Temperature-Switching Flexible Strain Sensors Based on Vanadium Dioxide for Intelligent Packaging Applications.

Flexible sensors are promising for intelligent packaging and artificial intelligence, but the required multistimulus response is still a challenge in external environments. A candidate material for such multistimulus response is VO2 due to its unique semiconducting properties. Herein, W-doped VO2(M) with a tunable phase transition temperature was prepared by the hydrothermal method, and then, VO2(M)-based flexible sensors were fabricated employing a direct-write strategy, where conductive inks with VO2(M) powders were patterned onto various substrates. These sensors achieve dual responses to temperature and strain and exhibit high stability (over 2000 stretch-release cycles) to accurately monitor various statuses (opening and closing, temperature changes, etc.) of intelligent packaging. The spatial pressure distribution of different objects was discerned by the prepared VO2(M)/poly(dimethylsiloxane) (PDMS) sponge flexible pressure sensor arrays, and the information was successfully edited using the Morse code. The sensing signals from the intelligent packaging were collected and remotely transmitted to intelligent terminals via a wireless local-area network to achieve real-time monitoring of the packaged contents. Therefore, in this work, we not only designed new flexible sensors with multiple stimulus responses but also demonstrated the potential applications of W-doped VO2(M)-based flexible sensors in intelligent packaging.

Fine extraction of cellulose from corn straw and the application for eco-friendly packaging films enhanced with polyvinyl alcohol.

Biomass materials substituting for petroleum-based polymers occupy an important position in achieving sustainable development. Cellulose, a typical biomass material, stands out as the primary choice for producing eco-friendly packaging materials. However, it is still a challenge to efficiently utilize cellulose from waste biomass materials in practice. Herein, cellulose-based films were prepared by pretreating waste corn straw, separating straw husk, straw pith and straw leaf, and extracting cellulose through alkali and sodium chlorite treatment to improve its mechanical properties using the cross-linked polyvinyl alcohol (PVA) method in this work. The prepared composite films were characterized by Fourier transform infrared spectrometer (FTIR), X-ray diffraction instrument (XRD), Scanning electron microscopy (SEM), Thermogravimetric (TG) and mechanical properties. The results indicated that corn straw husk exhibited the highest cellulose content of 31.67 wt%, and obtained husk cellulose had the highest crystallinity of 52.5 %. Compared to corn straw, the crystallinity of husk cellulose, pith cellulose and leaf cellulose increased by 19.5 %, 16.4 % and 44.1 %, respectively. Husk cellulose/PVA composite films were the most thermally stable, with a maximum weight loss temperature of 346.8 °C. In addition, the husk cellulose/PVA composite film had the best tensile strength of 37 MPa. Meanwhile, the composite films had good UV shielding, low water vapor transmission rate and biodegradability. Therefore, this work provides a fine utilization route of waste corn straw, and as-prepared cellulose based films have potential application in eco-friendly packaging materials.

Antimicrobial Properties of Carboxymethyl Cellulose/Starch/N'N Methylenebisacrylamide Membranes Endowed by Ultrasound and Their Potential Application in Antimicrobial Packaging.

Cellulose is used widely in antimicrobial packaging due to its abundance in nature, biodegradability, renewability, non-toxicity, and low cost. However, how efficiently and rapidly it imparts high antimicrobial activity to cellulose-based packaging materials remains a challenge. In this work, Ag NPs were deposited on the surface of carboxymethyl cellulose/starch/N'N Methylenebisacrylamide film using ultrasonic radiation. Morphology and structure analysis of as-prepared films were conducted, and the antibacterial effects under different ultrasonic times and reductant contents were investigated. These results showed that Ag NPs were distributed uniformly on the film surface under an ultrasonic time of 45 min. The size of Ag NPs changes as the reducing agent content decreases. The composite film demonstrated a slightly better antibacterial effect against E. coli than against S. aureus. Therefore, this work can provide valuable insights for the research on antimicrobial packaging.

Recent Progresses in Pyrolysis of Plastic Packaging Wastes and Biomass Materials for Conversion of High-Value Carbons: A Review.

