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J M Lema

Publications and source records attributed to J M Lema.

At least 37 records · Page 2Linked to original sources

Enzymatic membrane reactors for biodegradation of recalcitrant compounds. Application to dye decolourisation.

Membrane bioreactors are being increasingly used in enzymatic catalysed transformations. However, the application of enzymatic-based treatment systems in the environmental field is rather unusual. The aim of this paper is to overview the application of enzymatic membrane reactors to wastewater treatment, more specifically to dye decolourisation. Firstly, the basic aspects such as different configurations of enzymatic reactors, advantages and disadvantages associated to their utilisation are revised as well as the application of this technology to wastewater treatment. Secondly, dye decolourisation by white-rot fungi and their oxidative enzymes are discussed, presenting an overall view from for in vivo and in vitro systems. Finally, dye decolourisation by manganese peroxidase in an enzymatic membrane reactor in continuous operation is presented.

Azo Compounds↗

Biodegradation of a polymeric dye in a pulsed bed bioreactor by immobilised phanerochaete chrysosporium.

An immobilised fungal bioreactor operated with pulsation of the gas-phase is proposed and operated at variable conditions for the continuous biological degradation of complex structures. In order to test the system, a hardly biodegradable dye (Poly R-478) was selected as a model compound and Phanerochaete chrysosporium as the ligninolytic fungus. High percentages of decolourisation--between 65% and 80%--under optimal conditions were achieved. Moreover, the system proved to have high stability with long operational periods (at least, 90 days). During the operation Manganese Peroxidase was the sole ligninolytic enzyme detected which points out this enzyme as the main substance responsible for decolourisation. The optimal conditions established were the following: temperature of 37 degrees C, use of oxygen, Mn2+ concentrations between 33 and 330 microM and exogenous H2O2 added in periodical pulses (as chemical reagent, 1 microM or as H2O2 enzymatically generated by 0.6 U L(-1) glucose oxidase and residual glucose).

Biodegradation, Environmental↗

Nitrification in saline wastewater with high ammonia concentration in an activated sludge unit.

A nitrifying activated sludge reactor fed with a high salinity medium was operated efficiently at ammonia loading rates between 1 and 4 g NH4+ -N l(-1) d(-1). The system became completely inefficient at inlet salt concentrations higher than 525 mM due to the mixed inhibition effect of salts and ammonia. The final product was mainly nitrate although dissolved oxygen limitations caused sporadic ammonia and nitrite accumulations. Specific nitrifying activity decreased due to the saline effect. A set of activity tests showed that in the continuous reactor non-adapted biomass is rather more sensitive than biomass to the saline effect. Physical properties of biomass in the reactor (sludge volumetric index and zone settling velocity) were not affected by the saline concentration, a biomass concentration of 20 gVSS l(-1) was achieved.

Ammonia↗

An expert system for monitoring and diagnosis of anaerobic wastewater treatment plants.

In this paper, an expert system (ES) developed for the monitoring and diagnosis of anaerobic wastewater treatment plants (AWT), is presented. The system was evaluated in a hybrid pilot plant of 1.1 m3 located in an industrial environment for the treatment of wastewaters from a fibreboard production factory. The reactor is a hybrid USBF, combining an upflow anaerobic sludge blanket (UASB) in the lower part and an upflow anaerobic filter (UAF) at the top.

Bacteria, Anaerobic↗

The effect of kaolin particles on the behavior of nitrifying activated sludge units.

The effects of the addition of powered particles of kaolin to nitrifying activated sludge systems were studied. Kaolin was added to a nitrifying activated sludge reactor, during the operational phase, to observe the effects of this clay on reactor performance. The results were compared to those obtained from a similar unit operated without kaolin. The settling properties of the sludges from both units were similar (sludge volume index (SVI) of 14.5 ml/g VSS; zone settling velocity (ZSV) of 7.5 m/h), but the specific nitrifying activities of ammonia and nitrite oxidizing processes were enhanced up to 75% and 50%, respectively, when kaolin was added. The mechanism of action of kaolin was not clear. Additional ammonia, nitrite and nitrate adsorption tests showed that these compounds were not adsorbed by kaolin. This demonstrated that no beneficial effect was caused by adsorption of either substrates or products. Short-term activity tests also showed that the stimulating effects of kaolin on specific activity were not immediate. The effects of kaolin when nitrifying units were operated under unfavorable conditions were also evaluated: In a second set of experiments, a nitrifying unit was operated with low levels of dissolved oxygen (DO), with and without kaolin. The presence of kaolin exerted practically no effect on ammonia oxidation but nitrite oxidation slightly diminished. In a third set of experiments, a nitrifying unit was subjected to pH shocks (9, 10 and 11) over 3 h with pH then restored to 7.8. A pH shock of 11 caused a decrease of 60% in nitrifying activity for 12 days. When kaolin was added to this unit the efficiency of the system was completely restored in 4 days. Therefore, kaolin might be useful to restore damaged units.

