Determination Of Particle Size Distribution Research Articles

A novel method for predicting coarse aggregate particle size distribution based on segment anything model and machine learning

Particle size distribution (PSD) is an important index property of granular materials. The conventional mechanical sieve analysis for PSD determination is labor-intensive, time-consuming, and inefficient. With the development of computer vision, image-based gradation prediction methods gradually emerge. However, previous studies mainly focused on images where individual aggregate particles are separated from each other without overlapping (i.e., not densely packed together), thus limiting their applicability. This study proposed a novel framework to predict the PSD of densely packed coarse aggregate particles, which is based on visual foundation model and machine learning with appropriate feature engineering. First, the segment anything model, which is one of the visual foundation models, was used for the instance segmentation of the densely packed aggregate particles. Then, the feature engineering was implemented with the segmentation result. The major quantitative indicators related to particle sizes were extracted from each mask, such as the area, the diameter of minimum enclosing circle, and the major axes of the equivalent ellipse of particle contours. Subsequently, the cumulative distribution curves of these indicators were plotted, followed by the data sampling operation on these curves to generate the feature vectors. The artificial neural network (ANN) model was then trained for gradation prediction with each of the feature vectors and the data points extracted from PSD curves used as the inputs and data labels, respectively. The model-training dataset consisted of 8160 different sets of digitally generated particle samples with known PSDs. Finally, verification test results of additional five different groups of digital particle samples and real coarse aggregate samples with known PSDs show that the root mean squared error (RMSE) of predicted aggregate sizes is 1.79 mm and 1.86 mm for digital and real aggregate particle samples, respectively. Therefore, the efficacy and feasibility of the proposed method was validated in terms of predicting the PSD of densely packed coarse aggregates from two-dimensional image information. As compared to the Mask RCNN combined with empirical formula of which the RMSE values were 5.12 mm and 5.84 mm for digital and real aggregate particle samples, respectively, the proposed framework demonstrates improved particle segmentation applicability and better PSD prediction accuracy.

Determination of Particle Size Distribution: Comparison of Standard Hydrometer Method and Laser Diffraction Analysis for Use in Forestry

Laser diffraction analysis is an alternative to standard sedimentation methods designed to determine particle size distribution. In this article, five samples from the forested part of the floodplain of the Svitava River in the Czech Republic were analyzed. Laser diffraction analysis and sedimentation hydrometer method were performed for each sample. The samples were divided according to soil classification into two groups depending on their classification–group A and group B. The results of laser diffraction analysis and hydrometer method were compared. Correlation relationships between both methods were established, and values were recalculated from laser diffraction analysis to the hydrometer method according to correlation equations. The article is a part of the methodology under preparation, which will include the most common soil types in the Czech Republic. This methodology focuses on the use of laser diffraction for the establishment of structures in forest environments using the regional specific standards for particle size distribution determination.

Sediment imaging and factorized Haar wavelet transformation techniques for characterizing particle size distributions of granular soils

The particle size distribution (PSD) significantly influences various mechanical behaviors of granular soils. Advances in automation and camera technology allow for a rapid, green, and accurate PSD determination. This study develops a new sediment imaging system, mainly consisting of a sediment column filled with water and a line-scan camera driven by programmable logic controller, which can automatically capture high-resolution soil segregation images. The soil particles settle through the sediment column and segregate by size, which is scanned to generate sediment images. Naturally, the coarsest particles settle at the bottom of the image, while the finest particles are located at the top. Therefore, the analysis of the sediment image enables the determination of PSD. The higher sediment column, despite of poor operationality, yields better particle segregation quality and thus the more accurate PSD result. This study proposed a factorized Haar wavelet transformation (FHWT) algorithm that can account for less perfect segregation of particles by size, enabling to shorten the height of sediment column. The proposed hardware and FHWT are evaluated by six natural sands with different colors, internal textures, and geological origins. An excellent match between image-based PSDs and sieving-based PSDs are observed. Based on FHWT, four sediment columns with different heights of 2.1 m, 1.5 m, 1.0 m, 0.5 m are tested. The results indicate that columns higher than 1.0 m yield acceptable particle segregation results. Furthermore, the proposed FHWT is also adaptable to process high-resolution images captured by advanced cameras.