The recycling of plastic packaging wastes helps to alleviate the problems of white pollution and resource shortage. It is very necessary to develop high-value conversion technologies for plastic packaging wastes. To our knowledge, carbon materials with excellent properties have been widely used in energy storage, adsorption, water treatment, aerospace and functional packaging, and so on. Waste plastic packaging and biomass materials are excellent precursor materials of carbon materials due to their rich sources and high carbon content. Thus, the conversion from waste plastic packaging and biomass materials to carbon materials attracts much attention. However, closely related reviews are lacking up to now. In this work, the pyrolysis routes of the pyrolysis of plastic packaging wastes and biomass materials for conversion to high-value carbons and the influence factors were analyzed. Additionally, the applications of these obtained carbons were summarized. Furthermore, the limitations of the current pyrolysis technology are put forward and the research prospects are forecasted. Therefore, this review can provide a useful reference and guide for the research on the pyrolysis of plastic packaging wastes and biomass materials and the conversion to high-value carbon.

Divergence of trafficking and polarization mechanisms for PIN auxin transporters during land plant evolution.

The phytohormone auxin, and its directional transport through tissues, plays a fundamental role in the development of higher plants. This polar auxin transport predominantly relies on PIN-FORMED (PIN) auxin exporters. Hence, PIN polarization is crucial for development, but its evolution during the rise of morphological complexity in land plants remains unclear. Here, we performed a cross-species investigation by observing the trafficking and localization of endogenous and exogenous PINs in two bryophytes, Physcomitrium patens and Marchantia polymorpha, and in the flowering plant Arabidopsis thaliana. We confirmed that the GFP fusion did not compromise the auxin export function of all examined PINs by using a radioactive auxin export assay and by observing the phenotypic changes in transgenic bryophytes. Endogenous PINs polarize to filamentous apices, while exogenous Arabidopsis PINs distribute symmetrically on the membrane in both bryophytes. In the Arabidopsis root epidermis, bryophytic PINs have no defined polarity. Pharmacological interference revealed a strong cytoskeletal dependence of bryophytic but not Arabidopsis PIN polarization. The divergence of PIN polarization and trafficking is also observed within the bryophyte clade and between tissues of individual species. These results collectively reveal the divergence of PIN trafficking and polarity mechanisms throughout land plant evolution and the co-evolution of PIN sequence-based and cell-based polarity mechanisms.

Synthesis and Properties of Carbon Microspheres from Waste Office Paper.

As a kind of biomass resource, waste office paper can be used as a carbon precursor to prepare carbon materials. In this work, carbon microspheres with regular shape, uniform particle size and high carbon content were successfully prepared from waste office paper via a hydrothermal synthesis method with sulfuric acid as the catalyst. The effects of reaction temperature and sulfuric acid dosage on the morphology of the carbon microspheres were studied. The formation mechanism of the carbon microspheres was investigated by analyzing the structure and composition of the products. The results show that the hydrolysis of cellulose in waste paper under hydrothermal conditions was the key for the formation of carbon microspheres. The temperature of hydrothermal reaction and the use of sulfuric acid can affect the morphology of carbon microspheres. The carbon microspheres synthesized at 210 °C with 10 mL sulfuric acid have the best surface morphology, with uniform particle size and higher dispersion. Cyclic voltammetry and electrochemical impedance spectroscopy show that the carbon microspheres have good capacitance performance and can be used in capacitors. This study provides a low-cost precursor for carbon microspheres as well as a new method for the recycle of waste paper.

Surface charge regulation of imidazolium salts/starch/carboxymethyl cellulose ternary polymer blend films for controlling antimicrobial performance and hydrophobicity.

Starch (SR)/carboxymethyl cellulose (CMC) based antimicrobial films have been widely applied in packaging field. As a high-effect antimicrobial agent, the surface charge of imidazolium salt plays an important effect on antimicrobial performances of starch/carboxymethyl cellulose. Here in, the surface charge of dodecyl imidazolium bromide salt was regulated via thiol-ene reaction. Furthermore, antibacterial films were prepared by mixing imidazolium salts with SR/CMC via solution casting method. Under the optimized ratio of CMC to SR, the antibacterial activity for as-prepared ternary polymer blend films was enhanced with the increasing of surface charge of imidazolium salt. The sample of ADSC-01 film with highest surface charge showed best antibacterial properties for E. coli and S. aureus with the inhibition zone of 3.20 cm and 3.00 cm, respectively. In addition, hydrophobic property exhibited similar positive correlation with the surface charge. Therefore, this work provides a new route to regulate the antibacterial activity of bio-based ternary polymer blend films in the packaging.

Self-assembly of porous cellulose fibers and the incorporation of graphene carbon quantum dots for stable luminescence.

