Acidic
fracturing fluids, such as zirconium cross-linked carboxymethyl
hydroxypropyl guar gum (CMHPG), can not only adapt to formations treated
with CO2 but also protect such formations from the damage
that arises from the swelling and migration of clay particles during
the hydrofracturing process. However, the shortcomings of uncontrollable
viscosity growth and irreversible shear-thinning behavior limit the
large-scale application of acidic fracturing fluids. In this work,
a novel organic zirconium cross-linker was synthesized in the laboratory
and applied under acidic conditions to control and delay cross-linking
reactions. The ligands that were coordinated to the zirconium center
were l-lactate and ethylene glycol. A CMHPG thickener was
used at a low loading of 0.3% (approximately 25 pptg). Concentrated
hydrochloric acid was utilized as a buffer to adjust the fracturing
fluid pH to 3.0 for the majority of the tests and approximately simulate
the pH attained in formations treated with CO2 under high-temperature
(HT)/high-pressure (HP) conditions. Moreover, surface-functionalized
metallic-phase (1T) molybdenum disulfide (MoS2) nanosheets
were employed to improve the rheological performance of the zirconium
cross-linked CMHPG fracturing fluid. l-Cysteine was utilized
as a modification reagent. The morphologies, structures, and properties
of the fabricated functionalized 1T-MoS2 (Cys-1T-MoS2) nanosheets were systematically characterized using transmission
electron microscopy (TEM), scanning electron microscopy (SEM), Raman
spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy
(XPS), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric
analysis (TGA). The results of these characterization tests demonstrated
the successful functionalization of the 1T-MoS2 nanosheets
with l-cysteine. Then, the effects of this new nanosheet-enhanced
zirconium cross-linked CMHPG fracturing fluid system with different
cross-linker and nanosheet loadings on gelation performance were systematically
assessed through the Sydansk bottle testing method combined with a
rheometer under controlled-stress or controlled-rate modes. Microscopic
observations and gel-breaking, regained-permeability, and proppant-settling
tests were also carried out to further evaluate the fracturing fluid
properties of this new system. The results indicated that the nanosheet-enhanced
fracturing fluid had a desirable delayed cross-linking property. Compared
with the blank fracturing fluid (without nanosheet enhancement), the
nanosheet-enhanced fracturing fluid had a much better shear tolerance,
shear recovery, and proppant carrying performance. Micrograph observations
showed that an even and fine three-dimensional (3D) network structure
formed within the nanosheet-enhanced fracturing fluid sample. Additionally,
in contrast to the alkaline system, the acidic nanosheet-enhanced
zirconium cross-linked CMHPG fracturing fluid system had much less
formation damage induced by gel residues and clay swelling and dispersions.