CHEMICAL ENGINEERING JOURNAL
·
2018
·
IF 6.735
Mantang Chen,Zhimin Zhang,Lihua Zhu,Nan Wang,Heqing Tang
The present work aimed at using bisulfites (HSO 3 − ) to enhance the oxidative degradation of bisphenol A (BPA) in a Fenton process based on the Fe 3+ -H 2 O 2 reagents. It was confirmed that both the degradation and mineralization of BPA were drastically enhanced by the addition of HSO 3 − . Typically, the use of 0.1 mmol L −1 Fe 3+ , 0.3 mmol L −1 HSO 3 − and 10 mmol L −1 H 2 O 2 achieved a complete degradation of BPA (0.05 mmol L −1 ) in only 2 min. The addition of HSO 3 − increased the BPA degradation rate constant from 0.045 min −1 in the Fe 3+ -H 2 O 2 system to 2.71 min −1 in the Fe 3+ -HSO 3 − -H 2 O 2 system by 60 times. This drastic enhancement effect of HSO 3 − was attributed to its complexing and reducing abilities. The formation of FeSO 3 + complex prevented the precipitation of Fe 3+ and accelerated the cycling of Fe 3+ /Fe 2+ ; the reducing ability of HSO 3 − further favored the transformation of Fe 3+ to Fe 2+ . Several reactive species, including OH, SO 3 − and SO 4 − were responsible for the degradation of BPA, among which OH was the dominant one. The proposed Fe 3+ -HSO 3 − -H 2 O 2 system is suggested be able to act as the followed stage of a traditional Fe 2+ -H 2 O 2 system in the engineering setting.
研究领域:
环境科学
·
化学工程
·
污染控制
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产品关联
DOI
高影响因子
CHINESE CHEMICAL LETTERS
·
2024
·Vol. 36
·期 4
·109730
·
IF 9.4
Hongyuan Sha,Dongling Yang,Yanran Shang,Zujian Wang,Rongbing Su,Chao He,Xiaoming Yang,Xifa Long
Sulfates are always promising short-wave ultraviolet (UV) nonlinear optical (NLO) candidates, if their birefringence could be greatly improved. Here, in terms of the insufficient birefringence , the unity of heteroleptic tetrahedral groups and triangular ones was proposed and implemented. Thus, a new semi-organic crystal, [C(NH 2 ) 3 ]S 3 O 6 (G 2 S 3 O 6 ), was obtained, which is composed of [S 3 O 6 ] 2− and [C(NH 2 ) 3 ] + groups. It exhibits excellent optical properties with a short absorption cutoff edge of 218 nm, a strong NLO response of 1.4 × KH 2 PO 4 , and more especially, a large birefringence of 0.097@546 nm. This birefringence leap makes the G 2 S 3 O 6 crystal achieve a phase-matching behavior under a 532 nm laser. Thus, the synergy of [S 3 O 6 ] 2− and [C(NH 2 ) 3 ] + groups results in excellent optical performances. This finding opens a new horizon for exploring novel UV NLO crystals.
研究领域:
材料科学
·
光学工程
·
无机化学
·
晶体化学
·
非线性光学
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DOI
高影响因子
CORROSION SCIENCE
·
2018
·
IF 4.862
Jie Qiu,Bin Leng,Huajian Liu,Digby D. Macdonald,Angjian Wu,Yanyan Jia,Wandong Xue,Guojun Yu,Xingtai Zhou
The effect of SO 4 2− on the corrosion behavior of 316 L stainless steel (SS) in molten FLiNaK (LiF-NaF-KF: 46.5–11.5–42 mol.%) salt was studied. Results reveal that the SO 4 2− in the salt remarkably accelerates the corrosion of 316 L SS by promoting the dissolution of Cr, leading to increasing intergranular corrosion of the alloy. On the other hand, the results of structural characterization indicate that the SO 4 2− can react with Mn to form MnS at the grain boundaries of the alloy. The galvanic couple between MnS and steel matrix could further accelerate the intergranular corrosion of 316 L SS in molten fluoride salt environments.
