scholarly journals Ultrasonic irradiation of chemical compounds in aqueous solutions

1992 ◽  
Author(s):  
Αναστασία Κοτρωναρου

The ultrasonic irradiation of para-nitrophenol, S(-II), and parathion is studied in aqueous solutions at 20 kHz and ~ 75 W-cnT2. Para-nitrophenol was degraded primarily by denitration and secondarily by ΌΗ radical attack to yield N 02, NO3, benzoquinone, hydroquinone, 4-nitrocatechol, formate and oxalate. These reaction products and the kinetic observations are consistent with a model involving high-temperature reactions of p-nitrophenol in the interfa.cia.1 region of cavitation bubbles. The average effective temperature of the interfacial region surrounding the cavitation bubbles was estimated to be T ~ 800 K. Ultrasonic irradiation of S(-II) is studied in aqueous solutions over the pH range 7 - 12. The reaction of HS“ with OH is the principal pathway for theoxidation of S(-II) at pH > 10; the oxidation products are SO2“, SO2", and S20 Upon prolonged sonication, SO2" is the only observed product. At pH < 8.5, thermal decomposition of H2S within or near collapsing cavitation bubbles becomes the important pathway and elemental sulfur is found as an additional product of the sonolysis of S(-II). The sonolytic oxidation of H2S at pH > 10 was successfully modeled with an aqueous-phase free-radical chemistry mechanism and assumingcontinuous and uniform ΌΗ input into solution from the imploding cavitation bubbles. Parathion degradation occurred primarily by enhanced hydrolysis and secondarily by direct ΌΗ radical attack.The effect of various physical and chemical parameters on sonolytic yields is examined. The observed effects are in qualitative agreement with the sonolysis mechanisms proposed for the chemicals of interest and the existing hydrodynamic theories of acoustic cavitation. The formation of iodine upon ultrasonic irradiation of potassium iodide solutions and the sonolysis of S(-II) are used as probes to compare the sonochemical efficiency of different experimental set-ups. This work elucidates the mechanisms of the ultrasonic decomposition of typical organic and inorganic pollutants. It is shown that ultrasound has the potential to become a viable alternative for the destruction of chemical contaminants in water and wastewater. The current limitation of sonolysis is its low energy utilization efficiency, but there is room for improvement by optimizing reactor design and physical/chemical operation conditions. This work offers some recommendations and insight in that respect.

2012 ◽  
Vol 549 ◽  
pp. 238-241 ◽  
Author(s):  
Tao Zhu ◽  
Yan Dong Wan ◽  
Yu Jie Liu ◽  
Yu Yuan ◽  
Hai Rong Li ◽  
...  

Because of its wide pollution, large flow and low concentration, the waste gas containing volatile organic compound (VOCs) will be controlled more strictly on its emission, and new technologies for its treatment must be developed continuously. As an emerging technology for environmental protection, non-thermal plasma (NTP) has been subjected to extensive researches over the past 20 years. In the field of air pollution control, the NTP technology has been used for the abatement of various types of hazardous air pollutants due to its unique properties including the moderate operation conditions (normal temperature and atmospheric pressure), moderate capital cost, compact system, easy operations and short residence times, compared to the conventional technologies. Especially, combined plasma technology has multi-function effects, better pollutant degradation efficiency, better energy utilization efficiency and higher pollutant selectivity than single plasma technology. The research progresses in treatment of waste gas containing VOCs and the patents application by plasma technology combined with adsorbent, catalyst and ferroelectric are summarized and analyzed. From the review, we can come to a conclusion the synergistic technology result in greater enhancement of VOCs decomposition and energy efficiency. The development direction of combined plasma technology is prospected.


1983 ◽  
Vol 26 ◽  
Author(s):  
T. W. Newton ◽  
V. L. Rundberg

ABSTRACTThe rates of polymerization and disproportionation of Pu(IV) have been studied using low concentrations: (1.7 − 10) × 10−6M Pu, (0.8 − 12) × 10−4M HCI and 0.01M ionic strength. Osmium(II) complexes such as the tris−4,41−2,21−bipyridine complex were found to react rapidly with Pu(IV) but very slowly, if at all, with Pu(IV) polymer, Pu(lll), or Pu(V). Thus, it is possible to determine unreacted Pu(IV) in the presence of reaction products by using Os(II) complexes. Disproportionation reaction products, Pu(IlI) and Pu(V), were determined using their reactions with Ce(IV) sulfate. We find −d[Pu(IV)]/dt = k'[Pu(IV)]2 at constant pH. Log k1 varies from about 4.25 at pH 3 to about 7.0 at pH 4.1 (units for k1 are M−1min−1). The [H+] dependence varies from about −2 to −3 over the pH range studied. The measured rate is the sum of those for polymerization and disproportionation; the latter reaction amounts to about 75% of the total at pH 3 and 20% at pH 4. The second-order rate constants for disproportionation are very much larger than expected on the basis of extrapolation from 0.2 to 1.OM HClO, solutions. The products of the reaction do not affect the rate, but U(VI), aged Pu(IV) polymer, and CO2 increase the rate.


