Pretreatment of municipal landfill leachate by a combined process

Biodegradability enhancement of landfill leachate using air stripping followed by coagulation/ultrafiltration (UF) processes was introduced. The air stripping process obtained a removal efficiency of 88.6% for ammonia nitrogen (NH₄–N) at air-to-liquid ratio of 3500 (pH 11) for stripping 18 h. The single coagulation process increased BOD/COD ratio by 0.089 with the FeCl₃ dosage of 570 mg l^?1 at pH 7.0, and the single UF process increased the BOD/COD ratio to 0.311 from 0.049. However, the combined process of coagulation/UF increased the BOD/COD ratio from 0.049 to 0.43, and the final biological oxygen demand (BOD), chemical oxygen demand (COD), NH₄–N and colour of leachate were 1223.6 mg l^?1, 2845.5 mg l^?1, 145.1 mg l^?1 and 2056.8, respectively, when 3 kDa molecular weight cut-off (MWCO) membrane was used at the operating pressure 0.7 MPa. In ultrafiltration process, the average solution flux (J_V), concentration multiple (M_C) and retention rate (R) for COD was 107.3 l m^?2 h^?1, 6.3% and 84.2%, respectively.     

Effects of phosphorous on the stabilization of solid waste in anaerobic landfill

Anaerobic bioreactor attracted more attention in recent years because of its environmental and financial benefits. Nutrients and moisture could exert profound influences on the degradation of the pollutants and stabilization of solid waste in anaerobic landfill. The objective of this work was to investigate the effects of the activated sludge and phosphorous addition on the stabilization of solid waste. The experimental results indicated that phosphorous is the limiting nutrients in the landfill leachate; phosphorous and activated sludge simultaneously could stimulate the growth of the bacteria, enhance the attenuation of pollutants in landfill leachate and accelerate the stabilization of solid waste; the final removal efficiency of COD and NH₄⁺-N in R-C (phosphorous and activated sludge added simultaneously) was up to 95.13% and 73.4%, respectively. Therefore, phosphorous addition is an effective way to enhance the stabilization of solid waste in anaerobic landfill.     

Two-stage biodegradation coupled with ultrafiltration for treatment of municipal landfill leachate

The municipal landfill leachate was treated in a hydrolysis–acidification reactor (HAR)/aerobic bio-contact oxidation reactor (ABOR) following a pretreatment with ultrafiltration (UF) membrane. Experiments were conducted continuously for 44 days at a constant flow rate of 20 l d⁻¹ and organic loading rates (OLRs) from 0.75 to 1.5 kgCOD m⁻³ per day. The results showed that COD of the leachate steadily decreased from 20,015 mg l⁻¹ to less than 3000 mg l⁻¹, and NH₄-N decreased from 368.6 mg l⁻¹ to 259.3 mg l⁻¹ in the UF process. The COD and NH₄-N removal efficiency of HAR was 56.7% and 27.7%, and that of ABOR was 94.6% and 86.7%, respectively. The total COD and NH₄-N removal efficiency reached 99.6% and 93.2%, respectively. UF and HAR played a critical role in raising the biodegradability of the landfill leachate, while ABOR had an important function on removing the dissolved NH₄-N in leachate.     

Removal of humic substances from landfill leachate by Fenton oxidation and coagulation

In this study, chemical oxygen demand (COD) was characterized as total organic constituents and the isolated humic substances (HS) were characterized as an individual organic contaminant in landfill leachate. It was found that the HS content of landfill leachate was 83.3%. The results of laboratory tests to determine the roles of HS in reducing the organic content of landfill leachate during Fenton process are presented. Furthermore, the performances of oxidation and coagulation of Fenton reaction on the removal of HS and COD from leachate were investigated. The change curves of HS removal were similar to those of COD. The HS removal was 30% higher than COD removal, which indicated that HS were mostly degraded into various intermediate organic compounds but not mineralized by Fenton reagent. The oxidation removal was greatly influenced by initial pH relative to the coagulation removal. The oxidation and coagulation removals were linear dependent with hydrogen peroxide and ferrous dosages, respectively. Ferrous dosage greatly influenced the coagulation removal of COD at low ratio ([H₂O₂]/[Fe²⁺] < 3.0), but not at extremely high ratio ([H₂O₂]/[Fe²⁺] > 6.0). The coagulation removal of HS was not affected obviously by oxidation due to both Fenton oxidation and coagulation remove high molecular weight organics preferentially. Higher temperature gave a positive effect on oxidation removal at low Fe²⁺ dosage, but this effect was not obvious at high Fe²⁺ dosage.     

