Microwave-assisted and conventional hydrothermal carbonization of lignocellulosic waste material: comparison of the chemical and structural properties of the hydrochars

This study compares the chemical and structural properties of the hydrochars prepared from microwave-assisted and conventional hydrothermal carbonizations of Prosopis africana shell, a waste plant material. The preparation involved heating the raw material in de-ionized water at 200 °C for 5-20 min, and 120-240 min in the microwave and conventional oven respectively. The prepared hydrochars were characterized using the scanning electron microscope, nitrogen sorption measurement, Fourier transform infrared spectroscopy, CHN analyzer, thermogravimetric analysis, and nuclear magnetic resonance. The results showed that the microwave-assisted hydrothermal carbonization process is fast in the carbonization of the Prosopis africana shell as shown by the level of conversion attained within the short time. This study presents new data on the comparison of the hydrochars from microwave-assisted and conventional hydrothermal carbonization processes of the same lignocellulosic material in terms of their properties

Biomass derived mesoporous carbon monoliths via an evaporation-induced self-assembly

Evaporation-induced self-assembly has been applied in the synthesis of crack-free mesoporous carbon monolith with good mechanical stability using a waste plant material as carbon precursor and triblock copolymer F127 as template. The carbon monolith was characterized using transmission electron microscopy, scanning electron microscopy, nitrogen adsorption–desorption measurement, X-ray diffraction and Fourier transform infrared spectroscopy. The results showed that the carbon monolith is mesoporous, has a surface area of 219 m²/g, and a narrow pore size distribution of 6.5 nm

Microwave-assisted hydrothermal carbonization of rapeseed husk: A strategy for improving its solid fuel properties

Hydrothermal carbonization of a waste biomass material is a green and promising technique for improving its solid fuel properties, which does not require pretreatment procedure such as drying of the biomass. In this study, hydrothermal carbonization of rapeseed husk, a waste plant material was carried out under microwave heating and the effect of process parameters, such as reaction temperature and residence time on the mass yields and energy properties of the hydrochars was studied. The procedure involved the heating of the feedstock in deionized water in a microwave oven at temperatures of 150 to 200 °C for a specified period of time. The results indicated that the mass yields decreased, as the reaction temperature and residence time were increased, which led to improvement in the energy properties of the prepared hydrochars. The reaction was rapid within the first 20 min, and stabilized afterwards. The energy properties of the prepared hydrochars are consistent with previous studies, showing that the hydrochars have the potential of being used as solid fuel. The structural and morphological analysis carried out revealed that the feedstock was transformed during the process

Characterization of energy-rich hydrochars from microwave-assisted hydrothermal carbonization of coconut shell

In this study, microwave-assisted hydrothermal carbonization of waste coconut shell (feedstock) is reported. It is a thermo-conversion technique in which the feedstock was transformed into energy-rich carbonaceous material under mild conditions. The process was conducted in a microwave oven by heating the waste coconut shell in deionized water inside a pressurized vessel. The effects of different process conditions on the product yields, and the energy properties of the hydrochars were studied by varying the reaction temperature from 150 to 200 °C and residence time from 5 to 30 min. The results showed that there was transformation of the feedstock in the process due to the decarboxylation, dehydration, and demethanation reactions. This led to changes in the chemical and structural compositions, as well as increase in the energy properties of the prepared hydrochars. The higher heating value increased from 15.06 MJ/kg in the feedstock to 19.76 MJ/kg in the hydrochar. The energy properties of the hydrochars prepared in this study showed that microwave-assisted hydrothermal carbonization process could be a technique for converting waste coconut shell into high value-added product

Microwave-assisted hydrothermal synthesis of carbon monolith via a soft-template method using resorcinol and formaldehyde as carbon precursor and pluronic F127 as template

