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Paper sludge biomass represents an underutilized feedstock rich in pulped and processed cellulose which is currently a waste stream with significant disposal cost to industry for landfilling services. Effective fractionation of the cellulose from paper sludge presents an opportunity to yield cellulose as feedstock for value-added processes. A novel approach to cellulose fractionation is the sidehill screening system, herein studied at the pilot-plant scale. Composition analysis determined ash removal and carbohydrate retention of both sidehill and high-performance benchtop screening systems. Sidehill screening resulted in greater carbohydrates retention relative to benchtop screening (90% vs 66%) and similar ash removal (95% vs 98%). Techno-economic analysis for production of sugar syrup yielded a minimum selling price of $331/metric ton of sugar syrup including disposal savings, significantly less than a commercial sugar syrup without fractionation. Sensitivity analysis showed that screening conditions played a significant role in economic feasibility for cellulosic yield and downstream processes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

This study aims to understand the effect of micro- and nanofibrillated cellulose (MNFC) on the tensile index, softness, and water absorbency of tissue paper. MNFC was produced from four different fiber sources. The results show that MNFC acts as an effective strength enhancer at the expense of a reduced water absorbency and softness. The impact of the fiber source on MNFC manufacturing cost and the trade-off with performance was also investigated. MNFCs produced from southern bleached hardwood kraft, northern bleached softwood kraft, and deinked pulp exhibited similar performance trends with the MNFC from the deinked pulp having a significantly lower cost. This suggests that MNFCs with similar degrees of fibrillation may be used interchangeably regardless of the fiber source, revealing the possibility to minimize MNFC manufacturing costs based on fiber selection. MNFC produced from bleached Eucalyptus kraft showed the lowest degree of fibrillation and the lowest strength improvements among the MNFCs evaluated., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Hydrogels were synthesized by a copolymerization reaction of nanofibrillated cellulose (CNF) with acrylic acid (AA) and acrylamide (AM) and N , N -methylene-bis-acrylamide (MBA) as a cross-linker and their absorption performance as a function of composition was determined. Hydrogels with 4% by weight CNF had swelling of about 250 g/g and with 7% CNF about 200 g/g for water. Thermodynamic and kinetic studies of the reaction pathways and the electronic properties of the cellulose and monomers were investigated through density functional theory calculations. Thermodynamic investigations revealed that the radical formation of cellulose that initiates the hydrogel process can occur through the breaking of the homolytic covalent bonds C6-OH and C3-OH. The results show that the reaction of CNF with monomers is thermodynamically favorable in the decreasing order of AM, AA, and MBA. The kinetic study also indicates that the reaction kinetics of CNF with AM is faster than with AA which is much faster than with MBA. Overall, this study has elucidated some of the key chemical characteristics that impact the derivatization of nanocellulose structures to produce advanced renewable bioproducts.

The effect of fiber type (cotton, polyester, and rayon), temperature, and use of detergent on the number of microfibers released during laundering of knitted fabrics were studied during accelerated laboratory washing (Launder-Ometer) and home laundering experiments. Polyester and cellulose-based fabrics all shed significant amounts of microfibers and shedding levels were increased with higher water temperature and detergent use. Cellulose-based fabrics released more microfibers (0.2-4 mg/g fabric) during accelerated laundering than polyester (0.1-1 mg/g fabric). Using well-controlled aquatic biodegradation experiments it was shown that cotton and rayon microfibers are expected to degrade in natural aquatic aerobic environments whereas polyester microfibers are expected to persist in the environment for long periods of time., (Published by Elsevier Ltd.)

As one of the most abundant natural materials in nature, cellulose has revealed enormous potential for the construction of functional materials thanks to its sustainability, non-toxicity, biocompatibility, and biodegradability. Among many fascinating applications, functional surfaces based on cellulose-derived materials have attracted increasing interest recently, as platforms for diagnostics, sensoring, robust catalysis, water treatment, ultrafiltration, and anti-microbial surfaces. This mini-review attempts to cover the general methodology for the fabrication of functional cellulose surface and a few popular applications including bioactive and non-adhesive (i.e., anti-fouling and anti-microbial) surfaces.

