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High-strength nitrogen removal of opto-electronic industrial wastewater in membrane bioreactor--a pilot study.

The membrane bioreactor (MBR) system has become more and more attractive in the field of wastewater treatment. It is particularly attractive in situations where long solids retention times are required, such as nitrifying bacteria, and physical retention critical to achieving more efficiency for biological degradation of pollutant. Although it is a new technology, the MBR process has been applied for industrial wastewater treatment for only the past decade. The opto-electronic industry, developed very fast over the past decade in the world, is high technology manufacturing. The treatment of the opto-electronic industrial wastewater containing a significant quantity of organic nitrogen compounds with a ratio over 95% in organic nitrogen (Org-N) to total nitrogen (T-N) is very difficult to meet the discharge limits. This research is mainly to discuss the treatment capacity of high-strength organic nitrogen wastewater, and to investigate the capabilities of the MBR process. A 5 m3/day capacity of MBR pilot plant consisted of anoxic, aerobic and membrane bioreactor was installed for evaluation. The operation was continued for 150 days. Over the whole experimental period, a satisfactory organic removal performance was achieved. The COD could be removed with an average of over 94.5%. For TOC and BOD5 items, the average removal efficiencies were 96.3 and 97.6%, respectively. The nitrification and denitrification was also successfully achieved. Furthermore, the effluent did not contain any suspended solids. Only a small concentration of ammonia nitrogen was found in the effluent. The stable effluent quality and satisfactory removal performance mentioned above were ensured by the efficient interception performance of the membrane device incorporated within the biological reactor. The MBR system shows promise as a means of treating very high organic nitrogen wastewater without dilution. The effluent of TKN, NOx-N and COD can fall below 20 mg/L, 30 mg/L and 50 mg/L.

Bioreactors↗

Application of a membrane bioreactor system for opto-electronic industrial wastewater treatment--a pilot study.

The membrane bioreactor (MBR) system has become more and more attractive in the field of wastewater treatment. It is particularly attractive in situations where long solids retention times are required, such as nitrifying bacteria, and physical retention is critical to achieving more efficiency for biological degradation of pollutants. Although it is a new technology, the MBR process has been applied to industrial wastewater treatment for only the past decade. The opto-electronic industry, developed very fast over the past decade in the world, is a high technological manufacturing industry. The treatment of the opto-electronic industrial wastewater containing a significant quantity of organic nitrogen compounds, with a ratio over 95% in organic nitrogen (Org-N) to total nitrogen (T-N), is very difficult to meet the discharge limits. The purpose of this research is mainly to discuss the treatment capacity of high-strength organic nitrogen wastewater, and to investigate the capabilities of the MBR process. A 2 m3/day capacity MBR pilot plant consisting of anoxic and aerobic tanks and a membrane bioreactor was installed for evaluation. The operation was continued for 130 days. Over the whole experimental period, a satisfactory organic removal performance was achieved. The COD could be removed with an average of over 94.5%. For TOC and BOD5, the average removal efficiencies were 96.3 and 97.6%, respectively. The nitrification and denitrification were also successfully achieved. The effluent did not contain any suspended solids. Only a small concentration of ammonia nitrogen was found in the effluent. The stable effluent quality and satisfactory removal performance mentioned above were ensured by the efficient interception performance of the membrane device incorporated within the biological reactor. The MBR system shows promise as a means of treating very high organic nitrogen wastewater without dilution. The effluent of TKN, NOx-N and COD can fall below 20 mg/L, 30 mg/L and 50 mg/L.

Bioreactors↗

Responses of Sarcoptes scabiei (Acari: Sarcoptidae) to nitrogenous waste and phenolic compounds.

This study found that > or = 1 life stage(s) of Sarcoptes scabiei (L.) was significantly attracted to the nitrogenous compounds, guanine, purine, adenine, allantoin, hypoxanthine, xanthine, uric acid, ammonium chloride, ammonium nitrate, and ammonium sulfate. Females and larvae responded to all compounds. Males responded to all compounds except purine and allantoin. Nymphs responded to all compounds except allantoin. Some specific concentrations of compounds attracted only 1 life stage but other concentrations attracted multiple life stages. Also, some life stages were attracted by multiple concentrations of a compound. The concentration that induced the greatest response by a particular life stage varied between life stages. Overall, greater percentages of females were attracted to the nitrogenous compounds than any other life stage. Females responded to more concentrations of a compound compared to other life stages. Males responded to fewer concentrations then immatures. In addition, all life stages of S. scabiei were significantly attracted to the phenolic compounds, 2,6-dichlorophenol, methyl salicylate, and 2-nitrophenol. Nymphs followed by females responded to the most concentrations. The results indicated that these nitrogenous wastes and phenolic compounds acted in a pheromone-like manner that induced assembly of these ectoparasitic mites.

