The Relationship Between Iodine, Chlorinity, Ph, Reactive Phosphate, Nitrite and Organic Matter in the Coastal Water of Alexandria

Water samples were taken from 12 stations at El-Dikheila Harbour, El-Mex Bay, Western Harbour, Qayet Bey outfall, Eastern Harbour, El-Ibrahemiya, Gleem, Sidi Bishr and Mandara, during January, April, August and November 1995. the area lies between latitude 31˚ 8' and 31˚ 17' North and longitude 29˚ 47' and 30˚ East. the annual mean of chlorinity (11.69-20.5%₀), pH (7.9-8.3), reactive phosphate (0.31-2.24 μM), nitrite (0.18-1.98 μM), oxidizable organic matter (1.97-8.95 mgO₂ 1^-1), iodide (21.14-46.74 μg 1^-1) and iodate (4.61-2.04 μg 1^-1) were measured. Iodide content in water is three times higher than iodate. Iodide is positively correlated with chlorinity (r=0.65) and iodate (r=0.45), while it is negatively correlated with nitrite (r= -0.72), oxidizable organic matter (r= -0.55) and pH (r= -0.4).     

Discriminating zooplankton assemblages through multivariate methods: A case for a tropical polluted harbour and Bar-built estuary

A comparative study (June-July 2001) on zooplankton community structure amid polluted conditions in a stagnant harbour and relatively unaffected tidal estuary near Visakhapatnam, on the east coast of India, revealed a marked disparity in species composition and abundance. While the harbour supported a rich population of calanoids (46.4%), the estuary sustained mostly cyclopoids (55.2%). Univariate and multivariate techniques (species diversity, clustering, non-metric multi-dimensional scaling and one-way ANOSIM) revealed the existence of two differing zooplankton assemblages and associated water quality (similarity 50.6%). While the estuary is typified by high amounts of dissolved silica (67.4 ± 17.7 μmol l^-1) linked with monsoon influx, the harbour waters revealed abnormal levels of phosphate (40.9 ± 9.2 μmol l^-1) and nitrate (15.3 ± 5.41 μmol l^{- 1}) suggestive of intense eutrophication, caused by the discharge of fertilizer-factory waste and domestic sewage. On the basis of routines (e.g. BVSTEP, SIMPER) implemented in Plymouth Routines in Multivariate Ecological Research, it was possible to demonstrate that while species such as Oithona rigida, Oithona brevicornis, crustacean nauplii, gastropod veligers, Acartia spinicauda, and Acartia centrura played a key role in discriminating the zooplankton assemblage in the estuary, Acrocalanus spp. (mainly Acrocalanus gracilis) played a keyed role in harbour waters. Canonical Correspondence Analysis revealed species-environment relationships; for example, while the distribution of Oithona spp. and its associates in the estuary corresponded intimately with high silicate, temperature, and low salinity, it was high salinity, phosphate, and nitrate in the harbour channel that supported a different assemblage of copepods dominated by calanoids.     

Transport of Inorganic Phosphate in the Marine Seagrass Posidonia Oceanica By 32P-Phosphate As Tracer

Uptake and loss of inorganic phosphate by Posidonia oceanica leaf tissue has been studied in in vitro experiments. Experimental data have shown that a steady state of inorganic phosphate uptake (about 40 nmol mg^-1 dry wt.) is attained after 48 hours. in particular high accumulation (over 1000-fold the natural level in sea water) and slow loss (biological half-life, 65 days) of inorganic phosphate has been evaluated. Moreover the effect of three different metabolic inhibitors (sodium monovanadate, sodium azide, 2, 4-dinitrophenol) have been tested. Results of this effect and the high degree of inorganic phosphate accumulation in leaf tissue have demonstrated that inorganic phosphate carrier is energy dependent. Furthermore, the inorganic phosphate uptake is probably influenced by bivalent cations (Ca⁺², Mg⁺²) but the mechanism is still uncertain.

Preliminary kinetic study has shown interesting results. in particular, k_m estimated value (2.8 μmol 1^-1) has demonstrated the existence of a relatively high uptake rate (V_max) at low DIP concentration while the kinetic study of inorganic phosphate loss from leaf tissues has shown a low value of the biological half life (about 60-70 days). This evidence could be significant for the existence of a complex distribution of inorganic phosphate in the leaf tissues.     

