Recycling water from spent dialysate by osmotic dilution: Impact of urea rejection of forward osmosis membrane on hemodialysis duration
Introduction
Hemodialysis requires large volumes of purified water produced by the water purification system (primarily consists of a pretreatment unit and a reverse osmosis unit) to prepare dialysate, rinse and reprocess dialysis machines and membranes [1,2]. A typical facility-based patient uses about 80 tons of tap water to produce sufficient high-grade water per year for hemodialysis [2]. In 2010, the number of patients needing renal replacement therapy was estimated to range between 4.902 and 9.701 million worldwide, and is expected to increase dramatically in the coming decades [3]. Recycling water from spent dialysate with a low-cost method is of great significance for saving water resources and costs, as well as reducing the potential pollution risk of spent dialysate discharge, especially in the water shortage area.
A major challenge to recycle spent dialysate is the removal of urea, the main nitrogenous waste from metabolism [4]. Hydrolysis by enzymes to ammonia and subsequent adsorption by zirconium hydrophosphate is the most common technique to remove urea from spent dialysate [5]. The high cost and the frequent sorbent cartridge replacement are limiting for the wide application of the technique [6]. Electrochemical methods have been reported for efficient urea degradation [4,7], but the generation of toxic chlorine species, metal leaching from electrodes, and development of acidosis represent severe disadvantages of such an approach [7].
Forward osmosis (FO) is an emerging membrane technology utilizing natural osmotic process for water desalination [[8], [9], [10], [11], [12], [13]]. Without the energy-intensive draw solution recovery, osmotic dilution is a truly low-energy FO process with lower energy consumption than other desalination technologies [[14], [15], [16], [17], [18], [19], [20], [21], [22]]. In our recent work, osmotic dilution was reported to be promising to recover water from the spent dialysate [18]. Dialysis concentrate was used as the draw solution to extract water spontaneously from the spent dialysate (Fig. 1). Complete rejection of creatinine and uric acid by the FO membrane, as well as low membrane fouling and scaling were observed. Centralized treatment of spent dialysate from a dialysis center by FO would save substantial water and cost in case of complete urea rejection. Nonetheless, low urea rejection by the FO membrane raised great concerns since the small molecular weight (60 Da) and electroneutrality of urea presumably lead to a diluted dialysis concentrate containing urea. In hemodialysis, the urea concentration gradient between the blood and dialysate side represents the driving force for urea transport across the hemodialysis membrane [23]. As a consequence, the reduced urea concentration gradient leads to prolonged hemodialysis duration, which further results in increased dialysate consumption and costs.
Unfortunately, FO membranes reject urea only partially. To clarify the validity of FO technology in the application, we developed a mathematical model that correlates FO with hemodialysis to quantitatively determine the effect of partial urea rejection in osmotic dilution on the subsequent hemodialysis duration. The effect of three factors, i.e. average urea rejection in FO, water recovery, and the number of hemodialysis sessions, on the hemodialysis prolongation rate was systematically analyzed. This work provides a theoretical basis for the potential application of FO in water recovery from the spent dialysate.
Section snippets
Process and model assumptions
Fig. 1 schematically presents the combination of the hemodialysis process and spent dialysate recovery by FO (or osmotic dilution). A partial amount of water in the spent dialysate spontaneously moves towards the dialysis concentrate, as a consequence of the osmotic pressure gradient across the FO membrane. Thus the spent dialysate is concentrated and the dialysis concentrate is diluted. After FO, a certain amount of pure water is added to further dilute the dialysis concentrate. Dialysate
Analysis of A
Based on the physical meaning of A, A varies with the urea rejection of the FO membrane and water recovery, and the range of A can be roughly analyzed as [0, 1). A = 0 in case of an ideal FO membrane with a complete urea rejection (i.e., Rej = 100%) or a water recovery of zero (i.e., Rec = 0); A = 1 is only possible when the water is completely recovered (Rec = 100%), which is impossible due to the limitation of the osmotic pressure difference across the FO membrane (because there must be a
Conclusions
In this study, a mathematical model is developed to quantify the effect of incomplete urea rejection of an FO membrane during osmotic dilution on the subsequent hemodialysis duration. The impacts of three factors, i.e., the average urea rejection of the FO membrane in the osmotic dilution process, the water recovery in the osmotic dilution process, and the number of hemodialysis sessions, on the subsequent hemodialysis duration are systematically analyzed. The results demonstrate that a
Nomenclature
- A
reduction proportion of the urea amount in the spent dialysate after an osmotic dilution process, A = (1 - Rej)Rec(2 - Rec)/[2 - (1 + Rej)Rec]
- C
urea concentration
- D
urea dialysance of the dialyzer
- J
amount of urea removed from the blood per time unit
- M
amount of urea in the fresh dialysate/accumulated spent dialysate
- m
amount of urea transferred from a patient to dialysate per hemodialysis session
- Rec
water recovery in the osmotic dilution process
- Rej
average urea rejection of the FO membrane in the
Author statement
Pengjia Dou: Conceptualization; Methodology; Software; Formal analysis; Investigation; Data curation; Writing - original draft. Danilo Donato: Methodology; Software; Resources; Writing - review & editing. Hong Guo: Software; Visualization. Shuwei Zhao: Formal analysis; Writing - review & editing. Tao He: Conceptualization; Validation; Writing - review & editing; Supervision; Project administration; Funding acquisition.
Declaration of competing interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgments
The authors thank the National Natural Science Foundation of China (No. 51861145313, 21676290, 21808236, 21978315), Newton Advanced Fellowship (Grant No. NA170113), and Baxter Research Funding (2016–2017) for financial support.
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