Mechanical Property and Microstructure of Cement Mortar with Carbonated Recycled Powder

Carbonated recycled powder as cementitious auxiliary material can reduce carbon emissions and realize high-quality recycling of recycled concrete.In this paper,microscopic property of recycled powder with three carbonation methods was tested through XRD and SEM,the mechanical property and microstructure of recycled powder mortar with three replacement rates were studied by ISO method and SEM,and the strengthening mechanism was analyzed.The results showed that the mechanical property of recycled powder mortar decreased with the increasing of replacement rate.It is suggested that the replacement rate of recycled powder should not exceed 20%.The strength index and activity index of carbonated recycled powder mortar were improved,in which the flexural strength was increased by 27.85%and compressive strength was increased by 20%at the maximum.Recycled powder can be quickly and completely carbonated,and the improvement effect of CH pre-soaking carbonation was the best.The activity index of carbonated recycled powder can meet the requirements of Grade II technical standard for recycled powder.Microscopic results revealed the activation mechanism of carbonated recycled powder such as surplus calcium source effect,alkaline polycondensation effect and carbonation enhancement effect.

Experimental Observation of Cubic C_3N_4 Compound in Carbon Nitride Thin Films

Cubic C3N4 compound in the C-N thin films on Si and NaCl substrates was prepared by ion beam sputtering of a pure graphite target with discharge gas of pure N2. X-ray photoelectron spectroscopy indicated that nitrogen atoms combined with sp2- and sp3- coordinated C atoms in the film, respectively. X-ray diffraction, selected area electron diffraction and high-resolution electron microscopy were used to identify the cubic C3N4 phase. The results reconfirm the ab initio calculations on metastable structure in C-N compounds

Prediction of Henry Constants and Adsorption Mechanism of Volatile Organic Compounds on Multi-Walled Carbon Nanotubes by Using Support Vector Regression

Support vector regression （SVR） combined with particle swarm optimization for its parameter optimization is employed to establish a model for predicting the Henry constants of multi-walled carbon nanotubes （MWNTs） for adsorption of volatile organic compounds （VOCs）. The prediction performance of SVR is compared with those of the model of theoretical linear salvation energy relationship （TLSER）. By using leave-one-out cross validation of SVR test Henry constants for adsorption of 35 VOCs on MWNTs, the root mean square error is 0.080, the mean absolute percentage error is only 1.19~, and the correlation coefficient （R2） is as high as 0.997. Compared with the results of the TLSER model, it is shown that the estimated errors by SVR are ali smaller than those achieved by TLSER. It reveals that the generalization ability of SVR is superior to that of the TLSER model Meanwhile, multifactor analysis is adopted for investigation of the influences of each molecular structure descriptor on the Henry constants. According to the TLSER model, the adsorption mechanism of adsorption of carbon nanotubes of VOCs is mainly a result of van der Waals and interactions of hydrogen bonds. These can provide the theoretical support for the application of carbon nanotube adsorption of VOCs and can make up for the lack of experimental data.

ELECTROCARBOXYLATION OF ORGANIC COMPOUNDS WITH CARBON DIOXIDE CATALYTZED BY METALLOPORPHYRINS(Ⅳ)——EFFECT OF VARIOUS FACTORS ON ELECTROCARBOXYLATION

The effects of various factors on the electrocarboxylation of organic compounds with carbon dioxide catalyzed by metalloporphyrin are studied.The optimal potential of electrocar- boxylation is -1.6 V(vs.SCE).A weak protic solvent methanol can enhance catalytic activity. Tetrabutylammonium iodide is the best one of five electrolytes.The yields and current efficiencies of electrocarboxylation are increased slowly as the concentration of catalyst increases.

