Polyallylamine derivatives including 10 to 450 structural units represented by Formula (1):

##STR00001##

are useful for preparing dispersants, treated particles, particle-containing compositions, pigment-containing compositions, paints, ink compositions, liquid developers, and anti-blocking agents.

Polyallylamine derivatives including 10 to 450 structural units represented by Formula (1):

##STR00001##

are useful for preparing dispersants, treated particles, particle-containing compositions, pigment-containing compositions, paints, ink compositions, liquid developers, and anti-blocking agents.

A composition for enhancing fluid viscosity including a mixture of at least one cationic or cationizable polymer and at least one anionic or anionizable (hydrolysable) polymer. The composition has a zeta potential at 25° C. in the range of 0.5 to 100 mV or −0.5 to −100 mV, typically 1 to 60 mV or −1 to −60 mV, or is a precursor convertible at a temperature of 100 to 250° C. to the composition having a zeta potential at 25° C. of 0.5 to 100 mV or −0.5 to −100 mV, typically 1 to 60 mV or −1 to −60 mV. Typically the compositions exhibit salt tolerance and interaction of both polymers at very high temperatures (>300° F.) such that the system exhibits an increase of viscosity at extreme temperatures. The compositions are useful for hydraulic fracturing, enhanced oil recovery, subterranean acidization, personal care as well as home and industrial cleaners.

A composition for enhancing fluid viscosity including a mixture of at least one cationic or cationizable polymer and at least one anionic or anionizable (hydrolysable) polymer. The composition has a zeta potential at 25° C. in the range of 0.5 to 100 mV or −0.5 to −100 mV, typically 1 to 60 mV or −1 to −60 mV, or is a precursor convertible at a temperature of 100 to 250° C. to the composition having a zeta potential at 25° C. of 0.5 to 100 mV or −0.5 to −100 mV, typically 1 to 60 mV or −1 to −60 mV. Typically the compositions exhibit salt tolerance and interaction of both polymers at very high temperatures (>300° F.) such that the system exhibits an increase of viscosity at extreme temperatures. The compositions are useful for hydraulic fracturing, enhanced oil recovery, subterranean acidization, personal care as well as home and industrial cleaners.

Resin particles include mother particles containing a biodegradable resin and a plasticizer, in which an amount of a metal element having an ionic valence of 2 or more, obtained by fluorescent X-ray analysis, is 0.002% by mass or more and 2.0% by mass or less with respect to a total amount of the resin particles.

Resin particles include mother particles containing a biodegradable resin and a plasticizer, in which an amount of a metal element having an ionic valence of 2 or more, obtained by fluorescent X-ray analysis, is 0.002% by mass or more and 2.0% by mass or less with respect to a total amount of the resin particles.

Resin particles include mother particles containing a biodegradable resin and a plasticizer, in which an amount of a metal element having an ionic valence of 2 or more, obtained by fluorescent X-ray analysis, is 0.002% by mass or more and 2.0% by mass or less with respect to a total amount of the resin particles.

In a method for controlling shrinkage of a composite, a dried hydrophobically modified cellulose-based fiber is exposed to a slow acting resin system having a first curing time. An excess amount of the slow acting resin system is removed to separate out the pre-wetted hydrophobically modified cellulose-based fiber. The pre-wetted hydrophobically modified cellulose-based fiber is mixed with a fast acting resin system to form a mixture. The fast acting resin system has a second curing time that is less than the first curing time. The mixture is molded at a predetermined temperature. The fast acting resin system is cured prior to the slow acting resin system, and the slow acting resin system flows into free space within the curing fast acting resin system prior to the slow acting resin system being cured.

In a method for controlling shrinkage of a composite, a dried hydrophobically modified cellulose-based fiber is exposed to a slow acting resin system having a first curing time. An excess amount of the slow acting resin system is removed to separate out the pre-wetted hydrophobically modified cellulose-based fiber. The pre-wetted hydrophobically modified cellulose-based fiber is mixed with a fast acting resin system to form a mixture. The fast acting resin system has a second curing time that is less than the first curing time. The mixture is molded at a predetermined temperature. The fast acting resin system is cured prior to the slow acting resin system, and the slow acting resin system flows into free space within the curing fast acting resin system prior to the slow acting resin system being cured.

Disclosed herein are aqueous coating compositions containing an anionically stabilized polymer, one or more derivatized polyamines, and a volatile base. Coating compositions can further include one or more additional copolymers, which may or may not be anionically stabilized, and/or additional additives, including pigments, defoamers, pigment dispersing agents, thickeners, surfactants, and combinations thereof. By incorporating a derivatized polyamine, such as an alkoxylated polyamine, the setting time of the coating compositions can be decreased. Also provided are coatings formed from the coating compositions described herein, as well as methods of forming these coatings.