Journal of the Taiwan Institute of Chemical Engineers
·
2018
·
IF 3.849
Yafei Guo,Chang Tan,Peng Wang,Jian Sun,Junjie Yan,Weiling Li,Chuanwen Zhao,Ping Lu
Coal and biomass fly ash was impregnated with tetraethylenepentamine (TEPA) to prepare solid CO 2 sorbent. Experimental CO 2 adsorption capacities of the sorbent in fixed-bed column were fitted to several kinetic equations. The modified Avrami fractional kinetic model could accurately predict the CO 2 adsorption kinetic behaviors of the sorbent under different conditions. CO 2 adsorption rate increases with the increase in temperature, initial CO 2 concentration and gas flow rate, as a result of the decreased CO 2 diffusion resistance. A mathematical model was proposed and demonstrated to well predict the CO 2 adsorption breakthrough curves in the fixed-bed column. Effects of temperature, initial CO 2 concentration and gas flow rate on the mass transfer kinetic behaviors of the desired sorbent were investigated. The positive effect of these factors on promoting the overall mass transfer coefficient and the internal mass transfer coefficient is not significant. The external mass transfer coefficient will be remarkably reinforced with the increase in these operating parameters, due to the change in viscosity and density of the gas phase and the reduced external mass transfer resistance. Internal mass transfer process is determined as the rate-limiting step for CO 2 adsorption. The results will lay the groundwork for future scale-up application of the sorbent in post-combustion CO 2 capture.
研究领域:
环境科学
·
化学工程
·
能源工程
·
大气污染控制
·
碳捕集与封存
✓ 已验证
DOI
高影响因子
Desalination and Water Treatment
·
2024
·
IF 1
Yulong Yang,Jiao Feng,Shicui Zhu,Jinshu Zhou,Kejia Zhang,Xiaoyan Ma,Danial Gallagher,Andrea M. Dietrich
Nitrogenous disinfection by-products (N-DBPs) are more genotoxic and cytotoxic than the currently regulated carbonaceous DBPs (i.e., C-DBPs), and it has become a frontier issue of drinking water safety research. In this paper, the effect of granular activated carbon (GAC) on adsorption and its influencing factors was investigated for a typical N-DBP phenylacetonitrile, which is produced during chlorination of phenylalanine precursor during water treatment. The results showed that GAC had a high adsorption capacity (q max = 22.92 mg/g) for phenylacetonitrile, and the adsorption isotherm was fitted to the Langmuir isotherm model. Pseudo-second-order equation can well describe the behavior of phenylacetonitrile adsorption on activated carbon (R 2 > 0.990), and the adsorption rate constant k 2 = 0.7780–14.12 g/(mg h). Analysis of the influencing factors showed that higher phenylacetonitrile concentration improved the adsorption equilibrium capacity and the adsorption rate. Water temperature and pH had little effect on the capacity or rate of adsorption.
研究领域:
环境科学
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水处理工程
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毒理学
·
环境健康
✓ 已验证
DOI
高影响因子
Desalination and Water Treatment
·
2024
·
IF 1
Xu Zhang,Fan Yang,Jialing Qin,Huanghu Peng,Zezhou Chen,Lei Che,Shouxin Zhu,Wei Yang
The heterogeneous catalyst of CeO 2 /ZSM5 was applied to hydrolyze Congo red in subcritical water for the first time in the present study. The hydrolysis rate of Congo red could be significantly accelerated by introducing only 5 mg of 5% CeO 2 /ZSM5. The Congo red could be completely hydrolyzed at 220°C for 2 min—a reaction temperature 40°C lower than in the absence of 5% CeO 2 /ZSM5. In addition, the 5% CeO 2 /ZSM5 could be recycled for another run, and its Congo red hydrolysis efficiency and surface morphology showed no obvious change after 3 runs of recycling. The hydrolysis kinetics of Congo red in subcritical water could be well expressed by the Weibull model. The activation energy for hydrolysis of Congo red in subcritical water in the presence of 5% CeO 2 /ZSM5 (104.8 kJ mol –1 ) was much lower than in the absence of 5% CeO 2 /ZSM5 (155.9 kJ mol –1 ). The frequency factors were calculated to be 8.1 × 10 9 and 1.9 × 10 14 min –1 in the presence and absence of 5% CeO 2 /ZSM5, respectively. With these excellent properties, 5% CeO 2 /ZSM5 may prove to be an advantageous catalyst for the hydrolysis of Congo red in textile wastewater, in subcritical water.