ELECTROCARBOXYLATION OF ORGANIC COMPOUNDS WITH CARBON DIOXIDE CATALYZED BY METALLOPORPHYRINS(Ⅲ)——EFFECTS OF AXIAL LIGANDS ON CATALYTIC ACTIVITY OF CoTPP

The effects of peptides,amino acids and organic bases as an axial ligand on reaction ac- tivities in the electrocarboxylation of benzyl chloride with CO_2 catalyzed by CoTPP are reported. The imidazole organic base,peptide containing —SH and amino acid containing imidazolyl en- hance the catalytic activity.The effect of imidazole amounts on the catalytic activity of CoTPP is studied.

ELECTROCARBOXYLATION OF ORGANIC COMPOUNDS WITH CARBON DIOXIDE CATALYZED BY METALLOPORPHYRINS(Ⅱ)——ELECTROSYNTHESIS OF SOME ORGANIC COMPOUNDS WITH CO_2 CATALYZED BY CoTPP

The catalyzation of CoTPP for electrocarboxylation of alkyl halides, alkenes and ketones with CO_2 are studied. The electrocarboxylation of these organic compounds with CO_2 in the presenec of catalyst can occur at more positive potential than that of no catalyst. The products of electrocarboxylation were identified by UV, IR and GC-MS. The electrocarboxylation mechanisms of different organic compounds are discussed.

Anchoring Mo on C_(9)N_(4) monolayers as an efficient single atom catalyst for nitrogen fixation

Electrochemical nitrogen fixation via a convenient and sustainable manner,exhibits an intriguing prospect for ammonia generation under ambient conditions.Currently,the design and development of high-efficiency and low-cost electrocatalysts remains the major challenge confronting nitrogen reduction reaction(NRR).Herein,anchoring the single Mo atom on the C_(9)N_(4) substrate(Mo@C_(9)N_(4)) to form an efficient single-atom catalyst(SAC) is proposed for the conversion of N2 to NH3.By employing density functional theory(DFT) calculations,we demonstrated that gas phase N2 can be sufficiently activated and efficiently reduced to NH3 on the surface of Mo@C_(9)N_(4).Meanwhile,we found that the NRR dominantly occurred on the Mo center via a preferred distal pathway with favorable limiting potential of 0.40 V.Importantly,the as-established Mo@C_(9)N_(4) catalyst exhibits an outstanding structural stability and good selectivity toward NRR.These findings provide a promising platform for designing Mo-based SACs for electrochemical N2 fixation.

SOLID-STATE ELECTROCHROMIC DISPLAY

The catalyzation of CoTPP for electrocarboxylation of alkyl halides, alkenes and ketones with CO;are studied. The electrocarboxylation of these organic compounds with CO;in the presenec of catalyst can occur at more positive potential than that of no catalyst. The products of electrocarboxylation were identified by UV, IR and GC-MS. The electrocarboxylation mechanisms of different organic compounds are discussed.

In-situ fabrication of carbon compound NiFeMo-P anchored on nickel foam as bi-functional catalyst for boosting overall water splitting

The efficient non-noble metal-based bifunctional electrocatalyst for hydrogen evolution reaction(HER)and oxygen evolution reaction(OER)has attracted great interest,which is highly significant to enhance the efficiency of hydrogen production from water electrolysis.Herein,inspired by the appropriate hydrogen adsorption free energy of transition metal alloy and the strong corrosion resistance of phosphide in alkaline electrolyte,carbon compound NiFeMo-P anchored on nickel foam(NiFeMo-P-C)is obtained by simple one-pot hydrothermal and subsequent hydrogen reduction treatment.Remarkably,the NiFeMo-P-C exhibits excellent bifunctional electrocatalytic performances toward HER and OER with low overpotentials of 87 and 196 mV at 10 mA·cm^(-2),respectively.Moreover,the electrolyzer using NiFeMo-P-C as both cathode and anode only requires a cell voltage of 1.50 V to reach a current density of 10 mA·cm^(-2),along with an outstanding long-term stability for 50 h.The synergistic effect among alloys and phosphide,partially broken hollow morphology and porous nickel foam substrate jointly impart NiFeMo-P-C high electrocatalytic activity and superior durability.

