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Nitrogen, reactions

Table 4. Physical Properties of Less Common Nitrogen Reaction Products... Table 4. Physical Properties of Less Common Nitrogen Reaction Products...
The agronomic response of IBDU is compared to other nitrogen reaction products in Figure 4. In this study, various products were apphed to Kentucky bluegrass at 3 lb N /M (14.6 g/m ). Plant growth as measured by leaf fresh weight was monitored weekly. [Pg.133]

Fig. 4. Response of Kentucky bluegrass to select nitrogen reaction controUed release products. Apphcation of 3 lbs N/1000 ft (14.6 g/m ). A is IBDU B,... Fig. 4. Response of Kentucky bluegrass to select nitrogen reaction controUed release products. Apphcation of 3 lbs N/1000 ft (14.6 g/m ). A is IBDU B,...
Other Reaction Products. Nitrogen reaction fertilizers are commercially available that do not involve reactions between urea and aldehydes. These are oxamide and melamine. [Pg.134]

Two comments can be made on the second point. For a simple mathematical reason mistakes made with the LEL value are of little consequence to the calculated value of flashpoint cc . Indeed, this mistake is not that significant since there Is a logarithm involved. Secondly, in theory no mistake is made with the stoichiometric concentration (except for nitrogenous compounds where there is an ambiguous aspect with regard to the nitrogen reaction). This second approach (with Cg) can thus provide preliminary control of the model parameters (S or the group) and there... [Pg.63]

By chlorination, we observe that we are producing chlorides. We see that in the hypochlorous reaction, as well as in the nitrogenous reaction, where HC1 (chloric acid) is formed. [Pg.131]

The formation of the cyanopolyynes (HC2nCN) is closely tied to the synthesis of hydrocarbons. Both hydrocarbon ion-atomic nitrogen reactions 41 viz.,... [Pg.12]

Nitrification. The nitrogen reactions in the PROFILE model are very simple, since only nitrification and uptake are included explicitly. [Pg.52]

Thus, there is great similarity between the prompt NO reactions discussed and the fuel-nitrogen reactions. [Pg.432]

The general scheme of the fuel-nitrogen reactions is also represented in Fig. 8.7. [Pg.433]

The adducts of azodicarboxylate with EtsSi or PhsSi radicals [79], have been identified as hydrazyl radicals (Reaction 5.41). The addition of RsSi radical to alkyl azides takes place at the terminal nitrogen (Reaction 5.42) affording the triazenyl o-type radical in which the SOMO is in the NNN plane (only one canonical structure is shown) [80,81]. [Pg.112]

Where X is a poor leaving group, anomeric destabilization of the NX bond can lead to a novel rearrangement. The HERON (from Heteroatom Rearrangements On Nitrogen) reaction of anomeric amides was discovered in the mid-1990s and involves a concerted... [Pg.845]

The capability of NO to reduce nitrates, providing a pathway for the production of ammonium nitrite and thus of nitrogen, has also been demonstrated recently by Weitz and co-workers, mainly on the basis of IR data collected over BaNa-Y zeolite [75] however, according to a parallel additional route NO would also react with NO2 to form N2O3 and then nitrogen [reactions (13.25) and (13.26)], as already discussed. The oxidation of NO by surface nitrates over a Pt-Ba/Al2O3 catalyst has also been reported by Olsson et al. [76], whereas the formation of surface nitrates from NO2 on bare AI2O3 has been reported by Apostolescu et al. [77] and previously observed in our laboratories also [78]. [Pg.412]

The inclusion of aromatic rings as part of the side chains results in quite potent agents, possibly because the rigid rings better define the position of the basic nitrogen. Reaction of para-hydroxyacetanilide (19-1) with formaldehyde and diethylamine affords the corresponding Mannich product (19-2) hydrolysis of the acetamide then leads to the aniline (19-3). Treatment of that compound with dichloro-quinoline (17-6) leads to the displacement of chlorine on the heterocyclic ring and the formation of amodiaquine (19-4) [21]. [Pg.442]

