US2513659A - Recovery of alkyllead - Google Patents
Recovery of alkyllead Download PDFInfo
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- US2513659A US2513659A US61214A US6121448A US2513659A US 2513659 A US2513659 A US 2513659A US 61214 A US61214 A US 61214A US 6121448 A US6121448 A US 6121448A US 2513659 A US2513659 A US 2513659A
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- iron
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- sodium thiosulfate
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- 238000011084 recovery Methods 0.000 title description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 31
- 238000006243 chemical reaction Methods 0.000 claims description 23
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 claims description 19
- 235000019345 sodium thiosulphate Nutrition 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 16
- 239000007795 chemical reaction product Substances 0.000 claims description 15
- 230000015572 biosynthetic process Effects 0.000 claims description 7
- 238000003786 synthesis reaction Methods 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 238000004326 stimulated echo acquisition mode for imaging Methods 0.000 claims 1
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 24
- 229940001474 sodium thiosulfate Drugs 0.000 description 18
- 150000002505 iron Chemical class 0.000 description 15
- 229910052742 iron Inorganic materials 0.000 description 15
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 10
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000005054 agglomeration Methods 0.000 description 6
- 230000002776 aggregation Effects 0.000 description 6
- 238000004821 distillation Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000011790 ferrous sulphate Substances 0.000 description 5
- 235000003891 ferrous sulphate Nutrition 0.000 description 5
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 5
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 230000009286 beneficial effect Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 159000000014 iron salts Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 238000001256 steam distillation Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 229910000978 Pb alloy Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229960003750 ethyl chloride Drugs 0.000 description 2
- -1 ferrous lactate Chemical class 0.000 description 2
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 2
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 description 2
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- XDIDQEGAKCWQQP-OWOJBTEDSA-N (e)-2,3-dichloro-1,1,1,4,4,4-hexafluorobut-2-ene Chemical compound FC(F)(F)C(\Cl)=C(/Cl)C(F)(F)F XDIDQEGAKCWQQP-OWOJBTEDSA-N 0.000 description 1
- ZEYKLMDPUOVUCR-UHFFFAOYSA-N 2-chloro-5-(trifluoromethyl)benzenesulfonyl chloride Chemical compound FC(F)(F)C1=CC=C(Cl)C(S(Cl)(=O)=O)=C1 ZEYKLMDPUOVUCR-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- DKKCQDROTDCQOR-UHFFFAOYSA-L Ferrous lactate Chemical compound [Fe+2].CC(O)C([O-])=O.CC(O)C([O-])=O DKKCQDROTDCQOR-UHFFFAOYSA-L 0.000 description 1
- 229910000528 Na alloy Inorganic materials 0.000 description 1
- WBLCSWMHSXNOPF-UHFFFAOYSA-N [Na].[Pb] Chemical compound [Na].[Pb] WBLCSWMHSXNOPF-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- OLOAJSHVLXNSQV-UHFFFAOYSA-N diethyl(dimethyl)plumbane Chemical compound CC[Pb](C)(C)CC OLOAJSHVLXNSQV-UHFFFAOYSA-N 0.000 description 1
- 229960002089 ferrous chloride Drugs 0.000 description 1
- 239000004225 ferrous lactate Substances 0.000 description 1
- 235000013925 ferrous lactate Nutrition 0.000 description 1
- 229940037907 ferrous lactate Drugs 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- XOOGZRUBTYCLHG-UHFFFAOYSA-N tetramethyllead Chemical compound C[Pb](C)(C)C XOOGZRUBTYCLHG-UHFFFAOYSA-N 0.000 description 1
- SMHNCYOTIYFOKL-UHFFFAOYSA-N tetrapropylplumbane Chemical compound CCC[Pb](CCC)(CCC)CCC SMHNCYOTIYFOKL-UHFFFAOYSA-N 0.000 description 1
- 229940048910 thiosulfate Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/24—Lead compounds
Definitions
- This invention relates to the recovery of alkyllead compounds from the reaction products accompanying their synthesis. More specifically it relates to an improved method of steam distilling an alkyllead compound in the presence of other reaction products formed during its manufacture.
