Laboratory analyses of nutrient release processes from Haihe River sediment

Sediment samples were collected from the heavily contaminated Haihe River to conduct static nutrient release experiments with tap water,and to evaluate the effect of dredging depths,salinity and light ...     

澜沧江中下游泥沙微表面电荷特性与磷吸附关系研究

河流泥沙是水生态系统生源要素的重要附着载体,其微形貌及电荷特性直接关系着泥沙对溶解态营养盐或污染物的吸附能力。本研究选取澜沧江中下游干流及主要支流为考察对象,采集28个河流水库断面的悬移质泥沙,采用原子力显微镜测定泥沙微表面电荷量,探究澜沧江泥沙的微表面电荷性质,研究纳米尺度下泥沙的微表面特性。研究结果表明:(1)微观界面,形貌对表面电荷分布影响明显,在纳米尺度下电势图与相位差图均展现出明显非均匀分布特征;(2)在流域分布上,不同区域表面电荷存在较大差异,流域沿程变化对泥沙表面电荷产生重要影响,总体变化呈现先减小后增大的趋势,表面电势值变化范围为-201.47～35.34 mV,表面电荷密度范围为0.07～3.65 mC/m²,不同区域电荷特性差别明显;(3)在梯级水电筑坝影响下,坝上坝下泥沙颗粒电势差与水库库容存在较好的线性相关关系,相关系数为0.8214,且坝下电势普遍高于坝上区域;(4)泥沙表面电势与磷吸附之间具有较强相关性,其相关系数为0.6657,同时表现出较好的线性拟合关系。研究结论对深入理解水电大坝建设对流域内污染物的迁移转化及解释泥沙的表面电性特征...     

Phosphorus forms and distribution in Zhejiang coastal sediment in the East China Sea

Surface and core sediment samples were collected from Zhejiang coastal waters of the East China Sea to study phosphorus（P） forms and understand the potential release of P as well as adsorption.The sediments were extracted sequentially to determine four phosphorus fractions,and non-sequentially for total phosphorus（TP）.The total concentration of phosphorus in the surface sediments ranged from 527.2 to 680.5 mg kg-1.Inorganic P was the major form and accounted for 84-94%of TP.Among the four forms,P-Detrital was dominant（58.6-73.2%）,followed by P-CDB（10.5-20.9%）,P-Organic（6.1-15.9%）,and P-CFA（5.9-16.3%）.The distribution pattern of TP in the surface sediments was similar to that of P-Detrital and P-Organic,but different from P-CDB and P-CFA.A relatively high level of phosphorus was observed in estuarine sediments,reflecting the influence from terrestrial input.Phosphorus in all forms in core sediments at each station decreased with depth.In addition,potentially bio-available phosphorus accounted for 20-34%of TP.     

坦噶尼喀湖东北部入湖河流表层沉积物中磷的形态和分布特征

磷是坦噶尼喀湖生态系统中必不可少的营养元素,直接决定湖体初级生产力的高低,进而影响到周边居民对于动物蛋白的获取来源.为了解坦噶尼喀湖磷的外源输入,选择湖泊东北部的入湖河流,对表层沉积物(16个样点)中总磷(TP)和各形态磷含量及其分布特征进行分析,并探讨磷的形态分布特征与土地利用方式之间的相关关系.结果表明,入湖河流沉积物TP含量为73.05~239.94 mg/kg,平均含量为152.64±55.37 mg/kg,其中最高值出现在马拉加拉西河口.采用Psenner法对磷进行连续浸提并比较不同形态磷含量,由高及低依次为铁铝结合态磷(Fe/Al-P)钙结合态磷(CaP)有机磷(Org-P)残渣态磷(Res-P)弱吸附态磷(Labile-P).土地利用类型对TP及各形态磷含量影响较大,其中TP含量表现为河口湿地城镇附近林草地区,表明地表径流和人类活动会对TP含量产生影响,而对于不同形态磷含量,Laible-P、Fe/Al-P、Org-P含量均表现为河口湿地林草地城镇附近,Ca-P、Res-P含量均表现为城镇附近河口湿地林草地.分析沉积物理化性质与各磷形态之间的相关性,发现沉积物总氮(TN)、有机质和总有机碳与Fe/Al-P、LabileP和TP相关性较好,与Org-P、Ca-P和Res-P相关性较差,表明TN和有机质的输入,会伴随沉积物中磷含量的升高,其增量的赋存形态主要为氧化还原敏感态磷和Labile-P.沉积物粒径组成与各磷形态含量存在相关性,细粒径沉积物与各形态磷含量呈显著正相关,粗粒径沉积物与各形态磷呈显著负相关,表明细小颗粒更易吸附磷.     