Enzymatic hydrolysis of oat core flour improves physiochemical and sensory behaviors for oat milk

The aim of this study was to develop a novel plant-based milk using oat core flour (OCF) as the raw material. OCF was firstly treated with deep liquefaction and saccharification. After that, multienzyme treatments, including protease, lipase, and cellulase hydrolyzations, were optimized and applied. The physicochemical properties of the oat milk were characterized. Particle size distribution and zeta potential determinations showed that neutral protease and lipase could effectively prevent the phase separation of oat milk. The highest absolute zeta potential value and narrower particle distribution were obtained at pH 7. Microstructure analysis showed that neutral protease treatment prevented protein aggregations, whereas the cellulase treatment destroyed the network structures formed by the fibers. Multienzyme treatments decreased the centrifugal sedimentation rate (SR) of OCF and increased the water absorption index (WSI) and the denaturation temperature. Furthermore, multienzyme treatments improved the sensory acceptance of color and apparent viscosity. Above all, this research was of specific significance to the development, application, and industrialization of OCF.

Mechanism of Potassium Release from Feldspar by Mechanical Activation in Presence of Additives at Ordinary Temperatures.

To improve the potassium availability of feldspar at ordinary temperatures, the mechanical grinding and addition of sodium hydroxide/salts were employed to study the effects of mechanical activation and strong alkali addition on particle characteristics, water-soluble potassium, and the available potassium of feldspar. A laser particle size analyzer was utilized for the direct determination of particle size distribution (PSD) using ground samples. The Brunauer-Emmett-Teller (BET) method was employed for specific surface areas. X-ray diffraction (XRD) was employed for structural characterization, scanning electron microscopy (SEM) for morphology exploration, and energy dispersive spectroscopy (EDS) to determine the chemical composition of potassium feldspar powder. The results revealed that the mechanical activation of potassium feldspar could reduce the particle size and produce agglomerated nanoparticles in the later period. The addition of NaOH and sodium salt did not cause agglomeration, and NaOH dissolved the nanoparticles. The water-soluble potassium content of feldspar in each treatment increased during mechanical grinding, from 21.64 mg kg-1 to 1495.81 mg·kg-1, by adding NaOH 5% weight of potassium feldspar powder and to 3044.08 mg·kg-1 by adding NaOH 10% weight with effects different from those of mechanical shaking. By comparison, only 162.93 mg·kg-1 water-soluble potassium was obtained by adding NaOH 5% weight. The dissolved potassium in the former case was significantly higher than in the latter, and the addition of NaOH and sodium salts significantly enhanced the water-soluble potassium contents due to ion exchange. Furthermore, the addition of sodium hydroxide improved the water-soluble potassium due to its mechanochemical action on potassium feldspar. The mechanical energy changed the crystal structure of potassium feldspar, explaining the increase in available potassium. The addition of sodium salts did not promote change in the feldspar's structure, thereby did not raise the available potassium content. The reason for this was related to the mechanochemical action on sodium hydroxide and feldspar, which could promote the dissolution of fine particles, thereby incrementing the available potassium.

Assessment of waste hop (Humulus Lupulus) stems as a biosorbent for the removal of malachite green, methylene blue, and crystal violet from aqueous solution in batch and fixed-bed column systems: Biosorption process and mechanism

The discharge of industrial textile waters into water bodies leads to the accumulation of pollutants which are a serious threat to humans and the environment. The development of an efficient adsorbent for the removal of toxic organic dyes from water is of crucial importance. For that reason, this work aimed to elaborate on the potential application of a biosorbent obtained from waste Humulus lupulus stems (Hlup-BA) for the elimination of malachite green, methylene blue, and crystal violet from aqueous solution in batch and fixed-bed column systems. The Hlup-BA was characterized using chemical composition analysis, by determination of particle size distribution, the point of zero charge (pHpzc), SEM, BET, EDS, XRD, and FTIR. Comprehensive analysis of Hlup-BA adsorption efficiency in a batch study showed that at the optimal conditions (e.g. contact time, 120 min; biosorbent dose, 2 g/L; dye concentration, 100 g/L; pH, 8 and temperature, 298 K), even 98.4 %, 98.8 %, and 98.5 % of MG, MB, and CV were removed, respectively. The results showed that the biosorption process followed pseudo-second-order kinetics. The equilibrium data were modeled using Langmuir, Freundlich, Sips, and Dubinnin-Radushkevich biosorption isotherms. High values of Hlup-BA biosorption capacities obtained from Langmuir isotherm were 398.9 mg g−1, 209.8 mg g−1, and 133.2 mg g−1 for MG, MB, and CV, thus proving Hlup-BA as an excellent biosorbent for removal of the tested dyes. The thermodynamic study indicated that the biosorption of these three dyes on Hlup-BA from aqueous solution is an endothermic, spontaneous, and thermodynamically stable process. The proposed mechanism of the biosorption process covers π-π interactions, electrostatic interactions, and hydrogen bonding. Furthermore, the data obtained by modeling in the fixed-bed column were also successfully correlated with the Thomas, Bohart-Adams, and Yoon–Nelson models. The very good fit of the results obtained in this way will greatly contribute to optimizing the pilot-scale operations for future wastewater treatment. Consequently, Hlup-BA can be an effective, cheap, and environmentally friendly biosorbent to eliminate methylene blue, malachite green, and crystal violet dyes from the aqueous solution in batch and column systems.

