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Journal ArticleDOI

Fabrication of ceramic membrane supported palladium catalyst and its catalytic performance in liquid-phase hydrogenation reaction

Yefei Liu1, Minghua Peng1, Hong Jiang1, Weihong Xing1, Yong Wang1, Rizhi Chen1 
01 Apr 2017-Chemical Engineering Journal (Elsevier)-Vol. 313, Iss: 313, pp 1556-1566
TL;DR: Higher catalytic activity and stability were observed for the Pd NPs deposited on the polydopamine-functionalized membrane as compared to the membrane without modification, and a superior catalytic stability could be obtained.
About: This article is published in Chemical Engineering Journal.The article was published on 2017-04-01. It has received 33 citations till now. The article focuses on the topics: Ceramic membrane & Membrane.
Citations
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Journal ArticleDOI
TL;DR: In this article, the authors present a review on enzyme immobilization focusing on the three fundamental aspects to consider when dealing with the topic: catalytic properties, enzyme leakage and reusability.
Abstract: Transfer Challenges, Enzyme Leakage and Reuse of Materials DTU Orbit (04/08/2019) Enzyme Immobilization on Inorganic Surfaces for Membrane Reactor Applications: Mass Transfer Challenges, Enzyme Leakage and Reuse of Materials Enzyme immobilization is an established method for the enhancement of enzyme stability and reusability, two factors that are of great importance for industrial biocatalytic applications. Immobilization can be achieved by different methods and on a variety of carrier materials, both organic and inorganic. Inorganic materials provide the advantage of high stability and long service life which, together with the prolonged service life of the immobilized enzyme, can benefit the process economy. However, enzyme immobilization and increased stability often come at the cost of decreased enzyme activity. The main challenges involved in the design of an efficient immobilized enzyme system is to obtain both retention of high enzyme activity, enhanced stability and reusability, which is a complicated task, given the many variables involved, and the large numbers of methods and materials available. Simultaneously, new carrier materials and morphologies are constantly being developed. An investigation of enzyme immobilization systems on inorganic materials, with special emphasis on inorganic membranes, has been conducted in order to evaluate the effects of the immobilization system on the enzyme properties upon immobilization, i.e., activity, stability and reusability. The material properties of the enzyme carriers (particles and membranes) and their effects on the success of immobilization are described here. Furthermore, the reuse of inorganic membranes as enzyme carriers has been investigated and the reported examples show high ability of regeneration. To the best of our knowledge, this is the first review on enzyme immobilization focusing on the three fundamental aspects to consider when dealing with the topic: catalytic properties, enzyme leakage and reusability. Abbreviations: β‐Gal: β‐d‐galactosidase; ADH: alcohol dehydrogenase; AFM: atomic force microscopy; APTES: 3‐ aminopropyltriethoxysilane; APTMS: 3‐aminopropyltrimethoxysilane; BPA: bisphenol A; BSA: bovine serum albumin; CA: carbonic anhydrase; CALB: Candida antartica lipase B; CD: circular dichroism; CDI: carbonyldiimidazole; CLEA: cross‐ linked enzyme aggregates; CLSM: confocal laser scanning microscopy; CNT: carbon nanotube; CPG: controlled pore glass; CRL: Candida rugosa lipase; DMeDMOS: dimethyldimethoxysilane; DRIFT: diffuse reflectance Fourier transform infrared; E2: 17β‐estradiol; EDC: N‐(3‐dimethylaminopropyl)‐N′‐ethylcarbodiimide hydrochloride; EDS: electron dispersive spectroscopy; FDH: formate dehydrogenase; FESEM: field emission scanning microscopy; FT‐IR: Fourier transform infrared spectroscopy; GA: glutaraldehyde; GCSZn: coal fly ashes glass‐ceramic zinc sulfate; GOD: glucose oxidase; GPS: 3‐(glycidyloxypropyl)trimethoxysilane; HDMI: hexamethylene diisocyanate; HRP: horseradish peroxidase; IEP: isoelectric point; IPTES: (3‐isocyanatopropyl)triethoxysilane; IR: infrared spectroscopy; LbL: layer‐by‐layer: MCP: metallic ceramic powder; MeTEOS: methyltriethoxysilane; MF: microfiltration; MML: Mucor miehei lipase; MNP: magnetic nanoparticle; MPTMS: 3‐mercaptopropyltrimethoxysilane; NHS: N‐hydroxysuccinimidyl; PAH: poly(allylamine hydrochloride); PEI: polyethyleneimine; PEG: polyethylene glycol; PES: polyether sulfone; PM‐IRRAS: polarization modulation infrared reflection absorption spectroscopy; pNPA: para‐nitrophenyl acetate; pNPP: para‐nitrophenyl palmitate; PSS: polystyrene sulfonate; PTMS: phenyltrimethoxysilane; ROL: Rhizopus oryzae lipase; SCAD: Saccharomyces cerevisiae alcohol dehydrogenase; SDS: sodium dodecyl sulfate; SDS‐2: sodium dodecyl sulfonate; SEM: scanning electron microscopy; TEM: transmission electron microscopy; TEOS: tetraethoxysilane; TGA: thermogravimetric analysis; TLL: Thermomyces lanuginosa lipase; TMP: transmembrane pressure; TTIP: titanium tetraisoproxide; TVL: Trametes versicolor laccase; UF: ultrafiltration; VTMS: vinyltrimethylsilane

