4 research outputs found
Systematic Study of Nanohybrids of ZnO Nanoparticles toward Enhancement of Gas Hydrate Kinetics and the Application in Energy Storage
The search for efficient storage
and transportation systems
of
natural gas has led to the exploration of gas hydrate-based technologies
as a potential solution. The gas hydrate formation and development
have a propensity for occurrence under suitable conditions. The enhancement
in the hydrate growth kinetics through the usage of surfactants was
attributed to the enhanced heat and mass transfer, reactor design,
and ability of surfactants to promote the formation of hydrate crystals
but limited as a result of the generation of foam during the process
of hydrate dissociation. Apart from surfactants, studies emphasized
the utilization of selected nanoparticles as additives as a result
of the reduced nucleation barrier and improved heat transfer characteristics.
To establish the versatility of the observed behavior in the case
of reported nanoparticles, there is a requirement to launch a systematic
study focusing particularly on the chemical alterations of nanoparticles
and their impact on hydrate growth. Therefore, this study aims to
investigate the growth kinetics of methane hydrate formation by surfactant-modified
nanoparticles as nanohybrids and their synergistic effects. Zinc oxide
nanoparticles (ZnO NPs) were produced in the presence of sodium dodecyl
sulfate (SDS) and polyvinylpyrrolidone stabilizers, which are generally
known to enhance and reduce the pace of hydrate formation, respectively.
The comparative morphological study was conducted to visualize the
gas hydrate growth of all of the additive systems. The gas hydrate
yield reached its maximum level with minimal foam production when
0.5 wt % ZnO nanohybrids (with SDS) were used, thus surpassing the
methane gas hydrate promotion observed with SDS alone. Moreover, for
industrial applicability, the selected nanohybrids used for methane
gas hydrate formation were further tested with natural gas to investigate
the kinetic as well as gas hydrate storage behavior. Additionally,
for techno-commercial purposes, the reuse and recovery of ZnO NPs
was demonstrated
Systematic Study of Nanohybrids of ZnO Nanoparticles toward Enhancement of Gas Hydrate Kinetics and the Application in Energy Storage
The search for efficient storage
and transportation systems
of
natural gas has led to the exploration of gas hydrate-based technologies
as a potential solution. The gas hydrate formation and development
have a propensity for occurrence under suitable conditions. The enhancement
in the hydrate growth kinetics through the usage of surfactants was
attributed to the enhanced heat and mass transfer, reactor design,
and ability of surfactants to promote the formation of hydrate crystals
but limited as a result of the generation of foam during the process
of hydrate dissociation. Apart from surfactants, studies emphasized
the utilization of selected nanoparticles as additives as a result
of the reduced nucleation barrier and improved heat transfer characteristics.
To establish the versatility of the observed behavior in the case
of reported nanoparticles, there is a requirement to launch a systematic
study focusing particularly on the chemical alterations of nanoparticles
and their impact on hydrate growth. Therefore, this study aims to
investigate the growth kinetics of methane hydrate formation by surfactant-modified
nanoparticles as nanohybrids and their synergistic effects. Zinc oxide
nanoparticles (ZnO NPs) were produced in the presence of sodium dodecyl
sulfate (SDS) and polyvinylpyrrolidone stabilizers, which are generally
known to enhance and reduce the pace of hydrate formation, respectively.
The comparative morphological study was conducted to visualize the
gas hydrate growth of all of the additive systems. The gas hydrate
yield reached its maximum level with minimal foam production when
0.5 wt % ZnO nanohybrids (with SDS) were used, thus surpassing the
methane gas hydrate promotion observed with SDS alone. Moreover, for
industrial applicability, the selected nanohybrids used for methane
gas hydrate formation were further tested with natural gas to investigate
the kinetic as well as gas hydrate storage behavior. Additionally,
for techno-commercial purposes, the reuse and recovery of ZnO NPs
was demonstrated
Systematic Study of Nanohybrids of ZnO Nanoparticles toward Enhancement of Gas Hydrate Kinetics and the Application in Energy Storage
The search for efficient storage
and transportation systems
of
natural gas has led to the exploration of gas hydrate-based technologies
as a potential solution. The gas hydrate formation and development
have a propensity for occurrence under suitable conditions. The enhancement
in the hydrate growth kinetics through the usage of surfactants was
attributed to the enhanced heat and mass transfer, reactor design,
and ability of surfactants to promote the formation of hydrate crystals
but limited as a result of the generation of foam during the process
of hydrate dissociation. Apart from surfactants, studies emphasized
the utilization of selected nanoparticles as additives as a result
of the reduced nucleation barrier and improved heat transfer characteristics.
To establish the versatility of the observed behavior in the case
of reported nanoparticles, there is a requirement to launch a systematic
study focusing particularly on the chemical alterations of nanoparticles
and their impact on hydrate growth. Therefore, this study aims to
investigate the growth kinetics of methane hydrate formation by surfactant-modified
nanoparticles as nanohybrids and their synergistic effects. Zinc oxide
nanoparticles (ZnO NPs) were produced in the presence of sodium dodecyl
sulfate (SDS) and polyvinylpyrrolidone stabilizers, which are generally
known to enhance and reduce the pace of hydrate formation, respectively.
The comparative morphological study was conducted to visualize the
gas hydrate growth of all of the additive systems. The gas hydrate
yield reached its maximum level with minimal foam production when
0.5 wt % ZnO nanohybrids (with SDS) were used, thus surpassing the
methane gas hydrate promotion observed with SDS alone. Moreover, for
industrial applicability, the selected nanohybrids used for methane
gas hydrate formation were further tested with natural gas to investigate
the kinetic as well as gas hydrate storage behavior. Additionally,
for techno-commercial purposes, the reuse and recovery of ZnO NPs
was demonstrated
Study of the genetic structure of a Brassica napus canola population derived from six interspecific crosses of B. napus B. oleracea
Broadening the genetic base of the C genome of Brassica napus canola is needed for continued improvement of this crop. For this, we developed few hundred canola lines from B. napus B. oleracea interspecific crosses involving a B. napus canola line and six B. oleracea accessions belonging to four varieties, viz. vars. alboglabra, botrytis, capitata and italica, and following two breeding methods (F2- and BC1 (F1 B. napus)-derived lines). The objective of this study was to understand the genetic structure of this population regarding the alleles introgressed from B. oleracea by using SSR markers, and to investigate the inheritance of B. oleracea alleles in these re-constituted canola lines. Marker analysis showed that the four B. oleracea varieties were genetically quite distinct. Several canola lines derived from these six crosses tended to group together with their B. oleracea parent demonstrating that the wide diversity of the B. oleracea gene pool can be exploited for broadening the genetic base of the C genome of B. napus canola. Loss of several B. oleracea alleles occurred during the development of these inbred lines. While comparing the two breeding methods for introgression of B. oleracea alleles, significantly greater loss of alleles occurred in the F2-derived population as compared to the BC1-derived population. Thus, the knowledge from this study can be used for efficient introgression of exotic alleles from B. oleracea into B. napus for broadening the genetic base of this crop.The presentation of the authors' names and (or) special characters in the title of the pdf file of the accepted manuscript may differ slightly from what is displayed on the item page. The information in the pdf file of the accepted manuscript reflects the original submission by the author
