Separation of acid–water mixtures by pervaporation using nanoparticle filled mixed matrix copolymer membranes

BACKGROUND: Low energy and less expensive membrane based separation of acetic acid‐water mixtures would be a better alternative to conventional separation processes. However, suitable acid resistant membranes are still lacking. Thus, the objective of the present study was to develop mixed matrix membrane (MMM) which would allow high flux and water selectivity over a wide range of feed concentrations of acid in water. RESULTS: Three MMMs, namely PANBA0.5, PANBA1.5 and PANBA3 were made by emulsion copolymerization of acrylonitrile (AN) and butyl acrylate (BA) with 5.5:1 comonomer ratio and in situ incorporation of 0.5, 1.5 and 3 wt%, sodium montmorilonite (Na‐MMT) nanofillers, respectively. For a feed concentration of 99.5 wt% of acid in water the membranes show good permeation flux (2.61, 3.19, 3.97 kg m^?2 h^?1 µm^?1, for PANBA0.5, PANBA1.5 and PANBA3 membrane, respectively) and very high separation factors for water (1473, 1370, 1292 for PANBA0.5, PANBA1.5 and PANBA3 membrane, respectively) at 30 °C. Similarly for a dilute acid–water solution, i.e. for 71.6 wt% acid the membrane showed a very high thickness normalize flux (8.67, 9.44, 11.56 kg m^?2 h^?1 µm^?1, for PANBA0.5, PANBA1.5 and PANBA3 membrane, respectively) and good water selectivity (101.7, 95.3, 79 for PANBA0.5, PANBA1.5 and PANBA3 membrane, respectively) at the same feed temperature. The permeation ratio, permeability, diffusion coefficient and activation energy for permeation of the membranes were also estimated. CONCLUSION: Unlike most of the reported membranes, the present MMMs allowed high flux and selectivity over a wide range of feed concentrations. These membranes may also be effective for separating other similar organic‐water mixtures. Copyright © 2012 Society of Chemical Industry     

The Structures of Gd(III) Chelates Conjugated at the Periphery of 3-(1’-Hexyloxy)ethyl-3-devinylpyropheophorbide-a (HPPH) Have a Significant Impact on the Imaging and Therapy of Cancer

3-(1’-Hexyloxyethyl)-3-devinyl-pyropheophorbide-a (HPPH or Photochlor), a tumor-avid chlorophyll-a derivative currently undergoing human clinical trials, was conjugated at various peripheral positions (position-17 or 20) of HPPH with either Gd(III)-aminobenzyl-DTPA (Gd(III) DTPA) or Gd(III)-aminoethylamido-DOTA (Gd(III) DOTA). The corresponding conjugates were evaluated for in vitro PDT efficacy, T₁, T₂ relaxivities, in vivo fluorescence, and MR imaging under similar treatment parameters. Among these analogs, the water-soluble Gd(III)-aminoethylamido-DOTA linked at position-17 of HPPH, i. e., HPPH-17-Gd(III) DOTA, demonstrated strong potential for tumor imaging by both MR and fluorescence, while maintaining the PDT efficacy in BALB/c mice bearing Colon-26 tumors (7/10 mice were tumor free on day 60). In contrast to Gd(III) DTPA (Magnevist) and Gd(III) DOTA (Dotarem), the HPPH-Gd(III) DOTA retains in the tumor for a long period of time (24 to 48 h) and provides an option of fluorescence-guided cancer therapy. Thus, a single agent can be used for cancer-imaging and therapy. However, further detailed pharmacokinetic, pharmacodynamic, and toxicological studies of the conjugate are required before initiating Phase I human clinical trials.     

A Pyropheophorbide Analogue Containing a Fused Methoxy Cyclohexenone Ring System Shows Promising Cancer-Imaging Ability

