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Table 1 Summary of catalytic results obtained in liquid phase

From: Recent developments in maleic acid synthesis from bio-based chemicals

Catalyst

Conditions

Furfural or HMF conversion

MA yield

MA selectivity

References

H3PMo12O40

383 K, O2 20 bar, H2O + nitrobenzene

67 (furfural)

38

56

[30]

H3PMo12O40

383 K, O2 20 bar, H2O + toluene

73 (furfural)

37

50

[30]

H3PMo12O40

383 K, O2 20 bar, H2O + p-xylene

66 (furfural)

35

53

[30]

H3PMo12O40

383 K, O2 20 bar, H2O + cyclohexane

85 (furfural)

38

45

[30]

H3PMo12O40

383 K, O2 20 bar, H2O + tetradecane

82 (furfural)

38

46

[30]

H3PMo12O40

383 K, O2 20 bar, H2O

86 (Furfural)

38

44

[30]

VO(acac)2

363 K, O2 10 bar, CH3CN

99 (HMF)

52

52

[31]

Amberlyst 15

353 K, H2O2, H2O, 24 h

99 (furfural)

11

11

[33]

Nafion NR50

353 K, H2O2, H2O, 24 h

99 (Furfural)

11

11

[33]

Nb2O5

353 K, H2O2, H2O, 24 h

99 (furfural)

4

5

[33]

ZrO2

353 K, H2O2, H2O, 24 h

99 (furfural)

5

5

[33]

H6PV3MO9O40

383 K, O2 20 bar, CH3CN

99 (furfural)

12

12

[44]

VO(acac)2

363 K, O2 10 bar, DMF

96 (HMF)

7

7

[31]

H5PV2Mo10O40 + Pd(OAc)2 (1/1)

383 K, O2 20 bar, CH3CN

94 (furfural)

14

15

[44]

VO(acac)2

363 K, O2 10 bar, TFT

96 (HMF)

7

7

[31]

VO(acac)2

363 K, O2 10 bar, CH2Cl2

99 (HMF)

16

16

[31]

VOSO4

363 K, O2 10 bar, CH3CN

NC (furfural)

34

NC

[31]

Co(OAc)2

363 K, O2 10 bar, CH3CN

NC (furfural)

2

NC

[31]

Co(NO3)2

371 K, O2 20 bar, H2O

69 (furfural)

4

6

[32]

FeSO4

371 K, O2 20 bar, H2O

90 (furfural)

12

13

[32]

V2O5

371 K, O2 20 bar, H2O

72 (Furfural)

6

8

[32]

CuSO4

371 K, O2 20 bar, H2O

67 (furfural)

19

29

[32]

Cu(NO3)2

371 K, O2 20 bar, H2O

86 (furfural)

24

28

[32]

Cu(OAc)2

371 K, O2 20 bar, H2O

71 (furfural)

19

26

[32]

H3PMo12O40 + Cu(NO3)2 (2/1)

371 K, O2 20 bar, H2O

95 (furfural)

49

52

[32]

  1. NC Not communicated.