Reusable isotype heterojunction g-C3N4/alginate hydrogel spheres for photocatalytic wastewater treatment.

Various visible-light-driven photocatalysts have been studied for practical applications in photocatalytic wastewater treatment via solar irradiation. Among them, g-C3N4 has attractive features, including its metal-free and environmentally friendly nature; however, it is prone to charge recombination and has low photocatalytic activity. To solve these problems, isotype heterojunction g-C3N4 was recently developed; however, the methods employed for synthesis suffered from limited reproducibility and efficiency. In this study, isotype heterojunction g-C3N4 was synthesized from various combinations of precursor materials using a planetary ball mill. The isotype heterojunction g-C3N4 synthesized from urea and thiourea showed the highest photocatalytic activity and completely decolorized Rhodamine B (RhB; 10 ppm) in 15 min under visible-light irradiation. Furthermore, to improve recyclability, isotype heterojunction g-C3N4 was immobilized in alginate hydrogel spheres. The isotype heterojunction g-C3N4/alginate hydrogel beads were used in 10 repeated RhB degradation experiments and were able to maintain their initial photocatalytic activity and mechanical strength. These achievements represent an advance towards practical, sustainable photocatalytic wastewater treatment.

Optimization of method for cross section hydrogels preparation using high-pressure freezing.

High-pressure water freeze fracturing (HPWFF) is a method for preparing water-containing samples such as hydrogels for scanning electron microscopy, in which a sample is placed in a divisible pressure vessel, filled with water, sealed, frozen with liquid nitrogen, then vacuum dried after the vessel is divided. The pressure (about 200 MPa) generated by the phase transition from water to ice is expected to inhibit ice crystal formation that causes large deformation of microstructure in the sample. To maximize the useable sample size, where SEM observation is not affected by ice crystal growth, preparation conditions including the size of pressure vessel were examined in this work. Using pressure vessels 8.0 mm, 5.5 mm and 4.5 mm in diameter, agarose gel, gelatin gel, wheat starch hydrogel, wheat flour noodle and cellulose hydrogel were used to prepare SEM samples. With agarose gel, an area of 3.6 mm in diameter in the 5.5 mm vessel was achieved as the maximum size of the area observable without ice crystal growth. The observable size of other samples was comparable, except for gelatin gel. As a result, observation of the three-dimensional network structure of hydrogels could be performed over a wider range than with the conventional method without shredding or chemical treatment of the samples. Additionally, usability of agarose gel for sample support matrix in HPWFF was demonstrated.

Advanced light-tolerant microalgae-nitrifying bacteria consortia for stable ammonia removal under strong light irradiation using light-shielding hydrogel.

The consortium of microalgae and nitrifying bacteria has attracted attention owing to its advantages, such as energy- and cost-efficiency in terms of using only light irradiation without aeration. However, high light intensity can easily cause photoinhibition of nitrifying bacteria, resulting in process breakdown of the consortium. This challenge limits its practical application in outdoor environment. In a previous study, we developed a "light-shielding hydrogel" which entrapped nitrifying bacteria in carbon black-added alginate hydrogel beads and confirmed its effectiveness of protecting the nitrifying bacteria from intense light up to 1600 µmol photons m-2 s-1. However, the applicability of the light-shielding hydrogel to microalgae-nitrifying bacteria consortia under strong light irradiation has not yet been clarified. In this study, we aimed to establish consortia of Chlorella sorokiniana and nitrifying bacteria immobilised in light-shielding hydrogel and evaluate their nitrification performance under strong light. Three nitrifying bacteria conditions were used: light-shielding hydrogel, hydrogel containing only nitrifying bacteria without carbon black ('hydrogel'), and dispersed nitrifier without immobilisation ('dispersion') as a control. At 1600 µmol photons m-2 s-1, the dispersion afforded a significant decrease in nitrification activity and subsequent process breakdown. In contrast, light-shielding hydrogel achieved complete nitrification without nitrite accumulation and had nitrification rates of approximately nine and two times higher than those for the dispersion and hydrogel conditions, respectively. Based on the overall evaluation, a possible sequence of process breakdown under strong light was also proposed. This study demonstrated for the first time that the light-shielding hydrogel/consortia combination had potential for applications, which require mitigation of photoinhibition under strong light irradiation. Further, it is expected that the proposed method will contribute to realise the practical application of microalgae-nitrifying bacteria consortia in various countries that experience high sunlight intensity due to their location in the sunbelt areas.

The effect of the labile organic fraction in food waste and the substrate/inoculum ratio on anaerobic digestion for a reliable methane yield.

