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A highly sensitive electrochemical sensor was developed through a one-pot green synthesis method for nitrite detection based on the electrochemical technique. Xylan-based carbon quantum dots (CQDs) were used as green in situ reducing agent to prepare CQDs capped gold nanoparticles (Au@CQDs). MXene of good electrical conductivity was used as the immobilized matrix to fabricate Au@CQDs-MXene nanocomposites with the advantages of good electrical conductivity and electrocatalysis. An electrochemical sensor for nitrite monitor was obtained by loading the Au@CQDs-MXene on a glassy carbon electrode. The sensor presents high sensitivity, good stability, wide linear range, and excellent selectivity due to the high catalytic activity of AuNPs and CQDs, the large specific surface area of MXene, and exceptional electrical conductivity of AuNPs and MXene. Under the optimal condition, the linear detection range of the sensor was from 1 μM to 3200 μM with a detection limit of 0.078 μM (S/N = 3), which was superior to most reported sensors using differential pulse voltammetry (DPV) method. Furthermore, this sensor was successfully applied to detect nitrite in tap water and salted vegetables with satisfactory recoveries. This modified electrocatalytic sensor shows a new pathway to fabricate nitrite detection sensor with feasibility for practical application., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

Hypothesis: The synthesis and characterization of aminated nanocrystalline cellulose (ANCC), a new member of the hairy nanocellulose family, is reported. Hairy nanocelluloses consist of a crystalline rod-like body with amorphous cellulose chains ("hairs") at both ends, on which various functional groups can be accommodated. In ANCC these groups are reactive primary amine groups, which are useful for bioconjugation- and Schiff base-centered modifications. We hypothesize that a two-step oxidation-reductive amination of cellulose fibers followed by hydrothermal treatment will result in the formation of rod-like hairy ANCC., Experiments: ANCC was prepared by converting the aldehyde groups in cellulose, introduced by a periodate oxidation, to primary amines using ammonia and sodium borohydride, followed by a hot water treatment, during which diamine modified cellulose fibers were converted to ANCC. ANCC was characterized by AFM, TEM, DLS, ELS, FTIR, NMR, XPS and conductometric titration. Antibacterial activity of ANCC was assessed by the viable cell counting method., Findings: ANCC, with an amine content of 5.5 mmol g -1 is a bare nanocolloid (i.e. non-coated, without adsorbed polyelectrolytes or surfactants) which, as far as we know, has a positive charge density larger than any other bare cationic nanocolloid. It was observed that ANCC particles have a needle-like morphology with a width of ~ 5 nm and a length ~ 120 nm. DLS results proof that ANCC is hairy. Spectroscopic analysis confirmed the introduction of surface primary amine groups. ANCC showed promising bactericidal activities, against Gram-negative species due to their thinner and penetrable cell wall., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

In this work, a sulfonic acid-functionalized magnetic separable solid acid (Fe 3 O 4 @SiO 2 -SO 3 H) was synthesized, characterized, and tested for fructose conversion to 5-hydroxymethylfurfural (HMF). Results indicated that the prepared catalyst had a good efficacy for fructose dehydration to HMF due to its larger specific surface area, appropriate acid amount and homogeneous acid distribution. The maximum HMF yield of this work was 96.1 mol%. It was obtained at 120 °C for 1.5 h with 100 mol% fructose conversion. More importantly, the produced HMF could be further in-situ oxidized into 2,5-diformylfuran (DFF) after the replacing of the Fe 3 O 4 @SiO 2 -SO 3 H with a ZnFeRuO 4 catalyst, and the highest DFF yield of 90.2 mol% (based on initial fructose) was obtained after reaction another 8.5 h. The production of DFF from fructose through the above two consecutive steps avoids the intermediate HMF separation, which saves time and energy. In addition, both Fe 3 O 4 @SiO 2 -SO 3 H and ZnFeRuO 4 catalysts exhibited satisfied stability in the recycling experiments, which can be reused at least for five times with the HMF and DFF yield loss<5.3% and 3.3%, respectively. Finally, the plausible reaction mechanisms for fructose conversion to HMF or DFF over Fe 3 O 4 @SiO 2 -SO 3 H or/and ZnFeRuO 4 catalysts were also proposed in this work., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

It is expected that low-energy and scientific zero discharge of chemical-mechanical pulping wastewater will be achieved by applying the mechanical vapor recompression (MVR) technology. In this paper, the equal-standard pollution load model was introduced into pulp and paper field to parse the pollution sources for the first time. The results from the source apportionment indicated that the screw press and concentrating were the major pollution unit operations, and their cumulative load ratio reached 92.92%. The further survey demonstrated that the dominating pollution factors in the traditional chemical-mechanical pulping process were Chemical Oxygen Demand (COD), Biochemical Oxygen Demand (BOD 5 ), and Suspended Solids (SS), whose cumulative load ratio was 92.69%. The environmental analysis demonstrated the implementation of MVR technology significantly decreased the pollution load and reduce the pressure of subsequent wastewater treatment. In addition, a further economic performance indicated that the utilization of MVR technology possessed a smaller operating cost of 2.899 $/m 3 . The result of the given model provides a scientific gist and instruction for the future treatment of water pollutants in the chemical-mechanical pulping process. The MVR technology is conducive for wastewater treatment to minimize environmental effects and costs., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Lignin has been demonstrated to be green and effective for the modification of ZnO-based materials. In this work, quaternized lignin/zinc oxide nanostructured hybrid composites (QLS/ZnO NCs) were synthesized with good dispersion and uniform particle size via a facile hydrothermal method. Sodium lignosulfonate (LS) was modified by quaternization to endow the positive charges, which effectively captured bacteria due to the electrostatic interactions. Interestingly, QLS/ZnO NCs show a litchi-like morphology consisting of nanorods with diameters of 5-10 nm, which further resulted in damage to the bacterial cell membrane. Owing to the surface charge and rough surface topology for bacterial capture, QLS/ZnO NCs exhibited greatly enhanced antibacterial activity compared with bare ZnO. After being treated with QLS/ZnO NCs for 90 min, the sterilization rates of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) reached 97.54% and 99.55%, respectively. Due to the reactive oxygen species (ROS) produced by ZnO under light irradiation, the antibacterial activity of QLS/ZnO NCs could be further enhanced. In addition, the minimal inhibition concentrations (MICs) of QLS/ZnO NCs towards E. coli and S. aureus were both 100 μg/mL, and the minimum bactericidal concentrations (MBCs) were 100 μg/mL and 200 μg/mL, respectively. Moreover, with the incorporation of QLS/ZnO NCs into polyurethane films, the composite films showed excellent antibacterial activity, strong tensile strength and enhanced ultraviolet light blocking performance., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

With the increased awareness of reusing solid wastes for higher sustainability and the concern of water pollution associated with phosphorus over-emission, there are strong interests in developing solid waste based adsorbents for purifying phosphorus-containing wastewater. As a rich calcium resource, paper mill sludge (i.e., a major solid waste from pulping industry) can be used as phosphorus removal adsorbent after calcination. Thus, in this work, a simple and clean thermally treating route has been proposed for preparing calcium-containing biochar from paper mill sludge. The effect of the physicochemical properties of paper mill sludge and its carbonization condition on phosphorus adsorption has been analyzed. Moreover, the influence of some key adsorption parameters, e.g., biochar dosage, initial pH of solution, co-existing anions, initial phosphorus concentration and contact time has also been investigated. The results showed that the phosphorus adsorption data could be fitted well with pseudo-second-order kinetic and Langmuir isothermal models. The calculated maximum adsorption capacity of the as-prepared optimal calcium-containing biochar could reach to 68.49 mg·g -1 at 25 °C. Combined with the characterization results, it can be reasonably inferred that the adsorption process was chemisorption-dominated. Lastly, the application of this spent adsorbent in agriculture field has also been discussed. In brief, this work provided a feasible strategy for converting paper mill solid waste to an environmental functional material (i.e., calcium-rich biochar) for remediation of eutrophic water., Competing Interests: Declaration of Competing Interest The authors declared that there is no conflict of interest., (Copyright © 2021 Elsevier Inc. All rights reserved.)

