857. The partial molar heats of solution of water in dinitrogen pentoxide solutions and of potassium nitrate and sulphuric acid in nitric acid at 0°

1957 ◽  
Vol 0 (0) ◽  
pp. 4262-4267 ◽  
Author(s):  
L. Lloyd ◽  
P. A. H. Wyatt
1963 ◽  
Vol 16 (6) ◽  
pp. 943 ◽  
Author(s):  
NS Bayliss ◽  
DW Watts

The ultraviolet spectra of solutions of potassium nitrate in aqueous sulphuric acid have been studied. Three absorptions, those due to the species NO3-, HNO3, and NO2+, have been found. From this study a semiquantitative picture has been developed of the distribution of the total nitrate between these three species. It was found that in the sulphuric acid concentration range 0-15% by weight, the dissolved nitrate existed as nitrate ion and that from 15-70% sulphuric acid, nitrate ion, and molecular nitric acid were present in comparable amounts. In the sulphuric acid concentration range 72-82% nitric acid accounted for the total dissolved nitrate and as the sulphuric acid concentration was increased from 82-90% nitric acid was converted to nitronium ion.


2009 ◽  
Vol 13 ◽  
pp. 49-60 ◽  
Author(s):  
S. N. Jha ◽  
P. K. Jha

Freshly harvested seeds of the species (legumes: Alysicarpus vaginalis and Desmodium triflorum; grasses. Axonopus compressus and Chrysopogon aciculatus) failed to germinate even after acid scarification and incubation under different light qualities, whereas seven-nine-month old seeds exhibited germination in the order: D. triflorum (23%) > A. compresses (17%) > A. vaginalis (13%) > C. aciculatus (4%) without acid scarification or nutrient treatment. The legumes contained yellowish brown (Yb) and brick-red (Br) seeds in their pods in the ratio of 4:1. The Yb seeds had hard seed covering very slowly permeable to water. Storage of seeds under room conditions in sealed polythene pouches up to three years profoundly inhibited germination in Br seeds but had little effect on Yb seeds. The nine-month-old Br seeds had maximum germination (24 and 38%, respectively in A. vaginalis and D. triflorum) when submerged in water for 24 h before sowing, whereas germination in submerged in water for three days as a pretreatment. Germination in Yb seeds of the same age was 72 and 77%, respectively in A. vaginalis and 84% in D. triflorum when seven-eight-month old seeds were scarified with mixed (Yb and Br) seed lot was 71% in A. vaginalis and 84% in D. triforum when seven-eight-month old seeds were scarified with sulphuric acid for 10 min and incubated under red light for a week. The fresh seeds of A. compressus had 79% in viability (TTC test) which declined to 5% after storage for three years, and nine-month-old caryopses when treated with nitric acid for ten minute and incubated under red light for 18 days had maximum (45%) germination. In C. aciculatus. Seeds had only 37% viability when fresh, and they completely lost viability after storage for two years, and nine-month old caryopses had maximum (17%) germination when treated with 0.5% solution of potassium nitrate and incubated under ordinary condition for 25 days.Key words: Seed attributes; storage; viability; acid scarification; light; imbibition; potassium niratedoi: 10.3126/eco.v13i0.1629Ecoprint (An international Journal of Ecology) Vol.13, 2006 page 49-60 


2018 ◽  
Author(s):  
Hui Yun ◽  
Weihao Wang ◽  
Tao Wang ◽  
Men Xia ◽  
Chuan Yu ◽  
...  

Abstract. Nitrate (NO3−) has become a major component of fine particulate matter (PM2.5) during hazy days in China. However, the role of the heterogeneous reactions of dinitrogen pentoxide (N2O5) in nitrate formation is not well constrained. In January 2017, a severe haze event occurred in the Pearl River Delta (PRD) of southern China during which high levels of PM2.5 (~ 400 μg m−3) and O3 (~ 160 ppbv) were observed at a semi-rural site (Heshan) in the western PRD. Nitrate concentrations were up to 108 μg m−3 (1 h time resolution), and the contribution of nitrate to PM2.5 reached nearly 40 %. Concurrent increases in NO3− and ClNO2 (with a maximum value of 8.3 ppbv in 1 min time resolution) were observed in the first several hours after sunset, indicating an intense N2O5 heterogeneous uptake on aerosols. The formation potential of NO3− via N2O5 heterogeneous reactions was estimated to be 39.7 to 77.3 μg m−3 in the early hours (3 to 6 h) after sunset based on the measurement data, which could completely explain the measured increase in the NO3− concentration during the same time period. Daytime production of nitric acid from the gas-phase reaction of OH + NO2 was calculated with a chemical box model built using the Master Chemical Mechanism (MCM v3.3.1) and constrained by the measurement data. The integrated nocturnal nitrate formed via N2O5 chemistry was comparable to or even higher than the nitric acid formed during the daytime. This study confirms that N2O5 heterogeneous chemistry was a significant source of aerosol nitrate during hazy days in southern China.


2010 ◽  
Vol 10 (3) ◽  
pp. 396-400 ◽  
Author(s):  
Abdullah Abdullah ◽  
D.R. Wicakso ◽  
A.B. Junaidi ◽  
Badruzsaufari Badruzsaufari

Nitration of biodiesel from Jatropha curcas oil using mixture of HNO3 and H2SO4 had been done in an attempt to obtain a cetane improver or cetane number enhancer. The nitration was carried out by varying the numbers of moles of sulphuric acid, nitric acid, temperature and time. The process was conducted in a round bottom flask reactor that equipped with a magnetic stirrer and a ball cooler on a water batch. The mixture of H2SO4 and HNO3 was placed in the reactor and subsequently added slowly with biodiesel drop by drop. The results showed that increasing the mole numbers of sulphuric acid tends to reduce the yield or volume and total N of nitrated biodiesel. Increasing the number of moles of nitric acid tends to increase the yield, but decrease the value of total N. While increasing of temperature and reaction time tends to reduce the yield and total N. From FTIR spectra product was estimated as a mixture of esters of alkyl nitrates and nitro. From the testing of cetane number it can be predicted that nitrated biodiesel potentially as cetane improver.


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