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The appearance and quick spread of the new severe acute respiratory syndrome coronavirus disease, COVID-19, brought major societal challenges. Importantly, suitable medical diagnosis procedures and smooth clinical management of the disease are an emergent need, which must be anchored on novel diagnostic methods and devices. Novel molecular diagnostic tools relying on nucleic acid amplification testing have emerged globally and are the current gold standard in COVID-19 diagnosis. However, the need for widespread testing methodologies for fast, effective testing in multiple epidemiological scenarios remains a crucial step in the fight against the COVID-19 pandemic. Biosensors have previously shown the potential for cost-effective and accessible diagnostics, finding applications in settings where conventional, laboratorial techniques may not be readily employed. Paper- and cellulose-based biosensors can be particularly relevant in pandemic times, for the renewability, possibility of mass production with sustainable methodologies, and safe environmental disposal. In this review, paper-based devices and platforms targeting SARS-CoV-2 are showcased and discussed, as a means to achieve quick and low-cost PoC diagnosis, including detection methodologies for viral genomic material, viral antigen detection, and serological antibody testing. Devices targeting inflammatory markers relevant for COVID-19 are also discussed, as fast, reliable bedside diagnostic tools for patient treatment and follow-up., The authors acknowledge funding through projects Eco2Covid (POCI-01-02B7-FEDER-068174) and TecniCov (POCI-01-02B7-FEDER-069745), co-funded by FEDER through COMPETE2020 and Lisboa2020. T.P., A.R.C. and A.C.M. acknowledge funding to National Foundation for Science and Technology, I.P., FCT, through their PhD grants, references DFA/BD/8606/2020, SFRH/BD/130107/2017 and SFRH/BD/115173/2016, respectively, info:eu-repo/semantics/publishedVersion

Cellulose paper, a material that is naturally derived, low cost, lightweight, eco-friendly, and mechanically deformable, plays important roles in producing next-generation flexible electronics. Following the booms in the development of functional electronics, the soft actuators built from cellulose paper have attracted great attention. In this focused review, the milestones and recent achievements of cellulose paper-based actuators are summarized. Electro-, thermal, moisture and magnetic actuation mechanisms are utilized to acquire energy from external stimuli. Corresponding functional materials and available fabrication techniques like film assembly and layer deposition are described. Programmable actions for the emerging applications in bionics, paper grippers and robots are realized by pursuing different strategies to control the responding deformation. Along with a conclusion, the existing challenges and possible solutions in evaluating and improving the performance of cellulose paper are summarized in the final section.

Environmentally friendly and energy saving treatment of black liquor (BL), a massively produced waste in Kraft papermaking process, still remains a big challenge. Here, by adopting a Ni CaO Ca12Al14O33 bifunctional catalyst derived from hydrotalcite-like materials, we demonstrate the feasibility of producing high-purity H2 (∼96%) with 0.9 mol H2 mol−1 C yield via the sorption enhanced steam reforming (SESR) of BL. The SESRBL performance in terms of H2 production maintained stable for 5 cycles, but declined from the 6th cycle. XRD, Raman spectroscopy, elemental analysis and energy dispersive techniques were employed to rationalize the deactivation of the catalyst. It was revealed that gradual sintering and agglomeration of Ni and CaO and associated coking played important roles in catalyst deactivation and performance degradation of SESRBL, while deposition of Na and K from the BL might also be responsible for the declined performance. On the other hand, it was demonstrated that the SESRBL process could effectively reduce the emission of sulfur species by storing it as CaSO3. Our results highlight a promising alternative for BL treatment and H2 production, thereby being beneficial for pollution control and environment governance in the context of mitigation of climate change.

Coatings based on pigment and polymer binders are applied on paper surfaces to improve their surface, optical, and printing properties. Besides the coating composition, the structure and properties of the coated papers are influenced by the coating layer consolidation upon drying. In this study, the influence of drying conditions on the structure and properties of coating layers based on natural pigments (clay) and polymer binders (butadiene acrylonitrile latex) has been analyzed. Using a laboratory rod Mayer device, the coatings were applied as thin layer (about 15&ndash, 16 g/m2) on the paper surface and samples of coated paper were dried at 20 and 105 &deg, C temperatures. The optical, structural, and water absorption properties of the coating layer were evaluated by the measurement of gloss, opacity, void fraction, light scattering, and contact angle. The obtained results highlighted that both the drying temperature and latex content in the coating color have a synergic effect on the coated paper quality.

Over the past decades, paper-based lateral flow immunoassays (LFIAs) have been extensively developed for rapid, facile, and low-cost detection of a wide array of target analytes in a point-of-care manner. Conventional home pregnancy tests are the most significant example of LFAs, which detect elevated concentrations of human chorionic gonadotrophin (hCG) in body fluids to identify early pregnancy. In this work, we have upgraded these platforms to a higher version by developing a customized microfluidic paper-based analytical device (μPAD), as the new generation of paper-based point-of-care platforms, for colorimetric immunosensing. This will offer a cost-efficient and environmentally friendly alternative platform for paper-based immunosensing, eliminating the need for nitrocellulose (NC) membrane as the substrate material. The performance of the developed platform is demonstrated by detection of hCG (as a model case) in urine samples and subsequently indicating positive or negative pregnancy. A dual-functional silane-based composite was used to treat filter paper in order to enhance the colorimetric signal intensity in the detection zones of μPADs. In addition, microfluidic pathways were designed in a manner to provide the desired regulated fluid flow, generating sufficient incubation time (delays) at the designated detection zones, and consequently enhancing the obtained signal intensity. The presented approaches allow to overcome the existing limitations of μPADs in immunosensing and will broaden their applicability to a wider range of assays. Although, the application of the developed hCG μPAD assay is mainly in qualitative (i.e., positive or negative) detection of pregnancy, the semi-quantitative measurement of hCG was also investigated, indicating the viability of this assay for sensitive detection of the target hCG analyte within the related physiological range (i.e., 10–500 ng/mL) with a LOD value down to 10 ng/mL.