Characterization of spray dried cellulose nanofibrils produced by a disk refining process at different fineness levels

Three types of wood pulp feedstocks including bleached softwood kraft, unbleached softwood kraft and old corrugated containers were disk refined to produce cellulose nanofibrils at different fineness levels ranging from 50 to 100%, and the resulting aqueous suspensions of cellulose nanofibrils were spray dried. The spray drying experiments were carried out to examine different processing conditions for the different CNF feedstock types and fines level at various suspension concentrations to produce dry samples with free-flowing powder morphologies. The fineness levels and solids contents of CNF suspensions were set to 80% or more and 1.8% or less, respectively. If the solids content of the CNF solutions was high and the fibrillation level was low, plugging was experienced in the spray head because of the high viscosity of the suspensions, resulting in production of poor-quality powders. In terms of reduction in processing energy, even if the CNF suspension solids content was increased to 1.5 wt.%, the powder quality and the production yields were excellent. It was confirmed that high-quality powder under 20 µm were produced at a 90% fibrillation level of all CNF feedstocks. The resulting dry CNF powders were characterized to determine particle size distributions and morphological properties via a scanning electron microscope and a laser diffraction particle size analyzer. The particle sizes were smaller at higher fibrillation levels and lower solids content of the CNF suspensions. The CNF suspension derived from bleached kraft pulp, the average particle size decreased by 43% and 33% with the lowered solids contents from 1.8 to 1%, and the increased fineness levels from 80 to 100%, respectively.

Microencapsulation of Phenolic Compounds Extracted from Okra (Abelmoschus esculentus L.) Leaves, Fruits and Seeds

Several plants rich in phenolic compounds have many uses in the food and pharmaceutical fields. However, after extraction, these active biomolecules are susceptible to degradation. Microencapsulation is a possible solution to prevent this rapid degradation. In this study, phenolic compounds from the okra Abelmoschus esculentus L’s leaves, fruits and seeds were extracted using microwave-assisted extraction and then microencapsulated via the spray drying technique using maltodextrin combined with pectin (in a ratio of 10:1) as an encapsulation material. The total phenolic content, DPPH scavenging and antimicrobial activities of okra extracts and encapsulated samples were evaluated to verify the encapsulation efficiency. Particle size distribution determination and scanning electron microscopy of the microcapsules were also carried-out. The ethanolic leaf extract showed higher significant levels of total phenolic compounds (162.46 ± 4.48 mg GAE/g DW), and anti-oxidant (75.65%) and antibacterial activities compared to those of other aqueous and ethanolic extracts from fruits and seeds. Furthermore, the spray-dried ethanolic leaf extract had the highest total phenolic content. However, the encapsulated ethanolic fruit extract had the highest percentage of DPPH scavenging activity (30.36% ± 1.49). In addition, antibacterial activity measurements showed that the addition of ethanolic and aqueous seed microcapsules provided a significant zone of inhibition against the bacterium Brochotrix thermosphacta (38 mm and 30 mm, respectively). Okra aqueous leaf microcapsules showed the smallest Sauter mean diameter values (7.98 ± 0.12 µm). These data are applicable for expanding the use of okra leaves, fruits and seeds as food additives and/or preservatives in the food industry.