Partial nitritation of landfill leachate with varying influent composition under intermittent aeration conditions

The start-up and operation of a partial nitritation sequencing batch reactor for the treatment of landfill leachate were carried out on intermittent aeration mode. Partial nitrite accumulation was established in 15 days after the mode was changed from continuous aeration to intermittent aeration. Despite the varying influent composition, partial nitritation could be maintained by adjusting the hydraulic retention time (HRT) and the air flow rate. An increase in the air flow rate together with a decrease in air off duration can improve the partial nitritation capacity and eventually result in the development of granular sludge with fine diameters. A nitrogen loading rate of 0.71 ± 0.14 kg/m³/d and a COD removal rate of 2.21 ± 0.13 kg/m³/d were achieved under the conditions of an air flow rate of 19.36 ± 1.71 m³ air/m³/h and an air on/off duration of 1.5 min/0.7 min. When the ratio of total air flux (TAF) to the influent loading rate (ILR) was controlled at the range of 163–256 m³ air/kg COD, a stable effluent NO₃^?–N/NO_x^?–N (NO₂^?–N plus NO₃^?–N) ratio below 13% was achieved. Interestingly, the effluent pH was found to be a good indicator of the effluent NO₂^?–N/NH₄⁺–N ratio, which is an essential parameter for a subsequent anaerobic ammonium oxidation (Anammox) reactor.     

A novel pretreatment process of mature landfill leachate with ultrasonic activated persulfate: Optimization using integrated Taguchi method and response surface methodology

A novel advanced oxidation process (AOP) using ultrasonic activated persulfate oxidation was used to pretreat mature landfill leachate. The effects of different operating variables (e.g., the initial S₂O₈²⁻ concentration, pH, temperature, ultrasonic power and reaction time) on the oxidation performance were investigated regarding the total organic carbon (TOC) removal efficiency, and the variables were optimized using the integrated Taguchi method and response surface methodology (RSM). Based on the Taguchi method under L₁₆ (4⁵) arrays and a grey relational analysis, the most significant variables included the initial S₂O₈²⁻ concentration, temperature and reaction time. The concentrations of these variables were further optimized using RSM. Using the integrated optimization method, the optimal conditions included an initial S₂O₈²⁻ concentration of 8.5 mM, a reaction temperature of 70 °C and a reaction time of 2.46 h, which resulted in a TOC removal efficiency of 77.32%. The experimental results showed that the enhanced TOC removal from mature landfill leachate by sono-activated persulfate oxidation could be attributed to the combined effects of ultrasonic catalysis and sulfate radical-AOP. Overall, ultrasonic activated persulfate oxidation is a promising method for the pretreatment of landfill leachate.     

Effects of heavy metals on planting watercress in kailyard soil amended by adding compost of sewage sludge

Mixture of sewage sludge with organic garbage was alternatively composted by aerobic and anaerobic technology for 60 days. A basin-scale experiment was performed by planting watercress with kailyard (KY) soil amended with the compost. The results show that average total organic carbon (TOC) increases from 98.45% to 787.69%, and average total nitrogen (TN), total phosphorus (TP) and total potassium (TK) increases to 98.53%, 27.34%, and 41.62%, respectively. The results of watercress in 6 pot experiments with a control treatment show that biomass production increases from 76.47% to 312.00% with the increase of addition of compost from 50 g to 150 g per pot but decreases from 312.00% to 102.29% with the addition of compost to soil and further increases from 150 g to 400 g per pot. The optimal amount of compost added to KY soil is 0.4 g of compost 1 kg of KY soil. Heavy metals accumulated by watercress demonstrate that Cu, Ni, Cd, Pb, Cr, Zn in the crop are much lower than the limited levels of Chinese criteria for vegetables. KY soil is proper to be amended with compost of sewage sludge without threat of bio-magnification of heavy metals to planting watercress.     