111 citations

Journal ArticleDOI
TL;DR: In this article, a novel polyvinylidene fluoride-cohexafluoropropyle (PVDF-HFP)/catechol-polyethyleneimine (CA-PEI)/Ag/3-glycidyloxy propyltrimethoxysilane (KH560) tubular nanofiber membrane (TNM) for applications in dye degradation and oil/water separation was fabricated.

48 citations

Journal ArticleDOI
TL;DR: In this paper, bismuth nanoparticles supported by N-doped reduced graphene oxide (Bi/NG) and carbon black were synthesized using hydrazine as the reductant, and the resulting Bi/NG showed a superior catalytic activity towards the reduction of 4-nitrophenol (4-NP) with a high normalized rate constant (32.1 min−1·mg−1), which is 2.9

44 citations

Journal ArticleDOI
TL;DR: In this article, a ceramic membrane catalyst (Ni/Al2O3) was studied to control the CNTs growth, with reaction parameters, including catalytic temperature and Ni content investigated.

25 citations

Journal ArticleDOI
TL;DR: In this article, an analogue of mussel adhesive protein, polydopamine (PDA), was used as an active and green platform for the in situ Pd reduction by taking advantage of its high adhesion and reducing activity.
Abstract: We report a facile and green approach for the synthesis of novel Pd-loaded nanofibrous membrane and its catalytic performance for dechlorinating trichloroethylene. An analogue of mussel adhesive protein, polydopamine (PDA), was used as an active and green platform for the in situ Pd reduction by taking advantage of its high adhesion and reducing activity. A PDA layer was firstly coated on the surface of a nanofibrous membrane. Soaking this PDA-coated membrane into Pd solution led to spontaneous generation of Pd nanoparticles. The resulting membrane achieved a Pd loading of 4.56 wt.%. When applied for treating trichloroethylene in an aqueous solution, the Pd-loaded nanofibrous membrane showed excellent dechlorination performance (degree of TCE dechlorination can reach up to 96.5 (±0.32) %) with high recyclability.

