Current status and developing trends of the contents of heavy metals in sewage sludges in China

It is essential to determine the heavy metal concentrations in sewage sludge to select appropriate disposal methods. We conducted a national survey of heavy metal concentrations of sewage sludge samples from 107 municipal sewage treatment plants located in 48 cities covering the 31 provinces and autonomous regions, as well as Hong Kong, Macao and Taiwan by Xinjiang Production and Construction Corps in 2006, and identified the temporal trends of heavy metal contents in sewage sludge by comparison with surveys conducted in 1994-2001. In 2006, the average concentrations of As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn in sewage sludge were 20.2, 1.97, 93.1, 218.8, 2.13, 48.7, 72.3, and 1058mg.kg-1, respectively. Because of the decreased discharge of heavy metals into industrial wastewater in China and the increasingly stringent regulations governing the content of industrial wastes entering sewers, the average concentrations of Cd, Cr, Cu, Hg, Ni, Pb, and Zn have decreased by 32.3%, 49.7%, 54.9%, 25.0%, 37.2%, 44.8%, and 27.0%, respectively, during the past 12 years. The concentrations of Cd, Cr, Cu, Ni, and Zn in the samples exceeded the heavy metal limits of the Discharge Standard of Pollutants for Municipal Wastewater Treatment Plant in China （GB 18918-2002） by 6.5%, 3.7%, 6.5%, 6.5%, and 11.2%, respectively. From these results, 85 of the 107 municipal sludges analyzed would be considered suitable for land application.     

Effects of in situ biological treatments on heavy metal release of urban river sediment

A typical fiver in Yangzhou City was used to study the effects of artificial aeration, eco-brick cover, biological packing cover, and low-sited plant floating beds on the release of heavy metals from urban river sediments. This work showed that 1） the Cr release rate was decreased by 50.3%-89.6%, with an average of 59.3%, thereby reducing the Cr pollution load to the overlying water by 36.6%-82.7%, with an average of 53.3%; 2） the Zn release rate was reduced by 21.0%-88.9%, with an average of 42.3%, and the Zn pollution load of the overlying water was reduced by 38.0%-67.1%, with an average of 55.0%; 3） the Cu release rate was reduced by 27.5%-91.0%, with an average of 55.3%, and the Cu load of the overlying water was reduced by 57.1%-83.7%, with an average of 71.7%; 4） the Pb release rate was reduced by 11.8%- 79.3%, with an average of 41.2%, and the Pb pollution load of the overlying water was reduced by -1.3%-70.7%, with an average of 29.8%. We also found that the effects of in situ biological treatments on the release of heavy metals were affected by the extent of sediment disturbance. For integrated applications, high-disturbance treatments should be combined with low-disturbance treatments to reduce the explosive release of pollutants caused by sediment disturbance during the treatment operation to achieve better overall treatment effects.     

Occurrence of odor problems in drinking water of major cities across China

A comprehensive investigation into the occur-rence of odor problem at 111 drinking water treatment plants （DWTPs） in major cities across China was undertaken using both flavor profile analysis （FPA） and gas chromatography-mass spectrometry （GC-MS）. Eighty percent of source water samples exhibited odor problems, characterized by earthy/musty （41%） and swampy/septic （36%） odors, while the occurrence rate was lower （45%） in the finished water. Source water from rivers exhibited more pollution-origin odors, such as the swampy/septic odor, while that from lakes and reservoirs exhibited more algae- origin odors, such as earthy/musty odors. The occurrence rate of 2-methylisoborneol （2-MIB） in the surface source water samples was 75%, with 7% of samples containing 2- MIB concentrations of over 10 ng.L-1. The earthy/musty odor in the lake/reservoir water samples was mainly caused by 2-MIB （linear regression coefficient, R2= 0.69）, while the correlation between 2-MIB concentration and the earthy/musty odor intensity samples was weak （R2= 0.35） in the river-source water These results will be useful for the management of odor-quality problems in drinking water of China.     

