Organic Components Research Articles

Optimization of Recovery of Nutrients from Pig Manure Slurry through Combined Microbial Fuel Cell and Microalgae Treatment

Microbial fuel cells (MFCs) and microalgae–bacteria consortia represent two renewable and promising technologies of growing interest that enable wastewater treatment while obtaining high-value-added products. This study integrates MFCs and microalgae production systems to treat animal slurry, aiming to remove and recover organic and inorganic components while generating energy and producing biomass. The MFCs effectively eliminated Chemical Oxygen Demand (COD), organic nitrogen, and a portion of the suspended solids, achieving a maximum voltage of 195 mV and a power density of 87.03 mW·m−2. After pre-treatment with MFCs, the slurry was diluted to concentrations of 10%, 50%, and 100% and treated with microalgae–bacteria consortia. The results showed a biomass production of 0.51 g·L−1 and a productivity of 0.04 g·L−1·day−1 in the culture fed with 10% slurry, with significant removal efficiencies: 40.71% for COD, 97.76% for N-NH4+, 39.66% for N-NO2−, 47.37% for N-NO3−, and 94.37% for P-PO4−3. The combination of both technologies allowed for obtaining a properly purified slurry and the recovery of nutrients in the form of bioelectricity and high-value biomass. Increasing the concentration of animal slurry to be treated is essential to optimize and scale both technologies.

Comparative characterizations of plant and mineral dye as potential photosensitizer in Dye-Sensitized Solar Cell

The advent of dye-sensitized solar cells (DSSC) has expansively seen more studies as an alternative to silicon-based and thin-film solar cells due to their simple structure and relatively low production cost. In dye-sensitized solar cells, the dye is one of the major components for high power conversion efficiencies. The extracted dyes were characterized by powder x-ray diffraction, x-ray fluorescence, Scanning electron microscopy, UV-visible spectroscopy, and Gas Chromatography-Mass spectrometry analysis. The structure of the mineral dye contains constituents that enhance better absorption of solar radiation for use in a Dye-Sensitized Solar Cell (DSSC). The calcium and iron content of the mineral dye studied as revealed by the mineralogical analysis done using the powder x-ray diffraction (XRD) and the x-ray fluorescence (XRF) suggest this. These metals serve as bounding complexes to other organic components in the dye, like in the case of Ruthenium complexes dye for efficient absorption of solar radiation, especially in the visible light region. The functional groups present in the dye also confirm what favors good absorption of solar radiation for DSSC application. The Organic chemical compositions present in the mineral dye which were obtained by the Gas Chromatography-Mass spectrometry analysis also confirm the functional groups of carbonyl, Amine, and hydroxyl revealed by FTIR, which were responsible for solar radiation absorption. There are strong absorption narrow bands in the visible region with peaks at around 424 nm (2.903 a.u) and 486 nm (2.973 a.u). Optical band gaps of 1.66 eV and 2.27 eV for the mineral dye and plant dye respectively, were obtained. The properties of the dyes studied give potential substitutes to the relatively expensive ruthenium-based dyes for use in DSSC fabrication.

Retention factor variation on wide range of mobile phase compositions in reversed-phase high-performance liquid chromatography; a short tutorial

Mobile phase composition remains the major experimental parameter influencing the separation process in reversed-phase high-performance liquid chromatography (RP-HPLC). Its influence on the retention of solutes is explained by the Hildebrand solubility parameter and solvophobic theory, which also considers molecular characteristics of the participants in a separation process. The main empirical dependences (linear and polynomial) between the retention factor and the composition of mobile phase (retention function) are discussed taking into consideration a wide range of mobile phase compositions. Two direct chromatographic indices are resulting from these equations: the extrapolated value of retention factor for zero organic content in mobile phase composition (log kw) and the solvent strength parameter (S), which for a linear retention function is its slope being constant over the entire mobile phase compositions. Another chromatographic index could result from the retention function for zero content of water in mobile phase, but this situation can be applied only for very hydrophobic solutes. For large domains of mobile phase composition, the retention function cannot be described by a single type of dependence. This explains the paradox of generating by extrapolation different logkwvalues for different organic components. For the mobile phase close to pure water the retention function is different from that at average water concentration.

