Petrographic Studies on Hydrothermally Altered Conglomerates at Naer Creek, Sichuan Province, China

Based on analysing the wall rock alterations and related rocks which were used as a hint for mineral deposits and as a basis of mechanism research of fluid rock interaction, according to the results of petrographic analysis, the authors of this paper consider that the hydrothermally altered conglomerates have the following features. First, the conglomerates studied can be divided into two groups: Group A consists mainly of the gravels of granite and basalt; Group B is mainly composed of the gravels of basalt, limestone, mudstone and granite. Second, three distinct hydrothermal alterations or diagenesis were distinguished in Group A, that is, pre depositional hydrothermal alteration of the volcanic gravels (saussuritzation chloritization, epidotization chloritization, albitization and sericitization), mechanical diagenesis and post diagenetic hydrothermal alteration (epidote chlorite and prehnite calcite association). Third, the Group B is subjected mainly to pre depositional hydrothermal alteration; the alteration types are the same as of Type A. Last, the origin of the post diagenetic hydrothermal alteration of Group A is presumed to be related to the ascending of thermal water along the Naer Creek fault.

Estimate of Uniaxial Compressive Strength of Hydrothermally Altered Soft Rocks Based on Strength Index Tests

The purpose of this study was to clarify the relationships between results of index tests and uniaxial compressive strength (UCS) in hydrothermally altered soft rocks of the Upper Miocene, which are typical of the soft rock found in northeastern Hokkaido, Japan. Index tests were performed using point load testing machine and needle penetrometer with irregular lump specimens under forced-dry, forced-wet, and natural-moist states. The relationships between irregular lump point load strength (IPLS) index and UCS, and needle penetration (NP) index and UCS were “UCS = approximately 19 IPLS index” and “UCS = 0.848 (NP index)0.619”, respectively, in soft rocks with a UCS below 25 MPa. These relationships could be applied to on-site tests of rocks with natural moisture content. The UCS could be calculated from IPLS and NP tests on soft rocks only when UCS was below 25 MPa, using the equations obtained as a result of this study.

Effect of C/S Ratio on Morphology and Structure of Hydrothermally Synthesized Calcium Silicate Hydrate

The samples of the C-S-H series were synthesized by hydrothermal reaction of fumed silica, CaO and deionized water at initial C/S ratios between 1.0-1.7. Phase composition and structural and morphology characteristics of C-S-H samples were analyzed by XRD, IR and SEM. The experimental results showed that the d-spacing of （002）, （110） and （020） decreased, the d-spacing of （200） increased, and the d-spacing of （310） varied randomly, the polymerization of silica tetrahedra of C-S-H decreased, and morphology of C-S-H samples varied from sheet shapes to long reticular fibers as C/S ratio increased.

Researches on the Removal of Pb(Ⅱ) by Hydrothermally Modified Oyster Shells

A novel wastewater purification material was prepared by a hydrothermal method. It was mainly made from oyster shells with the merits of long service time, large surface area, high lead removal efficiency and excellent recyclable properties. The technological conditions were decided respectively based on the lead removal efficiencies. At pH = 5 and 30 ℃, for the wastewater with the initial concentration of Pb2＋ to be 5 mg/L, adsorption time 24 h, and 1 mg to 40 mL of mass ratio between adsorbent and Pb2＋, the maximum adsorption capacity can reach 0.19 mg/g. The lead removal material prepared by hydrothermal method has excellent recycle performance. The equilibrium adsorption capacity can get to 9.71 mg/g and the average Pb2＋ removal rate is as high as 66.39%. After reusing for 60 times, the SEM observation shows that the hydrates of reticular formation is formed after hydrothermal modification, which provides a good attachment position for Pb2＋, indicating the physical adsorption is dominant.

Structure and Shape Control of Hydrothermally Synthesized PbTiO_3 --Effects of pH and Complexing Agents

Tabular PE PbTiO 3, spherical PY PbTiO 3, and acicular PX PbTiO 3 powders were hydrothermally synthesized from triethanolamine(TEA) complexed precursor; clubbed PE PbTiO 3 powders were obtained from diethanolamine(DEA) complexed precursor. The effects of pH of the hydrolyzation as well as complexing agents including TEA, DEA, and MEA(monoethanolamine) on the structure and the morphology of PbTiO 3 powders are discussed. The optimal conditions for hydrothermal syntheses of acicular and clubbed PbTiO 3 powders have been established. The products were characterized by means of XRD, TEM and other techniques.

