Biohydrogen production with anaerobic sludge immobilized by granular activated carbon in a continuous stirred-tank

A continuous stirred-tank reactor （CSTR） process with granular activated carbon （GAC） was developed for fermentation hydrogen production from molasses-containing wastewater by mixed microbial cultures. Operation at 35℃, an initial biomass of 17.74 g·L^-1 and hydraulic retention time （HRT） of 6 h, the CSTR reactor presented a continuous hydrogen production ability of 5.9 L·d^-1 and the biogas was free of methane throughout the experiment. Dissolved fermehtation products were predominated by ethanol and acetate acid, with smaller quantities of propionic acid, butyric acid and valeric acid. It was found that GAC could make the immobilized system durable and stable in response to organic load impacting and low pH value. When the organic loading rate （OLR） ranged from 8 kgCOD/（m^3d） to 4 kgCOD/（m^3d）, stable ethanol-type fermentation was formed, and the ethanol and acetate concentrations account for 89% of the total liquid products.

Thermodynamics and kinetics of cadmium adsorption onto oxidized granular activated carbon

Cadmium sorption behavior of granular activated carbon oxidized with nitric acid was systematically studied by sets of the equilibrium and time-based experiments under various conditions. The cadmium adsorption capacity of oxidized granular activated carbon enlarged with an increase in pH, and reduced with an increase in ionic strength. Experimental data were evaluated to find out kinetic characteristics. Adsorption processes were found to follow pseudo-second order rate equation. Adsorption isotherms correlate well with the Langmuir isotherm model and the maximum sorption capacity of cadmium evaluated is 51.02 μmol/g. Thermodynamic parameters were calculated based on Van＇t Hoff equation. Equilibrium constant Kd was evaluated from Freundlich isotherm model constants, Langmuir isotherm model constants, and isotherms, respectively. The average change of standard adsorption heat ΔH^0 was -25.29 kJ/mol. Negative ΔH^0 and ΔG^0 values indicate the adsorption process for cadmium onto the studied activated carbon is exothermic and spontaneous. The standard entropy ΔS^0 was also negative, which suggests a decrease in the freedom of the system.

Combination of adsorption and biodegradation processes for textile effluent treatment using a granular activated carbon-biofilm configured packed column system

The objective of this study was to investigate the feasibility of using a granular activated carbon-biofilm configured packed column system in the deeolodzation of azo dye Acid Orange 7-containing wastewater.The Acid Orange 7-degrading microbial from anaerobic sequencing batch reactor which treating the azo dye-containing wastewater for more than 200 d was immobilized on spent granular activated carbon(GAC)through attachment.The GAC-biofilm configured packed column system showed the ability to decolorize 10...

Mechanisms of granular activated carbon anaerobic fluidized-bed process for treating phenols wastewater

Granular activated carbon (GAC) anaerobic fluidized bed reactor was applied to treating phenols wastewater. When influent phenol concentration was 1000 mg/L, volume loadings of phenol and COD Cr were 0 39 kg/(m 3·d) and 0 98 kg/(m 3·d), their removal rates were 99 9% and 96 4% respectively. From analyzing above results, the main mechanisms of the process are that through fluidizing GAC, its adsorption is combined with biodegradation, both activities are brought into full play, and phenol in wastewater is effectively decomposed. Meanwhile problems concerning gas liquid separation and medium plugging are well solved.

High-valued Utilization of China Fir Sawdust Extracted Essential Oil:Preparation of Granular Activated Carbons for n-Butane Adsorption

[Objective] The aim was to study on the high-valued utilization of China Fir sawdust extracted essential oil.[Method] In the field of fir essential oil extraction,the processed China fir sawdust was used to prepare low-valued products.The high-valued utilization of China fir sawdust extracted essential oil(CFSEEO),namely as a precursor to prepare granular activated carbons(GACs),was attempted.The materials were characterized by ultimate analysis,SEM and XRD.[Rusult] A butane working capacity(BWC)of 14.3 g/100 ml was obtained by using the GACs with apparent density of 0.25 g/ml.It was available to introduce the technology of extracting essential oil from the China fir sawdust(CFS)in the industrial production process of activated carbons with high BWC(12.0-16.5 g/100 ml)and high surface area(2 000-2 630 m2/g)using phosphoric acid based on previous studies of the authors.[Conclusion] The resulting carbon prepared with the raw materials containing lower moisture exhibited a better property on n-butane adsorption.

