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The effects of biosurfactants on gas hydrate formation in ocean sediments.

机译:生物表面活性剂对海洋沉积物中天然气水合物形成的影响。

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Recent discoveries of extensive gas hydrates in ocean sediments around the world center attention of researchers on vast amounts of natural gases and greenhouse gases in those hydrates. The extent of the discoveries were unexpected and inexplicable. In response to the discoveries, this research investigated the possible effect of microbial activities in promoting gas hydrate formation.; The critical micellar concentration (CMC) of rhamnolipid in distilled water at ambient conditions was found to be 1000 ppm by capillary surface tension measurement, but the value dropped drastically to 89 ppm at hydrate forming conditions. In seawater at ambient conditions, rhamnolipid was found to have a CMC as low as 400 ppm; it was estimated that the CMC drops to 36 ppm at hydrate-forming conditions.; At the CMC, hydrate formation was found to be greatly enhanced, determined by reduced induction time. Induction time in a sandpack was reduced from more than 100 hours for distilled water to 2 hours at the rhamnolipid CMC. Rhamnolipid in seawater also demonstrated very low induction times. This finding helps explain the occurrence of vast amounts of hydrates in ocean sediments.; Sodium dodecyl sulfate (SDS) and rhamnolipid at concentrations at or above CMC were found to generate micelles, solubilize gas, and to cause gas-laden micelles to rapidly migrate through a sandpack. This finding helps explain the connection of hydrates in a hydrate zone with activity outside the zone. Hydrate formation rate in a sandpack saturated with seawater increased 51% at the rhamnolipid CMC.; The results show that hydrate formation can be enhanced in sandpacks at very low biosurfactant concentrations (9 ppm for 100% active solution), which suggest that minimal microbial activity in ocean sediments could catalyze hydrate formation.
机译:最近在世界各地海洋沉积物中发现大量天然气水合物的发现,集中了研究人员对这些天然气水合物中大量天然气和温室气体的关注。发现的程度是出乎意料且无法解释的。针对这些发现,本研究调查了微生物活动在促进天然气水合物形成中的可能作用。通过毛细管表面张力测量发现,在室温下蒸馏水中鼠李糖脂的临界胶束浓度(CMC)为1000 ppm,但在水合物形成条件下,该值急剧下降至89 ppm。在环境条件下的海水中,鼠李糖脂的CMC值低至400 ppm。据估计,在水合物形成条件下,CMC降至36 ppm。在CMC处,发现水合物的形成大大增强,这取决于减少的诱导时间。在鼠李糖脂CMC中,沙袋中的诱导时间从蒸馏水的100多小时减少到2小时。海水中鼠李糖脂的诱导时间也很短。这一发现有助于解释海洋沉积物中大量水合物的发生。发现十二烷基硫酸钠(SDS)和鼠李糖脂的浓度等于或高于CMC会产生胶束,溶解气体,并导致载有气体的胶束快速通过沙袋。这一发现有助于解释水合物区域中水合物与该区域外部活性之间的联系。在鼠李糖脂CMC中,充满海水的沙袋中的水合物形成率增加了51%。结果表明,在非常低的生物表面活性剂浓度(100%活性溶液为9 ppm)下,沙袋中的水合物形成可以得到增强,这表明海洋沉积物中的最小微生物活性可以催化水合物的形成。

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