Phosphorus forms and bioavailability of lake sediments in the middle and lower reaches of Yangtze River

Forms of phosphorus in sediments from 25 lakes in the middle and lower reaches of Yangtze River were analyzed by the sequential extraction procedure. Contents and spatial distrubution of algal available phosphorus (AAP) in sediments of Lake Taihu, the third largest freshwater lake of China, were also studied. Relationships between phosphorus forms in sediment and macrophytes coverage in sample sites, as well as phosphorus forms in sediments and chlorophyal contents in lake water were discussed. Exchangeable form of phosphorus (Ex-P) in surface sediments was significantly positive correlative to total phosphorus (IP), dissolved total phosphorus (DTP) and soluble reactive phosphorus (SRP) contents in the lake water. Bioavailable phosphorus (Bio-P) contents in sediments from macrophytes dominant sites were significantly lower than that in no macrophyte sites. In Lake Taihu, Ex-P content in top 3 cm sediment was highest. However, content of ferric fraction phosphorus (Fe-P) was highest in 4 - 10 cm. Bioavalilble phosphorus (Bio-P) contents in surface sediments positively correlated to Chlorophyll a contents in water of Lake Taihu with significant difference. Therefore, contents of Bio-P and AAP could be acted as the indicators of risks of internal release of phosphorus in the shallow lakes. It was estimated that there were 268.6 ton AAP in top 1 cm sediments in Lake Taihu. Sediment suspension caused by strong wind-induced wave disturbance could carry plenty of AAP into water in large shallow lakes like Lake Taihu.     

Phosphorus forms and bioavailability of lake sediments in the middle and lower reaches of Yangtze River

Forms of phosphorus in sediments from 25 lakes in the middle and lower reaches of Yangtze River were analyzed by the sequential extraction procedure. Contents and spatial distrubution of algal available phosphorus (AAP) in sediments of Lake Taihu, the third largest freshwater lake of China, were also studied. Relationships between phosphorus forms in sediment and macrophytes coverage in sample sites, as well as phosphorus forms in sediments and chlorophyal contents in lake water were discussed. Exchangeable form of phosphorus (Ex-P) in surface sediments was significantly positive correlative to total phosphorus (TP), dissolved total phosphorus (DTP) and soluble reactive phosphorus (SRP) contents in the lake water. Bioavailable phosphorus (Bio-P) contents in sediments from macrophytes dominant sites were significantly lower than that in no macrophyte sites. In Lake Taihu, Ex-P content in top 3 cm sediment was highest. However, content of ferric fraction phosphorus (Fe-P) was highest in 4–10 cm. Bioavalilble phosphorus (Bio-P) contents in surface sediments positively correlated to Chlorophyll a contents in water of Lake Taihu with significant difference. Therefore, contents of Bio-P and AAP could be acted as the indicators of risks of internal release of phosphorus in the shallow lakes. It was estimated that there were 268.6 ton AAP in top 1 cm sediments in Lake Taihu. Sediment suspension caused by strong wind-induced wave disturbance could carry plenty of AAP into water in large shallow lakes like Lake Taihu.     

Biofilm effects on size gradation,drag coefficient and settling velocity of sediment particles

Sediment particles are often colonized by biofilm in a natural aquatic ecological system, especially in eutrophic water body. A series of laboratory experiments on particle size gradation, drag coefficient and settling velocity were conducted after natural sediment was colonized by biofilm for 5, 10, 15 and 20 days. Particle image acquisition, particle tracking techniques of Particle Image Velocimetry and Particle Tracking Velocimetry were utilized to analyze the changes of these properties. The experimental results indicate that the size gradation, the drag force exerted on bio-particles, and the settling velocity of bio-particles underwent significant change due to the growth of biofilm onto the sediment surface. The study proposes a characteristic particle size formula and a bio-particle settling velocity formula based on the regression of experiment results, that the settling velocity is only 50% to 60% as the single particle which has the same diameter and density. However, biofilm growth causes large particle which the settling velocities are approximately 10 times larger than that of primary particles. These results may be specifically used in the low energy reservoir or lake environment.     

