본 논문은 회분식 반응기에서 습식 산화법으로 합성한 칼륨 페레이트(VI)에 의한 난분해성 아조 염료Reactive Black 5의 분해 과정을 연구하는 것을 목적으로 한다. 수용액에서 RB5의 분해는 pH, Ferrate (VI) 투입량, 초기 농도, 수용액 온도 등 다양한 변수의 조건에서 연구되었다. RB5 경우에는 최대 분해 효율은 pH 7.0에서 63.2%가 달성되었으며, 이 실험 조건에서 얻은 kapp 값은 190.49 M-1s-1 으로 나타났다. 온도 또한 가장 중요한 매개 변수 중 하나로 연구되었으며, 그 결과로부터 온도(45°C까지)를 증가시키면 페레이트(VI)에 의한 아조 화합물 염료의 분해 효율이 증가하고, 온도가 45°C를 초과하면 분해 효율이 저하되는 것으로 나타났다.

본고는 『헨리 6세』 2부와 3부가 가부장제의 이념을 바탕으로 남녀 간의 뚜렷한 역할 구분에 기초하고 있다고 보고 전통적인 성 역할에 따르지 않는 마가렛과 같은 여성의 양상을 살핀다. 주로 마가렛의 용맹성, 전투력과 성적 매력과 방종이 주변 남성 인물의 가부장적인 가치에 대립되는 모습을 추적한다. 마가렛과 일리노어 등이 권력을 추구하는 과정에서 남성들, 특히 영국 남성을 대표하는 기사도적 영웅들과 대항하는 양상을 보이는데 이 여성 전사들이 대표하는 가치가 어떻게 남성들의 이상적 영웅주의나 부자간의 혈연 중심 관계에 대립하는지도 살핀다. 일부 남성 인물들이 감정에 치중하는 연인의 모습을 보이며 남성간의 유대를 약화시키는 결과에 이르는 아이러니한 상황 또한 살펴본다. 남성들이 이들 여성과 관련하여 남성성을 잃게 되는 과정을 분석함으로써 『헨리 6세』 2부와 3부에 담긴 가부장제의 양상과 여성 전사의 전복적 힘을 충실히 고찰하고자 한다.

Most of the radioactive wastes generated during the nuclear fuel processing activities conducted by KEPCO Nuclear Fuel Co., Ltd. are classified as the categories of intermediate and low-level radioactive waste. These radioactive waste materials are intended for permanent disposal at a designated disposal site, adhering strictly to the waste acceptance criteria. To facilitate the safe transportation of radioactive waste to the disposal site, it is necessary to ensure that the waste drums maintain a level of criticality that complies with the waste acceptance criteria. This necessitates the maintenance of subcritical conditions, under immersion or optimal neutron moderation conditions. This paper presents a criticality safety assessment of concrete radioactive waste under the most conservative conditions of immersion and moderation conditions for waste drums. Specifically, In order to send radioactive waste, which is the subject of criticality analysis, to a disposal facility, pre-processing operations must be performed to ensure compliance with waste accepatance criteria. To meet the physical characteristics required by the accepance criteria, particles below 0.2 mm should not be included. Thus, a 0.3 mm sieve is used to separate particles lager than 0.3 mm, and only those particles are placed in drums. The drums should be filled to achieve a filling ratio of at least 85%. A criticality analysis was conducted using the KENO-VI of SCALE. The Criticality Safety Analysis Results of varying the filling ratio of concrete drums from 85% to 100% presented in an effective multiplication factor of 0.22484. Additionally, the effective multiplication factor presented to be 0.25384 under the optimal moderation conditions. This demonstrates full compliance with the USL and criticality technology standards set as 0.95.

An optical fluorescence quenching sensor based on functionally modified iron-doped carbon nanoparticles was designed for the selective and sensitive Cr(VI) ion detection. Multifunctional iron-doped carbon nanoparticles were enclosed in the scaffolds of a promising stable nanocarrier system called hyperbranched polyglycerol (HPG), which has been fluorescently modified with 1-pyrene butyric acid using the Steglich esterification procedure. The therapeutic and diagnostic capabilities were boosted when these nanoparticles were enclosed in the fluorescently modified dendritic structure, HPG. Iron-doped carbon nanoparticles coupled with fluorescently modified hyperbranched polyglycerol can be used as a sensor for metal ions and can then be used to successfully remove them from a sample. Moreover, the synthesised nanoparticles demonstrated promising antimicrobial efficacy against bacteria and fungi. These results are also discussed in detail.

