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The features of the use of sizing emulsions of alkyl ketene dimers (AKD) and resin acids modified with monoethyl cellosolve maleate (TM) and monoethanolamine (TMAS-3N) for hydrophobization of fibrous suspensions containing primary (sulphate cellulose (unbleached and bleached) from coniferous and hardwood) and secondary (waste paper) semi-finished products, differing in fractional composition and degree of grinding (25-70 °SR). The content of particles of the dispersed phase of the emulsions varied from 0.08 to 0.30 % for the AKD emulsion and from 0.20 to 2.00 % for TM and TMAS-3N. It has been established that the hydrophobic effect of AKD, TM and TMAS-3N emulsions increases when secondary fibrous semi-finished products are replaced with primary ones; it depends on the grinding degree of the fibrous suspension and its fractional composition. A feature of the use of alkyl ketene dimers emulsion lies in the ability of its particles to form hydrophobic β-ketoether bonds with hydroxyl groups of fibers, the number of which increases singnificantly when cellulose fibers are used instead of recycled ones. A feature of the use of TM and TMAS-3N rosin emulsions is their ability to form sizing complexes in the presence of electrolyte, which makes it possible to ensure their electrostatic interaction with the surface of fibers (cellulose and waste paper). The advantage of the TMAS-3N emulsion as compared to TM is the possibility of reducing the content of particles of the dispersed phase by 1.8-6.6 times while achieving high hydrophobicity (absorption with one-sided wetting does not exceed 21 g/m2) and maintaining the original strength of paper and cardboard.

Fluoro-functionalized paper was prepared and applied in solid phase extraction (SPE) for the analysis of trace-level perfluorinated compounds (PFCs). The proposed fluoro-functionalized paper-based solid-phase extraction (Fp-SPE) exhibits significant advantages for sample preparation, such as the biodegradability of paper-based adsorbent, simple manipulation and low cost. Owing to the fluorous affinity, the Fp-SPE technique with high sensitivity and high selectivity is more suitable for the selective enrichment of fluorine-containing molecules from the background of non-fluorinated organic compounds in a real water sample. Combined with high-performance liquid chromatography coupled with electrospray ionization-tandem mass spectrometry analysis (HPLC-MS/MS), the linear range of the PFCs, including perfluorobutyric acid (PFBA), perfluorooctanic acid (PFOA), perfluorooctane sulfonic acid (PFOS), and perfluorodecanoic acid (PFDA), was 0.20–5.0 ng/L with the limits of detection (LOD) ranging from 0.04–0.05 ng/L and the limits of quantification (LOQ) ranging from 0.15-0.20 ng/L. The method was then applied to the analysis of tap water, river water and waste water samples. The results of the actual sample analysis are consistent with that by reverse phase SPE (RP-SPE).

WOS:000486383100017 One of the keys to improving print quality is to experimentally characterize the paper surface, structure and printability to obtain quality control mechanisms. In multi-color prints, determining the differences in the acceptance of the next color ink by the surface of the paper or the ink film that was previously printed is important for print quality. The criteria, such as ink setting, adhesion, color, gloss and density, in the printing process, depend on the wettability and absorbency of the paper. The surface structure of the paper is the most important factor in determining the hydrophobic properties. In this study, wetting and absorption dynamics of the printed partially hydrophobized paper surface were investigated. The aim was to measure the effect of the printed ink film on the wetting (surface free energy) and liquid absorption behavior of the paper. Liquid absorption changes on printed/unprinted paper surfaces were measured by the sessile drop method, using a contact angle-measuring device. The surface energies of the papers were calculated and evaluated according to the surface contact angle of the droplet. Marmara University, Commission of Scientific Research Project (M.U. BAPKO)Marmara University [FEN-B-100615-0271] This work was supported by Marmara University, Commission of Scientific Research Project (M.U. BAPKO) under grant FEN-B-100615-0271.

In recent years, there has been high interest in paper-based microfluidic sensors or microfluidic paper-based analytical devices (μPADs) towards low-cost, portable, and easy-to-use sensing for chemical and biological targets. μPAD allows spontaneous liquid flow without any external or internal pumping, as well as an innate filtration capability. Although both optical (colorimetric and fluorescent) and electrochemical detection have been demonstrated on μPADs, several limitations still remain, such as the need for additional equipment, vulnerability to ambient lighting perturbation, and inferior sensitivity. Herein, alternative detection methods on μPADs are reviewed to resolve these issues, including relatively well studied distance-based measurements and the newer capillary flow dynamics-based method. Detection principles, assay performance, strengths, and weaknesses are explained for these methods, along with their potential future applications towards point-of-care medical diagnostics and other field-based applications.

