Hydrostatic Pressure
This pressure is equal in all directions and acts perpendicular to any surface within the fluid.
Hydrostatic pressure is an important factor in numerous scientific and engineering applications, including the design of hydraulic systems, the study of biological processes, and the analysis of geological formations.
Understanding the principles of hydrostatic pressure is crucial for optimizing research protocols and enhancing the reproducibility of experiments in these fields.
PubCompare.ai's AI-driven platform can help researchers locate the best protocols from literature, pre-prints, and patents, as well as improve their research outcomes through intelligent comparisons and analysis of hydrostatic pressure experiments.
Most cited protocols related to «Hydrostatic Pressure»
The hydrostatic pressure of the urinary solution in the funnel pushes the solvent (water) through the mesh of dialysis membrane (filtration), together with all the analytes below the selected MWCO. After the first step resulting in sample concentration, the separating funnel was refilled with 200 ml of deionised filtrate (0.22 µm) water (R ≥ 18.2 MΩ·cm, mQ water) to rinse away remaining analytes below the MWCO until the volume of 5–8 ml of volume is reached. This filtration-concentration-dialysis process is called “hydrostatic filtration dialysis” (HFD).
HFD and differential centrifugation:The retained solution above the 1,000 kDa cut-off (HFDa) (5 ml) was then centrifuged at 5,000 g, 20,000 g and/or 40,000 g calculated at maximum radius 105 mm of a fixed angle JA-20 rotor (clearing factor or k factor = 770) (Beckman Coulter, Fullerton, Ca) for 1 h at RT. The retained 40,000 g supernatant (SN) fraction (5 ml) was then ultracentrifuged at 200,000 g calculated at maximum radius 91.9 mm of 70 Ti fixed-angle rotor (k factor = 44) (Beckman Coulter) for 2 h (RT) using a Beckman XL-80 Ultracentrifuge (Beckman Coulter). All the pellets were re-suspended in mQ water. For a pilot study, HFDa from the starting urinary volumes of 15, 50, 100 and 200 ml were concentrated to 3 ml. After determining the protein concentration, an equal amount of total protein was loaded in polycarbonate centrifugation tubes (3 ml). Ultracentrifugation was performed at 200,000 g calculated at the maximum radius 82.0 mm of 70.1Ti fixed-angle rotor (k factor = 36) (Beckman Coulter) for 2 h at RT.
Differential centrifugation and HFD: Comparative analysis was performed according to Fernández-Llama and colleagues15 (link). Pellets from 2,000 g and 17,000 g were resuspended in 10 ml of 250 mM sucrose, 10 mM triethanolamine pH7.6 and 200 mg/ml of DTT for 10 minutes at 37°C vortexing every 2 minutes. Centrifugations at 17,000 g (42 ml per tube of urine and 10 ml of dithiothreitol (DTT) fraction) were performed in a fixed angle JA-20 rotor (clearing factor or k factor = 770) (Beckman Coulter) for 30 min at RT. RCF were calculated at average radius of 70 mm. Ultracentrifugations (16,5 ml urine per tube and 10 ml of DTT fraction) were performed at 200,000 g calculated at maximum radius 91.9 mm of 70 Ti fixed-angle rotor (k factor = 44) (Beckman Coulter) for 2 h (RT) using a Beckman XL-80 Ultracentrifuge (Beckman Coulter). All the final pellets were resuspended in 1 ml of purified water. The final SNs were poured in HFD system and processed as described above. Conversely, the urine solution below the 1,000 kDa cut-off (HFDb) was ultracentrifuged (16.5 ml per tube) at 200,000 g calculated at maximum radius 91.9 mm of 70 Ti fixed-angle rotor (k factor = 44) (Beckman Coulter) for 2 h (RT) using a Beckman XL-80 Ultracentrifuge (Beckman Coulter).