Cellulose nanocrystals (CNCs) from ramie fibers are studied as stabilizers of oil-in-water emulsions. The phase behavior of heptane and water systems is studied, and emulsions stabilized by CNCs are analyzed by using drop sizing (light scattering) and optical, scanning, and freeze-fracture electron microscopies. Water-continuous Pickering emulsions are produced with cellulose nanocrystals (0.05-0.5 wt%) grafted with thermo-responsive poly(NIPAM) brushes (poly(NIPAM)-g-CNCs). They are observed to be stable during the time of observation of 4 months. In contrast, unmodified CNCs are unable to stabilize heptane-in-water emulsions. After emulsification, poly(NIPAM)-g-CNCs are observed to form aligned, layered structures at the oil-water interface. The emulsions stabilized by poly(NIPAM)-g-CNCs break after heating at a temperature above the LCST of poly(NIPAM), which is taken as indication of the temperature responsiveness of the brushes installed on the particles and thus the responsiveness of the Pickering emulsions. This phenomenon is further elucidated via rheological measurements, in which viscosities of the Pickering emulsions increase on approach of the low critical solution temperature of poly(NIPAM). The effect of temperature can be counterbalanced with the addition of salt which is explained by the reduction of electrostatic and steric interactions of poly(NIPAM)-g-CNCs at the oil-water interface., (Copyright © 2011 Elsevier Inc. All rights reserved.)

The colloidal stability and thermoresponsive behavior of poly(N-isopropylacrylamide) brushes grafted from cellulose nanocrystals (CNCs) of varying graft densities and molecular weights was investigated. Indication of the grafted polymer brushes was obtained after AFM imaging of CNCs adsorbed on silica. Also, aggregation of the nanoparticles carrying grafts of high degree of polymerization was observed. The responsiveness of grafted CNCs in aqueous dispersions and as an ultrathin film was evaluated by using light scattering, viscosimetry, and colloidal probe microscopy (CPM). Light transmittance measurements showed temperature-dependent aggregation originating from the different graft densities and molecular weights. The lower critical solution temperature (LCST) of grafted poly(NiPAAm) brushes was found to decrease with the ionic strength, as is the case for free poly(NiPAAm) in aqueous solution. Thermal responsive behavior of grafted CNCs in aqueous dispersions was observed by a sharp increase in dispersion viscosity as the temperature approached the LCST. CPM in liquid media for asymmetric systems consisting of ultrathin films of CNCs and a colloidal silica probe showed the distinctive effects of the grafted polymer brushes on interaction and adhesive forces. The origin of such forces was found to be mainly electrostatic and steric in the case of bare and grafted CNCs, respectively. A decrease in the onset of attractive and adhesion forces of grafted CNCs films were observed with the ionic strength of the aqueous solution. The decreased mobility of polymer brushes upon partial collapse and decreased availability of hydrogen bonding sites with higher electrolyte concentration were hypothesized as the main reasons for the less prominent polymer bridging between interacting surfaces.

Cellulose nanocrystals (CNCs) or nanowhiskers produced from sulfuric acid hydrolysis of ramie fibers were used as substrates for surface chemical functionalization with thermoresponsive macromolecules. The CNCs were grafted with poly(N-isopropylacrylamide) brushes via surface-initiated single-electron transfer living radical polymerization (SI-SET-LRP) under various conditions at room temperature. The grafting process was confirmed via Fourier transform IR spectroscopy and X-ray photoelectron spectroscopy and the different molecular masses of the grafts were quantified and found to depend on the initiator and monomer concentrations used. No observable damage occurred to the CNCs after grafting, as determined by X-ray diffraction. Size exclusion chromatography analyses of polymer chains cleaved from the cellulose nanocrystals indicated that a higher degree of polymerization was achieved by increasing initiator or monomer loading, most likely caused by local heterogeneities yielding higher rates of polymerization. It is expected that suspension stability, interfacial interactions, friction, and other properties of grafted CNCs can be controlled by changes in temperature and provide a unique platform for further development of stimuli-responsive nanomaterials.