Evaluation of Millability and Recyclability of Asphalt with Paving Interlayers

Abstract Reclaimed asphalt pavement (RAP) has been widely incorporated into roadway base and surface courses, as they provide economic and environmental benefits that lead to sustainable construction practices. However, because of the increasing use of paving interlayers (e.g., geotextiles, geogrids, and geocomposites) during roadway rehabilitation, the likelihood of milling projects involving asphalt layers with paving interlayers (referred to as GRAP) has significantly increased. Consequently, the assessment of potential GRAP reuse in geotechnical and pavement applications becomes essential. This research study aims at evaluating the millability and recyclability of asphalt layers with paving interlayers. Specifically, sections with and without paving interlayers were first milled to evaluate the millability of asphalt layers with paving interlayers. Subsequently, the recyclability of GRAP for the base and surface course of pavements was assessed by quantifying the geotechnical characteristics of millings collected from asphalt layers with paving interlayers, referred herein as geosynthetic RAP or GRAP, and those without paving interlayers (RAP). The evaluation of RAP and GRAP materials for road base suitability included blending them with virgin aggregates and investigating these blends via determination of particle size distribution, binder content, compaction characteristics, abrasion resistance, hydraulic conductivity, and resilient modulus. The evaluation of RAP and GRAP materials for surface course suitability involved preparing asphalt mixtures that incorporated RAP and GRAP and quantifying their particle size distribution, indirect tensile strength, and moisture susceptibility. Comparison of the results obtained from five different base course blends and five different asphalt mixtures demonstrated that the base course blends and asphalt mixtures with GRAP exhibited properties similar to those with RAP. Also, the results of this investigation indicate that asphalt mixtures (surface course) and granular base courses can incorporate up to 30 % and 50 % GRAP, respectively, thus leading to sustainable roadway construction practices.

Ethanol, not water, should be used as the dispersant when measuring microplastic particle size distribution by laser diffraction

Size distribution is a crucial characteristic of microplastics (MPs). A typical method for measuring this property is wet laser diffraction. However, when measuring size distributions of MPs, despite it being a poor dispersant for many MPs, water is commonly selected, potentially limiting the reliability of reported measurements. To evaluate dispersant suitability, different aqueous concentrations of ethanol (0, 10, 20, 30, 40, 50, 75, 100 wt%) and aqueous solutions of 0.001 wt% Triton X-100 and a mixture comprising 10 wt% sodium pyrophosphate and 10 wt% methanol were used as dispersants in a laser granulometer (Mastersizer 2000) to determine particle size distributions (PSDs) of granular polyethylene MP35, MP125 and MP500 particles (nominally <35, <125 and, < 500 μm in size). The reliability of the PSDs depended on the dispersant used and size of primary MPs. With increasing ethanol concentrations, PSD curves of MP35 particles shifted from multi-modal to mono-modal distributions. The measured size distribution reduced from 1588.7 to 4.5 μm in water to 39.9 to 0.1 μm in 100 wt% ethanol. Generally, as ethanol concentration increased, uncertainty associated with the PSD parameters decreased. Although Triton X-100 and the mixed solution also showed better dispersion than water, measured particle sizes and coefficient of variation (COV, %) were notably larger than those for 100 wt% ethanol. Similar trends were observed for larger-sized MP125 and MP500 particles, but differences in PSD curves, PSD parameters, and COV (%) among dispersants were less pronounced. In all dispersants, the volume weighted mean diameters (VWMD) in 100 wt% ethanol (MP35: 14.1 μm, MP125: 102.5 μm, MP500: 300.0 μm) were smallest and close to diameters determined from microscope observations (MP35: 14.6 μm, MP125: 109.0 μm, MP500: 310.6 μm). Therefore, for accurate determinations of the PSDs of MP by wet laser diffraction, ethanol rather than water should be used as the dispersant.