Simultaneous quantification of several classes of antibiotics in water,sediments, and fish muscles by liquid chromatography-tandem mass spectrometry

Precise and sensitive methods for the simultaneous determination of different classes of antibiotics, including sulphonamides, fluoroquinolones, macrolides, tetracyclines, and trimethoprim in surface water, sediments, and fish muscles were developed. In water samples, drugs were extracted with solid-phase extraction （SPE） by passing 1000 mL of water through hydrophilic lipophilic balanced （HLB） SPE cartridges. Sediment samples were solvent-extracted, followed by tandem SPE （strong anion exchange （SAX） ＋ HLB） clean-ups. Fish muscles were extracted by a mixture of acetonitrile and citric buffer （80：20, v/v） solution, and cleaned by SPE. Liquid chromatography-tandem mass spectrometry （LC-MS/ MS） with multiple reaction monitoring （MRM） detection was employed to quantify all compounds. The recoveries for the antibiotics in the spiked water, sediment, and fish samples were 60.2%-95.8%, 48.1%-105.3%, and 59.8%- 103.4%, respectively. The methods were applied to samples taken from Dianchi Lake, China. It showed that concentrations of the detected antibiotics ranged from limits of quantification （LOQ） to 713.6 ng- L1 （ofloxacin） in surface water and from less than LOQ to 344.8 μg·kg-1 （sulphamethoxazole） in sediments. The number of detected antibiotics and the overall antibiotic concentrations were higher in the urban area than the rural area, indicating the probable role of livestock and human activities as important sources of antibiotic contamination. In fish muscles, the concentration of norfioxacin was the highest （up to 38.5 μg·kg-1）, but tetracyclines and macrolides were relatively low. Results showed that the methods were rapid and sensitive, and capable of determining several classes of antibiotics from each of the water, sediment, and fish matrices in a single run.     

Adsorption of benzene and toluene from waste gas using activated carbon activated by ZnCl2

A series of activated carbons with high surface area were prepared from walnut shell using chemical activation with ZnCl2. In this research the carbonization stage was carried out at 500℃. The performance of the synthesized carbons evaluated in adsorption of benzene and toluene from waste gas. The influence of impregnation ratio on the characteristics of synthesized activated carbons as well as their adsorption capacity was investigated. The ratio of activation agent to walnut shell was selected in the range of 0.5-2.0 wt/wt. The synthesized activated carbons were characterized using XRD, SEM, BET and FTIR techniques. The highest activated carbon production yield was obtained at impregnation ratio of 1.5 wt/wt. The XRD analysis illustrated that peaks intensity decreased with increasing impregnation ratio showing that amorphous property of samples was increased. The SEM analysis revealed successful pore development in synthesized activated carbons obtained at high impregnation ratios. The surface area of the activated carbons increased with increasing impregnation ratio and its maximum value reached 2643 m2.g 1 at impregnation ratio of 2/1. FTIR analysis indicated that the relative amount of different acidic surface groups on synthesized carbons was a function of impregnation ratio. Experimental results for benzene and toluene adsorption showed a high potential of employing synthesized impregnated activated carbon for treatment of waste gas. Generally, the amount of VOC adsorbed on the surface was affected by physicochemical properties of synthesized activated carbons.     

Characterization of phosphorus species and modeling for its organic forms in eutrophic shallow lake sediments,North China

Variations of phosphorus （P） and its species in surface sediment of Baiyangdian Lake, a eutrophic shallow lake located in North China, were investigated through combination of field survey and numerical calculation based on cluster analysis. P fractionation was performed by a sequential extraction scheme, categorized as loosely bound P （NH4Cl-P）, reductant soluble P （BD-P）, metallic oxide bound P （NaOH-P）, calcium bound P （HCl-P） and organic P （Org-P）. P concentrations exhibited regional similarities and a total of four sub-areas were identified in which the same rank was HCl-P 〉 Org-P 〉 BD-P ,=NaOH-P 〉NH4Cl-E NH4Cl-P, BD-P and Org-P were found to contribute to P enrichment in overlying water column. Specifically, labile Org-P acted as a potential pool with a greater contribution in aerobic layer compared to anaerobic layer. A hysteresis （lag = 4 months） existed when labile Org-P concentration was negatively correlated with aerobic layer thickness. In view of magnitude of identified P contributors in sub-areas, higher potential of P release was present in Fuhe River and Tang River estuary areas. On the basis of calibration and verification, the mathematical model with parameter settings applied in this study was improved to serve as a tool for limnology management and eutrophic control.     

