v0.6.0 SOPs in docs

README.md

@@ -112,10 +112,10 @@ install as a special kernel when you are the user.
      found [here](https://janakiev.com/til/jupyter-virtual-envs/). 
 
 ## Change Log
-* 0.6.0dev
+* 0.6.0 (Mar. 29, 2023)
   * Documentation updates including Gutow Lab Standard Operating Procedures 
     (SOPs).
-  * Refactored everything to underneath the module `Trough`.
+  * Refactored everything to inside the module `Trough`.
 * 0.5.2 (Mar. 16, 2023) Now works in Jupyter Lab.
   * Adjusted widget updating/clearing to work in Jupyter lab.
   * Added JupyterLab >= 3.6.1 to requirements.
@@ -128,6 +128,9 @@ install as a special kernel when you are the user.
 ## Known issues
 * 0.5.0 - 0.6.0 The estimated error on values converted to metric units 
   based on calibration fits appears to be too pessimistic.
+* Inconsistent rendering of Latex ipywidget labels with ipywidgets >= 8.0. 
+  Until figured out requiring ipywidgets < 8.0.
+* Runs don't label graph axes reliably for x-axis units other than cm.
 
 ## Development
 

docs/Gutow_Lab_Trough_SOPs.md

@@ -20,6 +20,7 @@
 
 ## Checking Trough and Subphase Cleanliness
 **This need to be done before each experiment.**
+
 1. We usually use high-purity water as the subphase. Primarily this is 
    18+ M&Omega; de-ionized water mixed with KMnO<sub>4</sub> and redistilled.
    Depending on the status of the water polishers, it is sometimes possible 
@@ -100,6 +101,7 @@
 ## Handling Spreading Solvent(s)
 **It is extremely easy to contaminate the solvents with surface active 
 compounds at a level that will ruin experiments**
+
 * Generally HPLC grade solvents are adequately clean. We most commonly use 
   HPLC grade hexanes and absolute ethanol.
 * All glassware must be carefully cleaned before using to transfer or 
@@ -137,6 +139,7 @@ compounds at a level that will ruin experiments**
 For most molecules we want to spread about 3.00 X 10<sup>-8</sup> moles of 
 molecules on our trough to get a range of roughly 60 to 15 square Angstroms per 
 molecule during a compression.
+
 1. The ideal volume to spread is 50 &micro;L of solution. Thus we want a 
    concentration near (3.00 X 10<sup>-8</sup> moles)/(50.0 X 10<sup>-6</sup> L)
    = 6 X 10<sup>-4</sup> M. It is practical to spread anywhere between 20 
@@ -213,6 +216,7 @@ molecule during a compression.
 
 ## Calibrating the Wilhelmy Balance
 **This should be done at the beginning of any day real data is collected**
+
 1. If it is not already running launch the trough control and calibration 
    tool by running the command `Trough_GUI.Controls(Trough_GUI.calibrations)
    ` in an empty notebook cell.
@@ -222,6 +226,7 @@ molecule during a compression.
 ## Calibrating Barrier Position and Speed
 **This only needs to be done if a check of the measured barrier separation 
 is off by more than ±0.03 mm**
+
 1. If it is not already running launch the trough control and calibration 
    tool by running the command `Trough_GUI.Controls(Trough_GUI.calibrations)
    ` in an empty notebook cell.
@@ -230,6 +235,7 @@ is off by more than ±0.03 mm**
 
 ## Calibrating the Temperature Probe.
 **This is very stable so should not need to be done often**
+
 1. If it is not already running launch the trough control and calibration 
    tool by running the command `Trough_GUI.Controls(Trough_GUI.calibrations)
    ` in an empty notebook cell.

setup.py

@@ -5,7 +5,7 @@
 
 setuptools.setup(
     name="langmuir_trough",
-    version="0.6.0dev",
+    version="0.6.0",
     description="Controls and collects data from Gutow Lab Langmuir Trough.",
     long_description=long_description,
     long_description_content_type="text/markdown",