Microbial decolorization of synthetic dyes and reactive dyes of industrial effluents by using a novel fungus Aspergillus proliferans

A decolorizing fungal strain was isolated and identified by the morphology and genotypic characterization as Aspergillus proliferans. The effect of A. proliferans on decolorization of synthetic dyes (70 mg ml(-1)) and colored effluent was evaluated in liquid culture medium. A. proliferans expressed their effective decolorization activity in effectual decolorization of synthetic dyes and industrial effluent. Synthetic dyes were decolorized by 76 to 89% within 6 days of treatment and 73.5% of color was removed in industrial effluent within 8 days. The addition of optimum carbon and nitrogen sources were effectively stimulated the decolorization activity. The high concentration of glucose repressed the decolorization activity and supplementation of yeast extract has significantly enhanced the effluent decolorization at p < 0.05. Laccase enzyme was isolated from liquid state fermentation, which showed significant enzyme activity (10,200 Uml(-1)) at p < 0.005. The crude enzyme decolorizes the dyes aniline blue and congo red in 14 hours (40.9 to 70%) and the effluent in 14 hours (88.6%). Moreover, the culture free supernatant without the fungal biomass has also effectively decolorized the effluent and synthetic dyes. The fungi Aspergillus proliferans was used not only for decolorization but also for better bioremediation of industrial effluent.     

Trout farm effluents: characterization and impact on the receiving streams

Effluents from three rainbow trout (Oncorhynchus mykiss) farms located in Northern Portugal were characterized and their impact on the receiving streams was evaluated. Mean fish productions in the studied fish farms were 15, 55 and 500 t of trout per year, respectively. The feeding water was abstracted from Fornelo, Inha and Coura Rivers, at flow rates ranging from 1.2 (15 t year(-1) fish farm) to 4.8 litre s(-1) per ton annual fish production (500 t year(-1) fish farm). As the water flows through the farms, net variations in the chemical characteristics were observed: a mean reduction in the dissolved oxygen (DO) concentration between 0.7 and 2.4 mg litre(-1); mean increases between 1.9 and 3.2 mg CaCO3 litre(-1) for total alkalinity, between 0.9 and 14 mg litre(-1) for BOD5, between 0.27 and 1.46 mg litre(-1) for ammonia nitrogen (NH4-N), between 0.060 and 0.579 mg litre(-1) for soluble phosphorus (PO4-P) and less than 16 mg litre(-1) for suspended solids; variations in the pH value and nitrate nitrogen concentration were not statistically significant (p<0.05). At the 500 t year(-1) fish farm it was also possible to detect net increases of total hardness (3.2 mg CaCO3 litre(-1)), electric conductivity (19 mS cm(-1)) and permanganate value (3.6 mgO2 litre(-1)). At the other farms net variations in these parameters were not significant. Net mass flow variations reported to the annual fish production are presented. The DO mass flow decreased, on average, between 255 and 549 g t(-1) of fish per day. The mean daily BOD5 increase ranged from 353 to 1510 g t(-1) of fish. The corresponding ranges for the other parameters were 105-157 g t(-1) for NH4-N, 24-62 g t(-1) for PO4-P, 348-1035 g CaCO3 t(-1) for total alkalinity and 224 x 10(6)-506 x 10(6) t(-1) for mesophilic bacteria. Daily net variations of suspended solids, total hardness, electric conductivity and permanganate value were below 1753 g t(-1), 342 g CaCO3 t(-1), 2081 mS cm t(-1) and 392 gO2 t(-1), respectively. Longitudinal concentration profiles for the most relevant parameters show the impact of the effluent discharges on the physico-chemical and bacteriological river water quality downstream from the trout farms. Analyzing the situations from a purely chemical point of view, the polluted stretches were 3, 5 and 12 km long downstream from the effluent discharges, respectively. The microbiological contamination extended over longer distances.     

