TY  - JOUR
AU  - Hou, B.
AU  - Wang, H.
AU  - Yan, J.
AU  - Li, R.
AU  - Wu, S.
AU  - Wang, B.
AU  - Wang, Y.
AU  - Xu, T.
TI  - Bipolar membrane crystallization enables near zero-waste production of high-purity oxalic acid crystals
JF  - CHEMICAL ENGINEERING SCIENCE
J2  - CHEM ENG SCI
VL  - 293
PY  - 2024
SN  - 0009-2509
DO  - 10.1016/j.ces.2024.120032
UR  - https://m2.mtmt.hu/api/publication/34771049
ID  - 34771049
N1  - Export Date: 5 April 2024            
            CODEN: CESCA            
            Correspondence Address: Wang, Y.; Key Laboratory of Precision and Intelligent Chemistry, Anhui, China; email: ymwong@ustc.edu.cn
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Prasad, A.
AU  - Vijayan, K.S.
AU  - Rao, R.V.S.
AU  - Narasimhan, D.
AU  - Krishnamoorty, A.
TI  - Catalytic destruction of oxalate in the supernatant stream generated during plutonium reconversion process
JF  - RADIOCHIMICA ACTA
J2  - RADIOCHIM ACTA
PY  - 2024
SN  - 0033-8230
DO  - 10.1515/ract-2023-0211
UR  - https://m2.mtmt.hu/api/publication/34771050
ID  - 34771050
N1  - Export Date: 5 April 2024            
            CODEN: RAACA            
            Correspondence Address: Narasimhan, D.; Department of Atomic Energy, India; email: desi@igcar.gov.in
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Bashir, Shahid M.
AU  - Norhadif, Muhammad
AU  - Xia, Zhicheng
AU  - Qian, Linda
AU  - Gyenge, Elod L.
TI  - Improved Titrimetric Analysis of Formate/Formic Acid and Comparison with Ion Chromatography and Nuclear Magnetic Resonance Spectroscopy
JF  - ANALYTICAL LETTERS
J2  - ANAL LETT
PY  - 2023
PG  - 12
SN  - 0003-2719
DO  - 10.1080/00032719.2023.2297411
UR  - https://m2.mtmt.hu/api/publication/34596462
ID  - 34596462
N1  - Export Date: 28 February 2024; CODEN: ANALB
AB  - The advancements in renewable energy technologies brought about a significant interest in developing formic acid based chemical and electrochemical processes. These include the electroreduction of carbon dioxide to produce formic acid or direct electrooxidation of formic acid to generate electricity in a fuel cell. Considering the neutral to alkaline nature of electrolytes used in many of these processes, formic acid usually exists as a formate species. Unlike oxalate salt, the direct titration to quantify formate molarity using potassium permanganate (KMnO4) is difficult due to the formation of a suspended colored complex, which poses challenges in identifying the endpoint. Herein, we report two simple and efficient methods for formate and formic acid analysis, by back titration (FBT) using oxalate and iodine, respectively. These methods were shown to have an accuracy of more than 97% at a reduced cost when benchmarked against either nuclear magnetic resonance (NMR) spectroscopy or ion chromatography (IC). The effect of the analyte medium and optimization of the analytical procedure were also investigated. The formate quantification was found to vary insignificantly when different media, such as water, potassium hydroxide, potassium bicarbonate, or potassium sulfate, were used. This signifies the robustness and broader applicability of the FBT methods. Regarding the analytical steps, selecting the appropriate temperature, time, and molar ratio of participating species allowed the quantification of formate or formic acid with accuracy and precision. The analytical methods thus developed can provide alternative, cost-effective solutions for determining formate concentration for the research and development sector and for on-site analysis in industrial settings, where maintaining NMR and IC equipment may not be feasible.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - de Oliveira, C.M.S.
AU  - Grisi, C.V.B.
AU  - Silva, G.d.S.
AU  - Neto, J.H.P.L.
AU  - de Medeiros, L.L.
AU  - dos Santos, K.M.O.
AU  - Cardarelli, H.R.
TI  - Use of Lactiplantibacillus plantarum CNPC 003 for the manufacture of functional skimmed fresh cheese
JF  - INTERNATIONAL DAIRY JOURNAL
J2  - INT DAIRY J
VL  - 141
PY  - 2023
PG  - 9
SN  - 0958-6946
DO  - 10.1016/j.idairyj.2023.105628
UR  - https://m2.mtmt.hu/api/publication/33664096
ID  - 33664096
N1  - Postgraduate Program in Food Science and Technology, Department of Food Engineering, Centre of Technology, Federal University of Paraiba, Paraiba, João Pessoa, 58051-900, Brazil            
            Postgraduate Program in Agrifood Technology, Federal University of Paraiba, Campus Universitario III, Bananeiras, Paraiba58220-000, Brazil            
            Brazilian Agricultural Research Corporation – Embrapa Food Agroindustry, Rio de Janeiro, Rio de Janeiro, Brazil            
            Department of Food Technology, Centre of Technology and Regional Development, Federal University of Paraiba, Paraiba, João Pessoa, 58055-000, Brazil            
            Cited By :1            
            Export Date: 5 April 2024            
            CODEN: IDAJE            
            Correspondence Address: Cardarelli, H.R.; Department of Food Technology, Paraiba, Brazil; email: hrcarda@gmail.com
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Hovey, Tanden A.
AU  - Mishra, Disha
AU  - Singh, Manveer
AU  - Anaya, Grecia
AU  - Owusu, Chantele
AU  - Barvian, Nicole C.
AU  - Sorauf, Kellen J.
AU  - Patro, Mata Dambarudhar
AU  - Panigrahi, Akhil K.
AU  - Mahapatro, Surendra N.
TI  - Pathways in permanganate oxidation of mandelic acid: reactivity and selectivity of intermediate manganese species
JF  - DALTON TRANSACTIONS
J2  - DALTON T
VL  - 52
PY  - 2023
IS  - 48
SP  - 18268
EP  - 18286
PG  - 19
SN  - 1477-9226
DO  - 10.1039/d3dt02948d
UR  - https://m2.mtmt.hu/api/publication/34578657
ID  - 34578657
N1  - Department of Chemistry, Regis University, Denver, CO 80221, United States            
            Data Science, Anderson College of Business and Computing, Regis University, Denver, CO 80221, United States            
            Department of Chemistry, Khallikote University, Odisha, Berhampur, 760001, India            
            Participant, Regis University, Science Bridge Program, Legacy High School, Broomfield, CO, United States            
            Export Date: 5 April 2024            
            CODEN: DTARA            
            Correspondence Address: Mahapatro, S.N.; Department of Chemistry, United States; email: smahapat@regis.edu
AB  - We report a comprehensive kinetic and product study of the oxidation of mandelic acid (MA) by permanganate in the pH range of 1-13, including a full account of total oxidizing equivalents (five and three-electron change in acidic and basic media, respectively). In the entire pH range, the reaction shows a primary kinetic deuterium isotope effect (kH/kD >= 8-9), indicating rate-limiting hydride transfer. The deuterium label in alpha-deutero-mandelic acid is retained in benzaldehyde. Benzaldehyde (BZ) is formed in post-rate limiting steps due to reactions involving manganese intermediates. In alkaline pH (>= 13), in the presence of barium acetate, Mn(vi) is removed as insoluble blue barium manganate; the stoichiometry of the first step of reduction was found to be: MA + 2Mn(vii) -> PGA + 2Mn(vi). Manganate, MnO42-, is directly reduced to MnO2 giving an additional mole of phenylglyoxylic acid (PGA). The experimentally observed ratio of benzaldehyde to phenylglyoxylic (BZ/PGA) provides a basis for discrimination between mechanistic choices that include direct reduction of Mn(v) to Mn(iii) (in an acidic medium), disproportionation to Mn(iv) and Mn(vi) or oxidation to Mn(vi) by a second mole of permanganate. Interestingly, at pH 4, a stoichiometric, soluble Mn(iv) is observed for the first time for hydroxy-acid oxidation, reminiscent of the Guyard reaction. Because of the widespread use of permanganate as an environmentally green oxidant, results from mandelic acid oxidation have implications for the remediation of dissolved organic matter (DOM) including hydrocarbons and nitroaromatics in waste and groundwater.This study reports on the role of intermediates in permanganate oxidation of a model hydroxy-acid. It is significant in the context of wastewater treatment for contaminant abatement and water quality.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Huang, Jinbing
AU  - Liu, Xiaoyan
AU  - Xie, Shiwei
TI  - Efficient Mn(III)-oxalate generation for diclofenac oxidation by electro-reduction of potassium permanganate in the presence of oxalate
JF  - JOURNAL OF WATER PROCESSING ENGINEERING
J2  - J WATER PROCESS ENG
VL  - 56
PY  - 2023
PG  - 7
SN  - 2214-7144
DO  - 10.1016/j.jwpe.2023.104440
UR  - https://m2.mtmt.hu/api/publication/34596463
ID  - 34596463
N1  - Export Date: 28 February 2024
AB  - Although electrochemical activation of permanganate (E-PM) is a green and efficient method to degrade refractory organics by in-situ generated reactive Mn(III)aq, this process highlights on the presence of promoter and/ or stabilizer. Oxalate (OA) is a widespread organic chelate in natural water bodies (with concentrations up to 1 mM), but whose effect on the E-PM process is still unclear. In this study, we found electrolysis and the presence of OA both promote the activation of PM for the degradation of diclofenac (DCF), showing a high synergistic coefficient (3.23) and elevated reaction constant (0.1395 min-1). Nevertheless, this process is highly pHdependent, behaving decreased reactivity as pH value increasing from 3 to 11. Sufficient concentration of OA (>= 0.5 mM in this study) is required for stabilizing Mn(III). UV-vis spectra, visual evidence and quenching experiments identified the presence and dominant role of Mn(III)-OA on the degradation of DCF. Using chronoamperometry, we confirmed Mn(III)-OA was primarily generated from the electro-reduction of PM in the presence of OA at pH 5.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Kim, Namgyu
AU  - Lee, Sang-Hoon
AU  - Yang, Hanui
AU  - Park, Donghee
TI  - Mechanism of Permanganate Biosorption by Fermentation Biowaste
JF  - ADSORPTION SCIENCE & TECHNOLOGY
J2  - ADSORPT SCI TECHNOL
VL  - 2023
PY  - 2023
PG  - 7
SN  - 0263-6174
DO  - 10.1155/2023/4759123
UR  - https://m2.mtmt.hu/api/publication/34259996
ID  - 34259996
N1  - Export Date: 28 November 2023; CODEN: ASTEE
AB  - Biosorptive treatment of industrial wastewater contaminated with heavy metals has been recognized as one of the most effective green tools, competing with traditional physical/chemical treatment processes. This study delves into the detailed investigation of the biosorbent prepared from fermentation biowaste, particularly focusing on the mechanism behind permanganate (Mn(VII)) removal. Various parameters including pH, biosorbent dosage, initial concentration, and temperature were examined. Among these factors, solution pH emerged as the most crucial in removing Mn(VII) using the biosorbent. The significant removal of Mn(VII) was attributed to both reduction and adsorption, as confirmed by X-ray photoelectron spectroscopy. Depending on the experimental conditions, the removal of Mn(VII) was influenced not only by simple adsorption but also by oxidation-reduction and precipitation processes. This study not only advances our understanding of biosorptive treatment but also highlights the promising potential of fermentation biowaste-based biosorbents for effective Mn(VII) removal.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Peng, Z.