球磨零价镁/石墨(ZVMg/C)降解水中三氯乙烯

利用机械球磨法制备了零价镁/石墨(ZVMg/C)材料,并将其用于水溶液中三氯乙烯(TCE)的降解.研究通过SEM、BET和XRD等分析手段解析了ZVMg/C的表面形态结构和成分组成;采用正交实验方法优化了ZVMg/C的制备参数,比较了石墨含量对材料性能的影响;并考察了ZVMg/C投加量、溶液初始pH和地下水中常见阴(C...     

Comparing the adsorption behaviors of Cd,Cu and Pb from water onto Fe-Mn binary oxide,MnO2 and FeOOH

The adsorption potential of FMBO, FeOOH, MnO₂ for the removal of Cd²⁺, Cu²⁺ and Pb²⁺ in aqueous systems was investigated in this study. Comparing to FMBO and FeOOH, MnO₂ offered a much higher removal capacity towards the three metal ions. The maximal adsorption capacity of MnO₂ for Cd²⁺, Cu²⁺ and Pb²⁺ were 1.23, 2.25 and 2.60 mmol·g^-1, respectively. And that for FMBO were 0.37, 1.13, and 1.18 mmol·g^-1 and for FeOOH were 0.11, 0.86 and 0.48 mmol·g^-1, respectively. The adsorption behaviors of the three metal ions on the three adsorbents were all significantly affected by pH values and heavy metal removal efficiency increased with pH increased. The Langmuir and Freundlich adsorption models were used to describe the adsorption equilibrium of the three metal ions onto the three adsorbents. Results showed that the adsorption equilibrium data fitted well to Langmuir isotherm and this indicated that adsorption of metal ions occurred on the three metal oxides adsorbents limited to the formation of a monolayer. More negative charged of MnO₂ surface than that of FMBO and FeOOH could be ascribed by lower pH_iep of MnO₂ than that of FMBO and FeOOH and this could contribute to more binding sites on MnO₂ surface than that of FMBO and FeOOH. The higher metal ions uptake by MnO₂ than FMBO and FeOOH could be well explained by the surface charge mechanism.     

Influence of arsanilic acid,Cu2+, PO43− and their interaction on anaerobic digestion of pig manure

The methanogenesis was severely inhibited with 0.46 mM ASA addition.PO₄³⁻ didn’t attenuate the methanogenesis inhibition in the existence of ASA.ASA was transformed to As(III), As(V), MMA and DMA in anaerobic digestion.Cu²⁺ mitigated the methanogenesis inhibition via impeding the degradation of ASA.Arsanilic acid (ASA), copper ion (Cu²⁺) and phosphate (PO₄³⁻) are widely used as feed additives for pigs. Most of these three supplemented feed additives were excreted in feces and urine. Anaerobic digestion is often used for the management of pig manure. However, the interaction of ASA with Cu²⁺ or PO₄³⁻ on anaerobic digestion is still not clear. In this study, the influence of ASA, Cu²⁺, PO₄³⁻ and their interaction on anaerobic digestion of pig manure and the possible mechanisms were investigated. The initial concentrations of ASA, Cu²⁺ and PO₄³⁻ were 0.46 mM, 2 mM and 2 mM in the anaerobic digester, respectively. The methanogenesis was severely inhibited in the assays with only ASA addition, only Cu²⁺ addition and ASA+ PO₄³⁻ addition with the inhibition index of 97.8%, 46.6% and 82.6%, respectively, but the methanogenesis inhibition in the assay with ASA+ Cu²⁺ addition was mitigated with the inhibition index of 39.4%. PO₄³⁻ had no obvious impacts on the degradation of ASA. However, Cu²⁺ addition inhibited the degradation of ASA, mitigating the methanogenesis inhibition. The existence of ASA would inhibit methanogenesis and generate more toxic inorganic arsenic compounds during anaerobic digestion, implying the limitation of anaerobic digestion for ASA- contaminated animal manure. However, the co-existence of ASA and Cu²⁺ could mitigate the inhibition. These results could provide useful information for the management of anaerobic digestion of pig manure containing ASA with Cu²⁺.     