Influence of the labile organic fraction (LOF) on anaerobic digestion of food waste was investigated in different S/I ratio of 0.33, 0.5, 1.0, 2.0 and 4.0g-VSsubstrate/g-VSinoculum. Two types of substrate, standard food waste (Substrate 1) and standard food waste with the supernatant (containing LOF) removed (Substrate 2) were used. Highest methane yield of 435ml-CH4g-VS(-1) in Substrate 1 was observed in the lowest S/I ratio, while the methane yield of the other S/I ratios were 38-73% lower than the highest yield due to acidification. The methane yields in Substrate 2 were relatively stable in all S/I conditions, although the maximum methane yield was low compared with Substrate 1. These results showed that LOF in food waste causes acidification, but also contributes to high methane yields, suggesting that low S/I ratio (<0.33) is required to obtain a reliable methane yield from food waste compared to other organic substrates.

Maximum organic loading rate for the single-stage wet anaerobic digestion of food waste.

Anaerobic digestion of food waste was conducted at high OLR from 3.7 to 12.9 kg-VS m(-3) day(-1) for 225 days. Periods without organic loading were arranged between the each loading period. Stable operation at an OLR of 9.2 kg-VS (15.0 kg-COD) m(-3) day(-1) was achieved with a high VS reduction (91.8%) and high methane yield (455 mL g-VS-1). The cell density increased in the periods without organic loading, and reached to 10.9×10(10) cells mL(-1) on day 187, which was around 15 times higher than that of the seed sludge. There was a significant correlation between OLR and saturated TSS in the sludge (y=17.3e(0.1679×), r(2)=0.996, P<0.05). A theoretical maximum OLR of 10.5 kg-VS (17.0 kg-COD) m(-3) day(-1) was obtained for mesophilic single-stage wet anaerobic digestion that is able to maintain a stable operation with high methane yield and VS reduction.

New instrument for tribocharge measurement due to single particle impacts.

During particulate solid processing, particle-particle and particle-wall collisions can generate electrostatic charges. This may lead to a variety of problems ranging from fire and explosion hazards to segregation, caking, and blocking. A fundamental understanding of the particle charging in such situations is therefore essential. For this purpose we have developed a new device that can measure charge transfer due to impact between a single particle and a metal plate. The device consists of an impact test system and two sets of Faraday cage and preamplifier for charge measurement. With current amplifiers, high-resolution measurements of particle charges of approximately 1 and 10 fC have been achieved before and after the impact, respectively. The device allows charge measurements of single particles with a size as small as approximately 100 microm impacting on the target at different incident angles with a velocity up to about 80 m/s. Further analyses of the charge transfer as a function of particle initial charge define an equilibrium charge, i.e., an initial charge level prior to impact for which no net charge transfer would occur as a result of impact.

Triboelectrification of pharmaceutical powders by particle impact.

Pharmaceutical powders are very prone to electrostatic charging by colliding and sliding contacts with walls and other particles. In pharmaceutical formulation processes, particle charging is often a nuisance and can cause problems in the manufacture of products, such as affecting powder flow, and reducing fill and dose uniformity. For a fundamental understanding of the powder triboelectrification, it is essential to study charge transfer due to a single contact of a particle with a target plane under well-defined physical, mechanical and electrical conditions. In this study, charge transfer due to a single impact of a particle against a stainless steel target was measured for alpha-lactose monohydrate, aspirin, sugar granules and ethylcellulose. The amount of transferred charge is expressed as a function of impact velocity and impact angle as well as the initial charge. The maximum contact area during impact between a particle and a target plane is estimated by an elastic-plastic deformation model. It is found that the transferred charge is a linear function of the contact area. For a given material, there is an initial particle charge for which no charge transfer occurs due to impact. This is found to be independent of impact velocity and angle, and is hence viewed as a characteristic property, which is related to the contact potential difference and tribo-electric series of the sample powders.

Graphical comparison of image analysis and laser diffraction particle size analysis data obtained from the measurements of nonspherical particle systems.

The purpose of this paper is to describe results from the use of a set of Excel macros written to facilitate the comparison of image analysis (IA) and laser diffraction (LD) particle size analysis (psa) data. Measurements were made on particle systems of differing morphological characteristics including differing average aspect ratios, particle size distribution widths and modalities. The IA and LD psa data were plotted on the same graph treating both the weighting and the size unit of the LD psa data as unknowns. Congruency of the IA and LD plots was considered to indicate successful experimental determination of the weighting and size unit .The weighting of the resulting LD psa data (so-called volume-weighted) is shown to be better correlated with IA area-weighted data. The size unit of LD psa data is shown to be a function of particle shape. In the case of high aspect ratio particles characterized by approximately rectangular faces the LD psa data is shown to be a function of multiple particle dimensions being related to IA size descriptors through a simple variation of the law of mixtures. The results demonstrate that successful correlations between IA and LD psa data can be realized in the case of non-spherical particle systems even in the case of high aspect ratio particles; however, the inappropriateness of the application of the Equivalent Spherical Volume Diameter and the Random Particle Orientation assumptions to the interpretation of the LD psa results must first be acknowledged. Correlation permits cross validation of IA and LD psa results increasing confidence in the accuracy of the data from each orthogonal technique.