scholarly journals Effect of pH and concentration on the chemical stability and reaction kinetics of thiamine mononitrate and thiamine chloride hydrochloride in solution

BMC Chemistry ◽  
2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Adrienne L. Voelker ◽  
Lynne S. Taylor ◽  
Lisa J. Mauer
Keyword(s):  
Reaction Kinetics ◽  
High Performance ◽  
Degradation Kinetics ◽  
Degradation Pathway ◽  
Reaction Rate Constant ◽  
Solution Ph ◽  
Kinetics Of Degradation ◽  
One Year ◽  
Kinetics Of ◽  
Over Time

AbstractThiamine (vitamin B1) is an essential micronutrient in the human diet, found both naturally and as a fortification ingredient in many foods and supplements. However, it is susceptible to degradation due to heat, light, alkaline pH, and sulfites, among effects from other food matrix components, and its degradation has both nutritional and sensory implications as in foods. Thiamine storage stability in solution was monitored over time to determine the effect of solution pH and thiamine concentration on reaction kinetics of degradation without the use of buffers, which are known to affect thiamine stability independent of pH. The study directly compared thiamine stability in solutions prepared with different pHs (3 or 6), concentrations (1 or 20 mg/mL), and counterion in solution (NO3−, Cl−, or both), including both commercially available salt forms of thiamine (thiamine mononitrate and thiamine chloride hydrochloride). Solutions were stored at 25, 40, 60, and 80 °C for up to one year, and degradation was quantified by high-performance liquid chromatography (HPLC) over time, which was then used to calculate degradation kinetics. Thiamine was significantly more stable in pH 3 than in pH 6 solutions. In pH 6 solutions, stability was dependent on initial thiamine concentration, with the 20 mg/mL thiamine salt solutions having an increased reaction rate constant (kobs) compared to the 1 mg/mL solutions. In pH 3 solutions, kobs was not dependent on initial concentration, attributed to differences in degradation pathway dependent on pH. Activation energies of degradation (Ea) were higher in pH 3 solutions (21–27 kcal/mol) than in pH 6 solutions (18–21 kcal/mol), indicating a difference in stability and degradation pathway due to pH. The fundamental reaction kinetics of thiamine reported in this study provide a basis for understanding thiamine stability and therefore improving thiamine delivery in many foods containing both natural and fortified thiamine.

scholarly journals Reaction Kinetics of Iron Oxides in Ok Tedi Magnetite Skarn Ore

2020 ◽  
pp. 1-13
Author(s):  
Mary Kama ◽  
Kaul Gena ◽  
Tindi Seje Nuru
Keyword(s):  
Reaction Kinetics ◽  
Papua New Guinea ◽  
Iron Reduction ◽  
New Guinea ◽  
Reaction Rate Constant ◽  
Close Monitoring ◽  
Significant Difference ◽  
Different Temperatures ◽  
C 30 ◽  
Kinetics Of

Magnetic skarn ore (MSO) is one of the major copper bearing ore extracted by the Ok Tedi Copper Mine in Papua New Guinea (PNG). Copper minerals are recovered by flotation while the iron not associated with copper are discarded as tailings. The objective of this investigation was to determine the iron ore reduction kinetics for the Ok Tedi MSO and ascertain if it can be processed to produce sponge iron for a mini steel plant in Papua New Guinea. SEM-EDAX analyses of the Ok Tedi MSO indicated 10.1% C, 30% O, 0.6% Mg, 1.1% Si, 21.1% S, 0.8% Ca and 36.2 % Fe. Most of the iron is in sulfide form. Both naturally occurring and roasted sinters of Ok Tedi MSO samples of different particle sizes were reduced by charcoal carbon at three different temperatures and seven different reduction times. Analyses of the reduced products indicated a metallic iron content of more than 65 wt. % on average. Results showed that there was no significant difference in reduction between fluxed and control materials. Only a slight increase in kinetics with reduced particle size, hence the reaction rate constant (K) did not vary much within the temperatures investigated. Reaction kinetics increases with increasing reduction time at 900°C. Therefore, more iron reduction is observed with particles of 106 µm size. In addition, the results also confirmed that the reduction energy used was higher at 800°C and lower at 1000°C. In conclusion, iron reduction can be improved but close monitoring of temperature and reduction times are essential to determine the reaction kinetics of the Ok Tedi MSO.

