Octanoate grafted graphene oxide as an effective inhibitor against oil well acidizing corrosion

2021 ◽  
Vol 325 ◽  
pp. 115060
Author(s):  
Tawfik A. Saleh ◽  
K. Haruna ◽  
Abdul-Rashid I. Mohammed
2018 ◽  
Vol 916 ◽  
pp. 200-204 ◽  
Author(s):  
Hui Ting Liu ◽  
Jian Zhou Jin ◽  
Yong Jin Yu ◽  
Shuo Qiong Liu

The improvement of strength and ductility is a challenging task for application of oil well cement. As a 2D nanomaterial with high strength and toughness, graphene oxide (GO) was used as a reinforcing additive in oil well cement. The mechanical properties and micro-structure of oil well cement enhanced by GO were investigated. The compressive strength and flexrual strenghth of cement stone both showed a good enhancement effect when the content of GO was 0.02% -0.05%. The compressive strength and flexrual strength could increase by 15.8% and 33.5%, respectively. The results of SEM and MIP revealed that GO played a template role in promoting the formation of hydration products and further filled in the pores between the hydration products, which refined the micro-structure and improved mechanical properties of the cement consequently.


Author(s):  
E. A. Elfont ◽  
R. B. Tobin ◽  
D. G. Colton ◽  
M. A. Mehlman

Summary5,-5'-diphenyl-2-thiohydantoin (DPTH) is an effective inhibitor of thyroxine (T4) stimulation of α-glycerophosphate dehydrogenase in rat liver mitochondria. Because this finding indicated a possible tool for future study of the mode of action of thyroxine, the ultrastructural and biochemical effects of DPTH and/or thyroxine on rat liver mere investigated.Rats were fed either standard or DPTH (0.06%) diet for 30 days before T4 (250 ug/kg/day) was injected. Injection of T4 occurred daily for 10 days prior to sacrifice. After removal of the liver and kidneys, part of the tissue was frozen at -50°C for later biocheailcal analyses, while the rest was prefixed in buffered 3.5X glutaraldehyde (390 mOs) and post-fixed in buffered 1Z OsO4 (376 mOs). Tissues were embedded in Araldlte 502 and the sections examined in a Zeiss EM 9S.Hepatocytes from hyperthyroid rats (Fig. 2) demonstrated enlarged and more numerous mitochondria than those of controls (Fig. 1). Glycogen was almost totally absent from the cytoplasm of the T4-treated rats.


1983 ◽  
Vol 49 (02) ◽  
pp. 081-083 ◽  
Author(s):  
Vittorio Bertelé ◽  
Maria Carla Roncaglioni ◽  
Maria Benedetta Donati ◽  
Giovanni de Gaetano

SummaryIt has recently been reported that heparin neutralizes the inhibitory effect of prostacyclin (PGI2) on human platelet aggregation. The mechanism of this interaction has not yet been unequivocally established. We present here evidence that heparin (Liquemin Roche) does not react directly with PGI2 but counteracts its inhibitory effect by potentiating platelet aggregation. In the absence of heparin, PGI2 was a less effective inhibitor of platelet aggregation induced by the combination of ADP and serotonin than by ADP alone. Moreover, the inhibitory effect of PGI2 was similarly reduced when increasing the concentrations of ADP (in the absence of heparin). The lack of a specific interaction between heparin and PGI2 is supported by the observation that, in the presence of heparin, other prostaglandins such as PGD2 and PGE1, and a non-prostanoid compound such as adenosine also appeared to lose their inhibitory potency. It is concluded that heparin opposes platelet aggregation inhibitory effect of PGI2 by enhancement of platelet aggregation.


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