Elevated effect of hydrothermal treatment on phosphorus transition between solid-liquid phase in swine manure

The morphology and composition of phosphorus in biomass wastes are key factors in determining its potential for utilization. However, the morphological distribution and evolutionary mechanism of phosphorus during the hydrothermal conversion of biomass wastes are still unclear. In this study, swine manure was investigated as the research subject, and the changes in its solid-phase organic components, such as lignocellulose, and inorganic constituents, including metals and phosphorus, during the hydrothermal carbonization (HTC) processes were analyzed in relation to hydrothermal reaction severity (LnR0). A significant linear correlation in Phase II was observed between the solid-phase yield of swine manure and the LnR0. The rapid decline in the solid-phase yield during the initial phase (LnR0 < 9.72) was primarily attributed to the hydrolysis of hemicellulose and similar components. Similarly, solid phase phosphorus showed a very significant phase II with the decrease of solid phase yield. In the first stage, inorganic phosphorus and metal ions (calcium ions, magnesium ions) transferred to the liquid phase (LnR0<9.41). When LnR0 > 9.41, and the driving force of inorganic phosphorus and metal ions into solid phase is enhanced. As the LnR0 was further increased, the HTC could fix over 90 % of the total phosphorus content. XANES analysis indicated that hydroxyapatite emerged as the predominant phosphorus fraction in the solid-phase products, comprising more than 60 %, while magnesium ammonium phosphate components also appeared. This research elucidates the underlying mechanisms of component interaction and phosphorus transformation, providing a solid foundation for enhancing the reuse efficiency of phosphorus in wastes.

Surface tension prediction of pure organic components: An artificial neural network approach

Surface tension is an important thermodynamic property of fluids that impact several processes in the engineering. Accurate estimations of this parameter are required to correctly apply and develop operations such as flow processes and oil recovery. The present study proposes the applying of artificial neural network (ANN)-based approach to accurately predict the surface tension for 75 groups of pure organic compounds, encompassing 1,666 different compounds and 21,444 data points. The performance of the model was evaluated using the mean squared error (MSE) and the coefficient of determination (R2), with K-Fold cross-validation ensuring robustness. The optimal model (ArcD) achieved an average MSE of 8.27x10−5 during cross-validation and 1.55x10−5 during training, with an R2 value of 0.9955. Although training time for this model was 8.89 times longer than the second-best model (ArcA), which had an R2 of 0.9928. Comparative analyses with existing literature models were also realized and revealed an absolute relative deviation (ARD) value of 2.49% to ArcD, 18.39% to Brock and Bird, 23.97% to Curl and Pitzer, and 18.62% to Zuo and Stenby equations, demonstrating the applicability and precision of the developed model. The results highlighted the reliability, accuracy and robustness of the developed ANN-based model, providing a significant advancement in the prediction of surface tension for a wide range of pure organic compounds.

Stereospecific supramolecular polymerization of nanoclusters into ultra-long helical chains and enantiomer separation

During the construction of supramolecular polymers of smaller nanoparticles/nanoclusters bearing hierarchy and homochirality, the mechanism understanding via intuitive visualization and precise cross-scale chirality modulation is still challenging. For this goal, a cooperative self-assembly strategy is here proposed by using ionic complexes with uniform chemical composition comprising polyanionic nanocluster cores and surrounded chiral cationic organic components as monomers for supramolecular polymerization. The single helical polymer chains bearing a core-shell structure at utmost length over 20 μm are demonstrated showing comparable flexibility resembling covalent polymers. A nucleation-elongation growth mechanism that is not dealt with in nanoparticle systems is confirmed to be accompanied by strict chiral self-sorting. A permeable membrane prepared by simple suction of such supramolecular polymers displays high enantioselectivity (e.e. 98% after four runs) for separating histidine derivatives, which discloses a benefiting helical chain structure-induced functionalization for macroscopic supramolecular materials in highly efficient racemate separation.

