ACETALDEHYDE, acetic acid, acetic anhydride and acetone from acetylene at the Bunawerke, Schkopau, the production of, reported by W. L. Wood

199

50 ‘20-50 ‘35

“ from arc acetylene, preliminary estimate of cost of,

56

13-60

82-120

“ into acetaldol, conversion of

105

10513-10522

“ , manufacture of, reported by J. W. Fisher

226

50 ‘59-50 ‘66

“ , manufacture of, Schkopau, I.G. Farbenindustrie, reported by R. L. Hasche and R. H. Boundy

197

40 ‘51-40 ‘55

“ , modified Höchst process for the conversion of unpurified arc acetylene into

24

12..475-12..504

“ production, 1943/1944

54

667-671

ACETALDEHYDE without the use of mercury catalysts, studies on the synthesis of, by T. Yamamoto

231

20 ‘61-20 ‘76

ALDEHYDE samples, physical and chemical data on three

14

790

“ age, flow sheet of, Leuna M 4285d-2

195

31738

“ , oxidation of,

35

3440

62

0 ‘3-0 ‘9

42

653-654

Translation S-71

274

1730-1731

“ synthesis, alcohol formation in the

42

662-663

Translation S-76

274

1737

“ synthesis, technical use of the Gattermann, Hasche Reel 2, frame 404, translation by S.O. Co., Ind.

244

110 ‘27-110 ‘28

“ in the engine and their quantitative determination, by W. Kamm, the effect of

248

50 ‘83-50 ‘104

ALDOL condensation of acetaldehyde, drawings

27

2077

65..263-69..268

“ hydrogenation

105

10623-10637

“ “ at Huls

105

10638-10643

10656-10666

“ December 1942 - October 1943, production records of

155

714-781

“ , manufacture of, Schkopau (Auschwitz)

105

10644-10655

191

25104-25118

ALDOLIZATION

105

10564-10569

BUTYRALDEHYDE from crotonaldehyde by hydrogenation

154

176-178

315-317

“ , separation of,

31

2078

88.341

CROTONALDEHYDE to butyraldehyde, hydrogenation of,

154

176-178

315-317

CROTONALDEHYDE-ENOL acetate, production of

154

320-325

CROTONALDEHYDE, hydrogenation of the condensation products of

154

55-62

64-71

72-73

128-142

“ , Kd 1551 flow sheet for the manufacture of,

28

2167

90

“ , Kd 1553 material balance for the manufacture of

28

2167

89

“ plant, experimental

31

2170

19..1150-19.11**

“ production, flow sheet of,

29

15..724

CROTONALDEHYDE, 1942 status of condensation and hydrogenation of,

154

78-105

112-127

CYCLOHEXANONE process

116

70 ‘1-70 ‘70

ETHOXY propionaldehyde diethylacetal and methoxy propionaldehyde dimethylacetal, hydrogenation of

55

697-700

2-ETHYL hexanal-1, attempted pilot plant production of,

154

185-188

FORMALDEHYDE concentration, flow diagram

119

90 ‘89

“ , methanol, 1943/1944

54

672-673

“ from methanol and air, Leuna M 4573-1

195

31784

“ plant from methanol, flow diagram of a

119

90 ‘80

“ from methanol and air Leuna, production of, Leuna, M 4281-16, flow sheet

193

23459

“ by catalytic oxidation of methane with oxygen, theory of formation of, by Geib

195

31695-31702

“ “ by catalytic oxidation with ozone and oxygen, theory of, by Geib

192

22280-22289

“ and propionaldehyde preparation, flow sheet of, M3295-1, Leuna

194

30010

“ and propionic aldehyde flow sheets, Leuna

193

23456

“ , N9629-4 flow sheet for the manufacture of,

28

2167

79

“ plant, inspection of, Leuna

27

2169

16..106-16..107

FURFUROL, hydrogenation of,

55

648-651

“ , research on,

22

55..741-55..745

“ , separation from methylcyclopentanone

55

722-723

ISOMERIC aldehydes, method of separating

22

73..886-73..888

METHOXY-propionaldehyde dimethylacetal and ethoxy-propionaldehyde - diethylacetal, hydrogenation of,

55

697-700

OCTATRIENAL, hydrogenation of,

154

331-340

OXALDEHYDES for the production of fats

44

72

1180-1183

POLYENE aldehydes, hydrogenation of,

154

47-79

PRIMARY aldehydes, side reactions in the formation of,

42

660

Translation S-75

274

1736

PROPIONALDEHYDE and formaldehyde flow sheets, Leuna

193

23456

194

30010

PROPIONALDEHYDE, batch production of,

49

416-422

423-469

“ from propanol and air, Leuna M 4494a-1

195

31775

“ hydrogenation of acrolein to

55

639

“ , discussions of manufacture of,

119

70 ‘21-70 ‘26

“ manufacture

43

3439

34-35

154

289-294

“ production process, declaration of readiness for construction and brief description of,

116

40 ‘41-40 ‘64

“ reports

45

77

43-56

SYNTHESIS of aldehydes and other oxygen containing compounds starting with carbon monoxide and hydrogen, Ruhrbenzin A. G.

44

14

000176-000182

“ of organic compounds, aldehydes as starting material in the,

18

66..664-66..677

Translation

144

10 ‘34-10 ‘38