In　view　of　the　great　complexation　between　Copper(II)　and　cephalosporins,　and　excellent　ability　of　coordination　of　1,3,5-Benzenetricarboxylic　acid,　the　mesoporous　copper　based　metal　organic　framework　material　CS-X　was　synthesized　and　utilized　to　remove　ceftazidime　from　aqueous　solutions.　Templates　were　used　to　adjust　the　pore　sizes　of　CS-X　and　the　characterization　results　indicated　that　the　addition　of　templates　did　not　change　the　crystalline　structure.　The　optimum　CS-0.2　material　with　the　best　adsorption　capacity　had　the　pore　size　of　3.90　nm.　The　XPS　spectra　showed　that　the　hydrogen　bonds　were　formed　between　the　-NH2　groups　of　ceftazidime　and　the　adsorbent,　which　accelerated　the　adsorption　efficiency.　The　effect　of　ionic　strength,　pH　and　humic　acid　on　adsorption　was　studied.　The　kinetics　of　ceftazidime　adsorption　on　CS-0.2　demonstrated　that　the　adsorption　reached　equilibrium　in　the　first　20　min　and　corresponded　to　the　pseudo-second-order　model.　The　adsorption　mechanism　suggested　that　the　adsorption　of　ceftazidime　on　CS-0.2　is　spontaneous　and　endothermic,　predominating　by　the　chemical　adsorption,　in　good　conformity　with　the　Langmuir　and　Temkin　isotherm　models.　Besides,　the　studies　showed　that　the　CS-0.2　had　a　high　efficiency　and　selectivity　for　the　removal　of　the　numerous　cephalosporins　from　aqueous　solutions.