Research Regarding the Autochthonous Dissolved Organic Carbon to Recalcitrant Dissolved Organic Carbon Transformation Mechanism in a Typical Surface Karst River

Autochthonic recalcitrant organic carbon is the most stable component in karst aquatic systems. Still, the processes of its generation and transformation remain unclear, which hinders the study of the mechanisms and quantitative calculations of carbon sinks in karst aquatic systems. This study collected water samples from the Li River, a typical surface karst river in Southwest China. Through in situ microbial cultivation and the chromophoric dissolved organic matter (CDOM) spectrum, changes in organic carbon components and their contents during the transformation of autochthonic dissolved organic carbon (Auto-DOC) to autochthonic dissolved recalcitrant organic carbon (Auto-RDOC) were analyzed to investigate the inert transformation processes of endogenous organic carbon. This study found that microbial carbon pumps (MCPs) promote the tyrosine-like component condensed into microbial-derived fulvic and humic components via heterotrophic bacteria metabolism, forming Auto-RDOC. During the dry season, the high level of Auto-DOC provides abundant organic substrates for heterotrophic bacteria, resulting in significantly higher Auto-RDOC production compared to the rainy season. This study provides fundamental information on the formation mechanisms of Auto-DOC in karst aquatic systems, which contributes to the assessment of carbon sinks in karst aquatic systems.

Effects of Cultivar Factors on Fermentation Characteristics and Volatile Organic Components of Strawberry Wine.

Strawberry wine production is a considerable approach to solve the problem of the Chinese concentrated harvesting period and the short shelf life of strawberries, but the appropriative strawberry cultivars for fermentation are still undecided. In this study, the strawberry juice and wines of four typical strawberry cultivars named Akihime (ZJ), Sweet Charlie (TCL), Snow White (BX), and Tongzhougongzhu (TZ) were thoroughly characterized for their physicochemical indicators, bioactive compounds, and volatile organic components (VOCs) to determine the optimal strawberry cultivars for winemaking. The results showed that there were significant differences in the total sugar content, pH, total acid, and other physicochemical indexes in the strawberry juice of different cultivars, which further affected the physicochemical indexes of fermented strawberry wine. Moreover, the content of polyphenols, total flavonoids, vitamin C, and color varied among the four strawberry cultivars. A total of 42 VOCs were detected in the strawberry juice and wines using headspace solid-phase microextraction coupled with gas chromatography-mass spectrometry (HS-SPME-GC-MS), and 3-methyl-1-butanol, linalool, trans-2-pinanol, hexanoic acid, and hexanoic acid ethyl ester were the differential VOCs to identify the strawberry wine samples of different cultivars. Overall, strawberry cultivar ZJ had a relatively high VOC and bioactive compound content, indicating that it is the most suitable cultivar for strawberry wine fermentation. In addition to determining the relatively superior fermentation characteristics of cultivar ZJ, the results may provide a theoretical basis for the raw material quality control and quality improvement of strawberry wine.

Ultraviolet Nonlinear Optical Single Crystals of A Three‐Dimensional Chiral Covalent Framework Containing Te−O−B−O Bonds

AbstractExtending covalent organic frameworks (COFs) into crystalline carbon‐free covalent backbones is an important strategy to endow these materials with more exotic functions. Integrating metal‐free inorganic and organic components into one covalent framework is an effective way to address the issue of poor thermal/solvent stability in the field of nonlinear optics (NLO). However, constructing such structures is very challenging. Here, we linked 3‐connected nods (BO3) and 2‐connected organic building blocks (Te(Ph)2) together to produce colorless single crystals (size up to 400 μm) of a three‐dimensional (3D) chiral covalent framework (CityU‐22). The single‐crystal X‐ray diffraction (SCXRD) analysis reveals that CityU‐22 has a non‐carbon Te−O−B−O bond‐based network with the srs topology. The chiral CityU‐22 displays good stability under the treatment of different common solvents or heat (the decomposition temperature above 300 °C). Due to its non‐π‐conjugated backbone (−Te−O−B−O−), CityU‐22 shows an ultraviolet NLO behavior with a second‐harmonic generation (SHG) response similar to KH2PO4 (KDP).

