Heavy metal removal from water/wastewater by nanosized metal oxides: a review.

Covalent organic frameworks (COFs) are a class of crystalline porous organic polymers with permanent porosity and highly ordered structures. Unlike other polymers, a significant feature of COFs is that they are structurally predesignable, synthetically controllable, and functionally manageable. In principle, the topological design diagram offers geometric guidance for the structural tiling of extended porous polygons, and the polycondensation reactions provide synthetic ways to construct the predesigned primary and high-order structures. Progress over the past decade in the chemistry of these two aspects undoubtedly established the base of the COF field. By virtue of the availability of organic units and the diversity of topologies and linkages, COFs have emerged as a new field of organic materials that offer a powerful molecular platform for complex structural design and tailor-made functional development. Here we target a comprehensive review of the COF field, provide a historic overview of the chemistry of the COF field, survey the advances in the topology design and synthetic reactions, illustrate the structural features and diversities, scrutinize the development and potential of various functions through elucidating structure-function correlations based on interactions with photons, electrons, holes, spins, ions, and molecules, discuss the key fundamental and challenging issues that need to be addressed, and predict the future directions from chemistry, physics, and materials perspectives.

Covalent Organic Frameworks: Design, Synthesis, and Functions.

Polycyclic Hydrocarbons Vol. 1. Pp. xxvi + 487. 126S. (With a chapter on carcinogenesis by Regina Schoental.) Vol. 2. Pp. lvii + 487. 140s. By E. Clar. (London and New York: Academic Press; Berlin: Springer-Verlag, 1964.)

Polycyclic Aromatic Hydrocarbons

Amino-functionalized Fe3O4@SiO2 core–shell magnetic nanomaterial as a novel adsorbent for aqueous heavy metals removal

Hyperalgesia and allodynia are frequent symptoms of disease and may be useful adaptations to protect vulnerable tissues. Both may, however, also emerge as diseases in their own right. Considerable ...

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Models and Mechanisms of Hyperalgesia and Allodynia

Humic acid (HA) coated Fe3O4 nanciparticles (Fe3O4/HA) were developed for the removal of toxic Hg(II), Pb(II), Cd(II), and Cu(II) from water. Fe3O4/HA were prepared by a coprecipitation procedure with cheap and environmentally friendly iron salts and HA. TOC and XPS analysis showed the as-prepared Fe3O4/ HA contains similar to 11% (w/w) of HA which are fractions abundant in O and N-based functional groups. TEM images and laser particle size analysis revealed the Fe3O4/HA (with similar to 10 nm Fe3O4 cores) aggregated in aqueous suspensions to form aggregates with an average hydrodynamic size of similar to 140 nm. With a saturation magnetization of 79.6 emu/g, the Fe3O4/HA can be simply recovered from water with magnetic separations at low magnetic field gradients within a few minutes. Sorption of the heavy metals to Fe3O4/HA reached equilibrium in less than 15 min, and agreed well to the Langmuir adsorption model with maximum adsorption capacities from 46.3 to 97.7 mg/g. The Fe3O4/HA was stable in tap water, natural waters, and acidic/ basic solutions ranging from 0.1 M HCl to 2 M NaOH with low leaching of Fe (<= 3.7%) and HA (<= 5.3%). The Fe3O4/HA was able to remove over 99% of Hg(II) and Pb(II) and over 95% of COO and Cd(II) in natural and tap water at optimized pH. Leaching back of the Fe3O4/HA sorbed heavy metals in water was found to be negligible.

Coating Fe3O4 Magnetic Nanoparticles with Humic Acid for High Efficient Removal of Heavy Metals in Water

Effective heavy metal removal from aqueous systems by thiol functionalized magnetic mesoporous silica.

As the most complex halogenated contaminants, short chain chlorinated paraffins (SCCPs) are scarcely reported in marine environments. In this work, a total of 117 surficial sediment (0-3 cm) samples and two sediment cores were collected from the Chinese Bohai and Yellow Seas to systematically study the spatial and temporal trends of SCCPs at a large scale in the Chinese marine environment. Total SCCP concentrations in the surficial sediments were in the range of 14.5-85.2 ng g(-1) (dry weight, d.w.) with an average level of 38.4 ng g(-1) d.w. Spatial distribution showed a decreasing trend with the distance from the coast to the open waters. Compositional pattern analysis suggested that C10 was the most predominant homologue group, followed by C11, C12, and C13 homologue groups. The concentrations of total SCCPs in sediment cores ranged from 11.6 to 94.7 ng g(-1) d.w. for YS1 and from 14.7 to 195.6 ng g(-1) d.w. for YS2, with sharp rise from the early 1950s to present based on (210)Pb dating technique. The historical records in cores correspond well to the production and usage changes of CPs in China. Multivariate regression statistics indicate TOC, latitude and longitude are the major factors influencing surficial SCCP levels in the Chinese East Seas by combining analysis with the data from the East China Sea (R(2) = 0.332, p < 0.01). These findings indicated that the sources of SCCPs were mainly from river outflows via ocean current and partly from atmospheric depositions by East Asian monsoon in the sampling areas.

Spatial Distributions and Deposition Chronology of Short Chain Chlorinated Paraffins in Marine Sediments across the Chinese Bohai and Yellow Seas

Removal of heavy metal ions from aqueous solution using Fe3O4–SiO2-poly(1,2-diaminobenzene) core–shell sub-micron particles

An electrochemical bisphenol A sensor based on one step electrochemical reduction of cuprous oxide wrapped graphene oxide nanoparticles modified electrode

Zongshan Zhao

Papers

Coating Fe3O4 Magnetic Nanoparticles with Humic Acid for High Efficient Removal of Heavy Metals in Water

Effective heavy metal removal from aqueous systems by thiol functionalized magnetic mesoporous silica.

Spatial Distributions and Deposition Chronology of Short Chain Chlorinated Paraffins in Marine Sediments across the Chinese Bohai and Yellow Seas

Removal of heavy metal ions from aqueous solution using Fe3O4–SiO2-poly(1,2-diaminobenzene) core–shell sub-micron particles

An electrochemical bisphenol A sensor based on one step electrochemical reduction of cuprous oxide wrapped graphene oxide nanoparticles modified electrode