研究领域:
材料科学
·
腐蚀科学
·
无机化学
·
核工程材料
·
高温电化学
✓ 已验证
DOI
高影响因子
WATER RESEARCH
·
2024
·
IF 11.4
Jie Liu,Kexin Zhang,Xin Liu,Qiyong Xu,Weiyi Li
Despite being recognized as a promising technique for treating high salinity water, membrane distillation (MD) has been plagued by the scaling of sparingly soluble salts. The growth of crystals can not only create additional resistance to evaporating water at the feed-membrane interface, but also alter the hydrophobic network to bridge the feed and distillate (i.e., result in the phenomenon of wetting). When recognizing the uncertain behaviors of calcium sulfate (CaSO 4 ) scaling in MD, this study was motivated to ascertain whether the crystal-membrane interactions could be dependent on the variation in crystalline morphology. In particular, optical coherence tomography (OCT) was employed to characterize the scaling-induced wetting via a direct-observation-through-the-membrane (DOTM) mode, which mitigated the effects of developing an external scaling layer on resolving the crystal-membrane interactions. The improved in-situ characterization suggests that the crystalline morphology of CaSO 4 could be effectively regulated by varying the stoichiometry of crystallizing ions; the richness of calcium in the aqueous environment for crystallization would be in favor of weakening the crystal-membrane interactions. The stoichiometry-dependent growth of CaSO 4 crystals can be exploited to develop an effective strategy for preventing the hydrophobic network from being wetted or irreversibly damaged.
研究领域:
环境科学
·
膜科学与技术
·
化学工程
·
水处理技术
·
材料表征
·
结晶过程
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Hongyuan Xi,Song Zhou,Jinxi Zhou
NO is the main precursor of photochemical smog. Since the SCR system of marine diesel engines has many disadvantages, this paper proposes an effective wet method to remove NO from the exhaust gases of marine diesel engines. Experiments were performed in a bubble column reactor to study the absorption of NO using sodium persulfate (Na 2 S 2 O 8 )/urea ((NH 2 ) 2 CO) solutions from a simulated gas stream. The effects of various operating parameters on NO removal were investigated, including reaction temperature, urea concentration, Na 2 S 2 O 8 concentration and the initial pH value of Na 2 S 2 O 8 /urea solutions. The experimental results showed that the NO removal efficiency increased with increasing reaction temperature (25–80 °C) and increasing Na 2 S 2 O 8 concentration (0.01–0.2 mol/L). When the concentration of urea was higher than 0.5 mol/L at 60 °C, 1 mol/L at 70 °C or 2 mol/L at 80 °C, the NO removal efficiency increased with the increase of urea concentration (0.1–4 mol/L). The highest NO removal efficiency was 99.7%, occurring at 80 °C when the concentrations of Na 2 S 2 O 8 and urea were 0.1 mol/L and 4 mol/L, respectively, and the concentration of nitrate was 14.93 mg/L. The optimal urea conditions were well below the legal limit of 60 mg/L. The NO removal efficiency increased with the increase of initial pH value within the herein investigated range of 7–9. All the experimental data showed that the novel system not only achieved effective NO removal efficiency, but also reduced the nitrate in wastewater, which could thus be applied to denitrification of marine engine exhaust gases.
研究领域:
环境工程
·
大气污染控制
·
化学工程
·
海洋工程
·
能源与动力工程
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DOI
高影响因子
APPLIED ORGANOMETALLIC CHEMISTRY
·
2019
·Vol. 33
·期 9
·e5082
·
IF 3.259
Dongmei He,Li Zeng,Guiqing Zhang,Qinggang Li,Wenjuan Guan,Zuoying Cao,Shengxi Wu
A new compound, α-aminophosphonate derivative containing pyridine ring (PPDE), was designed and synthesized as an extractant for the separation of nickel from metal impurities. Over 94.5% of Ni (II) extraction from sulfuric acid solution was achieved by using PPDE with an equilibrium pH of 4.02. Meanwhile, high separation coefficients of 23.8 for Ni to Co, 84.9 for Ni to Mn, 254.1 for Ni to Ca and 696.7 for Ni to Mg, respectively, were obtained. It was noted that PPDE exhibited an excellent regenerability, and the extraction of Ni with the recycled organic phase ranged from 92.5% to 93.9% during six circulations. The extracted nickel complex was determined as [Ni (PPDE) 2 (DNNSA − ) 2 (H 2 O) 4 ], which was supported by the data obtained from Fourier transform-infrared, UV–Vis and electrospray ionization-mass spectrometry spectra.
