Efficient removal of per/polyfluoroalkyl substances from water using recyclable chitosan-coated covalent organic frameworks: Experimental and theoretical methods.

Covalent organic frameworks (COFs) demonstrate remarkable potential for adsorbing per/polyfluoroalkyl substances (PFAS). Nevertheless, the challenge of recycling powdered COFs hampers their practical application in water treatment. In this research, a quaternary amine COF with inherent positive surface charge was synthesised to adsorb perfluorooctanoic acid (PFOA) via electrostatic interactions. The COF was then combined with chitosan (CS) through a simple dissolution-evaporation process, resulting in a composite gel material termed COF@CS. The findings indicated that the adsorption capacity of COF@CS significantly surpassed that of the original COF and CS. According to the Langmuir model, COF@CS achieved a maximum PFOA capacity of 2.8 mmol g-1 at pH 5. Furthermore, the adsorption rate increased significantly to 6.2 mmol g-1 h-1, compared to 5.9 mmol g-1 h-1 for COF and 3.4 mmol g-1 h-1 for CS. Notably, COF@CS exhibited excellent removal efficacy for ten other types of PFAS. Moreover, COF@CS could be successfully regenerated using a mixture of 70% ethanol and 1 wt% NaCl, and it exhibited stable reusability for up to five cycles. X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) characterisation, and theoretical calculations revealed that the quaternary amine functional group in COF served as the primary adsorption site in the composite gel material, while the protonated amino group on CS enhanced PFOA adsorption through electrostatic interaction. This study highlights the significant practical potential of COF@CS in the removal of PFAS from aqueous solution and environmental remediation.

Effects of magnesium hydroxide morphology on Pb(ii) removal from aqueous solutions.

In this study, magnesium hydroxide (MH) particles with distinct morphologies were obtained through direct precipitation and subsequent hydrothermal treatment with various magnesium salts. The synthesized products were systematically characterized and utilized for the removal of Pb(ii) ions from aqueous solutions. The adsorption process of Pb(ii) by two different MH structures, namely flower globular magnesium hydroxide (FGMH) and hexagonal plate magnesium hydroxide (HPMH), adhered to the Langmuir isotherm and pseudo-second-order model. FGMH exhibited higher Pb(ii) removal capacity (2612 mg g-1) than HPMH (1431 mg g-1), attributable to the unique three-dimensional layered structures of FGMH that provide a larger surface area and abundant active sites. Additionally, metallic Pb was obtained by recycling the adsorbed Pb(ii) through acid dissolution-electrolysis. Furthermore, Pb(ii) removal mechanisms were investigated by analyzing adsorption kinetics and isotherms, and the adsorbed products were characterized. Based on the findings, the removal process occurs in two key stages. First, Pb(ii) ions bind with OH- ions on the surface upon diffusing to the MH surface, resulting in Pb(OH)2 deposits in situ. Concurrently, Mg(ii) ions diffuse into the solution, substituting Pb(ii) ions in the MH lattice. Second, the resultant Pb(OH)2, which is unstable, reacts with CO2 dissolved in water to yield Pb3(CO3)2(OH)2. Therefore, owing to its outstanding Pb(ii) adsorption performance and simple preparation method, FGMH is a promising solution for Pb(ii) pollution.

Synthesis of Zinc Oxide Doped Magnesium Hydrate and Its Effect on the Flame Retardant and Mechanical Properties of Polypropylene.

In this work, an effective flame retardant consisting of nanoscale zinc oxide doped on the surface of hexagonal lamellar magnesium hydrate (ZO@MH) has been successfully synthesized via a hydrothermal process. Approximately 3-methacryloxypropyltrimethoxysilane (KH-570) is chosen as a modifier of ZO@MH for the purpose of enhancing the interfacial interaction between ZO@MH and the polypropylene (PP) matrix and reducing the agglomeration of ZO@MH. Afterwards, ZO@MH and KH-570 modified ZO@MH (KZO@MH) filled PP (PP/ZO@MH and PP/KZO@MH) composites are respectively prepared via the melt blending method. The flame retardant and smoke suppression properties of PP/ZO@MH and PP/KZO@MH composites are estimated by a cone calorimetry test (CCT). The peak value of the heat release rate of the PP/40KZO@MH composite is 327.0 kW/m2, which is 6.1% and 31.2% lower than that of the PP/40ZO@MH and PP/40MH composites, respectively. The lowest peak values of CO and CO2 production, 0.008 and 0.62 g/s, also appeared in the PP/40KZO@MH composite, which are 11.1% and 10.1% lower than those of the PP/40ZO@MH composite. Analysis of char residues indicates that nanoscale ZO and modification of KH-570 improve the amount and quality of char residues, which should be the main reason for the good flame retardant and smoke suppression properties of KZO@MH. Impact strength and nominal strain at break results show that the PP matrix is toughened by ZO@MH rather than KZO@MH. Tensile properties and the quantitative interfacial interaction calculated by the Turcsányi equation both prove the reinforcement of KZO@MH on the PP matrix.

