Surface charge manipulation for improved humidity sensing of TEMPO-oxidized cellulose nanofibrils.

Cellulose-based humidity sensors have attracted great research interest due to their hydrophilicity, biodegradability, and low cost. However, they still suffer from relatively low humidity sensitivity. Due to the presence of negatively charged carboxylate groups, 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-oxidized cellulose nanofibril (CNF) exhibits enhanced hydrophilicity and ion conductivity, which is considered a promising candidate for humidity sensing. In this work, we developed a facile strategy to improve the humidity sensitivity of CNF films by regulating their surface charge density. With the increase in surface charge density, both water uptake and charge carrier densities of the CNF films can be improved, enabling a humidity sensitivity of up to 44.5 % (%RH)-1, higher than that of most polymer-based humidity sensors reported in the literature. Meanwhile, the sensor also showed good linearity (R2 = 0.998) over the 15-75 % RH at 1 kHz. With these features, the CNF film was further demonstrated for applications in noncontact sensing, such as human respiration, moisture on fingertips, and water leakage, indicating the great potential of CNF film in humidity monitoring.

Effect of hornification on the isolation of anionic cellulose nanofibrils from Kraft pulp via maleic anhydride esterification.

Cellulose nanofibrils (CNF) isolation based on a catalyst-free maleic anhydride esterification has proven to be effective, however, the effects of pulp hornification on CNF isolation by this strategy have yet to be explored, which could present significant impacts for CNF isolation. Herein, dried northern bleached softwood Kraft pulp (D-NBSK) and never-dried northern bleached softwood Kraft pulp (ND-NBSK) were selected as the substrates. After esterification with maleic anhydride (MA), the esterified ND-NBSK pulp (E-ND) shows a significantly smaller size and more fragmented structure than the esterified D-NBSK pulp (E-D). Meanwhile, higher degree of esterification can be realized for the never dried pulp as compared to the dried pulp, which is corroborated by the significantly stronger characteristic peaks of CO (1720 cm-1) and -COO- (1575 cm-1) from the FTIR spectra and the higher surface charge content (0.86 ± 0.04 mmol/g vs. 0.55 ± 0.05 mmol/g). A comparison of the characteristics of the resulting CNF similarly demonstrated the negative impact of hornification. Overall, this work indicates that hornification tends to reduce the accessibility of chemical reagents to the pulp, leading to insufficient deconstruction. Such negative impact of hornification should be considered when performing nanocellulose isolation, especially when using pulp as feedstock.

Multiscale Design for Robust, Thermal Insulating, and Flame Self-Extinguishing Cellulose Foam.

Cellulose foams are in high demand in an era of prioritizing environmental consciousness. Yet, transferring the exceptional mechanical properties of cellulose fibers into a cellulose network remains a significant challenge. To address this challenge, an innovative multiscale design is developed for producing cellulose foam with exceptional network integrity. Specifically, this design relies on a combination of physical cross-linking of the microfibrillated cellulose (MFC) networks by cellulose nanofibril (CNF) and aluminum ion (Al3+), as well as self-densification of the cellulose induced by ice-crystal templating, physical cross-linking, solvent exchange, and evaporation. The resultant cellulose foam demonstrates a low density of 40.7 mg cm-3, a high porosity of 97.3%, and a robust network with high compressive modulus of 1211.5 ± 60.6 kPa and energy absorption of 77.8 ± 1.9 kJ m-3. The introduction of CNF network and Al3+ cross-linking into foam also confers excellent wet stability and flame self-extinguish ability. Furthermore, the foam can be easily biodegraded in natural environments , re-entering the ecosystem's carbon cycle. This strategy yields a cellulose foam with a robust network and outstanding environmental durability, opening new possibilities for the advancement of high-performance foam materials.

Total mesialization of the mandibular dentition using a mini-implant-supported device : A finite element analysis.