Water Discoloration in Alexandria, Egypt, April 1993. I. Occurrence of Prorocentrum Triestinum Schiffer (Red Tide) Bloom and Associated Physical and Chemical Conditions

A yellow-brown coloration of water developed in the Eastern Harbour of Alexandria (Egypt) during April 1993. the dinoflagellate Prorocentrum triestinum, the causative organism, culminated in a population peak of 71-10⁶ cells 1^-1, chlorophyll a nearly 361 μgl^-1. the bloom occurred with a thermohaline stratified water column and low surface nutrient levels. Water temperature was considered a crucial environmental factor controlling the occurrence of P. triestinum and nitrate was significantly correlated with its counts. the high relative growth constant (3.4 d^-1), calculated just prior to the massive occurrence of the species, explains the rapid development of the bloom. A comparison with the earlier phytoplankton studies in the harbour is made.     

Selective recovery of Cu2+ and Ni2+ from wastewater using bioelectrochemical system

As the bioelectrochemical system, the microbial fuel cell (MFC) and the microbial electrolysis cell (MEC) were developed to selectively recover Cu²⁺ and Ni²⁺ ions from wastewater. The wastewater was treated in the cathode chambers of the system, in which Cu²⁺ and Ni²⁺ ions were removed by using the MFC and the MEC, respectively. At an initial Cu²⁺ concentration of 500 mg·L^-1, removal efficiencies of Cu²⁺ increased from 97.0%±1.8% to 99.0%±0.3% with the initial Ni²⁺ concentrations from 250 to 1000 mg·L^-1, and maximum power densities increased from 3.1±0.5 to 5.4±0.6 W·m^-3. The Ni²⁺ removal mass in the MEC increased from 6.8±0.2 to 20.5±1.5 mg with the increase of Ni²⁺ concentrations. At an initial Ni²⁺ concentration of 500 mg·L^-1, Cu²⁺ removal efficiencies decreased from 99.1%±0.3% to 74.2%±3.8% with the initial Cu²⁺ concentrations from 250 to 1000 mg·L^-1, and maximum power densities increased from 3.0±0.1 to 6.3±1.2 W·m^-3. Subsequently, the Ni²⁺ removal efficiencies decreased from 96.9%±3.1% to 73.3%±5.4%. The results clearly demonstrated the feasibility of selective recovery of Cu²⁺ and Ni²⁺ from the wastewater using the bioelectrochemical system.     

Heavy-metal adsorption by non-living biomass

The adsorption of some heavy metals onto the walls of harvested, washed, and dried non-living biomass cells of different Pseudomonas strains was studied at optimum experimental conditions using a simplified single component system. The Langmuir adsorption model was found to be a suitable approach to describe the system via multi-step processes. Isotherms measured at 30.0°C and pH 5.5 with [M]_total = 10-100 mM for tight, reversible Cr⁶⁺(aq), Ni²⁺(aq), Cu²⁺(aq) and Cd²⁺(aq) binding by the cell walls of the investigated biomass fit the Langmuir model and give the pH-independent stoichiometric site capacities ν_i and equilibrium constants K_i for metal binding at specific biomass sites i = A, B, C, and D. Tight binding sites A, B, and D of the non-living biomass are occupied by Cr^VI, sites A and C by Ni^II, sites A and D by Cd^II, and only site B by Cu^II. It is concluded that ν_i is a stoichiometric parameter that is independent of the magnitude of K_i for binding site i and that the studied heavy metals selectively and tightly bind at different biomass sites.     

The Influence of Varying Algal Biomass On Contaminant Exposure in Benthic-Planktonic Mesocosms: Copper (Ii)

A series of mesocosms was exposed to a suite of light treatments and nutrient enrichment in order to generate algal communities of varying biomass. the influence of this biomass on the speciation of copper (II) was studied. Distribution coefficients (_Kd,Lkg-1) were relatively high (log_Kd = 5 to 7), indicative of robust trace metal sequestration, and were likely controlled by the particulate organic carbon content (foc). Differences in _Kd over time and among treatments were significant, as was the relationship between _Kd and foc. Fluorescence quenching was used to determine binding capacities (_Lt, M) and their associated binding constants (_Kcond,M^-1) in order to model the solid phase copper speciation. the _Kcond ranged between 2.1 and 5.2 × 10¹²M^-1, indicating a very strong copper-ligand complex, and was higher in mesocosms that received more light. the light _Lt increased over time, dramatically after the nutrient enrichment, but did not vary systematically among light treatments. _Lt ranged from 7.2 × 10- 7 to 4.9 × 10- 5 M. the large magnitudes of _Kd, _Kcond and _Lt ensured that greater than 97% of total copper in the mesocosms was complexed by organic matter. the total copper concentration ([Cu]_T, M) needed to reach a target dissolved copper concentration of 10^-12.5 M (pCu = 12.5) was determined for each mesocosm over time. [Cu]_T was between 8.02 × 10^-5 and 3.41 × 10^-2 M, and increased over time. the [Cu]_T normalized to the target pCu (Effective Dose Ratio, EDR) increased directly with increases in algal biomass, indicating a direct link between system productivity and copper exposure. Approximately 45% of the variance in EDR was explained by variance in total biomass, while the residual variance in EDR was due likely to differences in the strengths of particle associations and magnitude of binding capacities.     

