Polystyrene Beads Research Articles

Assessment of Different Properties of Lightweight Concrete using Expanded Polystyrene Beads Extracted from Thermocol Wastage

Nepal is facing the problem of thermocol wastage, especially in the damping site nearby the urban areas. The thermocol wastage were crushed by a hammer and the extracted expanded polystyrene (EPS) beads was used as aggregates to produce the lightweight concrete. The content of EPS beads was 0, 20, 30, 40, 50, and 60 % by the total volume. Mechanical properties like density, different strengths, and Young’s modulus were experimentally evaluated on ranging percentages of EPS. The 28-day compressive, flexural, splitting tensile strengths and Young’s modulus of the control mixture were 59.9 MPa, 5.21 MPa, 4.43 MPa, and 20898 MPa respectively. The decrease on compressive strength was by 62 %, 72 %, 81 %, 88 %, and 93 % respectively for 20 %, 30 %, 40 %, 50 %, and 60 % EPS content respectively. It was 26 %, 41 %, 51 %, 57 %, and 69 % for flexural strength, 46 %, 60 %, 70 %, 80 %, and 88 % for the splitting tensile strength and 45 %, 56 %, 61 %, 70 %, and 77 % for Young’s modulus respectively. Drying shrinkage, freezing and thawing, and water absorption tests were conducted to evaluate the durability of EPS concrete. All properties were compared with the auto-cleaved lightweight concrete (ALC). It revealed that the EPS beads extracted from the thermocol wastage can be re-used to produce the structural and non-structural concrete depending on its percentages. It can easily solve the never-decomposing problems of thermocol wastage. Moreover, ALC can be replaced by EPS concrete for the in-fill and partition walls of the buildings.

Immune defense mechanisms against a systemic bacterial infection in the cat flea (Ctenocephalides felis)

A significant amount of work has been devoted towards understanding the cellular and humoral immune responses in arthropod vectors. Although fleas (Siphonaptera) are vectors of numerous bacterial pathogens, few studies have examined how these insects defend themselves from infection. In this study, we investigated the immune defense mechanisms in the hemocoel of cat fleas (Ctenocephalides felis), currently the most important flea pest of humans and many domestic animals. Using model species of bacteria (Micrococcus luteus, Serratia marcescens, and Escherichia coli), we delivered a systemic infection and measured the following: antimicrobial activity of hemolymph, levels of free radicals resulting from the induction of oxidase-based pathways, number of circulating hemocytes, phagocytosis activity of circulating hemocytes, and in vivo bacteria killing efficiency when phagocytosis activity is limited. Our results show that the antimicrobial activity of flea hemolymph increases in response to certain species of bacteria; yet, a systemic infection with the same bacterial species did not influence levels of hydrogen peroxide (H2O2), a reactive intermediate of oxygen, at the same time. Additionally, the number of circulating hemocytes increases in response to E. coli infection, and these cells display strong phagocytic activity against this bacterium. Moreover, limiting phagocytosis by injecting polystyrene beads subsequently increases flea susceptibility to E. coli infection when compared to injury controls; however, impairing the cellular immune response itself did not increase flea susceptibility to infection when compared to untreated fleas. Overall, this work yields significant insight into how fleas interact with bacterial pathogens in their hemocoel, and suggests that cellular and humoral immune responses cooperate to combat systemic bacterial infections.

Sensitive Label‐Free Immunoassay by Colorimetric Plasmonic Biosensors Using Silver Nanodome Arrays

The sensitive direct detection of biomolecules is demonstrated by a colorimetric plasmonic biosensor utilizing the surface colors of plasmonic metasurfaces named Ag nanodome arrays. The Ag nanodome arrays consist of polystyrene bead monolayers coated with Ag thin films whose surface colors are optimized by changing the size of the polystyrene beads. The bulk refractive index sensitivity of colorimetric detection evaluated using the hue angle is 590° RIU−1 (RIU: refractive index unit). For selected geometry, the refractive index resolution (5.0 × 10−5 RIU) obtained by colorimetric detection surpasses that of spectroscopic detection evaluated via the dip wavelength in the reflection spectrum. The numerical simulations predict an enhanced sensing performance when the hue angle of the surface colors of the Ag nanodome arrays changes from 300° to 200°, corresponding to changes in the dip wavelength from 570 to 600 nm in the reflection spectra. Furthermore, the detection sensitivity of the biomolecules is characterized using a direct IgG immunoassay format. The detection limit of the IgG concentration is as low as 134 pM using simple colorimetric detection. The feasibility of sensitive label‐free immunoassays using a colorimetric plasmonic biosensor is expected to accelerate the development of highly sensitive and reliable smartphone‐based plasmonic biosensors.