Additivity of pore structural parameters of granular activated carbons derived from different coals and their blends

A series of granular activated carbons （GACs） were prepared by briquetting method from Chinese coals of different ranks and their blends, with coal pitch as the binder. Pore structural parameters including BET specific surface area （SBEr）, total pore volume （Vr） and average pore diameter （da） were measured and cal- culated as well as process parameters such as yield of char （CY） and burn-off （B）. The relationship between the pore structural parameters of the GAC from coal blend （BC-GAC） and the ones of the GACs from corresponding single coals （SC-GACs） was analyzed, in which an index, the relative error （δ）, was presented to define the bias between fitted values and experimental values of these parameters of the BC-GACs. The results show that the BC-GAC keeps qualitatively the pore structural features of the SC-GACs; as concerned as the quantitative relationship, the pore structural parameters of the BC-GAC from coal blend consisting of non-caking coals can be obtained by adding proportionally the pore structural parameters of the SC-GACs with a less than 10%. Meanwhile, for the BC-GAC from coal blend containing weak caking bituminous coal, the δ increases up to 25% and the experimental pore size distribution differs greatly from the fitted one.

Effects of Dielectric Barrier Discharge Plasma Treatment on Pentachlorophenol Removal of Granular Activated Carbon

The pentachlorophenol （PCP） adsorbed granular activated carbon （GAC） was treated by dielectric barrier discharge （DBD） plasma. The effects of DBD plasma on the structure of GAC and PCP decomposition were analyzed by N2 adsorption, thermogravimetric, scanning electron microscopy （SEM）, X-ray photoelectron spectroscopy （XPS） and gas chromatographymass spectrometry （GC-MS）. The experimental data of adsorption kinetics and thermodynamics of PCP on GAC were fitted with different kinetics and isotherm models, respectively. The results indicate that the types of N2 adsorption isotherm of GAC are not changed by DBD plasma, while the specific surface area and pore volume increase after DBD plasma treatment. It is found that the weight loss of the saturated GAC is the highest, on the contrary, the weight loss of DBD treated GAC is the least because of reduced PCP residue on the GAC. The XPS spectra and SEM image suggest that some PCP on the GAC is removed by DBD plasma, and the surface of GAC treated by DBD plasma presents irregular and heterogeneous morphology. The GC-MS identification of by-products shows that two main dechlorination intermediate products, tetrachlorophenol and trichlorophenol, are distinguished. The fitting results of experimental data of adsorption kinetics and thermodynamics indicate that the pseudo-first-order and pseudo-second order models can be used for the prediction of the kinetics of virgin GAC and DBD treated GAC for PCP adsorption, and the Langmuir isotherm model fits better with the data of adsorption isotherm than the Freundlich isotherm in the adsorption of PCP on virgin GAC and DBD treated GAC.

Regeneration of Acid Orange 7 Exhausted Granular Activated Carbon Using Pulsed Discharge Plasmas

In this paper, a pulsed discharge plasma （PDP） system with a multi-needle-to-plate electrodes geometry was set up to investigate the regeneration of acid orange 7 （AO7） exhausted granular activated carbon （GAC）. Regeneration of GAC was studied under different conditions of peak pulse discharge voltage and water pH, as well as the modification effect of GAC by the pulse discharge process, to figure out the regeneration efficiency and the change of the GAC structure by the PDP treatment. The obtained results showed that there was an appropriate peak pulse voltage and an optimal initial pH value of the solution for GAC regeneration. Analyses of scanning electron microscope （SEM）, Boehm titration, Brunauer-Emmett-Teller （BET）, Horvath-Kawazoe （HK）, and X-ray Diffraction （XRD） showed that there were more mesopore and macropore in the regenerated GAC and the structure turned smoother with the increase of discharge voltage; the amount of acidic functional groups on the GAC surface increased while the amount of basic functional groups decreased after the regeneration process. From the result of the XRD analysis, there were no new substances produced on the GAC after PDP treatment.

Degradation of phenol using a combination of granular activated carbon adsorption and bipolar pulse dielectric barrier discharge plasma regeneration

A combined method of granular activated carbon（GAC） adsorption and bipolar pulse dielectric barrier discharge（DBD） plasma regeneration was employed to degrade phenol in water.After being saturated with phenol,the GAC was filled into the DBD reactor driven by bipolar pulse power for regeneration under various operating parameters.The results showed that different peak voltages,air flow rates,and GAC content can affect phenol decomposition and its major degradation intermediates,such as catechol,hydroquinone,and benzoquinone.The higher voltage and air support were conducive to the removal of phenol,and the proper water moisture of the GAC was 20%.The amount of H2 O2 on the GAC was quantitatively determined,and its laws of production were similar to phenol elimination.Under the optimized conditions,the elimination of phenol on the GAC was confirmed by Fourier transform infrared spectroscopy,and the total removal of organic carbons achieved 50.4%.Also,a possible degradation mechanism was proposed based on the HPLC analysis.Meanwhile,the regeneration efficiency of the GAC was improved with the discharge treatment time,which attained 88.5% after 100 min of DBD processing.

