Superabsorbent polymeric materials. IV. Swelling behavior of crosslinked poly [sodium acrylate-co-N,N-dimethyl (acrylamidopropyl) ammonium propane sulfonate] in aqueous salt solution

A series of xerogels based on sodium acrylate (SA), N,N-dimethyl(acrylamidopropyl)ammonium propane sulfonate (DMAAPS), and N,N′-methylene bisacrylamide (NMBA) were prepared by inverse suspension polymerization. The water absorbency or swelling behavior for these xerogels in water or various saline solutions was investigated. Results obtained from this study revealed a water absorbency of 721 g H₂O/g sample in deionized water and 83 g H₂O/g sample in 0.9 wt % NaCl solution for a gel containing a 1.50 × 10 ⁻² molar fraction of DMAAPS. The absorbency in the chloride salt solutions decreased with an increase in the ionic strength of the salt. For the same ionic strength of various salt solutions, the swelling amount had the following tendency: Co ²⁺ > Ni ²⁺ > Cu ²⁺ for the higher ionic strength of 2.44 × 10 ⁻⁵–1.8 × 10 ⁻² M. The Co ²⁺, Ni²⁺, and Cu ²⁺ solutions induce approximately the same degree of swelling at the lower ionic strength of <2.44 × 10 ^minus;5 M. The pH effect on the water absorbency for these xerogels was also investigated. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66:499–507, 1997     

Superabsorbent polymeric materials III. Effect of initial total monomer concentration on the swelling behavior of crosslinked poly(sodium acrylate) in aqueous salt solution

A series of xerogels based on sodium acrylate (SA) and N,N′-methylene-bisacrylamide (NMBA) were prepared by inverse suspension polymerization. The water absorbency or swelling behaviors for these hydrogels in water or various saline solutions was investigated. Experimental results indicate that the absorbency of poly(SA) in deionized water increases with decrease in the initial total monomer concentration. Results obtained from this study show that the water absorbency, respectively, exhibited a value of 992 g H₂O/g sample and 106 g H₂O/g sample in deionized water and a 0.9 wt % NaCl solution at an initial total monomer concentration of 3.03M. The absorbency in the chloride salt solutions decreases with increase in the ionic strength of the salt. For the same ionic strength of various salt solutions, the swelling amount has the following tendency: Co²⁺ > Ni²⁺ > Cu²⁺ for the higher ionic strength of 6.25 × 10⁻⁴ to 2.0 × 10⁻³M, and Co²⁺, Ni²⁺, and Cu²⁺ approximately have the same swelling amount for the lower ionic strength of < 6.25 × 10⁻⁴M. The influence of monovalent, divalent, and trivalent anions with a common cationic ion (Na⁺) on the water absorbency shows the tendency of monovalent < divalent < trivalent anions for the same ionic strength. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 64: 2371–2380, 1997     

Superabsorbent polymeric materials. VI. Effect of sulfobetaine structure on swelling behavior of crosslinked poly(sodium acrylate‐co‐sulfobetaines) in aqueous salt solutions

A series of xerogels based on sodium acrylate (SA), N,N‐dimethyl(acrylamidopropyl) ammonium propane sulfonate (DMAAPS) or dimethyl(methacryloyloxy ethyl) ammonium propane sulfonate (DMAPS), and N,N′‐methylene bisacrylamide (NMBA) was prepared by inverse suspension polymerization. The water absorbencies or swelling kinetic behaviors for these xerogels in water or various saline solutions were investigated. The swelling behaviors of these absorbents were related to their chemical structures, their compositions, and the nature of external salt solutions. The water absorbencies of these two copolymeric gel series in deionized water or in various salt solutions would be improved effectively by copolymerizing SA with a small amount of zwitterionic monomer (DMAAPS or DMAPS). The water absorbency of the gel containing DMAPS is larger than that of the gel containing DMAAPS when the amount of zwitterionic monomer in the copolymeric gel is <0.8 mol %, but a contrary result is observed when the zwitterionic monomer content is >0.8 mol %. The tendency of the absorbency for these gels in dilute solution is in the order Cu²⁺ > Zn²⁺ > Co²⁺ > Ni²⁺ for CuCl₂, ZnCl₂, CoCl₂, and NiCl₂ aqueous solution, respectively. The absorbency and initial absorption rate for those gels are related with gel compositions and salt concentrations. Finally, the adsorption of cupric ion by these gels is also investigated. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 72: 1221–1232, 1999     