Ultraviolet Nonlinear Optical Single Crystals of A Three-Dimensional Chiral Covalent Framework Containing Te-O-B-O Bonds.

Extending covalent organic frameworks (COFs) into crystalline carbon-free covalent backbones is an important strategy to endow these materials with more exotic functions. Integrating metal-free inorganic and organic components into one covalent framework is an effective way to address the issue of poor thermal/solvent stability in the field of nonlinear optics (NLO). However, constructing such structures is very challenging. Here, we linked 3-connected nods (BO3) and 2-connected organic building blocks (Te(Ph)2) together to produce colorless single crystals (size up to 400 µm) of a three-dimensional (3D) chiral covalent framework (CityU-22). The single-crystal X-ray diffraction (SCXRD) analysis reveals that CityU-22 has a non-carbon Te-O-B-O bond-based network with the srs topology. The chiral CityU-22 displays good stability under the treatment of different common solvents or heat (the decomposition temperature above 300 °C). Due to its non-π-conjugated backbone (-Te-O-B-O-), CityU-22 shows an ultraviolet NLO behavior with a second-harmonic generation (SHG) response similar to KH2PO4 (KDP).

Sorption and desorption behavior and mechanism of oxytetracycline on soil aggregates organic matter separated from soils and sediments in the Yellow River Delta

Soil aggregates organic matter (SAOM) is composed of free particulate organic matter (fPOM), intra-aggregate particulate organic matter (iPOM), and mineral-associated organic matter (mSOM), which are major antibiotic sorbents that play a significant role in the soil organic matter (SOM) turnover process. To date, the oxytetracycline (OTC) sorption and desorption behavior and mechanisms on SAOM have not been contrastively analyzed. SAOM organic components have been used to study scientific problems and to determine their influence on the fate and migration of OTC among the SOM turnover process. Results demonstrated that SAOM had great OTC sorption capacity ranging from approximately 12100–513,000 mg kg−1 and the desorption proportion was no more than 33.60%. The slow organic carbon pool (mSOM) had greater OTC accumulation capacity than the intermediate active pool (iPOM) and the active pool (fPOM), while OTC was more likely to reside in the active pool in wetlands (fPOM-w) and oil waste land (fPOM-o) than the organic carbon pool (mSOM-f) in farmland with human activity interference. The hysteresis was affected by SAOM's physical surface characteristics when the OTC initial equilibrium sorption concentration was higher than 200 mg L−1. When it was lower than that, it was affected by the organic carbon composition. Hydrogen bonds, electrostatic interactions, and π-π interactions dominated the SAOM-OTC interactions. The results of this study will be useful for evaluating the long-term behavior and migration of antibiotics in SOM turnover processes and could refine risk assessments of antibiotics contamination in soil environmental systems.

Controllable In situ Polymerization of 1,3‐Dioxolane via Sustained‐Release Effect for Solid‐State Lithium Metal Batteries

AbstractIn situ formed poly(1,3‐dioxolane) (PDOL) electrolytes are of great interest due to the facile process and the improved interface contact. However, the practical application of in situ PDOL electrolytes is still plagued by fast solidification time (liquid state) and poor high‐voltage stability (solid state). Herein, the slow‐release carriers triglycidyl isocyanurate (TGIC), which play dual roles as initiator sustained‐release and network confinement, can tune DOL curing time and cathode/electrolyte interface chemistry is demonstrated. Specifically, the electronegative C≐O and epoxy groups in TGIC have an affinity with BF3, the decomposition product of lithium bis(oxalate)borate (LiDFOB), delaying BF3 protonation reaction and thus extending DOL solidification time. In addition, the epoxy groups in TGIC serve as crosslinking sites to form in situ crosslinked polymer electrolytes (TPDOL@FEC). The corresponding network structure suppresses the contact reaction between high‐fluidity organic components and cathodes, generating a uniform and thin cathode electrolyte interface layer. As a result, the TPDOL@FEC precursor solution can remain its liquid state even after resting 24 h at room temperature. The assembled LiNi0.6Co0.2Mn0.2O2||TPDOL@FEC||Li cells display an impressive capacity retention of 91.5% after 100 cycles at 4.4 V (0.5 C). This study is expected to be a leap in the pursuit of practically feasible in situ formed PDOL electrolytes.

