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Mitigation of global warming, energy security and industrial competitiveness urge the energy-intensive pulp and paper industry (PPI) to transform energy use practices. This study investigates how the PPI has responded to the need for the energy transition in the 2000s. Finland and Sweden as forerunners of energy-efficient operation and decarbonization of the PPI are used as target countries. Understanding of changes in energy consumption is complemented using decomposition analysis (Logarithmic Mean Divisia Index Method) and the energy efficiency index approach. Analysis of companies’ investments in energy technologies is used for explaining changes in energy production. Evidence of significant development towards the more sustainable operation of the PPI was found. Energy consumption per produced unit has decreased, i.e., energy efficiency has improved. Fossil fuels have been partially replaced with bio-based alternatives. Thus, the CO2 intensity has decreased substantially. The generation of renewable electricity has increased in both countries. Examples of Finland and Sweden indicate that the PPI has great potential to contribute to CO2 emission reduction worldwide in the future as energy efficiency can be further improved, and the share of fossil fuels can be decreased increasing the use of biofuels and self-generated green electricity at least in kraft pulp mills.

The construction industry had approached a critical limit which led to the increase of cement production. The production of cement would cause a broader environmental implication. Cement production is a major source of carbon dioxide emission. Carbon dioxide gas contributes about 63.33% of global warming since the production of one ton of cement would emit about one ton of carbon dioxide to the environment. To mitigate this issue, the research community has investigated the use of waste materials that possess similar chemical properties with cement content as a material for partial cement replacement. The use of rice husk ash has shown to be a contending candidate in the literature. Therefore, this paper attempts at reviewing the performance of rice husk ash as partial cement replacement. It could be observed from the literature that concrete with 5% up to 15% of rice husk ash showed an equivalent performance to ordinary concrete in compressive, flexural, and tensile strength. Thus, rice husk ash can be used as a material replacement in concrete and reduces pollution that originates from cement production and open burning of rice husk.

Made available in DSpace on 2022-04-29T08:31:12Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-10-01 Organization and planning of reverse logistics networks make sustainable processes more efficient. Thus, an important sector for connecting the collection and waste paper recycling echelons is the intermediate center. In this study, a Mixed Integer Linear Programming model, which is multi-objective, multi-product, multi-level and multi-period, was developed to optimize the waste paper logistics processes of intermediate centers. The formulation includes the following echelons: collection, considering vehicle routing with different capacities; inventory of non-baling materials; baling sorted waste and inventory of bales; selling bales; disposal of non-recyclable waste. The aims of the model include: maximizing the collected waste; minimizing distances; maximizing both the production and sale of bales, and minimizing costs. According to research carried out in the literature, the developed model is a new proposal and to implement it, the Weighted Goal Programming and Revised Multi-Choice Goal Programming approaches were used to deal with multiple objectives and incorporate uncertainty into the quantity of waste available for collection. To analyze the proposed model, computational tests were executed with instances based on real data from a Brazilian company in the sector. For all performed tests, General Algebraic Modeling System 23.6.5 modeling language and CPLEX 12.2.0.2 solver were used for modeling and optimization. The results show that this study presents formulation and technological approaches that represent real situations and provide competitive solutions to the problem. Sáo Paulo State University “Júlio de Mesquita Filho” [Universidade Estadual Paulista Júlio de Mesquita Filho] School of Engineering of Guaratinguetá [Faculdade de Engenharia de Guaratinguetá] Production Department, Av. Ariberto Pereira da Cunha, 333, Portal das Colinas Agulhas Negras Military Academy [Academia Militar das Agulhas Negras] Rodovia Presidente Dutra, km 306, s/n Escola Preparatória de Cadetes do Exército Avenida Papa Pio XII 350 Jardim Chapadão Campinas - SP Brazil, Avenida Papa Pio XII, 350, Jardim Chapadão, Campinas - SP Sáo Paulo State University “Júlio de Mesquita Filho” [Universidade Estadual Paulista Júlio de Mesquita Filho] School of Engineering of Guaratinguetá [Faculdade de Engenharia de Guaratinguetá] Production Department, Av. Ariberto Pereira da Cunha, 333, Portal das Colinas

Graphene-based nanomaterials possess broad applications because of their excellent multi-functional properties. In this work, a facile self-assembling method was presented for preparing one kind of graphene oxide-based paper/hollow microspheres hybrid. It was found that most of the hollow microspheres can strongly anchored on the surface of graphene oxide paper (GOP) by an in-situ scanning electron microscope peeling testing combining with molecular dynamics (MD) simulation. In addition, the uniform distribution of hollow microspheres on the surface of GOP cannot only provide a better surface wettability, but also can effectively improve the interfacial stress-transfer capability between such hybrid and polymer matrix. Our work provides a guidance for the structural designs of graphene-based nanomaterials and broaden their applications.

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.

This study optimizes a novel surfactant-assisted green liquor dregs (GLD) pretreatment of paper mill sludge (PMS), both of which are wastes from the kraft pulping industry, using a combined Response Surface Methodology (RSM) design. Optimized conditions give a maximal reducing sugar release of 16.38 g/L. A substantial reduction in heavy metals aluminum, chromium, cobalt, arsenic, lead, and copper after pretreatment illustrates the enhancement of substrate digestibility by reducing toxic elements. Separate hydrolysis and fermentation (SHF) and simultaneous saccharification and fermentation (SSF) for hydrogen production are assessed. SSF produced a hydrogen yield of 3.72 mL/g, displaying a 36.26% increase from pretreated PMS compared to SHF. These findings provide insights into possible methods of reducing process duration, energy input, and costs incurred with waste disposal within the paper industry. Furthermore, improved hydrogen yield using an SSF process demonstrates the potential beneficiation of pulp and paper GLD and PMS wastes.

The fiber of paper mulberry, which is mostly grown in the East Asian region, varies in both length and width—even if from the same species—depending on the country, soil, and climate where it is grown. This accounts for differences in the quality of handmade paper between domestic and imported products. Once handmade paper is manufactured as sheets, its origin cannot be determined from a morphological perspective, regardless of macroscopic and microscopic observations. Therefore, this study attempted to determine the origin of Korean and imported products using mulberry bast fiber and handmade paper from a chemometrics perspective. The inorganic components of wood are absorbed from the soil and exist in the bark of trees; thus, metal and rare-earth elements in the bast fibers and handmade papers were quantitatively analyzed using inductively coupled plasma-atomic emission spectroscopy/mass spectrometry (ICP-AES/MS). Following this, a prediction model of their origin was constructed by applying multivariate statistical analysis, i.e., a partial least squares-discriminant analysis (PLS-DA) loading plot was constructed, which helped in identifying the discrimination factors resulting from their origin. According to the ICP-AES results, Pb was only detected in the Gyeongbuk Mungyeong dak sample of the Korean bast fibers. The Chinese bast fiber sample had high contents of Ca, and B and Zn were detected only in the Chinese bast fiber samples. Bast fiber samples from China, Japan, and Thailand showed relatively high contents of Al, Ca, and Na. Meanwhile, Cu and Zn were detected in the handmade paper manufactured from the imported materials. According to the ICP-MS results, among the Korean handmade papers, the products from Gyeongbuk Mungyeong, Andong, and Chungbuk Goesan exhibited a high U content and that from Gapyeong had high Sc, Rb, Sr, and Ba contents. Thus, the elemental analysis employed in this study effectively identified the origin of the papers. The origin prediction by PLS-DA for the domestic and imported products revealed an accuracy of 86.4% and 72.7% for ICP-AES and ICP-MS methods, respectively, which is deemed acceptable to assess the origin. We believe this method significantly contributes to determining the origin of paper mulberry bast fiber and handmade paper manufactured in East Asia.