Porous fibers as excellent carriers can be used to prepare photoluminescence materials. Herein, cellulose nanocrystals (CNCs) were derived from microcrystalline cellulose (MCC) by sulfuric acid hydrolysis. After CNCs were squeezed into a coagulating bath containing silicon precursors obtained by the hydrolysis of tetraethyl orthosilicate, porous cellulose fibers were constructed through self-assembly and then incorporated with graphene carbon quantum dots (GQDs) to prepare porous photoluminescence cellulose fibers. The silicon precursor amount, self-assembly time, and corrosion time were optimized. In addition, the morphology, structure and optical properties of the products were investigated. These results showed that as-prepared porous cellulose fibers with mesopores presented loose and porous mesh. Interestingly, the porous photoluminescence cellulose fibers exhibited blue fluorescence, and the maximum emission peak appeared at 430 nm under the excitation wavelength of 350 nm. Furthermore, the relative fluorescence intensity of the porous photoluminescence cellulose fibers was significantly enhanced compared with nonporous photoluminescence cellulose fibers. This work provided a new method to prepare environmentally and stably photoluminescence fibers, which had potential applications in anti-counterfeit packaging and smart packaging.

Research Progress of Treatment Technology and Adsorption Materials for Removing Chromate in the Environment.

Cr is used extensively in industry, so the number of Cr (VI) hazards is increasing. The effective control and removal of Cr (VI) from the environment are becoming an increasing research priority. In order to provide a more comprehensive description of the research progress of chromate adsorption materials, this paper summarizes the articles describing chromate adsorption in the past five years. It summarizes the adsorption principles, adsorbent types, and adsorption effects to provide methods and ideas to solve the chromate pollution problem further. After research, it is found that many adsorbents reduce adsorption when there is too much charge in the water. Besides, to ensure adsorption efficiency, there are problems with the formability of some materials, which impact recycling.

Research Progress on Up-Conversion Fluorescence Probe for Detection of Perfluorooctanoic Acid in Water Treatment.

Perfluorooctanoic acid (PFOA) is a new type of organic pollutant in wastewater that is persistent, toxic, and accumulates in living organisms. The development of rapid and sensitive analytical methods to detect PFOA in environmental media is of great importance. Fluorescence detection has the advantages of high efficiency and low cost, in which fluorescent probes have excellent fluorescence properties, excellent bio-solubility, and remarkable photostability. It is necessary to review the fluorescence detection routes for PFOA. In addition, the up-conversion of fluorescent materials (UCNPs), as fluorescent materials to prepare fluorescent probes with, has significant advantages and also attracts the attention of researchers, however, reviews related to their application in detecting PFOA and comparing them with other routes are rare. Furthermore, there are many strategies to improve the performance of up-conversion fluorescent probes including SiO2 modification and amino modification. These strategies can enhance the detection effect of PFOA. Thus, this work reviews the types of fluorescence detection, the design, and synthesis of UCNPs, their recognition mechanism, properties, and their application progress. Moreover, the development trend and prospects of these detection probes are given.

Photoluminescence Performance and Photocatalytic Activity of Modified Carbon Quantum Dots Derived from Pluronic F127.

The photocatalytic degradation of organic dyes in waste water using carbon quantum dots (CQDs) remains a hot topic due to the importance of environmental protection. However, identifying suitable carbon resources and successful surface modification are still challenging. Herein, the hydrothermal method and surface modification of ammonia and thionyl chloride were applied to synthesize CQDs with different surface groups using PEO106PPO70PEO106 (Pluronic F127) as a carbon source. The average particle size of the as-prepared CQDs was in the range of 2.3-3.5 nm. The unmodified CQDs had the highest relative photoluminescence intensity, while all as-prepared CQDs exhibited abnormal photoluminescence located outside the scope of the visible spectrum. Interestingly, CQDs modified with ammonia achieved a degradation rate of 99.13% (15 d) for 50 mg/L indigo carmine solution, while CQDs modified with thionyl chloride reached a degradation rate of 97.59% (15 d) for light green SF yellowish solution. Therefore, in this work, two typical organic dyes can be effectively photocatalytically degraded by as-prepared CQDs, with suitable surface modification.

Preparation of Low Volatile Organic Compounds Silver Paste Containing Ternary Conductive Fillers and Optimization of Their Performances.