Superabsorbent polymeric materials VIII: Swelling behavior of crosslinked poly[sodium acrylate‐co‐trimethyl methacryloyloxyethyl ammonium iodide] in aqueous salt solutions

A series of xerogels based on sodium acrylate (SA), cationic comonomer, trimethyl methacryloyloxyethyl ammonium iodide (TMMAI), and N,N‐methylene‐bis‐acrylamide (NMBA) were prepared by inverse suspension polymerization. The water absorbency and the swelling behavior for these high absorbent polymers in deionized water and various saline solutions were investigated. Results indicated that the water absorbency for the present copolymer gel increased when a small amount of TMMAI monomer was introduced into the SA gel, then decreased with increase in TMMAI content. The water absorbency was 583 g H₂O/g for a gel sample in deionized water containing 2.5 × 10⁻³ molar fraction TMMAI. But a contrary result was observed for initial absorption rate, that is, the initial absorption rates increased with an increase of TMMAI in deionized water and 0.9 wt % NaCl solution. The absorbency in the chloride salt solution decreased with an increase in the ionic strength of the salt solution. Finally, the adsorption of copper ion by these gels was also investigated. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 1665–1674, 2001     

Superabsorbent polymeric materials. I. Swelling behaviors of crosslinked poly(sodium acrylate-co-hydroxyethyl methacrylate) in aqueous salt solution

A series of crosslinked poly(sodium acrylate-co-hydroxyethyl methacrylate) based on sodium acrylate (SA), 2-hydroxyethyl methacrylate (HEMA), and N,N′-methylene-bis-acrylamide (NMBA) are prepared by inverse suspension polymerization. The resultant crosslinking polymers are xerogellants. This work investigates not only the absorbency or swelling behavior for these xerogellants composed of different ratios of HEMA/SA in water, but also the effects of various salts and pH values on the swelling properties. Experimental results indicate that the absorbency in deionized water decreases with an increase in the HEMA in copolymeric gel, which is related to the degree of expansion of the network and the strength of the hydrophilic group. The absorbency in the chloride salt solutions decreases with an increase in the salt concentration (swelling is 50 times for the IA group chloride salt solutions, but is less than 5 times for the IIA group salt solution), owing to the osmosis of water and ions between the polymeric gel and the external solution. A decrease in the extent of swelling occurs for divalent and trivalent chloride salt solutions. For the salt solutions of the same ionic strength, the swelling amount has the following tendency: LiCl(aq) = NaCl(aq) = KCl(aq), CaCl₂(aq) < SrCl₂(aq) < BaCl₂(aq), and Fe³⁺ > Ca²⁺ > Zn²⁺ > Cu²⁺. These orders are related to the complexing ability between metallic cations and the carboxylate group in the polymeric chains. Finally, the adsorption of ferric ion by these gels is also investigated. © 1996 John Wiley & Sons, Inc.     

Superabsorbent polymeric materials IX: Effect of cationic structure on swelling behavior of crosslinked poly(sodium acrylate‐co‐cationic monomers) in aqueous salt solutions