Achieving stable partial nitritation using endpoint pH control in an SBR treating landfill leachate

The feasibility of using endpoint pH control to achieve stable partial nitritation (PN) in an SBR for landfill leachate treatment was investigated. By imposing a fixed-time anoxia followed by variable-time aeration in an SBR cycle, successful partial nitritation was maintained for 182 days at a nitrogen loading rate of 0.30–0.89 kg/m³/day. The effluent NO₂⁻-N/NH₄⁺-N ratio and the effluent NO₃⁻-N concentration were 1.30 ± 0.22 and 16 ± 9 mg/L, respectively. High free ammonia (FA) and low dissolved oxygen (DO) concentrations were inhibition factors of nitrate formation. The termination of aeration at a suitable endpoint pH was the key to achieve an effluent NO₂⁻-N/NH₄⁺-N ratio close to the stoichiometric value. This endpoint pH control strategy represents practical potentials in the engineered application of combined PN–ANAMMOX processes.     

High nitrite accumulation and strengthening denitrification for old-age landfill leachate treatment using an autocontrol two-stage hybrid process

An autocontrol two-stage hybrid process was developed to treat landfill leachate. Biological nitrogen removal with nitrification and denitrification via nitrite pathway was split into two stages. The first stage was designed for the high nitrite accumulation and was composed of two hybrid bed reactors (Hybrid I and Hybrid II) and a coagulation–flocculation reactor having effective volumes of 120 L and 80 L, respectively. The second stage was designed for strengthening denitrification and included a single 80 L reactor. The carriers of the hybrid bed reactors were composed of fixed multiple flexible carriers and suspended particle carriers. Dissolved oxygen (DO), pH value, oxidation–reduction potential (ORP) and temperature were used as online fuzzy control parameters of the automatic control system. The concentration of nitrite in Hybrid I and Hybrid II could reach 411 mg L⁻¹ and 604 mg L⁻¹, respectively. Ammonia removal has reached maximal rates of 0.061 kgNH₄⁺-N (m³ h)⁻¹ and 0.041 kgNH₄⁺-N (m³ h)⁻¹, respectively. A maximum nitrite removal rate of 0.211 kgNO₂⁻-N (m³ h)⁻¹ was observed during the strengthening denitrification. The running time of one cycle was not fixed and was actually controlled by the system. The results indicated that the running period was more closely related to influent ammonia concentration than influent COD concentration. The aeration times could be shortened and the energy could be saved. The autocontrol two-stage hybrid process is therefore an economical and effective way for landfill leachate treatment.     

On–off control of aeration time in the simultaneous removal of ammonia and manganese using a biological aerated filter system

The biological aerated filter (BAF) system, a new alternative in drinking water treatment, was designed to remove NH₄⁺–N and Mn²⁺ simultaneously. This study aimed to control the aeration time in the BAF system for simultaneous NH₄⁺–N and Mn²⁺ removal to achieve the Malaysian effluent quality regulation for drinking water. The experiment was conducted under four strategies of S1, S2, S3 and S4. The results demonstrated that acceptable levels of NH₄⁺–N and Mn²⁺ were achieved over a 6 h aeration period (S1), producing effluent concentrations of 0.7 mg/L (93.2% removal) and 0.08 mg/L (79.6% removal), respectively. At the initial treatment of S1 and S2, the dissolved oxygen (DO) level rapidly increased until it reached a saturated concentration (6.8 mg/L DO) after 2 h period. Automatic on–off aeration time to maintain 3 mg/L DO set point (S4) resulted with a good effluent quality of NH₄⁺–N and Mn²⁺ compared with the 2 mg/L DO set point (S3) which did not meet the regulated standard limits. Through the automatic on–off aeration time, the saturated and excessive DO levels in the BAF system can be avoided consequently reduce the wastage of energy and electrical consumption for simultaneous NH₄⁺–N and Mn²⁺ removal from drinking water treatment.     