Animals↗

Biosynthesis and identification of volatiles released by the myxobacterium Stigmatella aurantiaca.

The volatiles released by agar plate cultures of two strains of the myxobacterium Stigmatella aurantiaca (strains Sg a15 and DW4/3-1) were collected in a closed-loop stripping apparatus (CLSA) and analyzed by GC-MS. Large numbers of substances from different compound classes (ketones, esters, lactones, terpenes, and sulfur and nitrogen compounds) were identified; several of them are reported from natural sources for the first time. The volatiles 2-methyltridecan-4-one (17), its isomer 3-methyltridecan-4-one (20), and the higher homologue 2-methyltetradecan-4-one (18) were identified in the extracts of both strains and were synthesized. In addition, strain Sg a15 produced 2,12-dimethyltridecan-4-one (19), 2-methyltridec-2-en-4-one (23), and a series of phenyl ketones, among them 1-phenyldecan-1-one (14) and 9-methyl-1-phenyldecan-1-one (16), whereas strain DW4/3-1 emitted traces of 10-methylundecan-2-one (21). The biosynthesis of 14 and 16 was examined in feeding experiments with deuterated precursors carried out on agar plate cultures. The leucine-derived starter unit isovalerate was shown to be incorporated into 16, as was phenylalanine-derived benzoic acid into both 14 and 16. The results point to formation both of the phenyl ketones and of the structurally related aliphatic ketones through an unusual head-to-head coupling between a starter unit such as benzoyl-CoA and a fatty acyl-CoA, followed by decarboxylation.

Benzoic Acid↗

Use of Monte Carlo analysis to characterize nitrogen fluxes in agroecosystems.

Intensive agricultural systems are largely responsible for the increase in global reactive nitrogen compounds, which are associated with significant environmental impacts. The nitrogen cycle in agricultural systems is complex and highly variable, which complicates characterization in environmental assessments. Appropriately representing nitrogen inputs into an ecosystem is essential to better understand and predict environmental impacts, such as the extent of seasonally occurring hypoxic zones. Many impacts associated with reactive nitrogen are directly related to annual nitrogen loads, and are not adequately represented by average values that de-emphasize extreme years. To capture the inherent variability in agricultural systems, this paper employs Monte Carlo analysis (MCA) to model major nitrogen exports during crop production, focusing on corn-soybean rotations within the U.S. Corn Belt. This approach yields distributions of possible emission values and is the first step in incorporating variable nutrient fluxes into life cycle assessments (LCA) and environmental impact assessments. Monte Carlo simulations generate distributions of nitrate emissions showing that 80% of values range between 15 and 90 kg NO39-) N/ha (mean 38.5 kg NO3(-) N/ha; median 35.7 kg NO3(-) N/ha) for corn fields and 5-60 kg NO3(-) N/ha (mean 20.8 kg NO3(-) N/ha; median 16.4 kg NO3(-) N/ha) for soybean fields. Data were also generated for grain and residue nitrogen, N2O, NO(x), and NH3. Results indicate model distributions are in agreement with available measured emissions.

Ecosystem↗

Novel 2-phenylimidazo[1,2-a]pyridine derivatives as potent and selective ligands for peripheral benzodiazepine receptors: synthesis, binding affinity, and in vivo studies.

The substituent effects at positions 6 and 8 (compounds 17-31) as well as at the amide nitrogen (compounds 32-40) of a series of 2-phenylimidazo[1,2-a]pyridineacetamides were evaluated at both central (CBR) and peripheral (PBR) benzodiazepine receptors. The structure-activity relationship studies detailed herein indicate the key structural features required for high affinity and selectivity for PBR. Substitution on the imidazopyridine nucleus at position 8 with lipophilic substituents and the presence of one chlorine atom at the para position of the phenyl ring at C(2) are crucial features for high binding affinity and selectivity toward PBR. A small subset of active ligands (i.e., 17, 20, 26, 34, and 35) were evaluated in vitro in Xenopus oocytes expressing cloned human GABA(A) receptors for their effects at CBR and in vivo for their ability to stimulate the synthesis of neurosteroids such as pregnenolone, progesterone, allopregnanolone, and allotetrahydrodeoxycorticosterone (THDOC). Compounds 17, 20, 26, and 34 markedly increased the levels of neuroactive steroids in plasma and cerebral cortex, unlike compound 35.

Animals↗

Nitrification-denitrification of opto-electronic industrial wastewater by anoxic/aerobic process.

