystallinity and good thermal stability were obtained from bagasse. The current work suggests a strategy with simplicity, mild conditions, and cost-effectiveness, which means that this method can contribute to sustainable development for the preparation of CNFs.

The low reactivity of lignin hinders its application as a phenol substitute in phenol–formaldehyde (PF) resin. Therefore, the combination of fractionation and phenolation was adopted to enhance the reactivity of lignin for preparing a phenol–formaldehyde resin adhesive. Sugarcane bagasse kraft lignin and its fractions were employed to replace 40 wt% of phenol to prepare a PF adhesive. The fractionation increased the reactivity of lignin, however the as-prepared lignin-based PF (LPF) hardly met its application requirements as an adhesive. Therefore, the phenolation of lignin under an acidic condition was adopted to further improve its reactivity. The phenolated lignin was characterized by FTIR, gel permeation chromatography, and NMR, indicating its active sites increased while its molecular weight decreased. The phenolated lignin was used to replace 40 wt% of phenol to prepare a PF adhesive (PLPF) which was further employed to prepare plywood. The results indicated that the combination of fractionation and phenolation effectively enhanced the reactivity of lignin, and eventually improved the properties of the PLPF and its corresponding plywood. The free formaldehyde content of PLPF decreased to 0.16%. The wet bonding strength of the as-prepared plywood increased to 1.36 MPa, while the emission of formaldehyde decreased to 0.31 mL/L.

The use of advanced and eco-friendly materials has become a trend in the field of food packaging. Cellulose nanofibrils (CNFs) were prepared from bleached bagasse pulp board by a mechanical grinding method and were used to enhance the properties of a chitosan/oregano essential oil (OEO) biocomposite packaging film. The growth inhibition rate of the developed films with 2% (w/w) OEO against E. coli and L. monocytogenes reached 99%. With the increased levels of added CNFs, the fibrous network structure of the films became more obvious, as was determined by SEM and the formation of strong hydrogen bonds between CNFs and chitosan was observed in FTIR spectra, while the XRD pattern suggested that the strength of diffraction peaks and crystallinity of the films slightly increased. The addition of 20% CNFs contributed to an oxygen-transmission rate reduction of 5.96 cc/m2·day and water vapor transmission rate reduction of 741.49 g/m2·day. However, the increase in CNFs contents did not significantly improve the barrier properties of the film. The addition of 60% CNFs significantly improved the barrier properties of the film to light and exhibited the lowest light transmittance (28.53%) at 600 nm. Addition of CNFs to the chitosan/OEO film significantly improved tensile strength and the addition of 60% CNFs contributed to an increase of 16.80 MPa in tensile strength. The developed chitosan/oregano essential oil/CNFs biocomposite film with favorable properties and antibacterial activity can be used as a green, functional material in the food-packaging field. It has the potential to improve food quality and extend food shelf life.

In this study, we investigated the barrier properties of a montmorillonite-reinforced biomass material, starch. Organically modified montmorillonite materials were prepared from natural montmorillonite by reacting it with dodecyl trimethyl ammonium chloride, dodecyl dimethyl benzyl ammonium chloride or octadecyl trimethyl ammonium chloride under ultrasonic conditions. The composite starch films incorporated with these organically modified montmorillonite samples were characterized by scanning electron microscopy, transmission electron microscopy, infrared spectroscopy and X-ray diffraction. The results showed that the introduction of montmorillonite decreases the transmittance of the composite film by 10% in the visible region and significantly inhibits UV-light transmittance. The decomposition temperature of the composite film ranges from 200 to 500 °C, with a weight loss rate of 80%. The distance between the montmorillonite layers increases from 0.14 nm in the non-magnetized state to 1.49 nm after magnetization. The oxygen permeability of the starch film modified by organic montmorillonite (0.067 cm3/m2·d) is lower than that of the montmorillonite starch film without magnetization (0.097cm3/m2·d). The oxygen barrier capacity is close to zero. Particularly in the ordered magnetic montmorillonite starch composite film, the oxygen barrier ability is the best. Therefore, modified montmorillonite could serve as an excellent reinforcing agent for cassava starch films and effectively improve the oxygen barrier performance of the films.

