Insight into the adsorption of tetracycline onto amino and amino–Fe functionalized mesoporous silica: Effect of functionalized groups

In order to study the influences of functionalized groups onto the adsorption of tetracycline (TC), we prepared a series of amino and amino–Fe^3 + complex mesoporous silica adsorbents with diverse content of amino and Fe^3 + groups (named N,N-SBA15 and Fe-N,N-SBA15). The resulting mesoporous silica adsorbents were fully characterized by X-ray powder diffraction, Fourier transform infrared spectrometer and N₂ adsorption/desorption isotherms. Furthermore, the effects of functionalized groups on the removal of TC were investigated. The results showed that the periodic ordered structure of SBA-15 was maintained after modification of amino/Fe^3 + groups. The functionalized amino groups decreased the adsorption capacity while the coordinated Fe^3 + increased the adsorption capacity. The adsorption kinetics of TC fitted pseudo-second-order model well and the equilibrium was achieved quickly. The adsorption isotherms fitted the Langmuir model well and with the Fe^3 + content increased from 3.93% to 8.26%, the Q_max of the adsorbents increased from 102 to 188 mmol/kg. The solution pH affected the adsorption of TC onto amino complex adsorbents slightly while influenced the adsorption onto Fe-amine complex adsorbents greatly. The adsorption of TC on SBA15 and N,N-SBA15 may be related to the formation of outer-sphere surface complexes, while the adsorption of TC onto Fe-N,N-SBA15 was mainly attributed to the inner-sphere surface complexes. This study could offer potential materials that have excellent adsorption behavior for environmental remediation and suggested useful information for the preparing other adsorbents in environmental applications.     

Insight into the mechanisms of trichloronitromethane formation by vacuum ultraviolet: QSAR model and FTICR-MS analysis

Vacuum ultraviolet(VUV) photolysis is recognized as an environmental-friendly treatment process. Nitrate(NO-3) and natural organic matter(NOM) are widely present in water source.We investigated trichloronitromethane(TCNM) formation during chlorination after VUV photolysis, because TCNM is an unregulated highly toxic disinfection byproduct. In this study:(1) we found reactive nitrogen species that is generated under VUV photolysis of NO-3react with organic matter to form nitrogen-containing compo...     

Underestimation of phosphorus fraction change in the supernatant after phosphorus adsorption onto iron oxides and iron oxide–natural organic matter complexes

The phosphorus(P) fraction distribution and formation mechanism in the supernatant after P adsorption onto iron oxides and iron oxide-humic acid(HA) complexes were analyzed using the ultrafiltration method in this study.With an initial P concentration of 20 mg/L(I =0.01 mol/L and pH = 7),it was shown that the colloid(1 kDa-0.45 μm) component of P accounted for 10.6%,11.6%,6.5%,and 4.0%of remaining total P concentration in the supernatant after P adsorption onto ferrihydrite(FH),goethite(GE),ferrihydrite-humic acid complex(FH-HA),goethite-humic acid complex(GE-HA),respectively.The 1 kDa component of P was still the predominant fraction in the supernatant,and underestimated colloidal P accounted for 2.2%,55.1%,45.5%,and 38.7%of P adsorption onto the solid surface of FH,FH-HA,GE and GE-HA,respectively.Thus,the colloid P could not be neglected.Notably,it could be interpreted that Fe~(3+) hydrolysis from the adsorbents followed by the formation of colloidal hydrous ferric oxide aggregates was the main mechanism for the formation of the colloid P in the supernatant.And colloidal adsorbent particles co-existing in the supernatant were another important reason for it.Additionally,dissolve organic matter dissolved from iron oxide-HA complexes could occupy large adsorption sites of colloidal iron causing less colloid P in the supernatant.Ultimately,we believe that the findings can provide a new way to deeply interpret the geochemical cycling of P,even when considering other contaminants such as organic pollutants,heavy metal ions,and arsenate at the sediment/soil-water interface in the real environment.     

Preparation and properties of chitosan–metal complex: Some factors influencing the adsorption capacity for dyes in aqueous solution

Chitosan–metal complexes have been widely studied in wastewater treatment, but there are still various factors in complex preparation which are collectively responsible for improving the adsorption capacity need to be further studied. Thus, this study investigates the factors affecting the adsorption ability of chitosan–metal complex adsorbents, including various kinds of metal centers, different metal salts and crosslinking degree. The results show that the chitosan–Fe( Ⅲ) complex prepared by sulfate salts exhibited the best adsorption efficiency(100%) for various dyes in very short time duration(10 min), and its maximum adsorption capacity achieved 349.22 mg/g. The anion of the metal salt which was used in preparation played an important role to enhance the adsorption ability of chitosan–metal complex. SO_4~(2-) ions not only had the effect of crosslinking through electrostatic interaction with amine group of chitosan polymer, but also could facilitate the chelation of metal ions with chitosan polymer during the synthesis process.Additionally, the p H sensitivity and the sensitivity of ionic environment for chitosan–metal complex were analyzed. We hope that these factors affecting the adsorption of the chitosan–metal complex can help not only in optimizing its use but also in designing new chitosan–metal based complexes.     

Simultaneous adsorption of As(Ⅲ) and Pb(Ⅱ) by the iron-sulfur codoped biochar composite:Competitive and synergistic effects

Simultaneous elimination of As(Ⅲ) and Pb(Ⅱ) from wastewater is still a great challenge.In this work,an iron-sulfur codoped biochar (Fe/S-BC) was successfully fabricated in a simplified way and was applied to the remediate the co-pollution of As(Ⅲ) and Pb(Ⅱ).The positive enthalpy indicated that the adsorption in As-Pb co-pollution was an endothermic reaction.The mechanism of As(Ⅲ) removal could be illustrated by surface complexation,oxidation and precipitation.In addition to precipitation and com...     

