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Preparation of calcium oxalate--bromopyrogaliol red inclusion sorbent and application to treatment of cationic dye and heavy metal wastewaters

机译:草酸钙-溴邻苯三酚红包合物吸附剂的制备及其在阳离子染料和重金属废水处理中的应用

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摘要

Dye pollutants are a major class of environmental contaminants. Over 100,000 dyes have been synthesized worldwide and more than 700,000 tons are produced annually and over 5 percent are discharged into aquatic environments. The adsorption or sorption is one of the most efficient methods to remove dye and heavy metal pollutants from wastewater. However, most of the present sorbents often bear some disadvantages, e.g. low sorption capacity, difficult separation of spoil, complex reproduction, or secondary pollution. Development of novel sorbents that can overcome these limitations is desirable. On the basis of the chemical coprecipitation of calcium oxalate (CaC_2O_4), bromopyro-gallol red (BPR) was embedded during the growing of CaC_2O_4 particles. The ternary C_2O_4~(2-)-BPR-Ca~(2+) sorbent was yielded by the centrifugation. Its composition was determined by spectrophotometry and AAS, and its structure and morphology were characterized by powder X-ray diffraction (XRD), laser particle-size analysis, and scanning electron microscopy (SEM). The adsorption of ethyl violet (EV) and heavy metals, e.g. Cu(II), Cd(II), Ni (II), Zn(II), and Pb(II) were carried out and their removal rate determined by spectrophotometry and ICP-OES. The adsorption performance of the sorbent was compared with powder activated carbon. The Langmuir isothermal model was applied to fit the embedment of BPR and adsorption of EV. The saturation number of BPR binding to CaC_2O_4 reached 0.0105 mol/mol and the adsorption constant of the complex was 4.70 X 10~5 M~(-1). Over 80 percent of the sorbent particles are between 0.7 and 1.02 mu m, formed by the aggregation of the global CaC_2O_4/BPR inclusion grains of 30-50 nm size. Such a material was found to adsorb cationic dyes selectively and sensitively. Ethyl violet (EV) was used to investigate the adsorption mechanism of the material. One BPR molecule may just bind with one EV molecule. The CaC_2O_4/BPR inclusion material adsorbed EV over two times more efficiently than the activated carbon. The adsorption of EV on the CaC_2O_4/BPR inclusion sorbent was complete in only 5 min and the sedimentation complete in 1 h. However, those of EV onto activated carbon took more than 1.5 and 5 h, respectively. The treatment of methylene blue and malachite green dye wastewaters indicated that only 0.4 percent of the sorbent adsorbed over 80 percent of color substances. Besides, the material can also adsorb heavy metals by complexation with BPR. Over 90 percent of Pb~(2+), and approximately 50 percent