Effects of phosphorus concentration on Cr（VI） sorption onto phosphorus-rich sludge biochar

To investigate effects of phosphorus content on Cr（VI） sorption onto phosphorus-rich biochar, sewage sludge of different phosphorus concentrations from 4 to 60 mg.g-1 by dry weight were prepared and carbonized to make biochar for batch sorption experiments. Test results revealed that different phosphorous concentration of raw sludge had respective impacts on surface area, pore surface area, average pore diameter and pH value of derived biochar. The adsorption kinetics of phosphorus-rich biochar could be described by the pseudo-second-order model. The sorption isotherm data followed Langmiur model better than Freundlich model. Biochar produced from sludge with phosphorus concentration of 20 mg. gl gave the largest chromium sorption capacity, which could be attributed to its largest surface area and pores surface area comparing with those of＇biochars from sludge with other phosphorus concentrations. The chromium loaded biochar was analyzed using Fourier Transform Infrared Spectroscopy and X-ray Diffraction measurement. The results indicated that chemical functional groups hydroxyl and methyl on surface of biochar were involved in Cr（VI） binding and its reducing to Cr（III）. Then, a portion of Cr （III） in form of various phosphate precipitates was bound onto biochar surface and the rest was released into the solution. The experimental results suggested that phos- phorus played an important role in pore and surface area development of sludge biochar during pyrolytic process. It also could react with Cr（III） on the biochar surface that impacted on capacity of Cr（VI） removal from solution by sludge biochar. Therefore, phosphorus concentration in sludge should be considered when sludge pyrolytic residue would be reused for heavy metals sorbing.     

Nitrogen pollution and source identification of urban ecosystem surface water in Beijing

Nitrogen contamination of surface water is a worldwide environmental problem with intensive agricul- ture and high population densities. We assessed the spatial and seasonal variation in concentrations of total nitrogen and different nitrogen species present in surface-water in Beijing, China. Also, chemical （NO3-N/C1-） and isotopic （615Nnitrate） indicators were used to identify nitrate sources. The results showed that, during 2009 and 2010, nitrate nitrogen concentrations ranged from 0.7 to 7.6 mg· L^-1, ammonium nitrogen from 0. I to 3.4 mg· L^-1, and total nitrogen from 2.4 to 17.0mg· L^-1. Inorganic nitrogen accounted for between 60 and 100% of total nitrogen at the ten monitoring sites. Nitrate nitrogen, ammonium nitrogen, and total nitrogen concentrations at the 2 downstream monitoring sites in south-eastern Beijing were significantly higher than those at the other eight upstream monitoring sites （P 〈 0.01）. Examination of seasonal variation showed that there was a significant inverse relationship between nitrate nitrogen concentrations and precipitation, and that nitrate nitrogen concentrations peaked in the dry seasons. The information given by the 15Nnitrate values and nitrate nitrogen concentrations, combined with the NO3-N/C1- ratio distribution, showed that domestic sewage was the major source of nitrate in Beijing. Methods to control and reduce sewage pollution are urgently needed to help manage surface water quality in Beijing.     

Laboratory study on high-temperature adsorption of HCI by dry-injection of Ca（OH）2 in a dual-layer granular bed filter

Combustion-generated hydrogen chloride （HCl） is considered to be a very hazardous acid gaseous pollutant. This paper presents a laboratory study on the dry adsorption of HCl. The experiments were conducted in a dual-layer granular bed filter, at gas temperatures of 500℃-700℃ and n（Ca）/n（Cl）molar ratios of 1.0-5.0 using the silver nitrate titration method by dry adsorbent powders Ca（OH）2. Mainly, the adsorption efficiency of HCI and utilization efficiency of Calcium were studied, by varying relevant factors including n（Ca）/n（Cl）, tempera- ture, feeding method, water vapor and CO2. With a relatively higher HCl concentration of 1000ppm, the experimental results revealed that 600℃ may be the optimum temperature for HCl adsorption when optimum n （Ca）/n（Cl） was 2.5 in our tests. The results also demonstrated that the feeding at a constant pressure was more effective, and the HCl adsorption efficiency could rapidly reach over 90% with n（Ca）/n（Cl） = 2.5 at 600℃. Furthermore, the HCl adsorption efficiency was found to be slightly promoted by water vapor, while could be impeded by CO2, and the utilization efficiency of calcium could be up to 74.4% without CO2, while was only 36.8% with CO2 when n（Ca）/n（Cl） was 2.5 at 600℃.     

