scholarly journals Recovery of Iron Nanoparticles from Mine Wastewater Using Plant Extracts of Eucalyptus Globulus, Callistemon Viminalis and Persea Americana

Minerals ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 859
Author(s):  
Lovasoa C. Razanamahandry ◽  
Assumpta C. Nwanya ◽  
Michael O. Akharame ◽  
Badeggi U. Muhammad ◽  
Seteno K.O. Ntwampe ◽  
...  

Mine wastewater (MW) is often rich in heavy metals that can have measurable effects on humans. The storage and treatment of MW remains a challenge for most mining companies. Iron (Fe) in MW was removed by using extracts from Eucalyptus globulus (EG); Callistemon viminalis (CV); and Persea americana (AS). Fe was removed from MW samples with an initial concentration of 5.53 mg Fe mL−1; 4.63 mg Fe mL−1 and 4.40 mg Fe mL−1 using EG leaves, CV flowers and AS seed extracts, respectively. Conditions of the MW decontamination were studied by varying the dosage of the plant extracts, the temperature of the medium and the contact time between the MW and the plant extracts. Undiluted plant extracts—which were mixed with the MW and heated at 45 °C for 3 h—gave the highest Fe-removal efficiency for CV (70%) and AS (53%) extracts, respectively. Similarly, EG extracts, albeit heated at 25 °C, showed a higher Fe-removal efficiency (85%) than the CV and AS extracts at low to high temperatures. The residual Fe concentration in the MW was 0.83 mg Fe mL−1, 1.39 mg Fe mL−1 and 2.07 mg Fe mL−1 for EG, CV and AS extracts, respectively. Residue solid-phase deposits from the precipitation reaction of the MW with the plant extracts were collected and analyzed. Fe was among the byproducts detected in the deposited material. The characterization of the annealed solid-phase deposits revealed Fe precipitates as maghemite-C (Fe2O3) and magnetite (FeFe2O4) nanoparticles. Therefore, the MW quality and form were improved, making it reusable for other purposes.

Author(s):  
Charles D. Humphrey ◽  
E. H. Cook ◽  
Karen A. McCaustland ◽  
Daniel W. Bradley

Enterically transmitted non-A, non-B hepatitis (ET-NANBH) is a type of hepatitis which is increasingly becoming a significant world health concern. As with hepatitis A virus (HAV), spread is by the fecal-oral mode of transmission. Until recently, the etiologic agent had not been isolated and identified. We have succeeded in the isolation and preliminary characterization of this virus and demonstrating that this agent can cause hepatic disease and seroconversion in experimental primates. Our characterization of this virus was facilitated by immune (IEM) and solid phase immune electron microscopic (SPIEM) methodologies.Many immune electron microscopy methodologies have been used for morphological identification and characterization of viruses. We have previously reported a highly effective solid phase immune electron microscopy procedure which facilitated identification of hepatitis A virus (HAV) in crude cell culture extracts. More recently we have reported utilization of the method for identification of an etiologic agent responsible for (ET-NANBH).


Author(s):  
N. David Theodore ◽  
Leslie H. Allen ◽  
C. Barry Carter ◽  
James W. Mayer

Metal/polysilicon investigations contribute to an understanding of issues relevant to the stability of electrical contacts in semiconductor devices. These investigations also contribute to an understanding of Si lateral solid-phase epitactic growth. Metals such as Au, Al and Ag form eutectics with Si. reactions in these metal/polysilicon systems lead to the formation of large-grain silicon. Of these systems, the Al/polysilicon system has been most extensively studied. In this study, the behavior upon thermal annealing of Au/polysilicon bilayers is investigated using cross-section transmission electron microscopy (XTEM). The unique feature of this system is that silicon grain-growth occurs at particularly low temperatures ∽300°C).Gold/polysilicon bilayers were fabricated on thermally oxidized single-crystal silicon substrates. Lowpressure chemical vapor deposition (LPCVD) at 620°C was used to obtain 100 to 400 nm polysilicon films. The surface of the polysilicon was cleaned with a buffered hydrofluoric acid solution. Gold was then thermally evaporated onto the samples.