Adsorption of Basic Dyes from Aqueous Solutions by Depolymerization Products of Post‐Consumer PET Bottles

The purpose of this work is the removal of basic dyes (Safranine T and Brilliant Green) from aqueous media by depolymerization products (DP) obtained from aminoglycolysis of waste poly(ethylene terephthalate) (PET). The surface morphology and physical properties of depolymerization product were also determined. Adsorption behaviors (adsorption capacities, adsorption kinetics and adsorption isotherms) of these samples were realized at room temperature. Then, the amounts of residual dye concentrations were measured using Visible Spectrophotometer at 530 and 618 nm for Safranine T (ST) and Brilliant Green (BG), respectively. All adsorption experiments were carried out for different depolymerization products (DP1, DP2, DP3, and DP4). Adsorption capacities of depolymerization products for both of dyes decrease with following order: DP2 > DP4 > DP1 > DP3. The maximum adsorption capacities for ST and BG onto DP2 sample were found to be 29 and 33 mg g^?1, respectively. In addition, the adsorption kinetic results show that the pseudo‐second‐order kinetic model is more suitable than pseudo‐first‐order model for the adsorption of basic dyes onto DP samples. Adsorption data were evaluated using Langmuir and Freundlich adsorption isotherm models. The results revealed that the adsorption of basic dyes onto DP sample fit very well Langmuir isotherm model. In conclusion, the depolymerization products of post‐consumer PET bottles can be used as low cost adsorbent for the removal of basic dyes from wastewaters.     

Characterization of phosphorus interaction with sediments affected by acid mine drainage-relation with the sediment composition

Phosphorus sorption capacity was investigated in surface sediments derived from an abandoned zinclead mine area located in northeastern Algeria. The forms and the distribution of phosphorus in the raw sediment were identified using the sequential chemical extractions method. Batch experiments were done to study the adsorption kinetics and isotherms. The pH effect was evaluated by macroscopic and infrared analyses. In raw sediment, speciation results show that phosphorus is dominantly bound to oxyhydroxides. Sorption experiments demonstrate that phosphorus uptake is principally related to sediment composition. The nature of the dominant iron oxyhydroxide has a substantial role in the adsorption capacity and the mechanism interaction. The adsorption kinetics can be described by the second order and Elovich models. The isotherms data are successfully modeled by the Temkin equation.The maximum phosphorus removal is reached under acidic pH. Spectroscopic analyses reveal that the predominance of jarosite implies electrostatic interaction with sediment particles. However, in the case of schwertmannite predominance, phosphate ions are adsorbed by the ligand exchange mechanism.     

Further discussion on the intercomparison of the trace metal concentrations and particle size of fluvial sediment recovered from two centrifuge systems

A single large volume water sample taken at the mouth of the Upper Rhone River on Lake Geneva was processed directly in parallel through two continuous flow centrifuges, a Westphalia and an Alfa-Laval. Sediment was recovered from the Westphalia, and separately from the bowl and brass core of the Alfa-Laval. The three sediment samples were analyzed for particle size and the following elements: Zn, Cu, Mn, Cr, P, Co, B, V, Be, Sr, Na, Pb, Ni, Ba, Fe, Ca, and Mg. Results indicate that the particle size recovery of both machines is similar when sediment from the brass core and bowl of the Alfa-Laval are combined, and that the recovery for all elements other than Cu, V, B, and Pb are the same when the particle size differences are taken into account. Sediment from the Alfa-Laval brass core is clearly contaminated by Cu, B and is also elevated in V and Pb but not to a significant extent. The sediment recovered from the bowl of the Alfa-Laval is contaminated only with Cu, with a 10 ppm increase over the 52 ppm recovered in the Westphalia sediment. Operating procedures involve the discarding of the brass core sediment and the mixing of the Alfa-Laval bowl sediment with that from the Westphalia. The consequent increase in Cu is estimated at less than 5 ppm or within the confidence level of the analysis. These procedures are recommended to all operators of non modified Alfa-Laval units.     