Paper-based analytical devices have been substantially developed in recent decades. Many fabrication techniques for paper-based analytical devices have been demonstrated and reported. Herein, we report a relatively rapid, simple, and inexpensive method for fabricating paper-based analytical devices using parafilm hot pressing. We studied and optimized the effect of the key fabrication parameters, namely pressure, temperature, and pressing time. We discerned the optimal conditions, including a pressure of 3.8 MPa, temperature of 80 °C, and 3 min of pressing time, with the smallest hydrophobic barrier size (821 µm) being governed by laminate mask and parafilm dispersal from pressure and heat. Physical and biochemical properties were evaluated to substantiate the paper functionality for analytical devices. The wicking speed in the fabricated paper strips was slightly lower than that of non-processed paper, resulting from a reduced paper pore size after hot pressing. A colorimetric immunological assay was performed to demonstrate the protein binding capacity of the paper-based device after exposure to pressure and heat from the fabrication. Moreover, mixing in a two-dimensional paper-based device and flowing in a three-dimensional counterpart were thoroughly investigated, demonstrating that the paper devices from this fabrication process are potentially applicable as analytical devices for biomolecule detection. Fast, easy, and inexpensive parafilm hot press fabrication presents an opportunity for researchers to develop paper-based analytical devices in resource-limited environments.

info:eu-repo/grantAgreement/EC/H2020/787410/EU The work was also partially funded by the Nanomark collaborative project between INCM (Imprensa Nacional - Casa da Moeda). Publisher Copyright: © 2021 The Author(s). Published by IOP Publishing Ltd. Titanium dioxide nanoparticles and nanostructured thin films were simultaneously synthesized using a microwave-assisted hydrothermal method. The synthesis formed very fine particles, appearing as nanospheres in the 11 nm size range. As for the nanostructured films, they have displayed similar structural characteristics to the nanoparticles, with thickness of 130 nm. These films covered uniformly and homogenously the Whatman paper, while maintaining its flexibility. The materials processed had their photocatalytic activity assessed from rhodamine B degradation under solar radiation (91% degradation after 40 min for the powder material and 68% after 6 h for the nanostructured thin films). Reusability experiments were also carried out, revealing superior performance concerning the Degussa P25, the most common photocatalyst used. The results of the present work can be thought as an option for the existing photocatalysts activated under solar light, namely for water purification, as it simultaneously produces enhanced photocatalytic powders and photocatalytic papers fully disposable and that can be easily recycled. publishersversion published

Paper sludge is a solid waste by-product abundantly produced in the paper industry and contains fine minerals and lignocellulosic biomass. In this contribution, the ex-situ catalytic fast pyrolysis of paper sludge with a high mineral content of ca. 71 wt% is reported for the first time and demonstrated in a pilot-scale unit (feeding rate of 11.3 kg h−1) using a granular Na2CO3/γ-Al2O3 catalyst (loading of 650 g) to produce a high-grade bio-oil at a fast pyrolysis temperature of 475 ± 5 °C (pre-screened using a pyroprobe) and a catalytic upgrading temperature of 500 °C. Besides, > 99 wt% minerals in the paper sludge could be recovered, including paper fillers such as CaCO3 (major) and talc. The bio-oil obtained at a carbon yield of 21 C.% has a low oxygen content of 3.2 wt%, a low total acidity number of 5.2 mg KOH g−1, low H2O content of 0.7 wt%, and a high higher heating value of 40.9 MJ kg−1. It consists of value-added bio-based chemicals such as paraffins, olefins, and low molecular weight aromatics. The results demonstrate that the use of paper sludge to recover minerals and to obtain fuels and chemicals using ex-situ catalytic pyrolysis is technically feasible at a pilot plant scale, which will be of importance for the development of future bio-based economy.

Diesel Particulate filters are considered one of the most efficient technologies to reduce particulate matter emitted by diesel engines. In this paper we study the development of catalytic ceramic papers based on Mn-Ce and their applications as soot particle filters in bench scale tests. Ceramic papers were prepared by a dual polyelectrolyte papermaking method and were impregnated with Mn and Ce precursors through a wet-spray procedure using a commercial fogger. Catalytic ceramic papers were tested as catalysts for the combustion of soot, which was obtained both from the burning of diesel fuel and directly from a bench test. In addition, the filtering capacity of catalytic ceramic papers was tested through opacity measurements by placing the ceramic papers in a suitable case at the end of the engine. Mn-Ce based catalysts were active in the soot combustion. The addition of citric acid considerably improved the catalytic performance of all the systems studied. This beneficial effect of citric acid is related to an improvement in the distribution of the catalytic material onto the ceramic fibers, being the mixed equimolar oxide Mn-Ce the most active catalyst.

Photonic crystals film that possesses periodic dielectric structure have shown great prospect in developing environmentally friendly paper alternatives due to the unique properties of dye free and non-photobleaching, but their practical application is limited by the weak interaction between colloidal particles. Although some progress has been obtained, it is still a challenge to develop photonic paper with the desired mechanical and optical properties. Herein, multifunctional hard core/soft shell nanoparticles with controlled size are fabricated by semi-continuous seed emulsion polymerization method. Compared with convention colloidal particles, these core/shell nanoparticles can facile self-assemble into large-scale dense ordered structure film via dried at room temperature due to the relatively low glass transition temperature (Tg) of the shell layers. The facile fabrication route enables the continuous high-through put production of the photonic papers. The as-formed papers not only possess the capacity to solvent (water/ethanol) rewritable and multicolor painting, but also can rapidly reversible mechanochromic. Moreover, due to the good compatibility of core/shell interface, these photonic films possess excellent mechanical properties, demonstrating that this multifunctional film makes the fabrication of novel robust rewritable papers possible and enables visual monitoring of deformation degree.

Highlights • Numerical simulations of acoustophoresis in pulp flow is conducted. • Parametric study of fiber characteristics, pulp flow regimes and acoustic parameters are conducted. • A feasibility study of industrial acoustophoresis for pulp concentration is performed. • A potential concentration gain of 15% is obtained experimentally., In pulp and paper mills, mechanical processes such as screening and washing are commonly used to remove accumulated solid suspensions and concentrate the pulp. For environmental reasons and to optimize paper production, an emerging challenge is to develop alternative methods to concentrate paper pulp between 3 % and 6 % consistency for which the mixed pulp-water flow is complex. Among the proposed solutions in the literature, solutions based on acoustic levitation, also referred as acoustophoresis, of low-consistency pulp have been demonstrated as a potential solution for efficient pulp concentration and water recirculation. However, no sensitivity analysis on the ultrasound and physical parameters was proposed, limiting the extension to a realistic application. Thus, this paper presents a numerical modeling of acoustophoresis for pulp flow concentration in a pipe. For this purpose, the pulp flow is defined as a pseudo-homogenous fluid with a turbulent Low Re k- ∊ formalism, and the pulp particles are considered spherical and deflected by two acoustic forces, namely the acoustic radiation force and the Stokes drag force, both induced by an ultrasound wave generated along the walls of a circular pipe. The combined action of these two forces in the pulp flow enables to concentrate the particles at the center of the pipe. The influences of particle size and mechanical properties, fluid properties and ultrasound parameters are analyzed within a parametric study to optimize the particle deflection and the pulp concentration. The experimental feasibility of the industrial use of acoustophoresis for the concentration of paper pulp is demonstrated with a concentration gain up to 15 %.