- reaction mass In the manufacture of tetraethyllead, a comminuted alloy of sodium and lead is reacted with ethyl chloride.
- the lead content of the alloy is in substantial excess of the quantity consumed for the tetraethyllead formation, so that the products of the reaction include excess metallic lead, as well as the tetraethyllead formed.
- the reaction products also include considerable quantitles of sodium chloride, plus minor quantities of unused sodium. This mixture of reaction products is usually referred to as reaction mass.
- My invention comprises conducting the steam distillation used for separating alkyllead products from reaction mass, in the presence of a dilute aqueous solution of a soluble iron salt and sodium thiosulfate.
- these materials, used in combination exhibit a morethan-additive effectiveness in preventing agglomeration and in minimizing steam distillation difficulties. This makes possible greatly improved performance of the steam distillation, even when the agglomerative tendency of reaction mass solids is quite severe.
- iron salts are suitable for combinin with sodium thiosulfate providing that they are water soluble. Salts of both inorganic or organic acids may be used. Thus an organic salt, such as ferrous lactate, is satisfactory. Mixed or double salts are effective also, providing that one of the cations is an iron ion, for example, ferric ammonium oxalate.
- the valence of the iron in the salt is not important, both ferrous and ferric salts being beneficial.
- Ferrous sulfate is especially desirable since it is not only effective but is readily available and inexpensive.
- beneficial soluble iron salts are ferric chloride, ferrous chloride, ferric nitrate, ferric phos-' phate and ferric sulfate.
- the iron salts of my invention are beneficial over a wide concentration range, when used in conjunction with sodium thiosulf-ate. Concentration is expressed herein in terms of the iron, Fe, introduced in the iron salt, as weight per cent based on the weight of lead present in the reaction mass.
- the iron salt can be used in con centrations between 0.003 and 0.12 weight per cent. with a high degree of effectiveness. Conce'ntrations, above 0. 2 weight per cent usually are not required ex ept when the agglomerative tendency of the reaction mass is especially severe. For the average reaction mass concentrations be- .tween 0.003 and 0.06 are satisfactory.
- the concentration of the sodium thiosulfate is not critical, but should be at least 0.1 per cent by weight based on the weight of the lead present in the reaction mass. Concentrations of sodium thiosulfate between 0.1 and 0.8'per cent by weight are satisfactory in most instances. Concentrations above 0.8 weight per cent are usually not. required. However where the agglomeration tendency of the reaction mass is severe higher concentrations are beneficial.
- the quantity of water used in the steam still may be varied widely and good results obtained.
- the amount of water should be sufflcient to submerge fully the reaction mass at the a start of the distillation.
- water solution of the still aids is preferable so that the dissolved salts will ,be in contact with all parts of the reaction mass at the start of the distillation.
- lead particles contained a small percentage of excess sodium, which was converted to sodium hydroxide by reaction with the water in the still.
- Line 0A shows the average efiectiveness of ferric chloride alone, within a concentration range of 0 to 0.06 per cent.
- line F0 sodium thiosulfate concentrations as iow as 0.4 weight per cent and in no case did the concentration exceed 0.8 weight per cent.
- shaded area HFCB represents the unpredictable and. unexpected more-than-additive benefits obtained by usin my combination of still aids.
- the line FC represents average eifectiveness in reaction masses having a normal tendency to agglomerate. Since complete effectiveness has been obtained at low concentrations of iron with sodium" thiosulfate, the higher concentrations were not fullyv utilized. However, higher concentrations of iron, in, combination with sodium thiosulfate, are advantageous when'the reaction mass exhibits especially severe tendency toward agglomeration.
- ferrous sulfate Similar surprising results were obtained with ferrous sulfate. For example, 0.06 per cent of ferrous sulfate used alone resulted in an effectiveness of about 30 per cent. However when the same concentration of ferrous sulfate was used with sodium thiosulfate in concentration between 0.6 and 0.8 per cent, the effectiveness consistently ranged between 90 and 95 per cent. In striking contrast, the effectiveness expected due to only an additiveeffect is only about 62 per cent.