Inactivation Removal for Excess Propagation of Copepod of Zooplankton in Ozone-Granular Activated Carbon Filter in Southern China

Comparative experiments on the inactivation of Copepod were investigated in southern China. The 100% of inactivation effect may be attained by 3.0 mg/L of ozone for contacting time of 25 min, whereas 0.5 mg/L of dosage resulted in only 30% of inactivation rate. Copepod may not be completely inactivated by ozone oxidation for feasible dosage limited by higher bromide in raw water. The favorable environment of granular activated carbon （GAC） filter provided Copepod with conditions for excess propagation, The disinfection experimental results show that the inactivation rate is 90% by 2.0 mg/L of chloramines for contacting time of 30 min, whereas only 70% is attained with chlorine. The GC-MS examination indicates that the total organic substance is increased to 92 specie： inciuding 13 sorts of halogenated hydrocarbon by chlorine disnfection, which is more than that of chloramines. More products of bromiinated trihalomethanes occur in treated water by chlorine, disinfection and total amount of THMs is 3 times as high as that of chloramines.

Removal of Heavy Metals （Copper, Manganese and Zinc） from Industrial Wastewater of Baiji Refinery by Granular Activated Carbon

The aim of the present work is to remove heavy metals （copper, manganese, and zinc） from industrial wastewater of Baiji refinery using GAC （granular activated carbon）. The most important factors affecting adsorption process have been studied, which are granular activated carbon thickness, H, inlet pollutant concentration, Cv, and liquid hourly space velocity, LHSV. All experiments were performed under constant temperature at 25℃ and pH = 7. The experimental apparatus was designed and constructed to enable controlling of the operating conditions. Employing five levels for each of H and LHSV and three levels for Co required 75 runs for each metal. Box-Wilson method was used to reduce the number of experiments to 15 for each metal. The results indicated that copper, manganese, and zinc can be completely removed from wastewater using activated carbon. However, breakthrough time for zinc is low. It is also shown that breakthrough time （TB） and exhaustion time （TE） are inversely proportional with pollutant concentration and LHSV （liquid hour space velocity） while it is directly proportional with the thickness of activated carbon column.

Interactions between H_(2)O_(2)and dissolved organic matter during granular activated carbon-based residual H_(2)O_(2)quenching from the upstream UV/H_(2)O_(2)process

Granular activated carbon(GAC)filtration can be employed to synchronously quench residual H_(2)O_(2)from the upstream UV/H_(2)O_(2)process and further degrade dissolved organicmatter(DOM).In this study,rapid small-scale column tests(RSSCTs)were performed to clarify the mechanisms underlying the interactions between H_(2)O_(2)and DOM during the GAC-based H_(2)O_(2)quenching process.It was observed that GAC can catalytically decompose H_(2)O_(2),with a long-lasting high efficiency(>80%for approximately 50,000 empty-bed volumes).DOM inhibited GAC-based H_(2)O_(2)quenching via a pore-blocking effect,especially at high concentrations(10 mg/L),with the adsorbed DOM molecules being oxidized by the continuously generated·OH;this further deteriorated the H_(2)O_(2)quenching efficiency.In batch experiments,H_(2)O_(2)could enhance DOM adsorption by GAC;however,in RSSCTs,it deteriorated DOM removal.This observation could be attributed to the different·OH exposure in these two systems.It was also observed that aging with H_(2)O_(2)and DOM altered the morphology,specific surface area,pore volume,and the surface functional groups of GAC,owing to the oxidation effect of H_(2)O_(2)and·OH on the GAC surface as well as the effect of DOM.Addi-tionally,the changes in the content of persistent free radicals in the GAC samples were insignificant following different aging processes.This work contributes to enhancing understanding regarding the UV/H_(2)O_(2)-GAC filtration scheme,and promoting the application in drinking water treatment.

