scholarly journals The Stabilization of Liquid Smoke through Hydrodeoxygenation Over Nickel Catalyst Loaded on Sarulla Natural Zeolite

2020 ◽  
Vol 10 (12) ◽  
pp. 4126
Author(s):  
Saharman Gea ◽  
Agus Haryono ◽  
Andriayani Andriayani ◽  
Junifa Layla Sihombing ◽  
Ahmad Nasir Pulungan ◽  
...  
Keyword(s):  
Natural Zeolite ◽  
Value Added ◽  
Catalyst System ◽  
Catalytic Performance ◽  
Gas Chromatography Mass Spectrometry ◽  
Metal Catalyst ◽  
Wet Impregnation ◽  
Liquid Smoke ◽  
Phenol Conversion ◽  
Catalyst Efficiency

Constituents of liquid smoke possess a huge potential to be converted as value-added chemicals, such as flavoring, antiseptics, antioxidants, or even fossil oil substitutes. However, liquid smoke instability, led by the presence of oxygenate compounds, is an obstacle for further utilization and processing. On the other hand, catalyst efficiency in hydrodeoxygenation (HDO) remains challenging. Sarulla natural zeolite (Z), with abundant availability, has not been comprehensively investigated in the catalytic performance of HDO. In this study, Sarulla natural zeolite with different Si/Al ratios, which are activated by several concentrations of hydrochloric acid and nickel supported by Z (Ni-Z) synthesized by wet impregnation, were evaluated for HDO of liquid smoke, particularly in reducing oxygenate compounds. Catalyst morphology, surface area, pores, and crystallinity are investigated. Catalytic performances were evaluated, particularly on reducing oxygenate compounds and the shifting of phenol and its derivatives. Furthermore, the liquid smoke product of HDO was analyzed by gas chromatography-mass spectrometry (GC-MS). The data obtained reveal that the HDO process of liquid smoke with the Z3 catalyst shows the best activity compared to Z5 and Z7, with phenol conversion of 62.39% and 11.93% of alkoxy reduction. Meanwhile, the best Ni metal catalyst system activity was given by the Ni-Z5 catalyst compared to Ni-Z3 and Ni-Z7, where phenol conversion and alkoxy reduction were at 60.06% and 11.49%, respectively.

scholarly journals Design of Silica Nanoparticles-Supported Metal Catalyst by Wet Impregnation with Catalytic Performance for Tuning Carbon Nanotubes Growth

Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 986
Author(s):  
Tairan da Cunha ◽  
Alberto Maulu ◽  
Jérôme Guillot ◽  
Yves Fleming ◽  
Benoit Duez ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Catalytic Efficiency ◽  
Sio2 Nanoparticles ◽  
Catalytic Performance ◽  
Metal Catalyst ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
Supported Metal Nanoparticles ◽  
Size Dispersion ◽  
Supported Metal

The catalytic activity of cobalt and iron nanoparticles for the growth of carbon nanotubes (CNTs) was studied by a specific reproducible and up-scalable fabrication method. Co and Fe catalysts were deposited over SiO2 nanoparticles by a wet-impregnation method and two different annealing steps were applied for the catalyst formation/activation. The samples were calcined at an optimal temperature of 450 °C resulting in the formation of metal oxide nano-islands without the detection of silicates. Further reduction treatment (700 °C) under H2 successfully converted oxide nanoparticles to Co and Fe metallic species. Furthermore, the catalytic efficiency of both supported-metal nanoparticles at 2 and 5% in weight of silica was evaluated through the growth of CNTs. The CNT structure, morphology and size dispersion were tailored according to the metal catalyst concentration.