Label-free single-cell counting and characterization in the GHz-range

Abstract We demonstrate operation of a micropore based flow cytometer in the radio-frequency range. Apart from simply counting micron sized particles, such as cells, with close to nano-second resolution this counter offers the additional benefit of delivering insight into the intracellular environment. Such non-invasive screening of the cell’s interior based on analysing amplitude and phase of the signal is helpful in characterizing the biological activity of cells. In detail we are using heterodyne mixing to demodulate the temporal impedance changes, which are induced by cells translocating through a micropore embedded in a radio-frequency circuit. This allows us to measure every amplitude and phase modulation induced by a translocation event. Herein, we compare the Jurkat cells (human T lymphocytes) recordings with a control group of polystyrene beads. As the cells are measured on a single cell level, the variations on the measured amplitude and phase signals are used, herein, to sense morphological cell changes in real time.

Plasmofluidic-Based Near-Field Optical Trapping of Dielectric Nano-Objects Using Gold Nanoislands Sensor Chips.

Near-field optical manipulation has been widely used for guiding and trapping nanoscale objects close to an optical-active interface. This near-field manipulation opens opportunities for next-generation biosensing with the capability of large-area trapping and in situ detection. In this article, we used the finite element method (FEM) to analyze the motion mechanism of nano-objects (50-500 nm) in the near-field optics, especially localized surface plasmon resonance (LSPR). The size-dependent optical forces and hydrodynamic forces of subwavelength nanoparticles (<500 nm) in different hydrodynamic velocity fields were calculated. When the strength of the local electric field was increased, LSPR with two-dimensional gold nanoislands (AuNIs) showed improved capability for manipulating nano-objects near the vicinity of the AuNI interface. Through the experiments of in situ interferometric testing 50-500 nm nano-objects with constant number concentration or volume fraction, it was confirmed that the local plasmonic near-field was able to trap the dielectric polystyrene beads smaller than 200 nm. The plasmofluidic system was further verified by testing biological nanovesicles such as exosomes (40-200 nm) and high- and low-density lipoproteins (10-200 nm). This concept of direct dielectric nano-objects manipulation enables large-scale parallel trapping and dynamic sensing of biological nanovesicles without the need of molecular binding tethers or labeling.

Subtle ecosystem effects of microplastic exposure in marine mesocosms including fish

For two months, communities in 5.8 m3 outdoor marine mesocosms were exposed to 700 μm sphere-shaped polystyrene (PS) beads in dosages between 0.08 and 80 g/m2. Barnacle (Semibalanus balanoides) densities were reduced at dosages of 0.8 g/m2 onwards without following a standard dose response curve. Lugworms and fish (Solea solea) ingested PS-beads without accumulating them. Lugworms (Arenicola marina) ingested the beads nonselective with the sediment without negative effects. The fish seemed to ingest the plastics only occasionally and at the final sampling day even in the highest dosed mesocosms (>30 beads/cm2) only 20% contained plastic. The condition index of the fish was slightly reduced in mesocosms with dosages of 0.8 g/m2 onwards. No difference in condition was found between fish with and without ingested plastic across mesocosms, illustrating the difficulty to relate plastic ingestion with condition from field data. The fish also ingested mollusks with shells exceeding the size of the PS-beads. Bivalves rejected the PS-beads as pseudofeces, without obvious impact on their condition. Mussel's (Mytilus edulis) pseudofeces present an effective matrix to monitor microplastic presence in the water column. Species richness and diversity of the pelagic and benthic community were not affected although, a trend was found that the lower microplastic dosages had a positive effect on the total abundance of benthic invertebrates. In general, the observed effects at even the highest exposure concentrations were that subtle that they will be obscured by natural variation in the field. This underlines the importance of experiments under semi-field conditions for meaningful assessment of the ecological impact of microplastics. This study was performed with the real life, non-toxic, sphere-shaped polystyrene beads as were lost during an actual spill near the Dutch Wadden sea in January 2019. We recommend future mesocosm studies with other types of microplastics, including microfibers, weathered microplastics from sea, and smaller sized particles down to nanoplastics.

