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Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format
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Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format Example of Reaction Kinetics, Mechanisms and Catalysis format
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open access Open Access

Reaction Kinetics, Mechanisms and Catalysis — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Physical and Theoretical Chemistry #99 of 169 down down by 1 rank
Catalysis #40 of 57 down down by 1 rank
journal-quality-icon Journal quality:
Medium
calendar-icon Last 4 years overview: 787 Published Papers | 2267 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 06/07/2020
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Related Journals

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Quality:  
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SJR: 2.337
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Wiley

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open access Open Access

Springer

Quality:  
Good
CiteRatio: 3.5
SJR: 0.385
SNIP: 0.741

Journal Performance & Insights

Impact Factor

CiteRatio

Determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

A measure of average citations received per peer-reviewed paper published in the journal.

1.52

6% from 2018

Impact factor for Reaction Kinetics, Mechanisms and Catalysis from 2016 - 2019
Year Value
2019 1.52
2018 1.428
2017 1.515
2016 1.264
graph view Graph view
table view Table view

2.9

16% from 2019

CiteRatio for Reaction Kinetics, Mechanisms and Catalysis from 2016 - 2020
Year Value
2020 2.9
2019 2.5
2018 2.3
2017 2.3
2016 2.2
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 6% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 16% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

0.398

15% from 2019

SJR for Reaction Kinetics, Mechanisms and Catalysis from 2016 - 2020
Year Value
2020 0.398
2019 0.345
2018 0.374
2017 0.409
2016 0.401
graph view Graph view
table view Table view

0.701

21% from 2019

SNIP for Reaction Kinetics, Mechanisms and Catalysis from 2016 - 2020
Year Value
2020 0.701
2019 0.581
2018 0.622
2017 0.647
2016 0.644
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 15% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 21% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Reaction Kinetics, Mechanisms and Catalysis

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Springer

Reaction Kinetics, Mechanisms and Catalysis

Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: • kinetics of homogeneous reactions in gas, liquid and solid phase; • Homogeneous catalysis; • Heterogeneous catalysis; • Adsorption in heterogeneous catalysis; • Transp...... Read More

Chemistry

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Last updated on
06 Jul 2020
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ISSN
1878-5190
i
Impact Factor
Medium - 0.775
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
SPBASIC
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Citation Type
Numbered
[25]
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Bibliography Example
Blonder GE, Tinkham M, Klapwijk TM (1982) Transition from metallic to tunneling regimes in superconducting mi-croconstrictions: Excess current, charge imbalance, and su- percurrent conversion. Phys Rev B 25(7):4515–4532, URL 10.1103/PhysRevB.25.4515

Top papers written in this journal

Journal Article DOI: 10.1007/S11144-010-0247-2
Adsorption kinetics and isotherm of methylene blue and its removal from aqueous solution using bone charcoal
Gh. Ghanizadeh1, Ghorban Asgari

Abstract:

This study aims at describing the removal of methylene blue (MB) from aqueous solution using bone charcoal (BC) as an adsorbent material. The effects of dye concentration, pH, contact time and the adsorbent dose were investigated. The chemical composition and solid structure of BC were analyzed using X-ray diffraction (XRD) a... This study aims at describing the removal of methylene blue (MB) from aqueous solution using bone charcoal (BC) as an adsorbent material. The effects of dye concentration, pH, contact time and the adsorbent dose were investigated. The chemical composition and solid structure of BC were analyzed using X-ray diffraction (XRD) and scanning electronic microscopy (SEM). The surface area was measured via the Brunauer–Emmett–Teller (BET) isotherm. The experimental data were analyzed with Langmuir, Freundlich and Temkin isotherm models. The results show that the main component of BC is calcium hydroxylapatite (Ca5(PO4)3OH). The BETSuface area of BC is approximately 100 m2/g. The experimental adsorption isotherm complies with Langmuir equation model (R 2 = 0.99) and the maximum amount of adsorption (q max) was 5 mg/g. The elevation of BC dose led to a decrease in q max, however, increasing the pH led to the elevation of dye adsorption. The kinetic studies revealed that the adsorption of MB is rapid and complies with the pseudo second-order kinetic (R 2 > 0.99). Apart from R 2, four error functions have been used for the validation of data. Analysis of data with Dubinin–Radushkevich isotherm showed that the energy of MB adsorption process onto BC was 2.65 kJ/mol, which implies that the adsorption of MB with BC is a physical adsorption. read more read less

Topics:

Freundlich equation (67%)67% related to the paper, Adsorption (59%)59% related to the paper, Langmuir (56%)56% related to the paper
82 Citations
Journal Article DOI: 10.1007/S11144-019-01623-8
Enhanced CO oxidation and toluene oxidation on CuCeZr catalysts derived from UiO-66 metal organic frameworks
Lu Wang1, Guangyi Yin1, Yiqiang Yang1, Xiaodong Zhang1

Abstract:

In this work, several MxOy-supported ZrO2 (MxOy = CuO, CeO2, CuO-CeO2) catalysts were prepared through the direct decomposition of metal organic frameworks UiO-66 in air. The catalysts were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), N2 adsorption–desorption isotherms and H2-temperature progr... In this work, several MxOy-supported ZrO2 (MxOy = CuO, CeO2, CuO-CeO2) catalysts were prepared through the direct decomposition of metal organic frameworks UiO-66 in air. The catalysts were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), N2 adsorption–desorption isotherms and H2-temperature programmed reduction (H2-TPR). The catalytic performance for CO oxidation and toluene oxidation over Zr based catalysts was investigated. Amongst the prepared catalysts, CuCeZr catalyst displayed excellent CO oxidation and toluene oxidation performance. The addition of Cu was favorable to the enhancement of catalytic performance. Importantly, the addition of cerium led to the formation of easily reducible surface copper species, consequently improving the CO oxidation and toluene oxidation performance. read more read less