Films of microfibrillated celluloses (MFCs) from pulps of different yields, containing varying amounts of extractives, lignin, and hemicelluloses, were produced by combining refining and high-pressure homogenization techniques. MFC films were produced using a casting-evaporation technique and the physical and mechanical properties (including density, roughness, fold endurance and tensile properties) were determined. Homogenization of bleached and unbleached Kraft pulps gave rise to highly individualized MFCs, but not for thermo-mechanical pulp (TMP). The resulting MFC films had a roughness equivalent to the surface upon which the films were cast. Interestingly, after homogenization, the presence of lignin significantly increased film toughness, tensile index, and elastic modulus. The hornification of fibers through a drying and rewetting cycle prior to refining and homogenization did not produce any significant effect compared to films from never-dried fibers, indicating that MFC films can potentially be made from low-cost recycled cellulosic materials., ((c) 2010 Elsevier Ltd. All rights reserved.)

We studied the use of cellulose nanocrystals (CNXs) obtained after acid hydrolysis of ramie cellulose fibers to reinforce poly(epsilon-caprolactone) (PCL) nanofibers. Chemical grafting with low-molecular-weight PCL diol onto the CNXs was carried out in an attempt to improve the interfacial adhesion with the fiber matrix. Grafting was confirmed via infrared spectroscopy and thermogravimetric analyses. The polymer matrix consisted of electrospun nanofibers that were collected as nonwoven webs. The morphology as well as thermal and mechanical properties of filled and unfilled nanofibers were elucidated by scanning electron microscopy, differential scanning calorimetry, and dynamic mechanical analysis, respectively. The addition of CNXs into PCL produced minimal changes in the thermal behavior of the electrospun fibers. However, a significant improvement in the mechanical properties of the nanofibers after reinforcement with unmodified CNXs was confirmed. Fiber webs from PCL reinforced with 2.5% unmodified CNXs showed ca. 1.5-fold increase in Young's modulus and the ultimate strength compared to PCL webs. Compared to the case of grafted nanocrystals, the unmodified ones imparted better morphological homogeneity to the nanofibrillar structure. The grafted nanocrystals had a negative effect on the morphology of nonwoven webs in which individual nanofibers became annealed during the electrospinning process and, therefore, could not be compared to neat PCL nonwoven webs. A rationalization for the different effects of grafted and unmodified CNXs in reinforcing PCL nanofibers is provided.

Producing environmentally benign and economically viable nanomaterials is critical for large-scale applications in energy and other industries. This study presents a modeling framework to identify environmentally greener and lower-cost pathways of large-scale nanomaterial production, which encompasses life cycle assessment, Green Chemistry principles, techno-economic analysis, and eco-efficiency analysis. The framework is demonstrated by case studies of cellulose nanomaterials produced in the U.S. For cellulose nanocrystals, the framework identifies pathways that simultaneously reduce the life-cycle global warming potential (GWP) from 17.7 to 2.6 kgCO2e per dry kg cellulose nanocrystals and the minimum selling price (MSP) from US$7540 to US$4587 per dry t cellulose nanocrystals. For cellulose nanofibrils, the strategies present trade-offs of reducing GWP from 7.8 to 0.1 kgCO2e per dry kg cellulose nanofibrils but increasing MSP slightly from US$2873 to US$2985 per dry t cellulose nanofibrils. Eco-efficiency analysis quantifies the magnitudes of co-benefits and trade-offs between the environmental and economic performance of different production strategies and supports decision making for sustainability-informed process optimization. [ABSTRACT FROM AUTHOR]