AU  - Adam, Z.R.
AU  - Fahrenbach, A.C.
AU  - Kaçar, B.
TI  - Assessment of Stoichiometric Autocatalysis across Element Groups
JF  - JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
J2  - J AM CHEM SOC
VL  - 145
PY  - 2023
IS  - 41
SP  - 22483
EP  - 22493
PG  - 11
SN  - 0002-7863
DO  - 10.1021/jacs.3c07041
UR  - https://m2.mtmt.hu/api/publication/34237329
ID  - 34237329
N1  - Department of Bacteriology, University of Wisconsin−Madison, Madison, WI 53706, United States            
            Department of Geoscience, University of Wisconsin−Madison, Madison, WI 53706, United States            
            School of Chemistry, Australian Centre for Astrobiology and the UNSW RNA Institute, University of New South Wales, Sydney, NSW 2052, Australia            
            Export Date: 3 November 2023            
            CODEN: JACSA            
            Correspondence Address: Peng, Z.; Department of Bacteriology, United States; email: zhen.peng@wisc.edu
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Ahmed, Ahmad A.
AU  - Aljarrah, Ihsan A.
AU  - Telfah, Mahmoud D.
AU  - Alsaad, Ahmad M.
AU  - Telfah, Ahmad
TI  - Optical, chemical, electrical, and morphological properties of PEO-Nb-doped KMnO4 thin films
JF  - JOURNAL OF MATERIALS SCIENCE: MATERIALS IN ELECTRONICS
J2  - J MATER SCI: MATER EL
VL  - 33
PY  - 2022
IS  - 13
SP  - 10585
EP  - 10595
PG  - 11
SN  - 0957-4522
DO  - 10.1007/s10854-022-08044-9
UR  - https://m2.mtmt.hu/api/publication/32969212
ID  - 32969212
N1  - Export Date: 3 August 2022
AB  - We report on the optical, chemical, and morphological properties of Polyethylene oxide (PEO) with Nb doped with (1%, 2%, 4%, and 8%) of potassium paramagnets (KMnO4) thin films. The as-prepared PEO-Nb-KMnO4 thin films are deposited using the casting technique on a glass substrate. The transmittance T% (i) and reflectance R% (lambda) of PEO-Nb-KMnO4 thin films are measured at room temperature in the (250-700) nm spectral range. Interestingly, increasing the doping level of KMnO4 decreases the transmittance slowly in the low-energy region and abruptly in the high-energy region. Furthermore, a redshift of the absorption edge is observed as the doping level of KMnO4 is increased, implying a significant reduction of the optical bandgap. Index of refraction n and extinction coefficient k for PEO-Nb-KMnO4 thin film are reported. Furthermore, a combination of classical models, namely, Tauc, Wemple-DiDomenico, and Sellmeier models are employed to measure and interpret the optical behavior, optical bandgaps, dispersion parameters, and optoelectronic parameters of PEO-Nb and PEO-Nb-doped KMnO4 thin films. The optical bandgap of PEO-Nb is found to be 4.00 eV. Incorporating 8% of KMnO4 into PEO-Nb matrix reduces the optical bandgap to 3.72 eV. To identify the major vibrational modes of the un-doped and doped thin films, Fourier transform infrared spectroscopy (FTIR) analysis is conducted. The major peak at 541 cm(-1) of PEO-Nb is associated with the Nb-3-O bond. Introducing KMnO(4)( )into PEO-Nb matrix leads to remarkable changes of the width, intensity, and the peak positions of the vibrational bands. Electrical properties of the investigated thin films are investigated and elucidated using the four-point probe. The measured conductivity of un-doped PEO-Nb is about1.82 x 10(-5)S/cm. Introduction different dopant levels of KMnO4 boosts the conductivity to 8.00 x 10(-5)S/cm at the highest concentration of KMnO4 (8%). The obtained Scanning Electron Microscopy (SEM) micrographs indicate that the amorphous PEO-Nb thin films exhibit a smooth surface. Inserting different concentrations of KMnO4 yields new aggregations on the constructed surfaces confirming the homogenous distribution of KMnO4 into PEO-Nb matrix. The drastic modifications of optical, chemical, and surface properties of PEO-Nb thin films caused by introducing KMnO4 imply that PEO-Nb-KMnO4 thin films indicate their potential for several optoelectronic applications.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Zeng, S.
AU  - Guo, P.
AU  - Zhang, K.
AU  - Hu, C.
AU  - Liu, Y.
AU  - Wang, Z.
TI  - Optimization and Validation of Ultraviolet-Visible Spectrophotometric Method for Determination of Potassium Permanganate Consumption for Migrants from Food Contact Rubber
JF  - SHIPIN KEXUE / FOOD SCIENCE
J2  - SHIPIN KEXUE / FOOD SCI
VL  - 43
PY  - 2022
IS  - 22
SP  - 334
EP  - 340
PG  - 7
SN  - 1002-6630
DO  - 10.7506/spkx1002-6630-20220114-133
UR  - https://m2.mtmt.hu/api/publication/34771051
ID  - 34771051
N1  - Key Laboratory of Product Packaging and Logistics of Guangdong Higher Education Institutes, College of Packaging Engineering, Jinan University, Zhuhai, 519070, China            
            School of Mechanics and Construction Engineering, Jinan University, Guangzhou, 510632, China            
            College of Science and Engineering, Jinan University, Guangzhou, 510632, China            
            Export Date: 5 April 2024            
            Correspondence Address: Wang, Z.; Key Laboratory of Product Packaging and Logistics of Guangdong Higher Education Institutes, China; email: wangzw@jnu.edu.cn            
            Correspondence Address: Wang, Z.; School of Mechanics and Construction Engineering, China; email: wangzw@jnu.edu.cn
LA  - Chinese
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Cao, Xin
AU  - Xu, Chunxiang
AU  - Zhang, Zhengwei
AU  - Yang, Wenfu
AU  - Zhang, Jinshan
TI  - Effect of I-phase morphology and microstructure transformation in biomedical Mg-3Zn-1Mn-1Y alloys on vitro degradation behavior in dynamic simulated body fluid
JF  - JOURNAL OF MATERIALS SCIENCE
J2  - J MATER SCI
VL  - 56
PY  - 2021
IS  - 21
SP  - 12394
EP  - 12411
PG  - 18
SN  - 0022-2461
DO  - 10.1007/s10853-021-06091-x
UR  - https://m2.mtmt.hu/api/publication/32377946
ID  - 32377946
N1  - College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan, 030024, China            
            Shanxi Province Magnesium Alloy Key Laboratory, Taiyuan, 030024, China            
            Cited By :9            
            Export Date: 5 April 2024            
            CODEN: JMTSA            
            Correspondence Address: Xu, C.; College of Materials Science and Engineering, China; email: xuchunxiang2012@126.com
AB  - The corrosion mechanism of as-cast, heat-treated (H400) and extruded (E30, E60, E90) Mg-3Zn-1Mn-1Y alloys with different microstructure is investigated by scan electron microscope (SEM), scan Kelvin probe force microscope (SKPFM), X-ray photoelectron spectroscopy (XPS), electrochemical impedance analysis and immersion experiments equipped with a dynamic corrosion device. The relevant results are as follows: continuously strip-like I-phase (Mg3Zn6Y) in as-cast alloy distributed along the grain boundary played a significant obstacle impact during corrosion, whereas this capability is weakened after heat treatment and large plastic extrusion deformation. However, extrusion deformation significantly improved alloy corrosion performance, the extruded E30 alloy performed superior anti-corrosion behavior among the three extruded alloys owing to the smaller potential difference between I-phase (2.59 V) and DRXed (2.51 V) or un-DRXed (2.54 V) grains. In addition, the corrosion obstacle effect of grains boundaries (the grain boundary has higher potential than the Mg substrate), dense corrosion products film protection (isolate the substrate from contact with SBF) and typical basal texture (lower reactivity of base atoms) have great influence on corrosion behavior.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Hanopolskyi, Anton I
AU  - Smaliak, Viktoryia A.
