Insight into the Alkali Resistance Mechanism of CoMnHPMo Catalyst for NH_(3) Selective Catalytic Reduction of NO

The existence of alkali metals in fl ue gases originating from stationary sources can result in catalyst deactivation in the low-temperature selective catalytic reduction(SCR)of nitrogen oxides(NO_(x)).It is widely accepted that alkali metal poisoning causes damage to the acidic sites of catalysts.Therefore,in this study,a series of CoMn catalysts doped with heteropolyacids(HPAs)were prepared using the coprecipitation method.Among these,CoMnHPMo exhibited superior catalytic performance for SCR and over 95%NO_(x) conversion at 150-300.Moreover,it exhibited excellent catalytic activity and stability after alkali poisoning,demonstrating outstanding alkali metal resistance.The characterization indicated that HPMo increased the specifi c surface area of the catalyst,which provided abundant adsorption sites for NO_(x) and NH_(3).Comparing catalysts before and after poisoning,CoMnHPMo enhanced its alkali metal resistance by sacrifi cing Brønsted acid sites to protect its Lewis acid sites.In situ DRIFTS was used to study the reaction pathways of the catalysts.The results showed that CoMnHPMo maintained high NH_(3) adsorption capacity after K poisoning and then reacted rapidly with NO intermediates to ensure that the active sites were not covered.Consequently,SCR performance was ensured even after alkali metal poisoning.In sum-mary,this research proposed a simple method for the design of an alkali-resistant NH_(3)-SCR catalyst with high activity at low temperatures.

Influence of TiO_2 on the Alkali Resistance and Structure of Invert Glass

Through measuring the alkali resistance of the invert glass and the quantity of SiO 2 and TiO 2 migrating fron the glass into the solution,the influence of TiO 2 on the alkali resistance of the glass is discussed and its structure is also analyzed by infrared spectroscopy.It is concluded that TiO 2 has double functions for the alkali resistance of the invert glass.On the one hand ,both TiO 2 polarizing the secondary ions in glass and TiO 2 isomorphism replacement of SiO 2 make the alkali resistance of the glass decrease.On the ther hand,TiO 2 patching network and anti erosion covering help to increase the alkali resistance.

Research on Alkali Resistance of Alumina-rich MgAl2O4 Spinel for Alkali Recovery Furnace

Chrame containing refractories are a kind of traditional material for the lining of alkali recovery furnaces, but the formation of hexavalent chrome compounds will give rise to detrimental effect on environment and human＇s health. With the gradual awakening of people＇s comciousness about environment protection, it is urgent to prepare environmental-friendly materials for alkali recovery jurnaces with high quality and long life. In this paper, alumina-rich MgAl2O4 spinel （ AR90 ） was used to replace chromite. The physical properties of dried （110 ℃ for 24 h） or fired （1 300 ℃ for 3 h） AR90 and chromite were studied, respectively. The alkali vapor method was used to determine the alkali resistance of the two materials. The results show that： （1） after drying at 110 ℃ for 24 h, AR90 specimens show higher apparent porosity and slightly lower bulk density than chromite specimens; after firing at 1 300 ℃ for 3 h, AR90 has significantly higher apparent porosity as well as higher bulk density; （2） after the alkali attack, the AR90 specimens sintered at 1 300 ℃ exhibit smaller strength change and much higher compressive strength than the chromite specimens; meanwhile, the permeability degree of alkali salt in chromite specimens is more serious than that in AR90 specimens, which indicates that AR90 possesses better alkali resistance.

Steric hindrance shielding viologen against alkali attack in realizing ultrastable aqueous flow batteries

Viologens known as a kind of promising negolyte materials for aqueous organic redox flow batteries,face a critical stability challenge due to the S_N2 nucleophilic attack by hydroxide ions(OH-)during the battery cycling.In this work,a N-cyclic quaternary ammonium-grafted viologen molecule,viz.1,1'-bis(4,4'-dime thylpiperidiniumyl)-4,4'-bipyridinium tetrachloride((DBPPy)Cl_(4)),is developed by the molecular engineering strategy.The obtained(DBPPy)Cl_(4) molecule shows a decent solubility of 1.84 M and a redox potential of-0.52 V vs.Ag/AgCl,Experimental and theoretical results reveal that the grafted N-cyclic quaternary ammonium groups act as the steric hindrance to prevent nucleophilic attack by OH~-,increasing the alkali resistance of the electroactive molecule.The symmetrical battery with 0.50 M(DBPPy)Cl4shows negligible decay during the 13-day cycling test.As demonstration,the flow battery utilizing 1.0 M(DBPPy)Cl_(4) as the negolyte and 1-(1-oxyl-2,2',6,6'-tetramethylpiperidin-4-yl)-1'-(3-(trimethylammonio)propyl)-4,4'-bipyridinium trichloride as the posolyte exhibits a high capacity retention rate of 99.99%per cycle at 60 mA cm^(-2).