Investigation of affecting parameters on treating high-strength compost leachate in a hybrid EGSB and fixed-bed reactor followed by electrocoagulation–flotation process

In this research, treatability of high-load compost leachate in a hybrid expanded granular sludge bed (EGSB) and fixed-bed (FB) bioreactor followed by electrocoagulation–flotation (ECF) system was examined. The operational factors in EGSB–FB were influent chemical oxygen demand (COD), hydraulic retention time (HRT) and COD/nitrogen ratio (COD/N). And, their interactive effects on the efficiency of COD removal and biogas production rate (BPR) as responses were analyzed and correlated by response surface methodology (RSM). The optimum conditions of the hybrid EGSB–FB reactor were acquired at COD = 7800 mg/L, HRT = 35 h, COD/N = 70, in which COD removal efficiency was 83% and BPR 94 mL/h. The amount of confidence interval was 95%. COD (relevant coefficient = 9.8) and HRT (relevant coefficient = −24) were resulted respectively as the most effective parameters on COD removal and BPR. Yet, COD/N parameter imposed negative effect on COD removal and BPR in values less than about 100. The outcomes indicated that operated ECF as post-treatment in constant conditions (electrolysis time = 75 min, electrodes distance = 3 cm, voltage = 20 V) successfully satisfied discharge criteria in the most part of experimental domains.     

Use of advance oxidation process to improve the biodegradability of olive oil mill effluents

In this study, recalcitrant total phenol (TPh) and organic matter removal were investigated at olive mill wastewater (OMW) in sequential Coagulation and Fenton system. This study focused on different operational parameters such as pH, H₂O₂, and Fe²⁺ dosages, and [Fe²⁺]/[H₂O₂] ratios. The optimum conditions were determined as; pH = 3; [Fe²⁺] = 2.5 g/L; [Fe²⁺]/[H₂O₂] = 2.5. A higher treatment efficiency was achieved at sequential Coagulation and Fenton system (COD, 65.5%) and TPh, 87.2%), compared to coagulation process (COD, 51.4%; total organic carbon (TOC), 38.6% and total nitrogen (TN) 52.1%). This study demonstrated that the Coagulation and Fenton process has a potential for efficient removal of phenolic pollutants from wastewater.     

Cushioning the impact of toxic release from runaway industrial accidents with greenbelts

The three aspects of accidents in chemical process industries which cause most serious damage—explosions, fires, and toxic releases—can all be controlled to some extent if greenbelts are present around the affected industry. We have recently developed and validated a system of methodologies for greenbelt design. In this paper we present the application of these models in designing greenbelts and forecasting their role in cushioning the impact of accidental release of toxic gases. With properly located and designed greenbelts as much as 33% of the accidental release of SO₂, 43% of H₂S, and 51% of NH₃ under stable atmospheric conditions (in which the dispersion is very slow and the release thus has maximum toxic impact) can be absorbed.     

Preparation of a metal-phosphate/chromium oxide nanocomposite from Cr(III)-containing electroplating sludge and its optical properties as a nanopigment

A nanocomposite composed of metal-phosphates and chromium oxide was prepared from a Cr(III)-containing electroplating sludge (CES) by a facile three-step (extraction–precipitation–calcination) process. Optimal process parameters were determined, and the structure of the metal-phosphate/chromium oxide nanocomposite (MPCON) was investigated by field-emission scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The results show that the optimal extraction pH is 2.0. The MPCON presents a polyhedral morphology with average particle size of around 100 nm. The components of MPCON vary from AlPO₄/Cr₂O₃ to Mg₃(PO₄)₂/AlPO₄/Cr₂O₃ at different solution pH during precipitation. Meanwhile, the optical performance of the nanocomposite as a pigment is discussed. The reflectance of MPCON-6.5 in the near-infrared range is around 56%, making it a strong prospect to be used as a functional pigment in energy-efficient buildings. This study proposes a novel recycling process for the conversion of CES into high-value products, which is beneficial for the treatment of waste.     