The bioreduction process from soluble U(VI) to insoluble U(IV) has been extensively studied in the field of radionuclides migration. Since acetic acid (AcOH) is widely used as an electron donor for bioreduction of U(VI), it is necessary to understand the effect of U(VI)-AcOH complexes that exist in different species depending on pH on this process. Changes in samples before and after bioreduction can be compared using time-resolved laser luminescence spectroscopy (TRLLS), which measures the characteristic luminescence spectra of different U(VI) species. Although luminescence properties of U(VI)-AcOH species were reported, experiments were conducted under conditions below pH 4.5. In this study, spectrophotometry and TRLLS for U(VI)-AcOH species (10−100 μM U(VI) and 20 mM AcOH) were performed in pH ranges extending to neutral and alkaline pH regions similar to groundwater conditions as well as acidic pH region. Two different complexes (UO2(AcO)+, UO2(AcO)2 with U(VI) and acetate ratios of 1:1, 1:2) were observed in the acidic pH region. The 1:1 complex, which appears as the pH increases, has no luminescence properties, but its presence can be confirmed because it serves to reduce the luminescence intensity of UO2 2+. In contrast, the 1:2 complex exhibits distinct luminescence properties that distinguish it from UO2 2+. The 1:3 complex (UO2(AcO)3 -) expected to appear with increasing pH was not observed. Two different complexes ((UO2)3(OH)5 +, (UO2)3(OH)7 - with U(VI) and OH ratios of 3:5, 3:7) were observed as the major species in the neutral pH region, but their luminescence lifetimes are remarkably short compared those in the absence of AcOH. Solid U(VI) particles were observed in the alkaline pH region, and they also had completely different luminescence properties from the aforementioned U(VI)-AcOH and U(VI)-hydrolysis species. Based on these results, the effect of pH in the presence of AcOH on the bioreduction process from U(VI) to U(IV) will be discussed.

Bacterial metabolisms influence the behavior of uranium (U) in deep geological repository (DGR) system because bacteria are ubiquitous in the natural environment. Nevertheless, most studies for the U(VI) bioreduction have focused on a few model bacterium, such as Shewanella putrefaciens, Desulfovibrio desulfuricans, and Geobacter sulfurreducens. In this study, the potential of aqueous U(VI) ((U(VI)aq) reduction by indigenous bacteria was examined under anaerobic conditions with addition of 20 mM sodium acetate for 24 weeks. Three different indigenous bacterial communities obtained from granitic groundwater at depths of 44–60 m (S1), 92–116 m (S2), and 234–244 m (S3) were applied for U(VI)aq reduction experiments. The S2 groundwater contained the highest U concentration of 885.4 μg/L among three groundwater samples, where U mainly existed in the form of Ca2UO2(CO3)3(aq). The S2 groundwater amended 20 mM of sodium acetate was used for the U(VI)aq bioreduction experiment. Variations in the U(VI)aq concentration and redox potential were monitored for 24 weeks to compare U(VI)aq removal efficiency in response to indigenous bacteria. The U(VI)aq removal efficiencies varied among three indigenous bacteria: 57.8% (S3), 43.1% (S2), and 37.7% (S1). The presence of the thermodynamically stable uranyl carbonate complex resulted in the incomplete U(VI)aq removal. Significant shifts in indigenous bacterial communities were observed through highthroughput 16S rRNA gene sequencing analysis. Two SRB species, Thermodesulfovibrio yellowstonii and Desulfatirhabdium butyrativorans, were dominant in the S3 sample after the anaerobic reaction, which enhanced the bioreduction of U(VI)aq. The precipitates produced by bacterial activity were determined to be U(IV)-silicate nanoparticles by a transmission electron microscope (TEM)-energy dispersive spectroscope (EDS) analysis. These results demonstrated that considerable U immobilization is possible by stimulating the activity of indigenous bacteria in the DGR environment.