研究领域:
无机化学
·
湿法冶金
·
分离科学
·
配位化学
·
环境化学
·
资源回收
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DOI
高影响因子
INTERNATIONAL BIODETERIORATION & BIODEGRADATION
·
2017
·
IF 2.962
Ee Li,Jiajia Wu,Dun Zhang,Yan Sun,Juna Chen
D-phenylalanine (D-Phe) was tested for its effect on the corrosion of Q235 carbon steel caused by Desulfovibrio sp. which belongs to sulfate reducing bacteria (SRB). Weight loss results indicated that the corrosion rate of Q235 coupons exposed to D-Phe was reduced. Much less pits were found on the surface of these coupons. It was found that pH and dissolved oxygen content of bacteria cultures as well as the growth of bacteria were not affected by D-Phe. However, the cell shape of D . sp. was changed to a more filamentous or spherical shape by treatment with D-Phe, and the structure of biofilms formed by bacteria with transformed shapes was looser and thinner. Moreover, the hydrogen sulfide production of D . sp. was inhibited by D-Phe. These results suggest that D-Phe may inhibit the corrosion process through two ways, i, D-Phe alters the bacteria shape, which inhibits the formation of biofilm and changes the structure of it consequently; ii, D-Phe reduces the production of hydrogen sulfide .
研究领域:
微生物腐蚀
·
材料科学
·
环境微生物学
·
金属腐蚀与防护
·
生物膜研究
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2015
·
IF 4.321
Yajie Qian,Xuefei Zhou,Yalei Zhang,Peizhe Sun,Weixian Zhang,Jiabin Chen,Xin Guo,Xiao Zhang
Calcium peroxide (CP) combined persulfate (PS) oxidation is an emerging in situ chemical oxidation (ISCO) technology for ground water remediation. Many field cases also confirm its effectiveness in ground water remediation while few research articles document it. This study investigated the performance of α-methylnaphthalene (MN) degradation by PS/CP to further understand this dual oxidant application in ISCO. Results showed that MN could be completely oxidized in 72 h with 1 g L −1 PS and 1 g L −1 CP. The degradation rates of MN increased with the increase of PS and CP concentration. MN degradation was significantly enhanced with the solution pH decrease, because CP was easier to dissolve and generated more radicals in acidic condition. Solutes in ground water including chloride ions, alkalinity and natural organic matters presented inhibitory effect on MN degradation in this dual oxidant system. Plausible mechanisms of the sulfate and hydroxyl radicals in the system were proposed based on the results of radical scavenging experiments and electron spin resonance (ESR) tests. It appeared that surface OH of CP was also responsible for the MN removal. The major oxidation products in this study were 1-naphthaldehdye, naphthalene-1-ylmethanol and 4-hydroxy-4-methylnaphthalen-1(4H)-one. To better understand PS/CP in ISCO, the degradation of MN was tested in ground water matrix, which showed satisfactory efficiency. The results of this study provided some detail information of PS/CP dual oxidant in degradation organic contaminants, which might provide some references for the application of this technology in ISCO.
研究领域:
环境工程
·
环境化学
·
污染控制
·
土壤与地下水修复
·
高级氧化技术
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DOI
高影响因子
ENVIRONMENTAL POLLUTION
·
2021
·
IF 8.071
Yanping Bao,Jinhao Lai,Yishun Wang,Zheng Fang,Yongshi Su,Daniel S. Alessi,Nanthi S. Bolan,Xiaolian Wu,Yan Zhang,Xueding Jiang,Zhihong Tu,Hailong Wang
Iron (III) co-precipitation with dissolved organic matter (DOM) is pervasive in many natural environments. However, the effects of DOM on the formation of Fe(III) hydroxysulfate (FHS) and its environmental implications are poorly understood. In this study, fulvic acid (FA) was used as a model DOM compound, and experiments were devised to investigate the effects of FA on the formation of FHS. In addition, the Pb(II) adsorption capabilities of FHSs biosynthesized under various FA dosages, including kinetics and sorption isotherm experiments, were conducted. These experiments showed that co-precipitation of FA promoted the formation of Fe-FA composites, FA-doped schwertmannite , and small particles of jarosite . Co-precipitates are more enriched in carboxyl (–COOH) functional groups due to their preferential binding with FHS. The adsorption kinetics , isotherms and mechanisms of Pb onto the biosynthesized FHSs were then comprehensively characterized and modeled. Though the specific surface area decreased with increasing FA loading, the introduction of FA into FHSs increased Pb(II) adsorption, with the highest concentration of FA addition improving the removal capacity of Pb(II) to 91.54%. Kinetics studies and intra-particle diffusion models indicated that the adsorption of Pb(II) onto the FHSs was correlated with the number of active sites, and two adsorption steps: surface adsorption and the diffusion of Pb(II) in channels inside the biosynthesized FHSs, are suggested. The adsorption mechanism was attributed to cation exchange between Pb(II) and –OH and –COOH functional groups, and the co-precipitated FA provided additional sites for Pb(II) adsorption by FHS.