Identification of Single Yeast Budding Using Impedance Cytometry with a Narrow Electrode Span.

Impedance cytometry is wildly used in single-cell detection, and its sensitivity is essential for determining the status of single cells. In this work, we focus on the effect of electrode gap on detection sensitivity. Through comparing the electrode span of 1 µm and 5 µm, our work shows that narrowing the electrode span could greatly improve detection sensitivity. The mechanism underlying the sensitivity improvement was analyzed via numerical simulation. The small electrode gap (1 µm) allows the electric field to concentrate near the detection area, resulting in a high sensitivity for tiny particles. This finding is also verified with the mixture suspension of 1 µm and 3 µm polystyrene beads. As a result, the electrodes with 1 µm gap can detect more 1 µm beads in the suspension than electrodes with 5 µm gap. Additionally, for single yeast cells analysis, it is found that impedance cytometry with 1 µm electrodes gap can easily distinguish budding yeast cells, which cannot be realized by the impedance cytometry with 5 µm electrodes gap. All experimental results support that narrowing the electrode gap is necessary for tiny particle detection, which is an important step in the development of submicron and nanoscale impedance cytometry.

The single and combined effects of mercury and polystyrene plastic beads on antioxidant-related systems in the brackish water flea: toxicological interaction depending on mercury species and plastic bead size

Plastics are considered as a major threat to marine environments owing their high usage, persistence, and negative effects on aquatic organisms. Although they often exist as mixtures in combination with other pollutants (e.g., mercury (Hg)) in aquatic ecosystems, the combined effects of plastics and ambient pollutants remain unclear. Therefore, in the present study, we investigated the toxicological interactions between Hg and plastics using two Hg species (HgCl2 and MeHgCl) and different-sized polystyrene (PS) beads (diameter: 0.05, 0.5, and 6-μm) in the brackish water flea Diaphanosoma celebensis. The single and combined effects of Hg and PS beads on mortality were investigated, and changes in the antioxidant system and lipid peroxidation were further analyzed. After 48-h exposure to single Hg, HgCl2 induced a higher mortality rate than MeHgCl. The combined exposure test showed that 0.05-μm PS beads can enhance the toxicity of both the Hg species. The expression of GST-mu, glutathione S-transferease (GST) activity and malondialdehyde (MDA) content increased significantly after exposure to Hg alone (HgCl2 or MeHgCl) exposure. Combined exposure with PS beads modulated the effects of Hg on the antioxidant system depending on bead size and the Hg species. In particular, the 0.05-μm beads significantly increased the expression level of GST-mu, GST activity and MDA content, regardless of Hg species. These findings suggest that toxicological interactions between Hg and PS beads depend on the type of Hg species and the size of PS beads; nano-sized 0.05-μm PS beads can induce synergistic toxicity with Hg.

Studying the Interaction Behavior of Protein Coronated Gold Nanorods with Polystyrene Nanoplastics