A new microwave-assisted hydrothermal synthesis of carbon monolith is reported in this work. The process uses microwave heating at 100 °C under acidic condition by employing a triblock copolymer F127 as the template, and resorcinol–formaldehyde as the carbon precursor. Scanning electron microscopy, Fourier transform infrared spectroscopy, nitrogen sorption measurements, transmission electron microscopy, X-ray studies and thermogravimetic analysis were used to characterize the synthesized material. The carbon monolith is crack-free, mesoporous and has a high surface area of 697 m²/g. The results demonstrate that the microwave-assisted hydrothermal synthesis is a fast and simple approach to obtain carbon monoliths, as it reduces effectively the synthesis time from hours to a few minutes which could be an advantage in the large scale production of the material

Electrochemical immunoassay for the detection of stress biomarkers

A rapid electrochemical immunoassay method was developed to detect and measure stress biomarkers (cortisol and cortisone) in two biological samples (Zebrafish whole-body and artificial saliva). This methodology utilizes an immunoassay approach taking advantage of the lock and key mechanism that is related to the antibody-antigen interaction depending on the reliable immobilization of the antibody labelled with ferrocene tags (Ab-Fc) on a modified tin-doped indium oxide (ITO) electrode using electrochemical instrumentation to build a POC platform. The limit of detection (LOD) obtained for this biosensor was 1.03 pg ml−1 for cortisol and 0.68 pg ml−1 for cortisone, respectively. The correlation coefficient was 0.9852 and 0.9841 for cortisol and cortisone, respectively with a linear concentration from (0-50 ng ml−1) which covers the standard levels of stress hormones in both selected biological samples. The incubation time was investigated and 30 min was found to be the optimum incubation time. This time would be acceptable for the POC system as total process time can be determined within 35 min

Controlling the nanotoxicity of polyelectrolyte-functionalized titania nanoparticles

This study gives important insights of the various factors controlling the nanotoxicity of titania nanoparticles (TiO2NPs). We studied the nanotoxicity of TiO2NPs of various hydrodynamic diameters and crystallite sizes on C. Reinhardtii (microalgae) and S. cerevisiae (yeast) upon illumination with UV/visible light [1]. The cell viability was assessed for a range of nanoparticle concentrations and incubation times. Bare TiO2NPs affect the microalgae viability at much lower particle concentrations than for yeast. We also found an increased nanotoxicity upon illumination with visible light which indicates that they may also interfere with the microalgae photosynthetic system leading to decreased chlorophyll content upon exposure to TiO2NPs. The results indicate that the larger the hydrodynamic diameter of the TiO2NPs the lower is their nanotoxicity, with anatase TiO2NPs generally being more cytotoxic than rutile TiO2NPs. We also prepared a range of polyelectrolyte-coated TiO2NPs using the layer by-layer method and studied their nanotoxicity on yeast and microalgae. The toxicity of the coated TiO2NPs alternates with their surface charge. TiO2NPs coated with cationic polyelectrolyte as an outer layer exhibit much higher nanotoxicity than the ones with an outer layer of anionic polyelectrolyte. TEM images of sectioned microalgae and yeast cells exposed to different polyelectrolyte-coated TiO2NPs confirmed the formation of a significant build-up of nanoparticles on the cell surface for bare- and cationic polyelectrolyte-coated TiO2NPs. The effect is coming from the increased adhesion of cationic nanoparticles to the cell walls. Significantly, coating the TiO2NPs with an anionic polyelectrolyte as an outer layer led to a reduced adhesion and much lower nanotoxicity due to electrostatic repulsion with the cell walls. This suggest a new way of making the TiO2NPs potentially safer for use in different formulations by pre-coating them with anionic polyelectrolytes. Please click Additional Files below to see the full abstract

Dual-functionalised shellac nanocarriers give a super-boost of the antimicrobial action of berberine

