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Family groups in the ancient cultures of China, Korea, and Japan have toiled for generations in an effort to out-compete their neighbors in the pursuit of handmade paper products having better strength performance, in addition to flatness, uniform appearance, and other desirable attributes. Study of the history of the papermaking craft reveals a remarkable ability of ancient peoples to discover advantageous ways to prepare the cellulosic pulp, to improve its brightness, and to form uniform and strong paper sheets. But though the ancients knew how to “beat” the pulp to improve its bonding ability, there is no evidence of any of them having attempted to greatly “over-beat” some of the fiber, thus making nanocellulose, for potential addition to the fiber mixture. Why not? In this editorial, it is proposed that the ancients may have discovered that adding very highly fibrillated cellulose material to paper was not a good idea.

Factors affecting the swelling of cellulosic fibers are considered in this review. Emphasis is placed on aqueous systems and papermaking fibers, but the review also considers cellulose solvent systems, nanocellulose research, and the behavior of cellulosic hydrogels. The topic of swelling of cellulosic fibers ranges from effects of humid air, continuing through water immersion, and extends to hydrogels and the dissolution of cellulose, as well as some of its derivatives. The degree of swelling of cellulose fibers can be understood as involving a balance between forces of expansion (especially osmotic pressure) vs. various restraining forces, some of which involve the detailed structure of layers within the fibril structure of the fibers. The review also considers hornification and its effects related to swelling. The expansive forces are highly dependent on ionizable groups, pH, and the ionic strength of solution. The restraining forces depend on the nature of lignin, cellulose, and their detailed structural arrangements.

This editorial considers three groups of individuals and how they often find themselves following common ways of thinking. Artists, especially those who become well known, are hard workers and somewhat stubborn. Once they have found a type of paper that works well for them, they tend to develop loyalty to it, regardless of what the label on the ream wrap may say. Papermakers, ancient and modern, likewise have tended to stick with practices that are convenient to them at the moment, whether or not they contribute to archival quality. Fortunately, the transition to alkaline papermaking practices means that modern printing papers tend to last a lot longer. Increasing knowledge of the importance of acid-free paper, as well as the principles of sustainability, are making positive contributions to our ongoing cultural heritage, at least to the part of that heritage that is related to cellulosic materials.

Size presses on paper machines are used to apply a solution of a polymer – usually starch – to the surface of the sheet and thereby to increase the stiffness, surface strength, and printing quality of the product. This article reviews publications dealing with the size press equipment, the materials, and factors affecting both the operating efficiency and attributes of the resulting paper. The emergence of film-press equipment (e.g. blade-metering size presses) in the 1980s has greatly decreased the frequency of web breaks and increased productivity. Starch technology at the size press, though relatively mature, continues to evolve. By adjustment of starch attributes, solids levels, and incorporating other additives, modern papermakers can tune size press outcomes to meet a range of paper product requirements, including strength, hydrophobicity, and the reduction of air permeability. By application of various synthetic polymers, mineral particles, and even nanocellulose in combination with starch or other base polymers, there is potential to extend the technology to meet a range of future needs for paper products.

Terminology plays a crucial role in shaping our understanding of a field. In this editorial, we focus on the widely used terms "wet end" and "wet end chemistry" within the realm of papermaking. By delving into historical records, our aim is to provide a deeper understanding and a clearer perspective on these terms. It is worth noting that exploring terminology can enhance comprehension and foster a more comprehensive understanding of the subject matter.

Picking up a discarded can or bottle and placing it in a recycling bin may seem like a very small step to take in the direction of making a better world. The scope of benefits that might accrue, by combining many such steps, and making careful plans, was highlighted in a recent Waste to Advanced Resources Matter (WARM) workshop hosted at this university. As shown during the discussions at the workshop, those who are deeply involved with issues of waste management, climate change issues, and care for our planet already know the “broad brush” answers regarding what needs to be done. Now is the time for action in implementing efficient and widespread recovery of valuable materials and energy from what we presently throw away.

This editorial considers hindrances that keep me from making sure that my used wooden furniture items don’t get thrown out at a point where their wooden content still has decades or hundreds of years of potential service left in them. I am a careless and lazy person, and I am not always appreciating the different ways in which other people might be ready to appreciate and utilize my cast-off items. Continued usage of a wooden item can be the ultimate in minimizing environmental impacts. I might envision that the only usage of an old, scuffed wooden dining room set is full restoration. But my niece might need it for her college apartment. A friend of a friend might need it for an informal basement art studio. Alternatively, if the set is really well beyond use in its original form, it could be converted into wood particles for particleboard or incinerated to generate renewable energy. Whether I use eBay, word of mouth, my church’s electronic bulletin board, or just put the item out by the curb on a sunny day, a wooden item of furniture has the potential to continue to provide valuable service for much longer than I might first imagine.

