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1.
Water Res ; 112: 137-146, 2017 04 01.
Artículo en Inglés | MEDLINE | ID: mdl-28157602

RESUMEN

Gas-permeable membrane technology is useful to recover ammonia (NH3) from liquid manures. In this study, phosphorus (P) recovery via MgCl2 precipitation was enhanced by combining it with NH3 recovery through gas-permeable membranes. Anaerobically digested swine wastewater containing approximately 2300 mg NH4+-N L-1 and 450 mg P L-1 was treated using submerged membranes plus low-rate aeration to recover the NH3 from within the liquid and MgCl2 to precipitate the P. The experiments included a first configuration where N and P were recovered sequentially and a second configuration with simultaneous recovery. The low-rate aeration reduced the natural carbonate, increased pH and accelerated NH3 uptake by the gas-permeable membrane system, which in turn benefited P recovery. Phosphorus removal efficiency was >90% and P recovery efficiency was about 100%. With higher NH3 capture, the recovered P contained higher P2O5 content (37-46%, >98% available), similar to the composition of the biomineral newberyite (MgHPO4·3H2O).


Asunto(s)
Amoníaco/química , Aguas Residuales/química , Animales , Estiércol , Minerales , Fosfatos , Fósforo , Porcinos
2.
Waste Manag ; 49: 372-377, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26739456

RESUMEN

Gas-permeable membrane technology is useful to recover ammonia from manure. In this study, the technology was enhanced using aeration instead of alkali chemicals to increase pH and the ammonium (NH4(+)) recovery rate. Digested effluents from covered anaerobic swine lagoons containing 1465-2097 mg NH4(+)-N L(-1) were treated using submerged membranes (0.13 cm(2) cm(-3)), low-rate aeration (120 mL air L-manure(-1) min(-1)) and nitrification inhibitor (22 mg L(-1)) to prevent nitrification. The experiment included a control without aeration. The pH of the manure with aeration rose from 8.6 to 9.2 while the manure without aeration decreased from 8.6 to 8.1. With aeration, 97-99% of the NH4(+) was removed in about 5 days of operation with 96-98% recovery efficiency. In contrast, without aeration it took 25 days to treat the NH4(+). Therefore, the recovery of NH4(+) was five times faster with the low-rate aeration treatment. This enhancement could reduce costs by 70%.


Asunto(s)
Compuestos de Amonio/análisis , Nitrificación , Administración de Residuos/métodos , Amoníaco/análisis , Anaerobiosis , Crianza de Animales Domésticos , Animales , Reactores Biológicos , Concentración de Iones de Hidrógeno , Estiércol/análisis , Membranas Artificiales , North Carolina , Porcinos , Administración de Residuos/instrumentación
3.
J Cardiovasc Pharmacol ; 37(1): 119-28, 2001 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11152369

RESUMEN

The JCR:LA-cp rat is obese and insulin resistant and develops a major vasculopathy, with associated ischemic damage to the heart. Male rats were treated with 17alpha-ethinylestradiol (EE), LY117018, and/or the nitric oxide synthase inhibitor, N(G)-nitro-L-arginine methyl ester (L-NAME). LY117018 decreased plasma cholesterol esters, with a 40% reduction in total cholesterol. EE increased triglyceride levels and modestly decreased cholesterol esters. L-NAME increased blood pressure and aortic contractile sensitivity to phenylephrine and inhibited acetylcholine-induced relaxation. LY117018 decreased the force of contraction. The L-NAME-mediated increase in force of contraction and decrease in response to acetylcholine was inhibited by LY117018. L-NAME-induced hypertension was prevented by LY117018. Platelet aggregation was not different between obese and lean rats and was unaffected by L-NAME. LY117018, both in the absence and presence of L-NAME, inhibited platelet aggregation. The effects of LY117018 are apparently mediated through both NO-dependent and -independent mechanisms. The changes induced by EE and LY117018 may reflect the activation of multiple mechanisms, both estrogen receptor-dependent and -independent. The changes induced by LY117018 are significant and may prove to be cardioprotective in the presence of the insulin resistance syndrome.


Asunto(s)
Congéneres del Estradiol/farmacología , Antagonistas de Estrógenos/farmacología , Etinilestradiol/farmacología , Metabolismo de los Lípidos , Agregación Plaquetaria/efectos de los fármacos , Pirrolidinas/farmacología , Tiofenos/farmacología , Vasoconstricción/efectos de los fármacos , Animales , Aorta/efectos de los fármacos , Aorta/fisiología , Presión Sanguínea/efectos de los fármacos , Presión Sanguínea/fisiología , Peso Corporal/efectos de los fármacos , Peso Corporal/fisiología , Ésteres del Colesterol/sangre , Ingestión de Alimentos/efectos de los fármacos , Ingestión de Alimentos/fisiología , Inhibidores Enzimáticos/farmacología , Resistencia a la Insulina/fisiología , Masculino , NG-Nitroarginina Metil Éster/farmacología , Óxido Nítrico/fisiología , Agregación Plaquetaria/fisiología , Ratas , Triglicéridos/sangre , Vasoconstricción/fisiología
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