Ammonia↗

Influence of pulsation on start-up of UASB reactors.

The aim of this work is to study the influence of pulsation on the start-up of lab-scale UASB reactors. Pulsation was produced by an Elastic Membrane Pulsator (EMP). The application of this device in previous works improved the performance of continuous fixed-bed fermentors and reduced the formation of preferential pathways, the retention of gas metabolites within the bed and the resistance to mass transfer. These characteristics seem to be suitable for feeding UASB reactors. In this work, the influence of pulsation frequency was studied in two pulsed UASB reactors operated in parallel with a non-pulsed one. One of them (P1) operated at high frequencies (periods of 50 and 200 s between each pulsation) and the other (P2) at low frequencies (periods of 3600 and 900 s between each pulsation). An important improvement of the removal efficiency for pulsed reactors with respect to the non-pulsed one was obtained. The structure of the biomass was observed at the end of the process by scanning electron microscopy. In general, granulation of biomass was improved when operating in pulsing form.

Bacteria, Anaerobic↗

Expert system for the on-line diagnosis of anaerobic wastewater treatment plants.

A diagnosis system for anaerobic wastewater treatment processes is presented. The system is able to recognise the state and trend of the operation and suggest the appropriate control action. The on-line variables measured were gas flow rate and composition (methane and carbon monoxide), feed and recycling flow rates, temperature and pH, while the manipulable inputs are feed, recycling and buffer-addition flow rates. The diagnosis system comprises a structured rule base, incorporating expert knowledge using fuzzy logic features. The structure of the system is based on the classification of information related to the process in three categories: i) the state of the process, ii) its trend and iii) the recommended set-point values for the inputs manipulated: feeding, buffer and recycling pumps. The system was applied to diagnose the operation of a 1.1 m3 hybrid UASB-UAF treating wastewater from a fibreboard production factory under different conditions (overload and underload), corresponding to some of the typical causes of destabilisation in anaerobic wastewater treatment plants. These situations require control action in order to maintain the stability and the treatment capacity of the reactor. The application of the system developed for the purpose of managing the situation proved to be reliable for supplying the actual state and trend of the process, as well as the adequate set point values to recover stable operation and/or to avoid further destabilisation.

Bacteria, Anaerobic↗

In vitro degradation of a polymeric dye (Poly R-478) by manganese peroxidase.

The aim of this study is the evaluation of the enzymatic action of the ligninolytic enzyme manganese peroxidase (MnP), through a suitable addition of H(2)O(2), as a feasible system for the in vitro degradation of complex structures. For this purpose, a highly recalcitrant polymeric dye (Poly R-478) was selected as a model compound. An amperometric technique was used to determine the H(2)O(2) requirement in the decolorization by nonpurified MnP. Two H(2)O(2) supply strategies-fed-batch (every hour) or semicontinuous (every 5 min)-were applied. The addition of H(2)O(2) in pulses led to a limited decolorization after the pulses and the instantaneous consumption or decomposition of H(2)O(2). Therefore, this way of addition may limit the actual H(2)O(2) concentration in the reaction mixture. In contrast, the semicontinuous strategy maintained lower and prolonged concentrations of H(2)O(2), which allowed a clearly greater decolorization (48% after 2 h). In addition, the effect of Mn(+2) concentration on the decolorization efficiency was investigated to establish the optimal application of the MnP-oxidative system. The enzymatic treatment provoked not only the destruction of the chromophoric groups but also a noticeable breakdown of the chemical structure of the dye. In experiments with pure enzyme, MnP proved to be the main factor responsible for the dye decolorization.