Herein we report the synthesis, photophysical properties, positron emission tomography (PET) imaging and photodynamic therapy (PDT) efficacy of methyl 3-(1′-m-iodobenzyloxy)ethyl-3-devinyl-verdin 4 (with or without the ¹²⁴I isotope). The PET imaging ability and ex vivo biodistribution of [¹²⁴I] 4 were compared with the well-studied methyl [3-(¹²⁴1′-m-iodobenzyloxy)ethyl]-3-devinyl-pyropheophorbide-a methyl ester (PET-ONCO or [¹²⁴I] 2 ) and [¹⁸F]fluorodeoxyglucose ([¹⁸F]FDG) in BALB/c mice bearing colon-26 tumors. Whole-body PET images of [¹²⁴I] 4 containing a fused methoxy cyclohexenone ring system showed excellent tumor contrast with time (72>48>24 h post-injection). Ex vivo biodistribution results indicate that relative to the current clinical standard [¹⁸F]FDG and [¹²⁴I] 2 in 2 % ethanol formulation, [¹²⁴I] 4 , at the same radioactive dose (25 μCi per mouse), showed higher tumor uptake at 24 h post-injection and longer tumor retention. In biological environments, compound 4 showed lower fluorescence and lower singlet oxygen yield than 2 , which is possibly due to higher aggregation caused by the presence of a fused cyclohexenone ring system, resulting in limited in vitro/in vivo PDT efficacy. Therefore, the chlorophyll-a analogue [¹²⁴I] 4 provides easy access to a novel PET imaging agent (with no skin phototoxicity) to image cancer types—brain, renal carcinomas, pancreas—in which [¹⁸F]FDG shows limitations.     

Inorganic thermoelectric materials: A review

Thermoelectric generator, which converts heat into electrical energy, has great potential to power portable devices. Nevertheless, the efficiency of a thermoelectric generator suffers due to inefficient thermoelectric material performance. In the last two decades, the performance of inorganic thermoelectric materials has been significantly advanced through rigorous efforts and novel techniques. In this review, major issues and recent advancements that are associated with the efficiency of inorganic thermoelectric materials are encapsulated. In addition, miscellaneous optimization strategies, such as band engineering, energy filtering, modulation doping, and low dimensional materials to improve the performance of inorganic thermoelectric materials are reported. The methodological reviews and analyses showed that all these techniques have significantly enhanced the Seebeck coefficient, electrical conductivity, and reduced the thermal conductivity, consequently, improved ZT value to 2.42, 2.6, and 1.85 for near-room, medium, and high temperature inorganic thermoelectric material, respectively. Moreover, this review also focuses on the performance of silicon nanowires and their common fabrication techniques, which have the potential for thermoelectric power generation. Finally, the key outcomes along with future directions from this review are discussed at the end of this article.     

微量元素添加对多元Sn-Bi系焊料合金组织与性能的影响

传统焊料合金由于熔点温度高,不能满足部分有机基板、温度敏感器件以及3D封装等多层封装形式的低温封装要求。以Sn-Bi合金为基体,通过添加微量Ag、Cu、Co和Ni元素形成新型多元合金,对多元合金的熔化性能、润湿性能、微观组织和力学性能进行研究。结果表明:微量元素的添加(质量分数0~1%)对多元Sn-Bi系合金的固相线温度影响很小,降低了SnBi57AgCuCo合金的液相线温度和熔程;添加微量元素降低了合金的表面能,提高了润湿性;多元Sn-Bi系合金的微观组织由SnBi共晶组织、β-Sn相和块状富Bi相组成,微量元素的添加细化了β-Sn相中的Bi相颗粒。组织中的金属间化合物颗粒提高了多元Sn-Bi系合金抗拉强度和延伸率;断口形貌表明合金主要沿Bi相晶界断裂,Bi相的细化可改善焊料合金的力学性能。     

Surface runoff estimation over heterogeneous foothills of Aravalli mountain using medium resolution remote sensing rainfall data with soil conservation system‐curve number method: A case of semi‐arid ungauged Manesar Nala watershed

