Abstract

A regenerable polyvinyl alcohol/organic boron fracturing fluid system with 1.6 wt% polyvinyl alcohol (PVOH) and 1.2 wt% organic boron (OBT) was studied, and its main regeneration mechanism is the reversible cross-linking reaction between B(OH)4 - and hydroxyl groups of PVOH as the change of pH. Results of rheology evaluations show that both the apparent viscosity and the thermal stability of the fracturing fluid decreased with the regeneration number of times increasing. In addition, the apparent viscosity of the fluid which was without regeneration was more sensitive to the shear action compared with that of the fluid with regeneration once or twice. When the fracturing fluid was without regeneration, the elasticity was dominating due to the three-dimensional network structure of the formed gel; the viscosity gradually occupied the advantage when the fracturing fluid was regenerated once or twice. The settling velocity of proppant was accelerated by both the regeneration process and the increasing temperature, but it was decelerated when the proppant ratio increased. Results of core damage tests indicate that less permeability damage was caused by the PVOH/OBT fracturing fluid compared with that caused by the guar gum fracturing fluid after gel breaking.

Highlights

  • Hydraulic fracturing is a favorable technique applied to the productivity improvement of oilwells located in reservoirs with the characteristics of low porosity and poor permeability

  • The present study described a regenerable polyvinyl alcohol/organic boron (PVOH/organic borate cross-linker (OBT)) fracturing fluid

  • A main purpose of this study is to develop a regenerable fracturing fluid system with favorable rheological properties and environmental-friendly performances

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Summary

Introduction

Hydraulic fracturing is a favorable technique applied to the productivity improvement of oilwells located in reservoirs with the characteristics of low porosity and poor permeability. When the (NH4)2S2O8 is added into the fracturing fluid, the H+ concentration increases and it contributes to the reverse reaction shown, i.e., the cross-linked PVOH/OBT gel structure is broken under acidic conditions.

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