Alkali Resistant Bricks for Cement Kiln

This standard specifies the classification, techni- cal requirements, test methods, inspection rules, marking, packing, transportation and storage of alkali resistant bricks.

Preparation and Properties of SiC Assembled Large Block for Blast Furnace Tuyeres

A SiC assembled large block for blast furnace tuyeres was prepared using silicon carbide particles(3-1 and 1-0.088 mm)and fine powder(<0.088 mm),silicon powder(<0.088 mm),industrial carbon black(N990),microsilica,ρ-Al_(2)O_(3) powder,etc.as raw materials.The developed block was compared with a silicon nitride bonded silicon carbide brick,a self-bonded silicon carbide brick and an imported self-bonded silicon carbide block to analyze and evaluate their service performance.The results show that:(1)in the 0-100 mm zone,the SiC large block mainly consists ofβ-SiC and nitrides such as O'-SiAlON,β-SiAlON,α-Si_(3)N_(4),and Si_(2)N_(2)O,the bulk density is 2.68-2.70 g·cm^(-3),the apparent porosity is 14%-15%,and the material structure is uniform;(2)in the 0-100 mm zone,β-SiC nano-whiskers intercalate with nitrides;with the depth increasing,the number of flocculentβ-SiC nano-whiskers increases,while the number of nitrides decreases;when the depth reaches 150 mm or more,the main bonding phases areβ-SiC and mullite;(3)compared with the reference products,the developed SiC large block has a good basic performance,and after alkali corrosion,the mass change rate is-0.1%,which is obviously superior to the imported self-bonded silicon carbide and the homemade silicon nitride bonded silicon carbide materials.

Physiological and Biochemical Changes of IrlVHA-c gene Transgenic Tobacco Seedlings and Self-crossed Progeny Under NaHCO_3 Stress

In order to study the alkali resistivity of VHA-c in Iris lacteal. （IrlVHA-c）, the transgenic tobacco seedlings harboring lrlVHA-c gene from Iris lactea （To）, the self-crossed progeny （T1）, and the non-transgenic lines of tobacco seedlings were grown in Hoagland nutrient solutions supplemented with 0, 100, 200, 300, 400 mmol.L^-1 NaHCO3. The MDA content, CAT, POD and SOD activity, electrical conductivity, chlorophyll content, soluble sugar content, proline content and polyphenol oxidase activity of the seedlings were determined. The results showed that the transgenic lines of tobacco maintained a high activity up to 200 mmol.L^-1 NaHCO3, and activity was slightly lower at 300 mmol.L^-1 NaHCOa. When the concentration of NaHCO3 was as high as 400 mmol.L^-1 the seedlings were badly hurt. In addition, the activity of To and T1 transgentic tobacoo was maintained more or less. While the non- transgenic lines of tobacco could maintain viably up to 100 mmol. L^-1 NaHCO3, and they could not survive at 400 mmol. L^-1 NaHCO3. The conclusion was drawn that the alkali resistance of the tobacoo transformed IrlVHA-c was noticeably improved.

Stretchable alkaline quasi-solid-state electrolytes created by super-tough, fatigue-resistant and alkali-resistant multi-bond network hydrogels

Hydrogel-based quasi-solid-state electrolytes(Q-SSEs) swollen with electrolyte solutions are important components in stretchable supercapacitors and other wearable devices. This work fabricates a supertough, fatigue-resistant, and alkali-resistant multi-bond network(MBN) hydrogel aiming to be an alkaline Q-SSE. To synthesize the hydrogel, a 2-ureido-4[1H]-pyrimidone(UPy) motif is introduced into a poly(acrylic acid) polymer chain. The obtained MBN hydrogels with 75 wt% water content exhibit tensile strength as high as 2.47 MPa, which is enabled by the large energy dissipation ability originated from the dissociation of UPy dimers due to their high bond association energy. Owing to the high dimerization constant of UPy motifs, the dissociated UPy motifs are able to partially re-associate soon after being released from external forces, resulting in excellent fatigue-resistance. More importantly, the MBN hydrogels exhibit excellent alkali-resistance ability. The UPy Gel-10 swollen with 1 mol/L KOH display a tensile strength as high as ~1.0 MPa with elongation at break of ~550%. At the same time, they show ionic conductivity of ~17 m S/cm, which do not decline even when the hydrogels are stretched to 500% strain.The excellent mechanical property and ionic conductivity of the present hydrogels demonstrate potential application as a stretchable alkaline Q-SSE.