This research focused on the biological treatment of high-strength organic nitrogen wastewater, and presented the results from the nitrification and denitrification of an actual industrial wastewater using anoxic/aerobic process. The opto-electronic industrial wastewater often contains a significant quantity of organic nitrogen compounds and has a ratio over 95% in organic nitrogen (Org-N) to total nitrogen (T-N). In this study, a 2-stage anoxic/aerobic process was established and evaluated the efficiency of wastewater treatment. Raw wastewater from an actual TFT-LCD manufacturing plant was obtained as the sample for looking into the feasibility of opto-electronic industrial wastewater treatment. After toxicity identification evaluation (TIE) test of raw wastewater. the inhibition was related to organic nitrogen (TMAH, MEA) and unionized ammonia (free ammonia, NH3) with high pH. Therefore, pH control is important for biological treatment of high-strength organic nitrogen industrial wastewater. Besides. hydraulic retention time (HRT) and mixed liquor recycled rate (MLR) were controlled independently to distinguish between the effects of these two factors. Under suitable HRT ( > 1.7 d) and mixed liquor recycled rate (< 4Q), effluent of NH4-N. NO3-N + NO2-N, and COD can fall below 20 mg/L, 30 mg/L, and 80 mg/L. The anoxic/aerobic process removed 92-98% of the carbon source, and approximately 80% of TKN, 70% of T-N.

Ammonia↗

[Research advances in soil nitrogen cycling models and their simulation].

Nitrogen is one of the necessary nutrients for plant, and also a primary element leading to environmental pollution. Many researches have been concerned about the contribution of agricultural activities to environmental pollution by nitrogenous compounds, and the focus is how to simulate soil nitrogen cycling processes correctly. In this paper, the primary soil nitrogen cycling processes were reviewed in brief, with 13 cycling models and 6 simulated cycling processes introduced, and the parameterization of models discussed.

Computer Simulation↗

Effect of the dietary exposure of rat to di(2-ethyl hexyl) phthalate on their metabolic efficiency.

The nutritional impact of di(2-ethyl hexyl) phthalate (DEHP), specifically its energy efficiency and nitrogen utilization, was studied in the experimental rat. Groups of male Wistar rats were fed over 21 days with a standard diet alone or a standard diet supplemented with 2% (w/w) DEHP. Food intake, body weight and nitrogen compounds excretion were measured daily. The composition and energetic content of the carcass were determined in animals of both dietary groups after the feeding period, as well as in a separate group on day 0. The food and energy intakes were similar in both groups, however, the efficiencies of energy and nitrogen use were significantly reduced in the DEHP-fed rat. These alterations were reflected by a reduction of 31% on carcass energy retention and a decrease of 26% on cumulative nitrogen balance, without changes in the body composition. The increase of urinary nitrogen excretion, mainly as urea compound, is the major contributing factor to the lower nitrogen retention. These results indicate that DEHP decreases energy efficiency and nitrogen utilization, leading to a pronounced reduction in body weight gain. In addition, this study provides a possible conceptual framework that could explain the metabolic changes induced by DEHP and related compounds in experimental animals.

Animals↗

Distribution and metabolism of xylem-borne ureido and amino compounds in developing soybean shoots.

Pulse-chase feeding (30-120 minutes) of (14)C-labeled nitrogenous compounds to cut transpiring shoots was used to investigate the early fate of the major xylem-borne solutes in N(2)-fixing soybean (Glycine max) plants at the V(4) growth stage. By comparison with the foliar distribution of [(14)C]inulin (a xylem marker), it was determined that the phloem supply of allantoin, allantoic acid, asparagine, glutamine, aspartate, and arginine, respectively, provided about 20, 10, three, two, five, and 20 times the (14)C delivered to the developing trifoliolate in the xylem stream. Recovery of unmetabolized asparagine, aspartate, and arginine in this indicator trifoliolate, and significant declines in the percentage of (14)C from allantoic acid and allantoin recovered in the first trifoliolate, provided some support for the direct xylem-to-phloem transfer of these compounds, but did not preclude the involvement of indirect transfer. Data on stem retention and foliar distribution, expressed as a function of the relative xylem sap composition, indicated that ureides provide the major sources of nitrogen to all plant parts. There was no consistent distinction in distribution patterns between pairs of similar anionic and neutral compounds. The extent of xylem-to-phloem transfer among the ureido or the amino compounds was inversely related to its prominence in xylem sap.

Journal Article↗

Chemical modification of lysine residues in cytochrome P450LM2 (P450IIB4): influence on heme liganding of arylamines.

