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1.
The chitosan–montmorillonite composites (CTS–MMT) were prepared by CTS in combination with Na-type montmorillonite (Na-MMT). The composites were characterized by X-ray diffraction and Fourier transform infrared spectroscopy. The effects of initial pH value of the solution, adsorbent dose, the mass ratio of CTS to Na-MMT, the adsorption temperature, and contact time on acid fuchsin (AF) removal efficiency were investigated. The results indicated that the CTS could be successfully intercalated into the interlayers of Na-MMT. With the increase in content of CTS, some of them may be distributed on the surfaces of the clay and the AF removal efficiency can reach 80.2% using CTS–MMT as adsorbent to treatment AF wastewater (the AF concentration 20?mg/L) under the condition of pH, 5; adsorbent dose, 5?g/L; the mass ratio of CTS to Na-MMT, 0.25:1; adsorption temperature, 40°C; and contact time, 90?min. Meanwhile, it was shown that the adsorption processes were better fitted by pseudo-second-order model and the Freundlich model. 相似文献
2.
《Marine Chemistry》2007,103(1-2):103-111
Particle–water interactions of selected platinum group elements (PGE) have been studied as a function of pH (between 5 and 10), salinity, and concentrations of Cl− and Ca2+. Rhodium(III), Pd(II) and Pt(IV) were added to water samples and sediment suspensions and, following a period of equilibration and subsequent phase separation, filtrates and HCl-digested filters were analysed by ICP-MS. PGE removal from the aqueous phase to the particulate phase appeared to proceed via both coagulation of organic/colloidal associations and adsorption to estuarine sediment particles. In river water, removal of Rh increased and Pt decreased with increasing pH, whereas Pd was not detected in the particulate phase throughout much of the pH range studied. In end-member estuarine water (salinity = 28), removal of Rh and Pt increased with increasing pH, but removal of Pd was relatively insensitive to pH. Conditional particulate-aqueous distribution coefficients, KDs (mL g− 1), were on the order of a few hundred (Pd and Pt) to several thousand (Rh) along the estuarine gradient. Increasing salinity and Cl− concentration were accompanied by an increase in KD for Rh and Pd, and a reduction in KD for Pt, while increasing Ca2+ concentration resulted in an increase in KD for all PGE. Experimental observations were qualitatively interpreted in terms of what is known about the aqueous speciation of PGE. Thus, Rh data were consistent with the adsorption of cationic species of the form: [RhCl6−x(H2O)x]x−3, where x = 0 to 6; although in river water complexation by additional (e.g. organic) ligands may have also occurred. Speciation of Pd was predicted to be dominated by organic complexes under all experimental conditions, consistent with its stabilisation in solution in freshwater and apparent salting out and/or coagulation in the presence of dissolved ions. The presence of hydroxychloride complexes of Pt(IV), whose ligand number (and negative charge) increases with increasing chlorinity, could explain most of the experimental observations for this element. 相似文献
3.
The extent and mechanisms of adsorption of marine pore water organic matter to montmorillonite were studied in a series of batch and sequential adsorption experiments. Pore water natural organic matter (pNOM) and easily extracted natural organic matter (eNOM) were collected from Liberty Bay (Puget Sound, WA, USA) sediments. The pNOM and eNOM were each divided into two size fractions using a 1000 D ultrafilter. Batch adsorption isotherms were approximately linear, and the >1000 D fractions of both pNOM and eNOM had larger partition coefficients (Kd) than the <1000 D fractions. A two-component fit of the sequential adsorption data indicated that pNOM and eNOM contained a similar amount of NOM (30%) that was not surface reactive toward montmorillonite. After correcting the batch adsorption Kds for the non-reactive components, the Kds estimated by batch and sequential adsorption were identical (2.7 l/kg for >1000 D pNOM and eNOM, and 1.6 l/kg for <1000 D pNOM and eNOM). Mechanisms of adsorption were investigated by systematically changing conditions (pH, temperature and ionic composition) of >1000 D fractions during batch isotherm experiments. Adsorption of NOM was found to decrease with increased temperature, suggesting that hydrophobic effects were not the dominant adsorption mechanisms in this system. Ion exchange was also not an important adsorption mechanism because adsorption increased with ionic strength. The observed enhancement in adsorption with ionic strength indicated that van der Waals interactions were important in the adsorption of NOM. Ligand exchange was found to be a significant mechanism since the presence of SO42− in solution reduced the amount of NOM adsorbed. Ca2+ enhanced adsorption slightly more than Na+, suggesting that cation bridging was involved. The relative contributions of van der Waals interactions, ligand exchange and cation bridging were estimated to be approximately 60%, 35% and 5%, respectively, for adsorption of NOM in a CaCl2 solution. 相似文献
4.