Separating the fibers, deconstructing both the interlamellar structures and the intermicrofibrils structures in the cell wall, and cleaving the amorphous regions of cellulose (all reached in one bath chemical-assisted treatment), then extracting cellulose nanofibers (CNFs) from biomass, is both challenging and imperative. A simple, cost-effective and green strategy for extracting CNFs from bamboo using nitric acid and hydrogen peroxide (NCHP), to enable fibrillation via a cooperative mechanism, is demonstrated herein. NCHP-CNFs 13.1 ± 2.0 nm wide, with a high aspect ratio, 74% crystallinity, excellent UV resistance and high thermal stability, were successfully extracted by treatment in HNO3 aqueous solution, at a concentration of 3.2 mol/L, and treatment with 60.00 mmol/g H2O2 at 50 °C for 48 h. The yields of NCHP-CNFs reached 73% and 99% based on biomass and cellulose, respectively, due to the high delignification selectivity of OH+ and the mild aqueous conditions during the NCHP treatment. These NCHP-CNFs with excellent UV resistance can potentially be applied in the field of UV-resistant coatings, to replace organic and inorganic materials.

Because of its non-toxic, pollution-free, and low-cost advantages, environmentally-friendly packaging is receiving widespread attention. However, using simple technology to prepare environmentally-friendly packaging with excellent comprehensive performance is a difficult problem faced by the world. This paper reports a very simple and environmentally-friendly method. The hydroxyl groups of cellulose nanofibrils (CNFs) were modified by introducing malic acid and the silane coupling agent KH-550, and the modified CNF were added to cassava starch as a reinforcing agent to prepare film with excellent mechanical, hydrophobic, and barrier properties. In addition, due to the addition of malic acid and a silane coupling agent, the dispersibility and thermal stability of the modified CNFs became significantly better. By adjusting the order of adding the modifiers, the hydrophobicity of the CNFs and thermal stability were increased by 53.5% and 36.9% ± 2.7%, respectively. At the same time, the addition of modified CNFs increased the tensile strength, hydrophobicity, and water vapor transmission coefficient of the starch-based composite films by 1034%, 129.4%, and 35.95%, respectively. This material can be widely used in the packaging of food, cosmetics, pharmaceuticals, and medical consumables.

Intimate coupling of photocatalysis and biodegradation (ICPB) has shown promise in removing unwanted organic compounds from water. In this study, bagasse cellulose titanium dioxide composite carrier (SBC-TiO2) was prepared by low-temperature foaming methods. The optimum preparation conditions, material characterization and photocatalytic performance of the composite carrier were then explored. By conducting a single factor test, we found that bagasse cellulose with a mass fraction of 4%, a polyvinyl alcohol solution (PVA) with a mass fraction of 5% and 20 g of a pore-forming agent were optimum conditions for the composite carrier. Under these conditions, good wet density, porosity, water absorption and retention could be realized. Scanning electron microscopy (SEM) results showed that the composite carrier exhibited good biologic adhesion. X-ray spectroscopy (EDS) results confirmed the successful incorporation of nano-TiO2 dioxide into the composite carrier. When the mass concentration of methylene blue (MB) was 10 mg L−1 at 200 mL, 2 g of the composite carrier was added and the initial pH value of the reaction was maintained at 6, the catalytic effect was best under these conditions and the degradation rate reached 78.91% after 6 h. The method of preparing the composite carrier can aid in the degradation of hard-to-degrade organic compounds via ICPB. These results provide a solid platform for technical research and development in the field of wastewater treatment.

MnO2-deposited lignin-based carbon fiber (MnO2-LCF) mats are fabricated for supercapacitor applications. LCF mats are produced from alkali lignin via electrospinning followed by stabilization and carbonization. The carbonization process is carried out at 800, 900, and 1000 °C, and the corresponding mats are denoted as MnO2-LCF-800, MnO2-LCF-900, and MnO2-LCF-1000, respectively. The LCF mats are immersed in a KMnO4 solution at room temperature for 72 h to obtain MnO2-LCF mats. The scanning electron microscopy and X-ray diffraction analysis confirm the deposition of MnO2 on the LCFs. The Brunauer−Emmett−Teller analysis, X-ray spectroscopy, and Raman spectroscopy reveal that MnO2-LCF-800 mat possesses a large number of mesopores and Mn vacancies as compared to MnO2-LCF-900 mat and MnO2-LCF-1000 mat. Consequently, MnO2-LCF-800 mat possesses the best electrochemical properties with a specific capacitance of 131.28 F∙g−1, an energy density of 14.77 Wh∙kg−1, and a power density of 135.01 W∙kg−1 at a specific current of 0.3 A∙g−1. Hence, MnO2-LCF-800 mat shows high potential to be used as a high-performance supercapacitor.