Subjects were screened to select a population of disease-free nonsmokers. Normal was defined as having no history of (1) smoking, (2) asthma, chronic bronchitis, pneumonia or cardiac disease, (3) persistent cough, (4) recent treatment for any respiratory or cardiac symptoms, (5) chest injury or operation, (6) working in a polluted atmosphere for any extended period, finally, no evidence of cardiopulmonary disease on a physical examination, an EKG, or a chest radiograph.
Height, weight, and hemoglobin concentration were measured. The DLCO was measured by the modified Krogh’s single-breath method, using the SRL 1000IV Computerized Pulmonary Function Laboratory, Gould Co., USA.
With the subjects in the sitting position, their noses were clamped and initial maximal exhalation was followed by maximal inhalation of the test gas (contained 0.3%CO and 10%He). After a 10-second holding of the breath the exhaled gas was collected in a sample bag, and the sampling was analyzed for CO and He. Then the DLCO was calculated as follows:
VA: Alveolar volume (STPD)
60: Correction from seconds to minutes
PB: Barometric pressure
47: Water vapor pressure (PH2O)
t2–t1: Breath holding interval
Ln: Natural logarithm
FACOt1: Fraction of CO in alveolar gas before diffusion
FACOt2: Fraction of CO in alveolar gas at the end of diffusion
The correlations based on the diffusion capacity of the lung and the physical characteristics, such as age, height, weight and body surface area were observed. And prediction formulas were derived from the variables for both sexes, using a computer system (SPSS Batch System).
Most recents protocols related to «Hydrostatic Pressure»
EXAMPLE 8
A protected particle was formed of a base particle having an average diameter of 20 μm. The base particle is a hollow sphere having a shell thickness of 1 μm. The interior pressure in the hollow cavity of the base particle is 14.7 psi. The density of the base particle is 0.38 g/cc and the crush strength of the base particle is 1,500 psi. The outer surface of the base particle was coated with a PLGA by suspension deposition. The coating thickness was 18 μm. The protected particle had a crush strength of about 8000 psi. The protected particles were subjected to well conditions of 30,000 ppm brine solution at a pH of 7.5, a temperature of 90° C., and under 6,000 psi hydrostatic pressure. After about 12 hours and over the period of 2 hours thereafter, the base particles were fractured or crushed. The acoustic sound or emission created by the fractured or crushed base particles had a traceable harmonic resonant frequency peak at 3,000 Hz. As is evident from Examples 7 and 8, the protected particle can be tailored by using different sized base particles to create a certain frequency or range of frequencies when the base particle fractures or crushes.
EXAMPLE 10
A protected particle was formed of a base particle having an average diameter of 40 μm. The base particle is a hollow sphere having a shell thickness of 1 μm. The interior pressure in the hollow cavity of the base particle is 1000 psi. The density of the base particle is 0.39 g/cc. The outer surface of the base particle was coated with a PVA by suspension deposition. The coating thickness was 68 μm. The protected particle had a crush strength of about 8000 psi. The protected particles were subjected to well conditions of 10,000 ppm brine solution at a pH of 8, a temperature of 80° C., and under 6,000 psi hydrostatic pressure. After about 36 hours and over the period of 72 hours thereafter, the base particles were fractured or crushed. The acoustic sound or emission created by the fractured or crushed base particles had a traceable harmonic resonant frequency peak at 600 Hz. As is evident from Examples 9 and 10, the protected particle can be tailored by using certain pressures in the hollow cavity of the base particle to create a certain frequency or range of frequencies when the base particle fractures or crushes.
EXAMPLE 7
A protected particle was formed of a base particle having an average diameter of 40 μm. The base particle is a hollow sphere having a shell thickness of 1 μm. The interior pressure in the hollow cavity of the base particle is 14.7 psi. The density of the base particle is 0.38 g/cc and the crush strength of the base particle is 1,500 psi. The outer surface of the base particle was coated with a PLGA by suspension deposition. The coating thickness was 60 μm. The protected particle had a crush strength of about 8000 psi. The protected particles were subjected to well conditions of 30,000 ppm brine solution at a pH of 7.5, a temperature of 90° C., and under 6,000 psi hydrostatic pressure. After about 12 hours and over the period of 2 hours thereafter, the base particles were fractured or crushed. The acoustic sound or emission created by the fractured or crushed base particles had a traceable harmonic resonant frequency peak at 1,500 Hz.
