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31.
To obtain new polymeric materials for environmental management, we used pine needles from the huge forest of the Western Himalayas as a source of cellulose. Cellulose was derivatized to hydroxypropyl cellulose (HPC), a useful water‐soluble cellulose ether. HPC was graft‐copolymerized with acrylamide (AAm) with benzoyl peroxide as the initiator. At optimum grafting conditions, five different concentrations of the comonomers glycidyl methacrylate, acrylic acid, 2‐hydroxyethyl methacrylate, and acrylonitrile were grafted with AAm. Networks of HPC and AAm were also synthesized by crosslinking reactions with glutaraldehyde as a crosslinker over a range of four different concentrations of crosslinker under acidic conditions. Crosslinked networks of HPC with AAm and a comonomer at one comonomer concentration were also synthesized. Graft copolymers were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and swelling behavior. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 545–555, 2004 相似文献
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Murari Lal Gupta Bhuvanesh Gupta Wilhelm Oppermann Gabriele Hardtmann 《应用聚合物科学杂志》2004,91(5):3127-3133
The alkaline hydrolysis of polyacrylonitrile staple fibers was investigated for evaluation as superabsorbent materials. Studies were performed to analyze the hydrolysis of fibers and the quantification of the developed functional groups, such as carboxyl and amide groups as well as changes in the nitrile content by means of Micro‐ATR. Dyeing of the samples with methylene blue was carried out to monitor the carboxyl groups formed during the hydrolysis. A gradual decrease in the nitrile groups and built up of the carboxyl and the amide groups was observed during the hydrolysis. Microscopic investigation carried out to investigate the surface structure of hydrolyzed fibers. Hydrolysis led to surface nonhomogeneity and erosion that was dependent on the hydrolysis conditions. The fibers showed good water retention behavior, making them superabsorbent materials. The dyeing showed more intense coloration in the surface region of the modified fibers. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3127–3133, 2004 相似文献
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Cornelius B. Bavoh Bhajan Lal Omar Nashed Muhammad S. Khan Lau K. Keong Mohd. Azmi Bustam 《中国化学工程学报》2016,24(11):1619-1624
Recently ionic liquids(ILs) are introduced as novel dual function gas hydrate inhibitors. However, no desired gas hydrate inhibition has been reported due to poor IL selection and/or tuning method. Trial error as well as selection based on existing literature are the methods currently employed for selecting and/or tuning ILs. These methods are probabilistic, time consuming, expensive and may not result in selecting high performance ILs for gas hydrate mitigation. In this work, COSMO-RS is considered as a prescreening tool of ILs for gas hydrate mitigation by predicting the hydrogen bonding energies(E_(HB)) of studied IL inhibitors and comparing the predicted E_(HB) to the depression temperature(?) and induction time. Results show that, predicted EHBand chain length of ILs strongly relate and significantly affect the gas hydrate inhibition depression temperature but correlate moderately(R = 0.70) with average induction time in literature. It is deduced from the results that, ? increases with increasing IL EHBand/or decreases with increasing chain length. However, the cation–anion pairing of ILs also affects IL gas hydrate inhibition performance. Furthermore, a visual and better understanding of IL/water behavior for gas hydrate inhibition in terms of hydrogen bond donor and acceptor interaction analysis is also presented by determining the sigma profile and sigma potential of studied IL cations and anions used for gas hydrate mitigation for easy IL selection. 相似文献
35.
We present a generic impedance model for the porous silicon|electrolyte structure that is valid for a range of interfacial layers and bias in these structures. The model is validated using three widely different porous structures: short irregular silicon columns and pores, long cylindrical silicon columns and pores; and branched interconnected silicon microchannels and voids in a mesh structure. The model incorporates appropriate RC or constant phase elements for the different parts of the porous structure, namely, the top of the silicon columns (channels)|electrolyte, the column (channel) walls|electrolyte in the pores/channels, and the electrolyte|semiconductor interface at the base of the pores/channels. This physical model underscores the effects of column/channel depletion and accumulation, either due to applied bias or change of surface charge, to the impedance spectra of the device. The model helps to explain why the porosity needs to be optimized for specific applications and helps as a measurement tool for optimization. 相似文献
36.
Microporous activated carbon spheres (ACSs) with a high specific Brunauer–Emmet–Teller (BET) surface area were prepared from resole‐type spherical crosslinked phenolic beads (PBs) by physical activation. The PBs used as precursors were synthesized in our laboratory through the mixing of phenol and formaldehyde in the presence of an alkaline medium by suspension polymerization. The effects of the gasification time, temperature, and flow rate of the gasifying agent on the surface properties of ACSs were investigated. ACSs with a controllable pore structure derived from carbonized PBs were prepared by CO2 gasification. Surface properties of ACSs, such as the BET surface area, pore volume, pore size distribution, and pore diameters, were characterized with BET and Dubinin–Reduchkevich equations based on N2 adsorption isotherms at 77 K. The results showed that ACSs with a 32–88% extent of burn‐off with CO2 gasification exhibited a BET surface area ranging from 574 to 3101 m2/g, with the pore volume significantly increased from 0.29 to 2.08 cm3/g. The pore size and its distribution could be tailored by the selection of suitable conditions, including the gasification time, temperature, and flow rate of the gasifying agents. The experimental results of this analysis revealed that ACSs obtained under different conditions were mainly microporous. The development of the surface morphology of ACSs was also studied with scanning electron microscopy. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
37.
Mohd Akram Hira Lal Mohammad Osama Farah Ansari Sana Anwar Kabir-ud-Din Ajaz Ahmad Samreen Naved Azum Hadi M. Marwani Abdullah M. Asiri 《Journal of surfactants and detergents》2021,24(1):35-49
In this study, we prepared a novel series of diester-functionalized cationic gemini surfactants (Cm-E2O2-Cm) containing ethylene oxide as a spacer with varying alkyl chain lengths and characterized by 1H NMR, FT-IR, elemental analysis, and ESI-MS. The physicochemical properties of the geminis were explored by tensiometry, fluorescence, dye solubilization, and Krafft point. These geminis acquire superior surface activity than the conventional surfactants. Fluorescence spectroscopy analysis affirmed that the micropolarity and aggregation number of micelles diminished with increase in the alkyl chain length. These geminis represent a new group of amphiphiles of considerably high biodegradability, better cleavability, and low toxicity as assessed by BOD test, FT-IR analysis, and HC50 analysis, respectively. They also showed significant level of antimicrobial activity toward some specified bacterial strains of Gram-positive and Gram-negative by using agar well diffusion method. Furthermore, the thermogravimetric analysis provided information regarding thermal stabilities of the newly synthesized gemini surfactants. 相似文献
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Shyam S. Shukla Alka S. Shukla Kwun-Chi Lee
Tejraj M. Aminabhavi
Ramachandra H. Balundgi 《Journal of hazardous materials》1992,30(3):317-331Solidification/stabilization of toxic pentachlorophenol (PCP) has been studied by using spectroscopic and electrochemical techniques. Portland type I c 相似文献