Efficient hydrothermal deoxygenation of methyl palmitate to diesel-like hydrocarbons on carbon encapsulated Ni–Sn intermetallic compounds with methanol as hydrogen donor

Porous carbon-encapsulated Ni and Ni-Sn intermetallic compound catalysts were prepared by the one-pot extended Stöber method followed by carbonization and tested for in-situ hydrothermal deoxygenation of methyl palmitate with methanol as the hydrogen donor.During the catalyst preparation,Sn doping reduces the size of carbon spheres,and the formation of Ni-Sn intermetallic compounds restrain the graphitization,contributing to larger pore volume and pore diameter.Consequently,a more facile mass transfer occurs in carbon-encapsulated Ni-Sn intermetallic compound catalysts than in carbonencapsulated Ni catalysts.During the in-situ hydrothermal deoxygenation,the synergism between Ni and Sn favors palmitic acid hydrogenation to a highly reactive hexadecanal that easily either decarbonylate to n-pentadecane or is hydrogenated to hexadecanol.At high reaction temperature,hexadecanol undergoes dehydrogenation-decarbonylation,generating n-pentadecane.Also,the C-C bond hydrolysis and methanation are suppressed on Ni-Sn intermetallic compounds,favorable for increasing the carbon yield and reducing the H_(2) consumption.The npentadecane and n-hexadecane yields reached 88.1%and 92.8%on carbon-encapsulated Ni_(3) Sn_(2) intermetallic compound at 330℃.After washing and H_(2) reduction,the carbon-encapsulated Ni_(3) Sn_(2) intermetallic compound remains stable during three recycling cycles.This is ascribed to the carbon confinement that effectively suppresses the sintering and loss of metal particles under harsh hydrothermal conditions.

A STUDY OF THE IMPOVEMENT OF TENACITY OF POLYACRYLONITRILE PREOXIDED FIBRE BY USING CUPROUS SALT

Polyacrylonitrile preoxided fibre PANOF is an intermediate in carbon fibre preparation. Thequality of PANOF is closely related to the property and structure of carbon fibre. In this paper, thermal mechanical analysis(TMA), thermogravimetric analysis(TGA), swell-ing differential scanning calorimetry(SDSC)and X-ray photoelectron spectroscopy(XPS)wereused to study the increase in tenacity of PANOF from the precursor treated with cuprous salt It has been discovered that the cuprous salt reacts strongly with the uncyclized CN of PANOF,resulting in an increase in the tenacity of PANOF by 30%. The results shwo that the cause of thistenacity improvement is the formation of coordinated complex. Cu^+is the central ion, and PANOFthe ligand. It is due to the coordinate bond that the network structure is formed from uncyclizedCN of PANOF. Therefore the tenacity of PANOF is remarkably increased.

Degradation products of different water content sevoflurane in carbon dioxide absorbents by gas chromatography-mass spectrometry analysis

Background Sevoflurane is currently used as a volatile inhalation anesthetic with many clinical advantages. A representative degradation product, compound A, was quantitatively measured to investigate whether there are different reactions between two kinds of water content sevoflurane formulations with different carbon dioxide （CO2） absorbents.

Long chain n-alkanes and their carbon isotopes in lichen species from western Hubei Province： implication for geological records

Five coticolous lichen samples were collected from western Hubei Province of China to analyze the long chain n-alkanes and their carbon isotope compositions. The n-alkanes range in carbon number from C17 to C33 with strong odd-over-even predominance between C21 and C33. Lichens are dominated by n-C29 in the samples of Dajiuhu, Shennongjia Mountain, but by both n-C23 and n- C29 at Qizimei Mountain. This difference may result from the different environmental conditions in these two sites. The δ13C values of long chain n-alkanes in lichen samples show the signature of C3 plants. Based on compound- specific carbon isotopic values and previous results, we state that alkane homologs 〉 C23 mainly originate from the symbiotic fungi, while symbiotic algae only contribute trace amount of long chain alkanes. Of great interesting is the occurrence of long chain 3-methylalkanes in the Qizimei samples. These anteiso compounds range from C24 to C32, displaying obvious even-over-odd predomi- nance. This study reveals that the association of long chain 3-methylalkanes with n-C23 alkane might be used as proxies to reconstruct the paleoecological implications of lichens in Earth history.