Two series of xerogels based on sodium acrylate (SA), trimethyl methacrylamidopropyl ammonium iodide (TMMAAI), trimethyl methacryloyloxyethyl ammonium iodide (TMMAI), and N,N′‐methylene‐bis‐acrylamide (NMBA) as a crosslinker were prepared by inverse suspension polymerization. The water absorbency and swelling kinetic behavior for these xerogels in water or various saline solutions were investigated. The results showed that the swelling behaviors of these absorbents are related to their chemical structures, their compositions, and the type of external salt solutions. There would be effective improvement in the water absorbency of these two gel series by copolymerizing SA with a small amount of cationic monomer (TMMAAI or TMMAI). The initial absorption rates in deionized water were found to be faster for TM series gels than for TA series gels. The two series of superabsorbents had a tendency to absorb water in dilute nitrate aqueous solutions in the order: Fe³⁺, Ni²⁺, Ca²⁺, Cu²⁺, and Na⁺ for Fe(NO₃)₃, Ni(NO₃)₂, Ca(NO₃)₂, Cu(NO₃)₂, and NaNO₃ aqueous solution, respectively. The absorbency and initial absorption rate for these gels were related to the gel compositions and salt concentrations. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 1827–1837, 2001     

Superabsorbent polymeric material. V. Synthesis and swelling behavior of sodium acrylate and sodium 2-acrylamido-2-methylpropanesulfonate copolymeric gels

A series of xerogels based on sodium acrylate (SA), sodium 2-acrylamido-2-methyl propanesulfonate (NaAMPS), and N,N-methylene-bis-acrylamide (NMBA) are prepared by inverse suspension polymerization. The water absorbency and swelling behavior for these high absorbent polymers in deionized water and transition salt solutions are investigated. Experimental results indicated that the absorbency in deionized water increases with an increase of the NaAMPS content in the copolymeric gels, which is related to the degree of charge density of the network and the strength of hydrophilic group. The extent of crosslinking agent also influenced the swelling capacity because of elastic chain force of the polymer chain. The absorbency in chloride salt solutions decreases with an increase in the ionic strength of salt. But the decrease of absorbency is different in monovalent and multivalent salt solution. This behavior can be accounted for in terms of counterion condensation or screening effect for monovalent cations, as well as complexation for multivalent cations. The swelling rates in various salt solutions for these xerogels are also investigated. At last, SA-NaAMPS copolymeric gels were used for ion adsorption. But the result showed that the adsorptive amount of transition metal ions for SA-NaAMPS copolymeric gels was lower than that for pure poly(SA) gel. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 229–237, 1998     

Synthesis and swelling behavior of crosslinked copolymers of neutralized maleic anhydride with other monomers

A series of novel copolymer superabsorbents based on maleic anhydride (MLN), acrylamide (AAM), hydroxyethyl methacrylate (HEMA), and N,N′‐methylenebisacrylamide (NMBA) were prepared by inverse‐suspension polymerization. The influence of the reaction parameters on the water absorption was investigated to improve the understanding and to identify the optimum reaction conditions. The water absorbences or swelling behaviors for these absorbents in various salt solutions and various alcohol solutions were studied. The tendency of the absorbency for these absorbents in salt and alcohol solutions is in the order Na⁺ > Ca²⁺ > Al³⁺ for NaCl, CaCl₂, and AlCl₃ aqueous solutions and a glycerol > glycol > methanol > ethanol solution, respectively. This article also explains the IR and SEM characterization of the water‐absorbing copolymers and their practical use in soil for water retention. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 12: 2725–2731, 2003     

Solidification of glass-ceramics of simulated fission products RE3+, Sr2+, Ba2+ in chlorine-containing waste molten salt