Green synthesis of silver nanoparticles (AgNPs) has received increasing attention. In this study, AgNPs were prepared through in-situ reduction by aminated alkaline lignin (AAL). Compared with alkaline lignin (AL), AAL exhibited stronger reduction capacity (increased by 36%) due to the introduced amine groups and better water solubility. Moreover, the coordination effect of amine groups on AAL improved the binding force between lignin and AgNPs. The content of AgNPs in AgNPs/AAL composite were 2.4 times higher than that in AgNPs/AL, such content could be further increased through increasing the reduction pH or prolonging the heating time. The results of XPS, XRD and TEM showed that the AgNPs were spherical and monodisperse with an average particle size about 17 nm. Additionally, the size of AgNPs was affected by the amination degree of lignin. AgNPs/AAL exhibited good catalytic performance for the reduction of 4-nitrophenol to 4-aminophenol, and this compound could be easily recovered and reused for at least eight cycles., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Nicotine contamination in tobacco waste effluent (TWE) from tobacco industry is a serious threat to public health and environment. Microbial degradation is an impending approach to remove nicotine and transform it into some other high value chemicals. Pseudomonas sp. JY-Q exhibits high efficiency of degradation, which can degrade 5 g/L of nicotine within 24 h. In strain JY-Q, we found the co-occurrence of two homologous key enzymes NicA2 and Nox, which catalyze nicotine to N-methylmyosmine, and then to pseudooxylnicotine via simultaneous hydrolysis. In this study, recombinant NicA2 and Nox were expressed in E. coli BL21(DE3) and purified. In vitro, the activity of recombinant NicA2 and Nox was accelerated by adding co-factor NAD + , suggesting that they worked as dehydrogenases. The optimal reaction conditions, substrate affinity, catabolism efficiency, pH-stability and thermal-stability were determined. Nox showed lower efficiency, but at a higher stability level than NicA2. Nox exhibited wider pH range and higher temperature as optimal conditions for the enzymatic reaction. In addition, The Nox showed higher thermo-stability and acid-stability than that of NicA2. The study on enzymatic reaction kinetics showed that Nox had a lower Km and higher substrate affinity than NicA2. These results suggest that Nox plays more significant role than NicA2 in nicotine degradation in TWE, which usually is processed at low pH (4-5) and high temperature (above 40 °C). Genetic engineering is required to enhance the affinity and suitability of NicA2 for an increased additive effect on homologous NicA2 and Nox in strain JY-Q., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Lignin has been considered as a green carrier with excellent biocompatibility for the biomedical applications in drug release, tissue engineering, etc. In this study, silver nanoparticles (AgNPs) incorporated quaternized lignin (QAL) composites (Ag@QAL) were synthesized in-situ with the assistance of the microwave radiation. The positive charged QAL, not only serves as reductive and stabilizing carriers, but also endows with electrostatic effect toward negatively charged Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), resulting in greatly enhanced antibacterial activity. It is worth mentioning that Ag@QAL exhibits the highest antibacterial activity, which causes 3.72 log 10 (>99.9%) and 5.29 log 10 (>99.999%) CFU/ml reduction against E. coli and S. aureus respectively after contacting for only 5 min. Furthermore, due to the strong interaction between Ag@QAL and Ag + /AgNPs, bacteria can be captured and co-precipitated by Ag@QAL fastly in 30 min with almost none silver ions detected in the supernatant, which prevents Ag + leaking with extremely low toxicity to the biological environment. This concept of electrostatic capture effect induced antibacterial activity enhancement and environmentally benign features may provide new insights into the design of highly effective antibacterial agents in a sustainable manner., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Inc. All rights reserved.)