Coprostanol as sewage tracer in McMurdo Sound, Antarctica

Sediment cores from the vicinity of sewage outfalls off McMurdo Station as well as surface grab samples from different locations in the McMurdo Sound, Antarctica were analysed for coprostanol (5β-cholestan-3β-ol) and epicoprostanol (5β-cholestan-3-ol) to assess the degree of sewage addition to the Sound. Sediment samples close to the point source contain as much as 3 mg g⁻¹ dry sediment of coprostanol, whereas samples farther from the source, for example from New Harbour and Granite Harbour, contain only trace levels to 40 ng g⁻¹. Coprostanol in the sediments of latter locations most likely originates from seals rather than from sewage outfalls. It appears that sewage particles are very quickly incorporated into the sediment layers close to the discharge point in the eastern Sound. However, significant levels (930 ng g⁻¹) of fecal sterols were detected in Cape Armitage surface sediments, indicating that the sewage plume could also have reached the seawater intake station, situated in between the outfall and Cape Armitage sampling site. These results suggest the need for a sound environmental monitoring and assessment of the existing wastewater practices in the region.     

Biopolymer-Based Nanocomposites for Removal of Cr(VI) from Aqueous Systems: A Review

Hexavalent chromium Cr(VI) has emerged as a contaminant of prime concern for the environmentalists because of its improper disposal by tannery, dye, and electroplating industries. Adsorption is the most exploited method for its removal from industrial wastewater because of its high removal efficiency even at low Cr(VI) concentration, minimal sludge, and ease of regeneration. In recent years, several adsorbents of biological origin such as plants, algae, fungi, and bacteria have been explored for Cr(VI) remediation. This review comprehends the recent studies involving usage of biopolymer-based nano-composites with respect to its adsorption mechanisms, adsorption capacities, isotherms, and kinetics. The conventional abiotic and biotic techniques for removal of Cr(VI) are also discussed with a comparative insight of their adsorption capacity and removal efficiency. Nano-biocomposites integrate the functional properties of both nanoparticles and biopolymers, which make them efficient biosorbents. Nano-biocomposites offer a large surface area, reduced particle loss, minimal particle agglomeration on the surface, and high stability. Common kinetic models among the nano-biocomposites,  and various equilibrium models are also analyzed to understand the mode of adsorption and associated factors. These materials are mostly found to follow monolayer adsorption with ion exchange, electrostatic interaction, and surface complexation as major players in the process.     

Catchment‐scale contribution of forest roads to stream exports of sediment,phosphorus and nitrogen

The relative contribution of forest roads to total catchment exports of suspended sediment, phosphorus, and nitrogen was estimated for a 13 451 ha forested catchment in southeastern Australia. Instrumentation was installed for 1 year to quantify total in‐stream exports of suspended sediment, phosphorus, and nitrogen. In addition, a total of 101 road–stream crossings were mapped and characterized in detail within the catchment to identify the properties of the road section where the road network and the stream network intersect. Sediment and nutrient generation rates from different forest road types within the catchment were quantified using permanent instrumentation and rainfall simulation. Sediment and nutrient generation rates, mapped stream crossing information, traffic data and annual rainfall data were used to estimate annual loads of sediment, phosphorus, and nitrogen from each stream crossing in the catchment. The annual sum of these loads was compared with the measured total catchment exports to estimate the proportional contribution of loads from roads within the catchment. The results indicated that 3·15 ha of near‐stream unsealed road surface with an average slope of 8·4% delivered an estimated 50 t of the 1142 t of total suspended sediment exported from the catchment, or about 4·4% of the total sediment load from the forest. Stream discharge over this period was 69 573 Ml. The unsealed road network delivered an estimated maximum of 22 kg of the 1244 kg of total phosphorus from the catchment, or less than 1·8% of the total load from the forest. The average sediment and phosphorous load per crossing was estimated at 0·5 t (standard deviation 1·0 t) and 0·22 kg (standard deviation 0·30 kg) respectively. The lower proportional contribution of total phosphorus resulted from a low ratio of total phosphorus to total suspended sediment for the road‐derived sediment. The unsealed road network delivered approximately 33 kg of the 20 163 kg of total nitrogen, about 0·16% of the total load of nitrogen from the forest. The data indicate that, in this catchment, improvement of stream crossings would yield only small benefits in terms of net catchment exports of total suspended sediment and total phosphorus, and no benefit in terms of total nitrogen. These results are for a catchment with minimal road‐related mass movement, and extrapolation of these findings to the broader forested estate requires further research. Copyright © 2007 John Wiley & Sons, Ltd.     

