Chemicals, Organic ACIDS

ACETIC, acetaldehyde, acetic anhydride, and acetone from acetylene, the production of, at the Bunawerke, Schkopau. Reported by W. L. Wood.

199

50 ‘20-50 ‘35

“ , additions to plant, Leuna, M7658-2

195

31731

“ , brief description of proposed additions to plant

116

40 ‘89-40 ‘107

“ , distillation flow sheet, Leuna M 4352a-1

195

31776

“ , flow sheet of, manufacture, Leuna M 8329a-2

195

31745

“ plant, flow sheet of 700 atm Leuna M 8308-2

195

31740

“ , flow sheet of production, Leuna, 700 atm.

193

23453

23455

“ , flowsheet of synthesis, Leuna, M 8469-2

195

31482

“ -formic acid mixtures, separation with toluene

55

744-751

“ , synthesis of, calculation of the equilibrium, by Schneider and Reitz

193

23426-23428

“ , synthesis of, thermodynamic calculations

253

363-365

“ , synthesis through the action of carbon monoxide on methanol

31

2078

91..540-91..518

“

119

90 ‘73-90 ‘74

ADIPIC

31

2078

90..427-90..449

54

677

119

70 ‘27-70 ‘30

“ and alkyl adipic acids, experiments on the preparation of,

18

53..454-53..509

Translation

144

0 ‘127-0 ‘128

“ and alkyl adipic acids, laboratory experiments for obtaining, by Froehlich

86

1588-1642

Translation

249

50 ‘44-50 ‘72

“ , description of manufacture of, with flow diagram, SK 31745

152

714-716

“ , plant flow diagram M-5463-2

116

10 ‘64

“ , preparation of from cyclohexane

47

994-995

Translation

243

30 ‘22-30 ‘23

“ , preparation of from tetrahydrofuran and carbon monoxide

32-II

208.1627-208.164*

“ , preparation of from tetrahydrofuran and carbon monoxide, reported by J. C. C. Gartshore

226

60 ‘20-60 ‘24

“ , production of 250 te/ann, flow sheet Leuna M 4242a-1

195

31733

ADIPIC, synthesis of through the reaction of carbon monoxide on cyclic ethers, lactones, and diols.

31

2078

90..344-90..416

ALKYL adipic and adipic acid, experiments on the preparation of,

18

53..454-53..509

Translation

144

0 ‘127-0 ‘128

“ adipic and adipic acid, laboratory experiments for obtaining, by Froehlich

86

1588-1642

Translation

249

50 ‘44-50 ‘72

ARYL thioglycollic and aryl mercaptans, new methods of production of

22

50..725-50..727

CARBOXYLIC, reported by J. G. Allen, D. A. Howes and H. Schindler

197

70 ‘73

“ , R-CH-(COONa) -CH3, synthetic

206

4981

CROTONIC, production of acetophenone, synthetic resin AP, with translations

176

206-218

DICARBOXYLIC, electrolytic preparation of,

55

392-396

183

8380-8384

DIGLYCOLLIC and ethyl methyl ketone, conden-sation with formaldehyde

154

192-193

FATTY and amines, vapor pressure diagrams of,

24

3391

50

“ and soaps by oxidation of oxo products

44

3441

11

70-125

“ , analysis of diesel oils for use in synthesis of,

44

3441

12

126

“ analysis of miscellaneous soaps and

44

71

1153-1179

“ , attempts at separation of the superoxidized,

24

10..382-10..388

“ , by distillation of synthesis products

44

3441

12

129-131

“ , chlorides, preparation of high molecular weight

54

48-54

“ , constants of C6-C20, compilation of,

16

2765-3018

“ , conversion of high molecular weight alcohols into high molecular weight

42

950-959

“ , data on,

122

25

102370-102380

“ , deliveries of,

70

686-689

“ , direct production of in large units

45

2-8

“ mixture (1 component), distillation installation for 2 te/day

71

816-826

“ , experimental installation Baton Rouge

54

628-638

“ , experimental oxidation of paraffin waxes to, Leuna, 1937

54

533-579

“ , fats and glycerine, order for synthetic work on

27

49..284

“ from alcohols by caustic fusion

14

692-693

“ , from Kogasin

71

802-809

FATTY from oil condensates

44

3441

12

127-128

“ “ paraffin wax

49

363-366

“ “ “ “ from pressure synthesis

67

1278-1292

1297-1299

1307-1317

“ from synthesis products

166

814-815

“ “ waste liquors of the synthesis plant in the Ruhr region

45

1

“ , high molecular weight, investigation of samples from the Ruhrchemie

29

16..726-16..727

“ , hydrogenation of oxidation products of crude soap to refine the,

24

10..373-10..381

“ , hydrogenation of, to alcohols

119

80 ‘91-80 ‘94

“ , identification and constitution of the branched shain acids from Fischer gatsch

