Spatio-temporal characteristics and mechanism of ecological degradation in a hilly southern area-a case study of Dongting Lake Basin.

Understanding the spatio-temporal characteristics of ecological degradation and its mechanism is the key to implementing national land space ecological restoration. Currently, there is a lack of knowledge about identifying ecologically degraded areas from a structure-function angle. This paper used the Dongting Lake Basin (DLB) as the research area, with the landscape pattern index and InVest model utilized to analyze the landscape distribution characteristics and ecosystem service functions in 2000 and 2018. Based on this, a fuzzy inference approach and geographic detectors were used to explore the characteristics and driving mechanism of ecological degradation in the DLB from 2000 to 2018. The results found are the following: (1) The overall landscape of the DLB was fragmented, the landscape shape tended to be complex, the degree of aggregation declined, and the landscape types were more discrete than before. In terms of the landscape-level index, the overall indicators of the landscape pattern in the DLB showed little change from 2000 to 2018, and the overall landscape pattern change was reasonably stable. (2) The three ecological services exhibited prominent spatial distribution features during the study period. In particular, food supply services showed a steady upward trend, while habitat quality and carbon storage services generally declined. (3) The ecological degradation in the DLB demonstrated striking spatial and temporal differences during the study period, and the ecological situation improved. The ecological degradation areas were mainly distributed in urban areas with denser populations and a higher level of urbanization, while the ecological restoration areas were mainly in the mountainous and hilly areas far away from the urban centers. (4) Among the influential factors, the production potential of urban land and farmland is the main factor that affects the ecological environment degradation and spatial distribution difference in the DLB. The interactive detection results indicate that the driving mechanism exhibits a two-factor enhancement or nonlinear increase.

Removal of 17ß-Estradiol from water by adsorption onto montmorillonite-carbon hybrids derived from pyrolysis carbonization of carboxymethyl cellulose.

In this work, we demonstrated the preparation of the carbonized montmorillonite/carboxymethyl cellulose (MMT/CMC) hybrids and their application as an adsorbent for efficient removal of 17ß-Estradiol (ßE2). X-ray diffractometer (XRD) results showed that CMC intercalation reached saturation at a CMC to MMT weight ratio of 1; transmission electron microscope (TEM) measurements clearly revealed that carbonization caused graphenes distribute on the MMT surfaces; pyrolysis temperature at 600 °C yielded novel MMT/CMC sample of high surface areas as reflected by Brunauer-Emmett-Teller (BET) surface area. The adsorbed amount of ßE2 under various conditions decreased in the order MMT/CMC1:1(600) > MMT/CMC1:1(450) > MMT/CMC1:1(300) ∼ MMT/CMC2:1(600) ∼ MMT > MMT/CMC5:1(600). The removal of ßE2 by MMT/CMC1:1(600) occurred very quickly, and the adsorption kinetics could be well fitted by the Ritchie nth-order kinetic model; the best-fit adsorption isotherm model was Freundlich model. The MMT/CMC1:1(600) also exhibited good regeneration performance after five adsorption/desorption cycles. The experimental results also showed that the adsorption of ßE2 on the MMT/CMC1:1(600) composite could contribute to hydrophobic partitioning, π-π staking interaction, H-bond interaction, pore-filling effect and simple van der Waals interaction. This highly effective and novel adsorbent can be easily synthesized and regenerated, indicating its great potential in drinking and wastewater purification for endocrine disruptor compounds.

Adsorption studies of 17ß-estradiol from aqueous solution using a novel stabilized Fe-Mn binary oxide nanocomposite.

The removal of 17ß-estradiol (E2) from contaminated water on nanoscale Fe-Mn binary oxide-loaded multiwalled carbon nanotubes (MWCNTs/FMBO) was evaluated in this work. The characterizations of the mesoporous adsorbent were analyzed by using SEM, TEM, VSM, XRD, XPS, and FTIR measurements. The effects of experimental conditions in E2 removal, including stabilizer additional level, adsorption time, initial E2 concentration, solution pH, reaction temperature, and foreign ions, were examined. The maximum monolayer adsorption capacity (qm) of MWCNTs/FMBO for E2 in the experiment was 47.25 mg/g as verified by the Langmuir sorption isotherm study. The adsorption process was pH-sensitive with an optimum pH of 7.0. On the kinetics study, the adsorption data could be satisfactorily fitted by the pseudo-second-order kinetics. Thermodynamic parameters indicated that the adsorption process was spontaneous and exothermal. In addition, the foreign ions did not show any noticeable inhibition for E2 removal from the water solution except for PO43- that was adversely affected for E2 uptake than other anions in a certain concentration. The adsorption capacities of the mesoporous adsorbent remained at 86.16% even after five adsorption-desorption cycles without significant loss of capacity, which demonstrated the stability and reusability for further removal of E2. Moreover, both hydrogen bond and π-π interaction might be the dominating adsorption mechanisms for E2 adsorption onto MWCNTs/FMBO.