By continuously varying the structure of graphene oxide paper (PRGP) using Joule heating annealing, we are able to tune its electrical conductivity (σ) and thermal diffusivity (α) in a very wide range: more than three orders of magnitude for σ (186–503009 S/m) and 10-fold for α (8.31 × 10−7 m2/s to 9.31 × 10−6 m2/s). Excellent coherency-linear relationship between σ and α is discovered although they are sustained by different carriers: electrons and phonons. Such coherency exists over two sections: σ > 2 × 104 S/m, and 103

Cellulose triacetate (CTA) forward osmosis (FO) membrane from Hydration Technology Innovation (HTI), USA was tested in a locally fabricated FO system to concentrate synthetic and pulp and paper mill wastewater. The industry is among the 17 most polluted industries with intensive water consumption and wastewater generation (MoEFCC, Government of India). The CTA membrane was studied with deionized water as feed solution and 1 M NaCl as draw solution, which resulted into water flux of 5.8 L/m2h and reverse salt flux of 0.2 g/L. A concentration stepping method was used to determine the critical draw concentration with lignin solution as the model feed. There was no deviation in flux between the baseline (deionized water feed) and the lignin solution up to 1.5 M NaCl, but a marginal deviation (8% and 21% respectively at 2 M and 3 M) was seen thereafter. The average water flux after 24 h FO study with synthetic wastewater as feed solution (draw solution 2 M NaCl) was 8 L/m2h, and 80% water recovery. Similar study with pulp and paper wastewater as feed solution (draw solution of 1.5 M NaCl) was 5.4 L/m2h was with 62% water recovery. Lignin and COD rejection in pulp and paper mill wastewater was 90% and 64% respectively. The preliminary results indicate that FO is promising for water and lignin recovery from waste streams.

Paper and pulp mills generate substantial quantities of cellulose-rich sludge materials that are disposed in landfills at a large scale. For sustainability purposes, sludge materials can be bioprocessed to produce renewable fuels and useful chemicals. The enzymatic hydrolysis of cellulose is the process bottleneck that affects the conversion economics directly by using zero-cost raw materials. In order to study and optimize the process, the characteristics of the sludge raw materials should be first evaluated. In this work, sludge samples were obtained from paper mills located at different locations in Wisconsin and Minnesota. Part of the sludge samples was washed (de-ashed) with hydrochloric acid while the other part remained unwashed. The samples were subjected to multiple spectroscopic analyses techniques to evaluate the morphological properties of cellulose fibers and to estimate the total structural carbohydrate content. The results showed that the de-ashing process changed some fiber characteristics and cellulose crystallinity structure in all sludge samples. Sludge sample A (obtained from Kraft pulp and recycled paper mill region) showed a high percentage of fiber, with crystalline cellulose, compared to the other two sludge samples suggesting that sludge A is a valuable source to make value-added products. Aspen Plus mass and energy calculations performed in view of the ‘zero’ cost and the reliable supply of sludge raw materials producing 2 mol H2/mol glucose. Moreover, the results showed that extracting crystalline cellulose from these sludge samples is more profitable than crystalline cellulose made from the other lignocellulosic feedstocks. The results reported here showed that the utilization of these sludge materials would be an economically attractive and promising alternative for the production of hydrogen.

Virgin pulp is made by splitting up cellulose fibers from the woods by mechanical and chemical process without adding any recycled pulp content. The demand for trees, which are the basic raw material for making virgin pulp, increasing constantly in enormously growing paper manufacturing industry. The paper, which is made from virgin pulp is called as virgin paper and this is considered as better quality paper than the recycled paper. Now there is a need to increase the quality of recycled paper to equalize the quality of virgin paper, to reduce the demand for trees to make virgin pulp. In recycling, dispersive system is responsible for the de-inking process, which is one of the pulp purifying process which removes the printing ink from fibers. Chemicals are added in this deinking process which causes a serious problem by increasing the chemical concentration level of industrial outlet water. In conventional deinking technology, dispersive system is controlled by DCS which is quite complicated to control complex loop of operations. To overcome these problems, the dispersive system operations are controlled by PLC along with sensors which make the process easier and replacing the chemicals with enzymes will reduce the chemical concentration level of industrial outlet water and increases the quality of paper.

Aim of the present work was to deepen the knowledge on the effects of funori on cellulose fibers with particular attention paid to their consolidation. Compared to canvas, paper samples (untreated or artificially aged) show different fiber packaging and liquid-absorbing properties. Herein, we conducted observations of cellulose fibers by scanning electron microscopy (SEM) in order to evaluate the seaweed extraction method employed in this work, as well the consolidation action had on the fibers through multiple additions of the prepared solutions. Surface homogeneity and fiber stiffness observed by us increased over time and the fibers, initially frayed and disordered, were eventually incorporated into the purified funori after several solution additions accompanied also by a progressive occlusion of the pores. The achieved consolidation effect was confirmed by means of mechanical tests. Moreover, the method herein developed was slightly modified in view of the application of the funori solution to a cultural asset of historical and botanical interest, still scarcely studied. Electronic microscopy allowed us to evaluate the consolidation and gluing effect obtained through subsequent funori applications.

Edible oils form an integral component in the human diet as well as in the industrial preparations. Any adulteration in oil is concerning from nutritional as well as economical perspective. Although analytical techniques exist for detection of adulterants in oil, most of them require sophisticated instruments, and trained professionals. Microfluidic based lab-on-a-chip technologies have rapidly progressed over the recent years and offer promising alternatives in this regard. In this work, we report development of a paper-based microfluidic lab-on-a-chip for detection of palm oil contamination in sunflower oil. We use the paper-based microfluidic colorimetric detection approach that indicates the presence of adulteration in a visual manner. The data is analyzed using digitally acquired images along with ultraviolet–visible spectrophotometry. The paper-based microfluidic device is fabricated and tested for 10–50% (v/v) palm oil adulteration in sunflower oil. Further, we employ the device for free fatty acid content tests in oil samples. Visual signal acquired from the device is optimized by varying phenolphthalein proportions. The stability of visual colorimetric signal is examined over time and is found to remain steady over the trial period of six days considered in this work. The integration of the detection device with smartphone imaging can prove to be useful for onsite data collection. We believe the approach presented here can be extended to food quality monitoring portable platforms.