A softer natural Pickering nanostabilizer, S-ovalbumin (S-OVA) was reported in this work, based on our previous researches about soft globular protein nanoparticles. Compared with native OVA, S-OVA has higher surface hydrophobicity, greater conformational flexibility and thinner tightly-bond water layer, which make it be unfolded more highly at the oil-water interface. However, S-OVA also possesses higher zeta-potential and thicker closely-surrounding water layer, offering it stronger electrostatic repulsion and steric hindrance between molecules and increased intramolecular cohesion. The improvements guarantee S-OVA undisintegrated particle structure and independent state on the interface and high refolding off the interface. The more flexible interior and firmer exterior together endow a higher softness to S-OVA. The HIPPE gels solely stabilized by S-OVA were fabricated using one-step shearing. These HIPPE gels own steady network structure mainly supported by bridging flocculation, strong self-supporting ability and moldability. The high storage stability and ability to inhibiting lipid oxidization provide the HIPPE gels an enormous potential in encapsulating and protecting volatile, easily-oxidized or dangerous organic liquids, during the storage and transportation. The attractive temperature responsiveness offers a high convenience to re-obtaining the organic liquids. And a re-encapsulation can be easily achieved via a re-shearing. The heat-enhanced gel intensity and moldability mean the HIPPE gels can be applied to produce dualistic gels or porous scaffolds with latent applications. These findings are helpful to explore more new Pickering stabilizers from the nature and extend the applications of HIPPEs in highly-demanded and high-tech industries., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Graphitic carbon nitride (CN) is considered as a promising photocatalyst for solar energy conversion. However, low specific surface area and fast electrons and holes recombination restrict the photocatalytic applications of CN material. Herein, a nitrogen defect-rich and highly porous CN nanostructure (CN-LT) was prepared by combining two strategies, i.e., LiOH treatment and heat etching. The as-prepared nitrogen defect-rich porous CN-LT not only has a larger specific surface area, as compared with pristine CN, but also the photogenerated electron-hole separation was boosted remarkably. Using Pt as a co-catalyst and lactic acid aqueous solutions as sacrificial reagent under visible light irradiation (λ > 400 nm), the hydrogen evolution reaction (HER) rate for CN-LT (1.54 mmol h -1 g -1 ) was 19.25 times higher than that for pristine CN (0.08 mmol h -1 g -1 ). While subjecting pristine CN to heat etching under the same experimental conditions, excepting the use of LiOH (CN-T), an increase in HER rate of 7.5 times was obtained. Our current study may shed more light on the enhancement of the photocatalytic activity of bulk CN materials by altering their microstructure., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Generally, the mechanical strength and stiffness of old corrugated cardboard (OCC) waste paper are decreased after multiple recycling procedures. Surface sizing starch, which is extensively used in the surface sizing of paper making, accumulates after dissolving from the fibers and is transformed into pollutant during the OCC re-pulping process. To overcome the pollution and reutilization problem of the waste starch during the recycling process of OCC paper, waste starch was ionized using hydrogen peroxide (H 2 O 2 ) to improve the mechanical properties of OCC paper during the reutilization. The results showed that the carboxyl group of waste starch increased with an increasing degree of ionization, resulting in enhanced copper ion adsorption capacity. Furthermore, the retention rate of the modified starch in the wet-end increased from 18.0% to 48.2%. The OCC paper presented the highest burst index and tensile strength of 8.94 kPa m 2 /g and 112.5 N m/g, respectively, when MS-2 was added. This work has great significance for implementation of the cleaning production of OCC waste papers and the reutilization of the waste starch., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Lignocellulosic hydrogels are valuable bio-products that have been considered widely in recent investigations. Also, application of low value recycled fibers for high value added products can be of much interest. In this respect, current research has focused on producing hydrogel from recycled old corrugated container (OCC) resources, using 1-butyl-3-methyl-imidazolium chloride ionic liquid (IL) as a green solvent. The results indicated that the IL successfully dissolved OCC fibers, allowing the production of lignocellulosic hydrogel. Considering total water absorption amount as a main criterion for evaluation of hydrogels, the fabricated hydrogel showed promising results (up to 4700% water absorption). X-ray diffraction analysis confirmed obvious reduction in cellulose material crystallinity and crystallite size as a result of the process. Field emission scanning electron microscopy also demonstrated the microstructure of the hydrogel, pore size and shape in the hydrogel, which well supported the laboratory research results. Furthermore, the effect of processing parameters showed that specimens washed with distilled water as the anti-solvent resulted in the highest water absorption. Infrared spectroscopy can be used to suggest the presence of more lignin content in the hydrogel washed with ethanol. Moreover, the best water re-absorption results were observed for the hydrogel washed with distilled water., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Objective: A cellulose-derived nano-toolbox has been developed via the chemical nano-trimming of electrosterically stabilized nanocrystalline celluloses (ENCCs). ENCC is a member of the class of hairy nanocellulose (HNC). The objective of this study is to determine the properties of chemically trimmed HNCs in order to establish whether or not they overcome the surface chemistry and size restrictions of conventional nanocelluloses. The newly "so-called crew-cut ENCCs" emerged by this approach address many technological and environmental challenges in colloidal systems, i.e., drug delivery, anti-scaling and self-assembly. Despite the importance of the crew-cut species, little is known about the systematic changes and the underlying mechanisms of the trimming of their hairs (the chains protruding from both ends of the cylindrical core)., Experiments: To quantify the effect of the hair trimming on the charge density as well as the kinetics of this process, the carboxylic acid content is determined by conductometric titration as a function of time and reaction conditions. We use electro-acoustic spectroscopy to elucidate the differences in colloidal properties of various crew-cut ENCCs. We focus on the interplay between the time of the acid-catalyzed hydrolysis reaction and tunable parameters, such as size and surface electric charge of ENCC, as well as their microrheological behavior., Findings: We show that a range of hairy ENCCs with various sizes and charge densities is easily obtained by taking advantages of the preferential hydrolysis of the amorphous chains protruding from both ends of the nanocrystals. The trimming mediated by a HCl-catalyzed hydrolysis is initially very fast, but slows down subsequently. The formation of crew-cut species with a smaller particle size and zeta potential was electro-acoustically verified by increasing the reaction time. The longitudinal viscosities of the trimmed ENCC suspensions also decreased with prolonging the reaction time. This research shows how manipulating HNCs enables both scientists and technologists to access a collection of nanocrystals with desired colloidal properties, based on the most abundant biopolymer in the world., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2019 Elsevier Inc. All rights reserved.)

Papermaking is a capital-intensive industry that requires a high consumption of plant fibers, energy, and water. Previous sustainability assessments of papermaking industry primarily focused on separate evaluations for multiple criteria without the integration for criteria and could not compare the overall priority of the production alternatives. The life cycle sustainability for the most representative boxboard production is analyzed as a case study in this work. Life cycle water consumption, energy consumption, greenhouse gas emissions, and internal costs are selected as the assessment criteria. The two multi-criteria decision-making methods are applied to integrate the above criteria to obtain the sustainability sequence under different production pathways. When the papermaking enterprises are regarded as decision-makers, the alternative using waste paper as raw material to manufacture boxboard is the most sustainable, following by mixed fiber. The sustainability sequence of the alternatives using wood and straw as raw materials is controversial due to the different calculation models. Changing the proportion of raw materials and the criteria weights might adjust sustainability sequence of the alternatives., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Psilocybin, the prodrug of the psychoactive molecule psilocin, has demonstrated promising results in clinical trials for the treatment of addiction, depression, and post-traumatic stress disorder. The development of a psilocybin production platform in a highly engineerable microbe could lead to rapid advances towards the bioproduction of psilocybin for use in ongoing clinical trials. Here, we present the development of a modular biosynthetic production platform in the model microbe, Escherichia coli. Efforts to optimize and improve pathway performance using multiple genetic optimization techniques were evaluated, resulting in a 32-fold improvement in psilocybin titer. Further enhancements to this genetically superior strain were achieved through fermentation optimization, ultimately resulting in a fed-batch fermentation study, with a production titer of 1.16 g/L of psilocybin. This is the highest psilocybin titer achieved to date from a recombinant organism and a significant step towards demonstrating the feasibility of industrial production of biologically-derived psilocybin., (Copyright © 2019 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.)

Flexible and conductive polypyrrole (PPy) paper shows the potential use in electromagnetic shielding, antistatic packaging, and electrochemical materials due to its low cost and facile manufacturing procedure. However, the poor mechanical strength and relatively low electrical stability of PPy paper is still challenging. In this study, we use horseradish peroxidase polymerized sulfonated alkaline lignin (HSAL) as a dispersant and dopant for PPy and demonstrate mechanically strong and electrically stable PPy paper by a combination of multiple impregnations and in-situ polymerization. The abundant sulfonic, carboxyl, and phenolic hydroxyl groups of HSAL could significantly improve the interfacial interaction between cellulose fibers and PPy. Meanwhile, its high molecular weight facilitated the uniform distribution of pyrrole along the fiber axial direction during in-situ polymerization. As a result, the resulting PPy paper exhibits enhanced mechanical properties and electrical stability, as well as high conductivity (24.84 S cm -1 ). More significantly, we investigated the influences of the dosage of HSAL and the cycles of multilayer impregnations on the electrical and mechanical properties of PPy paper. This work sheds light on the design and fabrication of flexible and conductive PPy paper with superior mechanical robustness and stable electrical performance., (Copyright © 2019 Elsevier Inc. All rights reserved.)

A practical and sustainable method to prepare polymeric hollow microcapsules (PHMs) using cellulose nanocrystal (CNC) stabilized Pickering emulsion polymerization was developed. Pristine CNCs hydrolyzed from wood pulp are hydrophilic and could be employed as emulsifiers to prepare oil-in-water (O/W) Pickering emulsions. The O/W Pickering emulsions were used as templates for the Pickering emulsion polymerization of hydrophobic monomers inside the emulsion droplets. The crosslinked hydrophobic polymers phase separated and partitioned to the interface of the Pickering emulsion, leading to the formation of hydrophobic PHMs. Correspondingly, cinnamate modified CNCs with less surface hydrophilicity were employed as emulsifiers to obtain water-in-oil (W/O) inverse Pickering emulsions, which were then used as templates for inverse Pickering emulsion polymerization of hydrophilic monomers to prepare hydrophilic PHMs. Therefore, both hydrophobic and hydrophilic PHMs could be obtained via this approach. Herein, polystyrene, poly(4-vinylpyridine), and poly(N-isopropyl acrylamide) hollow microcapsules were prepared as models, where the size, crosslinking density, shell structure and stimuli-responsive properties of PHMs could be tuned by varying the synthesis parameters., (Copyright © 2019 Elsevier Inc. All rights reserved.)