In this study, an physico-chemical method and enzymatic improvement were used to extract cassava dietary fiber from cassava residue. α-amylase, glucoamylase, lipase, and protease were added to the physically comminuted cassava residue to remove starch, fat, and protein. Then, with the aid of ultrasound, dietary fiber was bleached with hydrogen peroxide to increase its whiteness. Finally, the cassava dietary fiber was treated with cellulase to increase the amount of soluble dietary fiber. The yield of dietary fiber was 75.63%, 37.55% of which was soluble dietary fiber. Water-holding capacity, water-swelling capacity, and oil-holding capacity of cassava dietary fiber were 4.020 g/g, 2.091 mL/g, and 2.891 g/g, respectively, which were 11.14%, 52.85%, and 9.55% higher than those of raw tapioca. Thus, the physical and chemical properties of the dietary fiber were improved.

Wood–plastic composites were prepared from polyethylene terephthalate- 1,4-cyclohexanedimethanol ester (PETG) and waste-paper fiber that was unmodified, modified with alkyl-ketene-dimer (AKD), and modified with a silane-coupling agent. The mechanical properties, water absorption properties, surface structure, and thermal properties of the three prepared materials were compared. The results showed that the optimum amount of waste-paper powder is 10 wt%, while that of the waste-paper particles is 60–80 mesh. The use of AKD and coupling agent KH550 can reduce the water absorption of the composite; however, the reductive effect of the coupling agent is better, in that it is reduced by 0.3%. Modification using a 1-wt% KH550 coupling agent can effectively increase the tensile strength of a composite from 31.36 to 41.67 MPa (increase of 32.8%), while the bending strength increased from 86.47 to 98.31 MPa (increase of 13.7%). This also enhances the thermal stability of the composites. With the addition of the coupling agent, the composite material maintains good mechanical properties even after being immersed in water; this can enable the safe use of these composite materials in outdoor environments.

Nanocellulose was prepared by a mechanochemical method using cassava residue as a raw material and phosphoric acid as the auxiliary agent. The prepared nanocellulose was hydrophobically modified with stearic acid to improve its dispersibility. This modified nanocellulose was added to polylactic acid (PLA) film-forming liquids at concentrations of 0%, 0.5%, 1.0%, 1.5% and 2.0%, and the effect of modified nanocellulose on the mechanical properties of polylactic acid (PLA) films were investigated. When at least 0.5% modified nanocellulose is added, more active groups of modified nanocellulose are adsorbed onto the PLA molecular chain. Although the tensile strength of the film is only improved by 13.59%, the flexibility of the film decreases, and the elastic modulus decreases by 28.91%. When 1% modified nanocellulose is added, the modified nanocellulose and PLA are tangled together through molecular chains and they co-crystallize to form a stable network structure. The tensile strength of the nanocomposite films is enhanced by 40.03%, the elastic modulus is enhanced by 55.65%, and the flexibility of the film decreases.

The laccase-mediator system in laccase-aided chlorine dioxide bleaching of bagasse pulp was optimized using response surface methodology (RSM). The effects and interactions of the laccase enzyme dosage, the dosage of the mediator 1-hydroxybenzotriazole (HBT), and the reaction time on the adsorbed organic halogen (AOX) content of the wastewater as well as the brightness and kappa number of the pulp were examined. The optimal reaction conditions to achieve a balance of lower AOX content, higher brightness, and lower kappa number were as follows: laccase enzyme dosage of 20.3 U/g, HBT dosage of 1.51%, and reaction time of 154.5 min. Under these conditions, an AOX content of 20.67 mg/L, brightness of 58.94% ISO, and kappa number of 2.71 were observed. These results will offer a favorable option for pulp and paper mills as well as the natural environment and therefore provide a theoretical foundation for the industrial application of laccase in bleaching processes.