Seasonal and spatial distribution of matrix-bound phosphine and its relationship with the environment in the Changjiang River Estuary, China

Sediment is commonly considered as a source of phosphine, which is a highly toxic and reactive atmospheric trace gas. This study aims to investigate the seasonal and spatial distribution of matrix-bound phosphine (MBP) and its relationship with the environment in the Changjiang River Estuary. A total of 43 surface sediments were collected in four seasons of 2006, and concentrations of MBP and relative environmental factors were analyzed. MBP ranged from 1.93 to 94.86ngkg(-1) dry weight (dw) with an average concentration of 17.14ngkg(-1)dw. The concentrations of MBP in the upper estuary were higher than those in the lower estuary, which could be attributed to greater pollutant inputs in the upper estuary. The concentrations of MBP also varied with season, with November>August>May>February. Significant correlations existed between MBP and total phosphorus (TP), organic phosphorus (OP), inorganic phosphorus (IP), organic carbon (OC), total nitrogen (TN), the grain size, and redox potential (Eh), suggesting that these sedimentary environmental characteristics played an important role in controlling the MBP levels in the sediments. Notably, there were positive linear relationships between the concentrations of soluble reactive phosphorus (SRP), TP, and chlorophyll a (Chl a) in bottom water and MBP in sediments. These relationships might be very complicated and need further exploration. This work is the first comprehensive study of the seasonal and spatial distribution of MBP in sediments and its relationships with environmental factors in a typical estuary, and will lead to deeper understanding of the phosphorus (P) biogeochemical cycle.     

Distribution and source differentiation of PAHs and PCBs among size and density fractions in contaminated harbor sediment particles and their implications in toxicological assessment

Sediment samples collected from Kaohsiung Harbor (Taiwan) were analyzed for 15 priority polycyclic aromatic hydrocarbons (PAHs) and 118 individual polychlorinated biphenyl (PCB) congeners in various particle size fractions and two density fractions. The PAHs in the low density fraction were a much more sensitive and effective indicator of the PAH source than those in the sediment as a whole. Hierarchical cluster analysis of PAH analytes in the low density sediments revealed significant differences in compositional patterns between locations and among size fractions. In the sediment samples from both study sites, the low density fraction particles had up to 155 and 150 times higher concentrations of PAHs and PCBs, respectively, than those in the corresponding high density fractions. In addition, the total toxic benzo[a]pyrene and 2,3,7,8-tetrachlorodibenzodioxin (TCDD, dioxin) equivalents in the sediment low density fractions were much higher (up to 170 and 273 times, respectively) than the corresponding high density fractions.     

Fine scale distributions of porosity and particulate excessPb, organic carbon and CaCO3 in surface sediments of the deep equatorial Pacific

Sediment samples were recovered from the central equatorial Pacific Ocean, sectioned at 1-mm intervals, and analyzed for porosity, organic carbon, excess²¹⁰Pb and CaCO₃. Steep porosity gradients were measured in the upper 1 cm of the sediment column with extremely high values observed near the sediment surface. Similarly, particulate organic carbon contents are highest at the sediment surface, decrease sharply in the upper 1 cm, and are relatively constant between 1 and 5 cm. CaCO₃ values, on the other hand, are lowest at the sediment surface and increase to a constant value below 5–10 mm depth. At the carbonate ooze sites, excess²¹⁰Pb is present throughout the upper 5 cm of the sediments suggesting relatively rapid particle mixing rates. However, extremely high excess²¹⁰Pb activities (> 100 dpm/g) are observed at the sediment surface with sharp gradients present in the upper 1 cm which would suggest slow rates of mixing. This apparent contradiction along with the major features of the CaCO₃ and particulate organic carbon profiles can be explained by a particle-selective feeding mechanism in which organic carbon, excess²¹⁰Pb-enriched particles are preferentially maintained at the sediment surface via ingestion and defecation by benthic organisms.     