A novel, simple, and low-cost spray painting technique has been developed for the fabrication of microfluidic paper-based devices. The devices that we developed utilize aerosol spray paint to build hydrophobic barriers and employ a hole puncher to obtain paper-based patterned layers and paper dots without using any specialized instruments (e.g., without a laser cutter). The entire manufacturing process is extremely simple, inexpensive, and rapid, which means that it can be applied broadly. Furthermore, the application of the device to iron detection was demonstrated. A linear relationship between the colour value and the iron concentration was observed from 0 to 0.02 g/L. The developed microfluidic paper-based device for iron detection exhibited a low detection limit (0.00090 g/L), good selectivity, and acceptable recovery.

International audience; Despite its millennial age, cellulose paper remains the preferred material for domestic and professional printings, covering applications from simple office paperwork to fiducial solutions such as bills, passports, and head letters. The creation of robust photochromic patterns on cellulose papers for anti-counterfeiting applications is an important and still partially unaddressed challenge. In this contribution, we report the covalent printing of dibenzothienylethenes as photochromic compounds through a spatially-controlled light mediated thiol-X ligations. Photophysical and theoretical studies provide evidences for a reversible photochromism behavior, not affected significantly by the polar environment of the cellulose matrix, and demonstrates a high fatigue resistance over 18 successive write-erase cycles. The strong coloration-discoloration switch can be easily followed by a direct nakedeye readout.

The present study was conducted to form polysaccharide-based multilayers of cationic starch (CS)/anionic starch (AS), and CS/carboxymethyl cellulose (CMC) on broke chemi-mechanical pulp (BCMP) fibers. It aimed to examine the buildup of CS/AS and CS/CMC polyelectrolyte multilayers (PEM) on the fibers surface, and explore the effects of PEM formation on the properties of the resulting papers. The assembly of PEM was analyzed by using zeta (ζ-) potential, water retention value (WRV), SEM micrographs, and paper properties such as thickness and strength. The results of ζ-potential inversions indicated successful constitution of PEM on the BCMP fiber surface by assembling CS/AS or CS/CMC multilayers. Further, larger ζ-potential variations occurred in depositing CS/CMC PEM, due to more charge of CMC, which presumably formed a layer with greater potential of absorption. Based on the SEM images, the surface of PEM-treated fibers was rougher, compared to the untreated fibers due to the coating with starch. Furthermore, the PEM fabrication resulted in creating fibers with higher degree of WRV, which was consistent with the significant improvement of the sheet strengths. Finally, the strength enhanced papers made from PEM-treated fibers with tensile index of about 37.33 ± 1.47 N m/g vs 22.24 ± 1.23 N m/g or 11.60 ± 0.57 N m/g for the papers made from original CMP and untreated BCMP fibers, respectively, may diminish the challenges related to web breaks in the paper machine conveying BCMP broke fibers.

The aim of the present work has been to study the influence of chitosan addition into the composition of paper intended for documents on its ageing stability, with a view of enhancing the resistance of paper strength and optical properties over time. The chitosan solution was added during the formation of the paper sheets in various amounts: 0.2%, 1% and 2% o.d.f. Paper samples of different fibrous compositions were prepared from bleached sulphate softwood pulp (BSWP) and bleached sulphate hardwood pulp (BHWP) in the following ratios: 50% BSWP:50% BHWP, 80% BSWP:20% BHWP, 100% BSWP and 100% BHWP. Then, paper samples were subjected to accelerated thermal ageing for 24 hours at 105 °C. It was found that the use of chitosan as additive in the composition of bleached cellulose paper samples led to improved strength and hygroscopic properties. The study showed that chitosan could be used in the production of kraft document papers comprising aluminium sulphate, as the presence of aluminium sulphate had no negative effect on the action of the biopolymer. Regarding the complex evaluation of the properties of the obtained papers, it could be summarized that, for the studied fibrous compositions, the optimum amount of the additive was 1% chitosan for a fibrous composition of 50% bleached softwood pulp and 50% bleached hardwood cellulose. Therefore, preparing document paper with the addition of chitosan is a convenient procedure to enhance a number of paper properties, even after the ageing process.