AbstractThe formation of protein corona and their modulatory effects on the physicochemical and biological activity of the nanomaterial is well established. The active protein corona on the nanoparticles can further mediate interactions with trace amounts of exogenous entities present in the systemic circulation. In the present study, we utilize an in vitro simulation system wherein, protein corona is strategically engineered by varying the serum concentration on a model nanoparticle i. e. cationic‐gold nanorods (GNRs). Quantitative analysis indicated that the 4 nm cationic GNRs can accumulate as high as ∼1 mg/mL protein corona upon incubation with serum. The size distribution pattern of the bound corona and their subsequent impact on the physicochemical properties of GNRs were determined. To understand how these coronated nanorods would interact with a potent pollutant, the second layer of interaction was further introduced by interacting the coronated‐GNRs with 1 ppm nanoplastic. The impact of differently functionalized polystyrene beads (plain, aminated, and carboxylated) on the core size, hydrodynamic diameter, surface charge, and optical properties of the coronated GNRs is highlighted. A complex interplay of several interactive forces and amino acid‐mediated binding of the GNRs to the styrene and benzene rings of the nanoplastic leads to the formation of a coronated‐GNR‐PS complex (&gt;400 nm). Further, upon subjecting the hybrid‐conjugate system to acidic pH conditions (pH‐5.6 and 4.3), a considerable increase in protein leaching was observed. The novel approach of the present study aims to look into the layered interactive patterns for nanomaterials that are utilized for in vivo applications.

Parallel Impedance Cytometry for Real-Time Screening of Bacterial Single Cells from Nano- to Microscale.

The benefits of impedance cytometry include high-throughput and label-free detection, while long-term calibration is required to remove the effects of the detection circuits. This study presents a novel impedance cytometry system, called parallel impedance cytometry, to simplify the calibration and analysis of the impedance signals. Furthermore, target objects can be detected even when benchmarked against similar objects. Parallel dual microchannels allow the simultaneous detection of reference and target particles in two separate microchannels, without the premixing of reference and target suspensions. The impedance pulses of both can appear separately on the opposite sides of the same time series, which have been verified via simulation and experimental results. Raw impedance signals can easily distinguish target particles from reference ones. Polystyrene beads with different sizes ranging from nano- to microscale (e.g., 500, 750 nm, 1, 2, 3, and 4.5 μm) confirm the nanosensitivity of the system. In addition, the detection of antibiotic-treated Escherichia coli cells demonstrates that our system can be used for the quantitative assessment of the dielectric properties of individual cells, as well as for the proportion of susceptible cells. Through benchmarking against untreated E. coli cells in the other channel, our method enables the discrimination of susceptible cells from others and the comparison of susceptible and insusceptible cells in the target suspension. Those findings indicate that the parallel impedance cytometry can greatly facilitate the measurement and calibration of the impedances of various particles or cells and provide a means to compare their dielectric properties.

Visible-light photocatalytic degradation of dyes by TiO[formula omitted]–Au inverse opal films synthesized by Atomic Layer Deposition

TiO2–Au composite planar films and inverse opals were synthesized by Atomic Layer Deposition (ALD) using Direct Liquid Injection for TiO2 deposition and for the injection of preformed Au nanoparticles (NPs). A few nanometers thick layer of TiO2 was deposited after the Au NPs. Thermal annealing at 380 °C allowed to remove the polystyrene beads template and to form anatase TiO2.The obtained inverse opals have a layered structure of hollow TiO2 spheres interconnected by channels formed at the template beads contacts. Au NPs are homogeneously distributed on the surface. Their localized surface plasmon resonance (SPR) at 587 nm confirm that they are embedded in TiO2. These photocatalysts were tested for the degradation of methylene blue solutions under visible-light illumination. A significant photocatalytic effect is reported with a 95% degradation after 7 h of exposure only for the composite inverse opal. This results from the transfer of hot electrons from the NPs excited at their SPR to the conduction band of TiO2. They generate reactive oxygen species at the surface of TiO2 which are involved in the initial stage of MB degradation. These results highlight the potential of ALD for the fabrication of complex composite structures for application in photocatalysis.

Sperm selection with Annexin-V coated polystrene bead technique (APB-Tech): A novel and reliable method for the microscopic selection of viable and non-apoptotic sperm to be used for intracytoplasmic sperm injection

