Development and performance evaluation of high temperature resistant strong adsorption rigid blocking agent

As drilling wells continue to move into deep ultra-deep layers,the requirements for temperature resistance of drilling fluid treatments are getting higher and higher.Among them,blocking agent,as one of the key treatment agents,has also become a hot spot of research.In this study,a high temperature resistant strong adsorption rigid blocking agent(QW-1)was prepared using KH570 modified silica,acrylamide(AM)and allyltrimethylammonium chloride(TMAAC).QW-1 has good thermal stability,average particle size of 1.46μm,water contact angle of 10.5.,has a strong hydrophilicity,can be well dispersed in water.The experimental results showed that when 2 wt%QW-1 was added to recipe A(4 wt%bentonite slurry+0.5 wt%DSP-1(filtration loss depressant)),the API filtration loss decreased from 7.8to 6.4 m L.After aging at 240.C,the API loss of filtration was reduced from 21 to 14 m L,which has certain performance of high temperature loss of filtration.At the same time,it is effective in sealing 80-100mesh and 100-120 mesh sand beds as well as 3 and 5μm ceramic sand discs.Under the same conditions,the blocking performance was superior to silica(5μm)and calcium carbonate(2.6μm).In addition,the mechanism of action of QW-1 was further investigated.The results show that QW-1 with amide and quaternary ammonium groups on the molecular chain can be adsorbed onto the surface of clay particles through hydrogen bonding and electrostatic interaction to form a dense blocking layer,thus preventing further intrusion of drilling fluid into the formation.

Insights into the influence of temperature on the adsorption behavior of sodium oleate and its response to flotation of quartz

Temperature affects the flotation of quartz in the calcium/sodium oleate(Na OL)system,while there is a lack of understanding of its potential mechanism.Therefore,in this work,the flotation response of quartz to temperature was investigated via micro-flotation experiments,interface property analyses,and theoretical calculations.Flotation results demonstrated that increasing temperature contributed to higher flotation recovery of quartz,which enhanced the removal of quartz from hematite.Surface tension results revealed that higher temperatures lowered the critical micelle concentration(CMC)and surface tension of the Na OL solution,and thus enhanced its surface activity.Solution chemistry calculations and X-ray photoelectron spectroscopy(XPS)measurements confirmed that the increased content of Ca(OH)+achieved by increasing temperatures enhanced the adsorption amounts of calcium species(acting as activation sites)on the quartz surface.Dynamic light scattering(DLS)measurements verified that the association degree of RCOOàto form(RCOO)22àwas strengthened.Furthermore,adsorption density measurements and molecular dynamics(MD)simulations confirmed that increasing the temperature facilitated Na OL adsorption toward the surface of the quartz,which was attributed to the stronger interaction between Na OL and the calcium-activated quartz surface at higher temperatures.As a result,quartz flotation was improved by increasing temperatures.Accordingly,a possible adsorption model was proposed.

NH_4^+ Adsorption in a Eum-Orthic Anthrosol at Different Solution/Soil Ratios and Temperatures

Effects of NHj concentiation, solution/soil ratio and temperature on NH_4^+adsorption were studied in a Eum-Orthic Anthrosol. The slopes of the soil NH_4^+ adsorptionisotherms and the fitted n, the coefficient for the adsorption intensity, and kappa, the coefficientrelated to adsorption capacity, of the Freundlich equation increased with increasing solution/soilratio (SSR) and with decreasing temperature (T). For the range of experimental conditions, the valueof delta q/delta c, the rate of change of the amount of NH_4^+ adsorbed in the soil solid phase (q)with respect to the equilibrium concentration of NH_4^+ in soil solution (c), was 0.840, indicatingthat q increased with increasing c. From 2 to 45 deg C, delta q/delta SSR, the rate of change of qwith respect to SSR, decreased from 2.598 to 1.996, showing that q increased with increasing SSR,while its increasing rate decreased with temperature. From SSR 1:1 to 20:1, delta q/delta T, therate of change of q with respect to T, decreased from -- 0.095 to -- 0.361, indicating that qdecreased with increasing temperature, and at the same time the negative effect of temperaturebecame larger as SSR increased. Thus under the experimental conditions the order of importance indetermining the amount of NH_4^+ adsorbed in the soil solid phase was delta q/delta SSR > deltaq/delta c > |delta q/delta T|, indicating that the greatest effect on the amount of NH_4^+ adsorbedwas with the solution/soil ratio; the equilibrium concentration of NH_4^+ had a lesser effect; andtemperature had the least effect.