Karakterisasi Komponen Aktif Asap Cair Cangkang Sawit Hasil Pemurnian

2016 ◽  
Vol 9 (1) ◽  
pp. 64-72
Author(s):  
Fauziati Fauziati ◽  
Eldha Sampepana
Keyword(s):  
Acetic Acid ◽  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Activated Charcoal ◽  
Oil Refining ◽  
Gas Chromatography Mass Spectrometry ◽  
Antioxidant Compounds ◽  
Active Components ◽  
Liquid Smoke ◽  
Polycyclic Aromatic

Palm shell liquid smoke obtained by pyrolysis and redestilasi still produce a pungent smoke flavor and color of yellow to brownish yellow so that the necessary research purification of smoke that can be used as ingredients other than preservatives, such as antiseptic hand wash. The research objective is to reduce the stinging liquid smoke aroma, color is tawny and to identify the characterization of the active components of liquid smoke shell oil refining results in Gas Chromatography Mass Spectrometry (GC-MS). The purification process of liquid smoke with redistilled at a temperature of 2000C and by adding 4.5% zeolite adsorbent made three (3) times the resulting liquid smoke of distillate and residue. Liquid smoke produced from distillate and residue are added activated charcoal as much as 9%, 10.5% and 12%, then stirred with a shaker subsequently allowed to stand for 6 days and 10 days The results of the study showed that liquid smoke purification results of the residue by the addition of activated charcoal as 12% and the time saved for 10 days (A2B2C3) gives flavor and color by 1.94 of 1.84 is odorless, yellowish white color and clarity. While the characteristics of the active components of purification results are predominantly acetic acid and phenol compounds of residues that serve as preservatives, antibacterial and antioxidant compounds while PAH (Polycyclic Aromatic Hydrocarbon), namely tar, benzoperen, gualakol and siringoll (aroma causes) undetectedABSTRAKAsap cair cangkang sawit yang diperoleh melalui proses pirolisis dan redestilasi masih menghasilkan aroma asap menyengat dan warna kuning hingga kuning kecoklatan sehingga diperlukan penelitian pemurnian asap yang dapat digunakan sebagai bahan lain selain pengawet, seperti antiseptik pencuci tangan. Tujuan penelitian adalah  untuk mengurangi aroma asap cair yang menyengat, warna yang masih kuning kecoklatan dan untuk  mengidentifikasi karakterisasi komponen aktif asap cair cangkang sawit hasil pemurnian secara Kromatografi Gas Spektrometri Massa (GC-MS). Proses  pemurnian asap cair dengan  redistilasi pada suhu 2000C dan dengan menambahkan adsorben zeolit 4,5% yang dilakukan sebanyak 3 (tiga) kali  dihasilkan asap cair dari Destilat dan Residu . Asap cair  yang dihasilkan dari destilat dan residu ditambahkan arang aktif sebanyak 9%,10,5% dan 12%  kemudian diaduk dengan shaker selanjutnya didiamkan selama 6 hari dan 10 hari .Hasil penelitian menunjukkan bahwa asap cair hasil pemurnian dari residu dengan penambahan arang aktif sebanyak 12% dan waktu simpan selama 10 hari ( A2B2C3 ) memberikan aroma sebesar 1,94 dan warna sebesar 1,84 adalah tidak berbau ,  warna putih kekuningan dan jernih . Sedangkan  karakteristik  komponen aktif hasil pemurnian yang paling dominan  adalah  senyawa acetic acid dan phenol  dari residu yang berfungsi sebagai bahan pengawet, antibakteri dan antioksidan sedangkan senyawa PAH (Polycyclic Aromatic Hydrocarbon) yaitu tar, benzoperen,  gualakol  dan siringoll ( penyebab aroma ) tidak terdeteksi . Kata kunci : asap cair, cangkang sawit, komponen aktif, pemurnian, redestilasi 

scholarly journals Quasi-graphitic carbon shell-induced Cu confinement promotes electrocatalytic CO2 reduction toward C2+ products

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Ji-Yong Kim ◽  
Deokgi Hong ◽  
Jae-Chan Lee ◽  
Hyoung Gyun Kim ◽  
Sungwoo Lee ◽  
...  
Keyword(s):  
High Efficiency ◽  
Co2 Reduction ◽  
Value Added ◽  
Material Design ◽  
Catalyst System ◽  
Critical Issue ◽  
Reduction Reaction ◽  
Catalyst Design ◽  
Design Strategies ◽  
Faradaic Efficiency