Embedding nuclear waste in glass-ceramic and immobilizing nuclides in ceramic lattice is an effective way for the disposal of high-level radioactive waste. In this paper, a method of solidification of simulated various nuclides was proposed, i.e., RE³⁺(RE = La, Sm, Nd, Dy), Sr²⁺ and Ba²⁺ precipitated from waste molten salt in the form of REPO₄, SrCO₃ and BaCO₃ were solidified in glass-ceramics. To avoid the decomposition of SrCO₃ and BaCO₃ at high temperature, SrCO₃/BaCO₃ containing Cl⁻ salt was further sintered with NH₄H₂PO₄ to form Sr₅(PO₄)₃Cl/Ba₅(PO₄)₃Cl ceramics. It was found that the prepared REPO₄ belonged to monoclinic or tetragonal crystal system, while Sr₅(PO₄)₃Cl and Ba₅(PO₄)₃Cl belonged to hexagonal crystal system. REPO₄, Sr₅(PO₄)₃Cl and Ba₅(PO₄)₃Cl ceramics were co-solidified in iron phosphate glass. BET results showed that the ceramics had a dense structure without any pore inside. XRD, TEM and HRTEM results showed all ceramics had high crystallinity, and nuclides could enter the lattice structure of ceramics through isomorphic replacement, which made the nuclides stable in the crystal structure. The effects of embedding rate on the volume density, Vickers hardness and wettability of glass-ceramics were explored. It was found that the density of the glass-ceramics gradually increased with the increase of ceramic embedding rate, however, the Vickers hardness firstly increased and then decreased. When the embedding rate reached 20 wt%, the Vickers hardness of the glass-ceramics could reach 583.90 GPa. The water contact angles of glass-ceramics with an embedding rate 0–40 wt% were measured to be 70.45°–84.05°, indicating glass-ceramics having a good water leaching resistance. Furthermore, the normalized leaching rate NR_i of La³⁺, Sm³⁺, Nd³⁺, Dy³⁺, Sr²⁺, Ba²⁺, Cl⁻ on the 28th day were estimated to be 7.53 × 10⁻⁷, 5.02 × 10⁻⁷, 5.12 × 10⁻⁷, 4.04 × 10⁻⁷, 1.22 × 10⁻³, 1.59 × 10⁻⁴, 1.07 × 10⁻⁴ g‧m⁻²‧d⁻¹, which indicating that all elements remained good leaching resistance.     

Improved structural stability and ionic conductivity of Na3Zr2Si2PO12 solid electrolyte by rare earth metal substitutions

Sodium zirconium silicon phosphorus with the composition of Na₃Zr₂Si₂PO₁₂ (NZSP) was prepared by a facile solid state reaction method. The effects of the calcination temperature and rare earth element substitution on the structure and ionic conductivity of the NZSP material were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and AC impedance measurement. The results show that the microstructure and ionic inductivity of the NZSP was strongly affected by the aliovalent substitution of Zr⁴⁺ ions in NZSP with rare earth metal of La³⁺, Nd³⁺ and Y³⁺. At room temperature, the optimum bulk and total ionic conductivity of the pure NZSP solid electrolyte sintered under different conditions were 6.77×10⁻⁴ and 4.56×10⁻⁴ S cm⁻¹, respectively. Substitution of La³⁺, Nd³⁺ and Y³⁺ in place of Zr⁴⁺ exhibited higher bulk conductivity compared with that of pure NZSP. Maximum bulk and ionic conductivity value of 1.43×10⁻³ and 1.10×10⁻³ S cm⁻¹ at room temperature were obtained by Na_3+xZr_1.9La_0.1Si₂PO₁₂ sample. The charge imbalance created by aliovalent substitution improves the mobility of Na⁺ ions in the lattice, which leads to increase in the conductivity. AC impedance results indicated that the total ionic conductivity strongly depends on the substitution element and the feature of the grain boundary.     

Studies on poly(acrylic acid)/attapulgite superabsorbent composites. II. Swelling behaviors of superabsorbent composites in saline solutions and hydrophilic solvent–water mixtures