Influence of Synthesis Temperature on Phosphate Adsorption by Zn-Al Layered Double Hydroxides in Excess Sludge Liquor

A group of Zn-Al layered double hydroxides (LDHs) were synthesized at different temperatures from 25-90 °C in order to investigate the influence of synthesis temperature on characteristics of the LDHs and their phosphate adsorption behaviour. The results reveal that an increase in the synthesis temperature generally improves the specific surface area of the sample and the phosphate adsorption capacity. The significantly enhanced crystallin- ity of the Zn-Al-30, synthesized at 30 °C, leads to a remarkable decrease in the specific surface area and consequently a poor phosphate adsorption capacity. It is suggested that the surface adsorption plays an important role in the phosphate uptake by the Zn-Al LDHs. Zn-Al-70 presents a relatively higher crystallinity and a lower specific surface area, compared with Zn-Al-60 and Zn-Al-80, but the highest phosphate adsorption capacity, indicating that surface adsorption is only one of the pathways for phosphate removal. The phosphate adsorption by the Zn-Al follows a pseudo-second-order kinetic equation. The adsorption isotherms fit Langmuir models, and the maximum a dsorption capacities of the Zn-Al-25, Zn-Al-50 and Zn-Al-70 are estimated to be 17.82, 21.01 and 27.10 mg·g-1 adsorbent, respectively.

NO adsorption and temperature programmed desorption on K_2CO_3 modified activated carbons

Fuel cell stacks as the automotive power source can be severely poisoned by a trace amount of NOx in atmosphere,which makes it necessary to provide clean air for fuel cell vehicles.In this work,activating commercial activated carbons with K2CO3 for the large enhancement of NO capture was studied.K2CO3 modified activated carbons(K2CO3 ACs)were prepared by impregnating activate carbons in K2CO3 solution under ultrasound treatment,followed by temperature programmed baking at 800 oC.The dynamic NO flow tests on K2CO3 ACs at room temperature indicated that NO adsorption capacity reached the maximum(96 mg/g)when K2CO3 loading was 19.5 wt%,which corresponded to a specific surface area of 1196.1 m2/g and total pore volume of 0.70 cm3/g.The ten-fold enhancement of NO adsorption on K2CO3 ACs compared to the unimpregnated activated carbon was mainly attributed to the formation of potassium nitrite,which was confirmed by FTIR and temperature programmed desorption measurements.Regeneration tests of NO adsorption on the optimum sample revealed that 76%of the NO adsorption capacity could be remained after the fourth cycle.

Temperature effect on the dynamic adsorption of anionic surfactants and alkalis to silica surfaces

Chemical loss such as surfactants and alkalis by adsorption to reservoir rock surface is an important issue in enhanced oil recovery(EOR). Here, we investigated the adsorption behaviors of anionic surfactants and alkalis on silica for the first time as a function of temperature using quartz crystal microbalance with dissipation(QCM-D). The results demonstrated that the temperature dependent critical micelle concentration of alcohol alkoxy sulfate(AAS) surfactant can be quantitatively described by the thermodynamics parameters of micellization, showing a mainly entropy-driven process. AAS adsorption was mediated under varying temperature conditions, by divalent cations for bridging effect, monovalent cations competitive for adsorption sites but not giving cation bridging, pH regulation of deprotonated sites of silica, presence of alkoxy groups in the surfactants, and synergistic effect of surfactant coinjection. The addition of organic alkalis can enhance the overall adsorption of the species with AAS,whereas inorganic alkali of Na_(2)CO_(3) had capability of the sequestration of the divalent ions, whose addition would reduce AAS adsorption. The typical AAS adsorption indicated a non-rigid multilayer,estimated to have between 2 and 5 layers, with a likely compact bilayer followed by disorganized and unstable further layering. The new fundamental understanding about temperature effect on surfactants and alkalis adsorption contributes to optimizing the flooding conditions of chemicals and developing more efficient mitigation strategies.