Fabrication of Stabilized Fe⁻Mn Binary Oxide Nanoparticles: Effective Adsorption of 17ß-Estradiol and Influencing Factors.

Fe⁻Mn binary oxide nanoparticles (FMBON) were reported to be high performance as adsorbent for pollutants removal from aqueous solution. However, there are still limitations in practice application due to the FMBON tend to aggregate into the micro millimeter level. In order to avoid the agglomeration of nanoparticles, this work synthesized the stabilized Fe⁻Mn binary oxide nanoparticles (CMC-FMBON) by using water-soluble carboxymethyl celluloses (CMC) as the stabilizer. The characteristics of CMC-FMBON and FMBON were measured by using Transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and Zeta potential. This work systematically investigated the adsorption capacity of CMC-FMBON for 17ß-estradiol (E2) and the influences of external environmental factors on E2 removal. The results indicated that CMC-FMBON had much smaller particles, wider dispersion and larger surface area than the FMBON. CMC-FMBON showed better adsorption performance for E2 than FMBON with the maximum adsorption capacity of CMC-FMBON and FMBON were 124.10 and 98.14 mg/g at 298 K, respectively. The experimental data can be well fitted by the model of pseudo-second-order and Langmuir model. The E2 removal by CMC-FMBON was obviously dependent on pH with the maximum adsorption occurring when the pH was acidic. The removal capacity of CMC-FMBON increased when enhancing ionic strength in solution. Background electrolytes promoted slightly E2 adsorption process whereas the presence of humic acid inhibited the E2 removal. π-π interactions, hydrogen bonds, and oxidation might be responsible for E2 removal. This research suggested that the CMC-FMBON has been considered to be a cost-efficient adsorbent for removing E2 from water.

Influence of sodium dodecyl sulfate coating on adsorption of methylene blue by biochar from aqueous solution.

Biochar is regarded as a promising new class of materials due to its multifunctional character and the possibility of effectively coupling different properties. With increasing introduction into the environment, environmental chemicals such as surfactants will load onto the released biochar and change its physicochemical characteristics and adsorption behavior toward pollutants. In this study, sodium dodecyl sulfate (SDS), as one type of anionic surfactant, was coated onto biochar with different loading amounts. The influence of SDS loading onto biochar's physicochemical properties were investigated by Fourier transform infrared (FT-IR) spectroscopy, elemental analysis, zeta potential and Brunauer-Emmett-Teller (BET) surface area and pore size distribution analysis. Results showed that the pore size of the biochar decreased gradually with the increase of SDS loading because of the surface-adsorption and pore-blocking processes; the pH of the point of zero charge (pHPZC) decreased with increasing SDS loading. Although surface-coating with SDS decreased the pore size of the biochar, its adsorption capacity toward Methylene Blue (MB) significantly increased. The biochar-bound SDS introduced functional groups and negative charges to the biochar surface, which could thus enhance the adsorption of MB via hydrogen bonding and electrostatic interaction. The results can shed light on the underlying mechanism of the influence of anionic surfactants on the adsorption of MB by biochar.

Effect of Cu(II) ions on the enhancement of tetracycline adsorption by Fe3O4@SiO2-Chitosan/graphene oxide nanocomposite.

Fe3O4@SiO2-Chitosan/GO (MSCG) nanocomposite was investigated by various techniques (SEM, TEM, XRD, VSM, FT-IR, XPS) for the removal of tetracycline (TC). Effects of pH, zeta potential and initial contaminant concentration were studied in detail. Four background cations (Na+, K+, Ca2+ and Mg2+) with a concentration of 0.01M showed little influence on the TC adsorption at the studied pH range while the divalent heavy metal cation Cu(II) could significantly enhance the adsorption. The results indicated that the highest adsorption capacity of TC were 183.47mmol/kg and 67.57mmol/kg on MSCG with and without Cu(II), respectively. According to mechanism investigation for the adsorption of TC by pH impact study and XPS analysis, besides electrostatic interaction and π-π interactions, the Cu(II) also acts as a bridge between TC and MSCG, which significantly improve the adsorption of TC. This study provided valuable guidance and effective method for the removal of TC from aquatic environments.