Green Production of Phthalic Anhydride from Biobased Furan and Maleic Anhydride by an Acid Resin Catalyst

Author(s):  
Xiaojie Shao ◽  
Lijuan Su ◽  
Jiaojiao Zhang ◽  
Zishang Tian ◽  
Ning Zhang ◽  
...  
2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Amal Amin ◽  
Moshera Samy

Different polyesteramides hyperbranched polymers (HPEA1-6)/montomorillonite clay (MMT) nanocomposites were prepared with three different loading contents of clay (4, 10, and 15 wt%). The obtained nanocomposites were characterized via XRD, thermal analyses, and TEM. Generally, intercalation behavior was observed. The hyperbranched polyesteramides (HPEA1-6) were originally prepared by the bulky reaction between maleic anhydride (MAn), succinic anhydride (ScAn), and phthalic anhydride (PhAn) with either diethanolamine (DEA) or diisopropanolamine (DiPA). The resulting hyperbranched polyesteramides (HPEA1-6) were characterized by GPC, IR,1H-NMR, TGA, and DSC.


2012 ◽  
Vol 8 ◽  
pp. 227-233 ◽  
Author(s):  
Nan Wang ◽  
Ronghua Wang ◽  
Xia Shi ◽  
Gang Zou

A clean process has been developed for the synthesis of 2-adamantylphenol derivatives through adamantylation of substituted phenols with adamantanols catalyzed by commercially available and recyclable ion-exchange sulfonic acid resin in acetic acid. The sole byproduct of the adamantylation reaction, namely water, could be converted into the solvent acetic acid by addition of a slight excess of acetic anhydride during the work-up procedure, making the process waste-free except for regeneration of the ion-exchange resin, and facilitating the recycling of the resin catalyst. The ion-exchange sulfonic acid resin catalyst could be readily recycled by filtration and directly reused at least ten times without a significant loss of activity. The key intermediate of adapalene, 2-(1-adamantyl)-4-bromophenol, could be produced by means of this waste-free process.


1950 ◽  
Vol 28b (10) ◽  
pp. 652-659 ◽  
Author(s):  
R. W. Watson ◽  
N. H. Grace ◽  
J. L. Barnwell

New polyesters with basic units containing 6, 7, 8, 9, 10, 13, and 14 chain atoms have been prepared from levo-2,3-butanediol and ethyl oxalate, ethyl malonate, dimethyl terephthalate, maleic anhydride, succinic, glutaric, adipic, azelaic, and sebacic acids, and from meso-2,3-butanediol and o-phthalic anhydride. Esterification of 2,3-butanediol with a dibasic acid, or its anhydride, is accompanied by a side reaction, in which butanone-2 and the cyclic methyl ethyl ketal are formed. The purified polyesters, with the exception of the poly-malonate, appear to be composed of regularly recurring acid and diol segments over the molecular weight ranges investigated. Without exception they are amorphous resins or balsams. Polyesters formed from saturated aliphatic dibasic acids become progressively softer as the number of methylene groups in the acid segment increases. The polymeric oxalate, on distillation in vacuo, is converted to a macrocrystalline cyclic monomer.


2011 ◽  
Vol 239-242 ◽  
pp. 1721-1724 ◽  
Author(s):  
Xiao Qing Zheng ◽  
Li Ting Yang ◽  
Kun Peng Wang

Soybean oil-based alkyd resin was prepared using soy-based polyol, maleic anhydride and phthalic anhydride. The soy-based polyol was obtained through the epoxidization of soybean oil, followed by ring-opening with methanol and, the hydroxyl values of soybean oil-based polyols used in this reaction is 169.93 mgKOH/g. In the reactions of soy-based polyol, maleic anhydride and phthalic anhydride, the molar ratio of hydroxyl value is equal to carboxyl value and the molar ratio of maleic anhydride to phthalic anhydride is 2:1, 1:1 and 1:2, respectively. 1% hydroquinone based on total reactants was used as inhibitor of polymerization, 1% dibutyltin oxide was used as catalyst.


2018 ◽  
Vol 8 (2) ◽  
pp. 580-590 ◽  
Author(s):  
Fei Chen ◽  
Lei Shi ◽  
Jie Yao ◽  
Yan Wang ◽  
Dongxi Zhang ◽  
...  

The influence of H2O content on DMM carbonylation using a DICP-001 resin catalyst (Fig. 6).


1952 ◽  
Vol 30 (4) ◽  
pp. 291-294 ◽  
Author(s):  
M. F. Bartlett ◽  
S. K. Figdor ◽  
K. Wiesner

2-5-Octamethylene tetrahydrophthalic anhydride does not form even a trace of the corresponding phthalic anhydride on dehydrogenation, but partly dissociates back into cyclododecadiene and maleic anhydride. 2-5-Nonamethylene tetrahydrophthalic anhydride dehydrogenates with considerable difficulty.


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