Anthraquinones↗

A packed-bed fungal bioreactor for the continuous decolourisation of azo-dyes (Orange II).

The degradation of an azo dye, Orange II, by immobilised Phanerochaete chrysosporium in a continuous packed bed bioreactor for periods longer than 30 days has been carried out. Nearly complete decolourisation (>95%) was achieved when working at a high dye load rate of 0.2 g x l(-1) x d(-1), a temperature of 37 degrees C, a hydraulic retention time (HRT) of 24 h and applying oxygen gas in a pulsed flow. These conditions allowed Manganese peroxidase (MnP) production and the subsequently Orange II decolourisation. A correlation between residual MnP activity in the effluent and decolourisation was established. Apparently, for decolourisation to be effective, a minimum MnP activity was required, no substantial increase in efficiency at MnP activities higher than 10 U x 1(-1) was observed. The treatment caused, the breakdown of the chromophoric group as well as the cleavage of the aromatic ring.

Azo Compounds↗

Simultaneous methanogenesis and denitrification of pretreated effluents from a fish canning industry.

A lab-scale hybrid upflow sludge bed-filter (USBF) reactor was employed to carry out methanogenesis and denitrification of the effluent from an anaerobic industrial reactor (EAIR) in a fish canning industry. The reactor was initially inoculated with methanogenic sludge and there were two different operational steps. During the first step (Step I: days 1-61), the methanogenic process was carried out at organic loading rates (OLR) of 1.0-1.25 g COD l-1 d-1 reaching COD removal percentages of 80%. During the second step (Step II: days 62-109) nitrate was added as KNO3 to the industrial effluent and the OLR was varied between 1.0 and 1.25 g COD l-1 d-1. Two different nitrogen loads of 0.10 and 0.22 g NO3(-)-N l-1 d-1 were applied and these led to nitrogen removal percentages of around 100% in both cases and COD removal percentages of around 80%. Carbon to nitrogen ratio (C:N) in the influent was maintained at 2.0 and eventually it was increased to 3.0, by means of glucose addition, to control the denitrification process. From these results it is possible to establish that wastewater produced in a fish canning industry can be used as a carbon source for denitrification and that denitrifying microorganisms were present in the initially methanogenic sludge. Biomass productions of 0.23 and 0.61 g VSS:g TOC fed for Steps I and II, respectively, were calculated from carbon global balances, showing an increase in biomass growth due to denitrification.

Animals↗

Simultaneous urea hydrolysis, formaldehyde removal and denitrification in a multifed upflow filter under anoxic and anaerobic conditions.

A multifed upflow filter (MUF), working under anoxic or anaerobic conditions, coupled with an aerobic biofilm airlift suspension (BAS) reactor was operated in order to treat a wastewater with high formaldehyde (up to 1.5 g L-1) and urea (up to 0.46 g L-1) concentrations. In the MUF, formaldehyde removal, denitrification and urea hydrolysis took place simultaneously. The MUF was operated at 37 degrees C, at a hydraulic retention time (HRT) ranging from 1 to 0.3 d. An organic loading rate (OLR) of 0.5 kg-formaldehyde m-3 d-1 was efficiently eliminated during anaerobic operation and transformed into methane, while a much higher OLR (up to 2 kg-formaldehyde m-3 d-1) was oxidised under anoxic conditions by the nitrite or nitrate from the nitrifying airlift. However, only 80% of urea was hydrolysed to ammonia in an anoxic environment while complete conversion occurred under anaerobic conditions. Moreover, formaldehyde concentrations higher than 50 mg L-1 provoked a loss of efficiency of urea hydrolysis, decreasing to 10% at formaldehyde concentrations above 300 mg L-1. Methane production rate during the anaerobic stage was adversely affected by accumulations of formaldehyde in the reactor causing lower formaldehyde removal efficiency. However, denitrification proceeded properly even at a formaldehyde concentration of 700 mg L-1 in the reactor, although nitrous oxide appears in the off-gas. The COD/N ratios required for complete nitrite and nitrate denitrification with formaldehyde were estimated at 2.1 and 3.5 kg-COD/kg-N, respectively.