Metal Concentration in Oyster, Crassostrea Gigas, and Sediment in Ann-Ping Mariculture Ground, Taiwan

This study was to assess the metal contamination in oyster tissue grown in the Ann-ping mariculture ground in Taiwan. the information generated from this work also revealed general metal pollution problem for Taiwan's oyster farmers. Oysters, Crassostrea gigas, and surficial sediments collected from ten locations in Ann-ping mariculture ground in Taiwan for metals concentration (Cu, Zn, Pd, Cd, Fe and Mn) were performed. Analytical results indicated that the yearly averaged oyster copper concentrations (μg g^-1, wet weight) in oyster soft parts from Ann-ping increased from 21.3±4.1 in 1993; 24.1±6.8 in 1994; 36.8±11.9 in 1995 to 43.9±23.1 μg g^-1, wet weight, in the 1996 raising season. the mean oyster copper concentration reached a level of 50 μg g^-1, wet weight, in December 1996. This increasing trend of metal concentration in oyster tissue indicates a potential pollution source which may pose a potential disaster as green oyster incidence, which occurred on the Charting coast in 1986, in Taiwan. Sediment samples in Ann-ping mariculture ground were also collected and examined. the seasonal variation of the copper concentration in surficial sediment from Ann-ping did not show an increasing trend as observed in oyster tissue.     

Heavy Metal Concentrations in Sea Urchin Tissues From Egypt, Ireland and United Kingdom

Sea urchins (Paracentrotus lividus) were collected from the Mediterranean coast off Alexandria, Egypt and the Atlantic coast of Ireland to the west of Galway. Samples of another urchin species, Psammechinus miliaris, were collected from the entrance to Southampton Water, U.K. Both the Alexandria coast and Southampton Water receive domestic and industrial waste water inputs whilst the western Irish coast is relatively unpolluted.

Sampled animals were dissected to separate coelomic fluids, Aristotle's lantern, gonads and tissue (digestive tract plus connective tissue). the concentrations of heavy metals (cadmium, copper, lead, nickel and zinc) in the different parts were measured using flame atomic absorption spectroscopy.

Many levels of heavy metals in the different parts were similar in specimens taken across the wide range of sites and the two species. A notable exception was the high level of copper (33 μg g^-1 dry wt.) and zinc 328 μg g^-1- dry wt.) in urchin tissue from Southampton Water.

The metal concentrations in the gonads of Paracentrotus lividus are of particular interest because of human consumption of this species. the highest levels of copper (3.3-5.2 g^-1- dry wt.) and zinc (74-181 μ g^-1- dry wt.) dry wt.) in gonads were found in the samples from Egypt. Data from this study are compared with other results reported from the Mediterranean.

A simple, short term, elevated water column copper uptake experiment was undertaken with Paracentrotus lividus which showed an increase in gonad concentrations of this element.     

Origin and Distribution of Suspended Organic Matter As Inferred From Carbon Isotope Composition in A Mediterranean Semi-Enclosed Marine System

The origin and distribution of suspended organic matter, the trophic features and the stable carbon isotopic composition of particulate organic carbon (POC) were studied monthly in a Western Mediterranean semi-enclosed basin. Sampling stations were selected as a function of wind-exposure and the degree of vegetation cover and then compared with an adjacent unvegetated site. the predominant vegetation was seagrass (Posidonia oceanica and Cymodocea nodosa) and Caulerpa prolifera. Water samples were analyzed for total suspended matter (inorganic and organic fractions), photosynthetic pigments (chlorophyll-a and phaeopigments), dissolved organic carbon, particulate organic carbon and their isotopic composition. Temperature and salinity were also measured at the same sampling sites within range of Mediterranean limits. the suspended organic matter concentration was 1.77 ± 1.55 mg l^-1; the chlorophyll-a concentration was low (0.35 ± 0.24 μg l^-1); the disolved organic carbon concentration was 2,140 ± 2,010 μg l^-1; the particulate organic carbon concentration was 212 ± 106 μg l^-1 and the isotopic composition was 18.77 ± 2.51%_°. There were significant temporal differences except for phaeopigments, POC and its POC isotopic composition, and there were no spatial differences other than for δ¹³C. This picture highlighted a general seasonal trend and trophical features similar to adjacent sea.