Characterization of tire and road wear particles in urban river samples

Tire and road wear particles (TRWP) consist of tread rubber elastomers with pavement encrustations generated from tire-road friction. Our previous work utilized density separation and chemical mapping to characterize chemical and physical properties of individual TRWP. The current research extends the use of chemical mapping methods to urban river samples including sediment from the Seine River (France). TRWP were identified using a weight of evidence framework including density separation, optical imaging, scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM/EDX) mapping, and Fourier-transform infrared (FTIR) spectroscopy. River sediment collected immediately downstream of the Rouen urban area (with an average TRWP concentration of 930 mg TRWP/kg sediment; n = 3) subsequently density separated demonstrated an average TRWP size of 133 µm by number and 171 µm by volume. Sediment from a second location (190 mg TRWP/kg sediment; n = 1) was density separated and showed an overlap in features of tire tread and bitumen/asphalt in the FTIR signatures (operationally defined as weathered bitumen/TRWP). Average particle size for weathered bitumen/TRWP were 250 µm and 981 µm by number and volume, respectively. Pulverization pre-treatment of the second location sediment sample reduced larger particle agglomerates to an average weathered bitumen/TRWP particle size of 97 µm and 116 µm by number and volume, respectively. A quantitative TRWP or bitumen/TRWP size distribution in filtered suspended river solids (3300 mg TRWP/kg suspended solid) could not be determined due to lack of TRWP enrichment in pre- or post-density separation steps; however, average particle size for all collected river particles were 27 µm and 160 µm by number and volume, respectively. Additionally, TRWP were not identified in a river biota sample (bivalves) with or without chemical digestion and future research was discussed. Taken together, our single particle analysis methodologies were useful for the determination of particle size distribution (including bitumen and TRWP) in urban river sediment samples. These results are expected to help advance the methods for identification and characterization of TRWP and potentially other microplastics in various environmental matrices.

An automated algorithm for the determination of oil absorption strategy of magnetic nanoparticles from SEM images

In recent years, the magnetic iron oxide nanoparticles (MNPs) are employed as efficient absorbents for oil removal from water. In this research, the particle size (diameter) obtained from Scanning Electron Microscopy (SEM) images of MNPs, before and after oil-absorption, are utilized to determine the oil-absorption capacity. However, the manual evaluation of the particle size and particle size distribution (PSD) are highly time-consuming and needs expertised people for accurate analysis. Hence, an image processing algorithm is employed for the determination of particle size and PSD from the Scanning Electron Microscopy (SEM) images. The key objective revolves with the preparation of the Maleic Anhydride Grafted Polypropylene anchored Magnetic Nanoparticles (MAPP-a-MNPs) to absorb crude oil from the marine water. The shape, size, and size distribution of MAPP-a-MNPs were assessed by both manual and automated analysis. For this purpose, expertise people help with the manual analysis and Threshold Adaptive-Canny Edge Detection (TA-CED) and Accumulator Updated-Circular Hough Transform (AU-CHT) method is employed for automated analysis. All the automated process were conducted in MATLAB and the measurements were taken for both before and after the oil absorption images. These measurements aid us to determine the quantity of oil absorbed by MAPP-a-MNPs. The results demonstrates excellent oil removal capacity of MAPP-a-MNPs.

Soil texture analysis by laser diffraction and sedimentation and sieving–method and instrument comparison with a focus on Nordic and Baltic forest soils

PurposeLaser diffraction (LD) for determination of particle size distribution (PSD) of the fine earth fraction appeared in the 1990s, partly substituting the Sieving and Sedimentation Method (SSM). Whereas previous comparison between the two methods predominantly encompasses agricultural soils, less attention has been given to forest soils, including pre-treatment requirements related to their highly variable contents of carbon and Alox+ Feox. In this small collaborative learning study we compared (1) national SSM results with one type/protocol of LD analysis (Coulter), (2) LD measurements performed on three different LD instruments / laboratories, and (3) the replication error for LD Coulter analysis of predominantly sandy and loamy forest soils.MethodsWe used forest soil samples from Denmark, Norway and Lithuania and their respective national SSM protocols / results. LD analyses were performed on Malvern Mastersizer 2000, Sympatec HELOS version 1999, and Coulter LS230, located at University of Copenhagen, Aarhus University and Helsinki University, respectively. The protocols differed between laboratories, including the use of external ultrasonication prior to LD analysis.ResultsThe clay and silt fractions content (&amp;lt;20 μm) from the LD analysis were not comparable with SSM results, with differences ranging from −0.5 to 22.3 percentage points (pp) for clay. Preliminary results from loamy samples with spodic material suggested inconsistent effects of external ultrasonication to disperse aggregates. The comparison between the three LD instruments showed a range in the clay and silt fractions content of 1.9–5.3 and 6.2–8.1 pp, respectively. Differences may be related to the instruments, protocols, and content of a given particle size fraction. The replication error of the Coulter LD protocol was found to be &amp;lt;3 pp in sandy soils, but up to 10 pp in loamy soils.ConclusionDifferences in the clay fraction results partly affected the classification of soil types. The fast replication of the LD analysis enables more quality control of results. The pedological evaluation of non-silicate constituents and optional pre-treatment steps (e.g., soil organic matter or sesquioxides) remains the same for LD and SSM. For comparison of results, detailed descriptions of the analytical protocol including pre-treatments are needed irrespective of instrument and theoretical approach.