AbstractFor steady electroconversion to value-added chemical products with high efficiency, electrocatalyst reconstruction during electrochemical reactions is a critical issue in catalyst design strategies. Here, we report a reconstruction-immunized catalyst system in which Cu nanoparticles are protected by a quasi-graphitic C shell. This C shell epitaxially grew on Cu with quasi-graphitic bonding via a gas–solid reaction governed by the CO (g) - CO2 (g) - C (s) equilibrium. The quasi-graphitic C shell-coated Cu was stable during the CO2 reduction reaction and provided a platform for rational material design. C2+ product selectivity could be additionally improved by doping p-block elements. These elements modulated the electronic structure of the Cu surface and its binding properties, which can affect the intermediate binding and CO dimerization barrier. B-modified Cu attained a 68.1% Faradaic efficiency for C2H4 at −0.55 V (vs RHE) and a C2H4 cathodic power conversion efficiency of 44.0%. In the case of N-modified Cu, an improved C2+ selectivity of 82.3% at a partial current density of 329.2 mA/cm2 was acquired. Quasi-graphitic C shells, which enable surface stabilization and inner element doping, can realize stable CO2-to-C2H4 conversion over 180 h and allow practical application of electrocatalysts for renewable energy conversion.

Preparation of catalyst as Au doped Mn1Co9Ox/ceramic system for total oxidation of CO

2021 ◽  
Vol 10 (4) ◽  
pp. 39-45
Author(s):  
Phuong Pham Thi Mai ◽  
Hoan Nguyen Quoc ◽  
Quan Do Quoc ◽  
Hung Nguyen Thanh
Keyword(s):  
Sol Gel ◽  
Active Phase ◽  
Catalyst System ◽  
Oxidation Of Co ◽  
Sem Images ◽  
Total Oxidation ◽  
Wet Impregnation ◽  
Modern Analysis ◽  
Catalyst Powder ◽  
Xrd Patterns

In this paper, the Au doped Mn1Co9Ox was investigated for total oxidation of CO. The sol-gel method was applied to prepare this catalyst and some modern analysis methods as XRD, EPR, TPx, SEM were utilized to characterize its properties. The XRD patterns showed only Co3O4 phase without any peaks belonging to Mn or Au. However, the presence of Au and Mn was confirmed by EPR and O2-TPD results. With the aim to further apply catalyst in reality, the Au doped Mn1Co9Ox was deposited on ceramic by sol-gel, wet impregnation. The SEM images displayed the successful coating of active phase on substrate. However, the complete catalyst system didn’t have the high activity in total CO oxidation like the catalyst powder because of large agglomerations on coatings.

scholarly journals Maximizing Anhydrosugar Production from Fast Pyrolysis of Eucalyptus Using Sulfuric Acid as an Ash Catalyst Inhibitor

Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 609 ◽  
Author(s):  
Dongyan Zhang ◽  
Yuyang Fan ◽  
Anqing Zheng ◽  
Zengli Zhao ◽  
Fengyun Wang ◽  
...  
Keyword(s):  
Rank Order ◽  
Maximum Yield ◽  
Fast Pyrolysis ◽  
Value Added ◽  
Gas Chromatography Mass Spectrometry ◽  
Cellulose Content ◽  
Pyrolysis Gas ◽  
X Ray ◽  
Theoretical Yield ◽  
Pure Cellulose

