SORBENT FOR AT LEAST ONE METAL
This disclosure provides a sorbent for at least one metal. The sorbent includes a core particle and a ceramic nanoparticulate cation exchanger for at least one metal that is disposed about the core particle. The core particle is chosen from titanium dioxide, alumina, iron oxide, and combinations thereof.
1 . A sorbent for at least one metal, said sorbent comprising:
a core particle; and
a ceramic nanoparticulate cation exchanger for at least one metal that is disposed about said core particle,
wherein said core particle is chosen from titanium dioxide, alumina, iron oxide, and combinations thereof.
2 . The sorbent of claim 1 that is free of silica.
3 . The sorbent of claim 1 wherein said core particle is alumina having a D10 value of from about 4 to about 10, a D50 value of from about 10 to about 16, and a D90 value of from about 20 to about 42, micrometers, each determined using laser diffraction.
4 . The sorbent of claim 1 wherein said core particle is alumina having a D10 value, a D50 value, and a D90 value that are each independently of from about 1 to about 200, micrometers, each determined using laser diffraction.
5 . The sorbent of claim 1 wherein said ceramic nanoparticulate cation exchanger is chosen from aluminosilicates, titanosilicates, and combinations thereof.
6 . The sorbent of claim 1 wherein said ceramic nanoparticulate cation exchanger is amorphous titanosilicate (ATS).
7 . The sorbent of claim 1 wherein said ceramic nanoparticulate cation exchanger is crystalline titanosilicate.
8 . The sorbent of claim 1 wherein said core particle is present in an amount of from about 20 to about 80 weight percent based on a total weight percent of said sorbent and said ceramic nanoparticulate cation exchanger is present in an amount of from about 80 to about 20 weight percent based on a total weight percent of said sorbent.
9 . The sorbent of claim 1 wherein said core particle is present in an amount of from about 30 to about 70 weight percent based on a total weight percent of said sorbent and said ceramic nanoparticulate cation exchanger is present in an amount of from about 70 to about 30 weight percent based on a total weight percent of said sorbent.
10 . The sorbent of claim 1 wherein said core particle is present in an amount of from about 40 to about 60 weight percent based on a total weight percent of said sorbent and said ceramic nanoparticulate cation exchanger is present in an amount of from about 60 to about 40 weight percent based on a total weight percent of said sorbent.
11 . The sorbent of claim 1 wherein said core particle is present in an amount of about 50 weight percent based on a total weight percent of said sorbent and said ceramic nanoparticulate cation exchanger is present in an amount of about 50 weight percent based on a total weight percent of said sorbent.
12 . The sorbent of claim 1 wherein the at least one metal is lead,
wherein said core particle is alumina having a D10 value of from about 4 to about 10, a D50 value of from about 10 to about 16, and a D90 value of from about 20 to about 42, micrometers, each determined using laser diffraction;
wherein said ceramic nanoparticulate cation exchanger is amorphous titanosilicate (ATS); and
wherein said core particle is present in an amount of about 50 weight percent based on a total weight percent of said sorbent and said ceramic nanoparticulate cation exchanger is present in an amount of about 50 weight percent based on a total weight percent of said sorbent.
13 . A method of forming a sorbent for at least one metal, said method comprising the steps of:
providing a dispersion of a core particle and a ceramic nanoparticulate cation exchanger for at least one metal in water, and
spray-drying the dispersion to form the sorbent,
wherein the dispersion has a pH of greater than about 9.5,
wherein the ceramic nanoparticulate cation exchanger is disposed about the core particle,
wherein the core particle is chosen from titanium dioxide, alumina, iron oxide, and combinations thereof.
14 . The method of claim 13 wherein the sorbent is free of silica.
15 . The method of claim 13 wherein the ceramic nanoparticulate cation exchanger is chosen from aluminosilicates, titanosilicates, and combinations thereof.
16 . The method of claim 13 wherein the ceramic nanoparticulate cation exchanger is amorphous titanosilicate (ATS).
17 . The method of claim 13 wherein the ceramic nanoparticulate cation exchanger is crystalline titanosilicate.
18 . The method of claim 13 wherein the pH of the dispersion is about 9.6, wherein the dispersion has a viscosity of about 450 to about 500 cP determined at 25° C. using a Brookfield Viscometer, wherein the at least one metal is lead, wherein the core particle is alumina having a D10 value of from about 4 to about 10, a D50 value of from about 10 to about 16, and a D90 value of from about 20 to about 42, micrometers, each determined using laser diffraction; wherein the ceramic nanoparticulate cation exchanger is amorphous titanosilicate (ATS), and wherein the core particle is present in an amount of about 50 weight percent based on a total weight percent of the sorbent and the ceramic nanoparticulate cation exchanger is present in an amount of about 50 weight percent based on a total weight percent of the sorbent.
19 . A water treatment device comprising the sorbent of claim 1 .
20 . A method of treating water comprising at least one metal, said method comprising the step of contacting the water with the sorbent of claim 1 to adsorb the metal from the water onto the sorbent.