Efficient reduction and adsorption of Cr(Ⅵ) using FeCl3-modified biochar:Synergistic roles of persistent free radicals and Fe(Ⅱ)

Transition metal iron and persistent free radicals(PFRs) both affect the redox properties of biochar, but the electron transfer relationship between them and the coupling reduction mechanism of Cr(Ⅵ) requires further investigation. To untangle the interplay between iron and PFRs in biochar and the infuences on redox properties, FeCl₃-modified rice husk biochar(FBCs) was prepared and its reduction mechanism for Cr(Ⅵ) without light was evaluated. The FBCs had higher surface positive cha...     

An estimate of the conversion rates of SO_2 to SO_4~(2-)- and NO_2 to HNO_(3+) NO_3~- for the evaluation air pollution in Beijing

The conversion rates of SO2 to SO42- and NO2 to HNO3+NO3- are estimated from the field-data obtained in Beijing in summer, 1988. The results show that the conversion rate of NO2 is about four times as much as that of SO2; The conversion rates have a diurnal variation in a day. On the average, the rate of SO2 is estimated to be 4.7% h-1 during the daytime and 3.4% h-1 during the nighttime. Similarly, the rate of NO2 is estimated to be 17.2% h-1 and 12% h-1 respectively.     

Enhancement of the CO2 adsorption and hydrogenation to CH4 capacity of Ru–Na–Ca/γ–Al2O3 dual function material by controlling the Ru calcination atmosphere

Integrated CO₂capture and utilization (ICCU) technology requires dual functional materials(DFMs) to carry out the process in a single reaction system.The influence of the calcination atmosphere on efficiency of 4%Ru-8%Na₂CO₃-8%CaO/γ-Al₂O₃DFM is studied.The adsorbent precursors are first co-impregnated onto alumina and calcined in air.Then,Ru precursor is impregnated and four aliquotes are subjected to different calcination protocols:static a...     

Integrated modelling of climate control and air pollution: Methodology and results from one-way coupling of an energy–environment–economy (E3MG) and atmospheric chemistry model (p-TOMCAT) in decarbonising scenarios for Mexico to 2050

This paper reports the methodology and results of an one-way coupling of the E3 Model at the Global level (E3MG) model to the global atmospheric chemistry model, p-TOMCAT, to assess the effects on the concentrations of atmospheric gases over Mexico of a low-GHG scenario compared to an alternative reference case with higher use of fossil fuels. The paper covers the data and methods, changes in atmospheric gas concentrations, the macroeconomic effects of the policies, and the outcome for pollution. The results suggest that in the conditions of underemployment in Mexico, substantial investment in low-carbon technologies, such as electric vehicles, heat pumps and geo-thermal power, could improve employment prospects, maintain growth, as well as reduce some of the risks associated with prospective falls in oil revenues. The concentrations of low-level ozone, both for Mexico-only and global decarbonisation scenarios relative to the original reference case, show appreciable reductions, sufficient to bring concentrations close to the WHO guideline levels. An indication is given of the potential scale of the benefits on human health in Mexico City.     

Typologies of crop-drought vulnerability: an empirical analysis of the socio-economic factors that influence the sensitivity and resilience to drought of three major food crops in China (1961–2001)

Why is it that sometimes small droughts trigger serious crop losses while in other cases even large droughts do not have such a major effect? In this paper, we identify socio-economic indicators associated with sensitivity and resilience to drought for each of China's main grain crops (rice, wheat and corn). Provincial harvest and rainfall data (1961–2001) are used to calculate an annual “crop-drought vulnerability index”. We separate “sensitive cases” (where significant harvest losses occurred in years with only minor droughts) and “resilient cases” (where harvest losses were minimal despite there being a major drought) and explore the socio-economic characteristics of these different situations. Results show that sensitive cases were particularly common in economically poor landlocked provinces and in wealthy coastal areas that have a limited land base. In such “sensitive cases”, the size of the rural population and the quantity of agricultural inputs were negatively correlated with drought vulnerability, while for resilient cases, vulnerability was negatively correlated with the abundance of land. This leads us to propose a series of drought-vulnerability typologies based on the extent to which land, labour, capital, agricultural technology, and infrastructure buffer or exacerbate the effect of a drought event.     

First-principles study on the heterogeneous formation of environmentally persistent free radicals (EPFRs) over α-Fe2O3(0001) surface:Effect of oxygen vacancy

Metal oxides with oxygen vacancies have a significant impact on catalytic activity for the transformation of organic pollutants in waste-to-energy (WtE) incineration processes.This study aims to investigate the influence of hematite surface oxygen point defects on the formation of environmentally persistent free radicals (EPFRs) from phenolic compounds based on the first-principles calculations.Two oxygen-deficient conditions were considered:oxygen vacancies at the top surface and on the subsurf...     

Comments on “Efficient adsorption of Mn(II) by layered double hydroxides intercalated with diethylenetriaminepentaacetic acid and the mechanistic study. J. Environ. Sci. 85, 56–65”

正In the paper entitled Efficient adsorption of Mn(Ⅱ) by layered double hydroxides intercalated with di ethylenetriaminepentaacetic acid and the mechanistic study in Journal of Environmental Sciences,volume 85,page 56-65,there were problems with mathematical notation and dimensional errors in the calculation for Giibbs free energy.In Section 2.5:Adsorption isotherms and thermodynamics studies,authors calculated the Gibbs free energy change (△G°)