Biomimetic synthetic test system based on hydroxyapatite cement for adhesive strength evaluation of experimental mineral-organic bone adhesive materials.

The development of bone adhesive materials is a research field of high relevance for the advancement of clinical procedures. Despite this, there are currently no material candidates meeting the full range of requirements placed on such a material, such as biocompatibility, sufficient mechanical properties and bond strength under biological conditions, practical applicability in a clinical setting, and no adverse effect on the healing process itself. A serious obstacle to the advancement of the field is a lack in standardized methodology leading to comparable results between experiments and different research groups. Natural bone samples are the current gold-standard material used to perform adhesive strength experiments, however they come with a number of drawbacks, including high sample variability due to unavoidable natural causes and the impossibility to reliably recreate test conditions to repeat experiments. This paper introduces a valuable auxiliary test method capable of producing large numbers of synthetic test specimens which are chemically similar to bone and can be produced in different laboratories so to repeat experiments under constant conditions across laboratories. The substrate is based on a hydroxyapatite forming cement with addition of gelatine as organic component. Crosslinking of the organic component is performed to improve mechanical properties. In order to demonstrate the performance of the developed method, various experimental and commercial bone/tissue adhesive materials were tested and compared with results obtained by established methods to highlight the potential of the test system.

Advanced Organic–Inorganic Hybrid Materials for Optoelectronic Applications

AbstractResearch on organic–inorganic hybrid materials (OIHMs) has experienced explosive growth in the past decades. The diversity of organic components allows for the introduction of various spatial scales, functional groups, and polarities, while inorganic components provide higher hardness, heat resistance, and stability, their flexible combination facilitates the formation of diverse structures. Furthermore, simple and cost‐effective synthesis methods, such as room temperature solution processes and mechanochemical techniques, enable precise control over the materials' properties at different scales, thus achieving adjustable structure–performance relationships. This review will discuss the recent research progress of OIHMs within the field of optoelectronics and related optoelectronic device applications. According to the dimension of inorganic components and the nature of organic–inorganic interface, this review divides OIHMs into four structural categories. The ongoing research has revealed diverse applications for OIHMs in the fields of solar cells, light‐emitting devices, detectors, and memristors. As an outlook, the potential of perovskite and 0D metal halide materials, which are currently the most studied, for enhancing optoelectronic performance and stability is discussed.

Lead-free Cs3Bi2I9 perovskite hexagonal microplates: A promising material solution-processed for ultraviolet self-powered photodetectors

In recent times, hybrid organic-inorganic lead halide perovskites have garnered significant attention in the realm of optoelectronic devices. Metal halide perovskites are extensively researched for photodetection due to their exceptional optical and electrical properties. However, the toxicity of lead and the unstable nature of organic components are limiting its potential. Lead-free perovskites, on the other hand, have low toxicity and are being explored as a promising material for photodetector applications. However, achieving self-powered perovskite photodetectors with high photoresponse, broad spectral sensitivity, and long-term stability remains challenging Among them, Cs3Bi2I9 perovskites have emerged as standout, garnering attention for their environmentally friendly nature, impressive stability, and heightened photosensitivity. Herein, FTO/ Al-doped ZnO (AZO)/Cs3Bi2I9/P3HT/C self-powered ultra-violet (UV) photodetector. This device demonstrated outstanding self-powered photodetection capabilities with a photoresponsivity of 29 mA/W, a specific detectivity of 1.05×1011 Jones, and an impressive response rise and decay time of 90 ms /140 ms. Furthermore, the PDs device can function as a bias-based UV photodetector.

