Reconcile the contradictory wettability requirements for the reduction and oxidation half-reactions in overall CO_(2) photoreduction via alternately hydrophobic surfaces

The overall photocatalytic CO_(2) reduction reaction(OPCRR)that can directly convert CO_(2) and H_(2)O into fuels represents a promising renewable energy conversion technology.As a typical redox reaction,the OPCRR involves two half-reactions:the CO_(2) reduction half-reaction(CRHR)and the water oxidation half-reaction(WOHR).Generally,both half-reactions can be promoted by adjusting the wettability of catalysts.However,there is a contradiction in wettability requirements for the two half-reactions.Specifically,CRHR prefers a hydrophobic surface that can accumulate more CO_(2) molecules on the active sites,ensuring the appropriate ratio of gas-phase(CO_(2))to liquid-phase(H_(2)O)reactants.Conversely,the WOHR prefers a hydrophilic surface that can promote the departure of the gaseous product(O_(2))from the catalyst surface,preventing isolation between active sites and the reactant(H_(2)O).Here,we successfully reconciled the contradictory wettability requirements for the CRHR and WOHR by creating an alternately hydrophobic catalyst.This was achieved through a selectively hydrophobic modification method and a charge-transfer-control strategy.Consequently,the collaboratively promoted CRHR and WOHR led to a significantly enhanced OPCRR with a solar-to-fuel conversion efficiency of 0.186%.Notably,in ethanol production,the catalyst exhibited a 10.64-fold increase in generation rate(271.44μmol g^(-1)h~(-1))and a 4-fold increase in selectivity(55.77%)compared to the benchmark catalyst.This innovative approach holds great potential for application in universal overall reactions involving gas participation.

Efficient H_(2)O_(2)Electrosynthesis and Its Electro-Fenton Application for Refractory Organics Degradation

Hydrogen peroxide(H_(2)O_(2))in situ electrosynthesis by O_(2)reduction reaction is a promising alternative to the conventional Fenton treatment of refractory wastewater.However,O_(2)mass transfer limitation,cathodic catalyst selectivity,and electron transfer in O_(2)reduction remain major engineering obstacles.Here,we have proposed a systematic solution for efficient H_(2)O_(2)generation and its electro-Fenton(EF)application for refractory organic degradation based on the fabrication of a novel ZrO_(2)/CMK-3/PTFE cathode,in which polytetrafluoroethylene(PTFE)acted as a hydrophobic modifier to strengthen the O_(2)mass transfer,ZrO_(2)was adopted as a hydrophilic modifier to enhance the electron transfer of O_(2)reduction,and mesoporous carbon CMK-3 was utilized as a catalyst substrate to provide catalytic active sites.Moreover,feasible mass transfer of O_(2)from the hydrophobic to the hydrophilic layer was designed to increase the contact between O_(2)and the reaction interface.The H_(2)O_(2)yield of the ZrO_(2)/CMK-3/PTFE cathode was significantly improved by approximately 7.56 times compared to that of the co nventional gas diffusion cathode under the same conditions.The H_(2)O_(2)generation rate and Faraday efficiency reached125.98 mg·cm^(-2)·h^(-1)(normalized to 5674.04 mmol·g^(-1)·h^(-1)by catalyst loading)and 78.24%at-1.3 V versus standard hydrogen electrode(current density of-252 mA·cm^(-2)),respectively.The high H_(2)O_(2)yield ensured that sufficient OH was produced for excellent EF performance,resulting in a degradation efficiency of over 96%for refractory organics.This study offers a novel engineering solution for the efficient treatment of refractory wastewater using EF technology based on in situ high-yield H_(2)O_(2)electrosynthesis.

HYDROPHOBICITY－HYDROPHILICITY BALANCE RELATIONSHIPSFORCOLLECTORLESSFLOTATIONOFSULPHIDEMINERALS

ＨＹＤＲＯＰＨＯＢＩＣＩＴＹ－ＨＹＤＲＯＰＨＩＬＩＣＩＴＹＢＡＬＡＮＣＥＲＥＬＡＴＩＯＮＳＨＩＰＳＦＯＲＣＯＬＬＥＣＴＯＲＬＥＳＳＦＬＯＴＡＴＩＯＮＯＦＳＵＬＰＨＩＤＥＭＩＮＥＲＡＬＳＨＹＤＲＯＰＨＯＢＩＣＩＴＹ－ＨＹＤＲＯＰＨＩＬＩＣＩＴＹＢＡＬＡ...