AU  - Novichkov, Alexander I
AU  - Semenov, Sergey N.
TI  - Autocatalysis: Kinetics, Mechanisms and Design
JF  - CHEMSYSTEMSCHEM
J2  - CHEMSYSTEMSCHEM
VL  - 3
PY  - 2021
IS  - 1
PG  - 30
SN  - 2570-4206
DO  - 10.1002/syst.202000026
UR  - https://m2.mtmt.hu/api/publication/32829984
ID  - 32829984
N1  - Cited By :1            
            Export Date: 27 March 2024            
            Correspondence Address: Semenov, S.N.; Department of Organic Chemistry, Herzl, 234, Israel; email: sergey.semenov@weizmann.ac.il
AB  - The importance of autocatalysis spans from practical applications such as in chemically amplified photoresists, to autocatalysis playing a fundamental role in evolution as well as a plausible key role in the origin of life. The phenomenon of autocatalysis is characterized by its kinetic signature rather than by its mechanistic aspects. The molecules that form autocatalytic systems and the mechanisms underlying autocatalytic reactions are very diverse. This chemical diversity, combined with the strong involvement of chemical kinetics, creates a formidable barrier for entrance to the field. Understanding these challenges, we wrote this Review with three main goals in mind: (i) To provide a basic introduction to the kinetics of autocatalytic systems and its relation to the role of autocatalysis in evolution, (ii) To provide a comprehensive overview, including tables, of synthetic chemical autocatalytic systems, and (iii) To provide an in-depth analysis of the concept of autocatalytic reaction networks, their design, and perspectives for their development.
LA  - English
DB  - MTMT
ER  - 

TY  - GEN
AU  - Jakob, L. Andersen
AU  - Christoph, Flamm
AU  - Daniel, Merkle
AU  - Peter, F. Stadler
TI  - Defining Autocatalysis in Chemical Reaction Networks
PY  - 2021
UR  - https://m2.mtmt.hu/api/publication/32478460
ID  - 32478460
AB  - Autocatalysis is a deceptively simple concept, referring to the situation that a chemical species X catalyzes its own formation. From the perspective of chemical kinetics, autocatalysts show a regime of super-linear growth. Given a chemical reaction network, however, it is not at all straightforward to identify species that are autocatalytic in the sense that there is a sub-network that takes X as input and produces more than one copy of X as output. The difficulty arises from the need to distinguish autocatalysis e.g. from the superposition of a cycle that consumes and produces equal amounts of X and a pathway that produces X. To deal with this issue, a number of competing notions, such as exclusive autocatalysis and autocatalytic cycles, have been introduced. A closer inspection of concepts and their usage by different authors shows, however, that subtle differences in the definitions often makes conceptually matching ideas difficult to bring together formally. In this contribution we make some of the available approaches comparable by translating them into a common formal framework that uses integer hyperflows as a basis to study autocatalysis in large chemical reaction networks. As an application we investigate the prevalence of autocatalysis in metabolic networks.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Liu, Yali
AU  - Zhang, Sufeng
AU  - Lin, Rui
AU  - Li, Lei
AU  - Li, Min
AU  - Du, Min
AU  - Tang, Ruihua
TI  - Potassium permanganate oxidation as a carboxylation and defibrillation method for extracting cellulose nanofibrils to fabricate films with high transmittance and haze
JF  - GREEN CHEMISTRY
J2  - GREEN CHEM
VL  - 23
PY  - 2021
IS  - 20
SP  - 8069
EP  - 8078
PG  - 10
SN  - 1463-9262
DO  - 10.1039/d1gc02657g
UR  - https://m2.mtmt.hu/api/publication/32377944
ID  - 32377944
N1  - Export Date: 3 August 2022            
            CODEN: GRCHF
AB  - Cellulose-based films have attracted significant attention in the fields of flexible photoelectric products and energy equipment by virtue of their abundant sources, biodegradability, renewability, sustainability, and optical properties, of which high transmittance and high haze are important parameters. In this study, we proposed a green and efficient defibrillation and carboxylation method of KMnO4 synergized with slight homogenization to produce fine carboxylated cellulose nanofibrils (COOH-CNFs) with a high yield of 96%. The oxidation reaction was carried out under mild conditions (50 degrees C, 2 h). The as-prepared COOH-CNFs well-retained the crystalline structure of the pulp with coexisting crystalline and amorphous regions. This structure gave the COOH-CNF film unique optical properties, including a transmittance above 80% at a wavelength of 550 nm, a haze reaching 97.45%, and no obvious absorption in the ultraviolet-visible range. The resulting COOH-CNFs were characterized in terms of fibrillation yield, morphological features, crystal structure, surface chemistry, and mechanical behavior. This CNF preparation approach is advantageous over traditional methods owing to a reduced reactant dosage and enhanced efficiency, which represents a potential green route in industry and makes it a promising candidate for fabricating films for flexible lighting, energy, and sensing devices.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Jian, Shun-Yi
AU  - Chang, Ko-Lun
TI  - Effect of cerium ion on the microstructure and properties of permanganate conversion coating on LZ91 magnesium alloy
JF  - APPLIED SURFACE SCIENCE
J2  - APPL SURF SCI
VL  - 509
PY  - 2020
SN  - 0169-4332
DO  - 10.1016/j.apsusc.2019.144767
UR  - https://m2.mtmt.hu/api/publication/31359409
ID  - 31359409
N1  - Funding Agency and Grant Number: Ministry of Science and Technology of Taiwan, Republic of China [MOST 107-2623-E-606-004-D]
            Funding text: This study was financially supported by the Ministry of Science and Technology of Taiwan, Republic of China, under Grant No. MOST 107-2623-E-606-004-D. In addition, thanks to Ms. C. Y. Chien of Ministry of Science and Technology (National Taiwan University) for the assistance in FIB experiments.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Jian, S.-Y.
AU  - Tzeng, Y.-C.
AU  - Ger, M.-D.
AU  - Chang, K.-L.
AU  - Shi, G.-N.
AU  - Huang, W.-H.
AU  - Chen, C.-Y.
AU  - Wu, C.-C.
TI  - The study of corrosion behavior of manganese-based conversion coating on LZ91 magnesium alloy: Effect of addition of pyrophosphate and cerium
JF  - MATERIALS AND DESIGN
J2  - MATER DESIGN
VL  - 192
PY  - 2020
SN  - 0264-1275
DO  - 10.1016/j.matdes.2020.108707
UR  - https://m2.mtmt.hu/api/publication/31614066
ID  - 31614066
N1  - Department of Chemistry and Materials Engineering, Chung Cheng Institute of Technology, National Defense University, Dasi, Taoyuan, 335, Taiwan            
            Department of Power Vehicle and Systems Engineering, Chung Cheng Institute of Technology, National Defense University, Dasi, Taoyuan, 335, Taiwan            
            National Synchrotron Radiation Research Center, 101 Hsin-Ann Road, Hsinchu, 30076, Taiwan            
            Anti-Corrosion Chemistry Section, Chemical Research System Division, National Chung-Shan Institute of Science and Technology, Taiwan            
            System Engineering and Technology Program, National Chiao Tung University, Hsin-Chu, Taiwan            
            Cited By :28            
            Export Date: 5 April 2024            
            Correspondence Address: Jian, S.-Y.; Department of Chemistry and Materials Engineering, Taiwan; email: ftvko@yahoo.com.tw
AB  - A previous study by the authors reported that a Mn[sbnd]Ce based conversion coating protects the surface of LZ91 magnesium alloy from corrosion. However, the acidic permanganate solution decomposes after several days of storage and this significantly affects the properties of the coating. To address this problem, this study presents a method to stabilize the acidic permanganate bath by adding pyrophosphate into the bath. The results show that all conversion coatings are amorphous and comprise two layers: a porous layer that contacts the substrate and a compact overlay. Coatings that are produced using a bath with Ce are more resistant to corrosion than those that are produced in a bath without Ce ions. Coatings that are stored in the Mn[sbnd]Ce bath for 2 weeks are significantly less resistant to corrosion than coatings that are produced using an as-prepared Mn[sbnd]Ce bath. The salt spray test results of coatings that are produced using the as-prepared bath and stored for 2 weeks are found similar because the bath is rendered more stable by the addition of pyrophosphate. © 2020 The Authors
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Ali, H. Elhosiny
TI  - A novel optical limiter and UV-Visible filters made of Poly (vinyl alcohol)/KMnO4 polymeric films on glass-based substrate
JF  - JOURNAL OF MATERIALS SCIENCE: MATERIALS IN ELECTRONICS
J2  - J MATER SCI: MATER EL
VL  - 30
PY  - 2019
IS  - 7
SP  - 7043
EP  - 7053
PG  - 11
SN  - 0957-4522
DO  - 10.1007/s10854-019-01021-9
UR  - https://m2.mtmt.hu/api/publication/31070737
ID  - 31070737
N1  - Advanced Functional Materials & Optoelectronic Laboratory (AFMOL), Department of Physics, Faculty of Science, King Khalid University, P.O. Box 9004, Abha, Saudi Arabia            
            Physics Department, Faculty of science, Zagazig University, Zagazig, 44519, Egypt            
            Cited By :4            
            Export Date: 30 September 2020            
            Correspondence Address: Ali, H.E.; Physics Department, Faculty of science, Zagazig UniversityEgypt; email: hibrahim@kku.edu.sa
Funding Agency and Grant Number: Deanship of Scientific Research at King Khalid University [R.G.P.2/13/39]
            Funding text: The authors extend their appreciation to the Deanship of Scientific Research at King Khalid University for funding this work through the research group's program under grant number R.G.P.2/13/39.