The effect of the attapulgite content on the swelling for a series of poly(acrylic acid)/attapulgite superabsorbent composites in water was studied. The effects of the temperature and pH values on the water absorbency of the superabsorbent composites were investigated. The swelling behavior of the superabsorbent composites in various saline solutions was also investigated. The water absorbency in various salt solutions decreased with an increase in the ionic strength of the solutions. At a high ionic strength (>1 × 10^?3M), the water absorbency in monovalent cationic solutions was higher than that in multivalent cation solutions. This dramatic reduction of the water absorbency in multivalent cationic solutions of high ionic strength may have been due to the complexing ability of the carboxylate groups inducing the formation of intramolecular and intermolecular complexes, which resulted in an increased crosslink density of the network. The swelling behavior of the superabsorbent composites in mixtures of water and hydrophilic solvents, including methanol, acetone, ethanol, and dimethyl sulfoxide (DMSO), was also investigated. The water absorbency decreased with an increase in the concentration of any of the four organic solvents, and two transitions were observed in the superabsorbent composite/hydrophilic solvent–water mixture systems. The main transition for the four hydrophilic solvent–water mixtures was a collapse of the swollen gel (at 50–80% methanol, 30–80% acetone, 50–80% ethanol, and 50–80% DMSO). For the methanol–water system, the magnitudes of the first and second transitions for the poly(acrylic acid)/attapulgite superabsorbent composites containing lower proportions of attapulgite were larger than those for the superabsorbent composites with higher attapulgite contents. The effect of the mixture temperature on the water absorbency of the superabsorbent composites in 10 min was also reported. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1869–1876, 2004     

Superabsorbent polymeric materials. XII. Effect of montmorillonite on water absorbency for poly(sodium acrylate) and montmorillonite nanocomposite superabsorbents

A series of novel xerogels based on sodium acrylate (NaA), montmorillonite (MMT), and N,N′‐methylene‐bisacrylamide (NMBA) were prepared by inverse suspension polymerization and water solution polymerization. The influences of pure MMT, intercalated MMT, the method of polymerization, and the content of the MMT in the copolymeric gels on the water absorbency and the initial absorption rate in deionized water and various salt solutions were investigated. Results showed that the water absorbency was increased by adding a small amount of the pure MMT into the copolymeric gels, but decreased by adding intercalated MMT into the gels. In addition, the water absorbency of the gels prepared by water solution polymerization was lower than that prepared by inverse suspension polymerization. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3422–3429, 2004     

Effect of various environmental conditions on the swelling property of PAAm/PAAcK superabsorbent hydrogel prepared by ionizing radiation

Polyacrylamide/potassium polyacrylate (PAAm/PAAcK) superabsorbent hydrogels were prepared by using ionizing radiation for possible use in agricultural purposes. The influence of environmental conditions such as water quality, fertilizer salts, soil pH, and surrounding temperature on PAAm/PAAcK water absorbency and retention was investigated. The water absorbency apparently decreased with an increase in the valence and ionic strength of the salt solutions. The swelling of PAAm/PAAcK immersed in the solutions containing fertilizer of different nitrogen sources followed the order: Urea > NH₄NO₃ > (NH₄)₂SO₄. The PAAm/PAAcK water absorbency in solutions containing different types of phosphate sources was in the order: H₃PO₄ > KH₂PO₄ > K₂HPO₄. However, the water absorbency of PAAm/PAAcK in the solution of different types of potassium salts followed the order: KCl > K₂SO₄ > K₂HPO₄. PAAm/PAAcK hydrogel is fully swollen at pH 6. The relation between the ability of PAAm/PAAcK to retain water against time at different temperatures was studied. As the environmental temperature increases, the water retention of PAAm/PAAcK decreases. Potential application of PAAm/PAAcK in agriculture was evaluated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3955–3962, 2006     

Environmental-friendly economical cordierite-mullite-based ceramics for kiln furniture production and supports for CO2 hydrogenation towards C5+ fuels

In this study, lightweight cordierite-mullite ceramics with high strength and high thermal-shock resistance were successfully synthesized by solid-state method with the usage of hollow ceramic microspheres. After careful physico-chemical and mechanical characterization, we gained an economical cordierite material with a low bulk density of 1.40 g/cm³ with an apparent porosity of 44.78%, a flexural strength of 20.17 MPa and a coefficient of thermal expansion of 2.26 × 10^{−6 o}C⁻¹ compared to the bulk counterpart with a bulk density of 2.00 g/cm³ with an apparent porosity of 25.75%, a flexural strength of 23.69 MPa and a coefficient of thermal expansion of 2.47 × 10^{−6 o}C⁻¹. As a catalyst support of Na-FeO_x, the economical cordierite has proved the same stability and activity in CO₂ hydrogenation towards C₅₊ fuels as bulk cordierite-based catalyst counterparts.     