Adsorption of benzene, cyclohexane and hexane on ordered mesoporous carbon

Ordered mesoporous carbon（OMC） with high specific surface area and large pore volume was synthesized and tested for use as an adsorbent for volatile organic compound（VOC）disposal. Benzene, cyclohexane and hexane were selected as typical adsorbates due to their different molecular sizes and extensive utilization in industrial processes. In spite of their structural differences, high adsorption amounts were achieved for all three adsorbates, as the pore size of OMC is large enough for the access of these VOCs. In addition, the unusual bimodal-like pore size distribution gives the adsorbates a higher diffusion rate compared with conventional adsorbents such as activated carbon and carbon molecular sieve. Kinetic analysis suggests that the adsorption barriers mainly originated from the difficulty of VOC vapor molecules entering the pore channels of adsorbents. Therefore, its superior adsorption ability toward VOCs, together with a high diffusion rate, makes the ordered mesoporous carbon a promising potential adsorbent for VOC disposal.

Chinese Medicine Single-Walled Carbon Nanotube Targeting Compound for Antitumor Therapy:A Feasible Way?

Malignant cancer is the leading cause of death in man,exceeding cerebrovascular disease and heart disease.More than half of the total mortality due to malignant cancer is from lung,liver,intestinal and gastric cancer.Chemotherapy is one of the effective treatments for cancer.However,the great majority of Western anticancer medicines have considerable side effects.Herbal medicines offer many more advantages than synthesized compounds because they are made from purely natural compounds and have less adverse effects.However,the single administration methods used as standard in herbal medicine,and deficient drug targeting,severely limit their anticancer activity.Single-walled carbon nanotubes（SWNTs）can be used as drug carriers.They have been modified to form Chinese anticancer medicine-SWNT compounds which can specifically target tumors,thereby significantly increasing the therapeutic effectiveness of these medicines.Water-soluble SWNTs have high stability.As a drug carrier,SWNTs functional modification of the anticancer medicine may improve the targeting and killing of tumor cells.SWNTs have been attached to the Chinese antitumor medicines paclitaxel and plumbagin and have achieved excellent therapeutic effects.Furthermore,choosing the best administration methods such as internal iliac arterial infusion,intravesical infusion and embedment of a hypodermic chemotherapeutic pump,may also improve the anticancer effects of Chinese medicine.

Habitat Influence on the Molecular, Carbon and Hydrogen Isotope Compositions of Leaf Wax n-Alkanes in a Subalpine Basin, Central China

Epidermal leaf waxes of terrestrial higher plants have been widely utilized for the reconstructions of paleoenvironment and paleoclimate in peat deposits. In this study, specimens of four plant species growing in both peatland and non-peatland habitats were retrieved to compare their molecular, carbon(δ13 C) and hydrogen(δ2 H) isotopic compositions of leaf wax n-alkanes from a closed subalpine basin in Central China. Three of the four species show quite higher total concentrations of n-alkanes in the relatively dry non-peatland setting than in the peatland. In addition, the δ2 H values of long-chain n-alkanes are generally less depleted in the peatland and are comparable among different plant species, which is interpreted as the influence of inundation condition and the possible limited supply of photosynthetic products. This study reveals different patterns of plant wax molecular and isotopic compositions between peatland and the surrounding non-peatland conditions, and confirms the paleoenvironmental potential of leaf wax ratios on the peat sequences.