Microfibers and microplastics originating from wastewater treatment plant (WWTP) effluents are significant pollutants in freshwater sources and marine environments. This research investigated the biodegradation of cotton microfibers generated from bleached cotton jersey knit fabric and commercially available flushable wipes, polypropylene-based (PP) nonwoven wipes containing a cellulose component, and tissue paper. Biodegradation was tested in wastewater treatment plants (WWTP) solids, seawater, and lakewater according to the ISO 14852 and ASTM D6691 standard methods in an ECHO respirometer. Degradation experiments continued until a plateau in CO2 emissions was reached, and the final biodegradation extent was calculated relative to the theoretical CO2 produced based on elemental analysis. The results showed that the cotton and other cellulosic materials/components biodegrade to a great extent, as expected for all conditions, whereas the PP did not degrade. In general, for the cellulose polypropylene composite wipes, the cellulose biodegraded readily; the presence of the PP did not hinder the cellulose biodegradation. [ABSTRACT FROM AUTHOR]

The importance of renewable and environmentally friendly wood pulp fibers as an input material for single-use products has grown significantly. However, discarded single-use materials are found in the environment as litter and are sometimes disposed of in wastewater. It is important that these materials are biodegradable and environmentally benign. Wood pulp is mainly comprised of lignocellulosic material, and its composition and structure can vary depending on raw materials and processing, ultimately impacting the biodegradability. In this research, the aquatic biodegradation of five kinds of wood pulp and six different samples of isolated lignocellulosic components (cellulose, hemicellulose, and lignin) have been explored in a consistent detailed manner for the first time, and the effects of chemical composition on the biodegradation discussed. Several lignocellulosic materials were characterized using compositional analysis and were subjected to aquatic biodegradation with bio-solids from a wastewater treatment plant as an inoculum to indicate the potential to biodegrade in the environment. Cellulose and hemicellulose were readily biodegraded over a course of one month. The lignin samples were not biodegradable under these conditions, and the lignin within fibers decreased the biodegradability of the other components of the lignocellulosic fibers. It was also determined that ash and extractives negatively affect the biodegradability. The aerobic aquatic biodegradation results are useful for product designers to select different lignocellulosic materials for applications and for environmental scientists to understand the fate of these fibers in the environment. [ABSTRACT FROM AUTHOR]

Based on publications related to the use of micro- and nanofibrillated cellulose (MNFC) in papermaking applications, three sets of parameters (intrinsic and extrinsic variables, furnish composition, and degree of dispersion) were proposed. This holistic approach intends to facilitate understanding and manipulation of the main factors describing the colloidal behavior in systems comprising of MNFC, pulp fibers, and additives, which directly impact paper product performance. A preliminary techno-economic assessment showed that cost reductions driven by the addition of MNFC in paper furnishes could be as high as USD 149 per ton of fiber (up to 20% fiber reduction without adverse effects on paper's strength) depending on the cost of papermaking fibers. It was also determined that better performance in terms of strength development associated with a higher degree of MNFC fibrillation offset its high manufacturing cost. However, there is a limit from which additional fibrillation does not seem to contribute to further strength gains that can justify the increasing production cost. Further research is needed regarding raw materials, degree of fibrillation, and combination with polyelectrolytes to further explore the potential of MNFC for the reduction of weight of paper products. [ABSTRACT FROM AUTHOR]

A new Pd catalyst chemically bonded to cellulose nanocrystals surfaces (CNC-BIA-Pd) was developed. 2-(1H-Benzo[d]imidazol-2-yl) aniline (BIA), tosylated cellulose nanocrystals (CNC-TOS) and PdCl2 were the reactants for the synthesis of the new catalyst designed to be used for the Ullmann reaction. The modified cellulose nano catalyst was characterized with various analytical tools. The catalyst had excellent selectivity and activity in a short reaction time (45 min) and outstanding TON (490) and TOF (1960) values. The nano catalyst was determined to be reusable for at least eight cycles. The CNC-BIA-Pd catalyst indicated excellent catalytic efficiency for the Ullmann C–O reaction when it was compared to commercial palladium catalysts. A new Pd catalyst chemically bonded to cellulose nanocrystal surfaces (CNC-BIA-Pd) was developed and used for the Ullmann reactions. The catalyst had excellent selectivity and activity in a short reaction time and outstanding TON (490) and TOF (1960) values. The nano catalyst was determined to be reusable for at least eight cycles. [ABSTRACT FROM AUTHOR]