AB  - A poly (vinyl alcohol) polymeric films doped with various stages of concentrations (0, 0.037, 0.185, 0.37, 1.85 and 3.7 wt%) of KMnO4 salt were prepared by casting technique on glass substrate as a new optical limiting and laser filter application. Their structures, molecular complex formation and the morphology of the surface are analyzed by using XRD (X-ray diffraction), FTIR (Fourier transform-IR), and SEM (scanning electron microscopy), while the optical band gap as well as limiting characteristics is determined via UV-Vis spectroscopy, and optical limiting set-up for two laser sources, respectively. As a result of the increment of KMnO4 salt percentage inside the PVA polymer matrix, there is a significant decrease in the number of chain domains with a specific alignment (crystallizing degree) is observed through XRD diffraction and confirmed via Gaussian fitting and Fityk 0.9.8 software. FTIR spectra shows the complex interface interaction between KMnO4 and PVA. The numerical density as well as the size of the particles was increased as clearly seen in SEM images. In addition, the energy gap is markedly decreased from 3.6 eV to 1.1 eV for Pure PVA and 3.7 wt% of KMnO4 doped PVA (KMPVA5), respectively, on the glass substrate sample. The incident light was completely blocked in the UV range and extended to 555 nm in the visible region for the highest doping of KMnO4 in PVA. Moreover, a sharp decrease in the output and normalized power of the two laser sources via KMPVA5 film were detected. Therefore, for low cost optical limiting and laser filter technology, the PVA with the high concentration level of KMnO4 is considered as a promising candidate.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Ali, H. Elhosiny
AU  - Khairy, Yasmin
TI  - Microstructure and optical properties of Ni2+ doped PVA for optoelectronic devices
JF  - PHYSICA B-CONDENSED MATTER
J2  - PHYSICA B
VL  - 570
PY  - 2019
SP  - 41
EP  - 47
PG  - 7
SN  - 0921-4526
DO  - 10.1016/j.physb.2019.05.050
UR  - https://m2.mtmt.hu/api/publication/31070735
ID  - 31070735
N1  - Cited By :1            
            Export Date: 30 September 2020            
            CODEN: PHYBE            
            Correspondence Address: Khairy, Y.; Physics Department, Faculty of Science, Zagazig UniversityEgypt; email: yasmin_ph@yahoo.com
Funding Agency and Grant Number: Deanship of Scientific Research at King Khalid University [R.G.P.2/13/39]
            Funding text: The authors extend their appreciation to the Deanship of Scientific Research at King Khalid University for funding this work through the research group program under grant number R.G.P.2/13/39.
AB  - Different wt.% of Ni2+-doped Poly (vinyl alcohol), PVA, films are synthesized by a low-cost casting method. XRD, SEM and FTIR spectroscopy are used to study the microstructure of the composite samples. The degree of semi-crystallinity for all Ni2+-doped PVA (NPVA) and pure PVA films decreases and the amorphous order dominated in 3.7 wt% Ni2+-doped PVA (NPVA5) film as established by studying the spectroscopy of XRD and FT-IR. The increment of the Ni2+-doping level in PVA led to a formation of non-homogeneous particle size with an average value range from 1.03 mu m to 4.47 mu m for 0.027 wt% Ni2+-doped PVA (NPVA1), and NPVA5 films, respectively. UV-Vis-IR transmittance and absorption spectroscopies are specified for measuring the optical parameters. The indirect energy gap (E-ig) decreases to 4.85 eV for NPVA5 film, and the direct energy gap, Eg, to 1.36 eV for the same sample. However, owing to the complex construction between Ni2+-ions and the matrix of PVA, the transition strength (E-d), the indices of refraction (n, n(infinity)), and oscillator wavelength (lambda(0)) increase, while the excitation energy (E-s) decreases with further wt.% of Ni2+-ions. Due to the optical properties of the films, they are suitable to be inserted in different optoelectronic applications.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Ali, H. Elhosiny
AU  - Khairy, Yasmin
TI  - Optical and electrical performance of copper chloride doped polyvinyl alcohol for optical limiter and polymeric varistor devices
JF  - PHYSICA B-CONDENSED MATTER
J2  - PHYSICA B
VL  - 572
PY  - 2019
SP  - 256
EP  - 265
PG  - 10
SN  - 0921-4526
DO  - 10.1016/j.physb.2019.08.014
UR  - https://m2.mtmt.hu/api/publication/31070734
ID  - 31070734
N1  - Cited By :10            
            Export Date: 30 September 2020            
            CODEN: PHYBE            
            Correspondence Address: Ali, H.E.; Physics Department, faculty of science, Zagazig UniversityEgypt; email: hibrahim@kku.edu.sa
Funding Agency and Grant Number: Deanship of Scientific Research at King Khalid University [R.G.P.2/13/39]
            Funding text: The authors extend their appreciation to the Deanship of Scientific Research at King Khalid University for funding this work through the research group's program under grant number R. G. P. 2/13/39.
AB  - PVA composite films with different wt.% of CuCl2, by the cast method, were prepared. The semi-crystalline phases of PVA have been reduced by more addition of CuCl2 as confirmed with the help of X-ray diffraction, and Fourier transforms infrared spectroscopy. The thermal stability is surveyed by differential thermal analysis. The morphology of CuCl2 particles is studied by scanning electron microscopy, which shows the semi-spherical particles of size varied from (0.31-1.19) mu m to (3.1-5) mu m for 0.037 wt% CuCl2/PVA and 3.700 wt% CuCl2/PVA (CPVA5) films, respectively. With the increment of the additive, the absorptive property of the films is increased. The indirect and direct energy gap were estimated. The power with 632.8 nm and 533 nm of the laser sources has been reduced to 40% and 47% via CPVA5 films. The AC electrical conductivity follows the Jonscher's power law. The forward lnI (A) - lnV (V) behaviors show that the doped films have high voltage breakdown.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Colmenero, Francisco
TI  - Mechanical properties of anhydrous oxalic acid and oxalic acid dihydrate
JF  - PHYSICAL CHEMISTRY CHEMICAL PHYSICS
J2  - PHYS CHEM CHEM PHYS
VL  - 21
PY  - 2019
IS  - 5
SP  - 2673
EP  - 2690
PG  - 18
SN  - 1463-9076
DO  - 10.1039/c8cp07188h
UR  - https://m2.mtmt.hu/api/publication/30895932
ID  - 30895932
N1  - Cited By :14            
            Export Date: 30 September 2020            
            CODEN: PPCPF            
            Correspondence Address: Colmenero, F.; Instituto de Estructura de la Materia-Consejo Superior de Investigaciones Cientificas C/ SerranoSpain; email: francisco.colmenero@iem.cfmac.csic.es
AB  - The mechanical properties of oxalic acid dihydrate and anhydrous oxalic acid ( and polymorphic forms) were obtained by using rigorous theoretical solid-state methods based on density functional theory using plane waves and pseudopotentials. The calculated crystal structures and X-ray powder diffraction patterns of these materials were found to be in excellent agreement with the experimental information. Since the calculated elasticity matrices fullfilled the Born stability conditions, the corresponding crystal structures were found to be mechanically stable. A large number of relevant mechanical properties including the values of the bulk moduli and their pressure derivatives, shear and Young moduli, Poisson ratios, ductility and hardness indices, and mechanical anisotropy values of these materials were reported. The three forms of oxalic acid are highly anisotropic ductile materials having low hardness and bulk moduli. The three materials are shown to display small negative Poisson ratios (NPR) and to exhibit the phenomenon of negative linear compressibility (NLC) for applied pressures along the direction of the minimum Poisson ratio. In addition, they undergo pressure induced phase transitions for relatively small applied pressures. The analysis of the crystal structures of these materials as a function of pressure demonstrates that the mechanism of NLC of these materials is unrelated to the wine-rack structural mechanism commonly used to rationalize this phenomenon. The three forms of oxalic acid considered in this work are molecular crystals whose structures are characterized by structural elements which are not directly bonded but held together by weak van der Waals forces. The weak bonding between these elements is able to accommodate the structural variations originating from the application of pressure, but the resulting structural deformations appear to be counterintuitive and lead to the anomalous mechanical behavior of these materials.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Ibrahim, I.
AU  - Idris, S. O.
AU  - Abdulkadir, I.
AU  - Onu, A. D.
TI  - Kinetics and mechanism of the redox reaction of N,N-phenylenebis-(salicylideneiminato)iron(III) with oxalic acid in mixed aqueous medium
JF  - TRANSITION METAL CHEMISTRY
J2  - TRANSIT METAL CHEM
VL  - 44
PY  - 2019
IS  - 3
SP  - 269
EP  - 273
PG  - 5
SN  - 0340-4285
DO  - 10.1007/s11243-018-0291-8
UR  - https://m2.mtmt.hu/api/publication/31070738
ID  - 31070738
N1  - Department of Chemistry, Ahmadu Bello University, Zaria, Nigeria            
            Department of Chemistry, Federal College of Education, Zaria, Nigeria            
            Cited By :3            
            Export Date: 30 September 2020            
            CODEN: TMCHD            
            Correspondence Address: Ibrahim, I.; Department of Chemistry, Ahmadu Bello UniversityNigeria; email: ibrahimmismaila@gmail.com
AB  - The kinetics of electron transfer between N,N-phenylenebis-(salicylideneiminato)iron(III), hereafter referred to as [Fe(Salphen)](+), and oxalic acid was studied in mixed aqueous medium (DMSO:H2O; 1:4 v/v) under pseudo-first-order conditions at 26 +/- 1 degrees C, I=0.2coulomb(2)moldm(-3) (NaCl) and (max)=435nm. The reaction was found to be second order overall and acid independent, and displayed zero BrOnsted-Debye salt effect. There was no evidence for the formation of an intermediate complex or free radicals during the reaction. Overall, the kinetic data suggest an inner-sphere mechanism for the reaction, which is first order in both reactants. A plausible reaction mechanism is proposed.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - N. Ekeh, Humphrey
AU  - Odoemelam, Stevens A.