Facile fabrication of Fe3O4@Mg(OH)2 magnetic composites and their application in Cu(ii) ion removal.

In this study, we fabricated magnetic Fe3O4@Mg(OH)2 composites through the seed deposition technique to achieve Cu(ii) ion removal from aqueous solutions. As indicated by the characterization results, three-dimensional flower-like spheres composed of external Mg(OH)2 were formed, with nano-Fe3O4 particles uniformly embedded in the "flower petals" of the spheres. The efficacy of Fe3O4@Mg(OH)2-3 in Cu(ii) ion removal was examined through batch experiments. The impact of solution pH on removal efficiency was examined, and the pseudo-second-order model and the Langmuir model provided good fits to the adsorption kinetics and isotherm data, respectively. Remarkably, Fe3O4@Mg(OH)2-3 exhibited a significant removal capacity of 1051.65 mg g-1 for Cu(ii) ions. Additionally, the composite displayed a notable saturation magnetization value of 17.3 emu g-1, facilitating isolation from sample solutions through external magnetic fields after Cu(ii) ion absorption. At the solid-liquid interface, a mechanism involving ion exchange between Mg(ii) and Cu(ii) cations was realized as the mode of Cu(ii) ion removal. The composites' effective adsorption properties and rapid magnetic separation highlighted their suitability for use in treating copper-contaminated water.

Post-synthetic thiol modification of covalent organic frameworks for mercury(II) removal from water.

Various materials have been developed for environmental remediation of mercury ion pollution. Among these materials, covalent organic frameworks (COFs) can efficiently adsorb Hg(II) from water. Herein, two thiol-modified COFs (COF-S-SH and COF-OH-SH) were prepared, through the reaction between 2,5-divinylterephthalaldehyde and 1,3,5-tris-(4-aminophenyl)benzene, followed by post-synthetic modification using bis(2-mercaptoethyl) sulfide and dithiothreitol, respectively. The modified COFs showed excellent Hg(II) adsorption abilities with maximum adsorption capacities of 586.3 and 535.5 mg g-1 for COF-S-SH and COF-OH-SH, respectively. The prepared materials showed excellent selective absorbability for Hg(II) against multiple cationic metals in water. Unexpectedly, the experimental data showed that both co-existing toxic anionic diclofenac sodium (DCF) and Hg(II) performed positive effect for capturing another pollutant by these two modified COFs. Thus, a synergistic adsorption mechanism between Hg(II) and DCF on COFs was proposed. Moreover, density functional theory calculations revealed that synergistic adsorption occurred between Hg(II) and DCF, which resulted in a significant reduction in the adsorption system's energy. This work highlights a new direction for application of COFs to simultaneous removal of heavy metals and co-existing organic pollutants from water.

Efficient adsorption and degradation of dyes from water using magnetic covalent organic frameworks with a pyridinic structure.

Covalent organic frameworks (COFs) have promising applications in environmental remediation owing to their precise directional synthesis and superior adsorption ability. However, magnetic COFs with pyridinic N have not been studied as bifunctional materials for the adsorption and catalytic degradation of dyes. Therefore, in this study, a magnetic COF with a pyridinic structure (BiPy-MCOF) was successfully synthesized using a solvothermal method, which exhibited higher methyl orange (MO) removal than other common adsorbents. The best degradation efficiency via the Fenton-like reaction was obtained by pre-adsorbing MO for 3 h at pH 3.1. Both adsorption and catalytic degradation resulted in better removal of MO under acidic conditions. The introduction of pyridinic N improved MO adsorption and degradation on BiPy-MCOF. The electrostatic potential (ESP) showed that pyridinic N had a strong affinity for MO adsorption. Density functional theory calculations confirmed the potential sites on MO molecules that may be attacked by free radicals. Possible degradation pathways were proposed based on the experimental results. Moreover, BiPy-MCOF could effectively degrade MO at least four times, and a high degradation efficiency was obtained in other dyes applications. The coupling of adsorption and degradation demonstrated that the as-prepared BiPy-MCOF was an effective material for organic dyes removal from water.

