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Ginsenoside Rk3 Ameliorates Obesity-Induced Colitis simply by Regulatory involving Intestinal Flora and the TLR4/NF-κB Signaling Pathway inside C57BL/6 Rats.
Hence, more research is necessary to clarify the detailed impacts on FW management and wastewater treatment.Microplastic particles have been recognized as global hazardous pollutants in the last few decades pointing to the importance of analyzing and monitoring microplastics, especially in soils and sediments. This study focused on a multi-step approach for microplastic analysis combining grain size fractionation, density separation and identification by μ-FTIR-spectroscopy. Eight widely used polymers (polyethylene (PE), polypropylene (PP), polyvinylchloride (PVC), polystyrol (PS), polyethylenterephthalate (PET), polymethylmethacrylate (PMMA), polyurethane (PU) and polyamide (PA)) were fractionated into four groups of grain sizes (0.1-5 mm). Thereafter, sea sand was spiked with these particles to test a ZnCl2-based density separation for the polymer types and the various grain sizes. The obtained recovery rates were close to 100% showing that ZnCl2-based density separation is suitable to separate the polymer particles from a sandy matrix. learn more This approach was extended on three further environmental matrices and recovery rates for two of them (sandy-silty and fine-grained sediment) also provided reliable values (94-106%). Lastly, the developed multi-step approach was verified by analyzing an environmental sample (sediment from river Tiranë, Albania) characterized by smaller grain size and moderate organic matter content. Identification of two polymer types in different grain size classes verified the suitability of the developed approach for microplastic analyses on particulate matter such as soils and sediments.Modified walnut shell (MWS) was obtained using diethylenetriamine through a grafting reaction and its adsorption capacity toward Cr(VI) was enhanced. The adsorbent was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and elemental analysis and the results showed that the modification was effective. To optimize experimental conditions, the effect of temperature, solution pH, salinity, contact time, and Cr(VI) concentration on adsorption quantity were performed in batch mode. It showed that the adsorption ability for Cr(VI) onto MWH can reach 50.1 mg·g-1 at 303 K with solution pH 3. Both the solution pH and salinity had a great impact on the adsorption capacity. The Langmuir model can predict the equilibrium process while the pseudo-second-order model can describe the kinetic process. The Yan model can be used to predict the column process. Additionally, there was also some regeneration ability for Cr-loaded MWH. Consequently, MWS is effective for removing Cr(VI) from solution.A nitrogen-doped reduced graphene oxide/Fe3O4 composite (NGO-Fe3O4) was prepared through the simplified hydrothermal and deposition-precipitation method and characterized by X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy. The degradation efficiency of oxytetracycline (OTC) by NGO-Fe3O4 activated peroxodisulfate (PDS) under visible light irradiation was studied. The degradation efficiency reached 100% within 32.5 min (the initial OTC concentration 50 mg L-1 and PDS 1 mM; [NGO-Fe3O4][ PDS] = 41; pH = 3.0). No apparent decrease in degradation efficiency was observed after five cycles. SO4-· and ·OH were the main active oxides for OTC degradation in this system. Moreover, four degradation pathways were proposed, namely hydroxylation, dehydration, decarbonylation and demethylation according to the analysis results of high-performance liquid chromatography mass spectrometry.Electro-assisted adsorption was investigated for Pb2+, Cu2+ and Ni2+ removal using date seed biochar (DSB-Electro). Compared with pristine biochar, the results showed that DSB-Electro effectively increased the adsorption capacity of Pb2+, Cu2+ and Ni2+ by 21% to 94%. Significant differences were observed between Pb2+ and Cu2+ adsorption compared with Ni2+, which could be explained based on ion polarizing power. Under the same voltage, Ni2+ solution shows the highest electric conductivity; thereby more Ni2+ is transported to the biochar anode, giving them a greater chance to interact with the surface groups. Electro-assisted adsorption occurred rapidly as around 88% of Pb2+ and Ni2+ adsorbed within the first 3 h, while 96% of Cu2+ occurred within the first hour of contact. Reversing the polarity did not seem to cause significant desorption of the adsorbed ions as the amount released from reversing polarity was less than 38%, indicating that only a small fraction of the ions was held by the electrostatic charge introduced by the current. It was likely that the enhanced charge facilitated other adsorption mechanisms by bringing the ions in contact with the biochar initially via electrostatic force. Electro-assisted adsorption can improve the biochar economic feasibility for metals removal (particularly Ni2+) from industrial streams.In recent years, industrial contaminants and especially organic pollutions have been threatening both environmental safety and human health. Particularly, dibutyl phthalate (DBP) has been considered as one of the major hazardous contaminants due to its widespread production and ecological toxicities. Consequently, reliable methods toward the efficient and environmentally benign degradation of DBP in wastewater would be very desirable. To this end, a novel magnetically separable porous TiO2/Ag composite photocatalyst with magnetic Fe3O4 particles as the core was developed and successfully introduced to the photocatalytic degradation of DBP under visible irradiation with a fluorescent lamp. The presented work describes the grafting of Ag co-doped TiO2 composite on the silica-modified porous Fe3O4 magnetic particles with a simple and inexpensive chemical co-precipitation method. Through the investigation of the influencing factors including photocatalyst dosage, initial concentration of DBP, solution pH, and H2O2 content, we found that the degradation efficiency could reach 74%. The photodegradation recovery experiment showed that the degradation efficiency of this photocatalyst remained almost the same after five times of reuse. In addition, a plausible degradation process was also proposed involving the attack of active hydroxyl radicals generated from this photocatalysis system and production of the corresponding intermediates of butyl phthalate, diethyl phthalate, dipropyl phthalate, methyl benzoate, and benzoic acid.
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