AU  - U. Sonde, Christopher
TI  - Biosorption Studies of Cr(VI) Ion from Aqueous Solution using Unmodified and Oxalic Acid Modified African Yam Bean Pod and Groundnut Shell
JF  - INTERNATIONAL RESEARCH JOURNAL OF PURE AND APPLIED CHEMISTRY
J2  - INT RES J PURE APPL CHEM
VL  - 2019
PY  - 2019
SP  - 1
EP  - 14
PG  - 14
SN  - 2231-3443
DO  - 10.9734/irjpac/2019/v18i330091
UR  - https://m2.mtmt.hu/api/publication/32478477
ID  - 32478477
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Song, Dean
AU  - Jefferson, William A.
AU  - Cheng, Hanyang
AU  - Jiang, Xiaohua
AU  - Qiang, Zhimin
AU  - He, Hong
AU  - Liu, Huijuan
AU  - Qu, Jiuhui
TI  - Acidic permanganate oxidation of sulfamethoxazole by stepwise electron-proton transfer
JF  - CHEMOSPHERE
J2  - CHEMOSPHERE
VL  - 222
PY  - 2019
SP  - 71
EP  - 82
PG  - 12
SN  - 0045-6535
DO  - 10.1016/j.chemosphere.2019.01.113
UR  - https://m2.mtmt.hu/api/publication/31070736
ID  - 31070736
N1  - Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, China            
            State Agriculture Ministry Laboratory of Quality & Safety Risk Assessment for Tobacco, Tobacco Research Institute, Chinese Academy of Agricultural Sciences, Qingdao, 266101, China            
            College of Environmental Science and Engineering, Ocean University of China, Qingdao, 266100, China            
            Cited By :4            
            Export Date: 30 September 2020            
            CODEN: CMSHA            
            Correspondence Address: Liu, H.; Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of SciencesChina; email: hjliu@rcees.ac.cn            
            Chemicals/CAS: ammonia, 14798-03-9, 51847-23-5, 7664-41-7; sulfamethoxazole, 723-46-6; hydrogen, 12385-13-6, 1333-74-0; oxide, 16833-27-5; proton, 12408-02-5, 12586-59-3; Hydrogen; Manganese Compounds; Oxides; permanganic acid; Protons; Sulfamethoxazole
Funding Agency and Grant Number: Qingdao Postdoctoral Application Research Project [2016105]; Agricultural Science and Technology Innovation Program [ASTIPTRIC06]
            Funding text: This work was supported by the Qingdao Postdoctoral Application Research Project (2016105) and the Agricultural Science and Technology Innovation Program (ASTIPTRIC06).
AB  - Permanganate is a versatile chemical oxidant, and has undergone a dramatic evolution toward deep insight into its reaction mechanism. However, the hydrogen abstraction of the N-H bond by permanganate remains unclear. We studied the permanganate oxidation of the emerging micropollutant sulfamethoxazole in acidic aqueous solution. The reaction followed autocatalytic kinetics and demonstrated first-order with respect to each reactant. The presence of HMnO4 accelerated the reaction rate, which was four orders of magnitude higher than that of MnO4-. Based on the identified products, the rate-limiting step was determined to be simple N-H bond oxidation by metal-oxo species permanganate. The mechanism was then studied computationally by density functional theory (DFT) using ammonia as the simplest model. Results showed that the N-H bond oxidation by MnO4- (32.86 kcal/mol) was a concerted mechanism similar to that of C-H bond oxidation, whereas HMnO4 oxidation of the N-H bond (10.44 kcal/mol) was a stepwise electron-proton transfer. This reminds us that coordination of Bronsted acid could not only produce the stronger electrophile but also change the reaction mode by avoiding the bond cleavage in electron transfer process. (C) 2019 Elsevier Ltd. All rights reserved.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Zhou, Lijuan
AU  - Li, Na
AU  - Shu, Jie
AU  - Liu, Yunxiao
AU  - Wang, Kuntao
AU  - Cui, Xiang
AU  - Yuan, Yuan
AU  - Ding, BeiBei
AU  - Geng, Yong
AU  - Wang, Zhaolu
AU  - Duan, Yongxin
AU  - Zhang, Jianming
TI  - One-Pot Preparation of Carboxylated Cellulose Nanocrystals and Their Liquid Crystalline Behaviors
JF  - ACS SUSTAINABLE CHEMISTRY & ENGINEERING
J2  - ACS SUSTAIN CHEM ENG
VL  - 6
PY  - 2018
IS  - 9
SP  - 12403
EP  - 12410
PG  - 15
SN  - 2168-0485
DO  - 10.1021/acssuschemeng.8b02926
UR  - https://m2.mtmt.hu/api/publication/30526513
ID  - 30526513
N1  - Key Laboratory of Rubber-Plastics, Ministry of Education, Shandong Provincial Key Laboratory of Rubber-Plastics, Qingdao University of Science and Technology, Qingdao, 266042, China            
            Analysis and Testing Center, Soochow University, Renai Road 199, Suzhou, 215123, China            
            Cited By :14            
            Export Date: 30 September 2020            
            Correspondence Address: Zhang, J.; Key Laboratory of Rubber-Plastics, Ministry of Education, Shandong Provincial Key Laboratory of Rubber-Plastics, Qingdao University of Science and TechnologyChina; email: zjm@qust.edu.cn
Funding Agency and Grant Number: Natural Science Foundation of Shandong Province, ChinaNatural Science Foundation of Shandong Province [ZR2016EMB10]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [51573082, 21774068, 21604047, 21673148, 21303111, 51403095]
            Funding text: We acknowledge the financial support from the Natural Science Foundation of Shandong Province, China (Grant No. ZR2016EMB10) and the National Natural Science Foundation of China (Grant Nos. 51573082, 21774068, 21604047, 21673148, 21303111, and 51403095).
AB  - Carboxylated cellulose nanocrystals (CNCs-COOH) have attracted great attention for their potential applications in reinforcing polymer materials and surface modification. Herein, we developed a low-cost approach to prepare CNCs-COOH from pulp with high yield at mild reaction conditions (50 degrees C, 1 wt % sulfuric acid medium) using potassium permanganate (KMnO4) and oxalic acid (OA, H2C2O4) as the oxidizing and reducing agents, respectively. The oxidant dosage in this strategy is much lower than that in a conventional TEMPO method, and the yield of CNCs-COOH can reach as high as 68.0%, with a carboxylate content of 1.58 mmol/g. In this reaction system, the presence of the OA can complex with Mn3+ to form [Mn(C2O42-)](+) and prevent the Mn3+ from being reduced to Mn2+, leading to the strong oxidizing capacity of the reaction system maintained for a longer time. Atomic force microscopy analysis showed that rod-like CNCs were obtained with an average size of 10-22 nm in diameter and 150-300 nm in length. The crystal structure of as-prepared CNCs-COOH was nearly unchanged, and the crystallinity was 89.2% based on WAXD analysis. Of particular interest, CNCs-COOH suspension with high concentration (>6 wt %) also exhibited the same intriguing chiral nematic liquid crystalline self-assembly behaviors as sulfate CNCs prepared by traditional H2SO4 hydrolysis method. This study provides an efficient and cost-effective way to fabricate CNCs-COOH, leading to great potential applications in constructing advanced functional material.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Alves, Bezerra Taliana Kenia
AU  - de Oliveira, Arcanjo Narciza Maria
AU  - Garcia, Estefania Fernandes
AU  - Pereira, Gomes Ana Maria
AU  - Ramos, do Egypto Queiroga Rita de Cassia
AU  - de Souza, Evandro Leite
AU  - Madruga, Marta Suely
TI  - Effect of supplementation with probiotic lactic acid bacteria, separately or combined, on acid and sugar production in goat 'coalho' cheese
JF  - LWT-FOOD SCIENCE AND TECHNOLOGY
J2  - LWT-FOOD SCI TECHNOL
VL  - 75
PY  - 2017
SP  - 710
EP  - 718
PG  - 9
SN  - 0023-6438
DO  - 10.1016/j.lwt.2016.10.023
UR  - https://m2.mtmt.hu/api/publication/26368882
ID  - 26368882
N1  - Post Graduate Program in Food Science and Technology, Department of Food Engineering, Technology Centre, Federal University of Paraiba, Joao Pessoa, Paraiba 58051-900, Brazil            
            College of Biotechnology, Catholic University of Porto, Porto, Portugal            
            Cited By :23            
            Export Date: 5 April 2024            
            CODEN: LBWTA            
            Correspondence Address: Bezerra, T.K.A.; Post Graduate Program in Food Science and Technology, Brazil; email: taliana.kenia@hotmail.com
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Hue, Do Thi Kim
AU  - Shiba, Takumi
AU  - Maeda, Yasuaki
AU  - Takenaka, Norimichi
TI  - A 3-step chemiluminescence method for chemical oxygen demand measurement with dichromate oxidizing reagent
JF  - ANALYTICAL METHODS: ADVANCING METHODS AND APPLICATIONS
J2  - ANAL METHOD
VL  - 9
PY  - 2017
IS  - 39
SP  - 5797
EP  - 5805
PG  - 9
SN  - 1759-9660
DO  - 10.1039/c7ay01652b
UR  - https://m2.mtmt.hu/api/publication/27062303
ID  - 27062303
N1  - Cited By :5            
            Export Date: 5 April 2024            
            Correspondence Address: Hue, D.T.K.; Department of Applied Chemistry, 1-1 Gakuen-cho, Japan; email: huekim89@gmail.com
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Yin, Kai
AU  - Li, Fei
AU  - Wang, Ying
AU  - He, Qunying
AU  - Deng, Yongxiu
AU  - Chen, Shuo
AU  - Liu, Chengbin
TI  - Oxidative transformation of artificial sweetener acesulfame by permanganate: Reaction kinetics, transformation products and pathways, and ecotoxicity
JF  - JOURNAL OF HAZARDOUS MATERIALS
J2  - J HAZARD MATER
VL  - 330
PY  - 2017
SP  - 52
EP  - 60
PG  - 9
SN  - 0304-3894
DO  - 10.1016/j.jhazmat.2017.02.012
UR  - https://m2.mtmt.hu/api/publication/26729778
ID  - 26729778
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Pavel, Anatolyevich Nikolaychuk
AU  - Mariya, Mikhaylovna Vayner
TI  - The Decomposition of Tris-(Oxalato)-Manganate (III) Complex Ion as the Reaction Suitable for the Laboratory Practice on Chemical Kinetics
JF  - International Journal of Thermodynamics and Chemical Kinetics
VL  - 1
PY  - 2016
IS  - 2
SP  - 50
EP  - 59
PG  - 10
UR  - https://m2.mtmt.hu/api/publication/32478468
ID  - 32478468
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Jian, Shun-Yi
AU  - Chu, Yu-Ren
AU  - Lin, Chao-Sung
TI  - Permanganate conversion coating on AZ31 magnesium alloys with enhanced corrosion resistance
JF  - CORROSION SCIENCE
J2  - CORROS SCI
VL  - 93
PY  - 2015
SP  - 301
EP  - 309
PG  - 9
SN  - 0010-938X
DO  - 10.1016/j.corsci.2015.01.040
UR  - https://m2.mtmt.hu/api/publication/25683557
ID  - 25683557
N1  - Cited By :108            
            Export Date: 5 April 2024            
            CODEN: CRRSA            
            Correspondence Address: Lin, C.-S.; Department of Materials Science and Engineering, 1, Roosevelt Road, Section 4, Taiwan; email: csclin@ntu.edu.tw
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Otamonga, Jean-Paul
AU  - Abdel-Mageed, Amal
AU  - Agater, Irena B
AU  - Jewsbury, Roger A
TI  - A kinetic study of the enhancement of solution chemiluminescence of glyoxylic acid oxidation by manganese species
JF  - LUMINESCENCE
J2  - LUMINESCENCE
VL  - 30
PY  - 2015
IS  - 5
SP  - 507
EP  - 511
PG  - 5
SN  - 1522-7235
DO  - 10.1002/bio.2768
UR  - https://m2.mtmt.hu/api/publication/25683556
ID  - 25683556
N1  - Cited By :2            
            Export Date: 5 April 2024            
            CODEN: LUMIF            
            Correspondence Address: Jewsbury, R.A.; Department of Chemical and Biological Sciences, United Kingdom; email: r.a.jewsbury@hud.ac.uk
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Holdsworth, A.F.