The stabilization technology for the damaged spent fuel is being developed to process the damaged fuel into sound pellet suitable for dry re-fabrication. It requires several treatments including oxidative decladding followed by reduction treatment for oxidized powder closely related to the quality of oxidized powders for pellet fabrication. For the development of operating condition for the reduction treatment, in this study, we evaluated the effect of air-cylinder based vertical shaking previously applied to oxidative decladding on powder reduction. For U3O8 of 50-100 g, the reduction test were applied with and without vertical shaking at 700°C under reduction atmosphere (Ar + 4%H2) and the concentration of hydrogen in effluent was measured to evaluate the reduction reaction. It was found that the vertical shaking system has allowed the reaction time of 50 g and 100 g U3O8 reduced by 33% compared to the test in static mode. Based on XRD analysis, the better crystallinity of the products was also achieved.

2021년 우리나라 성범죄 발생은 6,321건, 범죄률 13.5%로 교정시설에서는 성범죄 예방을 위해 다양한 프로그램을 운영하고 있지만, 여전히 성범죄의 재범률은 증가하 고 있다. 그래서 본 연구에서는 변증법적 행동 치료이론을 기반으로 성범죄자의 재범 예방 프로그램을 개발하고자 한다. 프로그램의 개발은 선행연구와 요구조사를 바탕으 로 하였다. 프로그램은 변증법적 행동치료(DBT)의 4가지 핵심기술인 마음 챙김, 정서 조절훈련, 고통 감내, 대인 관계 증진 기술로 구성하였다. 연구설계는 비동등성 대조 군 사전-사후 설계(Nonequivalent control group pretest-posttest design)로 혼 합연구 방법(Mixed Methods Design)으로 프로그램의 효과를 검증하였다. 연구대상 자는 G*Power 3.1 program의 표본 크기에 맞게 G시 교정시설에 수감 된 남성 성범 죄자 중에서 총 28명 선정하고, 무작위 할당 표집으로 실험집단 14명과 대조집단 14 명으로 배정하였다. 하지만 이감과 중도 연구 참여 거부로 인한 탈락자를 뺀 실험집단 13명과 대조 집단 12명의 자료를 최종분석하였다. 양적 분석은 SPSS 27.0 프로그램 독립표본 검증(Independent t-test)으로 동질성을 확보를 확인하고, 집단 간 변화를 이원 혼합설계 반복측정 변량분석(Repeated measures ANOVA)으로 살펴보았다. 질적 자료는 Braun과 Clark(2006)가 제시한 주제 분석방법으로 분석하였다. 연구 결 과는 다음과 같다. 첫째, 변증법적 행동치료 프로그램에 참여한 실험집단이 대조집단 보다 대인 간의 공감 반응과 성인 애착에서 통계적으로 유의미하였으며, 변화의 효과 는 추후검사에서도 통계적으로 유의미하게 유지되었다. 둘째, 프로그램 참여 경험을 분석한 결과 36개의 하위 주제, 몇10개의 상위 주제가 나타났다. 이를 분석영역인 충 동성, 공격성, 자기통제력에 재배열하였다. 충동성에서는 이성에의 의지 폭력 행동의 자발적 제어, 예측 능력의 강화, 분노의 원인 탐색 주제가 돌출되었다. 공격성에서는 파괴 본능을 건강한 에너지로 전환, 타인에 대한 적대적 감정 없애기, 낮은 자리에 서 기라는 주제가 출연했다. 자기통제력에서는 유혹을 이길 수 있는 힘의 배양, 현재의 만족보다는 미래의 성공, 규범적인 행동 목표설정이 나타났다. 연구자들은 연구 결과에 근거하여 논의하였고, 교정기관 내에서 성범죄자들의 사회 재적응을 지지할 수 있는 실천적 접근을 제안함으로써 재범을 예방하고자 하였다. 본 연구는 기존의 교정시설 에서 시도하지 않은 변증법적 행동 치료이론을 접목한 프로그램의 개발하였기에 성범 죄자 프로그램에 새로운 패러다임을 시도하였다는 점에서 선행연구들과 차이가 있다.