Nature of Surface Layer and Electrochemical Behavior of NaOH Hydrothermally Treated NiTi Alloy

NiTi samples were hydrothermally treated in NaOH at 200℃ with different soaking times. The morphology of the surface layer formed was studied by scanning electron microscopy (SEM). The composition of the layer and the major phases present were determined by energy-dispersive spectroscopy (EDS) and X-ray diffractometry (XRD), respectively. In contrast to the results reported by some authors, the surface layer was essentially Ni(OH)2 instead of being TiO2. The electrochemical behavior of the samples was studied by electrochemical impedance spectroscopy (EIS) in 3.5% NaCl solution at 23℃, and analyzed using a simplified Randle circuit consisting of a resistance R and a capacitance C in parallel. After hydrothermal treatment, R was increased by a factor ranging from 1.5 to 5.0 times, depending on the treatment time. The value of R of all the samples became steady within a period of less than 15 h. Results of the present study indicate that alkaline treatment leads to the growth of an insulating layer on NiTi, but the method is not suitable for surface modification of NiTi implants due to the enhanced Ni content in the surface layer.

Hydrothermally induced diagenesis: Evidence from shallow marinedeltaic sediments, WilhelmØya, Svalbard

Sedimentary basins containing igneous intrusions within sedimentary reservoir units represent an important risk in petroleum exploration. The Upper Triassic to Lower Jurassic sediments at Wilhelm?ya(Svalbard) contains reservoir heterogeneity as a result of sill emplacement and represent a unique case study to better understand the effect of magmatic intrusions on the general burial diagenesis of siliciclastic sediments. Sills develop contact metamorphic aureoles by conduction as presented in many earlier studies. However, there is significant impact of localized hydrothermal circulation systems affecting reservoir sediments at considerable distance from the sill intrusions. Dolerite sill intrusions in the studied area are of limited vertical extent(～12 m thick), but created localized hydrothermal convection cells affecting sediments at considerable distance(more than five times the thickness of the sill)from the intrusions. We present evidence that the sedimentary sequence can be divided into two units:(1) the bulk poorly lithified sediment with a maximum burial temperature much lower than 60-70 ℃,and(2) thinner intervals outside the contact zone that have experienced hydrothermal temperatures(around 140 ℃). The main diagenetic alteration associated with normal burial diagenesis is minor mechanical plastic deformation of ductile grains such as mica. Mineral grain contacts show no evidence of pressure dissolution and the vitrinite reflectance suggests a maximum temperature of ～40 ℃. Contrary to this, part of the sediment, preferentially along calcite cemented flow baffles, show evidence of hydrothermal alteration. These hydrothermally altered sediment sections are characterized by recrystallized carbonate cemented intervals. Further, the hydrothermal solutions have resulted in localized sericitization(illitization) of feldspars, albitization of both K-feldspar and plagioclase and the formation of fibrous illite nucleated on kaolinite. These observations suggest hydrothermal alteration at T> 120-140 ℃ at distances considerably further away than expected from sill heat dissipation by conduction only, which commonly affect sediments about twice the thickness of the sill intrusion. We propose that carbonate-cemented sections acted as flow baffles already during the hydrothermal fluid mobility and controlled the migration pathways of the buoyant hot fluids. Significant hydrothermally induced diagenetic alterations affecting the porosity and hence reservoir quality was not noted in the noncarbonate-cemented reservoir intervals.

Highly Effective Propylene Epoxidation over TS-1/SiO_(2) Hydrothermally Treated

The propylene epoxidation over TS-1/SiO2 catalyst hydrothermally treated was investigated. It was found by EPR characterization that two types of Ti (IV)-superoxide radicals, A (gz=2.0271; gy=2.0074; gx=2.0010) and B (gz=2.0247; gy= 2.0074; gx= 2.0010), were observed for TS-1/SiO2. The superoxo species A converted to B after TS-1/SiO2 catalyst was hydrothermally treated. The results show that over TS-1/SiO2 catalyst hydrothermally treated at 170℃, about 95% conversion of H2O2 with above 94% PO selectivity is obtained during continuous running for 300 h under the conditions of reaction temperature 45℃, 0.5 h-1WHSV of propylene.