PURPOSE: Total mandibular arch mesialization using mini-implants is challenging due to anatomic limitations. The aim of this study was to introduce a mini-implant-supported device for total mesialization of the mandibular dentition and to analyze the biomechanical properties of the device. METHODS: Finite element models were constructed to explore the effect of friction and force direction on the force transmission efficiency of the device. In addition, the three-dimensional displacement of each tooth was evaluated with two force application points (2 or 8 mm hooks) under three force conditions (symmetric: 150 g of force on both sides, or asymmetric: 100 and 200 g of force on each side). RESULTS: The force transmission efficiency was 66.7% under a friction coefficient of 0.15 and parallel pushing and pulling forces. The force transmission efficiency was 65.90 and 66.63% when the pushing force was 15° away from the pulling force on the sagittal and horizontal planes, respectively. The mandibular dentition moved mesially with a greater tendency for incisor labial crown tipping, mesial molar rotation and buccal second molar crown tipping when using the 8 mm hook compared to that when using the 2 mm hook. Rigid archwires resulted in more consistent tooth mesialization than stainless steel archwires. Asymmetric forces resulted in asymmetric dental arch mesialization. CONCLUSION: The forces transmitted by the presented mini-implant-supported device varied depending on the friction level and force direction. The device should be able to achieve symmetric or asymmetric total mesialization of the mandibular dentition.

Cellulose-Based Ionic Conductor: An Emerging Material toward Sustainable Devices.

Ionic conductors (ICs) find widespread applications across different fields, such as smart electronic, ionotronic, sensor, biomedical, and energy harvesting/storage devices, and largely determine the function and performance of these devices. In the pursuit of developing ICs required for better performing and sustainable devices, cellulose appears as an attractive and promising building block due to its high abundance, renewability, striking mechanical strength, and other functional features. In this review, we provide a comprehensive summary regarding ICs fabricated from cellulose and cellulose-derived materials in terms of fundamental structural features of cellulose, the materials design and fabrication techniques for engineering, main properties and characterization, and diverse applications. Next, the potential of cellulose-based ICs to relieve the increasing concern about electronic waste within the frame of circularity and environmental sustainability and the future directions to be explored for advancing this field are discussed. Overall, we hope this review can provide a comprehensive summary and unique perspectives on the design and application of advanced cellulose-based ICs and thereby encourage the utilization of cellulosic materials toward sustainable devices.

Three-dimensional porous high boron-nitrogen-doped carbon for the ultrasensitive electrochemical detection of trace heavy metals in food samples.

Exposure to even trace amounts of Cd(II) and Pb(II) in food can have serious effects on the human body. Therefore, the development of novel electrochemical sensors that can accurately detect the different toxicity levels of heavy metal ions in food is of great significance. Based on the principle of green chemistry, we propose a new type of boron and nitrogen co-doped carbon (BCN) material derived from a metal-organic framework material and study its synthesis, characterization, and heavy-metal ion detection ability. Under the optimum conditions, the BCN-modified glassy carbon electrode was studied using square-wave anodic stripping voltammetry, which showed good electrochemical responses to Cd(II) and Pb(II), with sensitivities as low as 0.459 and 0.509 µA/µM cm2, respectively. The sensor was successfully used to detect Cd(II) and Pb(II) in Beta vulgaris var. cicla L samples, which is consistent with the results obtained using inductively coupled plasma-mass spectrometry. It also has a strong selectivity for complex samples. This study provides a novel approach for the detection of heavy metal ions in food and greatly expands the application of heteroatom-doped metal-free carbon materials in detection platforms.

Sprayable cellulose nanofibrils stabilized phase change material Pickering emulsion for spray coating application.