scholarly journals Desorption and re-adsorption of PAHS on aircraft soot surface

2020 ◽  
Vol 42 (4) ◽  
Author(s):  
Nguyen Mai Lan
Keyword(s):  
High Performance ◽  
Flow Reactor ◽  
Activation Energies ◽  
Binding Energies ◽  
Desorption Kinetics ◽  
Chemical Transformations ◽  
Polycyclic Aromatic ◽  
Kinetics Of Degradation ◽  
Kinetics Of ◽  
Pyrex Tube

Polycyclic Aromatic Hydrocarbons (PAHs) in aircraft soot are capable to distribute in the gas phase and particulate phase in chemical transformations in the atmosphere. The desorption of PAHs from the soot surface is a preliminary step in the study of the reactivity of particulate PAHs. The desorption kinetics of PAHs are measured from soot samples to determine desorption rate constants for different PAHs as a function of temperature and the binding energies between PAHs and soot. The kinetics of degradation of particulate PAHs were studied in the flow reactor. The soot samples previously deposited on a Pyrex tube are introduced into the reactor along its axis and the concentrations of PAHs adsorbed on soot are determined by the High-Performance Liquid Chromatography (HPLC) as a function of the desorption time. The results show a correlation between the size of PAHs and the thermodynamics of desorption: with the PAHs have the same number of carbon atoms, their energies of desorption are very similar and increase with this number. The activation energies EA and the number of carbon atoms in PAHs have a linear correlation. It is consistent with the additivity of the laws Van der Waals. The similarity between the activation energies of desorption of PAHs and the corresponding sublimation enthalpies is consistent with the similarity between the graphitic structure of soot and the structure of PAHs.

scholarly journals Degradation Kinetics of Anthocyanins in Shalgam Beverage

2019 ◽  
Vol 7 (2) ◽  
pp. 282
Author(s):  
Adnan Bozdoğan ◽  
Kurban Yaşar
Keyword(s):  
Activation Energy ◽  
Reaction Kinetics ◽  
Half Life ◽  
Degradation Kinetics ◽  
Production Method ◽  
Order Reaction ◽  
Different Temperatures ◽  
Traditional Production ◽  
Effects Of Temperature ◽  
Kinetics Of

This research was performed to elucidate the effects of temperature on the degradation kinetics of anthocyanins in shalgam beverage. Shalgam beverage was produced according to traditional production method. Then, it was kept at three different temperatures (65°C, 75°C, and 85°C) for 12 hours, and the relevant quantities of anthocyanins were determined thereafter. The research revealed that degradation of the anthocyanins was well described with a 1st-order reaction kinetics model and the R2 values varied in the range of 0.9059-0.9715. Activation energy of the reaction was determined to be 48537 Joule/mole. The half-lives of anthocyanins at 65°C and 75° C, and 85°C were found to be 138.63, 136.72, and 51.57, respectively. Compared the half-life periods at different temperatures, anthocyanins were found to be more resistant at 65°C and 75°C than at 85°C.

scholarly journals Supported TiO2 on Borosilicate Glass Plates for Efficient Photocatalytic Degradation of Fenamiphos

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
A. El Yadini ◽  
H. Saufi ◽  
P. S. M. Dunlop ◽  
J. Anthony Byrne ◽  
M. El Azzouzi ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Borosilicate Glass ◽  
High Performance ◽  
Order Kinetic ◽  
Degussa P25 ◽  
Plausible Mechanism ◽  
Kinetics Of Degradation ◽  
Glass Plates ◽  
Kinetics Of ◽  
Sulfonamide Group

Supported titanium dioxide (TiO2) was investigated for the photodegradation of the insecticide fenamiphos in water. The photocatalyst was immobilised on borosilicate glass plates and the kinetics of degradation were studied in a stirred tank reactor under UV irradiation. Two types of TiO2, for example, Millennium PC500 (100% anatase) and Degussa P25 (80% anatase, 20% rutile), were used. Their activities have been based on the rates of insecticide disappearance. Experiments were investigated to evaluate the effect of pH and initial concentrations of fenamiphos as well as catalyst doses on the photocatalytic degradation of fenamiphos. Kinetic parameters were experimentally determined and an apparent first-order kinetic was observed. For photolysis process of fenamiphos, two photoproducts were identified and characterized using high performance liquid chromatography/mass spectrometry (HPLC/MS). The plausible mechanism of photolysis involved is the oxidation of sulfonamide group. In presence of photocatalyst TiO2, photodegradation was observed. Under identical conditions, Degussa P25 shows higher photocatalytic activity in regard to PC500 Millennium and complete degradation was observed after 180 min.