Genesis of anhydrite in hydrothermally altered basalt from the East Pacific Rise near 13°N

This study reports the occurrence of anhydrite in hydrothermally altered pillow basalt （12°50.55＇N, 103°57.62＇W, water depth 2 480 m）, which may have been produced in the basalt during seawater-basalt interaction in the laboratory. The existence of anhydrite in the altered basalt indicates extensive high- temperature hydrothermal alteration at the surface of seafloor pillow basalt. Microprobe analysis shows significant chemical zoning in the hydrothermally altered pillow basalt, in which Ca, Si and A1 contents de- crease and P, Fe, Mn, Cr and S contents increase from fresh basalt to altered basalt. The negative correlation between Rb-Sr and Li-Sr, and negative correlation between Li-Ca and Rb-Ca in the high-temperature vent fuids show that these fluids underwent anhydrite precipitation before fluid jetting due to mixing with sea- water in the sub-seafloor. Based on these observations, we show that not all Ca in the anhydrite comes from basalt in the reaction zone, and that the basalts on the seafloor or in the upflow zone may also provide Ca for anhydrite.

Hydrothermally Synthesizing Nanospheres of Pd Loaded TiO_2 for Photocatalytically Reducing CO_2 in Isopropanol to Isopropyl Formate

Photocatalytic reduction of CO2 was carried out on villiform spherical catalysts of Pd-TiO2 in isopropanol solution.The catalysts were synthesized by hydrothermal method,their structures,morphologies and optical absorption properties were characterized by X-ray diffraction（XRD）,energy dispersive X-ray spectroscopy（EDS）,scanning electron microscopy（SEM）,transmission electron microscopy（TEM）,highresolution transmission electron microscopy（HRTEM）and UV-vis absorption spectroscopy（UV-vis）.The photocatalytic activities with different loading amounts and morphologies were evaluated for determining the dominant effect and optimizing the catalyst preparation.Based on a villiform spherical TiO2 with the largest specific surface area in our experiments,we prepared a set of catalysts with various loading amounts of palladium and tested them by bubbling CO2 through the slurry of catalyst and isopropanol.The highest formation rate of isopropyl formate was 276.6μmol/g？cat/h.Eventually we proposed the reaction mechanism.

Synthesis of Aluminum-doped Zinc Oxide Nanowires Hydrothermally Grown on Plastic Substrate

We report the synthesis of undoped ZnO and Al-doped ZnO (ZnO:Al) nanowires grown using a two-step process: (a) preparation of the seed layer, and (b) growth of the nanostructures. In the first step,? 10 mM solutions of zinc acetate dihydrate and 1-propanol were spin coated on polyethylene terephthalate? (PET) substrate at 2000 rpm by 30 s. Vertical nanowires were then grown by dipping the substrates in an equimolar solution of zinc nitrate hexahydrate and hexamethylenetetramine. As doping source, aluminum nitrate nonahydrate powders were added in the solution. In the solutions, Al doping concentrations were established as 0.5 At %, 1.0 At %, 2.0 At % and 3.0 At %, respectively. The hydrothermal process were carried out with a commercially microwave at 140 W power setting. The nanowires were characterized optically and morphologically. XRD patterns show the presence of ZnO, Zn(OH)2 and Zn6Al2O9. Scanning electron microscopy analysis showed that the size of ZnO nanowires was 50 nm in diameter. The undoped ZnO and ZnO:Al nanowires bandgap energy was obtained from optical transmission spectra.

Hydrothermally stable metal oxide-zeolite composite catalysts for low-temperature NO_(x) reduction with improved N_(2) selectivity

Development of hydrothermally stable,low-temperature catalysts for controlling nitrogen oxides emissions from mobile sources remains an urgent challenge.We have prepared a metal oxide-zeolite composite catalyst by depositing Mn active species on a mixture support of CeO_(2)/Al_(2)O_(3) and ZSM-5.This composite catalyst is hydrothermally stable and shows improved low-temperature SCR activity and significantly reduced N_(2)O formation than the corresponding metal oxide catalyst.Comparing with a Cu-CHA catalyst,the composite catalyst has a faster response to NH_(3) injection and less NH_(3) slip.Our characterization results reveal that such an oxide-zeolite composite catalyst contains more acidic sites and Mn^(3+)species as a result of oxide-zeolite interaction,and this interaction leads to the generation of more NH_(4)^(+)species bound to the Br?nsted acid sites and more reactive NOxspecies absorbed on the Mn sites.Herein,we report our mechanistic understanding of the oxide-zeolite composite catalyst and its molecular pathway for improving the low-temperature activity and N_(2) selectivity for NH_(3)-SCR reaction.Practically,this work may provide an alternative methodology for low-temperature NO_(x) control from diesel vehicles.

