Editorials

Lignocellulose-based self-assembled micelles have emerged as a new generation of value-added functional nanostructures that show promise to address issues concerning the depletion of non-renewable resources; also these materials may contribute to the growing enthusiasm of utilizing biomass resources. Lignocellulose micelles can be conveniently prepared by self-assembly of amphiphilic lignocellulose derivatives in aqueous solution. They show great potential for applications in disparate fields, e.g. drug delivery, bioimaging diagnosis, sensing, nanoreacting, and so on. However, as a new research topic, a lot of research work would be needed to find out the critical structural factors that correlate with the formation, stability, morphology, and flexibility of lignocellulose micelles.

A challenge in producing wood-plastic composites (WPCs) with a high wood content using extrusion processes is the poor processability, which gives rise to inadequate properties of the resulting WPC. Plasticizing the stiff wood cell walls can be a strategic response to this challenge. Two thoughts are addressed herein on improving the plasticity of wood particle cell walls: use of ionic liquids or use of low molecular weight organic thermal conductors. An ionic liquid can dissolve the cell wall surface and therefore reduce the stiffness of cell wall during an extrusion process. Organic thermal conductors can be incorporated into the cell wall (bulking) to improve the thermal conductivity, thereby sufficiently softening the lignin, a native plasticizer embedded in the cell walls. The potential issues that may arise as a result of these approaches are also presented and discussed.

Nonfood lignocellulosic biomass is an ideal substrate for biohydrogen production. By avoiding pretreatment steps (acid, alkali, or enzymatic), there is potential to make the process economical. Utilization of regional untreated lignocellulosic biomass by cellulolytic and fermentative thermophiles in a consolidated mode using a single reactor is one of the ways to achieve economical and sustainable biohydrogen production. Employing these potential microorganisms along with decentralized biohydrogen energy production will lead us towards regional and national independence having a positive influence on the bioenergy sector.

Based on its rich chemistry and broadly available raw material sources, hydroxymethylfurfural (HMF) has become one of the most promising platform compounds for chemicals and biofuels from renewable biomass, and its production has drawn much attention in recent years. However, it is currently still facing significant technical challenges to make it economically feasible in an industrial scale. Use of ionic liquids has provided a potential alternative to address such challenges. Some studies have shown that the use of ionic liquids and suitable catalysts can inhibit side reactions and decrease the formation of by-products, thus improving selectivity and yield during conversion of renewable biomass to HMF. Moreover, the use of ionic liquids also simplifies the HMF production procedures from crude biomass in a one-pot process.

The importance of teaching, for the development of economies, cultures, and the enrichment of people’s lives cannot be overstated. These days biomass and bioenergy teaching has a pivotal role to play in influencing all of the aforementioned areas of life, since fossil fuels are becoming depleted. However, what good is teaching if it cannot be communicated in an intelligible, persuading, and egalitarian manner? A dynamic educational construct between “teacher” and “student” will be the chief mode of promoting knowledge and provoking research for engendering more knowledge. This editorial attempts to show how teaching is a living and symbiotic discipline that we typically take for granted, but once we do it right, we have the power to change the world as we know it. We will briefly explore the example of BioSUCCEED, a platform at NC State University, as a means of communicating knowledge related to biomass and bioenergy.

The application of fillers at the surface of cellulosic paper is an interesting and industrially-commercialized but not very well-known concept, in which the filler particles are essentially added to the voids of the fibrous matrixes. This so-called “surface filling” can be achieved by the use of fillers together with a polymer solution via film press or size press, an approach that is distinct from both wet-end filling and conventional coating of paper. As an easily practicable process, surface filling has some advantages over direct wet-end addition of fillers, such as minimizing the adverse effects of filler addition on paper strength. Efficient surface filling is somewhat dependent on the specific characteristics of both fillers and fibrous matrixes. Surface filling may provide interesting possibilities for the papermaking discipline; for example, it would open the door to maximizing the cost-effectiveness of paper mills, and efficiently adding new functionalities to cellulosic paper. From both practical and fundamental points of view, systematic exploration and understanding of surface filling of cellulosic paper would be of great significance to the papermaking industry.

Since the introduction of the water footprint concept in 2002, in the context of humankind’s ever-increasing awareness of the valuable global freshwater resources, it has received more and more attention. The application of this relatively new concept has been expected to provide ecological and environmental benefits. For the water-intensive papermaking industry, it seems that water footprint needs to be addressed. The water footprint of cellulosic paper can be divided into three components, including its green water footprint, blue water footprint, and grey water footprint, which may be accounted for by considering the individual contributions of wood or non-wood materials, pulp production processes, effluent discharge to the receiving water bodies, process chemicals and additives, energy consumption, etc. In the literature, the accounting of water footprint during the whole production chain of cellulosic paper is already available, and relevant research findings can provide useful insights into the application of the concept; however, further development of the accounting methodologies is much needed, so that the quantitative and qualitative evaluation of water footprint can be internationally recognized, certified, and standardized. Although there are ongoing or upcoming debates and challenges associated with the concept, its application to papermaking industry may be expected to provide various encouraging possibilities and impacts.

The advances in manufactured fibers and textiles have garnered interest and excitement of textile artists and consumers alike for a myriad of reasons, including health, environmental, and fashion. The chemical and molecular nature of these advances, however leads to confusion and misunderstanding of the new fibers in the materials. This is exacerbated by the current climate of distrust for chemical words and desire for “green” products and the unregulated (mis)information and marketing on the web. Textile artists, consumers, and the clothing and household textile industry need clear names and labels to identify the materials they are using.

Although transport fuels are currently obtained mainly from petroleum, alternative fuels derived from lignocellulosic biomass (LB) have drawn much attention in recent years in light of the limited reserves of crude oil and the associated environmental issues. Lignocellulosic ethanol (LE) and lignocellulosic hydrocarbons (LH) are two typical representatives of the LB-derived transport fuels. This editorial systematically compares LE and LB from production to their application in transport fuels. It can be demonstrated that LH has many advantages over LE relative to such uses. However, most recent studies on the production of the LB-derived transport fuels have focused on LE production. Hence, it is strongly recommended that more research should be aimed at developing an efficient and economically viable process for industrial LH production.

Superhydrophobic materials have a lot of interesting potential applications. The self-cleaning property is a unique feature. Rendering the water-loving cellulosic paper superhydrophobic can open the door for value-added applications. Superhydrophobic paper is a fairly new area, and only very limited scientific publications are available in the literature. Among these publications, the topics on the use of mineral pigments in fabrication of superhydrophobic structures account for a large proportion. During the fabrication process, mineral pigments, e.g., silica, precipitated calcium carbonate, and clay, generally need to be hydrophobized, either directly or indirectly. Mineral pigments can be applied to cellulosic paper by surface treatment or wet-end filling, and good dispersabilities of these pigments are always highly demanded. A key mechanistic point is that by tunable particle packing or fabrication, mineral pigments may exhibit surface-roughening effects, which are critical for superhydrophobicity development. The roughening of a hydrophobic surface helps to enhance hydrophobicity. Possible concepts such as nano-structuring or controllable surface patterning of mineral pigments may help to improve superhydrophobicity. Environmental friendliness will also guide the scientific/technical development in this area.