2015
DOI: 10.1016/j.cjche.2014.10.021
|View full text |Cite
|
Sign up to set email alerts
|

Evaluation of an improved epichlorohydrin synthesis from dichloropropanol using a microchemical system

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
10
0

Year Published

2017
2017
2024
2024

Publication Types

Select...
5
1
1

Relationship

0
7

Authors

Journals

citations
Cited by 12 publications
(10 citation statements)
references
References 21 publications
0
10
0
Order By: Relevance
“…Drawbacks to this published method include that the functionalization procedures were chemically detrimental to cellulose, the indicator (1-naphthylamine) is carcinogenic, and that the sub-micromolar detection was only achieved via absorbance spectroscopy or by treating the paper repeatedly with the sample solution. A more favorable approach for the immobilization of N -(1-naphthyl)­ethylenediamine is the use of the linker epichlorohydrin, which has been reported in the grafting of small molecules and macrocycles , to cellulose, typically using aqueous sodium hydroxide conditions. , However, under these conditions, epichlorohydrin is known to undergo hydrolysis or form other unfavorable side products due to the presence of a strongly nucleophilic base and a nucleophilic solvent, which limits the efficacy of functionalization. Additionally, N -(1-naphthyl)­ethylenediamine is moisture sensitive and poorly water-soluble.…”
Section: Resultsmentioning
confidence: 99%
“…Drawbacks to this published method include that the functionalization procedures were chemically detrimental to cellulose, the indicator (1-naphthylamine) is carcinogenic, and that the sub-micromolar detection was only achieved via absorbance spectroscopy or by treating the paper repeatedly with the sample solution. A more favorable approach for the immobilization of N -(1-naphthyl)­ethylenediamine is the use of the linker epichlorohydrin, which has been reported in the grafting of small molecules and macrocycles , to cellulose, typically using aqueous sodium hydroxide conditions. , However, under these conditions, epichlorohydrin is known to undergo hydrolysis or form other unfavorable side products due to the presence of a strongly nucleophilic base and a nucleophilic solvent, which limits the efficacy of functionalization. Additionally, N -(1-naphthyl)­ethylenediamine is moisture sensitive and poorly water-soluble.…”
Section: Resultsmentioning
confidence: 99%
“…This causes not only the corrosion of the reaction equipment but also generates a large amount of by‐products and waste liquid. Besides, there are many problems with refining the main products and separating the catalysts from the reaction mixture . Compared with homogeneous catalysis, solid catalysis enables easier product separation, hence avoiding the production of large volumes of wastewater and increasing the cost efficiency, using less labor materials and financial resources …”
Section: Introductionmentioning
confidence: 99%
“…Besides, there are many problems with refining the main products and separating the catalysts from the reaction mixture. [8][9][10] Compared with homogeneous catalysis, solid catalysis enables easier product separation, hence avoiding the production of large volumes of wastewater and increasing the cost efficiency, using less labor materials and financial resources. [11][12][13][14] A solid base is a substance that can donate electron pairs or accept protons.…”
Section: Introductionmentioning
confidence: 99%
“…As an important chemical precursor and fine chemical product, epichlorohydrin (ECH) is used to synthesize epoxy resins, chlorohydrins rubber, pesticides, and plasticizers . Some current industrial processes to prepare ECH include propylene chlorination, propylene acetate chlorination, and glycerol chlorination .…”
Section: Introductionmentioning
confidence: 99%