2006
DOI: 10.1016/j.supflu.2005.11.004
|View full text |Cite
|
Sign up to set email alerts
|

Influence of salts on the dehydration of several biomass-derived polyols in sub- and supercritical water

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
13
1
1

Year Published

2007
2007
2016
2016

Publication Types

Select...
6

Relationship

2
4

Authors

Journals

citations
Cited by 20 publications
(15 citation statements)
references
References 23 publications
0
13
1
1
Order By: Relevance
“…The synthesis examples described in Section 4 were achieved with the help of a continuously driven high-pressure apparatus with a flow tube reactor made of stainless steel [12]. Temperatures up to 500 8C and pressures up to 35 MPa are feasible in this apparatus.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The synthesis examples described in Section 4 were achieved with the help of a continuously driven high-pressure apparatus with a flow tube reactor made of stainless steel [12]. Temperatures up to 500 8C and pressures up to 35 MPa are feasible in this apparatus.…”
Section: Methodsmentioning
confidence: 99%
“…The residence time range lies between 10 and 180 s. Quantitative analysis of the reaction products was carried out by GC-FID as well as HPLC with RI detector. A detailed description of the experiments carried out and of the apparatus are mentioned by Ott et al [12] and Jung [13].…”
Section: Methodsmentioning
confidence: 99%
“…7). The further refinement of polyols with adjacent hydroxyl groups, for example, to aldehydes and/or ketones occurs via pinacol-pinacolone rearrangement [75]: during the distillation of pinacol with concentrated sulfuric acid dehydration takes place, followed by an intramolecular rearrangement to pinacolone (methyl-tert-butylketone). This happens much more elegantly in hot high pressure water under the catalytic influence of acetic acid [76,77].…”
Section: Sorbit (1 Glucose + H 2 ( 1 Sorbit: Hydrogenation)mentioning
confidence: 99%
“…For this purpose, the use of 1,4-AHERY is promising as a starting material because it can be produced easily from erythritol by an acid catalyst, [23][24][25][26][27] and 1,4-AHERY can be converted into 1,2,3-butanetriol (1,2,3-BuT) because the ringopening hydrogenolysis of tetrahydrofuran to 1-butanol proceeds effectively over Rh-based catalysts. [36] This route provides the selective dissociation of one primary OH group in erythritol.…”
Section: Introductionmentioning
confidence: 99%