Search

Clean energy like hydrogen can be a promising strategy to solve problems of global warming. Photo-fermentation (PF) is an attractive technology for producing biohydrogen from various biowastes cost-effectively and environmentally friendly. However, challenges of low light conversion efficiency and small yields of biohydrogen production still limit its application. Thus, advanced strategies have been investigated to enhance photo-fermentative biohydrogen production. This review discusses advanced technologies that show positive outcomes in improving biohydrogen production by PF, including the following. Firstly, genetic engineering enhances light transfer efficiency, change the activity of enzymes, and improves the content of ATP, ammonium and antibiotic tolerance of photosynthetic bacteria. Secondly, immobilization technology is refined. Thirdly, nanotechnology makes great strides as a scientific technique and fourthly, integration of dark and photo-fermentation technology is possible. Some suggestions for further studies to achieve high levels of efficiency of photo-fermentative biohydrogen production are mentioned in this paper.

As a clean energy carrier, hydrogen is a promising alternative to fossil fuel so as the global growing energy demand can be met. Currently, producing hydrogen from biowastes through fermentation has attracted much attention due to its multiple advantages of biowastes management and valuable energy generation. Nevertheless, conventional dark fermentation (DF) processes are still hindered by the low biohydrogen yields and challenges of biohydrogen purification, which limit their commercialization. In recent years, researchers have focused on various advanced strategies for enhancing biohydrogen yields, such as screening of super hydrogen-producing bacteria, genetic engineering, cell immobilization, nanomaterials utilization, bioreactors modification, and combination of different processes. This paper critically reviews by discussing the above stated technologies employed in DF, respectively, to improve biohydrogen generation and stating challenges and future perspectives on biowaste-based biohydrogen production.

The ciprofloxacin (CIP) removal ability of a Fe-Cu electrolytic material was examined with respect to pH (2–9), time (15–150 min), shaking speed (100–250 rpm), material mass (0.2–3 g/L), temperature (298, 308, 323) and initial CIP concentration (30–200 mg/L). The Fe-Cu electrolytic materials were fabricated by the chemical plating method, and Fe-C materials were mechanically mixed from iron powder and graphite. The results show that at a pH value of 3, shaking time 120 min, shaking speed 250 rpm, a mass of Fe-Cu, Fe-C material of 2 g/L and initial CIP concentration of 203.79 mg/L, the CIP removal efficiency of Fe-Cu material reached 90.25% and that of Fe-C material was 85.12%. The removal of CIP on Fe-Cu and Fe-C materials follows pseudo-first-order kinetics. The activation energy of CIP removal of Fe-Cu material is 14.93 KJ/mol and of Fe-C material is 16.87 KJ/mol. The positive ΔH proves that CIP removal is endothermic. A negative entropy of 0.239 kJ/mol and 0.235 kJ/mol (which is near zero and is also relatively positive) indicated the rapid removal of the CIP molecules into the removed products.