Supercritical water oxidation for the destruction of toxic organic wastewaters:A review

The destruction of toxic organic wastewaters from munitions demilitarization and complex industrial chemical clearly becomes an overwhelming problem if left to conventional treatment processes. Two options, incineration and supercritical water oxidation （SCWO）, exist for the complete destruction of toxic organic wastewaters. Incinerator has associated problems such as very high cost and public resentment; on the other hand, SCWO has proved to be a very promising method for the treatment of many different wastewaters with extremely efficient organic waste destruction 99.99% with none of the emissions associated with incineration. In this review, the concepts of SCWO, result and present perspectives of application, and industrial status of SCWO are critically examined and discussed.

Degradation mechanism of 2,4,6-trinitrotoluene in supercritical water oxidation

The 2,4,6-trinitrotoluene （TNT） is a potential carcinogens and TNT contaminated wastewater, which could not be effectively disposed with conventional treatments. The supercritical water oxidation （SCWO） to treat TNT contaminated wastewater was studied in this article, The TNT concentration in wastewater was measured by high-performance liquid chromatograph （HPLC） and the degraded intermediates were analyzed using GC-MS. The results showed that SCWO could degrade TNT efficiently in the presence of oxygen. The reaction temperature, pressure, residence time and oxygen excess were the main contributing factors in the process. The decomposition of TNT was accelerated as the temperature or residence time increased. At 550℃, 24 MPa, 120 s and oxygen excess 300%, TNT removal rate could exceed 99.9%. Partial oxidation occured in SCWO without oxygen. It was concluded that supercritical water was a good solvent and had excellent oxidation capability in the existence of oxygen. The main intermediates of TNT during SCWO included toluene, 1,3,5-trinitrobenzene, nitrophenol, naphthalene, fluorenone, dibutyl phthalate, alkanes and several dimers based on the intermediate analysis. Some side reactions, such as coupled reaction, hydrolysis reaction and isomerization reaction may take place simultaneously when TNT was oxidized by SCWO.

Decomposition kinetics of dimethyl methylphospate(chemical agent simulant) by supercritical water oxidation

Supercritical water oxidation （SCWO） has been drawing much attention due to effectively destroy a large variety of high-risk wastes resulting from munitions demilitarization and complex industrial chemical. An important design consideration in the development of supercritical water oxidation is the information of decomposition rate. In this paper, the decomposition rate of dimethyl methylphosphonate（DMMP）, which is similar to the nerve agent VX and GB（Sarin） in its structure, was investigated under SCWO conditions. The experiments were performed in an isothermal tubular reactor with a H2O2 as an oxidant. The reaction temperatures were ranged from 398 to 633℃ at a fixed pressure of 24 MPa. The conversion of DMMP was monitored by analyzing total organic carbon （TOC） on the liquid effluent samples. It is found that the oxidative decomposition of DMMP proceeded rapidly and a high TOC decomposition up to 99.99% was obtained within 11 s at 555℃. On the basis of data derived from experiments, a global kinetic equation for the decomposition of DMMP was developed. The model predictions agreed well with the experimental data.

Effects of oxidants on the degradation of tributyl phosphate under supercritical water oxidation conditions

The effects of additional oxidants,such as NaNO_(3),Na_(2)S_(2)O_(3),KClO_(4),and K_(2)Cr_(2)O_(7),on the supercritical water oxidation(SCWO)of tributyl phosphate(TBP)were studied.The coupling of an ionic oxidant with SCWO can effectively enhance the oxidative degradation ability of the system,thus increasing its organic-matter-removal efficiency at a reduced reaction temperature.Moreover,the addition of NaNO_(3),KClO_(4),or K_(2)Cr_(2)O_(7)could improve this efficiency at a reaction temperature of 500℃compared with that of the original system at 550℃.Additionally,based on the conditions adopted in this study,the addition of either of these oxidants could reduce the final total organic carbon(TOC)of the effluent from~500 to<100 ppm.Concurrently,the ionic oxidants could effectively improve the processing capacity of the SCWO system to reduce the scale of the equipment,as well as the amount of produced wastewater.Compared with KClO_(4)and Na_(2)S_(2)O_(3),the addition of 10 mmol/L NaNO_(3)and K_(2)Cr_(2)O_(7)to the organic feed could increase the processing capacity of the system from 4 to 10%while maintaining the TOC removal at>99%.The effects of the ionic oxidants on the gas products,including CO_(2),CO,H_(2),and CH_(4),as well as other organic gases,have also been studied.Among these gas products,CO_(2)accounted for the main gas product with a proportion of more than half.At<500℃,temperature significantly affected the as products(CO,H_(2),CH_(4),and other organic gases).However,the gas product was mainly CO_(2)when the temperature was increased to≥500℃.This study initially revealed the enhancement effect of ionic oxidants on SCWO,which still requires further research.