The acute toxicity of phenol and unionized ammonia, separately and together, to the ephemeropteran Baetis rhodani (Pictet)

The acute toxicity of phenol and ammonia, singly and in combination, to larvae of the ephemeropteran, Baetis rhodani, was examined using a computerized continuous flow system in the laboratory. The 24 h LC50 values (with 95% confidence intervals) were calculated to be 29.9 (17.3-51.5) mg phenol litre(-1) and 8.2 (2.0-33.0) mg un-ionized ammonia litre(-1). When phenol and ammonia were together in low concentration (< 20 mg litre(-1) and < 3 mg litre(-1) [un-ionized], respectively), they expressed their toxicity additively, but at higher concentrations they behaved in a greater-than-additive manner. When the 24 h LC50 values were used to predict the toxicity of a coking plant effluent, containing principally ammonia and phenol, it was found that the B. rhodani larvae died quicker than expected indicating the presence of other toxic chemicals. This exemplifies the value of using direct toxicity assessments to detect the presence of unknown toxicants.     

氯化铁处理AB工艺二级出水中的磷

铁盐混凝剂因其高电荷、安全无毒、易于控制等优点,在城市污水厂除磷方面得到了进一步的发展和应用。为了考察FeCl3除磷的作用特征,探讨除磷效率随pH值、FeCl3投加量等混凝参数的变化规律,以氯化铁(FeCl3)为除磷剂,某城市污水处理厂二级出水为实验水样,进行了实验研究。研究结果表明,水样的硬度对混凝剂除磷性能有较大影响,在最佳工艺条件———不调节水样pH值、FeCl3投加量为75 mg/L时,可将废水中的总磷含量从4.95 mg/L降至0.44 mg/L以下,处理出水可达《城镇污水处理厂污染物排放标准》(GB 18918-2002)中的一级A排放标准(GB18918-2002)(TP<0.50 mg/L)。     

Benthic macroinvertebrate community structure in 20 streams of varying pH and humic content

The structure of stream benthic macroinvertebrate communities in relation to pH and humic content was studied in 20 second and third-order forest streams in southern Sweden. Streams varied in pH from 4.2 to 8.0, and in humic content from a colour of 5 to 1200 mg Pt litre(-1). There was a positive relationship between pH and species richness, with a discontinuity occurring at pH approximately 5.7. At pH > 5.7, species richness decreased with increasing colour. At pH < 5.7 there was a positive correlation between species richness and humic concentration up to a colour of about 200-300 mg Pt litre(-1). this may be explained by high concentrations, 0.4-0.9 mg litre(-1), of labile monomeric Al occurring in the low coloured acid streams. In streams with a colour > 200 mg Pt litre(-1) labile monomeric Al was less than 0.2 mg litre(-1). There was no significant change in species richness above this threshold, but a shift in species composition towards a dominance of Plecoptera and Chironomidae. This threshold model seems to explain the observed differences in stream benthic community structure better than a simple linear relationship with pH or humic content.     

Effects of ammonia on periphytic communities

Laboratory tests were conducted to evaluate the chronic effects of ammonia on periphytic communities. Species richness of the protozoan component of these communities was affected at un-ionized ammonia concentrations of 相似文献   

Biological denitrification of a highly nitrogenous industrial effluent: a case study in Zimbabwe

This paper describes the establishment and design of a scheme to denitrify industrial effluent with concentrations of N greater than 2000 mg litre(-1) to levels within the regulatory limits of the Zimbabwe Natural Resources Act which stipulates an upper limit of 10 mg litre(-1) of nitrate in effluent dumped in important catchment areas. The scheme was set up in 1978 and the data used in the discussion are for the year 1983, five years after the establishment of the scheme. The scheme consists of three impounding reservoirs in which effluent is held for at least 24 h in each case so that it undergoes biological denitrification at each stage. In some cases, the effluent is diverted after the second reservoir and is used to irrigate pastures on which dairy cattle are being grazed. In general, under this scheme, the N content of the effluent is within the regulatory limit by the time it enters the main river system, about 8 km away.     