研究领域:
环境化学
·
催化化学
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水处理技术
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绿色化学
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反应动力学
✓ 已验证
DOI
高影响因子
POLYMER
·
2018
·
IF 3.483
Dongxue Yang,Lingfeng Li,Binling Chen,Shuxian Shi,Jun Nie,Guiping Ma
In order to improve the removal ability of chitosan (CS) to heavy metal ions , in this study, rich amino-functionalized CS electrospun membranes have been prepared. During the efficient synthesis, poly (glycidyl methacrylate) (PGMA) and polyethylenimine (PEI) were sequentially grafted on the surface of CS electrospun membrane. The success of introduction of amino-group on the CS were confirmed by X-ray diffractometer (XRD), attenuated total reflection-fourier transform infrared (ATR-FTIR), and X-ray photoelectron spectroscopy (XPS). The ability of remove heavy metal ions (Cr(VI), Cu(II) and Co(II)) of the as-prepared membrane (CS-PGMA-PEI) was investigated. The adsorption equilibrium of the heavy metal ion solutions was rapidly established in 60 min. Adsorption kinetics analysis reveals that the adsorption process of CS-PGMA-PEI electrospun membrane was dominated by a Pseudo-second-order model. Its adsorption isotherm can be described by the Langmuir model. The maximum adsorption capacities calculated by Langmuir model were 138.96, 69.27 and 68.31 mg g −1 for Cr(VI), Cu(II) and Co(II), respectively. The adsorption ability of CS-PGMA-PEI electrospun membrane toward metal ions was found in an order of Cr(VI) > Cu(II) > Co(II). CS-PGMA-PEI membrane also exhibited a good reproducibility and stability. Our study may provide a way to synthesize membranes for water purification .
研究领域:
材料科学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
COMBUSTION AND FLAME
·
2024
·
IF 5.8
Hong Wang,Bingzhi Liu,Qiang Xu,Shijun Dong,Zhandong Wang,Long Zhu
Cyclopentanone (CPN) is a widely available biofuel with excellent combustion properties, but detailed speciation profiles during its pyrolysis have rarely been studied. This work examines the pyrolysis of CPN in a jet-stirred reactor (JSR) at atmospheric pressure, with residence time of 2 s and a temperature range from 830 K to 1100 K. Dozens of pyrolysis intermediates and products were measured using synchrotron vacuum ultraviolet photoionization mass spectrometry (SVUV-PIMS) and gas chromatography (GC). Among them, several new species were observed, including water, carbon dioxide , formaldehyde, indene , 1,2-dihydroindene, naphthalene , 1,2-dihydronaphthalene, 1-methylnaphthalene, acenaphthylene , biphenyl , and fluorene . A detailed kinetic model was developed based on the literature, and in general, it predicted the experimental results for most species well. Kinetic analyses indicated that the consumption of CPN was controlled by the bimolecular reactions with H atom. The formation of water, carbon dioxide and formaldehyde could be explained by the reaction pathways of OH radical. The pyrolysis of CPN yielded a significant number of alkenes and alkynes at higher temperatures; the bimolecular addition reactions of these species with resonantly stabilized radicals are important to the formation of polycyclic aromatic hydrocarbons (PAHs). Based on those, this work provides valuable insights into CPN pyrolysis chemistry and it promotes the development of a comprehensive CPN combustion model.
