<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao C</submitter><funding>National Natural Science Foundation of China</funding><funding>China Postdoctoral Science Foundation</funding><funding>Shandong Provincial Key Laboratory of Water Pollution Control and Resource Reuse, Shandong University</funding><pagination>16045-16052</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7346240</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(26)</volume><pubmed_abstract>Sludge-based activated carbon with doped &lt;i>Phragmites australis&lt;/i> was prepared using an environment-friendly method to treat waterworks sludge (WS) and obtain an economical adsorbing material for tetracycline (TC) elimination. For the WS, &lt;i>P. australis&lt;/i> was used as an additive to optimize the preparation of activated carbon. Optimum preparation conditions were as follows: activation temperature, 600 °C; ZnCl&lt;sub>2&lt;/sub> concentration, 3 mol/L; activation time, 50 min; impregnation ratio (weight of mix sample: weight of ZnCl&lt;sub>2&lt;/sub>) of 1:2.5; and the mixed ratio of &lt;i>P. australis&lt;/i> with WS, 40%. The obtained activated carbon owned well-developed Brunauer-Emmett-Teller surface area (949.90 m&lt;sup>2&lt;/sup>/g). The acidic and basic functional groups were improved to 0.762 and 0.016 mmol/g, respectively. The pseudo-second-order kinetic and Freundlich isotherm equations were more suitable models to simulate adsorption with the maximum adsorption capacity of 153.4 mg/g. According to the thermodynamic parameters, the adsorption process was spontaneous and endothermic. Electrostatic interaction, hydrogen bonding formation, and ion complexation adsorption mechanisms were the mechanisms underlying the adsorption of TC.</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Removal of Tetracycline from Water Using Activated Carbon Derived from the Mixture of &lt;i>Phragmites australis&lt;/i> and Waterworks Sludge.</pubmed_title><pmcid>PMC7346240</pmcid><funding_grant_id>2019KF11</funding_grant_id><funding_grant_id>51908343</funding_grant_id><funding_grant_id>2019M652458</funding_grant_id><pubmed_authors>Yin W</pubmed_authors><pubmed_authors>Zhao C</pubmed_authors><pubmed_authors>Guo Z</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Kong Q</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Shang D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Removal of Tetracycline from Water Using Activated Carbon Derived from the Mixture of &lt;i>Phragmites australis&lt;/i> and Waterworks Sludge.</name><description>Sludge-based activated carbon with doped &lt;i>Phragmites australis&lt;/i> was prepared using an environment-friendly method to treat waterworks sludge (WS) and obtain an economical adsorbing material for tetracycline (TC) elimination. For the WS, &lt;i>P. australis&lt;/i> was used as an additive to optimize the preparation of activated carbon. Optimum preparation conditions were as follows: activation temperature, 600 °C; ZnCl&lt;sub>2&lt;/sub> concentration, 3 mol/L; activation time, 50 min; impregnation ratio (weight of mix sample: weight of ZnCl&lt;sub>2&lt;/sub>) of 1:2.5; and the mixed ratio of &lt;i>P. australis&lt;/i> with WS, 40%. The obtained activated carbon owned well-developed Brunauer-Emmett-Teller surface area (949.90 m&lt;sup>2&lt;/sup>/g). The acidic and basic functional groups were improved to 0.762 and 0.016 mmol/g, respectively. The pseudo-second-order kinetic and Freundlich isotherm equations were more suitable models to simulate adsorption with the maximum adsorption capacity of 153.4 mg/g. According to the thermodynamic parameters, the adsorption process was spontaneous and endothermic. Electrostatic interaction, hydrogen bonding formation, and ion complexation adsorption mechanisms were the mechanisms underlying the adsorption of TC.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2024-11-15T16:12:14.167Z</modification><creation>2024-11-15T16:12:14.167Z</creation></dates><accession>S-EPMC7346240</accession><cross_references><pubmed>32656426</pubmed><doi>10.1021/acsomega.0c01524</doi></cross_references></HashMap>