Treatment of cytochrome P450LM2 with fluorescein isothiocyanate to introduce up to two equivalents of fluorophore per polypeptide chain resulted in the selective derivatization of lysine residues. CD-spectral measurements revealed the overall conformation as well as the immediate heme environment of the hemoprotein to remain unaffected by attachment of the label. Modification caused decreased affinity of p-phenylenediamine and other 4-substituted anilines for the heme site, whereas there was a rise in the extent of substrate interaction. Experiments with pigment containing acetylated lysines gave analogous results, suggesting that the observed phenomenon was due to charge neutralization. There was linear correlation between the Hammett sigma P values and both the optical dissociation constants for arylamine binding to intact enzyme and the dipole moments of the anilines, indicating that basicity along with electronic factors controlled heme liganding; lipophilicity appeared to be of minor importance. Introduction of fluorescein isothiocyanate into the oxygenase was found to influence the bond-making process through modulating basicity of the nitrogenous compounds, but perturbation of optimal spacial orientation of the amine nitrogen toward the heme iron also might have been operative. The lysines studied seem to represent metabolically inactive elements of the substrate channel located on the cytosolic surface of the aggregates, as evidenced by steady-state fluorescence measurements. A hydrophilic segment in the cytochrome P450LM2 molecule that would accommodate the critical residues is discussed.

Amines↗

[Effect of different nitrogen sources on the biosynthesis of lipase by Oospora lactis].

The effect of inorganic and organic nitrogen compounds on the synthesis of biomass and extracellular lipase by Oospora lactis was studied. Among the inorganic nitrogen sources ammonium sulphate and ammonium secondary phosphate and among the organic nitrogen sources yeast autolysate proved to be most beneficial for the lipase synthesis. Lipase activity and biomass accumulation in the medium containing yeast autolysate were greater than in the media containing the above ammonium salts. Lipase synthesis reached maximum in the nutrient medium containing yeast autolysate (0.7%) and ammonium sulphate (0.3%).

Ammonium Sulfate↗

Ammonia production from uric acid, urea, and amino acids and its absorption from the ceca of the cockerel.

Experiments were conducted in situ and in vitro in the ceca to measure ammonia production from uric acid, urea, and amino acids and its absorption. When uric acid was injected into a cecal sac containing mixed cecal microfloras, 77% disappeared within 1 hour, with a concomitant increase in ammonia concentration. When [15N]uric acid was added to the ceca in situ, 28% was converted to ammonia after 30 minutes. About 92% of the ammonia introduced into a cecal sac disappeared from the lumen fluid within 30 minutes. About 43% of each of urea nitrogen and glutamine-amide nitrogen was converted to ammonia-nitrogen, and 25% of uric acid-nitrogen and epsilon nitrogen of the arginine was found in ammonia. The conversion of aminonitrogen of glutamic acid and glycine to ammonia amounted to 19-20%, whereas that of alpha-alanine totaled 11%. It is concluded that dietary and urinary nitrogenous compounds that find their way into the ceca are useful nitrogen sources for ammonia production by microflora in the ceca of the chicken, and that ammonia is absorbed rapidly from the ceca.

Amino Acids↗

Activated chemical defense in aplysina sponges revisited.

Sponges of the genus Aplysina accumulate brominated isoxazoline alkaloids in concentrations that sometimes exceed 10% of their dry weight. We previously reported a decrease in concentrations of these compounds and a concomitant increase in concentrations of the monocyclic nitrogenous compounds aeroplysinin-1 and dienone in Aplysina aerophoba following injury of the sponge tissue. Further investigations indicated a wound-induced enzymatic cleavage of the former compounds into the latter, and demonstrated that these reactions also occur in other Aplysina sponges. A recent study on Caribbean Aplysina species, however, introduced doubt regarding the presence of a wound-induced bioconversion in sponges of this genus. This discrepancy motivated us to reinvestigate carefully the fate of brominated alkaloids in A. aerophoba and in other Aplysina sponges following mechanical injury. As a result of this study we conclude that (1) tissue damage induces a bioconversion of isoxazoline alkaloids into aeroplysinin-1 and dienone in Aplysina sponges, (2) this reaction is likely catalyzed by enzymes, and (3) it may be ecologically relevant as the bioconversion products possibly protect the wounded sponge tissue from invasion of bacterial pathogens.

Animals↗

Chromatographic retention relationships between aliphatic tertiary amines and their putative N-oxide metabolites--preliminary results.

The chromatography of a series of tertiary amines and the corresponding N-oxides have been studied and the Functional Group Contribution Approach used to describe retention correlations between them. Good correlations are observed between the behaviour of compounds on HPLC and with the exception of some alicyclic nitrogen compounds also on thin layer chromatography. The models produced are used to predict k' and Rf values for ranitidine N-oxide and tamoxifen N-oxide based upon those for the parent molecule. The deviation between actual and predicted values was larger than expected, presumably due to the structural or physico-chemical differences of ranitidine and tamoxifen compared to the model compounds.

Amines↗