We have developed highly efficient antimicrobial nanocarriers for berberine (BRB) based on shellac nanoparticles (NPs) which were surface-functionalised with a surface active polymer, Poloxamer 407 (P407), and the cationic surfactant octadecyltrimethylammonium bromide (ODTAB). These shellac nanocarriers were produced in a two-step process which involves: (i) a pH change from aqueous ammonium shellac solution using P407 as a steric stabilizer in the presence of berberine chloride, and (ii) addition of ODTAB to yield shellac nanocarriers of cationic surface. We determined the BRB encapsulation efficiency and release profiles from such nanocarriers. We explored the antimicrobial action of these nanocarriers at different stages of their preparation which allowed us gain better understanding how they work, fine tune their design and reveal the impact of the nanoparticle coatings on to its antimicrobial effect. The antimicrobial action of BRB loaded within such shellac NPs with cationic surface functionality was examined on three different microorganisms, C. reinhardtii, S. cerevisiae and E. coli and compared with the effect of free BRB as well as non-coated BRB-loaded nanocarriers at the same BRB concentrations. We found that the cationic surface coating of the shellac NPs strongly amplified the efficiency of the encapsulated BRB across all tested microorganisms. The effect was attributed to the increased attraction between the ODTAB-coated BRB-loaded NPs and the anionic surface of the cell walls which delivers locally high BRB concentration. This nanotechnological approach could lead to more effective antimicrobial and disinfecting agents, dental formulations for plaque control, wound dressings, antialgal/antibiofouling formulations and antifungal agents

Magnetic particles-based chemiluminescence immunoassay for progesterone determination

© 2017, Chiang Mai University. All rights reserved. A magnetic particles-based chemiluminescence immunoassay was investigated for progesterone detection by using luminometer. In this work, progesterone was determined based on the competitive binding between progesterone in the sample and progesterone-horseradish peroxidase (HRP) conjugate for a constant amount of rabbit anti-progesterone. Initially, anti-rabbit IgG coated magnetic particles conjugated with primary progesterone antibody were bound to progesterone in the samples. Then, the amount of proge sterone was quantified by reacting with the residual unoccupied antibody sites with HRP-progesterone, followed by HRP substrate (luminol, H 2 O 2 , and p-iodophenol (PIP)) and finally detection of the generated chemiluminescence by a luminometer. The intensity of the emitting light was proportional to the amount of enzyme present (HRP-progesterone) and was inversely related to the amount of unlabeled progesterone in the sample. The optimum conditions for determination of progesterone were obtained at 0.15 μg L -1 magnetic particles, 5.0x10-4 mol L -1 luminol, 5.0 × 10 -3 mol L -1 H 2 O 2 , 1.0 × 10 -3 mol L -1 PIP, and phosphate buffer saline buffer pH 9. The optimal dilutions of both anti-progesterone antibody and HRP-progesterone conjugate were 1:1000. The linear relationship between chemiluminescence intensity (RLU) and various concentrations of progesterone was over the concentration range of 0.5-50.0 μg L -1 . This proposed method had been successfully applied to the evaluation of progesterone in human sera

Interaction of temperature, salinity and extracellular polymeric substances controls trace element incorporation into tufa calcite

The influence of extracellular polymeric substances on carbonate mineral growth in natural settings remains one of the most poorly understood contributors to the growth of non-marine carbonate sediments. The influences of these materials are complicated by their association with living cells creating local microenvironments via metabolism and enzyme production, and by our uncertainty about the extracellular polymeric substances materials themselves. Different mixtures of extracellular polymeric substance molecules may behave in different ways, and differences in the local physical environment may alter how the mixtures influence mineral formation, and even result in different patterns of polymerization. Here, the influence of extracellular polymeric substances on calcite precipitation rate and Mg/Cacalcite in the absence of cells is investigated using extracts of extracellular polymeric substances from temperate fluvial tufa biofilm. The influence is complex, with the concentration of extracellular polymeric substances in solution altering deposition rate and trace element incorporation. Moreover, the results show interaction of the presence/absence of extracellular polymeric substances and both temperature and salinity. However, despite extracting extracellular polymeric substances from the same parent sample, a uniform influence was not found in these experiments, implying that the mixture is sufficiently variable within a sample for microenvironments within the biofilm to either promote or inhibit mineralization. As sedimentologists, we can no longer take the view that extracellular polymeric substances are a bystander material, or that they have a single set of coherent and predictable or intuitive influences. Rather, the emphasis must be on investigating the specific mixtures present in nature, and their complex and dynamic interaction with both mineral surfaces and hydrochemical conditions