1918
DOI: 10.1021/ja02238a012
|View full text |Cite
|
Sign up to set email alerts
|

The Action of Concentrated Sulfuric Acid on Olefins, With Particular Reference to the Refining of Petroleum Distillates.

Abstract: after a 6-day fast weighed 1600 g. gen whatever was found in the liver. of the carbohydrates in the litchi nut. The animal was killed and no glyco-'l'hese results show in a most marked way the glycogenetic properties SEW HAVEN, CONN.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

3
12
0

Year Published

1919
1919
1959
1959

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 61 publications
(16 citation statements)
references
References 1 publication
3
12
0
Order By: Relevance
“…In the analysis of dicyclopentadiene concentrates of the order of 50 to 80% purity, accuracy of the order of 1 or 2% may be obof hydrocarbon mixtures (7,8,10). Fisher and Eisner (8) have shown that adjustment of acid concentration and experimental conditions to overcome this failing has not been entirely successful.…”
mentioning
confidence: 99%
“…In the analysis of dicyclopentadiene concentrates of the order of 50 to 80% purity, accuracy of the order of 1 or 2% may be obof hydrocarbon mixtures (7,8,10). Fisher and Eisner (8) have shown that adjustment of acid concentration and experimental conditions to overcome this failing has not been entirely successful.…”
mentioning
confidence: 99%
“…As has been stated in the literature (1), several types of reaction. take place between sulfuric acid and olefinsnamely, esterification, alcohol formation, oxidation, polymerization, and condensation with aromatic hydrocarbons when the latter are present.…”
Section: Olefin-residue Ratiomentioning
confidence: 86%
“…Moreover, an excess of cyanogen chloride ought to aid in obtaining a higher yield of amine. Actually, adding cyanogen chloride to the alkyl hydrogen sulfate lowered the yield by one-half (Run 8) while an 100% excess of cyanogen chloride (Run 12) did not materially increase the yield (Table III).…”
Section: ^>Ch-c< Nh2 + Hc1 + C02mentioning
confidence: 98%
“…The material balance was quite low in most cases where attempts were made to evaluate the recovery, especially where some reaction did occur. This is believed to be a result of the formation of considerable amounts of stable water-soluble sulfuric acid esters, which are known to be stable up to boiling temperatures in aqueous solutions (12).…”
Section: ^>Ch-c< Nh2 + Hc1 + C02mentioning
confidence: 99%