- My invention is not limited to a process for the recovery of tetraethyllead but it is applicable to improving the recovery by steam-'distillation of other alkylleads such as tetramethyllead, tetra propyllead, dimethyldiethyllead, and trimethylphenyllead.
- a process of'recovering an alkyllead from the reaction products accompanying its synthesis comprising steam distilling the reaction mass in the presence of an aqueous. solution of an iron salt. and sodium thiosulfate.
- a process of recovering an alkyllead from the reaction products accompanying its synthesis comprising steam distilling the reaction mass in the presence of an; aqueous solution of an iron salt and sodium thiosulfate, said solution containing iron in an amount equivalent to at least 0.003 per cent byiweight of the lead present in the reaction products and sodium thiosulfate in an amount equivalent to at least 0.1 per cent by weight of the lead present 'in the reaction products.
- line HB represents the effectiveness expected due only to an additive effect for a com- 4.
- the iron salt comprises a sulfate of iron.
- a process of recovering tetraethyllead from the reaction products accompanyin its synthesis comprising steamdistilling the reaction mass in the presence of. an aqueous solution of iron salt and sodiumthiosulfate, said solution containing ,iron in anamount equivalent to 0.003 to 0.06 per bination of different concentrations of ferric sulfate, 9. per cent eifectiveness was obtained i at ferric chloride concentrations above 0.003 per cent, as shown by line FC.
- This is all themore f surprising because .the observed effectiveness cent by weightof the lead in' the reaction products and sodium thiosulfate in an amount equivalent to 0.1 to 0.8-per centiby weight of the lead presentin the reaction products, Y
- the process of claim 6 further defined in that the iron salt comprises ferric chloride.
- the process of claim 9 further defined in that the iron salt comprises a sulfate of iron.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
July 4, 1950 H. J. MADDEN RECOVERY OF ALKYLLEAD Filed NOV. 20, 1948 ACTUAL EFFECTIVENESS OF FERRIC CHLORIDE m C 0 E m T M L w m w T O. H T M m w 0 D O s m. W O. w v v ,w O v 4 u O. F l|ll l,l'l lll llllll ky o o. w 0 a 0 0 O 0 0 O y 0 V .0 00 9 8 7 6 5 .4 3 2 T I CONCENTRATION OF IRON-WEIGHT PERCENT BASED ON WEIGHT OF LEAD PRESENT INVENTQR. HAROLD MADDEN Patented July 4, 1950 RECOVERY OF 'ALKYLLEAD Harold J. Madden, Baton Rouge, La., assignor to Ethyl Corporation, New York, N. Y., a corpora.-
tion of Delaware Application November 20, 1948, Serial No. 61,214
12 Claims.
This invention relates to the recovery of alkyllead compounds from the reaction products accompanying their synthesis. More specifically it relates to an improved method of steam distilling an alkyllead compound in the presence of other reaction products formed during its manufacture.
In the manufacture of tetraethyllead, a comminuted alloy of sodium and lead is reacted with ethyl chloride. The lead content of the alloy is in substantial excess of the quantity consumed for the tetraethyllead formation, so that the products of the reaction include excess metallic lead, as well as the tetraethyllead formed. The reaction products also include considerable quantitles of sodium chloride, plus minor quantities of unused sodium. This mixture of reaction products is usually referred to as reaction mass.
Steam distillationis used to recover the tetraethyllead product from the reaction mass. The reaction mass is discharged into a still which is already partly full of water. The mixture is continuously agitated while steam is passed through the still. The mixture in the still, termed still sludge," tends to agglomerate forming a spongy porous mass in the shape of balls or forming a solid metallic mass. The solid metallic mass usually occurs as sheets or rings around the in-.
terior of the still. Such agglomerations cause considerable trouble such as overloading and jamming of the still agitator, making subsequent removal of the still sludge after distillation diflicult and in severe cases making it necessary to shut down the equipment so that this removal may be effected. The latter is a difficult task requiring unusual safety precautions due' to the toxic nature of thetetraethyllead.
