DOI: 10.1021/acsapm.6c02597 ISSN: 2637-6105

Development and Performance Evaluation of the Nanoparticle-Enhanced Seawater-Based High-Temperature-Resistant Guar Gum Fracturing Fluid System

Xin Li, Mingwei Zhao, Huan Zhang, Lixiao Zhang, Ruiqiong Liu, Xinjie Xu, Zhenfeng Ma, Zhongzheng Xu, Caili Dai

Abstract

To address the problems of low viscosity retention, and insufficient sand-carrying capacity for seawater-based fracturing fluids in deepwater high-temperature reservoirs, this study enhanced the fracturing fluid by adding modified nano-SiO2 (M-NS). A seawater-based, high-temperature-resistant fracturing fluid system was constructed from M-NS and carboxymethyl hydroxypropyl guar gum (CMHPG). The results showed that 3-aminopropyltriethoxysilane (APTES) modification improved, to a certain extent, the dispersion stability and interfacial compatibility of nano-SiO2 (NS) in the seawater-based CMHPG solution. The optimal formulation of the M-NS-enhanced system was 0.4 wt % CMHPG, 0.5 wt % organic zirconium crosslinker, 0.08 wt % M-NS, 0.1 wt % APS, and 0.05 wt % SDS. After shearing at 200 °C and 100 s–1 for 2 h, the retained viscosity was 60.03 mPa·s, which was 1.42 times that of the conventional system. At 95 °C, no proppant settling was observed at sand ratios of 10%, 20%, and 30%. In addition, the fracturing fluid exhibited favorable breaking and flowback performance, dynamic leak off control performance, and formation-damage performance. Investigation of the high-temperature-resistance mechanism revealed that the M-NS-enhanced fracturing fluid system demonstrated excellent viscosity recovery and nonlinear elastic response under large strain. This improvement is attributed to the formation of physical crosslinking through hydrogen bonding between the −NH2 on the M-NS surface and the hydroxyl and carboxymethyl groups on the polymer chains. This physical crosslinking mechanism likely synergizes with the organic zirconium chemical crosslinking to construct a dual-network structure. Moreover, M-NS is uniformly dispersed in the CMHPG base fluid, acting as rigid nucleation points and a skeleton. Consequently, the network skeleton of the enhanced gel is significantly thickened, and the structure of the gel is enhanced. This study provides a seawater-based, high-temperature-resistant guar gum fracturing fluid system for deepwater and ultra-deepwater high-temperature reservoirs, demonstrating significant engineering application potential.