An efficient Al-Fe cointercalated bentonite composite material (Al-Fe/Bent) which is capable of removing hexavalent chromium [Cr(VI)] from aqueous solutions was prepared. The batch experiment studies were conducted to evaluate the adsorption performance of Cr(VI) contained in aqueous solution. The XRD results showed the spacing of layers of bentonite was increased due to the aluminum and iron polycation intercalated into the layer of bentonite. The removal rate of Cr(VI) from the aqueous solution could be up 87.4% under the condition of the dosage of Al-Fe/Bent 8 g/L, pH 4, and a contact time of 60 min. The equilibrium data fitted well to the Freundlich model. The adsorption process could be well described by the pseudosecond order kinetic model. 相似文献
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7.
The reduction of heavy metals (cadmium, lead and zinc) in the presence of long-chain fatty acids (lauric, oleic and linoleic) in 0.55 mol dm?3 NaCl and 0.03 mol dm?3 NaHCO3 at pH 8.7 has been studied by differential pulse polarography. The increase of the peak height of investigated metals by up to tenfold the value obtained in electrolyte without fatty acid is due to adsorption of metal ions at the electrode surface. The accumulation of metal increases with the increase of adsorption time (at potentials more positive than the reduction potential of the particular metal) and with increase of salinity. The heavy-metal adsorption depends on the concentrations of both metal ions and fatty acids. The interaction of heavy metals with the unsaturated fatty acids in the bulk and/or in the adsorbed layer at different natural interfaces could be of considerable importance in an understanding of the fate and distribution of heavy metals in the natural aquatic environment. 相似文献
8.
The extent and kinetics of Np(V)O2+ adsorption from dilute aqueous solutions and seawater onto a variety of synthetic and natural solids were determined at 25°C and 1 atm total pressure. Extensive and complex adsorption reactions were found, contrary to speculations in the literature that NpO2+ should behave as a simple monovalent ion with a low affinity for surfaces. When normalized to adsorption per unit solid surface area, the ranking for the synthetic solids was aragonite ? calcite > goethite ? MnO2 ≈ clays. Natural materials generally followed the same behavior patterns as their synthetic counterparts. The dissolved/adsorbed ratio was found to be constant over a wide range (10?13–10?7M) of NpO2+ concentrations. At higher concentrations the extent of adsorption decreased until a solubility limit was reached at approximately 10?5 M.Solution composition had the most significant influence for NpO2+ adsorption on goethite, where much more extensive adsorption occurs in dilute solutions than in seawater. When seawater is added to a dilute solution, extensive desorption of NpO2+ from goethite occurs. Tests conducted on NpO2+ adsorbed on carbonates indicated that it remained in the V oxidation state.There is a growing consensus that Pu dissolved in natural waters also occurs dominantly in the V oxidation state as PuO2+ ion. Consequently, these results for NpO2+ may serve as a guide for Pu behavior when also in the V oxidation state. The fact that most adsorbed Pu is found in the III or IV oxidation states indicates that reduction of Pu may occur subsequent to adsorption in the V oxidation state. 相似文献
9.
S. R. Aston 《Marine Chemistry》1980,8(4):319-326
Thermodynamic considerations based on existing data from various laboratory studies of plutonium species in aqueous solution are used to predict the speciation of this radioactive pollutant in seawater. Oxidation-reduction data for plutonium suggest that Pu(VI) should be very dominant in seawater solution compared to Pu(IV), and that Pu(III) and Pu(V) should be absent. The disproportionation reactions and the alpha reduction mechanism are probably of no consequence to the oxidation state in seawater. However, the irreversible hydrolysis of Pu4+ and the associated formation of polymeric Pu(OH)4 colloids are important mechanisms of speciation control and plutonium removal to sediments, by adsorption onto suspended matter. Stability constants for plutonium complexation with inorganic ligands in seawater suggest that Pu(VI) dissolved in seawater will be dominantly PuO2CO3OH−.The theoretical predictions of plutonium speciation and behaviour in seawater are compared to the only available data on plutonium speciation in seawater (Nelson and Lovett, 1978). Good agreement between the predictions and field observations was obtained, within the limitations imposed by the scarcity of data on this subject. 相似文献
10.