2020 ◽  
Vol 4 (1) ◽  
Author(s):  
Kang Wang ◽  
Junsoo Han ◽  
Angela Yu Gerard ◽  
John R. Scully ◽  
Bi-Cheng Zhou

AbstractThe potential-pH diagram, a graphical representation of the thermodynamically predominant reaction products in aqueous corrosion, is originally proposed for the corrosion of pure metals. The original approach only leads to stoichiometric oxides and hydroxides as the oxidation products. However, numerous experiments show that non-stoichiometric oxide scales are prevalent in the aqueous corrosion of alloys. In the present study, a room temperature potential-pH diagram considering oxide solid solutions, as a generalization of the traditional potential-pH diagram with stoichiometric oxides, is constructed for an FCC single-phase multi-principal element alloy (MPEA) based on the CALculation of PHAse Diagram method. The predominant reaction products, the ions in aqueous solution, and the cation distribution in oxides are predicted. The oxide solid solution is stabilized by the mixing free energy (or mixing entropy) and the stabilizing effect becomes more significant as the temperature increases. Consequently, solid solution oxides are stable in large regions of the potential-pH diagram and the mixing free energy mostly affects the equilibrium composition of the stable oxides, while the shape of stable regions for oxides is mostly determined by the structure of the stable oxides. Agreements are found for Ni2+, Fe2+, and Mn2+ between the atomic emission spectroelectrochemistry measurements and thermodynamic calculations, while deviations exist for Cr3+ and Co2+ possibly due to surface complexation with species such as Cl− and the oxide dissolution. By incorporating the solution models of oxides, the current work presents a general and more accurate way to analyze the reaction products during aqueous corrosion of MPEAs.


Entropy ◽  
2020 ◽  
Vol 22 (12) ◽  
pp. 1337
Author(s):  
Xiangfeng Tian ◽  
Lemeng Wang ◽  
Pan Zhang ◽  
Dong Fu

The surface tension and viscosity values of N-methyldiethanolamine (MDEA) aqueous solutions promoted by tetramethylammonium arginate ([N1111][Arg]) were measured and modeled. The experimental temperatures were 303.2 to 323.2 K. The mass fractions of MDEA (wMDEA) and [N1111][Arg] (w[N1111][Arg]) were 0.300 to 0.500 and 0.025 to 0.075, respectively. The measured surface tension and viscosity values were satisfactorily fitted to thermodynamic models. With the aid of experimentally viscosity data, the activation energy (Ea) and H2S diffusion coefficient (DH2S) of MDEA-[N1111][Arg] aqueous solution were deduced. The surface entropy and surface enthalpy of the solutions were calculated using the fitted model of the surface tension. The quantitative relationship between the calculated values (surface tension, surface entropy, surface enthalpy, viscosity, activation energy, and H2S diffusion coefficient) and the operation conditions (mass fraction and temperature) was demonstrated.


2021 ◽  
pp. 1-18
Author(s):  
Jiahang Yuan ◽  
Yun Li ◽  
Xinggang Luo ◽  
Lingfei Li ◽  
Zhongliang Zhang ◽  
...  

