Talk:2,5-Dimethylfuran

From Wikipedia, the free encyclopedia

Chemicals WikiProject 2,5-Dimethylfuran is within the scope of WikiProject Chemicals, which aims to improve Wikipedia's coverage of chemicals. To participate, help improve this article or visit the project page for details on the project.
Chemistry WikiProject This article is also supported by WikiProject Chemistry.
Start This article has been rated as Start-Class on the quality scale.
Low This article has been rated as Low-importance on the importance scale.

Article Grading: The article has been rated for quality and/or importance but has no comments yet. If appropriate, please review the article and then leave comments here to identify the strengths and weaknesses of the article and what work it will need.

WikiProject Energy This article is within the scope of WikiProject Energy, which collaborates on articles related to energy.
Start This article has been rated as start-Class on the assessment scale.
Low This article is on a subject of low importance within energy.

This article has been rated but has no comments. If appropriate, please review the article and leave comments here to identify the strengths and weaknesses of the article and what work it will need.

WikiProject Environment
Portal
This environment-related article is part of the Environment WikiProject to improve Wikipedia's coverage of the environment.
The aim is to write neutral and well-referenced articles on environment-related topics, as well as to ensure that environment articles are properly categorized.
See WikiProject Environment and Wikipedia:Contributing FAQ.
B This article has been rated as B-Class on the assessment scale.
A story relating to the article 2,5-Dimethylfuran (or a previous version of it) was included in the news section of the Energy Portal. Please consider updating the portal news with any major developments on this topic.

Ref. for reaction with singlet oxygen: [1]

My search on the Internet for 2,5 Dimethylfuran was triggered by a page on eurekalert.org re: [James A. Dumesic's] work in converting sugars, notably fructose, to chemicals with properties of automotive fuels. Search on this topic yields roughly three insights, A) this chemical is a base for the synthesis of flavoring agents, B) little is known about it's biological effects, C) it behaves very much like gasoline in terms of flash points, boiling and freezing points, etc. I have pasted an MSDS into the main topic to publish at least something on the chemical.

[edit] "DMF"

I'm reading the nature paper and it seems quite dumb that they abbreviate this as "DMF". What about the possibility of mistaking this for N,N-dimethylformamide? --Rifleman 82 10:22, 21 June 2007 (UTC)

That's always the danger with abbreviations. :) --Itub 10:48, 21 June 2007 (UTC)

I'm *really* uncomfortable with this compound being associated with "DMF". Apart from the original paper discussing HMF and DMF (which could well be shorthand like compound 1 and 2), is there any widespread use of DMF for this compound? If not, perhaps such references should be removed. --Rifleman 82 02:49, 23 June 2007 (UTC)

I think too that this abbreviation has no widespread usage yet (the molecule itself had not been considered for widespread usage until recently!), but was just made up on the fly for the purpose of that paper. That is not unusual at all. I understand your reluctance to use this abbreviation in this page, but I'm not going to "vote" either way. My cynical approach to life doesn't make me uncomfortable with having confusing abbreviations because that happens all the time anyway and I have other things to worry about. ;-) The only thing I can tell you is that if this compound really gets used as a fuel and becomes commonly mentioned, it seems almost certain to me that people will refer to it as DMF, as it is the most obvious abbreviation, and its application domain doesn't overlap greatly with dimethylformamide (which is also sometimes abbreviated DMFA). --Itub 07:29, 23 June 2007 (UTC)

[edit] "Fuel Information"

For something to be considered a fuel, we should have some useful fuel information. This information is generally missing, eg here too http://cameochemicals.noaa.gov/chemical/20240#section4 These should include:-

Energy density in megajoules per kilogram,

so that we can know the sort of power we can expect from an engine running the fuel.

Autoignition temperature,

so that we know how much we can compress an air fuel mixture before it ignites automatically, thus giving us an idea of the highest compression ratios an engine could support (if not direct injection).

Heat of vaporization,

so that calculated temperatures can compensate for evaporative cooling if appropriate.

Oh, and this gives a figure for the potential fuel production from algae, http://en.wikipedia.org/wiki/Algaculture, eg 5000 gallons per acre per year. Maybe we should have a similar figure for this fuel so that people can determine its viability as a commerical fuel.

Crysta1c1ear 13:34, 24 June 2007 (UTC)

[edit] Start point for synthesis

I've heard that this is a "usual suspect" as a start point for a non-petroleum chemicals industry - ethanol is not even in the league. The article should mention this. --190.56.47.173 13:54, 25 June 2007 (UTC)

It would be great if you could add it yourself, together with a reference! Who mentions it as a usual suspect? --Itub 13:59, 25 June 2007 (UTC)

The real issue that makes 2,5 DMF a non starter as a 'biofuel' is that the synthesis requires large amounts of hydrogen, 3 moles per mole of 2,5 DMF. Hydrogen production is from oil products in Cracking Units in a refinery of from natural gas. A typical biorefinery making 50 million gallons of 2,5 DMF per year would required at least 7 Billion stnadard cubic feet of natural gas per year. At $7/million BTU, this is a cost of $50,000,000 per year. Therefore, 2,5 DMF has a significant CO2 footprint and is not such a nice biofuel. mtnclimber 16:26, 27 June 2007 (UTC)

Sounds reasonable. Do you have a good reliable source to add a referenced comment to the article? --Rifleman 82 16:35, 27 June 2007 (UTC)