Adsorption Kineties of Pb￣(2+) and Cu￣(2+) on Variable Charge Soils andMinerals V .Effects of Temperature and Ionic Strength￣*1

The study results of the effects of temperature and ionic strength on the adsorption kineties of Pb￣2+ and Cu￣2+ bylatosol, red soil and kaolinte coated with Mn oxide showed that Pb￣2+ and Cu￣2+ adsorption by all samples, as awhole, increased with missing temperature. Temperature also increased both values of X_m (the amount of ionadsorbed at equilibrium) and k (kinetica constant) of Pb￣2+ and Cu￣2+. The activation energies of Pb￣2+ adsorption werekaolin-Mn >red soil>goethite and those of Cu￣2+ were latosol> red soil > kaolin-Mn >goethite. For a given singlesample the activation energy of Cu￣2+ was greater than that of Pb￣2+. Raising ionic strength decreased the adsorptionof Pb￣2+ and Cu￣2+ by latosol, red soil and kaolinite coated with Mn oxide but increased Pb￣2+ and Cu￣2+ adsorption bygoethite. The contrary results could be explained by the different changes in ion forms of Pb￣2+ or Cu￣2+ and in surfacecbarge characteristics of latosol, red soil, kaolin-Mn and goethite. Increasing supporting electrolyte concentration in-creased X_m and k in goethite systems but decreased X_m and k in kaolin-Mn systems. All the time-dependent data fit-ted the surface second-order equation very well.

Regulating adsorption ability toward polysulfides in a porous carbon/Cu_(3)P hybrid for an ultrastable high-temperature lithium-sulfur battery

Lithium-sulfur batteries(LSBs)can work at high temperatures,but they suffer from poor cycle life stability due to the“shuttle effect”of polysulfides.In this study,pollen-derived porous carbon/cuprous phosphide(PC/Cu_(3)P)hybrids were rationally synthesized using a one-step carbonization method using pollen as the source material,acting as the sulfur host for LSBs.In the hybrid,polar Cu_(3)P can markedly inhibit the“shuttle effect”by regulating the adsorption ability toward polysulfides,as confirmed by theoretical calculations and experimental tests.As an example,the camellia pollen porous carbon(CPC)/Cu_(3)P/S electrode shows a high capacity of 1205.6 mAh g^(−1) at 0.1 C,an ultralow capacity decay rate of 0.038%per cycle after 1000 cycles at 1 C,and a rather high initial Coulombic efficiency of 98.5%.The CPC/Cu_(3)P LSBs can work well at high temperatures,having a high capacity of 545.9 mAh g^(−1) at 1 C even at 150℃.The strategy of the PC/Cu_(3)P hybrid proposed in this study is expected to be an ideal cathode for ultrastable high-temperature LSBs.We believe that this strategy is universal and worthy of in-depth development for the next generation energy storage devices.

Formation of AgI/Ag_3PO_4 solid solution on alumina for enhancing radioactive iodine adsorption at high temperatures

Radioiodine-131 is one of the pernicious radionuclides released during nuclear accidents, as its radioactivity can potentially affect public health and safety.To prevent radioiodine-131 from being released into the environment, the use of adsorbents that are highly efficient at high temperatures is significantly important. The radioactive gas from the nuclear core in an accident, such as the Fukushima nuclear accident, is usually released occurs under high-temperature conditions. Therefore, in this study, a 10 wt% silver phosphate-loaded alumina(Ag_3 PO_4/Al_2 O_3) adsorbent was prepared. Further, its performance toward radioiodine adsorption was tested at high temperatures up to 750 0 C, using Al_2 O_3 and traditional 10 wt% Ag/Al_2 O_3 adsorbent as controls. The results of the iodine adsorption test indicated that the 10 wt% Ag_3 PO_4/Al_2 O_3 adsorbent showed a higher decontamination factor than did the 10 wt% Ag/Al_2 O_3 adsorbent by two orders of magnitude at 650 and 750℃. Results of the iodine desorption test revealed that the new adsorbent could be effectively used at 750 ℃. The characteristic powder X-ray diffraction, nitrogen adsorption-desorption isotherm,X-ray photoelectron spectroscopy, and thermogravimetric analysis-differential scanning calorimetry data indicated that the enhanced adsorption ability at high temperatures was attributed to the formation of a solid solution between silver iodide and Ag_3 PO_4.