Evaluation of endocrine disruption and dioxin-like effects of organic extracts from sewage sludge in autumn in Beijing,China

Study on effective disposal and utilization of sewage sludge has recently been the target of growing interest in China. However, potential risks are associated with the use of sludge due to its contamination with toxic organics, heavy metals and pathogenic microorganisms. In this study, a screening assessment was conducted on sewage sludge samples collected from 17 different sewage treatment plants in Beijing, based on a batch of in vitro bioassays, including a set of recombinant gene yeast assays for endocrine disruption, and an ethoxy resorufin-O- deethylase （EROD） assay using H4IIE cells for aryl hydrocarbon receptor （Ah-R） agonistic activities. Our results suggested that moderate levels of estrogen receptor agonistic activities （0.9 ng E2. g-1 to 6.8 ng E2. gl, dw）, but relative higher androgen receptor antagonistic activ- ities （nd to 45%）, progestin receptor antagonistic activities （nd to 80%） and Ah-R agonistic activities （1390 to 6740 pg 2,3,7,8-tetrachlorodibenzo-p-dioxin （TCDD）·g-1, dw） were found in sewage sludge samples. However, there were no significant correlations between the toxic effects of sewage sludge and the sewage treatment processes. In addition, the 17β-estradiol （E2） equivalent quantity （EEQ） level of the sewage sludge was increased after the composting treatment, whereas the 2,3,7,8-tetrachlorodi- benzo-p-dioxin toxic equivalent quantity （TEQ） level of sewagesludge composted was much lower than that of sewage sludge.     

Recovery of NH 4 + by corn cob produced biochars and its potential application as soil conditioner

NH4^＋ ion, a main pollutant in aquatic systems, not only causes eutrophication in rivers and lakes but also contributes to fish toxicity. In this study, an eco-friendly biosorbent was prepared from the pyrolysis of corn cob, a low-cost agricultural residue. The biochars produced by pyrolysis of corn cob at 400℃ and 600℃ were characterized and investigated as adsorbents for NH4＋ -N from an aqueous solution. The biochars were characterized through elemental analysis, Brunauer-Emmett-Teller-N2 surface area analysis, scanning electron microscopy, and Fourier transform infrared spectroscopy. Batch experiments were conducted to investigate the NH4＋ adsorption process of the corn cob biochars. The Freundlich isotherm model fitted the adsorption process better than the Langmuir and Dubinin-Radushkevich isotherm models. Moreover, the adsorption process was well described by a pseudo-second-order kinetic model. Results of thermodynamic analysis suggested that adsorption was a nonspontaneous exothermic process. Biochars produced at 400℃ had higher adsorption capacity than those produced at 600℃ because of the presence of polar functional groups with higher acidity. The exhausted biochar can be potentially used as soil conditioner, which can provide 6.37 kg NH4＋-N-t^-1 （N fertilizer per ton of biochar）.     

Biosorption of Cr（VI） by carbonized Eupatorium adenophorum and Buckwheat straw： thermodynamics and mechanism

High quality and low cost carbon can be prepared from Eupatorium adenophorum （E. adenophorum） and Buckwheat straw. The biosorbent was used for Cr（VI） removal. The effect of experimental parameters, such as pH, sorbent dosage and temperature were examined and the optimal experimental condition was determned. Solution pH is found influencing the adsorp- tion. Cr（VI） removal efficiency is found to be maximum （98%） at pH= 1. Langmuir and Freundlich adsorption isotherms were applicable to the adsorption process and their constants were evaluated. The adsorption data obtained agreed well with the Langmuir sorption isotherm model. The maximum adsorption capacities for Cr（VI） ranged from 46.23 to 55.19mg.g^-1 for temperature between 298 K and 308 K under the condition of pH = 1.0. Thermodynamic parameters such as free energy change （AG）, enthalpy （AH） and entropy （AS） indicate a spontaneous, endothermic and increased randomness nature of Cr（VI） adsorption. Studies found that the raw E. adenophorum and buckwheat straw mixed materials with simple treatment had a high efficiency for the removal of Cr（VI） and would be a promising adsorbent.     