For about two millennia, paper has served as a main medium for preservation of people’s ideas, stories, contracts, and art. This article reviews what is known about the various components that make up paper from the perspective of their long-term stability under typical storage conditions. Literature evidence is considered relative to the susceptibility of different paper components to embrittlement, acid hydrolysis, microbiological attack, and discoloration, among others. The cellulose that makes up a majority of most paper items is demonstrably stable enough to persist for many hundreds of years on the shelves of archival collections, though it is susceptible to acid-catalyzed hydrolysis, which can be accelerated by byproducts of decomposition. Though less attention has been paid to the archival performance of various minor components of modern paper products, evidence suggests that at least some of them are subject to likely breakdown, embrittlement, or decay in the course of prolonged storage. Based on these considerations, one can envision different categories of paper that can be expected to meet different levels of storage stability: ancient recipes for handmade papermaking, e.g. washi and hanji, archival-grade paper products, ordinary modern alkaline paper products, and paper manufactured without concerns for its longevity.

Fire hazard is a constant risk in everyday life with the use of combustibles such as polymeric materials, wood, and fabrics, to name a few. Halogenated compounds have been widely used as efficient flame-retardants, often being applied as coatings or impregnations. With growing environmental concerns and regional bans on the use of halogenated flame-retardant compounds, bio-based alternatives are garnering significant research interest. Naturally occurring materials such as eggshells, DNA, and certain proteins have developed a self-defense mechanism against fire over millions of years of evolution. Cork, a naturally occurring biological tissue in outer bark, is of interest as it is often used as a heat shield and moisture repellent, specifically in spacecraft. A deeper look into the chemical structure of cork indicates the presence of suberin, a bio-polyester group that makes up as much as 40% of its chemical composition. These bio-polyester groups play a key role as a protective barrier between the plant and the surrounding external environment. Thus, the role of suberin in plants could be mimicked for the design of biobased flame-retardant materials.

This review article considers processes by which the main components of wood have been reported to arrange themselves into various kinds of organized structures, at least to a partial extent. The biosynthesis of wood provides the clearest examples of such self-organization. For example, even before a cellulose macromolecule has been completely synthesized in a plant organism, the leading parts of the polymer chains already will have assembled themselves into organized crystals, i.e., nano-fibrils. This review then considers a challenge that faces industrial engineers: how to emulate the great success of natural systems when attempting to achieve favorable materials properties, process efficiency, and environmental friendliness when developing new engineered wood structures, barrier films, and other desired products composed of lignocellulosic materials. Based on the reviewed literature, it appears that the main chemical components of wood, even after they have been isolated from each other, still have a remnant of their initial tendencies to come back together in a somewhat non-random fashion, following mechanisms that can be favorable for the production of engineered materials having potentially useful functions.

In many of its current and potential applications, technologists treat the surface of cellulose to render it more hydrophobic. By use of a variety of hydrophobic sizing treatment strategies, the bulk cellulose phase becomes covered up with a layer having lower polarity and less inclination to interact with water. Often, the goal is to use a relatively low amount of additive to cover up or change just the surface of the cellulosic material, while still benefiting from the strength, recyclability, relatively low cost, and other favorable features of the bio-based material. But what often gets forgotten is that the hydrophilic nature of pure cellulose is not very high, and there are ways to manipulate such characteristics without reacting the material or covering it up. Sometimes reacting the cellulose with hydrophobic substituent groups appears to make it more water-loving. So, when thinking broadly of processing options for new applications, there are several contrasting approaches to consider.

The release of soils and impurities from cellulosic surfaces plays a critical role in such processes as the laundering of clothes and the deinking of wastepaper pulps. This article reviews publications that provide evidence about factors that affect such release and the mechanisms by which such factors operate. In general, cellulosic substrates provide advantages for the release of contaminants due to their hydrophilic nature and due to their permeability, allowing the transport of surfactants to contact interfaces with dirt. However, the same permeability of cellulosic material also provides opportunities for contaminants to work themselves into internal crevices and pores, from which they are difficult to remove. The article also reviews aspects of theory related to detergency and how those theories relate to the laundering, deinking, and purifying of substrates based on cellulose and related plant materials. Cellulose and some of its derivatives also can play a role in detergent formulation, especially as builders or as finishes placed on textile surfaces, which sometimes aid in the release of dirt.

This editorial considers the use of images as a way to enhance the readability and possibly the impact of scientific writing. Readers are asked to envision effective scientific writing as a form of storytelling. Some stories can be enhanced by adding a diagram or a step-by-step procedure. Inherently dull results might be enlivened (in a cautious manner) with a non-typical graphical portrayal. A potentially tedious theoretical point might be lightened with a touch of humor, which might seem out of place if it were expressed in text. Keep these options in mind as you are creating your next story, i.e., your next research article.