Also the overall yields of tetraethyllead are adversely affected by such still troubles. When a tinuous problem. Many materials have been proposed and some used as additives to the still charge for prevention of agglomeration of the solids. These additives referred to as still aids, have not been suiiiciently effective as antiaggloinerants, and their use has frequently in- .2 troduced other difficulties, such as interference with the subsequent processing of the residue in the still for recovery of the lead content.
It is therefore an object of this invention to provide an improved still aid which greatly reduces the diificulties encountered during distillation due to the agglomeration of solid reaction products, another object is to obtain a better recovery of alkyllead products. A further object is to improve the safety and working conditions for the process.
These objects are attained by the use of two or more different materials which, when combined, exhibit a synergistic effect in their use as I still aids. My invention comprises conducting the steam distillation used for separating alkyllead products from reaction mass, in the presence of a dilute aqueous solution of a soluble iron salt and sodium thiosulfate. I have found that these materials, used in combination, exhibit a morethan-additive effectiveness in preventing agglomeration and in minimizing steam distillation difficulties. This makes possible greatly improved performance of the steam distillation, even when the agglomerative tendency of reaction mass solids is quite severe.
Generally, all of the iron salts are suitable for combinin with sodium thiosulfate providing that they are water soluble. Salts of both inorganic or organic acids may be used. Thus an organic salt, such as ferrous lactate, is satisfactory. Mixed or double salts are effective also, providing that one of the cations is an iron ion, for example, ferric ammonium oxalate. The valence of the iron in the salt is not important, both ferrous and ferric salts being beneficial. Ferrous sulfate is especially desirable since it is not only effective but is readily available and inexpensive. Among other beneficial soluble iron salts are ferric chloride, ferrous chloride, ferric nitrate, ferric phos-' phate and ferric sulfate.
The iron salts of my invention are beneficial over a wide concentration range, when used in conjunction with sodium thiosulf-ate. Concentration is expressed herein in terms of the iron, Fe, introduced in the iron salt, as weight per cent based on the weight of lead present in the reaction mass. The iron salt can be used in con centrations between 0.003 and 0.12 weight per cent. with a high degree of effectiveness. Conce'ntrations, above 0. 2 weight per cent usually are not required ex ept when the agglomerative tendency of the reaction mass is especially severe. For the average reaction mass concentrations be- .tween 0.003 and 0.06 are satisfactory.
3 The concentration of the sodium thiosulfate is not critical, but should be at least 0.1 per cent by weight based on the weight of the lead present in the reaction mass. Concentrations of sodium thiosulfate between 0.1 and 0.8'per cent by weight are satisfactory in most instances. Concentrations above 0.8 weight per cent are usually not. required. However where the agglomeration tendency of the reaction mass is severe higher concentrations are beneficial.
The quantity of water used in the steam still may be varied widely and good results obtained. In general the amount of water should be sufflcient to submerge fully the reaction mass at the a start of the distillation. At water solution of the still aids is preferable so that the dissolved salts will ,be in contact with all parts of the reaction mass at the start of the distillation.
To illustrate the surprising nature of the invention, an embodiment on a large scale is described. A still was charged with 3100 pounds of water, 2.5 pounds of ferric chloride added as FeClx-SHzO and 19 pounds of sodium thiosulfate added as Na2SzO3-5H2O. Then a charge of about 4500 pounds of reaction mass was introduced during agitation. The reaction mass contained about 2500 pounds of predominantly lead particles, about 1100 pounds of tetraethyllead and roughly 900 pounds of sodium chloride. The
lead particles contained a small percentage of excess sodium, which was converted to sodium hydroxide by reaction with the water in the still.
Open steam was passed through the still and the distillation continued for 90 to 120 minutes, :which was adequate for separation of the recoverable tetraethyllead. No "still trouble" was encountered in this procedure or in numerous the average effectiveness of ferric chloride alone,
, the expected effectiveness of ferric chloride with sodium thiosulfate based solely onan additive effect, and the observed effectiveness of the latter.