Fine scale distributions of porosity and particulate excess210Pb,organic carbon and CaCO3 in surface sediments of the deep equatorial Pacific

Sediment samples were recovered from the central equatorial Pacific Ocean, sectioned at 1-mm intervals, and analyzed for porosity, organic carbon, excess²¹⁰Pb and CaCO₃. Steep porosity gradients were measured in the upper 1 cm of the sediment column with extremely high values observed near the sediment surface. Similarly, particulate organic carbon contents are highest at the sediment surface, decrease sharply in the upper 1 cm, and are relatively constant between 1 and 5 cm. CaCO₃ values, on the other hand, are lowest at the sediment surface and increase to a constant value below 5–10 mm depth. At the carbonate ooze sites, excess²¹⁰Pb is present throughout the upper 5 cm of the sediments suggesting relatively rapid particle mixing rates. However, extremely high excess²¹⁰Pb activities (> 100 dpm/g) are observed at the sediment surface with sharp gradients present in the upper 1 cm which would suggest slow rates of mixing. This apparent contradiction along with the major features of the CaCO₃ and particulate organic carbon profiles can be explained by a particle-selective feeding mechanism in which organic carbon, excess²¹⁰Pb-enriched particles are preferentially maintained at the sediment surface via ingestion and defecation by benthic organisms.     

Comparison of granulometric methods and sampling strategies used in marine habitat classification and Ecological Status assessment

Sediment particle size analysis (PSA) is routinely used to support benthic macrofaunal community distribution data in habitat mapping and Ecological Status (ES) assessment. No optimal PSA Method to explain variability in multivariate macrofaunal distribution has been identified nor have the effects of changing sampling strategy been examined. Here, we use benthic macrofaunal and PSA grabs from two embayments in the south of Ireland. Four frequently used PSA Methods and two common sampling strategies are applied. A combination of laser particle sizing and wet/dry sieving without peroxide pre-treatment to remove organics was identified as the optimal Method for explaining macrofaunal distributions. ES classifications and EUNIS sediment classification were robust to changes in PSA Method. Fauna and PSA samples returned from the same grab sample significantly decreased macrofaunal variance explained by PSA and caused ES to be classified as lower. Employing the optimal PSA Method and sampling strategy will improve benthic monitoring.     

Isotherm Study of Phosphorus Uptake from Aqueous Solution Using Aluminum Oxide

Aluminum oxide, which could be an alternative filter media for phosphorus uptake from aqueous solution, was selected as an adsorbent for the isotherm study of phosphorus uptake from aqueous solution. Batch method was adopted to investigate the adsorption behavior of phosphorus onto aluminum oxide. The Langmuir, Freundlich, and Redlich–Peterson isotherms were used to analyze the experimental data by both the linear and nonlinear regression methods. The adsorption experiment was conducted at various temperatures, to choose the appropriate method and obtain the creditable adsorption parameters for phosphorus uptake studies. The results indicated that the nonlinear regression method might be a better way to compare the best‐fitting isotherm and obtain the parameters for the adsorption of phosphorus onto aluminum oxide. Both the Redlich–Peterson and the Freundlich isotherms have high coefficients of determination for the adsorption of phosphorus onto aluminum oxide at various temperatures. In addition, a new relationship between the Redlich–Peterson and the Freundlich isotherm parameters was presented.     

Biosorption of Dyes by Natural and Activated Vine Stem. Interaction between Biosorbent and Dye

In the present study, the vine stem and modified vine stem were used as low cost adsorbents for the removal of acidic and basic dyes from aqueous solutions. A comparative study was also carried out with activated carbon obtained from vine stem and then the adsorption capacities of all adsorbents were evaluated by batch adsorption process. The effects of various adsorption parameters (initial pH, particle size, and contact time) were investigated. The modification of the vine stem with nitric acid increased its adsorption capacity for the basic dye. Both, vine stem and modified vine stem exhibited higher adsorption capacities than activated carbon. The adsorption capacities were found to be 322.58, 250, and 200 mg g^?1 for modified, natural vine stem, and activated carbon, respectively. In the case of acidic dye, the pH strongly affected the adsorption capacity and the maximum dye uptake was observed at pH 2 for all adsorbents. The acidic dye adsorption was lower compared to basic dye on both biosorbents and activated carbon tested. The maximum acidic dye adsorption values (58.82 and 59.88 mg g^?1) were obtained with the vine stem and activated carbon, respectively. In the case of lignocellulosic adsorbents, both surface charge and surface groups had main effect on the adsorption of basic dye, while adsorption mechanism in activated carbon was mainly through the physical adsorption. The results of comparative adsorption capacity of adsorbents indicated that vine stem or modified vine stem can be used as a low cost alternative to activated carbon in aqueous solution for basic dye removal.