Spatial differences in δ¹³C showed that the source of suspended organic matter was different between stations as that between sources and wind-hydrodynamic constraints. In     

Dissolved trace-metal concentrations along the Mediterranean Sea, to the north of the Nile Delta Region, Egypt

This work focuses on four marine sites of the Mediterranean Sea, north of the Nile Delta, Egypt. Surface-water samples were collected seasonally during 2003. The aim of this study is to assess the levels of some dissolved trace metals (Fe, Mn, Zn, Cu, and Pb) in two environmental conditions. The metal concentrations in the coastal zone were in the following ranges: 11.92-30.45 μg l^-1 for Fe, 5.79-17.36 μg l^-1 for Mn, 0.87-7.80 μg l^-1 for Zn, 0.40-1.87 μg l^-1 for Cu, and 1.53-10.31 μg l^-1 for Pb. In the sites with continental water input (mixing zone), the metals were scattered in the following ranges: Fe (19.72-60.33 μg l^-1), Mn (12.63-35.60 μg l^-1), Zn (2.67-22.00), Cu (0.83-8.10 μg l^-1), and Pb (1.72-29.7 μg l^-1). The results for the metal concentrations showed a remarkable decrease in the levels of the different metals going from the estuaries and outlets into the coastal sea water. Generally, the levels of the metals in the two zones are higher than the background levels of the unpolluted area. A comparison of the trace-metal levels in the coastal zone of the Mediterranean Sea north of Nile Delta with the minimal risk concentration (reported by water-quality criteria, WQC) showed a significantly lower content at the coastal area of the Mediterranean sea of Egypt. The study also indicated that the impact of anthropogenic inputs was limited in the distribution of the metals, except that the Pb content was slightly higher in the area of the mixing zone than that reported for WQC. The relationships between the different trace-metal concentrations and the other parameters (salinity, chlorophyll a and suspended particulate matter) were discussed, and the simple regressions between them were evaluated.     

Shifts in Microbial Communities, Microbial Biomass and Organic Matter Mineralization for Three Mediterranean Soils Contaminated By Metals

Microbial communities (phospholipid fatty acid pattern, bacterial growing strategies, eco-physiological index (EPI) and total bacteria counts, as a number of heterotrophic cuhurable bacteria), substrate-induced respiration (SIR), and nitrogen mineralization were studied in three Mediterranean soils at three different depth levels (A, B and C). Soils were experimentally treated with a final concentration of 1000 ppm of trace metals (Cu²⁺, Zn²⁺, Al³⁺, Fe²⁺, Pb²⁺, Ni²⁺, Mn²⁺, Cr³⁺ and Cd²⁺). Soils were stored in 571 plastic containers for one year, and watered with 1001 during this period. Leachate was recovered through a bottom tap. Samples of the three depths were studied. Soil microbial communities showed different effects to other studies presented in the literature, but carried out on non-Mediterranean soils. Dramatic differences were found between treated soils and untreated ones, but not between soils or horizons. the treated soil displayed a decrease in CFUs, SIR N-mineralization and EPI together with a dominance of r-growing strategists. the relative moles percent of several PLFAs, especially 15:0, 16: 1ω7, cy17: 0, br18:0 and 18: 1ω7 decreased because of the pollution of soils, whereas 10Me16, 18:2ω6, cy19:0, i16:0 and br17:0 showed higher values than in untreated soils.     