Infertility is a growing health problem that affects 20% of couples who want to conceive. ‘Intracytoplasmic sperm injection’ (ICSI) is a commonly used assisted reproduction treatment technique that offers the couples to overcome a wide variety of infertility reasons, including female, male and unexplained infertility. A crucial step in ICSI is choosing the correct sperm with the highest potential to form a healthy embryo and thus a healthy offspring. The sperm selection strategies aim to obtain a sperm population with better motility and morphology, which are insufficient to predict a sperm's reproductive potential. The elimination of apoptotic sperms, which is shown to be higher in infertile males and which is shown to affect embryo development and reproductive cohort significantly should also be included in the selection strategies. Among all sperm selection methods, there are only a few which can eliminate apoptotic sperm, but because they need extra types of equipments, a long training period, and high costs, they couldn't find place in the most commonly used techniques in an IVF lab. Selecting the non-apoptotic sperm cells will help us choose a sperm that is more likely to be chosen by the natural selection mechanisms and thus will help to mimic the natural conception more.The study aimed to develop a novel, easy and a harmless individual sperm selection technique to enable choosing non-apoptotic viable sperm cells via light microscopy without any need for extra equipment, education and cost to be used for ''ICSI’. The technique is based on the binding ability of Annexin-V covered polystrene beads to the externalized phosphatidylserine at the outer leaflet of an apoptotic sperm's plasma membrane.After Annexin-V covered polystyrene beads were prepared, beads obtained were attached to BALB-c mice sperm, and the technique is optimized to obtain the most efficient attachment conditions. The results are then compared with the results of four well-known reliable apoptosis detection techniques to test the validity and sperm survival test to test the toxicity of the technique.The method is proven to be '''reliable’ by comparing it with the results of well-known techniques, including TUNEL and SCSA (sperm chromatin structure assay), and '''safe’ by showing its non-toxicity via sperm survival test (SST). In addition, the method enables the selection of sperm cells more closer to naturally-chosen ones from a pool of sperm that should not be allowed to be randomly chosen during microinjection. To date, it was impossible to distinguish a non-apoptotic sperm without harming it or without needing additional equipment other than a routine IVF lab and extra training other than routine andrology work.The technique is named as ‘Annexin-V coated polystyrene bead technique (APB-Tech)'. Based on our results, further studies on APB-Tech should be focused on the possible improvement of ICSI outcomes and, thus, success rates.

Growth and prevalence of antibiotic-resistant bacteria in microplastic biofilm from wastewater treatment plant effluents

It is accepted that Microplastic (MP) biofilms accumulates antibiotic-resistant bacteria (ARB) and antibiotic-resistant genes (ARGs) in water. ARB/ARGs and MPs are emerging pollutants of concern due to various associated health risks. The objective of this study was to 1) investigate the ARB community in a pilot-scale wastewater treatment plant (WWTP) effluent, 2) to study and visualize the ARB/ARGs in MP biofilm grown in WWTP effluent and tap water, and 3) to analyze microplastic adherent ARB/ARGs in the biofilm and planktonic ARB/ARGs in the filtrate under controlled conditions. Results indicated the dominance of Pseudomonas, Aeromonas, and Bacillus among isolated ARB in WWTP effluent. Representative resistance strains were incubated in 300 mL water containing commercial polystyrene beads of 300550 μm diameter (MP) in a series of batch experiments. Microbiological, molecular, and microscopic analyses were performed by enumeration, 16srRNA, real-time polymerase chain reaction (qPCR), and Field Emission-Scanning Electron Microscopy (FEG-SEM) techniques. The analyzed viable ARB indicated an increasing trend in MP biofilms between days 3 and 5. It further decreased on days 7 and 9. The prevalence of ARB in the filtrate and MP biofilm varied as a function of time and TOC level, while no significant impacts were observed for minor temperature variation, low antibiotic pressure, and increased MP mass with few exceptions. Relative abundance of ARGs (vanA, sul1) and integron integrase gene (intl1) in MP biofilm were significantly different across different TOC levels, time, and antibiotic pressure. ARGs and intl1 were detected in the MP biofilm in tap water and WWTP effluent on day 30.

Tilt-angle stimulated Raman projection tomography.