Line 0A shows the average efiectiveness of ferric chloride alone, within a concentration range of 0 to 0.06 per cent. For example, at a concen- :combined still aid is synergistic in nature, reference is made to the accompanying plot. This plot is based on large scale operations and shows shown by line F0, was obtained on sodium thiosulfate concentrations as iow as 0.4 weight per cent and in no case did the concentration exceed 0.8 weight per cent. Thus, shaded area HFCB represents the unpredictable and. unexpected more-than-additive benefits obtained by usin my combination of still aids.
The line FCrepresents average eifectiveness in reaction masses having a normal tendency to agglomerate. Since complete effectiveness has been obtained at low concentrations of iron with sodium" thiosulfate, the higher concentrations were not fullyv utilized. However, higher concentrations of iron, in, combination with sodium thiosulfate, are advantageous when'the reaction mass exhibits especially severe tendency toward agglomeration.
Similar surprising results were obtained with ferrous sulfate. For example, 0.06 per cent of ferrous sulfate used alone resulted in an effectiveness of about 30 per cent. However when the same concentration of ferrous sulfate was used with sodium thiosulfate in concentration between 0.6 and 0.8 per cent, the effectiveness consistently ranged between 90 and 95 per cent. In striking contrast, the effectiveness expected due to only an additiveeffect is only about 62 per cent.
Thus I have demonstrated that my still aids are outstanding in effectiveness and that a-more than an additive effect is obtained over the use of either an iron salt or sodium thiosulfate alone. My invention is not limited to a process for the recovery of tetraethyllead but it is applicable to improving the recovery by steam-'distillation of other alkylleads such as tetramethyllead, tetra propyllead, dimethyldiethyllead, and trimethylphenyllead. I
I claim: v v
1. A process of'recovering an alkyllead from the reaction products accompanying its synthesis comprising steam distilling the reaction mass in the presence of an aqueous. solution of an iron salt. and sodium thiosulfate.
2. A process of recovering an alkyllead from the reaction products accompanying its synthesis comprising steam distilling the reaction mass in the presence of an; aqueous solution of an iron salt and sodium thiosulfate, said solution containing iron in an amount equivalent to at least 0.003 per cent byiweight of the lead present in the reaction products and sodium thiosulfate in an amount equivalent to at least 0.1 per cent by weight of the lead present 'in the reaction products.
3. The process of claim 2 further defined in that the iron salt comprises a chloride of iron.
tration of 0.04 weight percent, ferric chloride alone is about 37 per cent effective. Line FC'is the observed effectiveness for varying concentrations of ferric chloride in combination with the sodium thiosulfate concentrations varying vorable concentration of 0.8 weight per cent results in an effectiveness of only 32 per cent.
Therefore line HB represents the effectiveness expected due only to an additive effect for a com- 4. The process of claim 2 further defined in that the iron salt comprises a sulfate of iron.
5. I'he process of claim 2 further defined in that the iron salt comprises a nitrate of iron.
6. A process of recovering tetraethyllead from the reaction products accompanyin its synthesis comprising steamdistilling the reaction mass in the presence of. an aqueous solution of iron salt and sodiumthiosulfate, said solution containing ,iron in anamount equivalent to 0.003 to 0.06 per bination of different concentrations of ferric sulfate, 9. per cent eifectiveness was obtained i at ferric chloride concentrations above 0.003 per cent, as shown by line FC. This is all themore f surprising because .the observed effectiveness cent by weightof the lead in' the reaction products and sodium thiosulfate in an amount equivalent to 0.1 to 0.8-per centiby weight of the lead presentin the reaction products, Y
. 7. Thep'rocess of claim-(ifurther define'dinb that the iron saltv comprises ferrous sulfate.
-a. The process of claim 6 further defined in that the iron salt comprises ferric chloride.
