New polymers that are stable in harsh environments (high salinity/hardness and high temperature) are in high demand because of the need for chemical EOR in oil reservoirs with these conditions. Commonly used partially hydrolyzed polyacrylamides (HPAM) have been successfully used in the field for decades, but they hydrolyze at high temperature and eventually precipitate in the presence of high concentrations of divalent cations. This paper mainly focuses on rheology and transport behavior of scleroglucan (non-ionic polysaccharide) and N-vinylpyrrolidone (NVP)-polyacrylamide (AM) co-polymer. The rigid, rod-like, triple helical structure of scleroglucan imparts exceptional stability and its non-ionic functionality makes it insensitivity to salinity and hardness. By a different mechanism, NVP in modified HPAM protects the polymer's amide group against thermal hydrolysis, i.e., by sterically hindering the amide group. This allows maintaining high viscosity even in high salinity brines at high temperature. Both scleroglucan and NVP co- or ter-polymers show good filterability and transport properties in sandstone and carbonate cores at high temperature and in brine with high salinity and hardness. Therefore, both polymers are promising candidates for polymer flooding, surfactant-polymer flooding and alkali-surfactant-polymer flooding in hard brine at high temperature, but must be evaluated under specific reservoir conditions.

A photoresponsive oil sorber (POS) with a hydrophobic, photoresponsive core and shell has been synthesized via suspension polymerization. Lauryl acrylate, isodecyl acrylate, and tert‐butylstyrene were used as monomers, 4‐(methacrylamino)azobenzene (Azo‐M) used as photoresponsive monomer, and bis(methacryloylamino)azobenzene (Azo‐CL‐M) used as photoresponsive surface crosslinker. The POS prefers nonpolar solvents. It absorbed 15 times its dry weight in toluene, 19 times its dry weight in chloroform, and 16 times its dry weight in dichloromethane. Rapid and photoresponsive desorption of solvent (86% of solvent expulsed in 30 min) was characteristic. POS is an excellent gasoline absorber rapidly increasing its body weight in its presence. The new POS is less dense than water, and can potentially be used for cleaning oil spills on water. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 55–62, 2010

Chemical EOR can be a very efficient enhanced oil recovery method when properly designed, but specialized laboratory tests must be done to tailor it to the specific reservoir fluids and mineralogy. The final step in the laboratory evaluation process is to test the chemicals in reservoir cores under reservoir conditions. Unfortunately, available reservoir cores are typically not in their native state. In particular, they are usually in a highly oxidized state (high E h ) compared to the reservoir formation. The oxidation state of the minerals affects the surfactants and polymers used for chemical EOR. In particular, at high E h some of the iron-containing minerals may have surficial ferric ions that were originally ferrous under the low E h conditions in the reservoir. Ferric ions can cause polymer degradation, poor polymer transport, and increased surfactant adsorption to the matrix, among other problems contributing to lower oil recovery. In general, to obtain valid test results, such cores must be restored to reservoir conditions to ensure valid results from core floods. We have investigated methods suitable for removing these ferric ions and restoring the core to reservoir condition. The new restoration method described in this paper dramatically improved polymer transport, reduced polymer and surfactant retention, and improved the oil recovery performance by the chemicals in several core floods. It should also be considered for other types of core floods to avoid getting laboratory results that are not representative of the behavior in the actual reservoir, which is in a reduced oxidation state compared to old cores.

Stimuli responsive hydrogels (PNIPAAm‐MSp) with a thermoresponsive backbone and photochromic pendant groups were synthesized via free radical polymerization using N‐isopropylacrylamide, modified spironaphthoxazines with a polymerizable double bond (MSp) as photochromic monomer, the crosslinker N,N′‐methylenebis(acrylamide) and the initiator 2,2′‐azobis(isobutyronitrile) in dimethylsulfoxide. The polymers are dual responsive, in that poly(N‐isopropylacrylamide) (PNIPAAm) responds to temperature changes whereas the pendant spironaphthoxazines respond to light. Irradiation enhanced the water absorption of the polymers while increases in temperature decreased it. The irradiated PNIPAAm‐MSp showed best water absorption at 0 °C (Q = 3.25) while water desorbed at higher temperatures (35 °C; Q = 0.30); where Q is the amount of water absorbed by a gram of dry polymer. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3318–3325, 2009

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