AU  - Horrocks, A.R.
AU  - Kandola, B.K.
AU  - Price, D.
TI  - The potential of metal oxalates as novel flame retardants and synergists for engineering polymers
JF  - POLYMER DEGRADATION AND STABILITY
J2  - POLYM DEGRAD STABIL
VL  - 110
PY  - 2014
SP  - 290
EP  - 297
PG  - 8
SN  - 0141-3910
DO  - 10.1016/j.polymdegradstab.2014.09.007
UR  - https://m2.mtmt.hu/api/publication/31614067
ID  - 31614067
N1  - Cited By :29            
            Export Date: 5 April 2024            
            CODEN: PDSTD            
            Correspondence Address: Horrocks, A.R.; Institute for Materials Research and Innovation (IMRI), University of Bolton, Deane Road, United Kingdom
AB  - Based on their known decomposition to carbon dioxide, carbon monoxide and the respective oxide, six metal (calcium, manganese (II), iron (II), copper (II), tin (II) and zinc) were synthesised and assessed for their potential flame retardant activity in the absence and presence of selected flame retardants. Initially they were assessed when impregnated on cotton as a screening process and then selectively compounded with polyamide 6.6 (PA66), as a typical engineering polymer. Only manganese (II) and iron (II) oxalates alone reduced the burning rate of cotton, whereas together with ammonium bromide, calcium and iron (II) oxalates showed an apparent additional burning rate reducing effect. Derived synergistic effectivity (Es) values fall within the limits 0 < Es < 1 indicating a less than additive interaction. TGA/DTA analysis of oxalate/PA66 blends suggested that only zinc oxalate (ZnOx) offers both possible flame retardant activity in terms of enhanced residue formation ≥500°C, coupled with acceptable stability in molten PA66. When compounded with PA66, in the presence and absence of either aluminium diethyl phosphinate (AlPi)-based or selected polymeric bromine-containing flame retardants, LOI values increased in most PA66/ZnOx/flame retardant blends but UL94 test ratings were disappointingly low and more likely than not, "fails". PA66/ZnOx blends with AlPi and AlPi/MPP gave poor plaques suggesting that thermal interactions were occurring during compounding. The bromine-containing blends had better processability and both TGA and cone calorimetric studies showed that the PA66/poly(pentabromobenzyl acrylate)/ZnOx sample not only yielded the highest residues in air and nitrogen at 500 and 580°C, but also the lowest peak heat release rate value of 398 compared with 1276 kW/m2 for pure PA66. The derived Es value for this blend is 1.17 suggesting a small level of synergy between the zinc oxalate and poly(pentabromobenzyl acrylate) flame retardant. The possible role of zinc bromide is discussed. © 2014 Elsevier Ltd. All rights reserved.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Smith, Zoe M
AU  - Terry, Jessica M
AU  - Barnett, Neil W
AU  - Francis, Paul S
TI  - Ethanol as an alternative to formaldehyde for the enhancement of manganese(IV) chemiluminescence detection
JF  - TALANTA
J2  - TALANTA
VL  - 130
PY  - 2014
SP  - 221
EP  - 225
PG  - 5
SN  - 0039-9140
DO  - 10.1016/j.talanta.2014.07.002
UR  - https://m2.mtmt.hu/api/publication/25683558
ID  - 25683558
N1  - Cited By :4            
            Export Date: 5 April 2024            
            CODEN: TLNTA            
            Correspondence Address: Francis, P.S.; School of Life and Environmental Sciences, Locked Bag 20000, Geelong, VIC 3220, Australia; email: paul.francis@deakin.edu.au
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Zhou, Tao
AU  - Peng, Leilei
AU  - Liu, Yongcheng
AU  - Zhan, Yanhui
AU  - Liu, Feiwei
AU  - Zhang, Aiming
TI  - An insight into the sequential order in 2D correlation spectroscopy using polymer transitions: Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, and Asymmetric Sigmoid. Findings in experiments and simulations
JF  - VIBRATIONAL SPECTROSCOPY
J2  - VIB SPECTROSC
VL  - 70
PY  - 2014
SP  - 137
EP  - 161
PG  - 25
SN  - 0924-2031
DO  - 10.1016/j.vibspec.2013.12.001
UR  - https://m2.mtmt.hu/api/publication/25683560
ID  - 25683560
N1  - Cited By :19            
            Export Date: 5 April 2024            
            CODEN: VISPE            
            Correspondence Address: Zhou, T.; State Key Laboratory of Polymer Materials Engineering of China, , Chengdu 610065, China; email: zhoutaopoly@scu.edu.cn
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Zhou, Tao
AU  - Peng, Leilei
AU  - Liu, Yongcheng
AU  - Zhang, Aiming
AU  - Huang, Yong
TI  - Transitions of monodisperse aPS studied by model-based 2D correlation infrared spectroscopy incorporating S-shaped function
JF  - JOURNAL OF MOLECULAR STRUCTURE
J2  - J MOL STRUCT
VL  - 1059
PY  - 2014
SP  - 8
EP  - 14
PG  - 7
SN  - 0022-2860
DO  - 10.1016/j.molstruc.2013.11.031
UR  - https://m2.mtmt.hu/api/publication/25683559
ID  - 25683559
N1  - Cited By :4            
            Export Date: 5 April 2024            
            CODEN: JMOSB            
            Correspondence Address: Zhou, T.; State Key Laboratory of Polymer Materials Engineering of China, , Chengdu 610065, China; email: zhoutaopoly@scu.edu.cn
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Опейда, Л.И.
AU  - Матвиенко, А.Г.
AU  - Симонов, М.А.