This work investigates the influence of blending waste paper and cement at fixed proportion with varying proportions of chicken feather fiber (CFF) and wood saw dust (WSD) as reinforcements. Samples produced were tested for flexural properties and water absorption potentials. The outcome showed that with increasing CFF content and reducing WSD content, water absorption reduced while flexural strength, modulus of ruptures (MOR) and modulus of elasticity (MOE) increases. MOR and MOE were at peaked when the ratio of CFF to WSD was 3:2 while flexural strength reached it crescendo at 4:1 of CFF to WSD. It was noticed that higher CCF content from 3 to 5 wt% gave better results in most of the investigated properties compared to WSD. Therefore, it was concluded that low quantity of WSD is needed to form a synergy with CFF in order to achieve optimum results. Well dispersed CFF-WSD phase in waste paper-cement based composites was observed to be responsible for the enhancement in the investigated properties.

The waste of paper or the paper dump is a serious problem and its occurrence is widespread in various institutions. Wastepaper can be recycled to produce some important and usable products that are ecological and biodegradable. For example, it is used to extract new paper from the old by chemical decomposition. Other products such as paper plates, paper cups, paper spoons, tiles, toys, crafts, etc. can be formed from the slurry. This project also initiates a mould that makes cups and plates from the wastepaper management circuit. With learning institutions being the main consumers, most paper are usually eliminated after its use. The waste remains undeveloped and unused, although is a valuable resource. Studying the design of a manual, economical and efficient paper recycling machine, it can be surmised that the design uses the integration of the knowledge gained about the recycling technology that exists manually from the paper recycling machines used to form a cheap but effective paper recycling system. The advantages of the machine are not only of recycled paper, but also the advantages of the interaction of the manual drive system, which will also reduce the high cost. As the design is not 100% effective, the transmission, belt and chain transmission correspond to the estimated 90% efficiency using the 90% for the design. The power consumption for the design is 450 W and since an average user can produce 100 W constant, it takes 5 people to drive the machine.

Wastewater containing heavy metal ions is considered as the serious environmental problem in human society. Adsorption as the widely used method plays an important role in wastewater treatment, which is based on the physical interaction between metal ions and sorbents. Drumsticks are reported to have efficient adsorbing property. It has been found that Moringa causes alteration in testosterone levels, preventing testicular damage and hence is capable of protecting against the toxic effect of hazardous material. Based on this phenomenon of adsorption by Moringa species, we are trying to remove heavy metals from aqueous sample. The bio sorption of heavy metals by non-living biomass of plant origin is an innovative and alternative technology for the removal of the pollutants from aqueous solution and offers several advantages such as low-cost bio sorbents, high efficiency, minimization of chemical and/or biological sludge, and regeneration of the bio sorbent. Moringa oleifera (drumsticks) has a number of advantages including low cost, biodegradable sludge production and lower sludge volume, and also it does not affect the pH of the water. Apart from turbidity removal, Moringa oleifera seeds also possess antimicrobial properties. Amount of adsorption is considerably larger when activated charcoal is used. Thus, this work reports preparation of activated charcoal from drumsticks seeds and fibres. These are generally part of kitchen waste; thus, its preparation and utilisation for heavy metal toxicity not only controls water pollution but also help in reduction of kitchen waste. It will serve as an effective, cheap and robust and green tool for toxicity control. The paper reports the removal of heavy metal (Pb, Ni, Cd, As in this study) by application of prepared activated charcoal tablets via MATLAB assisted paper based sensors. These tablets will surely serve as point-of- care devices for removal of heavy metal toxicity.

In recent years there has been increasing interest in the use of recycled paper waste in the production of concrete to reduce environmental pollution. This study aims to investigate the use of raw paper waste to produce lightweight cement mortar and to study the effect of the aluminium sulphate treatment of raw paper waste on the compressive strength, absorption ratio and hardened density of mortar. This study used raw paper waste as a replacement for fine aggregate, with percentages of 5%, 10%, 15%, 20% and 30%. The same percentages were examined for the aluminium-sulphate-treated paper waste. The study aims to achieve a similar workability and fixed flow rate for all mixes; therefore, the water–cement ratios were changed for mixes containing paper waste to balance the water absorbed by the paper waste. The study found that the treatment of paper waste with aluminium sulphate helps to reduce the amount of water absorbed by the paper waste and also reduces the amount of water required to maintain its workability, with a higher paper-waste content requiring a larger water content to achieve a similar workability. It was found that the higher the paper-waste content, the lower the wet and dry densities. The compressive strength at both an early and mature age decreased with the increased content of paper waste. Finally, the treatment of paper waste with aluminium sulphate increases the early age compressive strength for similar replacement percentages of up to 19%.

Cyanide ( CN - ) is a deleterious chemical and can cause serious health effects upon exposure even at low concentrations. Different sensors have been developed to monitor cyanide in water, which, however, suffers from complex mechanisms and high-cost. Curcuma longa or turmeric is a commercially available natural dye (usually in powder form) used as medicine. The phenolic substance curcumin is responsible for its yellow color and is capable of sensing environmentally significant analytes such as CN - . In this study, a colorimetric sensor for cyanide in aqueous solution was fabricated by the immobilization of crude curcumin on ordinary filter paper. The curcumin was extracted from locally available turmeric powder using a simple extraction method. Its successful integration in the filter paper was validated by FT-IR spectroscopy. UV–Vis analysis showed that the curcumin-based paper sensor was sensitive to CN - (down to 5.0 ppm), producing a visual change from yellow to dark red. The fabricated sensor also demonstrated high selectivity towards CN - in the presence of N a + , K + , and F - . Its response time was found to be inversely proportional to the concentration of the CN - in the solution. Assessment of reusability revealed that the sensor was reusable for up 8 cycles before significant changes in colorimetric response were observed. Importantly, the fabricated sensor exhibited applicability for actual cyanide monitoring in real water samples.

Food safety is always one of the most important issues for human being. With the variety of food, it is required to develop rapid, low-cost and convenient detection techniques for food safety. As a representative, paper-based detection techniques have developed rapidly from simple test papers to various microfluidic paper-based devices. The paper-based analytical devices combining paper platform with a variety of advanced analytical methods have shown great application prospects for rapid testing of food safety. In this review, the surface functionalization and modification of paper are introduced. Then, the construction and development of various detection techniques are discussed, including colorimetric analysis, fluorescent analysis, electrochemical analysis, surface enhanced Raman spectroscopic analysis, and multimethods on paper-based platforms for the application in rapid detection for food safety. Finally, the prospects and future challenges of rapid detection techniques in food safety are also discussed.

Paper money was first used in China as early as the sixth century AD. Since that time, counterfeits have circulated in parallel with authentic paper money. After WWII the interest of art collectors in historical emergency paper money surged and counterfeiting became a complex phenomenon. In fact, the use of scientific investigation for determining the authenticity of historical paper money is still limited to few cases. In this work nine pieces of Chinese paper money (from the fourteenth to nineteenth century) were investigated by combining non-invasive MA-XRF imaging and Raman spectroscopy. Analytical results on the paper money demonstrated how the complementary use of both non-invasive techniques can provide an excellent tool for discriminating modern materials from historical ones, allowing us to identify seven counterfeits in the set of nine investigated paper moneys.