Conductive silver paste is a key material in the fields of printed circuits and printed electronic devices. However, the preparation of conductive silver paste with low-cost and volatile organic compounds (VOCs) is still a challenge. In this work, conductive silver pastes with excellent comprehensive performances were developed by using water-borne polyurethane (WPU) as the bonding phase and using the ternary mixture of Ag microflakes (Ag MFs), Ag nanowires (Ag NWs), and Ag nanoparticles (Ag NPs) as the conductive phase. WPU endowed conductive silver pastes with the adhesion along with releasing a few VOCs during the curing. Results showed that a small amount of Ag NPs or Ag NWs dramatically enhanced the electrical conductivity of silver paste paint film filled only with Ag MFs. The electrical resistivity for optimal ternary mixture conductive silver paste was 0.2 × 10-3 Ω∙cm, and the conductive phase was composed of 20.0 wt% Ag MFs, 7.5 wt% Ag NWs, and 2.5 wt% Ag NPs. Meanwhile, the adhesive strength and hardness of silver paste paint film were effectively improved by increasing the curing temperature. The optimal overall performance of the conductive silver pastes was achieved at the curing temperature of 160 °C. Therefore, this work can provide a new route for preparing conductive silver pastes with high performances.

Preparation and Adsorption Performance Study of Graphene Quantum Dots@ZIF-8 Composites for Highly Efficient Removal of Volatile Organic Compounds.

Based on the large specific surface area and excellent adsorption potential of graphene quantum dots (GQDs) and zeolitic imidazolate framework-8 (ZIF-8) materials, a GQDs@ZIF-8 composite was constructed to achieve optimal matching of the microstructure and to acquire efficient adsorption of volatile organic compounds (VOCs). GQDs and ZIF-8 were synthesized and then compounded by the solution co-deposition method to obtain GQDs@ZIF-8 composites. GQDs were uniformly decorated on the surface of the ZIF-8 metal-organic framework (MOF), effectively restraining the agglomeration, improving the thermal stability of ZIF-8 and forming abundant active sites. Thus, the VOC removal percentage and adsorption capacity of the GQDs@ZIF-8 composites were significantly improved. Toluene and ethyl acetate were chosen as simulated VOC pollutants to test the adsorption performance of the composites. The results showed that, after the addition of GQDs, the adsorption property of GQDs@ZIF-8 composites for toluene and ethyl acetate was obviously improved, with maximum adsorption capacities of 552.31 mg/g and 1408.59 mg/g, respectively, and maximum removal percentages of 80.25% and 93.78%, respectively, revealing extremely high adsorption performance. Compared with raw ZIF-8, the maximum adsorption capacities of the composites for toluene and ethyl acetate were increased by 53.82 mg/g and 104.56 mg/g, respectively. The kinetics and isotherm study revealed that the adsorption processes were in accordance with the pseudo-first-order kinetic model and the Freundlich isotherm model. The thermodynamic results indicated that the adsorption process of the GQDs@ZIF-8 composites was a spontaneous, endothermic and entropy increase process. This study provides a new way to explore MOF-based adsorption materials with high adsorption capacity which have broad application prospects in VOC removal fields.

A Study on Doping and Compound of Zinc Oxide Photocatalysts.

As an excellent semiconductor photocatalyst, zinc oxide is widely used in the field of photocatalysis and is regarded as one of the most reliable materials to solve environmental problems. However, because its band gap energy limits the absorption of visible light and reduces the efficiency of catalytic degradation, it needs to be doped with other substances or compounded with other substances and precious metal. This paper summarizes the research on this aspect at home and abroad in recent years, introduces the doping of transition metal ions by zinc oxide, the compounding of zinc oxide with precious metals or other semiconductors, and the prospect of further improving the catalytic efficiency of zno photocatalyst is also put forward.

Structural optimization and antibacterial property of alkylimidazole salt/carboxymethyl cellulose/starch composite films.

As a green solvent, alkylimidazolium salt has attracted much attention due to high antibacterial activity and excellent biocompatibility. In this work, 1-allyl-3-alkylimidazolium bromide ionic liquids (AIMB) were synthesized in a closed system. Using carboxymethyl cellulose (CMC) and starch (SR) as carriers, 1-allyl-3-dodecylimidazolium bromide ionic liquid (AIMC12)/CMC/SR (AIMCS) films were prepared via solution casting method. The AIMC12 exhibited the highest antibacterial activity. Under the optimized ratio of CMC to SR, the AIMCS-1-1 film showed effective antibacterial properties for E. coli and S. aureus with the inhibition zone of 3.50 cm and 3.02 cm, respectively. In addition, the tensile strength and elongation at break of AIMCS-1-1 reached to 4.5 MPa and 111.6 %, and its Young's modulus was 1.4 GPa. Therefore, as-prepared AIMB will be expected to replace traditional antibacterial agents in antibacterial applications, and as-prepared AIMCS films as the green packaging materials have potential application in antibacterial packaging.

Recent Progresses in Adsorption Mechanism, Architectures, Electrode Materials and Applications for Advanced Electrosorption System: A Review.