The impact of inorganic tin on the planktonic cyanobacterium Synechocystis aquatilis: the effect of pH and humic acid

The influence of inorganic tin compounds on the unicellular cyanobacterium Synechocystis aquatilis was studied, and its dependence on changing pH of the surrounding medium and the presence of humic acid. Both Sn(II) and Sn(IV), used as chlorides (at the concentrations 1-10 mg litre(-1)), inhibit the growth and chlorophyll a content of the cyanobacterium cultures, but only under alkaline conditions. Generally, the observed tin toxicity increased with increase of metal concentration, time of exposure and pH value of the medium (in the range 7-9.8). Sn(II) seems to be more toxic than Sn(IV). At the lowest studied metal concentration (1 mg litre(-1)), Sn(II) caused a 36 and 40% decrease in growth and chl a content, respectively, after 96 h exposure at pH 9.8, while Sn(IV) caused even a slight increase of both physiological parameters (hormetic effect). Similar increases in growth and chl a content were also observed at a high Sn (II) and Sn(IV) concentration (10 mg litre(-1)), but only in cultures exposed to metal at pH 7. At high pH (9.8), 10 mg litre(-1) of Sn(II) and Sn(IV) significantly suppressed both the growth of the cyanobacterium (by 54.2 and 26.1%, respectively) and the chl a content in cultures (by 58.2 and 24%, respectively). Humic acid reduced the toxicity of tin towards the cyanobacterium. The observed effects of pH and complexing ligand on the inorganic tin toxicity are discussed in the context of changing, chemical metal speciation and bioavailability.     

高效菌藻塘系统对农村污水中磷的强化去除效果研究

研究了高效菌藻塘系统处理太湖地区农村生活污水除磷效果及其强化措施。高效菌藻塘和水生生物塘HRT分别为8 d和4 d,进水总磷浓度为1.7～17.1 mg/L,出水总磷浓度全年平均值为3.33 mg/L,高效菌藻塘系统的除磷能力欠佳。通过降低水生生物塘内水深、采用废弃石膏作为填料构建了新型复合水生生物塘,HRT=1.6 d条件下,复合水生生物塘出水总磷可保持在1 mg/L以下,可达到GB18918-2002一级B排放标准。     

Chemical and biological effects of acid, aluminium and lime additions to a Welsh Hill-stream

Chemical and biological responses to simultaneous additions of acid, aluminium and lime were investigated in contiguous 250m-reaches of a chronically acidic stream in Wales. Treatments were applied for 24 h, and from the upstream end were as follows: zone A-untreated, pH 5.0, 0.37 mg litre(-1) filterable Al; zone B-acidified to pH 4.5, 0.40 mg Al litre(-1) (47% of Al attributed to release from the stream bed due to acid additions); zone C-acidified to pH 4.5 and Al dosed to 0.67 mg litre(-1); zone D-dosed with limestone slurry, resulting in pH 7.2, 0.13 mg Al litre(-1). In all reaches, the chemistry of the interstitial water at depths of 0.15 and 0.3 m never fell below pH 5.5, with corresponding decreases in Al and increases in base cation concentrations. Brown trout, Salmo trutta, and crayfish, Austropotamobius pallipes, held in the stream showed decreases in plasma [Na(+)] and haemolymph [Na(+)], respectively, in all acidic zones (A, B, C): these responses were mitigated by liming (zone D). Thus both chronic and simulated episodic levels of pH and dissolved Al were sub-lethally toxic to test species of aquatic fauna. This experiment also demonstrates a stream bed source/sink of Al, and the availability of a possible refuge from acidic surface waters within the substratum.     

Acceleration of catalase and peroxidase activities in Lemna minor L. and Allium cepa L. in response to low levels of aquatic mercury