This study focuses on the mineral carbonation to capture CO2 using an alkaline industrial waste, the grits, formed during the kraft pulp production process. An indirect mineral carbonation route was adopted, composed by two steps: first the extraction of calcium from the grits and second the precipitation of calcium carbonate. Firstly, four solvents were analyzed (HNO3, CH3COOH, NaOH and NH4Cl). Only HNO3 and CH3COOH have shown significant extraction efficiencies of 79.4 and 73.2 %, respectively, after 2 h at 30 °C. Kinetic tests demonstrated that equilibrium conditions are reached after 60 min. Since the nitric acid is a corrosive acid and with high associated costs, the acetic acid was selected for the dissolution of grits and extraction of calcium. The optimal conditions determined were an acetic acid concentration of 2 M, solid/liquid ratio of 30 g/L and temperature of 45 °C with an efficiency approximately of 77 %. In the second step, carbonation experiments were performed contacting the Ca-rich liquor, obtained from the extraction step, with a flux of pure CO2 gaseous in a stainless inox reactor. The optimal conditions determined were 30 °C and 30 bar, reaching a carbonation efficiency of 74 %, corresponding a CO2 sequestration capacity of 460 kg CO2/ton of grits.

Competitive immunoassays comprise the standard means of detecting small molecules. However, conventional methods using microwells are difficult to apply during point-of-care tests (POCT) because they require complicated handling and are time consuming. Although paper-based analytical devices (PAD) have received considerable focus because of their rapid and straightforward operation, only a few devices have been proposed for competitive immunoassays. Herein, we describe a novel universal PAD format with a 3-dimensional configuration for competitive immunoassays that rapidly and sensitively detects small molecules. The proposed device comprised a layered structure with uniform color formation and high capture efficiency between antigen and antibody that results in rapid and reproducible results. The device rapidly (90 s) assayed biotin as a model target, with a limit of detection (LOD) of 5.08 ng mL−1, and detected progesterone with an LOD of 84 pg mL−1 within 5 min. Moreover, sample volumes and reagent consumption rates were minimized. Thus, our device could be applied to competitive immunoassays of various small molecules in POCT.

Photocatalytic materials have been widely used to remove dyes from printing and dyeing wastewater. However, difficulty in recycling of photocatalysts is the great concern in the real catalytic applications, which significantly raises the application cost. This study developed a low-cost catalyst by loading magnetic Ni onto filter paper (FP) via an easy going in-situ reaction. The characterization results displayed that the Ni particles were uniformly anchored onto the FP. The Ni@FP material presented a strong magnetic ability which was evidenced by a saturation magnetization (Ms) of 5.014 emu·g−1, a remanent magnetization (Mr) of 2.067 emu·g−1 and a coercivity (Hc) of 133.868 Oe. Meanwhile, the magnetic Ni@FP material displayed a recyclable advantage in photocatalytic degradation of methyl orange (MO) via an external magnetic field. There existed an optimal photocatalytic degradation rate of 93.40% within 5 min when MO concentration was 15 mg·L−1 at pH 8.0. Three cycle experiments confirmed that the Ni@FP possessed a satisfied stability and recycling ability. Moreover, the Ni@FP material presented a strong antibacterial activity which can prevent it from being contaminated by microorganisms. The versatility of the newly proposed photocatalyst in this study demonstrated its great application prospect in dyeing wastewater treatment.

Made available in DSpace on 2021-06-25T10:45:32Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-01-25 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG) Lactose (LAC) is a disaccharide - major sugar, present in milk and dairy products. LAC content is an important indicator of milk quality and abnormalities in food industries, as well as in human and animal health. The present study reports the development of an innovative imprinted voltammetric sensor for sensitive detection of LAC. The sensor was constructed using electropolymerized pyrrole (Py) molecularly imprinted polymer (MIP) on graphite paper electrode (PE). The MIP film was constructed through the electrosynthesis of polypyrrole (PPy) in the presence of LAC (template molecule) on PE (PPy/PE). To optimize the detection conditions, several factors affecting the PPy/PE sensor performance were assessed by multivariate methods (Plackett–Burman design and central composite design). Under optimized conditions, the proposed analytical method was applied for LAC detection in whole and LAC-free milks, where it demonstrated high sensitivity and selectivity, with two dynamic linear ranges of concentration (1.0–10 nmol L−1 and 25–125 nmol L−1) and a detection limit of 0.88 nmol L−1. The MIP sensor showed selective molecular recognition for LAC in the presence of structurally related molecules. The proposed PPy/PE sensor exhibited good stability, as well as excellent reproducibility and repeatability. Based on the results obtained, the PPy/PE is found to be highly promising for sensitive detection of LAC. Analytical Chemistry Department Institute of Chemistry São Paulo State University (UNESP), 55 Prof. Francisco Degni St., São Paulo State Institute of Exact and Natural Sciences of Pontal Federal University of Uberlandia, 1600 20 St., Ituiutaba, Minas Gerais State Bioenergy Research Institute (IPBEN) São Paulo State University (UNESP), 55 Prof. Francisco Degni St., São Paulo State Analytical Chemistry Department Institute of Chemistry São Paulo State University (UNESP), 55 Prof. Francisco Degni St., São Paulo State Bioenergy Research Institute (IPBEN) São Paulo State University (UNESP), 55 Prof. Francisco Degni St., São Paulo State FAPESP: 2017/25329–6 FAPESP: 2018/12131–6 FAPESP: 2019/13818–8 CNPq: 408783/2018–4 CNPq: 443315/2014–0 CNPq: 447668/2014–5 CAPES: 88887.368610/2019–00 FAPEMIG: APQ-02078-15 FAPEMIG: APQ-02905-15

SnO2 nanoparticles @ carbon nanoparticles (SnO2@carbon NPs) were synthesized by a facile route using SnCl2·2H2O and filter paper as precursors for lithium ion battery. The different sized nanoparticles of SnO2@carbon NPs were prepared at different temperatures (400, 450 and 500 °C). From the powder X-ray diffraction study the various size of prepared nanoparticles at different temperatures were found to be 16.5 nm (400 °C), 28.5 nm (450 °C), and 35.6 nm (500 °C). Scanning electron microscope (SEM) study reveals the particle nature of synthesized SnO2@carbon NPs. The presence of individual constituents such as Sn, O and C was confirmed by EDAX analysis. TG/DTA studies give assurance of the presence of carbon nanoparticles. FT-Raman spectral study also confirmed the phase and structure of SnO2 nanoparticles. The band gaps of SnO2@carbon NPs prepared at different temperatures (400, 450 and 500) were found to be 3.64 eV, 3.39 eV, and 3.17 eV, respectively by a UV–Vis spectral study. The capacity of SnO2@ carbon NPs prepared at 500 °C was found to be showing better electrochemical properties.