Molded cellulosic pulp products provide eco-friendly alternatives to various petroleum-based packaging systems. They have a long history of reliable usage for such applications as egg trays and the shipping of fruits. They have recently become increasingly used for the packaging of electronics, wine bottles, and specialty items. Molded pulp products are especially used in applications requiring cushioning ability, as well as when it is important to match the shapes of the packed items. Their main component, cellulosic fibers from virgin or recycled wood fibers, as well as various nonwood fibers, can reduce society’s dependence on plastics, including expanded polystyrene. However, the dewatering of molded pulp tends to be slow, and the subsequent evaporation of water is energy-intensive. The article reviews strategies to increase production rates and to lower energy consumption. In addition, by applying chemical treatments and processing approaches, there are opportunities to achieve desired end-use properties, such as grease resistance. New manufacturing strategies, including rapid prototyping and advances in tooling, provide opportunities for more efficient form factors and more effective packaging in the future.

Paper, nanocellulose, and other polysaccharide-based materials can be excellent candidates for food packaging barrier layers, except that they tend to be vulnerable to moisture. This article reviews published research describing various chemical treatments having the potential to render hydrophobic character to such layers. Emphasis is placed on systems in which hydrophobic monomers are used to treat either particles or sheets comprised largely of polysaccharides. A goal of this review is to identify combinations of materials and procedures having promise for scale-up to industrial production, while providing effective resistance to moisture. The idea is to protect the underlying polysaccharide-based barrier layers such that they can continue to impede the transfer of such permeants as oxygen, greases, flavor compounds, and water vapor. A further goal is to minimize any adverse environmental impacts associated with the treatments. Based on the research articles considered in this review, promising hydrophobic treatments can be achieved involving silanes, ester formation, other covalent interactions, plasma treatments, and to some extent by various treatments that do not require formation of covalent bonds. The article is designed such that readers can skip ahead to items of particular interest to them.

The pulp and paper industry is highly energy-intensive. In mills that use chemical pulping, roughly half of the higher heating value of the cellulosic material used to manufacture the product typically is incinerated to generate steam and electricity that is needed to run the processes. Additional energy, much of it non-renewable, needs to be purchased. This review considers publications describing steps that pulp and paper facilities can take to operate more efficiently. Savings can be achieved, for instance, by minimizing unnecessary losses in exergy, which can be defined as the energy content relative to a standard ambient condition. Throughout the long series of unit operations comprising the conversion of wood material to sheets of paper, there are large opportunities to more closely approach a hypothetical ideal performance by following established best-practices.

Wood-processing facilities, including pulp, paper, lumber, and engineered wood facilities, use large amounts of energy for such purposes as evaporative drying and the curing of adhesives. Much of that energy is already being supplied by the incineration of biomass, and there is opportunity to increase the proportion of renewable energy that is used. Specific changes can be made within such factories that allow them to come closer to what is thermodynamically possible in terms of avoiding the wastage of exergy, which can be defined as useful energy. Savings in exergy are often obtained by optimization of a network of heat exchangers within an integrated system. No steam should be allowed to leak to the atmosphere; rather the latent heat (due to phase transitions) and sensible heat (due to temperature changes) are recovered during the heating up of incoming air and water, ideally at a similar range of temperatures. Thus, by a combination of process integration and full utilization of cellulosic residues generated from the process, even bio-based industries can be made greener.

Due to its renewable nature, its inherent strength, and many other favorable attributes, nanocellulose (NC) has drawn increasing attention for many potential applications. A diverse and complex assortment of NC products have been reported, and these are most commonly classified based on some contrasting procedures of preparation. The research community is facing a continuing challenge to adequately measure and quantify morphological features of various NC products. In principle, it ought to be possible to quantify and name NC based on such attributes as “degree of branching,” “breadth of particle size,” and “aspect ratio distribution,” etc. However, the ability to measure and compute such quantities still lies beyond what can be achieved in practical amounts of time in typical laboratories. Meanwhile, there has been tension between researchers proposing additional descriptive names, while at the same time there have been efforts at achieving uniformity and simplicity in nomenclature. It is proposed in this essay that this state of affairs is largely a reflection of complexity itself, such that NC products that have the same nominal description can be very different from each other when examined closely. The diversity itself may turn out to be a good thing, as researchers work to come up with varieties of NC that can survive an expected relentless competition from existing plastic-based or cellulose-based materials.

Barrier films that are used on packages play an important role, especially in the protection of food products. Research is being carried out at an accelerating pace to replace petroleum-based plastic films, which do not biodegrade and are difficult to recycle. This review article considers publications related to the use of polyelectrolyte complexes (PECs) in barrier films as a strategy to decrease the permeation of oxygen and other substances into and out from packages. Research progress has been achieved in using combinations of positively and negatively charged polymers, sometimes together with platy mineral particles, as a way to restrict diffusion through packaging materials. In principle, the ionic bonds within PECs contribute to a relatively high cohesive energy density within such a barrier film, which can resist diffusion of various gases and greasy substances. Resistance to water vapor, as well as aqueous substances, represent important challenges for barrier concepts that depend on ionic bond contributions. Factors affecting barrier performance of PEC-based films are discussed in light of research findings.