Organic-Inorganic Modification of Magnesium Borate Rod by Layered Double Hydroxide and 3-Aminopropyltriethoxysilane and Its Effect on the Properties of Epoxy Resin.

To alleviate the safety hazards associated with the use of epoxy resin (EP), a multifunctional filler was designed. This study firstly combines the superior mechanical properties of magnesium borate rods (MBR) with the excellent smoke suppression and flame-retardant characteristics of layered double hydroxide (LDH). H2PO4- intercalated LDH (LDHP) was coated on the MBR surface to obtain inorganic composite particles MBR@LDHP. Subsequently, MBR@LDHP was modified with 3-aminopropyltriethoxysilane (APES) to obtain organic-inorganic composite particles MBR@LDHP-APES. Eventually, the hybrid particles were added to EP to prepare the composite materials. Thereafter, the morphology, composition, and structure of MBR@LDHP-APES were characterized utilizing scanning electron microscopy (SEM), Fourier transform infrared (FTIR), and X-ray diffraction (XRD). The results indicated the successful preparation of MBR@LDHP-APES, after which we investigated the effects of MBR@LDHP-APES on the smoke suppression, flame retardancy, and mechanical characteristics of EP. As observed, the EP composites containing 7.5 wt% MBR@LDHP-APES exhibited superior smoke suppression and flame retardancy abilities. The limiting oxygen index reached 33.5%, which is 36.73% greater than pure EP, and the lowest values of total heat and smoke release were observed for the composite materials. In addition, the mechanical properties test revealed that MBR@LDHP-APES considerably enhanced the tensile strength as well as the flexural strength of the composites. Furthermore, mechanistic studies suggested that the barrier effect of MBR, endothermic decomposition of LDHP, and the synergistic effect of LDHP and APES contributed essentially to the smoke suppression and flame-retardant properties of the material. The findings of this research point to a potential method for enhancing the EP's ability to suppress smoke and flames while enhancing its mechanical properties.

Controllable fabrication of a hybrid containing dodecyl dihydrogen phosphate modified magnesium borate whisker/hydrated alumina for enhancing the fire safety and mechanical properties of epoxy resin.

A composite particle with hydrated alumina deposited on the surface of magnesium borate whisker (MBW@HA) was prepared following a chemical liquid deposition method. Subsequently, dodecyl dihydrogen phosphate (DDP) was grafted onto the surface of the composite particles to synthesize an inorganic-organic hybrid (MBW@HA-DDP). The structure, morphology, and composition of MBW@HA-DDP were well characterized. The results revealed the hybrid of MBW@HA-DDP was successfully synthesized characterized by a hydrophobic surface. Subsequently, the obtained MBW@HA-DDP was incorporated into epoxy resin (EP) to fabricate flame retardant composites. The results revealed that the incorporation of MBW@HA-DDP significantly improved the fire safety of EP, for instance, the total heat release (THR) and peak heat release rate (PHRR) of the EP composite with 10-phr MBW@HA-DDP added were reduced by 28.1% and 32.0%, respectively, accompanied with lower total smoke production (TSP) and smoke production rate (SPR). The improved fire safety was due to the barrier function of MBW and HA, and the dilution effect of water vapor generated from HA. Meanwhile, the phosphorus oxoacids generated from DDP could function as catalysts and increase the degree of graphitization of the char residues, thus protecting the matrix effectively. In relation to mechanical properties, the incorporation of MBW@HA-DDP did not deteriorate the mechanical properties of EP but improved them to some extent. The results presented herein help develop a novel strategy for developing flame retardants characterized by good flame-retardant behavior and improved mechanical properties.

Rapid Removal of Perfluoroalkanesulfonates from Water by ß-Cyclodextrin Covalent Organic Frameworks.

