Sustainable treatment of boron industry wastewater with precipitation-adsorption hybrid process and recovery of boron species
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Tarih
2024
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Elsevier
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Boron removal from wastewater has been investigated by using various processes, including ion exchange resins, membrane processes and adsorption. Each method has various advantages and disadvantages, but most produce excessive waste in addition to high operational costs. Therefore, more sustainable methods are required for wastewater containing high concentrations of boron. In this study, a sustainable treatment process was developed for wastewater containing high concentrations of boron. This study investigated the removal of boron from wastewater by Al(OH)(3) sorption. The reuse of adsorbent (Al(OH)(3)) and the potential recovery of boric acid was the main goal of the study. It was observed that although lower concentrations of boron were obtained at pH 10.5 (980 mg/L and 635 mg/L at pH of 9.0 and 10.5, respectively), the amount of sorbed boron at pH 9 was substantially higher (94.7 mg B/g Al(OH)(3) and 27.8 mg B/g Al(OH)(3) at pH of 9.0 and 10.5, respectively). This was attributed to the higher initial boron concentrations and the formation of boric acid and polyborate complexes at pH 9.0. Results showed that polyborate species sorption was an outer sphere complex formation, which led to the desorption of boron as pH lowered. Adsorbed boron species to Al(OH)(3) could effectively be desorbed at low pH values (pH<5.0); which allows Al(OH)(3) to be used in successive adsorption studies. Approximately 55% of boron recovery from pretreated wastewater was possible with the effective reuse of adsorbent. A net profit of 2.85 $/m(3) could be obtained based on the amounts of chemical consumptions and boron recovery.
Açıklama
Anahtar Kelimeler
Boric acid recovery, Boron reuse, Polyborates sorption, Al(OH)(3), Sustainable treatment
Kaynak
Process Safety and Environmental Protection
WoS Q Değeri
Q1
Scopus Q Değeri
Q1
Cilt
182