This editorial considers the end fates of toxic materials, such as heavy metals, dyes, and synthetic organic compounds, which can be recovered from polluted water by using bio-based adsorbents. The point of the editorial is that insufficient research attention has been paid to the final fate of such contaminants. By contrast, much is known regarding factors affecting the adsorption capacities and rates of adsorption onto cellulose-based materials. Highly contaminated solutions are produced during the regeneration of biosorbent materials. Eutectic freeze crystallization potentially could be used to isolate relative pure compounds of heavy metals from such solutions. Alternatively, biochar can be prepared from cellulosic material in such a way as to achieve strong attachment to certain pollutants. Such biochar, after its use as an adsorbent, could be placed in the ground, where it can be expected to remain stable as sequestered carbon. A high ion exchange capacity of such biochar has potential to reduce the rates of leaching, which could otherwise lead to contamination of groundwater near to landfill sites. As shown by these examples, some promising answers to the final fate of contaminants may conform to a “circular economy” model, whereas other promising answers may conform to a “cradle-to-grave” viewpoint.

This article reviews publications with the goal of understanding the role of hydrophobic copolymers added to size-press starch as a means to make paper products more resistant to penetration by aqueous fluids. The underlying technology is considered, including background related to starch, size-press equipment, and various hydrophobic copolymers and latex products that have been evaluated. The resulting hydrophobization of the paper has been reported to depend not only on the dosage of the hydrophobic additive, but also on its molecular mass and ionic form. The mechanism appears to rely on an ability of starch to serve as a temporary host for hydrophobic compounds in aqueous solution. It has been proposed that hydrophobic copolymers added with size press starch tend to migrate to the air interface during drying of the starch film, thus allowing the low-energy functional groups, such as styrene or alkyl chains, to face outwards. Further research is needed to address various mechanistic questions. There may be opportunities to further raise the performance of this type of technology as practiced within paper production factories.

Society’s wish list for future packaging systems is placing some daunting challenges upon researchers: In addition to protecting contents during storage and shipping, the material must not bio-accumulate, and it should be readily recyclable by using practical processing steps. This article considers strategies employing bio-based plastics and reviews published information relative to their performance. Though bioplastics such as poly(lactic acid) (PLA) and poly(hydroxybutyrate) (PHB) can be prepared from plant materials, their default properties are generally inferior to those of popular synthetic plastics. In addition, some bioplastics are not easily decomposed in soil or seawater, and the polymers can undergo chemical breakdown during recycling. This review considers strategies to overcome such challenges, including the use of biodegradable cellulose-based reinforcing particles. In addition to contributing to strength, the cellulose can swell the bioplastic, allowing enzymatic attack. The rate-controlling step in bioplastic degradation also can be abiotic, i.e. not involving enzymes. Though there is much more work to be done, much progress has been achieved in formulating bioplastic composites that are biodegradable, recyclable, and higher in strength compared to the neat polymer. Emphasis in this review is placed on PLA and PHB, but not to the exclusion of other bioplastic matrix materials.

Because some of the critical events during the removal of water before the dryer section on a paper machine happen very rapidly within enclosed spaces – such as wet-press nips – there have been persistent challenges in understanding the governing mechanisms. In principle, a fuller understanding of the controlling mechanisms, based on evidence, should permit progress in achieving both higher rates of production of paper and more reliable control of paper attributes. In addition, energy can be saved, reducing environmental impacts. The goal of this article is to review published work dealing both with the concepts involved in water removal and evidence upon which existing and new theories can be based. The scope of this review includes all of the papermaking unit operations between the jet coming from the headbox and the final wet-press nip of an industrial-scale paper machine. Published findings support a hypothesis that dewatering rates can be decreased by densification of surface layers, plugging of drainage channels by fines, sealing effects, flocculation, and rewetting. Ways to overcome such effects are also reviewed.

Conventional rheological tests can be difficult to carry out in the case of suspensions of nanofibrillated cellulose (NFC). Such suspensions tend to migrate away from the walls of a rheometer device, leaving a low-viscosity layer. The very high aspect ratio of typical nanofibrillated cellulose particles favors formation of tangled clusters. But application of hydrodynamic shear can cause fragmentation of those clusters. It is proposed in this essay that some focus be placed on the fragments of entangled clusters of NFC and interactions between them at their fractured surfaces. The condition of near-uniform, defect-free structures of nanocellulose spanning the volume within a sheared suspension might be regarded as an unlikely circumstance. Isaac Newton started with a very simple equation to start to understand rheology. It is proposed that a similarly bold and simplified approach may be needed to account for the effects of broken entangled clusters of NFC on flow phenomena, their assessment, and their consequences related to industrial processes.

