US2123611A - Process for the manufacture of nitro-celluloses - Google Patents
Process for the manufacture of nitro-celluloses Download PDFInfo
- Publication number
- US2123611A US2123611A US81016A US8101636A US2123611A US 2123611 A US2123611 A US 2123611A US 81016 A US81016 A US 81016A US 8101636 A US8101636 A US 8101636A US 2123611 A US2123611 A US 2123611A
- Authority
- US
- United States
- Prior art keywords
- acid
- nitro
- celluloses
- nitrating
- manufacture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229920001220 nitrocellulos Polymers 0.000 title description 13
- 238000000034 method Methods 0.000 title description 10
- 238000004519 manufacturing process Methods 0.000 title description 6
- 239000002253 acid Substances 0.000 description 16
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- 230000000802 nitrating effect Effects 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 6
- 241000219146 Gossypium Species 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910017604 nitric acid Inorganic materials 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 238000006396 nitration reaction Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000005070 ripening Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 241001502381 Budorcas taxicolor Species 0.000 description 1
- 241000518994 Conta Species 0.000 description 1
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
- JOCBASBOOFNAJA-UHFFFAOYSA-N N-tris(hydroxymethyl)methyl-2-aminoethanesulfonic acid Chemical compound OCC(CO)(CO)NCCS(O)(=O)=O JOCBASBOOFNAJA-UHFFFAOYSA-N 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical compound OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 description 1
- 229940005991 chloric acid Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B5/00—Preparation of cellulose esters of inorganic acids, e.g. phosphates
- C08B5/02—Cellulose nitrate, i.e. nitrocellulose
- C08B5/04—Post-esterification treatments, e.g. densification of powders, including purification
Definitions
- This collodion cotton resin content of for example 0.8-1%, when niw s of a pure white color w ut t e s i htest trated with the aid of the hitherto normal nitrattinge f y and Completely qual to a 25 ing acids consisting of nitric acid, sulphuric acid COttOn made, p O d res nized celand water, furnish products having amore or less 1111058 as regards 0010 It could thus also be pronounced tinge of yellow, and that even when made into pr of a Cl White color.
- Example H as for example lacquers, plastic masses (cellu- 30 1 1 3 and t k Such products are t 5 kgs. of cotton linters were nitrated for 30 pletely white. Some grades of cotton that are not minutes at with 95 of nitrating acid a pure white also behave in similar fashion. p ed of H2804, 25% s and 5% However, when white cotton is used as the origin- After Washing and ripening which was ating material colorless products can be obtained.
- nitrocellulose in simple manner within certain which process comprises nitrating cellulose raw limits.
- acals fo about 30 minutes at about 30 C.
- cordance with the invention to make collodion with a nitrating acid Conta approximately 50 cottons direct, these being directly utilizable as furic a d, 243% n tric acid, and 3.7% lacquer cottons owing to the low viscosity of their hydrochloric acid. solutions, whereas a collodion cotton furnishing 2.
- Aprocess for manufacturing nitro-celluloses, highly viscous solutions is obtained without the which process compr ni rating cellulose raw addition of the hydrochloric acid, and the vlsmaterials for about 30 minutes at about 30 C. 55
- a process for manufacturing nitro-celluloses, chloric acid. 5 which process comprises nitrating cellulose raw AUGUST NOLL. 5
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Processing Of Meat And Fish (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented July 12, 1938 I I UNITED STATES P TENToFFIcs PROCESS FOR THE MANUFACTURE OF NITRO-CELLULOSES August Noll, Mannheim, Germany, assignor of one-half to Zellstofifabrik Waldhof, Mannheim-Waldhof, Germany, a German company No Drawing. Application May 21, 1936, Serial No. 81,016. In Germany June 11, 1935 3 Claims. (Cl. 260-145) This invention relates to a process for the cosity can only be reduced to the required extent manufacture of nitro-celluloses from chemical by subsequent treatment in an autoclave.
wood pulp. The process and the particular advantages In the nitration of cellulose use has hitherto arising therefrom will hereinafter be illustrated 5 been made of nitrating acids, consisting of sulwith the aid of the following examples: 5
phuric acid, nitric acid and water, in varying Example I proportions.