Hydrochemistry and dissolved nutrient flux of two small catchment rivers, south-western India

This paper deals with the water chemistry and dissolved nutrient flux of two small mountainous and heavily dammed rivers—Periyar and Chalakudy—of Kerala on the south-west coast of India. The lower reaches of these rivers are affected by sea-water ingression from the Arabian Sea during the non-monsoon season. Human interference through agriculture, urbanization, and industrialization in the lower and middle stretches of the river basins induces marked concentration variations in the hydro-chemical parameters. Except for N & P, all other chemical constituents exhibit high values during the non-monsoon season. Industrial contaminants in specific locations of the Periyar river reduce the pH to lower levels. Nutrients in the two rivers reveal marked seasonal and regional concentration variations. During the monsoon season, dissolved inorganic nitrogen (DIN) predominates over dissolved organic nitrogen (DON), but the reverse trend is observed during the non-monsoon season. The Periyar river shows higher average concentrations of DIN (monsoon 801 μg l^-1 and non-monsoon 292 μg l^-1) than Chalakudy river (monsoon 478 μg l^-1 and non-monsoon 130 μg l^-1). Dissolved inorganic phosphorus (DIP) has lower average values in the monsoon season (Periyar river, 38 μg l^-1; Chalakudy river, 42 μg l^-1) than dissolved organic phosphorus (DOP) values (Periyar river, 107 μg l^-1; Chalakudy, 62 μg l^-1). The rivers show a marked difference in nutrient flux due to its difference in water discharge/basin characteristics and point/non-point sources of contaminants. The flux rates of DIN, DIP, and DOP during the monsoon are higher than during the non-monsoon season, while those of dissolved silicon (DSi), dissolved Fe (DFe), and DON are lower. On average, the Periyar river discharges 4953 t y^-1 of DIN and 1626 t y^-1 of DON to the coastal waters, and the corres-ponding values of the Chalakudy river are 772 t y^-1 and 596 t y^-1. The Periyar and Chalakudy rivers discharge 245 t y^-1 and 70.8 t y^-1 of DIP, respectively. The total flux of DOP is considerably higher (Periyar river 703 t y^-1 and Chalakudy river 101 t y^-1). The discharge of DSi into the Periyar river (40 193 t y^-1) is nearly five times higher than that in the Chalakudy river (8275 t y^-1). The discharges of DFe through the Periyar and Chalakudy rivers are 257 t y^-1 and 36.7 t y^-1, respectively. To sum up, this study addresses the water quality and nutrient flux of two tropical rivers and discusses the impact of urbanization and industrialization on river-water quality.     

Nitrite and Freshwater Fish

Nitrite occurs naturally in fresh waters as a result of nitrification of ammonia and denitrification of nitrate, and its concentration can be enhanced by partial oxidation of ammoniacal discharges. Nitrite is toxic to vertebrates including fish and a principal effect is the conversion of haemoglobin to methaemoglobin which is incapable of oxygen transport although there are circulatory and tissue effects as well. The toxic species is the nitrite ion (NO₂) which is believed to enter the blood via the branchial chloride/bicarbonate exchange and fish such as salmonids with high chloride uptake rates are more susceptible than those with low chloride uptake rates, for example carp. Nitrite toxicity is strongly aleviated by chloride and the concentration ratio of these ions is of great importance in assessing toxicity. Short term and long term toxicity data for a variety of fish species are presented. There are no field data on fish populations in waters where nitrite was the only pollutant. However extensive field surveys indicated that, waters with a mean chloride concentration of 25 mg l^-1 in good salmon fisheries were associated with concentrations of nitrite below 50 μg l^-1 N · NO₂, good coarse fisheries below 100 μg l^-1 N · NO₂.     

Mass-transfer processes of chromium(VI) adsorption onto guava seeds

The chromium(VI) biosorption onto guava seeds, as an alternative method for Cr⁶⁺ removal from aqueous solutions, was investigated. The parameters affecting kinetics and equilibrium of Cr⁶⁺ adsorption onto guava seeds were studied. An external mass-transfer diffusion coefficient k and intra-particle diffusion coefficient k_i were determined to measure the rate-limiting step of adsorption. A single external mass-transfer diffusion model and intra-particle diffusion models were used. The effects of initial pH, sorbent mass, and initial Cr⁶⁺ concentrations on mass-transfer coefficients were investigated. The external mass-transfer coefficient has an average value of 7.2×10^-3 cm s^-1, while the intra-particle mass-transfer diffusion coefficient was 0.34 mg g^-1 min^-0.5. This indicates that external diffusion to the guava seeds surface and intra-particle diffusion are both involved in the sorption process. The isotherm equilibrium data were well fitted by the Langmuir and Freundlich models with an average correlation coefficient R²=0.98. The maximum removal of Cr⁶⁺ was obtained at pH 1 (about 100% for adsorbent dose of 15 g l^-1 and 25 mg l^-1 initial concentration of Cr⁶⁺). The results indicated that the guava seeds exhibit acceptable sorption capacity.     