This review article was prompted by a remarkable growth in the number of scientific publications dealing with the use of nanocellulose (especially nanofibrillated cellulose (NFC), cellulose nanocrystals (CNC), and bacterial cellulose (BC)) to enhance the barrier properties and other performance attributes of new generations of packaging products. Recent research has confirmed and extended what is known about oxygen barrier and water vapor transmission performance, strength properties, and the susceptibility of nanocellulose-based films and coatings to the presence of humidity or moisture. Recent research also points to various promising strategies to prepare ecologically-friendly packaging materials, taking advantage of nanocellulose-based layers, to compete in an arena that has long been dominated by synthetic plastics. Some promising approaches entail usage of multiple layers of different materials or additives such as waxes, high-aspect ratio nano-clays, and surface-active compounds in addition to the nanocellulose material. While various high-end applications may be achieved by chemical derivatization or grafting of the nanocellulose, the current trends in research suggest that high-volume implementation will likely incorporate water-based formulations, which may include water-based dispersions or emulsions, depending on the end-uses.

The pulp and paper (P&P) industry worldwide has achieved substantial progress in treating both process water and wastewater, thus limiting the discharge of pollutants to receiving waters. This review covers a variety of wastewater treatment methods, which provide P&P companies with cost-effective ways to limit the release of biological or chemical oxygen demand, toxicity, solids, color, and other indicators of pollutant load. Conventional wastewater treatment systems, often comprising primary clarification followed by activated sludge processes, have been widely implemented in the P&P industry. Higher levels of pollutant removal can be achieved by supplementary treatments, which can include anaerobic biological stages, advanced oxidation processes, bioreactors, and membrane filtration technologies. Improvements in the performance of wastewater treatment operations often can be achieved by effective measurement technologies and by strategic addition of agents including coagulants, flocculants, filter aids, and optimized fungal or bacterial cultures. In addition, P&P mills can implement upstream process changes, including dissolved-air-flotation (DAF) systems, filtration save-alls, and kidney-like operations to purify process waters, thus reducing the load of pollutants and the volume of effluent being discharged to end-of-pipe wastewater treatment plants.

Wet-laid forming, which can be regarded as being analogous to conventional papermaking processes but with use of chopped synthetic or staple fibers, continues to draw attention as an advantageous way to prepare advanced nonwoven textile products. This review of the literature considers scientific advances in the field, with emphasis placed on applications involving cellulosic fibers as a significant component of the product. Some primary challenges with respect to wet-laid processing concern the dispersion of the synthetic fibers in aqueous media and methods for avoiding their subsequent entanglement. Both mechanical and chemical strategies have been employed in order to achieve well-formed sheets of high uniformity and binding among the fibers to meet a variety of end-use specifications. The incorporation of cellulosic fibers has been shown to facilitate fiber dispersion and to impart certain beneficial characteristics and properties to wet-laid fabrics. The contrasting attributes of synthetic and cellulosic fibers contribute to some unique challenges during the processing of their mixtures during wet-laid forming.

Issues of cost and product quality have caused papermakers to place increased attention on the use of mineral additives, which are the subject of this review article. Technologists responsible for the production of paper can choose from a broad range of natural and synthetic mineral products, each of which has different characteristic shapes, size distributions, and surface chemical behavior. This article considers methods of characterization, and then discusses the distinguishing features of widely available filler products. The mechanisms by which fillers affect different paper properties is reviewed, as well as procedures for handling fillers in the paper mill and retaining them in the paper. Optical properties of paper and strategies to maintain paper strength at higher filler levels are considered. The goal of this review is to provide background both for engineers working to make their paper products more competitive and for researchers aiming to achieve effects beyond the current state of the art.

Contact angle methods are widely used to evaluate the wettability of cellulose-based surfaces and to judge their suitability for different applications. Wettability affects ink receptivity, coating, absorbency, adhesion, and frictional properties. There has been a continuing quest on the part of researchers to quantify the thermodynamic work of adhesion between cellulosic surfaces and various probe liquids and to account for such components of force as the London/van der Waals dispersion force, hydrogen bonding, and acid and base interactions. However, due in part to the rough, porous, and water-swellable nature of cellulosic materials, poor fits between various theories and contact angle data have been observed. Such problems are compounded by inherent weaknesses and challenges of the theoretical approaches that have been employed up to this point. It appears that insufficient consideration has been given to the challenging nature of cellulosic materials from the perspective of attempting to gain accurate information about different contributions to surface free energy. Strong hysteresis effects, with large differences between advancing and receding contact angles, have been overlooked by many researchers in attempting to quantify the work of adhesion. Experimental and conceptual approaches are suggested as potential ways to achieve more reliable and useful results in future wettability studies of cellulosic surfaces.

Major libraries have been placing increasing reliance upon non-aqueous mass deacidification in an effort to avoid hydrolytic decomposition of the cellulose during storage of bound volumes. Such decomposition is especially a problem when the printing papers used in manufacture of the books have been prepared under acidic conditions, using aluminum sulfate. But there is reason to doubt that the widely used non-aqueous treatments, in which “alkaline reserve” particles are deposited in the void spaces of the paper, can achieve neutralization of acidity throughout the paper structure under the conditions most commonly used for treatment and storage. Anecdotal evidence suggests that alkaline particles such as CaCO3, MgO, Mg(OH)2, or ZnO can be present for long periods of time adjacent to acidic parts of cellulosic fibers without neutralization of the acidity, especially the acidity within the fibers. If these phenomena can be better understood, then there may be an opportunity to use a high-humidity treatment of certain “deacidified” books in order to achieve more pervasive protection against acid-induced degradation.