Adsorption is an effective method for the removal of perfluoroalkanesulfonates (PFSAs) from water, and the limitation of the adsorption rate of existing adsorbents motivates efforts to develop novel adsorbents. Here, we developed four ß-cyclodextrin covalent organic frameworks (ß-CD-COFs) with a rapid removal rate and high adsorption capacity for four PFSAs in water including perfluorooctanesulfonate (PFOS), perfluorobutanesulfonate (PFBS), perfluorohexanesulfonate (PFHxS), and chlorinated polyfluorinated ether sulfonate (F53B). All ß-CD-COFs exhibited extremely fast adsorption (adsorption equilibrium <2 min) for PFSAs with high adsorption capacities (0.33-1.51 mmol/g), which were significantly better than those of traditional resins and activated carbons, probably due to the ordered pores of ß-CD-COFs and the electron-deficient cavity ß-CD. Density functional theory (DFT) calculations also showed that PFSAs could be captured in the ß-CD cavity through strong interactions with a high binding energy. The novel ß-CD-COFs were highly selective to PFSAs in simulated wastewater impacted by aqueous film-forming foams, and they could also rapidly remove them from an actual chrome plating wastewater within 2 min. Additionally, the ß-CD-COFs could be regenerated by methanol with relatively good reusability in four cycles, further highlighting their application potential as PFAS adsorbents in water or wastewater.

Granular reduced graphene oxide/Fe3O4 hydrogel for efficient adsorption and catalytic oxidation of p-perfluorous nonenoxybenzene sulfonate.

The catalytic performance of Fe3O4/reduced graphene oxide (Fe3O4/rGO) nanocomposite makes it attractive for the removal of emerging pollutants from water, but the combination of its efficient adsorption and degradation of per- and polyfluoroalkyl substances has not been studied. Here we report the optimal granular Fe3O4/rGO with high thermal and acid resistance stability through controlling its self-assembly for the adsorption and degradation of sodium p-perfluorous nonenoxybenzene sulfonate (OBS) from water. The maximum adsorption capacity for OBS was calculated to be 362.4 µmol/g according to Langmuir fitting. Electrostatic, π-π and hydrogen bonding interactions were involved in OBS adsorption, and the quaternary N in Fe3O4/rGO was a key adsorption site. The efficiency of the utilization of free radicals generated in Fenton-like and persulfate (PS) systems increased with the increase of OBS adsorbed onto the Fe3O4/rGO, while the increase of OBS amount adsorbed on Fe3O4/rGO would casue a slow OBS removal in the adsorption-degradation process due to the slow adsorption process. The Fenton-like oxidation was more efficient for OBS removal than PS oxidation. The spent Fe3O4/rGO was able to be reused in the Fenton-like system at least ten times, while the OBS removal in the PS reaction system was reduced to 47.8 % after six reuse cycles.

Adsorption behaviour and mechanism of the PFOS substitute OBS (sodium p-perfluorous nonenoxybenzene sulfonate) on activated carbon.

Perfluorooctane sulfonate (PFOS) was listed as a persistent organic pollutant by the Stockholm Convention. As a typical alternative to PFOS, sodium p-perfluorous nonenoxybenzene sulfonate (OBS) has recently been detected in the aquatic environment which has caused great concern. For the first time, the adsorption behaviour and mechanism of OBS on activated carbon (AC) with different physical and chemical properties were investigated. Decreasing the particle size of AC can accelerate its adsorption for OBS, while AC with too small particle size was not conducive to its adsorption capacity due to the destruction of its pore structure during the mechanical crushing process. Intra-particle diffusion had a lesser effect on the adsorption rate of AC with smaller particle size, higher hydrophilicity and larger pore size. Reactivation of AC by KOH can greatly enlarge their pore size and surface area, greatly increasing their adsorption capacities. The adsorption capacity of two kinds of R-GAC exceeded 0.35 mmol g-1, significantly higher than that of other ACs. However, increasing the hydrophilicity of AC would decrease their adsorption capacities. Further investigation indicated that a larger pore size and smaller particle size can greatly enhance the adsorptive removal of OBS on AC in systems with other coexisting PFASs and organic matter due to the reduction of the pore-blocking effect. The spent AC can be successfully regenerated by methanol, and it can be partly regenerated by hot water and NaOH solution. The percentage of regeneration for the spent AC was 70.4% with 90°C water temperature and up to 95% when 5% NaOH was added into the regeneration solution. These findings are very important for developing efficient adsorbents for the removal of these newly emerging PFASs from wastewater and understanding their interfacial behaviour.