Electrochemical oxidation of humic acid at the antimony- and nickel-doped tin oxide electrode

This work investigated the degradation of humic acid （HA） in aqueous solution by electrochemical oxidation with Antimony- and Nickel-doped Tin oxide electrode （Ni-Sb-SnO2/Ti electrode） as the anode. Initial concentrations of HA ranged from 3 to 9 mg-L 1. Under such a concentration scope, the degradation of HA was a mass transfer controlled process. Degradation rate increased with the increase of HA initial concentration. Test on the effect of tert-butanol revealed that · OH played an important role in the oxidation of HA. The absence of cation Ca2＋ was beneficial to HA degradation, which suggested that both indirect and direct electrolyze happened during the whole electrochemical oxidation process. Alkaly （pH = 12） and neutral （pH = 7） conditions were benefical to HA degradation.     

Production of N2O in two biologic nitrogen removal processes: a comparison between conventional and short-cut nitrogen removal processes

The N2O production in two nitrogen removal processes treating domestic wastewater was investigated in laboratory-scale aerobic-anoxic sequencing batch reactors （SBRs）. Results showed that N2O emission happened in the aerobic phase rather than in the anoxic phase. During the aerobic phase, the nitrogen conversion to N2O gas was 27.7% and 36.8% of NH＋-N loss for conventional biologic N-removal process and short-cut biologic N-removal process. The dissolved N2O was reduced to N2 in the anoxic denitrification phase. The N2O production rate increased with the increasing of nitrite concentration and ceased when NH＋-N oxidation was terminated. Higher nitrite accumulation resulted in higher NEO emission in the short-cut nitrogen removal process. Pulse-wise addition of 20 mg NO2 -N. L- 1 gave rise to 3-fold of N2O emission in the conventional N-removal process, while little change happened with 20 mg NOS-N L-1 was added to SBR1.     

Application of probabilistic risk assessment at a coking plant site contaminated by polycyclic aromatic hydrocarbons

Application of Probabilistic Risk Assessment （PRA） and Deterministic Risk Assessment （DRA） at a coking plant site was compared. By DRA, Hazard Quotient （HQ） following exposure to Naphthalene （Nap） and Incremental Life Cancer Risk （ILCR） following exposure to Benzo（a）pyrene （Bap） were 1.87 and 2.12 × 104. PRA revealed valuable information regarding the possible distribution of risk, and risk estimates of DRA located at the 99.59th and 99.76th percentiles in the risk outputs of PRA, which indicated that DRA overestimated the risk. Cleanup levels corresponding acceptable HQ level of 1 and ILCR level of 104 were also calculated for both DRA and PRA. Nap and Bap cleanup levels were 192.85 and 0.14mg.kg-1 by DRA, which would result in only 0.25% and 0.06% of the exposed population to have a risk higher than the acceptable risk, according to the outputs of PRA. The application of PRA on cleanup levels derivation would lift the cleanup levels 1.9 times for Nap and 2.4 times for Bap than which derived by DRA. For this coking plant site, the remediation scale and cost will be reduced in a large portion once the method of PRA is used. Sensitivity analysis was done by calculating the contribution to variance for each exposure parameter and it was found that contaminant concentration in the soil （Cs）, exposure duration （ED）, total hours spent outdoor per day （ETout）, soil ingestion rate （IRs）, the air breathing rate （IRa） and bodyweight （BW） were the most important parameters for risk and cleanup levels calculations.     

CO2 adsorption performance of ZIF-7 and its endurance in flue gas components

Porous ZIF-7 with the sodalite （SOD） cage structure （ZIF, Zeolitic imidazolate framework） were synthesized by the solvothermal method. Synthesized material was characterized by powder X-ray diffraction （PXRD）, thermal gravity （TG）, scanning electron micro- scopy （SEM） and Na adsorption analysis. ZIF-8 with the SOD structure and a littl larger pore window was synthesized in a similar way and was characterized for comparisons. Thermal stability and structural stability of ZIF-7 were tested through PXRD analysis, and the capability of the material for CO2 capture from simulated flue gas was investigated through physical adsorption method. The results showed that CO： adsorption capacity on ZIF-7 was about 48 mL. gl while the capacity on ZIF-8 was about 18mg.g-1 （at 12C and 0.98 P/Po relative pressure）. Furthermore, the impact of flue gas components on adsorption capacity of ZIF-7 and the selectivity of CO2 against N2 on ZIF-7 was also investigated in this work     

Assessment of metals in dry-toilet collected matters from suburban areas of Ulaanbaatar,Mongolia, using biosolids quality guidelines and potential ecological risk index