Hydrophilic/hydrophobic characters of antimicrobial peptides derived from animals and their effects on multidrug resistant clinical isolates

Multidrug resistant（MDR） pathogen infections are serious threats to hospitalized patients because of the limited therapeutic options. A novel group of antibiotic candidates, antimicrobial peptides（AMPs）, have recently shown powerful activities against both Gram-negative and Gram-positive bacteria. Unfortunately, the viability of using these AMPs in clinical settings remains to be seen, since most still need to be evaluated prior to clinical trials and not all of AMPs are potent against MDR clinical isolates. To find a connection between the characteristics of several of these AMPs and their effects against MDR pathogens, we selected 14 AMPs of animal origin with typical structures and evaluated their in vitro activities against clinical strains of extensive drugresistant Acinetobacter baumannii, methicillinresistant Staphylococcus aureus, extended spectrum β-lactamase-producing Pseudomonas aeruginosa and extended spectrum β-lactamase-producing Escherichia coli. Our results showed that these peptides＇ hydrophilic/hydrophobic characteristics, rather than their secondary structures, may explain their antibacterial effects on these clinical isolates. Peptides that are amphipathic along the longitudinal direction seemed to be effective against Gramnegative pathogens, while peptides with hydrophilic terminals separated by a hydrophobic intermediate section appeared to be effective against both Gramnegative and Gram-positive pathogens. Among these, cathelicidin-BF was found to inhibit all of the Gram-negative pathogens tested at dosages of no more than 16 mg/L, killing a pandrug-resistant A. baumannii strain within 2 h at 4×MICs and 4 h at 2×MICs. Tachyplesin III was also found capable of inhibiting all Gram-negative and Gram-positive pathogens tested at no more than 16 mg/L, and similarly killed the same A. baumannii strain within 4 h at 4×MICs and 2×MICs. These results suggest that both cathelicidin-BF and tachyplesin III are likely viable targets for the development of AMPs for clinical uses.

A Metal-organic Framework with Alternately Hydrophilic and Hydrophobic Layers Based on Tetrazole Derivative:Synthesis,Structure and Luminescent Property

A new metal-organic framework based on ethyl 1H-tetrazole-5-acetate （Hetza）, [Ag4（etza）4] （1）, has been synthesized and characterized by elemental analysis, IR, thermal gravimetric and X-ray structural analysis. Crystal data for the title complex are as follows： triclinic system, space group P1 with a = 11.0771（6）, b = 11.6636（6）, c = 13.2925（8）, a = 102.3710（10）, β =103.3810（10）, γ = 90.0890（10）°, V = 1629.60（16） A3, Mr = 1052.06, Z = 2, F（000） = 1024, Dc = 2.144 g/cm3, μ（MoKa） = 2.438 mm^-1, the final R = 0.0538 and wR = 0.1475 （I 〉 2σ（I））. Complex 1 adopts the （4.82） topological network and the alternately hydrophilic-hydrophilic and hydropho- bic-hydrophobic arrangements. The luminescent properties of complex 1 and the free Hetza ligand have been studied in the solid states.

Synthesis and Characterization of a HydrophilicHydrophobic IPN Composed of Poly(vinyl alcohol)and Polystyrene

A hydrophilic/hydrophobic interpenetrating polymer network （IPN） of poly （vinyl alcohol） / polystyrene was prepared by conversion of the IPN of poly （vinyl acetate）/polystyrene. The hydrophilic/hydrophobic IPN was characterized by FT-IR and DSC, and the swelling ratios of the IPN in different solvents were measured.

The Rise and Fall of the Hydrophobic Effect in Protein Folding and Protein-Protein Association, and Molecular Recognition

In the beginning everything was explained in Biochemistry in terms of hydrogen-bonds (HB). Then, the devastating blow, known as the HB-inventory argument came;hydrogen bonding with water molecules compete with intramolecular hydrogen-bonds. As a result, the HBs paradigm fell from grace. The void created was immediately filled by Kauzmann’s idea of hydrophobic (HφO) effect which reigned supreme in biochemical literature for over 50 years (1960-2010). Cracks in the HB-inventory argument on one hand, and doubts about the adequacy of Kauzmann’s model for the HφO effect, have led to a comeback of the HBs, along with a host of new hydrophilic (HφI) effects. The HφO effects lost much of its power - which it never really had - in explaining protein folding and protein-protein association. Instead, the more powerful and richer repertoire of HφI effects took over the reins. The interactions also offered simple and straightforward answers to the problems of protein folding, and protein-protein association.

