Methods may include contacting a degradable polymer in a wellbore traversing a subterranean formation with a treatment fluid, wherein the treatment fluid is formulated with one or more polymer degrading catalysts; and allowing the degradable polymer composite to at least partially degrade. In another aspect, methods may be directed to designing a wellbore treatment that includes determining at least one degradation characteristic for one or more degradable polymers; formulating an aqueous treatment fluid based on the determined values, wherein the aqueous treatment fluid comprises one or more polymer degrading catalysts; contacting the degradable polymer with an aqueous fluid; and allowing the degradable polymer to at least partially degrade the degradable polymer.

The present invention relates to a process for modifying a layered double hydroxide (LDH), the process comprising, a. providing a water-wet layered double hydroxide of formula:
[M.sup.z+.sub.1-xM.sup.y+.sub.x(OH).sub.2].sup.a+(X.sup.n).sub.a/r.bH.sub.2O(1) wherein M and M are metal cations, z=1 or 2; y=3 or 4, x is 0.1 to 1, preferably x<1, more preferably x=0.1-0.9, b is 0 to 10, X is an anion, r is 1 to 3, n is the charge on the anion X and a is determined by x, y and z, preferably a=z(1x)+xy2; b. maintaining the layered double hydroxide water-wet, and c. contacting the water-wet layered double hydroxide with at least one solvent, the solvent being miscible with water and preferably having a solvent polarity (P) in the range 3.8 to 9,
as well as to a layered double hydroxide prepared according to that process.

The present invention relates to a process for modifying a layered double hydroxide (LDH), the process comprising, a. providing a water-wet layered double hydroxide of formula:
[M.sup.z+.sub.1-xM.sup.y+.sub.x(OH).sub.2].sup.a+(X.sup.n).sub.a/r.bH.sub.2O(1) wherein M and M are metal cations, z=1 or 2; y=3 or 4, x is 0.1 to 1, preferably x<1, more preferably x=0.1-0.9, b is 0 to 10, X is an anion, r is 1 to 3, n is the charge on the anion X and a is determined by x, y and z, preferably a=z(1x)+xy2; b. maintaining the layered double hydroxide water-wet, and c. contacting the water-wet layered double hydroxide with at least one solvent, the solvent being miscible with water and preferably having a solvent polarity (P) in the range 3.8 to 9,
as well as to a layered double hydroxide prepared according to that process.

A novel mixed metal molybdate useful as a hydroprocessing catalyst has been created. The hydroprocessing using the novel mixed metal molybdate material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

A hydroprocessing catalyst has been developed. The catalyst is a unique transition metal tungsten oxy-hydroxide material. The hydroprocessing using the transition metal tungsten oxy-hydroxide material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

A hydroprocessing catalyst has been developed. The catalyst is a unique crystalline ammonia transition metal molybdotungstate material. The hydroprocessing using the crystalline ammonia transition metal molybdotungstate material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

A hydroprocessing catalyst has been developed. The catalyst is a unique transition metal tungstate material. The hydroprocessing using the crystalline transition metal molybdotungstate material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

A catalytic converter includes a catalyst. The catalyst includes a supporting oxide layer. The catalyst also includes platinum group metal (PGM) particles partially embedded in the supporting oxide layer such that a portion of each PGM particle is surrounded by the supporting oxide layer and an other portion of each PGM particle remains exposed.

The invention relates to a process for the metathesis of olefins implemented with a catalyst comprising a mesoporous matrix and at least the elements molybdenum and aluminium, said elements being incorporated into said matrix by means of at least one precursor comprising molybdenum and aluminium.

The invention relates to a process for the metathesis of olefins implemented with a catalyst comprising a mesoporous matrix and at least the elements molybdenum and aluminium, said elements being incorporated into said matrix by means of at least one precursor comprising molybdenum and aluminium.