Anhydrosugars, such as levoglucosan (LG), are high value-added chemicals which are mainly derived from fast pyrolysis of pure cellulose. However, fast pyrolysis of raw lignocellulosic biomass usually produces a very low amount of levoglucosan, since alkali and alkaline earth metals (AAEM) present in the ash can serve as the catalysts to inhibit the formation of levoglucosan through accelerating the pyranose ring-opening reactions. In this study, eucalyptus was impregnated with H2SO4 solutions with varying concentrations (0.25–1.25%). The characteristics of ash derived from raw and H2SO4-impregnated eucalyptus were characterized by X-ray fluorescence spectroscopy (XRF) and X-ray diffraction (XRD). The pyrolysis behaviors of raw and H2SO4-impregnated eucalyptus were performed on the thermogravimetric analysis (TGA) and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). TG analysis demonstrated that the H2SO4-impregnated eucalyptus produced less char than raw eucalyptus. Py-GC/MS analysis showed that even small amounts of H2SO4 can obviously improve the production of anhydrosugars and phenols and suppressed the formation of carboxylic acids, aldehydes, and ketones from fast pyrolysis of eucalyptus. The rank order of levoglucosan yield from raw and impregnated eucalyptus was raw < 1.25% H2SO4 < 1% H2SO4 < 0.75% H2SO4 < 0.25% H2SO4 < 0.5% H2SO4. The maximum yield of levoglucosan (21.3%) was obtained by fast pyrolysis of eucalyptus impregnated with 0.5% H2SO4, which was close to its theoretical yield based on the cellulose content. The results could be ascribed to that H2SO4 can react with AAEM (e.g., Na, K, Ca, and Mg) and lignin to form lignosulfonate, thus acting as an inhibitor to suppress the catalytic effects of AAEM during fast pyrolysis of eucalyptus.

scholarly journals Characterization of selected pyrolysis products of diseased orange wood

BioResources ◽  
2020 ◽  
Vol 15 (3) ◽  
pp. 7118-7126
Author(s):  
Carolina Kravetz ◽  
Carlos Leca ◽  
José Otávio Brito ◽  
Daniel Saloni ◽  
David C. Tilotta
Keyword(s):  
Value Added ◽  
Chemical Compounds ◽  
Gas Chromatography Mass Spectrometry ◽  
Pyrolysis Products ◽  
Bio Oil ◽  
Potential Applications ◽  
Domestic Use ◽  
Immediate Analysis ◽  
Orange Trees

Orange trees in Brazil are often burned as a means of eradication when they become infected with Huanglongbing disease. Rather than destroying them, which is a low-value proposition, one potential option is to utilize the biomass through pyrolysis. In this preliminary work, orange trees (Citrus sinensis) otherwise selected for purging, were sampled and pyrolyzed at 500 °C, and the charcoal and bio-oil were evaluated for potential value-added use. The results showed that the pyrolysis process resulted in 26.3% charcoal, 57.6% bio-oil, and 16.0% non-condensable gases. Qualitative analysis of the bio-oil by gas chromatography/mass spectrometry found 178 chemical compounds; however, only 25% of those compounds could be reliably identified. Potential applications of the compounds identified in the bio-oil were determined by examining the published literature, and it was found that at least 73% of them showed promise. Finally, initial studies on the immediate analysis of the pyrolysis charcoal showed that it potentially meets the standards set forth for Brazilian domestic use.

scholarly journals Spatial reactant distribution in CO2 electrolysis: Balancing CO2 utilization and Faradaic Efficiency

2021 ◽  
Author(s):  
Siddhartha Subramanian ◽  
Joost Middelkoop ◽  
Thomas Burdyny
Keyword(s):  
Value Added ◽  
Catalytic Performance ◽  
Process Performance ◽  
Co2 Utilization ◽  
Faradaic Efficiency ◽  
Co2 Electrolysis ◽  
Reactant Distribution

The production of value added C1 and C2 compounds within CO2 electrolyzers has reached sufficient catalytic performance that system and process performance – such as CO2 utilization – have come...

scholarly journals THE PARAFFIN CRACKING REACTION WITH NiMo/ACTIVE NATURAL ZEOLITE CATALYST: THE EFFECT TEMPERATURE ON CATALYTIC ACTIVITYTHE PARAFFIN CRACKING REACTION WITH NiMo/ACTIVE NATURAL ZEOLITE CATALYST: THE EFFECT TEMPERATURE ON CATALYTIC ACTIVITY