Cellulose extracted from recycled pulverized cotton in nanocrystalline cellulose (CNC) and nanofibrillated cellulose (NFC) forms is investigated as a reinforcing agent in low-density polyethylene (LDPE) nanocomposites. The effect of extraction processing on the pulverized cotton is shown to influence the degree of crystallinity, morphology, and thermal stability of cellulose nanomaterials. Melt compounding of CNC with LDPE resulted in polymer nanocomposites with no discoloration at 170 °C. Significant differences observed in transparency, mechanical, and thermal properties of LDPE nanocomposite films, are demonstrated to be a result of the microstructure and the content of cellulose nanomaterials. Thermal analysis using thermogravimetric analyzer and differential scanning calorimeter showed higher thermal stability and degree of crystallinity of NFC/LDPE comparing to CNC/LDPE nanocomposite films. Tensile analysis exhibited a higher elastic modulus and tensile strength for the NFC material. 10 wt% of NFC reinforcing agent showed 32% improved strength and higher transparency over the one with CNC. [ABSTRACT FROM AUTHOR]

There has been great attention focused on the effects of first and second generation biofuels on global warming. The Energy Independence and Security Act (EISA) and the Renewable Fuel Standard (RFS) have mandated production levels and performance criteria of biofuels in the United States. The thermochemical conversion of biomass to ethanol shows potential as a biofuel production pathway. The objective of this research was to examine the alcohol yields and GHG emissions from the thermochemical conversion process for six different feedstocks on a gate-to-gate basis. GHG analyses and life cycle assessments were performed for natural hardwood, loblolly pine, eucalyptus, miscanthus, corn stover, and switchgrass feedstocks using a NREL thermochemical model and SimaPro. Alcohol yield and GHG emission for the hybrid poplar baseline feedstock conversion were 105,400 L dry metric ton-1 and 2.8 kg CO2 eq. per liter, respectively. Compared with the baseline, loblolly pine produced the highest alcohol yields, an 8.5% increase, and the lowest GHG emissions per liter of ethanol, a 9.1% decrease. Corn stover, due to its high ash content, had the lowest yields and the highest GHG emissions per liter of ethanol. The results were highly sensitive to the ash and water content of the biomass, indicating that biomass properties can significantly affect the environmental impact of the thermochemical ethanol conversion process. [ABSTRACT FROM AUTHOR]

Microfibrillated celluloses (MFCs) have mechanical properties sufficient for packaging applications but lack water vapor barrier properties in comparison to petroleum-based plastics. These properties can be modified by the use of mineral fillers, added within the film structure, or waxes, as surface coatings. In this investigation it was determined that addition of fillers resulted in films with lower densities but also lower water vapor transmission rates (WVTR). This was hypothesized to be due to decreased water vapor solubility in the films. Associated transport phenomena were analyzed by the Knudsen model for diffusion but due to the limited incorporation of chemical factors in the model and relatively large pore sizes, accurate prediction of pore diameters for filled films was not possible with this model. Modeling the filled-films with Fick's equation, however, takes into account chemical differences, as observed by the calculated tortuosity values. Interestingly, coating with beeswax, paraffin, and cooked starch resulted in MFC films with water vapor transmission rates lower than those for low density polyethylene. These coatings were modeled with a three-layer model which determined that coatings were more effective in reducing WVTR. [ABSTRACT FROM AUTHOR]