Adsorption of gaseous iodine-131 at high temperatures by silver impregnated alumina

To prevent radioactive iodides from releasing into the environment in an accident of a nuclear power plant,silver-impregnated alumina(Ag/Al2O3)was fabricated,and its performance of radioactive iodine adsorption from high-temperature gas was tested.The silver loadings on alumina were obtained by ICP-OES and the texture properties of Ag/Al2O3were characterized by N2adsorption-desorption.The Ag/Al2O3was of reduced specific surface(107.2 m2/g at 650?C).Crystalline phases of Ag/Al2O3were confirmed through XRD characterization.After calcination at 650?C for 2 h,the crystalline phase of Ag/Al2O3changed.The131I-removal efficiency of Ag/Al2O3was tested at 100,250,350,450 and 650?C,with good decontamination factor values for the radioactive iodine.Silver-impregnated alumina can be applied as adsorbents to remove radioactive iodine at high temperatures in nuclear accident.

Synthesis of SAPO-34/graphite composites for low temperature heat adsorption pumps

Low temperature heat adsorption pumps represent the innovative cooling systems, where cold is generated through adsorption/desorption cycle of water by a suitable adsorbent with good adsorption and high thermal conductive properties. In this work, the hydrothermal synthesis of zeolite SAPO-34 on thermal conductive grapbitic supports, aiming at the development of highly pertbrming adsorbent materials, is reported. The synthesis was carried out using as-received and oxidized commercial carbon papers, and graphite plate. Composites were characterized by XRD, SEM and also by a thermogravimetric method, using a Cahn microbalance. The water adsorbing capacity showed typical S-shape trend and the maximum water loading was around 25 wt%, a value close to water adsorption capability of pure SAPO-34. These results are very promising for their application in heat adsorption pumps.

Systematic investigation of SO_(2) adsorption and desorption by porous powdered activated coke:Interaction between adsorption temperature and desorption energy consumption

Porous carbon materials have been widely used for the removal of SO_(2) from flue gas.The main objective of this work is to clarify the effects of adsorption temperature on SO_(2) adsorption and desorption energy consumption.Coal-based porous powdered activated coke(PPAC)prepared in the drop-tube reactor was used in this study.The N_(2) adsorption measurements and Fourier transform infrared spectrometer analysis show that PPAC exhibits a developed pore structure and rich functional groups.The experimental results show that with a decrease in adsorption temperature in the range of 50–150℃,the adsorption capacity of SO_(2) increases linearly;meanwhile,the adsorption capacity of H_(2)O increases,resulting in the increase in desorption energy consumption per unit mass of adsorbent.The processes of SO_(2) and H_(2)O desorption were determined by the temperature-programmed desorption test,and the desorption energies for each species were calculated.Considering the energy consumption per unit of desorption and the total amount of adsorbent,the optimal adsorption temperature yielding the minimum total energy consumption of regeneration is calculated.This study systematically demonstrates the effect of adsorption temperature on the adsorption–desorption process,providing a basis for energy saving and emission reduction in desulfurization system design.

Adsorption Enthalpy Calculations of Hydrogen Adsorption at Ambient Temperature and Pressures Exceeding 300 bar

Hydrogen adsorption isotherms were measured at ambient temperature to pressures exceeding 300 bar for three benchmark adsorbents: two metal-organic frameworks, Cu3(btc)2 (btc = 1,3,5-benzenetricarboxylate) and Zn4O(btb)2 (btb = 1,3,5-benzenetribenzoate), and the activated carbon MSC-30. The Dubinin-Astakhov model was applied to calculated absolute adsorption isotherms as a function of the fugacity to determine the adsorption enthalpy at ambient temperature. Comparisons of the calculated enthalpies and the surface excess concentration (excess adsorption per square meter of surface) show that Zn4O(btb)2 has an adsorption enthalpy comparable to MSC-30, but that the spacing between adsorbed molecules is much larger.