Manesar Nala watershed, having an aerial extent of 71.53 km², was subjected to modelling of its hydrological behaviour for assessing its water resource potential. Modern tools and techniques of Remote Sensing (RS) and Geographic Information System (GIS) were used for assessment of runoff generating potential using the Hydrologic Soil Cover Complex (HSCC) Method [U.S. Department of Agriculture (USDA)‐Soil Conservation System‐Curve Number (SCS‐CN) approach]. RS and GIS were used in generation and integration of thematic maps [such as Land use/Land cover (using LISS‐III data) and Hydrologic Soil Group (HSG), (using soil map of study area) to derive the Curve Number (CN) for simulating Runoff (R_o)]. The daily rainfall (P) data for the study period 2002–2015 were acquired from NOAA Climate Prediction Center (NCPC). Corresponding R_o from the watershed for intense storm events for 14 years were calculated through RS and GIS. GIS and SCS‐CN model was employed for modelling the runoff production to study its hydrological behaviour. The study showed that the Manesar Nala watershed was having a composite Curve Number – II (CN_II) value of 82.5 for normal conditions. For dry and wet conditions these values were estimated at 66.44 (CN_I) and 91.56 (CN_III), respectively. This investigation showed that Manesar Nala watershed exhibited an annual average (of 14 years, 2002–2015) R_o volume of 4 542 514.37 m³ based on the average annual rainfall (P) of 0.72 m (720 mm). The average annual surface runoff (R_o) was predicted to be approximately 0.21 m with annual runoff coefficient (C_R) of 0.29. During the study, we also found a strong correlation ‘r’ between satellite driven P and R_o from NRCS‐CN method of the order of 0.94. The methodology so developed has the potential to be used in other similar ungauged watersheds in the same agro‐climatic conditions for the purpose of planning of watershed conservation measures and other developmental activities.     

LSI implementation of a low-power 4×4-bit array two-phase clocked adiabatic static CMOS logic multiplier

As the density and operating speed of complementary metal oxide semiconductor (CMOS) circuits increases, dynamic power dissipation has become a critical concern in the design and development—of personal information systems and large computers. The reduction of supply voltage, node capacitance, and switching activity are common approaches used in conventional CMOS. In adiabatic switching circuits, the current flow through transistors can be significantly reduced by ensuring uniform charge transfer over the entire available time. This paper presents the simulation of this current in two-phase clocked adiabatic static CMOS logic (2PASCL) and conventional CMOS. From the SPICE simulations, at transition frequencies from 1 to 12 MHz, a 4×4-bit array 2PASCL multiplier shows a maximum reduction in power dissipation of 77% relative to that of a static CMOS. The measurement results of a 4×4-bit array 2PASCL multiplier demonstrate a 57% reduction compared to a 4×4-bit array two-phase clocked adiabatic dynamic CMOS logic (2PADCL). These results indicate that 2PASCL technology can be advantageous when applied to low-power digital devices operated at low frequencies, such as radio-frequency identification (RFID) tags, smart cards, and sensors.     

Recovery of pyridine from water by pervaporation using filled and crosslinked EPDM membranes

Organoselective membrane was prepared from ethylene propylene diene monomer (EPDM) rubber. Crosslinked EPDM rubber was filled with 2, 4 and 6 wt% N330 carbon black filler to produce three different filled membranes designated as EPDMCV2, EPDMCV4 and EPDMCV6, respectively. These filled rubber membranes were used for pervaporative recovery of low concentration of pyridine from water. These filled membranes were characterized by crosslink density, SEM, XRD and mechanical properties. Sorption thermodynamics were discussed. Partial permeability, intrinsic membrane selectivity and diffusion coefficients of solvents were also determined. The filled membranes showed much higher pyridine selectivity than most of the membranes reported for similar system.     

Synthesis,characterization and biophysical evaluation of the 2D Ti2CTx MXene using 3D spheroid-type cultures

MXenes are novel 2-D materials which have been extensively investigated for use in advanced biocomposites, water purification, biosensors, bioimaging and antibacterial systems. However, the knowledge associated with the mechanism of cytotoxic response is still limited to lack of verification against 3D spheroid-type cultures. Herein, we present a report on the in vitro cytotoxicity of Ti₂CT_x MXene against cervical cancer cell lines (HeLa) in a form of 3D spheroid with comparison to 2D cell culture system. Ti₂CT_x MXenes can be characterized by their multi-layered structure that is produced by the efficient elimination of Al and appearance of the surface functional groups. The biological results with 2D and 3D HeLa indicated that the Ti₂CT_x MXene was moderately cytotoxic to cells and the cytotoxicity was dose dependent. Our results showed that the toxicity of MXenes is potentially due to direct contact of the Ti₂CT_x MXene with the cell membrane wall. The Raman spectra suggested that the Ti₂CT_x MXenes interfered with the cytoplasmic proteins’ conformation and the surrounding microenvironment. This inherently modified the biochemistry of the cell membrane and caused cell apoptosis. This paper contributes to the pool of knowledge regarding the biocompatibility and biophysical properties of Ti₂CT_x MXene.