Many current and potential uses of cellulosic materials depend critically on the character of their surfaces. This review of the scientific literature considers both well-established and emerging strategies to change the outermost surfaces of cellulosic fibers or films not only in terms of chemical composition, but also in terms of outcomes such as wettability, friction, and adhesion. A key goal of surface modification has been to improve the performance of cellulosic fibers in the manufacture of composites through chemistries such as esterification that are enabled by the high density of hydroxyl groups at typical cellulosic surfaces. A wide variety of grafting methods, some developed recently, can be used with plant-derived fibers. The costs and environmental consequences of such treatments must be carefully weighed against the potential to achieve similar performances by approaches that use more sustainable methods and materials and involve less energy and processing steps. There is potential to change the practical performances of many cellulosic materials by heating, by enzymatic treatments, by use of surface-active agents, or by adsorption of polyelectrolytes. The lignin, hemicelluloses, and extractives naturally present in plant-based materials also can be expected to play critical roles in emerging strategies to modify the surfaces characteristics of cellulosic fibers with a minimum of adverse environmental impacts.

By exercising of one’s curiosity, in combination with a lot of persistence, it is possible to solve some seemingly intractable problems. Many readers of this journal will have spent much, if not all of their careers, in university laboratories. In such settings there is an understandable emphasis on understanding underlying reasons. In other words, one is expected to focus on “why things happen” rather than just getting results. But if such an approach works well at the university, how about applying it at the production facility? This editorial features the stories of a man who was brave enough to spend his career asking “why” questions while working to improve the operations of paper mills.

Residents in localities throughout the world voluntarily participate in the routine recycling of household wastes, such as paper, metals, and plastics containers. But when a house in their neighborhood gets built or torn down, most of the debris – including wood waste – gets landfilled. Such a waste of material suggests that there are opportunities to add value to these under-utilized resources. The great variability, as well as contamination, pose major challenges. It is recommended that reclaimed wood be primarily used in the manufacture of durable goods, and then whatever is left over be used for energy (or heat) generation.

Dissolved petroleum-based compounds, e.g. solvents, pesticides, and chemical reagents such as phenolic compounds, can pose significant hazards to the health of humans and ecosystems when they are released to the environment. This review article considers research progress related to the biosorption and removal of such contaminants from water using cellulose-derived materials. The fact that cellulosic materials show promise in removing such sparingly soluble materials from water lends support to a hypothesis that lignocellulosic materials can be broad-spectrum adsorbents. Also, the hydrophobic character and sorption capabilities can be increased through thermal treatment and the preparation of activated carbons. As shown in many studies, the efficiency of uptake of various petrochemical products from water also can be increased by chemical treatments of the adsorbent. It appears that more widespread adoption of biosorption as a means of removing petroleum-based products from water has been limited by concerns about the used, loaded biosorbent. Disposal or regeneration options that need to be considered more in future research include enzymatic and biological treatments, taking advantage of the fact that the biosorbent material is able to collect, immobilize, and concentrate various contaminants in forms that are suited for a number of packed bed or batch-type degradative treatment systems.

Paper production requires large amounts of cellulosic fiber, whereas the world’s forested lands and croplands have a finite capacity to supply such resources. To deal with likely future pressure on forest resources, as well as to hold down costs of materials, publications examined in the preparation of this review suggest that the paper industry will need to implement several concurrent strategies. In particular, the industry can be expected to view recycling as a central part of its activities. Basis weights of various paper-based products can be expected to decrease over the coming decades, and more of the fiber content will be replaced with fillers such as calcium carbonate. Such trends will place intense demands upon chemical-based strategies to enhance the bonding within paper and paperboard. Based on the literature, further progress in reducing the amount of new forest resources used to meet a given set of paper product requirements will require a combined approach, taking into account various fiber attributes, nanostructures, novel concepts in bond formation, and advances in the unit operations of papermaking.

Dissolved and colloidal substances (DCS) in the process waters of paper machine systems can interfere with the retention of fine particles, retard the drainage of water from the wet web, and generally hurt the intended functions of various polyelectrolytes that are added to the process. This review considers publications that have attempted to characterize the nature and effects of different DCS fractions, in addition to some of the ways that paper technologists have attempted to overcome related problems. The consequences of DCS in a paper machine system can be traced to their ability to form complexes with various polyelectrolytes. Such tendencies can be understood based on a relatively strong complexing ability of multivalent materials, depending on the macromolecular size and charge density. Continuing research is needed to more fully understand the different contributions to cationic demand in various paper machine systems and to find more efficient means of dealing with DCS.