There is growing demand for simple to operate, sensitive, on-site quantitative assays to investigate concentrations of drug molecules in pharmaceutical preparations for quality assurance. Here, we report on the development of two colorimetric analysis methods for the study the antibiotic doxycycline hyclate (DOX) and the nasal decongestant oxymetazoline hydrochloride (OXY), in solution as well as in their respective formulations. We compare a UV/vis spectrophotometry method with a color change recorded on a microfluidic paper-based analytical device (μPAD). Detection is based on the pharmaceutical compounds coupling with diazotized 4-aminoacetophenone (DAAP) under alkaline conditions to produce colored azo-dye products. These azo-compounds were monitored by absorbance at 425 nm for DOX and 521 nm for OXY, with linear calibration graphs in the concentration range of 0.5–35 mg L−1 (DOX) and 1.0–40 mg L−1 (OXY) and limits of detection of 0.24 mg L−1 (DOX) and 0.32 mg L−1 (OXY). For the μPAD method, color intensity was measured from photographs and a linear increase was observed at concentrations from above approximately 15 mg L−1 for both compounds and up to 35 mg L−1 for DOX and 40 mg L−1 for OXY. The developed methods were also applied to the formulated pharmaceuticals and no interference was found from the excipient. Thus, the paper-based device provides an inexpensive, simple alternative approach for use outside centralized laboratories with semi-quantitative capability.

Paper-based colorimetric sensor array has attracted extensive attention due to its low-cost, easy-operation, powerful discrimination, good selectivity, rapid response and versatility. It combines the advantages of paper-based analytical devices and colorimetric sensor array, and extends its application fields in analytical chemistry. This review described the recent progress in paper-based colorimetric sensor array and summarized its applications in biomedicine, environmental and food safety. Moreover, the sensing materials, characteristics and performances of different paper-based colorimetric sensor arrays were investigated. The prospects of future research for the paper-based colorimetric sensor array were discussed.

The growing need for reliable analytical tools to perform measurements at the point-of-need has prompted the development of novel sensors that are low cost, portable, sensitive, easy to use, and capable of multiplexed analysis. Miniaturization of the sensors into microfluidic platforms has become a promising approach to achieve these self-contained sensors. However, traditional microfluidics often require relatively expensive and complicated pumping mechanisms that increase the cost and limit the portability of the sensors. From a material perspective, paper is an attractive substrate for constructing point-of-need sensors because of its affordability, vast availability, and self-pumping ability, particularly when combined with electrochemical detection. In this mini-review, we discuss various strategies to achieve multiplexing or simultaneous detection of multiple analytes in electrochemical paper-based devices and provide a brief guide on selecting the detection strategy based on the electrochemical property of the analytes.

A novel nacre-like flame-retardant paper based on graphene oxide (GO), and phytic acid (PTA) is fabricated via evaporation-induced self-assembly. This facile method is time saving and low energy consuming. A facile approach is proposed to improve thermal oxidative stability of GO paper by in situ phosphorus doping during flame exposure. Then fire-alarm system is designed based on the high-temperature thermal reduction characteristic of GO. The GO paper functionalized with PTA (GO-PTA) can provide ultrasensitive, reliable and longtime fire early-warning signal. Fire alarm can be triggered at approximately 0.50 s when GO-PTA samples are attacked by fire. Phosphorus atoms are in situ doped into graphene layers during fire exposure, endowing GO-PTA paper with outstanding thermal oxidative stability, and thus alarm duration time of GO is greatly improved. The work develops advanced fire detection and early-warning sensors that provide reliable and continuous signals, which provide more available time for fire evacuation.

Simultaneous enhancement in water flux and removal efficiency during the filtration process remains a big challenge for separation membranes. The porous structure of the filter paper can provide many channels for water transportation, but the separation performance is generally poor. The purpose of this study is to develop a new kind of filter paper consisting of ultralong hydroxyapatite (HAP) nanowires, cellulose fibers (CFs) and double metal oxide (LDO) nanosheets, and to achieve the simultaneous enhancement of both water flux and removal efficiency for high-performance dye separation. In this work, a novel kind of LDO/HAP/CF nanocomposite filter paper consisting of ultralong HAP nanowires and CFs and LDO nanosheets has been developed for rapid water filtration and highly efficient dye adsorption. Positively charged LDO nanosheets can adsorb on the surface of negatively charged ultralong HAP nanowires and embed in the porous networked structure of the LDO/HAP/CF nanocomposite filter paper, which can provide a porous structure for rapid water transportation and can adjust the pore size of the nanocomposite filter paper. As a result, the pure water flux of the LDO/HAP/CF nanocomposite filter paper can be adjusted. The optimized pure water flux of the LDO/HAP/CF nanocomposite filter paper can reach 783.6 L m-2 h-1 bar-1, which is 1.51 times that of the HAP/CF filter paper without LDO nanosheets (518.6 L m-2 h-1 bar-1). More importantly, the adsorption capacity of LDO nanosheets is high for dye molecules, the rejection percentage of Congo red (CR) by the as-prepared HAP/CF filter paper is only 59.8%, and its water flux is 534.7 L m-2 h-1 bar-1. The optimized rejection percentage and water flux of the LDO/HAP/CF nanocomposite filter paper for CR are significantly enhanced (98.3% and 736.8 L m-2 h-1 bar-1, respectively) compared to those of the HAP/CF filter paper. The size of LDO nanosheets has a significant effect on the water flux and dye rejection percentage of the LDO/HAP/CF nanocomposite filter paper. The as-prepared LDO/HAP/CF nanocomposite filter paper is promising for the applications in highly efficient purification of wastewater containing dye molecules.

The dispute over the paternity of western paper is a longstanding problem. In Italy, a country that has a long tradition of papermaking, many cities compete for the leadership in the production of this material; on the other hand, several studies attribute to Fabriano (13th century), a little center in Marche region, the birth of modern paper and its diffusion throughout Europe. During the 14thcentury, the nearby town of Camerino imposed itself on the paper market, triggering a historic rivalry with the manufacture of Fabriano. As scientific studies on these different productions are missing, a comparative, multidisciplinary investigation has been carried out to characterize a set of thirteenth-fifteenth century handmade papers from Camerino-Fabriano area. Several analytical techniques–some non-invasive such as Fourier-transform infrared spectroscopy (FTIR) and portable magnetic resonance (unilateral NMR), joined to micro-destructive ones such as scanning electron microscopy (SEM), 13C CPMAS NMR spectroscopy, thermo-gravimetric analysis (TGA), sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and reverse-phase liquid chromatography (RP-HPLC)–have been employed in order to study the morphology of the paper documents, to identify the substances used in production process and to define their preservation state. Moreover principal component analysis (PCA) has been applied to the spectroscopic data, allowing the clustering of Fabriano documents with respect to Camerino ones and dividing the samples in two sets. This work improves and confirms knowledges on paper production in Marche region, and the experimental data collected highlight similarities and differences between Camerino and Fabriano manufactures.