[Pharmacological research of wild and cultivated Atractylodes lancea].

OBJECTIVE: To explore the differences of the main pharmacological action in wild and cultivated Atractylodes lancea. METHOD: Study the effect of the 70% ethanol extracts from the wild and the culticated A. lancea on the mice with gastriculcer induced by absolute ethyl alcohol or HCl. Stdudy the effect on intestinal propulsive function in mice by measuring the length of intestine and distance of Indian ink. Observe anti-bacteria effect in vitro of the A. lancea by determining the minimum inhibitory concentrations. RESULT: The pharmacological action, which made a little difference in the sane productive places, and made significant differences in different productive places. Compared to Jurong, it has better actions in Luotian on small intestinal propulsive function and bacteriostatic action. There was not an obvious difference in protective effect on gastric ulcer induced by absolute ethyl alcohol and 0.6 mol x L(-1) HC1 between different locations. CONCLUSION: To the main effect, cultvated A. lancea had no significant difference on the whole but having better result in some respects, which can provide the pharmacodynamics evidence of cultivated A. lancea being used instead of the wild.

[Effects of alternate partial root-zone subsurface drip irrigation on potato yield and water use efficiency].

Field experiment was conducted to investigate the effects of alternate partial root-zone subsurface drip irrigation (APRSDI) on the physiological responses, yield, and water use efficiency of potato. Compared with conventional drip irrigation (CDI), APRSDI had less negative effects on the potato leaf photosynthesis rate (P(n)), but decreased the transpiration rate and stomatal conductance significantly. The slightly higher P(n) under CDI was at the expense of consuming more water. No significant difference was observed in the potato yield under APRSDI and CDI, but APRSDI saved the irrigation amount by 25.8% and increased the irrigation water use efficiency and total water use efficiency by 27.5% and 15.3%, respectively, suggesting that APRSDI would be a feasible water-saving irrigation technique for the planting of potato.

[Advances in chemistry, molecular biology and pharmacological of Cangzhu].

We described chemical composition in Cangzhu in recent years, volatile oil is the important chemical composition, The beta-eudesmol, hinesol are active ingredient in volatile oil and there are 38 kind of glycosides. At the same time, we overview the applying of RAPD technology in atractylodes lancea. The results is that there are correlation in chemical composition, genetic differentiation and geographical distribution, there is some truth in bounded by a territorial division of the north-south Cangzhu, and genetic differentiation has been happened in atractylodes lancea to adapting the environment. We described advances of pharmacological in dampness spleen, cardiovascular system, genitourinary system, nervous system, and the results show that there are pharmacological activity in digestive system, cardiovascular system, genitourinary system of atractylodes lancea.

[Effects of infrasound exposure on several enzymes activities of spleen and liver in rats].

AIM: To investigate the changes of several enzymes activities in the spleen and liver of rats after exposure to 8 Hz 130 dB infrasound for different time. METHODS: Thirty-five male SD rats were randomly divided into five groups. Rats of group 1 served as control, rats from group 2 to 5 were exposed to 8 Hz 130 dB infrasound, 2 hours per day, for 1 wk, 2 wk, 3 wk, and 4 wk, respectively. The changes of enzymes activities in spleen and liver of rats were observed. RESULTS: Monoamine oxidase activities in spleen were significantly increased at 1 wk and 2 wk, it was decreased at 3 wk, and increased again at 4 wk (P < 0.05). There were no changes in the liver compared with the control group. Glutathione peroxides activities in spleen were significantly increased at 4 wk (P < 0.05) and it also increased in liver at 1 wk (P < 0.05). Superoxide dismutase activities in spleen were increased significantly from 1 wk to 4 wk, but there were no markedly changes in liver. The level of malondialdehyde in spleen were increased at 3 wk and 4 wk. In the liver, it were increased at 1 wk and 2 wk, and decreased at 3 wk, but it increased again at 4 wk (P < 0.05). CONCLUSION: The results indicated that lipid peroxidation and oxygen free radicals in spleen and liver were increased after infrasound exposure and it might induce the damage in tissue or cells.