Dyes used in the coloration of textiles, paper, and other products are highly visible, sometimes toxic, and sometimes resistant to biological breakdown; thus it is important to minimize their release into aqueous environments. This review article considers how biosorption of dyes onto cellulose-related materials has the potential to address such concerns. Numerous publications have described how a variety of biomass-derived substrates can be used to absorb different classes of dyestuff from dilute aqueous solutions. Progress also has been achieved in understanding the thermodynamics, kinetics, and chemical factors that control the uptake of dyes. Important questions remain to be more fully investigated, such as those involving the full life-cycle of cellulosic substrates that are used for the collection of dyes. Also, more work needs to be done in order to establish whether biosorption should be implemented as a separate unit operation, or whether it ought to be integrated with other water treatment technologies, including the enzymatic breakdown of chromophores.

A communications scholar at our university asked me recently whether I would take part in a debate about academic social media services such as ResearchGate. Yes, I responded, as long as I don’t have to argue the affirmative – that such online systems are necessarily a good thing. Personally I do not count myself as a user of academic social media, but I can easily understand why others could make an opposite decision. Academic social media can provide a way to get copies of full-length published articles, to pose questions to other researchers, to get various questions answered, and in general to foster relationships with well-networked and possibly influential people within one’s academic field. Or, like me, you might just enjoy having something mildly annoying that is fun to complain about.

Recent years have seen explosive growth in research concerning the use of cellulosic materials, either in their as-recieved state or as modified products, for the removal of heavy metal ions from dilute aqueous solutions. Despite highly promising reports of progress in this area, important questions remain. For instance, it has not been clearly established whether knowledge about the composition and structure of the bioadsorbent raw material is equally important to its availability at its point of use. Various physical and chemical modifications of biomass have been shown to boost the ability of the cellulose-based material to bind various metal ions. Systems of data analysis and mechanistic models are described. There is a continuing need to explain the mechanisms of these approaches and to determine the most effective treatments. Finally, the article probes areas where more research is urgently needed. For example, life cycle analysis studies are needed, comparing the use of renewable biosorbents vs. conventional means of removing toxic metal ions from water.

Plant-derived cellulosic materials play a critical role when organic wastes are composted to produce a beneficial amendment for topsoil. This review article considers publications dealing with the science of composting, emphasizing ways in which the cellulosic and lignin components of the composted material influence both the process and the product. Cellulose has been described as a main source of energy to drive the biological transformations and the consequent temperature rise and chemical changes that are associated with composting. Lignin can be viewed as a main starting material for the formation of humus, the recalcitrant organic matter that provides the water-holding, ion exchange, and bulking capabilities that can contribute greatly to soil health and productivity. Lignocellulosic materials also contribute to air permeability, bulking, and water retention during the composting process. Critical variables for successful composting include the ratio of carbon to nitrogen, the nature of the cellulosic component, particle size, bed size and format, moisture, pH, aeration, temperature, and time. Composting can help to address solid waste problems and provides a sustainable way to enhance soil fertility.

Embrittlement threatens the useful lifetime of books, maps, manuscripts, and works of art on paper during storage, circulation, and display in libraries, museums, and archives. Past studies have traced much of the embrittlement to the Brønsted-acidic conditions under which printing papers have been made, especially during the period between the mid 1800s to about 1990. This article reviews measures that conservators and collection managers have taken to reduce the acidity of books and other paper-based materials, thereby decreasing the rates of acid-catalyzed hydrolysis and other changes leading to embrittlement. Technical challenges include the selection of an alkaline additive, selecting and implementing a way to distribute this alkaline substance uniformly in the sheet and bound volumes, avoiding excessively high pH conditions, minimizing the rate of loss of physical properties such as resistance to folding, and avoiding any conditions that cause evident damage to the documents one is trying to preserve. Developers have achieved considerable progress, and modern librarians and researchers have many procedures from which to choose as a starting point for further developments.

For over 2000 years the manual craft of papermaking has been practiced all over the world utilizing a variety of techniques. This review describes the evolution of hand papermaking and its cultural significance. Paper’s evolution has been shaped by the structure and chemical composition of the fibers. Almost every aspect of modern papermaking technology has been foreshadowed by traditional practices. Such practices were passed down for many generations within families of papermakers. The main sources of cellulosic fiber evolved as the ancient craft migrated from its birthplace in China to Korea and Japan, the Islamic world, and then to Europe and America. Though most paper made today comes from automated, continuous production systems, handmade paper has enjoyed a resurgence, both as a traditional craft and as an art-form. In addition, traditional papermaking methods can provide insights to help in modern applications involving cellulosic fibers.

