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中国化学工程学报(英文版)
中国化学工程学报(英文版)

廖叶华

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1004-9541

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中国化学工程学报(英文版)/Journal Chinese Journal of Chemical EngineeringCSCDCSTPCD北大核心EISCI
查看更多>>The Chinese Journal of Chemical Engineering (Bimonthly, started in 1982) is the official journal of the Chemical Industry and Engineering Society of China and published by the Chemical Industry Press. The aim of the journal is to develop the international exchange of scientific and technical information in the field of chemical engineering. It publishes original research papers that cover the major advancements and achievements in chemical engineering in China as well as some articles from overseas contributors. The topics of journal include chemical engineering, chemical technology, biochemical engineering, energy and environmental engineering and other relevant fields. Papers are published on the basis of their relevance to theoretical research, practical application or potential uses in the industry as Research Papers, Research Notes, Chemical Engineering Data and Reviews. Prominent domestic and overseas chemical experts and scholars have been invited to form an International Advisory Board and the Editorial Committee. It enjoys recognition among Chinese academia and industry as a reliable source of information of what is going on in chemical engineering research, both domestic and abroad.
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    Co3O4 as an efficient passive NOx adsorber for emission control during cold-start of diesel engines

    Jinhuang CaiShijie HaoYun ZhangXiaomin Wu...
    1-7页
    查看更多>>摘要:The Co3O4 nanoparticles,dominated by a catalytically active(110)lattice plane,were synthesized as a low-temperature NOx adsorbent to control the cold start emissions from vehicles.These nanoparticles boast a substantial quantity of active chemisorbed oxygen and lattice oxygen,which exhibited a NOx uptake capacity commensurate with Pd/SSZ-13 at 100 ℃.The primary NOx release temperature falls within a temperature range of 200-350 ℃,making it perfectly suitable for diesel engines.The charac-terization results demonstrate that chemisorbed oxygen facilitate nitro/nitrites intermediates formation,contributing to the NOx storage at 100 ℃,while the nitrites begin to decompose within the 150-200 ℃ range.Fortunately,lattice oxygen likely becomes involved in the activation of nitrites into more stable nitrate within this particular temperature range.The concurrent processes of nitrites decomposition and its conversion to nitrates results in a minimal NOx release between the temperatures of 150-200 ℃.The nitrate formed via lattice oxygen mainly induces the NOx to be released as NO2 within a temperature range of 200-350 ℃,which is advantageous in enhancing the NOx activity of downstream NH3-SCR catalysts,by boosting the fast SCR reaction pathway.Thanks to its low cost,considerable NOx absorption capacity,and optimal release temperature,CO3O4 demonstrates potential as an effective material for passive NOx adsorber applications.

    Hydrothermal hydrogenation/deoxygenation of palmitic acid to alkanes over Ni/activated carbon catalyst

    Min LinYuhao YanXiaoxian LiRui Li...
    8-18页
    查看更多>>摘要:To produce paraffin from hydrogenation/deoxygenation of palmitic acid,model compound of bio-oil obtained by hydrothermal liquefaction(HTL)of microalgae has been an attractive focus in recent years.In order to avoid energy-intensive separation process of water and bio-oil,it is of importance that deoxygenation upgrading of fatty acids under hydrothermal conditions similar to HTL process.Herein,it is the first time to explore the application of activated carbon(AC)-supported non-noble-metal catalysts,such as Ni,Co,and Mo,and so on,in the hydrothermal hydrogenation/deoxygenation of long-chain fatty acids,and the obtained Ni/AC-H(the Ni/AC was further H2 pre-reduced)is one of the best catalysts.In addition,it is found that the catalytic activity can be further improved by H2 pre-reduction of catalyst.Characterization results that are more low valences of nickel and oxygen vacancy can be obtained after H2 pre-reduction,thus significant promoting the deoxygenation especially the decarbonylation pathway of fatty acids.The total alkanes yield can reaches 95.9%at optimal conditions(280 ℃,360 min).This work confirmed that the low-priced AC-supported non-noble-metal catalysts have great potential compared with the noble-metal catalyst,in hydrothermal upgrading of bio-oil.