It has now been ascertained that substantial 5 of a bleached pi o d ce lu ose wit a advantages are obtained by using a nitrating acid resin Content of We t d fo 30 mincontaining in an amount corresponding su t utes at a temperature of 30 C. with 95 kgs. of an 10 tially to about one fifth of the weight of the wood acid mixture Consisting Of 60% H2804, 25% I-INO3 pulp chlorine, such as can be obtained for ex- After the usual Washing and ample by adding small quantities of hydrochloric ripening, there was obtained a collodion cotton acid to a normal nitrating acid mixture containing of nitrogen having a distinct yel- 15 In this manner the advantage is obtained in low tinge, and a viscosity of 203 taking acetone 15 t fir t place that the product obtained is f a as unity (measured in a 2% acetone solution). lighter color, which is particularly important in When the treatment was Carried-.0111? in the t nitration of less pure raw materia1s Moresame manner but with the addition of 3 litres of over the process of the present invention enables hydrochloric a'Cid p cifi ravity 1.19) to the the viscosity of the solutions made from the reabove-Specified quantity of nitrating cid, there 20 sulting nitrocelluloses to be varied within certain Was Obtained. a collodion Cotton Containing limits, in imple manhen of nitrogen and having a relative viscosity of 4'7 t is known t t wood pulps th th usual taking acetone as unity. This collodion cotton resin content, of for example 0.8-1%, when niw s of a pure white color w ut t e s i htest trated with the aid of the hitherto normal nitrattinge f y and Completely qual to a 25 ing acids consisting of nitric acid, sulphuric acid COttOn made, p O d res nized celand water, furnish products having amore or less 1111058 as regards 0010 It could thus also be pronounced tinge of yellow, and that even when made into pr of a Cl White color.
these products are made into other products, such Example H as for example lacquers, plastic masses (cellu- 30 1 1 3 and t k Such products are t 5 kgs. of cotton linters were nitrated for 30 pletely white. Some grades of cotton that are not minutes at with 95 of nitrating acid a pure white also behave in similar fashion. p ed of H2804, 25% s and 5% However, when white cotton is used as the origin- After Washing and ripening which was ating material colorless products can be obtained. carried out in the usual manner, collodion 35 It is true that lighter products have been obtained ton was obtained which contained 12.1% nitro en by removing the resin from the raw cellulose and a relative Viscosity a 2% acetone prior to nitration, but apart from the fact that Solution) 294, taking acetone as ty. the effect thus achieved was often still incom- By Operating in the Same a but adding 40 plete, the additional cost of the resin extraction 3 litres of hydrochimic acid p fic gravity 40 renders the process commercially impracticable. 1.19) to the above-spe fi q y of nitrat- In carrying out the invention, te t ad h v ing acid, there was obtained a collodion cotton shown that the viscosity of the solutions made w chcontaincd 10.9% of nitrogen and which from the resulting nitrocellulose falls as the prohad a relative viscosity of 90, takin acet as portion of chlorine contained in the nitrating unity. 5
acid rises, so that it is possible to regulate the I claim: viscosity of the solutions to be made from the s 1. Aprocess for manufacturing nitro-celluloses,
nitrocellulose in simple manner within certain which process comprises nitrating cellulose raw limits. In particular it is easily possible in acals fo about 30 minutes at about 30 C.
cordance with the invention to make collodion with a nitrating acid Conta approximately 50 cottons direct, these being directly utilizable as furic a d, 243% n tric acid, and 3.7% lacquer cottons owing to the low viscosity of their hydrochloric acid. solutions, whereas a collodion cotton furnishing 2. Aprocess for manufacturing nitro-celluloses, highly viscous solutions is obtained without the which process compr ni rating cellulose raw addition of the hydrochloric acid, and the vlsmaterials for about 30 minutes at about 30 C. 55
with a nitrating acid containing approximately with about 20 times its weight quantity of a ni- 57.8% sulfuric acid, 24.3% nitric acid, 3.7% hytrating acid containing approximately 57.8% suldroch'loric acid, and 14.2% water. furic acid, 24.3% nitric acid and 3.7 hydro- 3. A process for manufacturing nitro-celluloses, chloric acid. 5 which process comprises nitrating cellulose raw AUGUST NOLL. 5
materials for about 30 minutes at about 30 0.,
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2123611X | 1935-06-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2123611A true US2123611A (en) | 1938-07-12 |
Family
ID=7986045
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US81016A Expired - Lifetime US2123611A (en) | 1935-06-11 | 1936-05-21 | Process for the manufacture of nitro-celluloses |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2123611A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3534018A (en) * | 1967-12-20 | 1970-10-13 | Army France | Methods for making nitrocellulose |
-
1936
- 1936-05-21 US US81016A patent/US2123611A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3534018A (en) * | 1967-12-20 | 1970-10-13 | Army France | Methods for making nitrocellulose |
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