A laboratory investigation was developed to confirm and to quantify the reductions in absorbable organic halide (AOX) discharge when sodium sulphide was added during elemental chlorine-free (ECF) bleaching of sugarcane bagasse pulp. After the chlorine dioxide bleaching stage, the pulp was sent directly into the extraction stage without washing. FTIR was employed to determine the breakage of chemical bonds in the pulp, and GC-MS was used to measure the composition of the bleaching effluent. The addition of sodium sulphide caused a reduction in AOX of up to 46.7%. The AOX reduction reached this maximum when the sodium sulphide was added 30 min after the start of the extraction stage and when the pH was higher than 12. FTIR spectroscopy showed that the phenolic lignin of the pulp was degraded by the sodium sulphide and that the syringyl lignin and C-O-C, C=O structure of the pulp holocellulose of the pulp was preserved during the extraction stage. The GC-MS showed that the chlorobenzene and chlorophenol contents decreased noticeably after the addition of sodium sulphide.

This paper aimed to investigate the reasons for improved properties of bamboo alkaline peroxide mechanical pulp (APMP), such as relatively high brightness and low post-colour number, by alkali hydrogen peroxide pre-extraction (AHPP) treatment. It was found that AHPP could affect the dissolution of 1% sodium hydroxide extractives, benzene-ethanol extractives, and acid-soluble lignin. The results of Fourier transform infrared (FTIR) and 13C-nuclear magnetic resonance spectroscopy (13C-NMR) illustrated that carboxyl, syringyl, guaiacyl, acetyl, and methoxyl groups of the milled wood lignin (MWL) in bamboo were degraded slightly after AHPP treatment. However, some lignin-like structures, the links of α-O-4, β-O-4, and some carbohydrates such as xylan, α-glucose, β-glucose, α-mannose, and β-mannose in lignin-carbohydrate complexes (LCCs) were degraded noticeably. The analysis of UV spectrophotometry indicated that AHPP treatment was conductive to the degradation of some chromophores in MWL. The degradation of MWL and LCC under simulated AHPP conditions showed consistency with the above results.

The aims of this study were response surface modeling and optimization of Cr(VI) removal from solution using formaldehyde-modified eucalyptus bark. A high removal rate of Cr(VI) was achieved under the conditions of low adsorbent dosing quantity and high initial concentration of Cr(VI). Analysis of variance showed a high multiple coefficient of determination (R2=0.9875), adjusted determination coefficient (R2Adj=0.9714), and the good second order regression equation. The initial concentration of Cr(VI) was 40.15 mg/L, adsorbent dosing quantity 3.40 g/L, and initial reaction pH 2.78, and the largest removal rate was 99.998% under the optimum reaction conditions. Langmuir and Freundlich isothermal models described well adsorption of Cr(VI) by the modified stringy bark. Adsorption kinetics studies showed that the adsorption was controlled by multiple factors, dominated by chemical adsorption. The adsorption was found to be spontaneous and endothermic, with △G0 < 0, △H0 > 0, and △S0 > 0. Adsorption of Cr(VI) by formaldehyde-modified stringy bark was partly controlled by REDOX reactions. The adsorbents were characterized by SEM and FTIR.

In this paper, a kinetic model of the first chlorine dioxide bleaching stage (D0) in an elemental chlorine-free (ECF) bleaching sequence is presented for bagasse pulps. The model is based on the rate of adsorbable organic halogen (AOX) formation. The effects of the chlorine dioxide dosage, the sulfuric acid dosage, and the reaction temperature on the AOX content of wastewater are examined. The reaction of AOX formation could be divided into two periods. A large amount of AOX was formed rapidly within the first 10 min. Ten minutes later, the AOX formation rate significantly decreased. The kinetics could be expressed as: dW⁄dt=660.8•e^(-997.98/T) 〖•[ClO〗_2 ]^0.877•[H2SO4 ]^0.355•W^(-1.065), where W is the AOX content, t is the bleaching time (min), T is the temperature (K), [ClO2] is the dosage of chlorine dioxide (kg/odt), and [H2SO4] is the dosage of sulfuric acid (kg/odt). The fit of the experiment results obtained for different temperatures, initial chlorine dioxide dosages, initial sulfuric acid dosages, and AOX content were very good, revealing the ability of the model to predict typical mill operating conditions.