    Dual-functional poly(2-methyl-2-oxazoline)/poly(2-(dimethylamine)ethyl methacrylate)mixed brushes with switchable protein adsorption and antibacterial properties

    Kang HeLiangyu ZhuYanmei Wang
    19-30页
    查看更多>>摘要:Herein,binary mixed brushes consisting of poly(2-methyl-2-oxazoline)(PMOXA)and poly(2-(dime-thylamine)ethyl methacrylate)(PDMAEMA)with different chain lengths were fabricated by successive grafting of NH2-terminated PMOXA and SH-terminated PDMAEMA onto polydopamine-anchored sub-strates.The mixed-brush coating was characterized by variable-angle spectroscopic ellipsometry,X-ray photoelectron spectroscopy,Fourier transform infrared spectroscopy,zeta potential measurements,water contact angle,and atomic force microscopy.The mixed brushes showed tunable surface charge,wettability,and surface roughness,depending on the degree of PDMAEMA swelling under varying pH and ionic strength(I).Then the adsorption behaviors of pepsin,bovine serum albumin(BSA),γ-globulin,and lysozyme,four very different proteins with regard to isoelectric point,on the mixed brushes coating were studied by using fluorescence microscopy and surface plasmon resonance.When the chain length of PDMAEMA was about twice as long as PMOXA,the mixed brushes not only had high adsorption ca-pacity for pepsin,BSA,and y-globulin but also had a desorption efficiency of 86.9%,87.1%,and 93.5%,respectively.It is explained that electrostatic attraction between the protonated PDMAEMA and posi-tively charged acidic proteins(pepsin and BSA,whose isoelectric points were below the pKa of PDMAEMA)would drive the intensive adsorption(at pH 3,I=10-3 mol·L-1 for pepsin,and pH 5,I=10-5 mol·L-1 for BSA),while desorption was dominated by the hydrophilic PMOXA when PDMAEMA was shrinking(at pH 7,I=10-1mol·L-1 for pepsin,and pH 9,I=10-1 mol·L-1 for BSA).Furthermore,the isoelectric precipitation led to the adsorption of neutral protein(γ-globulin,whose isoelectric point was near the pKa of PDMAEMA)at pH 7,I=10-5 mol·L-1,while electrostatic repulsion and antifouling PMOXA triggered the desorption of y-globulin at pH 3,I=10-1 mol·L-1.However,alkaline protein(lysozyme,whose isoelectric point was higher than the pKa of PDMAEMA)exhibited slight adsorption on PMOXA/PDMAEMA mixed brushes under test conditions,regardless of whether PMOXA or PDMAEMA occupied the outermost layer.The antibacterial property of the mixed brushes against Escherichia coli was investigated.PMOXA/PDMAEMA mixed brushes showed significant bactericidal activity at pH 3,I=10-3 mol·L-1,while the rinse of pH 9,1=10-1 mol·L-1 solution could remove most of the residual bacteria.This work not only enables controlled adsorption of proteins with different isoelectric points but also ensures that the surface of the coating is minimized from bacterial contamination.

    High performance photodegradation resistant PVA@TiO2/carboxyl-PES self-healing reactive ultrafiltration membrane

    Yu LiangYuanfang FanZhongmin SuMingxin Huo...
    31-39页
    查看更多>>摘要:The occurrence of ultrafiltration(UF)membrane fouling frequently hampers the sustainable advancement of UF technology.Reactive self-cleaning UF membranes can effectively alleviate the problem of membrane fouling.Nevertheless,the self-cleaning process may accelerate membrane aging.Addressing these con-cerns,we present an innovative design concept for composite self-healing materials based on self-cleaning UF membranes.To begin,TiO2 nanoparticles were incorporated into the polymer molecular structure via molecular design,resulting in the synthesis of TiO2/carboxyl-polyether sulfone(PES)hybrid materials.Subsequently,the nonsolvent-induced phase inversion technique was employed to prepare a novel of UF membrane.Lastly,a polyvinyl alcohol(PVA)hydrogel coating was applied to the hybrid UF membrane surface to create PVA@TiO2/carboxyl-PES self-healing reactive UF membranes.By establishing a covalent bond,the TiO2 nanoparticles were effectively and uniformly dispersed within the UF membrane,leading to exceptional self-cleaning properties.Furthermore,the water-absorbing and swelling properties of PVA hydrogel,along with its capacity to form hydrogen bonds with water molecules,resulted in UF membranes with improved hydrophilicity and active self-healing abilities.The results demonstrated that the water contact angle of PVA@5%TiO2/carboxyl-PES UF membrane was 43.1 °.Following a 1-h exposure to simulated solar exposure,the water flux recovery ratio increased from 48.16%to 81.03%.Moreover,even after un-dergoing five cycles of 12-h simulated sunlight exposure,the UF membranes exhibited a consistent retention rate of over 97%,thus fully demonstrating their exceptional self-cleaning,antifouling,and self-healing capabilities.We anticipate that the self-healing reactive UF membrane system will serve as a pioneering and comprehensive solution for the self-cleaning antifouling challenges encountered in UF membranes while also effectively mitigating the aging effects of reactive UF membranes.