Time-resolved laser fluorescence spectroscopy (TRLFS) and excitation-emission matrix (EEM) spectroscopy were used to study the interaction of U(VI) and natural organic matters (NOMs) in groundwater. Various types of groundwaters (DB-1, DB-3 from KURT site and OB-1, OB-3 from a U deposit in Ogcheon metamorphic belt) were used as samples. Pulsed Nd-YAG laser at 266 nm (Continuum Minilite) was used as the light source of TRLFS. The laser pulse energy of 1.0 mJ was fixed for all measurements. The luminescence spectrum was recorded using a gated intensified chargecoupled device (Andor, DH-720/18U03 iStar 720D) attached to the spectrograph (Andor, SR-303i). EEM spectra were measured using a spectrofluorometer (Horiba Scientific, Aqualog) equipped with a 150 W ozone-free xenon arc lamp. Excitation spectra were recorded by scanning the excitation wavelength from 200 to 500 nm. Emission spectra were measured using a CCD in the wavelength range of 242–823 nm. In the case of the recently collected DB-1 samples, it was observed that the U and NOM quantities decreased compared to the samples collected before 2016. For some DB-1 samples, the amount of dissolved organic carbon indicating the presence of NOM was significantly reduced, and changes consistent with this phenomenon were observed in the EEM spectrum. The time-resolved luminescence characteristics (peak wavelengths and lifetime) of U(VI) in the DB-1 samples agree well with those of Ca2UO2(CO3)3(aq). This U(VI) species remains stable, even in samples taken five years ago. The estimated amounts of U and NOM from the spectroscopic data of DB-3, OB-1, and OB-3 samples are relatively low compared to DB-1 samples. When a known amount of U(VI) was mixed in each groundwater, the time-resolved luminescence spectrum exhibited a characteristic spectral shape different from the expected luminescence intensity. This phenomenon is presumed to be due to the interaction between U(VI) and NOM in groundwater. The results of this study suggest that the chemical speciation of NOM as well as U(VI) is required to understand U behavior in groundwater.

Montmorillonite plays a key role in engineered barrier systems in the high-level radioactive waste repository because of its large sorption capacity and high swelling pressure. However, the sorption capacity of montmorillonite can be largely varied dependent on the surrounding environments. This study conducted the batch simulation for U(VI) sorption on Na-montmorillonite by utilizing the cation exchange and surface complexation coupled (2SP-NE-SC/CE) model and evaluated the effects of physicochemical properties (i.e., pH, temperature, competing cations, U(VI) concentration, and carbonate species) on U(VI) sorption. The simulation demonstrated that the U(VI) sorption was affected by physicochemical properties: the pH and temperature relate to aqueous U(VI) speciation, the competing cations relate to the cation exchange process and selectivity, the U(VI) concentration relates to saturation at sorption sites. For example, the Kd (L kg−1) of Na-montmorillonite represented the largest values of 2.7×105 L kg−1 at neutral pH condition and had significantly decreased at acidic pH<3, showing non-linear and diverse U(VI) sorption at the ranged pH from 2 to 11. Additionally, the U(VI) sorption on montmorillonite significantly decreased in presence of carbonate species. The U(VI) sorption for long-term in actual porewater chemistry and temperature of high-level radioactive waste repository represented that the sorption capacity of Na-montmorillonite was affected by various external properties such as concentration of competing cation, temperature, pH, and carbonate species. These results indicate that geochemical sorption capacity of bentonite should be evaluated by considering both geological and aquifer environments in the high-level radioactive waste repository.

수용액에서 EBT의 분해는 pH, Ferrate (VI) 투입량, 초기 농도, 수용액 온도 등 다양한 변수의 조건에서 연구되었다. 최대 분해 효율은 pH 7.0에서 95.42%가 달성되었으며, 이 실험 조건에서 얻은 kapp 값은 872.87 M-1s-1 이었다. EBT 분해율은 Ferrate (VI)의 투입량이 증가함에 따라 증가하였으며 EBT 초기 농도가 감소함에 따라 EBT 분해의 초기 속도 상수가 증가하였다. 또한 EBT의 분해율은 온도가 10°C에서 45°C에 도달할 때까지 수용액의 온도에 따라 증가하였으며 이 실험조건에서 활성화 에너지 값은 EBT 분해에 대해 11.9 kJ/mol의 값이 도출되었다. 따라서 분해 실험의 결과는 Ferrate (VI)가 수용액상에서 EBT를 효과적으로 분해시킬 수 있음을 보여주고 있다.