Changes in Soil Aggregate Carbon Components and Responses to Plant Input during Vegetation Restoration in the Loess Plateau, China.

Vegetation restoration is an effective measure to cope with global climate change and promote soil carbon sequestration. However, during vegetation restoration, the turnover and properties of carbon within various aggregates change. The effects of plant source carbon input on surface soil and subsurface soil may be different. Thus, the characteristics of carbon components in aggregates are affected. Therefore, the research object of this study is the Robinia pseudoacacia forest located in 16-47a of the Loess Plateau, and compared with farmland. The change characteristics of organic carbon functional groups in 0-20 cm, 20-40 cm, and 40-60 cm soil layers were analyzed by Fourier near infrared spectroscopy, and the relationship between the chemical structure of organic carbon and the content of organic carbon components in soil aggregates was clarified, and the mechanism affecting the distribution of organic carbon components in soil aggregates was revealed in the process of vegetation restoration. The results show the following: (1) The stability of surface aggregates is sensitive, while that of deep aggregates is weak. Vegetation restoration increased the surface soil organic carbon content by 1.97~3.78 g·kg-1. (2) After vegetation restoration, the relative contents of polysaccharide functional groups in >0.25 mm aggregates were significantly reduced, while the relative contents of aromatic and aliphatic functional groups of organic carbon were significantly increased. The opposite is true for aggregates smaller than 0.25 mm. (3) With the increase in soil depth, the effect of litter on organic carbon gradually decreased, while the effect of root input on the accumulation of inert carbon in deep soil was more lasting.

Inorganic/organic sublattice roles in band edge photodynamics of isoelectronically substituted hybrid semiconductors

Zero-dimensional organic–inorganic hybrid metal halides are unique semiconductors with fruitful physical properties. Usually, only the inorganic polyhedrons dominate the band edge electronic and photophysical properties of such hybrid semiconductors, whereas the organic components mainly act as structure-stabilizing units. Herein, we study the electronic structures and photodynamics of isoelectronically Br-substituted (I) zero-dimensional organic–inorganic copper halide semiconductors (C9H14N)3Cu3(BrxI1−x)6. They are composed of both inorganic [Cu3(BrxI1−x)6]3− units and organic C9H14N+ skeletons. It is surprising to find that unlike usual organic–inorganic metal halides, although the heavily isoelectronic substitution of halogen atoms in the (C9H14N)3Cu3I6 crystal leads to significant shrinkage of the lattice, it does not remarkably alter the bandgap and luminescence peak owing to the site-projected density of states as revealed by the density functional theory calculation. The inorganic units dominate the valence band edge quantum states, whereas the organic skeletons dominate the conduction-band edge states. However, the isoelectronic substitution significantly lowers the symmetry of the crystal, and as a result, the quantum transition probability at the band edge increases first and decreases then with increasing concentration of substituting bromine atoms. The (C9H14N)3Cu3(BrxI1−x)6 crystals exhibit dual-band luminescence with large Stokes shift and near-unity quantum yield. It arises from the excitons trapped by two kinds of centers. The critical participation of the organic skeletons in the electronic structures and band edge photodynamics refresh our knowledge of their roles in the hybrid semiconductors.

Construction of a 2D/2D Vs-ZnIn2S4/Zn-TCPP heterojunction for effective charge transfer to enhance photocatalytic hydrogen evolution