Electrochemical Oxidation of Chlorimuron-ethyl on Ti/SnO_2-Sb_2O_5/PbO_2 Anode for Waste Water Treatment

The electrochemical oxidation of chlorimuron-ethyl on metry. The electrochemical behaviour of the electrode in a sodium Ti/SnO2-Sb2O5/PbO2 electrode was studied by cyclic voltamsulfate solution and in the mixture solution of sodium sulfate and chlorimuron-ethyl was studied. The experimental results of cyclic voltammetry show that the acidic medium was suitable for the efficient electrochemical oxidation of chlorimuron-ethyl. Some electro-generated reagent was formed in the electrolysis process and chlorimuron-ethyl could be oxidized by the electro-generated reagent. A Ti/SnO2-Sb2O5/PbO2 electrode was used as the anode and the electrolysis experiment was carried out under the optimized conditions. The electrolysis process was monitored by UV-Vis spectrometry and high performance liquid chromatography（HPLC）, and the chemical oxygen demand（COD） was determined by the potassium dichromate method. The mechanism of chlorimuron-ethyl to be oxided was studied primarily by the cyclic voltammetry and UV-Vis spectrometry. The results of electrolysis experiment demonstrate the possibility of the electrode to be used as an anode for the electrochemical treatment of chlorimuron-ethyl contained in waste water.

Decomposition of oil cleaning agents from nuclear power plants by supercritical water oxidation

Oil cleaning agents generated from nuclear power plants(NPPs)are radioactive organic liquid wastes.To date,because there are no satisfactory industrial treatment measures,these wastes can only be stored for a long time.In this work,the optimization for the supercritical water oxidation(SCWO)of the spent organic solvent was investigated.The main process parameters of DURSET(oil cleaning agent)SCWO,such as temperature,reaction time,and excess oxygen coefficient,were optimized using response surface methodology,and a quadratic polynomial model was obtained.The determination coefficient(R^(2))of the model is 0.9812,indicating that the model is reliable.The optimized process conditions were at 515 C,66 s,and an excess oxygen coefficient of 211%.Under these conditions,the chemical oxygen demand removal of organic matter could reach 99.5%.The temperature was found to be the main factor affecting the SCWO process.Ketones and benzene-based compounds may be the main intermediates in DURSET SCWO.This work provides basic data for the industrialization of the degradation of spent organic solvents from NPP using SCWO technology.

Treatment of Acetonitrile by Catalytic Supercritical Water Oxidation in Compact-Sized Reactor

The objective of this research was to study the treatment of acetonitrile by catalytic supercritical water oxi-dation in a compact-sized tubular reactor, with an internal volume of 4.71 mL. Manganese dioxide was used as the catalyst and H2O2 was used as the oxidant. The oxidation of acetonitrile in supercritical water was studied at 400-500 oC, 25-35 MPa, the flow rate of 2-4 mL/min, the initial concentration of acetonitrile 0.077-0.121 M and the %excess O2 of 50-200%. As a result, the products were mainly N2, CO2 and CO and acetonitrile can be decomposed > 93 % within a very short contact time (1.45-6.19 s). The oxidation process was carried out with respect to the conversion of acetonitrile by 25 factorial design. Regression models were obtained for correlating the conversion of acetonitrile with temperature and flow rate. The complete oxida-tion can be achieved at a condition as moderate as 400 oC, 25 MPa with the flow rate of 2 mL/min.

COD Removal Efficiencies of Some Aromatic Compounds in Supercritical Water Oxidation

Some aromatic compounds, phenol, aniline and nitrobenzene, were oxidized in supercritical water. It was experimentally found that the chemical oxygen demand (COD) removal efficiency of these organic compounds can achieve a high level more than 90% in a short residence time at temperatures high enough. As temperature, pressure and residence time increase, the COD removal efficiencies of the organic compounds would all increase. It is also found that temperature and residence time offer greater influences on the oxidation process than pressure. The difficulty in oxidizing these three compounds is in the order of nitrobenzene ＞ aniline ＞ Phenol. In addition, it is extremely difficult to oxidize aniline and nitrobenzene to CO2 and H2O at the temperature lower than 873.15 K and 923.15 K, respectively. Only at the temperature higher than 873.15 K and 923.15 K, respectively, the COD removal efficiencies of 90% of aniline and nitrobenzene can be achieved.