    Pt nanoclusters modified porous g-C3N4 nanosheets to significantly enhance hydrogen production by photocatalytic water reforming of methanol

    Yi-Fei LiangJin-Rong LuShang-Kun TianWen-Quan Cui...
    40-50页
    查看更多>>摘要:For the use of green hydrogen energy,it is crucial to have efficient photocatalytic activity for hydrogen generation by water reforming of methanol under mild conditions.Much attention has been paid to g-C3N4 as a promising photocatalyst for the generation of hydrogen.To improve the separation of pho-togenerated charge,porous nanosheet g-C3N4 was modified with Pt nanoclusters(Pt/g-C3N4)through impregnation and following photo-induced reduction.This catalyst showed excellent photocatalytic activity of water reforming of methanol for hydrogen production with a 17.12 mmol·g-1·h-1 rate at room temperature,which was 311 times higher than that of the unmodified g-C3N4.The strong interactions of Pt-N in Pt/g-C3N4 constructed effective electron transfer channels to promote the separation of photo-generated electrons and holes effectively.In addition,in-situ infrared spectroscopy was used to inves-tigate the intermediates of the hydrogen production reaction,which proved that methanol and water eventually turn into H2 and CO2 via formaldehyde and formate.This study provides insights for un-derstanding the photocatalytic hydrogen production in the water reforming of methanol.

    OSDA-free synthesis of FeZSM-22 zeolite from natural minerals for n-octane hydroisomerization

    Tiesen LiTing ChenYinghui YePeng Dong...
    51-59页
    查看更多>>摘要:A seed-directed approach to synthesizing FeZSM-22 zeolite without organic structure directing agent(OSDA)was developed by using Fe-rich diatomite as all aluminum and iron sources.The FeZSM-22 zeolite with optimal crystallinity and purity can be obtained by systematically adjusting feed composi-tion and synthesis conditions.Characterizations show that FeZSM-22 zeolite synthesized with OSDA-free owns high crystallinity,obvious thin needle-shaped morphology and high Bronsted/Lewis acid ratio.Significantly,when used for n-octane hydroisomerization reaction,its derived catalyst exhibits the best catalytic performance reflected by the highest selectivity to C8 isomers compared to the two reference catalysts prepared based on a Fe-containing and a Fe-free ZSM-22 synthesized through an OSDA-directed route from natural diatomite and conventional chemicals,respectively.This work provides an alternative route to sustainably synthesizing heteroatomic zeolites with high performance.

    The flow behavior of droplet adsorption on a liquid-liquid interface accompanied by cross-linking reaction and phase separation in a microchannel

    Haozhe YiTaotao FuChunying ZhuYouguang Ma...
    60-70页
    查看更多>>摘要:The adsorption process of droplets on the liquid-liquid interface and phase separation process can regulate the spatial distribution of the fluid system,which are crucial for chemical engineering.However,the cross-linking reaction,which is widely used in the field of polymers,can change the physical properties of the fluids and affect the flow behavior accordingly.A configuration of microchannels is designed to conveniently generate uniform droplets in one phase of the parallel flow.The flow behavior of the adsorption process of sodium alginate droplets on the liquid-liquid interface is investigated,and the subsequent process of phase separation is studied.In the process of droplet adsorption,the cross-linking reaction occurs synchronously,which makes the droplet viscosity and the elasticity modules of the droplet surface increase,thus affecting the dynamics of the adsorption process and the equilibrium shape of the droplet.The variation of the adsorption length with time is divided into three stages,which all conform to power law relationship.The exponents of the second and third stages deviate from the results of the Tanner's law.The flow pattern maps of droplet adsorption and phase separation are drawn,and the operating ranges of complete adsorption and complete separation are provided.This study provides a theoretical basis for further studying the flow behavior of droplets with cross-linking reaction in a microchannel.