The integration of inorganic and organic semiconductor components in composites has tremendous potential in photocatalysis, owing to the ultrafast photogenerated exciton dissociation and slow carrier recombination kinetics at their interfaces, which can result in enhanced photocatalytic performances. By exploiting the synergy among morphology modulation, sulfur vacancy (Vs) engineering, and close interface control, a novel inorganic–organic Vs-ZnIn2S4/ tetrakis (4-carboxyphenyl) zinc porphyrin (Zn-TCPP) composite for photocatalytic hydrogen evolution (PHE) was successfully synthesized via microwave-assisted solvothermal and self-assembly methods. The cocatalyst-free PHE rate of Vs-ZnIn2S4/Zn-TCPP (ZZT-20 %) reaches 8.997 mmol h−1 g−1 under visible light irradiation, which is 10.9, 2.2, and 67.1 times that of ZnIn2S4, Vs-ZnIn2S4, and Zn-TCPP, respectively. Moreover, the apparent quantum yield of ZZT-20 % under 420 nm monochromatic light (1.11 %) clearly exceeds that of Vs-ZnIn2S4. Testing experiments and DFT calculations revealed that the significantly enhanced PHE activity can be mainly attributed to the Z-scheme charge transfer mechanism, which greatly improves the visible light response range and redox potentials. Remarkably, Vs sites act as electron traps, inducing the vertical transport of electrons within the bulk phase and their accumulation at the surface Zn–S bonds. Simultaneously, van der Waals forces and weak hydrogen bonds between Vs-ZnIn2S4 and the Zn-TCPP interface cause the rapid migration of photogenerated electrons to Zn-TCPP. This work not only reveals new insights into the structure–property relationships of inorganic–organic Vs-ZnIn2S4 and Zn-TCPP composites, but also provides an appropriate strategy for cleaner water resourcelization and sustainable solar energy conversion.

Condensable and filterable particulate matter emitted from typical diesel vehicles in steady and transient driving conditions

Condensable particulate matter (CPM) and filterable particulate matter (FPM) emitted from industrial sources have been well studied, but their emissions from vehicles have not yet been covered. This study explores the emission characteristics of CPM and FPM from typical diesel vehicles under various driving conditions. The emission factors (EFs) of CPMs under driving conditions were 5.4–10.4 times higher than those of FPMs, while CPMs EFs under transient driving conditions were about 2.5 times higher than those under steady driving conditions. CPM and FPM are mainly composed of organic matter accounting for 53.3 %−92.9 %, while the intermediate and semi-volatile organic compounds dominate the organic matter accounting for 86.3 %−98.6 %. Similar to industrial sources, alkanes are the predominant organic species emitted by diesel vehicles, comprising 42.0 %−64.0 % of the detected organic components. Inorganic CPM is primarily composed of NH4+ , representing 84.9 %−87.6 % of the total, in contrast to industrial sources where SO42- and Cl- dominate. Interestingly, the air pollution control devices installed on diesel vehicles under steady driving conditions perform better in removing organic CPM and producing higher inorganic CPM emissions than those under transient driving conditions. These findings will enhance the comprehensive understanding of particulate matter emitted from diesel vehicles and provide a scientific foundation for the development of related control technologies.

Genetic Characteristics and Volatile Organic Compounds of Leaves and Fruit Edible Parts of Citrus depressa Hayata from Different Geographic Origins

Citrus depressa Hayata is a citrus cultivar grown in Japan and Taiwan. To assess the differences in genetic characteristics and volatile organic components (VOCs) in the leaves and edible parts of the fruits of 23 C. depressa accessions from different geographic origins, the tissues were analyzed using cleaved amplified polymorphic sequence markers and gas chromatography-mass spectrometry. A phylogenetic cluster analysis demonstrated that Kagoshima accessions had a close genetic relationship with one another, with Okinawan “Izumi kugani-like” being the most distinct accession. The predominant volatiles in the leaves were γ-terpinene, p-cymene, limonene, and linalool. Multivariate analysis and volcano plots revealed distinct volatiles in the leaves of each cultivation region: piperitone and citronellal (Kagoshima); 5,9,9-trimethyl-spiro[3.5]non-5-en-1-one (Okinawa); and hexanal (Taiwan). Furthermore, the edible parts of Taiwanese fruits contained abundant amounts of monoterpenes, including linalool and 1,8-cineole. In contrast, Kagoshima and Okinawa accessions were rich in aldehydes and esters, respectively. In conclusion, the genetic and volatile profiles of 23 C. depressa accessions of different origins could be distinguished, and multivariate analysis suggested that C. depressa contains diverse VOCs depending on where it is cultivated. These findings demonstrate the exclusivity of C. depressa resources in each region, which could assist farmers and agro-industries in promoting food products derived from C. depressa fruits.