The purpose of this study was to assess certain physiological responses of Lemna minor L. (duckweed) and Allium cepa L. (onion) to aquatic mercury at low concentrations. Following a 96-h exposure of plants to nutrient medium contaminated with known levels of mercuric chloride (HgCl(2)), 0.001 to 4 mg litre(-1) (0.0007 to 2.95 mg Hg litre(-1)) or methyl mercuric chloride (MeHgCl(2)), 0.0001 to 0.1 mg litre(-1) (0.0007 to 0.07 mg Hg litre(-1)), the physiological endpoints measured were the growth of fronds (Lemna minor) or roots (Allium cepa), and catalase and peroxidase activities in both plant assays. The EC(50) for HgCl(2) on the basis of the growth curve of Lemna minor was found to be 2.1 mg litre(-1). HgCl(2) and MeHgCl(2) were lethal to L. minor at concentrations of 4 and 0.01 mg litre(-1), respectively. The range of low concentrations that accelerated growth as well as enzymic activities in L. minor was 0.004 to 0.04 mg litre(-1) for HgCl(2) and 0.001 mg litre(-1) for MeHgCl(2). HgCl(2) and MeHgCl(2) induced maximum enzymic activity in Lemna fronds at concentrations of 0.008 and 0.0005 mg litre(-1), respectively. In Allium roots, catalase activity was accelerated at all the concentrations of HgCl(2) (0.001-2 mg litre(-1)) and MeHgCl(2) (0.0001-0.1 mg litre(-1)) tested. The activity of peroxidase was, however, accelerated by HgCl(2) at concentration range 0.01-1.0 mg litre(-1), or by MeHgCl(2) at 0.001 mg litre(-1). The concentrations of HgCl(2) and MeHgCl(2) that induced the highest enzymic activity in Allium roots were 0.05 mg litre(-1) and 0.001 mg litre(-1), respectively.     

Waste Fe(III)/Cr(III) hydroxide as adsorbent for the removal of Cr(VI) from aqueous solution and chromium plating industry wastewater

Fe(III)/Cr(III) hydroxide, a waste material from the fertilizer industry, has been used for the adsorption of Cr(VI) from aqueous solution, over a range of initial metal ion concentrations (5-30 mg litre(-1)), agitation times (1-180 min), adsorbent dosages (100-1200 mg per 50 ml), temperatures (24, 29 and 38 degrees C) and pH values (4.5-10). The adsorption of Cr(VI) increased with the initial concentration of Cr(VI) and with temperature. The process of uptake follows both the Langmuir and the Freundlich isotherm models. The applicability of Lagergren and empirical kinetic models has also been investigated. Almost quantitative removal of Cr(VI) at 10 mg litre(-1) in a 50-ml solution by 500 mg of adsorbent was found at an equilibrium pH of 5.6. The efficiency of chromium removal was also tested using wastewater from the chromium plating industry.     

淀粉基黄原酸盐处理重金属废水的条件优化研究

采用淀粉基黄原酸盐处理含重金属的电镀废水 ,对淀粉基黄原酸盐的用量、pH值和反应时间等条件进行了研究。结果发现 ,1L含氰电镀废水 (含Cr3+15mg/L、Cu2 +3mg/L、Ni2 +9.2mg/L和Zn2 +6mg/L) ,加入 1g淀粉基黄原酸盐 ,调节 pH为 8,搅拌 1h ,过滤 ,处理后的废水中Cr3+、Cu2 +、Zn2 +和Ni2 +残余浓度分别为 0 .0 8mg/L、0 .0 1mg/L、0 .1mg/L和 0 .0 8mg/L。含有重金属盐的残渣 ,可用硝酸处理 ,以回收重金属     

Abundance and population structure of perch (Perca fluviatilis L.) in some acidic Norwegian lakes

Abundance (catch per unit effort, n=3752) and population structure of perch Perca fluviatilis were studied in 30 acidic Norwegian lakes with relation to pH (4.3-5.9), calcium (0.41-2.44 mg litre(-1)), labile aluminium (24-255 microg litre(-1)) and total organic carbon (TOC, 1.7-13.8 mg C litre(-1)). Standard series of bottom gill-nets were used to sample fish populations. A multiple regression analysis showed that abundance was significantly correlated to TOC (P<0.05) and, to a smaller extent, to the Ca in lakes with concentrations between 0.41 and 1.70 mg litre(-1) (P=0.07). The lakes which were inhabited by pike were excluded from the analysis. Recruitment failure seems to be the main cause of reductions in perch numbers in the lakes studied. However, high mortality among adult individuals was also evident, and an episode of fish kill was observed in one of the lakes.     

Phosphorus release in aerobic sludge digestion.

