Description: Gas production from gas hydrate-bearing sediments has been attracting global interests because of its potential to meet growing energy demand. Methane (CH4) gas can be extracted from CH4 hydrates by depressurization, thermal stimulation or chemical activation. However, it has never been produced on a commercial scale and the past field trials faced premature termination due to the technical difficulties such as excessive sand flow into the well, a phenomenon known as sand production. One exception is the trial at the Ignik Sikumi, Alaska in 2012, which was conducted by chemical activation followed by depressurization. During the trial, initial sand production ceased after two weeks while CH4 gas production continued for five weeks. The mitigation of sand production is deemed attributed to mechanical or hydraulic effects through formation of CO2-rich gas hydrates. This incident has highlighted the favorable effect of CO2 hydrate formation and needs to incorporate the chemo-processes into existing thermo-hydro-mechanical formulations. This paper presents an analytical formulation to capture the coupled thermo-hydro-chemo-mechanical behavior of gas hydrate-bearing sediments during gas production via CO2 injection. The key features of the formulation include hydrate formation and dissociation, gas dissolution and multiphase flow for both CH4 and CO2, facilitating CH4-CO2 hydrate conversion.

Description: Due to its remoteness, the deep-sea floor remains an understudied ecosystem of our planet. The patchiness of existing data sets makes it difficult to draw conclusions about processes that apply to a wider area. In our study we show how different settings and processes determine sediment heterogeneity on small spatial scales. We sampled solid phase and porewater from the upper 10 m of an approximately 7.4×13 km2 area in the Peru Basin, in the southeastern equatorial Pacific Ocean, at 4100 m water depth. Samples were analyzed for trace metals, including rare earth elements and yttrium (REY), as well as for particulate organic carbon (POC), CaCO3, and nitrate. The analyses revealed the surprisingly high spatial small-scale heterogeneity of the deep-sea sediment composition. While some cores have the typical green layer from Fe(II) in the clay minerals, this layer is missing in other cores, i.e., showing a tan color associated with more Fe(III) in the clay minerals. This is due to varying organic carbon contents: nitrate is depleted at 2–3 m depth in cores with higher total organic carbon contents but is present throughout cores with lower POC contents, thus inhibiting the Fe(III)-to-Fe(II) reduction pathway in organic matter degradation. REY show shale-normalized (SN) patterns similar to seawater, with a relative enrichment of heavy REY over light REY, positive LaSN anomaly, negative CeSN anomaly, and positive YSN anomaly and correlate with the Fe-rich clay layer and, in some cores, also correlate with P. We therefore propose that Fe-rich clay minerals, such as nontronite, as well as phosphates, are the REY-controlling phases in these sediments. Variability is also seen in dissolved Mn and Co concentrations between sites and within cores, which might be due to dissolving nodules in the suboxic sediment, as well as in concentration peaks of U, Mo, As, V, and Cu in two cores, which might be related to deposition of different material at lower-lying areas or precipitation due to shifting redox boundaries.