1998 ◽  
Vol 79 (01) ◽  
pp. 104-109 ◽  
Author(s):  
Osamu Takamiya

SummaryMurine monoclonal antibodies (designated hVII-B101/B1, hVIIDC2/D4 and hVII-DC6/3D8) directed against human factor VII (FVII) were prepared and characterized, with more extensive characterization of hVII-B101/B1 that did not bind reduced FVIIa. The immunoglobulin of the three monoclonal antibodies consisted of IgG1. These antibodies did not inhibit procoagulant activities of other vitamin K-dependent coagulation factors except FVII and did not cross-react with proteins in the immunoblotting test. hVII-DC2/D4 recognized the light chain after reduction of FVIIa with 2-mercaptoethanol, and hVIIDC6/3D8 the heavy chain. hVII-B101/B1 bound FVII without Ca2+, and possessed stronger affinity for FVII in the presence of Ca2+. The Kd for hVII-B101/B1 to FVII was 1.75 x 10–10 M in the presence of 5 mM CaCl2. The antibody inhibited the binding of FVII to tissue factor in the presence of Ca2+. hVII-B101/B1 also inhibited the activation of FX by the complex of FVIIa and tissue factor in the presence of Ca2+. Furthermore, immunoblotting revealed that hVII-B101/B1 reacted with non-reduced γ-carboxyglutaminic acid (Gla)-domainless-FVII and/or FVIIa. hVII-B101/B1 showed a similar pattern to that of non-reduced proteolytic fragments of FVII by trypsin with hVII-DC2/D4 on immunoblotting test. hVII-B101/B1 reacted differently with the FVII from the dysfunctional FVII variant, FVII Shinjo, which has a substitution of Gln for Arg at residue 79 in the first epidermal growth factor (1st EGF)-like domain (Takamiya O, et al. Haemosta 25, 89-97,1995) compared with normal FVII, when used as a solid phase-antibody for ELISA by the sandwich method. hVII-B101/B1 did not react with a series of short peptide sequences near position 79 in the first EGF-like domain on the solid-phase support for epitope scanning. These results suggested that the specific epitope of the antibody, hVII-B101/B1, was located in the three-dimensional structure near position 79 in the first EGF-like domain of human FVII.


2021 ◽  
Vol 9 (4) ◽  
pp. 105452
Author(s):  
Jianhua Zhang ◽  
Hongjiao Pang ◽  
Stephen Gray ◽  
Shaoheng Ma ◽  
Zongli Xie ◽  
...  

Metabolites ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 21
Author(s):  
Yanhang Chen ◽  
Musavvara Kh. Shukurova ◽  
Yonathan Asikin ◽  
Miyako Kusano ◽  
Kazuo N. Watanabe

Curcuma amada Roxb. (Zingiberaceae), commonly known as mango ginger because its rhizome and foliar parts have a similar aroma to mango. The rhizome has been widely used in food industries and alternative medicines to treat a variety of internal diseases such as cough, bronchitis, indigestion, colic, loss of appetite, hiccups, and constipation. The composition of the volatile constituents in a fresh rhizome of C. amada is not reported in detail. The present study aimed to screen and characterize the composition of volatile organic compound (VOC) in a fresh rhizome of three C. amada (ZO45, ZO89, and ZO114) and one C. longa (ZO138) accessions originated from Myanmar. The analysis was carried out by means of headspace solid-phase microextraction (HS-SPME) coupled with gas chromatography-time-of-flight-mass spectrometry (GC-TOF-MS). As a result, 122 VOCs were tentatively identified from the extracted 373 mass spectra. The following compounds were the ten most highly abundant and broadly present ones: ar-turmerone, α-zingiberene, α-santalene, (E)-γ-atlantone, cuparene, β-bisabolene, teresantalol, β-sesquiphellandrene, trans-α-bergamotene, γ-curcumene. The intensity of ar-turmerone, the sesquiterpene which is mainly characterized in C. longa essential oil (up to 15.5–27.5%), was significantly higher in C. amada accession ZO89 (15.707 ± 5.78a) compared to C. longa accession ZO138 (0.300 ± 0.08b). Cis-α-bergamotene was not detected in two C. amada accessions ZO45 and ZO89. The study revealed between-species variation regarding identified VOCs in the fresh rhizome of C. amada and C. longa.


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