International audience; Despite predictions of the paperless office, global demand for printing and writing paper remains strong, and paper appears to be here to stay for some time. Not only firms, but also governments, libraries, and archives are in possession of large collections of legacy documents that still must be sorted and scanned. In this study, terahertz-based techniques are demonstrated to address several routine tasks related to the automated paper handling of unsorted legacy documents. Specifically, we demonstrate terahertz-based counting of the number of sheets in unconsolidated paper stacks, as well as locating stapled documents buried in paper stacks.

Ambient ionization of glycans is simply and efficiently achieved by spraying from an alkali metal salt-impregnated paper surface. Monosaccharides, oligosaccharides and ring glycans easily form abundant alkali metal adduct ions, and give simple and clean high-quality mass spectra. The enhancement is specific for glycans, compared to a wide variety of non-glycan compounds present in a matrix. In addition, molecular weight of unknown glycans can be further identified based on the ion mass difference of various alkali metal adduct ions from a certain compound when using a mixed salt-impregnated paper containing five cation salts. Successful determination of glycans and glycoconjugates in plant extracts, honey, blood and urine demonstrates the practicability of this approach to complicated matrices, especially biological matrices.

The development of low-cost analytical devices for on-site water quality monitoring is a critical need, especially for developing countries and remote communities in developed countries with limited resources. Microbial electrochemical cell-based (MXC) biosensors have been quite promising for quantitative and semi-quantitative (often qualitative) measurements of various water quality parameters due to their low cost and simplicity compared to traditional analytical methods. However, conventional MXC biosensors often encounter challenges, such as the slow establishment of biofilms, low sensitivity, and poor recoverability, making them unable to be applied for practical cases. In response, MXC biosensors assembled with paper-based materials demonstrated tremendous potentials to enhance sensitivity and field applicability. Furthermore, the paper-based platforms offer many prominent features, including autonomous liquid transport, rapid bacterial adhesion, lowered resistance, low fabrication cost (

Graphene-based papers have recently triggered considerable interests in developing the application as thermal interface materials (TIMs) for addressing the interfacial heat transfer issue, but their low through-plane thermal conductivity (κ⊥), resulting from the layer-by-layer stacked architecture, limits the direct use as TIMs. Although various hybrid graphene papers prepared by combining the graphene sheets and the thermally conductive insertions have been proposed to solve this problem, achieving a satisfactory κ⊥ higher than that of commercial TIMs (>5 W m−1 K−1) remains challenging. Here, a strategy aimed at the construction of heat pathways along the through-plane direction inside the graphene paper for achieving a high κ⊥ was demonstrated through the simultaneous filtration of graphene sheets with two different lateral sizes. The as-prepared graphene paper presented a hierarchical structure composed of loosely stacked horizontal layers formed by large graphene sheets, intercalated by a random arrangement of small graphene sheets. Due to the heat pathways formed by small graphene sheets along the through-plane direction, the hierarchically structured graphene paper exhibited an improved κ⊥ as high as 12.6 W m−1 K−1 after a common graphitization post-treatment. In the practical test, our proposed paper as an all-graphene TIM achieved an enhancement in cooling efficiency of ≈ 2.2 times compared to that of the state-of-the-art TIM, demonstrating its superior performance to meet the ever-increasing heat dissipation requirement.

Uniformly dispersing silver nanowires (AgNWs) in polymer matrices is of paramount importance for developing high-performance electromagnetic interference (EMI) shielding materials. Herein, new flexible and robust high-efficiency bacterial cellulose (BC)-based EMI shielding papers were developed via a modified step-by-step in situ biosynthesis method, in which, AgNWs were well distributed in the BC network. The BC nanofibers and AgNWs could form an effective entangled network with hydrogen bonding, efficiently strengthening the produced BC/AgNW papers. An electrical conductivity of 608365 S m1 was achieved for a BC/AgNW paper with a AgNW content of 36.5 wt%, which is superior to almost all AgNW-containing papers reported so far. Moreover, the BC/AgNW paper could sustain mechanical deformation and vigorous washing, without losing electrical conductivity. Additionally, this paper presents an ultrahigh specific EMI shielding effectiveness of 6400 dB mm1, which is higher than almost all previously reported AgNW-based polymer composites. The proposed approach in this study provides a facile and scalable fabrication route for producing flexible and highly conductive BC/AgNW papers, which are of great potential as electrically conductive components and EMI shielding elements in advanced applications., This work was supported by the National Natural Science Foundation of China (Grant Nos. 51973058 and 31870963), Jiangxi Provincial Natural Science Foundation (Grant No. 20202ACBL214007), Key Research and Development Program of Jiangxi Province (Grant No. 20192ACB80008) and the Key Project of Natural Science Foundation of Jiangxi Province (20202ACBL204013)., info:eu-repo/semantics/publishedVersion

This paper presents a critical review of laser pyrolysis. Although this technology is almost 60 years old, in literature many researchers, both from academia and industry, are still developing and improving it. On the contrary industrial applications are struggling to take off, if not in very restricted areas, although the technology has undoubted advantages that justify future development. The aim of this work consists in analysing a representative pool of scientific papers (230) and patents (121), from the last 20 years, to have an overview about the evolution of the method and try to understand the efforts spent to improve this technology effectively in academia and in industry. This study is important to provide a complete review about the argument, still missing in the literature. The objective is to provide an overview sufficiently broad and representative in the sources and to capture all the main ways in which laser pyrolysis has been used and with what distribution. The main focuses of the study are the analyses of the functions carried out by laser technologies, the application fields, and the types of used laser (i.e. models, power and fluence). Among the main results, the study showed that the main use of laser pyrolysis is to produce nanoparticles and coatings, the main materials worked by laser pyrolysis are silicon and carbon dioxide and the main searched properties in the products of laser pyrolysis are catalysts activity and electrical conductivity. CO2 lasers are the most used and the have high versatility compared to others. In conclusion, the study showed that laser pyrolysis is a consolidated technology within its main application fields (nanoparticles and coatings) for several years. Within this context, the technology has been developed on very different sizes and processes, obtaining a very wide range of results. Finally, these results may also have stimulated new areas of experimentation that emerged mainly in recent years and which concern biomedical applications, additive manufacturing, and waste disposal. Graphical abstract

International audience; We clarify some analytical expressions existing in the literature, • Within the correct formulae we conclude that there is no need for an ad hoc improvement on the opposite to the title paper, • We highlight the symmetry properties of the function to be integrated in order to agree with the usual assumptions made to derive the Kramers-Kronig relations, • The analytical formula we provide may be used to increase the accuracy of the "Poor Man's Kramers-Kronig analysis" method and the "Kramers-Kronig constrained variational analysis" method.