Nondestructive testing and assessment of consolidation effects of earthen sites

Earthen sites are widely distributed throughout China, and most of them belong to archaeological sites with significant values, which not only directly witness the origin, formation and development of Chinese civilization, but also possess important values for conservation and exhibition. Many researches and practices on their conservation and consolidation have been carried out; however, the consolidation effect is mainly judged by visual observation and expert evaluation. Scientific assessment of conservation and consolidation effects is a challenging issue. Many instruments in other fields cannot be directly applied to the conservation of cultural relics due to their peculiarity. In order to assess the effects of field conservation experiments, this paper tries to understand the consolidation effects at Liangzhu site using nondestructive or micro-damage methods, including thermo-physical parameters testing, infrared thermal imaging, high-density microelectrode resistivity testing, portable microscope observation, and hydrophilic and hydrophobic testing, and thereby explores the practicable methods for evaluating the properties of consolidation materials for earthen sites treatment.

Synthesis and Properties of Fumed Silicas Modified with Mixtures of Poly(methylphenylsiloxane) and Dimethyl Carbonate

Effect of the concentration ratios of organosiloxane/initiator and treatment temperature on the characteristics of hydrophobic products obtained by modification of surface of fumed silica with poly(methylphenylsiloxane) (PMPS) in the presence of dimethyl carbonate has been studied. Morphology, particle size, surface area and coating microstructure of modified silicas were analyzed by methods of transmission electron and atomic force microscopies, nitrogen adsorption-desorption data. Carbon contents in the grafted modifying layer of organosilicas were determined using IR spectroscopy and elemental analysis. Hydrophilic-hydrophobic properties of surface of the obtained modified silicas were estimated by measurements of contact angles of wetting. It was shown that modification of pyrogenic silicas with mixtures of poly(methylphenylsiloxane) and dimethyl carbonate allows to obtain the homogeneous hydrophobic products and serve their nanodispersity.

Surface-state controlled synthesis of hydrophobic and hydrophilic carbon dots

It is of great significance to synthesize carbon dots(CDs)with desirable hydrophilicity for the ever-growing application of CDs in different fields.In this study,the hydrophilic and hydrophobic CDs were facilely prepared by solvothermal treatment of o-dihydroxybenzene and urea in N,N-dimethylformamide(DMF).Optimization experiments revealed that the solvothermal temperature has a great impact on the surface states of the CDs.The hydrophobic CDs with a contact angle of 110.7°was obtained at 200℃.The structural and optical characterizations,along with theoretical calculations elucidated that the lipophilic nature of the CDs was resulting from the formation of polymer chains.The presence of extended conjugated sp^(2)-domains and amino groups contributed to the red emission of the CDs synthesized at low reaction temperatures(160-200℃).With the further increase of solvothermal temperature,the hydrophobic CDs were gradually transformed to the hydrophilic state accompanying the blue shift of the fluorescence of the CDs.The highly hydrophilic CDs with a contact angle of 25.9°were obtained at 240℃ due to the increased formation of hydrophilic functional groups on the surface of CDs.The red emissive CDs exhibited a sensitive color and fluorescence response to ethanol content while the fluorescence of the blue emissive CDs remained constant.By combining the two kinds of CDs,a dual-emission sensor was constructed,which was successfully applied for the evaluation of the alcoholic strength in commercial Baijiu commodities in both fluorometric and colorimetric modes.

Studies on the Surface Properties of MCM-41

MCM 41 materials with a well ordered long range structure, a large pore size and a high surface area have been synthesized. Their surface properties including the number and the nature of the surface hydroxyl groups and surface hydrophobicity/hydrophilicity have been investigated by means of 29 Si MAS NMR and FT IR spectra and TPD of probe molecules. The results clearly show that the surface of MCM 41 has an abundance of acidic silanol groups, and that the hydrophobicity/hydrophilicity can be modified by the introduction of Al and transition metals Ti, Cr, Ni and Fe into it.

Determination of hydrophilic–lipophilic balance value and emulsion properties of sacha inchi oil