Study into influence of different types of igniters on the explosion parameters of dispersed nitrocellulose powder

Nitrocellulose is a flammable compound produced by cellulose nitration. The nitrocellulose production and handling are associated with a risk of fire and explosion. Nitrocellulose is used as either collodion cotton (<12.5% N) or as an explosive (>12.5% N). Nitrocellulose is a fibrous or powdered substance and may detonate or burn upon certain conditions. The article compares the combustion parameters of dry nitrocellulose in the KV-150M2-UIBE explosion chamber at the concentrations of 250, 500 and 750 g m⁻³. To ignite a nitrocellulose sample, six different types of igniters were used. A commercially available 5 kJ pyrotechnic igniter was used as the standard. Also used were a nitrocellulose igniter, a pyrotechnic igniter with magnesium powder and KNO₃/KClO₃, and an exploding wire (Kanthal and tungsten wire). The examined igniters were found to affect the explosion parameters of dispersed nitrocellulose. The deviation of the explosion constant K_st reached 50% of the standard value. The highest pressure of 12.73 bar g was reached at a concentration of 750 g m⁻³ and an igniter exploding wire with Kanthal wire. The highest K_st value of 287.9 bar.m.s⁻¹ was achieved at a concentration of 750 g m⁻³, when using the pyrotechnic igniter with KClO₃ and magnesium powder.     

Life cycle analysis of a biogas-centred integrated dairy farm-greenhouse system in British Columbia

This study investigates the potential integration of a dairy farm and a greenhouse into an eco-industrial system to promote waste-to-energy and waste-to-material exchanges. Natural gas consumption is substituted by renewable biogas generated from anaerobic digestion (AD) of the dairy manure; CO₂ for plant enrichment in greenhouses is supplied by biogas combustion and the digestate (digestion residue) from digesters is used as animal bedding, plant growing media and liquid fertilizers.A life cycle analysis (LCA) was conducted to quantify the environmental impacts of the eco-industrial system in comparison to the conventional agriculture practices. The results show that the integrated system reduces non-renewable energy consumption, climate change impact, acidification, respiratory effects from organic emissions, and human toxicity by more than 40%. If the digestate surplus is treated as a waste, the integrated system shows an increase in eutrophication and respiratory effects from inorganic emissions while all the analyzed impacts are reduced if the digestate can be used for substituting chemical fertilizers.     

Comparisons of TGA and DSC approaches to evaluate nitrocellulose thermal degradation energy and stabilizer efficiencies

This study investigated the thermal degradation energy (activation energy, E_a) for nitrocellulose (NC) with low nitrogen content of 11.71 mass%, so-called NC3, by using two different kinds of thermal analysis instruments: thermogravimetric analyzer (TGA) and differential scanning calorimetry (DSC). A comparison of E_a for various nitrogen content NC samples at two scanning rates (5 and 10 °C min^?1) tested by TGA and DSC is also discussed in this paper. Meanwhile, our aim was to analyze the anti-degradation of E_a for NC with high nitrogen content, as so-called NC1. Thermal stability for NC1 with diphenylamine (DPA) was tested via DSC with 10 DPA concentrations in weights of 0, 0.25, 0.50, 0.75, 1.0, 1.25, 1.50, 1.75, 2.0, and 3.0 mass%. Experimental results indicated that E_a of NC3s was 319.91 kJ mol^?1. Moreover, that while dosing DPA into NC1 the best recipe could be employed to avoid any violent NC1 runaway and also can be used to distinguish the differences of thermal decomposition E_a between NC with different nitrogen contents. This study established a fast and efficient procedure for thermal decomposition properties of NC, and could be applied as an intrinsically safer design during relevant operations.     