An elevated temperature is expected at the deep geological repository (DGR) due to the decay heat from spent nuclear fuel and the positive geothermal gradient. The resulting elevated temperature would change the aqueous speciation and surface complexation of uranium, which is the major component in spent nuclear fuel. Since sorption reactions of uranium species on natural minerals determine the extent of uranium retardation, in this work the temperature-dependent adsorption of hexavalent uranium, U(VI), was studied by choosing alumina as the basic component mineral for complex aluminosilicates. Time-resolved laser fluorescence spectroscopy (TRLFS) was used to assess the dissolved and adsorbed U(VI) species on γ-Alumina in the pH range of 6.5–9.0 at temperatures of 25 to 70°C. Initial concentrations of U(VI), carbonate and calcium were 89 μM, 25 mM, and 3.0 mM, respectively. The parallel factor analysis (PARAFAC) was used for chemical speciation by spectrum deconvolution. In addition, a separate solution system with higher U(VI) concentrations (0.1 mM, 1.0 mM) and carbonate concentration of 25 mM was studied with attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy for adsorbed species at 25°C. The electrophoretic mobility measurements were also conducted at 25°C to assess the coordination mechanism of adsorbed species at 25°C. The uranyl hydrolysis species and uranyl tricarbonato species coexist in solution at 25°C. At the same temperature, both species were found to be adsorbed. ATR-FTIR could confirm the adsorption of uranyl tricarbonato species at 25°C, and the electrophoretic mobility measurements suggested that the reaction mechanism is an inner-sphere coordination. However, in comparison with aqueous speciation at 25°C, at elevated temperatures the available pH range of uranyl tricarbonato species was narrow and that for uranyl hydrolysis species was wider. It was evident that two hydrolysis species are adsorbed at elevated temperatures, but no tricarbonato species. The enhanced U(VI) adsorption was observed with temperatures. This could result from the transition of dominance from the concurrent adsorption of uranyl hydrolysis species and uranyl tricarbonato species to two hydrolysis species. It was seen that the trend of enthalpy of adsorption was endothermic. Combining the present results with temperature-dependent adsorption studies on silica and aluminosilicates, a reliable SCM for the subsurface system can be proposed to explain U(VI) migration.

To predict the long-term behaviors of actinides in aqueous environments, complexation behaviors of actinides should be understood. Various organic ligands of chelating aromatic structure appearing in humic substances are known to form stable aqueous complexes. In this study, a benzene diol (or catechol) derivative, i.e., 4-nitrocatechol (nCA) is selected and its chemical equilibria including acid dissociation and complexation with U(VI) ion were examined using spectroscopic methods. In addition, the effect of ionic strength (Is) on those equilibria was evaluated by adjusting the level of NaClO4 in aqueous solutions. First, the experiments to determine the acid dissociation constant (pKa) of nCA were carried out in aqueous solutions with different ionic strengths from 0.01–2.0 M. The acid dissociation constants of nCA (pKa1) were measured to 6.73 ± 0.07, 6.69 ± 0.03, 6.38 ± 0.03, 6.09 ± 0.12, and 6.04 ± 0.07 at Is = 0.01, 0.1, 0.5, 1.0, and 2.0, respectively. These results were confirmed through the UV-Vis absorption spectral data analysis using the HypSpec program. As the pKa1 decreases as the ionic strength increases, except for Is = 2.0, these data were further analyzed with SIT (Specific ion Interaction Theory). Typically, as the solution becomes basic, a red shift is shown in the absorption spectrum. This effect can be understood from the intramolecular charge transfer (ICT) occurring in the deprotonated structures of nCA. At higher pH similar trends were also observed for measurement of pKa2. However, the determination of pKa2 is found not to be straightforward since a dimer formation equilibrium of nCA was observed as the ionic strength increased. This phenomenon will be discussed in detail with other supporting experimental results. Second of all, the complexation between the U(VI) and nCA in aqueous solutions was also examined. It was shown that nCA can easily form complexes with U(VI) ions at a wide range of pH via the deprotonation of their hydroxyl groups. U(VI)-nCA complexation will be further characterized by UV-Vis spectroscopy, IR and NMR by varying the solution ionic strength. The metal-ligand binding stoichiometry will be confirmed, for example, through the Job’s method. Finally, the acid dissociations constant and stability constants that were determined in this study will be used to provide species diagrams of aqueous U(VI)-nCA systems at a wide range of pH considering the effect of solution ionic strengths.

