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Performance of Conformance Gels Under Harsh Conditions

机译:苛刻条件下一致性凝胶的性能

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Permeability reduction provided by conventional polymer gels is affected by harsh reservoir conditions. Harsh conditions are defined by high temperature (> 75°C), high salinity, high divalent ions and the presence of H2S. Polymer gels undergo syneresis when exposed to high salinity and hardness reservoir brines. We evaluated conventional polyacrylamide-based polymer (HPAM)-gels and other modified HPAM- gels with molecular weights between 2-20MM Daltons for gelation time and long-term gel stability under harsh conditions. In addition to polymer degradation, the cross-linkers are also sensitive to harsh reservoir conditions. Specifically, H2S can consume cross-linkers and inhibit gelation. The cross-linkers tested were Chromium (III) Acetate and Chevron Unogel formulation consisting of a combination of hexamethylenetetramine (HMTA) and hydroquinone (HQ). High performing gels were tested for sensitivity to high salinity brines and H2S in a limited number of experiments. The gels were observed for gel strength, and syneresis with time. The goal of our work was to identify a combination of polymer and cross-linker that would provide effective conformance under harsh conditions. Sulfonated polyacrylamide (ATBS) polymers were found to provide better resistance to high salinity/ hardness brines than partially hydrolyzed polyacrylamides in high temperature conditions. The addition of hydrophobic groups to the sulfonated-acrylamide backbone does not increase the hardness tolerance of the polymer. Higher concentration, low molecular weight sulfonated polymers are recommended for use at high temperature and salinity. Polymer gels made with 2MM Dalton polymer show less syneresis with time compared to higher molecular weight polymer at the same polymer concentration. HMTA/HQ ATBS polymer gels are preferable to chromium (III) ATBS polymer gel for high temperature and salinity conditions. Chromium (III) ATBS polymer gels show more susceptibility to syneresis compared to organic crosslinked gels at same polymer concentration. HMTA/HQ crosslinker is ineffective in the presence of hydrogen sulfide. Gelants consisting of HMTA/HQ do not mature into rigid gels after 14 days of exposure to sour gas. Preformed HMTA/HQ gels lose strength upon exposure to sour crude. This is mostly due to HMTA ability as a sour gas/crude sweetener. Chromium (III) gels form weak gels in the presence of sour gas. Chromium competes with sulfide ions to produce insoluble chromium sulfide leading to consumption of crosslinker and poor gelation. Malonate and tartrate are effective gel retardants for chromium (III) polymer gels. Malonate is better at extending onset of gelation for longer periods of time. Tartrate is more effective for shorter gelation time at lower concentrations.
机译:通过常规的聚合物凝胶提供渗透性的减少是通过苛刻贮存条件的影响。恶劣的条件下通过高温(> 75℃),高盐度,高的二价离子和H 2 S的存在限定。当暴露于高盐度和硬度贮存盐水聚合物凝胶经历脱水收缩。我们评估了常规的基于聚丙烯酰胺的聚合物(HPAM)-gels并用2-20MM道尔顿之间的分子量为在恶劣条件下凝胶化的时间和长期凝胶稳定性其它修饰HPAM-凝胶。除了聚合物降解,所述交联剂是也恶劣储层条件敏感。具体地,H 2 S可以消耗交联剂和抑制凝胶化。测试的交联剂是铬(III)乙酸盐和Chevron Unogel制剂选自由六亚甲基四胺(HMTA)和氢醌(HQ)的组合。高执行凝胶在实验有限数量的高盐度的盐水和H 2 S的敏感性进行测试。观察到对于凝胶强度,并随着时间的脱水收缩的凝胶。我们工作的目标是确定聚合物和交联剂的组合,将提供恶劣条件下有效的一致性。发现磺化聚丙烯酰胺(ATBS)聚合物,以提供高盐度/硬度盐水更好电阻比在高温条件下部分水解的聚丙烯酰胺。将疏水性基团与磺化 - 丙烯酰胺主链不增加聚合物的硬度耐受性。浓度较高时,低分子量的磺化聚合物被推荐用于在高温和盐度使用。与2MM道尔顿制成的聚合物凝胶聚合物显示出与相比在相同的聚合物浓度较高分子量的聚合物的时间少的脱水收缩。 HMTA / HQ ATBS聚合物凝胶是优选的铬(III)ATBS用于高温和盐度条件聚合物凝胶。铬(III)ATBS聚合物凝胶表现出更多的易感性脱水收缩相比在相同的聚合物浓度的有机交联的凝胶。 HMTA / HQ交联剂是在硫化氢存在下是无效的。由HMTA / HQ的Gelants后暴露于酸性气体的14天内不成熟为刚性凝胶。预制HMTA / HQ胶凝暴露于高硫原油失去力量。这主要是由于HMTA能力作为酸性气体/粗甜味剂。铬(III)的凝胶形成的酸性气体的存在弱凝胶。与硫化物离子铬竞争以生成不溶性的铬硫化物导致交联剂和凝胶化较差的消耗。丙二酸盐和酒石酸盐是铬(III)的聚合物凝胶有效凝胶阻燃剂。丙二酸二乙酯是在发病凝胶的延长更长的时间更好。酒石酸盐是在较低浓度下更短的胶凝时间更有效。

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