5 9. In the process of preparing tetraethyllead by reacting sodium-lead alloy and ethyl chloride, and recovering tetraethyllead from the products of reaction accompanying its synthesis,
the step of steam distilling tetraethyllead there- 5 from in the presence of aqueous solution containing an iron salt having an iron content in amount equivalent to from 0.003 to 0.12 per cent by weight of the lead present in the reaction products, and sodium thiosulfate in an amount equivalent to from 0.1 to 0.8 per cent by Weight of the lead present in the reaction products.
10. The process of claim 9 further defined in that the iron salt comprises a sulfate of iron.
11. The process of claim 9 further defined in that the iron salt comprises a nitrate of iron.
12. The process of claim 9 further defined in that the iron salt comprises a chloride of iron.
HAROLD J. MADDEN.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,645,375 Daudt Oct. 11, 1927 2,004,160 Downing June 11, 1935 2,038,703 Bake et a1. Apr. 28, 1936 2,038,704 Bake et a1. Apr. 28, 1936 FOREIGN PATENTS Number Country Date 214,221 Great Britain July 22, 1925 516,875 Great Britain Jan. 15, 1940
Claims (1)
1. A PROCESS OF RECOVERING AN ALKYLLEAD FROM THE REACTION PRODUCTS ACCOMPANYING ITS SYNTHESIS COMPRISING STEAM DISTILLING THE REACTION MASS IN THE PRESENCE OF AN AQUEOUS SOLUTION OF AN IRON SALT AND SODIUM THIOSULFATE.
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US61214A US2513659A (en) | 1948-11-16 | 1948-11-20 | Recovery of alkyllead |
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Application Number | Priority Date | Filing Date | Title |
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US60391A US2513654A (en) | 1948-11-16 | 1948-11-16 | Recovery of alkyllead compounds |
US61214A US2513659A (en) | 1948-11-16 | 1948-11-20 | Recovery of alkyllead |
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US2513659A true US2513659A (en) | 1950-07-04 |
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US61214A Expired - Lifetime US2513659A (en) | 1948-11-16 | 1948-11-20 | Recovery of alkyllead |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2777867A (en) * | 1953-08-03 | 1957-01-15 | Ethyl Corp | Recovery of alkyllead compounds |
Citations (6)
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---|---|---|---|---|
GB214221A (en) * | 1923-04-13 | 1925-07-22 | Standard Dev Co | An improved process of making metallo-organic compounds |
US1645375A (en) * | 1925-11-02 | 1927-10-11 | Du Pont | Manufacture of tetra-ethyl lead |
US2004160A (en) * | 1932-03-09 | 1935-06-11 | Du Pont | Tetra alkyl lead |
US2038703A (en) * | 1933-03-30 | 1936-04-28 | Du Pont | Recovery of alkyl lead compounds from their reaction masses |
US2038704A (en) * | 1934-03-30 | 1936-04-28 | Du Pont | Recovery of alkyl lead compounds |
GB516875A (en) * | 1938-02-16 | 1940-01-15 | Ethyl Gasoline Corp | Improvements in or relating to manufacture of methyl and ethyl lead compounds |
-
1948
- 1948-11-20 US US61214A patent/US2513659A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB214221A (en) * | 1923-04-13 | 1925-07-22 | Standard Dev Co | An improved process of making metallo-organic compounds |
US1645375A (en) * | 1925-11-02 | 1927-10-11 | Du Pont | Manufacture of tetra-ethyl lead |
US2004160A (en) * | 1932-03-09 | 1935-06-11 | Du Pont | Tetra alkyl lead |
US2038703A (en) * | 1933-03-30 | 1936-04-28 | Du Pont | Recovery of alkyl lead compounds from their reaction masses |
US2038704A (en) * | 1934-03-30 | 1936-04-28 | Du Pont | Recovery of alkyl lead compounds |
GB516875A (en) * | 1938-02-16 | 1940-01-15 | Ethyl Gasoline Corp | Improvements in or relating to manufacture of methyl and ethyl lead compounds |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2777867A (en) * | 1953-08-03 | 1957-01-15 | Ethyl Corp | Recovery of alkyllead compounds |
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