研究领域:
燃烧化学
·
能源化学
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反应动力学
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分析化学
·
环境化学
✓ 已验证
DOI
高影响因子
BIORESOURCE TECHNOLOGY
·
2020
·
IF 7.539
Kaijun Wang,Sining Yun,Tian Xing,Bingjie Li,Yasir Abbas,Xinming Liu
The effects of binary and ternary trace elements (TEs) (Fe/Co, Fe/Ni, and Fe/Co/Ni) on the anaerobic digestion (AD) of cattle manure were investigated using kinetic models (first-order, logistic, modified Gompertz, and Coats-Redfern) and experimental measurements. Binary and ternary TEs can significantly improve the biogas production rate and yield potential. The deviation between the predicted and measured data for biogas yield with logistic model (2.1%–5.3%) and modified Gompertz model (0.32%–2.9%) was smaller than that with first-order kinetic model (6.9%–9.9%). The Coats-Redfern model fitting indicated that the activation energy of digestates with trace elements during pyrolysis was reduced by 3.9%–26.2% compared with the control group. Meanwhile, digestates with TEs showed remarkable fertility (5.72%–5.95%). The combination of kinetic models and experimental measurements can effectively quantify the effect of TEs on AD performance and provide an informed choice for industrial production.
研究领域:
环境科学
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农业工程
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生物质能源
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废物资源化
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生物化学工程
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2014
·
IF 4.058
Ming-Xia Wang,Qi-Lei Zhang,Shan-Jing Yao
Mycelial pellets prepared using a marine-derived Penicillium janthinellum sp. strain (P1) were applied as biosorbents to remove dyes from aqueous solutions. Nine different dyes were studied and the effects of pH and salt concentration on the decolorization processes were investigated. The results showed that the mycelial pellet was effective in removing dyes from their water solutions. Moreover, it was found that pH was an important factor of the decolorization process and the best dye removal performance was achieved when pH = 5.0. The adsorption process of the live mycelial pellets was not affected by high salt concentrations. In addition, the mycelial pellets retained 91.3% of the original decolorization activity after five reusing cycles without any desorption treatments. The adsorption isotherms indicated that the biosorption process agreed well with the Langmuir isotherm model with a maximum biosorption capacity of 344.83 mg g(dry) − 1 and the kinetic adsorption results showed that the biosorption process followed a pseudo-second-order kinetic model.
研究领域:
环境微生物学
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环境工程
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生物吸附
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水污染控制
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应用微生物学
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环境化学
✓ 已验证
DOI
高影响因子
PROCEEDINGS OF THE COMBUSTION INSTITUTE
·
2022
·Vol. 39
·期 1
·315-324
·
IF 6.535
Qianjin Lin,Wanxiong Liao,Jia Cheng,Chun Zou,Bin Yang,Wenxiang Xia
Few studies on the low-temperature combustion behavior of MIPK, being a promising fuel additive , have been conducted. In this work, ignition delay times (IDTs) of MIPK were measured in the temperatures ranging between 780–910 K and pressures of 20 and 25 bar using a rapid compression machine (RCM). Oxy-fuel combustion combined with biofuel could remove CO 2 from the atmosphere. The IDTs of MIPK were measured in the temperatures ranging between 1125–1600 K under the O 2 /CO 2 atmosphere at the pressures of 1 and 10 bar using a shock tube . A low to high-temperature MIPK kinetic model (HUST-MIPK model) was proposed, in which the low-temperature sub-model consists of 19 low-temperature reaction classes and was constructed by analogy-based method, the high-temperature sub-model was adapted from the works of Cheng et al.. The predictions of HUST-MIPK model are in good agreement with the present low-temperature IDTs, high-temperature O 2 /CO 2 atmosphere IDTs, and the literature experimental data. The negative temperature coefficient (NTC) behavior was not observed in the temperature range from 790 to 910 K in the present RCM experiments, but was observed for methyl propyl ketone (MPK) and diethyl ketone (DEK) under similar conditions. The low-temperature chemistry of three pentanone isomers (MIPK, MPK, and DEK) was compared using the flux and sensitivity analysis. The comparison of the experimental high-temperature IDTs between O 2 /CO 2 and O 2 /Ar atmospheres indicates the IDTs of MIPK under O 2 /CO 2 atmosphere are longer than those under O 2 /Ar atmosphere at 1 bar, and the effects of CO 2 are almost independent of the pressure. The physical and chemical effects of CO 2 on the ignition were studied in detail.