Preparation and properties of a salt‐resistant superabsorbent polymer

Crosslinked sodium polyacrylate was prepared by solution polymerization with N,N‐methylene‐bisacrylamide (bisAM) as crosslinking agent; it was subsequently surface‐crosslinked by ethylene glycol diglycidyl ether (EGDE) and then was modified with inorganic salt to obtain a superabsorbent with water absorbency in 0.9 wt % NaCl aqueous solution at atmosphere and applied pressure (P ≈ 2 × 10³ Pa) of 55 and 20 g.g^?1, respectively. Moreover, it also had excellent hydrogel strength. The effects of reaction temperature, reaction time, neutralization degree (ND) of acrylic acid, amount of initiator, crosslinking agent, and surface‐crosslinking agent, mass ratio of inorganic salt to initial superabsorbent, molar ratio of sodium aluminate (NaAlO₂) to potassium dihydrogen hyphosphate (KH₂PO₄) on water absorbency (WA) in 0.9 wt % NaCl aqueous, and the hydrogel modulus were investigated and optimized. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2532–2541, 2004     

Superabsorbent polymeric materials. XIV. Preparation and water absorbency of nanocomposite superabsorbents containing intercalated hydrotalcite

A series of novel xerogels, based on sodium acrylate (NaA), intercalated hydrotalcite (IHT), and N,N′‐methylene‐bisacrylamide (NMBA), were prepared by inverse suspension polymerization. The influences of the HT intercalated with acrylic acid (AA–IHT) and with 2‐acryloylamido‐2‐methyl propane sulfonic acid (AMPS–IHT), the content of the IHT in the poly(NaA) gel on the water absorbency, and the initial absorption rate in deionized water and various salt solutions were investigated. Results showed that adding a small amount of IHT could effectively increase the water absorbency of the gels, but adding excess IHT could decrease the water absorbency of the gels. In addition, the water absorbency of the gels containing AA–IHT was lower than that containing AMPS–IHT. The initial absorption rate, for the present gels, increased with increasing content of IHT in the copolymeric gels. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2417–2424, 2004     

Immobilization of strontium by crystalline zirconium phosphate

Mixtures of HZr₂(PO₄)₃ with varying amounts of Sr(NO₃)₂ were thermally treated at 600–1200 °C in order to investigate the immobilization of radioactive Sr. When the Sr(NO₃)₂ / HZr₂(PO₄)₃=0.2 mixture was thermally treated at 700 °C, the main product was postulated to be SrZr₄(PO₄)₆ from the XRD results. The Sr(NO₃)₂/HZr₂(PO₄)₃=0.2 immobilized product thermally treated at 700 °C containing the maximum amount of immobilized Sr (a 0.2 molar ratio of Sr(NO₃)₂/HZr₂(PO₄)₃ equates to approximately 4 wt.% of Sr) had minimal Sr leaching rates in several solvents at 160 °C in an autoclave. The leaching rate of Sr ion from that product was <10⁻⁶, 1.3×10⁻⁴, 1.4×10⁻⁴, 1.1×10⁻³, 2.0×10⁻³, 8.8×10⁻³ and <10⁻⁶ g m⁻² day⁻¹ in deionized water, sea water, 0.1 mol l⁻¹- HCl, 0.5 mol l⁻¹- HCl, 1 mol l⁻¹- HCl, 1.5 mol l⁻¹- HCl and 1 mol l⁻¹- NH₃ in an autoclave at 160 °C, respectively, indicating that HZr₂(PO₄)₃ reacts with Sr(NO₃)₂ to give a stable Sr-immobilized product.     

