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where f i is the stoichiometric coefficient for the i th parallel reaction component, and w i and wi, 0 are the reacted amount and the initial amount of the i th component, respectively (Sweeney and Burnham 1990).
If this calculation of ΔVOC results in a reacted amount less than the VOC injected during that time step, then the residual VOC builds up in the chamber and contributes to the instantaneous rate calculation for the next timsestep.
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The off-line data, shown in Electronic Supplementary Material Figure S 3, are not consistent with an intermediate reaction with the LC eluent because, if it would be reacting, the amount of methoxylated product should be the same or less after storage (depending on the stability of the intermediate).
The results from the designs states that this additional oxidation was responsible for 40% of the total amount of α-pinene reacted, 33% of the total amount of Δ3-carene reacted and 41% of the total amount of limonene reacted at the settings 20 ppb terpene, 75 ppb ozone, 20% RH and a reaction time of 213 s.
Three difunctional azo chromophores (DR19, NDPD and DNDA) were, respectively, reacted with excessive amount of 4,4′-methylene-diphenylisocyanate (MDI) to form poly-CDI, and subsequently trimellitic anhydride (TMA) was added to obtain an intermediate, poly N-acylurea).
Each of 1a d reacted with equimolar amount of monobromomalononitrile (2), in ethanolic potassium hydroxide solution, yielded in each case a single product which could be formulated to be either 5H-thiazolo[3,2-a]pyrimidine structure 3 or its isomeric structure 7H-thiazolo[3,2-a]pyrimidine 4 (Scheme 2).
Comparison of the measured and simulated data shows that this simple model adequately describes the data and captures the effects of reacting varying amounts of cement with the CO2-rich brine.
The metal complexes were prepared by reacting calculated amounts corresponding to 2 1 ratio [M L] in 50 mL EtOH and the mixture was heated under reflux for 6 8 h.
The kinetics of PAP phosphatase activity were measured by reacting various amounts of substrate with Rv2131c and quantifying product formation by the ESI-MS assay.
Thus by reacting equimolar amounts of 2,4,6-trichloro-1,3,5-triazine and sulfamerazinesulfamerazine (1b), sulfaquinoxaline (2b), sulfadiazine (3b), sulfadimidine (4b), and sulfachloropyrazine (5b), products of type (a) (see Scheme 1) were easily obtained without interference from di- or tri-substituted products.
In short fractal pores, the amounts reacted are seven times larger than in smooth cylindrical pores of the same length.
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