The objectives of this study are to examine the phosphorus release in aerobic sludge digestion and to better understand its governing mechanisms. In this study, phosphorus release was examined using the secondary sludge from both conventional and biological nutrient removal processes. The experiments were carried out at room temperature (22 +/- 2 degrees C), with or without automatic control of pH (4.5 to 7.8), and under three aeration schemes: fully aerobic (dissolved oxygen [DO] at 3 to 4 mg/L), low DO (0.2 to 0.8 mg/L), and cyclic (with alternate on/off aeration). The released phosphorus concentrations were 20 to 80 mg/L for the conventional sludge and 60 to 130 mg/L for the biophosphorus sludge. Higher phosphorus release also occurred at low pH (<6.0). As for the effect of DO, fully aerobic digestion caused higher phosphorus release than the low-DO and cyclic operations. For better understanding, the solid phosphorus in sludge was conceptually categorized into three forms: inorganic phosphorus precipitates, organic cellular phosphorus, and polyphosphate (poly-P) in polyphosphate-accumulating organisms. Dissolution of inorganic phosphorus precipitates is controlled by physical and chemical conditions, with pH being the most important in this study. Lowering the pH to 4 to 6 clearly promoted the release of inorganic phosphorus. Polyphosphate hydrolysis, on the other hand, was found to be regulated biologically (sensitive to occurrence of anaerobic conditions) and was insignificant in the glutaraldehyde-fixed sludge. Phosphorus release from organic phosphorus should correlate with the volatile solid (VS) digestion, which lyses the cells and frees the phosphorus covalently bonded with the organic matters. The amounts of phosphorus released per unit VS digested (deltaP/deltaVS) were therefore calculated for experiments with long periods of constant pH (to minimize interferences from dissolution/precipitation of inorganic phosphorus). The results suggested that some poly-P was hydrolyzed and released accompanying the aerobic VS digestion, but at rates far lower than those under anaerobic conditions.     

方解石粉钝化太湖水中磷的能力及影响因素

利用轻质、重质和纳米方解石粉进行了去除太湖水中磷的实验研究,单位重量方解石粉除磷量与溶液中磷浓度正相关,轻质和重质方解石粉除磷规律符合Langmuir吸附等温式,极限除磷量分别为0.387 mg/g和0.351 mg/g,纳米方解石粉除磷规律符合Freundlich吸附等温式.方解石粉BET比表面积是影响方解石粉除磷能...     

Color and COD removal from wastewater containing Reactive Black 5 using Fenton's oxidation process

In this study, Reactive Black 5 (RB5) was removed from synthetic wastewater using Fenton's oxidation (FO) process. Experiments were conducted on the samples containing 100 and 200 mg l(-1) of RB5 to remove the dye toxicity. Seventy-five milligram per litre of RB5 caused 25% toxicity on 24-h born daphnids whereas 100 mg l(-1) of RB5 displayed 100% toxicity on Daphnia magna. The study was performed in a systematic approach searching optimum values of FeSO(4) and H(2)O(2) concentrations, pH and temperature. Optimum pH and temperature for 100 mg l(-1) of RB5 were observed as 3.0 and 40 degrees C, respectively, using 100 mg l(-1) of FeSO(4) and 400 mg l(-1) of H(2)O(2) resulted in 71% chemical oxygen demand (COD) and 99% color removal. For 200 mg l(-1) of RB5, 84% COD removal was obtained using 225 mg l(-1) of FeSO(4) and 1000 mg l(-1) of H(2)O(2) yielding 0.05 molar ratio at pH 3.0 and 40 degrees C. Color removal was also more than 99%. The optimum conditions determined in accordance with the literature data. The H(2)O(2) requirement seems to be related to initial COD of the sample. FeSO(4)/H(2)O(2) ratios found were not changed for both concentrations. The temperature affected the COD removal significantly at high degrees. Toxicity was completely removed for each concentration of RB5 at optimum removal conditions.     