The paper industry is an important sector annually consuming kilotons of nanoforms and non-nanoforms of fillers and pigments. Fillers accelerate the rate of drying (less energy needed) and product cost (increasing the load of low-cost fillers). The plastic industry is another use sector, where coloristic pigments can be in nanoform, and many food containers are made of plastic. Use of paper to wrap both wet and dry food is consumer practice, but not always intended by producers. Here we compare the release behavior of different nano-enabled products (NEPs) by changing a) nanoform (NF) characteristics, b) NF load, c) the nano-enabled product (NEP) matrix, and d) food simulants. The ranking of these factors enables an assessment of food contact by concepts of analogy, specifically via the similarities of the rate and form of release in food during contact. Three types of matrices were used: Paper, plastic ((Polylactic Acid (PLA), Polyamide (PA6), and Polyurethane (PU)), and a paint formulation. Two nanoforms each of SiO2, Fe2O3, Cu-Phthalocyanine were incorporated, additionally to the conventional form of CaCO3 that is always contained in paper to reduce cellulose consumption. Tests were guided by the European Regulation EC 1935/2004 and EU 10/2011. No evidence of particle release was observed: the qualitative similarity (the form of release) was high regarding the food contact of all NEPs with embedded NFs. Quantitative similarity of releases depended primarily on the NEP matrix, as this controls the penetration of the simulant fluid into the NEP. The solubility of the NF and impurities in the simulant fluid was the second decisive factor, as dissolution of the NF inside the NEP is the main mechanism of release. This led to complete removal of CaCO3 in acidic medium, whereas Fe and Si signals remained in the paper, consistent with the low release rates in an ionic form. In our set of 16 NEPs, only one NEP showed a dependence on the REACH NF descriptors (substance, size, shape, surface treatment, crystallinity, impurities), specifically attributed to differences in soluble impurities, whereas for all others the substance of the nanoform was sufficient to predict a similarity of food contact release, without influences of size, shape, surface treatment and crystallinity. European Union [760840] Published version The GRACIOUS project has received funding from the European Union's Horizon 2020 Research and Innovation Programme under grant agreement No. 760840. We sincerely thank Tim Duncan of the US-FDA for providing specimen of Quantum-Dot-polymer films that enabled benchmarking of our methodology. Hubert Rauscher of EC-JRC and Danail Hristozov of GD are gratefully acknowledged for critical presubmission review. We thank Kai Werle and Svenja Berit Seiffert for performing single-particle-ICPMS analyses, Philipp Muller for supervising electron microscopy, and Elke Schumacher for performing UVVis analyses.

A flexible Pt/TiO2/γ-Al2O3 nanfiber paper (PTA) was successfully prepared by an electrospinning-coating-NaBH4 reduction method. The catalytic performance for formaldehyde (HCHO) oxidation over PTA with different Pt contents was investigated at room temperature. The results show that PTA exhibits higher catalytic activity and stability than Pt/γ-Al2O3. The TiO2 coating can promote the transformation of intermediate species and the desorption of CO2. The PTA1 with 1 wt% Pt shows the best catalytic activity and good stability. In the view of activity and cost, 0.5 wt% Pt is the optimal Pt content. The TiO2 coating not only plays an important role in improving the activity and stability of PTA, but also acts as a protective shell of γ-Al2O3 fiber, which greatly reduces the risk of alkali etching during preparation and maintains the good flexibility of PTA. The dioxymethylene (DOM), formate/carbonate species, CO are the intermediate species in HCHO oxidation over PTA. In addition, PTA exhibits good filtration performance for fine particles as well as good fluid permeability. Because of the high efficiency and flexibility of PTA composite catalytic material for HCHO oxidation with good filtration performance for fine particles, it will be a promising candidate in air purification.

The authors of the title paper (J Photochem & Photobio A:Chem 393 (2020) 112413) claim to have synthesized a toluidine tartrate (TT) crystal and examined its nonlinear optical (NLO) behavior by experimental and theoretical studies. In this critique, it is shown that the so-called TT crystal is a surface degraded material and the experimental and theoretical data contradict literature reports on the 1:1 salt of p-toluidine and l -tartaric acid.

In this study, eco-friendly and disposable paper-based membraneless microfluidic enzymatic fuel cells (EFCs) were developed without any mediators to reduce the toxicity and cost of EFCs. Glucose oxidase and laccase were immobilized on multi-walled carbon nanotube electrodes to catalyze the redox reaction of glucose and oxygen. Micromachining techniques well-suited for mass production were used to precisely fabricate micro-scale Y-shaped and cross-shaped EFCs. Experimental measurements showed that the concentration of glucose in the fuel solution affects the cell performance, which occurs because the flow speed of the fuel stream decreases as the concentration of glucose increases. The highest performance of power density (104.2 ± 3.35 μW cm−2) and current density (615.6 ± 3.14 μA cm−2) were obtained with the Y-shaped channel configuration at a glucose concentration of 100 mM. This performance is the best of all paper-based single EFCs reported to date. The new paper-based co-laminar flow mediatorless EFC exhibits strong potential to power miniaturized and portable on-site diagnostic devices.

Rational design of photoelectrode architectures is deemed as an effective solution to enhance efficiency of photoelectrochemical water splitting for conquering increasingly prominent environmental problems. Herein, a programmable flexible photoanode with built-in tandem Z-scheme configuration fabricated by in-situ growth of MoSe2-CdS-ZnO array with ultrathin nanosheet-interlaced-nanorod structure on the Au paper electrode, is firstly reported. By taking advantages of the interwoven nanonetwork structure, high conductivity as well as larger porosity of the as-fabricated Au paper electrode, a stable light-harvesting paper chip with fast transfer/separate mediators of the charge/carriers is thus integrated. By virtue of double internal electric fields (IEFs) and photothermal effect, the developed MoSe2-CdS-ZnO photoanode exhibits incident-photon-to-current efficiency of 52 % under 460 nm of light irradiation, and the current density reaches 2.4 mA cm−2 at 0.3 V versus normal hydrogen electrode, which is comparable with respect to current state-of-the-art “type-II-scheme”, “surface-scheme”, and cocatalyst-free photocatalysts (0.03–2.4 mA cm−2). Consequently, the paper-based photoanode achieves admirable photoelectrocatalytic hydrogen generation property (39.7 μmol cm−2 h-1). The synergistic effect of tailorable tandem Z-scheme configuration with double IEFs and delineating of 3D cross-linked network structure of the proposed photoanode in this work may open an avenue for constructing high-performance photoelectrochemical water splitting devices.