为了阐释鱼、蚌生态混养的可行性,通过建立微型生态系统,探索不同养殖密度和处理时间的背角无齿蚌(Anodonta woodiana)对池塘底泥释放营养盐的净化效果。结果表明:背角无齿蚌对pH、DO和总固溶物的影响总体不明显,但能够显著降低浊度和Chl-a含量(P0.05),最大去除率分别为79.2%和83.4%;背角无齿蚌对营养盐的净化效果受到处理时间、养殖密度的显著影响(P0.05);TN、NO_3~–-N和NO_2~–-N呈现升高的趋势,而能够显著降低NH_4~+-N、TP和PO_4~(3–)的含量(P0.05),最大去除率分别为90.9%、55.6%和52.9%。响应面优化分析显示蚌养殖密度和处理时间的配比分别为27个/m~3和22.63 d、25个/m~3和23.69 d时,对TP和PO_4~(3–)的去除率可进一步提升至68.9%和58.1%。本研究表明背角无齿蚌有潜力用于养殖池塘底泥富营养化的防控。 相似文献
11.
The adsorption of Pb2+ and of Cd2+ ions from calcareous Krka river water of various salinities (3, 14, 20 and 38 psu) on calcite (CaCO3, Merck p.a.) was investigated. Simultaneous adsorption of Pb2+ and Cd2+ ions was studied as well. The results suggest that the two ions are adsorbed at different calcite surface sites; Pb2+ remained firmly bound to calcite at all salinities, whereas Cd2+ was firmly bound at low salinities and released at high salinities. Dissolved natural organic ligands at the freshwater-seawater interface (FSI; at 14 psu) promoted and below the FSI (at 20 psu) decreased the adsorption of Cd2+. The experiments were performed at metal concentrations of 8 × 10−8 mol l−1 and at natural pH values around pH 8. Adsorbed amounts of trace metal ions were determined in filtered samples by differential pulse anodic stripping voltammetry (DPASV) with a three-electrode system, after 24 h of equilibration with calcite. Several adsorption models were tested, such as Freundlich's, Langmuir's and Schindler-Stumm's surface coordination model. Adsorption isotherms belong to S-1 class of empirical adsorption isotherms. None gave reasonable values of adsorption constants. The fractional partitioning of adsorbent to the solid phase when normalized to the quantity of adsorbent present (Kd) declined as solid concentration increased. It was found that the surface charge is not responsible for the observed effect. Instead, aggregate size increased, which effected a loss in surface area. This is a reasonable explanation for the observed S-shaped adsorption isotherms curves. 相似文献
12.
Experiments have been conducted to investigate the effects of temperature on the interfacial surface area and on the rate of oxygen transfer from air bubbles dispersed in aqueous NaCl solutions. Tests were also conducted to estimate the effects of salt concentration on the size of the bubbles. In addition to NaCl solutions, seawater was used in some tests. The temperature effects were investigated at 5, 10, 15, 20, 25, and 30°C. The results showed a pronounced effect of the salt on the size of the bubbles, which first decreased sharply with increasing concentration, but showed no further drop when the concentration was increased beyond 0.6 M. Both in seawater and in the 0.6 M solution, the mass transfer rate, KLA, increased almost linearly when temperature was increased within the range from 5 to 25°C. The salt solution, as well as the seawater, showed an increase of KLA of 60–70% over that in pure water at the same temperatures. This effect was the result of increased surface area of bubbles because of decreased coalescence. The increase in surface area was strongly temperature dependent, especially between 15 and 20°C. Contrary to this behavior the surface area in pure water showed, practically, no temperature dependence. The results are explained and discussed on the basis of ion-water interactions. 相似文献
13.
The choice of convenient basic constituents for evaluating pH stability of aqueous systems is discussed, and two useful interaction parameters are defined and related to the buffer capacity: the interaction capacity, , and the interaction intensity, ; for pH and TOTH, δ′H, H = ?βH?1, where βH is the pH buffer capacity. A method is presented for the computation of exact values of all interaction capacities and intensities through inversion of the Jacobian matrix of the system of non-linear equations describing the aqueous system. The major species of an aqueous system (H2O, H+, solid phases, gases, and the most abundant solute species) are shown to constitute a useful set of basic constituents for evaluation of approximate pH buffer capacities according to a simple rule: the major-minor species rule for zeroth order pH-TOTH interaction. The concepts of buffering and pH-statting are examined and contrasted; it is demonstrated that the buffer capacity of an aqueous system cannot be infinite: it is limited by the concentration of solutes in solution. The effect upon pH of variations in constituents other than H+ is described in terms of first order interactions via complex formation and solid formation; approximate formulas for calculation are derived. Higher order interactions are derived from combinations of first order ones. The pH stability of the ocean system is examined in terms of an aqueous phase model including ion-association reactions and a heterogeneous model incorporating CO2 in the gas phase, quartz, kaolinite, calcite, chlorite, and illite, in addition to the aqueous phase. There is an approximately three-fold enhancement of buffer capacity in the aqueous model as a consequence of ion-association. Only a few interaction pathways are of quantitative significance in establishing the buffer capacity. Results for the heterogeneous ocean model lend quantitative support to Sillén's notion of pH stability: the buffer capacity is about four hundred times greater than that of the aqueous phase model. 相似文献
14.