Supercritical water oxidation of spent extraction solvent simulants

The rapid development of nuclear technology has led to more liquid organic radioactive wastes. Different from the regular aqueous radioactive wastes, these liquids possess a higher hazard potential and cannot be disposed through the conventional methods due to their radioactivity and chemical nature. Spent extraction solvent is a kind of common liquid organic radioactive wastes. In this work, tri-butyl phosphate(TBP), which is more difficult to degrade in the spent extraction solvent, was used as the model compound. Influences of reaction conditions on total organic carbon(TOC) removal and the volume percentage of each gas component under supercritical water oxidation(SCWO) were studied. The SCWO behaviors of spent extraction solvent simulants were studied under the optimal conditions derived from the TBP experiment. The SCWO experiments were studied at 400–550℃, oxidant stoichiometric ratio of 0–200%, feed concentration of 1.5%–4% and pressure of25 MPa for 15–75 s. The results show that the TOC removal of the simulants was greater than 99.7% and CH4,H2 and CO were not detected at 550℃, 25 MPa, oxidant stoichiometric ratio of 150%, feed concentration of3%, and residence time of 30 s.

Corrosion of titanium in supercritical water oxidation environments

Supercritical water oxidation (SCWO) can effectively destroy many kinds of civilian and military wastes. The high temperature and high pressure SCWO operation conditions generate very corrosive environment that many engineering materials fail to withstand. Preliminary test shows that titanium may be a promising material in most of SCWO conditions. Commercially pure titanium is tested in four kinds of SCWO environments. Phenol, sodium dodecyl benzosulfonate, n amine phenol, and chlorpyrifos were chosen as typical target pollutants. The results show that titanium is only superficially attacked in the first three SCWO environments while in chlorpyrifos SCWO medium titanium is corroded. The corrosion is temperature dependent, with heavier corrosion occurring at near critical temperature. X ray diffraction analysis shows that the corrosion products consist of titanium oxy phosphates and titanium oxide, in which Ti 5O 4(PO 4) 4 is the main phase.

Supercritical water oxidation of polyvinyl alcohol and desizing wastewater: Influence of NaOH on the organic decomposition

Polyvinyl alcohol is a refractory compound widely used in industry. Here we report supercritical water oxidation of polyvinyl alcohol solution and desizing wastewater with and without sodium hydroxide addition. However, it is difficult to implement complete degradation of organics even though polyvinyl alcohol can readily crack under supercritical water treatment. Sodium hydroxide had a significant catalytic effect during the supercritical water oxidation of polyvinyl alcohol. It appears that the OH ion participated in the C-C bond cleavage of polyvinyl alcohol molecules, the CO2-capture reaction and the neutralization of intermediate organic acids, promoting the overall reactions moving in the forward direction. Acetaldehyde was a typical intermediate product during reaction. For supercritical water oxidation of desizing wastewater, a high destruction rate （98.25%） based on total organic carbon was achieved. In addition, cases where initial wastewater was alkaline were favorable for supercritical water oxidation treatment, but salt precipitation and blockage issues arising during the process need to be taken into account seriously.

Destruction of methylphosphonic acid in a supercritical water oxidation bench-scale double wall reactor

The destruction of methylphosphonic acid （MPA）, a final product by hydrolysis/neutralization of organophosphorus agents such as sarin and VX （O-ethyl S-[2-（diisopropylamino）ethyl] methylphosphonothionate）, was investigated in a a bench-scale, continuous concentric vertical double wall reactor under supercritical water oxidation condition. The experiments were conducted at a temperature range of 450–600°C and a fixed pressure of 25 MPa. Hydrogen peroxide was used as an oxidant. The destruction efficiency （DE） was monitored by analyzing total organic carbon （TOC） and MPA concentrations using ion chromatography on the liquid effluent samples. The results showed that the DE of MPA up to 99.999% was achieved at a reaction temperature of 600°C, oxygen concentration of 113% storichiometric requirement, and reactor residence time of 8 sec. On the basis of the data derived from experiments, a global kinetic rate equation for the DE of MPA and DE of TOC were developed by nonlinear regression analysis. The model predictions agreed well with the experimental data.

Waste Management in Propylene Epoxidation Process with the Use of Supercritical Fluid Media

Experimental results on solubility of the styrene, phenol, methylphenylcarbinol, acetophenone, ethyl benzene, propylene glycol and molybdenum as a complex with Trilon B in supercritical CO2 obtained using a dynamic (flow) method are presented. The obtained data are described in the framework of Peng-Robinson equation. The results of the experients on the extraction of organic components from waste formed in the olefin epoxidation process at Nizhnekam-skneftekhim Inc., on the analysis of extract composition, and on the testing of the extract as an epoxidation catalyst are presented. The supercritical water oxidation (SCWO) process of epoxidation process waste was conducted in periodical and continuous mode. The analysis results of reaction product are given. Pilot experiments on dry sediment formation were conducted using Radio Frequency (RF) Inductively Coupled Plasma (ICP) of low pressure.