Objective: To determine hydrophilic–lipophilic balance(HLB) value, stability of formulate emulsion and properties of sacha inchi oil.Methods: The physiochemical characteristics of sacha inchi oil were first investigated.Free radical scavenging property was studied by DPPH assay. HLB value of sacha inchi oil was experimentally determined by preparing the emulsion using emulsifiers at different HLB value. Sacha inchi oil emulsion was prepared using the obtained HLB and its stability was conducted by centrifugation, temperature cycling, and accelerated stability test. The efficiency of the prepared emulsion was clinically investigated by 15 volunteers. The primary skin irritation was performed using closed patch test. Subjective sensory assessment was evaluated by using 5-point hedonic scale method.Results: Peroxide value of sacha inchi oil was 18.40 meq O2/kg oil and acid value was1.86 KOH/g oil. The major fatty acids are omega-3(44%), omega-6(35%) and omega-9(9%). The vitamin E content was 226 mg/100 g oil. Moreover, sacha inchi oil(167 ppm)and its emulsion showed 85% and 89% DPPH inhibition, respectively. The experimental HLB value of sacha inchi oil was 8.5. The sacha inchi oil emulsion exhibited good stability after stability test. The emulsion was classified as non-irritant after tested by primary skin irritation method. The skin hydration value significantly increased from38.59 to 45.21(P < 0.05) after applying sacha inchi oil emulsion for 1 month and the overall product satisfaction of volunteers after use was with score of 4.2.Conclusions: This work provides information on HLB value and emulsion properties of sacha inchi oil which is useful for cosmetic and pharmaceutical application.

THE DISTRIBUTION FUNCTION OF RESIDUE-RESIDUE CONTACTS IN PROTEIN MOLECULES

In protein molecules each residue has a different ability to form contacts.In this paper,we calculated the number of contacts per residue and investigated the distribution of residue-residue contacts from 495 globular protein molecules using Contacts of Structural Units(CSU)software.It was found that the probability P(n)of amino acid residues having n pairs of contacts in all contacts fits Gaussian distribution very well.The distribution function of residue-residue contacts can be expressed as:P(n)=P_0+aexp[-b(n-n_c)~2].In our calculation,P_0=-0.06,α=11.4,b=-0.04 and n_c=9.0.According to distribution function,we found that those hydrophobic(H)residues including Leu,Val,Ile,Met,Phe,Tyr,Cys,and Trp residues have large values of the most probable number of contact n_c,and hydrophilic(P)residues including Ala,Gly,Thr, His,Glu,Gln,Asp,Asn,Lys,Ser,Arg,and Pro residues have the small ones.We also compare with Fauchere-Pliska hydrophobicity scale(FPH)and the most probable number of contact n_c for 20 amino acid residues,and find that there exists a linear relationship between Fauchere-Pliska hydrophobicity scale(FPH)and the most probable number of contact n_c, and it is expressed as:n_c=a+b×FPH,here α=8.87,and b=1.15.It is important to further explain protein folding and its stability from residue-residue contacts.

Theory of cold denaturation of proteins

A new approach to the problem of cold denaturation is presented. It is based on solvent-induced effects operating on hydrophilic groups along the protein. These effects are stronger than the corresponding hydrophobic effects, and they operate on the hydrophilic groups which are plentiful than hydrophobic groups. It is shown that both heat and cold denaturation can be explained by these hydrophilic effects.

Osteoconductivity Control Based on the Chemical Properties of the Implant Surface

Metallic materials, such as Ti, Zr, Nb, Ta, and their alloys, and also stainless steels are widely attractive as osteoconductive materials in the dental and orthopedic fields. Ceramics and polymers are also commonly used as biomaterials. However, they do not have high osteoconductivity in their pure form, and surface coatings with bioactive substances, such as hydroxyapatite or TiO2, are needed before implantation into the bone. Many reports claim that the surface chemical properties of implants, in particular, hydrophilicity and hydrophobicity, strongly affect the biological reactions. However, the effect of surface properties on osteoconductivity is not clear. In this review, we focus on the relationship between the surface hydrophilicity of metallic implants and osteoconductivity using in vivo evaluation, and the control of the osteoconductivity is discussed from the viewpoint of protein adsorption in implants.

Study the effect of formulation variables in the development of timed-release press-coated tablets by Taguchi design

In this investigation, the effect of formulation variables on the release properties of timed- release press-coated tablets was studied using the Taguchi method of experimental design. Formulations were prepared based on Taguchi orthogonal array design with different types of hydrophilic polymers (X1), varying hydrophilic polymer/ethyl cellulose ratio (X2), and addition of magnesium stearate (X3) as independent variables. The design was quantitatively evalu-ated by best fit mathematical model. The results from the statistical analysis revealed that factor X1, X3 and interaction factors between X1X2 and X1X3 were found to be significant on the re-sponse lag time (Y1), where as only factor X1 was found to be significant on the response percent drug release at 8 hrs (Y2). A numerical optimization technique by desirability function was used to optimize the response variables, each having a different target. Based on the re-sults of optimization study, HPC was identified as the most suitable hydrophilic polymer and incorporation of hydrophobic agent magnesium stearate, could significantly improve the lag time of the timed-release press-coated tablet.