22 citations

References
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Journal ArticleDOI
19 Oct 2007-Science
TL;DR: Inspired by the composition of adhesive proteins in mussels, dopamine self-polymerization is used to form thin, surface-adherent polydopamine films onto a wide range of inorganic and organic materials, including noble metals, oxides, polymers, semiconductors, and ceramics.
Abstract: We report a method to form multifunctional polymer coatings through simple dip-coating of objects in an aqueous solution of dopamine. Inspired by the composition of adhesive proteins in mussels, we used dopamine self-polymerization to form thin, surface-adherent polydopamine films onto a wide range of inorganic and organic materials, including noble metals, oxides, polymers, semiconductors, and ceramics. Secondary reactions can be used to create a variety of ad-layers, including self-assembled monolayers through deposition of long-chain molecular building blocks, metal films by electroless metallization, and bioinert and bioactive surfaces via grafting of macromolecules.

8,669 citations

Journal ArticleDOI
TL;DR: The present review describes the use of metal-organic frameworks as porous matrices to embed metal nanoparticles (MNPs) and occasionally metal oxide clusters, which are subsequently used as heterogeneous catalysts, according to the embedded metal.
Abstract: The present review describes the use of metal–organic frameworks (MOFs) as porous matrices to embed metal nanoparticles (MNPs) and occasionally metal oxide clusters, which are subsequently used as heterogeneous catalysts. The review is organized according to the embedded metal including Pd, Au, Ru, Cu, Pt, Ni and Ag. Emphasis is also given in the various methodologies reported for the formation of the NPs and the characterization techniques. The reactions described with this type of solid catalysts include condensation, hydrogenations, carbon–carbon coupling, alcohol oxidations and methanol synthesis among others. Remaining issues in this field have also been indicated.

883 citations

Journal ArticleDOI
TL;DR: The developed ZIF-8 membranes show high hydrogen selectivity and thermal stability, and are promising for hydrogen separation and purification.
Abstract: Inspired by the bioadhesive ability of the marine mussel, a simple, versatile, and powerful synthesis strategy was developed to prepare highly reproducible and permselective molecular sieve membranes by using polydopamine as a novel covalent linker. Attributing to the formation of strong covalent and noncovalent bonds, ZIF-8 nutrients are attracted and bound to the support surface, thus promoting the ZIF-8 nucleation and the growth of uniform, well intergrown, and phase-pure ZIF-8 molecular sieve membranes. The developed ZIF-8 membranes show high hydrogen selectivity and thermal stability. At 150 °C and 1 bar, the mixture separation factors of H2/CO2, H2/N2, H2/CH4, and H2/C3H8 are 8.9, 16.2, 31.5 and 712.6, with H2 permeances higher than 1.8 × 10–7 mol·m–2·s–1·Pa–1, which is promising for hydrogen separation and purification.

416 citations

Journal ArticleDOI
TL;DR: In this article, nano-sized nickel catalysts were characterized by XRD, EDS, SEM, HRTEM and Mastersizer 2000, and it was shown that as-prepared catalysts are pure f.c. nickel and are prone to aggregation.
Abstract: p-Aminophenol was synthesized by catalytic hydrogenation of p-nitrophenol on nano-sized nickel catalysts prepared by a chemical reduction method from aqueous solutions. The catalysts were characterized by XRD, EDS, SEM, HRTEM and Mastersizer 2000. Analysis results show that as-prepared catalysts are pure f.c.c. nickel and are prone to aggregation; the average particle size of nickel catalysts is 57 nm and there are high-density defects on particle surfaces. In hydrogenation reactions of p-nitrophenol, the hydrogenation rate is zero-order dependent on nitro aromatics and increases with increasing of hydrogen pressure. Compared with commercial Raney Ni, catalytic properties (activity, selectivity, and stability) of the as-prepared nickel are superior. The reason proposed for higher catalytic activity of nano-sized nickel is a combination effect of the small particle size and high-density surface defects. The partial sintering of nano-sized nickel might lead to the deactivation of the catalytic activity of nano-sized nickel.

297 citations

Journal ArticleDOI
TL;DR: In this article, a novel membrane material was synthesized through graphene oxide modification on the commercial 19 channels Al2O3 ceramic microfiltration membrane to achieve both high permeate flux and high oil rejection in the oil/water emulsion micro-filtration.

172 citations

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