Understanding the hydroxyl adsorption behavior at Pt electrode surface in high-temperature alkaline solutions

Since the application in fuel cell,the electrochemical adsorption of hydroxyl has received considerable attention in recent years.While most research mainly focus on the room temperature,in this paper,the electrochemical adsorption of hydroxyl in alkaline solution at high temperature was investigated.An unusual oxidation peak was observed at-0.27 V,suggesting new behavior of hydroxyl adsorption occurred.As is known two kinds of cation hydrated clusters exist in alkaline solution,(H_(2)O)_(x-1)M^(+)-H_(2)O-O_(ad)H and(H_(2)O)_xM^(+)-O_(ad)H.For K^(+)and Cs^(+),the cluster shows unstable structure due to the weak interaction between hydrated cation and OH^(-)especially at high temperature.However,For Li^(+),Na^(+)the cluster structure would be stable,as the interaction force between the hydrated cation and OH^(-)is so strong.It was revealed that the unusual oxidation peak has some relationship with the(H_(2)O)_(x-1)M^(+)-H_(2)O-O_(ad)H cluster(K^(+)and Cs^(+))absorbed at Pt electrode surface.When the temperature was raised,(H_(2)O)_(x-1)M^(+)-H_(2)O-and-O_(ad)H was disconnected,then the O_(ad)H absorbed at Pt surface got oxidated.Based on the SEM observation,it was showed the unusual electrochemical oxidation reaction would generate platinum oxides,blocking the reactive sites at Pt electrode surface,thus reducing the electrochemical reactivity of Pt electrode.Accordingly,parameters of alkaline concentration and temperature were systematically studied,it was found that increase temperature or alkaline concentration was in favor of the unusual oxidation reaction.This study provides more understanding of hydroxyl adsorption behavior at Pt electrode surface for the high temperature water solution environment.

K^+ Adsorption Kinetics of Fluvo-Aquic and Cinnamon Soil Under Different Temperature

The K+ adsorption kinetics of fluvo-aquic soil and cinnamon soil under different temperatureswere studied. The results showed: 1) The first order equations were the most suitable forfitting the adsorption under various temperature levels with constant K+ concentration indisplacing fluid. With temperature increasing, the fitness of Elovich equation increased,while those of power equation and parabolic diffusion equation decreased; 2)the apparentadsorption rate constant ka and the product of ka multiplied by the apparent equilibriumadsorption qincreased when temperature increased, while the apparent equilibrium adsorptionqreduced; 3)temperature influenced hardly the reaction order, the order of concentrationand adsorpton site were always 1 under various temperatures, if they were taken intoaccount simultaneously, the adsorption should be a two-order reaction process; 4)theGibbs free energy change △G of potassium adsorption were negative, ranged from -4444.56to -2450.63Jmol-1,and increased with temperature increasing, while enthalpy change △H,entropy change △S, apparent adsorption activation Ea, adsorption activation energy E1and desorption activation energy E2 were temperature-independent; 5)the adsorption wasspontaneous process with heat releasing and entropy dropping, fluvo-aquic soil releasedmore heat than cinnamon soil.

Effects of Low Temperature and Ultra-low Temperature on Pollen Viability of Tomato(Lycopersicon esculentum Mill.)

The pollen of two tomato varieties, Ryau961721 and Ryau9327D, was adopted in our research. The two tomato varieties were bred by College of Land- scape and Horticulture, Yunnan Agricultural University. The collected pollen was stored in low-temperature （4 ℃） and ultra-low-temperature （-196 ℃） circumstances. Then it was inoculated to the medium and cultured at 28 ℃ in thermostat incubator. The pollen viability was determined by electron microscope. The results showed that compared to that of pollen stored in control （25 ℃） circumstance, the viability of pollen stored in low-temperature （4 ℃） and ultra-low-temperature （-196 ℃） circum- stances for 1 -3 d did not change significantly. In addition, pollen viability trended to decrease with the increase of freeze-thaw cycle and storage time. The pollen lost basically the viability by the 7th d in the storage.