An assessment of the efficacy of sodium carbonate for semi-passive treatment of circumneutral zinc-bearing mine waters

This study reports on the novel application of sodium carbonate dosing specifically for the semi-passive precipitation of Zn from circum-neutral mine water and demonstrates the use of Na2CO3 as a readily available, safe to handle reagent which can precipitate Zn at pH within environmental quality standards. >95 % Zn removal was achieved for each mine drainage investigated, requiring differing dosages of Na2CO3 with residual Zn concentrations <1 mgL−1. Geochemical modelling and precipitate characterisation using XRD, SEM-EDS, TGA and full chemical digest suggests that the precipitate predominantly comprised of hydrozincite. Laboratory trials demonstrated that (i) adding the precipitant dropwise could reduce the sludge volume by circa 50 %, and (ii) That following a laboratory protocol for simulating type II High Density Sludge (HDS) process resulted in substantial decreases in sludge volumes compared to single pass sludge, with 5.3 mL per litre mine water treated compared to 55.3 mL per litre for conventional single pass treatment after 25 cycles. Such reductions in sludge volume are a very advantageous outcome for practical applications. Particle size distribution and zeta potential determinations on the resultant HDS sludge suggest that increased heterogenous precipitation and decrease in zeta potential are important in the formation of HDS when using sodium carbonate to treat zinc-bearing waters. This work demonstrates that sodium carbonate is an efficacious reagent for semi-passive treatment of zinc-bearing mine waters and as such could find widescale application to this pressing global problem.

Synthesized Approach for Evaluating the Integral Suspension Pressure (ISP) Method and the Hydrometer in the Determination of Particle Size Distribution

Different techniques have been developed in the 20th and 21st centuries to address the study of particle size distribution in fine materials. Most of these techniques are based on gravitational sedimentation processes. The modern method used in this research bases the measurement on the change in pressure of the aqueous medium caused by the progressive settling of fine particles. Different materials were evaluated within the study to compare the results of the integral suspension pressure (ISP) method with a traditional approach used worldwide, such as hydrometers. Although the ISP method is considered promising and reliable in measuring the particle size distribution of the fine fraction, current literature lacks comparisons with traditional methods. This aspect would help in the definitive validation of the technique and its use in practical engineering. The hydrometer recorded silt content was greater than ISP over the whole range of measurements, especially in yellow kaolin, in which the silt content is more than 40%. Compared to the hydrometer method, the ISP presented a tendency to misclassify the soil texture of bentonite due to the high clay content. The considerable differences, especially in clays with finer particles such as bentonite, demonstrate that the modern ISP technique can detect very fine projected materials within the particle size distribution compared to conventional methodologies. The study’s objective is mainly to compare both methods, given the important technological evolution that the ISP method presents in relation to the hydrometer.

Extended wet sieving method for determination of complete particle size distribution of general soils

The traditional standard wet sieving method uses steel sieves with aperture ≥0.063 mm and can only determine the particle size distribution (PSD) of gravel and sand in general soil. This paper extends the traditional method and presents an extended wet sieving method. The extended method uses both the steel sieves and the nylon filter cloth sieves. The apertures of the cloth sieves are smaller than 0.063 mm and equal 0.048 mm, 0.038 mm, 0.014 mm, 0.012 mm, 0.0063 mm, 0.004 mm, 0.003 mm, 0.002 mm, and 0.001 mm, respectively. The extended method uses five steps to separate the general soil into many material sub-groups of gravel, sand, silt and clay with known particle size ranges. The complete PSD of the general soil is then calculated from the dry masses of the individual material sub-groups. The extended method is demonstrated with a general soil of completely decomposed granite (CDG) in Hong Kong, China. The silt and clay materials with different particle size ranges are further examined, checked and verified using stereomicroscopic observation, physical and chemical property tests. The results further confirm the correctness of the extended wet sieving method.