研究领域:
燃烧化学
·
燃料化学
·
反应动力学
·
能源工程
·
大气环境影响
✓ 已验证
DOI
高影响因子
Journal of the Taiwan Institute of Chemical Engineers
·
2016
·
IF 2.848
Zhanjing Guo,Xiongmin Liu,Hongmiao Huang,Lingfeng Jiang
The strong acidic cationic exchange fiber (SACEF) was used to adsorb yohimbine from alcoholic solution. Batch experiments were performed to examine the effects of adsorbent dosage, solution pH and temperature in the adsorption process. The thermodynamics and kinetics of adsorption were also analyzed. The optimum yohimbine adsorption onto the SACEF was found at pH = 5 of solution and equilibrium could be attained within 20 min. The equilibrium adsorption data were preferably modeled with the Freundlich isotherm model and the thermodynamic parameters were calculated to be: 11.99 kJ/mol < Δ H < 13.72 kJ/mol, −21.17 kJ/mol < Δ G < −17.87 kJ/mol and 63.18 J/mol K < Δ S < 65.60 J/mol K. The results demonstrated that the adsorption was an endothermic, spontaneous and feasible process of physisorption . Meanwhile, yohimbine adsorption on SACEF fitted well to the pseudo-second-order kinetic model and the adsorption rate was limited by film diffusion. The activation energy Ea was calculated to be 14.39 kJ/mol. Furthermore, the surface morphologies of the SACEF before and after yohimbine adsorption were analyzed by SEM and the adsorption mechanism was discussed by FTIR analysis. SACEF could effectively adsorb yohimbine from alcoholic solution and could be used repeatedly for more than five cycles.
研究领域:
药物化学
·
药剂学
·
物理化学
·
分离科学
·
吸附科学
·
天然产物提取
·
药物代谢
✓ 已验证
DOI
高影响因子
COMBUSTION AND FLAME
·
2021
·
IF 4.185
Zhi-Hao Jin,Jin-Tao Chen,Wang Li,Shu-Bao Song,Jiu-Zhong Yang,Zhen-Yu Tian
Owing to significant advantages over traditional biofuels, 2-methylfuran (MF) has arisen extensive interest as next generation biofuels . Atmospheric pressure pyrolysis of a 1:1 blend of MF with a three-component (3C) surrogate jet fuel was conducted in a flow tube using synchrotronphotoionization and molecular beam mass spectrometry techniques within a temperature range of 898–1223 K. Therein, the 3C surrogate fuel consists of 66.2% n-dodecane (NC 12 H 26 ), 18.0% 1,3,5-trimethylcyclohexane (T135MCH) and 15.8% n-propylbenzene (NPB, A1C 3 H 7 ). The detailed kinetic model including 579 species and 3474 reactions was developed via validating against both measured and literature data with reasonable agreement. MF exhibits no obvious influence on the 3C components pyrolysis . However, 3C mixtures play an important roles in MF decomposition: lower initial temperature and different decomposition pathways. In the meantime, n-propylbenzene (NPB) pyrolysis curve in 3C and 3C+MF significantly transfers to low temperature zone after 1000 K in contrast to pure NPB, while smaller change was found in the decomposition curve of n-dodecane. Compared with 3C pyrolysis, 3C+MF blends have less formation of aromatic species and light hydrocarbons except for vinylacetylene (C 4 H 4 ) and acetylene (C 2 H 2 ). Allyl radical (C 3 H 3 ) has significant roles in benzene ring formation. The combination of allyl radical with propargyl radical producing benzene and H radical (aC 3 H 5 + C 3 H 3 = A1 + 2H) has the highest contribution to the benzene formation in both 3C and 3C+MF. Moreover, most of naphthalene (A2) formation is also related to C 3 H 3 radical via reaction: A1CH 2 + C 3 H 3 = A2 + H, rather than via HACA (hydrogen abstraction carbon addition) reaction. Interaction of fuel blends was mainly presented through the common and important sensitive reactions which are much to do with CH 3 and H radicals. The overview of product distribution was investigated by providing comparisons of carbon conversion rates during the pyrolysis of 3C and 3C+MF. These results will be helpful to better understand the pyrolysis properties of MF/jet fuel surrogate blends and could contribute to developing new generation biofuels for aviation.