TI  - OXIDATION OF N HYDROXYPHTALIMIDE BY POTASSIUM PERMANGANATE IN NEUTRAL MEDIUM
JF  - NAUKOVI PRACI DONECKOGO NACIONALNOGO TEHNICNOGO UNIVERSITETU. SERIA HIMIA I HIMICNA TEHNOLOGIA
J2  - NAUKOVI PRACI DONECKOGO NACIONALNOGO TEHNICNOGO UNIVERSITETU. SERIA HIMIA I HIMICNA TEHNOLOGIA
VL  - 2
PY  - 2014
IS  - 23
SP  - 104
EP  - 110
PG  - 7
SN  - 2074-6652
UR  - https://m2.mtmt.hu/api/publication/32478473
ID  - 32478473
LA  - Russian
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Hindson, Christopher M
AU  - Smith, Zoe M
AU  - Barnett, Neil W
AU  - Hanson, Graeme R
AU  - Lim, Kieran F
AU  - Francis, Paul S
TI  - Autocatalytic Chemiluminescence Sheds New Light on the Classic Permanganate-Oxalate Reaction
JF  - JOURNAL OF PHYSICAL CHEMISTRY A
J2  - J PHYS CHEM A
VL  - 117
PY  - 2013
IS  - 19
SP  - 3918
EP  - 3924
PG  - 7
SN  - 1089-5639
DO  - 10.1021/jp312603m
UR  - https://m2.mtmt.hu/api/publication/25683562
ID  - 25683562
N1  - Centre for Chemistry and Biotechnology, Faculty of Science and Technology, Deakin University, Geelong, VIC 3216, Australia            
            Centre for Advanced Imaging, University of Queensland, Brisbane, QLD 4072, Australia            
            Alfred Deakin Research Institute and School of Life and Environmental Sciences, Faculty of Science and Technology, Deakin University, Burwood, VIC 3125, Australia            
            Cited By :7            
            Export Date: 5 April 2024            
            CODEN: JPCAF            
            Correspondence Address: Francis, P.S.; Centre for Chemistry and Biotechnology, , Geelong, VIC 3216, Australia; email: paul.francis@deakin.edu.au
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Puyol, D
AU  - Carvajal-Arroyo, J M
AU  - Garcia, B
AU  - Sierra-Alvarez, R
AU  - Field, J A
TI  - Kinetic characterization of Brocadia spp.-dominated anammox cultures
JF  - BIORESOURCE TECHNOLOGY
J2  - BIORESOUR TECHNOL
VL  - 139
PY  - 2013
SP  - 94
EP  - 100
PG  - 7
SN  - 0960-8524
DO  - 10.1016/j.biortech.2013.04.001
UR  - https://m2.mtmt.hu/api/publication/25683561
ID  - 25683561
N1  - Cited By :72            
            Export Date: 5 April 2024            
            CODEN: BIRTE            
            Correspondence Address: Puyol, D.; Department of Chemical and Environmental Engineering, 1133 E. James E. Rogers Way, Harshbarger 108, Tucson, AZ, United States; email: daniel.puyol@uam.es
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Bahrami, Homayoon
AU  - Bigdeli, Moghadas
AU  - Davari, Mehdi D.
AU  - Zahedi, Mansour
AU  - Moosavi-Movahedi, Ali A.
TI  - Kinetics and Mechanism of the Permanganate-Induced Autocatalytic Dehydration Reaction of L-Y-Amino-N-Butyric Acid to Give 2-Pyrrolidone through a Radical Intermediate in Moderately Concentrated Acidic Medium
JF  - PROGRESS IN REACTION KINETICS AND MECHANISM
J2  - PROG REACT KINET MEC
VL  - 36
PY  - 2011
IS  - 2
SP  - 120
EP  - 138
PG  - 19
SN  - 1468-6783
DO  - 10.3184/146867810X12925913885141
UR  - https://m2.mtmt.hu/api/publication/32478463
ID  - 32478463
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Cheng, HP
AU  - Huang, YH
AU  - Lee, C
TI  - Decolorization of reactive dye using a photo-ferrioxalate system with brick grain-supported iron oxide
JF  - JOURNAL OF HAZARDOUS MATERIALS
J2  - J HAZARD MATER
VL  - 188
PY  - 2011
IS  - 1-3
SP  - 357
EP  - 362
PG  - 6
SN  - 0304-3894
DO  - 10.1016/j.jhazmat.2011.01.131
UR  - https://m2.mtmt.hu/api/publication/22000605
ID  - 22000605
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Davari, MD
AU  - Bahrami, H
AU  - Zahedi, M
AU  - Jadidi, K
TI  - Kinetics and mechanism of the KMnO(4)-oxidative catalysed condensation reaction of L-proline to a diketopiperazine: evidence for delayed autocatalytic behaviour
JF  - PROGRESS IN REACTION KINETICS AND MECHANISM
J2  - PROG REACT KINET MEC
VL  - 36
PY  - 2011
IS  - 2
SP  - 95
EP  - 119
PG  - 25
SN  - 1468-6783
DO  - 10.3184/146867810X12894108189486
UR  - https://m2.mtmt.hu/api/publication/22000601
ID  - 22000601
N1  - Cited By :2            
            Export Date: 5 April 2024            
            CODEN: PRKNA            
            Correspondence Address: Davari, M.D.; Department of Chemistry, , Evin, 19839-6313, Tehran, Iran
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Francis, PS
AU  - Hindson, CM
AU  - Terry, JM
AU  - Smith, ZM
AU  - Slezak, T
AU  - Adcock, JL
AU  - Fox, BL
AU  - Barnett, NW
TI  - Enhanced permanganate chemiluminescence
JF  - ANALYST
J2  - ANALYST
VL  - 136
PY  - 2011
IS  - 1
SP  - 64
EP  - 66
PG  - 3
SN  - 0003-2654
DO  - 10.1039/c0an00588f
UR  - https://m2.mtmt.hu/api/publication/22000603
ID  - 22000603
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Haus, UU
AU  - Hemmecke, R
AU  - Pokutta, S
TI  - Reconstructing biochemical cluster networks
JF  - JOURNAL OF MATHEMATICAL CHEMISTRY
J2  - J MATH CHEM
VL  - 49
PY  - 2011
IS  - 10
SP  - 2441
EP  - 2456
PG  - 16
SN  - 0259-9791
DO  - 10.1007/s10910-011-9892-6
UR  - https://m2.mtmt.hu/api/publication/22000620
ID  - 22000620
N1  - Megjegyzés-23576355
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Kelland, MA
TI  - A Neat Trick Using Oxalic Acid Dihydrate and Potassium Permanganate and Other Experiments with Small Organic Amine or Oxygenated Compounds
JF  - JOURNAL OF CHEMICAL EDUCATION
J2  - J CHEM EDUC
VL  - 88
PY  - 2011
IS  - 3
SP  - 276
EP  - 278
PG  - 3
SN  - 0021-9584
DO  - 10.1021/ed1004118
UR  - https://m2.mtmt.hu/api/publication/22000622
ID  - 22000622
N1  - Cited By :1            
            Export Date: 5 April 2024            
            CODEN: JCEDA            
            Correspondence Address: Kelland, M. A.; Department of Mathematics and Natural Sciences, , 4036 Stavanger, Norway; email: malcolm.kelland@uis.no
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Li, YY
AU  - Zhao, Y
AU  - Zhu, ZL
TI  - Kinetic Investigation of the Autocatalytic Reaction between Potassium Permanganate and Hydrogen Peroxide with Soft-modeling Methods
JF  - ANALYTICAL SCIENCES
J2  - ANAL SCI
VL  - 27
PY  - 2011
IS  - 1
SP  - 37
EP  - 41
PG  - 5
SN  - 0910-6340
DO  - 10.2116/analsci.27.37
UR  - https://m2.mtmt.hu/api/publication/22000602
ID  - 22000602
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Perez-Benito, JF
TI  - Permanganate Oxidation of alpha-Amino Acids: Kinetic Correlations for the Nonautocatalytic and Autocatalytic Reaction Pathways
JF  - JOURNAL OF PHYSICAL CHEMISTRY A
J2  - J PHYS CHEM A
VL  - 115
PY  - 2011
IS  - 35
SP  - 9876
EP  - 9885
PG  - 10
SN  - 1089-5639
DO  - 10.1021/jp2043174
UR  - https://m2.mtmt.hu/api/publication/24390414
ID  - 24390414
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Terry, JM
AU  - Zammit, EM
AU  - Slezak, T
AU  - Barnett, NW
AU  - Olson, DC
AU  - Wolcott, DK
AU  - Edwards, DL
AU  - Francis, PS
TI  - Solution mixing and the emission of light in flow-cells for chemiluminescence detection
JF  - ANALYST
J2  - ANALYST
VL  - 136
PY  - 2011
IS  - 5
SP  - 913
EP  - 919
PG  - 7
SN  - 0003-2654
DO  - 10.1039/c0an00591f
UR  - https://m2.mtmt.hu/api/publication/22000598
ID  - 22000598
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Zhang, QH
AU  - Feng, XW
AU  - Zhang, DJ
AU  - Zhao, Y
AU  - Zhu, ZL
TI  - Determination and resolution of non-UV-visible absorptive component during a kinetic process with modified soft modeling methods
JF  - CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS
J2  - CHEMOMETR INTELL LAB
VL  - 109
PY  - 2011
IS  - 2
SP  - 131
EP  - 138
PG  - 8
SN  - 0169-7439
DO  - 10.1016/j.chemolab.2011.08.012
UR  - https://m2.mtmt.hu/api/publication/22000621
ID  - 22000621
N1  - Department of Chemistry, Tongji University, 1239 Siping Road, Shanghai 200092, China            
            School of Chemistry and Molecular Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China            
            Cited By :3            
            Export Date: 5 April 2024            
            CODEN: CILSE            
            Correspondence Address: Zhu, Z.; Department of Chemistry, 1239 Siping Road, Shanghai 200092, China; email: zhuzl@tongji.edu.cn
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Furuya, T
AU  - Benitez, D
AU  - Tkatchouk, E
AU  - Strom, AE
AU  - Tang, PP
AU  - Goddard, WA
AU  - Ritter, T
TI  - Mechanism of C-F Reductive Elimination from Palladium(IV) Fluorides
JF  - JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
J2  - J AM CHEM SOC
VL  - 132
PY  - 2010
IS  - 11
SP  - 3793
EP  - 3807
PG  - 15
SN  - 0002-7863
DO  - 10.1021/ja909371t
UR  - https://m2.mtmt.hu/api/publication/22000608
ID  - 22000608
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Haus, UU
AU  - Hemmecke, R