The In Vitro Degradation Kinetics of Polyurethane Prodrug Materials

2011 ◽  
Vol 399-401 ◽  
pp. 1067-1070
Author(s):  
Chun Yan Li ◽  
Cong Cong Hu ◽  
Zhi Guo Wen ◽  
Sheng Xiong Dong
Keyword(s):  
Drug Release ◽  
High Performance ◽  
Degradation Kinetics ◽  
Hplc Method ◽  
In Vitro Degradation ◽  
Erosion Mechanism ◽  
First Order ◽  
First Order Kinetics ◽  
Kinetics Of

The method of high performance liquid chromatography (HPLC) is established to determine the content of antibacterial agent — ciprofloxacin (CF) in the degradation solution of ciprofloxacin-polyurethane (CFPU) and investigate the in vitro degradation kinetics by plotting and fitting the cumulative release curves to inspect the effects of different medium and different concentrations on drug release. The results showed that the HPLC method is accurate, reliable and simple. The drug-release of CFPU was bioresponsive and could be accorded with first order kinetics. It was observed that CF was released from CFPU by a combination of diffusion and erosion mechanism, mainly in the manner of diffusion in the absence of infection while erosion mechanism in the presence of infection.

Dissipation rates of some selected pesticides from the soil of tea agroecosystem in Assam, India

2016 ◽  
Author(s):  
Yumnam Devashree ◽  
B. K. Dutta ◽  
S. B. Paul ◽  
Sudip Choudhury
Keyword(s):  
High Performance ◽  
Negative Impact ◽  
Degradation Kinetics ◽  
Cost Benefit ◽  
Sampling Period ◽  
Application Rate ◽  
Tea Plantations ◽  
Tea Plants ◽  
One Year ◽  
The Impact

An experiment was carried out in Rosekandy Tea Estate, Barak Valley, Assam to investigate the persistence of some selected pesticides (i.e Endosulfan, Fipronil, Paraquat and 2,4-D) on the soil. These pesticides were applied in the soil as per the application rate, where one year old tea plants were growing and the residue were analysed for a period of 50 days. Their degradation kinetics in soil was also studied and described. Soil samples were collected with the help of soil corer. The samples were brought to the laboratory, air dried in room temperature and extracted for analysis with high performance liquid chromatography (HPLC). Among the pesticides 2,4-D was highly persistent with half life of 57.75 days followed by Endosulfan which lost 42.64% of its initial concentration by the last sampling period (i.e 50 days) after the spraying. Fipronil and paraquat lost 65% and 70.32% of initial residue in soil making them the least persistent amongst these pesticides in the studied soil. Considering the impact of pesticide residues on human health, the less persistent pesticides may be used in tea plantations to minimize the potential negative impact of pesticides in the environment. The cost benefit ratios of the use of the pesticides should be also worked out.

scholarly journals Photo degradation kinetics of insensitive munitions constituents nitroguanidine, nitrotriazolone, and dinitroanisole in natural waters

2021 ◽  
Author(s):  
Lee Moores ◽  
Stacy Jones ◽  
Garrett George ◽  
David Henderson ◽  
Timothy Schutt
Keyword(s):  
Laboratory Experiments ◽  
Natural Waters ◽  
Matrix Effects ◽  
Degradation Kinetics ◽  
Relative Rate ◽  
Ph Dependence ◽  
Degradation Pathway ◽  
Quantum Yields ◽  
The Individual ◽  
Kinetics Of