研究领域:
燃料化学
·
燃烧动力学
·
生物燃料
·
能源化学
·
反应机理
·
质谱分析
✓ 已验证
DOI
高影响因子
PROCEEDINGS OF THE COMBUSTION INSTITUTE
·
2018
·Vol. 37
·期 1
·565-573
·
IF 5.336
Xiaoyuan Zhang,Yuyang Li,Chuangchuang Cao,Jiabiao Zou,Yan Zhang,Wei Li,Tianyu Li,Jiuzhong Yang,Philippe Dagaut
The kinetics of propanal oxidation was studied in a jet-stirred reactor (JSR) at atmospheric pressure. The investigated temperature range is from 450 to 800 K at two different equivalence ratios (0.35 and 4.0). Thanks to the synchrotron vacuum ultraviolet photoionization mass spectrometry (SVUV-PIMS), critical intermediates were identified, including methylperoxy, methyl hydroperoxide , ethylperoxy, ethyl hydroperoxide, α-lactone, β-propiolactone and ketohydroperoxides. A kinetic model for propanal oxidation was also developed and validated against the present experimental results, as well as those available from the literature. Main chain-branching pathways under the investigated conditions were analyzed based on present experimental data and kinetic model . The O 2 addition reaction to the propanoyl radical and subsequent oxidation reactions play an important role in determining the oxidation rate of propanal under fuel-lean conditions, especially in the low-temperature oxidation region. Under fuel-rich conditions, the decomposition of the propanoyl radical is predominant and C 2 H 5 relevant reactions consequently determine the kinetics of oxidation of propanal.
研究领域:
物理化学
·
燃烧化学
·
反应动力学
·
分析化学
·
能源化学
✓ 已验证
DOI
高影响因子
COMBUSTION AND FLAME
·
2021
·
IF 4.185
Jizhen Zhu,Sixu Wang,Mohsin Raza,Yuan Feng,Jing Li,Yebing Mao,Liang Yu,Yong Qian,Xingcai Lu
Methanol is an attractive oxygenate increasingly used as primary fuel for dual-fuel combustion technology yielding beneficial thermal-efficiency and emissions in modern engines. As such, it is significant to fundamentally understand the autoignition behavior of methanol/diesel mixtures. This study measured the ignition delay times (IDTs) of methanol/diesel blends with different mixing ratios (30%, 50%, 70% methanol by mol.) on a heated shock tube and a heated rapid compression machine at temperatures of 650−1450 K, pressures of 6−20 bar, and equivalence ratios of 0.5, 1.0 and 2.0. The typical two-stage ignition characteristics with the negative temperature coefficient response were observed for dual-fuel mixtures. In general, both the total and first-stage IDTs decrease with the increment of pressure and equivalence ratio as well as diesel proportion in mixtures. The simulation results performed with a published detailed mechanism in conjunction with a tri-component diesel surrogate demonstrate generally good agreement with the experimental data at all test conditions. Moreover, a crossover of IDTs occurs at a higher temperature (~1500 K) for varying equivalence ratios, and experiment and simulation both exhibit a non-linear mixing effect of methanol addition on diesel ignition. Interestingly, simulation results clearly suggest a crossover (~940 K) for mixtures with varying methanol content at an intermediate-temperature, where the IDT of the mixture with a lower methanol ratio becomes longer as the temperature is higher than that of the crossover. Furthermore, brute-force sensitivity analyses assisted with reaction path analysis were conducted to gain deeper insights into the autoignition chemistry of dual-fuel mixtures, especially for the chemical interaction between both fuels during the low-temperature oxidation process . It is found that methanol hardly generates •OH, whereas •OH is mainly produced by the low-temperature reaction pathways of diesel. Thus, •OH is the bridge for both fuels during the ignition process. At the high methanol ratio, the H-abstraction of diesel is mainly via •HO 2 while CH 3 OH consumes a large percentage of •OH. Consequently, the competition between methanol and diesel for •OH radicals inhibits the overall reactivity of reaction network. In addition, the original data reported here lay a foundation for the development and validation of more accurate and robust dual-fuel kinetic schemes.
研究领域:
燃烧化学
·
燃料科学
·
化学动力学
·
内燃机工程
·
替代燃料技术
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）