Inorganic salt modified paper substrates were developed and utilized in microfluidic paper based sampling coupled with potentiometric ion sensors for the determination of heavy metals, such as Cd2+ and Pb2+. The application of paper based sampling without any paper substrate pre-treatment were characterized with super Nernstian response, while the paper substrates with inorganic salt pre-treatment were characterized with standard Nernstian response. The application of inorganic salt modified paper substrates was found advantageous when the cation of the salt in the conditioning solution was the same as the primary cations of the ion-selective electrodes (ISEs). A relatively high concentration of inorganic salts during pre-treatment of the paper substrates, namely Cd(NO3)2 or Pb(NO3)2 with subsequent measurement of cadmium(II) and lead(II), by Cd2+- and Pb2+-ISEs, respectively was needed to sustain Nernstian response of sensors. It was also found that paper substrates facilitate sorption of metal ions onto the paper substrates, with stronger binding strength given to Pb2+ over Cd2+. Moreover, the metal-paper interactions suggest concentration dependent sorption-desorption of metal ion, which can have direct limitations of the use of paper based analytics for the determination of low analyte concentration of heavy metals. Nanyang Technological University The authors would like to thank NTU-India Connect Research Internship Program for financial support of Ms Tharini Saravana Sundaram from Coimbatore Institute of Technology, India.

With the rapid emergence of wearable devices, flexible lithium-ion batteries (LIBs) are much more needed than ever. Free-standing graphene-based composite paper electrodes with various active materials have appealed wide applications in flexible LIBs. However, due to the prone-to-restacking feature of graphene layers, a long cycle life at high current densities is rather difficult to be achieved. Herein, a unique three-dimensional (3D) hierarchically porous NiO micro-flowers/graphene paper (fNiO/GP) electrode is successfully fabricated. The resulting fNiO/GP electrode shows superior long-term cycling stability at high rates (e.g., storage capacity of 359 mAh/g after 600 cycles at a high current density of 1 A/g). The facile 3D porous structure combines both the advantages of the graphene that is highly conductive and flexible to ensure rapid electrons/ions transfer and buffer the volume expansion of NiO during charge/discharge, and of the micro-sized NiO flowers that induces hierarchical between-layer pores ranging from nano-micro meters to promote the penetration of the electrolyte and prevent the re-stacking of graphene layers. Such structural design will inspire future manufacture of a wide range of active materials/graphene composite electrodes for high performance flexible LIBs.

Serish (Eremurus) paste, made of Eremurus genus roots, is a strongly adherent substance which had traditionally been used for book binding and paper restoration in Iran for centuries. The proper pH of Serish and its quality of being reversible after long times has made it a good choice in restoring paper. However, it leaves yellow-brown stains on paper due to its own color, which had negatively affected conservator's desire to make use of this adhesive. Therefore the present study was intended to investigate the process of eliminating color from Serish, as a way of improving its quality for paper restoration. The study adopted solvent extraction method to eliminate color from Serish adherent polysaccharide. Extracted adhesives were coated on paper. Humid-thermal accelerated aging was carried out to investigate the effects of adhesives on pH, color change, tensile strength and cellulose structure of papers. It was found that stabilizing enzyme, using 70% boiling ethanol before extracting adhesive, is an effective method to inhibit enzyme operation and prevent creating new chromophores through enzymatic molecules degradation. This approach, on one hand, is useful in removing color and on the other hand proves effective in increasing pH of adhesives. Furthermore, it leads neither to paper acidification nor to damaging polymeric structure of paper after accelerated aging. The results confirmed that the adhesive extracted from the enzymatic stabilized roots by ethanol provides appropriate pH and color; it also improves the tensile strength of paper and yields more desirable results for conservation of paper-based documents, compared to the other examined samples.

This work presents an unconventional use of capacitively coupled contactless conductivity detector (C4D) for detection of gas absorption by moist paper with potential application for chemical analysis. To be suitable for measuring conductivity of moist paper absorbent, the C4D sensor was therefore designed in planar configuration. A layer of dry filter paper, only 20 mm × 25 mm in size, was placed on the C4D sensor and the device installed inside a specifically designed vaporization chamber. A vial (16 mm i.d., 8 mm high) containing a 150-μL solution of sodium bicarbonate was placed alongside. The filter paper was loaded with 110 μL of deionized water through an injection hole in the cover lid. A 100-μL aliquot of 2 M hydrochloric acid solution was directly dispensed into the vial through a second hole in the lid to generate CO2 gas from the bicarbonate solution. It was observed that the C4D sensor gave real-time response that corresponded to the absorption of the gas and subsequent production of H+ and HCO3− in the moist paper. The monitored signal reached a constant value at 160 s after the addition of the acid. Chemistry of the absorption process and equivalent circuit for the C4D are proposed. Direct measurement of cement powder was chosen to demonstrate the potential use of this device for quantifying the CaCO3 content of the cement. The calibration curve for 0.5–3 mg CaCO3 was linear for signals recorded at 160 s: Vdc = (0.172 ± 0.005) · (mg CaCO3) + (0.016 ± 0.009), with coefficient of determination of 0.9965. Linear calibrations were also observed when the signals were monitored at various time less than 160 s. The limit of quantitation (3 SD of intercept/slope) was 0.17 mg CaCO3. The method provided acceptable precision with %RSD of 4.6 (2 mg CaCO3, n = 10).

Background Surface enhanced Raman scattering (SERS) based on highly sensitive, flexible, solid-state sensors can provide molecular vibrational fingerprints of targeted substances in point-of-care (POC) analysis. Cellulose paper offers many advantages for the build-up of silver and gold nanostructures on a three-dimensional scaffold. Such composites can be made to contain SERS hot spots required for sensitive SERS detection in an active solid-state sensor. Scope and approach In this review, we discuss the key technical issues involved in the fabrication of SERS sensors combining a metallic SERS substrate and a cellulose paper support. We then survey recent literature for methods designed to address these issues with applications to support food safety where POC analysis serves as a valuable tool. Key findings and conclusions Sensitivity of detection is a primal challenge in the development of a paper-based SERS substrate. The fibril structures of paper materials, a suitable modification for improved bonding at the paper-metal interface, and the surface conditions of metal nanostructures all contribute to sensitive SERS performance on paper. Continuing expansion of spectrum collection in a database format, diverse methods for the statistical analyses of Raman spectra, and advanced integration of portable Raman instruments with the mobile tele-networks are critical in the further development of flexible SERS sensor in POC testing of food-borne substances.

Advancements in technology have led to the use of smartphones as biosensor detectors. However, it is difficult to obtain stable color information of colorimetric sensors using multiple smartphones owing to different light conditions and image correction operations. In this study, we attempted color detection of the colorimetric paper chip using smartphone-embedded light-emitting diode (LED) and simple transformation calculation. This method enables the acquisition of stable color information using different smartphones by reducing the influence of external light sources. Moreover, we studied characteristics such as convergence and distinction of detection result details by the manufacturers and smartphones. These findings suggested the necessity of classification criteria for the use of smartphones to achieve optimal detection. In addition, white and black references were used to set the standard for color correction of various light sources. Based on our results, we conclude that this approach presents the possibility of smartphone-based colorimetric detection in practical applications.