Oil-in-oil emulsions are ideal systems for water-sensitive reactions such as polymerizations and catalytic reactions, which has received extensive attention in recent years. The application of oil-in-oil emulsions has been developed slowly due to the limited types of surfactants and complicated synthesis process. Herein, we proposed a simple method to prepare poly(amide-thioether)-based surfactant for oil-in-oil emulsions via taking advantage of single-pot multicomponent and click characters of thiolactone chemistry. Using a combination of alkyl amine and acrylamide thiolactone, the aminolysis of thiolctone occurred first, generating thiol group in-situ, and then the generated thiol group would sequentially react with the double bonds of acrylamide to form polythioether in the presence of amine. The hydrophobicity of the surfactant could be effectively adjusted by the chain length of the alkyl amine and thus this polymer could serve as a promising surfactant for oil-in-oil emulsion. Notably, the emulsion types could be switched by changing the chain length of the alkyl amine. In addition, the effects of surfactant loading, volume ratio of oil phases, oil types on the size and stability of oil-in-oil emulsions were further investigated. It was demonstrated that the oil-in-oil emulsion stabilized by poly(amide-thioether)s kept stable after more than five months. Besides, we preliminarily explored the application of the oil-in-oil emulsion to prepare closed cell foam and porous particles via photo-initiated thiol-ene polymerization. It is believed that this super-stable oil-in-oil emulsion could offer more possibilities for highly potential water-sensitive systems., (Copyright © 2019 Elsevier Inc. All rights reserved.)

Hypothesis: The present paper investigates, for the first time, the potential of cationic hairy cellulose nanocrystals (CNCC) to induce the flocculation of a model suspension of kaolinite. CNCC belong to a brand new family of nanocelluloses characterized for presenting a crystalline rod-like body and functionalized amorphous chains at both ends. Given that these chains can be easily tuned, these nanocelluloses present a high potential as fit-to-purpose flocculants., Experiments: CNCC were produced through periodate oxidation, cationization and thermal treatment of cellulose. Flocculation was monitored by both photometric dispersion analysis and laser reflectance. Flocs were characterized by the determination of zeta potential, supernatant turbidity removal and optical microscopy. A recently developed machine learning random forest regression model was used to estimate fractal dimension (D f ) from chord length distribution data., Findings: Although a high efficiency was achieved for CNCC dosages between 7.5 and 75 mg/g, the maximum floc size and the fastest flocculation were found near the isoelectric point (10-30 mg/g). Thus, CNCC acted through charge neutralization mechanism. The model used to estimate flocs D f was found very successful to describe the flocculation process. The clay/CNCC flocs D f values suggest a relation between floc conformation and CNCC dosage, presenting an opener structure when closer to the isoelectric point., (Copyright © 2019 Elsevier Inc. All rights reserved.)

The pulp and paper industry is highly dependent on forest and water resources. It has more concerns on fair utilization of these resources and their conservation for its further expansion. Present study emphasizes on the use of rice straw (agro waste) in papermaking to protect wood based resources. It further deals with ozone bleaching (Z) prior to elemental chlorine free bleaching that proved to be significant in terms of reducing the effluent load specially the reduction in toxic, recalcitrant and carcinogenic compounds. Z based sequences resulted in pulp brightness of ∼85% that was 3.6% higher than the elemental chlorine free bleaching. Bleached pulps of Z based sequences were found to be having better strength properties than elemental chlorine based sequence and thus may be adopted as improved bleaching technology. The analysis of handsheets prepared after pulp bleaching was performed using X-Ray diffraction, ATR-FTIR and SEM. Incorporating ozone stage resulted in marked reduction of 58% and 63% in total solids in bleaching wastewater. Reduction of more than 80% in BOD, COD and adsorbable organic halides was achieved in Z based bleaching in comparison to chlorine bleaching. The amount of chlorophenols, guaiacols, catechols, vanillins and syringols became negligible (approx. 90% reduction) in effluents of Z based bleaching sequences. The chlorine dioxide followed by peroxide bleaching after Z stage was found to be the most promising to reduce the effluent load., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Hypothesis: Dendrimer-directed assembly of electrosterically stabilized nanocrystalline cellulose (ENCC) to form network structures was studied. ENCC is a member of the family of hairy nanocelluloses and consists of a crystalline rod and dicarboxylated cellulose chains ("hairs") protruding from both ends, which are very reactive. We hypothesized that covalent linking of ENCC and dendrimers should lead to self-assembled hybrid network structures in which dendrimeric nodes connect cellulose nanorods., Experiments: Polyamidoamine (PAMAM) dendrimers were covalently linked to ENCC by a bioconjugation reaction with different ratios of ENCC to PAMAM. To control the self-assembly process and prevent aggregation, acid hydrolysis of ENCC was performed to obtain crew-cut ENCC with shorter hairs and less negative charge. The formation of self-assembled structures from different PAMAM concentrations were analyzed using atomic force microscopy., Findings: It was observed that depending on the concentration of PAMAM, various linear, star-shaped, and closed-loop structures were formed. Also, networks were formed with dendrimers acting as the nodes, connecting long cellulose rods, thus producing a network with a characteristic length of around 100-200 nm, which is difficult to obtain otherwise. We have demonstrated that the reactions of dendrimers with ENCC are solely occurring at the hairs and not at the crystalline regions., (Copyright © 2019 Elsevier Inc. All rights reserved.)

High strength hydrogels open new possibilities in the fields of bioengineering and biomedical. In this paper, a highly efficient one-pot strategy was developed to prepare carboxymethyl xylan-g-poly (acrylic acid) (CMX-g-PAA) hydrogels with high compression strength, high elongation and high elasticity by using the metal coordination and the reinforcement of hydroxylate multi-walled carbon nanotubes (HCNTs). Prepared hydrogels were characterized by means of FTIR, XRD, SEM, rheological measurements as well as their swelling and mechanical properties. Results showed that the Fe 3+ -carboxyl coordination and HCNTs imparted hydrogels with high strength and good rapid recovery properties, in which the maximum high compressive strength and elongation at break were achieved to 10.4 MPa and 1032%, and the shape of hydrogels almost returned to the original shape after the external force was removed after 30 cycles of compression. These hydrogels also exhibited Fe 3+ -triggered shape memory properties. Therefore, as-prepared hydrogels possessing high strength, rapid recovery and shape memory properties, could broaden access for application in intelligent toys, electronic skin, biosensing, and tissue engineering., (Copyright © 2018 Elsevier Inc. All rights reserved.)