Integrating graphene with other kinds of biochemical molecules is an effective way to improve the properties of graphene film. Proteins are promising candidates for graphene hybridization. We create an effective method to prepare multifunctional graphene hybrid film by incorporation of antibacterial protamine. Protamine could be stably adsorbed on the surface of GO as both a reductant and an antibiotic to realize antimicrobial protamine/RGO conjugates. The presence of decorated protein layers makes it possible to adjust the physical performance of the composite. The obtained hybrid papers show improved hydrophilic property of reduced GO paper. These freestanding papers have a reversible humidity response shape-memory effect and great antibacterial property. The facile strategy possesses a promising way to develop multifunctional antibacterial materials.

Cellulose-based materials have attracted tremendous interest recently due to their fascinating merits of renewability, biodegradability, and low cost, holding great promise in electromagnetic protection, clean energy harvesting, and thermal management. However, the simple and effective integration of multiple functions into single cellulose material remains a challenge. Herein, we report the fabrication of a multifunctional and superhydrophobic cellulose composite paper (CCP) via coated MXene modified by in-situ polymerized polypyrrole and PDMS/candle soot on the opposite surface of the paper. CCP exhibits high-performance electromagnetic interference shielding effectiveness (~40 dB) while maintaining high electrical conductivity (1467 S/m). Moreover, the superhydrophobic surface of CCP can be used as the hydraulic triboelectric nanogenerator (H-TENG) to harvest water energy due to the liquid–solid contact triboelectrification and electrostatic induction. The hydraulic triboelectric energy can be captured and released when water droplets drop from a height of 2 cm and roll at a tilt angle of 20°, the output current can reach a peak of 0.8 nA. Furthermore, the surface saturation temperature of CCP can reach 140 °C with a low applied voltage of 6 V enabled by the Joule effect. Thus, CCP holds great potentials in applications of integrated smart electronics, clean energy harvesting, and thermal management.

Developing 3D printable waste paper based biocomposites is a potentially greener alternative to traditional waste paper recycling methods. In this paper, waste office paper (WOP) filled polylactide acid (PLA) biocomposites were prepared as filaments for Fused Filament Fabrication (FFF). The morphology, rheology, thermal properties, and physical properties of PLA-WOP composites were investigated. Results revealed that the addition of WOP improved the composites’ melt flow abilities. The Tg and Tm of composites remained similar to the neat PLA. However, tensile strengths of the prints decreased with the increase of WOP content, which could be attributed to the heterogeneous dispersion and aggregation caused by the abundance of WOP in the system. When 5% WOP was used, the elongation at break increased in comparison with pure PLA specimens. Nonetheless, when the WOP content was increased to 15%, the elongation at break decreased. To improve the mechanical properties of the prints, a silane coupling agent (γ-methacryloxypropyltrimethoxylsilane, KH570) was used to modify WOP granules. The mechanical properties were clearly enhanced post KH570 treatment. Furthermore, FTIR analyses demonstrated that the hydrogen bonding improved interfacial adhesion between WOP fillers and the PLA matrix. Thermal decomposition showed that the PLA-WOP composites had virtually no degradation below 260 °C, indicating that the composite filaments are safe for indoor 3D printing.

Bacteria identification has predominantly been conducted using specific bioreceptors such as antibodies or nucleic acid sequences. This approach may be inappropriate for environmental monitoring when the user does not know the target bacterial species and for screening complex water samples with many unknown bacterial species. In this work, we investigate the supervised machine learning of the bacteria-particle aggregation pattern induced by the peptide sets identified from the biofilm-bacteria interface. Each peptide is covalently conjugated to polystyrene particles and loaded together with bacterial suspensions onto paper microfluidic chips. Each peptide interacts with bacterial species to a different extent, leading to varying sizes of particle aggregation. This aggregation changes the surface tension and viscosity of the liquid flowing through the paper pores, altering the flow velocity at different extents. A smartphone camera captures this flow velocity without being affected by ambient and environmental conditions, towards a low-cost, rapid, and field-ready assay. A collection of such flow velocity data generates a unique fingerprinting profile for each bacterial species. Support vector machine is utilized to classify the species. At optimized conditions, the training model can predict the species at 93.3% accuracy out of five bacteria: Escherichia coli, Staphylococcus aureus, Salmonella Typhimurium, Enterococcus faecium, and Pseudomonas aeruginosa. Flow rates are monitored for less than 6 s and the sample-to-answer assay time is less than 10 min. The demonstrated method can open a new way of analyzing complex biological and environmental samples in a biomimetic manner with machine learning classification.

Flexible all-solid-state supercapacitors (FASSCs) have attracted much attention as power supplies for portable and wearable electronic products. Herein, we report the fabrication of a foldable, extra lightweight, flexible chopped carbon fiber paper (CFP) with a porous network structure prepared via wet-mold papermaking that can serve as a conductive substrate. The conductivity and pseudocapacitance of the electrode were improved by controlling the growth of 3D Cu(OH)2 nanorod arrays on CFP substrate. The Cu(OH)2@CFP electrode has a high specific capacitance of 421.8 mF cm−2 at a current density of 0.5 mA cm−2 with capacitance retention of 82.98% at a current density of 10 mA cm−2 after 5000 charge-discharge cycles. The FASSC manifested not only a large capacitance of 196.1 mF cm−2 at 2 mA cm−2, as well as energy and power densities of 6.97 × 10−2 mWh cm−2 and 1.6 mW cm−2, respectively, but also excellent stability of 80.3% over 5000 cycles at 5 mA cm−2. In addition, we confirmed that the FASSC has a large bending angle and can be twisted into various shapes, thereby indicating its applicability in portable and wearable electronic devices.

Lithium metal is the most attractive and promising anode for next-generation high energy batteries. However, uncontrollable dendrite growth of lithium remains a detrimental safety challenge. To tackle this problem, a 3D flexible MXene@Au host is designed by depositing an ultra-fine and robust Au layer on MXene paper via ion-sputtering. The Au layer acts as lithiophilic nuclear agent to ensure homogeneous lithium deposition and suppress the lithium dendrites growth. The as-prepared flexible 3D MXene@Au@Li anode shows significantly enhanced performance. Full lithium metal cell with LFP cathode delivers high capacity retention of 98.47% even after 200 cycles with good rate capability. These results may be useful for other metallic battery system and has potential applications in sensors, super-capacitor and catalyst etc.