R. Herrero B. Cordero P. Lodeiro C. Rey-Castro M.E. Sastre de Vicente 《Marine Chemistry》2006,99(1-4):106
Samples of dead biomass from the marine brown algae Fucus ceranoides, Fucus vesiculosus and Fucus serratus were studied for their ability to remove cadmium from aqueous solutions. The metal sorption process is rapid, with 90% of the metal uptake completed within the first 25 min of contact. The kinetic data was described successfully by a pseudo second order chemical sorption process with rate constants of ca. 0.6 g mmol− 1 min− 1. At pH 4.5, the raw biomass of the three species exhibited equilibrium uptake capacities for Cd as high as 0.8 mmol g− 1 (90 mg g− 1), on a dry weight basis, without chemical pretreatment. These sorption capacities are much higher than those reported for activated carbon and chitin. The sorption of Cd was found to increase as pH increases, reaching a plateau at pH 5.Batch sorption experiments and continuous potentiometric titrations of acid-treated biomass samples in 0.05 M NaNO3 were used to derive thermodynamic binding parameters according to the NICCA model. The total amount of acid sites was 2.4–2.9 mmol g− 1, with median values of the affinity distribution for protons and cadmium ions, log K˜H and log K˜Cd, of 3.7 and 2.69, respectively (conditional values). The apparent heterogeneity of the sorbent was successfully taken into account by the empirical NICCA isotherm, which described very well the competition between protons and metal ions, in contrast with a simpler discrete competitive Langmuir model.The experimental results demonstrate that these seaweeds constitute a promising, efficient, cheap and biodegradable sorbent biomaterial for cadmium removal from wastewaters. This use would represent an example of exploitation of a renewable marine resource in water treatment technologies for the prevention of heavy metal pollution in the environment. 相似文献
15.
Yoshiyuki Nakano Hideshi Kimoto Shuichi Watanabe Koh Harada Yutaka W. Watanabe 《Journal of Oceanography》2006,62(1):71-81
We have developed new systems capable of profiling to >1000 m for measuring in situ pH and fugacity of CO2 (fCO2) in the ocean using spectrophotometric analysis (pH and CO2 profilers). The in situ pH is determined by detecting the color change of the pH indicator (m-cresol purple). It can withstand ambient pressure to 1000 m depth. The CO2 profiler analyzed in situ fCO2 by detecting the change of pH in an inner solution, equilibrated with the seawater through a gas permeable membrane. It can
be operated to 2500 m depth. We used an amorphous fluoropolymer tubing form of AF-2400 for the gas permeable membrane due
to its high gas permeability coefficients. The inner solution was a mixture of 2 μM bromocresol purple (BCP) and 5 μM sodium
hydroxide. This system gave us a response time of 1 minute, which is twice as fast as previous systems. The precisions of
pH and CO2 profilers were within 0.002 and 2.5% respectively. We have used these profilers to study the North Pacific, obtaining good
agreement with the difference between the data from profilers and a discrete bottle of 0.002 ± 0.005 pH (SE, n = 25) and −0.4
± 3 μatm (SE, n = 31). 相似文献
16.
为获得反硝化脱氮效率较好的菌株,实验从海水螺旋藻培养体系中分离获得一株嗜碱兼性好氧反硝化菌, 通过观察细菌形态以及16S rRNA基因序列的同源性分析, 鉴定该菌株为海杆菌属, 命名为Marinobacter sp. B3。为明确该海杆菌的反硝化性能及氮转化途径, 研究开展了溶解氧(DO), 碳氮摩尔比(C/N), pH和温度等不同单因素对反硝化性能影响实验和氮平衡实验。单因素影响实验结果表明, 当硝酸钾(KNO3)作为唯一氮源, NO3--N的初始浓度为100 mg/L, 盐度32, 振荡速度为150 r/min (初始DO质量浓度是5.6 mg/L), C/N=10, pH=8.0±0.2, 温度为35 °C时, 可获得最大脱氮效果。氮平衡实验结果得出, 在好氧环境下, 有20.11%的NO3--N转化为胞内氮, 5.58 mg/L的NO3--N转化为其他形态(NO2--N、NO4+-N和有机氮), 74.72%转化为N2释放; 厌氧环境下, 有26.65%的NO3--N转化为胞内氮, 72.86%的NO3--N转化为气态产物释放。最终实验结果表明, Marinobactersp. B3在好氧和厌氧条件下, 48 h对NO3--N的去除率分别为99.89%和93.80%, 具有较好的反硝化脱氮能力, 且在好氧条件下NO3--N去除效率更高, 在海水工厂化循环水养殖尾水处理方面具有良好的应用前景。 相似文献
17.