Phase change materials (PCM) have been increasingly used over the past decades in applications requiring thermal energy storage or maintaining temperature uniformity, in particular in the textile industry. Organic PCM is desired in temperature control, but it suffers from thermal leaking and unstable form during phase transition. Here, cellulose nanofibrils (CNFs) were used as emulsifiers to stabilize paraffin Pickering emulsion by ultrasonication. Results indicated uniform PCM emulsion particles of 4.2 ± 2.1 µm could be obtained using 0.8 wt% CNF suspension sonicated at 100%A and 7 mins with 2:8 paraffin to CNF ratio. The CNF-stabilized paraffin emulsion showed excellent long-term stability with unchanged particle size when stored at 45 °C for 28 days. In addition, differential scanning calorimetry (DSC) results showed high thermal stability after 51 heating-cooling cycles with high latent heat of 117.6 J/g. The CNF-stabilized paraffin emulsion can be facilely spray-coated onto fabric to prepare thermal regulating textile.

Sustainable isolation of nanocellulose from cellulose and lignocellulosic feedstocks: Recent progress and perspectives.

As a type of sustainable nanomaterials, nanocellulose has drawn increasing attention over the last two decades due to its great potential in diverse value-added applications such as electronics, sensors, energy storage, packaging, pharmaceuticals, biomedicine, and functional food. Sourcing nanocellulose from lignocellulose is commonly accomplished via the use of mineral acids, oxidizers, enzymes, and/or intensive mechanical energy. Yet, the economic and environmental concerns associated with these conventional isolation techniques pose major obstacles for commercialization. Considerable progress has been achieved in the last few years in developing sustainable nanocellulose isolation technologies involving organic acid/anhydride, Lewis acid, solid acid, ionic liquid, and deep eutectic solvent. This paper provides a comprehensive review of these alternatives with regard to general procedures and key advantages. Important knowledge gaps, including total biomass utilization, complete life cycle analysis, and health/safety, require urgently bridging in order to develop economically competitive and operationally feasible nanocellulose isolation technology for commercialization.

Advanced Switchable Molecules and Materials for Oil Recovery and Oily Waste Cleanup.

Advanced switchable molecules and materials have shown great potential in numerous applications. These novel materials can express different states of physicochemical properties as controlled by a designated stimulus, such that the processing condition can always be maintained in an optimized manner for improved efficiency and sustainability throughout the whole process. Herein, the recent advances in switchable molecules/materials in oil recovery and oily waste cleanup are reviewed. Oil recovery and oily waste cleanup are of critical importance to the industry and environment. Switchable materials can be designed with various types of switchable properties, including i) switchable interfacial activity, ii) switchable viscosity, iii) switchable solvent, and iv) switchable wettability. The materials can then be deployed into the most suitable applications according to the process requirements. An in-depth discussion about the fundamental basis of the design considerations is provided for each type of switchable material, followed by details about their performances and challenges in the applications. Finally, an outlook for the development of next-generation switchable molecules/materials is discussed.

Using Specified Risk Materials-Based Peptides for Oil Sands Fluid Fine Tailings Management.

Fluid fine tailings are produced in huge quantities by Canada's mined oil sands industry. Due to the high colloidal stability of the contained fine solids, settling of fluid fine tailings can take hundreds of years, making the entrapped water unavailable and posing challenges to public health and the environment. This study focuses on developing value-added aggregation agents from specified risk materials (SRM), a waste protein stream from slaughterhouse industries, to achieve an improved separation of fluid fine tailings into free water and solids. Settling results using synthetic kaolinite slurries demonstrated that, though not as effective as hydrolyzed polyacrylamide, a commercial flocculant, the use of SRM-derived peptides enabled a 2-3-fold faster initial settling rate than the blank control. The pH of synthetic kaolinite tailings was observed to be slightly reduced with increasing peptides dosage in the test range (10-50 kg/ton). The experiments on diluted fluid fine tailings (as a representation of real oil sands tailings) demonstrated an optimum peptides dosage of 14 kg/ton, which resulted in a 4-fold faster initial settling rate compared to the untreated tailings. Overall, this study demonstrates the novelty and feasibility of using SRM-peptides to address intractable oil sands fluid tailings.