Influence of potassium humate on the swelling properties of a poly(acrylic acid‐co‐acrylamide)/ potassium humate superabsorbent composite

A novel superabsorbent composite, poly(acrylic acid‐co‐acrylamide)/potassium humate (PAA‐AM/KHA), was prepared by aqueous solution polymerization from acrylic acid, acrylamide, and potassium humate (KHA) with N,N′‐methylenebisacrylamide as a crosslinker and potassium peroxydisulfate as an initiator. The effects of incorporated KHA on the water absorbency, swelling rate, and reswelling capability were investigated. The swelling property of PAA‐AM/KHA in various saline solutions was studied systematically. The results show that the comprehensive properties and especially salt‐resistant ability of PAA‐AM/KHA were enhanced. There was a linear relationship between the saturated water absorbency and the minus square root of the ionic strength of the external medium, and the water absorbency of PAA‐AM/KHA in various salt solutions had the following order: NH₄Cl_(aq) = KCl_(aq) = NaCl_(aq) > MgCl_2(aq) > CaCl_2(aq) > AlCl_3(aq) > FeCl_3(aq). Moreover, the polymeric net structure of PAA‐AM/KHA was examined with respect to that of poly(acrylic acid‐co‐acrylamide). The results indicate that the polymeric net of PAA‐AM/KHA was improved by the introduction of a moderate amount of KHA into the superabsorbent composite and made more suitable for agriculture and horticulture applications. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

The ablation behavior and mechanical property of C/C-SiC-ZrB2 composites fabricated by reactive melt infiltration

In order to improve the ablation resistance of carbon/carbon (C/C) composites, SiC-ZrB₂ di-phase ceramic were introduced by reactive melt infiltration. The ablation properties of these composites were evaluated by oxyacetylene torch with a heat flux of 2.38 MW/m² for 60 s. Compared with the pure C/C composites, the C/C-SiC-ZrB₂ composites show a significant improvement in the ablation resistance, and the linear and mass ablation rates decreased from 10.28×10⁻³ mm/s to 6.72×10⁻³ mm/s and from 3.08×10⁻³ g/s to 0.61×10⁻³ g/s, respectively. After ablation test, the flexural strength retentions of the C/C and C/C-SiC-ZrB₂ composites near the ablated center region are 39.7% and 81.6%, respectively. The higher strength retention rate of C/C-SiC-ZrB₂ composites was attributed to the introduction of SiC-ZrB₂ ceramic phases, which have excellent ablation resistant property. During ablation test, an ‘embedding structure’ of Zr-O-Si glass layer was formed, which could act as an effective barrier for oxygen and heat. The oxide ceramic coating could protect the C/C-SiC-ZrB₂ composites from further ablation, and thus contribute to retaining the mechanical property of C/C-SiC-ZrB₂ composites after ablation.     

Irradiation damage in xenon-irradiated α-Al2O3 before and after annealing

The irradiation damage build-up of α-Al₂O₃ under Xe²⁰⁺ ion irradiation has been investigated by a combination of Raman spectroscopy and transmission electron microscopy. α-Al₂O₃ crystalline was irradiated with 5 MeV Xe²⁰⁺ ions to fluences of 1 × 10¹⁴ cm⁻², 5 × 10¹⁴ cm⁻², 1 × 10¹⁵ cm⁻² and 5 × 10¹⁵ cm⁻² at room temperature. No amorphous phase was formed under the experimental condition. The Raman intensities of feature peaks of Al₂O₃ decrease after Xe ion irradiation. The interstitial-type dislocation loops with Burgers vectors of b = 1/3 < 10-11> on the {10-10} and (0001) habit planes were found. The formation of basal and prism dislocation loops is related to the lattice damage and position. After annealing, the Raman intensities of feature peaks of Al₂O₃ increases with annealing temperature. With annealing at 1500℃ for 30 min, lattice defects were completely annealed out in the near surface region. Meanwhile, long dislocations and facet cavities on long dislocations were found in the Xe deposition region. Some lattice defects beyond the projected region were found due to the diffusion toward deep region during thermal annealing.