Low-energy-consumption temperature swing system for CO_(2) capture by combining passive radiative cooling and solar heating

Temperature-swing adsorption(TSA)is an effective technique for CO_(2) capture,but the temperature swing procedure is energy-intensive.Herein,we report a low-energy-consumption system by combining passive radiative cooling and solar heating for the uptake of CO_(2) on commercial activated carbons(CACs).During adsorption,the adsorbents are coated with a layer of hierarchically porous poly(vinylidene fluoride-co-hexafluoropropene)[P(VdF-HFP)HP],which cools the adsorbents to a low temperature under sunlight through radiative cooling.For desorption,CACs with broad absorption of the solar spectrum are exposed to light irradiation for heating.The heating and cooling processes are completely driven by solar energy.Adsorption tests under mimicked sunlight using the CACs show that the performance of this system is comparable to that of the traditional ones.Furthermore,under real sunlight irradiation,the adsorption capacity of the CACs can be well maintained after multiple cycles.The present work may inspire the development of new temperature swing procedures with little energy consumption.

Innovation for forming aluminum alloy thin shells at ultra-low temperature by the dual enhancement effect

Integral thin shells made of high strength aluminum alloys are urgently needed in new generation transportation equipment. There are challenges to overcoming the co-existing problems of wrinkling and splitting by the cold forming and hot forming processes. An innovative technology of ultra-low temperature forming has been invented for aluminum alloy thin shells by the new phenomenon of ‘dual enhancement effect’. That means plasticity and hardening are enhanced simultaneously at ultra-low temperatures. In this perspective, the dual enhancement effect is described, and the development, current state and prospects of this new forming method are introduced. This innovative method can provide a new approach for integral aluminum alloy components with large size, ultra-thin thickness, and high strength. An integral tank dome of rocket with 2 m in diameter was formed by using a blank sheet with the same thickness as the final component, breaking through the limit value of thickness-diameter ratio.

Anisotropic Rock Poroelasticity Evolution in Ultra-low Permeability Sandstones under Pore Pressure,Confining Pressure,and Temperature:Experiments with Biot's Coefficient

This study aimed to show anisotropic poroelasticity evolution in ultra-low permeability reservoirs under pore pressure,confining pressure,and temperature.Several groups of experiments examining Biot's coefficient under different conditions were carried out.Results showed that Biot's coefficient decreased with increased pore pressure,and the variation trend is linear,but the decreasing rate is variable between materials.Biot's coefficient increased with increased confining pressure;the variation trend is linear,but the increasing rate varies by material as well.Generally,Biot's coefficient remains stable with increased temperature.Lithology,clay mineral content,particle arrangement,and pore arrangement showed impacts on Biot's coefficient.For strong hydrophilic clay minerals,expansion in water could result in a strong surface adsorption reaction,which could result in an increased fluid bulk modulus and higher Biot's coefficient.For skeleton minerals with strong lipophilicity,such as quartz and feldspar,increased oil saturation will also result in an adsorption reaction,leading to increased fluid bulk modulus and a higher Biot's coefficient.The study's conclusions provide evidence of poroelasticity evolution of ultra-low permeability and help the enhancing oil recovery(EOR)process.

Low-temperature collecting performance of a new combined collector on scheelite flotation

The reduced ability of fatty acids to dissolve and disperse at low temperatures limits their effectiveness in winter applications.In this study,a green and environment-friendly reagent,polyethylene glycol 2000(PEG-2000),was used to evaluate its effect on the collecting performance of sodium oleate during scheelite flotation at low temperatures.The effect of PEG-2000 on the flotation of scheelite with the collector sodium oleate(NaOL)was studied by flotation tests,surface tension tests,infrared spectral analysis,and zeta potential measurements.Flotation tests showed that adding PEG-2000 can enhance the collecting ability of NaOL on scheelite at low temperature(5℃).The recovery of scheelite with the mixed collector of PEG-200 and NaOL is 4.39%higher than that with NaOL only.The surface tension tests,infrared spectral analysis and zeta potential measurements revealed that PEG-2000 and OL^(−)are co-adsorbed on the scheelite surface at low temperatures.The presence of PEG-2000 promoted the increase of the adsorption concentration of oleate ions(OL^(−))on the scheelite surface.The reason was that PEG-2000 has a shielding effect on the electrostatic repulsion between the OL^(−)groups,which changes the micellar configuration of OL^(−)in the solution system and makes the OL^(−)gather more tightly on the surface of scheelite,leading to the enhancement of its hydrophobicity.This discovery provides a reference for the development of collecting reagents for efficient flotation recovery of scheelite under low temperature environment.