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Bioleaching of copper from large printed circuit boards for synthesis of organic-inorganic hybrid

机译:来自大型印刷电路板的铜的生物浸出,用于合成有机无机杂种

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The present study described a process for copper (Cu) bioleaching from waste printed circuit boards (PCBs). The 45 (+/- 0.18) mg/g Cu was found in waste PCBs. Acidiphilium acidophilum (NCIM 5344) (A. acidophilum) and hydrogen peroxide (H2O2) were used for two-step Cu bioleaching. A. acidophilum showed growth in 9K medium containing glucose and sulfur. During the growth the bacteria decreased medium pH from 3.5 (+/- 0.01) to 1.0 (+/- 0.02) in 10 days. The results showed that it required 2.5 h to leach all of the Cu from single PCB piece using 60 mL culture supernatant + 15 mL H2O2 at 60 degrees C temperature and static condition. The leached Cu was further used to synthesize the organic-inorganic hybrid (OIH). For this study, egg white was used as a polyphenol oxidase (PPO) enzyme source. The morphological, elemental, and structural analysis was carried out using scanning electron microscopy (SEM)-energy dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). Further the PPO enzyme activity was tested in OIH and crude enzyme (egg white). The egg white showed 0.00014 (+/- 0.00001) U/mg/min PPO activity while OIH showed 0.005 (+/- 0.00016) U/mg/min PPO activity. The pH 7 and 30 degrees C temperature were found to be optimum for PPO enzyme activity. The OIH was applied for phenol degradation. It degraded 95 (+/- 0.49)% of phenol (5 mM). The efficiency of phenol degradation decreased with an increase in phenol concentration.
机译:本研究描述了废物印刷电路板(PCB)的铜(Cu)生物浸出的方法。在废PCB中发现45(+/- 0.18)mg / g Cu。酸双嗜酸性(NCIM 5344)(A. acidophilum)和过氧化氢(H2O2)用于两步Cu Boolaping。 A. acidophilum显示出含有葡萄糖和硫的9K培养基的生长。在生长过程中,细菌在10天内从3.5(+/- 0.01)降低3.5(+/- 0.01)至1.0(+/- 0.02)。结果表明,它需要2.5小时,从使用60毫升培养物上清液+ 15mL的H 2 O 2在60度的温度和静态条件单个PCB片浸出所有的Cu制成。浸出的Cu进一步用于合成有机 - 无机杂交(OIH)。对于本研究,用作多酚氧化酶(PPO)酶源的蛋白。使用扫描电子显微镜(SEM)的分散X射线光谱(EDS),傅里叶变换红外光谱(FTIR)和X射线衍射(XRD)进行形态学,元素和结构分析。此外,在OIH和粗酶(蛋白)中测试PPO酶活性。蛋清显示0.00014(+/- 0.00001)U /毫克/分PPO活性,同时显示出OIH 0.005(+/- 0.00016)U /毫克/分PPO活性。发现pH 7和30℃温度为PPO酶活性最佳。 oih被施用于酚类降解。它降解了95(+/- 0.49)%的苯酚(5mm)。苯酚降解的效率随苯酚浓度的增加而降低。

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