259

655-664

“ , improvements in manufacture of,

54

275-283

“ , installation for distillation of, into two fractions (cost estimate)

71

810-815

“ , investigation of soap from TTH paraffin wax

16

2718-2736

“ , mechanism of formation of, by interaction of carbon monoxides and alcohols

134

80 ‘15-80 ‘18

“ , oxidization of alcohols to,

13

3043

3

70 ‘17-70 ‘19

“ , “ sludges produced in the oxidation of paraffin wax, attempts to work up,

24

10..366-10..372

“ , oxidation tests and the use of oxidation products

164

546-550

“ , paraffin wax mixtures for the conversion to, by catalytic oxidation, determination of suitability of, reported by H. S. Coith and F. O. Robitchek

240

10 ‘43-10 ‘85

“ plant calculations

36

3452

41

0 ‘73-0 ‘83

“ , preparation of from alcohols

42

673

Translation S-78

274

1739

“ , preparation of from neutralization alkalies, by Ohme

67

648-653

Translation (S. O.)

243

50 ‘14-50 ‘18

“ , production of,

38

3450

17

10 ‘65-10 ‘69

42

657

Translation S-83

274

1733

“ , production of, discussion in Leuna, March 1943

29

11..652-11..6**

“ , production from by-products of the Fischer-Tropsch process. Reported by P. L. Pavcek

198

60 ‘17-60 ‘19

FATTY production from gasoline synthesis products

36

3451

5

70 ‘113-70 ‘118

39

3450

44

60 ‘73-60 ‘91

71

798-801

“ , production form the neutralization lye in synthesis, 1943

46

434-441

“ production from pressure synthesis paraffin wax

67

1307-1317

“ , properties of paraffin gatch for the synthesis of,

36

3451

5

80 ‘30-80 ‘33

48

521-526

“ , recovery of from alkaline wash, by Ohme

67

648-658

180

6075-6081

“ , recovery of from waste utilization liquors

45

100-106

Translation

225

50 ‘29-50 ‘33

“ , the “Renal” installation for the production of low molecular weight, (C₄-C₆)

31

2170

22..1189-22..1210

“ sample

44

3441

10

68-69

“ , semi-commercial production in Leuna

54

580-627

“ , synthesis of,

43

3439

94

36-40

44

66-67

“ , “ “ and fatty acid esters by the interaction of carbon monoxide upon olefins and alcohols or water

26

10..481-10..564

Do., by Pistor, Kroper and Schlenk

219

20 ‘80-20 ‘111

“ , synthesis of, workup detail

56

9

950-954

“ “ “ unsaturated,

155

110-112

“ , testing of soft paraffin wax for its suitability for the production of,

201

766-773

“ three ton per day production plant for,

49

402-407

“ , vapor pressure diagrams of amines and

24

3391

50

FERULIC and ammonium ferulate, hydrogenation of,

55

706-710

FORMIC - acetic acid mixtures, separation with toluene

55

744-751

“ , flow sheet for the manufacture of,

28

2167

78

GAMMA ketodicarboxylic, and spirodilactones

22

76..894-76..902

HYDROCYANIC, I. G. Oppau and Ludwigshafen,, reported by W. Hunter

239

30 ‘60-30 ‘65

“ , manufacture of, I. G. Farbenindustrie Oppau. Reported by R. H. Boundy and R. L. Hasche

196

20 ‘38-20 ‘41

KETO, as building blocks in organic synthesis

193

23447

MALEIC anhydride, experiments on, by Theilacker

69

184-189

METHYL adipic, flow sheet of production, Leuna M 5334-1

195

31713

MONO carboxylic acids, aliphatic, plant for the production of

116

60 ‘56-60 ‘78

MUCONIC, oxidative ring fission of the o-dioxy benzenes to derivatives, by Spangler

152

718-738

PERACETIC, preparation of,

127 & 128

1286-1288

PHTHALIC, description of the production, Schkopau, Oct. 1945

151

942-961

“ , naphthalene, 1943/1944

54

675-676

PIMELIC, ethylhexanol esters of, and related acids as plasticizers

27

2077

11..27-11..28

“ , preliminary economic balance in manu-facture of,

27

2077

13..48-13..49

“ , process for the manufacture of,

27

2077

12..29-12..47

PROPIONIC, flow sheet for the manufacture of Leuna, M 3652-1

195

31780

SEBACIC, electro synthesis of dimethyl esters of,

55

397-407

“ , production of,

22

75..892-75..893

“ , theory of electrolytic synthesis of from adipic acid

18

56..529-56..534

STEARIC, preparation of pure

79

2877-2879

“ , octa-decyl alcohol from,

79

2864-2867

SUCCINIC, industrial production of,

119

80 ‘95-80 ‘96

TARTARIC, continuous production from tetrahydrofuran

3

2168

13

20 ‘64-20 ‘83

26

10..355-10..373

TOLUIC, m-, o- and p-, chlorinated products of,

22

66..818-66..827