    A data-driven model of drop size prediction based on artificial neural networks using small-scale data sets

    Bo WangHan ZhouShan JingQiang Zheng...
    71-83页
    查看更多>>摘要:An artificial neural network(ANN)method is introduced to predict drop size in two kinds of pulsed columns with small-scale data sets.After training,the deviation between calculate and experimental results are 3.8%and 9.3%,respectively.Through ANN model,the influence of interfacial tension and pulsation intensity on the droplet diameter has been developed.Droplet size gradually increases with the increase of interfacial tension,and decreases with the increase of pulse intensity.It can be seen that the accuracy of ANN model in predicting droplet size outside the training set range is reach the same level as the accuracy of correlation obtained based on experiments within this range.For two kinds of columns,the drop size prediction deviations of ANN model are 9.6%and 18.5%and the deviations in correlations are 11%and 15%.

    A green cross-linking method for the preparation of renewable three-dimensional graphene sponges for efficient adsorption of Congo red dye

    Zhuang LiuBo GaoHaoyuan HanYuling Li...
    84-93页
    查看更多>>摘要:Graphene-based materials possess significant potential for the treatment of dye wastewater due to their exceptional adsorption properties toward stubborn pollutants.However,their utilization is hindered by high preparation costs,low yields,environmental pollution during synthesis,and challenges in regenerating the adsorbent.This study proposes a novel approach to address these limitations by developing nitrogen-doped three-dimensional(3D)polyvinyl alcohol(PVA)cross-linked graphene sponges(N-PGA)using a cross-linking method with ammonium carbonate.This method offers a relatively mild,environmentally friendly approach.Ammonium carbonate serves as both a reducing and modifying agent,facilitating the formation of the intrinsic structure of N-PGA and acting as a nitrogen source.Meanwhile,PVA is utilized as the cross-linking agent.The results demonstrate that N-PGA exhibits a favorable internal 3D hierarchical porous structure and possesses robust mechanical properties.The measured specific surface area(BET)of N-PGA was as high as 406.538 m2·g-1,which was favorable for its efficient adsorption of Congo red(CR)dye molecules.At an initial concentration of 50 mg·L-1,N-PGA achieved an impressive removal rate of 89.6%and an adsorption capacity of 112 mg·g1 for CR dye.Furthermore,it retained 79%of its initial adsorption capacity after 10 cycles,demonstrating excellent regeneration performance.In summary,the syn-thesized N-PGA displays remarkable efficacy in the adsorption of CR dye in wastewater,opening up new possibilities for utilizing 3D porous graphene nanomaterials as efficient adsorbents in waste-water treatment.

    Modeling and analysis of air combustion and steam regeneration in methanol to olefins processes

    Jinqiang LiangDanzhu LiuShuliang XuMao Ye...
    94-103页
    查看更多>>摘要:Light olefins is the incredibly important materials in chemical industry.Methanol to olefins(MTO),which provides a non-oil route for light olefins production,received considerable attention in the past decades.However,the catalyst deactivation is an inevitable feature in MTO processes,and regeneration,therefore,is one of the key steps in industrial MTO processes.Traditionally the MTO catalyst is regenerated by removing the deposited coke via air combustion,which unavoidably transforms coke into carbon dioxide and reduces the carbon utilization efficiency.Recent study shows that the coke species over MTO catalyst can be regenerated via steam,which can promote the light olefins yield as the deactivated coke species can be essentially transferred to industrially useful synthesis gas,is a promising pathway for further MTO processes development.In this work,we modelled and analyzed these two MTO regeneration methods in terms of carbon utilization efficiency and technology economics.As shown,the steam regeneration could achieve a carbon utilization efficiency of 84.31%,compared to 74.74%for air combustion regen-eration.The MTO processes using steam regeneration can essentially achieve the near-zero carbon emission.In addition,light olefins production of the MTO processes using steam regeneration is 12.81%higher than that using air combustion regeneration.In this regard,steam regeneration could be considered as a potential yet promising regeneration method for further MTO processes,showing not only great environmental benefits but also competitive economic performance.