Nitrate removal from groundwater using chemically modified coconut husk based granular activated carbon:characterization of the adsorbent,kinetics and mechanism

In this study,a highly porous chemically activated granular activated carbon(GAC)was prepared from coconut husk and tested as an adsorbent to remove nitrate from contaminated groundwater.The prepared GAC was characterized by Fouriertransform infrared spectroscopy(FTIR),thermogravimetric and differential thermal analysis(TGA/DTA),scanning electron microscopy(SEM)and the Brunauer-Emmett-Teller(BET)surface area(SBET)analysis.The effects of various process parameters such as initial nitrate concentration,contact time and adsorbent dose on nitrate removal efficiency(response)by the modified GAC were investigated using the statistically significant response surface methodology and Box-Behnken design of experiments.The experimental data were fitted to well-known adsorption isotherms and kinetic models to ascertain the mechanism of the adsorption process.Analysis of variance(ANOVA)was performed to determine the significance of the individual and the interactive effects of process variables on the response.The BET surface area(SBET)and micropore volume of the prepared GAC from coconut husk was 1120 m^(2)/g and 0.392 cm^(3)/g,respectively.The experimental results showed that physisorption was the main adsorption mechanism governing the process,while the rate of adsorption was limited at initial nitrate concentrations>10 mg/L.The Langmuir mono-layer adsorption isotherm best fitted the experimental data with a maximum adsorption capacity of 6.0±1.3 mg/g(~92.5%)with an adsorbent dose of 0.1 g/50 mL,an equilibrium time of 6 h at 28±2℃,and at pH 7.6(±0.2).Among the tested process variables,the adsorbent dose and initial nitrate concentration showed significant effects on the nitrate removal efficiency.

Anaerobic tapered fluidized bed reactor for starch wastewater treatment and modeling using multilayer perceptron neural network

treatability of synthetic sago wastewater was investigated in a laboratory anaerobic tapered fluidized bed reactor （ATFBR） with a mesoporous granular activated carbon （GAC） as a support material. The experimental protocol was defined to examine the effect of the maximum organic loading rate （OLR）, hydraulic retention time （HRT）, the efficiency of the reactor and to report on its steady- state performance. The reactor was subjected to a steady-state operation over a range of OLR up to 85.44 kg COD/（m^3·d）. The COD removal efficiency was found to be 92% in the reactor while the biogas produced in the digester reached 25.38 m^3/（m^3·d） of the reactor. With the increase of OLR from 83.7 kg COD/（m^3·d）, the COD removal efficiency decreased. Also an artificial neural network （ANN） model using multilayer perceptron （MLP） has been developed for a system of two input variable and five output dependent variables. For the training of the input-output data, the experimental values obtained have been used. The output parameters predicted have been found to be much closer to the corresponding experimental ones and the model was validated for 30% of the untrained data. The mean square error （MSE） was found to be only 0.0146.

Degradation kinetics and mechanism of trace nitrobenzene by granular activated carbon enhanced microwave/hydrogen peroxide system

The kinetics of thedegradation of trace nitrobenzene （NB） by a granular activated carbon （GAC） enhanced microwave （MW）/hydrogen peroxide （H202 ） systemwas studied. Effects of pH, NB initial concentration and tert-butyl alcohol on the removal efficiencywere examined. Itwas found that the reaction rate fitswell to first-order reaction kinetics in the MW/GAC/H202 process. Moreover, GAC greatly enhanced thedegradation rate of NB inwater. Under a given condition （MW power300 W, H202dosage 10 mg/L, pH 6.85 and temperature （60 ± 5）°C）, thedegradation rate of NBwas 0.05214 min 1when4 g/L GACwas added. In general, alkaline pHwas better for NBdegradation; however, the optimum pHwas 8.0 in the tested pH value range of4.0-12.0. At H202dosage of 10 mg/L and GACdosage of4 g/L, the removal of NBwasdecreasedwith increasing initial concentrations of NB, indicating that a low initial concentrationwas beneficial for thedegradation of NB. These results indicated that the MW/GAC/H202 processwas effective for trace NBdegradation inwater. Gas chromatography-mass spectrometry analysis indicated that a hydroxyl radical addition reaction anddehydrogenation reaction enhanced NBdegradation.

Fluorescence spectroscopic studies of the effect of granular activated carbon adsorption on structural properties of dissolved organic matter fractions

