Estimation of biodegradation parameters of phenolic compounds on activated sludge by respirometry

The bio-oxidation of phenol, catechol, resorcinol, m-cresol and 5-methylresorcinol on activated sludge was investigated by oxygen uptake measurements. In addition, the degradation of acetate with the same microbial population was studied. The substrate-dependent oxygen uptake data were analysed on the basis of the Michaelis-Menten kinetics. The extant kinetic parameters, the maximum rates of oxygen consumption and half-saturation constants for the processes with different substrates were determined. The simple respirometric approach also made it possible to determine the short-term oxygen demands of the substrates which formed 23-38% of the theoretical oxygen demand of the studied compounds.     

Effect of textile auxiliaries on the biodegradation of dyehouse effluent in activated sludge

The textile industry is confronted with serious environmental problems associated with its immense wastewater discharge, substantial pollution load, extremely high salinity, and alkaline, heavily coloured effluent. Particular sources of recalcitrance and toxicity in dyehouse effluent are two frequently used textile auxiliaries; i.e. dye carriers and biocidal finishing agents. The present experimental work reports the observation of scientific and practical significance related with the effect of two commercially important textile dye carriers and two biocidal finishing agents on biological activated sludge treatment at a textile preparation, dyeing and finishing plant in Istanbul. Respirometric measurements of the dyehouse effluent spiked with the selected textile chemicals were carried out for the assessment of the "readily biodegradable COD fraction" of the wastewater. The respirometric data obtained to visualize the effect of the selected textile auxiliaries on biomass activity was evaluated by an adopted activated sludge model. Results have indicated that the tested biocides did not exert any significant inhibitory effect on the treatment performance of the activated sludge reactor at the concentrations usually encountered in the final, total dyehouse effluent. The situation with the dye carriers was inherently different; one dye carrier appeared to be highly toxic and caused serious inhibition of the microbial respirometric activity, whereas the other dye carrier, also known as the more ecological alternative, i.e. the "Eco-Carrier", appeared to be biodegradable. Finally, the respirometric profile obtained for the Eco-Carrier was described by a simplified respirometric model.     

Synthesis of polychlorinated [14C]alkanes (PCA) of high specific activity

The synthesis of certain ¹⁴C-labelled polychlorinated alkanes is described. The compounds used as starting material were [1-¹⁴C]lauric acid, [1-¹⁴C]hexadecane and [U-¹⁴C]palmitic acid. The carboxylic acids were reduced with lithium aluminium hydride. The alcohol obtained was treated with triphenylphosphine dichloride which gave the corresponding 1-chloroalkane. The chlorination of the alkanes was performed in tetrachloromethane by use of sulphuryl chloride with benzoyl peroxide or UV-light as initiators. Three mixtures of polychlorinated dodecanes (45.9%, 55.9% and 68.5% chlorine) and two polychlorinated hexadecanes (34.1% and 69% chlorine) were synthesized. The products of higher chlorine content prepared were only available via the photoinduced chlorination.     

Study on 14C-BHA absorption and distribution in rat

BHA was administered to rats at doses of 5 or 500 mg/kg for seven days. ¹⁴C-BHA absorption was investigated on the eighth day and compared with animals receiving a single dose of 5 or 500 mg/kg BHA. Absorption of ¹⁴C-BHA was proportionately greater at the high dose rats. ¹⁴C distribution was 3–6 times higher in the forestomach than in the pyloric region of the stomach. The urinary excretion of BHA conjugates was not dependent on pretreatment with BHA or on the dose.     

A new method to study biodegradation kinetics of organic trace pollutants by activated sludge

A reliable prediction of the behaviour of organic trace compounds in activated sludge plants requires an accurate input of the biodegradation kinetics. Often these kinetics are extrapolated from the results of standardised biodegradation tests. However, these tests generally are not designed to yield kinetic information and do not reflect the conditions in activated sludge plants. To overcome these problems a new test method was developed which is referred to as a 'by-pass' test. The test methodology is explained and examples are given for three compounds: the C(12)-homologue of linear alkylbenzene sulfonate, nitrilotriacetic acid and toluene. More experience with the test is required, particularly with respect to selection of the proper test settings, which are compound related. The test is a suitable tool in a research environment, for example to investigate the effect of plant operational parameters on the biodegradation kinetics.     

Adsorption/desorption of linear alkylbenzenesulfonate (LAS) and azoproteins by/from activated sludge flocs

Our study investigated the adsorption/desorption by/from activated sludge flocs, dispersed in river water or in diluted wastewater, of organic compounds (C(11)-LAS, azoalbumin and azocasein) at concentrations relevant to environmental conditions. Activated sludge flocs, used as a model of biological aggregates, are characterized by a very heterogeneous matrix able to sorb the three organic compounds tested at 4 degrees C. The adsorbed amount of C(11)-LAS by activated sludge flocs was higher than that of azocasein or azoalbumin, as shown by the Freundlich parameters (K(ads)=8.6+/-1.7, 1.6+/-0.3 and 0.3+/-0.1 micromol(1-1/n)g(-1)l(1/n) for C(11)-LAS, azocasein and azoalbumin, respectively; n=3 sludges). C(11)-LAS sorption from activated sludge appeared to be partially reversible in river water, while a marked hysteresis phenomenon was observed for azocasein and azoalbumin, implying a low degree of reversibility in their exchange between activated sludge and river water. It has also been displayed that the conductivity variation of bulk water (comprised between 214 and 838 microS cm(-1)) exerted no dramatic effect on the C(11)-LAS desorption from activated sludge flocs, while a little effect of it on azocasein desorption was observed. Thus, biological aggregates as activated sludge flocs can serve as an intermediate carrier for C(11)-LAS, while it represents a sink for proteins.     