Graphitic carbon nitride with nitrogen defects (g-C 3 N 4-x ) is prepared by a facile and effective solid-state chemical reduction technique at mild temperature conditions. The cyano groups and nitrogen vacancies, as evidenced by electron paramagnetic resonance (EPR), X-ray photoelectron spectrometer (XPS), Fourier transform infrared spectra (FTIR) and Solid-state 13 C MAS NMR spectra, are controllable via adjusting chemical reduction temperature. Comparing to the pristine g-C 3 N 4 , the as-prepared g-C 3 N 4-x shows much enhanced photocatalytic H 2 evolution activity under visible-light irradiation. The maximum H 2 evolution rate of 3068 μmol·g -1 ·h -1 is achieved with g-C 3 N 4-x after chemical reduction treatment at 400 °C for 1 h, which is 4.85 times that of the pristine g-C 3 N 4. Moreover, excellent reusability and storage stability have been shown by this photocatalyst as well. It is discovered that nitrogen defects can result in both the up-shift of the valance band and the down-shift of the conduction band, which benefit the absorption of longer wavelength photons and trapping of the photoinduced electrons, therefore reducing the recombination losses of the generated carriers. It is because of this improved visible-light absorption and charge carrier separation, g-C 3 N 4-x displays better visible-light photocatalytic activity compared to the pristine g-C 3 N 4 . It is then concluded that the synthetic strategy presented here represents a straightforward and efficient way to synergistically optimize the chemical composition, optical response, and photocatalytic characteristics of g-C 3 N 4 -based photocatalysts., (Copyright © 2018 Elsevier Inc. All rights reserved.)

The importance of water pollutants on human health has been the subject of intense study and constitutes perhaps the most significant grand challenge for the future of human society. Water remediation faces many challenges in effectively combating pollution, especially for low income populations where poor water sanitation and little to no access to technically competent and cost effective remediation are nearly insurmountable issues. In an effort to provide low-cost adsorbents, research over the last few years has focused on biological residual materials from plants and animal biomass to not only to add value, but to remediate water at a lower cost with the same or improved efficiency as commercially available option. Crustacean shells are among a class of biological residues that are commonly treated as a waste product of the sea food industry. However, potential valorization by remediation of heavy metal ions, organic matter, and anionic species is a topic of high interest in the current eco-friendly environment. The aim of this review is to provide insight on the state of the art of crustacean shells for addressing water remediation and to offer some perspective regarding challenges and the future of this type of biomass., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

This study was done with the aim of lignosulfonate and ethanol production from different spent liquors of bagasse pulping process. For this purpose, alkali lignin from bagasse alkali liquor was separated and was sulfomethylated to produce soda lignosulfonate (SLig). Furthermore, raw bagasse was directly treated with sodium sulfite in acidic and neutral conditions to produce BLig and NLig bagasse lignosulfonate, respectively. In addition, the pentoses and hexoses impurities in lignosulfonates were fermented to ethanol using Candida guilliermondii. Results showed that the molecular weight of NLig lignosulfonate was considerably high comparing to the SLig and BLig lignosulfonates. A high level of thermal resistance was found in case of SLig regarding to the other samples at 500 °C. Fermentation of the spent liquors with Candida guilliermondii led to a maximum ethanol yield of 7.0, 1.0 and 5.1 g L -1 in NLig, SLig and BLig, respectively., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Hypothesis: Amphiphilic character of surfactants drives them at the interface of dispersed systems, such as emulsions. Hemicellulose-rich wood extracts contain assemblies (lignin-carbohydrate complexes, LCC) with natural amphiphilicity, which is expected to depend on their chemical composition resulting from the isolation method. Lignin-derived phenolic residues associated with hemicelluloses are hypothesized to contribute to emulsions' interfacial properties and stability., Experiments: We investigated the role of phenolic residues in spruce hemicellulose extracts in the stabilization of oil-in-water emulsions by physical and chemical approach. Distribution and changes occurring in the phenolic residues at the droplet interface and in the continuous phase were studied during an accelerated storage test. Meanwhile, the physical stability and lipid oxidation in emulsions were monitored., Findings: Naturally associated lignin residues in GGM act as vehicles for anchoring these hemicelluloses into the oil droplet interface and further enable superior stabilization of emulsions. By adjusting the isolation method of GGM regarding their phenolic profile, their functionalities, especially interfacial behavior, can be altered. Retaining the native interactions of GGM and phenolic residues is suggested for efficient physical stabilization and extended protection against lipid oxidation. The results can be widely applied as guidelines in tailoring natural or synthetic amphiphilic compounds for interfacial stabilization., (Copyright © 2017 Elsevier Inc. All rights reserved.)

Cellulose grafted with soy protein isolate (SPI), sustainable and cost effective material, was investigated as a bioactive material for calcium phosphate mineralization. The formation of hydroxyapatite rod-like nanocrystals with ∼50nmdiameter was confirmed by different characterization tools. Cellulose grafted SPI/hydroxyapatite hybrid was evaluated as recyclable adsorbent for methylene blue (MB) from aqueous solutions using batch adsorption technique. The new sustainable material exhibited adsorption capacity up to 454mg/g. Adsorption data were examined using different kinetics and isotherms to investigate the adsorption mechanism. After four adsorption-desorption cycles, the efficiency of MB removal is ∼95%. These results present new sustainable, cost effective and reusable hybrid material as a promising adsorbent for organic dyes removal from waste water., (Copyright © 2016 Elsevier Inc. All rights reserved.)

Luminescent hydroxyapatite nanoparticles, which have excellent biocompatibility, excellent photostability, and strong fluorescence, have received increasing attention as bioprobes in cell imaging. However, they are also excellent candidates for use in ink-jet security printing. Successful products for related applications usually require highly crystalline, mono-dispersible hydroxyapatite nanorods with good colloidal stability and high fluorescence in aqueous media. These requirements are hard to simultaneously satisfy using most synthetic methods. In this paper, we report a simple and versatile hydrothermal method that incorporates the use of sodium citrate to prepare water-dispersible Eu(3+)-doped hydroxyapatite nanorods. The hydroxyapatite nanorods obtained using this method are highly crystalline rod-shaped particles with an average length of 50-80 nm and an average diameter of 15-30 nm. Dispersions of these hydroxyapatite nanorods, which are transparent with a slightly milky color under natural light and a bright red color when excited with 241 nm UV light, display zeta potentials of -35 mV and hydrodynamic diameters of 120 nm. These dispersions remain colloidally stable for a few months. Dispersions with these properties could be easily applied to security printing for confidential information storage and anti-counterfeiting technologies., (Copyright © 2016 Elsevier Inc. All rights reserved.)

The adsorption of polyalkylene glycols and co-polymers of ethylene oxide and propylene oxide on substrates relevant to textiles with varying surface energies (cellulose, polypropylene, nylon and polyester) was studied by using quartz crystal microgravimetry. Langmuirian-type isotherms were observed for the adsorption profiles of nonionic block polymers of different architectures. The affinity with the surfaces is discussed based on experimental observations, which highlights the role of hydrophobic effects. For a given type of block polymer, micellar and monomeric adsorption is governed by the balance of polymer structure (mainly, chain length of hydrophobic segments) and substrate's surface energy., (Copyright © 2015 Elsevier Inc. All rights reserved.)