Oxidation behavior of ferritic/martensitic steels in flowing supercritical water

The oxidation behavior of two Ferritic/Martensitic(F/M)steels including novel SIMP steel and commercial P91 steel were investigated by exposure to flowing deaerated supercritical water(SCW)at 700℃for up to 1000 h.The kinetic weight gain curves follow parabolic and near-cubic rate equations for SIMP and P91 steels,respectively.X-Ray Diffraction analysis showed the presence of magnetite and a spinel phase in flowing SCW for both steels.The morphology and structure of the oxide scales formed on these two steels were analyzed.The relationship between the microstructure and oxidation behavior and the reason that SIMP steel showed better oxidation resistance than P91 steel were discussed.

Supercritical Water Technology Applied to the Purification of Waters Contaminated by Toxic Micro-Polluting Organic Compounds

Purification of water contaminated by toxic organic compounds at low and very low concentration is a quite interesting challenge from both the technical and the economical point of view. In fact, the direct destruction of organic compounds dissolved in very diluted aqueous solution is very costly and hardly achievable. To overcome this problems it was studied and developed a new water purification process which is made of three steps: a) removal of the diluted and toxic polluting compounds by adsorption on activated carbon beds operating at ambient P ant T;b) regeneration of the exhausted carbon bed with supercritical water in order to obtain a mixture of water and polluting compounds signifi-cantly more concentrated than the contaminated liquid water;c) destruction of the toxic compounds in a continuous Supercritical Water Oxidation Reactor. Step a) was studied at laboratory scale in order to obtain all the required information for modeling the adsorption operation;step b) was modeled by using literature experimental data and, step c) was validated at pilot plant scale. In all the above mentioned steps, phenol was used as representative of polluting compounds.

Corrosion of candidate materials for supercritical water-cooled reactor

Supercritical water reactor(SCWR) was proposed as a GenerationⅣconcept for building large capacity nuclear power plants.Comparing with the present GenerationⅡandⅢlight water reactors,SCWR possesses great advantages of 10%higher efficiency,simpler system design,better sustainability,and so on. However,the selection of materials for fuel cladding and reactor internals of SCWR is facing a great challenge. Corrosion in supercritical steam is of the first important issue to be solved to meet the stringent requirement of the reactor internal components.Corrosion screening tests were conducted on candidate materials for nuclear fuel cladding and reactor internals of supercritical water reactor(SCWR) in static and re-circulating autoclave at the temperatures of 550,600 and 650℃,pressure of about 25 MPa,deaerated or saturated dissolved hydrogen(STP). Nickel base alloy type Hastelloy C276,austenitic stainless steels type 304NG,AL-6XN,HR3C.NF709 and SAVE 25,ferritic/martensitic(F/M) steel type P92,P122 and 410,and oxide dispersion strengthened steel MA 956,are tested.This paper presents corrosion rate,and focuses on the formation and breakdown of corrosion oxide film,and proposes the future trend for the development of SCWR internal structure materials.

The Combination of Coagulation-Flocculation Method and the SCWO in the Waste Water Treatment Problems

The influence of the degree of wastewater coagulation-flocculation and supercritical water oxidation (SCWO) methodsisconsidered. The regularities of changes in the composition of the purity of the reagents used and the parameters of SCWO are established. Based on the results of chromatographic analysis of the effluent after washing the mass rape, it is found that the achievement of the required parameters is achieved by treatment with a combination of coagulation-flocculation method and supercritical water oxidation (SCWO). The necessity of combining techniques is insufficient oxidation in SCWO lignin conducted at T = 400oC and P = 25 MPa, T = 500oC and P = 30 MPa. Effluent treatment of process of styrene and propylene oxide“Nizhnekamskneftekhim”conducted by the SCWO, using an oxidant (H2O2), and without an oxidant showed the possibility of cleaning without the use of an oxidizing agent in the process parameters T = 500oC, P = 30 MPa.

Characteristics of Oxidation and Oxygen Penetration of Alloy 690 in 600°C Aerated Supercritical Water

The oxide films formed on Alloy 690 exposed to 600 ℃ supercritical water were characterized using mass measurement, X-ray diffraction. Raman spectroscopy, scanning electron microscopy equipped with energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. It was found that the mass gain of the alloy in supercritical water decreased with increasing exposure time. The oxide films have a double-layer structure, with an inner layer rich in Cr and outer layer rich in Ni and Fe after short time and long time exposure. The penetration of the oxide along the grain boundaries was observed, and the penetration depth increased with increasing exposure time. The grain boundaries and voids are the short-path of oxygen diffusion into the metal.