Herein the matrix effects on the kinetics of aqueous photolysis for the individual munitions constituents of IMX-101: nitroguanidine (NQ), dinitroanisole (DNAN), and nitrotriazolone (NTO) are reported along with the environmentally relevant kinetics and quantum yields. Photolysis potentially represents a major degradation pathway for these munitions in the environment and further understanding the complex matrices effects on photolytic kinetics was needed. Aqueous systems are of particular interest due to the high solubility of NQ (3,800 ppm) and NTO (16,642 ppm) compared to the traditional munitions trinitrotoluene (TNT, 100.5 ppm) and 1,3,5-trinitro-1,3,5-triazine (RDX, 59.9 ppm). Environmental half-lives (and quantum yields) were found to be 0.44 days, 0.83 days, and 4.4 days for NQ, DNAN, and NTO, respectively, under natural sunlight. In laboratory experiments using nominally 300 nm bulbs in a merry-go-round style reactor in DI water the relative rate of photolysis for the three munitions constituents followed the same order NQ > DNAN > NTO, where DNAN and NTO reacted 57 and 115 times more slowly, respectively, than NQ. In the various environmentally relevant matrices tested in the laboratory experiments NQ was not significantly affected, DNAN showed a faster degradation with increasing ionic strength, and NTO showed a modest salinity and pH dependence on its rate of photolysis.

Development of the mobile bag technique to determine the degradation kinetics of purified starch sources in the pre-caecal segment of the equine digestive tract

1999 ◽  
Vol 1999 ◽  
pp. 138-138 ◽  
Author(s):  
B M L McLean ◽  
J J Hyslop ◽  
A C Longland ◽  
D Cuddeford ◽  
T Hollands
Keyword(s):  
Pore Size ◽  
Digestive Tract ◽  
Dry Matter ◽  
Degradation Kinetics ◽  
Grass Hay ◽  
Ad Libitum ◽  
Kinetics Of ◽  
Over Time ◽  
Digestive Processes

Previous work has shown that the mobile bag technique (MBT) can be used to study the dynamics of digestive processes in the whole tract of ponies (Hyslopet al, 1998). This experiment further develops the MBT as a method to study feed degradation dynamics over time in the pre-caecal segment of the digestive tract of ponies.Two caecally-fistulated mature Welsh-cross pony geldings (LW 270kg) were offered 4kg of dry matter (DM) per day of a 1:3 rolled barley:hay cube mix plus minerals, in 2 equal meals per day at 09:00 and 17:00h. Grass hay was also offeredad libitumbetween 17:00 and 09:00h. Two sizes of mobile bag (6 x 1 cm Ø-large and 4 x 1 cm Ø- small) made from monofilament polyester with a 7 μm pore size were used.

scholarly journals pH-Dependent Degradation of Diclofenac by a Tunnel-Structured Manganese Oxide

Water ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 2203
Author(s):  
Ching-Yao Hu ◽  
Yu-Jung Liu ◽  
Wen-Hui Kuan
Keyword(s):  
Formation Control ◽  
High Performance ◽  
Degradation Kinetics ◽  
Removal Rate ◽  
Solution Ph ◽  
Mn Oxide ◽  
Highly Active ◽  
Alkaline Conditions ◽  
Acidic Conditions ◽  
Key Parameter

The mechanism of diclofenac (DIC) degradation by tunnel-structured γ-MnO2, with superior oxidative and catalytic abilities, was determined in terms of solution pH. High-performance liquid chromatography with mass spectroscopy (HPLC–MS) was used to identify intermediates and final products of DIC degradation. DIC can be efficiently oxidized by γ-MnO2 in an acidic medium, and the removal rate decreased significantly under neutral and alkaline conditions. The developed model can successfully fit DIC degradation kinetics and demonstrates electron transfer control under acidic conditions and precursor complex formation control mechanism under neutral to alkaline conditions, in which the pH extent for two mechanisms exactly corresponds to the distribution percentage of ionized species of DIC. We also found surface reactive sites (Srxn), a key parameter in the kinetic model for mechanism determination, to be exactly a function of solution pH and MnO2 dosage. The main products of oxidation with a highly active hydroxylation pathway on the tunnel-structured Mn-oxide are 5-iminoquinone DIC, hydroxyl-DIC, and 2,6-dichloro-N-o-tolylbenzenamine.

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