Regional integrated energy system (RIES) provides a platform for coupling utilization of multi-energy and makes various energy demand from client possible. The suitable RIES composition scheme will upgrade energy structure and improve integrated energy utilization efficiency. Based on a RIES construction project in Jiangsu province, this paper proposes a new multi criteria decision-making (MCDM) method for the selection of RIES schemes. Because that subjective evaluation on RIES schemes benefit under criteria has uncertainty and hesitancy, intuitionistic trapezoidal fuzzy number (ITFN) which has the better capability to model ill-known quantities is presented. In consideration of risk attitude and interdependency of criteria, a new decision model with risk coefficients, Mahalanobis-Taguchi system and Choquet integral is proposed. Firstly, the decision matrices given by experts are normalized, and then are transformed to minimum expectation matrices according to different risk coefficients. Secondly, the weights of criteria from different experts are calculated by Mahalanobis-Taguchi system. Mobius transformation coefficients based on interaction degree are to calculate 2-order additive fuzzy measures, and then the comprehensive weights of criteria are obtained by fuzzy measures and Choquet integral. Thirdly, based on group decision consensus requirement, the weights of experts are obtained by the maximum entropy and grey correlation. Fourthly, the minimum expectation matrices are aggregated by the intuitionistic trapezoidal fuzzy Bonferroni mean operator. Thus, the ranking result according to the comparison rules using the minimum expectation and the maximum expectation is obtained. Finally, an illustrative example is taken in the present study to make the proposed method comprehensible.


2014 ◽  
Vol 13 (1) ◽  
Author(s):  
Dariusz Wyrzykowski ◽  
Joanna Pranczk ◽  
Dagmara Jacewicz ◽  
Aleksandra Tesmar ◽  
Bogusław Pilarski ◽  
...  

AbstractA potentiometric titration method (PT) and a stopped-flow kinetic technique monitored by a UV−Vis spectroscopy have been used to characterize the stability of series of Co(II)- and Ni(II)-thiodiacetato complexes, M(TDA), in the presence of 1,10-phenanthroline (phen) or 2,2’-bipyridine (bipy) in aqueous solutions. The stability constants of the binary (1:1), ternary (1:1:1) as well as the resulting hydroxo complexes were evaluated and compared to the corresponding oxydiacetate complexes. Based on the species distribution as a function of pH the relative predominance of the species in the system over a pH range was discussed. Furthermore, the kinetic measurements of the substitution reactions of the aqua ligands to phen or bipy in the coordination sphere of the binary complexes M(TDA) were performed in the 288–303 K temperature range, at a constant concentration of phen or bipy and at seven different concentrations of the binary complexes (0.2–0.5 mM). The kinetic stability of the M(TDA) complexes was discussed in relation to the experimental conditions and the kind of the auxiliary ligands (phen/bipy). Moreover, the influence of the type of primary ligand (thiodiacetate/oxydiacetate) on the substitution rate of the auxiliary ligands was also compared.


1978 ◽  
Vol 33 (3) ◽  
pp. 293-299 ◽  
Author(s):  
Joachim Stauff ◽  
Wolfgang Jaeschke

Abstract The reactions of diluted aqueous solutions of SO2 resp. HSO3-ions with MnO4-or Ce4+ ions in the pH range 1-4 produce chemiluminescence in the spectral region of 450-600 nm. Measurements of the time course of the light emission and their simulation on an analog computer led to a reaction scheme in which a recombination product of primarily formed HSO3 radicals -of a lifetime of about 1 second -appears as precursor of electronically excited SO2 molecules. The participation of singlet oxygen can be excluded because at least the reaction with Ce4+ ions proceeds also in the absence of oxygen.


Author(s):  
H. X. Liang ◽  
Q. W. Wang

This paper deals with the problem of energy utilization efficiency evaluation of a microturbine system for Combined Cooling, Heating and Power production (CCHP). The CCHP system integrates power generation, cooling and heating, which is a type of total energy system on the basis of energy cascade utilization principle, and has a large potential of energy saving and economical efficiency. A typical CCHP system has several options to fulfill energy requirements of its application, the electrical energy can be produced by a gas turbine, the heat can be generated by the waste heat of a gas turbine, and the cooling load can be satisfied by an absorption chiller driven by the waste heat of a gas turbine. The energy problem of the CCHP system is so large and complex that the existing engineering cannot provide satisfactory solutions. The decisive values for energetic efficiency evaluation of such systems are the primary energy generation cost. In this paper, in order to reveal internal essence of CCHP, we have analyzed typical CCHP systems and compared them with individual systems. The optimal operation of this system is dependent upon load conditions to be satisfied. The results indicate that CCHP brings 38.7 percent decrease in energy consumption comparing with the individual systems. A CCHP system saves fuel resources and has the assurance of economic benefits. Moreover, two basic CCHP models are presented for determining the optimum energy combination for the CCHP system with 100kW microturbine, and the more practical performances of various units are introduced, then Primary Energy Ratio (PER) and exergy efficiency (α) of various types and sizes systems are analyzed. Through exergy comparison performed for two kinds of CCHP systems, we have identified the essential principle for high performance of the CCHP system, and consequently pointed out the promising features for further development.


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