TI  - Decomposition of reaction networks: the initial phase of the permanganate/oxalic acid reaction
JF  - JOURNAL OF MATHEMATICAL CHEMISTRY
J2  - J MATH CHEM
VL  - 48
PY  - 2010
IS  - 2
SP  - 305
EP  - 312
PG  - 8
SN  - 0259-9791
DO  - 10.1007/s10910-010-9670-x
UR  - https://m2.mtmt.hu/api/publication/22000624
ID  - 22000624
N1  - Cited By :1            
            Export Date: 5 July 2023            
            Correspondence Address: Haus, U.-U.; Institut für Mathematische Optimierung, Universitätsplatz 2, 39106 Magdeburg, Germany; email: haus@imo.math.uni-magdeburg.de
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Hindson, CM
AU  - Francis, PS
AU  - Hanson, GR
AU  - Adcock, JL
AU  - Barnettlt, NW
TI  - Mechanism of Permanganate Chemiluminescence
JF  - ANALYTICAL CHEMISTRY
J2  - ANAL CHEM
VL  - 82
PY  - 2010
IS  - 10
SP  - 4174
EP  - 4180
PG  - 7
SN  - 0003-2700
DO  - 10.1021/ac100363s
UR  - https://m2.mtmt.hu/api/publication/22000623
ID  - 22000623
N1  - School of Life and Environmental Sciences, Deakin University, Geelong, VIC 3217, Australia            
            Institute for Technology Research and Innovation, Deakin University, Geelong, VIC 3217, Australia            
            Centre for Advanced Imaging, University of Queensland, St. Lucia, QLD 4072, Australia            
            Cited By :51            
            Export Date: 5 April 2024            
            CODEN: ANCHA            
            Correspondence Address: Barnett, N. W.; School of Life and Environmental Sciences, , Geelong, VIC 3217, Australia; email: neil.barnett@deakin.edu.au
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Khatti, Z
AU  - Davari, MD
AU  - Bahrami, H
AU  - Zahedi, M
TI  - KINETICS AND MECHANISM OF THE PERMANGANATE-INDUCED OXIDATIVE CATALYTIC CONDENSATION OF SARCOSINE TO A DIKETOPIPERAZINE
JF  - PROGRESS IN REACTION KINETICS AND MECHANISM
J2  - PROG REACT KINET MEC
VL  - 35
PY  - 2010
IS  - 1
SP  - 1
EP  - 26
PG  - 26
SN  - 1468-6783
DO  - 10.3184/146867809X472125
UR  - https://m2.mtmt.hu/api/publication/22000609
ID  - 22000609
N1  - Cited By :2            
            Export Date: 5 April 2024            
            CODEN: PRKNA            
            Correspondence Address: Khatti, Z.; Department of Chemistry, P.O. Box 19395-4716, Tehran, 19839-6313, Iran
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Slezak, T
AU  - Terry, JM
AU  - Francis, PS
AU  - Hindson, CM
AU  - Olson, DC
AU  - Wolcott, DK
AU  - Barnett, NW
TI  - Autocatalytic Nature of Permanganate Oxidations Exploited for Highly Sensitive Chemiluminescence Detection
JF  - ANALYTICAL CHEMISTRY
J2  - ANAL CHEM
VL  - 82
PY  - 2010
IS  - 6
SP  - 2580
EP  - 2584
PG  - 5
SN  - 0003-2700
DO  - 10.1021/ac9028399
UR  - https://m2.mtmt.hu/api/publication/22000611
ID  - 22000611
N1  - School of Life and Environmental Sciences, Deakin University, Geelong, VIC 3217, Australia            
            Institute for Technology Research and Innovation, Deakin University, Geelong, VIC 3217, Australia            
            Global FIA, P.O. Box 480, Fox Island, WA 98333, United States            
            Cited By :23            
            Export Date: 5 April 2024            
            CODEN: ANCHA            
            Correspondence Address: Francis, P. S.; School of Life and Environmental Sciences, , Geelong, VIC 3217, Australia; email: psf@deakin.edu.au
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Bahrami, H
AU  - Davari, MD
AU  - Keshavari, M
AU  - Zahedi, M
AU  - Bazgir, A
AU  - Moosavi-Movahedi, AA
TI  - Kinetics and Mechanism of the Dehydration Reaction of Sarcosine to a Bislactame through Diacyclperoxide Intermediate in Strong Acidic Medium
JF  - INTERNATIONAL JOURNAL OF CHEMICAL KINETICS
J2  - INT J CHEM KINET
VL  - 41
PY  - 2009
IS  - 11
SP  - 689
EP  - 703
PG  - 15
SN  - 0538-8066
DO  - 10.1002/kin.20441
UR  - https://m2.mtmt.hu/api/publication/22000613
ID  - 22000613
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Bordjiba, T
AU  - Belanger, D
TI  - Direct Redox Deposition of Manganese Oxide on Multiscaled Carbon Nanotube/Microfiber Carbon Electrode for Electrochemical Capacitor
JF  - JOURNAL OF THE ELECTROCHEMICAL SOCIETY
J2  - J ELECTROCHEM SOC
VL  - 156
PY  - 2009
IS  - 5
SP  - A378
EP  - A384
SN  - 0013-4651
DO  - 10.1149/1.3090012
UR  - https://m2.mtmt.hu/api/publication/22000614
ID  - 22000614
N1  - Cited By :97            
            Export Date: 5 April 2024            
            CODEN: JESOA            
            Correspondence Address: B́langer, D.; D́partement de Chimie, , Montŕal, QC H3C 3P8, Canada; email: belanger.daniel@uqam.ca
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Perez-Benito, JF
TI  - Autocatalytic Reaction Pathway on Manganese Dioxide Colloidal Particles in the Permanganate Oxidation of Glycine
JF  - JOURNAL OF PHYSICAL CHEMISTRY C
J2  - J PHYS CHEM C
VL  - 113
PY  - 2009
IS  - 36
SP  - 15982
EP  - 15991
PG  - 10
SN  - 1932-7447
DO  - 10.1021/jp9014178
UR  - https://m2.mtmt.hu/api/publication/22000615
ID  - 22000615
N1  - Cited By :37            
            Export Date: 5 April 2024            
            Correspondence Address: Perez-Benito, J. F.; Departamento de Quimica Fisica, Marti i Franques, 1, 08028 Barcelona, Spain; email: jfperezdebenito@ub.edu
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Rolison, DR
AU  - Long, RW
AU  - Lytle, JC
AU  - Fischer, AE
AU  - Rhodes, CP
AU  - McEvoy, TM
AU  - Bourga, ME
AU  - Lubers, AM
TI  - Multifunctional 3D nanoarchitectures for energy storage and conversion
JF  - CHEMICAL SOCIETY REVIEWS
J2  - CHEM SOC REV
VL  - 38
PY  - 2009
IS  - 1
SP  - 226
EP  - 252
PG  - 27
SN  - 0306-0012
DO  - 10.1039/b801151f
UR  - https://m2.mtmt.hu/api/publication/22000612
ID  - 22000612
N1  - Surface Chemistry Branch, US Naval Research Laboratory, Code 6170, Washington, DC, 20375, United States            
            Nova Research, Inc., 1900 Elkin Street, Suite 230, Alexandria, VA, 22308, United States            
            Lynntech, Inc., College Station, TX, 77840, United States            
            Air Products and Chemicals, Inc., 7201 Hamilton Boulevard, Allentown, PA, 18195, United States            
            Cited By :713            
            Export Date: 31 May 2023            
            Correspondence Address: Rolison, D.R.; Surface Chemistry Branch, Code 6170, Washington, DC, 20375, United States
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Bahrami, H
AU  - Zahedi, M
TI  - Conclusive Evidence for Delayed Autocatalytic Behavior of Mn(II) Ions at a Critical Concentration
JF  - JOURNAL OF THE IRANIAN CHEMICAL SOCIETY
J2  - J IRAN CHEM SOC
VL  - 5
PY  - 2008
IS  - 4
SP  - 535
EP  - 545
PG  - 11
SN  - 1735-207X
DO  - 10.1007/BF03246131
UR  - https://m2.mtmt.hu/api/publication/22000616
ID  - 22000616
N1  - Cited By :14            
            Export Date: 5 April 2024            
            CODEN: JICSC            
            Correspondence Address: Zahedi, M.; Department of Chemistry, , Evin, Tehran, 19839, Iran; email: m-zahedi@cc.sbu.ac.ir
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Fischer, AE
AU  - Pettigrew, KA
AU  - Rolison, DR
AU  - Stroud, RM
AU  - Long, JW
TI  - Incorporation of homogeneous, nanoscale MnO2 within ultraporous carbon structures via self-limiting electroless deposition: Implications for electrochemical capacitors
JF  - NANO LETTERS
J2  - NANO LETT
VL  - 7
PY  - 2007
IS  - 2
SP  - 281
EP  - 286
PG  - 6
SN  - 1530-6984
DO  - 10.1021/nl062263i
UR  - https://m2.mtmt.hu/api/publication/22000617
ID  - 22000617
N1  - Surface Chemistry Branch (Code 6170), Naval Research Laboratory, Washington, DC 20375, United States            
            Materials and Sensors Branch (Code 6360), Naval Research Laboratory, Washington, DC 20375, United States            
            Cited By :577            
            Export Date: 5 April 2024            
            Correspondence Address: Long, J.W.; Surface Chemistry Branch (Code 6170), , Washington, DC 20375, United States; email: jeffrey.long@nrl.navy.mil
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Davies, M B
TI  - Mechanisms of reactions in solution
JF  - ANNUAL REPORTS ON THE PROGRESS OF CHEMISTRY SECTION A: INORGANIC CHEMISTRY
J2  - AN REP PROG CHEM A INORG CHEM
VL  - 101
PY  - 2005
SP  - 548
EP  - 584
PG  - 37
SN  - 0260-1818
DO  - 10.1039/b413628b
UR  - https://m2.mtmt.hu/api/publication/20827270
ID  - 20827270
N1  - Export Date: 5 April 2024            
            Correspondence Address: Davies, M.B.; Department of Forensic Science and Chemistry, East Road, Cambridge, CB1 1PT, United Kingdom
LA  - English
DB  - MTMT
ER  -