Ca(II)在活性污泥生物絮凝中的作用研究

采用4个平行的序批式反应器(SBR),研究了进水Ca²⁺浓度对活性污泥絮体表面特性和结构稳定性的影响,并由此来确定Ca²⁺在生物絮凝中的作用。结果表明：随着进水Ca²⁺浓度的增加,污泥中的Ca含量逐渐增大。进水中Ca²⁺的加入,增大了污泥絮体的粒径和密度,进而改善了污泥的沉降性能;Ca²⁺的加入,使可供结合的蛋白质数量最高增至近1倍,污泥表面疏水性也相应增强;污泥絮凝性能的改善,主要和可供Ca²⁺结合的蛋白质含量增加有关,而非多糖;EDTA通过络合污泥絮体中的Ca²⁺,破坏了由Ca²⁺架桥形成的污泥絮体结构,这说明Ca²⁺可通过和胞外聚合物（extracellular polymeric substances, EPS）中的负电官能团架桥来促进污泥絮体的形成并维持絮体结构的稳定性。     

Effect of mixed liquor suspended solids concentration on the biodegradation of nitrilotriacetic acid in the activated sludge process

The biodegradation of nitrilotriacetic acid in laboratory simulations of the activated sludge process has been studied at two different concentrations of mixed liquor suspended solids. Responses to changes in the influent nitrilotriacetic acid concentration such as those which might be associated with a “wash day” have been examined.     

Effect of ultrasonication and Fenton oxidation on biodegradation of bis(2-ethylhexyl) phthalate (DEHP) in wastewater sludge

The presence of bis(2-ethylhexyl) phthalate (DEHP) and its metabolites, i.e. 2-ethylhexanol, 2-ethylhexanal, and 2-ethylhexanoic acid in wastewater sludge (WWS) were investigated during aerobic digestion and Bacillus thuringiensis (Bt)-based fermentation of WWS. Ultrasonication and Fenton oxidation pre-treatment was applied to improve biodegradability of WWS and bioavailability of the target compounds for digestion and fermentation. DEHP and 2-ethylhexanoic acid were observed at higher concentration, meanwhile 2-ethylhexanol and 2-ethylhexanal were observed at lower concentration in WWS. After 20-day aerobic digestion, DEHP removal was 72%, 89%, and 85%, and 2-ethylhexanoic acid removal was 71%, 84%, 79%, respectively for raw, ultrasonicated, and Fenton-oxidized sludges. Bt was found to degrade DEHP, leading to DEHP removal of 21%, 40%, and 30%, respectively for raw, ultrasonicated, and Fenton-oxidized sludges in the fermentation. The results suggested that aerobic stabilization and Bt-based fermentation can remove the phthalates, and pre-treatment of WWS was also effective in improvement of DEHP biodegradation. Hence, Bt-based biopesticide production from WWS can be applied safely when taking into consideration the phthalate contaminants.     

Effects of nano-copper(II) oxide and nanomagnesium oxide particles on activated sludge

Effects of nano-copper(II) oxide (nano-CuO) and nanomagnesium oxide (nano-MgO) particles on activated sludge endogenous respiration (aerobic digestion), biochemical oxygen demand (BOD) biodegradation, and nitrification were investigated through respiration rate measurement. For comparison, the effects of Cu(II) and Mg(II) ions on activated sludge were also studied. Results indicated that soluble Cu(II) has half maximum inhibitory concentration (IC50) values of 19, 5.5, 53, and 117 mg Cu/L for endogenous respiration, BOD biodegradation, ammonium oxidation, and nitrite oxidation, respectively. However, nano-CuO only inhibited BOD biodegradation at 240 mg Cu/L or more, and its associated toxicity was primarily caused by soluble Cu(II). In contrast, soluble Mg(II) was not toxic to activated sludge in the experimental concentration range, but nano-MgO inhibited BOD biodegradation and nitrification with IC50 values of 70 and 143 mg Mg/L, respectively. Further study indicated that the toxicity of nano-MgO resulted primarily from increased pH following MgO hydrolysis.     

Investigation of Cr(VI) reduction in continuous-flow activated sludge systems

The aim of this research was to investigate hexavalent chromium, Cr(VI), reduction by activated sludge and to evaluate the use of continuous-flow activated sludge systems for the treatment of Cr(VI)-containing wastewater. Three series of experiments were conducted using two parallel lab-scale activated sludge systems. During the first experiment, one system was used as a control, while the other received Cr(VI) concentrations equal to 0.5, 1, 3 and 5mg l(-1). For all concentrations added, approximately 40% of the added Cr(VI) was removed during the activated sludge process. Determination of chromium species in the dissolved and particulate phase revealed that the removed Cr(VI) was sorbed by the activated sludge flocs mainly as trivalent chromium, Cr(III), while the residual chromium in the dissolved phase was mainly detected as Cr(VI). Activated sludge ability to reduce Cr(VI) was independent of the acclimatization of biomass to Cr(VI) and it was not affected by the toxic effect of Cr(VI) on autotrophic and heterotrophic microorganisms. During the second experiment, both systems were operated under two different hydraulic residence time (theta equal to 20 and 28h) and three different initial organic substrate concentration (COD equal to 300, 150 and 0mg l(-1)). Cr(VI) reduction was favored by an increase of theta, while it was limited by influent COD concentration. Finally, at the last experiment the effect of anoxic and anaerobic reactors on Cr(VI) reduction was investigated. It was observed that the use of an anoxic zone or an anaerobic-anoxic zone ahead of the aerobic reactor favored Cr(VI) reduction, increasing mean percentage Cr(VI) reduction to almost 80%.