A reliable, robust, and resilient water recovery system is of paramount importance on board the International Space Station (ISS). Such a system must be able to treat all sources of water, thereby reducing resupply costs and allowing for longer-term space missions. As such, technologies able to dewater urine in microgravity have been investigated by different space agencies. However, despite over 50 years of research and advancements on water extraction from human urine, the Urine Processing Assembly (UPA) and the Water Processor Assembly (WPA) now operating on the ISS still achieve suboptimal water recovery rates and require periodic consumables resupply. Additionally, urine brine from the treatment is collected for disposal and not yet reused. These factors, combined with the need for a life support system capable of tolerating even dormant periods of up to one year, make the research in this field ever more critical. As such, in the last decade, extensive research was conducted on the adaptation of existing or emerging technologies for the ISS context. In virtue of having a strong chemical resistance, small footprint, tuneable selectivity and versatility, novel membrane-based processes have been in focus for treating human urine. Their hybridisation with thermal and biological processes as well as the combination with new nanomaterials have been particularly investigated. This article critically reviews the UPA and WPA processes currently in operation on the ISS, summarising the research directions and needs, highlighted by major space agencies, necessary for allowing life support for missions outside the Low Earth Orbit (LEO). Additionally, it reviews the technologies recently proposed to improve the performance of the system as well as new concepts to allow for the valorisation of the nutrients in urine or the brine after urine dewatering.
Re-thinking our approach to dealing with waste is one of the major challenges in achieving a more sustainable society. However, it could also generate numerous opportunities. Specifically, in the context of wastewater, nutrients, energy and water could be mined from it. Because of its exceptionally high nitrogen (N) and phosphorous (P) concentration, human urine is particularly suitable to be processed for fertiliser production. In the present study, forward osmosis (FO) was employed to mine the P and N from human urine. Two Mg-fertilisers, i.e. MgSO and Mg(NO) were selected as draw solution (DS) to dewater synthetic non-hydrolysed urine. In this process, the Mg reverse salt flux (RSF) were used to recover P as struvite. Simultaneously, the urea was recovered in the DS as it is poorly rejected by the FO membrane. The results showed that, after concentrating the urine by 60%, about 40% of the P and 50% of the N were recovered. XRD and SEM - EDX analysis confirmed that P was precipitated as mineral struvite. If successfully tested on real urine, this process could be applied to treat the urine collected in urban areas e.g., high-rise building. After the filtration, the solid struvite could be sold for inland applications whereas the diluted fertiliser used for direct fertigation of green walls, parks or for urban farming. Finally, reduction in the load of N, P to the downstream wastewater treatment plant would also ensure a more sustainable urban water cycle.
Due to high phosphorus (P) and nitrogen (N) content, human urine has often proven to suitable raw material for fertiliser production. However, most of the urine diverting toilets or male urinals dilute the urine 2 to 10 times. This decreases the efficiency in the precipitation of P and stripping of N. In this work, a commercial fertiliser blend was used as forward osmosis (FO) draw solution (DS) to concentrate real diluted urine. During the concentration, the urea in the urine is recovered as it diffuses to the fertiliser. Additionally, the combination of concentrate PO4 3-, reverse Mg 2+ flux from the DS and the Mg 2+ presents in the flushing water, was able to recover the PO4 3as struvite. With 50% concentrated urine, 93% P recovery was achieved without the addition of an external Mg 2+ . Concurrently, 50% of the N was recovered in the diluted fertiliser DS. An economic analysis was performed to understand the feasibility of this process. It was found that the revenue from the produced fertilisers could potentially offset the operational and capital costs of the system.Additionally, if the reduction in the downstream nutrients load is accounted for, the total revenue of the process would be over 5.3 times of the associated costs.
The high concentration of nitrogen, phosphorous and potassium in human urine makes it a suitable raw material for fertiliser production. However, urine is often diluted with a significant amount of flushing water which increases the costs for the downstream nutrients recovery process. Re-using the water and the nutrients in the urine is paramount for enhancing the sustainability of our waste management system. In this work, a combination of forward osmosis (FO) and membrane distillation (MD) was used to extract distilled water from human urine. FO was chosen as MD pre-treatment to increase the overall nitrogen rejection and to prevent wetting of the MD membrane. The goal of this investigation was to tune the FO and MD operating parameters to reduce the nitrogen transport to the MD permeate. Urine pH, draw solution (DS) salt concentration and operating pressure were varied as a means to enhance the FO performances. On the other hand, feed temperature, nitrogen concentration and membrane characteristics were investigated to optimise the MD process. With 2.5 M NaCl as DS commercial FO membranes achieved a water flux between 31.5-28.7 L.m-2 .h-1 and a minimum nitrogen flux of 1.4 g.L-1. An additional 33% reduction in the nitrogen transport was observed by applying minimal hydraulic pressure on the DS. However, this was also found to significantly reduce the net transmembrane water flux. Acidification of the feed was also beneficial for both FO and MD nitrogen rejection. Finally, we demonstrated that, by tuning the MD membrane porosity and thickness, higher MD permeate quality could be achieved. To conclude, the hybrid FO-MD process is expected to be an effective solution for the production of clean water and concentrated fertiliser from human urine. This double barrier separation process could be suitable for both water reclamation in space application and resource recovery in urban application.
The production of the existing nitrogen fertilizer is costly and less environmental-friendly. Various green technologies are currently emerging toward providing alternative options. In this study, a liquid/liquid hydrophobic hollow-fiber membrane contactor was employed at ambient temperature and natural urine pH ~ 9.7 to recover ammonium fertilizers from human urine. Results showed that permeate side chemistry was one of the major factors affecting the ammonia mass transfer. The study on the ammonia capturing performance of diluted sulfuric acid, phosphoric acid, nitric acid, and DI water confirmed that acid type, acid concentration, and permeate side operating pH were the most important parameters affecting the ammonia capturing tendency. Sulfuric acid was slightly better in capturing more ammonia than other acid types. The study also identified increasing acid concentration didn’t necessarily increase ammonia mining tendency because there was always one optimum concentration value at which maximum ammonia extraction was possible. The best permeate side operating pH to extract ammonia for fertilizer purposes was selected based on the dissociation equilibrium of different types of acids. Accordingly, the analysis showed that the membrane process has to be operated at pH > 3 for sulfuric acid, between 3.5 to 11.5 for phosphoric acid, and above 0.5 for nitric acid so as to produce their respective high-quality liquid ammonium sulfate, ammonium monophosphate/diphosphate, and ammonium nitrate fertilizer. Therefore, permeate side acid concentration, pH, and acid type has to always be critically optimized before starting the ammonia mining experiment.
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