Nanocomposites consisting of cellulose nanofibrils (CNFs) and nano-aluminum nitride (AlN) were prepared using a simple vacuum-assisted filtration process. Bleached sugarcane bagasse pulp was treated with potassium hydroxide and sodium chlorite, and was subsequently ultra-finely ground and homogenized to obtain CNFs. Film nanocomposites were prepared by mixing CNFs with various AlN amounts (0−20 wt.%). X-ray diffraction revealed that the crystal form of CNF-AlN nanocomposites was different to those of pure CNFs and AlN. The mechanical performance and thermal stability of the CNF-AlN nanocomposites were evaluated through mechanical tests and thermogravimetric analysis, respectively. The results showed that the CNF-AlN nanocomposites exhibited excellent mechanical and thermal stability, and represented a green renewable substrate material. This type of nanocomposite could present great potential for replacing traditional polymer substrates, and could provide creative opportunities for designing and fabricating high-performance portable electronics in the near future.

Owing to the implementation of increasingly stringent water conservation policies and regulations, the pulp and paper mill industry must make increased efforts to meet the limits for pollutant emissions. The primary pretreatment and secondary biochemical treatment methods used currently generally fail to meet the country-specific environmental regulations, and the wastewater must be processed further even after being subjected to secondary biochemical treatments. In this work, we synthesized Fe3O4/MnO2 nanocomposites (FMNs) with a flower-like structure for use in the heterogeneous photocatalytic treatment of biotreated papermaking wastewater. FMNs1.25, which were formed using a KMnO4/Fe3O4 molar ratio of 1.25, could be separated readily using an external magnetic field and exhibited higher photocatalytic activity than those of the other samples as well as MnO2 and Fe3O4. The effects of various experimental parameters on the photocatalytic activity of FMNs1.25, including the initial pH of the wastewater and the catalyst dosage, were determined. The common chemical oxygen demand (CODCr) reduction rate in the case of this sample reached 56.58% within 120 min at a pH of 3, the CODCr of effluent after treatment was 52.10 mg/L. Further, even under neutral conditions, the CODCr of the treated effluent was below the current limit for discharge in China. Moreover, the nanocomposites exhibited good recyclability, and their catalytic activity did not decrease significantly even after five usage cycles. This study should serve as a platform for the fabrication of effective photocatalysts for the advanced treatment of biotreated papermaking effluent and refractory organic wastewater.

Lignin is the second largest naturally renewable resource and is primarily a by-product of the pulp and paper industry; however, its inefficient use presents a challenge. In this work, Fe3O4 nanoparticles loaded on lignin nanoparticles (Fe3O4@LNPs) were prepared by the self-assembly method and it possessed an enhanced peroxidase-like activity. Fe3O4@LNPs catalyzed the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) in the presence of H2O2 to generate a blue color, was observable by the naked eye. Under the optimal conditions, Fe3O4@LNPs showed the ability of sensitive colorimetric detection of H2O2within a range of 5⁻100 μM and the limit of detection was 2 μM. The high catalytic activity of Fe3O4@LNPs allows its prospective use in a wide variety of applications, including clinical diagnosis, food safety, and environmental monitoring.

Acetylated nanofibrillated cellulose (ANFC)/acrylic resin ABPE-10 composite film was prepared by impregnating ABPE-10 into ANFC films under negative pressure, which can enhance properties of ANFC films by forming an interpenetrating polymer network structure between ABPE-10 and the ANFC film. The ANFC/ABPE-10 composite film met the high performance flexible organic light-emitting diode substrate requirement, even when the ANFC dosage was as high as approximately 70%. The transparency of films with different ANFC dosages significantly increased from 67% (42 µm) to 88% (45 µm), as determined by ultraviolet-visible analysis. The composite film inherited the properties of AFNC, with a low coefficient of thermal expansion and a ductile compact structure. The contact angles of ANFC films increased from 49.2° to 102.9° after dipping in ABPE-10. Additionally, the composite films had good surface smoothness and mechanical properties.

