in this work, a series of polyphenol porous polymers were derived from biomass polyphenols via a facile azo-coupling method. the structure and morphologies of the polymer were characterized by Bet, teM, SeM, XRD, tGA and ft-iR techniques. Batch experiments demonstrated their potentialities for adsorptive separation of cs + from aqueous solution. Among them, porous polymers prepared with gallic acid as starting material (GApp) could adsorb cs + at wide pH value range effectively, and the optimal adsorption capacity was up to 163.6 mg/g, placing it at top material for Cs + adsorption. GApp exhibited significantly high adsorption performance toward Cs + compared to na + and K + , making it possible in selective removal of cs + from ground water in presence of co-existing competitive ions. Moreover, the cs-laden GApp could be facilely eluted and reused in consecutive adsorption-desorption processes. As a result, we hope this work could provide ideas about the potential utilization of biomass polyphenol in environmental remediation. Growing concern about the remediation of radioactive waste generated from nuclear power plants and unforeseen accidents have been given worldwide for the sake of human health and environmental issues 1-4. Among them, radio-isotope 137 Cs is considered as the most hazardous nuclide due to the serious gamma radiation, long half-life as well as high solubility being an alkaline element 5,6. The generation of hazardous 137 Cs by nuclear waste and unforeseen nuclear plant accidents has seriously threatened the global environment and human health. In addition, long-term exposure to 137 Cs-contanining wastewater would lead to horrible diseases such as cancer, leukemia and genetic disorder 7. For example, the accidents occurred at Chernobyl in 1986 and Fukushima in 2011 severely impacted the local environments, and the surrounding areas are still classified as dangerous regions due to the leakage and serious emission of 137 Cs and other radio-isotopes 8,9. Therefore, effective techniques for the decontamination of radioactive Cs + from wastewater are indispensable and highly desirable. So far, considerable efforts have been made to explore available methodologies for hazardous Cs + removal from radioactive wastewater, such as liquid-liquid solvent extraction, chemical precipitation, electrochemical techniques and adsorption process 10-12. Taking disposal cost and removal efficiency into consideration, adsorption is considered as one of the most effective and clean techniques, and has been widely used in Cs + removal. To date, Prussian blue (PB) analogues 12,13 , titanate nanomaterials 14 , metal oxides and sulfides 15 , natural zeolites 16 , ammonium molybdophosphate 17,18 and other adsorbents 19 were developed and used for the removal of Cs + from radioactive effluents. Unfortunately, they still suffered from several problems, such as considerable preparation cost, unsatisfactory adsorption performance and insufficient stability, thus majority of the adsorbents aforementioned were not environment...