Topics:

Toluene oxidation (73%)73% related to the paper, Catalysis (52%)52% related to the paper, Metal-organic framework (52%)52% related to the paper
80 Citations
Journal Article DOI: 10.1007/S11144-013-0587-9
Methanol synthesis from CO2 hydrogenation over copper based catalysts

Abstract:

A series of Cu–ZnO/Al2O3 catalysts prepared by coprecipitation were used for methanol synthesis by CO2 hydrogenation in a fixed bed reactor system. The effect of the catalysts composition and the reaction temperature on the catalytic activity was investigated. The main results show that the highest CO2 conversion and the best... A series of Cu–ZnO/Al2O3 catalysts prepared by coprecipitation were used for methanol synthesis by CO2 hydrogenation in a fixed bed reactor system. The effect of the catalysts composition and the reaction temperature on the catalytic activity was investigated. The main results show that the highest CO2 conversion and the best yield of methanol are obtained with the catalyst containing 51 wt% Cu and 22 wt% Zn. This result is assigned to the highest metallic copper surface area and to the interaction between copper and zinc oxide. However, the reaction temperature increase is disadvantageous for the methanol synthesis reaction. read more read less

Topics:

Catalysis (58%)58% related to the paper, Methanol (55%)55% related to the paper, Copper (54%)54% related to the paper, Coprecipitation (52%)52% related to the paper
78 Citations
Journal Article DOI: 10.1007/S11144-011-0291-6
A novel Ag/BiOBr nanoplate catalyst with high photocatalytic activity in the decomposition of dyes
Changlin Yu1, Caifeng Fan1, Xiangjie Meng1, Kai Yang1, Fangfang Cao1, Xin Li1

Abstract:

A novel Ag/BiOBr composite catalyst has been synthesized by a solution combination with photodeposited method. The as-synthesized catalysts were characterized by powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and UV–Vis diffuse reflectance spectra. T... A novel Ag/BiOBr composite catalyst has been synthesized by a solution combination with photodeposited method. The as-synthesized catalysts were characterized by powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and UV–Vis diffuse reflectance spectra. The photocatalytic reaction tests in the degradation of the dyes of acid orange II, rhodamine B and methyl orange showed that the deposition of optimal amount of 1–2 wt% Ag could bring about a big increase in the activity under visible light irradiation. The high photocatalytic performance could be attributed to the strong visible light absorption and low recombination rate of the e−/h+ pairs resulted in by the presence of metal silver nanoparticles. read more read less

Topics:

Methyl orange (57%)57% related to the paper, Photocatalysis (55%)55% related to the paper, Rhodamine B (54%)54% related to the paper, Visible spectrum (52%)52% related to the paper, Silver nanoparticle (50%)50% related to the paper
71 Citations
open accessOpen access Journal Article DOI: 10.1007/S11144-015-0889-1
The influence of different agitation techniques on the adsorption kinetics of 4-chlorophenol on granular activated carbon

Abstract:

The influence of different agitation techniques on the adsorption of organic compounds, represented by 4-chlorophenol, onto granular activated carbon was investigated. The effect of the flask type and the type of agitator, including a laboratory shaker, mechanical agitator, magnetic stirrer as well as mixing with gas bubbles,... The influence of different agitation techniques on the adsorption of organic compounds, represented by 4-chlorophenol, onto granular activated carbon was investigated. The effect of the flask type and the type of agitator, including a laboratory shaker, mechanical agitator, magnetic stirrer as well as mixing with gas bubbles, was studied. The results of adsorption kinetics demonstrate that the adsorption process of 4-chlorophenol on the activated carbon follows a pseudo-second order kinetic model closely. The adsorption equilibrium was reached faster in the Erlenmeyer flask than in the round-bottomed flask. At the same agitation speed (200 rpm), the better adsorption rate and adsorption efficiency were observed using the mechanical and magnetic stirrers than the laboratory shaker. At the gas flow rate of 1.5 dm3 min−1, the mixing with the air or nitrogen bubbles was comparable with the agitation when using mechanical and magnetic stirrers at 200 rpm. The effect of the agitation speed on the adsorption of the 4-chlorophenol by the activated carbon was also tested. The kinetic experiments were carried out at 100, 200, 300 and 500 rpm and it was found that the adsorption rate increases with the increase in the agitation speed. As the stirring rate increased from 100 to 500 rpm, the adsorption rate constants increased from 0.577 to 1.264 g mmol−1 h−1 (mechanical agitator) and from 0.560 to 1.231 g mmol−1 h−1 (magnetic stirrer), respectively. The experimental results demonstrate that the agitation affects the adsorption kinetics significantly as well as the adsorption equilibrium of the organic compounds on the activated carbon, and should be taken into account in such studies. read more read less

Topics:

Adsorption (59%)59% related to the paper, Activated carbon (57%)57% related to the paper, Agitator (55%)55% related to the paper, Erlenmeyer flask (51%)51% related to the paper
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70 Citations
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13. What is Sherpa RoMEO Archiving Policy for Reaction Kinetics, Mechanisms and Catalysis?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Reaction Kinetics, Mechanisms and Catalysis. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Reaction Kinetics, Mechanisms and Catalysis?

The 5 most common citation types in order of usage for Reaction Kinetics, Mechanisms and Catalysis are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

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