Simple fabrication of carboxymethyl cellulose and κ-carrageenan composite aerogel with efficient performance in removal of fluoroquinolone antibiotics from water

● A composite aerogel was simply obtained to remove various fluoroquinolones (FQs). ● The structural and textural properties of this composite aerogel are improved. ● Its adsorption capacity was improved at a low content of coexisting Cu²⁺ or Fe³⁺ ion. ● Two substructural analogs of FQs are compared to explore the adsorption mechanisms. ● This aerogel after saturated adsorption can be reused directly for Cu²⁺ adsorption. 3D composite aerogels (CMC-CG) composed of carboxymethyl cellulose and κ-carrageenan were designed and fabricated using the one-pot synthesis technique. The optimized CMC-CG showed a good mechanical property and a high swelling ratio due to its superior textural properties with a proper chemically cross-linked interpenetrating network structure. CMC-CG was utilized for the removal of various fluoroquinolones (FQs) from water and exhibited high adsorption performance because of effective electrostatic attraction and hydrogen bonding interactions. Ciprofloxacin (CIP), a popular FQ, was used as the representative. The optimized CMC-CG had a theoretically maximal CIP uptake of approximately 1.271 mmol/g at the pH of 5.0. The adsorption capacity of CMC-CG was improved in the presence of some cations, Cu²⁺ and Fe³⁺ ions, at a low concentration through the bridging effect but was reduced at a high concentration. The investigation of adsorption mechanisms, based on the adsorption kinetics, isotherms and thermodynamic study, Fourier transform infrared spectrometry and X-ray photoelectron spectroscopy analyses before and after adsorption, and changes in the adsorption performance of CMC-CG toward two molecular probes, further indicated that electrostatic attraction was the dominant interaction rather than hydrogen bonding in this adsorption. CMC-CG after saturated adsorption of CIP could be easily regenerated using a dilute NaCl aqueous solution and reused efficiently. Moreover, the disused aerogel could still be reused as a new adsorbent for effective adsorption of Cu²⁺ ion. Overall, this study suggested the promising applications of this composite aerogel as an eco-friendly, cost-effective, and recyclable adsorbent for the efficient removal of FQs from water.     

Multistep conversion of cresols by phenol hydroxylase and 2,3-dihydroxy-biphenyl 1,2-dioxygenase

A mulfistep conversion system composed of phenol hydroxylase （PHrND） and 2,3-dihydroxy-biphenyl 1,2-dioxygenase （BphCLA_4） was used to synthesize methylcatechols and semialdehydes from o- and m-cresol for the first time. Docking studies displayed by PyMOL predicted that cresols and methylcatechols could be theoretically transformed by this multistep conversion system~ High performance liquid chromatography mass spectrometry （HPLC-MS） analysis also indicated that the products formed from multistep conversion were the corresponding 3-methylcatechol, 4-methylcatechol, 2- hydroxy-3-methyl-6-oxohexa-2,4-dienoic acid （2- hydroxy-3-methyl-ODA） and 2-hydroxy-5-methyl-6-oxo- hexa-2,4-dienoic acid （2-hydroxy-5-methyl-ODA）. The optimal cell concentrations of the recombinant E. coli strain BL21 （DE3） expressing phenol hydroxylase （PHrND） and 2,3-dihydroxy-biphenyl 1,2-dioxygenase （BphCLA_4） and pH for the multistep conversion of o- and m-cresol were 4.0 （g-L-1 cell dry weight） and pH 8.0, respectively. For the first step conversion, the formation rate of 3- methylcatechol （0.29μmol·L-1·min-1·mg-1cell dry weight） from o-cresol was similarly with that ofmethylca- techols （0.28 μmol·L-1·min-1·mg-1 cell dry weight） from m-cresol by strain PHrND. For the second step conversion, strain BphCLA_4 showed higher formation rate （0.83 μmol·L-1·min-1·mg-1 cell dry weight） for 2-hydroxy-3-methyl- ODA and 2-hydroxy-5-methyl-ODA from m-cresol, which was 1.1-fold higher than that for 2-hydroxy-3-methyl- ODA （0.77 μmol·L-1·min-1·mg-1. mglcell dry weight） from ocresol. The present study suggested the potential application of the multistep conversion system for the production of chemical synthons and high-value products.