Microfibrillated celluloses (MFCs) with diameters predominantly in the range of 10-100 nm liberated from larger plant-based fibers have garnered much attention for the use in composites, coatings, and films due to large specific surface areas, renewability, and unique mechanical properties. Energy consumption during production is an important aspect in the determination of the 'green' nature of these MFC-based materials. Bleached and unbleached hardwood pulp samples were processed by homogenization, microfluidization, and micro-grinding, to determine the effect of processing on microfibril and film properties, relative to energy consumption. Processing with these different methods affected the specific surface area of the MFCs, and the film characteristics such as opacity, roughness, density, water interaction properties, and tensile properties. Apparent film densities were approximately 900 kg/m for all samples and the specific surface area of the processed materials ranged from approximately 30 to 70 m/g for bleached hardwood and 50 to 110 m/g for unbleached hardwood. The microfluidizer resulted in films with higher tensile indices than both micro-grinding and homogenization (148 Nm/g vs. 105 Nm/g and 109 Nm/g, respectively for unbleached hardwood). Microfluidization and micro-grinding resulted in films with higher toughness values than homogenization and required less energy to obtain these properties, offering promise for producing MFC materials with lower energy input. It was also determined that a refining pretreatment required for microfluidization or homogenization can be reduced or eliminated when producing MFCs with the micro-grinder. A summary of the fiber and mechanical energy costs for different fibers and processing conditions with economic potential is presented. [ABSTRACT FROM AUTHOR]

The interactions with water and the physical properties of microfibrillated celluloses (MFCs) and associated films generated from wood pulps of different yields (containing extractives, lignin, and hemicelluloses) have been investigated. MFCs were produced by combining mechanical refining and a high pressure treatment using a homogenizer. The produced MFCs were characterized by morphology analysis, water retention, hard-to-remove water content, and specific surface area. Regardless of chemical composition, processing to convert macrofibrils to microfibrils resulted in a decrease in water adsorption and water vapor transmission rate, both important properties for food packaging applications. After homogenization, MFCs with high lignin content had a higher water vapor transmission rate, even with a higher initial contact angle, hypothesized to be due to large hydrophobic pores in the film. A small amount of paraffin wax, less than 10%, reduced the WVTR to a similar value as low density polyethylene. Hard-to-remove water content correlated with specific surface area up to approximately 50 m2/g, but not with water retention value. The drying rate of the MFCs increased with the specific surface area. Hornified fibers from recycled paper also have the potential to be used as starting materials for MFC production as the physical and optical properties of the films were similar to the films from virgin fibers. In summary, the utilization of lignin containing MFCs resulted in unique properties and should reduce MFC production costs by reducing wood, chemical, and energy requirements. [ABSTRACT FROM AUTHOR]

Abstract: Atomic force microscopy with chemically modified cantilever tips (chemical force microscopy) was used to study the pull-off forces (adhesion forces) on cellulose model surfaces and bleached softwood kraft pulp fibers in aqueous media. It was found that for the –COOH terminated tips, the adhesion forces are dependent on pH, whereas for the –CH3 and –OH terminated tips adhesion is not strongly affected by pH. Comparison between the cellulose model surfaces and cellulosic fibers under our experimental conditions reveal that surface roughness does not affect adhesion strongly. X-ray photoelectron spectroscopy (XPS) and Fourier Transformed Infrared (FTIR) spectroscopy reveal that both substrate surfaces have homogeneous chemical composition. The results show that chemical force microscopy can be used for the chemical characterization of cellulose surfaces at a nano-level. [Copyright &y& Elsevier]

The aerobic biodegradation of common textiles that shed microfibers during laundering was evaluated under the action of microbes found in the environment, such as lake and seawater, and activated sludge at a low concentration from a wastewater treatment plant (WWTP). Under these conditions, the biodegradation potential was the same in all the experiments: Microcrystalline Cellulose (MCC) > Cotton > Rayon > Polyester/Cotton ≫ Polyester. Nevertheless, for cotton and rayon yarns, >70% biodegradation was achieved with activated sludge at low concentration and lake water, whereas in seawater, about 50% degradation was reached. Polyester did not appreciably degrade. The biodegradation results herein indicate potential not absolutes in nature. The bacterial diversity analyses in the different biodegradation inoculums show that there are distinct bacterial communities related to the assimilation and mineralization of complex carbohydrates that were promoted with the cellulosic MCC, cotton, and rayon samples different than the polyester sample. Unlabelled Image • The biodegradability was as follows: Microcrystalline Cellulose (MCC) > Cotton > Rayon > Polyester/Cotton >> Polyester. • The biodegradability depends on the chemical nature of the fibers and the microorganisms present in the environment. • The biodegradation achieved with activated sludge from the WWTP and lake water was higher than with the seawater. • The bacterial diversity analyses show that there are different communities developed in each inoculum system. • • There are distinct communities related to the biodegradable and non-degraded samples. [ABSTRACT FROM AUTHOR]

