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Firstly, a large number of thiol functional groups were introduced on the surface of adsorbent.

and took advantage of the property that CuS was insoluble in water, having it "fixed" on sulfhydryl active site, and then made the amount of S2- was in excess to make it ¡°adsorbed¡± on the surface of CuS. Achieved removal of Cu (II) from aqueous solution as well as completed the preparation of adsorbent through the above process.

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The copper ion was affixed to the sulfhydryl active site of an absorbent via the adsorption of the copper ion to the absorbent . Then, excess S2 was introduced to form micrometer or nanomter CuS. The obtained CuS was evenly distributed within the pores of the adsorbent, as the CuS is insolube in water. In another aspect, copper £¨II£© was removed from the aqueous solution by this process,   which sucessfully prepared the (Cu loaded) adsorbent at the same time.
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Initially, Cu2+ were immobilized on the surface of the absorbent through thiol groups, then an excess of S2- was added to form micro - and nano copper sulfide, which precipitated and evenly distributed on the surface of internal cavities. In other words, this method simultaneously accomplished the removal of Cu2+ and the preparation of the  absorbent.
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Cu2+ was initially  immobilized on the surface of the absorbent through thiol groups, then an excess of S2- was added to form micro - and nano copper sulfide, which precipitated and evenly distributed on the surface of internal cavities. In other words, this method simultaneously accomplished the removal of Cu2+ and the preparation of the  absorbent.
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