The rate and extent of transport of macromolecules and other solutes into cellulosic materials and fibers have important applications in such fields as papermaking, textiles, medicine, and chromatography. This review considers how diffusion and flow affect permeation into wood, paper, and other lignocellulosic materials. Because pore sizes within such materials can range from nanometers to millimeters, a broad perspective will be used, also considering some publications related to other porous materials. Factors that limit the rate or extent of polymer or other solute transport into pores can involve thermodynamics (affecting the driving motivation for permeation), kinetics (if there is insufficient time for the system to come to equilibrium), and physical barriers. Molecular flow is also affected by the attributes of the solute, such as molecular mass and charge, as well as those of the substrate, such as the pore size, interconnectedness, restricted areas, and surface characteristics. Published articles have helped to clarify which of these factors may have a controlling influence on molecular transport in different situations.

Retention aids can be defined as very-high-mass, water-soluble polymers that are added to cellulosic fiber slurries before the formation of paper in order to improve the efficiency with which fine particles, including cellulosic fines, are retained in the paper product. Optimization of retention aid performance can be a key to achieving efficient and environmentally responsible papermaking objectives. This article reviews various published theories related to retention aid use. Findings related to three main classes of retention aid polymers are considered: cationic acrylamide copolymers (cPAM), anionic acrylamide copolymers (aPAM), and polyethylene oxide (PEO). While many aspects of the interactions of each of these classes of retention aid products can be understood based on colloid chemistry principles, further research is needed in order to more fully bridge the gap between theory and practice.

Filter media, including those prepared from cellulosic materials, often suffer from permeability loss during continued use. To help understand such issues, one can take advantage of an extensive body of related research in such fields as industrial filtration, water purification, enhanced oil recovery, chromatography, paper manufacture, and the leaching of pollutants from impoundments. Though the mechanisms that appear to govern permeability-loss phenomena depend a lot on the details of various applications, the published research has revealed a number of common features. In particular, flow through a porous bed or fiber mat can be markedly reduced by deposition of particles or colloidal matter in positions that either block or partially restrict fluid flow. Progress has been achieved in the development of mechanistic models, as well as the use of such models in numerical simulations to explain various experimental findings. Further research of this type needs to be applied to cellulosic materials, which tend to be much more elongated in comparison to the bed materials and suspended matter considered most often by most researchers active in research related to permeability loss.

Aqueous dispersions of lignocellulosic materials are used in such fields as papermaking, pharmaceuticals, and preparation of cellulose-based composites. The present review article considers published literature dealing with the ability of cellulosic particle dispersions (fiber, fines, nanorods, etc.) to either remain well dispersed or to agglomerate in response to changes in the composition of the supporting electrolyte solution. In many respects, the colloidal stability and coagulation of lignocellulosics can be understood in terms of well-known concepts, including effects due to osmotic pressure arising from overlapping electrostatic double layers at the charged surfaces. Details of the morphology and surface properties of lignocellulosic materials give rise to a variety of colloidal behaviors that make them unique. Adjustments in aqueous conditions, including the pH, salt ions (type and valence), polymers (charged or uncharged), and surfactants can be used to control the dispersion stability of cellulose, lignin, or wood-extractive materials to serve a variety of applications.

Because of their wide abundance, their renewable and environmentally benign nature, and their outstanding mechanical properties, a great deal of attention has been paid recently to cellulosic nanofibrillar structures as components in nanocomposites. A first major challenge has been to find efficient ways to liberate cellulosic fibrils from different source materials, including wood, agricultural residues, or bacterial cellulose. A second major challenge has involved the lack of compatibility of cellulosic surfaces with a variety of plastic materials. The water-swellable nature of cellulose, especially in its non-crystalline regions, also can be a concern in various composite materials. This review of recent work shows that considerable progress has been achieved in addressing these issues and that there is potential to use cellulosic nano-components in a wide range of high-tech applications.

This review article highlights progress in understanding the optical properties of paper. Paper’s appearance can be defined in terms of its opacity, brightness, color, fluorescent properties, gloss, and various quantities related to its uniformity. The phenomena that give rise to paper’s optical properties, especially its ability to scatter and absorb visible light, are highly dependent on paper’s structure and its chemical composition. In an effort to engineer low-cost products having relative high opacity and brightness, it is necessary to optimize the material selection and processing conditions. The dimensions of solid materials and void structures within the paper are key factors for optimizing the optical properties. In addition, additives including bleaching agents, mineral particles, dyes, and fluorescent whitening agents can impact paper’s optical properties Paper’s appearance depends, in subtle ways, on the processes of its manufacture.

Both reversible and irreversible changes take place as cellulosic fibers are manufactured into paper products one or more times. This review considers both physical and chemical changes. It is proposed that by understanding these changes one can make better use of cellulosic fibers at various stages of their life cycles, achieving a broad range of paper performance characteristics. Some of the changes that occur as a result of recycling are inherent to the fibers themselves. Other changes may result from the presence of various contaminants associated with the fibers as a result of manufacturing processes and uses. The former category includes an expected loss of swelling ability and decreased wet-flexibility, especially after kraft fibers are dried. The latter category includes effects of inks, de-inking agents, stickies, and additives used during previous cycles of papermaking.