2016 ◽  
Vol 11 (2) ◽  
pp. 111 ◽  
Author(s):  
Khoirina Dwi Nugrahaningtyas ◽  
Eko Cahyono ◽  
Dian Maruto Widjonarko
Keyword(s):  
Gas Chromatography ◽  
Natural Zeolite ◽  
Zeolite Catalyst ◽  
Catalyst Activity ◽  
Gas Chromatography Mass Spectrometry ◽  
Hydrogen Flow ◽  
Catalyst Temperature ◽  
Cracking Reaction ◽  
Active Natural ◽  
Cracking Products

This research deals with the study of the paraffin cracking reaction with termal reaction, active natural zeolite (ZAA) and NiMo / active natural zeolite (ZAA) catalyst. Temperature variation was done in order to study the optimum temperature of paraffin cracking reactions. Paraffin cracking reaction carried out at temperatures of 200 - 400 °C and a hydrogen flow rate of 30 mL / min. Cracking products obtained, and then analyzed by gas chromatography (GC) and gas chromatography-mass spectrometry(GCMS). Catalyst activity (%) was defined as the amount of lighter fractions/the amount of feed (paraffin) (%). The results showed that the catalyst NiMo/ZAA has the highest activity (31.33 %) at the cracking reaction temperature of 300 ºC

SnO2 nano-rods with superior CO oxidation performance

2014 ◽  
Vol 2 (16) ◽  
pp. 5616-5619 ◽  
Author(s):  
Xiang Wang ◽  
Lihong Xiao ◽  
Honggen Peng ◽  
Wenming Liu ◽  
Xianglan Xu
Keyword(s):  
Co Oxidation ◽  
Noble Metal ◽  
Catalytic Performance ◽  
Metal Catalyst ◽  
Noble Metal Catalyst ◽  
Catalytic Behavior ◽  
Oxidation Performance ◽  
Nano Rods

SnO2 with a nano-rod morphology shows a superior catalytic performance over SnO2 with other morphologies for CO oxidation. The SnO2-rods’ catalytic behavior is very similar to that of a noble metal catalyst.

scholarly journals Environmentally benign chemical recycling of polycarbonate wastes: comparison of micro- and nano-TiO2 solid support efficiencies

2019 ◽  
Vol 8 (1) ◽  
pp. 108-117 ◽  
Author(s):  
Samira Emami ◽  
Mir Mohammad Alavi Nikje
Keyword(s):  
Titanium Dioxide ◽  
Solid Support ◽  
Conventional Heating ◽  
Gas Chromatography Mass Spectrometry ◽  
Metal Catalyst ◽  
Chemical Recycling ◽  
Solid Supports ◽  
H Nmr ◽  
Optical Discs ◽  
Green System

Abstract Polycarbonate (PC) wastes, including optical discs (CDs) and digital optical discs (DVDs), were chemically recycled into valuable materials such as 4,4′-(propane-2,2-diyl)diphenol (BPA) and etherified derivatives of BPA using sodium hydroxide (NaOH) as the alkali metal catalyst and nanostructured titanium dioxide (nano-TiO2) and microstructured titanium dioxide (micro-TiO2) as the solid supports in the binary green system consisting of water and 2,2′-oxydi(ethan-1-ol) (DEG) under conventional heating method, and data were compared. In this study, the effects of various parameters, such as solvent composition, concentration of NaOH, and solid support, were studied on the reaction progress. In these reactions, the importance of water as the green solvent was investigated in achieving pure BPA as the valuable material. When used with 20% aqueous DEG (pbw), a pure BPA can be obtained at 70% yield in the presence of nano-TiO2 and micro-TiO2 as the solid supports. According to the results, the use of nano-TiO2 in comparison with micro-TiO2 accelerates the chemical recycling of PC wastes. The nano-TiO2 catalyst recovery shows that the recovered solid support is applicable for four cycles. The obtained products were characterized using spectroscopic methods, namely, 1H NMR, 13C NMR, and Fourier transform infrared spectroscopy as well as gas chromatography-mass spectrometry.

Sign in / Sign up

Export Citation Format

Share Document