Application of silica-alumina as hydrothermally stable supports for Pt catalysts for acid-assisted soot oxidation

In this work,silica-alumina mixed oxides with different SiO_(2)contents(5%and 30%)were adopted as acidic supports for platinum catalysts for soot oxidation.The obtained catalysts were hydrothermally aged in 10%H_(2)0/air at 750℃for 20 h.The catalysts were characterized by X-ray diffraction(XRD),N_(2)adsorption,inductively coupled plasma(ICP),CO chemisorption,NH3temperature-programmed desorption(TPD),infrared(IR)spectroscopy of CO adsorption,temperature-programmed oxidation(TPO)of NO,and TPD of NO_(x).The surface acidity of catalyst was positive correlated with the content of SiO_(2),which kept platinum in metallic and partially oxidized states in an oxidizing atmosphere.Compared with sulfation treatment on the alumina support,the application of SiO_(2)-Al_(2)O_(3)mixed oxides does not result in the coverage of Pt active sites and the prepared catalysts exhibit excellent activity for NO oxidation.They promote NOxpreferential adsorption on soot and decomposition of surface oxygenated compounds(SOCs)as the sulfated Pt/Al_(2)O_(3)catalyst does.

Assessing the Performance of CMIP6 Models in Simulating Droughts across Global Drylands

Both the attribution of historical change and future projections of droughts rely heavily on climate modeling. However,reasonable drought simulations have remained a challenge, and the related performances of the current state-of-the-art Coupled Model Intercomparison Project phase 6(CMIP6) models remain unknown. Here, both the strengths and weaknesses of CMIP6 models in simulating droughts and corresponding hydrothermal conditions in drylands are assessed.While the general patterns of simulated meteorological elements in drylands resemble the observations, the annual precipitation is overestimated by ~33%(with a model spread of 2.3%–77.2%), along with an underestimation of potential evapotranspiration(PET) by ~32%(17.5%–47.2%). The water deficit condition, measured by the difference between precipitation and PET, is 50%(29.1%–71.7%) weaker than observations. The CMIP6 models show weaknesses in capturing the climate mean drought characteristics in drylands, particularly with the occurrence and duration largely underestimated in the hyperarid Afro-Asian areas. Nonetheless, the drought-associated meteorological anomalies, including reduced precipitation, warmer temperatures, higher evaporative demand, and increased water deficit conditions, are reasonably reproduced. The simulated magnitude of precipitation(water deficit) associated with dryland droughts is overestimated by 28%(24%) compared to observations. The observed increasing trends in drought fractional area,occurrence, and corresponding meteorological anomalies during 1980–2014 are reasonably reproduced. Still, the increase in drought characteristics, associated precipitation and water deficit are obviously underestimated after the late 1990s,especially for mild and moderate droughts, indicative of a weaker response of dryland drought changes to global warming in CMIP6 models. Our results suggest that it is imperative to employ bias correction approaches in drought-related studies over drylands by using CMIP6 outputs.

Episodic hydrothermal alteration on Middle Permian carbonate reservoirs and its geological significance in southwestern Sichuan Basin,SW China

To analyze the episodic alteration of Middle Permian carbonate reservoirs by complex hydrothermal fluid in southwestern Sichuan Basin,petrology,geochemistry,fluid inclusion and U-Pb dating researches are conducted.The fractures and vugs of Middle Permian Qixia–Maokou formations are filled with multi-stage medium-coarse saddle dolomites and associated hydrothermal minerals,which indicates that the early limestone/dolomite episodic alteration was caused by the large-scale,high-temperature,deep magnesium-rich brine along flowing channels such as basement faults or associated fractures under the tectonic compression and napping during the Indosinian.The time of magnesium-rich hydrothermal activity was from the Middle Triassic to the Late Triassic.The siliceous and calcite fillings were triggered by hydrothermal alteration in the Middle and Late Yanshanian Movement and Himalayan Movement.Hydrothermal dolomitization is controlled by fault,hydrothermal property,flowing channel and surrounding rock lithology,which occur as equilibrium effect of porosity and permeability.The thick massive grainstone/dolomites were mainly altered by modification such as hydrothermal dolomitization/recrystallization,brecciation and fracture-vugs filling.Early thin-medium packstones were mainly altered by dissolution and infilling of fracturing,bedding dolomitization,dissolution and associated mineral fillings.The dissolved vugs and fractures are the main reservoir space under hydrothermal conditions,and the connection of dissolved vugs and network fractures is favorable for forming high-quality dolomite reservoir.Hydrothermal dolomite reservoirs are developed within a range of 1 km near faults,with a thickness of 30–60 m.Hydrothermal dolomite reservoirs with local connected pore/vugs and fractures have exploration potential.