Performace of a Kind of Organic Emulsion Coated Phosphogypsum Particles

The phosphogypsum particles coated with organic emulsion were prepared by coating three kinds of organic emulsion of silicone-acrylic,styrene-acrylic and acrylic.The structure and mineralogical characteristics,acid and alkali resistance,water resistance and dissociation degree of coated phosphogypsum were studied by means of SEM-EDAX,optical microscope,gravimetric analysis and chemical detection.The results showed that the initial emulsion can be used directly for coating and granulation of phosphogypsum.The spray re-coating was carried out by using diluted emulsion with the water-to-emulsion mass ratio of 1∶1.The organic emulsion coated phosphogypsum crystal can be clearly observed,and the mixing zone at internal boundary between the organic emulsion and phosphogypsum crystal was distinguishable under the optical microscope.SEM photos showed that the surface of coated phosphogypsum particles was smooth.And the basic elements of C,O,S and Ca can be detected by EDAX.Organic emulsion can be solidified into film-network between the phosphogypsum crystals inside of the coated particles,and it can play a protective role in improving the acid resistance,alkali resistance and water resistance of phosphogypsum,and reduce the degree of dissociation of phosphogypsum in water.

Ca^(2+)-dependent TaCCD1 cooperates with TaSAUR215 to enhance plasma membrane H^(+)-ATPase activity and alkali stress tolerance by inhibiting PP2C-mediated dephosphorylation of TaHA2 in wheat

Alkali stress is a major constraint for crop production in many regions of saline-alkali land.However,little is known about the mechanisms through which wheat responds to alkali stress.In this study,we identified a calcium ion-binding protein from wheat,TaCCD1,which is critical for regulating the plasma membrane(PM)H^(+)-ATPase-mediated alkali stress response.PM H+-ATPase activity is closely related to alkali tolerance in the wheat variety Shanrong 4(SR4).We found that two D-clade type 2C protein phosphatases,TaPP2C.D1 and TaPP2C.D8(TaPP2C.D1/8),negatively modulate alkali stress tolerance by dephosphorylating the penultimate threonine residue(Thr926)of TaHA2 and thereby inhibiting PM H+-ATPase activity.Alkali stress induces the expression of TaCCD1 in SR4,and TaCCD1 interacts with TaSAUR215,an early auxin-responsive protein.These responses are both dependent on calcium signaling triggered by alkali stress.TaCCD1 enhances the inhibitory effect of TaSAUR215 on TaPP2C.D1/8 activity,thereby promoting the activity of the PM H^(+)-ATPase TaHA2 and alkali stress tolerance in wheat.Functional and genetic analyses verified the effects of these genes in response to alkali stress,indicating that TaPP2C.D1/8 function downstream of TaSAUR215 and TaCCD1.Collectively,this study uncovers a new signaling pathway that regulates wheat responses to alkali stress,in which Ca^(2+)-dependent TaCCD1 cooperates with TaSAUR215 to enhance PM H+-ATPase activity and alkali stress tolerance by inhibiting TaPP2C.D1/8-mediated dephosphorylation of PM H+-ATPase TaHA2 in wheat.

Marine urease with higher thermostability, pH and salinity tolerance from marine sponge-derived Penicillium steckii S4-4

Urease has a broad range of applications,however,the current studies on urease mainly focus on terrestrial plants or microbes.Thus,it is quite necessary to determine if marine-derived ureases have diferent characteristics from terrestrial origins since the fnding of ureases with superior performance is of industrial interest.In this study,the marine urease produced by Penicillium steckii S4-4 derived from marine sponge Siphonochalina sp.was investigated.This marine urease exhibited a maximum specifc activity of 1542.2 U mg protein−1.The molecular weight of the enzyme was 183 kDa and a single subunit of 47 kDa was detected,indicating that it was a tetramer.The N-terminal amino acid sequence of the urease was arranged as GPVLKKTKAAAV with greatest similarity to that from marine algae Ectocarpus siliculosus.This urease exhibited a K_(m) of 7.3 mmol L^(−1) and a V_(max) of 1.8 mmol urea min^(−1) mg protein^(−1).The optimum temperature,pH and salinity are 55℃,8.5 and 10%,respectively.This urease was stable and more than 80%of its maximum specifc activity was detected after incubating at 25–60℃for 30 min,pH 5.5–10.0 or 0–25%salinity for 6 h.Compared with the terrestrial urease from Jack bean,this marine urease shows higher thermostability,alkaline preference and salinity tolerance,which extends the potential application felds of urease to a great extent.