Laser scattering centrifugal liquid sedimentation method for the accurate quantitative analysis of mass-based size distributions of colloidal silica.

This paper proposes a laser scattering centrifugal liquid sedimentation (LS-CLS) method for the accurate quantitative analysis of the mass-based size distributions of colloidal silica. The optics comprised a laser diode light source and multi-pixel photon-counting detector for detecting scattered light intensity. The unique optics can only detect the light scattered by a sample through the interception of irradiated light. The developed centrifugal liquid sedimentation (CLS) method comprised a light-emitting diode and silicon photodiode detector for detecting transmittance light attenuation. The CLS apparatus could not accurately measure quantitative volume- or mass-based size distribution of poly-dispersed suspensions, such as colloidal silica, because the detecting signal includes both transmitted and scattered light. The LS-CLS method exhibited improved quantitative performance. Moreover, the LS-CLS system allowed the injection of samples with concentrations higher than that permitted by other particle size distribution measurement systems with particle size classification units using size-exclusion chromatography or centrifugal field-flow fractionation. The proposed LS-CLS method achieved an accurate quantitative analysis of the mass-based size distribution using both centrifugal classification and laser scattering optics. In particular, the system could measure the mass-based size distribution of approximately 20mgmL-1 poly-dispersed colloidal silica samples, such as in a mixture of the four mono-dispersed colloidal silica, with high resolution and precision, thereby demonstrating high quantitative performance. The measured size distributions were compared with those observed through transmission electron microscopy. The proposed system can be used in practical setups to achieve a reasonable degree of consistency for determining particle size distribution in industrial applications.

Physicomechanical properties of raw and comminuted pine and poplar shavings: energy consumption, particle size distribution and flow properties

The aim of this study was to assess the energy consumption during milling and cutting-milling of pine and poplar shavings and the determination of particle size distribution (PSD) characteristics and mechanical properties of these materials. Cutting-milling process required less energy (in kJ·kg–1) than milling but maximum mass flow rate of shavings was significantly higher and thus the effective power requirement of the knife mill during cutting also was higher. Comminution of plastic poplar shavings was more energy-consuming than harder pine shavings. These features influenced PSD, which was approximated with four mathematical models: Rosin–Rammler-Sperling-Bennett (RRSB), normal, logistic and lognormal. On the basis of the best fitting (Radj2) for RRSB, detailed PSD parameters were calculated and all PSDs were described as ‘mesokurtic’, ‘fine skewed’ and ‘well-graded’. In comparison to milled shavings, cut-milled shavings had higher density, but were less compressible and had lower unconfined yield strength. However, cut-milled shavings had higher flowability because of lower cohesion and internal friction angles, because after cutting-milling particles were more spherical than elongated particles after milling. Cut-milled poplar shavings had more favourable mechanical parameters and better PSD characteristics, but required more energy for comminution than pine shavings.

Determination of 2D Particle Size Distributions in Plasmonic Nanoparticle Colloids via Analytical Ultracentrifugation: Application to Gold Bipyramids

Multidimensional particle properties determine the product properties in numerous advanced applications. Accurate and statistically meaningful measurements of complex particles and their multidimensional distributions are highly challenging but strongly needed. 2D particle size distributions of plasmonic nanoparticles of complex regular shape can be obtained from analytical ultracentrifugation experiments via the optical back coupling method. A workflow for the calculation of frictional properties of arbitrarily shaped nanoparticles was developed based on bead shell models and applied to gold bipyramids with a pentagonal cross-section. The obtained 2D particle length-diameter distributions and the reduced cumulative 1D length and diameter distributions were compared to transmission electron microscopy measurements. While we find very good agreement for most measurements, the obtained length and diameter distributions were shifted by a few nanometers for some samples. Transmission electron microscopy, energy-dispersive X-ray spectroscopy, electron tomography, and finite element modeling indicate that the shift originated from a slight mismatch between the assumed shape of the simulated perfect bipyramids and the real particle shape and composition due to the presence of silver in the particles. This study demonstrates the feasibility of the applied techniques for complex shape analysis of nanoparticle ensembles with unmatched particle count numbers.

Development of soil Particle size distribution model and determination of all related coefficients

Development of soil Particle size distribution model and determination of all related coefficients