Deep geological repository (DGR) has been considered as a globally accepted strategy to dispose high-level radioactive wastes. During long storage periods of 100,000 years, uranium (U) could be migrated through fractures in deep granite aquifers and interact with indigenous bacteria under anaerobic condition. Anaerobic bacteria can reduce U(VI) and further precipitate in the form of U(IV)-oxide minerals by transferring electrons through c-type cytochrome. In this point of view, a comprehensive understanding of uranium-microorganisms interaction is necessary to guarantee the safety of high-level radioactive waste disposal. Although diverse bacterial communities are present in DGR environment, a number of studies have been focused on some model bacteria, such as Desulfovibrio, Geobacter, and Shewanella spp.. In this study, indigenous bacterial community in deep granitic groundwater at 234–244 m was inoculated to sterile uranium-contaminated granitic groundwater amended with 20 mM of sodium acetate, and then incubated under anaerobic condition for 12 weeks. Bio-reduction of U(VI) to U(IV) by indigenous bacteria in uranium-contaminated groundwater was investigated during whole operation period. Initial U(VI) concentration of 885.4 μg·L−1 gradually decreased to 586.1 μg·L−1, resulting in approximately 33.8% of aqueous U(VI) removal efficiency. Oxidation-reduction potential (ORP) value was gradually decreased from 175.4 mV to –243.0 mV after the incubation of 12 weeks. The decrease in ORP value was attributed to the presence of aerobic bacteria and facultative anaerobic bacteria in indigenous bacterial community. The shift in bacterial community structure was observed by 16S rRNA gene high-throughput sequencing analysis. Proteobacteria (55.6%), Firmicutes (24.1%), Actinobacteria (5.5%), and Bacteroidetes (5.4%) were dominant in initial indigenous bacterial community, while Proteobacteria (94.8%) was found to be the only abundant phylum after the reaction. In addition, great increase in the relative abundance of sulfate-reducing bacteria (SRB) was observed: the relative abundance of SRB increased from 11.4% to 44.3% after the reaction. This result indicates that the SRB played a key role in the removal of aqueous U(VI). This finding shows the potential of aqueous U(VI) removal by indigenous bacteria in DGR environment.

In this study, Ni nanoparticle supported by graphene oxide (GO) (Ni-GO) is successfully synthesized through hydrothermal synthesis and calcination, and Cr(VI) is extracted from aqueous solution. The morphology and structure of Ni- GO composites are characterized by scanning electron microscopy (SEM), trans mission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). High-resolution transmission electron microscopy (HRTEM) and XRD confirms the high dispersion of Ni nanoparticle after support by GO. Loading Ni on GO can obviously enhance the stability of Ni-GO composites. It can be calculated from TGA that the mass percentage of Ni is about 60.67%. The effects of initial pH and reaction time on Cr(VI) removal ability of Ni-GO are investigated. The results indicate that the removal efficiency of Cr(VI) is greater than that of bared GO. Ni-GO shows fast removal capacity for Cr(VI) (<25 min) with high removal efficiency. Dynamic experiments show that the removal process conforms to the quasi-second order model of adsorption, which indicates that the rate control step of the removal process is chemical adsorption. The removal capacity increases with the increase of temperature, indicating that the reaction of Cr(VI) on Ni-GO composites is endothermic and spontaneous. Combined with tests and characterization, the mechanism of Cr(VI) removal by rapidly adsorption on the surface of Ni-GO and reduction by Ni nanoparticle is investigated. The above results show that Ni-GO can be used as a potential remediation agent for Cr(VI)-contaminated groundwater.

Tetracycline is one of the most commonly used as antibiotics for the livestock industry and it is still widely used nowadays. Tetracycline and its metabolites are excreted with excrement, which is difficult to completely removed with conventional sewage treatment, therefore it is apprehended that the tetracycline-resistant bacteria occurs. In this study, the oxidant named ferrate(VI) was used to degrade the tetracycline and investigate the reaction between ferrate(VI) and tetracycline under various aqueous conditions. The highest degradation efficiency of tetracycline occurred in basic condition (pH 10.1 ± 0.1) because of the pKa values of tetracycline and ferrate(VI). The results also showed the effect of water temperature on the degradation of tetracycline was not significant. In addition, the dosage of ferrate(VI) was higher, the degradation of tetracycline and the self-degradation of ferrate(VI) also higher, finally the efficiency of ferrate(VI) was lower. The results said that the various mechanisms effects the reaction of ferrate(VI) oxidation, it required the consideration of the characteristics of the target compound for optimal degradation efficiency. Additionally, intermediate products were detected with LC/MS/MS and three degradation pathways were proposed.