of Cd~(2+) and Cu~(2+), were removed in a high Zn~(2+)-electroplating wastewater when 3 percent of the material was added. Eighty-six percent of Cu~(2+), and 60 percent of Ni~(2+) and Cd~(2+), were removed in a high Cd~(2+)-electroplating wastewater. The embedment of BPR into CaC_2O_4 particles responded to the Langmuir isothermal adsorption. As the affinity ligand of Ca~(2+), BPR with sulfonic groups may be adsorbed into the temporary electric double layer during the growing of CaC_2O_4 particles. Immediately, C_2O_4~(2-) captured the Ca~(2+) to form the CaC_2O_4 outer enclosed sphere. Thus, BPR may be released and embedded as a sandwich between CaC_2O_4 layers. The adsorption of EV on the sorbent obeyed the Langmuir isothermal equation and adsorption is mainly due to the ion-pair attraction between EV and BPR. Different from the inclusion sorbent, the activated carbon depended on the specific surface area to adsorb organic substances. Therefore, the adsorption ca-pacity, equilibrium, and sedimentation time of the sorbent are much better than activated carbon. The interaction of heavy metals with the inclusion sorbent responded to their coordination. By characterizing the C_2O_4~(2-) - BPR-Ca~(2+) inclusion material using various modern instruments, the ternary in situ embedment particle, [(CaC_2O_4)_(95) (BPR)]_n~(2n-), an electronegative, micron-sized adsorbent was synthesized. It is selective, rapid, and highly effective for
机译:染料污染物是环境污染物的主要类别。全世界已经合成了超过100,000种染料,每年生产超过700,000吨,超过5%的染料排入水生环境。吸附或吸附是从废水中去除染料和重金属污染物的最有效方法之一。然而,大多数目前的吸附剂通常具有一些缺点,例如,吸附剂的缺点。吸附能力低,难以分离的残渣,繁复的繁殖或二次污染。期望开发能够克服这些限制的新型吸附剂。在草酸钙(CaC_2O_4)化学共沉淀的基础上,溴化吡咯洛尔红(BPR)在CaC_2O_4颗粒的生长过程中被嵌入。通过离心产生三元C_2O_4〜(2-)-BPR-Ca〜(2+)吸附剂。通过分光光度法和原子吸收光谱法确定其组成,并通过粉末X射线衍射(XRD),激光粒度分析和扫描电子显微镜(SEM)表征其结构和形态。吸附乙基紫(EV)和重金属,例如进行了Cu(II),Cd(II),Ni(II),Zn(II)和Pb(II)的分离,并通过分光光度法和ICP-OES测定了它们的去除率。将吸附剂的吸附性能与粉末活性炭进行了比较。应用Langmuir等温模型拟合BPR的嵌入和EV的吸附。 BPR与CaC_2O_4结合的饱和数达到0.0105 mol / mol,复合物的吸附常数为4.70 X 10〜5 M〜(-1)。超过80%的吸附剂颗粒介于0.7和1.02μm之间,这是由30-50 nm大小的整体CaC_2O_4 / BPR夹杂物颗粒的聚集形成的。发现这种材料选择性地且灵敏地吸附阳离子染料。乙基紫(EV)用于研究材料的吸附机理。一个BPR分子可能只与一个EV分子结合。 CaC_2O_4 / BPR夹杂物吸附EV的效率是活性炭的两倍。 EV在CaC_2O_4 / BPR夹杂物吸附剂上的吸附仅在5分钟内完成,而沉降在1 h内完成。但是,将EV应用于活性炭的时间分别超过了1.5和5小时。亚甲蓝和孔雀石绿染料废水的处理表明,只有0.4%的吸附剂吸附了80%以上的有色物质。此外,该材料还可以通过与BPR络合来吸附重金属。当高浓度的Zn〜(2+)电镀废水中有90%的Pb〜(2+)和大约50%的Cd〜(2+)和Cu〜(2+)被去除加入。在高Cd〜(2+)电镀废水中去除了86%的Cu〜(2+)和60%的Ni〜(2+)和Cd〜(2+)。 BPR在CaC_2O_4颗粒中的嵌入对Langmuir等温吸附有响应。作为Ca〜(2+)的亲和配体,在CaC_2O_4粒子生长过程中,带有磺酸基的BPR可能被吸附到临时双电层中。 C_2O_4〜(2-)立即捕获Ca〜(2+),形成CaC_2O_4外部封闭球。因此,BPR可以作为CaC_2O_4层之间的夹层被释放和嵌入。 EV在吸附剂上的吸附遵循Langmuir等温方程,吸附主要是由于EV和BPR之间的离子对吸引。与夹杂物吸附剂不同,活性炭取决于比表面积来吸附有机物质。因此,吸附剂的吸附容量,平衡和沉降时间比活性炭好得多。重金属与夹杂物吸附剂的相互作用对它们的配位反应。通过使用各种现代仪器表征C_2O_4〜(2-)-BPR-Ca〜(2+)夹杂物,可得到三元原位包埋粒子[(CaC_2O_4)_(95)(BPR)] _ n〜(2n-)合成了负电的微米级吸附剂。它具有选择性,快速和高效

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