The file attached to this record is the author's final peer reviewed version. The Publisher's final version can be found by following the DOI link. The enhancement of fingermarks on thermal paper can be challenging due to background staining caused by polar solvents used in fingermark enhancement techniques such as ninhydrin. This study explored a commercial one-step superglue fuming process, Lumicyano™, and Vacuum Metal Deposition (VMD) to develop fingermarks on this substrate and overcome this issue. Different sequential treatments involving Lumicyano™ and a combination of VMD methods were investigated with varying degrees of success with some sequences being highly sensitive. The VMD processes, however, were observed to generally be more effective at enhancing marks, whereas Lumicyano™ provided little or no benefit on this paper type. The results indicate that Lumicyano™ is only beneficial as a pre-treatment when the entire sequence of gold/zinc and silver/zinc is taken to completion. The gold/zinc and silver/zinc VMD processes were optimised on five different thermal papers, and the optimised techniques were then directly compared to determine which was more successful on each thermal paper type as a single treatment.

Point-of-care (POC) detection is crucial in clinical diagnosis in order to provide timely and specific treatment. Combining polyamidoamine (PAMAM) dendrimer, p-phenylene diisothiocyanate (PDITC) and superparamagnetic beads, a novel method to activate the surface of filter paper to bind DNA molecules has been developed. The method is based on the primary amination of the filter paper surface with PAMAM dendrimer, followed by generation of isothiocyanate groups via PDITC, and subsequent repetition of these two steps. Different parameters of the process have been optimized, including probe printing, preparation of target DNAs and detection. The result shows that, due to the highly porous structure of filter paper, high amounts of printed probes, target DNAs and magnetic beads can provide high signal intensities in the detection area via probe/target duplex formation. This method is suitable for rapid, specific and cost-efficient DNA detection on cellulose filter paper. It can be used as a POC device, in particular for diagnosis and treatment management of infectious diseases and identification of antimicrobial drug resistance genes.

Enormous quantities of bagasse are being used as raw material in agro based large integrated pulp and paper mills. Anaerobic technology is an effective means of biodegradation of organic substance in wastewater and energy production of biogas that can be used as an alternative fuel. This study illustrates the effect of HRT on performance of lab scale hybrid upflow anaerobic sludge blanket (HUASB) reactor on treatment of pulp and paper mill bagasse wash water. The lab scale HUASB reactor was designed for an effective volume of 0.013 m3 with bio balls as packing media at the top of reactor and operated under mesophilic condition. After startup period, the reactor was operated with HRTs of 23.55, 15.98, 12.00, 10.03 and 7.97 h for the average influent COD concentrations of 2503.6 mg/L, 3918 mg/L, 5432 mg/L, 6608 mg/L and 7996 mg/L respectively. The results showed that the maximum COD removal efficiencies and TSS removal efficiencies were in the range of 68.60–92.19% and 89.56–94.66% respectively. The minimum and maximum biogas yield of 0.32 and 0.53 m3/kg CODa were obtained at influent concentration of 2503.6 mg/L and 7996 mg/L respectively.

A novel all-in-one paper-based sampling concept for mass spectrometric bottom-up protein analysis is here demonstrated in a chip format integrating instant immunocapture, protein reduction, - alkylation and tryptic digestion all in-device. Conventional laboratory grade filter paper was coated with the polymer 2-hydroxyethyl methacrylate-co-2-vinyl-4,4-dimethyl azlactone (pHEMA-VDM) with a subsequent covalent immobilization of the monoclonal antibody E27 targeting the biomarker human chorionic gonadotropin (hCG). In-device protein reduction and alkylation was optimized with regards to reagent concentration and reaction pH. The sampling concept showed a high degree of performance between 10 and 1000 ng/mL (R2 > 0.99) by a five-point calibration curve sampled with hCG spiked to human serum samples and freshly collected whole blood samples, respectively. LOD (experimentally obtained at 100 pg/mL (2.64 pM/0.9 IU/L)) was demonstrated to be up to ten times lower with more than six times faster sample preparation than what has previously been reported for on-paper analysis of hCG in human serum samples.

The adulteration of herbal medicines by dexamethasone or prednisolone is regarded as a serious problem in many communities. Herein, a novel platform for the separation and quantification of both target steroids in herbal medicines based on electrochemical paper-based analytical devices (ePADs) has been created. The ePAD was composed of Whatman SG81 chromatography paper, 3D-printed devices and a commercial screen-printed electrode. Whatman SG81 silica-coated paper was used for the separation of dexamethasone and prednisolone based on the difference in their partition coefficients during the flow of the mobile phase. The optimal mobile phase was composed of 60% ethyl acetate in cyclohexane and required 7 min for separation. The separated steroids on the paper were then quantified by electrochemical detection using differential pulse voltammetry, in which the 3D-printed devices facilitated the measurement. Analytical detection ranges of 10–500 μg mL−1 were obtained for both dexamethasone and prednisolone (r2 = 0.988 and 0.994, respectively). The limits of detection for dexamethasone and prednisolone were 3.59 and 11.98 μg mL−1, respectively, whereas the limits of quantification were 6.00 and 20.02 μg mL−1, respectively. The amounts of both target steroids derived from real herbal medicine samples determined by the proposed method were comparable to those obtained with assays using standard high-performance liquid chromatography. In addition, a simple evaporation step can be used to increase the concentration of the samples before analysis. These ePADs are simple, low-cost, rapid, and very promising for on-site quantitative detection.

Paper based assays are paving the way to automated, simplified, robust and cost-effective point of care testing (POCT). We propose a method for fabricating three dimensional (3D) microfluidic paper based analytical devices (μPADs) via combining thin adhesive films and paper folding, which avoids the use of cellulose powders and the complex folding sequence and simultaneously permits assays in several layers. To demonstrate the effectiveness of this approach, a 3DμPADs was designed to conduct more assays on a small footprint, allowing dual colorimetric and electrochemical detections. More importantly, we further developed a 3D platform for implementing automated and multiplexed ELISA in parallel, since ELISA, a routine and standard laboratory method, has rarely been used in practical analyses outside of the laboratory. In this configuration, complex and multistep diagnostic assays can be carried out with the addition of the sample and buffer in a simple fashion. Using Troponin I as model, the device showed a broad dynamic range of detection with a detection limit of 0.35 ng/mL. Thus, the developed platforms allow for various assays to be cost-effectively carried out on a single 3D device, showing great potential in an academic setting and point of care testing under resource-poor conditions.