Fabricating low-cost and high-efficiency oil-water separation superwetting materials for the demand of oil spilling treatment remains a great challenge. Herein, a superwetting aluminosilicate fiber paper decorated by flower-like nickel-cobalt carbonate hydroxide (NiCo-CH) nanostructures was prepared via the hydrothermal method and chemical modification with stearic acid (SA) or 1H, 1H, 2H, 2H-Perfluoroalkyltriethoxysilane (FAS-17). The superhydrophilic multi-layers nanoflowers combing with nanoflakes were uniformly distributed on the surface of aluminosilicate fiber. The superhydrophilic aluminosilicate fiber was then modified by the SA to obtain the superhydrophobic aluminosilicate fiber (SA-NiCo-CH@Al2SiO5 FP). The SA-NiCo-CH@Al2SiO5 FP revealed high separation efficiency (> 95.4%) for both light oils and heavy oils, and high oil flux (417 L m−2 h−1–71,656 L m−2 h−1). Furthermore, the SA-NiCo-CH@Al2SiO5 FP can also remain superhydrophobicity under various harsh conditions, such as dust, sand impact, acid or alkali, and low-temperature environments. This study revealed an inexpensive and simple-fabricated multifunctional superwetting material, which provides promising avenue for future applications in oil-water separation.

Lignin, the second most plentiful biopolymer, is produced on a large scale as the waste of the pulp and paper industries. Conventionally, lignin is incinerated for energy generation, while less tha...

Iron gall Inks corrosion causes paper degradation (browning, embrittlement) and treatments were developed to tackle this issue. They often include resizing with gelatin to reinforce the paper and its cellulosic fibers (of diameter approx. 10 µm). This work aimed at measuring the distribution of ink components at the scale of individual paper fibers so as to give a better understanding of the impact of gelatin (re-)sizing on iron gall ink corrosion. For this purpose, scanning transmission X-ray microscopy (STXM) was used at the Canadian light source synchrotron (CLS, Saskatoon). This technique combines nano-scale mapping (resolution of 30 nm) and near edge X-ray absorption fine structure (NEXAFS) analysis. Fe L-edge measurements enabled to map iron distribution and to locate iron(II) and iron(III) rich areas. N K-edge measurement made it possible to map gelatin distribution. C K-edge measurements allowed mapping and discrimination of cellulose, gallic acid, iron gall ink precipitate and gelatin. Three fibers were studied: an inked fiber with no size, a sized fiber that was afterwards inked and an inked fiber sprayed with gelatin. Analysis of gelatin and ink ingredients distribution indicated a lower amount of iron inside the treated cellulosic fiber, which may explain the beneficial effect of gelatin on iron gall ink corrosion.

Lignin is a potential renewable raw material for synthesis of aromatic molecules and materials. Particularly, Kraft-type lignins are abundantly available as a byproduct of wood and paper industries. Currently, there are practically no valuable products made using this highly complex polymer. Within this work, we have investigated the straightforward, high-yield depolymerization of two different technical lignins (Indulin AT and alkaline lignin) using only a mixture of green short-chain (C-1-C-3) alcohols and water as solvents. As shown here, at a temperature of 220 degrees C, autogenous pressure, and isopropanol/water as a co-solvent medium, it is possible to cleave Kraft lignin without char-forming side reactions. The obtained so-called "light" oil contains guaiacol-based monomeric units of 23 wt % yield together with liquid oligomers of 13 wt % yield combining liquid-liquid and solid-liquid extraction. Two-dimensional nuclear magnetic resonance analysis of lignin residues showed that the isopropanol/water treatment caused a marked breakdown of the intermolecular beta-O-4 and beta-beta bonds; thus, the depolymerization produced monomers and lignin residues with lower molecular weight. The results suggested a synergistic effect between isopropanol and water. No sign of repolymerization reactions could be observed with this process.

As an aromatic polymer in nature, lignin has recently attracted gross attention because of its advantages of high carbon content, low cost and bio-renewability. However, most lignin is directly burnt for power generation to satisfy the energy demand of the pulp mills. As a result, only a handful of isolated lignin is used as a raw material. Thus, increasing value addition on lignin to expand its scope of applications is currently a challenge demanding immediate attention. Many efforts have been made in the valorization of lignin, including the preparation of precursors for carbon fibers. However, its complex structure and diversity significantly restrict the spinnability of lignin. In this review, we provide elaborate knowledge on the preparation of lignin-based carbon fibers ranging from the relationships among chemical structures, formation conditions and properties of fibers, to their potential applications. Specifically, control procedures for different spinning methods of lignin, including melt spinning, solution spinning and electrospinning, together with stabilization and carbonization are deeply discussed to provide an overall understanding towards the formation of lignin-based carbon fibers. We also offer perspectives on the challenges and new directions for future development of lignin-based carbon fibers.

Graphical abstract, Introduction Face masks are regarded as effective Personal Protective Equipment (PPE) during the COVID-19 pandemic. However, the dominant polypropylene (PP)-based masks are devoid of antiviral/antibacterial activities and create enormous environmental burdens after disposal. Objectives Here we report a facile and potentially scalable method to fabricate biodegradable, breathable, and biocidal cellulose nonwovens (BCNWs) to address both environmental and hygienic problems of commercially available face masks. Methods TEMPO-oxidized cellulose nonwovens are rendered antiviral/antibacterial via covalent bonding with disinfecting polyhexamethylene guanidine or neomycin sulfate through carbodiimide coupling chemistry. Results The obtained results showed that the BCNWs have virucidal rate of >99.14%, bactericidal efficiency of >99.51%, no leaching-out effect, and excellent air permeability of >1111.5 mm s−1. More importantly, the as-prepared BCNWs can inactivate SARS-CoV-2 instantly. Conclusions This strategy provides a new platform for the green fabrication of multifunctional cellulose nonwovens as scalable bio-protective layers with superior performance for various PPE in fighting COVID-19 or future pandemics. Additionally, replacing the non-biodegradable non-antimicrobial PP-based masks with the cellulose-based masks can reduce the plastic wastes and lower the greenhouse gas production from the incineration of disposed masks.

