Surfactant based small molecules for reducing aluminosilicate scale in the Bayer process
The invention provides methods and compositions for inhibiting the accumulation of DSP scale in the liquor circuit of Bayer process equipment. The method includes adding one or more GPS-surfactant based small molecules to the liquor fluid circuit. These scale inhibitors reduce DSP scale formation and thereby increase fluid throughput, increase the amount of time Bayer process equipment can be operational and reduce the need for expensive and dangerous acid washes of Bayer process equipment. As a result, the invention provides a significant reduction in the total cost of operating a Bayer process.
1. A method of reducing aluminosilicate containing scale in a Bayer process comprising:
adding to a Bayer liquor a non-polymeric reaction product resulting from the reaction of dodecyl-1,3-propanediamine, tetraethylenepentamine, ethylenediamine, and an epoxide binder;
and a glycidoxyalkyltrimethoxysilane.
2. The method of claim 1 , wherein the epoxide binder is selected from epichlorohydrin and ethylene glycol diglycidylether.
3. The method of claim 1 , wherein the epoxide binder is epichlorohydrin.
4. The method of claim 1 , wherein the epoxide binder is ethylene glycol diglycidylether.
5. The method of claim 1 , wherein the glycidoxyalkyltrimethoxysilane is 3-glycidoxypropyltrimethoxysilane.
6. The method of claim 1 , wherein the epoxide binder is a molecule according to formulas (I), (II), and any combination thereof:
7. The method of claim 1 , wherein the epoxide binder is a composition according to formula (I):
8. The method of claim 1 , wherein the epoxide binder is a composition according to formula (II):
9. The method of claim 1 , the non-polymeric reaction product resulting from the reaction of items further comprising a hydrophobe, wherein the hydrophobe is a C8-C10 aliphatic glycidyl ether.
10. The method of claim 1 , wherein the non-polymeric reaction product has a molecular weight of less than 500 daltons.
11. The method of claim 1 , wherein the non-polymeric reaction product is formed according to one of the methods selected from the group consisting of Methods I, II, III, IV, V, VI, VII, VIII, IX, X, XI, XII, and XIII, and any combination thereof.
12. The method of claim 1 , wherein the non-polymeric reaction product is added to the Bayer liquor upstream of or at a heat exchanger.
13. The method of claim 1 , wherein the dodecyl-1,3-propanediamine, the tetraethylenepentamine, the ethylenediamine, the epoxide binder, and the glycidoxyalkyltrimethoxysilane are reacted at a molar ratio of about 2:1:1:3:1, respectively.
14. The method of claim 1 , wherein the dodecyl-1,3-propanediamine, the tetraethylenepentamine, the ethylenediamine, the epoxide binder, and the glycidoxyalkyltrimethoxysilane are reacted at a molar ratio of about 2:1:1:3:2, respectively.
15. The method of claim 1 , wherein the dodecyl-1,3-propanediamine, the tetraethylenepentamine, the ethylenediamine, the epoxide binder, and the glycidoxyalkyltrimethoxysilane are reacted at a molar ratio of about 2:1:1:3:3, respectively.