Justify the choice of rate constants for the key reactions. Implement the nitrogen reactions in the starting mechanism. Be careful that the rate constant format and units are consistent with the H2-O2 starting mechanism. [Pg.580]

Lithium azide 0.570 7xl07 4.01xl022 2xl07 2xl06 Nitrogen reaction 6Li (n,a)3H, 2.1 MeV ol and 2.7 MeV3H... [Pg.32]

Silver azide 0.745 1x10s 1.21xl022 iO7Ag4xl06 1O9Aglxl07 lxlO6 Silver and nitrogen reactions... [Pg.32]

Lead azide 1.875 2xl07 2.71xl022 17 8xl05 Lead reactions unimportant, nitrogen reaction... [Pg.32]

The butadiene (80%)-acrylonitrile(17%)-aerylamidoxime(3%) terpolymer was prepared by reacting 2.5g butadiene 80%)-acrylo-nitrile(20%) copolymer (Aldrich) in 150 ml xylene with 1.61g hydro-xylamine hydrochloride in 12 ml n-butanol (freed of HC1 immediately before addition by method of Hurd (4) by dropwise addition under nitrogen. Reaction time and temperature were 23 hr. and 90-95°C. The polymer product was worked up by slowly adding the reaction mixture to 500 ml ether with rapid stirring. The precipitated polymer was allowed to settle, the supernate decanted and the polymer resuspended and washed with two 100 ml portions of ether followed by vacuum drying. Yield 2.04g (81%). Conversion of nitrile functional groups to amidoxime groups was 15% by infrared absorption. [Pg.310]

Regiospecific 1,3-dipolar cycloaddition reactions of dihydropyridines and some organic azides lead to high yields of fused aziridines—2,7-diazabicy-cli[4.1.0]hept-3-enes 337 [365, 366, 367] (Scheme 3.112). The reaction proceeds via the preliminary formation of an intermediate 336 and the elimination of nitrogen. Reaction of pyrimidine 334 with less reactive methoxycarbonyl and benzoyl azides does not occur [367]. Compounds 337 exhibit significant analgesic, antibacterial and antifungal activities [367]. [Pg.121]

Zero-Order Reactions. Zero-order reactions have been applied to describe potassium (Mortland, 1958 Burns and Barber, 1961), chromium (Amacher and Baker, 1982), and nitrogen reactions in soils (Patrick, 1961 Broadbent and Clark, 1965 Keeney, 1973). [Pg.17]

Modeling of Inorganic Reactions 174 Nitrogen Reactions 174 Phosphorus Reactions 177 Potassium Reactions 181 Aluminum Reactions 183 Modeling of Soil-Pesticide Interactions 183 Modeling of Organic Pollutants in Soils 186 Supplementary Reading 189... [Pg.173]

A number of kinetically based models to describe nitrogen reactions in soils are presented in Table 9.1. The model of Mehran and Tanji (1974) will be elaborated on since it includes many aspects of nitrogen dynamics in soils. [Pg.174]

More investigations of nitrogen reactions with transition metal compounds [162] confirmed the capability of nitrogen to readily enter reactions and reduction by many organometallic and inorganic coordination compounds of transition metals [163],... [Pg.137]

By reactions of l,2,3(5-tetramethyl-4,6-di (alkylamino)borazines with several diamines and 4,4 -diisocyanatodiphenylmethane, it was shown that the thermal stability of the bis(alkylamino)borazine depends on the substituents at the exocyclic nitrogens. Reactions with diamines led to polycondensates such as the ones cited above. However, reaction with diisocyanates gave different results depending on the substitution pattern of the exocyclic amino groups 140,141),... [Pg.81]

N-Donor Ligands. Stable products of nitrogen reaction with have been established... [Pg.61]


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