Recovery of phosphates from wastewater using converter slag: Kinetics analysis of a completely mixed phosphorus crystallization process

A phosphorus crystallization process for recovering phosphates was developed using a completely mixed reactor and powdered converter slag as a seed crystal. This completely mixed phosphorus crystallization process achieved a stable and high phosphorus recovery: the average PO4-P removal efficiency during 200 d of operation was 87%, with a range of 70-98%. The apparent volume of the slag doubled due to crystal growth during the long-term phosphorus-removal experiments. The Ca2+ concentration, slag dosage, and temperature were found to govern the phosphorus recovery system for a given condition of pH and hydraulic retention time. The equations for the rate constant and reaction order were obtained by evaluating the model parameters. The model developed in this study was observed to successfully simulate the behavior of effluent PO4-P in a completely mixed phosphorus crystallization reactor over a wide variety of operating conditions of temperature, Ca2+ concentration, and influent PO4-P. Model investigations of design factors suggest that the completely mixed phosphorus crystallization process with influent PO4-P concentrations of less than 10 mg l(-1) could ensure effluent PO4-P concentrations of less than 0.5 and 1.0 mg l(-1) during summer and winter in Korea, respectively.     

Coagulation and precipitation as post-treatment of anaerobically treated primary municipal wastewater.

The main objective of this study was to investigate the feasibility of coagulation as a post-treatment method of anaerobically treated primary municipal wastewater. Both mesophilic and ambient (20 degrees C) temperature conditions were investigated in a laboratory-scale upflow anaerobic sludge bed (UASB) reactor. In addition, optimization of the coagulant, both in terms of type and dose, was performed. Finally, phosphorus removal by means of aluminum and iron coagulation and phosphorus and ammonia nitrogen removal by means of struvite precipitation were studied. Anaerobic treatment of primary effluent at low hydraulic retention times (less than 15 hours) resulted in mean chemical oxygen demand (COD) removals ranging from 50 to 70%, while, based on the filtered treated effluent, the mean removals increased to 65 to 80%. Alum coagulation of the UASB effluent gave suspended solids removals ranging from approximately 35 to 65%. Turbidity removal reached up to 80%. Remaining COD values after coagulation and settling were below 100 mg/L, while remaining total organic carbon (TOC) levels were below 50 mg/L. Filterable COD levels were generally below 60 mg/L, while filterable TOC levels were below 40 mg/L. All coagulants tested, including prepolymerized aluminum and iron coagulants, demonstrated similar efficiency compared with alum for the removal of suspended solids, COD, and TOC. Regarding struvite precipitation, optimal conditions for phosphorus and nitrogen removal were pH 10 and molar ratio of magnesium: ammonia-nitrogen: phosphate-phosphorus close to the stoichiometric ratio (1:1:1). During struvite precipitation, removal of suspended solids reached 40%, while turbidity removal reached values up to 80%. The removal of COD was approximately 30 to 35%; yet, when removal of organic matter was based on the treated filterable COD, the removal increased to approximately 65%. In addition, nitrogen was removed by approximately 70%, while phosphorus removal ranged between approximately 30 and 45% on the basis of the initial phosphorus concentration. Finally, size fractionation of the organic matter (COD) showed that the various treatment methods were capable of removing different fractions of the organic matter.     

Limited compensation of ozone stress by potassium in Norway spruce

The effects of potassium fertilization and ozone stress were investigated in a clone of Picea abies (L.) Karst, by studies of the uptake of CO(2) by the crowns, the element content, on leaching of the youngest needles, and the longevity of the needles. All plants were exposed to 0.075 microl litre(-1) SO(2) from January to April 1986. The average ozone concentrations applied during the subsequent growing season (May-December) were 0, 0.027, 0.050 and 0.100 microl litre(-1). Half of the trees received liquid fertilizer applications from April to July 1986. CO(2) uptake by the crowns was significantly reduced in non-fertilized plants at ozone doses of 100-200 microl litre(-1) h, whereas similar reductions were recorded in fertilized plants only above an ozone dose of 300 microl litre(-1) h. Independent of the fertilization, however, the concentrations of calcium, magnesium and nitrogen in the needles increased in parallel with the ozone dose, whilst potassium, phosphorus and sulphur showed little response to ozone. In both nutrient regimes, the diffusive loss of elements from chloroform-washed needles was similar and tended to be reduced at the highest ozone concentration, when relating the leachate to the corresponding element content in the needles. Needles formed in the highest ozone treatment were significantly shed during the succeeding year, regardless of the nutrient supply. It appears that increased potassium supply has little compensating effect on ozone stress in spruce.