Dry-toilet collected matter （DCM） from traditional dry-toilet pits are a potential health and ecological risk in suburban areas. In this study, the characteristics of metals in DCMs from suburban areas of Ulaanbaatar were surveyed. The results indicate that DCMs contain a high percentage of organic matter and nutrients, while heavy metals are at low levels, which shows good agricultural potential. The concentration ranges of Cr, Cu, Hg, Ni, Pb, and Zn were 11±5, 46±9, 0.08±0.05, 9±3, 17±9, and 338±86mg·kg^-1, respectively. The concentration of Cd was below 0.5 mg.kgl, and a high positive relation was shown between chromium and nickel concentrations. The heavy metals in DCMs were safe for land application but Zn in DCMs was close to the effects range median （ERM）, which is toxic in some cases, such as amphipod bioassays. Because it is mandatory to treat DCMs to reduce pathogens, in the case of heavy metal enrichment and agricultural reuse, composting or pyrolysis are better choices than incinera- tion. Compared with global soil background values, the heavy metals in DCMs showed a low level of ecological risk, but a medium level when compared with Mongolian soil background values. The ecological risk of six heavy metals was in the descending order Hg 〉 Cu 〉 Zn 〉 Pb 〉 Ni 〉 Cr and the contribution rate of Hg exceeded 60%.     

A red water occurrence in drinking water distribution systems caused by changes in water source in Beijing,China: mechanism analysis and control measures

A red water phenomenon occurred in several communities few days after the change of water source in Beijing, China in 2008. In this study, the origin of this problem, the mechanism of iron release and various control measures were investigated. The results indicated that a significant increase in sulphate concentration as a result of the new water source was the cause of the red water phenomenon. The mechanism of iron release was found that the high-concentration sulphate in the new water source disrupted the stable shell of scale on the inner pipe and led to the release of iron compounds. Experiments showed that the iron release rate in the new source water within pipe section was over 11-fold higher than that occurring within the local source water. The recovery of tap water quality lasted several months despite ameliora- tive measures being implemented, including adding phosphate, reducing the overall proportion of the new water source, elevating the pH and alkalinity, and utilizing free chlorine as a disinfectant instead of chloramine. Adding phosphate was more effective and more practical than the other measures. The iron release rate was decreased after the addition of 1.5 mg. L-1 orthophosphate- P, tripolyphosphate-P and hexametaphosphate-P by 68%, 83% and 87%, respectively. Elevating the pH and alkalinity also reduced the iron release rate by 50%. However, the iron release rate did not decreased after replacing chloramine by 0.5-0.8 mg. L-1 of free chlorine as disinfectant.     

Microalgae Scenedesmus obliquus as renewable biomass feedstock for electricity generation in microbial fuel cells （MFCs）

Renewable algae biomass, Scenedesmus obliquus, was used as substrate for generating electricity in two chamber microbial fuel cells （MFCs）. From polarization test, maximum power density with pretreated algal biomass was 102mW·m^2 （951mW·m^3） at current generation of 276mA·m^-2. The individual electrode potential as a function of current generation suggested that anodic oxidation process of algae substrate had limitation for high current generation in MFC. Total chemical oxygen demand （TCOD） reduction of 74% was obtained when initial TCOD concentration was 534mg · L^-1 for 150 h of operation. The main organic compounds of algae oriented biomass were lactate and acetate, which were mainly used for electricity generation. Other byproducts such as propionate and butyrate were formed at a negligible amount. Electrochemical Impedance Spectroscopy （EIS） analysis pinpointed the charge transfer resistance （112Ω ） of anode electrode, and the exchange current density of anode electrode was 1214 nA·cm^-2.     

Removal of Cu（ll） ions from aqueous solution by activated carbon impregnated with humic acid

Humic acid （HA） was impregnated onto powdered activated carbon to improve its Cu（II） adsorption capability. The optimum pH value for Cu（II） removal was 6. The maximum adsorption capacity of HAimpregnated activated carbon was up to 5.98mg.g-1, which is five times the capacity of virgin activated carbon. The adsorption processes were rapid and accompanied by changes in pH. In using a linear method, it was determined that the equilibrium experimental data were better represented by the Langmuir isotherm than by the Freundlich isotherm. Surface charges and surface functional groups were studied through zeta potential and FTIR measurements to explain the mechanism behind the humicacid modification that enhanced the Cu（II） adsorption capacity of activated carbon.