This work investigated the effect of granular activated carbon adsorption （GACA） on fluorescence characteristics of dissolved organic matter （DOM） in secondary effluent, by means of excitation-emission matrix （EEM） spectra, the fluorescence regional integra- tion （FRI） method, synchronous spectra, the fluorescence index defined as the ratio of fluorescence emission intensity at wavelength 450nm to that at 500nm at excitation （λex）= 370 am, and the wavelength that corre- sponds to the position of the normalized emission band at its half intensity （λ0.5）. DOM in the secondary effluent from the North Wastewater Treatment Plant （Shenyang, China） was fractionated using XAD resins into 5 fractions： hydrophobic acid （HPO-A）, hydrophobic neutral （HPO- N）, transphilic acid （TPI-A）, transphi｜ic neutral （TPI-N） and hydrophilic fraction （HPI）. Results showed that fluorescent materials in HPO-N and TPI-N were less readily removed than those in the other fractions by GACA. The relative content of fluorescent materials in HPO-A, TPI-A and HPI decreased whereas that in HPO- N and TPI-N increased as a consequence of GACA. Polycyclic aromatics in all DOM fractions were preferen- tially absorbed by GACA, in comparison with bulk DOM expressed as DOC. On the other hand, the adsorption of aromatic amino acids and humic acid-like fluorophores exhibiting fluorescence peaks in synchronous spectra by GACA seemed to be dependent on the acid/neutralproperties of DOM fractions. All five fractions had decreased fluorescence indices as a result of GACA. GACA led to a decreased λ0.5 value for HPO-A, increased ,λ0.5 values for HPO-N, TPI-A and HPI, and a consistent λ0.5 value for TPI-N.

Evaluate HAA removal in biologically active carbon filters using the ICR database

The effects of biologically active carbon(BAC)filtration on haloacetic acid(HAA)levels in plant effluents and distribution systems were investigated using the United States Environmental Protection Agency’s Information Collection Rule(ICR)database.The results showed that average HAA5 concentrations in all locations were 20.4μg·L^(-1)and 29.6μg·L^(-1)in ICR plants with granular activated carbon(GAC)and ICR plants without GAC process,respectively.For plants without GAC,the highest HAA levels were observed in the quarters of April to June and July to September.However,for plants with GAC,the highest HAA levels were observed in the quarters of April to June and January to March.This HAA level profile inversely correlated well with water temperature,or biologic activity.For GAC plants,simulated distribution samples matched well with distribution system equivalent samples for Cl3AA and THMs.For plants with and without GAC,simulated distribution samples overestimated readily biodegradable HAAs in distribution systems.The study indicated that through HAA biodegradation,GAC process plays an important role in lowering HAA levels in finished drinking water.

Pilot Study on Drinking Water Advanced Treatment by GAC-MF System

The pilot performance of the combined GAC-MF membrane process for drinking water advanced treatment was described. In the process of GAC adsorption, under the conditions of 20 min HRT and 6 m/h filtration rate, the removal efficiencies of UV_(254) and trichloromethane could reach 40% and 50% respectively and the UV_(254) and trichloromethane in system effluent was less than 0.015 cm^(-1) and 5μg/L respectively. In the post MF membrane process, MF membrane effectively retained the particles and bacteria in raw water. The effluent turbidity was less than 0.2 NTU and no bacteria were detected at all in permeate. A computer-controlled system was employed to control this system. The membrane operating parameters of backwash interval, duration and flux were studied. The backwash interval of 10-min, 20-min and 60-min was researched respectively, and the variation of trans-membrane pressure was also analyzed. Consequently short backwash interval was recommended under the same water consume.

Novel FGBAC reactor for controlling the leakage of microfauna in drinking water treatment

In order to reduce the microfauna leakage risk from a granular biological activated carbon （GBAC） reactor which employs granular activated carbon （GAC） as adsorption media in drinking water advanced treatment, a novel fiber and granular biological activated carbon （FGBAC） reactor which employs both GAC and activated carbon fiber （ACF） as adsorption media, was developed. The results showed that the species composition of microfauna leaking from FGBAC reactor is almost similar to that leaking from GBAC reactor, however the densities of microfauna leaking from FGBAC reactor is reduced by 26%-81% compared to those leaking from GBAC reactor. In addition, compared to GBAC reactor, FGBAC reactor can increase the removal efflciencies of chemical oxygen demand （COD） and turbidity by 7% and 10%, respectively, during the stable operation period of reactor.

Study on enhanced filtration for the 2-methylisoborneol removal in drinking water treatment processes

Pilot plant studies on 2-methylisoborneol(2-MIB)removal in drinking water by biological activated carbon-sand filter(BACSF)were conducted in this paper.The biological activated carbon was chosen from a BAC filter of an advanced treatment plant which has operated for 1 year.The results showed that the BACSF worked effectively when high concentrations of MIB in raw water especially in summer season.Most of the MIB was removed within 450 mm of the top packed media and the removal rate was 75.24%.The biomass on the surface of activated carbon increased to 103 nmolP/g carbon in August.In addition to MIB,turbidity,UV254 and DOC consumption value are also effectively removed by BACSF.The micro flocculation in combination with BACSF enhanced filtration test provided the evidence that the micro-flocculation made the contaminant in water forming the colloidal matter and it improved the BACSF removal ability of MIB.The optimum PACl dosage was 0.2 mg/L and the PACl contact time was 2-4 min.