Anaerobiosis↗

Anaerobic treatment of fibreboard manufacturing wastewaters in a pilot scale hybrid usbf reactor.

The treatment of fibreboard manufacturing (FBM) wastewaters was carried out in an industrial pilot plant, which consisted of a hybrid upflow sludge bed filter (USBF) anaerobic reactor and a coagulation-flocculation unit as a pre-treatment. COD removal efficiencies of 90-93% were attained in the anaerobic reactor operating at 37degrees C at organic loading rates (OLR) of 6.5-8.5 kg COD/m3 d. Flocculant sludges were used as inoculum, and granulation was observed in the USBF reactor after 120 days of operation. The overall linear upward velocity (result of liquid and gas flow) was the key factor controlling biomass retention and, therefore, a stable operation at high OLR. According to ecotoxicity values (measured by means of bioluminescence assays), the wastewaters were partially detoxified, being EC50 values for the liquid effluent 25 times lower than those corresponding to the influent. Besides, phenolic compounds removal efficiencies of 90% were attained. The hybrid reactor configuration is an interesting alternative to treat these wastewaters since it is less sensitive to biomass clogging or floatation.

Bacteria, Anaerobic↗

Oxidation of lignin in eucalyptus kraft pulp by manganese peroxidase from Bjerkandera sp. strain BOS55.

The white rot fungus Bjerkandera sp. strain BOS55 was shown in previous studies to cause high levels of kraft pulp bleaching and delignification under culture conditions in which manganese peroxidase (MnP) occurs as the dominant oxidative enzyme. In this study, the MnP of Bjerkadera was isolated and tested in vitro with eucalyptus oxygen-delignified kraft pulp (ODKP) based on measuring the reduction in kappa number as an indicator of lignin oxidation. The MnP preparation applied at 60 U/g pulp for 6 h caused a significant decrease of 11-13% in the kappa number in the ODKP under optimal conditions compared to parallel-incubated controls lacking enzyme. The effects of MnP dosage, Mn2+ concentration, organic acid buffer selection, pH and H2O2 addition were evaluated. The optimal Mn2+ concentration range for lignin oxidation in ODKP was 100-500 microM. In the presence of low oxalate concentrations (0.3-2 mM) the Bjerkandera MnP also significantly reduced the kappa number of ODKP by 6% without any Mn. This observation is in agreement with the fact that purified Bjerkandera MnP has Mn-independent activities. Under incubation conditions with added Mn2+, buffers composed of metal-complexing organic acids provided two-fold better kappa number reductions compared to the inert acetic acid. The optimal H2O2 dosage was found to be 0.017 micromol/min ml when added as semi-continuous pulses (every 30 min) or 0.2 micromol/min ml when generated continuously by glucose oxidase. Excess H2O2 caused severe inactivation of MnP during the incubations. Factors that improved the turnover of the enzyme, such as Mn2+ and metal-chelating acids, stabilized MnP against rapid inactivation.

Biotechnology↗

Effect of two broad-spectrum antibiotics on activity and stability of continuous nitrifying system.

The effects of two broad-spectrum antibiotics, chloramphenicol and oxytetracycline hydrochloride, on the microbial activity and biofilm stability of a mixed nitrifying culture were studied. These antibiotics are present in some wastewaters generated in cattle farms or pharmaceutical industries. A 1-L fermentor, in which nitrifiers grew both in suspension and in a biofilm, was used during the experiments. Chloramphenicol (10-250 mg/L) barely had any effect on biofilm stability and nitrification. Ammonia was fully oxidized to nitrate. However, oxytetracycline caused biofilm sloughing at concentrations of 10 mg/L, but nitrification was not inhibited at antibiotic concentrations up to 100 mg/L. When the concentration of oxytetracycline chlorohydrate was increased stepwise from 100 to 250 mg/L, nitrification was inhibited by 50%. The dissolved organic carbon measurements in both the influent and effluent showed that the antibiotics were neither mineralized by the mixed nitrifying culture nor accumulated in the system. Furthermore, the microbial tests did not reveal the presence of active antibiotics in the effluent. This fact indicates that both cloramphenicol and oxytetracycline were degraded by the nitrifying sludge but not mineralized.