Optimizing drying energy in the forest products industry is critical for integrating lignocellulosic feedstocks across all manufacturing sectors. Despite substantial efforts to reduce thermal energy consumption during drying, further enhancements are possible. Cellulose, the main component of forest products, is Earth's most abundant biopolymer and a promising renewable feedstock. This study employs all-atom molecular dynamics (MD) simulations to explore the structural dynamics of a small I β -cellulose microcrystallite and surrounding water layers during drying. Molecular and atomistic profiles revealed localized water near the cellulose surface, with water structuring extending beyond 8 Å into the water bulk, influencing solvent-accessible surface area and solvation energy. With increasing temperature, there was a ∼20 % reduction in the cellulose surface available for interaction with water molecules, and a ∼22 % reduction in solvation energy. The number of hydrogen bonds increased with thicker water layers, facilitated by a "bridging" effect. Electrostatic interactions dominated the intermolecular interactions at all temperatures, creating an energetic barrier that hinders water removal, slowing the drying processes. Understanding temperature-dependent cellulose-water interactions at the molecular level will help in designing novel strategies to address drying energy consumption, advancing the adoption of lignocellulosics as viable manufacturing feedstocks. [Display omitted] [ABSTRACT FROM AUTHOR]

Abstract: Drywall, which is made primarily of a calcium sulfate dihydrate (gypsum) core with paper on both sides, is one of the most widely used construction materials. Because board failure often occurs at the gypsum core/paper interface, it has become important to know the exact nature of the gypsum/cellulose bond and how crystal morphology affects it. This study provides data about the nature of this interaction by means of AFM and Colloidal Probe Microscopy. These methods made it possible to distinguish among the different crystal faces and their respective interactions with cellulose. Measured in air, the adhesive forces between the AFM tip and the different faces varied according to f(010)

Efficient utilization of forestry, agriculture, and marine resources in various manufacturing sectors requires optimizing fiber transformation, dewatering, and drying energy consumption. These processes play a crucial role in reducing the carbon footprint and boosting sustainability within the circular bioeconomy framework. Despite efforts made in the paper industry to enhance productivity while conserving resources and energy through lower grammage and higher machine speeds, reducing thermal energy consumption during papermaking remains a significant challenge. A key approach to address this challenge lies in increasing dewatering of the fiber web before entering the dryer section of the paper machine. Similarly, the production of high-value-added products derived from alternative lignocellulosic feedstocks, such as nanocellulose and microalgae, requires advanced dewatering techniques for techno-economic viability. This critical and systematic review aims to comprehensively explore the intricate interactions between water and lignocellulosic surfaces, as well as the leading technologies used to enhance dewatering and drying. Recent developments in technologies to reduce water content during papermaking, and advanced dewatering techniques for nanocellulosic and microalgal feedstocks are addressed. Existing research highlights several fundamental and technical challenges spanning from the nano- to macroscopic scales that must be addressed to make lignocellulosics a suitable feedstock option for industry. By identifying alternative strategies to improve water removal, this review intends to accelerate the widespread adoption of lignocellulosics as feasible manufacturing feedstocks. Moreover, this review aims to provide a fundamental understanding of the interactions, associations, and bonding mechanisms between water and cellulose fibers, nanocellulosic materials, and microalgal feedstocks. The findings of this review shed light on critical research directions necessary for advancing the efficient utilization of lignocellulosic resources and accelerating the transition towards sustainable manufacturing practices. [Display omitted] • One key strategic issue facing the forest products industry is the high energy requirements. • The nature of interactions, association, and bonding of lignocelluloses is essential. • Alternative enzymatic treatments targeting the fiber surface can increase dryness while reducing the need for refining. • An understanding of floc formation and micro and nano-fines migration mechanisms is required. • Nanocellulose and microalgal dewatering is critical to enable braoder applicaitons. [ABSTRACT FROM AUTHOR]