Oxidation of kerosene components in a soil matrix by a dielectric barrier discharge reactor

This paper discusses some aspects of the kerosene components oxidation in a soil matrix by a dielectric barrier discharge reactor at atmospheric pressure. The total kerosene components abatement can reaches 90% for an energy density of 960 J g_soil^?1. The analyses of the discharge cell outlet gas reveals that CO_x and hydrocarbon compounds selectivity is close to 10%. A semi-quantitative approach by GC-FID shows that the carbon content in the oxidized compounds in soil is about 20% of the carbon content in the initial kerosene components. The polar species formed in soil are a mixture of aliphatic and aromatic molecules containing alcohol and carboxylic acid groups. The process of kerosene oxidation in soil matrix is more promoted than kerosene desorption followed by an oxidation in gas phase.     

Effect of pyrolysis and oxidation characteristics on lauric acid and stearic acid dust explosion hazards

The effect of pyrolysis and oxidation characteristics on the explosion sensitivity and severity parameters, including the minimum ignition energy MIE, minimum ignition temperature MIT, minimum explosion concentration MEC, maximum explosion pressure P_max, maximum rate of pressure rise (dP/dt)_max and deflagration index K_st, of lauric acid and stearic acid dust clouds was experimentally investigated. A synchronous thermal analyser was used to test the particle thermal characteristics. The functional test apparatuses including the 1.2 L Hartmann-tube apparatus, modified Godbert-Greenwald furnace, and 20 L explosion apparatus were used to test the explosion parameters. The results indicated that the rapid and slow weight loss processes of lauric acid dust followed a one-dimensional diffusion model (D1 model) and a 1.5 order chemical reaction model (F1.5 model), respectively. In addition, the rapid and slow weight loss processes of stearic acid followed a 1.5 order chemical reaction model (F1.5 model) and a three-dimensional diffusion model (D3 model), respectively, and the corresponding average apparent activation energy E and pre-exponential factor A were larger than those of lauric acid. The stearic acid dust explosion had higher values of MIE and MIT, which were mainly dependent on the higher pyrolysis and oxidation temperatures and the larger apparent activation energy E determining the slower rate of chemical bond breakage during pyrolysis and oxidation. In contrast, the lauric acid dust explosion had a higher MEC related to a smaller pre-exponential factor A with a lower amount of released reaction heat and a lower heat release rate during pyrolysis and oxidation. Additionally, due to the competition regime of the higher oxidation reaction heat release and greater consumption of oxygen during explosion, the explosion pressure P_m of the stearic acid dust was larger in low concentration ranges and decayed to an even smaller pressure than with lauric acid when the concentration exceeded 500 g/m³. The rate of explosion pressure rise (dP/dt)_m of the stearic acid dust was always larger in the experimental concentration range. The stearic acid dust explosion possessed a higher P_max, (dP/dt)_max and K_st mainly because of a larger pre-exponential factor A related to more active sites participating in the pyrolysis and oxidation reaction. Consequently, the active chemical reaction occurred more violently, and the temperature and overpressure rose faster, indicating a higher explosion hazard class for stearic acid dust.     

Experimental study on the suppression of gas explosion using the gas–solid suppressant of CO2/ABC powder

Gas explosion is the leading accident in underground coal mining in China. Using the self-improved 20 L spherical experimental system, the impacts of 8% CO₂, ABC powder at various concentrations and mixture of them on the suppression of mine gas explosion were investigated. The results indicate that cooperative synergism exists between ABC powder and CO₂. Their combination has a better effect than each of the two components acting alone, especially for the gas of larger concentration. When 0.25 g/L ABC powder was mixed with 8% CO₂, the explosion limits were reduced by about 55%, the time to reach the peak explosion pressure was prolonged 3.56 times on average. Meanwhile, the maximum explosion pressure declined on an average of 59.4% and the maximum explosion overpressure rising rate decreased on an average of 91.1%. A combination of 0.20 g/L ABC powder and 8% CO₂ completely suppressed 11% gas explosion. The explosion suppression mechanism of CO₂ and ABC powder were probed theoretically. CO₂ plays a key part in the whole explosion processes, and it can effectively suppress the forward reaction between gas and oxygen. While it is during the middle-later period of explosion processes that ABC powder plays a critical role. The particles decomposed from heated ABC powder such as nitrogen and phosphor will react with free radicals rapidly. Besides, atoms as N, P are capable of participating in chain reaction and reacting with active groups, significantly suppressing the gas explosion.