Embargado hasta 30/11/2023 Lithium–sulfur batteries have been recognised as highly promising next-generation batteries, due to their low cost and high theoretical energy density. Despite numerous advances in this technology over the last decade, its commercialisation is still a challenge that has not yet been achieved. Many efforts have been made to improve the problems that these batteries present, mainly by investigating different cathode manufacturing strategies, testing novel Li anodes, new additives in the electrolytes, and modified separators or interlayers. However, the characteristics of the current collectors used in the preparation of the electrodes have been rarely addressed. Three commercial collectors are commonly used in basic research on Li–S batteries: Al foil, carbon coated Al foil (Al-C), and carbon paper (gas diffusion layer, GDL). In this work, a detailed study of the electrochemical response of these commercial collectors has been carried out. The tests were carried out on two S composites formed by carbons of a different natures, commercial carbon black and synthetic N-doped graphene. In addition, the S impregnation method was different, using either melt diffusion at 155 °C or ethylenediamine as S solvent, respectively. In both systems, the results were similar – the electrodes supported on GDL delivered higher specific capacities than those supported on Al and Al-C, with minimal differences between the two. Of the different collector properties examined to explain this behaviour, namely Al corrosion, electrical conductivities, surface-level composition, and surface texture, only the latter had a significant effect in the performance of GDL-based electrodes. SEM images revealed a rough and cracked surface formed by the agglomerated carbon particles that give rise to a complex pore system, predominantly consisting of macropores. All of these features are beneficial for a better anchoring of the active material on the collector surface, in addition to enhancing the wettability of the electrolyte and favouring reaction kinetics. In contrast, the Al-based collector possesses a very smooth and non-porous surface, detrimental to both the active material-substrate interface and the active material impregnation by the electrolyte.

Chemical and spectroscopic characterization of the mononuclear photosensitizers [(DPEPhos)Cu(I)(MPyrT)]0/+ (CuL, CuLH) and their dinuclear analogues (Cu2L’, Cu2L'H2 ), backed by (TD)DFT and high‐level GW‐Bethe‐Salpeter equation calculations, exemplifies the complex influence of charge, nuclearity and structural flexibility on UV‐induced photophysical pathways. Ultrafast transient absorption and step‐scan FTIR spectroscopy reveal flattening distortion in the triplet state of CuLH as controlled by charge, which also appears to have a large impact on the symmetry of the long‐lived triplet states in Cu2L’ and Cu2L'H2 . Time‐resolved luminescence spectroscopy (solid state), supported by transient photodissociation spectroscopy (gas phase), confirm a lifetime of some tens of μs for the respective triplet states, as well as the energetics of thermally activated delayed luminescence, both being essential parameters for application of these materials based on earth‐abundant copper in photocatalysis and luminescent devices., The comprehensive results on two mononuclear pyridyl‐triazole/DPEPhos based Cu(I) complexes and its extension to their two dinuclear analogues paves the road to addressing the complex coupling of the respective monomeric units, involving various physical and chemical properties as charge, (electronic) structure and (long‐lived) excited state properties, relevant for applications.

Biorefinery is pivotal to the sustainability of modern chemical industry. However, since biomass is oxygen-enriched, new and green chemical strategies are required for expanding the biomass derived chemical space. In this work, synthesis of natural products dihydrocapsaicin and dihydrocapsiate was achieved exclusively from lignocellulosic platform chemicals. Natural products dihydrocapsaicin and dihydrocapsiate were synthesized exclusively from lignocellulosic platform chemicals, using furfural (from hemicellulose) and methyl isopropyl ketone (from cellulose) through aldol condensation-hydrolysis-hydrodeoxygenation to synthesize 8-methylnonanoic acid and then combined with vanillin derivates (from lignin). This synthesis demonstrates the feasibility of constructing natural products entirely from renewable biomass platform through green processes. The utilization of inherent functional groups of biomass demonstrates their potential to open up chemical space.

In order to investigate the effect of washing water pH on textile damage for delicate garments, the study was conducted such that a customer survey was first applied to randomly selected users to analyze domestic washing machine using habits of Turkish consumers. Based on the findings of the survey, the experimental study was designed in two successive phases to investigate the dimensional and mechanical behavior of certain types of delicate textiles against varying washing conditions by taking in particular, water properties, namely pH, hardness, and temperature into account, and accordingly to determine the optimized washing conditions for such textiles. Firstly, tergotometer was employed as a washing machine simulator. Within the light of the results obtained, the experimental work of the second phase of the study was conducted, which involved a domestic washing machine as a real-life scenario. All of the results, including the correlation between the data sets obtained from the tergotometer and domestic washing machine trials, were statistically analyzed using Minitab 17. The study produced some important findings regarding the effect of washing water pH on delicate textiles, in addition to an algorithm for improving the present washing program, minimizing textile damage for mainly wool and silk garments.

Flexible thermoelectric materials are presented with potential applications in electronic devices and energy conversion due to their convenient preparation, good flexibility, and various forms. However, as ductility is rarely observed in inorganic semiconductors and ceramic insulators, reports on applications of inorganic oxide materials in flexible thermoelectric materials are sparse. Here, we report a new method for the synthesis of a flexible Na1.4Co2O4 thermoelectric material based on Na1.4Co2O4 bulk materials, which are prepared by a self-flux method and painted on print paper. Seebeck coefficient and power factor of the obtained thermoelectric material are 78–102 μVK-1 and 159–223 μWm-1K-2, respectively, in a temperature range of 303–522 K, which are superior to those values of other conductive polymers and their compounds. More interestingly, the n-type Na1.4Co2O4 flexible material is obtained in the painting process at higher pressure with Seebeck coefficients of –109 to –183 μVK-1 in a temperature range of 303–522 K. The convenient preparation method of these novel flexible thermoelectric materials may be expanded to the synthesis of other flexible thermoelectric materials, which will be the focus of future work.

Serial femtosecond crystallography (SFX) is a powerful technique that exploits X-ray free-electron lasers to determine the structure of macromolecules at room temperature. Despite the impressive exposition of structural details with this novel crystallographic approach, the methods currently available to introduce crystals into the path of the X-ray beam sometimes exhibit serious drawbacks. Samples requiring liquid injection of crystal slurries consume large quantities of crystals (at times up to a gram of protein per data set), may not be compatible with vacuum configurations on beamlines or provide a high background due to additional sheathing liquids present during the injection. Proposed and characterized here is the use of an immiscible inert oil phase to supplement the flow of sample in a hybrid microfluidic 3D-printed co-flow device. Co-flow generation is reported with sample and oil phases flowing in parallel, resulting in stable injection conditions for two different resin materials experimentally. A numerical model is presented that adequately predicts these flow-rate conditions. The co-flow generating devices reduce crystal clogging effects, have the potential to conserve protein crystal samples up to 95% and will allow degradation-free light-induced time-resolved SFX.