A thermo-responsive cellulose-based material (cellulose-g-PNIPAAm) was prepared by grafting N-isopropylacrylamide (NIPAAm) onto bagasse pulp cellulose via Ce (IV)-initiated free radical polymerization. The surfaces of the obtained cellulose-g-PNIPAAm paper showed a rapid wettability conversion from being hydrophilic (water contact angles (WCA) of 0°) at 25 °C to becoming hydrophobic (WCA of 134.2°) at 45 °C. Furthermore, the thermo-responsive mechanism of cellulose-g-PNIPAAm was examined by the in situ variable-temperature 13C NMR, 1H NMR and AFM analysis. At the same time, the resulting cellulose paper was applied for a switchable separation of oil/water mixtures. Water can pass through the paper under 45 °C, while oil is kept on the paper. When the temperature is above 45 °C, oil can permeate through the paper, while water cannot pass through the water. Moreover, the paper exhibited excellent regeneration performance after five cycles and maintained its switchable wettability.

A biomass-based catalyst with amine groups (–NH2), viz., amine-functionalized sugarcane bagasse (SCB-NH2), was prepared through the amination of sugarcane bagasse (SCB) in a two-step process. The physicochemical properties of the catalyst were characterized through FT-IR, elemental analysis, XRD, TG, and SEM-EDX techniques, which confirmed the –NH2 group was grafted onto SCB successfully. The catalytic performance of SCB-NH2 in Knoevenagel condensation reaction was tested in the batch and continuous flow reactions. Significantly, it was found that the catalytic performance of SCB-NH2 is better in flow system than that in batch system. Moreover, the SCB-NH2 presented an excellent catalytic activity and stability at the high flow rate. When the flow rate is at the 1.5 mL/min, no obvious deactivation was observed and the product yield and selectivity are more than 97% and 99% after 80 h of continuous reaction time, respectively. After the recovery of solvent from the resulting solution, a white solid was obtained as a target product. As a result, the SCB-NH2 is a promising catalyst for the synthesis of fine chemicals by Knoevenagel condensation reaction in large scale, and the modification of the renewable SCB with –NH2 group is a potential avenue for the preparation of amine-functionalized catalytic materials in industry.

Modification of chemithermomechanical pulp (CTMP) by fungal treatment was investigated. Eucalyptus CTMP was treated with three different types of white-rot fungi, namely, Phanerochaete chrysosporium (P.c-1767), Trametes hirsute 19-6 (T.h-19-6), and Trametes hirsute19-6w (T.h-19-6w), under a stationary culture condition. Pulp total weight loss, lignin loss, and cellulose loss were determined to compare the different enzymes secreted by the three fungal strains. Pulp physical strengths, optical properties, and bleachability after the fungal treatment were investigated to compare the effect of fungal treatment on the pulp quality improvement. The results show that lignin reduction by both T.h-19-6 and T.h-19-6 (w) was about twice as much as that by P.c-1767. However, the selectivity of T.h-19-6 (w) towards lignin over cellulose was only 0.82, while that of T.h-19-6 was as high as 4.43. After T.h-19-6 treatment, pulp tensile, tear, and internal bonding strength increased by about 27%, 38%, and 40%, respectively.

Black liquor is generated in Kraft pulping of wood or non-wood raw material in pulp mills, and regarded as a renewable resource. The objective of this paper was to develop an effective means to remove the water pollutants by recovery of both lignin and sodium hydroxide from black liquor, based on electrolysis. The treatment of a 1000 mL of black liquor (122 g/L solid contents) consumed 345.6 kJ of electric energy, and led to the generation of 30.7 g of sodium hydroxide, 0.82 g of hydrogen gas and 52.1 g of biomass solids. Therefore, the recovery ratios of elemental sodium and biomass solids are 80.4% and 76%, respectively. Treating black liquor by electrolysis is an environmentally friendly technology that can, in particular, be an alternative process in addressing the environmental issues of pulping waste liquor to the small-scale mills without black liquor recovery.