Biomedical subjects

Mari Shin

Publications and source records attributed to Mari Shin.

4 recordsLinked to original sources

PubMed2005

Effect of surfactant alkyl chain length on soil cadmium desorption using surfactant/ligand systems.

The effect of surfactant alkyl chain length on soil Cd desorption was studied using nonionic surfactants of polyethylene oxide (PEO) of PEO chain lengths of 7.5 (Triton X-114), 9.5 (Triton X-100), 30 (Triton X-305), or 40 units (Triton X-405) in combination with the I- ligand. Triplicate 1 g soil samples were equilibrated with 15 ml of surfactant-ligand mixture, at concentrations of 0.025, 0.50 or 0.10, and 0.0, 0.168 or 0.336 mol/l, respectively. After shaking the samples for 24 h, the supernatant fraction was analyzed for Cd content to determine the percent of Cd desorbed from the soil. After five successive washings, 53%, 40% and 25% of Cd had been desorbed by 0.025, 0.050 or 0.10 mol/l of Triton X-114, respectively, in the presence of 0.336 mol/l of I-, whereas with the same conditions, Triton X-100 desorbed 61%, 57% and 56% Cd and either Triton X-305 or Triton X-405 desorbed 51, 40 and 14 to 16% Cd. The most efficient Cd desorption was obtained using 0.025 mol/l Triton X-100 in admixture with 0.336 mol/l I-. Increased surfactant concentration was detrimental to Cd desorption consistent with a process that blocked ligand access to the soil particle surface. After 5 washings,the cumulative cadmium desorption decreased with increasing surfactant alkyl chain length, indicating that the metal-ligand complexes are preferably stabilized by the micelles' hydrophobic octyl phenyl (OP) group rather than by the hydrophilic PEO group. In the absence of ligand, the surfactants alone desorbed less than 1% Cd from the contaminated soil, suggesting that the ligand, rather than the surfactant, extracts the metal, to be subsequently stabilized within the surfactant micelles.

Cadmium↗

PubMed2004

Simultaneous soil Cd and PCB decontamination using a surfactant/ligand solution.

The simultaneous desorption of Cd and PCBs, from a contaminated soil, was investigated using a surfactant/ligand solution. The test surfactants were combinations of a nonionic surfactant [polyethylene oxide (PEO) of chain length 7.5 (Triton X-114), 9.5 (Triton X-100), 30 (Triton X-305), or 40 units (Triton X-405)], with iodide (I-). Triplicate 1 g soil samples were equilibrated, during 24h, with 15 mL of surfactant/ligand solution, at 0.025 or 0.50 and 0.0, 0.168, or 0.336 mol L(-1), respectively. The supernatant fraction was then separated from the particulates by centrifugation and analyzed for Cd to determine Cd desorption efficiency. After five consecutive washings, the treated soil samples were analyzed for PCB content to determine the desorption efficiency of this class of toxicant. Desorption of Cd increased with both increasing ligand concentration and decreasing surfactant chain length and concentration. The maximum Cd desorption efficiency (61%), was obtained with Triton X-100 at 0.025 mol L(-1), in the presence of I at 0.336 mol L(-1). After 5 successive washings, virtually quantitative PCB desorption (below limits of detection for tetra-, penta-, and hexachloro biphenyl compounds) had been achieved with most of surfactant/ligand combinations. Maximum desorption efficiency was achieved using either shorter chain length surfactant (n = 7.5 or 9.5) in combination with a higher ligand concentration, or using longer chain length surfactants (n = 30 and 40) with a lower ligand concentration. Thus, heavy metals and PCBs can be desorbed simultaneously from a contaminated soil with the same washing reagents, namely a surfactant-ligand combination. The optimum surfactant-ligand combination for the simultaneous desorption of both heavy metals and PCBs was a short chain length (n = 7.5 or 9.5) surfactant at low concentration admixed with 0.336 mol L(-1) I-.

Adsorption↗

PubMed2002

Precipitation of swine and cattle manure phosphorous using limestone dust.

The effectiveness of SPS and PULPRO, fine limestone dusts, in precipitating swine and dairy manure phosphorous (P) was determined in the laboratory. Both manures were sieved before being treated with limestone, to reproduce the treatment of mechanically separated manure and to observe the precipitation effect of limestone without that of the large manure solid particles. P precipitation was optimized by varying precipitation conditions (propeller blade speeds, mixing time and limestone levels) and limestone particle size. P precipitation was optimized using a propeller blade mixing speed of 0.3 m s(-1) for at least 5 minutes, using 3% limestone (dry limestone mass over wet manure mass). In terms of particle size, PULPRO 20 (limestone with a particle size of 0.02 mm) produced the most P precipitation and the smallest volume and mass of sludge, as compared to PULPRO 10, PULPRO 3 and SPS (limestone with a particle size of 0.01, 0.003 and 0.3 to 0.003 mm, respectively). For both 9.5% TS (total solids) dairy and 8.8% TS swine manure, mechanical separation followed by limestone precipitation concentrated 90% of manure TS and TP in a sludge volume representing 45% of the initial raw manure mass.

Animals↗

PubMed2001

Thermodynamics of

Formation of cobalt(II)-thiocyanato complexes in nonionic surfactant solutions of poly(ethylene oxide) type with varying poly(ethylene oxide) chain lengths of 7.5 (Triton X-114), 30 (Triton X-305), and 40 (Triton X-405) has been studied by titration spectrophotometry and calorimetry at 298 K. Data were analyzed by assuming formation of a series of ternary complexes Co(NCS)(n)Y(m)((2-n)+) (Y=surfactant) with an overall formation constant beta(nm). In all the surfactant systems examined, data obtained can be explained well in terms of formation of Co(NCS)(+) and Co(NCS)(2) in an aqueous phase (aq), and Co(NCS)(4)Y(2-) in micelles, and their formation constants, enthalpies, and entropies have been determined. The beta(41)/beta(20) ratio increases and the corresponding enthalpy becomes significantly less negative with an increasing number of ethylene oxide groups. This suggests that micelles of these nonionic surfactants have a heterogeneous inner structure consisting of ethylene oxide and octylphenyl moieties. Indeed, on the basis of molar volumes of ethylene oxide and octylphenyl groups, intrinsic thermodynamic parameters have been extracted for the reaction Co(NCS)(2)(aq)+2NCS(-)(aq)=Co(NCS)(4)Y(2-) (Delta(r)G degrees, Delta(r)H degrees, and Delta(r)S degrees ) at each moiety. The Delta(r)G degrees, Delta(r)H degrees, and Delta(r)S degrees values are -16 kJ mol(-1), -15 kJ mol(-1), and 3 J K(-1) mol(-1), respectively, for the ethylene oxide moiety, and -15 kJ mol(-1), -70 kJ mol(-1), and -183 J K(-1) mol(-1) for octylphenyl. Significantly less negative Delta(r)H degrees and Delta(r)S degrees values for ethylene oxide imply that the hydrogen-bonded network structure of water is extensively formed at the ethylene oxide moiety, and the structure is thus broken around the Co(NCS)(4)(2-) complex with weak hydrogen-bonding ability. Copyright 2001 Academic Press.

Journal Article↗