Lubricants are widely used in macroscopic mechanical systems to reduce friction and wear. However, on the microscopic scale, it is not clear to what extent lubricants are beneficial. Therefore, in this study, we consider two diamond solid-state gears at the nanoscale immersed in different lubricant molecules and perform classical MD simulations to investigate the rotational transmission of motion. We find that lubricants can help to synchronize the rotational transmission between gears regardless of the molecular species and the center-of-mass distance. Moreover, the influence of the angular velocity of the driving gear is investigated and shown to be related to the bond formation process between gears.

Various detrimental effects of petroleum-based lubricants have encouraged the use of vegetable oil as a replacement due to its better lubricity and environmental friendliness. This study evaluated the performance of virgin and emulsified vegetable oil as cutting fluid for the turning of titanium alloy with ceramic inserts. The performance was determined using signal to noise (S/N) ratio with few input parameters such as lubricant type, cutting speed, feed rate, and depth of cut. Palm oil and coconut oil were used as the vegetable oil. The virgin oil was mixed with a portion of water to produce emulsified oil. The machining operation applied minimum quantity lubrication (MQL) throughout the experiment. The performance of each type of oil was evaluated in terms of S/N ratio for cutting temperature, and chip reduction coefficient, and percentage of cutting tool wear in order to obtain the best cutting condition. Results showed that the virgin palm oil had better performance on the cutting temperature, tool wear, and chip reduction coefficient. Furthermore, the virgin coconut produced better performance compared to emulsified coconut oil. Hence, it is concluded that virgin vegetable oils perform better as cutting fluid compared to emulsified vegetable oil.

We demonstrate the possibility of using a CMOS 2D sensor for time-resolved pump–probe XUV FEL experiments. We gained a factor of 30 in acquisition time compared to the use of a commercial CCD-BSI., The latest Complementary Metal Oxide Semiconductor (CMOS) 2D sensors now rival the performance of state-of-the-art photon detectors for optical application, combining a high-frame-rate speed with a wide dynamic range. While the advent of high-repetition-rate hard X-ray free-electron lasers (FELs) has boosted the development of com­plex large-area fast CCD detectors in the extreme ultraviolet (EUV) and soft X-ray domains, scientists lacked such high-performance 2D detectors, principally due to the very poor efficiency limited by the sensor processing. Recently, a new generation of large back-side-illuminated scientific CMOS sensors (CMOS-BSI) has been developed and commercialized. One of these cost-efficient and com­petitive sensors, the GSENSE400BSI, has been implemented and characterized, and the proof of concept has been carried out at a synchrotron or laser-based X-ray source. In this article, we explore the feasibility of single-shot ultra-fast ex­peri­ments at FEL sources operating in the EUV/soft X-ray regime with an AXIS-SXR camera equipped with the GSENSE400BSI-TVISB sensor. We illustrate the detector capabilities by performing a soft X-ray magnetic scattering experiment at the DiProi end-station of the FERMI FEL. These measurements show the possibility of integrating this camera for collecting single-shot images at the 50 Hz operation mode of FERMI with a cropped image size of 700 × 700 pixels. The efficiency of the sensor at a working photon energy of 58 eV and the linearity over the large FEL intensity have been verified. Moreover, on-the-fly time-resolved single-shot X-ray resonant magnetic scattering imaging from prototype Co/Pt multilayer films has been carried out with a time collection gain of 30 com­pared to the classical start-and-stop acquisition method performed with the conventional CCD-BSI detector available at the end-station.

Developing new energy sources is of critical significance to satisfy the growing energy demand and also reduce the emissions of carbon dioxide (CO2) gas. The conversion of CO2 into value-added prod...

The authors would like to thank the financial support from Stora Enso and Aalto University. D.S. gratefully acknowledges funding from the Academy of Finland’s Flagship Programme under the projects no. 318890 and 318891 (Competence Center for Materials Bioeconomy, FinnCERES). Prehydrolysis kraft (PHK) pulps account for more than half of the global market of dissolving pulp. Characterized by high reactivity toward dissolution, their performances can still be improved by activation treatments. This study compares the dissolution kinetics in cupriethylenediamine of a hardwood and a softwood PHK pulps before and after their activation by high-solid-content mechano-enzymatic treatments. Three enzyme combinations were tested: endoglucanase (E), xylanase and mannanase (XM), and endoglucanase, xylanase, and mannanase (EXM). Xylanase and mannanase reduced the hemicellulose content of only hardwood (by max. 2.4%). Mixing and carbohydrate depolymerization decreased the dissolution time of hardwood and softwood pulps by a maximum of 63 and 30% with E, 37 and 16% with XM, and 44 and 30% with EXM, respectively. The shortening of the dissolution time was partially hindered by hornification, which increased with hemicellulose degradation. Interestingly, XM accelerated the dissolution while preserving a high weight-average molecular mass.

The motor gasoline production mixing flows ratios determination considering feedstock quality and quantity is the one of the most complex and multifactorial problems of catalyst crude oil processing. Mixing compounds ratios determination taking into account hydrocarbon feedstock properties and composition changes, as well as optimal catalyst process conditions will reduce the end products cost by reducing quality giveaway. The catalyst process isomerization C7-C8 implementation allows to increase low-octane fractions supply in commercial gasoline compounding by 7–10 % of the produced amount. At the same time, increasing the octane number of these fractions causes reducing the consumption of MTBE by 9 %, toluene by over 3% and alkylbenzene by 15 %. These changes can significantly reduce the cost of commercial gasoline while maintaining the quality.

Three-dimensional (3D) extrusion-based bioprinting is widely used in tissue engineering and regenerative medicine to create cell-incorporated constructs or scaffolds based on the extrusion technique. One critical issue in 3D extrusion-based bioprinting is printability or the capability to form and maintain reproducible 3D scaffolds from bioink (a mixture of biomaterials and cells). Research shows that printability can be affected by many factors or parameters, including those associated with the bioink, printing process, and scaffold design, but these are far from certain. This review highlights recent developments in the printability assessment of extrusion-based bioprinting with a focus on the definition of printability, printability measurements and characterization, and printability-affecting factors. Key issues and challenges related to printability are also identified and discussed, along with approaches or strategies for improving printability in extrusion-based bioprinting., Graphical abstract Image 1, Highlights • Focusing on one of the critical challenges in 3D bioprinting called “printability”. • Investigating factors, including those associated with bioink, printing process, and scaffold design affecting printability. • Highlights the recent development in the discovery of printability for the extrusion bioprinting. • Providing a systematic review on “how printability is measured and characterized”. • Identifying key challenges in the printability discovery.