Adsorptions are commonly of monolayer coverage of adsorbate molecules on adsorbent sites, in particular for chemisorptions, where Langmuir adsorption isotherm equation and kinetics are adequate. The Langmuir adsorption is termed ideal adsorption as the surface active centers are uniformly distributed, the molecules are of point-sizes and the interactions between adsorbate molecules and the adsorbent are uniform. However, there are more cases where Langmuir adsorption isotherm and/or kinetics are inadequate in describing the adsorption behavior. Apparent multilayer adsorption has been shown to be descriptive of both physisorptions and chemisorptions as a means of idealization to nonideal adsorptions. The deviation of adsorption isotherm and/or kinetics from (ideal) Langmuir adsorption is due to cooperative adsorption, or interactions between adsorbates or between adsorbate and adsorbent caused deviation from "uniform" interactions. The multi-layer or apparent multilayer behavior of adsorption is an excellent model to describe cooperative adsorption. Adsorption kinetics and isotherms have been derived for adsorptions without differentiating the different types of adsorptions. The simplistic approach can explain majority of the adsorption isotherms and kinetic behaviors., (Copyright © 2015 Elsevier Inc. All rights reserved.)

The photocatalytic degradation of sulfanethazine (SMT), one of the sulfonamide antibiotics, in aqueous solution by TiO2 was investigated. The time courses of SMT concentration, the amount of non-purgeable organic carbon, and the concentrations of ions such as SO4(2-), NH4(+), and NO3(-) formed during the photocatalytic reaction were measured and the structures of seven intermediates formed with the disappearance of SMT were also estimated by LC/MS/MS analyses. In addition to that of SMT, the decomposition behaviors of model compounds sulfanilic acid (SA) and 4-amino-2, 6-dimethylpyrimidine (ADMP) were investigated using the TiO2/UV system. The observed photocatalytic degradation behaviors of SMT, SA, and ADMP gave new insight into the degradation pathway of SMT. Especially, the formation of p-aminophenol during SMT decomposition, which until now has not been reported in previous studies concerning the photocatalytic decomposition of SMT and other sulfonamide antibiotics. These results indicate the existence of a novel photocatalytic degradation pathway for sulfonamides. The direct substitution of the sulfonamide group with a hydroxyl group is suggested., (Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Experimentally we explore the potential of using pre-defined motion of a receding contact line to control the deposition of nanoparticles from suspension. Stripe-patterned wettability gradients are employed, which consist of alternating hydrophilic and hydrophobic stripes with increasing macroscopic surface energy. Nanoparticle suspensions containing nanorods and nanospheres are deposited onto these substrates and left to dry. After moving over the pattern and evaporation of the solvent, characteristic nanoparticle deposits are found. The liquid dynamics has a pronounced effect on the spatial distribution. Nanoparticles do not deposit on the hydrophobic regions; there is high preference to deposit on the wetting stripes. Moreover, the fact that distributed nanoparticle islands are formed suggests that the receding of the contact line occurs in a stick-slip like fashion. Furthermore, the formation of liquid bridges covering multiple stripes during motion of the droplet over the patterns is modeled. We discuss their origin and show that the residue after drying, containing both nanoparticles and the stabilizing surfactant, also resembles such dynamics. Finally, zooming into individual islands reveals that highly selective phase separation occurs based on size and shape of the nanoparticles., (Copyright © 2014 Elsevier Inc. All rights reserved.)

Nanoparticles are widely used as drug carriers, texturizing agents, fat replacers, and reinforcing inclusions. Because of a growing interest in non-renewable materials, much research has focused on nanocellulose derivatives, which are biodegradable, biocompatible, and easily synthesized. Among nanocellulose derivatives, nanocrystalline cellulose (NCC) has been known for half a century, but its utility is limited because its colloidal stability is challenged by added salt. On the other hand, electrosterically stabilized nanocrystalline cellulose (ENCC) has recently been observed to have superior colloidal stability. Here, we use electrokinetic-sonic-amplitude (ESA) and acoustic attenuation spectroscopy to assess NCC and ENCC ζ-potentials and sizes over wide ranges of pH and ionic strength. The results attest to a soft, porous layer of dicarboxylic cellulose (DCC) polymers that expands and collapses with ionic strength, electrosterically stabilizing ENCC dispersions at ionic strengths up to at least 200mmol L(-1)., (Copyright © 2014 Elsevier Inc. All rights reserved.)

Surface modification enables fiber lubrication and processing but little is known about the extent and dynamics of adsorption of typical adsorbates applied for such purposes, which often includes water-soluble block nonionic amphiphilic polymers. In this work we used quartz crystal microgravimetry (QCM) to investigate the adsorption on poly(ethylene terephthalate) (PET) of polyalkyl glycol ethers and triblock molecules of ethylene oxide and propylene oxide. The adsorption from aqueous solution of the block nonionic amphiphilic polymers strongly correlated with the self-association driven by the chain length of the respective hydrophobic blocks. This was demonstrated for the different adsorbing polymers using hydrophobic numbers calculated from simple group contribution methods. Hydrophobic and van der Waals interactions explain the affinity of the nonionic polymers with PET, which lead to adsorption isotherms that follow Langmuir-based and one-step empirical adsorption models., (Copyright © 2014 Elsevier Inc. All rights reserved.)

Fe/S doped granular activated carbon (Fe/SGAC) was synthesized with ferric nitrate, Na2S2O3 and (NH4)2S2O8 via an impregnation-precipitation, reduction-oxidation combining with aqueous-phase synthesis method treatment. Surface density of functional groups, surface area changes as well as the chemical state inside Fe/SGAC catalyst were studied by Boehm titration, N2 adsorption and X-ray photoelectron spectroscopy (XPS). The reactivity of the catalysts was tested by degrading Orange G (OG) and diethyl phthalate (DEP). The Fe/SGAC catalysts could significantly enhance the removal rate of OG as compared to persulfate alone and PS/GAC. And the catalytic capacity was also enhanced by S doping. But the degradation of DEP under the similar condition was inhibited by adsorption process because of the different hydrophobicities of OG and DEP molecule. Fe2O3/FeOOH (Fe(3+)) (represents ferrihydrite) together with FeO/Fe3O4 (Fe(2+)) and Fe2O3-satellite, which provide the new active site for persulfate catalyst was found to be the major components of iron element in Fe/SGAC catalyst; the existence of FeS2(S(-)) for sulfur element verified the assumption that the doped S element promoted the electron transfer between the persulfate species and iron oxide at the interface. COD removal experiment further confirmed that mostly contaminant removal was owed to the Fe/SGAC catalytic persulfate oxidation process., (Copyright © 2013 Elsevier Inc. All rights reserved.)

Mechanisms controlling short time water absorption and the effect of temperature on water absorption into paper were investigated by analyzing previously published data. A dynamic contact angle effect caused by contact line friction explained the liquid uptake dynamics at short times. The water absorption rate increase with temperature is suggested to be controlled by the molecular processes occurring in front of the advancing liquid front. The increase in the non-equilibrium vapor pressure at air-liquid interface leads to higher water molecule adsorption onto fibers and associated lowering of the solid-gas interfacial tension, thereby increasing the wetting velocity and water absorption. The classical Lucas-Washburn equation was found to be inadequate for predicting water absorption into paper both at short times and as a function of temperature., (Copyright © 2013 Elsevier Inc. All rights reserved.)