医用介入导丝用疏水和亲水涂层的研究进展

医用介入导丝被广泛应用于各类介入手术,是目前经皮冠状动脉成形(PTCA)术及经皮血管成形术(PTA)中常用的医疗器械之一。在医用介入导丝表面添加亲水或疏水涂层,可以减小导丝在临床应用中的组织摩擦和组织损伤,有效提高导丝的通过性、抗菌性和生物相容性,减少炎症。综述了近年来国内外医用介入导丝亲水和疏水涂层材料,介绍了这些涂层的机理、附着力优化、抗菌修饰等方面内容,重点介绍了聚四氟乙烯、聚乙烯吡咯烷酮、聚丙烯酰胺、聚乙二醇、聚对二甲苯等涂层材料体系的研究进展,介绍了不同材料体系在医用导丝亲水和疏水涂层的作用机理和实际应用,同时介绍了亲疏水涂层的制备工艺,重点阐述了层层自组装、紫外光接枝、等离子体接枝和化学气相沉积等制备方法的可操作性、优势和劣势。最后在总结前人研究成果的基础上,对医用介入导丝涂层的现状及面临的问题进行了探讨,并对医用介入导丝涂层的发展方向及提高涂层综合性能等方面进行了展望。

一步水热改性石英砂支撑剂及性能研究

为提高石英砂在压裂液中的分散稳定性,采用十六烷基三甲基氯化铵(CTAC)对传统石英砂表面进行改性。结果表明,CTAC质量分数为0.6%,在80℃中性条件下与石英砂反应120 min,可以使石英砂的沉降速度降低44.85%。改性前后石英砂与水的接触角由28.233°增至87.853°,表明石英砂表面的疏水性有大幅度改善,石英砂颗粒与水分子之间的排斥力增大。表面自由能由83.342 mJ/m^(2)降至22.379 mJ/m^(2),表面自由能降低使系统更加稳定,从能量的角度解释了改性后石英砂沉降速度降低的原因。改性后石英砂的zeta电位是改性前的2倍,石英砂颗粒之间的静电斥力明显增大,从而使颗粒之间不容易聚沉,体系更加稳定。

单,双脂肪酸酯与吐温80复配亲水亲油平衡值对搅打稀奶油品质的影响

利用单,双脂肪酸甘油酯及吐温-80研究不同亲水亲油平衡(hydrophilic lipophilic balance,HLB)值对稀奶油稳定性及搅打特性的影响,对稀奶油打发硬度、打发率、表观黏度、稳定性及微观结构等指标进行检测。结果表明,随着HLB值的增加,乳液表观黏度下降,所有的稀奶油组均出现了剪切稀化现象,离心乳析率和稳定性指数先降低后增加,Zeta电位绝对值先增加后降低。搅打特性分析结果显示,随着HLB值的增加,稀奶油搅打时间缩短,打发率降低,打发后硬度先增加后降低,当HLB值为9时硬度最大(1150.1 g)。HLB值在9~11范围内,稀奶油具有较短的搅打时间、较高的打发硬度、适宜的打发率,且裱花性能良好、无坍塌变形;此时微观结构观察结果显示打发后奶油气泡大小相对均匀,气泡周围的脂肪球致密且彼此接近,形成了更紧密的网络结构保护气泡,使得泡沫较为稳定。因此,复配乳化剂HLB值应控制在9~11的范围内,可获得稳定性及搅打特性良好的稀奶油。

表面润湿性对球体斜射入水过程的影响研究

针对球体表面润湿性对倾斜入水空泡演化过程及球体动力特性的影响开展研究,以便能够进一步理解润湿性对入水过程的影响并且能够为多种情况下的入水现象提供理论依据.基于球体入水过程空泡形态观察、采集与测量实验平台,分析了亲水性和疏水性球体入水过程中入水喷溅和空泡的演变规律,并深入讨论了不同速度下球体表面润湿性对球体入水过程中动力特性的影响.研究表明,不同表面润湿性球体在入水过程中的喷溅及入水空泡演化与动力特性存在明显区别.在相同入水速度下,亲水性球体的三相接触点远高于疏水性球体,而喷溅的高度却低于疏水性球体,但该差异随入水速度的增加反而减小.随着入水速度的增大,亲水性球体依次经历了无空泡、浅闭合和面闭合3种闭合方式,而疏水性球体先后只出现了深闭合和面闭合两种.但是,随着入水速度的增加,球体表面润湿性对空泡演化过程的影响逐渐减弱,当速度增加到11.25 m/s时,二者不存在区别.同时发现,在入水过程中,在相同速度下生成入水空泡较无入水空泡其总流动阻力系数降低49.94%;亲水性球体生成空泡体积更小,空泡带来的附加质量力也更小,减阻效果更好.