采用化学沉淀法成功制备了Cu2+/SnO2复合纳米光催化剂,采用XRD、SEM等测试手段对复合纳米光催化剂的粒径、形态等进行表征。在紫外光条件下,分别改变催化剂掺杂比、催化剂煅烧温度、催化剂投加量、柴油初始含量和光照时间等单因素,探究不同条件对Cu2+/SnO2复合纳米光催化剂降解海洋柴油污染物的影响。结果表明,自制复合纳米光催化剂可以有效降解海水中的柴油污染物,在紫外光作用下,于400℃下煅烧Cu/Sn掺杂比为0. 03的Cu2+/SnO2复合纳米光催化剂、投加量为0. 2 g/dm3、柴油初始含量为0. 15 g/dm3、H2O2溶液含量为0. 2 g/dm3、溶液的p H为7、光照时间3 h时效果最好,海水中柴油的去除率最高,达到86. 98%。Cu2+/SnO2复合纳米光催化剂用聚丙烯纳米球负载后可以实际应用于海洋中,便于回收。 相似文献
18.
Preliminary measurements of sulfide in seawater using cathodic stripping voltammetry and a hanging mercury drop electrode (HMDE) in batch-mode showed that the sulfide peak decreased rapidly with time. This decrease was not caused by O2, H2O2 or IO3−, and the sulfide peak was not stabilised by trace metal additions. A home-made flow-cell was constructed to enable the determination of sulfide in seawater using voltammetry with an HMDE. A stable sulfide peak was obtained by flow-analysis with voltammetric detection, with a precision of 2.8% and detection limit of 0.5 nM at a 60 s adsorption time. Several thiol compounds were found to produce a peak at, or very close to, the peak potential for sulfide. Their interference was evaluated by allowing the sulfide peak in conventional (batch) voltammetry to decay. Comparative experiments showed that waste metallic mercury is responsible for removal of sulfide in batch-mode analysis due to formation of insoluble mercuric sulfide salts causing the rapid decay of the sulfide peak. The problem is circumvented by using flow-analysis to determine sulfide. 相似文献
19.
水环境中抗生素污染日益严重。本研究制备了掺杂氮、硫的新型石墨烯材料(GO-NS),研究了其对磺胺类抗生素(Sulfonamides,SAs)的吸附和去除能力,并阐明吸附机制。研究发现,GO-NS对SAs的最大吸附量达100.26 mg·g^-1,吸附能力优于多层石墨烯(Multilayer graphene,MG)和还原氧化石墨烯(Reduced graphene oxide,rGO)这两种传统石墨烯材料。疏水作用和氢键作用是GO-NS吸附SAs的主要机理。相比于MG和rGO,GO-NS适用的pH范围最广,在pH=2~10范围内均具有较强的吸附效果,并且离子强度和腐殖酸(Humicacid,HA)的加入提升了GO-NS的吸附性能。此外,GO-NS仅通过短时间超声可实现有效的剥离分散,使吸附量增加。故该新型石墨烯材料GO-NS具有优越地吸附SAs的能力和广泛的环境适应性,可作为治理水环境中SAs污染的一种有效吸附剂。 相似文献
20.
利用湿法纺丝技术制备了琼胶/SiO2复合纤维，对琼胶分子在溶液中的分散性、纺丝液流变性、纤维的形貌、化学结构分别用DLS、旋转黏度计、SEM、FTIR和XRD进行了表征，并对纤维的力学性能、热性能和吸湿性能进行了测定。研究结果表明：琼胶分子在溶液中呈纳米尺度分布，纺丝液具有良好的流动性；琼胶/纳米SiO2复合纤维具有良好的形态。随着纳米SiO2的添加量逐渐提高，复合纤维的力学拉伸强度先增强后降低，复合纤维的吸水性降低，复合纤维的热稳定性逐渐增强。结合复合纤维综合性能，纳米SiO2的最佳添加质量分数为0.5%。 相似文献