Microfluidic paper-based analytical devices (μPADs) for detection of hydrogen peroxide and glucose have been developed. The analytical performance of colorimetric detection using the conventional starch-iodine color reaction has been significantly improved by using gelatin as the surface modifier which retains the enzyme activity in the dry filter paper strip, improves antioxidability, as well as decreases the strong background signal. Under optimal conditions, the color intensities show a good linear relationship with glucose concentration ranging from 0.5 to 5 mM and hydrogen peroxide concentration from 0.5 to 6 mM, with the detection limit of 0.05 mM and 0.1 mM, respectively. In addition, the accuracy of colorimetric sensor has been successfully assessed in detecting glucose from real human serum samples and recovery value ranges from 95.7% to 97%, which are approaching to the glucose oxidase endpoint. The new colorimetric assay exhibits high sensitivity, good selectivity, acceptable stability and reproducibility. The present approach is promising for monitoring glucose for point of care diagnostic applications, especially in regions with resource-limited settings.

The application of microfluidics for largescale rapid analytics holds great promise in the pharmaceutical diagnostics and analytical chemistry. Here we report a paper based microfluidic substrate designed by the impregnation of Silver nanoparticles. This study demonstrates the achievement of a thousand-fold increase in the successful detection level up to 10 ppb (90.8 nM) by employing Surface Enhanced Raman Spectroscopy (SERS) for the detection of Catechol. The presented sensor exhibits the following main features: (i) high specificity of enzyme (Hemocyanin)-based sensing, (ii) effective SERS sensitivity, (iii) easiness and cost-effectiveness of a paper-based platform. We rationalize these findings using the ab initio DFT simulations using Gaussian 09 whose theoretical calculations reflect the observed experimental Raman peaks.

In this study, an internal circulation-anoxic/aerobic (IC-A/O) process followed by ultrafiltration (UF) and reverse osmosis (RO) system was applied for paper wastewater reclamation. The IC-AO system presented a stable and efficient performance, achieving high removal of chemical oxygen demand (COD), total organic carbon (TOC) and total nitrogen (TN) with methane production rate of 132.8 mL/d. Acute toxicity to Daphnia magna (D. magna) was reduced significantly (83.2%) and the spearman's rank correlation analysis indicated that the toxicity of effluents from each reactor were positively correlated with COD and TOC. Hexadecanoic acid, octadecanoic acid and benzophenone were the main toxic contributors for biological effluent. Microbial community revealed that Anaerolinea was significantly related with organic pollutants. The UF-RO system further removed pollutants and toxicity with the final effluent COD, TOC, ammonium nitrogen (NH4+-N) and TN of 32.6, 18.8, 0.3 and 9.2 mg/L, respectively, which proved that it was feasible for paper wastewater reuse. This study presented an efficient, practical and environmentally competitive system, and paved a foundation for the treatment and reuse of paper wastewater.

Made available in DSpace on 2019-10-06T17:04:31Z (GMT). No. of bitstreams: 0 Previous issue date: 2019-06-01 Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Development and application of a new, simple, inexpensive, and eco-friendly method is presented for the quantification of bumetanide in human urine samples for the detection of doping in sports. The method involves the use of a paper platform and digital image detection and is based on the reaction between bumetanide, p-dimethylaminocinnamaldehyde (p-DAC), and HCl in a methanolic medium, yielding a colored compound in a delimited area on a qualitative filter paper. The concentrations of p-DAC and HCl were optimized by a chemometric experimental design. After the addition of the reagents to the paper, digital images were obtained by scanning in a multifunctional printer and analyzed using the RGB pattern. The linear bumetanide concentration range was 6.90 × 10 −5 –1.37 × 10 −3 mol L −1 with R 2 = 0.993 and the limits of detection (LOD) and quantification (LOQ) were 3.60 × 10 −4 and 1.09 × 10 −4 mol L −1 , respectively. A SPE clean-up step for the samples were required to eliminate the interference of urinary urea. The recoveries obtained varied from 94% to 105%, indicating the absence of significant matrix effects or interferences in urine samples after clean-up step. The proposed method was successfully applied to the analysis of bumetanide in human urine samples. Instituto de Química Universidade Estadual Paulista “Júlio de Mesquita Filho” UNESP, R. Prof. Francisco Degni 55, P.O. Box 355 Instituto de Química Universidade Estadual Paulista “Júlio de Mesquita Filho” UNESP, R. Prof. Francisco Degni 55, P.O. Box 355 CAPES: 001 FAPESP: 2015/21733-1

Micro-cracks are inherently present in concrete, leads to debilitation of structures. Methods used for managing micro-cracks have a certain degree of toxicity and also possesses certain drawbacks that made them not completely efficient. Bacterial technique when used in fresh concretes results in calcite precipitation in voids and consequently improves the strength and lowers permeability of concrete. Bio- cement is the combination of Bacillus pasteurii 5% and nutrients Urea, Calcium Lactate 95%. In this study by adding 0.5, 1, 1.5 and 2% Bio- cement by weight of cement and observed compressive strength, flexural strength values after 7 and 28 days of curing for M25 grade of concrete.

Microfluidic paper-based analytical devices (μPADs) as a potentially powerful analytical platform have recently gained significant attention for on-site monitoring of heavy metal ions, which are one of the most significant environmental concern because of non-degradability and high toxicity. The commonly applied μPADs suffers from some defects, such as heterogeneous deposition of reagent, resulting in poor detection limits and low sensitivity. So, in this work, a three-dimensional origami μPAD combined with PVC Membrane was developed, which can manage problems of movement of colored products or leaching out the dye and leading to color heterogeneity in the detection zones. Furthermore, a waste layer was added to μPAD for loading of more amounts of the analyte, which results in improvement of detection limit. As a proof of concept, the μPAD was used for the analysis of Cu2+ ion. For this purpose, pyrocatechol violet and chrome azurol S as colorimetric reagents were doped into PVC membrane and injected in the detection zone. The proposed μPAD was presented good linearity in the ranges of 5.0–1400.0 and 5.0–200.0 mg L−1, and the limits of detections of 1.7 and 1.9 mg L−1 in presence of chrome azurol S and pyrocatechol violet, respectively.

Polygalacturonase (PG) activity in plants can serve as an important index for plant disease. However, the conventional method to detect PG activity is a complex process and requires a skilled technician and expensive analytical equipment. In this study, a paper-based colorimetric sensor was developed based on the principle of the ruthenium red (RR) dye method for easy and simple measurement of PG activity. The proposed paper-based sensor has a three-layer structure for detection of PG activity in samples. The sensor sensitivity was enhanced by optimizing the pH of the sodium acetate buffer used in polygalacturonic acid (PGA)-RR complex formation and the reaction temperature for PG and the PGA-RR complex. Further, for quantitative analysis of PG activity, Delta RGB analysis was conducted to detect color changes in the sensing window of the sensor. Results presented that the linear measurement range of the paper sensor was 0.02-0.1 unit with the limit of detection of 0.02 unit, which showed a similar detection range, but a lower detection limit, compared to the spectrophotometry. Furthermore, PG activity based on culture condition was measured using samples from Sclerotium cepivorum to verify the potential application of the developed paper-based sensor in the field. The measured activity showed no statistically significant difference from the values obtained from the spectrophotometry at 95% confidence level. Therefore, the paper-based colorimetric sensor can be used to predict plant diseases in Allium crops during the stage of pathogen invasion, potentially contributing to the improvement of crop production.