To obtain effective adsorbent that can remove emerging organic pollutant of triclosan (TCS) in aquatic environment, different ester-containing Gemini surfactant-modified MMT (EMMT) were prepared under microwave irradiation. The whole process was rapid, uniform, easy and energy-efficient. The structures and morphology of EMMT were characterized by XRD, TEM, FT-IR, SEM and TGA. The results revealed that the saturated intercalation amount of this surfactant was 0.8 times to cation exchange capacity (CEC) of MMT, and there was electrostatic interaction between ester-containing Gemini surfactant and MMT. In addition, they bound in the ways of intercalation, intercalation-adsorption or adsorption, which relied on the dosage of the surfactant. The surface of EMMT was hydrophobic, rough and fluffy, which contributed to its strong adsorption capacity. The adsorption equilibrium data of EMMT for TCS were fitted to Langmuir and Freundlich isothermal adsorption model. The result showed that Langmuir isothermal adsorption model could describe the adsorption behavior better, the adsorption behavior of TCS on EMMT was confirmed to a surface monolayer adsorption, and notably the theoretical maximum adsorption capacity was up to 133 mg/g. Therefore, this work lays important foundation on developing effective and safe absorbent materials for the treatment of emerging organic pollutants., (Copyright © 2013 Elsevier Inc. All rights reserved.)

Bioactive papers are usually challenged by four major limitations: sensitivity, selectivity, simplicity and strength (4S). Gold nanoparticles (AuNPs) treated paper has previously been demonstrated as a Surface Enhanced Raman Scattering (SERS) active substrate, capable of addressing the 4S issues. In this study, AuNPs on paper substrate were functionalized by a series of biomolecules to develop a generic SERS platform for antibody-antigen detection. The functionalization steps were performed by taking advantage of the high affinity association between Streptomyces avidinii-derived protein, streptavidin, and biotin. Streptavidin was firstly bound onto the AuNPs treated paper using biotinylated-thiol. Subsequently, desired biotinylated-antibody was bound onto the streptavidin. SERS spectra of each functionalization step were obtained to ensure specific adsorption of the bio-molecules. The binding interaction of the antibody with its specific antigen was detected using SERS. Shifts of Raman band associated with α-helix and β-sheet structures indicated structural modification of the antibody upon interaction with its antigen. Predominant tryptophan and tyrosine residue bands were also detected, confirming the presence of antigen. Reproducible spectral features were quantified as AuNP papers were subjected to different concentrations of antigen; the spectra intensity increased as a function of the antigen concentration. The retention of AuNPs on paper remained constant after all the consecutive washing and functionalization steps. The feasibility of AuNPs paper as a low-cost and generic SERS platform for bio-diagnostic applications was demonstrated., (Crown Copyright © 2013. Published by Elsevier Inc. All rights reserved.)

This work reports a simple method to form and visualize individual polyelectrolyte-nanoparticle necklace-like structures on paper, which is applicable to other porous surfaces. In this work, one-dimensional necklaces of negatively charged gold nanoparticles (AuNPs) have been electrostatically assembled along the backbone of a cationic polyacrylamide (CPAM) chain adsorbed on paper. The process involves rapidly passing a dilute CPAM solution through filter paper, adsorbing the polyelectrolyte on the surface, followed by the immediate filtration of an AuNP suspension through the same filter paper. The nanoparticles used were negatively charged, citrate ion capped AuNPs with an average diameter of 20 nm. Scanning electron microscopy images of the dried paper sample showed that the AuNP necklaces were adsorbed in a perpendicular direction to that of the cellulose fibers and along the length of the CPAM molecules which were draped over the fibers. The effects of CPAM polymer concentration, charge density, and molecular weight on such assembly of AuNPs were studied. This technique enables the visualization of polyelectrolyte molecules and the formation of very well organized and reproducible polyelectrolyte-nanoparticle necklaces on a porous, three-dimensional substrate., (Copyright © 2013 Elsevier Inc. All rights reserved.)

This work assesses the effects of white rice husk ash (WRHA) as pozzolanic material, virgin kraft pulp (VKP), old corrugated container (OCC) and fibers derived from fiberboard (FFB) as reinforcing agents on some properties of blended cement composites. In the sample preparation, composites were manufactured using fiber-to-cement ratio of 25:75 by weight and 5% CaCl(2) as accelerator. Type II Portland cement was replaced by WRHA at 0%, 25% and 50% by weight of binder. A water-to-binder ratio of 0.55 was used for all blended cement paste mixes. For parametric study, compressive strength, water absorption and density of the composite samples were evaluated. Results showed that WRHA can be applied as a pozzolanic material to cement and also improved resistance to water absorption. However, increasing the replacement level of WRHA tends to reduce the compressive strength due to the low binding ability. The optimum replacement level of WRHA in mortar was 25% by weight of binder; this replacement percentage resulted in better compressive strengths and water absorption. OCC fiber is shown to be superior to VKF and FFB fibers in increasing the compressive strength, due to its superior strength properties. As expected, the increase of the WRHA content induced the reduction of bulk density of the cement composites. Statistical analysis showed that the interaction of above-mentioned variable parameters was significant on the mechanical and physical properties at 1% confidence level., (Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.)

This study examines and quantifies the effect of cationic polyelectrolyte adsorption on paper on the aggregation and retention of gold nanoparticles (AuNPs) to optimize their Surface Enhanced Raman Scattering (SERS) enhancement factor and sensitivity. Aggregation of metallic nanoparticles is known as a key factor for intense SERS enhancement. Paper substrates were treated with aqueous solutions of cationic polyacrylamide (CPAM) varying in concentration, charge density, and molecular weight to control the AuNPs' aggregate size distribution and surface coverage on paper. The Raman Enhancement Factor of AuNPs-CPAM paper was almost an order of magnitude greater than for the untreated AuNPs paper. The high loading and uniform distribution of AuNPs aggregates on CPAM pre-treated paper contributed toward the excellent SERS reproducibility, sensitivity, and high enhancement factor. This configuration of AuNP on paper was favoured by treating the substrate with CPAM solutions of higher concentrations, higher charge density, and greater molecular weight., (Crown Copyright © 2012. Published by Elsevier Inc. All rights reserved.)

The hydrodynamic diameter (D(h)) of cationic polyacrylamides (c-PAM) in water can either decrease or increase dramatically in the presence of small amounts of beta-cyclodextrin (beta-CD). It is proposed that the CD partially disperses the charge on the polymer thereby promoting associations within or among neighboring polymer strands. Turbidity measurements show that beta-CD enhances the c-PAM induced flocculation of wood pulp fibers, which is in keeping with previous observations on sludge dewatering. The CD-polymer combinations that are the most effective for fiber flocculation are also those for which D(h) of the polymer is reduced the most. In situations where the CD compacts the c-PAM, the fiber network associated with the c-PAM is also compacted giving rise to a tighter floc.

Lignosulfonate is an anionic surfactant from pulp processing industries. Alcohols are often used as cosurfactants in the application of surfactant. The improvement of straight-chain alcohols with different alkyl chain lengths as cosurfactant on the physicochemical properties of calcium lignosulfonate (CL) aqueous solution has been investigated. The results indicate that small amounts of straight-chain alcohols with longer alkyl chains are helpful in improving the surface activity of CL, especially when the number of carbon atoms in alcohols is 10 or larger. The adsorption amount of CL solutions with additives of longer chain alcohols on TiO(2) particles increases greatly, and the zeta potential of TiO(2) particles adsorbing CL rises significantly. It can be concluded that there is a cooperative effect of the longer chain alcohols on lignosulfonate to form a tighter adsorption layer at the interface. The steric hindrance increases with the increasing amount of adsorption, and the static repulsive force increases with the increasing zeta potential. Therefore, the effect of CL on the stability of the TiO(2) suspension is enhanced dramatically by addition of longer chain alcohols. This understanding can lead to further development in expanding the functionalities of the lignosulfonate through manipulation of the adsorption capacity of CL on solid particles and enhance the dispersive ability of CL on solid suspensions by adding longer straight-chain alcohols.