Ammonia↗

Carbon and nitrogen removal from a wastewater of an industrial dairy laboratory with a coupled anaerobic filter-sequencing batch reactor system.

A set of two reactors, an Anaerobic Filter (AF) of 12 m3 and a Sequencing Batch Reactor (SBR) of 28 m3, coupled in series, were used to treat the wastewaters from an industrial milk analysis laboratory. The characteristics of these effluents are similar to those discharged by dairy factories (average values around 10 kg COD/m3 and 0.20 kg N/m3). These wastewaters were produced as the result of the final mixture of the analysed milk samples, with a very high organic load, and other low strength effluents, such as sewage and other minor liquid streams generated in the laboratory. Two microbial growth inhibitors, sodium azide and chloramphenicol, were systematically added to the milk before its analysis. Preliminary results have shown that these compounds did apparently not inhibit the methanogenic activity of the anaerobic sludge. Toxicity determination, using the Microtox method, resulted in EC50 values for the wastewaters of 20 g/L, whereas the final effluent from the SBR was non toxic. A maximum OLR of 8 kg COD/m3.d was treated in the AF, being the maximum OLR in the SBR around 1.5-2 kg COD/m3.d. During operation, the soluble COD of the final effluent from the SBR was usually below 200 mg/L, and total nitrogen (mainly nitrate) below 10 mg N/L. Assimilation of nitrogen for growth and nitrification-denitrification were the main mechanisms of nitrogen removal from the wastewater. In the anaerobic system between 50-85% of the organic matter was converted into methane, being the remaining COD and most of the nitrogen removed in the suspended culture system. Overall COD removal in the treatment system was 98% and the nitrogen removal up to 99%. The combination of the AF and the SBR was advantageous resulting in a lower energy consumption and sludge generation in the treatment system.

Anaerobiosis↗

Advanced monitoring and control of anaerobic wastewater treatment plants: diagnosis and supervision by a fuzzy-based expert system.

A fuzzy-based expert system (ES) for the diagnosis and supervision for anaerobic digesters is presented. The system was developed in a Microsoft Windows support using fuzzy logic inference together with a rule base for the implementation of expert knowledge. The ES runs on-line through three main modules, which determine the state and trend of the process, and the best set points for the actuation on the final control elements of the plant. Two further modules run in parallel, when they are required by the operator, using off-line and on-line information for the detection of inhibition due to toxic compounds in the process and for the validation of the on-line diagnosis. The diagnosis and supervision ES was tuned up in order to adjust the membership functions describing the process, and lately tested, running on-line, to study the response of the rule base.

Anaerobiosis↗

Anaerobic treatment: a key technology for a sustainable management of wastes in Europe.

Environmental regulations in the European Union, based on the concept of integrated prevention and control of pollution, are oriented towards the sustainability of the production processes, and this leads to better recovery of resources from raw materials, energy saving, etc. This philosophy introduces a new framework to Environmental Engineers, who have to make efforts concerning waste minimisation. During the last few decades technologies based on the anaerobic treatment of wastewaters and organic wastes have been applied successfully to a wide variety of problems. A case study on the impact of applying anaerobic technology to the treatment of wastewaters from the sugar industry in Spain is presented. Nowadays, processes based on anaerobic treatment appear to be an excellent option as the core of an integrated process for waste and wastewater treatment.

Bacteria, Anaerobic↗

Different fungal manganese-oxidizing peroxidases: a comparison between Bjerkandera sp. and Phanerochaete chrysosporium.

Two manganese-oxidizing peroxidases differing in glycosylation degree were purified from fermenter cultures of Bjerkandera sp. They were characterized and compared with the three manganese-oxidizing peroxidase isoenzymes obtained from the well-known ligninolytic fungus Phanerochaete chrysosporium. All the enzymes showed similar molecular masses but those from P. chrysosporium had less acidic isoelectric point. Moreover, the latter strictly required Mn2+ to oxidize phenolic substrates whereas the Bjerkandera peroxidases had both Mn-mediated and Mn-independent activity on phenolic and non-phenolic aromatic substrates. Taking into account these results, and those reported for Bjerkandera adusta and different Pleurotus species, we concluded that two different types of Mn(2+)-oxidizing peroxidases are secreted by ligninolytic fungi.

Amino Acid Sequence↗