Stimulated Raman projection tomography is a label-free volumetric chemical imaging technology allowing three-dimensional (3D) reconstruction of chemical distribution in a biological sample from the angle-dependent stimulated Raman scattering projection images. However, the projection image acquisition process requires rotating the sample contained in a capillary glass held by a complicated sample rotation stage, limiting the volumetric imaging speed, and inhibiting the study of living samples. Here, we report a tilt-angle stimulated Raman projection tomography (TSPRT) system which acquires angle-dependent projection images by utilizing tilt-angle beams to image the sample from different azimuth angles sequentially. The TSRPT system, which is free of sample rotation, enables rapid scanning of different views by a tailor-designed four-galvo-mirror scanning system. We present the design of the optical system, the theory, and calibration procedure for chemical tomographic reconstruction. 3D vibrational images of polystyrene beads and C. elegans are demonstrated in the C-H vibrational region.

Machine learning-based impedance system for real-time recognition of antibiotic-susceptible bacteria with parallel cytometry

Impedance cytometry has enabled label-free and fast antibiotic susceptibility testing of bacterial single cells. Here, a machine learning-based impedance system is provided to score the phenotypic response of bacterial single cells to antibiotic treatment, with a high throughput of more than one thousand cells per min. In contrast to other impedance systems, an online training method on reference particles is provided, as the parallel impedance cytometry can distinguish reference particles from target particles, and label reference and target particles as the training and test set, respectively, in real time. Experiments with polystyrene beads of two different sizes (3 and 4.5 µm) confirm the functionality and stability of the system. Additionally, antibiotic-treated Escherichia coli cells are measured every two hours during the six-hour drug treatment. All results successfully show the capability of real-time characterizing the change in dielectric properties of individual cells, recognizing single susceptible cells, as well as analyzing the proportion of susceptible cells within heterogeneous populations in real time. As the intelligent impedance system can perform all impedance-based characterization and recognition of particles in real time, it can free operators from the post-processing and data interpretation.

A Solid Alkylation: Highly Recyclable, Flow Chemistry‐Ready, Resin‐Supported Thioimidazoliums Alkylate Sulfur‐Centered Nucleophiles

AbstractA series of readily regenerable thioimidazolium‐based ionic liquids, which can transfer alkyl groups to nucleophiles, are immobilized on crosslinked polystyrene beads. Different alkyl groups can be loaded onto the resin, highlighting the tunability of the material. The efficiency of these materials is demonstrated by their screening against a series of nucleophiles, showing a particular preference for thiols. Finally, these materials were evaluated for use under continuous flow conditions. The flexibility, ease of use, safety, and recyclability of these alkylating resins shows promise for their use in large scale and automated applications.

Modulation of ecdysteroid and juvenile hormone signaling pathways by bisphenol analogues and polystyrene beads in the brackish water flea Diaphanosoma celebensis

Owing to its high production and world-wide usage, plastic pollution is an increasing concern in marine environments. Plastic is decomposed into nano- and micro-sized debris, which negative affect reproduction and development in aquatic organisms. Bisphenol A (BPA), an additive of plastic, is released into the water column upon plastic degradation, and is known as a representative endocrine-disrupting chemical. However, the reproductive effects of plastics and bisphenols at the molecular level have not yet been explored in small marine crustaceans. In this study, we investigated the effects of polystyrene (PS) beads (0.05, 0.5, and 6 - μm) and bisphenol analogues (BPs; BPA, BPS, and BPF) on reproduction and development of small marine crustaceans. Effects on transcriptional changes in ecdysteroid and juvenile hormone (JH) signaling pathway-related genes were examined in the brackish water flea Diaphanosoma celebensis exposed to PS beads and BPs for 48 h. As results, BPs and PS beads delayed emergence time of first offspring, and increased fecundity in a concentration-dependent manner. BPs differentially modulated the expression of ecdysteroid and JH signaling pathway-related genes, indicating that BP analogs can disrupt endocrine systems via mechanisms different from those of BPA. PS beads was also changed the gene expression of both pathway, depending on their size and concentration. Our findings suggest that BP analogues and PS beads disrupt the endocrine system by modulating the hormonal pathways, affecting reproduction negatively. This study provides a better understanding of the molecular mode of action of BPs and PS beads in the reproduction of small crustaceans.