As an advanced strategy for water treatment, electrosorb technology has attracted extensive attention in the fields of seawater desalination and water pollution treatment due to the advantages of low consumption, environmental protection, simplicity and easy regeneration. In this work, the related adsorption mechanism, primary architectures, electrode materials, and applications of different electrosorption systems were reviewed. In addition, the developments for advanced electrosorb technology were also summarized and prospected.

Electrochemically enhanced adsorption of organic dyes from aqueous using a freestanding metal-organic frameworks/cellulose-derived porous monolithic carbon foam.

Monolithic carbon foams are promising materials for adsorption due to the easy recyclability and without secondary-pollution. However, poor adsorption efficiency for organic pollutants limits its practical application. Hence, this work proposed a novel monolithic porous carbon foam by a facile carbonization approach as freestanding electrodes to remove the organic dyes. The prepared carbon foam derived from waste cigarette filters and zeolitic-imidazolate frameworks-8 with well-developed pores, and the calculated surface area is 1457 m2·g-1, and exhibited an outstanding removal efficiency for methylene blue in aqueous. The maximum adsorption capacity for methylene blue can reach up to 1846.7 mg·g-1 under the applied voltage of -1.2 V. Importantly, as-prepared carbon foams possessed excellent stability, and the removal efficiency can remain above 85% after 5 cycles. Thus, obtained porous carbon foams in this paper as a free standing electrode is expected to be promising materials of adsorbent besides supercapacitors.

Author Correction: Various nanoparticle morphologies and surface properties of waterborne polyurethane controlled by water.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Synthesis and structure of carboxymethylcellulose with a high degree of substitution derived from waste disposable paper cups.

The cost of the cellulose derived from some raw materials was high. In addition, the dispersion of the cellulose with special shape and a low degree of substitution (DS) in water-soluble polymers was poor. To resolve this problem, cellulose was separated from waste disposable paper cups (WDPC) and then the carboxymethylcellulose (CMC) was synthesized by etherification. Under the optimized conditions (the etherification temperature of 70 ℃, the etherification time of 1.5 h, the monochloroacetic acid mass (C2H3ClO2) of 7 g), the DS of CMC was as high as 1.21. As-prepared CMC showed ribbon and rod-like shapes with a diameter of 25-50 µm. In addition, they exhibited an excellent thermal stability. Compared with other CMC, we could infer that as-prepared CMC in this paper will have potential applications in flexible composites and functional materials.

Facile synthesis of mesoporous carbon microspheres/graphene composites in situ for application in supercapacitors.

Mesoporous carbon/graphene composites (MCG) have exhibited good electrochemical performances; however, the fixed mesoporous carbon, the low specific surface area, and porosity are the main obstacles in their application in supercapacitors. In this paper, mesoporous carbon microspheres/graphene composites (MCMG) were synthesized in situ via a soft template method and subsequent thermal reduction by using cetyltrimethylammonium bromide (CTAB) as the structure-directing agent, and aqueous mesophase pitch (AMP) and graphene oxide (GO) as the carbon sources. The strong electrostatic interaction between GO/CTAB and AMP promoted the self-assembly of CTAB and AMP to form the MCMG precursor. The results showed that the CTAB concentration and aging temperature have an important effect on the morphology and pore structure of the synthesized MCMG. The high aging temperature promoted the formation of mesoporous carbon spheres and its diameter increased with the increase in the concentration of CTAB. The as-prepared MCMG at the aging temperature of 140 °C had obvious spherical and layered carbon materials after carbonization at 900 °C. When the concentration of CTAB was 10.6 g L-1, the formed mesoporous carbon spheres with the diameter of 30-40 nm were uniformly dispersed among the layered graphenes in MCMG-140-0.2 (the aging temperature of 140 °C and the CTAB content of 0.2 g). In addition, its specific surface area was 1150.5 m2 g-1 and the mesopore size was centered at 4.3 nm, 7.9 nm, and 17.1 nm. Compared with the MCMG precursor, the ordered degree of the mesopores for MCMG was reduced due to the high temperature carbonization. Importantly, the specific capacitance of MCMG-140-0.2 at the current density of 0.1 A g-1 was as high as 356.3 F g-1. Moreover, the specific capacitance of MCMG-140-0.2 at 1 A g-1 remained at 278.5 F g-1, the capacitance retention was 92.1% after 6000 cycles, and the coulombic efficiency was over 98% at a high current density of 2 A g-1. Therefore, the as-prepared MCMG can be an excellent candidate for electrode materials in supercapacitors.