研究领域:
环境地球化学
·
水处理技术
·
胶体与界面化学
·
污染控制化学
·
功能材料
·
吸附科学
✓ 已验证
DOI
高影响因子
International Journal of Electrochemical Science
·
2023
·Vol. 11
·期 12
·10135-10149
·
IF 1.5
Lijuan Gong,Kangquan Qiao
The corrosion inhibition performances of Diantipyrylmethane (DAM) for mild steel in 0.5 M H 2 SO 4 were investigated using weight loss, electrochemical impedance spectroscopy (EIS), potentiodynamic polarization, scanning electron microscope (SEM) and quantum chemical calculation. The obtained results reveal that DAM acts as a mixed-type inhibitor with a predominantly anodic reaction, and the inhibition efficiency increases with increasing inhibitor concentration whereas decreases with increasing temperature. The adsorption of DAM on steel surface is found to obey Langmuir isotherm, and the adsorption mechanism is mixed physical and chemical adsorption. The results of quantum chemical calculation demonstrate that pyrazolone rings within molecular structure of DAM play a dominant role in corrosion inhibition of mild steel.
研究领域:
材料腐蚀与防护
·
物理化学
·
电化学
·
表面科学
·
量子化学
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2017
·
IF 2.714
Zhilin Xi,Zhenya Feng,Ang Li
For the control of pulverized coal, we propose a dust suppressant by applying a blend of mixed polyethylene oxide (g-PEO) and sodium dodecyl sulfate ( SDS ). In our experimental study, the thermal characteristics, critical micelle concentration ( CMC ), wettability and adhesion of the dust suppressant are investigated. It was found that g-PEO had a low fusing temperature and its combustion temperature was close to that of coal, thus, the solution containing g-PEO applied coal dust control did not affect the use of the coal. Based on steady-state fluorescence using pyrene as a fluorescent label, quantitative analysis revealed that the CMC s of g-PEO and SDS were 1 and 20 g/L in g-PEO& SDS solution, respectively. The solution containing SDS had the best wettability, but it only had a short-term effect. The solution containing g-PEO showed negligible wetting ability to wet coal dust. The solution containing g-PEO& SDS had better wetting ability and adhesion. Scanning electron microscopy showed that the coal dust covered by g-PEO& SDS on its surface could form a thin layer of armor by holding the particles together after air-drying. It was concluded that the g-PEO& SDS solution containing g-PEO for 1 g/L and SDS for 20 g/L could suppress coal dust and maintain a long-term effect.
研究领域:
环境工程
·
矿业安全
·
颗粒物控制
·
表面化学
·
燃烧科学
✓ 已验证
DOI
高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2018
·
IF 6.578
Shaosuo Bing,Jiaqian Wang,Hao Xu,Yanyan Zhao,Yong Zhou,Lin Zhang,Congjie Gao,Li’an Hou
Polyamide (PA) thin-film composite (TFC) reverse osmosis membrane is widely used for desalination , but the selectivity-permeability trade-off and oxidation are two major restrictions on the membrane application. By modifying PA TFC membrane with potassium persulfate (K 2 S 2 O 8 ), we overcame the trade-off relation (the water flux and salt rejection increased by 43.2% and 0.2%, respectively) and improved the chlorine resistance. The modification was demonstrated to be a combination of the interfacial crosslinking between PA layer and polysulfone support with the surficial oxidation of PA layer. The dense crosslinked interface enabled the membrane with higher solute rejection, better chlorine tolerance and long-term stability. Meanwhile, the thinner PA layer contributed to the increase of membrane permeability. Furthermore, the modification method has the application potential in high-performance membrane fabrication in terms of simplicity and high efficiency.
研究领域:
材料科学
·
膜分离技术
·
高分子化学
·
环境工程
·
水处理
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）