Based on the analysis of its genome sequence, the ectomycorrhizal (ECM) basidiomycetous fungus Laccaria bicolor was shown to be lacking many of the major classes of secreted enzymes that depolymerize plant cell wall polysaccharides. To test whether this is also a feature of other ECM fungi, we searched a survey genome database of Amanita bisporigera with the proteins found in the secretome of Trichoderma reesei (syn. Hypocrea jecorina), a biochemically well-characterized industrial fungus. Additional proteins were also used as queries to compensate for major groups of cell-wall-degrading enzymes lacking in the secretome of T. reesei and to substantiate conclusions drawn from the T. reesei collection. By MS/MS-based "shotgun" proteomics, 80 proteins were identified in culture filtrates of T. reesei strain RUTC30 grown on corn cell walls and in a commercial "cellulase" preparation, Spezyme CP. The two T. reesei enzyme preparations were qualitatively and quantitatively similar, the most striking difference being the lack of at least five major peptidases from the commercial enzyme mixture. Based on our analysis of A. bisporigera, this ECM fungus is deficient in many major classes of cell-wall-degrading enzymes, including both glycosyl hydrolases and carbohydrate esterases. By comparison, the genomes of the saprophytic basidiomycetes Coprinopsis cinerea and Galerina marginata (using a genome survey sequence approximately equivalent in depth to that of A. bisporigera) have, like T. reesei, a much more complete complement of cell-wall-degrading enzymes.

We describe the synthesis of cellulose fibers densely grafted with the cationic polymer poly[2-(methacryloyloxy)ethyl]-trimethylammoniumchloride (PMeDMA) through aqueous ATRP. The hydroxyl groups present on the cellulose surface were exploited to initiate the ATRP polymerization of MeDMA. We first grafted a bromide initiator, known to be an efficient initiator for ATRP, on the cellulose surface from which the polymer was then directly grown. The resulting fibers/PMeDMA complex was analyzed with infra-red, XPS and SEM techniques and present clear evidences that the polymer is present on the cellulose surface. In order to better characterize the polymer, sacrificial initiators were also added in the mixture and subsequently recovered for analysis. Size exclusion chromatography shows that the polymerization in this heterogeneous medium was controlled. Finally, we show that the mechanical properties of test hand sheets made from modified pulp are markedly improved by the grafting of the cationic PMeDMA.

The consolidation of pigment coating layers was simulated using a three-dimensional particle dynamics model. The model included hydrodynamic interactions as well as colloidal force models and the Brownian motion. The impact of various colloidal model parameters on the z-direction solids profile development and coating layer thickness was investigated. Also, the influence of continuous (liquid) phase viscosity was tested. Particle systems resembling a polydisperse ground calcium carbonate (GCC) distribution were studied. Results show that a lower particle surface potential on pigments increased the thickness of the coating layer, while the electrostatic double layer thickness influenced the internal coating structure. An increased viscosity of the continuous phase slowed the consolidation down, but did not have a significant impact on the final microstructure. The work contributes to the understanding of the influence of colloidal system properties on the consolidation and structure development of coating layers. The results may aid in the understanding of the impact of chemical additives on coating layer structure formation.

The synthesis of cationically modified poly(vinyl alcohol), CPVA, by copolymerization of vinyl acetate and diallyldimethyl ammonium chloride (DADMAC), followed by alkaline hydrolysis was systematically studied. The application of the resulting polymer to the fine clay flocculation was also reported. The charge density and the structure of the resulting CPVA were characterized by polyelectrolyte titration and NMR. A photometric dispersion analyzer was used to conduct the dynamic flocculation experiments. Under fine clay experimental conditions, the CPVA alone contributed little to inducing clay flocculation. However, in conjunction with anionic polyacrylamide-based polymer with high molecular weight and low charge density, significant improvement in the flocculation of fine clay particles was achieved. The influence of factors such as pH and shear force on clay flocculation was also investigated to identify optimum application conditions for clay flocculation. The electrostatic interactions between the clay and CPVA, as well as those between the CPVA pre-treated clay and anionic polymer, were studied to explore the flocculation mechanism.

Myocilin is a 55-57kDa secreted glycoprotein and member of the olfactomedin family, which is mutated in some forms of primary open-angle glaucoma. To assess the effects of elevated amounts of myocilin on aqueous humor outflow dynamics in an in vivo system, transgenic betaB1-crystallin-MYOC mice have been developed that strongly overexpress myocilin in their eyes. The transgenic overexpression of myocilin results in an almost five-fold increase of secreted normal myocilin in the aqueous humor of betaB1-crystallin-MYOC mice. In the present study, we wanted to use betaB1-crystallin-MYOC as a tool to identify the response of ocular tissues to the presence of higher than normal amounts of myocilin, and to identify changes in gene expression that could help to shed light on the functional in vivo properties of myocilin. RNA was isolated from ocular tissues of betaB1-crystallin-MYOC mice and wild-type littermates. Changes in gene expression were determined by hybridization of gene microarrays and confirmed by real time RT-PCR and Western blotting. The expression of genes that had been found to be differentially regulated in betaB1-crystallin-MYOC mice was further analyzed in cultured human trabecular meshwork (HTM) cells treated with recombinant myocilin. Although betaB1-crystallin-MYOC mice do not have an obvious phenotype, a statistically significant up- and downregulation of several distinct genes was found when compared to gene expression in wild-type littermates. Among the genes that were found to be differentially regulated were Wasl, Ceacam1, and Spon2, which are involved in cell adhesion and cell-matrix interactions. Differences in expression were also found for Six1 which encodes for a transcription factor, and for Pftk1 whose gene product is a cdc2-related protein kinase. The expression of these genes was also found to be regulated in vitro in HTM cells treated with recombinant myocilin. Substantially higher amounts in ocular tissues of betaB1-crystallin-MYOC mice were found for connexin 46 and alphaB-crystallin. In addition, several genes that encode for olfactomedin proteins showed distinct changes in expression. Olfml3 was significantly downregulated, while Lphn1, Lphn2, and Lphn3 were significantly upregulated. Our findings support a role for myocilin in modulating cellular adhesion, and suggest functional processes that involve other proteins of the olfactomedin family.

The flocculation of paper fibers by cationic polyacrylamides (c-PAM) was studied by imaging the fibers that remain free during flocculation. Studies with fibers of different lengths showed that the degree of flocculation increases with fiber length, with the best flocs being formed with mixtures of short and long fibers. Short fibers did not flocculate by themselves but were captured by flocs formed with longer fibers. The short fibers strengthen the floc and give it shear resistance. Shear had the expected effect of promoting flocculation at low Reynolds number but disrupting it at higher values. For a given polymer the maximum floc size for a mixture of fibers is dictated by the length distribution of the fibers. The polymer dose governs the rate of flocculation. The technique is especially useful in following the tail end of the flocculation process. At this stage a floc is almost fully grown and a small increase in its size would be very difficult to measure by conventional techniques. In contrast, the number of free fibers measured by single fiber imaging decreases rapidly at this point.