Polystyrene microplastic particles in combination with pesticides and antiviral drugs: Toxicity and genotoxicity in Ceriodaphnia dubia

Freshwater ecosystems are recognized as non-negligible sources of plastic contamination for the marine environment that is the final acceptor of 53 thousand tons of plastic per year.In this context, microplastic particles are well known to directly pose a great threat to freshwater organisms, they also indirectly affect the aquatic ecosystem by adsorbing and acting as a vector for the transport of other pollutants (“Trojan horse effect”). Polystyrene is one of the most widely produced plastics on a global scale, and it is among the most abundant microplastic particles found in freshwaters. Nevertheless, to date few studies have focused on the eco-genotoxic effects on freshwater organisms caused by polystyrene microplastic particles (PS-MPs) in combination with other pollutants such as pharmaceuticals and pesticides.The aim of this study is to investigate chronic and sub-chronic effects of the microplastic polystyrene beads (PS-MP, 1.0 μm) both as individual xenobiotic and in combination (binary/ternary mixtures) with the acicloguanosine antiviral drug acyclovir (AC), and the neonicotinoid broad-spectrum insecticide imidacloprid (IMD) in one of the most sensitive non-target organisms of the freshwater food chain: the cladoceran crustacean Ceriodaphnia dubia. Considering that the individually selected xenobiotics have different modes of action and/or different biological sites, the Bliss independence was used as reference model for this research. Basically, when C. dubia neonates were exposed for 24 h to the mixtures during Comet assay, mostly an antagonistic genotoxic effect was observed. When neonates were exposed to the mixtures for 7 days, mostly an additive chronic toxic effect occurred at concentrations very close or even overlapping to the environmental ones ranging from units to tens of ng/L for PS-MPs, from tenths/hundredths to units of μg/L for AC and from units to hundreds of μg/L for IMD, revealing great environmental concern.

Thermal performance evaluation of two types of wall panels under dynamic weather conditions

Thermal performance of two types of wall panels were evaluated under dynamic weather conditions. The thermal performance of wall pane ls (61 x 61 cm) prepared in the laboratory with a 5.0 cm extruded polystyrene (XPS) board sandwiched between two 7.5 cm concrete layers and 5.0 cm layer of foam-mortar containing expanded polystyrene (EPS) beads sandwiched between two 7.5 cm concrete layers were evaluated simultaneously in a specially designed air conditioned test box. The thermal transmittance (U-value) and resistance (R-value) of the two wall samples were determined and compared. The thermal transmittance (air to air) of sandwiched XPS concrete and EPS beads foam-mortar concrete wall panel samples are 0.836 and 2.526 W/m2 K, respectively. The corresponding mean thermal resistance values (surface to surface) of the wall panels are 1.142 and 0.292 m2 K/W, respectively. Thermal performance indicates that the wall panel sample with the XPS insulation board sandwiched between concrete is much more effective than the wall panel sample made of foam-mortar containing EPS beads sandwiched between concrete. The results also indicate that the time lag between the maximum exterior surface temperature and the maximum heat transmission on the interior surface is about 4.5 hours for both samples.

Acoustophoretic particle manipulation in hybrid solid/gel resonators

This study presents a proof of concept to demonstrate the ability of ultrasounds to perform acoustophoretic processes in hybrid millifluidic resonators that include channels laterally embedded in extremely soft media with physical properties close to those of liquids. In our experiments, particles are driven by acoustic radiation forces toward hydrodynamic/acoustic equilibrium positions in a similar way to that produced in conventional microfluidic resonators with solid structures; 20 um-sized polystyrene beads immersed in deionized water flow channelized throughout an aqueous-based gel between an inlet and outlet in a resonant chamber while being exposed to ultrasounds at a frequency of 1.54 MHz. The liquid channel formed presents irregular walls and variable geometry defined by the sample injection pressure. Particles collect rapidly along a central line equidistant from the walls, regardless of whether they are parallel or not, as observed for different channel geometries and cross-sectional dimensions. Only when the flow stops, the particles collect in acoustic pressure nodes established with the 2D spatial distribution. These results break the paradigm of solid structures as essential physical elements to support acoustophoresis, demonstrating the ability to produce these processes in media without a consolidated structure. It opens a door to bioprinting applications.