Efficient Removal of Phosphate from Aqueous Solutions Using Corundum-hollow-spheres Supported Caclined Hydrotalcite Porous Thin Films

Phosphate was removed from aqueous environment by corundum-hollow-spheres supported caclined hydrotalcite (cHT) thin films. Mg-Al-CO3 hydrotalcite (HT) thin films were deposited on corundumhollow-sphere substrates by hydrothermal homogeneous precipitation at 120℃for 30-240 min and cHT thin films were obtained by annealing of the HT thin films at 500℃for 180 min. Their crystal phase, morphology and microstructure were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM).The results show that homogeneous, well-crystallized and hierarchical flower-like thin films were deposited firmly on the surface of the corundum. The mechanism of nucleation and growth of the HT thin films was fitted well with the anion coordination polyhedron growth unit model. To determine the absorption of phosphate by this adsorbent, different bed depth (10-30 cm) and flow rate (1.0-3.0 m L/min) were examined by column experiments. The highest removal efficiency of phosphate amounted to 98.5%under optimum condition (pH=7.2). The adsorption capacity increased as the bed depth increased and decreased as the flow rate increased.

An effective strategy of constructing multi-metallic oxides of ZnO/ CoNiO_(2)/CoO/C microflowers for improved supercapacitive performance

In this work,a new ZnO/CoNiO_(2)/CoO/C metal oxides composite is prepared by cost-effective hydrothermal method coupled with annealing process under N_(2) atmosphere.Notably,the oxidation-defect annealing environment is conducive to both morphology and component of the composite,which flower-like ZnO/CoNiO_(2)/CoO/C is obtained.Benefited from good chemical stability of ZnO,high energy capacity of CoNiO_(2) and CoO and good conductivity of C,the as-prepared sample shows promising electrochemical behavior,including the specific capacity of 1435 C·g^(-1) at 1 A·g^(-1),capacity retention of 87.3%at 20 A·g^(-1),and cycling stability of 90.5%for 3000 cycles at 5 A·g^(-1),respectively.Furthermore,the prepared ZnO/CoNiO_(2)/CoO/C/NF//AC aqueous hybrid supercapacitors device delivers the best specific energy of 55.9 W·h·kg^(-1) at 850 W·kg^(-1).The results reflect that the as-prepared ZnO/CoNiO_(2)/CoO/C microflowers are considered as high performance electrode materials for supercapacitor,and the strategy mentioned in this paper is benefit to prepare mixed metal oxides composite for energy conversion and storage.

High-stable and High-capacity Sn/SnO_(2)@C as Anode of Lithium-ion Batteries

We synthesized size-controllable nanoparticles with homogeneous distribution of carbon and Sn/SnO_(2)by a solvothermal method.The effects of different carbon content and hydrothermal time on the composition,morphology and electrochemical properties of the materials were investigated.Compared with bulk materials,nanoparticles materials not only have high specific surface area,but also can provide abundant reaction sites,thus enhancing the electrochemical activity of electrode materials.More importantly,the optimized microspheres Sn/8C-24 delivers a superior electrochemical performance,achieving a specific discharge capacity of 700.4 mAh·g^(-1)after 150 cycles at 0.5 A·g^(-1),and the Coulomb efficiency reaches 98.65%,which is promising for anode of LIBs.

Hydrothermal hydrogenation/deoxygenation of palmitic acid to alkanes over Ni/activated carbon catalyst

To produce paraffin from hydrogenation/deoxygenation of palmitic acid,model compound of bio-oil obtained by hydrothermal liquefaction(HTL)of microalgae has been an attractive focus in recent years.In order to avoid energy-intensive separation process of water and bio-oil,it is of importance that deoxygenation upgrading of fatty acids under hydrothermal conditions similar to HTL process.Herein,it is the first time to explore the application of activated carbon(AC)-supported non-noble-metal catalysts,such as Ni,Co,and Mo,and so on,in the hydrothermal hydrogenation/deoxygenation of long-chain fatty acids,and the obtained Ni/AC-H(the Ni/AC was further H_(2)pre-reduced)is one of the best catalysts.In addition,it is found that the catalytic activity can be further improved by H_(2)pre-reduction of catalyst.Characterization results that are more low valences of nickel and oxygen vacancy can be obtained after H_(2)pre-reduction,thus significant promoting the deoxygenation especially the decarbonylation pathway of fatty acids.The total alkanes yield can reaches 95.9%at optimal conditions(280℃,360 min).This work confirmed that the low-priced AC-supported non-noble-metal catalysts have great potential compared with the noble-metal catalyst,in hydrothermal upgrading of bio-oil.