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Table 4 Results of combustion energy determination for investigated compounds

From: Thermodynamic properties of some isomeric 5-(nitrophenyl)-furyl-2 derivatives

m(cpd), g

ΔT, V

ΔUfuse, J

ΔUHNO3, J

ΔUcarbon, J

ΔUter, J

− cU(cpd), J g−1

m exp /m cal

5-(2-Nitrophenyl)-2-furaldehyde oxime

0.13947

0.25347

106.7

7.7

22.3

412.4

23,464

0.9996

0.18548

0.33140

119.5

11.8

27.6

473.7

23,510

1.0002

0.16006

0.28787

106.2

4.1

20

434.6

23,520

0.9985

0.20085

0.35193

124.4

8.9

39.5

427.2

23,515

0.9961

0.17080

0.30603

118.1

8.9

23.6

441.8

23,507

0.9998

0.17019

0.30680

111.2

9.4

38.2

488

23,510

0.9987

0.19456

0.34651

121.3

11.2

43.5

505.5

23,483

0.9959

− cU(cpd)average = 23,501 ± 17 J g−1

5-(3-Nitrophenyl)-2-furaldehyde oxime

0.15358

0.31158

82.0

10.0

28.5

982.4

23,421

0.9968

0.26843

0.46052

94.5

14.8

28.2

499.8

23,400

0.9952

0.14936

0.27347

82.4

7.1

48.4

534.1

23,431

0.9998

0.14361

0.26148

121.2

7.1

25.1

424.5

23,456

1.0000

0.15737

0.28468

120.7

7.1

27.4

453.2

23,438

0.9987

0.18331

0.32799

99.5

8.9

28.2

510.2

23,400

0.9990

0.13068

0.24331

99.4

7.7

25.3

483.8

23,416

0.9991

− cU(cpd)average = 23,429 ± 16 J g−1

5-(4-Nitrophenyl)-2-furaldehyde oxime

0.20572

0.36079

106.5

14.2

27.7

486.0

23,319

1.0000

0.12488

0.23304

104.1

4.7

23.9

473.6

23,335

0.9989

0.17515

0.34180

117.1

8.3

32.3

902.4

23,395

0.9999

0.21358

0.40512

120.3

13.0

27.2

946.7

23,335

0.9992

0.18755

0.36144

136.0

9.4

21.3

884.7

23,338

0.9999

0.24203

0.44750

127.9

13.6

31.7

913.2

23,324

0.9987

0.16330

0.32067

120.1

8.9

23.6

858.2

23,360

0.9965

− cU(cpd)average = 23,344 ± 22 J g−1

3-[5-(2-Nitrolphenyl)-2-furyl]acrylic acid

0.31440

0.49265

82.0

3.5

29.9

23,172

0.9968

0.37839

0.59087

72.3

4.7

28.4

23,140

0.9992

0.33991

0.53119

85.7

8.9

53.3

23,165

0.9973

0.36358

0.56796

78.7

9.4

30.8

23,120

0.9965

0.41155

0.64234

74.8

9.4

30.8

23,127

0.9978

0.13428

0.21518

129.3

4.7

34.1

23,134

0.9995

0.12360

0.19809

113.3

4.1

28.2

23,160

0.9997

− cU(cpd)average = 23,145 ± 20 J g−1

3-[5-(3-Nitrolphenyl)-2-furyl]acrylic acid

0.21935

0.3439

97.3

7.1

46.9

23,100

0.9985

0.23066

0.36164

103.8

8.9

24.9

23,062

0.9962

0.19197

0.30458

110.9

7.7

21.3

23,135

1.0000

0.27004

0.42269

80.2

13.0

24.3

23,069

0.9998

0.24827

0.39045

97.7

10.6

22.8

23,090

0.9986

0.24804

0.38918

84.7

12.4

28.5

23,103

0.9991

0.24000

0.37684

91.5

10.0

24.4

23,076

0.9979

− cU(cpd)average = 23,091 ± 22 J g−1

3-[5-(4-Nitrolphenyl)-2-furyl]acrylic acid

0.16072

0.25432

106.7

5.9

22.8

23,020

0.9999

0.17773

0.27984

101.4

7.7

25.1

22,989

0.9999

0.23568

0.37014

115.7

10.0

27.2

22,985

0.9996

0.16126

0.25492

101.1

5.9

23.3

23,036

0.9998

0.19640

0.30968

99.9

8.3

23.0

23,062

0.9997

0.16949

0.26797

112.3

6.5

23.5

22,997

0.9999

0.16084

0.25462

102.3

4.7

20.3

23,050

0.9995

− cU(cpd)average = 23,020 ± 26 J g−1