Utilization of paper wastes as renewable resource of lignocellulosic constituents has the opportunity to promote a cleaner environment and to prepare valuable materials. This paper describes our study on an isolation of low-fiber powder cellulose from two grades of wastes as feedstocks: waste newsprint paper and cardboard wrapper through recycling including a thermal defibration, an alkali treatment with a solution of NaOH with a concentration from 0.03 to 1.00 М, a bleaching with a solution of Н2О2 with a concentration from 0.8 to 2.6 М followed with an acid hydrolysis of the pretreated species with a solution of HNO3 of 1.5 and 3.0 M. An impact of the pretreatment on sizes of fibers was evaluated with a stereoscopic microscopy. The powder celluloses obtained as a result of the acid hydrolysis exhibited the structure of cellulose I revealed with a WAXS method and were of a high-grade purity, according to EDXA. Sorption capacities of the powder celluloses from the waste cardboard and newsprint towards a dye methylene blue were 6.67 mg∙g-1 and 8.75 mg∙g-1 correspondingly., Использование макулатурной массы как источника лигноцеллюлозных продуктов для получения низковолокнистых порошковых целлюлоз перспективно как с экономической, так и с экологической точки зрения. Настоящая работа посвящена изучению процесса получения низковолокнистых порошковых целлюлоз из макулатурной массы (отходы газетной бумаги и картона) для дальнейшего их применения в качестве функциональных материалов. Процесс переработки макулатуры состоял из предварительной обработки и кислотного гидролиза. Предварительную обработку проводили путем терморазволокнения макулатурной массы в воде, затем мацерации раствором NaOH с концентрацией от 0.03 до 1.00 М и отбелки раствором Н2О2 с концентрацией от 0.8 до 2.6 М. В результате кислотного гидролиза предобработанных образцов в 1.5 и 3.0 М растворах HNO3 получены порошковые образцы, структура которых по данным рентгенофазового анализа соответствовала структуре целлюлозы I. Выделенные порошковые целлюлозы имели высокую степень чистоты, что было подтверждено с помощью энергодисперсионного микрорентгеноспектрального анализа. Методом стереоскопической микроскопии показано влияние обработок на размеры волокон. Сорбционная способность порошковых целлюлоз из макулатурной массы картона и бумаги по отношению к метиленовому голубому составляла 6.67 мг∙г-1 и 8.75 мг∙г-1 соответственно.

The production of human-generated wastes is increasing with the rise in the world’s population. Under this scenario, sustainable management of large quantities of waste is becoming an increasingly challenging task. The present study carried out the anaerobic co-digestion of food waste (FW), human feces (HF), and toilet paper (TP) to evaluate its potential for use in the on-site treatment of household organic wastes. The biochemical methane potential (BMP) was determined for these wastes and their mixtures, confirming the effective methanation of each substrate and its mixtures, with FW showing significantly higher BMP than HF or TP. Response surface analysis of the BMP data successfully produced two models describing the effect of the substrate mixing ratio on the overall methane yield and the synergistic effect of co-digestion (in terms of methane yield). The obtained models revealed that methane yield and the synergistic effect of co-digestion are influenced in different ways by variations in the substrate mixing ratio. Importantly, the effect of interactions between individual substrates is not substantial in magnitude regardless of the substrate mixture composition (synergy index close to 1). This indicates that FW, HF, and TP can be co-digested without compromising the overall methane yield (i.e., no antagonistic effect) at any desired substrate mixing ratio, which makes the application of co-digestion in the field more flexible. The overall results suggest that anaerobic co-digestion is a feasible means for the on-site treatment and valorization of mixed FW, HF, and TP, the major household organic wastes.

Focusing on eco-friendly materials, cellulose nanocrystal (CNC) extracted from office waste paper was used to reinforce waterborne polyurethane (WPU) with varying content by two incorporation routes including blending method by sonication after WPU synthesis (BCNC/WPU) and the alternative in-situ during the WPU synthesis process (CNC/WPU). The results showed that new interaction between CNC and WPU through hydrogen bonds in the interfacial area was formed and CNC reinforced hard segments effectively. However, the interaction in BCNC/WPU was not as stronger as that in CNC/WPU. Besides, CNC improved thermal stability of WPU remarkably, especially BCNC/WPU. The addition of CNC caused a delay around 50 °C in the start of the degradation process, and a delay of 5–18 °C and 2–20 °C in the temperatures at 10 and 50 wt% weight loss, respectively. These eco-friendly and biodegradable novel materials have potential applications in medical and biologic fields.

Since the monumental work conducted by Whitesides et al. in 2007, research and development of paper-based microfluidics has been widely carried out, with its applications ranging from chemical and biological detection and analysis, to environmental monitoring and food-safety inspection. Paper-based microfluidics possesses several competitive advantages over other substrate materials, such as being simple, inexpensive, power-free for fluid transport, lightweight, biodegradable, biocompatible, good for colorimetric tests, flammable for easy disposal of used paper-based diagnostic devices by incineration, and being chemically modifiable. Myriad methods have been demonstrated to fabricate paper-based microfluidics, such as solid wax printing, cutting, photolithography, microembossing, etc. In this study, fabrication of paper-based microfluidics was demonstrated by spray on the printed paper. Different from the normally used filter papers, printing paper, which is much more accessible and cheaper, was utilized as the substrate material. The toner was intended to serve as the mask and the patterned hydrophobic barrier was formed after spray and heating. The processing parameters such as toner coverage on the printing paper, properties of the hydrophobic spray, surface properties of the paper, and curing temperature and time were systematically investigated. It was found that, after repetitive printing four times, the toner was able to prevent the hydrophobic spray (the mixture of PDMS and ethyl acetate) from wicking through the printing paper. The overall processing time for fabrication of paper-based microfluidic chips was less than 10 min and the technique is potentially scalable. Glucose detection was conducted using the microfluidic paper-based analytical devices (µPADs) as fabricated and a linear relationship was obtained between 1 and 10 mM.