EXAMPLE 9
A protected particle was formed of a base particle having an average diameter of 40 μm. The base particle is a hollow sphere having a shell thickness of 1 μm. The interior pressure in the hollow cavity of the base particle is 14.7 psi. The density of the base particle is 0.38 g/cc. The outer surface of the base particle was coated with a PVA by suspension deposition. The coating thickness was 68 μm. The protected particle had a crush strength of about 8000 psi. The protected particles were subjected to well conditions of 10,000 ppm brine solution at a pH of 8, a temperature of 80° C., and under 6,000 psi hydrostatic pressure. After about 36 hours and over the period of 72 hours thereafter, the base particles were fractured or crushed. The acoustic sound or emission created by the fractured or crushed base particles had a traceable harmonic resonant frequency peak at 1,500 Hz.
The experimental conditions are summarized in Supplementary Table
The sheathed thermocouple of 0.5 mm in diameter was used to monitor the temperature evolution in selected experiments. The thermocouple hole of 2 mm in diameter was drilled through the stationary rock cylinder, and the thermocouple was fixed in the hole by using the high-temperature waterproof adhesive, with its tip end exposing on the slip surface (Supplementary Fig.
In each experiment, before shearing the dolerite samples at the equivalent slip rate24 (link) of 2.0 m/s, we preslid the samples for two revolutions (~166 mm in equivalent displacement) under the slip rate of 5 mm/s and the normal stress same as that in the main test. This adjusts the alignment of rock cylinders and helps to get better quality experimental data.
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More about "Hydrostatic Pressure"
It refers to the pressure exerted by a fluid or liquid at rest, which is equal in all directions and acts perpendicular to any surface within the fluid.
This pressure is an important factor in numerous applications, including the design of hydraulic systems, the study of biological processes, and the analysis of geological formations.
Understanding the principles of hydrostatic pressure is crucial for optimizing research protocols and enhancing the reproducibility of experiments in these fields.
One key application of hydrostatic pressure is in the design and operation of hydraulic systems, such as those used in industrial machinery, heavy equipment, and even in everyday household appliances.
The principles of hydrostatic pressure are used to transfer and amplify force, enabling the efficient operation of these systems.
In the biological sciences, hydrostatic pressure plays a crucial role in various physiological processes, such as the transport of fluids and nutrients within the body, the regulation of cell volume, and the maintenance of tissue integrity.
Understanding the effects of hydrostatic pressure on these processes is essential for research in areas like cell biology, physiology, and biomedicine.
Geological formations, such as sedimentary rocks and underground aquifers, are also influenced by hydrostatic pressure.
This pressure can affect the properties and behavior of these formations, including their permeability, porosity, and the flow of fluids through them.
Studying hydrostatic pressure in geological contexts is important for applications like oil and gas exploration, groundwater management, and the assessment of natural hazards.
To optimize research protocols and enhance the reproducibility of hydrostatic pressure experiments, researchers can utilize advanced tools and technologies, such as PubCompare.ai's AI-driven platform.
This platform can help researchers locate the best protocols from literature, pre-prints, and patents, as well as improve their research outcomes through intelligent comparisons and analysis of hydrostatic pressure experiments.
Additionally, researchers may employ a variety of other techniques and instruments, such as Collagenase D for tissue dissociation, MATLAB for data analysis, STS-VIS for visualization, FITC-dextran for permeability measurements, Quanta 200 FEG for high-resolution imaging, DNase I for nucleic acid removal, CO2 flow meters for gas flow control, PPMS for physical property measurements, and Transwell cell culture inserts for in vitro experiments.
By leveraging these tools and technologies, researchers can deepen their understanding of hydrostatic pressure and its applications, ultimately leading to more robust, reproducible, and impactful research in their respective fields.